T Cell Immunosenescence in Aging, Obesity, and Cardiovascular Disease

Although advances in preventive medicine have greatly improved prognosis, cardiovascular disease (CVD) remains the leading cause of death worldwide. This clearly indicates that there remain residual cardiovascular risks that have not been targeted by conventional therapies. The results of multiple a...

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Main Authors: Kohsuke Shirakawa, Motoaki Sano
Format: Article
Language:English
Published: MDPI AG 2021-09-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/10/9/2435
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spelling doaj-0b075e051e994e17ab1b0ef64bc92ed32021-09-25T23:53:10ZengMDPI AGCells2073-44092021-09-01102435243510.3390/cells10092435T Cell Immunosenescence in Aging, Obesity, and Cardiovascular DiseaseKohsuke Shirakawa0Motoaki Sano1Department of Cardiovascular Medicine, Graduate School of Medicine, Juntendo University, Bunkyo-ku, Tokyo 1138421, JapanDepartment of Cardiology, Keio University School of Medicine, Shinjuku-ku, Tokyo 1608582, JapanAlthough advances in preventive medicine have greatly improved prognosis, cardiovascular disease (CVD) remains the leading cause of death worldwide. This clearly indicates that there remain residual cardiovascular risks that have not been targeted by conventional therapies. The results of multiple animal studies and clinical trials clearly indicate that inflammation is the most important residual risk and a potential target for CVD prevention. The immune cell network is intricately regulated to maintain homeostasis. Ageing associated changes to the immune system occurs in both innate and adaptive immune cells, however T cells are most susceptible to this process. T-cell changes due to thymic degeneration and homeostatic proliferation, metabolic abnormalities, telomere length shortening, and epigenetic changes associated with aging and obesity may not only reduce normal immune function, but also induce inflammatory tendencies, a process referred to as immunosenescence. Since the disruption of biological homeostasis by T cell immunosenescence is closely related to the development and progression of CVD via inflammation, senescent T cells are attracting attention as a new therapeutic target. In this review, we discuss the relationship between CVD and T cell immunosenescence associated with aging and obesity.https://www.mdpi.com/2073-4409/10/9/2435obesitycardiovascular diseaseimmunosenescenceT cell
collection DOAJ
language English
format Article
sources DOAJ
author Kohsuke Shirakawa
Motoaki Sano
spellingShingle Kohsuke Shirakawa
Motoaki Sano
T Cell Immunosenescence in Aging, Obesity, and Cardiovascular Disease
Cells
obesity
cardiovascular disease
immunosenescence
T cell
author_facet Kohsuke Shirakawa
Motoaki Sano
author_sort Kohsuke Shirakawa
title T Cell Immunosenescence in Aging, Obesity, and Cardiovascular Disease
title_short T Cell Immunosenescence in Aging, Obesity, and Cardiovascular Disease
title_full T Cell Immunosenescence in Aging, Obesity, and Cardiovascular Disease
title_fullStr T Cell Immunosenescence in Aging, Obesity, and Cardiovascular Disease
title_full_unstemmed T Cell Immunosenescence in Aging, Obesity, and Cardiovascular Disease
title_sort t cell immunosenescence in aging, obesity, and cardiovascular disease
publisher MDPI AG
series Cells
issn 2073-4409
publishDate 2021-09-01
description Although advances in preventive medicine have greatly improved prognosis, cardiovascular disease (CVD) remains the leading cause of death worldwide. This clearly indicates that there remain residual cardiovascular risks that have not been targeted by conventional therapies. The results of multiple animal studies and clinical trials clearly indicate that inflammation is the most important residual risk and a potential target for CVD prevention. The immune cell network is intricately regulated to maintain homeostasis. Ageing associated changes to the immune system occurs in both innate and adaptive immune cells, however T cells are most susceptible to this process. T-cell changes due to thymic degeneration and homeostatic proliferation, metabolic abnormalities, telomere length shortening, and epigenetic changes associated with aging and obesity may not only reduce normal immune function, but also induce inflammatory tendencies, a process referred to as immunosenescence. Since the disruption of biological homeostasis by T cell immunosenescence is closely related to the development and progression of CVD via inflammation, senescent T cells are attracting attention as a new therapeutic target. In this review, we discuss the relationship between CVD and T cell immunosenescence associated with aging and obesity.
topic obesity
cardiovascular disease
immunosenescence
T cell
url https://www.mdpi.com/2073-4409/10/9/2435
work_keys_str_mv AT kohsukeshirakawa tcellimmunosenescenceinagingobesityandcardiovasculardisease
AT motoakisano tcellimmunosenescenceinagingobesityandcardiovasculardisease
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