| Literature DB >> 29330114 |
Aditi Narsale1, Rosita Moya1, Joanna Davida Davies2.
Abstract
CD4+ T cells that co-express CD25 and CD127 (CD25+CD127+) make up around 20% of all circulating CD4+ memory T cells in healthy people. The clinical significance of these cells is that in children with type 1 diabetes their relative frequency at diagnosis is significantly and directly correlated with rate of disease progression. The purpose of this study was to further characterize the CD25+CD127hi cells. We show that they are a mix of Th1 and Th2 cells however, they have a significantly higher relative frequency of pre-committed and committed Th2 cells, and secrete significantly higher levels of Th2-type cytokines than CD25- memory T cells. Further, these cells are neither exhausted nor senescent and proliferate to the same extent as CD25- memory cells. Thus, CD25+CD127hi cells are a highly active subset of memory T cells that might play a role in controlling inflammation via anti-inflammatory Th2-type deviation.Entities:
Keywords: CD25(+)CD127(hi) cells; Chemokine receptors; Cytokines; T cell subsets; Th1 and Th2
Mesh:
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Year: 2018 PMID: 29330114 PMCID: PMC5826897 DOI: 10.1016/j.clim.2018.01.003
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969