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Stress ; 12(2): 134-43, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18609297

RESUMEN

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.


Asunto(s)
Linfoma de Células T/inmunología , Estrés Psicológico/inmunología , Linfocitos T/inmunología , Animales , Conducta Animal , Linfocitos T CD4-Positivos/inmunología , Proliferación Celular , Femenino , Interferón gamma/biosíntesis , Células Asesinas Naturales/inmunología , Linfoma de Células T/patología , Ratones , Ratones Endogámicos BALB C , Restricción Física , Factor de Necrosis Tumoral alfa/biosíntesis
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