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About:
B cell clonal expansion and convergent antibody responses to SARS-CoV-2
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schema:ScholarlyArticle
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
B cell clonal expansion and convergent antibody responses to SARS-CoV-2
Creator
Yang, Fan
Rogers, Angela
Lee, Ji-Yeun
Kim, Peter
Pinsky, Benjamin
Roeltgen, Katharina
Blish, Catherine
Article, Research
Boyd, Scott
Hoh, Ramona
Jackson, Katherine
Nielsen, Sandra
Powell, Abigail
Rustagi, Arjun
Wang, Taia
source
Medline; PMC
abstract
During virus infection B cells are critical for the production of antibodies and protective immunity. Establishment of a diverse antibody repertoire occurs by rearrangement of germline DNA at the immunoglobulin heavy and light chain loci to encode the membrane-bound form of antibodies, the B cell antigen receptor. Little is known about the B cells and antigen receptors stimulated by the novel human coronavirus SARS-CoV-2. Here we show that the human B cell compartment in patients with diagnostically confirmed SARS-CoV-2 and clinical COVID-19 is rapidly altered with the early recruitment of B cells expressing a limited subset of V genes, and extensive activation of IgG and IgA subclasses without significant somatic mutation. We detect expansion of B cell clones as well as convergent antibodies with highly similar sequences across SARS-CoV-2 patients, highlighting stereotyped naïve responses to this virus. A shared convergent B cell clonotype in SARS-CoV-2 infected patients was previously seen in patients with SARS. These findings offer molecular insights into shared features of human B cell responses to SARS-CoV-2 and other zoonotic spillover coronaviruses.
has issue date
2020-05-06
(
xsd:dateTime
)
bibo:doi
10.21203/rs.3.rs-27220/v1
bibo:pmid
32702737
has license
cc-by
sha1sum (hex)
658608215fcb44553b086a2ece196daacb65af5f
schema:url
https://doi.org/10.21203/rs.3.rs-27220/v1
resource representing a document's title
B cell clonal expansion and convergent antibody responses to SARS-CoV-2
has PubMed Central identifier
PMC7336706
has PubMed identifier
32702737
schema:publication
Res Sq
resource representing a document's body
covid:658608215fcb44553b086a2ece196daacb65af5f#body_text
is
schema:about
of
named entity 'antibodies'
named entity 'antibody'
named entity 'clonal expansion'
named entity 'SARS-CoV-2'
named entity 'COVID-19'
named entity 'HTS'
named entity 'SARS-CoV-2'
named entity 'IgD'
named entity 'IgM'
named entity 'IGH'
named entity 'IGHV'
named entity 'p-value'
named entity 'receptor'
named entity 'gDNA'
named entity 'speci'
named entity 'serology'
named entity 'IgA'
named entity 'RNA'
named entity 'cell clones'
named entity 'IgG'
named entity 'IgG'
named entity 'p-value'
named entity 'IGH'
named entity 'isotypes'
named entity 'Qiagen'
named entity 'Invitrogen'
named entity 'homologous'
named entity 'SARS-CoV-2'
named entity 'antibody response'
named entity 'EBOV'
named entity 'IGHV'
named entity 'antibodies'
named entity 'plasma'
named entity 'antigen'
named entity 'SARS-CoV-2'
named entity 'COVID'
named entity 'Qubit'
named entity 'infection'
named entity 'virus'
named entity 'SARS-CoV-2'
named entity 'p-value'
named entity 'clone'
named entity 'antibody'
named entity 'IgG2'
named entity 'gDNA'
named entity 'COVID'
named entity 'isotype'
named entity 'IGH'
named entity 'IgE'
named entity 'HKU1'
named entity 'p-value'
named entity 'gDNA'
named entity 'Clonal'
named entity 'SARS-CoV-2'
named entity 'coronaviruses'
named entity 'Qiagen'
named entity 'speci'
named entity 'antibody'
named entity 'somatic mutation'
named entity 'RT-qPCR'
named entity 'SHM'
named entity 'SARS-CoV'
named entity 'humoral'
named entity 'heavy chain'
named entity 'constant region'
named entity 'primers'
named entity 'infection'
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