Immune Checkpoint Inhibitors in Recipients of Renal Allografts

IF 2.8 3区 医学 Q2 UROLOGY & NEPHROLOGY
Karthik Venkataraman MBBS , Tania Salehi MBBS , Robert P. Carroll MD, PhD, FRACP, A(ACHI)
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引用次数: 0

Abstract

Kidney transplant recipients are at increased risk of malignancy as a result of immunosuppression and are increasingly exposed to checkpoint inhibitors (CPIs). However, CPI therapy can precipitate allograft rejection. This review aims to summarize the current literature describing the epidemiology, immunological mechanisms, diagnosis, and treatment of CPI-associated allograft rejection.Initial studies of CPIs suggested allograft rejection post commencement of CPIs occured commonly (40-60%), occurring between 2 and 6 weeks after CPI initiation, with a cancer response rate approaching 50%. More recent studies with predefined, structured immunosuppressive regimens have seen rejection rates of 0-12.5%, with rejection occurring later. Allograft biopsy remains the mainstay of diagnosis; however, noninvasive tools are emerging, including donor-derived cell-free DNA, urinary chemokine assessment, and defining alloreactive T-cell clones prior to or during CPI therapy.

免疫检查点抑制剂在肾移植受者中的应用
肾移植受者因免疫抑制而罹患恶性肿瘤的风险增加,并越来越多地接触到检查点抑制剂(CPI)。然而,CPI疗法可能会诱发异体移植排斥反应。本综述旨在总结目前描述CPI相关异体移植物排斥反应的流行病学、免疫学机制、诊断和治疗的文献。最初的CPI研究表明,CPI开始后的异体移植物排斥反应发生率很高(40-60%),发生在CPI开始后的2-6周,癌症反应率接近50%。最近采用预定义、结构化免疫抑制方案进行的研究发现,排斥反应发生率为 0-12.5%,排斥反应发生时间较晚。同种异体移植物活检仍是诊断的主要方法;然而,非侵入性工具也在不断涌现,包括供体来源的无细胞 DNA、尿液趋化因子评估以及在 CPI 治疗前或治疗期间确定异体反应性 T 细胞克隆。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Seminars in nephrology
Seminars in nephrology 医学-泌尿学与肾脏学
CiteScore
5.60
自引率
0.00%
发文量
27
审稿时长
6-12 weeks
期刊介绍: Seminars in Nephrology is a timely source for the publication of new concepts and research findings relevant to the clinical practice of nephrology. Each issue is an organized compendium of practical information that serves as a lasting reference for nephrologists, internists and physicians in training.
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