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SARS-CoV-2 infection severity is linked to superior humoral immunity against the spike
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is currently causing a global pandemic. The antigen specificity and kinetics of the antibody response mounted against this novel virus are not understood in detail. Here, we report that subjects with a more severe SARS-CoV- 2 infection exh...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7491512/ https://www.ncbi.nlm.nih.gov/pubmed/32935099 http://dx.doi.org/10.1101/2020.09.12.294066 |
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author | Guthmiller, Jenna J. Stovicek, Olivia Wang, Jiaolong Changrob, Siriruk Li, Lei Halfmann, Peter Zheng, Nai-Ying Utset, Henry Stamper, Christopher T. Dugan, Haley L. Miller, William D. Huang, Min Dai, Ya-Nan Nelson, Christopher A. Hall, Paige D. Jansen, Maud Shanmugarajah, Kumaran Donington, Jessica S. Krammer, Florian Fremont, Daved H. Joachimiak, Andrzej Kawaoka, Yoshihiro Tesic, Vera Madariaga, Maria Lucia Wilson, Patrick C. |
author_facet | Guthmiller, Jenna J. Stovicek, Olivia Wang, Jiaolong Changrob, Siriruk Li, Lei Halfmann, Peter Zheng, Nai-Ying Utset, Henry Stamper, Christopher T. Dugan, Haley L. Miller, William D. Huang, Min Dai, Ya-Nan Nelson, Christopher A. Hall, Paige D. Jansen, Maud Shanmugarajah, Kumaran Donington, Jessica S. Krammer, Florian Fremont, Daved H. Joachimiak, Andrzej Kawaoka, Yoshihiro Tesic, Vera Madariaga, Maria Lucia Wilson, Patrick C. |
author_sort | Guthmiller, Jenna J. |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is currently causing a global pandemic. The antigen specificity and kinetics of the antibody response mounted against this novel virus are not understood in detail. Here, we report that subjects with a more severe SARS-CoV- 2 infection exhibit a larger antibody response against the spike and nucleocapsid protein and epitope spreading to subdominant viral antigens, such as open reading frame 8 and non-structural proteins. Subjects with a greater antibody response mounted a larger memory B cell response against the spike, but not the nucleocapsid protein. Additionally, we revealed that antibodies against the spike are still capable of binding the D614G spike mutant and cross-react with the SARS-CoV-1 receptor binding domain. Together, this study reveals that subjects with a more severe SARS-CoV-2 infection exhibit a greater overall antibody response to the spike and nucleocapsid protein and a larger memory B cell response against the spike. |
format | Online Article Text |
id | pubmed-7491512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-74915122020-09-16 SARS-CoV-2 infection severity is linked to superior humoral immunity against the spike Guthmiller, Jenna J. Stovicek, Olivia Wang, Jiaolong Changrob, Siriruk Li, Lei Halfmann, Peter Zheng, Nai-Ying Utset, Henry Stamper, Christopher T. Dugan, Haley L. Miller, William D. Huang, Min Dai, Ya-Nan Nelson, Christopher A. Hall, Paige D. Jansen, Maud Shanmugarajah, Kumaran Donington, Jessica S. Krammer, Florian Fremont, Daved H. Joachimiak, Andrzej Kawaoka, Yoshihiro Tesic, Vera Madariaga, Maria Lucia Wilson, Patrick C. bioRxiv Article Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is currently causing a global pandemic. The antigen specificity and kinetics of the antibody response mounted against this novel virus are not understood in detail. Here, we report that subjects with a more severe SARS-CoV- 2 infection exhibit a larger antibody response against the spike and nucleocapsid protein and epitope spreading to subdominant viral antigens, such as open reading frame 8 and non-structural proteins. Subjects with a greater antibody response mounted a larger memory B cell response against the spike, but not the nucleocapsid protein. Additionally, we revealed that antibodies against the spike are still capable of binding the D614G spike mutant and cross-react with the SARS-CoV-1 receptor binding domain. Together, this study reveals that subjects with a more severe SARS-CoV-2 infection exhibit a greater overall antibody response to the spike and nucleocapsid protein and a larger memory B cell response against the spike. Cold Spring Harbor Laboratory 2020-09-13 /pmc/articles/PMC7491512/ /pubmed/32935099 http://dx.doi.org/10.1101/2020.09.12.294066 Text en http://creativecommons.org/licenses/by-nc/4.0/It is made available under a CC-BY-NC 4.0 International license (http://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Article Guthmiller, Jenna J. Stovicek, Olivia Wang, Jiaolong Changrob, Siriruk Li, Lei Halfmann, Peter Zheng, Nai-Ying Utset, Henry Stamper, Christopher T. Dugan, Haley L. Miller, William D. Huang, Min Dai, Ya-Nan Nelson, Christopher A. Hall, Paige D. Jansen, Maud Shanmugarajah, Kumaran Donington, Jessica S. Krammer, Florian Fremont, Daved H. Joachimiak, Andrzej Kawaoka, Yoshihiro Tesic, Vera Madariaga, Maria Lucia Wilson, Patrick C. SARS-CoV-2 infection severity is linked to superior humoral immunity against the spike |
title | SARS-CoV-2 infection severity is linked to superior humoral immunity against the spike |
title_full | SARS-CoV-2 infection severity is linked to superior humoral immunity against the spike |
title_fullStr | SARS-CoV-2 infection severity is linked to superior humoral immunity against the spike |
title_full_unstemmed | SARS-CoV-2 infection severity is linked to superior humoral immunity against the spike |
title_short | SARS-CoV-2 infection severity is linked to superior humoral immunity against the spike |
title_sort | sars-cov-2 infection severity is linked to superior humoral immunity against the spike |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7491512/ https://www.ncbi.nlm.nih.gov/pubmed/32935099 http://dx.doi.org/10.1101/2020.09.12.294066 |
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