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用免疫抑制和供体特异性血液对肾移植受者进行预处理。

Pretreatment of renal allograft recipients with immunosuppression and donor-specific blood.

作者信息

Anderson C B, Tyler J D, Sicard G A, Anderman C K, Rodey G E, Etheredge E E

出版信息

Transplantation. 1984 Dec;38(6):664-8. doi: 10.1097/00007890-198412000-00023.

Abstract

The induction of immunologic unresponsiveness to improve renal allograft survival was attempted in 64 patients by the pretransplant administration of donor-specific whole blood or buffy coat in conjunction with continuous azathioprine immunosuppression. All donor/recipient combinations were at least one-haplotype-disparate. Presensitization, defined as a positive Amos or antiglobulin crossmatch or a high-titer (greater than 1:8) B-cell-positive crossmatch, was present in 6 patients and not present in 58 patients. Attempts at desensitization of the already sensitized group were uniformly unsuccessful. Treatment of the 58 nonpresensitized patients resulted in transient sensitization in 2 patients, permanent sensitization in 1 patient, and no evidence of sensitization in 55 patients. Fifty-three patients underwent renal transplantation from the specific blood donor, and only two have experienced renal allograft rejection loss during a mean follow-up period of 22 months (5-45 months); 57% have never experienced a rejection episode. The two-year renal allograft survival rate was 85%. This is significantly (P less than 0.01) better than our historical experience of 64% with one-haplotype living-related transplants. The low rate of sensitization (5%) has permitted almost all patients to undergo eventual renal transplantation from the specific blood donor. This and the low rate of rejection (4%) argues for a modification of the immunologic response, rather than a selecting-out process as the mechanism for improved allograft survival.

摘要

通过移植前给予供者特异性全血或富含白细胞层,并联合持续使用硫唑嘌呤免疫抑制,对64例患者尝试诱导免疫无反应性以提高肾移植存活率。所有供者/受者组合至少有一个单倍型不相配。6例患者存在预致敏,定义为阿莫斯试验或抗球蛋白交叉配型阳性或高滴度(大于1:8)B细胞阳性交叉配型,58例患者不存在预致敏。对已致敏组进行脱敏的尝试均未成功。对58例未预致敏患者的治疗导致2例患者出现短暂致敏,1例患者出现永久致敏,55例患者无致敏证据。53例患者接受了来自特定献血者的肾移植,在平均22个月(5 - 45个月)的随访期内,只有2例经历了肾移植排斥失败;57%的患者从未经历过排斥反应。两年肾移植存活率为85%。这显著(P小于0.01)优于我们单倍型活体亲属移植64%的历史经验。低致敏率(5%)使几乎所有患者最终都能接受来自特定献血者的肾移植。这一点以及低排斥率(4%)表明免疫反应发生了改变,而非筛选过程是移植存活率提高的机制。

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