Costanzo Maria Rosa
Department of Medicine, Rush Medical College, Chicago, Illinois, USA.
Curr Control Trials Cardiovasc Med. 2001;2(1):45-53. doi: 10.1186/cvm-2-1-045.
Only a few randomized clinical trials have been performed so far in heart transplant recipients, mainly because of the relatively small number of heart transplants performed worldwide each year. The main focus of the few controlled trials that have been completed has been the prevention and treatment of heart allograft rejection. In the area of pharmacologic immunosuppression, both biological agents and drugs have been the subject of investigation. Among the biological agents, chimeric monoclonal antibodies directed against the interleukin (IL)-2 receptor, which have been found to be safe and effective in renal transplant recipients, are now undergoing the test of controlled trials in heart transplant recipients. Immunosuppressive drugs that have been studied in controlled trials include calcineurin inhibitors (such as the microemulsion formulation of cyclosporine and tacrolimus) and inhibitors of purine synthesis, such as mycophenolate mofetil. Non-pharmacologic prophylactic immunosuppression with photopheresis has also been tested in a prospective, multicenter, randomized trial. New immunosuppressive regimens, such as mycophenolate mofetil combined with a monoclonal antibody against the IL-2 receptor, are being tested with the aim to reduce or eliminate calcineurin inhibitors or corticosteroids. Although clinical approaches to the induction of tolerance have undergone preliminary clinical evaluation, the ability to induce tolerance to an allograft in humans remains an elusive goal.
到目前为止,针对心脏移植受者仅开展了少数随机临床试验,主要原因是全球每年进行的心脏移植数量相对较少。已完成的少数对照试验的主要重点是心脏移植排斥反应的预防和治疗。在免疫抑制药物领域,生物制剂和药物均已成为研究对象。在生物制剂中,针对白细胞介素(IL)-2受体的嵌合单克隆抗体在肾移植受者中已被证明安全有效,目前正在心脏移植受者中进行对照试验测试。在对照试验中研究过的免疫抑制药物包括钙调神经磷酸酶抑制剂(如环孢素微乳剂和他克莫司)以及嘌呤合成抑制剂,如霉酚酸酯。光分离置换法的非药物预防性免疫抑制也已在一项前瞻性、多中心、随机试验中进行了测试。新的免疫抑制方案,如霉酚酸酯与抗IL-2受体单克隆抗体联合使用,正在进行测试,目的是减少或消除钙调神经磷酸酶抑制剂或皮质类固醇。尽管诱导免疫耐受的临床方法已进行了初步临床评估,但在人类中诱导对移植器官的免疫耐受能力仍然是一个难以实现的目标。