Mueller Xavier M
Department of Cardiovascular Surgery, Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke, Quebec, Canada.
Ann Thorac Surg. 2004 Jan;77(1):354-62. doi: 10.1016/j.athoracsur.2003.07.006.
In the early days of transplantation, immunosuppression therapy was rather broad and nonspecific, mainly using high-dose corticosteroids and azathioprine. Thereafter we progressively narrowed the target of immunosuppressive strategy starting with polyclonal antibodies. The introduction of cyclosporine, OKT3, and tacrolimus further narrowed the target on the T-cell pathways. More recently mycophenolate mofetil progressively took the place of azathioprine with its higher lymphocyte specificity and sirolimus and interleukin-2 receptor antibodies were introduced. In this field in constant movement the aim is to find a drug or a regimen that provides optimal immunosuppression therapy with minimal side effects, in other words to find the right balance between overimmunosuppression and underimmunosuppression therapy. This review is divided into two parts. The first part will provide a basic understanding of the immunologic response to allograft and explain how conventional and recently introduced immunosuppressive agents work. The second part will describe the clinical application of immunosuppressive drugs to provide practical information for those in charge of heart transplant recipients.
在移植早期,免疫抑制治疗相当宽泛且缺乏特异性,主要使用大剂量皮质类固醇和硫唑嘌呤。此后,我们从多克隆抗体开始逐步缩小免疫抑制策略的靶点。环孢素、OKT3和他克莫司的引入进一步将靶点缩小到T细胞途径。最近,霉酚酸酯因其更高的淋巴细胞特异性逐渐取代了硫唑嘌呤,并且引入了西罗莫司和白细胞介素-2受体抗体。在这个不断发展的领域中,目标是找到一种药物或方案,以最小的副作用提供最佳的免疫抑制治疗,换句话说,就是在过度免疫抑制和免疫抑制不足之间找到正确的平衡。本综述分为两部分。第一部分将提供对同种异体移植免疫反应的基本理解,并解释传统和最近引入的免疫抑制剂的作用机制。第二部分将描述免疫抑制药物的临床应用,为负责心脏移植受者的人员提供实用信息。