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HLA 不相容的肾移植。

HLA incompatible renal transplantation.

机构信息

Department of Surgery, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA.

出版信息

Curr Opin Organ Transplant. 2012 Aug;17(4):386-92. doi: 10.1097/MOT.0b013e328356132b.

DOI:10.1097/MOT.0b013e328356132b
PMID:22790073
Abstract

PURPOSE OF REVIEW

Human leukocyte antigen (HLA) sensitization is a major public health problem that limits access to renal transplantation for 30% of the patients awaiting a kidney transplant. This review describes the transplantation modalities available to the sensitized patient and discusses aspects of the donor/recipient phenotypes that determine the most suitable option for a particular patient.

RECENT FINDINGS

Patients, who undergo desensitization have a significant survival benefit compared with similar patients, who either remain on dialysis or wait for a compatible donor. The initial donor-specific antibody (DSA) strength is the best predictor of outcome and cost of desensitization. In small, uncontrolled single center trials, complement inhibitors, proteasome inhibitors and anti-CD20 have been used to both prevent and reverse antibody-mediated rejection (AMR).

SUMMARY

With new agents being introduced into the armamentarium, which have not undergone rigorous investigation, it is important to emphasize that plasmapheresis, intravenous immunoglobulin, increased sharing, and kidney-paired donation are very effective strategies for transplanting sensitized patients. However, a significant population of patients will not benefit from either kidney-paired donation or desensitization and will require a hybrid technique in which the goal of matching is to reduce the strength of the DSA to facilitate desensitization.

摘要

目的综述

人类白细胞抗原(HLA)致敏是一个主要的公共卫生问题,限制了 30%等待肾移植患者的移植机会。本篇综述描述了可供致敏患者选择的移植方式,并讨论了决定患者最适合选择的供体/受者表型的各个方面。

最近的发现

与仍在透析或等待匹配供体的相似患者相比,接受脱敏治疗的患者具有显著的生存获益。初始的供体特异性抗体(DSA)强度是预测脱敏治疗效果和成本的最佳指标。在小型、非对照的单中心试验中,补体抑制剂、蛋白酶体抑制剂和抗 CD20 已被用于预防和逆转抗体介导的排斥反应(AMR)。

总结

随着新的治疗药物的出现,尽管这些药物尚未经过严格的研究,但需要强调的是,血浆置换、静脉注射免疫球蛋白、增加共享和肾配对捐赠是移植致敏患者的非常有效的策略。然而,仍有相当一部分患者将不能从肾配对捐赠或脱敏治疗中获益,而需要采用混合技术,其匹配目标是降低 DSA 的强度,以促进脱敏治疗。

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