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2000
Volume 18, Issue 27
  • ISSN: 1381-6128
  • E-ISSN: 1873-4286

Abstract

The capacity of the immune system to distinguish foreign from self-antigen, and to subsequently eliminate the threat of disease without injuring the host is crucial for survival. It also serves to defend against tumor formation and progression via a process termed cancer immunosurveillance. Innate and adaptive immune cell types and effector molecules collectively function as extrinsic tumorsuppressor mechanisms. However, tumors may escape immunesurveillance through a variety of mechanisms that create a local microenvironment that is unfavorable for effective tumor immunity. Transforming growth factor β (TGF-β) has pleiotropic effects on the immune system, and is recognized as one of the most potent immunosuppressive agents in facilitating oncogenesis. The TGF-β pathway promotes cancer progression by concomitantly enhancing tumor metastases while inhibiting the protective host immunity. In this review, we discuss mechanisms through which TGF-β interferes with the development of an anti-tumor immunity and potential means through which to circumvent its activity in order to define more effective cancer immunotherapies.

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/content/journals/cpd/10.2174/138161212802430378
2012-09-01
2024-10-11
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/content/journals/cpd/10.2174/138161212802430378
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  • Article Type: Research Article
Keyword(s): anti-tumor immunity; cancer; CD8+ T cells; dendritic cells; natural killer; TGF-β; Th1; Th17; Th2; treg cells
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