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About:
Dynamics of B-cell repertoires and emergence of cross-reactive responses in COVID-19 patients with different disease severity
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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
has title
Dynamics of B-cell repertoires and emergence of cross-reactive responses in COVID-19 patients with different disease severity
Creator
Lv, Huibin
Peiris, J
Wilson, Ian
Wu, Nicholas
Tak, Owen
Tsang, Yin
Yip, Garrick
Yuan, Meng
Ka, Chris
Mok, Pun
Isacchini, Giulio
Liu, Hejun
Montague, Zachary
Ng, Wilson
Nourmohammad, Armita
Otwinowski, Jakub
Dewitt, William
Source
MedRxiv; Medline; PMC
abstract
COVID-19 patients show varying severity of the disease ranging from asymptomatic to requiring intensive care. Although a number of monoclonal antibodies against SARS-CoV-2 have been identified, we still lack an understanding of the overall landscape of B-cell receptor (BCR) repertoires in COVID-19 patients. Here, we used high-throughput sequencing of BCR repertoires collected over multiple time points during an infection to characterize statistical and dynamical signatures of the B-cell response to SARS-CoV-2 in 19 patients with different disease severities. Based on principled statistical approaches, we determined differential sequence features of BCRs associated with different disease severity. We identified 34 significantly expanded rare clonal lineages shared among patients as candidates for a specific response to SARS-CoV-2. Moreover, we identified natural emergence of a BCR with cross-reactivity to SARS-CoV and SARS-CoV-2 in a number of patients. Overall, our results provide important insights for development of rational therapies and vaccines against COVID-19.
has issue date
2020-07-15
(
xsd:dateTime
)
bibo:doi
10.1101/2020.07.13.20153114
bibo:pmid
32699862
has license
cc-by-nc-nd
sha1sum (hex)
5edd0b8d2e4aad4927bef804dbfa08a73527ac0a
schema:url
https://doi.org/10.1101/2020.07.13.20153114
resource representing a document's title
Dynamics of B-cell repertoires and emergence of cross-reactive responses in COVID-19 patients with different disease severity
has PubMed Central identifier
PMC7373151
has PubMed identifier
32699862
schema:publication
medRxiv
resource representing a document's body
covid:5edd0b8d2e4aad4927bef804dbfa08a73527ac0a#body_text
is
schema:about
of
named entity 'high-throughput sequencing'
named entity 'patients'
named entity 'specific'
named entity 'infection'
named entity 'responses'
named entity 'DIFFERENT'
named entity 'SEVERITY'
named entity 'sequence'
named entity 'SARS-CoV-2'
named entity 'intensive care'
named entity 'development'
named entity 'patients'
named entity 'B-cell receptor'
named entity 'intensive care'
named entity 'Bcell'
named entity 'B-cell'
named entity 'COVID-19'
named entity 'false discovery rate'
named entity 'mAbs'
named entity 'BCR'
named entity 'recombination'
named entity 'GenBank'
named entity 'BCR'
named entity 'BCR'
named entity 'SARS-CoV-2'
named entity 'sample size'
named entity 'Hamming distance'
named entity 'probability'
named entity 'heavy chain'
named entity 'SARS-CoV-2'
named entity 'SONIA'
named entity 'stop codons'
named entity 'COVID'
named entity 'BCR'
named entity 'dashed'
named entity 'primer'
named entity 'antibody'
named entity 'probability'
named entity 'SARS-CoV-2'
named entity 'mRNA'
named entity 'cysteine'
named entity 'antibodies in the blood'
named entity 'medRxiv'
named entity 'probability'
named entity 'COVID'
named entity 'p-value'
named entity 'Hong Kong West Cluster'
named entity 'dashed'
named entity 'PCR'
named entity 'gene'
named entity 'nucleoprotein'
named entity 'medRxiv'
named entity 'infection'
named entity 'Pall Corporation'
named entity 'molecular mechanism'
named entity 'paratope'
named entity 'medRxiv'
named entity 'probability'
named entity 'infectious diseases'
named entity 'clusterable'
named entity 'human plasma'
named entity 'single-linkage clustering'
named entity 'COVID-19'
named entity 'complementarity-determining regions'
named entity 'RBD'
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