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Regulatory T Cell as a Target for Cancer Therapy
被引:38
|作者:
Dias de Rezende, Lucas Cunha
[1
]
Silva, Ian Victor
[2
]
Azevedo Rangel, Leticia Batista
[1
]
Cunegundes Guimaraes, Marco Cesar
[1
]
机构:
[1] Univ Fed Espirito Santo, Lab Cellular & Mol Biol Human Canc, Dept Pharmaceut Sci, BR-29040090 Vitoria, ES, Brazil
[2] Univ Fed Espirito Santo, Dept Morphol, Lab Ageing Cell Biol, BR-29040090 Vitoria, ES, Brazil
关键词:
Cancer;
Immunotherapy;
Regulatory lymphocytes;
Foxp3;
TRANSCRIPTION FACTOR FOXP3;
CHRONIC LYMPHOCYTIC-LEUKEMIA;
GROWTH-FACTOR-BETA;
PHASE-I TRIAL;
TUMOR-IMMUNITY;
POSITIVE SELECTION;
FUSION-PROTEIN;
MEDIATED SUPPRESSION;
METASTATIC MELANOMA;
DENILEUKIN DIFTITOX;
D O I:
10.1007/s00005-010-0075-0
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Advances in our understanding of CD4(+) CD25(+)Foxp3(+) regulatory T cells (T-Regs) enabled the characterization of their activities in maintaining peripheral tolerance, preventing autoimmune diseases, and limiting chronic inflammatory diseases. Ironically, an effective action of these cells during tumor development can limit beneficial responses by suppressing immunity and limiting antitumor resistance, whereas one of the main functions of the immune system is to eliminate malignant cells. During the last years, the immunological role, mechanism of action, and clinical importance of these cells were profoundly characterized and the relationship between this subset of lymphocytes and cancerous cells arises as a key factor that influences tumor development. Recent insights obtained from clinical studies and experimental mouse models expand our perception of the potential role of T-Regs in cancer treatment. In this review we describe the basic mechanisms of T-Reg origin and differentiation, their potential role in cancer, as well as the future perspectives concerning the modulation of these cells as a potential approach for anticancer strategies.
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页码:179 / 190
页数:12
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