| Literature DB >> 25713993 |
Ming-Song Li1, Zhenzhen Liu, Jin-Qing Liu, Xiaotong Zhu, Zhihao Liu, Xue-Feng Bai.
Abstract
Accumulating evidences from animal studies have indicated that both endogenous and exogenous IL-27, an IL-12 family of cytokine, can increase antitumor T-cell activities and inhibit tumor growth. IL-27 can modulate Treg responses, and program effector T cells into a unique T-effector stem cell (TSEC) phenotype, which enhances T-cell survival in the tumor microenvironment. However, animal studies also suggest that IL-27 induces molecular pathways such as IL-10, PD-L1 and CD39, which may downregulate tumor-specific T-cell responses. In this review paper, we will discuss the Yin and Yang aspects of IL-27 in the induction of tumor-specific T-cell responses, and the potential impacts of these functions of IL-27 in the design of cancer immunotherapy.Entities:
Keywords: IL-12; IL-27; T-effector stem cells; cancer immunotherapy; regulatory T cells
Mesh:
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Year: 2015 PMID: 25713993 PMCID: PMC4356131 DOI: 10.2217/imt.14.95
Source DB: PubMed Journal: Immunotherapy ISSN: 1750-743X Impact factor: 4.196