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Individuals with obesity who survive SARS‐CoV‐2 infection have preserved antigen‐specific T cell frequencies

OBJECTIVE: Obesity is a major risk factor for severe disease in COVID‐19, with increased hospitalization, intensive care unit admission, and mortality. This increased impact of COVID‐19 in people with obesity (PWO) is likely driven, in part, by the well‐described obesity‐induced immune dysregulation...

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Autores principales: Wrigley Kelly, Neil E., Kenny, Grace, Cassidy, Féaron C., Garcia‐Leon, Alejandro A., De Barra, Conor, Mallon, Patrick W. G., Hogan, Andrew E., O'Shea, Donal
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/PMC9350216/
https://www.ncbi.nlm.nih.gov/pubmed/35766325
http://dx.doi.org/10.1002/oby.23526
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author Wrigley Kelly, Neil E.
Kenny, Grace
Cassidy, Féaron C.
Garcia‐Leon, Alejandro A.
De Barra, Conor
Mallon, Patrick W. G.
Hogan, Andrew E.
O'Shea, Donal
author_facet Wrigley Kelly, Neil E.
Kenny, Grace
Cassidy, Féaron C.
Garcia‐Leon, Alejandro A.
De Barra, Conor
Mallon, Patrick W. G.
Hogan, Andrew E.
O'Shea, Donal
author_sort Wrigley Kelly, Neil E.
collection PubMed
description OBJECTIVE: Obesity is a major risk factor for severe disease in COVID‐19, with increased hospitalization, intensive care unit admission, and mortality. This increased impact of COVID‐19 in people with obesity (PWO) is likely driven, in part, by the well‐described obesity‐induced immune dysregulation. Obesity has also been associated with impaired immune memory in many settings, including weakened responses to hepatitis B, tetanus, rabies, and influenza vaccination. Recently, it was reported that PWO who have COVID‐19 have reduced IgG antibody titers with defective neutralizing capabilities. However, it remains unknown whether PWO generate durable T cell immunity to SARS‐CoV‐2. METHODS: This study investigated SARS‐CoV‐2‐specific T cell responses in a cohort of 40 patients (n = 20 PWO and n = 20 matched control individuals) who had recovered from COVID‐19. T cell (CD4(+), CD8(+)) cytokine responses (IFNγ, TNFα) to SARS‐CoV‐2 peptide pools (spike, membrane) were determined using multicolor flow cytometry. RESULTS: Circulating T cells specific for SARS‐CoV‐2 were readily detected in the total cohort. PWO displayed comparable levels of SARS‐CoV‐2 spike‐ and membrane‐specific T cells, with both T cell subsets responding. CONCLUSIONS: These data indicate that PWO who survive COVID‐19 generate robust and durable SARS‐CoV‐2‐specific T cell immunity that is equivalent to that seen in those without obesity.
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spelling pubmed-93502162022-08-04 Individuals with obesity who survive SARS‐CoV‐2 infection have preserved antigen‐specific T cell frequencies Wrigley Kelly, Neil E. Kenny, Grace Cassidy, Féaron C. Garcia‐Leon, Alejandro A. De Barra, Conor Mallon, Patrick W. G. Hogan, Andrew E. O'Shea, Donal Obesity (Silver Spring) BRIEF CUTTING EDGE REPORTS OBJECTIVE: Obesity is a major risk factor for severe disease in COVID‐19, with increased hospitalization, intensive care unit admission, and mortality. This increased impact of COVID‐19 in people with obesity (PWO) is likely driven, in part, by the well‐described obesity‐induced immune dysregulation. Obesity has also been associated with impaired immune memory in many settings, including weakened responses to hepatitis B, tetanus, rabies, and influenza vaccination. Recently, it was reported that PWO who have COVID‐19 have reduced IgG antibody titers with defective neutralizing capabilities. However, it remains unknown whether PWO generate durable T cell immunity to SARS‐CoV‐2. METHODS: This study investigated SARS‐CoV‐2‐specific T cell responses in a cohort of 40 patients (n = 20 PWO and n = 20 matched control individuals) who had recovered from COVID‐19. T cell (CD4(+), CD8(+)) cytokine responses (IFNγ, TNFα) to SARS‐CoV‐2 peptide pools (spike, membrane) were determined using multicolor flow cytometry. RESULTS: Circulating T cells specific for SARS‐CoV‐2 were readily detected in the total cohort. PWO displayed comparable levels of SARS‐CoV‐2 spike‐ and membrane‐specific T cells, with both T cell subsets responding. CONCLUSIONS: These data indicate that PWO who survive COVID‐19 generate robust and durable SARS‐CoV‐2‐specific T cell immunity that is equivalent to that seen in those without obesity. John Wiley and Sons Inc. 2022-09-01 2022-10 /pmc/articles/PMC9350216/ /pubmed/35766325 http://dx.doi.org/10.1002/oby.23526 Text en © 2022 The Authors. Obesity published by Wiley Periodicals LLC on behalf of The Obesity Society (TOS). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle BRIEF CUTTING EDGE REPORTS
Wrigley Kelly, Neil E.
Kenny, Grace
Cassidy, Féaron C.
Garcia‐Leon, Alejandro A.
De Barra, Conor
Mallon, Patrick W. G.
Hogan, Andrew E.
O'Shea, Donal
Individuals with obesity who survive SARS‐CoV‐2 infection have preserved antigen‐specific T cell frequencies
title Individuals with obesity who survive SARS‐CoV‐2 infection have preserved antigen‐specific T cell frequencies
title_full Individuals with obesity who survive SARS‐CoV‐2 infection have preserved antigen‐specific T cell frequencies
title_fullStr Individuals with obesity who survive SARS‐CoV‐2 infection have preserved antigen‐specific T cell frequencies
title_full_unstemmed Individuals with obesity who survive SARS‐CoV‐2 infection have preserved antigen‐specific T cell frequencies
title_short Individuals with obesity who survive SARS‐CoV‐2 infection have preserved antigen‐specific T cell frequencies
title_sort individuals with obesity who survive sars‐cov‐2 infection have preserved antigen‐specific t cell frequencies
topic BRIEF CUTTING EDGE REPORTS
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350216/
https://www.ncbi.nlm.nih.gov/pubmed/35766325
http://dx.doi.org/10.1002/oby.23526
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