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首页> 外文期刊>Clinical & developmental immunology. >De Novo Donor-Specific HLA Antibodies Developing Early or Late after Transplant Are Associated with the Same Risk of Graft Damage and Loss in Nonsensitized Kidney Recipients
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De Novo Donor-Specific HLA Antibodies Developing Early or Late after Transplant Are Associated with the Same Risk of Graft Damage and Loss in Nonsensitized Kidney Recipients

机译:在移植后早期或晚期发育的De Novo供体特异性HLA抗体与未敏化的肾脏接受者发生移植物损坏和丢失的风险相同

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De novo posttransplant donor-specific HLA-antibody ( dn 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 dn DSA occurrence by Luminex platform. dn DSAs occurred in 39 patients at a median time of 24.6 months. In 15 patients, dn DSAs developed within 1 year ( early-onset group), while the other 24 seroconverted after the first posttransplant year ( late-onset 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 dn DSA development. Late AMR was diagnosed in 47% of the early group and in 58% of the late group. Graft loss occurred in 3/15 (20%) and 4/24 (17%) patients in early- and late-onset groups, respectively ( p = ns). In our pediatric kidney recipients, dn DSAs predict AMR and graft loss irrespective of the time elapsed between transplantation and antibody occurrence.
机译:现在公认从头移植后供体特异性HLA抗体(dn DSA)检测是鉴定有抗体介导排斥(AMR)和移植物丢失风险的患者的工具。尚不清楚从移植到DSA发生的时间间隔是否影响移植物损伤。利用纵向收集的血清,我们评估了2002年至2013年之间通过Luminex平台移植的dn DSA发生的114例连续的小儿肾脏原发性受体。 dn DSA发生于39例患者,中位时间为24.6个月。在15例患者中,dn DSA在1年内发生(早发组),而其他24例在移植后的第一年后发生血清转换(晚发组)。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,两组具有可比性。在这两个队列中,只有移植时的接受者年龄显着不同,年轻的患者显示出dn DSA的发展较早。早期组的47%和晚期组的58%被诊断为晚期AMR。在早期和晚期发病组中,分别有3/15(20%)和4/24(17%)患者发生移植物丢失(p = ns)。在我们的儿科肾脏接受者中,dn DSA可以预测AMR和移植物的丢失,而与移植和抗体出现之间的时间无关。

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