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作 者:张川[1] 邵勇[1] 高治忠[1] 张明刚[1] 王文涛[1] 刘云力[1]
机构地区:[1]哈尔滨医科大学附属第二医院泌尿外利,150086
出 处:《中国综合临床》2013年第7期714-717,共4页Clinical Medicine of China
基 金:黑龙江省科技计划项目(GC07C35304)
摘 要:目的探讨器官移植术后应用核酸基础序列扩增法(NASBA)检测即刻早期抗原(IE)-mRNA对人外周血中巨细胞病毒(HCMV)感染的诊断价值,以评价和推广CMV活动性感染的诊断方法。方法肾移植术后患者32例,分别于术后3、7周采血5~7ml,每次同时进行针对CMV感染的NASBA、实时荧光定量PCR(Realtime—PCR)、ELISA法检测。比较三者的敏感度和特异度。结果32例肾移植术后受体CMV检测结果显示,采用NASBA法外周血IE-mRNA阳性率为45.8%(15/32);Realtime.PCR法检测HCMV—DNA阳性率45.8%(15/32);ELISA法检测HCMV-(IgG+IgM)阳性率37.5%(14/32)。IE-mRNA、HCMV—DNA灵敏度和特异度明显优于HCMV-(IgG+IgM),且可以降低后者存在的假阳性率。有CMV症状者共14例,其中NASBA法IE—mRNA检测阳性患者占92.8%(13/14);RealtimePCR、ELISA法阳性率分别为71.5%(10/14)和42.8%(6/14)。结论NASBA和Realtime—PCR是一种敏感、快速诊断HCMV感染的方法,灵敏度及特异性均高于传统ELISA法,并能弥补ELISA的假阴性。NASBA检测IE—mRNA对于辅助临床诊断具有很好的价值。Objective To investigate the diagnostic value of the immediate early antigen (IE) mRNA by nucleic acid sequence-based amplification(NASBA) in peripheral blood cytomegalovirus (CMV) infection, and to establish and promote the diagnosis method for CMV. Methods Five to seven ml blood was taken from 32 patients at 3 week and 7 week after renal transplantation to detect serum cytomegalovirus antigen and antibody expression by NASBA, Real time-PCR and enzyme-linked immunosorbent assay (ELISA) sensitivity and specificity were compared. Results The results of CMV detection in 32 renal transplanted patients respectively showed that the positive rate of peripheral blood IE-mRNA by NASBA was 45.8% (15/32) ;The positive rate of HCMV-DNA in blood by Real time-PCR was 45. 8% (15/32). Using ELISA,the positive rate of HCMV-( IgG + IgM) was 37. 5% (14/32). IE-mRNA and HCMV-DNA had higher sensitivity and specificity and lower false positive rate than HCMV-( IgG + IgM). The positive rates of IE-mRNA by NASBA, Real time-PCR and ELISA were 92. 8% ,71.5% and 42. 8% respectively in the 14 cases. Conclusion The nucleic acid amplification method (NASBA based sequence ) and Real time-PCR are sensitive, rapid diagnosis methods of HCMV infection, with higher sensitivity and specificity and lower false positive rate than traditional ELISA. And NASBA detection of IE-mRNA has good value for auxiliary clinical diagnosis.
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