Adimab, LLC, Lebanon, NH 03766, USA.
U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD 21702, USA; Geneva Foundation, Tacoma, WA 98042, USA.
Cell Rep. 2024 Jul 23;43(7):114502. doi: 10.1016/j.celrep.2024.114502. Epub 2024 Jul 13.
Crimean-Congo hemorrhagic fever virus can cause lethal disease in humans yet there are no approved medical countermeasures. Viral glycoprotein GP38, exclusive to Nairoviridae, is a target of protective antibodies and is a key antigen in preclinical vaccine candidates. Here, we isolate 188 GP38-specific antibodies from human survivors of infection. Competition experiments show that these antibodies bind across 5 distinct antigenic sites, encompassing 11 overlapping regions. Additionally, we show structures of GP38 bound with 9 of these antibodies targeting different antigenic sites. Although these GP38-specific antibodies are non-neutralizing, several display protective efficacy equal to or better than murine antibody 13G8 in two highly stringent rodent models of infection. Together, these data expand our understanding regarding this important viral protein and may inform the development of broadly effective CCHFV antibody therapeutics.
克里米亚-刚果出血热病毒可在人类中引起致命疾病,但目前尚无经过批准的医疗对策。病毒糖蛋白 GP38 是纳罗病毒科所特有的,是保护性抗体的靶标,也是临床前候选疫苗的关键抗原。在这里,我们从感染后幸存的人类患者中分离出 188 种 GP38 特异性抗体。竞争实验表明,这些抗体跨越 5 个不同的抗原结合位点,涵盖 11 个重叠区域。此外,我们展示了 9 种与不同抗原结合位点结合的 GP38 结构,这些抗体靶向不同的抗原结合位点。尽管这些 GP38 特异性抗体是非中和性的,但在两种高度严格的感染啮齿动物模型中,有几种抗体的保护效果与鼠源抗体 13G8 相当或更好。这些数据扩展了我们对这种重要病毒蛋白的认识,并可能为开发广泛有效的 CCHFV 抗体治疗方法提供信息。