期刊
ONCOIMMUNOLOGY
卷 3, 期 6, 页码 -出版社
LANDES BIOSCIENCE
DOI: 10.4161/onci.29126
关键词
BRAF; melanoma; T cell; CD40L; IFN gamma
资金
- Howard Hughes Medical Institute Funding Source: Medline
- NCI NIH HHS [P50 CA121974] Funding Source: Medline
- NIAID NIH HHS [R01 AI074699] Funding Source: Medline
The establishment of an immunosuppressive tumor microenvironment is a hallmark feature driving cancer cell evasion of immunosurveillance. In a murine melanoma model, we recently demonstrated that decreased intratumoral CD4(+) T-cell expression of CD40L and interferon gamma (IFN gamma) is critical to maintain this immunosuppressive microenvironment. Altered effector functions of tumor-associated CD4(+) T cells is essential for B-Raf(V600E) inhibitor-mediated restoration of antitumor immunity.
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