Matches in SemOpenAlex for { <https://semopenalex.org/work/W2022164982> ?p ?o ?g. }
- W2022164982 endingPage "638" @default.
- W2022164982 startingPage "627" @default.
- W2022164982 abstract "Despite the high frequency of CD4+ T cells with a regulatory phenotype (CD25+CD127(low) FoxP3+) in the joints of patients with rheumatoid arthritis (RA), inflammation persists. One possible explanation is that human Treg cells are converted into proinflammatory interleukin-17 (IL-17)-producing cells by inflammatory mediators and thereby lose their suppressive function. The aim of this study was to investigate whether activated monocytes, which are potent producers of inflammatory cytokines and are abundantly present in the rheumatic joint, induce proinflammatory cytokine expression in human Treg cells and impair their regulatory function.The presence and phenotype of CD4+CD45RO+CD25+CD127(low) T cells (memory Treg cells) and CD14+ monocytes in the peripheral blood (PB) and synovial fluid (SF) of patients with RA were investigated by flow cytometry. Memory Treg cells obtained from healthy control subjects underwent fluorescence-activated cell sorting and then were cocultured with autologous activated monocytes and stimulated with anti-CD3 monoclonal antibodies. Intracellular cytokine expression, phenotype, and function of cells were determined by flow cytometry, enzyme-linked immunosorbent assay, and proliferation assays.In patients with RA, the frequencies of CD4+CD45RO+CD25+CD127(low) Treg cells and activated CD14+ monocytes were higher in SF compared with PB. In vitro-activated monocytes induced an increase in the percentage of IL-17-positive, interferon-γ (IFNγ)-positive, and tumor necrosis factor α (TNFα)-positive Treg cells as well as IL-10-positive Treg cells. The observed increase in IL-17-positive and IFNγ-positive Treg cells was driven by monocyte-derived IL-1β, IL-6, and TNFα and was mediated by both CD14+CD16- and CD14+CD16+ monocyte subsets. Despite enhanced cytokine expression, cells maintained their CD25+FoxP3+CD39+ Treg cell phenotype and showed an enhanced capacity to suppress T cell proliferation and IL-17 production.Treg cells exposed to a proinflammatory environment show increased cytokine expression as well as enhanced suppressive activity." @default.
- W2022164982 created "2016-06-24" @default.
- W2022164982 creator A5002707998 @default.
- W2022164982 creator A5011305212 @default.
- W2022164982 creator A5021013876 @default.
- W2022164982 creator A5038031232 @default.
- W2022164982 creator A5041537684 @default.
- W2022164982 creator A5066693323 @default.
- W2022164982 creator A5068862016 @default.
- W2022164982 creator A5085234051 @default.
- W2022164982 date "2013-02-25" @default.
- W2022164982 modified "2023-10-11" @default.
- W2022164982 title "Interaction with activated monocytes enhances cytokine expression and suppressive activity of human CD4+CD45ro+CD25+CD127<sup>low</sup>regulatory T cells" @default.
- W2022164982 cites W1509117621 @default.
- W2022164982 cites W1520953238 @default.
- W2022164982 cites W1560623534 @default.
- W2022164982 cites W1561046927 @default.
- W2022164982 cites W1969021940 @default.
- W2022164982 cites W1980564318 @default.
- W2022164982 cites W1982243301 @default.
- W2022164982 cites W1985516890 @default.
- W2022164982 cites W1987735044 @default.
- W2022164982 cites W1993292726 @default.
- W2022164982 cites W2001740313 @default.
- W2022164982 cites W2007631222 @default.
- W2022164982 cites W2009649694 @default.
- W2022164982 cites W2011446655 @default.
- W2022164982 cites W2022785778 @default.
- W2022164982 cites W2024490058 @default.
- W2022164982 cites W2025035158 @default.
- W2022164982 cites W2029520442 @default.
- W2022164982 cites W2029640857 @default.
- W2022164982 cites W2029682692 @default.
- W2022164982 cites W2036383793 @default.
- W2022164982 cites W2038026702 @default.
- W2022164982 cites W2042073660 @default.
- W2022164982 cites W2042586707 @default.
- W2022164982 cites W2043776488 @default.
- W2022164982 cites W2044247010 @default.
- W2022164982 cites W2045236396 @default.
- W2022164982 cites W2045311357 @default.
- W2022164982 cites W2068529443 @default.
- W2022164982 cites W2072853625 @default.
- W2022164982 cites W2075326117 @default.
- W2022164982 cites W2080935386 @default.
- W2022164982 cites W2081585219 @default.
- W2022164982 cites W2084007358 @default.
- W2022164982 cites W2092713406 @default.
- W2022164982 cites W2093383759 @default.
- W2022164982 cites W2098919737 @default.
- W2022164982 cites W2104369318 @default.
- W2022164982 cites W2115768311 @default.
- W2022164982 cites W2116701250 @default.
- W2022164982 cites W2122939321 @default.
- W2022164982 cites W2123166427 @default.
- W2022164982 cites W2123249923 @default.
- W2022164982 cites W2142877732 @default.
- W2022164982 cites W2147172932 @default.
- W2022164982 cites W2150901150 @default.
- W2022164982 cites W2155702314 @default.
- W2022164982 cites W2166731586 @default.
- W2022164982 cites W2167297937 @default.
- W2022164982 cites W2167815562 @default.
- W2022164982 cites W2169969151 @default.
- W2022164982 doi "https://doi.org/10.1002/art.37832" @default.
- W2022164982 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3947722" @default.
- W2022164982 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23280063" @default.
- W2022164982 hasPublicationYear "2013" @default.
- W2022164982 type Work @default.
- W2022164982 sameAs 2022164982 @default.
- W2022164982 citedByCount "79" @default.
- W2022164982 countsByYear W20221649822013 @default.
- W2022164982 countsByYear W20221649822014 @default.
- W2022164982 countsByYear W20221649822015 @default.
- W2022164982 countsByYear W20221649822016 @default.
- W2022164982 countsByYear W20221649822017 @default.
- W2022164982 countsByYear W20221649822018 @default.
- W2022164982 countsByYear W20221649822019 @default.
- W2022164982 countsByYear W20221649822020 @default.
- W2022164982 countsByYear W20221649822021 @default.
- W2022164982 countsByYear W20221649822022 @default.
- W2022164982 countsByYear W20221649822023 @default.
- W2022164982 crossrefType "journal-article" @default.
- W2022164982 hasAuthorship W2022164982A5002707998 @default.
- W2022164982 hasAuthorship W2022164982A5011305212 @default.
- W2022164982 hasAuthorship W2022164982A5021013876 @default.
- W2022164982 hasAuthorship W2022164982A5038031232 @default.
- W2022164982 hasAuthorship W2022164982A5041537684 @default.
- W2022164982 hasAuthorship W2022164982A5066693323 @default.
- W2022164982 hasAuthorship W2022164982A5068862016 @default.
- W2022164982 hasAuthorship W2022164982A5085234051 @default.
- W2022164982 hasBestOaLocation W20221649822 @default.
- W2022164982 hasConcept C123982805 @default.
- W2022164982 hasConcept C153911025 @default.
- W2022164982 hasConcept C164027704 @default.
- W2022164982 hasConcept C17991360 @default.
- W2022164982 hasConcept C187316574 @default.
- W2022164982 hasConcept C203014093 @default.