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자료유형
학술저널
저자정보
Da-Sol Kuen (Seoul National University) Byung-Seok Kim (Seoul National University) Yeonseok Chung (Seoul National University)
저널정보
대한면역학회 Immune Network Immune Network Vol.20 No.1
발행연도
2020.2
수록면
74 - 93 (20page)

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IL-17 is produced by RAR-related orphan receptor gamma t (RORγt)-expressing cells including Th17 cells, subsets of γδT 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.

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ABSTRACT
INTRODUCTION
PRODUCERS OF IL-17 IN THE TUMOR MICROENVIRONMENT
TISSUE-SPECIFIC NICHE DIVERSIFIES TYPE 17 RESPONSES
TYPE 17 CELLS AS PROGNOSIS FACTORS AND THERAPEUTIC TARGETS
CONCLUSIONS AND FUTURE PERSPECTIVES
REFERENCES

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