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作 者:潘卫东[1] 王东升[1] 李燕[2] 谷淑燕[2]
机构地区:[1]河南医科大学微生物学与免疫学教研室,郑州450052 [2]中国预防医学科学院病毒所免疫室,北京100052
出 处:《河南医科大学学报》1999年第2期51-54,共4页Journal of Henan Medical University
摘 要:获得足够的EB病毒壳抗原,建立ELISA方法用于鼻咽癌的诊断。方法:将 BALF4基因克隆进入 载体pUR291,在大肠杆菌中表达EB病毒壳抗原与β-半乳糖苷酶的融合蛋白,并通过DEAE-Sepharose Fast Flow离子 交换柱层析对融合蛋白进行纯化,将纯化的蛋白用于 ELISA方法检测人血清中的IgG/VCA和 IgA/VCA抗体,用带 有pUR291质粒的宿主菌裂解液吸收待检血清中的抗β-半乳糖苷酶抗体。结果:ELISA方法与免疫荧光方法检测的 结果呈正相关(r=0.6236,P<0.001;r=0.9225,P<0.001)。免疫荧光方法检测为阳性的血清,ELISA检测均为 阳性;IgG/VCA和IgA/VCA抗体的几何平均滴度(GMT)分别是免疫荧光方法的13倍和15倍。在40份免疫荧光检 测IgA/VCA阴性的血清中,ELISA检测有3例阳性,表明ELISA方法比免疫荧光方法更敏感。结论:在原核系统中 表达抗原,为ELISA方法在鼻咽癌的诊断和大规模血清学普查中的应用提供了一个有效手段。Aim:To obtain sufficient Epstein-Barr viral capsid antigen and apply it to the diagnosis of Nasopharyngeal Carcinoma based on ELISA.Methods:Using the recombinant DNA technique,a fragment of gene BALF_4 was cloned into vector plasmid pUR291 and a fusion protein consisting of β-galactosidase and the major polypeptide of Epstein-Barr viral capsid antigen (VCA)was expressed in E.coli.After determining the specificity of the fusion protein,the product was purified by DEAESepharose Fast Flow ion-exhange column chromatography.ELISAswere established with the purified product,using rabbit antiserum to block β-galactosidase in human sera.Results:There was a close correlation between results of the immunofluorescence and ELISA(r=0.6236,P<0.001;R=0.9225,p<0.001).The IgG and IgA positive sera determined by immunofluoresence were also positive when determined by ELISAs,and GMT were respectively 13 times and 15 times as immunofluorescence.Three positive sera were detected by ELISA in 40 IgA negative sera determined by immunofluorescence,suggesting that ELISA is more sensitiv than immunofluorescence assay.Conclusion:The Epstein-Barr viral capsid antigen expressed in prokaryotic is useful in the application of the diagnosis of Nasopharyngeal Carcinoma based on ELISA.
分 类 号:R373.1[医药卫生—病原生物学]
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