CD4+CD25+ regulatory T cells limit the risk of autoimmune disease arising from T cell receptor crossreactivity

Leigh A Stephens, David Gray, Stephen M Anderton

Research output: Contribution to journalArticlepeer-review

Abstract

The molecular-mimicry theory proposes that immune crossreactivity between microbial and self-antigen is the initiating event in the activation of autoaggressive immune responses leading to autoimmune disease. In support of this possibility, it is now accepted that T cell recognition of antigen is highly degenerate. However, it is to be expected that the immune system would have evolved mechanisms to counter such a potential danger. We studied the influence of CD4(+)CD25(+) regulatory T cells (Treg) on the ability of suboptimal T cell receptor ligands to provoke autoimmunity. By using CD4(+) T cell-driven experimental autoimmune encephalomyelitis as a model, it was found that depletion of CD4(+)CD25(+)Foxp3(+) Treg allowed pathology to develop in response to suboptimal T cell stimulation. These data demonstrate the importance of Treg in raising the threshold of triggering of autoreactive T cell responses, thus limiting the risk of autoimmune disease due to molecular mimicry.
Original languageEnglish
Pages (from-to)17418-23
Number of pages6
JournalProceedings of the National Academy of Sciences
Volume102
Issue number48
DOIs
Publication statusPublished - 2005

Keywords

  • experimental autoimmune encephalomyelitis (EAE)
  • multiple sclerosis
  • regulation
  • tolerance

Fingerprint

Dive into the research topics of 'CD4+CD25+ regulatory T cells limit the risk of autoimmune disease arising from T cell receptor crossreactivity'. Together they form a unique fingerprint.

Cite this