significance of Treg cells in defective tumor immunity
Regulatory T cells (Treg) enriched in FoxP3⁺, glucocorticoid-induced TNF receptor⁺, and cytotoxic T-lymphocyte-associated antigen-4⁺ exert a potential to suppress effector T cells in the periphery. These cells exist in markedly higher proportions within tumor-infiltrating lymphocytes, peripheral blo...
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Published in | Archivum Immunologiae et Therapiae Experimentalis Vol. 56; no. 3; pp. 181 - 191 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Basel
Basel : Birkhäuser-Verlag
01.06.2008
Birkhäuser-Verlag Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Regulatory T cells (Treg) enriched in FoxP3⁺, glucocorticoid-induced TNF receptor⁺, and cytotoxic T-lymphocyte-associated antigen-4⁺ exert a potential to suppress effector T cells in the periphery. These cells exist in markedly higher proportions within tumor-infiltrating lymphocytes, peripheral blood lymphocytes, and/or regional lymph node lymphocytes of patients with cancer and their frequencies are suggested to be strongly related to tumor progression and inversely correlated with the efficacy of treatment. Tumor-specific Treg cells require ligand-specific activation and cell-to-cell contact to exert their suppressive activity on tumor-specific effector cells (CD8⁺ cytotoxic T lymphocytes and CD4⁺ Th cells), which includes decreased cytotoxity, proliferation, and Th1 cytokine secrection. Depletion or blockade of Treg cells can enhance immune protection from tumor-associated antigens that are expressed as self antigens. Recent studies revealed that lymphoma T cells might adopt a Treg profile as well. Studies assessing the influence of chemotherapy on Treg cells have also been included in this review. |
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Bibliography: | http://dx.doi.org/10.1007/s00005-008-0018-1 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-3 ObjectType-Review-1 |
ISSN: | 0004-069X 1661-4917 |
DOI: | 10.1007/s00005-008-0018-1 |