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出 处:《武汉大学学报(医学版)》2014年第1期106-109,共4页Medical Journal of Wuhan University
基 金:武汉市卫生局资助课题(编号:WG10B03)
摘 要:目的:探讨3种结核分枝杆菌保守抗原Ag85A、Ag85B和HspX抗原特异性细胞免疫反应对结核性胸膜炎的辅助诊断价值。方法:收集我院收治的胸腔积液患者30例,根据胸水性质,分为结核性胸膜炎组20例,非结核性胸膜炎组10例。收集胸水样本,分离胸水样本中细胞成分。原核表达、纯化并鉴定结核分枝杆菌Ag85A、Ag85B、HspX蛋白。用Ag85A、Ag85B及HspX蛋白分别刺激2组患者的胸水细胞成分,通过ELISA技术检测IFN-γ表达水平并进行组间比较。结果:Ag85A蛋白刺激后,非结核性胸膜炎组IFN-γ为(15.50±2.41)ng/L,结核性胸膜炎组IFN-γ为(1 775.00±362.86)ng/L;Ag85B蛋白刺激后,非结核性胸膜炎组IFN-γ为(14.89±2.30)ng/L,结核性胸膜炎组IFN-γ为(2 442.50±418.94)ng/L;HspX蛋白刺激后,非结核性胸膜炎组IFN-γ为(14.20±2.30)ng/L,结核性胸膜炎组IFN-γ为(3 570.00±496.41)ng/L;两组比较均P<0.01。结核性胸膜炎组中,不同患者对不同抗原刺激所产生的IFN-γ水平有一定差别。结论:结核性胸膜炎患者胸水中的细胞成分经Ag85A、Ag85B及HspX蛋白刺激后,IFN-γ水平均不同程度明显升高,该方法对结核性胸膜炎有一定的辅助诊断价值。Objective. To construct a method to diagnosis tuberculosis pleurisy based on specific cellular immune response induced by Mycobacterium tuberculosis Ag85A, Ag85B, and HspX antigens. Methods: Thirty samples of pleurisy, including twenty tuberculosis pleurisy samples (group A) and ten non-tuberculosis pleurisy samples (group B), were collected to separate cell component and supernatant. Mycobacterium tuberculosis Ag85A, Ag85B, and HspX antigens were ex- pressed in pET30A procaryotic expression system and purified. Cell components of samples were stimulated with Ag85A, Ag85B, and HspX proteins for 72 h and the concentrations of induced IFN-γ were detected with human IFN-γ/ELISA kit. Results: In group A, the level of IFN-γ were (1 775.00±362.86) ng/L, (2 442.50±418.94) ng/L and (3 570.00±496.41) ng/L respectively significant increase of IFN-γ after stimulation method is potent to be developed as a kind of culosis pleurisy. with Ag85A, Ag85B and HspX antigens, and this specific and fast method for the diagnosis of tuberculosis pleurisy.
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