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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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Detalles Bibliográficos
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
Descripción
Sumario: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.