作者
Zijun Wang, Julio CC Lorenzi, Frauke Muecksch, Shlomo Finkin, Charlotte Viant, Christian Gaebler, Melissa Cipolla, Hans-Heinrich Hoffmann, Thiago Y Oliveira, Deena A Oren, Victor Ramos, Lilian Nogueira, Eleftherios Michailidis, Davide F Robbiani, Anna Gazumyan, Charles M Rice, Theodora Hatziioannou, Paul D Bieniasz, Marina Caskey, Michel C Nussenzweig
发表日期
2021/1/20
期刊
Science translational medicine
卷号
13
期号
577
页码范围
eabf1555
出版商
American Association for the Advancement of Science
简介
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes coronavirus disease 2019 (COVID-19), primarily infects cells at mucosal surfaces. Serum neutralizing antibody responses are variable and generally low in individuals that suffer mild forms of COVID-19. Although potent immunoglobulin G (IgG) antibodies can neutralize the virus, less is known about secretory antibodies such as IgA that might affect the initial viral spread and transmissibility from the mucosa. Here, we characterize the IgA response to SARS-CoV-2 in a cohort of 149 convalescent individuals after diagnosis with COVID-19. IgA responses in plasma generally correlated with IgG responses. Furthermore, clones of IgM-, IgG-, and IgA-producing B cells were derived from common progenitor cells. Plasma IgA monomers specific to SARS-CoV-2 proteins were demonstrated to be twofold less potent than IgG equivalents …
引用总数
学术搜索中的文章
Z Wang, JCC Lorenzi, F Muecksch, S Finkin, C Viant… - Science translational medicine, 2021