| Literature DB >> 24952375 |
Fumichika Matsuki1, Jun Saegusa2, Keisuke Nishimura3, Yasushi Miura4, Masahiro Kurosaka4, Shunichi Kumagai5, Akio Morinobu3.
Abstract
Increased numbers of regulatory T (Treg) cells are found in synovial fluid from patients with rheumatoid arthritis (RASF) compared with peripheral blood. However, Treg cells in RASF have been shown to have a decreased capacity to suppress T cells. Here we phenotypically classified CD4+ T cells in RASF into six subsets based on the expression of CD45RA, CCR7, CD27 and CD28, and demonstrated that the CCR7-CD45RA-CD27+CD28+ TEM subset was significantly increased in synovial fluid compared with peripheral blood. In addition, the proportion of Foxp3+ Treg cells in the CCR7-CD45RA-CD27+CD28+ TEM subset was significantly increased in RASF. Furthermore, most of the Foxp3+ Treg cells in RASF were non-suppressive CD45RA-Foxp3(low) non-Treg cells, and the frequency of the non-Treg cells in the CCR7-CD45RA-CD27+CD28+ TEM subset was significantly increased in RASF. Our findings suggest that the pro-inflammatory environment in RA joints may induce the increase of CD45RA-Foxp3(low) non-Treg cells in synovial fluid.Entities:
Keywords: Central memory T cells; Effector memory T cells; Regulatory T cells; Rheumatoid arthritis; Synovial fluid
Mesh:
Substances:
Year: 2014 PMID: 24952375 DOI: 10.1016/j.cellimm.2014.05.011
Source DB: PubMed Journal: Cell Immunol ISSN: 0008-8749 Impact factor: 4.868