4.6 Review

Functional stability of Foxp3+ regulatory T cells

Journal

TRENDS IN MOLECULAR MEDICINE
Volume 18, Issue 8, Pages 454-462

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.molmed.2012.06.001

Keywords

-

Funding

  1. Canadian Institutes for Health Research (CIHR) [MOP 67211, MOP 84037]
  2. CIHR doctoral award

Ask authors/readers for more resources

Significant evidence demonstrates that CD4(+) regulatory T cells (T-reg) expressing the Forkhead box P3 (Foxp3) transcription factor are a distinct lineage of CD4(+) T cells that are essential for maintaining self-tolerance and modulating immunity to various nonself-antigens under changing inflammatory settings. Stable Foxp3 expression ensures T-reg function in a variety of inflammatory contexts. However, the model of T-reg cells as a stable, long-lived lineage is controversial. Whereas some studies have observed long-lived T-reg, function, recent studies suggest that T-reg cells adapt to microenvironmental changes and consequently manifest functional plasticity by reprogramming into inflammatory T cells. Here, we review the evidence addressing the functional stability or plasticity of Foxp3(+) T-reg cells and the implications for immune homeostasis and disease.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available