Department of Immunology, Leiden University Medical Center, Leiden, Netherlands.
Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, Netherlands.
Front Immunol. 2024 May 16;15:1288597. doi: 10.3389/fimmu.2024.1288597. eCollection 2024.
Complement activation protects against infection but also contributes to pathological mechanisms in a range of clinical conditions such as autoimmune diseases and transplant rejection. Complement-inhibitory drugs, either approved or in development, usually act systemically, thereby increasing the risk for infections. We therefore envisioned a novel class of bispecific antibodies (bsAbs) which are capable of site-directed complement inhibition by bringing endogenous complement regulators in the vicinity of defined cell surface antigens. Here, we analyzed a comprehensive set of obligate bsAbs designed to crosslink a specific target with either complement regulator factor H (FH) or C4b-binding protein (C4BP). The bsAbs were assessed for their capacity to inhibit complement activation and cell lysis in an antigen-targeted manner. We observed that the bsAbs inhibited classical, lectin, and alternative pathway complement activation in which sufficient endogenous serum FH and C4BP could be recruited to achieve local inhibition. Importantly, the bsAbs effectively protected antigen-positive liposomes, erythrocytes, and human leukocytes from complement-mediated lysis. In conclusion, localized complement inhibition by bsAbs capable of recruiting endogenous human complement regulators (such as FH or C4BP) to cell surfaces potentially provides a novel therapeutic approach for the targeted treatment of complement-mediated diseases.
补体激活可预防感染,但在多种临床情况下(如自身免疫性疾病和移植排斥)也会导致病理性机制。补体抑制药物,无论是已批准的还是正在开发的,通常都会全身性作用,从而增加感染的风险。因此,我们设想了一类新型双特异性抗体(bsAbs),它们能够通过将内源性补体调节剂带到特定细胞表面抗原附近,实现靶向补体抑制。在这里,我们分析了一套综合的必需 bsAbs,旨在通过补体调节因子 H (FH) 或 C4 结合蛋白 (C4BP) 与特定靶标交联。这些 bsAbs 的抗原靶向抑制补体激活和细胞裂解的能力进行了评估。我们观察到,bsAbs 抑制经典、凝集素和替代途径补体激活,在此过程中可募集足够的内源性血清 FH 和 C4BP 以实现局部抑制。重要的是,bsAbs 可有效保护抗原阳性的脂质体、红细胞和人白细胞免受补体介导的裂解。总之,能够将内源性人补体调节剂(如 FH 或 C4BP)募集到细胞表面的 bsAbs 进行局部补体抑制,可能为靶向治疗补体介导的疾病提供一种新的治疗方法。