| Literature DB >> 35675766 |
Emily N Gallichotte1, Sandra Henein1, Usha Nivarthi1, Matthew Delacruz1, Trevor Scobey2, Matthew Bonaparte3, Janice Moser4, Alina Munteanu3, Ralph Baric5, Aravinda M de Silva6.
Abstract
The four dengue virus serotypes (DENV1-4) are mosquito-borne flaviviruses of humans. Several live-attenuated tetravalent DENV vaccines are at different stages of clinical development and approval. In children with no baseline immunity to DENVs, a leading vaccine (Dengvaxia) is efficacious against vaccine-matched DENV4 genotype II (GII) strains but not vaccine-mismatched DENV4 GI viruses. We use a panel of recombinant DENV4 viruses displaying GI or GII envelope (E) proteins to map Dengvaxia-induced neutralizing antibodies (NAbs) linked to protection. The vaccine stimulated antibodies that neutralize the DENV4 GII virus better than the GI virus. The neutralization differences map to 5 variable amino acids on the E protein located within a region targeted by DENV4 NAbs, supporting a mechanistic role for these epitope-specific NAbs in protection. In children with no baseline immunity to DENVs, levels of DENV4 serotype- and genotype-specific NAbs induced by vaccination are predictive of vaccine efficacy.Entities:
Keywords: CP: Immunology; antibodies; dengue virus; immune correlate; live-attenuated tetravalent dengue vaccine; vaccines
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Year: 2022 PMID: 35675766 PMCID: PMC9326871 DOI: 10.1016/j.celrep.2022.110930
Source DB: PubMed Journal: Cell Rep Impact factor: 9.995