Understanding T cell aging to improve anti-viral immunity

2021 ◽  
Vol 51 ◽  
pp. 127-133
Author(s):  
Huimin Zhang ◽  
Cornelia M Weyand ◽  
Jörg J Goronzy ◽  
Claire E Gustafson
Keyword(s):  
T Cell ◽  
Author(s):  
Kristen Orumaa ◽  
Margaret R. Dunne

AbstractCOVID-19 is a respiratory disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It was first documented in late 2019, but within months, a worldwide pandemic was declared due to the easily transmissible nature of the virus. Research to date on the immune response to SARS-CoV-2 has focused largely on conventional B and T lymphocytes. This review examines the emerging role of unconventional T cell subsets, including γδ T cells, invariant natural killer T (iNKT) cells and mucosal associated invariant T (MAIT) cells in human SARS-CoV-2 infection.Some of these T cell subsets have been shown to play protective roles in anti-viral immunity by suppressing viral replication and opsonising virions of SARS-CoV. Here, we explore whether unconventional T cells play a protective role in SARS-CoV-2 infection as well. Unconventional T cells are already under investigation as cell-based immunotherapies for cancer. We discuss the potential use of these cells as therapeutic agents in the COVID-19 setting. Due to the rapidly evolving situation presented by COVID-19, there is an urgent need to understand the pathogenesis of this disease and the mechanisms underlying its immune response. Through this, we may be able to better help those with severe cases and lower the mortality rate by devising more effective vaccines and novel treatment strategies.


2021 ◽  
Author(s):  
Maria Mittelbrunn ◽  
Guido Kroemer
Keyword(s):  
T Cell ◽  

Blood ◽  
2003 ◽  
Vol 102 (9) ◽  
pp. 3244-3251 ◽  
Author(s):  
Vladimir Janković ◽  
Ilhem Messaoudi ◽  
Janko Nikolich-Žugich

AbstractA prominent theory of immune senescence holds that repeated antigenic stimulation and decreased production of naive cells combine to progressively exhaust the reserve of lymphocytes available to fight new pathogens, culminating in an accumulation of lymphocytes that achieved replicative senescence. A well-defined primate model of immune senescence in vivo would greatly facilitate testing of this theory. Here, we investigated phenotypic and functional T-cell aging in the rhesus macaques (RMs), currently the dominant primate model of AIDS. Our results show that sharp differences exist between the CD8 and CD4 T-cell subsets in (1) cell-cycle programs (as assessed by both in vitro proliferation and in vivo turnover measurement); (2) CD28 regulation on cell-cycle entry; and (3) accumulation of immediate effector cells among the CD28– cells, believed to be close to or at replicative senescence. These results further suggest poor reliability of CD28 as a marker for senescence. We suggest that some of the T-cell aging phenomenology in RMs can be ascribed to accentuation over time of the inherent differences in activation programs in CD8 and CD4 T cells.


Immunity ◽  
2017 ◽  
Vol 46 (3) ◽  
pp. 364-378 ◽  
Author(s):  
Jörg J. Goronzy ◽  
Cornelia M. Weyand
Keyword(s):  
T Cell ◽  

PLoS ONE ◽  
2014 ◽  
Vol 9 (2) ◽  
pp. e89379 ◽  
Author(s):  
Ting-Ting Sheu ◽  
Bor-Luen Chiang ◽  
Jui-Hung Yen ◽  
Wen-Chi Lin

1998 ◽  
Vol 33 (3) ◽  
pp. 267-282 ◽  
Author(s):  
Nathalie Boucher ◽  
Tania Dufeu-Duchesne ◽  
Eric Vicaut ◽  
Dominique Farge ◽  
Rita B Effros ◽  
...  
Keyword(s):  
T Cell ◽  

2019 ◽  
Vol 208 (3-4) ◽  
pp. 281-287 ◽  
Author(s):  
TienYu Owen Yang ◽  
Yi-Fang Chuang ◽  
Yen-Ling Chiu

Immunity ◽  
2016 ◽  
Vol 45 (4) ◽  
pp. 903-916 ◽  
Author(s):  
Yinyin Li ◽  
Yi Shen ◽  
Philipp Hohensinner ◽  
Jihang Ju ◽  
Zhenke Wen ◽  
...  

Oncotarget ◽  
2014 ◽  
Vol 6 (1) ◽  
pp. 171-184 ◽  
Author(s):  
Xuekai Zhu ◽  
Shruthi Prasad ◽  
Simone Gaedicke ◽  
Michael Hettich ◽  
Elke Firat ◽  
...  

2013 ◽  
Vol 4 ◽  
Author(s):  
Dietmar Herndler-Brandstetter ◽  
Harumichi Ishigame ◽  
Richard A. Flavell
Keyword(s):  
T Cell ◽  

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