肾移植后供者特异性HLA抗体监测的影响。

Clinical transplants Pub Date : 2014-01-01
Swati Rao, Mythili Ghanta, Iris J Lee, Avrum Gillespie, Hemant K Parekh, Steven S Geier, Xu Zeng, Andreas Karachristos, Kwan N Lau, Sunil Karhadkar, Antonio Di Carlo, Nicole M Sifontis, Serban Constantinescu
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引用次数: 0

摘要

具有供体特异性HLA抗体(DSA)的肾移植(KT)受者会遇到较高的急性排斥反应率和较差的同种异体移植存活率。我们报告了单中心前瞻性DSA监测的经验,并提供了用于克服DSA潜在影响的治疗细节,主要是非洲裔美国成人KT接受者。75名流动交叉配型阴性KT受体在移植后3、6、9和12个月采用单抗原珠测定法定期筛查DSA。在存在DSA和/或移植物功能障碍的证据时进行同种异体移植物活检。DSA的发生率为23%,以II类抗体为主。DSA阳性KT受体的排异率是DSA阴性患者的6倍(41%对7%,p = 0.004)。在DSA阳性组中,排斥反应仅发生在新生DSA存在的情况下,主要是抗体介导的或混合排斥反应。尽管接受DSA的KT受体的排斥发生率较高,但在中位随访18个月时,DSA阳性和阴性受体的血清肌酐、移植物存活率和患者存活率没有显著差异。在6个月、1年和3年的随访中,DSA阳性患者的蛋白尿明显高于DSA阴性患者。总之,DSA对同种异体移植物功能的有害影响可以通过连续的DSA监测、方案活检和免疫抑制的改变来减轻。通过这些措施,至少在短期内,DSA阳性KT受体移植物存活的改善是令人鼓舞的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Donor Specific HLA Antibody Monitoring After Kidney Transplantation.

Kidney transplantation (KT) recipients with donor specific HLA antibodies (DSA) encounter higher rates of acute rejection and inferior allograft survival. We report our single center experience with prospective DSA monitoring and provide details of treatments utilized to overcome the potential impact of DSA in a cohort of predominantly African American adult KT recipients. Seventy-five flow crossmatch negative KT recipients underwent periodic screening for DSA utilizing the single antigen bead assay at 3, 6, 9, and 12 months post-transplant. Allograft biopsies were performed in the presence of DSA and/or evidence of graft dysfunction. The incidence of DSA was 23%, with a predominance of Class II antibodies. The rate of rejection was 6 times higher in DSA positive KT recipients compared to DSA negative patients (41% versus 7%, p = 0.004). In the DSA positive group, rejections occurred exclusively in the presence of de novo DSA and were predominantly antibody-mediated or mixed rejections. Despite a higher incidence of rejection in KT recipients with DSA, there were no significant differences in serum creatinine, graft survival, and patient survival between DSA positive and negative recipients at median follow-up of 18 months. DSA positive patients had significantly higher proteinuria compared to DSA negative recipients at 6 months, 1 year, and 3 years of follow-up. In conclusion, the detrimental effects of DSA on allograft function could be mitigated by serial DSA surveillance, protocol biopsies, and alterations in immunosuppression. With these measures, the improvement in graft survival in DSA positive KT recipients, at least at short-term, is encouraging.

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