Fung John, Kelly Dympna, Kadry Zakiyah, Patel-Tom Kusum, Eghtesad Bijan
Thomas E. Starzl Transplantation Institute, Department of Surgery, University of Pittsburgh, 3459 Fifth Avenue, N755 MUH, Pittsburgh, PA 15213, USA.
Liver Transpl. 2005 Mar;11(3):267-80. doi: 10.1002/lt.20373.
Although calcineurin inhibitors (CNIs) remain the mainstay of immunosuppression in liver transplantation (LTX), their long-term toxicity significantly contributes to morbidity and mortality. The elucidation of mechanisms of alloimmunity and leukocyte migration have provided novel targets for immunosuppression development. The toxicities of these agents differ from that of the CNI and act additively or synergistically. CNI avoidance protocols in LTX have not been achieved routinely; however, pilot trials have begun to delineate the limitations and promises of such approaches. CNI-sparing protocols appear to be much more promising in balancing the early need for minimizing rejection while tapering doses and minimizing long-term toxicity.
尽管钙调神经磷酸酶抑制剂(CNIs)仍是肝移植(LTX)免疫抑制的主要药物,但其长期毒性显著导致了发病率和死亡率。对同种免疫和白细胞迁移机制的阐明为免疫抑制药物的研发提供了新靶点。这些药物的毒性与CNIs不同,具有相加或协同作用。肝移植中常规避免使用CNI的方案尚未实现;然而,试点试验已开始明确此类方法的局限性和前景。在平衡早期尽量减少排斥反应的需求、逐渐减少剂量并将长期毒性降至最低方面,避免使用CNI的方案似乎更具前景。