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在韩国利用NS-4肽和丙型肝炎病毒基因组检测丙型肝炎病毒的型特异性抗体。

Type-specific antibody for hepatitis C virus detected by use of NS-4 peptide and hepatitis C virus genome in Korea.

作者信息

Son Han-Chul, Yoon Man-Soo, Kim Yoon-Jin, Kim In-Hoo, Kim You-Sun

机构信息

Department of Clinical Pathology, College of Medicine, Pusan National University, Korea.

出版信息

Rinsho Byori. 2002 May;50(5):533-40.

Abstract

Hepatitis C virus, often possessing mutant genes, have the features that allow them to avoid host's immunologic response and further cause chronic progressive infections. Therefore, it is essential for those patients infected of HCV to receive improved diagnostic procedures. And it is equally important to investigate the course of disease progression and the response to treatment. The goal of this study is to review the efficacy of the third generation immunoblot assay and standardized RT-PCR-Hybridization assay, and in contrast with genotype identification(genotyping), the followings were briefly evaluated for the efficacy of serotype identification(serotyping) by using NS-4 peptide in the observation of the course and in the treatment of patients with HCV hepatitis. 1. The true positive rate in 132 cases showing repeated positives with 3rd generation anti-HCV EIA are 81.8% by immunoblot assay and 75.8% by RT-PCR-Hybridization assay. 2. The 79.5% concordance of immunoblot and RT-PCR-Hybridization assay is shown. The negative results from immunoblot assay are also negative in RT-PCR-Hybridization assay. 3. Among 95 patients with HCV hepatitis patients in 95 cases, the serotype 1, 2 and 4 were 53.2%, 45.2%, and 1.6%, respectively. In 29 cases, the genotypes of patients with HCV showed 1b in 15 cases, 2a/2c in 8 cases, 2b in 2 cases and mixed type in 4 cases. 4. In comparison between serotype and genotype, they showed 75.9% concordance. But serotyping showed higher efficacy in experimental procedures and sampling conditions, with more convenience. Based on above evaluation and reference review, it is reasonable to check with 3rd generation immunoblot assay the samples producing repeated positive results from anti-HCV EIA. For more definitive diagnosis of HCV infection, it is appropriate to confirm and double-check with standardized RT-PCR-Hybridization assay. Lastly, it is strongly suggested that for observation of progression and for choice of interferon treatment, serotype identification(serotyping) is more useful in practice than genotype identification (genotyping).

摘要

丙型肝炎病毒通常携带突变基因,具有能够逃避宿主免疫反应并进而导致慢性进行性感染的特征。因此,对于那些感染丙肝病毒的患者来说,接受改进的诊断程序至关重要。研究疾病进展过程以及对治疗的反应同样重要。本研究的目的是回顾第三代免疫印迹法和标准化逆转录聚合酶链反应-杂交法的疗效,并且与基因型鉴定(基因分型)相比,在丙肝病毒肝炎患者病程观察和治疗中,简要评估使用NS-4肽进行血清型鉴定(血清分型)的疗效。1. 在132例第三代抗丙肝病毒酶免疫测定呈反复阳性的病例中,免疫印迹法的真阳性率为81.8%,逆转录聚合酶链反应-杂交法的真阳性率为75.8%。2. 免疫印迹法和逆转录聚合酶链反应-杂交法的一致性为79.5%。免疫印迹法的阴性结果在逆转录聚合酶链反应-杂交法中也为阴性。3. 在95例丙肝病毒肝炎患者中,血清型1、2和4分别占53.2%、45.2%和1.6%。在29例中,丙肝病毒患者的基因型为1b的有15例,2a/2c的有8例,2b的有2例,混合型的有4例。4. 血清型和基因型之间的一致性为75.9%。但血清分型在实验程序和采样条件方面显示出更高的疗效,且更方便。基于上述评估和参考文献回顾,用第三代免疫印迹法检查抗丙肝病毒酶免疫测定产生反复阳性结果的样本是合理的。为了更明确地诊断丙肝病毒感染,用标准化逆转录聚合酶链反应-杂交法进行确认和复查是合适的。最后,强烈建议在观察病程和选择干扰素治疗时,血清型鉴定(血清分型)在实际应用中比基因型鉴定(基因分型)更有用。

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