Myeloid-derived suppressor cells exert immunosuppressive function on the T helper 2 in mice infected with Echinococcus granulosus

Exp Parasitol. 2020 Aug:215:107917. doi: 10.1016/j.exppara.2020.107917. Epub 2020 May 22.

Abstract

Cystic echinococcosis (CE) is a worldwide hazardous zoonotic parasitosis caused by Echinococcus granulosus. CE development involves complex immunological mechanisms, including participation of multiple immune cells and effector molecules. Myeloid-derived suppressor cells (MDSCs) are known to be involved in chronic and acute inflammatory conditions. In this study, we aimed to characterize the immune function of MDSCs in CE to improve the understanding, prevention and treatment of CE. Our results indicated that MDSCs overexpressing Ly6C and Ly6G inhibit the formation and activity of T helper 2 cells in a NO-dependent manner during E. granulosus infection.

Keywords: Echinococcus granulosus; Immunosuppressive function; Myeloid-derived suppressor cells (MDSCs).

MeSH terms

  • Analysis of Variance
  • Animals
  • Antibodies, Monoclonal
  • Arginase / analysis
  • Bone Marrow / drug effects
  • Bone Marrow / immunology
  • Cytokines / analysis
  • Echinococcosis / immunology*
  • Echinococcus granulosus / immunology*
  • Female
  • Flow Cytometry
  • Humans
  • Keratolytic Agents / pharmacology
  • Mice
  • Myeloid-Derived Suppressor Cells / drug effects
  • Myeloid-Derived Suppressor Cells / enzymology
  • Myeloid-Derived Suppressor Cells / immunology*
  • Nitric Oxide / analysis
  • Reactive Oxygen Species / analysis
  • Specific Pathogen-Free Organisms
  • Spleen / cytology
  • Spleen / drug effects
  • Spleen / immunology
  • Th2 Cells / immunology*
  • Tretinoin / pharmacology

Substances

  • Antibodies, Monoclonal
  • Cytokines
  • Keratolytic Agents
  • Reactive Oxygen Species
  • Nitric Oxide
  • Tretinoin
  • Arginase