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CD4 and CD8 T lymphocyte interplay in controlling tumor growth

期刊

CELLULAR AND MOLECULAR LIFE SCIENCES
卷 75, 期 4, 页码 689-713

出版社

SPRINGER BASEL AG
DOI: 10.1007/s00018-017-2686-7

关键词

Crosstalk; Immunotherapy; Immune escape; T cell exhaustion; Neoantigen; Oncolytic virotherapy; Cancer vaccine; Immune response; Clinical study; Cancer mouse model

资金

  1. Deutsche Forschungsgemeinschaft [WO 1933/1-2] Funding Source: Medline

向作者/读者索取更多资源

The outstanding clinical success of immune checkpoint blockade has revived the interest in underlying mechanisms of the immune system that are capable of eliminating tumors even in advanced stages. In this scenario, CD4 and CD8 T cell responses are part of the cancer immune cycle and both populations significantly influence the clinical outcome. In general, the immune system has evolved several mechanisms to protect the host against cancer. Each of them has to be undermined or evaded during cancer development to enable tumor outgrowth. In this review, we give an overview of T lymphocyte-driven control of tumor growth and discuss the involved tumor-suppressive mechanisms of the immune system, such as senescence surveillance, cancer immunosurveillance, and cancer immunoediting with respect to recent clinical developments of immunotherapies. The main focus is on the currently existing knowledge about the CD4 and CD8 T lymphocyte interplay that mediates the control of tumor growth.

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