Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Adimab, LLC, Lebanon, NH 03766, USA.
Cell. 2021 Jun 24;184(13):3486-3501.e21. doi: 10.1016/j.cell.2021.05.001. Epub 2021 Jun 1.
Crimean-Congo hemorrhagic fever virus (CCHFV) is a World Health Organization priority pathogen. CCHFV infections cause a highly lethal hemorrhagic fever for which specific treatments and vaccines are urgently needed. Here, we characterize the human immune response to natural CCHFV infection to identify potent neutralizing monoclonal antibodies (nAbs) targeting the viral glycoprotein. Competition experiments showed that these nAbs bind six distinct antigenic sites in the Gc subunit. These sites were further delineated through mutagenesis and mapped onto a prefusion model of Gc. Pairwise screening identified combinations of non-competing nAbs that afford synergistic neutralization. Further enhancements in neutralization breadth and potency were attained by physically linking variable domains of synergistic nAb pairs through bispecific antibody (bsAb) engineering. Although multiple nAbs protected mice from lethal CCHFV challenge in pre- or post-exposure prophylactic settings, only a single bsAb, DVD-121-801, afforded therapeutic protection. DVD-121-801 is a promising candidate suitable for clinical development as a CCHFV therapeutic.
克里米亚-刚果出血热病毒(CCHFV)是世界卫生组织的优先病原体。CCHFV 感染可引起高度致命的出血热,急需特定的治疗方法和疫苗。在这里,我们描述了人类对自然 CCHFV 感染的免疫反应,以鉴定针对病毒糖蛋白的有效中和单克隆抗体(nAb)。竞争实验表明,这些 nAb 结合 Gc 亚基中的六个不同的抗原位点。通过突变和映射到 Gc 的预融合模型进一步描绘了这些位点。通过对协同 nAb 对的可变结构域进行双特异性抗体(bsAb)工程,对非竞争 nAb 进行了配对筛选,确定了协同中和的组合。通过物理连接协同 nAb 对的可变结构域,进一步提高了中和的广度和效力。尽管多种 nAb 在预防或暴露后预防性治疗中可保护小鼠免受致死性 CCHFV 挑战,但只有一种 bsAb,即 DVD-121-801,可提供治疗保护。DVD-121-801 是一种有前途的候选药物,适合作为 CCHFV 的治疗药物进行临床开发。