Identification of a Novel Subset of Myeloid-Derived Suppressor Cells During Chronic Staphylococcal Infection That Resembles Immature Eosinophils

J Infect Dis. 2017 Dec 12;216(11):1444-1451. doi: 10.1093/infdis/jix494.

Abstract

We have previously reported that myeloid-derived suppressor cells (MDSC), which are a heterogeneous population of immunosuppressive immature myeloid cells, expanded during chronic Staphylococcus aureus infection and promoted bacterial persistence by inhibiting effector T cells. Two major MDSC subsets, including monocytic MDSC and granulocytic MDSC, have been described to date. Here, we identified a new subset of MDSC (Eo-MDSC) in S. aureus-infected mice that phenotypically resembles eosinophils. Eo-MDSC exhibit eosinophilic cytoplasmic granules and express CD11b, the eosinophil marker Syglec-F, variable levels of CCR3, and low levels of interleukin-5Rα. Furthermore, Eo-MDSC accumulated at the site of infection and exerted a potent immunosuppressive effect on T-cell responses that was mediated by nitric oxide-dependent depletion of l-arginine. Increases in the number of Eo-MDSC by adoptive transfer caused a significant exacerbation of infection in S. aureus-infected mice. This study sheds new light on the heterogeneity and complexity of MDSC during chronic infection.

Keywords: Staphylococcus aureus; chronic infection; eosinophils; immunosuppression; myeloid-derived suppressor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer
  • Animals
  • Arginine
  • CD11b Antigen / metabolism
  • CD4-Positive T-Lymphocytes / immunology
  • Cell Proliferation
  • Cytokines / biosynthesis
  • Cytokines / metabolism
  • Disease Models, Animal
  • Eosinophils / drug effects*
  • Female
  • Gene Expression
  • Immune Tolerance / immunology
  • Interleukin-5 Receptor alpha Subunit / metabolism
  • Kidney / pathology
  • Mice
  • Mice, Inbred C57BL
  • Myeloid-Derived Suppressor Cells / metabolism*
  • Myeloid-Derived Suppressor Cells / microbiology*
  • Myeloid-Derived Suppressor Cells / pathology
  • Nitric Oxide
  • Phenotype
  • Receptors, CCR3 / metabolism
  • Spleen / microbiology
  • Spleen / pathology
  • Staphylococcal Infections / immunology*
  • Staphylococcal Infections / metabolism*
  • Staphylococcus aureus / pathogenicity
  • Staphylococcus aureus / physiology
  • T-Lymphocytes / drug effects
  • T-Lymphocytes, Regulatory

Substances

  • CD11b Antigen
  • Ccr3 protein, mouse
  • Cytokines
  • Interleukin-5 Receptor alpha Subunit
  • Receptors, CCR3
  • interleukin-5- receptor alpha, mouse
  • Nitric Oxide
  • Arginine