β-Glucan-Induced Trained Immunity Protects against Leishmania braziliensis Infection: a Crucial Role for IL-32

Cell Rep. 2019 Sep 3;28(10):2659-2672.e6. doi: 10.1016/j.celrep.2019.08.004.

Abstract

American tegumentary leishmaniasis is a vector-borne parasitic disease caused by Leishmania protozoans. Innate immune cells undergo long-term functional reprogramming in response to infection or Bacillus Calmette-Guérin (BCG) vaccination via a process called trained immunity, conferring non-specific protection from secondary infections. Here, we demonstrate that monocytes trained with the fungal cell wall component β-glucan confer enhanced protection against infections caused by Leishmania braziliensis through the enhanced production of proinflammatory cytokines. Mechanistically, this augmented immunological response is dependent on increased expression of interleukin 32 (IL-32). Studies performed using a humanized IL-32 transgenic mouse highlight the clinical implications of these findings in vivo. This study represents a definitive characterization of the role of IL-32γ in the trained phenotype induced by β-glucan or BCG, the results of which improve our understanding of the molecular mechanisms governing trained immunity and Leishmania infection control.

Keywords: BCG; IL-32; IL-32 transgenic mouse; Leishmania braziliensis; proinflammatory cytokines; trained immunity; β-glucan.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Aged
  • Animals
  • BCG Vaccine / immunology
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / metabolism
  • Female
  • Hematopoietic Stem Cells / drug effects
  • Hematopoietic Stem Cells / metabolism
  • Humans
  • Immunity* / drug effects
  • Interleukin-1 / metabolism
  • Interleukins / metabolism*
  • Leishmania braziliensis / drug effects
  • Leishmania braziliensis / physiology*
  • Leishmaniasis, Cutaneous / prevention & control*
  • Macrophages / drug effects
  • Macrophages / parasitology
  • Male
  • Mice, Transgenic
  • Middle Aged
  • Monocytes / drug effects
  • Monocytes / metabolism
  • Signal Transduction / drug effects
  • Transcription, Genetic / drug effects
  • Up-Regulation / drug effects
  • Vaccination
  • Young Adult
  • beta-Glucans / pharmacology*

Substances

  • BCG Vaccine
  • IL32 protein, human
  • Interleukin-1
  • Interleukins
  • beta-Glucans