CD25+Foxp3+ regulatory T cells facilitate CD4+ T cell clonal anergy induction during the recovery from lymphopenia

J Immunol. 2006 May 15;176(10):5880-9. doi: 10.4049/jimmunol.176.10.5880.

Abstract

T cell clonal anergy induction in lymphopenic nu/nu mice was found to be ineffective. Exposure to a tolerizing peptide Ag regimen instead induced aggressive CD4(+) cell cycle progression and increased Ag responsiveness (priming). Reconstitution of T cell-deficient mice by an adoptive transfer of mature peripheral lymphocytes was accompanied by the development of a CD25(+)Foxp3(+)CTLA-4(+)CD4(+) regulatory T cell population that acted to dampen Ag-driven cell cycle progression and facilitate the induction of clonal anergy in nearby responder CD25(-)CD4(+) T cells. Thus, an early recovery of CD25(+) regulatory T cells following a lymphopenic event can prevent exuberant Ag-stimulated CD4(+) cell cycle progression and promote the development of clonal anergy.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adoptive Transfer
  • Animals
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism
  • CD4-Positive T-Lymphocytes / pathology
  • CD4-Positive T-Lymphocytes / transplantation
  • Cell Proliferation
  • Cells, Cultured
  • Clonal Anergy / genetics
  • Clonal Anergy / immunology*
  • Forkhead Transcription Factors / biosynthesis*
  • Lymphopenia / genetics
  • Lymphopenia / immunology*
  • Mice
  • Mice, Transgenic
  • Receptors, Interleukin-2 / biosynthesis*
  • T-Lymphocytes, Regulatory / immunology
  • T-Lymphocytes, Regulatory / physiology*

Substances

  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Receptors, Interleukin-2