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在交叉配型阳性、经二硫苏糖醇处理后血清阴性的受者中成功进行肾移植。种族、移植史和HLA - DR1表型。

Successful renal allografts in recipients with crossmatch-positive, dithioerythritol-treated negative sera. Race, transplant history, and HLA-DR1 phenotype.

作者信息

Barger B, Shroyer T W, Hudson S L, Deierhoi M H, Barber W H, Curtis J J, Julian B A, Luke R G, Diethelm A G

机构信息

Department of Surgery/Histocompatibility Laboratory, University of Alabama, Birmingham 35233.

出版信息

Transplantation. 1989 Feb;47(2):240-5. doi: 10.1097/00007890-198902000-00008.

Abstract

Graft survival was examined in 15 renal allograft recipients from a group of 20 patients with IgM autolymphocytotoxic antibody that could be removed in a crossmatch assay using a reducing agent, dithioerythritol (DTE). The significant differences in this group of 20 patients compared with end-stage renal disease (ESRD) patients lacking autolymphocytotoxic antibodies included an increased frequency of black patients (P = 0.002), a lack of previous transplants (P = 0.003), and an increased frequency of the HLA-DR1 phenotype (P = 0.0001). Sex and the number of transfusions did not appear significant, whereas the cause of ESRD was primarily systemic lupus erythematosus. Fifteen of the 20 patients were transplanted against a positive donor crossmatch. Eleven were recipients of cadaveric kidneys, nine of which are still functioning for periods ranging from 0.5 to 40 months. Two fo the cadaveric recipients died with functional grafts. Four received living-related donor transplants, one of which was lost to acute rejection one month posttransplant, while the remaining three have survived 1.5, 9, and 21 months, respectively. Fourteen patients had immediate allograft function with no hyperacute rejection and only one case of acute tubular necrosis (ATN) was found. In summary, a negative crossmatch using DTE-treated, autologous reactive recipient sera may identify a group of patients who can be transplanted with minimal concern for hyperacute rejection or ATN. In addition to cause of ESRD, race, transplant history, and HLA-DR phenotype may further define this group of transplant candidates having IgM autolymphocytotoxic antibody. Extrapolation of these conclusions to transplant candidates lacking autolymphocytotoxic antibodies is not warranted.

摘要

在一组20例患有IgM自身淋巴细胞毒性抗体的患者中,对15例肾移植受者的移植物存活情况进行了检查。这些抗体在使用还原剂二硫苏糖醇(DTE)的交叉配型试验中可被清除。与缺乏自身淋巴细胞毒性抗体的终末期肾病(ESRD)患者相比,这20例患者的显著差异包括黑人患者频率增加(P = 0.002)、既往无移植史(P = 0.003)以及HLA - DR1表型频率增加(P = 0.0001)。性别和输血次数似乎无显著差异,而ESRD的主要病因是系统性红斑狼疮。20例患者中有15例在供者交叉配型阳性的情况下进行了移植。11例接受了尸体肾移植,其中9例仍在发挥功能,时间从0.5个月至40个月不等。2例尸体肾移植受者在移植物仍有功能时死亡。4例接受了亲属活体供肾移植,其中1例在移植后1个月因急性排斥反应移植失败,其余3例分别存活了1.5个月、9个月和21个月。14例患者移植后立即具备移植物功能,无超急性排斥反应,仅发现1例急性肾小管坏死(ATN)。总之,使用DTE处理的自身反应性受者血清进行阴性交叉配型,可能识别出一组患者,他们在移植时对超急性排斥反应或ATN的担忧最小。除了ESRD的病因外,种族、移植史和HLA - DR表型可能进一步界定这组患有IgM自身淋巴细胞毒性抗体的移植候选者。将这些结论外推至缺乏自身淋巴细胞毒性抗体的移植候选者是不合理的。

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