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晚期心脏移植排斥反应的治疗

The treatment of advanced cardiac allograft rejection.

作者信息

Sweeney M S, Macris M P, Frazier O H, Sinnott J T, Peric M, McAllister H A

机构信息

Division of Surgery, Texas Heart Institute, Houston 77225.

出版信息

Ann Thorac Surg. 1988 Oct;46(4):378-81. doi: 10.1016/s0003-4975(10)64645-0.

Abstract

Severe cardiac allograft rejection remains a serious problem despite the advances of cyclosporine-based immunosuppression. This study analyzes our experience with 202 recipients of cardiac allografts who were treated primarily with cyclosporine and prednisone. Failure of such therapy in 86 patients (43%) resulted in 105 episodes of advanced cardiac allograft rejection as diagnosed by endomyocardial biopsy. Of 101 rejection episodes that were initially treated with intravenous pulse therapy, 48 (48%) were successfully resolved, yet 60% of these successes were associated with major infections. Patients in whom steroid therapy failed or was contra-indicated received intravenous antithymocyte globulin (ATG) or intravenous monoclonal antibody (OKT3). ATG and OKT3 successfully reversed severe rejection in 26 (81%) of 32 and in 13 (93%) of 14 episodes, respectively. Infectious complication rates were 54% and 21%, respectively. Because the majority (87%) of these rejection episodes occurred within the first 30 days after treatment, many of them may have resulted from inadequate immunosuppressive induction therapy. Based on our results, we believe that advanced cardiac allograft rejection may be managed best by individualizing immunosuppressive therapy, thus enhancing prevention, and by adding OKT3 to the regimen when rejection occurs.

摘要

尽管基于环孢素的免疫抑制疗法取得了进展,但严重的心脏移植排斥反应仍然是一个严重的问题。本研究分析了我们对202例心脏移植受者的治疗经验,这些受者主要接受环孢素和泼尼松治疗。86例患者(43%)的这种治疗失败,导致通过心内膜心肌活检诊断出105次晚期心脏移植排斥反应发作。在最初接受静脉脉冲治疗的101次排斥反应发作中,48次(48%)成功缓解,但这些成功案例中有60%与严重感染有关。类固醇治疗失败或有禁忌证的患者接受了静脉注射抗胸腺细胞球蛋白(ATG)或静脉注射单克隆抗体(OKT3)。ATG和OKT3分别在32次发作中的26次(81%)和14次发作中的13次(93%)成功逆转了严重排斥反应。感染并发症发生率分别为54%和21%。由于这些排斥反应发作的大多数(87%)发生在治疗后的前30天内,其中许多可能是由于免疫抑制诱导治疗不足所致。基于我们的结果,我们认为晚期心脏移植排斥反应可能通过个体化免疫抑制疗法得到最佳管理,从而加强预防,并在发生排斥反应时在治疗方案中添加OKT3。

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