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[上海慢性丙型肝炎患者NS5A基因序列与干扰素治疗反应的相关性]

[Association between NS5A gene sequence and response to interferon therapy in chronic hepatitis C patients in Shanghai].

作者信息

Hu Yunwen, Tang Meifang, Jiang Weilun, Wu Ying, Yuan Zhenghong, Wen Yumei

机构信息

Department of Molecular Virology, Medical Center of Fudan University, Shanghai 200032, China.

出版信息

Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2002 Jun;16(2):114-8.

Abstract

BACKGROUND

To elucidate relationship between amino acid sequence of non-structural protein 5A (NS5A) and outcome of HCV (1 b) patients after interferon (IFNa) therapy.

METHODS

Sera of 24 patients were collected before, during and after IFNa therapy. Pretreatment RNA levels and the sequences of HCV NS5A interferon sensitivity determining region (ISDR) were determined. NS5A full-length sequences of 5 HCV isolates from 3 patients with different response types were also analyzed. Phylogenetic tree analysis and protein secondary structure prediction were undertaken.

RESULTS

Pretreatment RNA levels of sustained response group were significantly lower than that of non-response group and relapse group (4.50X104 copies/ml versus 1.82X107 copies/ml, P < 0.01).ISDR sequences of NS5A from pretreatment sera were compared with HCV-J strain (prototype). Thirteen of 24 isolates were wild type,11 of 24 were intermediate type and none of them was mutant type. 3 of 6 sustained responders were infected with wild-type isolates, the rest with intermediate type isolates. Phylogenetic tree based on NS5A full-length sequences classified 5 isolates with 3 different response types into 3 groups. Non-response isolates belonged to the same group as HCV-J. Secondary structure prediction of 5 isolates revealed significant differences existing in 2 255- 2 289. This region was partly overlapped with PKR-binding domain.

CONCLUSIONS

Low HCV RNA levels in serum are associated with favorable outcome of IFNa therapy. ISDR sequence alone could not predict outcome of IFN treatment. Combination of determination of HCV RNA levels in serum with sequence analysis of PKR-binding domain may be helpful in predicting the efficacy of IFN therapy.

摘要

背景

阐明非结构蛋白5A(NS5A)的氨基酸序列与丙型肝炎病毒(HCV,1b型)患者接受干扰素(IFNα)治疗后的疗效之间的关系。

方法

收集24例患者在IFNα治疗前、治疗期间及治疗后的血清。测定治疗前RNA水平及HCV NS5A干扰素敏感性决定区(ISDR)序列。对3例不同反应类型患者的5株HCV分离株的NS5A全长序列也进行了分析。进行了系统发育树分析和蛋白质二级结构预测。

结果

持续应答组治疗前RNA水平显著低于无应答组和复发组(4.50×10⁴拷贝/ml对1.82×10⁷拷贝/ml,P<0.01)。将治疗前血清中NS5A的ISDR序列与HCV-J株(原型)进行比较。24株分离株中13株为野生型,24株中11株为中间型,无突变型。6例持续应答者中有3例感染野生型分离株,其余感染中间型分离株。基于NS5A全长序列的系统发育树将5株具有3种不同反应类型的分离株分为3组。无应答分离株与HCV-J属于同一组。5株分离株的二级结构预测显示,在2255-2289区域存在显著差异。该区域与PKR结合域部分重叠。

结论

血清中低HCV RNA水平与IFNα治疗的良好疗效相关。仅ISDR序列不能预测IFN治疗的疗效。血清中HCV RNA水平测定与PKR结合域序列分析相结合可能有助于预测IFN治疗的疗效。

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