An overview of the immune response and Arginase I on CHIKV immunopathogenesis

Microb Pathog. 2019 Oct:135:103581. doi: 10.1016/j.micpath.2019.103581. Epub 2019 Jun 6.

Abstract

Chikungunya virus (CHIKV) is mosquito-borne alphavirus that has caused epidemics around the world. Many individuals affected by the disease may experience joint pain that persists for months after the acute phase. The pathophysiology of viral arthritis is not completely elucidated. And it is important to emphasize that the effects of the viral infection in each host may depend on host factors that include immune response, as well as factors specific to the virus as tissue tropism. The main pathway for the response against viral infection is through induction of type I interferon (IFN-I), whose function is important to control viral replication. Beside this, T cell and macrophage mediated immunopathology in CHIKV infections has been reported. It has been demonstrated that some association with the Arginase I and macrophages type II are involved in the infection profile along with myeloid-derived suppressor cells (MDSC) that are responsible for T cell suppression. Therefore, in this review, will be discuss an overview on CHIKV immunopathogenesis and the importance of Arginase I.

Keywords: Arginase I; Chikungunya virus; Cytokines; Immune cells.

Publication types

  • Review

MeSH terms

  • Arginase / metabolism*
  • Chikungunya Fever / immunology*
  • Chikungunya virus / pathogenicity*
  • Cytokines / metabolism
  • Host-Pathogen Interactions / immunology*
  • Humans
  • Interferon Type I
  • Macrophages
  • Myeloid-Derived Suppressor Cells / immunology
  • Myeloid-Derived Suppressor Cells / metabolism
  • Suppressor Factors, Immunologic
  • T-Lymphocytes
  • Viral Tropism / immunology
  • Virus Replication

Substances

  • Cytokines
  • Interferon Type I
  • Suppressor Factors, Immunologic
  • ARG1 protein, human
  • Arginase