Aging and CMV Infection Affect Pre-existing SARS-CoV-2-Reactive CD8+ T Cells in Unexposed Individuals

Age is a major risk factor for COVID-19 severity, and T cells play a central role in anti-SARS-CoV-2 immunity. Because SARS-CoV-2-cross-reactive T cells have been detected in unexposed individuals, we investigated the age-related differences in pre-existing SARS-CoV-2-reactive T cells. SARS-CoV-2-re...

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Main Authors: Norihide Jo, Rui Zhang, Hideki Ueno, Takuya Yamamoto, Daniela Weiskopf, Miki Nagao, Shinya Yamanaka, Yoko Hamazaki
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-08-01
Series:Frontiers in Aging
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fragi.2021.719342/full
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spelling doaj-0972f62376b243a7af034d4589a3463d2021-08-10T05:12:32ZengFrontiers Media S.A.Frontiers in Aging2673-62172021-08-01210.3389/fragi.2021.719342719342Aging and CMV Infection Affect Pre-existing SARS-CoV-2-Reactive CD8+ T Cells in Unexposed IndividualsNorihide Jo0Norihide Jo1Rui Zhang2Hideki Ueno3Hideki Ueno4Takuya Yamamoto5Takuya Yamamoto6Daniela Weiskopf7Miki Nagao8Shinya Yamanaka9Shinya Yamanaka10Yoko Hamazaki11Yoko Hamazaki12Department of Life Science Frontiers, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, JapanAlliance Laboratory for Advanced Medical Research, Graduate School of Medicine, Kyoto University, Kyoto, JapanDepartment of Life Science Frontiers, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, JapanDepartment of Immunology, Graduate School of Medicine, Kyoto University, Kyoto, JapanInstitute for the Advanced Study of Human Biology (WPI-ASHBi), Kyoto University, Kyoto, JapanDepartment of Life Science Frontiers, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, JapanInstitute for the Advanced Study of Human Biology (WPI-ASHBi), Kyoto University, Kyoto, JapanCenter for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, CA, United StatesDepartment of Clinical Laboratory Medicine, Graduate School of Medicine, Kyoto University, Kyoto, JapanDepartment of Life Science Frontiers, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, JapanGladstone Institute of Cardiovascular Disease, San Francisco, CA, United StatesDepartment of Life Science Frontiers, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, JapanLaboratory of Immunobiology, Graduate School of Medicine, Kyoto University, Kyoto, JapanAge is a major risk factor for COVID-19 severity, and T cells play a central role in anti-SARS-CoV-2 immunity. Because SARS-CoV-2-cross-reactive T cells have been detected in unexposed individuals, we investigated the age-related differences in pre-existing SARS-CoV-2-reactive T cells. SARS-CoV-2-reactive CD4+ T cells from young and elderly individuals were mainly detected in the central memory fraction and exhibited similar functionalities and numbers. Naïve-phenotype SARS-CoV-2-reactive CD8+ T cell populations decreased markedly in the elderly, while those with terminally differentiated and senescent phenotypes increased. Furthermore, senescent SARS-CoV-2-reactive CD8+ T cell populations were higher in cytomegalovirus seropositive young individuals compared to seronegative ones. Our findings suggest that age-related differences in pre-existing SARS-CoV-2-reactive CD8+ T cells may explain the poor outcomes in elderly patients and that cytomegalovirus infection is a potential factor affecting CD8+ T cell immunity against SARS-CoV-2. Thus, this study provides insights for developing effective therapeutic and vaccination strategies for the elderly.https://www.frontiersin.org/articles/10.3389/fragi.2021.719342/fullSARS-CoV-2COVID-19T-cell immunitycross-reactive T cellssenescent T cellscytomegalovirus
collection DOAJ
language English
format Article
sources DOAJ
author Norihide Jo
Norihide Jo
Rui Zhang
Hideki Ueno
Hideki Ueno
Takuya Yamamoto
Takuya Yamamoto
Daniela Weiskopf
Miki Nagao
Shinya Yamanaka
Shinya Yamanaka
Yoko Hamazaki
Yoko Hamazaki
spellingShingle Norihide Jo
Norihide Jo
Rui Zhang
Hideki Ueno
Hideki Ueno
Takuya Yamamoto
Takuya Yamamoto
Daniela Weiskopf
Miki Nagao
Shinya Yamanaka
Shinya Yamanaka
Yoko Hamazaki
Yoko Hamazaki
Aging and CMV Infection Affect Pre-existing SARS-CoV-2-Reactive CD8+ T Cells in Unexposed Individuals
Frontiers in Aging
SARS-CoV-2
COVID-19
T-cell immunity
cross-reactive T cells
senescent T cells
cytomegalovirus
author_facet Norihide Jo
Norihide Jo
Rui Zhang
Hideki Ueno
Hideki Ueno
Takuya Yamamoto
Takuya Yamamoto
Daniela Weiskopf
Miki Nagao
Shinya Yamanaka
Shinya Yamanaka
Yoko Hamazaki
Yoko Hamazaki
author_sort Norihide Jo
title Aging and CMV Infection Affect Pre-existing SARS-CoV-2-Reactive CD8+ T Cells in Unexposed Individuals
title_short Aging and CMV Infection Affect Pre-existing SARS-CoV-2-Reactive CD8+ T Cells in Unexposed Individuals
title_full Aging and CMV Infection Affect Pre-existing SARS-CoV-2-Reactive CD8+ T Cells in Unexposed Individuals
title_fullStr Aging and CMV Infection Affect Pre-existing SARS-CoV-2-Reactive CD8+ T Cells in Unexposed Individuals
title_full_unstemmed Aging and CMV Infection Affect Pre-existing SARS-CoV-2-Reactive CD8+ T Cells in Unexposed Individuals
title_sort aging and cmv infection affect pre-existing sars-cov-2-reactive cd8+ t cells in unexposed individuals
publisher Frontiers Media S.A.
series Frontiers in Aging
issn 2673-6217
publishDate 2021-08-01
description Age is a major risk factor for COVID-19 severity, and T cells play a central role in anti-SARS-CoV-2 immunity. Because SARS-CoV-2-cross-reactive T cells have been detected in unexposed individuals, we investigated the age-related differences in pre-existing SARS-CoV-2-reactive T cells. SARS-CoV-2-reactive CD4+ T cells from young and elderly individuals were mainly detected in the central memory fraction and exhibited similar functionalities and numbers. Naïve-phenotype SARS-CoV-2-reactive CD8+ T cell populations decreased markedly in the elderly, while those with terminally differentiated and senescent phenotypes increased. Furthermore, senescent SARS-CoV-2-reactive CD8+ T cell populations were higher in cytomegalovirus seropositive young individuals compared to seronegative ones. Our findings suggest that age-related differences in pre-existing SARS-CoV-2-reactive CD8+ T cells may explain the poor outcomes in elderly patients and that cytomegalovirus infection is a potential factor affecting CD8+ T cell immunity against SARS-CoV-2. Thus, this study provides insights for developing effective therapeutic and vaccination strategies for the elderly.
topic SARS-CoV-2
COVID-19
T-cell immunity
cross-reactive T cells
senescent T cells
cytomegalovirus
url https://www.frontiersin.org/articles/10.3389/fragi.2021.719342/full
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