4.7 Article

Immune consequences of the spontaneous pro-inflammatory status in depressed elderly patients

Journal

BRAIN BEHAVIOR AND IMMUNITY
Volume 18, Issue 2, Pages 135-148

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/S0889-1591(03)00111-9

Keywords

CMV; depression; immune attrition; inflammation; ageing; anti-influenza vaccination; cytokines

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Introduction. The aim of the study was to describe the interrelationship between senescence, depression, and immunity. Methods. We assessed 10 elderly patients with depression and 10 age- and sex-matched controls: before, at one and at six month intervals after the anti-influenza vaccination. Levels of TNFalpha, IL6, ACTH, and cortisol, titres of anti-hemagglutinins and anti-neuraminidases, lymphocytes secreting IFNgamma, IL2, IL4, and IL10, cytotoxicity of NK and CD3(+)CD8(+)IFNgamma(+) cells, anti-CMV antibodies, and CD28(-)CD57(+) lymphocytes known to be associated with the CMV carrier status were evaluated. Results. Higher levels of anti-CMV, higher percentage of the CD28(-)CD57(+) cells, and elevated levels of TNFalpha, IL6, and cortisol concomitant with decreased levels of ACTH and insufficient production of IL10 (which increased the IFNgamma(+)/IL10(+) ratio) were found in the patients suffering from depression, in comparison to healthy controls. The subjects with depression revealed a low NK cytotoxicity, while a level of CD3(+)CD8(+)IFNgamma(+) cells was comparable between the groups. Although the levels of anti-hemagglutinins and anti-neuraminidases were low in the depressed patients, they reached the protective titres. The majority of these differences disappeared when CMV titres were entered into the analyses as a covariate. Discussion. The results suggest that the elderly depressed patients were characterised by increased exposure to CMV in the past, which could have resulted in a pro-inflammatory profile demonstrated as elevated levels of TNFalpha, IL6 and deficiency of suppressive IL10(+) cells. These changes negatively affect humoral and innate response in the depressed patients. (C) 2003 Elsevier Inc. All rights reserved.

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