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Nucleocapsid protein-specific monoclonal antibodies protect mice against Crimean-Congo hemorrhagic fever virus.
Garrison, Aura R; Moresco, Vanessa; Zeng, Xiankun; Cline, Curtis R; Ward, Michael D; Ricks, Keersten M; Olschner, Scott P; Cazares, Lisa H; Karaaslan, Elif; Fitzpatrick, Collin J; Bergeron, Éric; Pegan, Scott D; Golden, Joseph W.
  • Garrison AR; United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA. aura.r.garrison.civ@health.mil.
  • Moresco V; Division of Biomedical Sciences, University of California Riverside, Riverside, CA, USA.
  • Zeng X; United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.
  • Cline CR; United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.
  • Ward MD; United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.
  • Ricks KM; United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.
  • Olschner SP; United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.
  • Cazares LH; United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.
  • Karaaslan E; Viral Special Pathogens Branch, Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Fitzpatrick CJ; United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD, USA.
  • Bergeron É; Viral Special Pathogens Branch, Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Pegan SD; Division of Biomedical Sciences, University of California Riverside, Riverside, CA, USA.
  • Golden JW; Department of Chemistry & Life Science, United States Military Academy, West Point, NY, USA.
Nat Commun ; 15(1): 1722, 2024 Feb 26.
Article en En | MEDLINE | ID: mdl-38409240
ABSTRACT
Crimean-Congo hemorrhagic fever virus (CCHFV) is a WHO priority pathogen. Antibody-based medical countermeasures offer an important strategy to mitigate severe disease caused by CCHFV. Most efforts have focused on targeting the viral glycoproteins. However, glycoproteins are poorly conserved among viral strains. The CCHFV nucleocapsid protein (NP) is highly conserved between CCHFV strains. Here, we investigate the protective efficacy of a CCHFV monoclonal antibody targeting the NP. We find that an anti-NP monoclonal antibody (mAb-9D5) protected female mice against lethal CCHFV infection or resulted in a significant delay in mean time-to-death in mice that succumbed to disease compared to isotype control animals. Antibody protection is independent of Fc-receptor functionality and complement activity. The antibody bound NP from several CCHFV strains and exhibited robust cross-protection against the heterologous CCHFV strain Afg09-2990. Our work demonstrates that the NP is a viable target for antibody-based therapeutics, providing another direction for developing immunotherapeutics against CCHFV.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Virus de la Fiebre Hemorrágica de Crimea-Congo / Fiebre Hemorrágica de Crimea Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Virus de la Fiebre Hemorrágica de Crimea-Congo / Fiebre Hemorrágica de Crimea Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article