首页> 外文期刊>The Journal of rheumatology >Increased in vitro production of interleukin 6 in response to trimethoprim among persons with trimethoprim induced systemic adverse reactions.
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Increased in vitro production of interleukin 6 in response to trimethoprim among persons with trimethoprim induced systemic adverse reactions.

机译:甲氧苄啶诱导的全身性不良反应患者中对甲氧苄啶反应的白细胞介素6的体外产生增加。

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OBJECTIVE: Trimethoprim occasionally triggers a systemic adverse reaction including fever, malaise, head and backache, and even overt meningeal irritation, particularly in women with an autoimmune rheumatic disease. To study the unknown pathogenesis of the reaction we measured the effect of trimethoprim upon the cytokine [interleukin (IL) 2, 6, 10, and tumor necrosis factor-alpha] production of trimethoprim reactive and tolerant persons' peripheral blood mononuclear cells in vitro. METHODS: Peripheral blood mononuclear cells from 12 women reactive to trimethoprim (3 with primary Sjogren's syndrome, 3 with systemic lupus erythematosus, 1 with systemic scleroderma, 5 with no rheumatic disease) were cultured in the presence of trimethoprim, and the cytokine production was measured. Eleven women who tolerated trimethoprim (6 with Sjogren's syndrome and 5 with no rheumatic disease) served as controls. RESULTS: Therapeutic trimethoprim concentration induced in the mononuclear cells of the trimethoprim reactive patients significantly higher IL-6 production [mean +/- SD (median), 2034+/-2965 (572) pg/ml] versus cells of the trimethoprim tolerant subjects [954+/-2552 (89) pg/ml; p = 0.036]. No significant differences in the production of other cytokines were detected. CONCLUSION: Trimethoprim induces IL-6 production in the peripheral blood mononuclear cells of trimethoprim reactive persons. We suggest that IL-6 production is the probable trigger leading to the clinical reaction.
机译:目的:甲氧苄啶有时会引起全身性不良反应,包括发烧,全身乏力,头疼和腰酸,甚至明显的脑膜刺激,特别是在患有自身免疫性风湿病的女性中。为了研究该反应的未知发病机理,我们在体外测量了甲氧苄啶对甲氧苄啶反应性和耐受性人外周血单核细胞的细胞因子[白介素(IL)2、6、10和肿瘤坏死因子-α]产生的影响。方法:在甲氧苄啶存在的情况下,培养了对甲氧苄啶有反应的12名妇女的外周血单个核细胞(原发性干燥综合征3例,系统性红斑狼疮3例,全身性硬皮病1例,无风湿性疾病5例),并测量了细胞因子产生。耐受甲氧苄啶的11名妇女(6名患有干燥综合征,5名无风湿病)作为对照。结果:在甲氧苄啶反应性患者的单核细胞中诱导的治疗性甲氧苄啶浓度明显高于耐甲氧苄啶的受试者的细胞中IL-6的产生[平均+/- SD(中位数),2034 +/- 2965(572)pg / ml]。 [954 +/- 2552(89)pg / ml; p = 0.036]。在其他细胞因子的生产中未检测到显着差异。结论甲氧苄啶可诱导甲氧苄啶反应性人外周血单个核细胞产生IL-6。我们认为IL-6的产生可能是导致临床反应的诱因。

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