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基线抗血型抗体滴度及其对脱敏和肾移植的反应。

Baseline Anti-blood Group Antibody Titers and their Response to Desensitization and Kidney Transplantation.

作者信息

Shah B V, Rajput P, Virani Z A, Warghade S

机构信息

Institute of Renal Sciences, Global Hospitals, Mumbai, Maharashtra, India.

Department of Haematopathology, Metropolis Healthcare Ltd., Mumbai, Maharashtra, India.

出版信息

Indian J Nephrol. 2017 May-Jun;27(3):195-198. doi: 10.4103/0971-4065.202402.

Abstract

In recent years, immunological barriers historically considered as absolute contraindications to transplantation are being reevaluated. One such barrier is the ABO blood group incompatibility. With better understanding of immunological mechanisms and effective various regimens for controlling it, ABO-incompatible (ABO-I) kidney transplantation is now being performed with increasing frequency. For good outcome, most important is to achieve and maintain low anti-blood group antibody titers (ABGATs). Twenty-two patients with ABO-I donors have been studied. The anti-A and anti-B antibody titers (IgG and IgM) were estimated by column agglutination technology using Automated Ortho BioVue System. For desensitization, pretransplant plasmapheresis and/or immunoadsorption and rituximab were used. ABGAT was determined before transplant and periodically after transplant. It was observed that one-third of the patients have low baseline ABGAT. In these cases with low ABGAT, transplant can be performed without any desensitization. In those with titers <1:256, rituximab (two doses of 200 mg weekly) and 3-6 sessions of plasmapheresis can bring down titers to <1:32. In those with titers >1:256, immunoadsorption may be used from the beginning to reduce ABGAT. After transplant, the titers drop to <1:8 in majority. Rise in titers to >1:64 require close observation and biopsy. If there is evidence of antibody-mediated rejection, treatment should be promptly started. Rise in titers 4-6 weeks after transplant is not associated with any graft dysfunction, and hence not of any clinical significance.

摘要

近年来,一些历史上被视为移植绝对禁忌的免疫屏障正在重新评估。ABO血型不相容就是这样一种屏障。随着对免疫机制的更好理解以及控制它的各种有效方案的出现,ABO不相容(ABO-I)肾移植目前的开展频率越来越高。为了获得良好的结果,最重要的是实现并维持低抗血型抗体滴度(ABGATs)。对22例ABO-I供体的患者进行了研究。使用自动化奥森BioVue系统,通过柱凝集技术估计抗A和抗B抗体滴度(IgG和IgM)。为了进行脱敏,采用了移植前血浆置换和/或免疫吸附以及利妥昔单抗。在移植前和移植后定期测定ABGAT。观察到三分之一的患者基线ABGAT较低。在这些ABGAT较低的病例中,可以在不进行任何脱敏的情况下进行移植。在滴度<1:256的患者中,利妥昔单抗(每周两剂200mg)和3 - 6次血浆置换可将滴度降至<1:32。在滴度>1:256的患者中,可从一开始就使用免疫吸附来降低ABGAT。移植后,大多数患者的滴度降至<1:8。滴度升至>1:64需要密切观察并进行活检。如果有抗体介导的排斥反应的证据,应立即开始治疗。移植后4 - 6周滴度升高与任何移植功能障碍无关,因此不具有任何临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ffb/5434685/5f1e5ddabecd/IJN-27-195-g001.jpg

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