4.4 Article

Age-dependent alterations in serum cytokines, peripheral blood mononuclear cell cytokine production, natural killer cell activity, and prostaglandin F2α

Journal

IMMUNOLOGIC RESEARCH
Volume 65, Issue 5, Pages 1009-1016

Publisher

HUMANA PRESS INC
DOI: 10.1007/s12026-017-8940-0

Keywords

Aging; Serum cytokine; PBMC cytokine; NK cell activity; Oxidative stress; Inflammation

Categories

Funding

  1. Coorperative Research Program for Agriculture Science & Technology Development, Rural Development Administration, Republic of Korea [PJ010835]

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This study aimed to determine age-dependent alterations in serum cytokines, peripheral blood mononuclear cell (PBMC) cytokine production, natural killer (NK) cell activity, and urinary 8-epi-prostaglandin F-2 alpha (PGF(2 alpha)). Nine hundred eighty-seven healthy and nonobese subjects were divided into five age groups: 20-34 (group 1), 35-44 (group 2), 45-54 (group 3), 55-64 (group 4), and 65-80 (group 5) years of age. After adjusting for BMI, sex, and smoking and drinking status, serum interferon (IFN)-gamma levels decreased in groups 3, 4, and 5 compared with those in groups 1 and 2. Production of IFN-gamma by unstimulated PBMCs was lower in the older groups (groups 4 and 5) than in the younger groups (groups 1 and 3). Serum interleukin (IL)-12 was lower in group 5 than in groups 1 and 2. In contrast, both serum and PBMC IL-6 were higher in group 5 than in groups 1, 2, and 3. Urinary 8-epi-PGF(2 alpha) increased in group 3 compared with that in group 1 and further increased in group 5. Multiple linear regression analysis revealed that serum IFN-gamma levels were negatively affected by age, and NK cell activity at a ratio of E:T = 5:1 was positively affected by PBMC IFN-gamma. This study shows the age-related reductions in serum and PBMC IFN-gamma and serum IL-12 and age-related increases in serum and PBMC IL-6 and oxidative stress in healthy nonobese subjects. Additionally, circulating IL-6 levels may be a better marker of the chronic low-grade inflammatory activity associated with aging than systemic levels of high-sensitivity C-reactive protein, TNF-alpha, and IL-1 beta.

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