Gender specificity of altered human immune cytokine profiles in aging

免疫系统 细胞因子 免疫学 医学 心理学 生物
作者
Edward J. Goetzl,Mei‐Chuan Huang,Junko Kon,Kalpesh Patel,Janice B. Schwartz,Katharine Fast,Luigi Ferrucci,Karen Madara,Dennis D. Taub,Dan L. Longo
出处
期刊:The FASEB Journal [Wiley]
卷期号:24 (9): 3580-3589 被引量:107
标识
DOI:10.1096/fj.10-160911
摘要

Cytokine generation by T cells and monocytes was determined for 50 subjects aged 65 yr or older and concurrently studied young subjects individually matched to each old subject for sex, race, and national origin. Highly significant differences between cytokine levels of old and young subjects all were gender specific. For T cells stimulated with anti-CD3 plus anti-CD28 antibodies, mean ratios of IFN-gamma generation for healthy old to young subjects were 0.22 for men (P<0.001; n=15) and 3.35 for women (P<0.001; n=13), and those of IL-17 were 0.30 for men (P<0.001) and no difference for women. CD8 T cells were the source of high IFN-gamma in healthy old women. For old men with an inflammatory or immune disease (n=10), mean old to young ratios of T-cell-generated IFN-gamma and IL-17 increased with disease severity up to 5.78 and 2.97 (both P<0.01), respectively, without changes for old women with similar diseases (n=12). For differentiated LPS-stimulated monocytes, old to young ratios of TNF-alpha and IL-6 generation were high only in women with immune or inflammatory disease (2.38, P<0.05 and 1.62, P<0.01, respectively), whereas ratios of IFN-gamma-evoked IP-10 chemokine were low in all groups. Alterations in immune cytokine profiles with aging show significant gender specificity.
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