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Carbamylation of vimentin is inducible by smoking and represents an independent autoantigen in rheumatoid arthritis

机译:波形蛋白的氨基甲酸酯化可通过吸烟诱导,并代表类风湿关节炎中的独立自身抗原

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摘要

OBJECTIVES: Smoking has been connected to citrullination of antigens and formation of anti-citrullinated peptide antibodies (ACPAs) in rheumatoid arthritis (RA). Since smoking can modify proteins by carbamylation (formation of homocitrulline), this study was conducted to investigate these effects on vimentin in animal models and RA.\udMETHODS: The efficiency of enzymatic carbamylation of vimentin was characterised. B-cell response was investigated after immunisation of rabbits with different vimentin isoforms. Effects of tobacco smoke exposure on carbamylation of vimentin and formation of autoantibodies were analysed in mice. The antibody responses against isoforms of vimentin were characterised with respect to disease duration and smoking status of patients with RA.\udRESULTS: Enzymatic carbamylation of vimentin was efficiently achieved. Subsequent citrullination of vimentin was not disturbed by homocitrullination. Sera from rabbits immunised with carbamylated vimentin (carbVim), in addition to carbVim also recognised human IgG-Fc showing rheumatoid factor-like reactivity. Smoke-exposed mice contained detectable amounts of carbVim and developed a broad immune response against carbamylated antigens. Although the prevalence of anti-carbamylated antibodies in smokers and non-smokers was similar, the titres of carbamylated antibodies were significantly increased in sera of smoking compared with non-smoking RA. CarbVim antibodies were observed independently of ACPAs in early phases of disease and double-positive patients for anti-mutated citrullinated vimentin (MCV) and anti-carbVim antibodies showed an extended epitope recognition pattern towards MCV.\udCONCLUSIONS: Carbamylation of vimentin is inducible by cigarette smoke exposure. The polyclonal immune response against modified antigens in patients with RA is not exclusively citrulline-specific and carbamylation of antigens could be involved in the pathogenesis of disease.\udTRIAL REGISTRATION NUMBER: ISRCTN36745608; EudraCT Number: 2006-003146-41.
机译:目的:吸烟与类风湿关节炎(RA)中抗原的瓜氨酸化和抗瓜氨酸肽抗体(ACPAs)的形成有关。由于吸烟可以通过氨基甲酰化(高瓜氨酸的形成)修饰蛋白质,因此进行了这项研究,以研究在动物模型和RA中对波形蛋白的这些作用。\ udMETDS:表征波形蛋白的酶式氨基甲酸酯化的效率。用不同波形蛋白同工型免疫兔后,研究了B细胞反应。在小鼠中分析了烟草烟雾暴露对波形蛋白的氨基甲酰化和自身抗体形成的影响。针对RA患者的病程和吸烟状况,对针对波形蛋白同工型的抗体反应进行了表征。\结果:有效地实现了波形蛋白的酶促氨基甲酰化。随后波形蛋白的瓜氨酸化不受同瓜氨酸化的干扰。除了使用carbVim免疫了氨基甲酰化波形蛋白(carbVim)免疫的兔的血清外,还识别了类人风湿因子反应性的人IgG-Fc。暴露于烟雾的小鼠含有可检测量的carbVim,并产生了针对氨甲酰化抗原的广泛免疫反应。尽管吸烟者和非吸烟者中抗氨基甲酸酯化抗体的患病率相似,但与非吸烟RA相比,吸烟者血清中氨基甲酰化抗体的滴度显着增加。在疾病早期和双阳性患者的抗突变瓜氨酸波形蛋白(MCV)和抗carbVim抗体显示出对MCV扩展的表位识别模式,独立于ACPAs观察到CarbVim抗体。冒烟。 RA患者对修饰抗原的多克隆免疫反应并非仅对瓜氨酸具有特异性,抗原的氨甲酰化可能与疾病的发病机制有关。\\注册号:ISRCTN36745608; EudraCT编号:2006-003146-41。

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