Division of Nephrology and Dialysis, Department of Internal Medicine III, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Section of Transplantation Immunology, Department of Surgery, Medical University of Vienna, Währinger Gürtel 18-20, 1090 Vienna, Austria.
Nat Rev Nephrol. 2015 Dec;11(12):732-47. doi: 10.1038/nrneph.2015.144. Epub 2015 Sep 1.
Kidney transplantation across the ABO blood group barrier was long considered a contraindication for transplantation, but in an effort to increase donor pools, specific regimens for ABO-incompatible (ABOi) transplantation have been developed. These regimens are now widely used as an integral part of the available treatment options. Various desensitization protocols, commonly based on transient depletion of preformed anti-A and/or anti-B antibodies and modulation of B-cell immunity, enable excellent transplant outcomes, even in the long-term. Nevertheless, the molecular mechanisms behind transplant acceptance facilitated by a short course of anti-humoral treatment are still incompletely understood. With the evolution of efficient clinical programmes, tailoring of recipient preconditioning based on individual donor-recipient blood type combinations and the levels of pretransplant anti-A/B antibodies has become possible. In the context of low antibody titres and/or donor A2 phenotype, immunomodulation and/or apheresis might be dispensable. A concern still exists, however, that ABOi kidney transplantation is associated with an increased risk of surgical and infectious complications, partly owing to the effects of extracorporeal treatment and intensified immunosuppression. Nevertheless, a continuous improvement in desensitization strategies, with the aim of minimizing the immunosuppressive burden, might pave the way to clinical outcomes that are comparable to those achieved in ABO-compatible transplantation.
将 ABO 血型不相容的肾脏移植用于临床曾被认为是一种禁忌,但为了增加供体库,已经开发出了针对 ABO 血型不相容(ABOi)移植的特定方案。这些方案现在已被广泛用作现有治疗方案的重要组成部分。各种脱敏方案通常基于短暂耗尽预先形成的抗-A 和/或抗-B 抗体以及调节 B 细胞免疫,即使在长期内,也能实现出色的移植效果。然而,通过短期抗体液治疗促进移植接受的分子机制仍不完全清楚。随着高效临床方案的发展,基于供体-受者血型组合和移植前抗-A/B 抗体水平对受者预处理进行个体化定制已成为可能。在低抗体滴度和/或供体 A2 表型的情况下,免疫调节和/或血浆置换可能是不必要的。然而,人们仍然担心 ABOi 肾脏移植与手术和感染并发症的风险增加有关,部分原因是体外治疗和强化免疫抑制的影响。尽管如此,不断改进脱敏策略,旨在最小化免疫抑制负担,可能为临床结果铺平道路,使其与 ABO 血型相容移植相当。