Broadly neutralizing antibody cocktails targeting Nipah virus and Hendra virus fusion glycoproteins

被引:0
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作者
Ha V. Dang
Robert W. Cross
Viktoriya Borisevich
Zachary A. Bornholdt
Brandyn R. West
Yee-Peng Chan
Chad E. Mire
Sofia Cheliout Da Silva
Antony S. Dimitrov
Lianying Yan
Moushimi Amaya
Chanakha K. Navaratnarajah
Larry Zeitlin
Thomas W. Geisbert
Christopher C. Broder
David Veesler
机构
[1] University of Washington,Department of Biochemistry
[2] University of Texas Medical Branch,Department of Microbiology and Immunology
[3] University of Texas Medical Branch,Galveston National Laboratory
[4] Mapp Biopharmaceutical,Department of Microbiology and Immunology
[5] Inc.,Department of Molecular Medicine
[6] Uniformed Services University,undefined
[7] Mayo Clinic,undefined
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摘要
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.
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页码:426 / 434
页数:8
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