Special Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada.
Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, Manitoba, Canada.
J Infect Dis. 2023 Nov 13;228(Suppl 7):S691-S700. doi: 10.1093/infdis/jiad205.
Filoviruses, including ebolaviruses and marburgviruses, can cause severe and often fatal disease in humans. Over the past several years, antibody therapy has emerged as a promising strategy for the treatment of filovirus disease. Here, we describe 2 distinct cross-reactive monoclonal antibodies (mAbs) isolated from mice immunized with recombinant vesicular stomatitis virus-based filovirus vaccines. Both mAbs recognized the glycoproteins of multiple different ebolaviruses and exhibited broad but differential in vitro neutralization activities against these viruses. By themselves, each mAb provided partial to full protection against Ebola virus in mice, and in combination, the mAbs provided 100% protection against Sudan virus challenge in guinea pigs. This study identified novel mAbs that were elicited through immunization and able to provide protection from ebolavirus infection, thus enriching the pool of candidate therapeutics for treating Ebola disease.
丝状病毒,包括埃博拉病毒和马尔堡病毒,可导致人类严重且常常致命的疾病。在过去的几年中,抗体疗法已成为治疗丝状病毒病的一种有前途的策略。在这里,我们描述了两种从用重组水疱性口炎病毒为基础的丝状病毒疫苗免疫的小鼠中分离出的不同的交叉反应性单克隆抗体(mAb)。这两种 mAb 都识别多种不同埃博拉病毒的糖蛋白,并对这些病毒表现出广泛但有差异的体外中和活性。单独使用时,每种 mAb 都能为小鼠提供针对埃博拉病毒的部分至完全保护,而联合使用时,mAb 能为豚鼠提供针对苏丹病毒的 100%保护。本研究鉴定了通过免疫接种诱导产生的新型 mAb,这些 mAb 能提供针对埃博拉病毒感染的保护,从而丰富了治疗埃博拉病的候选治疗药物库。