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techniques&#44; inclusion in either cross-transplant lists &#40;living donor&#41; or in exclusive list of cadaveric donor for sensibilized patients&#46;<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">3&#8211;6</span></a> Survival is better in DS patients than in those who remain on the waiting list and are transplanted with a compatible donor and it is even better than those in the list that remain on dialysis&#46;<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">7</span></a> Two review manuscripts compare the results of different DS techniques&#58; Immunoglobulins &#40;IgV&#41;&#44; high dose IgV&#44; plasmapheresis &#40;PF&#41; or immunoadsorption &#40;IA&#41; with or without IgV&#44; rituximab &#40;RTX&#41;&#44; bortezomib&#44; but there is great heterogeneity in&#58; patient selection &#40;live donor versus cadaver&#41;&#44; the method used for <span class="elsevierStyleItalic">cross-match</span> selection &#40;complement dependent cytotoxicity &#91;CDC&#93;&#44; flow cytometry &#91;FC&#93;&#44; specific donor antibodies &#91;SDA&#93; by Luminex&#41;&#44; follow up and type of monitorization to assess the response to desensitization&#46; In these groups of transplant patients the rate of rejection varies from 0&#37; to 100&#37; &#8211; and depends on the treatment used and the selection criteria&#46; Patient survival ranges from 80 to 100&#37; and graft survival between 69 and 100&#37;&#46; In 2014&#44; Riella et al&#46;&#44; using a DS protocol based on PF&#44; IgV and RTX&#44; reported a 61&#37; of antibody-mediated rejection rate&#44; after 5 years the patient survival was 86&#37; and the renal survival was 84&#37;&#46;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">9</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">In 2012&#44; within our area of health care&#44; there were only 24 transplanted patients who presented reactivity against the panel of 70&#37;&#46; This group of patients had been in the transplant waiting list for the longest period of time&#46;<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">10</span></a> Only 3 patients were transplanted under the network renal transplant program&#59; the National Plan of Renal Exchange for Hyperimmunized Patients &#40;PATHI&#41; was not started in Spain until 2015&#46; Therefore&#44; taking into consideration the results of the other series above described&#44; we started a DS program in 2007&#44; the objective was to open up the possibility of transplantation to this group of patients&#46; The aim of the present study is to show our results obtained from &#8220;A Coru&#241;a University Hospital&#8221; in patients&#44; with HLA incompatible living donors&#44; who underwent desensitization &#40;DS&#41;&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Methods</span><p id="par0020" class="elsevierStylePara elsevierViewall">The study began in January 2007 and it was completed in 2014&#46; During this period&#44; 100 patients received a kidney transplant from a living donor&#46; We evaluated 32 patients on pre-transplantation DS protocol&#59; 21 of them were on hemodialysis&#44; 5 in peritoneal dialysis&#44; and 6 were in predialysis&#46; All patients had a positive cross-reactivity against their donor as assessed by CDC&#44; FC or Luminex&#46; Prior to the onset of DS&#44; patients and donors were informed about the procedure and gave their official consent form authorized in our center&#46; In addition&#44; the donors signed the consent in court&#44; according to the protocol of live donation&#46;</p><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Desensitization</span><p id="par0025" class="elsevierStylePara elsevierViewall">The DS protocol consisted in administration of RTX 375<span class="elsevierStyleHsp" style=""></span>mg&#47;m<span class="elsevierStyleSup">2</span> &#40;Roche Farma AG&#44; Grenzach-Wyhlen&#44; Germany&#41; one month prior to transplantation&#46; Tacrolimus&#44; MMF or MFS and prednisone were initiated one week before starting PF&#47;IA&#46; PF or non-specific IA was performed initially on a daily basis&#44; except on Sundays&#46; IA was performed in 19 patients using Therasorb columns&#44; PF in 12 patients and in one patient both procedure were used&#46; After each PF&#47;AI session the patients received specific anti-CMV IgV 100<span class="elsevierStyleHsp" style=""></span>mg&#47;kg &#40;Cytotect Biotest Pharma GmbH&#44; Germany&#41;&#46; Hemodialysis was performed every 48<span class="elsevierStyleHsp" style=""></span>h after the apheresis session or 4 daily exchanges of peritoneal dialysis&#46; Once the apheresis sessions were started&#44; we either monitored the antibody count or performed cross-reaction tests&#46; When CDC or FC cross-reaction test was negative and SDA levels reached a mean fluorescence intensity &#40;MFI&#41; of less than 1000&#44; the patient was accepted for transplantation&#46; Once transplanted&#44; PF or IA was performed on days &#43;3&#44; &#43;5 and &#43;8 after transplantation&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Immunosuppression</span><p id="par0030" class="elsevierStylePara elsevierViewall">Induction with basiliximab was performed in 13 patients &#40;56&#46;5&#37;&#41;&#46; Tacrolimus levels were set at 10&#8211;12<span class="elsevierStyleHsp" style=""></span>ng&#47;ml during the first week&#44; and were reduced progressively to reach 7&#8211;8<span class="elsevierStyleHsp" style=""></span>ng&#47;ml from the 6th month&#46; The initial dose of MMF &#40;Cellcept&#41; was 2<span class="elsevierStyleHsp" style=""></span>g&#47;day&#44; followed by reduction of 1<span class="elsevierStyleHsp" style=""></span>g&#47;day per month&#46; The dose of MFS &#40;Myfortic&#41; was 1440<span class="elsevierStyleHsp" style=""></span>mg per day&#44; which was reduced to 720<span class="elsevierStyleHsp" style=""></span>mg&#47;day per month&#46; Prednisone was started at 20<span class="elsevierStyleHsp" style=""></span>mg&#47;day&#44; and it was progressively reduced to 5<span class="elsevierStyleHsp" style=""></span>mg by month 6&#46; Prophylaxis was performed using co-trimoxazole for 6 months&#44; itraconazole for 4&#8211;6 months&#44; and valganciclovir &#40;Valcyte&#59; Roche Farma&#44; Madrid&#44; Spain&#41; in CMV donor positive patients&#44; CMV negative receptor &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Follow up</span><p id="par0035" class="elsevierStylePara elsevierViewall">After discharge&#44; patients were followed in the out patient clinic with monitorization of renal function&#44; tacrolimus levels&#44; CMV infection first with pp55 antigenemia and presently using PCR of CMV and BK virus&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">If deterioration of renal function was evidenced&#44; a biopsy was obtained and SDA were determined&#46; In our transplant unit protocol biopsies or systematic follow-up of SDA are not performed&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">The diagnosis of rejection in the biopsy was made based on Banff classification&#44; adapted to the date in which this classification was published&#46;<a class="elsevierStyleCrossRefs" href="#bib0190"><span class="elsevierStyleSup">11&#44;12</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Antibody-mediated rejection was treated with steroids &#40;3 boluses of 500<span class="elsevierStyleHsp" style=""></span>mg for 3 consecutive days&#41;&#44; PF or IA&#44; IgV&#44; RTX and eculizumab &#40;in refractory cases&#41;&#46; Treatment of T-cell mediated rejection included steroid boluses &#40;3 boluses of 500<span class="elsevierStyleHsp" style=""></span>mg for 3 consecutive days&#41;&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Variables evaluated&#58; Efficacy of DS&#44; delayed graft function&#44; acute rejection&#44; graft and patient survival&#44; renal function&#44; number of procedures of PF&#47;IA&#44; MFI against class I and II pre and postapheresis&#44; Number of antibodies against class I and II&#44; relative intensity scale &#40;RIS&#41; as reported by Jordan et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">10</span></a> CMV and BK infections&#44; diabetes posttransplant&#44; neoplasias and urological complications&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">E-statistics analysis&#58; Quantitative variables were compared by Student <span class="elsevierStyleItalic">t</span> test and ANOVA&#46; Mann&#8211;Whitney was used to compare variables without normal distribution&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Chi square and Fisher&#39;s test was used for qualitative variables&#46; Survival was calculated according to Kaplan&#8211;Meier and log rank test&#46; For the multivariate study we used the Cox regression and for the sensitivity and specificity analysis&#44; the ROC curves&#46; The statistical analysis was performed using the program SPSS &#40;version 15&#46;0&#46;1&#44; Chicago&#44; IL&#44; USA&#41;&#46;</p></span></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Results</span><p id="par0070" class="elsevierStylePara elsevierViewall">The study included 32 patients &#40;15 males&#41;&#44; with a mean age of 46<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>14 years&#46; The relationship between donor and recipient was&#58; parent&#44;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">9</span></a> spouse&#44;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">14</span></a> sibling&#44;<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">5</span></a> child<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">1</span></a> and others&#46;<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">3</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">At baseline&#44; patients presented a number of antibodies against class I&#58; 0&#46;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;7 &#40;0&#8211;3&#41; with MFI 7979<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>40 and class II&#58; 0&#46;6<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;5 &#40;0&#8211;2&#41; with MFI 6825<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4182&#59; RIS 8&#46;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&#46;7 &#40;2&#8211;30&#41;&#46; CDC cross-match was positive in 18 patients&#59; by FC&#44; in 7&#46; Another 7 patients had only SDA using solid phase techniques &#40;Luminex&#44; One Lambda&#44; Thermo Fisher Scientific&#44; Canoga Park&#44; CA&#44; USA&#41;&#46; DS was considered effective when CDC and FC cross-tests were negative and the MFI less than 1000 &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0080" class="elsevierStylePara elsevierViewall">After 8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3 sessions of PF&#47;IA4-15&#44; it was possible to perform transplantation in 23 patients &#40;71&#46;9&#37;&#41;&#44; but in 9 patients the transplant failed&#46; Desensitization was not successful in 9 patients&#59; 8 of these patients presented a previous cross-match by CDC and one by SDA &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;02&#41;&#46; Class I MFI and RIS were predictors of efficacy by ROC curves &#40;area of 0&#46;949 and 0&#46;848&#44; respectively&#41;&#46; A cutoff point of MFI and RIS was set at 9300 and 8&#46;5 points respectively&#44; with provides 100&#37; sensitivity and 93&#37; specificity for the first and 88&#37; sensitivity and 74&#37; specificity for the second&#46; DS was not effective above these values &#40;<a class="elsevierStyleCrossRefs" href="#fig0010">Figs&#46; 2 and 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0085" class="elsevierStylePara elsevierViewall">In the postoperative period&#44; 13 patients had hematoma-hemorrhage&#44; requiring reintervention in 6 &#40;26&#37;&#41;&#46; Blood transfusion was necessary in 16 &#40;69&#37;&#41;&#46; In 3 patients &#40;13&#37;&#41; there was a delay the initial function of the graft&#46;</p><p id="par0090" class="elsevierStylePara elsevierViewall">After 43<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>30 months &#40;range 0&#46;1&#8211;104&#41; of follow-up&#44; 4 patients &#40;17&#46;4&#37;&#41; had acute rejection&#59; in one patient it was antibody-mediated&#44; in two T-mediated and in the last of four it was mixed &#40;antibodies and T cells mediated rejection&#41;&#46; Patients with rejection had a higher baseline MFI&#44; higher values of RIS&#44; and a positive CDC cross-match &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a>&#41;&#44; but in the Cox analysis&#44; RIS was the only parameter that reached statistical significance&#46;</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia><p id="par0095" class="elsevierStylePara elsevierViewall">Patient survival at 1 and 5 years were 96&#37; and 90&#37; respectively &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a>&#41;&#46; One patient died during sepsis of urinary origin &#40;during the first week postransplantation&#41; and one died after subarachnoid hemorrhage &#40;during the second year&#41;&#46; Graft survival was 86&#37; at year 1 and 5 after transplantation &#40;<a class="elsevierStyleCrossRef" href="#fig0030">Fig&#46; 6</a>&#41;&#44; being worse in patients with acute rejection mediated by antibodies &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>0&#46;02&#41;&#46; The causes of graft loss were antibody-mediated rejection in 2 patients &#40;one of them also had T cell mediated rejection&#41;&#44; chronic nephropathy in one patient&#44; and arterial thrombosis in another&#46;</p><elsevierMultimedia ident="fig0025"></elsevierMultimedia><elsevierMultimedia ident="fig0030"></elsevierMultimedia><p id="par0100" class="elsevierStylePara elsevierViewall">The mean serum creatinine &#40;mg&#47;dl&#41; was 1&#46;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;3&#44; after one year&#44; 1&#46;4<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;4 the 3rd year and 1&#46;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;04<span class="elsevierStyleHsp" style=""></span>at the end of the 5 years of follow-up&#46; Mean values of proteinuria &#40;mg&#47;day&#41; at years 1&#44; 3 and 5 post transplantation were 0&#46;3<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;3&#44; 0&#46;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;2 and 0&#46;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;7 respectively</p><p id="par0105" class="elsevierStylePara elsevierViewall">There were six CMV infections &#40;26&#37;&#41; and one BK viremia &#40;4&#37;&#41;&#46; The frequency of post-transplant diabetes was 26&#37;&#44;<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">6</span></a> lymphocele 13&#37;<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">3</span></a> and renal artery stenosis 4&#37;&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">1</span></a></p><p id="par0110" class="elsevierStylePara elsevierViewall">Two post-transplant neoplasia were diagnosed&#44; one chronic lymphatic leukemia and one cutaneous squamous cell carcinoma&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Discussion</span><p id="par0115" class="elsevierStylePara elsevierViewall">Renal transplantation is the best therapeutic option for patients with end stage renal disease&#46;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">14</span></a> In hypersensitized patients the rate of transplantation is low &#40;&#60;6&#46;5&#37; per year in USA&#44; up to the last year&#41;&#44; they remain in the waiting list for long periods of time and the mortality is high&#46; The options of a patient with an incompatible living donor are DS&#44; joining cross-renal donation programs which is valid option if a living donor is available&#44; or being included in special exchange and prioritization programs&#46;<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">3&#8211;6</span></a></p><p id="par0120" class="elsevierStylePara elsevierViewall">Our DS protocol is similar to others being used during the last years by different groups&#46; However there is a lot of heterogeneity between the series&#44; especially when defining selection criteria for desensitization and transplantation&#46;<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">1&#44;8</span></a> In our serie&#44; cross-match was positive for CDC in 18 of the 32 patients and it was not possible to desensitize 44&#37; of them&#46; The results were more favorable in those who presented a positive cross-reaction by FC or only with SDA by Luminex&#44; in fact we managed to transplant 100 and 86&#37; of those respectively&#46; Orandi et al&#46; showed that DS improves the prognosis of patients as compared with those who remain on the waiting list and finally are transplanted or those remaining on dialysis&#46; These differences were maintained for any level of baseline DS &#40;CDC&#43;&#44; CF&#43; or only SDA&#43; by Luminex&#41;&#44; although the prognosis was worse in those with cross-reaction test was positive by CDC&#44;<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">7</span></a> which could mean that these patients positive by CDC have a higher number of antibodies or higher affinity and this allows them to be detected by techniques that are less sensitive with respect to CF or Luminex&#46;<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">3</span></a></p><p id="par0125" class="elsevierStylePara elsevierViewall">Another factor that could influence the results is the amount of antibodies&#44; interpreted as the level of MFI&#44; which is not well known in most of the series&#46; We used RIS to homogenize the number of antibodies in each patient and their MFI&#44; as described by Jordan et al&#46;<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">13</span></a> Our results demonstrate that DS was not effective in patients with MFI greater than 9300 in class I&#44; or in those with an RIS greater than 8&#46;5&#46;</p><p id="par0130" class="elsevierStylePara elsevierViewall">In our study&#44; at year 5 the survival of patient &#40;90&#37;&#41; and graft &#40;86&#37;&#41; was similar to that reported by others and illustrate the possibility of performing this type of treatment in HY patients who would otherwise remain for a long time in the waiting list&#46; Marfo et al&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">1</span></a> reports a 95&#37; patient survival and 85&#37; graft survival&#59; Orandi at year 3&#44; 91&#46;7&#37; and at year 8 a 76&#46;5&#37;<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">6</span></a>&#59; Yang et al&#46; in Taiwan&#44;<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">15</span></a> at year 5&#44; they report 100&#37; of the patient and 92&#46;3&#37; of the graft survival&#59; and De Sousa et al&#46;&#44; 95&#46;9&#37; of patients and 85&#37; of grafts survived after 5 years&#46;<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">16</span></a> Morath et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">17</span></a> using PF or AI&#44; reported a 95&#46;8&#37; patient survival and 92&#46;4&#37; graft survival&#44; after one year&#46; Bentall et al&#46;<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">18</span></a> reported a 5-year patient survival rate of 83&#46;5&#37;&#44; lower than in the control group &#40;92&#46;5&#37;&#41; and a graft survival of 70&#46;7&#37;&#44; lower than in the control group &#40;88&#37;&#41;&#44; and Thielke et al&#46;<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">19</span></a> showed 95&#37; patient survival and 93&#37; of the graft survival after one year&#46;</p><p id="par0135" class="elsevierStylePara elsevierViewall">The incidence of acute rejection was 17&#37;&#44; in 2 cases antibody-mediated &#40;AMR&#41;&#44; one of them also had T-cell mediated rejection with no response to treatment&#44; and 2 other patients had rejections mediated only by T cells&#44; Banff IA&#44; with good response to steroids&#46; In our serie&#44; the probability of rejection was greater in patients with CDC-positive cross-match and in those with higher RIS&#46; Our low frequency of rejection contrasts with others that have reported from 17 to 80&#37; rejections&#44; using different protocols and different degrees of DS &#40;CDC&#44; CF&#44; SDA&#41;&#46;<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">1&#44;8</span></a> We do not perform biopsies by protocol and only monitor SDA if there is a suspicion of antibody-mediated rejection&#44; so we may not have detected subclinical rejections or chronic rejections mediated by antibodies&#44; which could explain this difference&#46; Riella et al that uses a DS protocol similar to ours&#44;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">9</span></a> has reported a 61&#37; rejection&#59; 100&#37; of patients had CDC-positive cross-match pre-transplantation and the monitorization of titers differs from ours in that we used MFI and they used antibody titers&#59; in addition&#44; only 21 of 39 received RTX&#46; After DS with bortezomib&#44; Aubert et al&#46;<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">20</span></a> found no acute rejection after 18 months and Woodle et al&#46;<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">21</span></a> reported 31&#37;&#46; Recently&#44; Moreno Gonzales et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">2</span></a> using 32 doses of bortezomib only found moderate reduction of antibody without negativization of the cross-match&#44; and it was not well tolerated&#46;</p><p id="par0140" class="elsevierStylePara elsevierViewall">There is little information on the incidence of post-transplant SDA in the series of desensitized patients&#46; Morath et al&#46;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">17</span></a> monitored antibodies during one year and these remained positive at low titers&#46; De Sousa et al&#46;<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">16</span></a> monitored the antibodies in 18 patients&#44; in one of them were positive and developed AMR&#46; Kauke et al&#46;<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">22</span></a> demonstrated that in 6 out of 8 desensitized patients the antibodies persisted and 3 of them developed AMR&#46; Stegall et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">23</span></a> in patients treated with eculizumab&#44; found that 50&#37; of the patients developed SDA with MFI &#62;10&#44;000&#44; although the incidence of acute rejection was 7&#46;7&#37; as compared with 41&#46;1&#37; in the group without eculizumab&#46; In our series&#44; 8 patients had SDA at follow-up&#58; 3 of them were positive&#44; 2 developed AMR and another patient had transplant glomerulopathy&#46;</p><p id="par0145" class="elsevierStylePara elsevierViewall">In our study&#44; despite the high load of immunosuppression&#44; the rate of infectious complications was acceptable&#44; with an incidence of CMV of 26&#37; and BK of 4&#37;&#46; Vo et al&#46;<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">24</span></a> reported a 16&#46;5&#37; CMV infection and 0&#37; BK viremia&#46; Kauke et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">22</span></a> reported 2&#47;8 &#40;25&#37;&#41; of BK viremia&#46; Yang et al&#46;<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">15</span></a> reported 3 cases of BK nephropathy &#40;13&#46;6&#37;&#41; and 2 CMV pneumonitis &#40;9&#37;&#41;&#46; De Sousa et al&#46;<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">16</span></a> reported 3 CMV reactivations &#40;13&#37;&#41; and one case of BK &#40;4&#46;3&#37;&#41;&#46; Morath et al&#46;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">17</span></a> describe 10&#37; CMV and 0&#37; BK&#46; Thielke et al&#46;<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">19</span></a> 7&#37; CMV and 4&#46;9&#37; BK&#46; Stegall et al&#46;<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">23</span></a> used eculizumab without reporting no CMV or BK virus infections&#46;</p><p id="par0150" class="elsevierStylePara elsevierViewall">The incidence of neoplasias is not usually reported&#46; Two patients in our series had de novo neoplasia &#40;a chronic lymphatic leukemia and a skin squamous cell carcinoma&#41;&#46; The Taiwan group reported 3 cases of urothelial cancer&#46; Stegall et al&#46;&#44; in patients desensitized with eculizumab&#44; reported one case of Burkitt&#39;s lymphoma&#46;</p><p id="par0155" class="elsevierStylePara elsevierViewall">A relatively frequent complication following transplantation is the occurrence of hematoma&#47;hemorrhage&#46; It could be related to PF or IA in incompatible ABO transplants due to the loss of coagulation factors&#44; including factor XIII&#44; the decrease in the number of platelets or the use of anticoagulants to perfuse the graft&#46;<a class="elsevierStyleCrossRefs" href="#bib0260"><span class="elsevierStyleSup">25&#8211;27</span></a> In our patients we did not identify a factor that could favor bleeding &#40;although we did not measure factor XIII&#41;&#44; perhaps due to the limited number of patients&#46; There might be a number of factors that acting together may facilitate hemorrhage&#46;</p><p id="par0160" class="elsevierStylePara elsevierViewall">The limitations of our study are the sample size&#44; the absence of protocol biopsy and the low number of SDA monitored&#46; Despite this&#44; the clinical results are acceptable in a group of patients who would have to be maintained on the waiting list for a long time&#46; We detected markers that identify patients in whom DS is ineffective&#44; these are MFI class I or RIS&#44; which would suggest to avoid the initiation a costly treatment with potential adverse effects&#46; We conclude that the HLA DS with the protocol shown in this study is an option to consider in those patients sensitized against a living donor&#46;</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Conflict of interests</span><p id="par0165" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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            0 => "Renal transplantation from HLA-incompatible live donors"
            1 => "Desensitization"
            2 => "Plasmapheresis"
            3 => "Immunoadsorption"
            4 => "Rituximab"
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            0 => "Trasplante renal de donante vivo HLA incompatible"
            1 => "Desensibilizaci&#243;n"
            2 => "Plasmaf&#233;resis"
            3 => "Inmunoadsorci&#243;n"
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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Desensitization is a procedure undergone by the recipient of a kidney transplant from a donor who is cross-match positive&#46; The aim of this study was to present the outcomes from our hospital of kidney transplant recipients from HLA-incompatible live donors after desensitization&#46;</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">We studied 32 patients aged 46<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>14 years with a mean fluorescence intensity &#40;MFI&#41; versus class I HLA of 7979<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4089 and 6825<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4182 MFI versus class II and relative intensity scale &#40;RIS&#41; of 8&#46;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&#46;6&#46; The complement-dependent cytotoxicity &#40;CDC&#41; cross-matching test was positive in 18 patients&#44; flow cytometry was positive in 7 patients and donor-specific antibodies &#40;DEA&#41; were detected in 7&#46; The protocol used was rituximab&#44; plasmapheresis&#47;immunoadsorption&#44; immunoglobulins&#44; tacrolimus&#44; mycophenolic acid derivatives and prednisone&#46;</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">After 8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3 sessions of plasmapheresis&#47;immunoadsorption&#44; 23 patients were transplanted &#40;71&#46;9&#37;&#41; and desensitization was ineffective in 9&#46; There were baseline differences in MFI class I &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#44; RIS &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;008&#41;&#44; and CDC cross-matching&#44; DSA and flow cytometry &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;05&#41;&#46; MFI class I and RIS were predictors of inefficiency in ROC curves&#46; After follow-up of 43<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>30 months&#44; 13 patients &#40;56&#37;&#41; presented postoperative bleeding&#44; 3 &#40;13&#37;&#41; delayed graft function&#44; 4 &#40;17&#46;4&#37;&#41; acute rejection&#44; 6 &#40;26&#37;&#41; CMV viremia and 1 &#40;4&#37;&#41; BK viremia&#46; Five-year patient survival was 90&#37;&#44; with 86&#37; allograft survival&#46; Five-year creatinine was 1&#46;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;4 and proteinuria was 0&#46;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;7&#46;</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conclusions</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Kidney transplantation from HLA-incompatible live donors after desensitization was possible in 71&#46;9&#37; of patients&#46; MFI class I and RIS predict the inefficiency of desensitization&#46; Five-year allograft survival &#40;86&#37;&#41; was acceptable with a low incidence of acute rejection &#40;17&#46;4&#37;&#41;&#44; although with a greater trend toward postoperative bleeding&#46;</p></span>"
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        "resumen" => "<span id="abst0015" class="elsevierStyleSection elsevierViewall"><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">La desensibilizaci&#243;n es un m&#233;todo empleado en trasplante renal para tratar de trasplantar a pacientes que presentan una prueba cruzada positiva frente a su donante&#46; El objetivo del estudio es mostrar los resultados de nuestro hospital en pacientes trasplantados renales con donantes vivos HLA incompatibles&#44; tras un protocolo de desensibilizaci&#243;n&#46;</p><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Estudiamos a 32 pacientes de 46<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>14 a&#241;os que presentaban una intensidad media de fluorescencia &#40;MFI&#41; frente a HLA de clase I de 7&#46;979<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4&#46;089 y de 6&#46;825<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4&#46;182 para MFI frente a clase II y <span class="elsevierStyleItalic">relative intensity scale</span> &#40;RIS&#41; de 8&#44;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&#44;6&#46; La prueba cruzada fue positiva por citotoxicidad dependiente del complemento &#40;CDC&#41; en 18 pacientes&#44; citometr&#237;a de flujo &#40;CF&#41; en 7 y anticuerpos donante espec&#237;ficos &#40;ADE&#41; en 7&#46; El protocolo empleado fue&#58; rituximab&#44; plasmaf&#233;resis&#47;inmunoadsorci&#243;n&#44; inmunoglobulinas&#44; tacrolimus&#44; derivados &#225;cido micofen&#243;lico y prednisona&#46;</p><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Tras 8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3 sesiones de plasmaf&#233;resis&#47;inmunoadsorci&#243;n se trasplant&#243; a 23 pacientes &#40;71&#44;9&#37;&#41; y result&#243; ineficaz en 9&#46; Exist&#237;an diferencias basales en MFI clase I &#40;p<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#44;001&#41;&#44; RIS &#40;p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;008&#41; y <span class="elsevierStyleItalic">cross-match</span> por CDC&#44; ADE o CF &#40;p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;05&#41;&#46; El MFI de clase I y el RIS resultaron predictores de eficacia en curvas COR&#46; Tras un seguimiento de 43<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>30 meses&#44; 13 pacientes &#40;56&#37;&#41; presentaron sangrado postoperatorio&#44; 3 &#40;13&#37;&#41; funci&#243;n retrasada injerto&#44; 4 &#40;17&#44;4&#37;&#41; rechazo agudo&#44; 6 &#40;26&#37;&#41; viremia CMV y uno &#40;4&#37;&#41; viremia BK&#46; Al 5&#46;&#176; a&#241;o&#44; la supervivencia del paciente fue del 90&#37; y la supervivencia renal del 86&#37;&#46; En ese mismo a&#241;o&#44; la creatinina fue de 1&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#44;4 y la proteinuria de 0&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#44;7&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Conclusiones</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">El trasplante renal de donante vivo HLA incompatible tras la desensibilizaci&#243;n fue posible en el 71&#44;9&#37; de los pacientes&#46; MFI de clase I y RIS predicen ineficacia de la desensibilizaci&#243;n&#46; La supervivencia renal &#40;86&#37; al 5&#46;&#176; a&#241;o&#41; es aceptable con baja incidencia de rechazo agudo &#40;17&#44;4&#37;&#41;&#44; aunque con una mayor tendencia al sangrado postoperatorio&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0015">Please cite this article as&#58; Fern&#225;ndez C&#44; Calvo M&#44; Leite N&#44; L&#243;pez A&#44; Ferreiro T&#44; Ribera R&#44; et al&#46; Trasplante renal procedente de donante vivo HLA incompatible&#58; Eficacia y pron&#243;stico en 32 pacientes tras desensibilizaci&#243;n&#46; Nefrologia&#46; 2017&#59;37&#58;638&#8211;645&#46;</p>"
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                  \t\t\t\t</th><th class="td" title="table-head  " align="center" valign="top" scope="col" style="border-bottom: 2px solid black">Efficacy&#58; <span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>23&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="center" valign="top" scope="col" style="border-bottom: 2px solid black">Without efficacy&#58; <span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>9&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">NS&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Age of recipient &#40;years&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">48&#46;6<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>14&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">38&#46;6<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>12&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;07&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Dialysis vintage &#40;months&#41;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;07&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">No&#46; of antibodies class I and II&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">5840<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3002&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;001&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">MFI class II&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">6048<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4145&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">9169<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3725&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">NS&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">RIS<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a>&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">15<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;005&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Pregnancy&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;86<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;33<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;07&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">NS&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">No&#46; of HLA incompatibilities&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">3&#46;7<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>11&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">3&#46;3<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#46;6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">NS&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Number of PFS&#47;IA sessions&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">8&#46;1<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>2&#46;7&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">8&#46;7<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3&#46;3&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">NS&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Cross-match&#58; CDC&#47;FC&#47;SDA &#40;n&#176;&#41;<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">10&#47;7&#47;6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">8&#47;0&#47;1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;02&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr></tbody></table>
                  """
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          "en" => "<p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Desensitization efficacy&#46;</p>"
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                  ]
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                            0 => "R&#46; Wolfe"
                            1 => "V&#46; Ashby"
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Original article
Kidney transplantation of 32 patients from HLA-incompatible live donors: Efficacy and outcome after desensitization
Trasplante renal procedente de donante vivo HLA incompatible: Eficacia y pronóstico en 32 pacientes tras desensibilización
Constantino Fernándeza,
Corresponding author
, María Calvoa, Natacha Leitea, Andrés Lópeza, Tamara Ferreiroa, Roi Riberaa, Rocío Seijob, Ángel Alonsoa
a Servicio de Nefrología, Complexo Hospitalario Universitario A Coruña, La Coruña, Spain
b Unidad de Bioestadística y Epidemiología, Complexo Hospitalario Universitario A Coruña, La Coruña, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Patients that have developed hypersensitivity &#40;HY&#41; have increasing difficulty to access to a kidney transplant because of the high incidence of pre-transplant positive cross-match&#46; In USA&#44; 35&#37; of the patients on the waiting list for renal transplantation are sensibilized and 15&#37; are highly sensibilized&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">1</span></a> Recently&#44; it has been reported that 6&#37; of patients on the waiting list have a 100&#37; of calculated reactivity against the panel&#46;<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">2</span></a> In Spain&#44; in 2014&#44; 11&#46;5&#37; of patients on the transplant waiting list are HY&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">The remedy for these patients is to use desensitization &#40;DS&#41; 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Roche Farma&#44; Madrid&#44; Spain&#41; in CMV donor positive patients&#44; CMV negative receptor &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Follow up</span><p id="par0035" class="elsevierStylePara elsevierViewall">After discharge&#44; patients were followed in the out patient clinic with monitorization of renal function&#44; tacrolimus levels&#44; CMV infection first with pp55 antigenemia and presently using PCR of CMV and BK virus&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">If deterioration of renal function was evidenced&#44; a biopsy was obtained and SDA were determined&#46; In our transplant unit protocol biopsies or systematic follow-up of SDA are not performed&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">The diagnosis of rejection in the biopsy was made based on Banff classification&#44; adapted to the date in which this classification was published&#46;<a class="elsevierStyleCrossRefs" href="#bib0190"><span class="elsevierStyleSup">11&#44;12</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Antibody-mediated rejection was treated with steroids &#40;3 boluses of 500<span class="elsevierStyleHsp" style=""></span>mg for 3 consecutive days&#41;&#44; PF or IA&#44; IgV&#44; RTX and eculizumab &#40;in refractory cases&#41;&#46; Treatment of T-cell mediated rejection included steroid boluses &#40;3 boluses of 500<span class="elsevierStyleHsp" style=""></span>mg for 3 consecutive days&#41;&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Variables evaluated&#58; Efficacy of DS&#44; delayed graft function&#44; acute rejection&#44; graft and patient survival&#44; renal function&#44; number of procedures of PF&#47;IA&#44; MFI against class I and II pre and postapheresis&#44; Number of antibodies against class I and II&#44; relative intensity scale &#40;RIS&#41; as reported by Jordan et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">10</span></a> CMV and BK infections&#44; diabetes posttransplant&#44; neoplasias and urological complications&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">E-statistics analysis&#58; Quantitative variables were compared by Student <span class="elsevierStyleItalic">t</span> test and ANOVA&#46; Mann&#8211;Whitney was used to compare variables without normal distribution&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Chi square and Fisher&#39;s test was used for qualitative variables&#46; Survival was calculated according to Kaplan&#8211;Meier and log rank test&#46; For the multivariate study we used the Cox regression and for the sensitivity and specificity analysis&#44; the ROC curves&#46; The statistical analysis was performed using the program SPSS &#40;version 15&#46;0&#46;1&#44; Chicago&#44; IL&#44; USA&#41;&#46;</p></span></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Results</span><p id="par0070" class="elsevierStylePara elsevierViewall">The study included 32 patients &#40;15 males&#41;&#44; with a mean age of 46<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>14 years&#46; The relationship between donor and recipient was&#58; parent&#44;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">9</span></a> spouse&#44;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">14</span></a> sibling&#44;<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">5</span></a> child<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">1</span></a> and others&#46;<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">3</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">At baseline&#44; patients presented a number of antibodies against class I&#58; 0&#46;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;7 &#40;0&#8211;3&#41; with MFI 7979<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>40 and class II&#58; 0&#46;6<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;5 &#40;0&#8211;2&#41; with MFI 6825<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4182&#59; RIS 8&#46;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&#46;7 &#40;2&#8211;30&#41;&#46; CDC cross-match was positive in 18 patients&#59; by FC&#44; in 7&#46; Another 7 patients had only SDA using solid phase techniques &#40;Luminex&#44; One Lambda&#44; Thermo Fisher Scientific&#44; Canoga Park&#44; CA&#44; USA&#41;&#46; DS was considered effective when CDC and FC cross-tests were negative and the MFI less than 1000 &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0080" class="elsevierStylePara elsevierViewall">After 8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3 sessions of PF&#47;IA4-15&#44; it was possible to perform transplantation in 23 patients &#40;71&#46;9&#37;&#41;&#44; but in 9 patients the transplant failed&#46; Desensitization was not successful in 9 patients&#59; 8 of these patients presented a previous cross-match by CDC and one by SDA &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;02&#41;&#46; Class I MFI and RIS were predictors of efficacy by ROC curves &#40;area of 0&#46;949 and 0&#46;848&#44; respectively&#41;&#46; A cutoff point of MFI and RIS was set at 9300 and 8&#46;5 points respectively&#44; with provides 100&#37; sensitivity and 93&#37; specificity for the first and 88&#37; sensitivity and 74&#37; specificity for the second&#46; DS was not effective above these values &#40;<a class="elsevierStyleCrossRefs" href="#fig0010">Figs&#46; 2 and 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0085" class="elsevierStylePara elsevierViewall">In the postoperative period&#44; 13 patients had hematoma-hemorrhage&#44; requiring reintervention in 6 &#40;26&#37;&#41;&#46; Blood transfusion was necessary in 16 &#40;69&#37;&#41;&#46; In 3 patients &#40;13&#37;&#41; there was a delay the initial function of the graft&#46;</p><p id="par0090" class="elsevierStylePara elsevierViewall">After 43<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>30 months &#40;range 0&#46;1&#8211;104&#41; of follow-up&#44; 4 patients &#40;17&#46;4&#37;&#41; had acute rejection&#59; in one patient it was antibody-mediated&#44; in two T-mediated and in the last of four it was mixed &#40;antibodies and T cells mediated rejection&#41;&#46; Patients with rejection had a higher baseline MFI&#44; higher values of RIS&#44; and a positive CDC cross-match &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a>&#41;&#44; but in the Cox analysis&#44; RIS was the only parameter that reached statistical significance&#46;</p><elsevierMultimedia ident="fig0020"></elsevierMultimedia><p id="par0095" class="elsevierStylePara elsevierViewall">Patient survival at 1 and 5 years were 96&#37; and 90&#37; respectively &#40;<a class="elsevierStyleCrossRef" href="#fig0025">Fig&#46; 5</a>&#41;&#46; One patient died during sepsis of urinary origin &#40;during the first week postransplantation&#41; and one died after subarachnoid hemorrhage &#40;during the second year&#41;&#46; Graft survival was 86&#37; at year 1 and 5 after transplantation &#40;<a class="elsevierStyleCrossRef" href="#fig0030">Fig&#46; 6</a>&#41;&#44; being worse in patients with acute rejection mediated by antibodies &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span><span class="elsevierStyleHsp" style=""></span>0&#46;02&#41;&#46; The causes of graft loss were antibody-mediated rejection in 2 patients &#40;one of them also had T cell mediated rejection&#41;&#44; chronic nephropathy in one patient&#44; and arterial thrombosis in another&#46;</p><elsevierMultimedia ident="fig0025"></elsevierMultimedia><elsevierMultimedia ident="fig0030"></elsevierMultimedia><p id="par0100" class="elsevierStylePara elsevierViewall">The mean serum creatinine &#40;mg&#47;dl&#41; was 1&#46;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;3&#44; after one year&#44; 1&#46;4<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;4 the 3rd year and 1&#46;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;04<span class="elsevierStyleHsp" style=""></span>at the end of the 5 years of follow-up&#46; Mean values of proteinuria &#40;mg&#47;day&#41; at years 1&#44; 3 and 5 post transplantation were 0&#46;3<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;3&#44; 0&#46;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;2 and 0&#46;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;7 respectively</p><p id="par0105" class="elsevierStylePara elsevierViewall">There were six CMV infections &#40;26&#37;&#41; and one BK viremia &#40;4&#37;&#41;&#46; The frequency of post-transplant diabetes was 26&#37;&#44;<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">6</span></a> lymphocele 13&#37;<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">3</span></a> and renal artery stenosis 4&#37;&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">1</span></a></p><p id="par0110" class="elsevierStylePara elsevierViewall">Two post-transplant neoplasia were diagnosed&#44; one chronic lymphatic leukemia and one cutaneous squamous cell carcinoma&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Discussion</span><p id="par0115" class="elsevierStylePara elsevierViewall">Renal transplantation is the best therapeutic option for patients with end stage renal disease&#46;<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">14</span></a> In hypersensitized patients the rate of transplantation is low &#40;&#60;6&#46;5&#37; per year in USA&#44; up to the last year&#41;&#44; they remain in the waiting list for long periods of time and the mortality is high&#46; The options of a patient with an incompatible living donor are DS&#44; joining cross-renal donation programs which is valid option if a living donor is available&#44; or being included in special exchange and prioritization programs&#46;<a class="elsevierStyleCrossRefs" href="#bib0150"><span class="elsevierStyleSup">3&#8211;6</span></a></p><p id="par0120" class="elsevierStylePara elsevierViewall">Our DS protocol is similar to others being used during the last years by different groups&#46; However there is a lot of heterogeneity between the series&#44; especially when defining selection criteria for desensitization and transplantation&#46;<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">1&#44;8</span></a> In our serie&#44; cross-match was positive for CDC in 18 of the 32 patients and it was not possible to desensitize 44&#37; of them&#46; The results were more favorable in those who presented a positive cross-reaction by FC or only with SDA by Luminex&#44; in fact we managed to transplant 100 and 86&#37; of those respectively&#46; Orandi et al&#46; showed that DS improves the prognosis of patients as compared with those who remain on the waiting list and finally are transplanted or those remaining on dialysis&#46; These differences were maintained for any level of baseline DS &#40;CDC&#43;&#44; CF&#43; or only SDA&#43; by Luminex&#41;&#44; although the prognosis was worse in those with cross-reaction test was positive by CDC&#44;<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">7</span></a> which could mean that these patients positive by CDC have a higher number of antibodies or higher affinity and this allows them to be detected by techniques that are less sensitive with respect to CF or Luminex&#46;<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">3</span></a></p><p id="par0125" class="elsevierStylePara elsevierViewall">Another factor that could influence the results is the amount of antibodies&#44; interpreted as the level of MFI&#44; which is not well known in most of the series&#46; We used RIS to homogenize the number of antibodies in each patient and their MFI&#44; as described by Jordan et al&#46;<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">13</span></a> Our results demonstrate that DS was not effective in patients with MFI greater than 9300 in class I&#44; or in those with an RIS greater than 8&#46;5&#46;</p><p id="par0130" class="elsevierStylePara elsevierViewall">In our study&#44; at year 5 the survival of patient &#40;90&#37;&#41; and graft &#40;86&#37;&#41; was similar to that reported by others and illustrate the possibility of performing this type of treatment in HY patients who would otherwise remain for a long time in the waiting list&#46; Marfo et al&#46;<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">1</span></a> reports a 95&#37; patient survival and 85&#37; graft survival&#59; Orandi at year 3&#44; 91&#46;7&#37; and at year 8 a 76&#46;5&#37;<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">6</span></a>&#59; Yang et al&#46; in Taiwan&#44;<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">15</span></a> at year 5&#44; they report 100&#37; of the patient and 92&#46;3&#37; of the graft survival&#59; and De Sousa et al&#46;&#44; 95&#46;9&#37; of patients and 85&#37; of grafts survived after 5 years&#46;<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">16</span></a> Morath et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">17</span></a> using PF or AI&#44; reported a 95&#46;8&#37; patient survival and 92&#46;4&#37; graft survival&#44; after one year&#46; Bentall et al&#46;<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">18</span></a> reported a 5-year patient survival rate of 83&#46;5&#37;&#44; lower than in the control group &#40;92&#46;5&#37;&#41; and a graft survival of 70&#46;7&#37;&#44; lower than in the control group &#40;88&#37;&#41;&#44; and Thielke et al&#46;<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">19</span></a> showed 95&#37; patient survival and 93&#37; of the graft survival after one year&#46;</p><p id="par0135" class="elsevierStylePara elsevierViewall">The incidence of acute rejection was 17&#37;&#44; in 2 cases antibody-mediated &#40;AMR&#41;&#44; one of them also had T-cell mediated rejection with no response to treatment&#44; and 2 other patients had rejections mediated only by T cells&#44; Banff IA&#44; with good response to steroids&#46; In our serie&#44; the probability of rejection was greater in patients with CDC-positive cross-match and in those with higher RIS&#46; Our low frequency of rejection contrasts with others that have reported from 17 to 80&#37; rejections&#44; using different protocols and different degrees of DS &#40;CDC&#44; CF&#44; SDA&#41;&#46;<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">1&#44;8</span></a> We do not perform biopsies by protocol and only monitor SDA if there is a suspicion of antibody-mediated rejection&#44; so we may not have detected subclinical rejections or chronic rejections mediated by antibodies&#44; which could explain this difference&#46; Riella et al that uses a DS protocol similar to ours&#44;<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">9</span></a> has reported a 61&#37; rejection&#59; 100&#37; of patients had CDC-positive cross-match pre-transplantation and the monitorization of titers differs from ours in that we used MFI and they used antibody titers&#59; in addition&#44; only 21 of 39 received RTX&#46; After DS with bortezomib&#44; Aubert et al&#46;<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">20</span></a> found no acute rejection after 18 months and Woodle et al&#46;<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">21</span></a> reported 31&#37;&#46; Recently&#44; Moreno Gonzales et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">2</span></a> using 32 doses of bortezomib only found moderate reduction of antibody without negativization of the cross-match&#44; and it was not well tolerated&#46;</p><p id="par0140" class="elsevierStylePara elsevierViewall">There is little information on the incidence of post-transplant SDA in the series of desensitized patients&#46; Morath et al&#46;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">17</span></a> monitored antibodies during one year and these remained positive at low titers&#46; De Sousa et al&#46;<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">16</span></a> monitored the antibodies in 18 patients&#44; in one of them were positive and developed AMR&#46; Kauke et al&#46;<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">22</span></a> demonstrated that in 6 out of 8 desensitized patients the antibodies persisted and 3 of them developed AMR&#46; Stegall et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">23</span></a> in patients treated with eculizumab&#44; found that 50&#37; of the patients developed SDA with MFI &#62;10&#44;000&#44; although the incidence of acute rejection was 7&#46;7&#37; as compared with 41&#46;1&#37; in the group without eculizumab&#46; In our series&#44; 8 patients had SDA at follow-up&#58; 3 of them were positive&#44; 2 developed AMR and another patient had transplant glomerulopathy&#46;</p><p id="par0145" class="elsevierStylePara elsevierViewall">In our study&#44; despite the high load of immunosuppression&#44; the rate of infectious complications was acceptable&#44; with an incidence of CMV of 26&#37; and BK of 4&#37;&#46; Vo et al&#46;<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">24</span></a> reported a 16&#46;5&#37; CMV infection and 0&#37; BK viremia&#46; Kauke et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">22</span></a> reported 2&#47;8 &#40;25&#37;&#41; of BK viremia&#46; Yang et al&#46;<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">15</span></a> reported 3 cases of BK nephropathy &#40;13&#46;6&#37;&#41; and 2 CMV pneumonitis &#40;9&#37;&#41;&#46; De Sousa et al&#46;<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">16</span></a> reported 3 CMV reactivations &#40;13&#37;&#41; and one case of BK &#40;4&#46;3&#37;&#41;&#46; Morath et al&#46;<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">17</span></a> describe 10&#37; CMV and 0&#37; BK&#46; Thielke et al&#46;<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">19</span></a> 7&#37; CMV and 4&#46;9&#37; BK&#46; Stegall et al&#46;<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">23</span></a> used eculizumab without reporting no CMV or BK virus infections&#46;</p><p id="par0150" class="elsevierStylePara elsevierViewall">The incidence of neoplasias is not usually reported&#46; Two patients in our series had de novo neoplasia &#40;a chronic lymphatic leukemia and a skin squamous cell carcinoma&#41;&#46; The Taiwan group reported 3 cases of urothelial cancer&#46; Stegall et al&#46;&#44; in patients desensitized with eculizumab&#44; reported one case of Burkitt&#39;s lymphoma&#46;</p><p id="par0155" class="elsevierStylePara elsevierViewall">A relatively frequent complication following transplantation is the occurrence of hematoma&#47;hemorrhage&#46; It could be related to PF or IA in incompatible ABO transplants due to the loss of coagulation factors&#44; including factor XIII&#44; the decrease in the number of platelets or the use of anticoagulants to perfuse the graft&#46;<a class="elsevierStyleCrossRefs" href="#bib0260"><span class="elsevierStyleSup">25&#8211;27</span></a> In our patients we did not identify a factor that could favor bleeding &#40;although we did not measure factor XIII&#41;&#44; perhaps due to the limited number of patients&#46; There might be a number of factors that acting together may facilitate hemorrhage&#46;</p><p id="par0160" class="elsevierStylePara elsevierViewall">The limitations of our study are the sample size&#44; the absence of protocol biopsy and the low number of SDA monitored&#46; Despite this&#44; the clinical results are acceptable in a group of patients who would have to be maintained on the waiting list for a long time&#46; We detected markers that identify patients in whom DS is ineffective&#44; these are MFI class I or RIS&#44; which would suggest to avoid the initiation a costly treatment with potential adverse effects&#46; We conclude that the HLA DS with the protocol shown in this study is an option to consider in those patients sensitized against a living donor&#46;</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Conflict of interests</span><p id="par0165" class="elsevierStylePara elsevierViewall">The authors have no conflicts of interest to declare&#46;</p></span></span>"
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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Desensitization is a procedure undergone by the recipient of a kidney transplant from a donor who is cross-match positive&#46; The aim of this study was to present the outcomes from our hospital of kidney transplant recipients from HLA-incompatible live donors after desensitization&#46;</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">We studied 32 patients aged 46<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>14 years with a mean fluorescence intensity &#40;MFI&#41; versus class I HLA of 7979<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4089 and 6825<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4182 MFI versus class II and relative intensity scale &#40;RIS&#41; of 8&#46;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&#46;6&#46; The complement-dependent cytotoxicity &#40;CDC&#41; cross-matching test was positive in 18 patients&#44; flow cytometry was positive in 7 patients and donor-specific antibodies &#40;DEA&#41; were detected in 7&#46; The protocol used was rituximab&#44; plasmapheresis&#47;immunoadsorption&#44; immunoglobulins&#44; tacrolimus&#44; mycophenolic acid derivatives and prednisone&#46;</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">After 8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3 sessions of plasmapheresis&#47;immunoadsorption&#44; 23 patients were transplanted &#40;71&#46;9&#37;&#41; and desensitization was ineffective in 9&#46; There were baseline differences in MFI class I &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#46;001&#41;&#44; RIS &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;008&#41;&#44; and CDC cross-matching&#44; DSA and flow cytometry &#40;<span class="elsevierStyleItalic">p</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#46;05&#41;&#46; MFI class I and RIS were predictors of inefficiency in ROC curves&#46; After follow-up of 43<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>30 months&#44; 13 patients &#40;56&#37;&#41; presented postoperative bleeding&#44; 3 &#40;13&#37;&#41; delayed graft function&#44; 4 &#40;17&#46;4&#37;&#41; acute rejection&#44; 6 &#40;26&#37;&#41; CMV viremia and 1 &#40;4&#37;&#41; BK viremia&#46; Five-year patient survival was 90&#37;&#44; with 86&#37; allograft survival&#46; Five-year creatinine was 1&#46;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;4 and proteinuria was 0&#46;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;7&#46;</p></span> <span id="abst0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conclusions</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Kidney transplantation from HLA-incompatible live donors after desensitization was possible in 71&#46;9&#37; of patients&#46; MFI class I and RIS predict the inefficiency of desensitization&#46; Five-year allograft survival &#40;86&#37;&#41; was acceptable with a low incidence of acute rejection &#40;17&#46;4&#37;&#41;&#44; although with a greater trend toward postoperative bleeding&#46;</p></span>"
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        "titulo" => "Resumen"
        "resumen" => "<span id="abst0015" class="elsevierStyleSection elsevierViewall"><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">La desensibilizaci&#243;n es un m&#233;todo empleado en trasplante renal para tratar de trasplantar a pacientes que presentan una prueba cruzada positiva frente a su donante&#46; El objetivo del estudio es mostrar los resultados de nuestro hospital en pacientes trasplantados renales con donantes vivos HLA incompatibles&#44; tras un protocolo de desensibilizaci&#243;n&#46;</p><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Estudiamos a 32 pacientes de 46<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>14 a&#241;os que presentaban una intensidad media de fluorescencia &#40;MFI&#41; frente a HLA de clase I de 7&#46;979<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4&#46;089 y de 6&#46;825<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4&#46;182 para MFI frente a clase II y <span class="elsevierStyleItalic">relative intensity scale</span> &#40;RIS&#41; de 8&#44;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&#44;6&#46; La prueba cruzada fue positiva por citotoxicidad dependiente del complemento &#40;CDC&#41; en 18 pacientes&#44; citometr&#237;a de flujo &#40;CF&#41; en 7 y anticuerpos donante espec&#237;ficos &#40;ADE&#41; en 7&#46; El protocolo empleado fue&#58; rituximab&#44; plasmaf&#233;resis&#47;inmunoadsorci&#243;n&#44; inmunoglobulinas&#44; tacrolimus&#44; derivados &#225;cido micofen&#243;lico y prednisona&#46;</p><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Tras 8<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3 sesiones de plasmaf&#233;resis&#47;inmunoadsorci&#243;n se trasplant&#243; a 23 pacientes &#40;71&#44;9&#37;&#41; y result&#243; ineficaz en 9&#46; Exist&#237;an diferencias basales en MFI clase I &#40;p<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>0&#44;001&#41;&#44; RIS &#40;p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;008&#41; y <span class="elsevierStyleItalic">cross-match</span> por CDC&#44; ADE o CF &#40;p<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>0&#44;05&#41;&#46; El MFI de clase I y el RIS resultaron predictores de eficacia en curvas COR&#46; Tras un seguimiento de 43<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>30 meses&#44; 13 pacientes &#40;56&#37;&#41; presentaron sangrado postoperatorio&#44; 3 &#40;13&#37;&#41; funci&#243;n retrasada injerto&#44; 4 &#40;17&#44;4&#37;&#41; rechazo agudo&#44; 6 &#40;26&#37;&#41; viremia CMV y uno &#40;4&#37;&#41; viremia BK&#46; Al 5&#46;&#176; a&#241;o&#44; la supervivencia del paciente fue del 90&#37; y la supervivencia renal del 86&#37;&#46; En ese mismo a&#241;o&#44; la creatinina fue de 1&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#44;4 y la proteinuria de 0&#44;5<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#44;7&#46;</p></span> <span id="abst0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Conclusiones</span><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">El trasplante renal de donante vivo HLA incompatible tras la desensibilizaci&#243;n fue posible en el 71&#44;9&#37; de los pacientes&#46; MFI de clase I y RIS predicen ineficacia de la desensibilizaci&#243;n&#46; La supervivencia renal &#40;86&#37; al 5&#46;&#176; a&#241;o&#41; es aceptable con baja incidencia de rechazo agudo &#40;17&#44;4&#37;&#41;&#44; aunque con una mayor tendencia al sangrado postoperatorio&#46;</p></span>"
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    "NotaPie" => array:1 [
      0 => array:2 [
        "etiqueta" => "&#9734;"
        "nota" => "<p class="elsevierStyleNotepara" id="npar0015">Please cite this article as&#58; Fern&#225;ndez C&#44; Calvo M&#44; Leite N&#44; L&#243;pez A&#44; Ferreiro T&#44; Ribera R&#44; et al&#46; Trasplante renal procedente de donante vivo HLA incompatible&#58; Eficacia y pron&#243;stico en 32 pacientes tras desensibilizaci&#243;n&#46; Nefrologia&#46; 2017&#59;37&#58;638&#8211;645&#46;</p>"
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                  <table border="0" frame="\n
                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head  " align="" valign="top" scope="col" style="border-bottom: 2px solid black">&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="center" valign="top" scope="col" style="border-bottom: 2px solid black">Efficacy&#58; <span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>23&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="center" valign="top" scope="col" style="border-bottom: 2px solid black">Without efficacy&#58; <span class="elsevierStyleItalic">n</span><span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>9&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th><th class="td" title="table-head  " align="center" valign="top" scope="col" style="border-bottom: 2px solid black"><span class="elsevierStyleItalic">p</span>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Age of donor &#40;years&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">50&#46;3<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>9&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">49&#46;6<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">NS&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Age of recipient &#40;years&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">48&#46;6<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>14&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">38&#46;6<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>12&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;07&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Dialysis vintage &#40;months&#41;&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">84&#46;9<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>77&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">39&#46;3<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>46&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;07&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">No&#46; of antibodies class I and II&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">1&#46;47<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;79&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">1&#46;66<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;70&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">NS&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">MFI class I&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">5840<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3002&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">12&#44;258<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>2044&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;001&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">MFI class II&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">6048<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>4145&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">9169<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3725&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">NS&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">RIS<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">6&#46;2<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>6&#46;6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">15<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>7&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;005&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Pregnancy&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;86<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;33<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>0&#46;07&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">NS&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">No&#46; of HLA incompatibilities&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">3&#46;7<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>11&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">3&#46;3<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>1&#46;6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">NS&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Number of PFS&#47;IA sessions&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">8&#46;1<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>2&#46;7&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">8&#46;7<span class="elsevierStyleHsp" style=""></span>&#177;<span class="elsevierStyleHsp" style=""></span>3&#46;3&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">NS&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Cross-match&#58; CDC&#47;FC&#47;SDA &#40;n&#176;&#41;<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</span></a>&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">10&#47;7&#47;6&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">8&#47;0&#47;1&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="table-entry  " align="left" valign="top">0&#46;02&nbsp;\t\t\t\t\t\t\n
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ISSN: 20132514
Original language: English
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Nefrología (English Edition)