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Human Monoclonal Antibodies Potently Neutralize Zika Virus and Select for Escape Mutations on the Lateral Ridge of the Envelope Protein
Author(s) -
Mark Bailey,
Felix Broecker,
Alec W. Freyn,
Angela Choi,
Julia A. Brown,
Nadia Fedorova,
Viviana Simon,
Jean K. Lim,
Matthew J. Evans,
Adolfo Garcı́a-Sastre,
Peter Palese,
Gene S. Tan
Publication year - 2019
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.00405-19
Subject(s) - biology , virology , zika virus , monoclonal antibody , envelope (radar) , ridge , antibody , mutation , virus , genetics , gene , radar , telecommunications , paleontology , computer science
Zika virus (ZIKV) is a global health threat causing severe disease in humans, including microcephaly in newborns and Guillain-Barré syndrome in adults. Here, we analyzed the human monoclonal antibody response to acute ZIKV infection and found that neutralizing antibodies could not elicit Fc-mediated immune effector functions but could potentiate antibody-dependent enhancement of disease. We further identified critical epitopes involved with neutralization by generating and characterizing escape variants by whole-genome sequencing. We demonstrate that the lateral ridge region, particularly the S368 amino acid site, is critical for neutralization by domain III-specific antibodies.

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