TY - JOUR
T1 - Increased percentages of regulatory T cells are associated with inflammatory and neuroendocrine responses to acute psychological stress and poorer health status in older men and women
AU - Ronaldson, Amy
AU - Gazali, Ahmad M.
AU - Zalli, Argita
AU - Kaiser, Frank
AU - Thompson, Stephen J.
AU - Henderson, Brian
AU - Steptoe, Andrew
AU - Carvalho, Livia
N1 - Publisher Copyright:
© 2015 The Author(s).
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Rationale: The percentage of regulatory T cells (TRegs) - a subtype of T lymphocyte that suppresses the immune response - appears to be reduced in a number of stress-related diseases. The role of the TReg in stress-disease pathways has not yet been investigated. Objectives: The aim of the study was to investigate the association between biological responsivity to acute psychosocial stress and the percentage of TRegs in healthy older adults. The secondary purpose was to measure the associations between TReg percentage and psychological and physical well-being in the participants. Methods: Salivary cortisol and plasma interleukin (IL)-6 samples were obtained from 121 healthy older men and women from the Whitehall II cohort following acute psychophysiological stress testing. Three years later at a follow-up visit, we measured TReg percentages and psychological and physical well-being were recorded using the Short Form 36 Health Survey and the Center for Epidemiologic Studies Depression Scale. Results: Blunted cortisol responses (p = 0.004) and elevated IL-6 responses (p = 0.027) to acute psychophysiological stress were associated with greater TReg percentage independently of age, sex, BMI, smoking status, employment grade, time of testing, and baseline measures of cortisol and IL-6, respectively. Percentage of TRegs was associated cross-sectionally with lower physical (p = 0.043) and mental health status (p = 0.008), and higher levels of depressive symptoms (p = 0.002), independently of covariates. Conclusions: Increased levels of TRegs may act as a defence against increased inflammation and may be a pre-indication for chronically stressed individuals on the cusp of clinical illness.
AB - Rationale: The percentage of regulatory T cells (TRegs) - a subtype of T lymphocyte that suppresses the immune response - appears to be reduced in a number of stress-related diseases. The role of the TReg in stress-disease pathways has not yet been investigated. Objectives: The aim of the study was to investigate the association between biological responsivity to acute psychosocial stress and the percentage of TRegs in healthy older adults. The secondary purpose was to measure the associations between TReg percentage and psychological and physical well-being in the participants. Methods: Salivary cortisol and plasma interleukin (IL)-6 samples were obtained from 121 healthy older men and women from the Whitehall II cohort following acute psychophysiological stress testing. Three years later at a follow-up visit, we measured TReg percentages and psychological and physical well-being were recorded using the Short Form 36 Health Survey and the Center for Epidemiologic Studies Depression Scale. Results: Blunted cortisol responses (p = 0.004) and elevated IL-6 responses (p = 0.027) to acute psychophysiological stress were associated with greater TReg percentage independently of age, sex, BMI, smoking status, employment grade, time of testing, and baseline measures of cortisol and IL-6, respectively. Percentage of TRegs was associated cross-sectionally with lower physical (p = 0.043) and mental health status (p = 0.008), and higher levels of depressive symptoms (p = 0.002), independently of covariates. Conclusions: Increased levels of TRegs may act as a defence against increased inflammation and may be a pre-indication for chronically stressed individuals on the cusp of clinical illness.
UR - http://www.scopus.com/inward/record.url?scp=84922697099&partnerID=8YFLogxK
U2 - 10.1007/s00213-015-3876-3
DO - 10.1007/s00213-015-3876-3
M3 - Journal articles
C2 - 25678193
AN - SCOPUS:84922697099
SN - 0033-3158
VL - 233
SP - 1661
EP - 1668
JO - Psychopharmacology
JF - Psychopharmacology
IS - 9
ER -