期刊
AGING AND DISEASE
卷 12, 期 1, 页码 277-296出版社
INT SOC AGING & DISEASE
DOI: 10.14336/AD.2020.0627
关键词
sepsis; aging; immunosenescence; immune cell; dysfunction
资金
- China National Key Research Program [2018ZX09201013]
- China PLA Key Research Program [BLB18J008]
Sepsis is a life-threatening organ dysfunction caused by dysregulated host responses to infection, with elderly individuals displaying increased susceptibility and mortality due to immune dysfunction. Alterations in immune cells of elderly sepsis patients, including endothelial cells, neutrophils, monocytes, macrophages, natural killer cells, dendritic cells, T lymphocytes, and B lymphocytes, largely contribute to their poor prognosis and increased mortality. Recent studies on elderly mice and sepsis patients have investigated changes affecting both innate and adaptive immune cells, shedding light on potential new therapeutic strategies.
Sepsis is a form of life-threatening organ dysfunction caused by dysregulated host responses to an infection that can be partly attributed to immune dysfunction. Although sepsis affects patients of all ages, elderly individuals display increased susceptibility and mortality. This is partly due to immunosenescence, a decline in normal immune system function associated with physiological aging that affects almost all cell types in the innate and adaptive immune systems. In elderly patients with sepsis, these alterations in immune cells such as endothelial cells, neutrophils, monocytes, macrophages, natural killer cells, dendritic cells, T lymphocytes, and B lymphocytes, are largely responsible for their poor prognosis and increased mortality. Here, we review recent studies investigating the events affecting both innate and adaptive immune cells in elderly mice and patients with sepsis, including alterations in their number, phenotype, and function, to shed light on possible new therapeutic strategies.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据