Department of Medicine, Division of Nephrology.
Ajmera Transplant Centre, University Health Network, Toronto, Ontario, Canada.
Curr Opin Organ Transplant. 2022 Oct 1;27(5):405-414. doi: 10.1097/MOT.0000000000001011. Epub 2022 Aug 11.
Antibody-mediated rejection (AMR) has emerged as the leading cause of late graft loss in kidney transplant recipients. Donor-specific antibodies are an independent risk factor for AMR and graft loss. However, not all donor-specific antibodies are pathogenic. AMR treatment is heterogeneous due to the lack of robust trials to support clinical decisions. This review provides an overview and comments on practical but relevant dilemmas physicians experience in managing kidney transplant recipients with AMR.
Active AMR with donor-specific antibodies may be treated with plasmapheresis, intravenous immunoglobulin and corticosteroids with additional therapies considered on a case-by-case basis. On the contrary, no treatment has been shown to be effective against chronic active AMR. Various biomarkers and prediction models to assess the individual risk of graft failure and response to rejection treatment show promise.
The ability to personalize management for a given kidney transplant recipient and identify treatments that will improve their long-term outcome remains a critical unmet need. Earlier identification of AMR with noninvasive biomarkers and prediction models to assess the individual risk of graft failure should be considered. Enrolling patients with AMR in clinical trials to assess novel therapeutic agents is highly encouraged.
抗体介导的排斥反应(AMR)已成为肾移植受者晚期移植物丢失的主要原因。供体特异性抗体是 AMR 和移植物丢失的独立危险因素。然而,并非所有供体特异性抗体都是致病性的。由于缺乏强有力的临床试验来支持临床决策,AMR 的治疗存在异质性。本综述概述并评论了在管理 AMR 肾移植受者时,医生在实践中遇到的但相关的困境。
有供体特异性抗体的活动性 AMR 可采用血浆置换、静脉注射免疫球蛋白和皮质类固醇治疗,根据具体情况考虑其他治疗方法。相反,没有治疗方法被证明对慢性活动性 AMR 有效。各种生物标志物和预测模型可评估移植物衰竭的个体风险和对排斥反应治疗的反应,显示出前景。
为特定的肾移植受者制定个性化管理方案并确定可改善其长期预后的治疗方法仍然是一个关键的未满足需求。应考虑使用非侵入性生物标志物和预测模型更早地识别 AMR,以评估移植物衰竭的个体风险。强烈鼓励将 AMR 患者纳入临床试验,以评估新的治疗药物。