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他克莫司治疗肺移植后持续性或复发性急性排斥反应。

Tacrolimus therapy for persistent or recurrent acute rejection after lung transplantation.

作者信息

Horning N R, Lynch J P, Sundaresan S R, Patterson G A, Trulock E P

机构信息

Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

J Heart Lung Transplant. 1998 Aug;17(8):761-7.

PMID:9730424
Abstract

BACKGROUND

Because the severity, frequency, and duration of acute rejection have been linked to the risk of chronic allograft rejection, controlling persistent or recurrent acute rejection is paramount. Tacrolimus has been effective in the management of recalcitrant rejection in other solid organ transplants, and the initial experience in lung transplantation has been favorable. In this study, the impact of changing from a cyclosporine-based to a tacrolimus-based immunosuppressive regimen in lung transplant recipients with persistent or recurrent acute rejection was analyzed.

METHODS

The incidence and severity of acute rejection were retrospectively analyzed in 14 lung transplant recipients who were switched from cyclosporine to tacrolimus maintenance immunosuppression because of persistent or recurrent, biopsy-proven acute rejection.

RESULTS

Recipients had been treated for acute rejection an average of 2.6 times before changing from cyclosporine to tacrolimus, and 3 recipients had a course of OKT3 therapy. Tacrolimus therapy was begun 238+/-180 days after transplantation, and the mean follow-up period on tacrolimus treatment was 330+/-201 days. After the changeover from cyclosporine to tacrolimus, the number of episodes of acute rejection per recipient decreased (4.3+/-2.1 to 0.4+/-0.5; p=.0001), the average histologic grade of rejection receded (1.3+/-0.4 to 0.3+/-0.4; p=.0001), and the incidence of acute rejection declined (2.4+/-1.5 to 0.1+/-0.3 episodes per 100 patient-days; p=.0001).

CONCLUSIONS

Conversion from a cyclosporine- to a tacrolimus-based maintenance immunosuppressive regimen is an effective approach for managing persistent or recurrent allograft rejection after lung transplantation.

摘要

背景

由于急性排斥反应的严重程度、发生频率和持续时间与慢性移植物排斥反应的风险相关,控制持续性或复发性急性排斥反应至关重要。他克莫司在其他实体器官移植中治疗顽固性排斥反应有效,在肺移植中的初步经验也很乐观。本研究分析了肺移植受者从基于环孢素的免疫抑制方案转换为基于他克莫司的免疫抑制方案对持续性或复发性急性排斥反应的影响。

方法

回顾性分析14例因持续性或复发性、经活检证实的急性排斥反应而从环孢素转换为他克莫司维持免疫抑制治疗的肺移植受者急性排斥反应的发生率和严重程度。

结果

受者在从环孢素转换为他克莫司之前平均接受了2.6次急性排斥反应治疗,3例受者接受了OKT3治疗疗程。他克莫司治疗在移植后238±180天开始,他克莫司治疗的平均随访期为330±201天。从环孢素转换为他克莫司后,每位受者的急性排斥反应发作次数减少(4.3±2.1至0.4±0.5;p = 0.0001),平均排斥反应组织学分级降低(1.3±0.4至0.3±0.4;p = 0.0001),急性排斥反应发生率下降(每100患者日2.4±1.5至0.1±0.3次发作;p = 0.0001)。

结论

从基于环孢素的维持免疫抑制方案转换为基于他克莫司的方案是治疗肺移植后持续性或复发性移植物排斥反应的有效方法。

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