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心脏移植血管病变:当前概念与治疗

Cardiac allograft vasculopathy: current concepts and treatment.

作者信息

Waller Julian, Brook Nicholas R, Nicholson Michael L

机构信息

Division of Transplant Surgery, Professorial Unit, Leicester General Hospital, Leicester, Leicestershire, UK.

出版信息

Transpl Int. 2003 Jun;16(6):367-75. doi: 10.1007/s00147-003-0580-8. Epub 2003 May 17.

Abstract

Cardiac allograft vasculopathy (CAV) remains the leading limiting factor of patient and graft survival after the first post-operative year. The pathogenesis involves both immunological and non-immunological factors. Here, we present recent advances and discuss potential preventative and treatment regimens. A review of the current literature of heart transplantation, detailing molecular mechanisms, pharmacological risk factors and novel immunosuppression regimens was performed. Recent findings demonstrate the pivotal role of the endothelium, resulting in release of pro-fibrotic cytokines, recruitment of circulating leucocytes, proliferation of vascular smooth muscle cells, and deposition of extracellular matrix proteins (ECMs). The role of HMG-CoA reductase inhibitors and anti-hypertensives remains controversial, but there is increasing evidence advocating their prophylactic use. We can conclude that novel immunosuppressive agents such as rapamycin, mycophenolate mofetil and FTY-720 are experimental immunosuppressive agents that are undergoing evaluation in clinical trials. The prophylactic use of statins and anti-hypertensive drugs needs to be defined but needs to suggest potential strategies to prolong cardiac allograft survival.

摘要

心脏移植血管病变(CAV)仍然是术后第一年之后影响患者和移植物存活的主要限制因素。其发病机制涉及免疫和非免疫因素。在此,我们介绍近期进展并讨论潜在的预防和治疗方案。我们对当前心脏移植文献进行了综述,详细阐述了分子机制、药理学危险因素和新型免疫抑制方案。近期研究结果表明内皮细胞起关键作用,可导致促纤维化细胞因子释放、循环白细胞募集、血管平滑肌细胞增殖以及细胞外基质蛋白(ECM)沉积。HMG-CoA还原酶抑制剂和抗高血压药物的作用仍存在争议,但越来越多的证据支持预防性使用它们。我们可以得出结论,新型免疫抑制剂如雷帕霉素、霉酚酸酯和FTY-720是正在临床试验中接受评估的实验性免疫抑制剂。他汀类药物和抗高血压药物的预防性使用需要进一步明确,但需要提出延长心脏移植物存活的潜在策略。

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