Mankidy Babith, Kesavan Ramesh B, Silay Yavuz S, Haddad Tarik J, Seethamraju Harish
Baylor College of Medicine, Department of Medicine, Pulmonary and Critical Care, Lung transplant program, Houston, Texas, USA.
Expert Opin Emerg Drugs. 2007 Mar;12(1):61-73. doi: 10.1517/14728214.12.1.61.
The balance between immunosuppression to ensure graft tolerance while preventing emergence of infectious complications is key in lung transplantation. Although opportunistic infection may appear to be the most important of these complications, malignancies and severe drug toxicities significantly affect the short- and long-term outcomes of the patients. The present practice is combination therapy using drugs with complementary immunosuppressive action, to achieve synergistic immunosuppression with the lowest possible toxicity. Components of immunosuppression include induction and maintenance regimens. Primary graft failure remains an important cause of mortality and morbidity in the immediate post-transplant period. Acute rejection is a common complication after lung transplant, but responds well to augmented immunosuppression and immunomodulation. Chronic rejection still is the major cause of mortality in patients who survive the initial year post-transplantation. Several new drugs have shown promise in decreasing the rate of loss of graft function. This review discusses the current and emerging therapeutic regimens.
在肺移植中,关键在于平衡免疫抑制以确保移植物耐受,同时预防感染性并发症的出现。尽管机会性感染似乎是这些并发症中最重要的,但恶性肿瘤和严重的药物毒性会显著影响患者的短期和长期预后。目前的做法是使用具有互补免疫抑制作用的药物进行联合治疗,以在尽可能低的毒性下实现协同免疫抑制。免疫抑制的组成部分包括诱导和维持方案。原发性移植物功能衰竭仍然是移植后即刻死亡率和发病率的重要原因。急性排斥是肺移植后的常见并发症,但对强化免疫抑制和免疫调节反应良好。慢性排斥仍然是移植后第一年存活患者死亡的主要原因。几种新药在降低移植物功能丧失率方面显示出前景。本综述讨论了当前和新兴的治疗方案。