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钙调磷酸酶抑制剂在 HIV 患者肾移植前的剂量探索。

Calcineurin inhibitor dose-finding before kidney transplantation in HIV patients.

机构信息

Division of Nephrology, Medizinische Klinik und Poliklinik IV, Ludwig-Maximilians-University, Munich, Germany.

出版信息

Transpl Int. 2013 Mar;26(3):254-8. doi: 10.1111/tri.12020. Epub 2012 Dec 10.

DOI:10.1111/tri.12020
PMID:23227980
Abstract

Kidney transplantation in HIV-infected patients is associated with a higher rate of graft rejection as well as an increased toxicity of the immunosuppressive therapy. Specifically, the use of the calcineurin inhibitor tacrolimus is problematic because of a narrow therapeutic range, a high interindividual variability of trough levels, and multiple interactions with combination antiretroviral therapy (cART). Our objective was to establish the optimal individual immunosuppressive dose for the time after kidney transplantation. We administered a temporary course of immunosuppressive therapy in three HIV-infected patients with end-stage renal disease (ESRD) after wait-listing and prior to transplantation for deceased donor kidney transplantation. Starting with a tacrolimus dose of 1 mg twice daily, the dose was titrated to reach a tacrolimus trough level of 8-12 ng/ml. HIV had been diagnosed 7-14 years prior. All patients had no detectable HIV-1 RNA while on cART. All three patients had been on chronic dialysis for 4, 7, and 10 years. In two patients, the intended tacrolimus trough levels of 8-12 ng/ml were achieved within a month. The required tacrolimus dose ranged from 0.5 mg thrice weekly to 10 mg daily. In one case, ventricular tachycardia occurred, so the immunosuppressive therapy was switched to cyclosporine A. So far, two patients have been transplanted successfully. In summary, dose-finding of immunosuppressive therapy with tacrolimus in patients on cART before renal transplantation is feasible and appears useful to minimize immunosuppressive therapy-related complications in the post-transplantation period.

摘要

肾移植在 HIV 感染患者中与更高的移植物排斥率以及免疫抑制治疗的毒性增加有关。具体而言,由于治疗窗狭窄、谷浓度个体间变异性高以及与联合抗逆转录病毒治疗(cART)的多种相互作用,钙调磷酸酶抑制剂他克莫司的使用存在问题。我们的目标是确定肾移植后时间内的最佳个体免疫抑制剂量。我们对 3 名等待名单上的终末期肾病(ESRD)HIV 感染患者进行了临时免疫抑制治疗,然后进行了死亡供体肾移植。起始剂量为他克莫司每日两次,1 毫克,然后滴定剂量以达到他克莫司谷浓度 8-12ng/ml。HIV 诊断时间为 7-14 年前。所有患者在 cART 期间均未检测到 HIV-1 RNA。所有 3 名患者均已进行慢性透析 4、7 和 10 年。在 2 名患者中,在一个月内达到了预期的他克莫司谷浓度 8-12ng/ml。所需的他克莫司剂量范围为每周 3 次 0.5 毫克至每日 10 毫克。在一个病例中,发生了室性心动过速,因此将免疫抑制治疗转换为环孢素 A。迄今为止,已有 2 名患者成功移植。总之,在肾移植前 cART 患者中使用他克莫司进行免疫抑制治疗的剂量确定是可行的,并且似乎有助于最大限度地减少移植后免疫抑制治疗相关并发症。

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