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Concordance of B‐ and T‐cell responses to SARS‐CoV‐2 infection, irrespective of symptoms suggestive of COVID‐19

This study assessed T‐cell responses in individuals with and without a positive antibody response to SARS‐CoV‐2, in symptomatic and asymptomatic individuals during the COVID‐19 pandemic. Participants were drawn from the TwinsUK cohort, grouped by (a) presence or absence of COVID‐associated symptoms...

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Autores principales: Österdahl, Marc F., Christakou, Eleni, Hart, Deborah, Harris, Ffion, Shahrabi, Yasaman, Pollock, Emily, Wadud, Muntaha, Spector, Tim D., Brown, Matthew A., Seow, Jeffrey, Malim, Michael H., Steves, Claire J., Doores, Katie J., Duncan, Emma L., Tree, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349709/
https://www.ncbi.nlm.nih.gov/pubmed/35864567
http://dx.doi.org/10.1002/jmv.28016
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author Österdahl, Marc F.
Christakou, Eleni
Hart, Deborah
Harris, Ffion
Shahrabi, Yasaman
Pollock, Emily
Wadud, Muntaha
Spector, Tim D.
Brown, Matthew A.
Seow, Jeffrey
Malim, Michael H.
Steves, Claire J.
Doores, Katie J.
Duncan, Emma L.
Tree, Timothy
author_facet Österdahl, Marc F.
Christakou, Eleni
Hart, Deborah
Harris, Ffion
Shahrabi, Yasaman
Pollock, Emily
Wadud, Muntaha
Spector, Tim D.
Brown, Matthew A.
Seow, Jeffrey
Malim, Michael H.
Steves, Claire J.
Doores, Katie J.
Duncan, Emma L.
Tree, Timothy
author_sort Österdahl, Marc F.
collection PubMed
description This study assessed T‐cell responses in individuals with and without a positive antibody response to SARS‐CoV‐2, in symptomatic and asymptomatic individuals during the COVID‐19 pandemic. Participants were drawn from the TwinsUK cohort, grouped by (a) presence or absence of COVID‐associated symptoms (S+, S−), logged prospectively through the COVID Symptom Study app, and (b) anti‐IgG Spike and anti‐IgG Nucleocapsid antibodies measured by ELISA (Ab+, Ab−), during the first wave of the UK pandemic. T‐cell helper and regulatory responses after stimulation with SARS‐CoV‐2 peptides were assessed. Thirty‐two participants were included in the final analysis. Fourteen of 15 with IgG Spike antibodies had a T‐cell response to SARS‐CoV‐2‐specific peptides; none of 17 participants without IgG Spike antibodies had a T‐cell response (χ (2): 28.2, p < 0.001). Quantitative T‐cell responses correlated strongly with fold‐change in IgG Spike antibody titer (ρ = 0.79, p < 0.0001) but not to symptom score (ρ = 0.17, p = 0.35). Humoral and cellular immune responses to SARS‐CoV‐2 are highly correlated. We found no evidence of cellular immunity suggestive of SARS‐CoV2 infection in individuals with a COVID‐19‐like illness but negative antibodies.
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spelling pubmed-93497092022-08-04 Concordance of B‐ and T‐cell responses to SARS‐CoV‐2 infection, irrespective of symptoms suggestive of COVID‐19 Österdahl, Marc F. Christakou, Eleni Hart, Deborah Harris, Ffion Shahrabi, Yasaman Pollock, Emily Wadud, Muntaha Spector, Tim D. Brown, Matthew A. Seow, Jeffrey Malim, Michael H. Steves, Claire J. Doores, Katie J. Duncan, Emma L. Tree, Timothy J Med Virol Research Articles This study assessed T‐cell responses in individuals with and without a positive antibody response to SARS‐CoV‐2, in symptomatic and asymptomatic individuals during the COVID‐19 pandemic. Participants were drawn from the TwinsUK cohort, grouped by (a) presence or absence of COVID‐associated symptoms (S+, S−), logged prospectively through the COVID Symptom Study app, and (b) anti‐IgG Spike and anti‐IgG Nucleocapsid antibodies measured by ELISA (Ab+, Ab−), during the first wave of the UK pandemic. T‐cell helper and regulatory responses after stimulation with SARS‐CoV‐2 peptides were assessed. Thirty‐two participants were included in the final analysis. Fourteen of 15 with IgG Spike antibodies had a T‐cell response to SARS‐CoV‐2‐specific peptides; none of 17 participants without IgG Spike antibodies had a T‐cell response (χ (2): 28.2, p < 0.001). Quantitative T‐cell responses correlated strongly with fold‐change in IgG Spike antibody titer (ρ = 0.79, p < 0.0001) but not to symptom score (ρ = 0.17, p = 0.35). Humoral and cellular immune responses to SARS‐CoV‐2 are highly correlated. We found no evidence of cellular immunity suggestive of SARS‐CoV2 infection in individuals with a COVID‐19‐like illness but negative antibodies. John Wiley and Sons Inc. 2022-07-30 2022-11 /pmc/articles/PMC9349709/ /pubmed/35864567 http://dx.doi.org/10.1002/jmv.28016 Text en © 2022 The Authors. Journal of Medical Virology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Österdahl, Marc F.
Christakou, Eleni
Hart, Deborah
Harris, Ffion
Shahrabi, Yasaman
Pollock, Emily
Wadud, Muntaha
Spector, Tim D.
Brown, Matthew A.
Seow, Jeffrey
Malim, Michael H.
Steves, Claire J.
Doores, Katie J.
Duncan, Emma L.
Tree, Timothy
Concordance of B‐ and T‐cell responses to SARS‐CoV‐2 infection, irrespective of symptoms suggestive of COVID‐19
title Concordance of B‐ and T‐cell responses to SARS‐CoV‐2 infection, irrespective of symptoms suggestive of COVID‐19
title_full Concordance of B‐ and T‐cell responses to SARS‐CoV‐2 infection, irrespective of symptoms suggestive of COVID‐19
title_fullStr Concordance of B‐ and T‐cell responses to SARS‐CoV‐2 infection, irrespective of symptoms suggestive of COVID‐19
title_full_unstemmed Concordance of B‐ and T‐cell responses to SARS‐CoV‐2 infection, irrespective of symptoms suggestive of COVID‐19
title_short Concordance of B‐ and T‐cell responses to SARS‐CoV‐2 infection, irrespective of symptoms suggestive of COVID‐19
title_sort concordance of b‐ and t‐cell responses to sars‐cov‐2 infection, irrespective of symptoms suggestive of covid‐19
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9349709/
https://www.ncbi.nlm.nih.gov/pubmed/35864567
http://dx.doi.org/10.1002/jmv.28016
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