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...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-09-01
|
Series: | Cells |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4409/10/9/2435 |
id |
doaj-0b075e051e994e17ab1b0ef64bc92ed3 |
---|---|
record_format |
Article |
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 |
_version_ |
1717367635007504384 |