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IL-33/regulatory T cell axis triggers the development of a tumor-promoting immune environment in chronic inflammation
Author(s) -
Amir H. Ameri,
Sara Moradi Tuchayi,
Anniek Zaalberg,
Jong Ho Park,
Kenneth Ngo,
Tiancheng Li,
E López,
Marco Colonna,
Richard Lee,
Mari MinoKenudson,
Shadmehr Demehri
Publication year - 2019
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1815016116
Subject(s) - inflammation , immune system , cancer research , medicine , immunology , biology
Significance Chronic inflammatory diseases are well-recognized causes of cancer and account for up to 20% of all cancer deaths worldwide. However, the mechanism that initiates the development of a tumor-promoting immune environment in chronic inflammation is not known. Using mouse models of chronic skin and colon inflammation and human samples, we show IL-33 triggers the transition from tumor-suppressive immunity to chronic, tumor-promoting inflammation through a regulatory T cell-dependent mechanism. Our findings demonstrate a generalized dependency of tumor-promoting immune environments on the IL-33/Treg axis both in the skin and colon. Based on these findings, IL-33/Treg axis blockade may be an attractive therapeutic strategy for the treatment and prevention of cancers associated with chronic inflammatory diseases and potentiating the antitumor immunity induced by cancer immunotherapeutics.

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