Functional and molecular characterization of B cell-responsive V delta 1+ gamma delta T cells

Eur J Immunol. 1994 Dec;24(12):3199-204. doi: 10.1002/eji.1830241243.

Abstract

Cells expressing the V delta 1+ gene segment are a minor gamma delta T cell population in human peripheral blood but predominate in epithelial and (inflamed) tissues. The characteristic dendritic-like morphology of these gamma delta T cells is consistent with their putative immune surveillance role in epithelia. Their function, however, remains unknown. We and others previously reported that a subset of V delta 1+ gamma delta T cells proliferates after stimulation with Epstein-Barr virus (EBV)-transformed B lymphoblastoid cell lines (LCL), but not with fresh peripheral blood-derived B cells. These responses were independent of the type of T cell receptor (TcR) gamma chain co-expressed with the V delta 1 chain. The in vivo relevance of this LCL-mediated activation as well as the nature of the stimulatory ligand on the LCL is not well established. In this study, we tested the proliferative response of V delta 1+ LCL-responsive T cells against non-EBV-transformed B cells, activated through CD40 by murine EL4 B5 cells, and to a panel of B cell lines differing in the expression of EBV nuclear antigen proteins and adhesion/co-stimulatory molecules. The role of the Epstein-Barr virus-derived antigen in the induction of this response could be excluded as the activated (non-EBV-transformed) peripheral blood B cells were also able to induce a proliferative response in the LCL-responsive V delta 1+ T cells. Therefore, the stimulatory ligand on B cells is of cellular rather than of viral origin, and its expression is up-regulated upon activation of B cells. The expression of B7 and CD39 molecules on the surface of activated B cells appeared to be crucial since antibodies to these structures could block the induction of proliferation of the V delta 1+ T cells. Finally, we investigated the diversity of the responding V delta 1+ gamma delta T cell clones by sequence analysis of the TcR delta junctional regions. No restricted V-D-J sequences were found among the LCL-responsive V delta 1+ T cell clones, arguing strongly against a mono- or oligoclonal V delta 1+ gamma delta T cell response to LCL. These findings may explain the presence of polyclonally activated V delta 1+ T cells in inflamed tissues where activated B cells are often present.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases*
  • Amino Acid Sequence
  • Antigens, CD / physiology
  • Apyrase
  • B-Lymphocytes / immunology
  • B7-1 Antigen / physiology
  • Base Sequence
  • Cell Transformation, Viral
  • Clone Cells
  • DNA Primers / chemistry
  • Gene Rearrangement, delta-Chain T-Cell Antigen Receptor
  • Herpesvirus 4, Human
  • Humans
  • In Vitro Techniques
  • Lymphocyte Activation
  • Molecular Sequence Data
  • Receptors, Antigen, T-Cell, gamma-delta / chemistry
  • Receptors, Antigen, T-Cell, gamma-delta / immunology*
  • T-Lymphocyte Subsets / immunology*

Substances

  • Antigens, CD
  • B7-1 Antigen
  • DNA Primers
  • Receptors, Antigen, T-Cell, gamma-delta
  • Adenosine Triphosphatases
  • Apyrase
  • CD39 antigen