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隐匿性乙型肝炎病毒感染:S蛋白变体的影响

Occult hepatitis B virus infection: influence of S protein variants.

作者信息

Zhang Zhenhua, Zhang Ling, Dai Yu, Zhang Yafei, Li Jun, Li Xu

机构信息

Department of Infectious Diseases, the First Affiliated Hospital, Anhui Medical University, Hefei, 230022, China.

School of Pharmacy, Anhui Medical University, Hefei, China.

出版信息

Virol J. 2016 Jan 19;13:10. doi: 10.1186/s12985-016-0464-z.

Abstract

BACKGROUND

In occult hepatitis B viral infection (OBI), the persistence of hepatitis B virus (HBV) DNA is associated with a lack of hepatitis B surface antigen (HBsAg). To assess the possible role of HBsAg immune escape variants in OBI patients, variability in the HBV S gene was evaluated for OBI patients as well as chronic HBV infection patients from the same families.

METHODS

We selected 17 HBV DNA-positive/HBsAg-negative patients (OBI group) and 15 HBV DNA- and HBsAg-positive patients from OBI families (control group). The S gene was amplified and cloned, and at least 15 clones per patient were sequenced and analyzed.

RESULTS

Although the incidence of stop codon mutations within the S region was higher in the OBI group (13.6 %) than in the control group (1.5 %, P < 0.001), this type of mutation, together with insertion and deletion mutations, was prevalent in only three OBI patients. In the major hydrophilic region (MHR), a median of 0.75 residues were altered in every 100 residues for the OBI patients, whereas 0.95 out of 100 residues were changed in the control group (P = 0.428). Furthermore, some variants that are generally considered immune escape variants, such as mutations at positions s145, s147, and s123, were only observed in less than 5 % of all the clones sequenced, in either OBI or control group.

CONCLUSIONS

Our data suggest that HBsAg variants may not play a major role in OBI pathogenesis.

摘要

背景

在隐匿性乙型肝炎病毒感染(OBI)中,乙型肝炎病毒(HBV)DNA的持续存在与乙型肝炎表面抗原(HBsAg)的缺乏有关。为了评估HBsAg免疫逃逸变异体在OBI患者中的可能作用,我们对OBI患者以及来自同一家族的慢性HBV感染患者的HBV S基因变异性进行了评估。

方法

我们选择了17例HBV DNA阳性/HBsAg阴性患者(OBI组)和15例来自OBI家族的HBV DNA和HBsAg阳性患者(对照组)。扩增并克隆S基因,对每位患者至少15个克隆进行测序和分析。

结果

虽然OBI组S区域内终止密码子突变的发生率(13.6%)高于对照组(1.5%,P<0.001),但这种类型的突变以及插入和缺失突变仅在3例OBI患者中普遍存在。在主要亲水区(MHR),OBI患者每100个残基中平均有0.75个残基发生改变,而对照组每100个残基中有0.95个残基发生改变(P=0.428)。此外,一些通常被认为是免疫逃逸变异体的变体,如s145、s147和s123位点的突变,在OBI组或对照组所有测序克隆中仅在不到5%的克隆中观察到。

结论

我们的数据表明,HBsAg变异体可能在OBI发病机制中不起主要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e672/4717550/9976f42107b1/12985_2016_464_Fig1_HTML.jpg

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