Immunosenescence: A Critical Factor Associated With Organ Injury After Sepsis

Progressive immune dysfunction associated with aging is known as immunosenescence. The age-related deterioration of immune function is accompanied by chronic inflammation and microenvironment changes. Immunosenescence can affect both innate and acquired immunity. Sepsis is a systemic inflammatory re...

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Main Authors: Xuan Lu, Yun-Mei Yang, Yuan-Qiang Lu
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-07-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2022.917293/full
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author Xuan Lu
Xuan Lu
Yun-Mei Yang
Yun-Mei Yang
Yuan-Qiang Lu
Yuan-Qiang Lu
author_facet Xuan Lu
Xuan Lu
Yun-Mei Yang
Yun-Mei Yang
Yuan-Qiang Lu
Yuan-Qiang Lu
author_sort Xuan Lu
collection DOAJ
description Progressive immune dysfunction associated with aging is known as immunosenescence. The age-related deterioration of immune function is accompanied by chronic inflammation and microenvironment changes. Immunosenescence can affect both innate and acquired immunity. Sepsis is a systemic inflammatory response that affects parenchymal organs, such as the respiratory system, cardiovascular system, liver, urinary system, and central nervous system, according to the sequential organ failure assessment (SOFA). The initial immune response is characterized by an excess release of inflammatory factors, followed by persistent immune paralysis. Moreover, immunosenescence was found to complement the severity of the immune disorder following sepsis. Furthermore, the immune characteristics associated with sepsis include lymphocytopenia, thymus degeneration, and immunosuppressive cell proliferation, which are very similar to the characteristics of immunosenescence. Therefore, an in-depth understanding of immunosenescence after sepsis and its subsequent effects on the organs may contribute to the development of promising therapeutic strategies. This paper focuses on the characteristics of immunosenescence after sepsis and rigorously analyzes the possible underlying mechanism of action. Based on several recent studies, we summarized the relationship between immunosenescence and sepsis-related organs. We believe that the association between immunosenescence and parenchymal organs might be able to explain the delayed consequences associated with sepsis.
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spelling doaj.art-77280bd7faf642218d57ce38c73c160a2022-12-22T02:12:11ZengFrontiers Media S.A.Frontiers in Immunology1664-32242022-07-011310.3389/fimmu.2022.917293917293Immunosenescence: A Critical Factor Associated With Organ Injury After SepsisXuan Lu0Xuan Lu1Yun-Mei Yang2Yun-Mei Yang3Yuan-Qiang Lu4Yuan-Qiang Lu5Department of Geriatric and Emergency Medicine, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, ChinaThe Key Laboratory for Diagnosis and Treatment of Aging and Physic-chemical Injury Diseases of Zhejiang Province, Hangzhou, ChinaDepartment of Geriatric and Emergency Medicine, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, ChinaThe Key Laboratory for Diagnosis and Treatment of Aging and Physic-chemical Injury Diseases of Zhejiang Province, Hangzhou, ChinaDepartment of Geriatric and Emergency Medicine, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, ChinaThe Key Laboratory for Diagnosis and Treatment of Aging and Physic-chemical Injury Diseases of Zhejiang Province, Hangzhou, ChinaProgressive immune dysfunction associated with aging is known as immunosenescence. The age-related deterioration of immune function is accompanied by chronic inflammation and microenvironment changes. Immunosenescence can affect both innate and acquired immunity. Sepsis is a systemic inflammatory response that affects parenchymal organs, such as the respiratory system, cardiovascular system, liver, urinary system, and central nervous system, according to the sequential organ failure assessment (SOFA). The initial immune response is characterized by an excess release of inflammatory factors, followed by persistent immune paralysis. Moreover, immunosenescence was found to complement the severity of the immune disorder following sepsis. Furthermore, the immune characteristics associated with sepsis include lymphocytopenia, thymus degeneration, and immunosuppressive cell proliferation, which are very similar to the characteristics of immunosenescence. Therefore, an in-depth understanding of immunosenescence after sepsis and its subsequent effects on the organs may contribute to the development of promising therapeutic strategies. This paper focuses on the characteristics of immunosenescence after sepsis and rigorously analyzes the possible underlying mechanism of action. Based on several recent studies, we summarized the relationship between immunosenescence and sepsis-related organs. We believe that the association between immunosenescence and parenchymal organs might be able to explain the delayed consequences associated with sepsis.https://www.frontiersin.org/articles/10.3389/fimmu.2022.917293/fullsepsisimmune agingimmunosenescenceimmunosuppressionmyeloid-derived suppressor cells
spellingShingle Xuan Lu
Xuan Lu
Yun-Mei Yang
Yun-Mei Yang
Yuan-Qiang Lu
Yuan-Qiang Lu
Immunosenescence: A Critical Factor Associated With Organ Injury After Sepsis
Frontiers in Immunology
sepsis
immune aging
immunosenescence
immunosuppression
myeloid-derived suppressor cells
title Immunosenescence: A Critical Factor Associated With Organ Injury After Sepsis
title_full Immunosenescence: A Critical Factor Associated With Organ Injury After Sepsis
title_fullStr Immunosenescence: A Critical Factor Associated With Organ Injury After Sepsis
title_full_unstemmed Immunosenescence: A Critical Factor Associated With Organ Injury After Sepsis
title_short Immunosenescence: A Critical Factor Associated With Organ Injury After Sepsis
title_sort immunosenescence a critical factor associated with organ injury after sepsis
topic sepsis
immune aging
immunosenescence
immunosuppression
myeloid-derived suppressor cells
url https://www.frontiersin.org/articles/10.3389/fimmu.2022.917293/full
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