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Stress ; 12(2): 134-43, 2009 Mar.
Article in English | MEDLINE | ID: mdl-18609297

ABSTRACT

Long-term exposure to stressful situations can affect the immune system. The T-cell response is an important component of anti-tumoral immunity. Hence, impairment of the immune function induced by a chronic stressor has been postulated to alter the immunosurveillance of tumors, thus leading to a worse neoplastic prognosis. Here, we show that chronic restraint stress affects T-cell mediated immunity in mice. This was evidenced by a decrease of mitogen-induced T-cell proliferation, a reduction in CD4(+)T lymphocyte number and a decrease of tumor necrosis factor-alpha (TNF-alpha) and Interferon-gamma (IFN-gamma) production in stressed mice. Additionally, mice subjected to chronic restraint stress displayed an enhancement of tumor growth in a syngeneic lymphoma model, i.e. an increase of tumor proliferation and a reduction of animal survival. Finally, stressed mice had a reduced specific cytotoxic response against these tumor cells. These results suggest that chronic exposure to stress promotes cancer establishment and subsequent progression, probably by depressing T-cell mediated immunity. The T-cell immunity impairment as well as the tumor progression enhancement emphasize the importance of the therapeutic management of stress to improve the prognosis of cancer patients.


Subject(s)
Lymphoma, T-Cell/immunology , Stress, Psychological/immunology , T-Lymphocytes/immunology , Animals , Behavior, Animal , CD4-Positive T-Lymphocytes/immunology , Cell Proliferation , Female , Interferon-gamma/biosynthesis , Killer Cells, Natural/immunology , Lymphoma, T-Cell/pathology , Mice , Mice, Inbred BALB C , Restraint, Physical , Tumor Necrosis Factor-alpha/biosynthesis
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