TY - JOUR
T1 - Social stress and asthma
T2 - The role of corticosteroid insensitivity
AU - Haczku, Angela
AU - Panettieri, Reynold A.
N1 - Funding Information:
A.H. receives grant support from NIH R01AI055593, R01HL076646 , and ALA CI. R.A.P. is supported by the Mind, Body, Brain, and Health Initiative .
Funding Information:
Disclosure of potential conflict of interest: A. Haczku receives research support from Sepracor . R. A. Panettieri receives research support from the NIH-NHLBI and AstraZeneca .
PY - 2010/3
Y1 - 2010/3
N2 - Psychosocial stress alters susceptibility to infectious and systemic illnesses and may enhance airway inflammation in asthma by modulating immune cell function through neural and hormonal pathways. Stress activates the hypothalamic-pituitary-adrenal axis. Release of endogenous glucocorticoids, as a consequence, may play a prominent role in altering the airway immune homeostasis. Despite substantial corticosteroid and catecholamine plasma levels, chronic psychosocial stress evokes asthma exacerbations. Animal studies suggest that social stress induces corticosteroid insensitivity that in part may be a result of impaired glucocorticoid receptor expression and/or function. Such mechanisms likely promote and amplify airway inflammation in response to infections, allergen, or irritant exposure. This review discusses evidence of an altered corticosteroid responsive state as a consequence of chronic psychosocial stress. Elucidation of the mechanisms of stress-induced impairment of glucocorticoid responsiveness and immune homeostasis may identify novel therapeutic targets that could improve asthma management.
AB - Psychosocial stress alters susceptibility to infectious and systemic illnesses and may enhance airway inflammation in asthma by modulating immune cell function through neural and hormonal pathways. Stress activates the hypothalamic-pituitary-adrenal axis. Release of endogenous glucocorticoids, as a consequence, may play a prominent role in altering the airway immune homeostasis. Despite substantial corticosteroid and catecholamine plasma levels, chronic psychosocial stress evokes asthma exacerbations. Animal studies suggest that social stress induces corticosteroid insensitivity that in part may be a result of impaired glucocorticoid receptor expression and/or function. Such mechanisms likely promote and amplify airway inflammation in response to infections, allergen, or irritant exposure. This review discusses evidence of an altered corticosteroid responsive state as a consequence of chronic psychosocial stress. Elucidation of the mechanisms of stress-induced impairment of glucocorticoid responsiveness and immune homeostasis may identify novel therapeutic targets that could improve asthma management.
KW - Airway inflammation
KW - corticosteroids
KW - innate immune system
KW - psychosocial stress
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U2 - 10.1016/j.jaci.2009.11.005
DO - 10.1016/j.jaci.2009.11.005
M3 - Article
C2 - 20153032
AN - SCOPUS:77649270933
SN - 0091-6749
VL - 125
SP - 550
EP - 558
JO - Journal of Allergy and Clinical Immunology
JF - Journal of Allergy and Clinical Immunology
IS - 3
ER -