Cargando…

SARS-CoV-2 spike conformation determines plasma neutralizing activity

Numerous safe and effective COVID-19 vaccines have been developed that utilize various delivery technologies and engineering strategies. The influence of the SARS-CoV-2 spike (S) glycoprotein conformation on antibody responses induced by vaccination or infection in humans remains unknown. To address...

Descripción completa

Detalles Bibliográficos
Autores principales: Bowen, John E., Walls, Alexandra C., Joshi, Anshu, Sprouse, Kaitlin R., Stewart, Cameron, Tortorici, M. Alejandra, Franko, Nicholas M., Logue, Jennifer K., Mazzitelli, Ignacio G., Tiles, Sasha W, Ahmed, Kumail, Shariq, Asefa, Snell, Gyorgy, Iqbal, Najeeha Talat, Geffner, Jorge, Bandera, Alessandra, Gori, Andrea, Grifantini, Renata, Chu, Helen Y., Van Voorhis, Wesley C., Corti, Davide, Veesler, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722597/
https://www.ncbi.nlm.nih.gov/pubmed/34981060
http://dx.doi.org/10.1101/2021.12.19.473391
Descripción
Sumario:Numerous safe and effective COVID-19 vaccines have been developed that utilize various delivery technologies and engineering strategies. The influence of the SARS-CoV-2 spike (S) glycoprotein conformation on antibody responses induced by vaccination or infection in humans remains unknown. To address this question, we compared plasma antibodies elicited by six globally-distributed vaccines or infection and observed markedly higher binding titers for vaccines encoding a prefusion-stabilized S relative to other groups. Prefusion S binding titers positively correlated with plasma neutralizing activity, indicating that physical stabilization of the prefusion conformation enhances protection against SARS-CoV-2. We show that almost all plasma neutralizing activity is directed to prefusion S, in particular the S(1) subunit, and that variant cross-neutralization is mediated solely by RBD-specific antibodies. Our data provide a quantitative framework for guiding future S engineering efforts to develop vaccines with higher resilience to the emergence of variants and longer durability than current technologies.