CD154-dependent priming of diabetogenic CD4(+) T cells dissociated from activation of antigen-presenting cells

Immunity. 2002 May;16(5):719-32. doi: 10.1016/s1074-7613(02)00315-1.

Abstract

We followed the fate of K(d)- or I-A(g7)-restricted beta cell-autoreactive T cells in monoclonal TCR-transgenic NOD mice expressing or lacking CD154. 8.3-NOD.RAG-2(-/-)/CD154(-/-) mice, which bear autoreactive CD8(+) T cells, developed diabetes with the same incidence and tempo as 8.3-NOD.RAG-2(-/-)/CD154(+) mice. Recruitment of CD154(-/-) 8.3-CD8(+) CTL was accelerated by CD154(+)CD4(+) T cells, by expression of a B7.1 transgene in beta cells or by treatment of the mice with CpG-DNA or an agonistic anti-CD40 antibody. In contrast, the autoreactive CD4(+) T cells maturing in 4.1-NOD.RAG-2(-/-) mice lost their diabetogenic potential if they lacked CD154, even in the presence of CD154(+)CD4(+) T cells, B7.1 molecules on beta cells, CpG-DNA treatment, or systemic CD40 ligation. These results demonstrate the existence of a novel, CD154-dependent pathway of CD4(+) T cell activation that is independent of CD40-mediated activation of APCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen-Presenting Cells / drug effects
  • Antigen-Presenting Cells / immunology*
  • B7-1 Antigen / genetics
  • B7-1 Antigen / metabolism
  • CD40 Antigens / metabolism
  • CD40 Ligand / genetics
  • CD40 Ligand / physiology*
  • Cell Line
  • Cells, Cultured
  • DNA-Binding Proteins / genetics
  • Diabetes Mellitus, Type 1 / immunology*
  • Female
  • Genes, T-Cell Receptor
  • Islets of Langerhans / immunology
  • Lymph Nodes / immunology
  • Lymphocyte Activation*
  • Male
  • Mice
  • Mice, Inbred NOD
  • Mice, Knockout
  • Mice, Transgenic
  • Oligodeoxyribonucleotides / pharmacology
  • Pancreas / immunology
  • T-Lymphocytes, Cytotoxic / immunology
  • T-Lymphocytes, Helper-Inducer / immunology*

Substances

  • B7-1 Antigen
  • CD40 Antigens
  • CPG-oligonucleotide
  • DNA-Binding Proteins
  • Oligodeoxyribonucleotides
  • Rag2 protein, mouse
  • V(D)J recombination activating protein 2
  • CD40 Ligand