Significance Hepatitis C virus (HCV) infects 58 million people worldwide, with an estimated 1.5 million new infections annually. Despite remarkable advances in treatment, new infections outpace cures, and a prophylactic vaccine is needed to achieve HCV elimination. Vaccine development has been impeded, however, by the extreme genetic variability of HCV. Our previous work indicates that even in highly variable epitopes, HCV is limited by phenotypic constraints that can be exploited by rational vaccine design. Here, we applied a unique measure of genetic distance to model these constraints into a network describing the global HCV sequence space. By combining variants from across this space to immunize mice, we elicited broadly neutralizing antibodies with greater neutralization breadth and potency than a classical vaccine candidate.
Polyvalent immunization elicits a synergistic broadly neutralizing immune response to hypervariable region 1 variants of hepatitis C virus
Alexander I. Mosa,Davis S. Campo,Y. Khudyakov,M. AbouHaidar,A. Gehring,A. Zahoor,J. Ball,R. Urbanowicz,J. Feld
Published 2023 in Proceedings of the National Academy of Sciences of the United States of America
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PUBLICATION RECORD
- Publication year
2023
- Venue
Proceedings of the National Academy of Sciences of the United States of America
- Publication date
2023-06-05
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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