Abstract

Chronic stress is known to suppress the immune system, but the influence of stress on the pathogenesis of Chlamydia trachomatis genital infection and host immune response remains unexplored A stress mouse model has been developed in our lab and we have demonstrated that cold-induced stress (CIS) suppresses the immune system and subsequently leads to increased intensity of Chlamydia muridaum in mice. We have started feeding mice with Active hexose correlated compound (AHCC) that may restore the function of the immune system and result in reduced C. muridarum shedding from the genital tract. During the feeding of stressed mice with AHCC, dendritic cells (DCs) and macrophages bring the AHCC to T cells in the lymph node; however, the specific functions of DCs subsets in our stress model are not defined. We determined the production of cytokines by macrophages, CDs, and CD4+T in the AHCC-fed stress mice during C. muridarum genital infection. CD4+ T cells isolated from the spleen or lymph node of stressed-AHCC-fed, PBS-stressed, or non-stressed mice proliferated, and cytokine secretion was measured by ELISA. AHCC-feeding led to lower production of IL-5, IL-13, IL-10 and higher IL-12 (P<0.01) and IFN-

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