丙型肝炎病毒RNA包膜区E2的高变区1的变异似乎与病毒的持久性无关,与肝脏疾病有关。

M R Brunetto, T Suzuki, H Aizaky, D Flichman, P Colombatto, M L Abate, F Oliveri, Y Matsuura, F Bonino, T Miyamura
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引用次数: 0

摘要

丙型肝炎病毒(HCV) RNA包膜蛋白编码区E2 (HVR1 E2) 5'末端的高遗传变异性已被许多作者认为在病毒的持续存在和肝脏疾病的结局中发挥重要作用。我们研究了8例慢性HCV携带者(男5例,女3例,中位年龄41岁,平均随访时间3年)HVR1 E2变异与HCV基因型、HCV- rna水平和肝脏疾病的关系。4例为ALT水平持续正常、肝脏组织学正常的健康HCV携带者,4例为慢性肝病患者。在每位患者中,通过直接测序评估间隔至少12个月获得的2个血清HCV-RNA分离株的HVR1 E2变异性。健康携带者的核苷酸和氨基酸同源性分别为97.6%-57.1%和92.8%-25%,患者的核苷酸和氨基酸同源性分别为95.2%-55.9%和89.3%-32.1%。我们没有观察到HVR1 E2异质性与HCV基因型、病毒血症水平、肝坏死炎症的存在和程度之间的任何相关性。我们的研究结果表明,hvr1e2异质性与肝炎的发病机制没有直接关系,但它可能在病毒的持久性中起主要作用。
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Variations in the hypervariable region 1 of the envelope region E2 of hepatitis C virus RNA appear associated with virus persistence independently of liver disease.

The high genetic variability of the 5' end of the envelope protein-coding region E2 (HVR1 E2) of Hepatitis C Virus (HCV) RNA has been suggested by many authors to play an important role in both virus persistence and outcome of liver disease. We studied the relations between HVR1 E2 variability and HCV genotypes, HCV-RNA levels and liver disease in 8 chronic HCV carriers (5 males and 3 females, median age 41 years, followed-up for a mean period of 3 years). Four were healthy HCV carriers with persistently normal ALT levels and normal liver histology and 4 patients with chronic liver disease. In each patient, the HVR1 E2 variability of 2 serum HCV-RNA isolates obtained at least 12 months apart were evaluated by direct sequencing. Nucleotide and amino acid homologies ranged between 97.6%-57.1% and 92.8%-25% in healthy carriers and 95.2%-55.9% and 89.3%-32.1% in patients, respectively. We did not observe any correlation between HVR1 E2 heterogeneity and HCV genotypes, viraemia levels, presence and extent of liver necroinflammation. Our findings suggest that HVR1 E2 heterogeneity has no direct implications in hepatitis, pathogenesis but it could play a major role in virus persistence.

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