Vincenti Flavio
University of California, San Francisco, Calif., USA.
Contrib Nephrol. 2005;146:22-29. doi: 10.1159/000082058.
Induction therapy with biological agents was introduced the in the 1970s and the rationale, concepts and approach have remained almost unchanged for 30 years. However, the novel biological agents being developed for induction therapy are being designed for chronic rather than short-term therapy with several objectives: reduce dependence on toxic and nephrotoxic agents, improve outcome and ultimately facilitate the emergence of tolerance. The biological agents include efalizumab, a humanized anti-CD11a (anti-LFA1), anti- CD154, anti-CD40, a number of agents targeting IL-15 and its receptor, and costimulation blockade with humanized antibodies to CD80/CD86 and the fusion receptor protein LEA29Y, a second generation CTLA4Ig. The past decade has witnessed an unprecedented number of small molecules/oral drugs that have been developed and approved for renal transplantation; the next decade, however, may witness the emergence of a new class of biological induction agents that may displace some of the currently used drugs.
生物制剂诱导疗法于20世纪70年代引入,其基本原理、概念和方法在30年里几乎没有变化。然而,正在研发用于诱导疗法的新型生物制剂是为慢性治疗而非短期治疗设计的,有几个目标:减少对有毒和肾毒性药物的依赖,改善治疗结果并最终促进耐受性的出现。生物制剂包括依法利珠单抗,一种人源化抗CD11a(抗LFA1)、抗CD154、抗CD40,多种靶向IL-15及其受体的药物,以及用针对CD80/CD86的人源化抗体和融合受体蛋白LEA29Y(第二代CTLA4Ig)进行共刺激阻断。过去十年见证了前所未有的大量小分子/口服药物被研发并批准用于肾移植;然而,未来十年可能会出现一类新的生物诱导剂,它们可能会取代一些目前使用的药物。