Double Positive CD4+CD8+ (DP) T-Cells Display Distinct Exhaustion Phenotype in Chronic Hepatitis C

Cells. 2023 May 22;12(10):1446. doi: 10.3390/cells12101446.

Abstract

In chronic hepatitis C (CHC), characterized by exhaustion of T-cell function, increased frequencies of double-positive (DP) (CD4+CD8+) cells are present in peripheral blood. We compared the exhaustion phenotype between DP and single positive (SP) T-cells, including HCV-specific cells, and assessed the effect of successful HCV treatment on inhibitory receptors expression. Blood samples from 97 CHC patients were collected before and six months post-treatment. PD-1 (programmed cell death protein 1) and Tim-3 (T-cell immunoglobulin and mucin domain-containing molecule-3) expression was assessed by flow cytometry. DP T-cells displayed significantly higher PD-1 expression, lower Tim-3 expression than CD8+ SP T-cells and lower percentages of PD-1-Tim-3- cells than CD4+ SP T-cells, both before and after treatment. PD-1+Tim-3+ DP T-cells decreased following treatment. HCV-specific cells were more frequent among DP than SP T-cells, both before and after treatment. HCV-specific DP T-cells were characterized by lower PD-1 expression, higher PD-1 and Tim-3 co-expression, and lower percentages of PD-1-Tim-3- cells (both before and after treatment) and higher post-treatment Tim-3 than HCV-specific SP T-cells. Their percentages decreased following treatment, but the exhaustion phenotype remained unchanged. DP T-cells in CHC exhibit a distinct exhaustion phenotype from SP T-cells, and these changes mostly persist following successful treatment.

Keywords: CD4+CD8+ double positive (DP) T-cells; DAA; PD-1; T-cell exhaustion; Tim-3; antiviral treatment; hepatitis C virus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD8-Positive T-Lymphocytes / metabolism
  • Hepatitis A Virus Cellular Receptor 2 / metabolism
  • Hepatitis C, Chronic* / immunology
  • Hepatitis C, Chronic* / metabolism
  • Humans
  • Phenotype
  • Programmed Cell Death 1 Receptor / metabolism
  • T-Cell Exhaustion*

Substances

  • Hepatitis A Virus Cellular Receptor 2
  • Programmed Cell Death 1 Receptor

Grants and funding

The work was supported by grant UMO-2015/19/D/NZ6/01303 from the National Science Center, Poland.