A role for the transcription factor Helios in human CD4+CD25+ regulatory T cells

  • Derese Getnet
  • , Joseph F. Grosso
  • , Monica V. Goldberg
  • , Timothy J. Harris
  • , Hung Rong Yen
  • , Tullia C. Bruno
  • , Nicholas M. Durham
  • , Edward L. Hipkiss
  • , Kristin J. Pyle
  • , Satoshi Wada
  • , Fan Pan
  • , Drew M. Pardoll
  • , Charles G. Drake*
  • *Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

204 Scopus citations

Abstract

Relative upregulation of the Ikaros family transcription factor Helios in natural regulatory T cells (Tregs) has been reported by several groups. However, a role for Helios in regulatory T cells has not yet been described. Here, we show that Helios is upregulated in CD4+CD25+ regulatory T cells. Chromatin-immunoprecipitation (ChIP) experiments indicated that Helios binds to the FoxP3 promoter. These data were further corroborated by experiments showing that knocking-down Helios with siRNA oligonucleotides results in down-regulation of FoxP3. Functionally, we found that suppression of Helios message in CD4+CD25+ T cells significantly attenuates their suppressive function. Taken together, these data suggest that Helios may play an important role in regulatory T cell function and support the concept that Helios may be a novel target to manipulate Treg activity in a clinical setting.

Original languageEnglish
Pages (from-to)1595-1600
Number of pages6
JournalMolecular Immunology
Volume47
Issue number7-8
DOIs
StatePublished - 04 2010
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • FoxP3
  • Helios
  • Regulatory T cells

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