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免疫抑制的未来发展方向。

Future directions in immunosuppression.

作者信息

Beckebaum S, Cicinnati V R, Broelsch C E

机构信息

Department of General and Transplant Surgery, University Hospital Essen, Essen, Germany.

出版信息

Transplant Proc. 2004 Mar;36(2 Suppl):574S-576S. doi: 10.1016/j.transproceed.2004.01.044.

Abstract

As liver transplantation is now being performed with an excellent 5-year survival rate of approximately 70% at selected centers, attention has been shifted to reduce long-term complications of calcineurin inhibitors including diabetes, hypertension, and hyperlipidemia, which have a major effect on morbidity and mortality within the transplant setting. Cyclosporine (CsA) monitoring has been performed traditionally by measurement of predose "trough" blood concentrations (C0). Recent development of 2 hour postdose CsA (C2) monitoring strategy has emerged as a much more sensitive approach for assessing the pharmacokinetics and providing greater precision in the optimization of Neoral dosing than C0 measurements. Furthermore, a reduction of risk factors for atherosclerotic vascular disease and in the incidence and severity of acute cellular rejection have been associated with the adoption of C2 monitoring. However, further data from multicenter trials are required to evaluate the long-term benefits of this new therapeutic monitoring strategy.

摘要

由于目前在选定的中心进行肝移植的5年生存率约为70%,效果良好,因此人们的注意力已转向减少钙调神经磷酸酶抑制剂的长期并发症,包括糖尿病、高血压和高脂血症,这些并发症对移植患者的发病率和死亡率有重大影响。传统上,通过测量给药前的“谷值”血药浓度(C0)来监测环孢素(CsA)。最近出现的给药后2小时CsA(C2)监测策略,是一种比C0测量更敏感的评估药代动力学的方法,并且在优化新山地明剂量方面能提供更高的精确度。此外,采用C2监测与降低动脉粥样硬化性血管疾病的危险因素以及急性细胞排斥反应的发生率和严重程度有关。然而,需要多中心试验的进一步数据来评估这种新的治疗监测策略的长期益处。

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