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ABO 血型不相容的肾移植。

ABO-incompatible kidney transplantation.

机构信息

Division of Urology, Department of Regenerative and Transplant Medicine, Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan.

出版信息

Transplant Rev (Orlando). 2013 Jan;27(1):1-8. doi: 10.1016/j.trre.2012.07.003. Epub 2012 Aug 15.

Abstract

Owing to the shortage of deceased donors in Japan, since 1989, we have performed ABO-incompatible kidney transplantation (ABO-IKTx) to expand the indication for living donor kidney transplantation. During the past two decades, about 2000 ABO-IKTxs were performed. Since 2001 the success rate for these kidney transplants has reached 96% for 1-year, 91% for 5-year and 83% for 9-year graft survival, similar to outcomes of ABO-compatible kidney transplantation (ABO-CKTx). This dramatic improvement in results means that ABO-IKTx has become accepted as a therapeutic alternative for end-stage renal failure. Today ABO-IKTx accounts for approximately 30% of all living donor kidney transplantations performed in Japan. We have been making a lot of efforts to elucidate the mechanism of acute antibody-mediated rejection in ABOI-KTx in order to overcome the ABO barrier and to improve the outcome. From careful and precise clinical observations, proteomic analysis of ABO histo-blood group antigens in graft endothelial cells and deep insight into immunology and biology, we have reached the hypothesis that the structural difference of ABO histo-blood group antigens and de novo corresponding antibody production would be the key and keyhole of the development of acute AMR in ABOI-KTx. Preoperative desensitization therapy would be the best solution for the suppression of acute AMR and graft loss, which is now widespread and improves the outcome.

摘要

由于日本供体短缺,自 1989 年以来,我们已经进行了 ABO 不相容肾移植(ABO-IKTx)以扩大活体供肾移植的适应证。在过去的二十年中,大约进行了 2000 例 ABO-IKTx。自 2001 年以来,这些肾移植的成功率达到了 1 年时 96%、5 年时 91%和 9 年时 83%的移植物存活率,与 ABO 相容肾移植(ABO-CKTx)的结果相似。结果的显著改善意味着 ABO-IKTx 已成为治疗终末期肾衰竭的一种治疗选择。如今,ABO-IKTx 约占日本所有活体供肾移植的 30%。为了克服 ABO 障碍并改善结果,我们一直在努力阐明 ABOI-KTx 中急性抗体介导排斥反应的机制。通过仔细和精确的临床观察、移植内皮细胞中 ABO 组织血型抗原的蛋白质组学分析以及对免疫学和生物学的深入了解,我们提出了这样的假设,即 ABO 组织血型抗原的结构差异和新产生的相应抗体的产生将是 ABOI-KTx 中急性 AMR 发展的关键和关键。术前脱敏治疗将是抑制急性 AMR 和移植物丢失的最佳解决方案,目前已广泛应用并改善了结果。

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