Fungus Regulates CD8 T Cell Exhaustion Through Involvement of T-Bet/Eomes in the Tumor Microenvironment.

Targeting exhausted T (Tex) cells is a promising strategy for anti-tumour treatment. Previously, we demonstrated that s fungus (HSF) could significantly increase T cell infiltration and the effector T cell ratio in the tumor microenvironment, activating systemic immune responses. However, we do not know how HSF regulates Tex cells in the tumor microenvironment. Here, we explored the mechanism underlying HSF inhibition of Tex cells and tumor growth and metastasis in breast cancer. We examined the effects of HSF on various tumor mouse models using imaging technology. Lung metastasis was detected by H&E staining and the T cell subsets in the tumor microenvironment were assayed with flow cytometry. The proliferation, function and apoptosis of CD8 T cells were measured, as well as the and mRNA expressions. HSF inhibited tumor growth and lung metastasis in the mice, and had significantly higher CD44CD62L and CD44CD62Lpopulations in the tumour-infiltrating CD8 T cells. However, HSF significantly reduced levels of inhibitory receptors, such as PD-1, TIGIT, CTLA-4, and regulatory T cells. , HSF inhibited the CD8 T cell apoptosis rate, and promoted CD8 T cell proliferation and secretion of interferon (IFN)-γ and granzyme B. Furthermore, HSF treatment both and significantly increased Eomes expression, while decreasing T-bet expression. HSF exerted anti-tumour effects mainly through the immune system, by promoting effector/memory T cells and reducing Tex cell production in the tumor microenvironment. The specific mechanisms involved inhibiting T-bet and promoting Eomes to decrease the expression of immune inhibitor receptors and enhance the T cell function, respectively.