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作 者:陈文碧[1] 张锡林[2] 王光西[1] 许颖[2] 张跃辉[1] 毛樱逾[1] 湛蜀燕[1]
机构地区:[1]泸州医学院人体寄生虫学教研室,四川泸州646000 [2]第三军医大学基础部病原生物学教研室
出 处:《泸州医学院学报》2004年第4期292-295,共4页Journal of Luzhou Medical College
基 金:四川省教育厅重点科研资助项目 (2 0 0 3A0 6 2 )
摘 要:目的 :建立一种检测斯氏狸殖吸虫病患者血清抗体的快速、敏感和特异的新方法。方法 :以斯氏狸殖吸虫成虫可溶性抗原为上样抗原 ,胶体金标记羊抗人IgG为显色剂 ,建立检测斯氏狸殖吸虫病患者血清抗体的斑点金免疫渗滤法 (DIGFA) ;并以ELISA作平行对照。结果 :DIGFA和ELISA分别检测 83例斯氏狸殖吸虫病患者血清抗体 ,其阳性率分别为 95 .2 % (79/ 83)和 91 .6 % (76 / 83) ,两法差异无显著性 (P >0 .0 5 )。DIGFA分别检测正常人血清32例、华支睾吸虫病患者血清 2 3例和日本血吸虫病患者血清 36例 ,前者均为阴性 ,后两者的交叉反应率分别为 4 .3% (1 / 2 3)和 8.3% (3/ 36 ) ;DIGFA和ELISA两法的总符合率达 92 .3% (36 / 39)。结论 :DIGFA的特异性和敏感性与ELISA相近 ,但方法快速、试剂稳定 ,且不需特殊设备 。Objective: To establish a new, fast, sensitive and specific assay for detecting antibodies in pagumogonimiasis skrjabini. Method: Using pagumogonimus skrjabini adult worm antigen and IgG Labelled with colloidal gold as color developing agent, a dot immunogold filtration assay(DIGFA) for detecting pagumogonimus skrjabini antibodies was tested. ELISA was used as the parallel control. Result: The positive rates of DIGFA and ELISA in testing the sera from 83 proved cases were 95.2%(79/83) and 91.6%(76/83),respectively, the difference between the two assays being insignificant(P>0.05). The negative rate of DIGFA in healthy people was 100%(32/32). The cross reaction rates in 36 schistosomiasis cases and 23 clonorchiasis cases were 8.3%(3/36) and 4.3%(1/23), respectively. Both coincidence rates in comparison of DIGFA with ELISA were 92.3%(36/39). Conclusion: DIGFA is as sensitive and specific as the ELISA, and thus has the advantages of simplicity and saving specific equipment. Therefore, this method is fitful to diagnosis of Pagumogonimiasis skrjabini as well as epidemiological investigation.
分 类 号:R38[医药卫生—医学寄生虫学]
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