Porcine reproductive and respiratory syndrome virus induces CD4+CD8+CD25+Foxp3+ regulatory T cells (Tregs)

Virology. 2012 Aug 15;430(1):73-80. doi: 10.1016/j.virol.2012.04.009. Epub 2012 May 18.

Abstract

The aim of this study was to analyze the regulatory T cells (Tregs) induced by the porcine reproductive and respiratory syndrome virus (PRRSV) in pigs. Serum, blood, tonsil, and mediastinal lymph nodes' samples were obtained at different time post-infection (dpi). The frequencies of CD4(+)CD8(-)CD25(+)Foxp3(+), CD4(+)CD8(+)CD25(+)Foxp3(+), or CD4(-)CD8(+)CD25(+)Foxp3(+) phenotypes were determined in PBMC and lymph node cells, and cells producing IL-10 or TGF-β were analyzed. PRRSV increased the number of CD4(+)CD8(+)CD25(+)Foxp3(+) cells at 14 dpi, whereas CD4(+)CD8(-)CD25(+)Foxp3(+) remained constant until 28 dpi. Positive correlation exists between viremia and induced regulatory cells. CD4(+)CD8(+)CD25(+)Foxp3(+)-induced Treg cells were consistently observed in lymphoid tissues. Analysis of IL-10- and TGF-β-producing cell demonstrated that in response to PRRSV, CD4(+)CD8(-)Foxp3(low) and CD4(+)CD8(+)Foxp3(high) cells increase moderately the proportion of IL-10(+) cells. TGF-β was only observed in the CD4(+)CD8(+)Foxp3(high) population after PRRSV stimulation. In conclusion, PRRSV infection increases the frequency of Tregs with the phenotype CD4(+)CD8(+)CD25(+)Foxp3(high) and produces TGF-β.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood / immunology
  • CD4 Antigens / analysis
  • CD8 Antigens / analysis
  • Hepatocyte Nuclear Factor 3-gamma / analysis
  • Interleukin-10 / metabolism
  • Interleukin-2 Receptor alpha Subunit / analysis
  • Lymph Nodes / immunology
  • Palatine Tonsil / immunology
  • Porcine Reproductive and Respiratory Syndrome / immunology*
  • Porcine respiratory and reproductive syndrome virus / immunology*
  • Swine
  • T-Lymphocytes, Regulatory / chemistry
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / virology*
  • Time Factors
  • Transforming Growth Factor beta / metabolism

Substances

  • CD4 Antigens
  • CD8 Antigens
  • Interleukin-2 Receptor alpha Subunit
  • Transforming Growth Factor beta
  • Interleukin-10
  • Hepatocyte Nuclear Factor 3-gamma