Decreased Tim-3 and its correlation with Th1 cells in patients with immune thrombocytopenia

Thromb Res. 2014 Jan;133(1):52-6. doi: 10.1016/j.thromres.2013.10.029. Epub 2013 Oct 24.

Abstract

Here we evaluate the expression of Tim-3 in CD4+ T cells from patients with immune thrombocytopenia (ITP). We also counted platelets and evaluated plasma IFN-γ, IL-18 and IL-4 levels in patients with active ITP (n=26), patients with ITP in remission (n=23) and in healthy subjects (n=34) by enzyme linked immunosorbent assay (ELISA). Using real-time quantitative polymerase chain reaction (RT-PCR), the mRNA expression of IL-18, IFN-γ, IL-4, T-box (T-bet) and Tim-3 was studied in the blood. The CD4+ Tim-3+ cells in blood were evaluated by flow cytometry and are expressed as a percentage of the total number of CD4+ cells. The Tim-3 positive cells within the circulating CD4+ population of newly diagnosed patients were significantly decreased compared to controls. However, T-bet, IL-18 and IFN-γ levels were significantly elevated in patients. Tim-3 mRNA expression was significantly lower in the peripheral mononuclear cells (PBMCs) of ITP patients compared to controls. The decreased levels of Tim-3 during active stages of disease suggest a possible role in the pathogenesis and course of ITP and restoration of Tim-3 may be a reasonable therapeutic strategy for ITP.

Keywords: Immune thrombocytopenia; T-bet; T-cell immunoglobulin- and mucin- domain-containing molecule 3; Th1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Case-Control Studies
  • Female
  • Flow Cytometry
  • Hepatitis A Virus Cellular Receptor 2
  • Humans
  • Interleukin-18 / immunology
  • Interleukin-18 / metabolism
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / immunology
  • Membrane Proteins / metabolism*
  • Middle Aged
  • Th1 Cells / immunology*
  • Th1 Cells / metabolism
  • Th1 Cells / pathology
  • Thrombocytopenia / blood
  • Thrombocytopenia / immunology*
  • Thrombocytopenia / metabolism
  • Thrombocytopenia / pathology
  • Young Adult

Substances

  • HAVCR2 protein, human
  • Hepatitis A Virus Cellular Receptor 2
  • Interleukin-18
  • Membrane Proteins