Sanofi Research, Immunology & Inflammation Therapeutic Area, Cambridge, MA.
Blood Adv. 2023 Aug 22;7(16):4258-4268. doi: 10.1182/bloodadvances.2022009028.
Dysregulated activation of the complement system is implicated in the onset or progression of several diseases. Most clinical-stage complement inhibitors target the inactive complement proteins present at high concentrations in plasma, which increases target-mediated drug disposition and necessitates high drug levels to sustain therapeutic inhibition. Furthermore, many efforts are aimed at inhibiting only terminal pathway activity, which leaves opsonin-mediated effector functions intact. We describe the discovery of SAR443809, a specific inhibitor of the alternative pathway C3/C5 convertase (C3bBb). SAR443809 selectively binds to the activated form of factor B (factor Bb) and inhibits alternative pathway activity by blocking the cleavage of C3, leaving the initiation of classical and lectin complement pathways unaffected. Ex vivo experiments with patient-derived paroxysmal nocturnal hemoglobinuria erythrocytes show that, although terminal pathway inhibition via C5 blockade can effectively inhibit hemolysis, proximal complement inhibition with SAR443809 inhibits both hemolysis and C3b deposition, abrogating the propensity for extravascular hemolysis. Finally, intravenous and subcutaneous administration of the antibody in nonhuman primates demonstrated sustained inhibition of complement activity for several weeks after injection. Overall, SAR443809 shows strong potential for treatment of alternative pathway-mediated disorders.
补体系统的失调激活与几种疾病的发生或进展有关。大多数处于临床阶段的补体抑制剂针对的是血浆中高浓度存在的无活性补体蛋白,这增加了靶介导的药物处置,并需要高药物水平来维持治疗抑制。此外,许多努力旨在仅抑制末端途径活性,这使得调理素介导的效应功能保持完整。我们描述了 SAR443809 的发现,这是一种补体旁路 C3/C5 转化酶(C3bBb)的特异性抑制剂。SAR443809 选择性地结合到激活形式的因子 B(因子 Bb),并通过阻断 C3 的切割来抑制旁路途径活性,而不影响经典和凝集素补体途径的起始。用源自阵发性夜间血红蛋白尿患者的红细胞进行的离体实验表明,尽管通过 C5 阻断的末端途径抑制可以有效地抑制溶血,但通过 SAR443809 的旁路抑制可以抑制溶血和 C3b 沉积,从而消除血管外溶血的倾向。最后,在非人类灵长类动物中静脉和皮下给予该抗体后,在注射后数周内持续抑制补体活性。总体而言,SAR443809 具有治疗旁路途径介导的疾病的巨大潜力。