Suppression, subversion and escape: the role of regulatory T cells in cancer progression (original) (raw)

Oleinika, K., Nibbs, R.J. ORCID: https://orcid.org/0000-0002-8150-0044, Graham, G.J. ORCID: https://orcid.org/0000-0002-7801-204X and Fraser, A.R.(2013) Suppression, subversion and escape: the role of regulatory T cells in cancer progression.Clinical and Experimental Immunology, 171(1), pp. 36-45. (doi: 10.1111/j.1365-2249.2012.04657.x)

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Publisher's URL: http://dx.doi.org/10.1111/j.1365-2249.2012.04657.x

Abstract

Regulatory T cells (T_regs) are crucial in mediating immune homeostasis and promoting the establishment and maintenance of peripheral tolerance. However, in the context of cancer their role is more complex, and they are thought to contribute to the progress of many tumours. As cancer cells express both self- and tumour-associated antigens, T_regs are key to dampening effector cell responses, and therefore represent one of the main obstacles to effective anti-tumour responses. Suppression mechanisms employed by T_regs are thought to contribute significantly to the failure of current therapies that rely on induction or potentiation of anti-tumour responses. This review will focus on the current evidence supporting the central role of T_regs in establishing tumour-specific tolerance and promoting cancer escape. We outline the mechanisms underlying their suppressive function and discuss the potential routes of T_regs accumulation within the tumour, including enhanced recruitment, in-situ or local proliferation, and de-novo differentiation. In addition, we review some of the cancer treatment strategies that act, at least in part, to eliminate or interfere with the function of T_regs. The role of T_regs is being recognized increasingly in cancer, and controlling the function of these suppressive cells in the tumour microenvironment without compromising peripheral tolerance represents a significant challenge for cancer therapies.

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Funder and Project Information

2

Regulation of the adaptive immune response by chemokine scavenging receptors

Gerard Graham

G0901113

III -IMMUNOLOGY

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