The mechanisms shaping the repertoire of CD4+ Foxp3+ regulatory T cells

Piotr Kraj, Leszek Ignatowicz

Research output: Contribution to journalReview article

10 Scopus citations

Abstract

Regulatory T (Treg) cells expressing Foxp3 transcription factor control homeostasis of the immune system, antigenic responses to commensal and pathogenic microbiota, and immune responses to self and tumour antigens. The Treg cells differentiate in the thymus, along with conventional CD4+ T cells, in processes of positive and negative selection. Another class of Treg cells is generated in peripheral tissues by inducing Foxp3 expression in conventional CD4+ T cells in response to antigenic stimulation. Both thymic and peripheral generation of Treg cells depends on recognition of peptide/MHC ligands by the T-cell receptors (TCR) expressed on thymic Treg precursors or peripheral conventional CD4+ T cells. This review surveys reports describing how thymus Treg cell generation depends on the selecting peptide/MHC ligands and how this process impacts the TCR repertoire expressed by Treg cells. We also describe how Treg cells depend on sustained signalling through the TCR and how they are further regulated by Foxp3 enhancer sequences. Finally, we review the impact of microbiota-derived antigens on the maintenance and functionality of the peripheral pool of Treg cells.

Original languageEnglish (US)
Pages (from-to)290-296
Number of pages7
JournalImmunology
Volume153
Issue number3
DOIs
StatePublished - Mar 2018

Keywords

  • T cell
  • T-cell receptors
  • regulation/suppression

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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