IL-17-Producing Cells in Tumor Immunity: Friends or Foes?

被引:88
作者
Kuen, Da-Sol [1 ,2 ]
Kim, Byung-Seok [1 ]
Chung, Yeonseok [1 ,2 ]
机构
[1] Seoul Natl Univ, Inst Pharmaceut Sci, Lab Immune Regulat, 1 Gwanak Ro, Seoul 08826, South Korea
[2] Seoul Natl Univ, Inst Pharmaceut Sci, BK21 Plus Program, 1 Gwanak Ro, Seoul 08826, South Korea
基金
新加坡国家研究基金会;
关键词
Tumor microenvironment; Th17; cells; Interleukin-17; T-lymphocytes; CD8(+) T-CELLS; HELPER; 17; CELLS; TH17; SUPPRESSOR-CELLS; POOR-PROGNOSIS; LUNG-CANCER; INFILTRATING LYMPHOCYTES; DIFFERENTIATION PROGRAM; INTERLEUKIN-17; RECEPTOR; METASTATIC MELANOMA;
D O I
10.4110/in.2020.20.e6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-17 is produced by RAR-related orphan receptor gamma t (ROR gamma t)-expressing cells including Th17 cells, subsets of gamma delta T cells and innate lymphoid cells (ILCs). The biological significance of IL-17-producing cells is well-studied in contexts of inflammation, autoimmunity and host defense against infection. While most of available studies in tumor immunity mainly focused on the role of T-bet-expressing cells, including cytotoxic CD8(+) T cells and NK cells, and their exhaustion status, the role of IL-17-producing cells remains poorly understood. While IL-17-producing T-cells were shown to be anti-tumorigenic in adoptive T-cell therapy settings, mice deficient in type 17 genes suggest a protumorigenic potential of IL-17-producing cells. This review discusses the features of IL-17-producing cells, of both lymphocytic and myeloid origins, as well as their suggested pro-and/or antitumorigenic functions in an organ-dependent context. Potential therapeutic approaches targeting these cells in the tumor microenvironment will also be discussed.
引用
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页数:20
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