Crimean-Congo hemorrhagic fever virus protein GP38 from isolate M18-China confers broad immunological breadth
Abstract
Crimean-Congo hemorrhagic fever virus (CCHFV) is a tick-borne, negative-strand RNA virus that causes outbreaks of lethal hemorrhagic fever. No approved vaccines or specific antiviral treatments are available. CCHFV glycoprotein GP38 is an integral component of the pre-fusion glycoprotein entry complex, plays roles in viral pathogenesis, and is a key target of antibody-mediated protection. Herein, we investigated the hypothesis that recombinant GP38 itself could elicit protection against divergent CCHFV isolates/strains in an animal model. Accordingly, we generated GP38 immunogens from six CCHFV clades and showed that GP38 from the isolate M18-China induces a broad immunological response in mice despite its lower amino acid sequence similarity to other isolates. We identified sequences in M18-China GP38 associated with this immunological breadth and evaluated it as a vaccine candidate. Although M18-China GP38 was not protective in isolation, our findings warrant further exploration of its utility as one component of a broadly protective CCHFV vaccine.
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Authors: Albert Wang, Stephanie R. Monticelli, Jacob Berrigan, Christy K. Hjorth, Thomas Batchelor, Alexandra L. Tse, Ana I. Kuehne, Russell R. Bakken, N. A. Saavedra-Avila, Gorka Lasso, Steven A. Porcelli, Jason S. McLellan, Andrew S. Herbert, Kartik Chandran
Institutions: Albert Einstein College of Medicine, The University of Texas at Austin, Oak Ridge Associated Universities, Oak Ridge Institute for Science and Education, Henry M. Jackson Foundation, United States Army Medical Research Institute of Infectious Diseases