首页> 外文期刊>Transfusion: The Journal of the American Association of Blood Banks >Sensitivity of HCV core antigen and HCV RNA detection in the early infection phase.
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Sensitivity of HCV core antigen and HCV RNA detection in the early infection phase.

机译:HCV核心抗原的敏感性和HCV RNA在感染初期的检测。

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BACKGROUND: Various countries have introduced HCV NAT to exclude infectious donations collected during the preseroconversion window phase (PWP). For the same purpose, an ELISA has also been developed to detect HCV core antigen (cAg). STUDY DESIGN AND METHODS: Using sequential samples from regular plasma donors with very recent HCV infections, a total of 494 samples from 52 anti-HCV-negative donors were collected. These panels were used for direct comparison of the performance of PCR and ELISA in detecting viral markers (RNA and cAg) during the PWP of HCV infection. The panels were genotyped, and each sample was analyzed by qualitative and quantitative HCV PCR and by cAg ELISA. The HCV RNA doubling time was calculated from quantitation of viral RNA in consecutive samples during the earliest outbreak of viremia. RESULTS: Concurrent detection of HCV RNA and cAg in 218 and nondetection in 185 samples yielded 81.6-percent concordance in the results of 494 samples. Unidirectional discrepancy of results (i.e., PCR positive and cAg negative) was seen in 91 of 494 (18.4%) samples, which was consistent with 65 specimens with RNA concentrations ranging between 300 and 100,000 IU per mL and 26 specimens with less than 300 IU per mL (limit of quantitative PCR). Individual genotyped panels had different kinetics and courses of viremia. The mean doubling time in the early PWP at the onset of viremia was derived to be 10.8 (range, 5.8-21.0) hours. CONCLUSION: A majority of HCV RNA-positive samples were also cAg-positive during the PWP. The current cAg detection corresponds to 100,000 IU per mL of HCV RNA. Since low-titer samples would be identified only by single-donation NAT, which is often affordable only in developed countries, the cAg ELISA could offer a practical alternative for some countries. The doubling time for HCV RNA at the onset of viremia corresponds to a calculated mean delay of cAg detection during the virus burst phase of 2 or 5 days, when compared with minipool (5000 IU/mL) or single-donation NAT (50 IU/mL), respectively.
机译:背景:各国已经引入了HCV NAT,以排除在血清转换前窗口阶段(PWP)期间收集的传染性捐赠。出于相同的目的,还开发了用于检测HCV核心抗原(cAg)的ELISA。研究设计和方法:使用来自具有近期HCV感染的常规血浆供体的连续样本,共收集了来自52个抗HCV阴性供体的494个样本。这些面板用于直接比较PCR和ELISA在HCV感染PWP期间检测病毒标志物(RNA和cAg)的性能。对面板进行基因分型,并且通过定性和定量HCV PCR和cAg ELISA分析每个样品。 HCV RNA倍增时间是根据病毒血症最早爆发期间连续样本中病毒RNA的定量计算得出的。结果:并发检测218个样本中的HCV RNA和cAg以及185个样本中未检测到494个样本,结果一致性为81.6%。在494个样本中的91个(18.4%)中发现了结果的单向差异(即PCR阳性和cAg阴性),这与65个样本(RNA浓度在每毫升300到100,000 IU之间)和26个样本(300 IU以下)一致每毫升(定量PCR的极限)。各个基因分型的小组具有不同的动力学和病毒血症病程。病毒血症发作初期PWP的平均倍增时间为10.8小时(范围5.8-21.0)小时。结论:在PWP期间,大多数HCV RNA阳性样品也均为cAg阳性。当前的cAg检测量相当于每毫升HCV RNA 100,000 IU。由于低滴度样品只能通过单次捐赠NAT来识别,而这通常仅在发达国家才能买到,因此cAg ELISA可以为某些国家提供实用的替代选择。与微型池(5000 IU / mL)或单次捐赠NAT(50 IU / mL)相比,病毒血症发作时HCV RNA的倍增时间对应于在病毒爆发阶段2或5天计算出的cAg检测平均延迟。毫升)。

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