Natural and TGF-β-induced Foxp3+CD4+ CD25+ regulatory T cells are not mirror images of each other

David A. Horwitz, Song Guo Zheng, J. Dixon Gray

Research output: Contribution to journalReview articlepeer-review

277 Scopus citations


Foxp3+ CD4+ CD25+ regulatory cell (Treg) subsets that maintain immunologic homeostasis have been considered to be a homogeneous population of naturally occurring, thymus-derived CD4+CD25+ cells (nTregs). However, similar Foxp3+ Tregs can be induced from CD25- precursors in vivo, and ex vivo with interleukin 2 (IL-2) and transforming growth factor β (TGF-β) (iTregs). These two subsets differ in their principal antigen specificities and in the T-cell receptor signal strength and co-stimulatory requirements needed for their generation. However, whether iTregs have any unique functions in vivo has been unclear. Although IL-6 can convert nTregs to Th17 cells, iTregs induced by IL-2 and TGF-β are resistant to this cytokine and thereby might retain suppressive function at inflammatory sites. Thus, nTregs and iTregs may have different roles in the adaptive immune response.

Original languageEnglish (US)
Pages (from-to)429-435
Number of pages7
JournalTrends in Immunology
Issue number9
StatePublished - Sep 2008

All Science Journal Classification (ASJC) codes

  • Immunology and Allergy
  • Immunology


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