Ricklin Daniel, Lambris John D
Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, USA.
Semin Immunol. 2016 Jun;28(3):208-22. doi: 10.1016/j.smim.2016.06.001. Epub 2016 Jun 16.
The complement system is a powerful effector arm of innate immunity that typically confers protection from microbial intruders and accumulating debris. In many clinical situations, however, the defensive functions of complement can turn against host cells and induce or exacerbate immune, inflammatory, and degenerative conditions. Although the value of inhibiting complement in a therapeutic context has long been recognized, bringing complement-targeted drugs into clinical use has proved challenging. This important milestone was finally reached a decade ago, yet the clinical availability of complement inhibitors has remained limited. Still, the positive long-term experience with complement drugs and their proven effectiveness in various diseases has reinvigorated interest and confidence in this approach. Indeed, a broad variety of clinical candidates that act at almost any level of the complement activation cascade are currently in clinical development, with several of them being evaluated in phase 2 and phase 3 trials. With antibody-related drugs dominating the panel of clinical candidates, the emergence of novel small-molecule, peptide, protein, and oligonucleotide-based inhibitors offers new options for drug targeting and administration. Whereas all the currently approved and many of the proposed indications for complement-targeted inhibitors belong to the rare disease spectrum, these drugs are increasingly being evaluated for more prevalent conditions. Fortunately, the growing experience from preclinical and clinical use of therapeutic complement inhibitors has enabled a more evidence-based assessment of suitable targets and rewarding indications as well as related technical and safety considerations. This review highlights recent concepts and developments in complement-targeted drug discovery, provides an overview of current and emerging treatment options, and discusses the new milestones ahead on the way to the next generation of clinically available complement therapeutics.
补体系统是固有免疫的强大效应分支,通常能抵御微生物入侵者和清除堆积的碎片。然而,在许多临床情况下,补体的防御功能可能会转而攻击宿主细胞,引发或加剧免疫、炎症和退行性疾病。尽管在治疗背景下抑制补体的价值早已得到认可,但将补体靶向药物应用于临床却颇具挑战。这一重要里程碑终于在十年前达成,但补体抑制剂在临床上的可及性仍然有限。尽管如此,补体药物的长期积极经验及其在各种疾病中的已证实疗效,重新激发了人们对这种方法的兴趣和信心。事实上,目前有各种各样几乎作用于补体激活级联反应任何水平的临床候选药物正在进行临床开发,其中几种正在进行2期和3期试验。随着抗体相关药物在临床候选药物中占据主导地位,新型小分子、肽、蛋白质和基于寡核苷酸的抑制剂的出现为药物靶向和给药提供了新选择。虽然目前所有已批准的以及许多针对补体的抑制剂的拟用适应症都属于罕见病范畴,但这些药物正越来越多地被评估用于更常见的疾病。幸运的是,治疗性补体抑制剂临床前和临床应用经验的不断积累,使得人们能够更基于证据地评估合适的靶点、有价值的适应症以及相关的技术和安全考量。本综述重点介绍了补体靶向药物研发的最新概念和进展,概述了当前和新兴的治疗选择,并讨论了在开发下一代临床可用补体疗法的道路上的新里程碑。