| Literature DB >> 26000107 |
Alessia Alunno1, Elena Bartoloni1, Giuseppe Nocentini2, Onelia Bistoni1, Simona Ronchetti2, Maria Grazia Petrillo2, Carlo Riccardi2, Roberto Gerli1.
Abstract
Regulatory T cells (Treg) are a CD4(+) lymphocyte subset involved in self-tolerance and autoimmunity prevention. There is evidence for a phenotypic and/or functional impairment of this cell subset during the natural history of several chronic autoimmune/inflammatory diseases, including rheumatoid arthritis (RA). Although the intracellular transcription factor FoxP3 is thought to be the master regulator of Treg cell function, a number of other molecules expressed on the cell surface have been proposed for the identification of Treg cells. This is important in order to favour their possible selective isolation and in the development of new therapeutic strategies. In the present paper, available data on phenotypic and functional characterization of Treg cells in both peripheral blood and synovial fluid from RA patients are reviewed and their possible pathogenic role in triggering and perpetuating rheumatoid joint inflammation is discussed.Entities:
Keywords: FoxP3 GITR; Rheumatoid arthritis; Treg cells
Year: 2010 PMID: 26000107 PMCID: PMC4389058 DOI: 10.1007/s13317-010-0008-2
Source DB: PubMed Journal: Auto Immun Highlights ISSN: 2038-0305