4.5 Review

Group 3 innate lymphoid cells: regulating host-commensal bacteria interactions in inflammation and cancer

Journal

INTERNATIONAL IMMUNOLOGY
Volume 28, Issue 1, Pages 43-52

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/intimm/dxv056

Keywords

cancer; commensal bacteria; innate lymphoid cells; intestinal homeostasis

Categories

Funding

  1. National Institutes of Health [DP5OD012116, R56AI114724]
  2. NIAID Mucosal Immunology Studies Team Scholar Award in Mucosal Immunity
  3. Institute for Translational Medicine and Therapeutics Transdisciplinary Program in Translational Medicine and Therapeutics from the US National Center for Research Resources [UL1-RR024134]
  4. Crohn's and Colitis Foundation of America [297365]

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ILC3s regulate inflammation, the microbiota and cancer.A delicate balance exists between the mammalian immune system and normally beneficial commensal bacteria that colonize the gastrointestinal tract, which is necessary to maintain tissue homeostasis. Dysregulation of these interactions between the host and commensal bacteria is causally associated with chronic inflammation and the development of cancer. In contrast, recent reports have highlighted that commensal bacteria also play an essential role in promoting anti-tumor immune responses in several contexts, highlighting a paradox whereby interactions between the host and commensal bacteria can influence both pro- and anti-tumor immunity. Given the critical roles for group 3 innate lymphoid cells (ILC3s) in regulating inflammation, tissue repair and host-microbe interactions in the intestine, here we discuss new evidence that ILC3s may profoundly influence the development, progression and control of tumors. In this review, we provide an overview of recent advances in understanding the impact of commensal bacteria on tumorigenesis, discuss recent findings identifying ILC3s as critical regulators of host-microbe interactions and highlight the emerging role of this immune cell population in cancer and their potential implication as a therapeutic target.

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