Rapid and transient activation of γδ T cells to IFN-γ production, NK cell-like killing, and antigen processing during acute virus infection

J Immunol. 2011 Apr 15;186(8):4853-61. doi: 10.4049/jimmunol.1003599. Epub 2011 Mar 7.

Abstract

γδ T cells are the majority peripheral blood T cells in young cattle. The role of γδ T cells in innate responses against infection with foot-and-mouth disease virus was analyzed on consecutive 5 d following infection. Before infection, bovine WC1(+) γδ T cells expressed a nonactivated phenotype relative to CD62L, CD45RO, and CD25 expression and did not produce IFN-γ ex vivo. Additionally, CD335 expression was lacking and no spontaneous target cell lysis could be detected in vitro, although perforin was detectable at a very low level. MHC class II and CD13 expression were also lacking. Following infection with foot-and-mouth disease virus, expression of CD62L and CD45RO was greatly reduced on WC1(+) γδ T cells, and unexpectedly, CD45RO expression did not recover. A transient increase in expression of CD25 correlated with production of IFN-γ. Expression of CD335 and production of perforin were detected on a subset of γδ T cells, and this correlated with an increased spontaneous killing of xenogeneic target cells. Furthermore, increased MHC class II expression was detected on WC1(+) γδ T cells, and these cells processed protein Ags. These activities are rapidly induced, within 3 d, and wane by 5 d following infection. All of these functions, NK-like killing, Ag processing, and IFN-γ production, have been demonstrated for these cells in various species. However, these results are unique in that all these functions are detected in the same samples of WC1(+) γδ T cells, suggesting a pivotal role of these cells in controlling virus infection.

MeSH terms

  • Acute Disease
  • Animals
  • Antigen Presentation / immunology*
  • Cattle
  • Cytotoxicity, Immunologic / immunology
  • Female
  • Flow Cytometry
  • Foot-and-Mouth Disease / blood
  • Foot-and-Mouth Disease / immunology*
  • Foot-and-Mouth Disease / virology
  • Foot-and-Mouth Disease Virus / immunology
  • Foot-and-Mouth Disease Virus / physiology
  • Host-Pathogen Interactions / immunology
  • Humans
  • Immunophenotyping
  • Interferon-gamma / immunology*
  • Interferon-gamma / metabolism
  • Interleukin-2 Receptor alpha Subunit / immunology
  • Interleukin-2 Receptor alpha Subunit / metabolism
  • K562 Cells
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism
  • Lymphocyte Activation / immunology
  • Lymphocyte Count
  • Male
  • Membrane Glycoproteins / immunology
  • Membrane Glycoproteins / metabolism
  • Natural Cytotoxicity Triggering Receptor 1 / immunology
  • Natural Cytotoxicity Triggering Receptor 1 / metabolism
  • Receptors, Antigen, T-Cell, gamma-delta / immunology*
  • Receptors, Antigen, T-Cell, gamma-delta / metabolism
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism
  • Time Factors

Substances

  • DMBT1 protein, Bos taurus
  • Interleukin-2 Receptor alpha Subunit
  • Membrane Glycoproteins
  • Natural Cytotoxicity Triggering Receptor 1
  • Receptors, Antigen, T-Cell, gamma-delta
  • Interferon-gamma