共 112 条
T-Regulatory Cells: Key Players in Tumor Immune Escape and Angiogenesis
被引:655
作者:

Facciabene, Andrea
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机构:
Univ Penn, Ovarian Canc Res Ctr, Philadelphia, PA 19104 USA Univ Penn, Ovarian Canc Res Ctr, Philadelphia, PA 19104 USA

Motz, Gregory T.
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机构:
Univ Penn, Ovarian Canc Res Ctr, Philadelphia, PA 19104 USA Univ Penn, Ovarian Canc Res Ctr, Philadelphia, PA 19104 USA

Coukos, George
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机构:
Univ Penn, Ovarian Canc Res Ctr, Philadelphia, PA 19104 USA Univ Penn, Ovarian Canc Res Ctr, Philadelphia, PA 19104 USA
机构:
[1] Univ Penn, Ovarian Canc Res Ctr, Philadelphia, PA 19104 USA
基金:
美国国家卫生研究院;
关键词:
CHRONIC LYMPHOCYTIC-LEUKEMIA;
LOW-DOSE CYCLOPHOSPHAMIDE;
COLON-CANCER PATIENTS;
STAGE OVARIAN-CANCER;
PHASE-I TRIAL;
METASTATIC MELANOMA;
ANTITUMOR IMMUNITY;
TGF-BETA;
MEDIATED SUPPRESSION;
MONOCLONAL-ANTIBODY;
D O I:
10.1158/0008-5472.CAN-11-3687
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
T-regulatory cells (Tregs) are found infiltrating tumors in a vast array of tumor types, and tumor-infiltrating Tregs are often associated with a poor clinical outcome. Tregs are potent immunosuppressive cells of the immune system that promote progression of cancer through their ability to limit antitumor immunity and promote angiogenesis. Here, we discuss the ways in which Tregs suppress the antitumor immune response and elaborate on our recent discovery that Tregs make significant direct contributions to tumor angiogenesis. Further, we highlight several current therapies aimed at eliminating Tregs in cancer patients. Given the multifaceted role of Tregs in cancer, a greater understanding of their functions will ultimately strengthen future therapies. Cancer Res; 72(9); 2162-71. (C) 2012 AACR.
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页码:2162 / 2171
页数:10
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