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Broadly neutralizing antibody cocktails targeting Nipah virus and Hendra virus fusion glycoproteins.
Dang, Ha V; Cross, Robert W; Borisevich, Viktoriya; Bornholdt, Zachary A; West, Brandyn R; Chan, Yee-Peng; Mire, Chad E; Da Silva, Sofia Cheliout; Dimitrov, Antony S; Yan, Lianying; Amaya, Moushimi; Navaratnarajah, Chanakha K; Zeitlin, Larry; Geisbert, Thomas W; Broder, Christopher C; Veesler, David.
Afiliação
  • Dang HV; Department of Biochemistry, University of Washington, Seattle, WA, USA.
  • Cross RW; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
  • Borisevich V; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, USA.
  • Bornholdt ZA; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
  • West BR; Mapp Biopharmaceutical, Inc., San Diego, CA, USA.
  • Chan YP; Mapp Biopharmaceutical, Inc., San Diego, CA, USA.
  • Mire CE; Department of Microbiology and Immunology, Uniformed Services University, Bethesda, MD, USA.
  • Da Silva SC; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
  • Dimitrov AS; Galveston National Laboratory, University of Texas Medical Branch, Galveston, TX, USA.
  • Yan L; Department of Microbiology and Immunology, Uniformed Services University, Bethesda, MD, USA.
  • Amaya M; Department of Microbiology and Immunology, Uniformed Services University, Bethesda, MD, USA.
  • Navaratnarajah CK; Department of Microbiology and Immunology, Uniformed Services University, Bethesda, MD, USA.
  • Zeitlin L; Department of Microbiology and Immunology, Uniformed Services University, Bethesda, MD, USA.
  • Geisbert TW; Department of Molecular Medicine, Mayo Clinic, Rochester, MN, USA.
  • Broder CC; Mapp Biopharmaceutical, Inc., San Diego, CA, USA.
  • Veesler D; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX, USA.
Nat Struct Mol Biol ; 28(5): 426-434, 2021 05.
Article em En | MEDLINE | ID: mdl-33927387
Hendra virus (HeV) and Nipah virus (NiV) are henipaviruses (HNVs) causing respiratory illness and severe encephalitis in humans, with fatality rates of 50-100%. There are no licensed therapeutics or vaccines to protect humans. HeV and NiV use a receptor-binding glycoprotein (G) and a fusion glycoprotein (F) to enter host cells. HNV F and G are the main targets of the humoral immune response, and the presence of neutralizing antibodies is a correlate of protection against NiV and HeV in experimentally infected animals. We describe here two cross-reactive F-specific antibodies, 1F5 and 12B2, that neutralize NiV and HeV through inhibition of membrane fusion. Cryo-electron microscopy structures reveal that 1F5 and 12B2 recognize distinct prefusion-specific, conserved quaternary epitopes and lock F in its prefusion conformation. We provide proof-of-concept for using antibody cocktails for neutralizing NiV and HeV and define a roadmap for developing effective countermeasures against these highly pathogenic viruses.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Virais de Fusão / Vírus Hendra / Vírus Nipah / Anticorpos Amplamente Neutralizantes / Anticorpos Antivirais Limite: Animals / Humans Idioma: En Revista: Nat Struct Mol Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Virais de Fusão / Vírus Hendra / Vírus Nipah / Anticorpos Amplamente Neutralizantes / Anticorpos Antivirais Limite: Animals / Humans Idioma: En Revista: Nat Struct Mol Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos