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- W2097353137 abstract "T-cell responses are induced by antigen presenting cells (APC) and signals from the microenvironment. Antigen persistence and inflammatory microenvironments in chronic infections and cancer can induce a tolerant state in T-cells resulting in hyporesponsiveness, loss of effector function, and weak biochemical signaling patterns in response to antigen stimulation. Although the mechanisms of T-cell tolerance induced in chronic infection and cancer may differ from those involved in tolerance to self-antigen, the impaired proliferation and production of IL-2 in response to antigen stimulation are hallmarks of all tolerant T cells. In this review, we will summarize the evidence that the immune responses change from non-self to self-like in chronic infection and cancer, and will provide an overview of strategies for re-balancing the immune response of antigen-specific T cells in chronic infection and cancer without affecting the homeostasis of the immune system." @default.
- W2097353137 created "2016-06-24" @default.
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- W2097353137 date "2014-06-17" @default.
- W2097353137 modified "2023-09-25" @default.
- W2097353137 title "Modulation of Antigen-Specific T-Cells as Immune Therapy for Chronic Infectious Diseases and Cancer" @default.
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- W2097353137 doi "https://doi.org/10.3389/fimmu.2014.00293" @default.
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