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首页> 外文期刊>Journal of Medical Virology >Anti-HCV RIBA/LiaTek reactivity and HCV genotype in EIA-negative patients with viremia.
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Anti-HCV RIBA/LiaTek reactivity and HCV genotype in EIA-negative patients with viremia.

机译:EIA阴性病毒血症患者的抗HCV RIBA / LiaTek反应性和HCV基因型。

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Individuals infected with hepatitis C virus (HCV) usually produce anti-HCV antibodies detectable by enzyme immunoassay (EIA); however, in certain viremic cases this antibody does not appear. To investigate whether anti-HCV in these cases is detectable by Western blot (WB), 38 HCV RNA positive/anti-HCV EIA-negative sera were tested by RIBA 3.0 or LiaTek III. The HCV genotypes (INNO-LiPA) were analyzed to determine whether the variance in these genotypes can be the reason for the late, weak antibody production or its absence. As the control group, 282 EIA-positive/HCV RNA-positive patients were examined. A single band reactivity of various intensities by RIBA or LiaTek was observed in 16/38 EIA negative sera. Positive results with NS3 were detected in 4 sera and weak positive (+/-) with core, NS3, and NS5 in 5, 6, and 1 sera, respectively. In 3 cases with anti-NS3, the seroreversion was observed in follow-up. The distribution of genotypes in anti-HCV-negative versus anti-HCV-positive groups was: 1b alone, 50.0% vs. 78.0%; 3a alone, 13.2% vs. 15.6%; and mixed (1b+3a), 36.8% vs. 5.0%, respectively. The follow-up studies showed that viremia was lost spontaneously in 12/35 patients. In some patients infected with two genotypes, the spontaneous loss of the 3a genotype was observed. The study showed that WB tests are useful for serological confirmation of HCV infection in some EIA negative/HCV RNA-positive patients but, because seroreversion may occur, sequential sera samples should be tested. No unusual HCV genotype was detected in anti-HCV-negative/HCV RNA-positive cases, but the frequency of mixed infection with the 1b+3a genotypes in this group was found to be higher than that in anti-HCV-positive hepatitis patients. Copyright 1999 Wiley-Liss, Inc.
机译:感染了丙型肝炎病毒(HCV)的个体通常会产生可通过酶免疫分析(EIA)检测到的抗HCV抗体;但是,在某些病毒血症情况下,这种抗体不会出现。为了研究在这些情况下抗HCV是否可通过Western blot(WB)检测到,通过RIBA 3.0或LiaTek III测试了38 HCV RNA阳性/抗HCV EIA阴性血清。分析了HCV基因型(INNO-LiPA),以确定这些基因型的差异是否可能是抗体产生较弱或迟发的原因。作为对照组,检查了282位EIA阳性/ HCV RNA阳性患者。在16/38 EIA阴性血清中观察到RIBA或LiaTek产生的各种强度的单条带反应性。在3个血清中检测到NS3阳性结果,在5个,6个和1个血清中分别检测到核心,NS3和NS5弱阳性(+/-)。在3例抗NS3病例中,在随访中观察到了血清逆转。抗HCV阴性组和抗HCV阳性组的基因型分布分别为:单独1b,50.0%vs. 78.0%;仅3a,分别为13.2%和15.6%;和混合(1b + 3a)分别为36.8%和5.0%。后续研究表明,病毒血症在12/35患者中自发消失。在一些感染了两种基因型的患者中,观察到了3a基因型的自发丧失。该研究表明,WB检测对于某些EIA阴性/ HCV RNA阳性患者的HCV感染的血清学确诊非常有用,但由于可能发生血清逆转,因此应测试顺序的血清样品。在抗HCV阴性/ HCV RNA阳性的病例中未检测到异常的HCV基因型,但发现该组中1b + 3a基因型的混合感染频率高于抗HCV阳性肝炎患者。版权所有1999 Wiley-Liss,Inc.

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