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作 者:黄超[1] 张文帅[1] 张黎[1] 温恬[1] 史凤娟[1] 曾晓燕[1] 迟莹[1] 史智扬[1] 焦永军[1]
出 处:《江苏预防医学》2015年第4期1-3,共3页Jiangsu Journal of Preventive Medicine
基 金:江苏医学重点人才基金项目(RC2011082);江苏省科技支撑计划项目(BE2012768);科技部传染病重大专项(2013ZX09102029)
摘 要:目的基于上转化发光(UPT)免疫层析技术,建立发热伴血小板减少综合征病毒(SFTSV)总抗体的现场快速检测方法。方法将SFTSV重组NP蛋白与上转化发光颗粒(UCP)偶联,制备UCP-NP免疫层析试纸条,评价该试纸条检测SFTSV总抗体的灵敏性、特异性和稳定性,并检测SFTSV血清254份,与酶联免疫法(ELISA)比较。结果该方法可在15min内完成SFTSV总抗体检测,可检测1∶500稀释度的SFTSV阳性血清,与其他出血热病毒无交叉反应,加样14d内稳定性较高。UPT免疫层析法与ELISA法检测临床血清样品一致性极高(Kappa=0.967),约登指数为0.973。结论建立了基于UPT免疫层析技术的SFTSV总抗体快速检测方法,该方法灵敏、特异,且操作简便、快速,结果稳定,适合在基层门诊和体检现场推广。Objective To develop a method for rapid and on-site detection of severe fever with thrombocytopenia syndrome virus (SFTSV) total antibodies by up-converting phosphor technology (UPT) -based lateral-flow assay. Methods SFTSV re- combinant NP protein was conjugated to up-converting phosphor particles (UCP), UPT-NP analysis strips were assembled. The sensitivity, specificity and stability of UPT method to detect total antibodies were evaluated; 254 clinical sera were tested by UPT method and ELISA to study the consistence of above 2 methods. Results UPT method can analyze total antibodies a- gainst SFTSV in 15 minutes, with the detection limit of 1:500 dilution of original positive SFTSV sera samples; no cross reac- tion with other hemorrhagic fever virus were detected. UPT method exhibited high stability in 14 days upon sample loading. The results of UPT method were highly consistent with ELISA (Kappa=0. 967), with Youden's index of 0. 973. Conclusion Rapid detection of SFTSV total antibodies by UPT-based lateral-flow assay was developed successfully, which was sensitive , specific , rapid ,stable and easy to operate. It is especially suitable to be promoted in local clinics and on-site physical examina- tions.
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