Incidence and hazards of alloantibodies in renal transplantation.

Clinical transplants Pub Date : 2013-01-01
Matthew J Everly
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引用次数: 0

Abstract

In the last 10 years, many reports on the impact of antibodies against human leukocyte antigens (HLA) have been published. Now, in 2014, the overwhelming consensus is that antibodies cause allograft failure. Based on reports from East Carolina University, we now know that approximately 10% of patients will develop de novo donor specific anti-HLA antibodies (DSA) by 1-year post-transplant. Within 5 years, 20% of all transplanted patients will have de novo DSA. In those who develop de novo DSA, allograft failure rates are significantly higher than that of patients who do not develop DSA. By 1-year post-DSA appearance, 9% of patients' allografts will fail. By 3-years post-DSA appearance, 24% of patients' allografts will fail. In 2014, with estimates of incidence and risk defined for de novo DSA in renal transplantation, the focus is now on how to treat DSA. Currently, the options are limited. Future trials to investigate regimens that can durably remove de novo DSA and protect the allograft from antibody mediated damage are needed.

肾移植中同种异体抗体的发生率和危害。
在过去的十年中,许多关于抗人类白细胞抗原(HLA)抗体影响的报告已经发表。现在,在2014年,压倒性的共识是抗体会导致同种异体移植失败。根据东卡罗莱纳大学的报告,我们现在知道大约10%的患者在移植后1年内会产生供体特异性hla抗体(DSA)。在5年内,20%的移植患者将重新发生DSA。在那些新发DSA的患者中,同种异体移植失败率明显高于未发生DSA的患者。在dsa出现后1年,9%的患者同种异体移植物会失败。dsa出现3年后,24%的患者同种异体移植物会失败。2014年,随着肾移植中新生DSA的发生率和风险的估计,现在的重点是如何治疗DSA。目前,选择是有限的。未来的试验需要研究能够持久地去除新生DSA并保护同种异体移植物免受抗体介导的损伤的方案。
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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