GP38-targeting monoclonal antibodies protect adult mice against lethal Crimean-Congo hemorrhagic fever virus infection

作者：Joseph W. Golden, Charles J. Shoemaker, Michael E. Lindquist, Xiankun Zeng, Sharon P. Daye, Janice A. Williams, Jun Liu, Kayla M. Coffin, Scott P. Olschner, Olivier Flusin, Louis A. Altamura, Kathleen Kuehl, Collin J. Fitzpatrick, Connie S. Schmaljohn, Aura R. Garrison · 发表于：Science Advances · 年份：2019 · DOI：10.1126/sciadv.aaw9535 · 被引用次数：107 · 研究领域：Viral Infections and Vectors、Vector-Borne Animal Diseases、Viral Infections and Outbreaks Research

Crimean-Congo hemorrhagic fever virus (CCHFV) is an important human pathogen. Limited evidence suggests that antibodies can protect humans against lethal CCHFV disease but the protective efficacy of antibodies has never been evaluated in adult animal models. Here, we used adult mice to investigate the protection provided against CCHFV infection by glycoprotein-targeting neutralizing and non-neutralizing monoclonal antibodies (mAbs). We identified a single non-neutralizing antibody (mAb-13G8) that protected adult type I interferon-deficient mice >90% when treatment was initiated before virus exposure and >60% when administered after virus exposure. Neutralizing antibodies known to protect neonatal mice from lethal CCHFV infection failed to confer protection regardless of immunoglobulin G subclass. The target of mAb-13G8 was identified as GP38, one of multiple proteolytically cleaved glycoproteins derived from the CCHFV glycoprotein precursor polyprotein. This study reveals GP38 as an important antibody target for limiting CCHFV pathogenesis and lays the foundation to develop immunotherapeutics against CCHFV in humans.