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10.1111/cei.12606 http://scihub22266oqcxt.onion/10.1111/cei.12606 C4449774!4449774 !25683200     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=25683200 &cmd=llinks): Failed to open stream: HTTP request failed! 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Specific overexpression of tumour necrosis factor-?-induced protein (TNFAIP)9 in CD14(+) CD16(-) monocytes in patients with rheumatoid arthritis: comparative analysis with TNFAIP3 |pdf=|usr=}}{{25683200 }} gab.com Text Specific overexpression of tumour necrosis factor- -induced protein (TNFAIP)9 in CD14(+) CD16(-) monocytes in patients with rheumatoid arthritis: comparative analysis with TNFAIP3 JO: Clin Exp Immunol http://www.kidney.de/pget.php?&tw=1&pmid=25683200 #FOAvip The tumour necrosis factor (TNF)-?-induced proteins (TNFAIP)9 and TNFAIP3 play an important pathogenic role in murine arthritis. To clarify their pathophysiological roles in patients with rheumatoid arthritis (RA), we examined their expression and localization in peripheral blood mononuclear cells (PBMC). TNFAIP9 and TNFAIP3 mRNA expression was determined in PBMC of RA patients and healthy subjects (control). Flow cytometry was used to analyse the main TNFAIP9- and TNFAIP3-expressing cell populations. TNFAIP9 and TNFAIP3 mRNA expression levels were examined in vitro on CD14(+) cells stimulated with TNF-? and lipopolysaccharide (LPS). The expression levels of TNFAIP9 and TNFAIP3 mRNA were also measured before and 12 weeks after treatment with tocilizumab and abatacept. TNFAIP9 expression was significantly higher, while TNFAIP3 expression was lower in PBMC of RA (n=36) than the control (n=24) (each P?<?0.05). TNFAIP9 was expressed on CD14(+) cells, especially in human leucocyte antigen D-related (HLA-DR)(+) CD14(bright) CD16(-) cells, while TNFAIP3 was expressed mainly on CD3(+) T cells. TNF-? and LPS induced TNFAIP9 and TNFAIP3 in human CD14(+) monocytes in vitro. Treatment with tocilizumab (n=13), but not abatacept (n=11), significantly reduced TNFAIP9 mRNA expression in PBMC, which was associated with reduction in the number of circulating CD14(bright) monocytes. The expression of TNFAIP9 in CD14(+) cells was specifically elevated in patients with RA, regulated by TNF-? and LPS, and suppressed by tocilizumab, while TNFAIP3 in PBMC showed different localization and induction patterns. Twit Text FOAVip Specific overexpression of tumour necrosis factor- -induced protein (TNFAIP)9 in CD14(+) CD16(-) monocytes in patients with rheumatoid arthritis: comparative analysis with TNFAIP3 ????Clin Exp Immunol http://www.kidney.de/pget.php?&tw=1&pmid=25683200 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25683200 #FOAvip English Wikipedia <ref>{{Cite pmid|25683200 }}</ref> Specific overexpression of tumour necrosis factor-?-induced protein (TNFAIP)9 in CD14(+) CD16(-) monocytes in patients with rheumatoid arthritis: comparative analysis with TNFAIP3 #MMPMID25683200 Takai C ; Matsumoto I ; Inoue A ; Umeda N ; Tanaka Y ; Kurashima Y ; Wada Y ; Narita I ; Sumida T Clin Exp Immunol 2015[Jun]; 180 (3 ): 458-66 PMID25683200 show ga The tumour necrosis factor (TNF)-?-induced proteins (TNFAIP)9 and TNFAIP3 play an important pathogenic role in murine arthritis. To clarify their pathophysiological roles in patients with rheumatoid arthritis (RA), we examined their expression and localization in peripheral blood mononuclear cells (PBMC). TNFAIP9 and TNFAIP3 mRNA expression was determined in PBMC of RA patients and healthy subjects (control). Flow cytometry was used to analyse the main TNFAIP9- and TNFAIP3-expressing cell populations. TNFAIP9 and TNFAIP3 mRNA expression levels were examined in vitro on CD14(+) cells stimulated with TNF-? and lipopolysaccharide (LPS). The expression levels of TNFAIP9 and TNFAIP3 mRNA were also measured before and 12 weeks after treatment with tocilizumab and abatacept. TNFAIP9 expression was significantly higher, while TNFAIP3 expression was lower in PBMC of RA (n=36) than the control (n=24) (each P? |*Gene Expression [MESH] |Adult [MESH] |Aged [MESH] |Antibodies, Monoclonal, Humanized/pharmacology [MESH] |Antirheumatic Agents/therapeutic use [MESH] |Arthritis, Rheumatoid/diagnosis/drug therapy/*genetics/*immunology [MESH] |Case-Control Studies [MESH] |DNA-Binding Proteins/genetics [MESH] |Female [MESH] |Humans [MESH] |Immunophenotyping [MESH] |Intracellular Signaling Peptides and Proteins/genetics [MESH] |Leukocytes, Mononuclear/drug effects/immunology/metabolism [MESH] |Lipopolysaccharide Receptors/metabolism [MESH] |Lipopolysaccharides/pharmacology [MESH] |Male [MESH] |Membrane Proteins/*genetics [MESH] |Middle Aged [MESH] |Monocytes/drug effects/*immunology/*metabolism [MESH] |Nuclear Proteins/genetics [MESH] |Oxidoreductases/*genetics [MESH] |RNA, Messenger/genetics [MESH] |Receptors, IgG/metabolism [MESH] |Tumor Necrosis Factor alpha-Induced Protein 3 [MESH]Specific overexpression of tumour necrosis factor-?-induced protein (T(epmc).pdf DeepDyve Pubget Overpricing