TNF contributes to T-cell exhaustion in chronic L. mexicana infections of mice through PD-L1 up-regulation

Cell Immunol. 2020 Dec:358:104196. doi: 10.1016/j.cellimm.2020.104196. Epub 2020 Sep 14.

Abstract

Leishmania mexicana can produce chronic infections leading to exhausted T cell phenotypes, mediated by PD-1/PD-L1. Little is known on mechanisms that induce these inhibitory molecules in chronic leishmaniasis. We analyzed factors that contribute to exhausted phenotypes in chronic L. mexicana infections of mice. Our results show that draining lymph node cells express enhanced levels of PD-1/PD-L1. T lymphocytes producing low cytokine levels were also found. L. mexicana infection of dendritic cells (DCs) produced elevated amounts of TNF and showed up-regulation of PD-L1 expression. We provide evidence that T cells of chronic L. mexicana infections in mice are functionally exhausted due to chronic TNF production, which leads to PD-L1 up-regulation in DCs. We conclude that TNF has a fundamental role in promoting T cell exhaustion during chronic L. mexicana infections, which contributes to the inability of T cells to proliferate and produce pro-inflammatory cytokines, thus favoring disease progression.

Keywords: Chronic infection; Exhausted phenotype; Leishmania mexicana; Mouse model; PD-1; PD-L1; TNF.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B7-H1 Antigen / genetics
  • B7-H1 Antigen / immunology*
  • CD8-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / metabolism
  • Cytokines / genetics
  • Cytokines / immunology
  • Dendritic Cells / immunology
  • Disease Models, Animal
  • Female
  • Leishmania mexicana / immunology
  • Leishmania mexicana / isolation & purification
  • Leishmaniasis, Cutaneous / immunology*
  • Leishmaniasis, Cutaneous / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Programmed Cell Death 1 Receptor / genetics
  • Programmed Cell Death 1 Receptor / immunology*
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism
  • Tumor Necrosis Factor-alpha / metabolism*
  • Tumor Necrosis Factor-alpha / physiology
  • Up-Regulation

Substances

  • B7-H1 Antigen
  • Cd274 protein, mouse
  • Cytokines
  • Pdcd1 protein, mouse
  • Programmed Cell Death 1 Receptor
  • Tumor Necrosis Factor-alpha