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Dysregulated metal ion homeostasis underscores non-canonical function of CD8(+) T cell during COVID-19

INTRODUCTION: Several efforts have been made to describe the complexity of T cell heterogeneity during the COVID-19 disease; however, there remain gaps in our understanding in terms of the granularity within. METHODS: For this attempt, we performed a single-cell transcriptomic analysis of 33 individ...

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Autores principales: Khare, Kriti, Chattopadhyay, Partha, Devi, Priti, Mehta, Priyanka, Raina, Aakarshan, Liu, Chinky Shiu Chen, Tardalkar, Kishore, Joshi, Meghnad G., Pandey, Rajesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598344/
https://www.ncbi.nlm.nih.gov/pubmed/37886355
http://dx.doi.org/10.3389/fmed.2023.1282390
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author Khare, Kriti
Chattopadhyay, Partha
Devi, Priti
Mehta, Priyanka
Raina, Aakarshan
Liu, Chinky Shiu Chen
Tardalkar, Kishore
Joshi, Meghnad G.
Pandey, Rajesh
author_facet Khare, Kriti
Chattopadhyay, Partha
Devi, Priti
Mehta, Priyanka
Raina, Aakarshan
Liu, Chinky Shiu Chen
Tardalkar, Kishore
Joshi, Meghnad G.
Pandey, Rajesh
author_sort Khare, Kriti
collection PubMed
description INTRODUCTION: Several efforts have been made to describe the complexity of T cell heterogeneity during the COVID-19 disease; however, there remain gaps in our understanding in terms of the granularity within. METHODS: For this attempt, we performed a single-cell transcriptomic analysis of 33 individuals (4 healthy, 16 COVID-19 positive patients, and 13 COVID-19 recovered individuals). RESULTS: We found CD8(+) T cell-biased lymphopenia in COVID-19 patients compared to healthy and recovered individuals. We also found an optimal Th1/Th2 ratio, indicating an effective immune response during COVID-19. Expansion of activated CD4(+) T and NK T was detected in the COVID-19-positive individuals. Surprisingly, we found cellular and metal ion homeostasis pathways enriched in the COVID-19-positive individuals compared to the healthy and recovered in the CD8(+) T cell populations (CD8(+) TCM and CD8(+) TEM) as well as activated CD4(+) T cells. DISCUSSION: In summary, the COVID-19-positive individuals exhibit a dynamic T cell mediated response. This response may have a possible association with the dysregulation of non-canonical pathways, including housekeeping functions in addition to the conventional antiviral immune response mediated by the T cell subpopulation. These findings considerably extend our insights into the heterogeneity of T cell response during and post-SARS-CoV-2 infection.
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spelling pubmed-105983442023-10-26 Dysregulated metal ion homeostasis underscores non-canonical function of CD8(+) T cell during COVID-19 Khare, Kriti Chattopadhyay, Partha Devi, Priti Mehta, Priyanka Raina, Aakarshan Liu, Chinky Shiu Chen Tardalkar, Kishore Joshi, Meghnad G. Pandey, Rajesh Front Med (Lausanne) Medicine INTRODUCTION: Several efforts have been made to describe the complexity of T cell heterogeneity during the COVID-19 disease; however, there remain gaps in our understanding in terms of the granularity within. METHODS: For this attempt, we performed a single-cell transcriptomic analysis of 33 individuals (4 healthy, 16 COVID-19 positive patients, and 13 COVID-19 recovered individuals). RESULTS: We found CD8(+) T cell-biased lymphopenia in COVID-19 patients compared to healthy and recovered individuals. We also found an optimal Th1/Th2 ratio, indicating an effective immune response during COVID-19. Expansion of activated CD4(+) T and NK T was detected in the COVID-19-positive individuals. Surprisingly, we found cellular and metal ion homeostasis pathways enriched in the COVID-19-positive individuals compared to the healthy and recovered in the CD8(+) T cell populations (CD8(+) TCM and CD8(+) TEM) as well as activated CD4(+) T cells. DISCUSSION: In summary, the COVID-19-positive individuals exhibit a dynamic T cell mediated response. This response may have a possible association with the dysregulation of non-canonical pathways, including housekeeping functions in addition to the conventional antiviral immune response mediated by the T cell subpopulation. These findings considerably extend our insights into the heterogeneity of T cell response during and post-SARS-CoV-2 infection. Frontiers Media S.A. 2023-10-10 /pmc/articles/PMC10598344/ /pubmed/37886355 http://dx.doi.org/10.3389/fmed.2023.1282390 Text en Copyright © 2023 Khare, Chattopadhyay, Devi, Mehta, Raina, Liu, Tardalkar, Joshi and Pandey. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Khare, Kriti
Chattopadhyay, Partha
Devi, Priti
Mehta, Priyanka
Raina, Aakarshan
Liu, Chinky Shiu Chen
Tardalkar, Kishore
Joshi, Meghnad G.
Pandey, Rajesh
Dysregulated metal ion homeostasis underscores non-canonical function of CD8(+) T cell during COVID-19
title Dysregulated metal ion homeostasis underscores non-canonical function of CD8(+) T cell during COVID-19
title_full Dysregulated metal ion homeostasis underscores non-canonical function of CD8(+) T cell during COVID-19
title_fullStr Dysregulated metal ion homeostasis underscores non-canonical function of CD8(+) T cell during COVID-19
title_full_unstemmed Dysregulated metal ion homeostasis underscores non-canonical function of CD8(+) T cell during COVID-19
title_short Dysregulated metal ion homeostasis underscores non-canonical function of CD8(+) T cell during COVID-19
title_sort dysregulated metal ion homeostasis underscores non-canonical function of cd8(+) t cell during covid-19
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10598344/
https://www.ncbi.nlm.nih.gov/pubmed/37886355
http://dx.doi.org/10.3389/fmed.2023.1282390
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