Expression of K2P5.1 potassium channels on CD4+ T lymphocytes correlates with disease activity in rheumatoid arthritis patients.
Expression of K2P5.1 potassium channels on CD4+ T lymphocytes correlates with disease activity in rheumatoid arthritis patients.
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DOI:
10.1186/ar3245
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发表时间:
2011-02-11
影响因子:
4.9
通讯作者:
Meuth SG
中科院分区:
文献类型:
--
作者:
Bittner S;Bobak N;Feuchtenberger M;Herrmann AM;Göbel K;Kinne RW;Hansen AJ;Budde T;Kleinschnitz C;Frey O;Tony HP;Wiendl H;Meuth SG
CD4+ T cells express K2P5.1 (TWIK-related acid-sensitive potassium channel 2 (TASK2); KCNK5), a member of the two-pore domain potassium channel family, which has been shown to influence T cell effector functions. Recently, it was shown that K2P5.1 is upregulated upon (autoimmune) T cell stimulation. The aim of this study was to correlate expression levels of K2P5.1 on T cells from patients with rheumatoid arthritis (RA) to disease activity in these patients. Expression levels of K2P5.1 were measured by RT-PCR in the peripheral blood of 58 patients with RA and correlated with disease activity parameters (C-reactive protein levels, erythrocyte sedimentation rates, disease activity score (DAS28) scores). Twenty patients undergoing therapy change were followed-up for six months. Additionally, synovial fluid and synovial biopsies were investigated for T lymphocytes expressing K2P5.1. K2P5.1 expression levels in CD4+ T cells show a strong correlation to DAS28 scores in RA patients. Similar correlations were found for serological inflammatory parameters (erythrocyte sedimentation rate, C-reactive protein). In addition, K2P5.1 expression levels of synovial fluid-derived T cells are higher compared to peripheral blood T cells. Prospective data in individual patients show a parallel behaviour of K2P5.1 expression to disease activity parameters during a longitudinal follow-up for six months. Disease activity in RA patients correlates strongly with K2P5.1 expression levels in CD4+ T lymphocytes in the peripheral blood in cross-sectional as well as in longitudinal observations. Further studies are needed to investigate the exact pathophysiological mechanisms and to evaluate the possible use of K2P5.1 as a potential biomarker for disease activity and differential diagnosis.
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影响因子:
27.4
作者:
Wells G;Becker JC;Teng J;Dougados M;Schiff M;Smolen J;Aletaha D;van Riel PL
通讯作者:
van Riel PL
影响因子:
4.9
作者:
Goronzy JJ;Weyand CM
通讯作者:
Weyand CM
影响因子:
27.4
作者:
Jones G;Sebba A;Gu J;Lowenstein MB;Calvo A;Gomez-Reino JJ;Siri DA;Tomsic M;Alecock E;Woodworth T;Genovese MC
通讯作者:
Genovese MC
影响因子:
4.8
作者:
Meuth, Sven G.;Bittner, Stefan;Wiendl, Heinz
通讯作者:
Wiendl, Heinz
影响因子:
2.2
作者:
Matsui, Toshihiro;Komiya, Akiko;Tohma, Shigeto
通讯作者:
Tohma, Shigeto