Th1-Th2 Cross-Regulation Controls Early Leishmania Infection in the Skin by Modulating the Size of the Permissive Monocytic Host Cell Reservoir

Cell Host Microbe. 2020 May 13;27(5):752-768.e7. doi: 10.1016/j.chom.2020.03.011. Epub 2020 Apr 15.

Abstract

The impact of T helper (Th) 1 versus Th2 immunity on intracellular infections is attributed to classical versus alternative activation of macrophages leading to resistance or susceptibility. However, observations in multiple infectious settings demonstrate deficiencies in mediators of Th1-Th2 immunity, which have paradoxical or no impact. We report that prior to influencing activation, Th1/Th2 immunity first controls the size of the permissive host cell reservoir. During early Leishmania infection of the skin, IFN-γ- or STAT6-mediated changes in phagocyte activation were counteracted by changes in IFN-γ-mediated recruitment of permissive CCR2+ monocytes. Monocytes were required for early parasite expansion and acquired an alternatively activated phenotype despite the Th1 dermal environment required for their recruitment. Surprisingly, STAT6 did not enhance intracellular parasite proliferation, but rather modulated the size and permissiveness of the monocytic host cell reservoir via regulation of IFN-γ and IL-10. These observations expand our understanding of the Th1-Th2 paradigm during infection.

Keywords: CCR2; IFN-γ; IL-10; Leishmania; STAT6; Th1; Th2; iNOS; monocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Female
  • Interferon-gamma / deficiency
  • Interferon-gamma / genetics
  • Interleukin-10 / deficiency
  • Interleukin-10 / genetics
  • Leishmaniasis / immunology*
  • Macrophages / immunology
  • Mice
  • Mice, Inbred C57BL / genetics
  • Mice, Knockout
  • Monocytes / immunology*
  • Permissiveness
  • Psychodidae
  • Receptors, CCR2 / deficiency
  • Receptors, CCR2 / genetics
  • STAT6 Transcription Factor / deficiency
  • STAT6 Transcription Factor / genetics
  • STAT6 Transcription Factor / metabolism
  • Skin / immunology*
  • Th1 Cells / immunology*
  • Th2 Cells / immunology*
  • Virus Replication

Substances

  • Ccr2 protein, mouse
  • IL10 protein, mouse
  • Receptors, CCR2
  • STAT6 Transcription Factor
  • Interleukin-10
  • Interferon-gamma