肾移植受者BK病毒血症后重新发生DSA的发生率及相关因素。

Clinical transplants Pub Date : 2016-01-01
Samir J Patel, Samantha A Kuten, Richard J Knight, Edward A Graviss, Duc Nguyen, A Osama Gaber
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引用次数: 0

摘要

BK多瘤病毒感染和新生供体-人白细胞抗原(HLA)特异性抗体(dnDSA)是肾移植后发生的两种众所周知的独特并发症。最近的文献表明这两件事之间存在联系。本研究旨在探讨肾移植受者BKV病毒血症(BKV)与dnDSA之间的关系,并确定BKV后dnDSA的潜在危险因素。对休斯顿卫理公会医院1019例受助人进行回顾性分析。所有患者都接受了BKV和dnDSA的常规筛查。中位随访时间为44个月。移植后中位时间为107(82-205)天,186例(18%)患者检测到BKV。283例(28%)患者在移植后272(62-575)天发生dnDSA。在69例dnDSA阳性/BKV阳性患者中,46例患者在BKV发病后检测到dnDSA。因此,46例(28%)先前dsa阴性的患者在BKV后变为dnsa阳性,与BKV阴性患者(26%;p = 0.5)。BKV发病后到DSA检测的中位时间为BKV检测后232天(四分位数间距为119-460)。多变量分析显示,大量HLA错配和病毒清除是BKV后发生dnDSA的危险因素,而移植功能延迟与dnDSA的风险较低相关。总之,尽管被认为是过度免疫抑制的结果,但在相当比例的患者中,BKV仍然可以伴随dnDSA。对BKV患者进行dnDSA监测可能是有必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Incidence and Factors Associated with De Novo DSA After BK Viremia in Renal Transplant Recipients.

BK polyomavirus infection and de novo donor-human leukocyte antigen (HLA) specific antibodies (dnDSA) are two well-known and distinct complications occurring after kidney transplantation. Recent literature suggests an association between the two events. This study aims to examine the relationship between BK viremia (BKV) and dnDSA and to identify potential risk factors for dnDSA following BKV in kidney transplant recipients. A retrospective review of 1019 recipients from Houston Methodist Hospital was conducted. All patients underwent routine screening for BKV and dnDSA. Median follow-up was 44 months. BKV was detected in 186 (18%) patients at a median of 107 (82-205) days post-transplant. dnDSA occurred in 283 (28%) patients at a median of 272 (62-575) days post-transplant. Of the 69 dnDSA-positive/BKV-positive patients, dnDSA detection occurred after BKV onset in 46 patients. Thus, 46 (28%) previously DSA-negative patients later became dnDSA-positive following BKV, not significantly different from the rate seen in BKV-negative patients (26%; p=0.5). Median time to DSA detection following BKV onset was 232 days (interquartile range, 119-460) post-BKV detection. Multivariate analysis revealed a greater number of HLA mismatches and viral clearance as risk factors for development of dnDSA following BKV, whereas delayed graft function was associated with a lower risk of dnDSA. In conclusion, despite being considered a result of over-immunosuppression, BKV can still be followed by dnDSA in a substantial proportion of patients. Monitoring for dnDSA in patients being managed for BKV may be warranted.

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