Nephrology, Dialysis and Transplantation Unit, IRCCS Istituto G. Gaslini, Genova, Italy.
Clinical Nephrology Unit and Transplant Immunology Research Laboratory, Department of Internal Medicine, University of Genova and IRCCS San Martino University Hospital IST, Genova, Italy.
J Immunol Res. 2017;2017:1747030. doi: 10.1155/2017/1747030. Epub 2017 Mar 6.
De novo posttransplant donor-specific HLA-antibody (DSA) detection is now recognized as a tool to identify patients at risk for antibody-mediated rejection (AMR) and graft loss. It is still unclear whether the time interval from transplant to DSA occurrence influences graft damage. Utilizing sera collected longitudinally, we evaluated 114 consecutive primary pediatric kidney recipients grafted between 2002 and 2013 for DSA occurrence by Luminex platform. DSAs occurred in 39 patients at a median time of 24.6 months. In 15 patients, DSAs developed within 1 year ( group), while the other 24 seroconverted after the first posttransplant year ( group). The two groups were comparable when considering patient- and transplant-related factors, as well as DSA biological properties, including C1q and C3d complement-binding ability. Only recipient age at transplant significantly differed in the two cohorts, with younger patients showing earlier DSA development. Late AMR was diagnosed in 47% of the group and in 58% of the group. Graft loss occurred in 3/15 (20%) and 4/24 (17%) patients in and groups, respectively ( = ns). In our pediatric kidney recipients, DSAs predict AMR and graft loss irrespective of the time elapsed between transplantation and antibody occurrence.
目前,新出现的移植后供体特异性 HLA 抗体(DSA)检测被认为是识别发生抗体介导的排斥反应(AMR)和移植物丢失风险的一种工具。目前尚不清楚从移植到 DSA 出现的时间间隔是否会影响移植物损伤。本研究利用纵向采集的血清,通过 Luminex 平台评估了 2002 年至 2013 年间连续 114 例原发性儿科肾移植患者的 DSA 发生情况。39 例患者在中位数 24.6 个月时出现 DSA。15 例患者(组)在 1 年内出现 DSA,而另外 24 例患者(组)在移植后第 1 年之后发生血清学转换。在考虑患者和移植相关因素以及 DSA 生物学特性(包括 C1q 和 C3d 补体结合能力)时,两组之间无差异。只有移植时受者年龄在两组之间存在显著差异,年轻患者更早出现 DSA 发展。组和组中分别有 47%和 58%的患者发生晚期 AMR(=ns)。在 15 例组和 24 例组患者中,分别有 3/15(20%)和 4/24(17%)发生移植物丢失(=ns)。在我们的儿科肾移植患者中,DSA 可预测 AMR 和移植物丢失,而与移植到抗体出现之间的时间无关。