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一名丙型肝炎病毒感染患者在接受索磷布韦和维帕他韦治疗期间乙肝核心抗体呈阳性,其体内由乙肝病毒表面抗原免疫逃逸突变株维持的乙肝病毒再激活:病例报告

Hepatitis B virus reactivation sustained by a hepatitis B virus surface antigen immune-escape mutant isolate in a patient who was hepatitis B core antibody positive during treatment with sofosbuvir and velpatasvir for hepatitis C virus infection: a case report.

作者信息

Foroghi Biland Luca, Ferrari Ludovica, Malagnino Vincenzo, Teti Elisabetta, Cerva Carlotta, Gentile Adele, Aragri Marianna, Salpini Romina, Svicher Valentina, Andreoni Massimo, Sarmati Loredana

机构信息

Infectious Diseases Clinic, Policlinico Tor Vergata, Rome, Italy.

Department of Experimental Medicine and Surgery, University of Rome Tor Vergata, Rome, Italy.

出版信息

J Med Case Rep. 2019 Sep 22;13(1):299. doi: 10.1186/s13256-019-2232-3.

Abstract

BACKGROUND

Although several cases of hepatitis B virus reactivation have been described in patients with a history of hepatitis B virus infection while undergoing treatment for hepatitis C virus infection with direct acting antivirals, the question of whether hepatitis B virus surface antigen immune-escape mutations might play a role has not been addressed so far.

CASE PRESENTATION

We report a case of hepatitis B virus reactivation in a Caucasian patient infected with hepatitis C virus during treatment with sofosbuvir and velpatasvir. A 50-year-old man with a genotype 1a hepatitis C virus infection was considered for therapy. His serological profile was hepatitis B virus surface antigen-negative, hepatitis B virus core antibody-positive, hepatitis B virus surface antibody-negative, and anti-hepatitis D virus-positive. The detection of hepatitis B virus deoxyribonucleic acid (DNA) indicated active viral replication during the direct acting antiviral treatment that spontaneously returned to undetectable levels after treatment completion. Starting from week 12 after the end of treatment, hepatitis B virus surface antibody titers and hepatitis B virus e antibody developed. Sequencing analysis revealed the hepatitis B virus genotype D3 and the presence of two relevant immune-escape mutations (P120S and T126I) in the major hydrophilic region by analyzing the S region.

CONCLUSIONS

We speculate that the presence of the hepatitis B virus surface antigen mutations, endowed with the enhanced capability to elude the immune response, could play a role in hepatitis B virus reactivation. This observation confirms that occult hepatitis B infection should also be carefully monitored, through surveillance of the hepatitis B virus viral load before and during direct acting antiviral treatment of hepatitis C virus.

摘要

背景

尽管已有数例乙型肝炎病毒(HBV)感染病史患者在接受丙型肝炎病毒(HCV)直接抗病毒药物治疗时出现HBV再激活的病例报道,但HBV表面抗原免疫逃逸突变是否起作用的问题迄今尚未得到解决。

病例报告

我们报告1例在接受索磷布韦和维帕他韦治疗期间丙型肝炎病毒感染的白种人患者发生HBV再激活的病例。一名基因型为1a的丙型肝炎病毒感染50岁男性被考虑进行治疗。其血清学特征为HBV表面抗原阴性、HBV核心抗体阳性、HBV表面抗体阴性及抗丁型肝炎病毒阳性。HBV脱氧核糖核酸(DNA)检测表明在直接抗病毒治疗期间病毒呈活跃复制,治疗结束后自发恢复至检测不到的水平。从治疗结束后第12周开始,出现HBV表面抗体滴度及HBe抗体。通过分析S区测序分析显示为HBV D3基因型,且在主要亲水区存在两个相关的免疫逃逸突变(P120S和T126I)。

结论

我们推测,具有增强免疫逃逸能力的HBV表面抗原突变可能在HBV再激活中起作用。这一观察结果证实,在HCV直接抗病毒治疗前和治疗期间通过监测HBV病毒载量,对隐匿性HBV感染也应进行仔细监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52d0/6754855/11965f0c3aa4/13256_2019_2232_Fig1_HTML.jpg

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