Functions of adipose-resident immune subsets and the impact on metabolic syndrome

Immunology. 2018 Dec;155(4):405-406. doi: 10.1111/imm.13015.

Abstract

There is a growing appreciation of the role in the aetiology of metabolic syndrome that is played by the interplay of diet, microbiota and the interactions of immune cells and adipose cells in visceral adipose tissue. Recent studies have highlighted the programmes, properties and roles of the specialized, resident immune subsets that are abundant in adipose tissue, which may be considered a newly identified lymphoid compartment for immunology research. The findings indicate important roles for resident T effector and regulatory cells, innate lymphoid cells (ILCs), invariant natural killer T (iNKT) cells and macrophages, among others. Immunologists are at the very beginning of trying to narrate a story of complex interactions, with the need to unravel cause from effect. The enterprise will require studies in humans as well as mice, and needs to bring together the collaborative efforts of scientists and clinicians from diverse spheres including metabolic disease, diet and microbiology.

Publication types

  • Editorial

MeSH terms

  • Animals
  • Humans
  • Interleukin-23 / immunology
  • Interleukin-33 / immunology
  • Intra-Abdominal Fat / cytology
  • Intra-Abdominal Fat / immunology*
  • Macrophages / immunology*
  • Metabolic Syndrome / etiology*
  • Metabolic Syndrome / immunology*
  • Metabolic Syndrome / microbiology
  • Mice
  • Natural Killer T-Cells / immunology*
  • T-Lymphocytes, Regulatory / immunology*
  • Th17 Cells / immunology

Substances

  • Interleukin-23
  • Interleukin-33