CD4 T Lymphocytes from Patients with Chronic Fatigue Syndrome Have Decreased Interferon‐γ Production and Increased Sensitivity to Dexamethasone
Author(s) -
Jeroen Visser,
Bep Blauw,
B. Hinloopen,
E.J.P. Brommer,
E. R. de Kloet,
Cornelis Kluft,
Lex Nagelkerken
Publication year - 1998
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/517373
Subject(s) - endocrinology , medicine , dexamethasone , chronic fatigue syndrome , immune system , interferon , t cell , cytokine , interleukin , immunology , biology
A disturbed hypothalamus-pituitary-adrenal gland axis and alterations at the immune system level have been observed in patients with chronic fatigue syndrome (CFS). Glucocorticoids are known to modulate T cell responses; therefore, purified CD4 T cells from CFS patients were studied to determine whether they have an altered sensitivity to dexamethasone (DEX). CD4 T cells from CFS patients produced less interferon-gamma than did cells from controls; by contrast, interleukin-4 production and cell proliferation were comparable. With CD4 T cells from CFS patients (compared with cells from controls), a 10- to 20-fold lower DEX concentration was needed to achieve 50% inhibition of interleukin-4 production and proliferation, indicating an increased sensitivity to DEX in CFS patients. Surprisingly, interferon-gamma production in patients and controls was equally sensitive to DEX. A differential sensitivity of cytokines or CD4 T cell subsets to glucocorticoids might explain an altered immunologic function in CFS patients.
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