Association of Donor-Specific Antibodies with Rejection and Graft Outcomes in Pediatric Kidney Transplant Recipients: A Single-Center Retrospective Study.
{"title":"Association of Donor-Specific Antibodies with Rejection and Graft Outcomes in Pediatric Kidney Transplant Recipients: A Single-Center Retrospective Study.","authors":"Begüm Avcı, Gönül Parmaksız, Aytül Noyan, Kenan Çalışkan, Esra Baskın, Bilkay Baştürk, Mehmet Haberal","doi":"10.6002/ect.MESOT2025.O42","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>De novo donor -specific antibodies are recognized mediators of alloimmune injury after kidney transplant, yet their clinical significance in pediatric recipients remains incompletely defined. We evaluated the incidence of de novo donor -specific antibodies and the associated rejection patterns and graft outcomes in a pediatric kidney transplant cohort.</p><p><strong>Materials and methods: </strong>This retrospective single -center study included pediatric kidney transplant recipients who underwent transplants between 2009 and June 2024. Donor -specific antibody positivity was determined using Luminex -based assays (mean fluorescence intensity >1000 ). Clinical, immunologic, and functional outcomes were compared between patients positive for donor -specific antibodies and patients negative for donor -specific antibodies, including rejection phenotype, estimated glomerular filtration rate, graft loss, and duration of follow -up.</p><p><strong>Results: </strong>Among 78 recipients, 15 recipients (19.2 % ) developed de novo donor -specific antibodies during a mean follow -up of approximately 4 years. Acute rejection occurred more frequently in patients positive for donor -specific antibodies versus patients negative for donor -specific antibodies (80 % vs 32 %, respectively; P = .053 ), predominantly antibody -mediated or mixed phenotypes. Graft loss rates were comparable between groups (13.3 % vs 14.2 %; P = 1.000 ). Although not statistically significant, recipients positive for donor -specific antibodies demonstrated numerically lower eGFR values at 1 year and at last follow -up (49.6 ± 22.2 vs 57.1 ± 29.8 mL /min /1.73 m ² at last visit, respectively; P - .445 ).</p><p><strong>Conclusions: </strong>In this pediatric cohort, de novo development of donor -specific antibodies was associated with a higher tendency toward antibody -mediated rejection, without a significant difference in short -term to mid -term graft survival. Continued surveillance of donor -specific antibodies and longer follow -up are warranted to clarify the long -term clinical effect of donor -specific antibodies in pediatric kidney transplants.</p>","PeriodicalId":50467,"journal":{"name":"Experimental and Clinical Transplantation","volume":"24 Suppl 2","pages":"110-114"},"PeriodicalIF":0.7000,"publicationDate":"2026-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental and Clinical Transplantation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.6002/ect.MESOT2025.O42","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"TRANSPLANTATION","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: De novo donor -specific antibodies are recognized mediators of alloimmune injury after kidney transplant, yet their clinical significance in pediatric recipients remains incompletely defined. We evaluated the incidence of de novo donor -specific antibodies and the associated rejection patterns and graft outcomes in a pediatric kidney transplant cohort.
Materials and methods: This retrospective single -center study included pediatric kidney transplant recipients who underwent transplants between 2009 and June 2024. Donor -specific antibody positivity was determined using Luminex -based assays (mean fluorescence intensity >1000 ). Clinical, immunologic, and functional outcomes were compared between patients positive for donor -specific antibodies and patients negative for donor -specific antibodies, including rejection phenotype, estimated glomerular filtration rate, graft loss, and duration of follow -up.
Results: Among 78 recipients, 15 recipients (19.2 % ) developed de novo donor -specific antibodies during a mean follow -up of approximately 4 years. Acute rejection occurred more frequently in patients positive for donor -specific antibodies versus patients negative for donor -specific antibodies (80 % vs 32 %, respectively; P = .053 ), predominantly antibody -mediated or mixed phenotypes. Graft loss rates were comparable between groups (13.3 % vs 14.2 %; P = 1.000 ). Although not statistically significant, recipients positive for donor -specific antibodies demonstrated numerically lower eGFR values at 1 year and at last follow -up (49.6 ± 22.2 vs 57.1 ± 29.8 mL /min /1.73 m ² at last visit, respectively; P - .445 ).
Conclusions: In this pediatric cohort, de novo development of donor -specific antibodies was associated with a higher tendency toward antibody -mediated rejection, without a significant difference in short -term to mid -term graft survival. Continued surveillance of donor -specific antibodies and longer follow -up are warranted to clarify the long -term clinical effect of donor -specific antibodies in pediatric kidney transplants.
目的:新生供者特异性抗体是公认的肾移植后同种免疫损伤的介质,但其在儿科受体中的临床意义仍不完全明确。我们评估了儿童肾移植队列中新生供者特异性抗体的发生率以及相关的排斥模式和移植结果。材料和方法:本回顾性单中心研究纳入了2009年至2024年6月间接受肾移植的儿童肾移植受者。采用基于Luminex的检测方法测定供体特异性抗体阳性(平均荧光强度bbb1000)。比较供体特异性抗体阳性患者和供体特异性抗体阴性患者的临床、免疫和功能结果,包括排斥表型、肾小球滤过率估计、移植物损失和随访时间。结果:78名受者中,15名受者(19.2%)在平均约4年的随访期间产生了供者特异性抗体。供体特异性抗体阳性的患者比供体特异性抗体阴性的患者更频繁发生急性排斥反应(分别为80%对32%;P = 0.053),主要是抗体介导或混合表型。两组间移植物失取率具有可比性(13.3% vs 14.2%; P = 1.000)。虽然没有统计学意义,但供体特异性抗体阳性的受体在1年和最后随访时的eGFR数值较低(分别为49.6±22.2 vs 57.1±29.8 mL /min /1.73 m²;P - 0.445)。结论:在这个儿童队列中,供体特异性抗体的新生发展与抗体介导的排斥反应的更高倾向相关,在短期和中期移植物存活方面没有显著差异。供体特异性抗体的持续监测和长期随访是必要的,以明确供体特异性抗体在儿童肾移植中的长期临床效果。
期刊介绍:
The scope of the journal includes the following:
Surgical techniques, innovations, and novelties;
Immunobiology and immunosuppression;
Clinical results;
Complications;
Infection;
Malignancies;
Organ donation;
Organ and tissue procurement and preservation;
Sociological and ethical issues;
Xenotransplantation.