摘要
目的 用丙型肝炎病毒(HCV)核心抗原酶联免疫吸附技术(HCV-cAg ELIsA)检测抗-HCV ELISA阳性无偿献血血标本,了解丙型肝炎病毒核心抗原筛查献血者应用价值.方法 将225份抗-HCV ELISA检测阳性标本分别用HCV-cAgELISA和HCV RT-PCR检测.结果 225份抗-HCVELISA检测不合格标本HCV-cAgELISA和HCV RT-PCR阳性率分别为39.1%和38.7%,阳性率差异无统计学意义(P>0.05).复检双试剂均阳性、初或复检单试剂阳性和S/CO值在灰区标本抗-HCVELISA的假阳性率分别为31.4%、90.4%和83.0%,总假阳性率为61.3%.HCV-cAgELISA的假阳性率分别为1.4%、0和0,总假阳性率为1.1%.HCV cAg ELISA检测不同样本假阳性率为0-1.4%明显低于抗-HCV ELISA检测的阳性率31.4% -90.4%(P<0.01).结论 HCV-cAg ELISA敏感性与HCV RT-PCR类似,假阳性率明显低于抗-HCV ELISA,HCV-cAg ELISA具有简便、快速、可靠优点,较适用于安全输血中献血者的血液筛检.
Objective To detect anti-hepatitis C virus enzyme-linked immunoassay (anti-HCV ELISA) positive blood specimens by HCV core antigen ELISA(HCV-cAgELISA),and to investigate the value of detecting of HCV-cAg for screening blood donor.Methods All anti-HCV ELISA positive specimens were identified by using HCV-cAgELISA and HCV RT-PCR methods.Results In 225 anti-HCV positive specimens,the positive rates of HCV-cAgELISA and HCV RT-PCR were 39.1% and 38.7%,respectively,the positive rates were no significant difference.Among anti-HCV screening unqualified samples,the false positive rates of anti-HCV ELISA in both positive,single positive,and grey area were 31.4%,90.4% and 83.0%,respectively.The total false positive rate was 61.3%.The false positive rate of HCV-cAgELISA in both positive,single positive,and grey area were 1.4%,0 and 0,respectively.The total false positive rate was 1.1%.The false positive rate of HCV-cAgELISA was significantly lower antiHCV ELISA (P 〈 0.01).Conclusion Sensitivity of HCVcAg ELISA is silllilar to HCV RT-PCR (P 〉 0.05).The total false positive rate of HCVcAg ELISA was significantly lower anti-HCV ELISA (P 〈 0.01).HCVcAg ELISA is a simple,fast,and reliable memod to screen donor with HCV infection in blood transfusion medicine.
出处
《中华实验和临床病毒学杂志》
CAS
CSCD
2015年第1期68-70,共3页
Chinese Journal of Experimental and Clinical Virology
基金
衢州市科技计划项目(2013J063)