Double positive CD4+CD8+ T cells are part of the adaptive immune response against Candida albicans

Hum Immunol. 2019 Dec;80(12):999-1005. doi: 10.1016/j.humimm.2019.09.008. Epub 2019 Sep 24.

Abstract

Although multiple immune cells participate in the innate and adaptive immune response against Candida albicans, the elucidation of cellular and inflammation kinetics may be a promising strategy to decipher events propitious to infection eradication. We used an in vitro Candida-human leucocyte coculture approach to study the dynamics of rare CD4+CD8+ double positive T lymphocytes (DP T) produced in response to this fungus. Our results highlight the presence of two phenotypically distinct subsets of DP T cells: CD4hiCD8lo and CD4loCD8hi, and that the different ratio of these cells correlates with infection outcome. The ratio of CD4hiCD8lo over CD4loCD8hi by day 6 was significantly higher in controlled infections and decreased when infection persisted due to a significant increase in the proportion of CD4loCD8hi. When infection was controlled, CD4hiCD8lo T cells secreted IFNγ, TNFα, IL-4 and IL-10 cytokines two days after challenge. By day 2, under conditions of persistent infection, CD4hiCD8lo and CD4loCD8hi T cells secreted significant levels of IL-4 and IL-10, respectively, compared to uninfected cultures. Frequency kinetics and original cytokine profiles detailed in this work indicate that DP T cells could participate in the adaptive immune response to C. albicans.

Keywords: C. albicans; CD4+CD8+ double positive T cells; Host-Candida interaction; tSNE.

MeSH terms

  • Adaptive Immunity
  • Adult
  • CD4 Antigens / metabolism
  • CD8 Antigens / metabolism
  • Candida albicans / physiology*
  • Candidiasis / immunology*
  • Cells, Cultured
  • Cytokines / metabolism
  • Female
  • Host-Pathogen Interactions
  • Humans
  • Immunophenotyping
  • Lymphocyte Activation
  • Male
  • Middle Aged
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocytes / immunology*
  • Young Adult

Substances

  • CD4 Antigens
  • CD8 Antigens
  • Cytokines