tetano
Editor, Senior Moderator
Sci Transl Med
. 2020 Dec 7;eabf1555.
doi: 10.1126/scitranslmed.abf1555. Online ahead of print.
Enhanced SARS-CoV-2 neutralization by dimeric IgA
Zijun Wang[SUP] 1 [/SUP], Julio C C Lorenzi[SUP] 1 [/SUP], Frauke Muecksch[SUP] 2 [/SUP], Shlomo Finkin[SUP] 1 [/SUP], Charlotte Viant[SUP] 1 [/SUP], Christian Gaebler[SUP] 1 [/SUP], Melissa Cipolla[SUP] 1 [/SUP], Hans-Heinrich Hoffmann[SUP] 3 [/SUP], Thiago Y Oliveira[SUP] 1 [/SUP], Deena A Oren[SUP] 4 [/SUP], Victor Ramos[SUP] 1 [/SUP], Lilian Nogueira[SUP] 1 [/SUP], Eleftherios Michailidis[SUP] 3 [/SUP], Davide F Robbiani[SUP] 5 [/SUP], Anna Gazumyan[SUP] 1 [/SUP], Charles M Rice[SUP] 3 [/SUP], Theodora Hatziioannou[SUP] 2 [/SUP], Paul D Bieniasz[SUP] 2 6 [/SUP], Marina Caskey[SUP] 1 [/SUP], Michel C Nussenzweig[SUP] 7 6 [/SUP]
Affiliations
Abstract
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 IgG antibodies can neutralize the virus, less is known about secretory antibodies such as IgA that might impact 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 following diagnosis with COVID-19. IgA responses in plasma generally correlated with IgG responses. Further, 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 two-fold less potent than IgG equivalents. However, IgA dimers, the primary form of antibody in the nasopharynx, were on average fifteen times more potent than IgA monomers against the same target. Thus, dimeric IgA responses may be particularly valuable for protection against SARS-CoV-2 and for vaccine efficacy.
. 2020 Dec 7;eabf1555.
doi: 10.1126/scitranslmed.abf1555. Online ahead of print.
Enhanced SARS-CoV-2 neutralization by dimeric IgA
Zijun Wang[SUP] 1 [/SUP], Julio C C Lorenzi[SUP] 1 [/SUP], Frauke Muecksch[SUP] 2 [/SUP], Shlomo Finkin[SUP] 1 [/SUP], Charlotte Viant[SUP] 1 [/SUP], Christian Gaebler[SUP] 1 [/SUP], Melissa Cipolla[SUP] 1 [/SUP], Hans-Heinrich Hoffmann[SUP] 3 [/SUP], Thiago Y Oliveira[SUP] 1 [/SUP], Deena A Oren[SUP] 4 [/SUP], Victor Ramos[SUP] 1 [/SUP], Lilian Nogueira[SUP] 1 [/SUP], Eleftherios Michailidis[SUP] 3 [/SUP], Davide F Robbiani[SUP] 5 [/SUP], Anna Gazumyan[SUP] 1 [/SUP], Charles M Rice[SUP] 3 [/SUP], Theodora Hatziioannou[SUP] 2 [/SUP], Paul D Bieniasz[SUP] 2 6 [/SUP], Marina Caskey[SUP] 1 [/SUP], Michel C Nussenzweig[SUP] 7 6 [/SUP]
Affiliations
- PMID: 33288661
- DOI: 10.1126/scitranslmed.abf1555
Abstract
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 IgG antibodies can neutralize the virus, less is known about secretory antibodies such as IgA that might impact 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 following diagnosis with COVID-19. IgA responses in plasma generally correlated with IgG responses. Further, 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 two-fold less potent than IgG equivalents. However, IgA dimers, the primary form of antibody in the nasopharynx, were on average fifteen times more potent than IgA monomers against the same target. Thus, dimeric IgA responses may be particularly valuable for protection against SARS-CoV-2 and for vaccine efficacy.