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A bivalent HCV peptide vaccine elicits pan-genotypic neutralizing antibodies in mice

Mosa, Alexander I.; Urbanowicz, Richard A.; AbouHaidar, Mounir G.; Tavis, John E.; Ball, Jonathan K.; Feld, Jordan J.

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Authors

Alexander I. Mosa

Richard A. Urbanowicz

Mounir G. AbouHaidar

John E. Tavis

Jonathan K. Ball

Jordan J. Feld



Abstract

© 2020 Elsevier Ltd Vaccine development for antigenically variable pathogens has faltered because extreme genetic diversity precludes induction of broadly neutralizing antibodies (nAB) with classical vaccines. Here, using the most variable epitope of any known human pathogen (HVR1 of HCV), we describe a novel approach capable of eliciting broadly neutralizing antibodies targeting highly variable epitopes. Our proof-of-concept vaccine elicited pan-genotypic nAB against HCV variants differing from the immunogen sequences by more than 70% at the amino acid level. These findings suggest broadly nAB to highly variable pathogens can be elicited by vaccines designed to target physicochemically conserved residues within hypervariable epitopes.

Citation

Mosa, A. I., Urbanowicz, R. A., AbouHaidar, M. G., Tavis, J. E., Ball, J. K., & Feld, J. J. (2020). A bivalent HCV peptide vaccine elicits pan-genotypic neutralizing antibodies in mice. Vaccine, 38(44), 6864-6867. https://doi.org/10.1016/j.vaccine.2020.08.066

Journal Article Type Article
Acceptance Date Aug 25, 2020
Online Publication Date Sep 6, 2020
Publication Date Oct 14, 2020
Deposit Date Jan 5, 2021
Publicly Available Date Sep 7, 2021
Journal Vaccine
Print ISSN 0264-410X
Electronic ISSN 1873-2518
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 38
Issue 44
Pages 6864-6867
DOI https://doi.org/10.1016/j.vaccine.2020.08.066
Keywords Infectious Diseases; Public Health, Environmental and Occupational Health; General Veterinary; General Immunology and Microbiology; Molecular Medicine
Public URL https://nottingham-repository.worktribe.com/output/4913610
Publisher URL https://www.sciencedirect.com/science/article/pii/S0264410X2031118X?via%3Dihub

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