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SARS-CoV-2 Beta variant infection elicits potent lineage-specific and cross-reactive antibodies

SARS-CoV-2 Beta variant of concern (VOC) resists neutralization by major classes of antibodies from COVID-19 patients and vaccinated individuals. Here, serum of Beta-infected patients revealed reduced cross-neutralization of wildtype virus. From these patients, we isolated Beta-specific and cross-re...

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Detalles Bibliográficos
Autores principales: Reincke, S. Momsen, Yuan, Meng, Kornau, Hans-Christian, Corman, Victor M., van Hoof, Scott, Sánchez-Sendin, Elisa, Ramberger, Melanie, Yu, Wenli, Hua, Yuanzi, Tien, Henry, Schmidt, Marie Luisa, Schwarz, Tatjana, Jeworowski, Lara Maria, Brandl, Sarah E., Rasmussen, Helle Foverskov, Homeyer, Marie A., Stöffler, Laura, Barner, Martin, Kunkel, Désirée, Huo, Shufan, Horler, Johannes, von Wardenburg, Niels, Kroidl, Inge, Eser, Tabea M., Wieser, Andreas, Geldmacher, Christof, Hoelscher, Michael, Gänzer, Hannes, Weiss, Günter, Schmitz, Dietmar, Drosten, Christian, Prüss, Harald, Wilson, Ian A., Kreye, Jakob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8939768/
https://www.ncbi.nlm.nih.gov/pubmed/35076281
http://dx.doi.org/10.1126/science.abm5835
Descripción
Sumario:SARS-CoV-2 Beta variant of concern (VOC) resists neutralization by major classes of antibodies from COVID-19 patients and vaccinated individuals. Here, serum of Beta-infected patients revealed reduced cross-neutralization of wildtype virus. From these patients, we isolated Beta-specific and cross-reactive receptor-binding domain (RBD) antibodies. The Beta-specificity results from recruitment of VOC-specific clonotypes and accommodation of mutations present in Beta and Omicron into a major antibody class that is normally sensitive to these mutations. The Beta-elicited cross-reactive antibodies share genetic and structural features with wildtype-elicited antibodies, including a public VH1-58 clonotype targeting the RBD ridge. These findings advance our understanding of the antibody response to SARS-CoV-2 shaped by antigenic drift with implications for design of next-generation vaccines and therapeutics.