Dysregulation of ILC3s unleashes progression and immunotherapy resistance in colon cancer. Academic Article uri icon

Overview

abstract

  • Group 3 innate lymphoid cells (ILC3s) regulate immunity and inflammation, yet their role in cancer remains elusive. Here, we identify that colorectal cancer (CRC) manifests with altered ILC3s that are characterized by reduced frequencies, increased plasticity, and an imbalance with T cells. We evaluated the consequences of these changes in mice and determined that a dialog between ILC3s and T cells via major histocompatibility complex class II (MHCII) is necessary to support colonization with microbiota that subsequently induce type-1 immunity in the intestine and tumor microenvironment. As a result, mice lacking ILC3-specific MHCII develop invasive CRC and resistance to anti-PD-1 immunotherapy. Finally, humans with dysregulated intestinal ILC3s harbor microbiota that fail to induce type-1 immunity and immunotherapy responsiveness when transferred to mice. Collectively, these data define a protective role for ILC3s in cancer and indicate that their inherent disruption in CRC drives dysfunctional adaptive immunity, tumor progression, and immunotherapy resistance.

publication date

  • August 17, 2021

Research

keywords

  • Colonic Neoplasms
  • Disease Progression
  • Immunity, Innate
  • Immunotherapy
  • Lymphocytes

Identity

PubMed Central ID

  • PMC8454863

Scopus Document Identifier

  • 85115026856

Digital Object Identifier (DOI)

  • 10.1016/j.cell.2021.07.029

PubMed ID

  • 34407392

Additional Document Info

volume

  • 184

issue

  • 19