Reduced Foxp3 protein expression is associated with inflammatory disease during human t lymphotropic virus type 1 Infection

J Infect Dis. 2006 Jun 1;193(11):1557-66. doi: 10.1086/503874. Epub 2006 Apr 28.

Abstract

The Foxp3 protein is a specific marker of CD4(+)CD25(+) regulatory T (T(reg)) cells, and its expression is critical to their development and function. Several studies have demonstrated the dysregulation of Foxp3 expression during human inflammatory diseases. Infection with human T lymphotropic virus type 1 (HTLV-1) is associated with the development of a number of inflammatory conditions, including myelopathy, although the majority of individuals who are infected with HTLV-1 remain asymptomatic. To examine the role played by T(reg) cells in the development of inflammatory disease during HTLV-1 infection, we examined Foxp3 expression by flow cytometry. Our analysis showed that HTLV-1-associated myelopathy/tropical spastic paraparesis was associated with a lower expression (compared with that in asymptomatic HTLV-1 carriers and healthy donors) of Foxp3 in peripheral-blood leukocytes. In individuals infected with HTLV-1, Foxp3 expression was inversely correlated with HTLV-1 tax proviral DNA load. These results suggest that impaired Foxp3 expression may contribute to the development of inflammatory disease during HTLV-1 infection.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • CD4 Antigens / analysis
  • DNA, Viral / blood
  • Female
  • Flow Cytometry
  • Forkhead Transcription Factors / biosynthesis*
  • Genes, pX
  • HTLV-I Infections / immunology*
  • HTLV-I Infections / metabolism
  • Humans
  • Lymphocyte Subsets / immunology
  • Male
  • Middle Aged
  • Paraparesis, Tropical Spastic / immunology*
  • Paraparesis, Tropical Spastic / metabolism
  • Receptors, Interleukin-2 / analysis
  • Statistics as Topic
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism
  • Tumor Necrosis Factor Receptor Superfamily, Member 7 / analysis
  • Viral Load

Substances

  • CD4 Antigens
  • DNA, Viral
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Receptors, Interleukin-2
  • Tumor Necrosis Factor Receptor Superfamily, Member 7