Moudgil Asha, Puliyanda Dechu
Department of Nephrology, Children's National Medical Center, Washington, District of Columbia 20010, USA.
Paediatr Drugs. 2007;9(5):323-41. doi: 10.2165/00148581-200709050-00005.
Induction therapy to prevent the acute rejection of mismatched allografts with the ultimate aim of prolonging the life of the allograft has been the cornerstone of immunosuppression since the introduction of renal transplantation. Agents used for induction therapy have changed over time. Their role in transplantation is expanding to include corticosteroid avoidance and immunosuppression minimization. This review provides an overview of induction therapies for renal transplantation including historic therapies such as total lymphoid irradiation and Minnesota antilymphocyte globulin, and current therapies with polyclonal and monoclonal antibodies and chemical agents, with special emphasis on children. Data from adult studies, and pediatric studies whenever available, are summarized. A brief summary of experimental therapies with fingolimod and belatacept is provided. Historically, induction therapies were targeted at T cells. The role of induction therapies targeted at B cells is emerging in select groups of patients that include highly sensitized recipients and those receiving transplants from blood group incompatible donors. With the advent of newer maintenance immunosuppressive medications and with very low rates of acute rejection, induction protocols for renal transplantation need to be targeted so that excessive immunosuppression and infections are avoided. Several single-center and registry data analyses in children suggest that the addition of an interleukin (IL)-2 receptor antagonist may improve graft survival compared with no induction. The safety profile of IL-2 receptor antagonists is indistinguishable from that of placebo, with no apparent difference in the incidence of infection or post-transplant lymphoproliferative disease. IL-2 receptor antagonists and polyclonal lymphocyte-depleting antibodies offer equivalent efficacy in standard-risk populations. However, in high-risk patients, acute rejection rates and graft outcomes may be improved with the use of lymphocyte-depleting agents such as Thymoglobulin. However, cytomegalovirus infection and other infections may be more common with this therapy. Therefore, in patients at high risk of graft loss, Thymoglobulin may be the preferred choice for induction therapy, while for all other patients, IL-2 receptor antagonists should be considered the first-line choice for induction therapy. Newer lymphocyte-depleting agents such as alemtuzumab may be better utilized in minimization regimens involving one or two oral maintenance immunosuppressive agents.
自肾移植开展以来,诱导治疗一直是免疫抑制的基石,其目的是预防不匹配同种异体移植物的急性排斥反应,最终延长移植物的存活时间。用于诱导治疗的药物随着时间推移而发生了变化。它们在移植中的作用正在扩大,包括避免使用皮质类固醇以及尽量减少免疫抑制。本综述概述了肾移植的诱导治疗方法,包括诸如全身淋巴照射和明尼苏达抗淋巴细胞球蛋白等传统疗法,以及目前使用多克隆和单克隆抗体及化学药物的疗法,特别强调了儿童患者。总结了来自成人研究以及在可得情况下的儿科研究的数据。还简要介绍了用芬戈莫德和贝拉西普进行的实验性治疗。从历史上看,诱导治疗主要针对T细胞。针对B细胞的诱导治疗作用正在一些特定患者群体中显现出来,这些患者群体包括高度致敏受者以及接受来自血型不相合供体移植的患者。随着更新的维持性免疫抑制药物的出现以及急性排斥反应发生率极低,肾移植的诱导方案需要有针对性,以避免过度免疫抑制和感染。几项针对儿童的单中心和登记数据分析表明,与不进行诱导治疗相比,添加白细胞介素(IL)-2受体拮抗剂可能会提高移植物存活率。IL-2受体拮抗剂的安全性与安慰剂无异,在感染或移植后淋巴细胞增生性疾病的发生率上没有明显差异。在标准风险人群中,IL-2受体拮抗剂和多克隆淋巴细胞清除抗体具有同等疗效。然而,在高危患者中,使用诸如抗胸腺细胞球蛋白等淋巴细胞清除剂可能会改善急性排斥反应发生率和移植物结局。然而,这种治疗方法可能会使巨细胞病毒感染和其他感染更为常见。因此,对于有高移植失败风险的患者,抗胸腺细胞球蛋白可能是诱导治疗的首选,而对于所有其他患者,IL-2受体拮抗剂应被视为诱导治疗的一线选择。诸如阿仑单抗等更新的淋巴细胞清除剂可能更适合用于涉及一种或两种口服维持性免疫抑制药物的最小化方案。