Host Resistance and Immune Aging

被引:48
作者
Bandaranayake, Thilinie [1 ]
Shaw, Albert C. [1 ]
机构
[1] Yale Sch Med, Infect Dis Sect, Dept Internal Med, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
Aging; Immunosenescence; Innate immunity; Inflammation; T cell; B cell; B-CELL RESPONSES; DENDRITIC CELLS; T-CELLS; CYTOMEGALOVIRUS-SEROPOSITIVITY; NLRP3; INFLAMMASOME; INFLUENZA VACCINE; SECRETORY PHENOTYPE; AGED SUBJECTS; NK CELLS; DEPENDENT ALTERATIONS;
D O I
10.1016/j.cger.2016.02.007
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Human immune system aging results in impaired responses to pathogens or vaccines. In the innate immune system, which mediates the earliest pro inflammatory responses to immunologic challenge, processes ranging from Toll-like Receptor function to Neutrophil Extracellular Trap formation are generally diminished in older adults. Dysregulated, enhanced basal inflammation with age reflecting activation by endogenous damage associated ligands contributes to impaired innate immune responses. In the adaptive immune system, T and B cell subsets and function alter with age. The control of cytomegalovirus infection, particularly in the T lineage, plays a dominant role in the differentiation and diversity of the T cell compartment.
引用
收藏
页码:415 / +
页数:19
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