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标题: 乙型肝炎感染:确定最有可能对Peginterferon Alfa作出反应的患 [打印本页]

作者: StephenW    时间: 2020-12-19 21:50     标题: 乙型肝炎感染:确定最有可能对Peginterferon Alfa作出反应的患

Hepatitis B Infection: Progress in Identifying Patients Most Likely to Respond to Peginterferon Alfa.
Ming-Lun Yeh , Jee-Fu Huang , Ming-Lung Yu & Wan-Long Chuang
Received 08 Nov 2020, Accepted 17 Dec 2020, Accepted author version posted online: 18 Dec 2020

    Download citation https://doi.org/10.1080/17474124.2021.1866985 CrossMark Logo CrossMark

Accepted author version
Abstract

Introduction: Despite the potential disadvantage of side effects, pegylated interferon alpha (Peg-IFN α) remains an indispensable agent for the treatment of chronic hepatitis B (CHB) due to its immunomodulatory effect. The selection of a patient most likely to have a favorable response becomes an essential issue for Peg-IFN α therapy.

Areas covered: Recent progress in the prediction of the treatment response to Peg-IFN α.

Expert opinion: Before initiating Peg-IFN α therapy, baseline host and viral factors, including female sex, younger age, a high alanine aminotransferase level, HBV genotype A or B, and low viral load, predict a favorable response. In addition, on-treatment viral kinetics of hepatitis B surface antigen (HBsAg), e antigen (HBeAg) and HBV DNA help clinicians determine whether to continue or discontinue Peg-IFN α therapy. The novel HBV markers hepatitis B core-related antigen and HBV RNA have also recently been investigated as useful predictors. The limited efficacy of Peg-IFN α monotherapy facilitated the development of new strategies of “add-on” or “switch to” Peg-IFN α in patients receiving long-term nucleot(s)ide analog treatment, which may lead to an increase in HBeAg and HBsAg loss. In summary, tailored Peg-IFN α therapeutic strategies based on predictors extended the landscape for CHB treatment.

Keywords: Chronic hepatitis BHepatitis B virusPegylated interferonPredictorResponse
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Acknowledgements

This study was supported partially by Kaohsiung Medical University Research Center Grant (Center for Cancer Research KMU Global Networking Talent Plan Grant 105KMUOR08) and Kaohsiung Medical University Hospital (grant number KMUH108-8R08). The authors thank secretary help from Taiwan Liver Research Foundation (TLRF), Kaohsiung, Taiwan. They did not influence how the study was conducted or the approval of the manuscript. All the authors have read and approved the submitted manuscript.
Article highlights

    Peg-IFN α remains an indispensable anti-HBV agent, as it is the only agent that achieves a functional HBV cure.

    Host and viral predictors (baseline and on-treatment) of Peg-IFN α effectiveness as a treatment for HBV exist. The combination of these predictors further identifies patients with the most favorable response.

    Novel HBV markers, HBcrAg and HBV RNA, have recently been identified as promising predictors of Peg-IFN α therapy.

    Strategies of an “add-on” or “switch to” Peg-IFN α in patients already receiving steady NUC treatment obviously increase the treatment response. A careful consideration of the advantages and disadvantages before the application of these strategies is recommended.

    Physicians should consider all aspects of patients using the described predictors to obtain the optimal treatment strategy and response and to identify patients most likely to respond to Peg-IFN α.

Declaration of Interests

Jee-Fu Huang consults for Roche, Sysmex, Gilead Sciences, PharmaEssentia, and has received honoraria from Bristol-Myers Squibb, Abbvie, Sysmex, Gilead Sciences, PharmaEssentia, Merck. Ming-Lung Yu has received research support (grant) from Abbott, BMS, Gilead and Merck; served as a consultant of Abbvie, Abbott, Ascletis, BMS, Gilead, Merck and Roche and served as a speaker of Abbvie, Abbott, BMS, Gilead, Merck, and IPSEN. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed

作者: StephenW    时间: 2020-12-19 21:51

乙型肝炎感染:确定最有可能对Peginterferon Alfa作出反应的患者的进展。
叶明伦,黄洁夫,于明龙和庄万龙
于2020年11月8日接收,于2020年12月17日接受,在线接受作者版本:2020年12月18日

    下载引文https://doi.org/10.1080/17474124.2021.1866985 CrossMark徽标CrossMark

接受的作者版本
抽象

简介:尽管有潜在的副作用副作用,但聚乙二醇化干扰素α(Peg-IFNα)的免疫调节作用仍然是治疗慢性乙型肝炎(CHB)不可或缺的药物。选择最有可能产生良好反应的患者成为Peg-IFNα治疗的重要问题。

涵盖领域:预测对Peg-IFNα的治疗反应的最新进展。

专家意见:在开始使用Peg-IFNα治疗之前,基线宿主和病毒因素,包括女性,年轻,丙氨酸转氨酶水平高,HBV基因型A或B和病毒载量低,预示良好的反应。此外,乙型肝炎表面抗原(HBsAg),e抗原(HBeAg)和HBV DNA的治疗中病毒动力学有助于临床医生确定是否继续或终止Peg-IFNα治疗。最近还研究了新颖的HBV标记乙肝核心相关抗原和HBV RNA作为有用的预测因子。在接受长期核苷酸类似物治疗的患者中,Peg-IFNα单一疗法的疗效有限,促进了“附加”或“转换为” Peg-IFNα的新策略的开发,这可能导致治疗增加HBeAg和HBsAg丢失。总之,基于预测因子的量身定制的Peg-IFNα治疗策略扩大了CHB治疗的前景。

关键词:慢性乙型肝炎乙型肝炎病毒聚乙二醇干扰素预测因子反应
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致谢

这项研究得到了高雄医科大学研究中心拨款(癌症研究中心KMU全球网络人才计划拨款105KMUOR08)和高雄医科大学医院(拨款号KMUH108-8R08)的部分支持。作者感谢台湾高雄市台湾肝脏研究基金会(TLRF)的秘书帮助。它们不影响研究的进行方式或手稿的批准。所有作者均已阅读并批准了提交的手稿。
文章重点

    PEG-IFNα仍然是必不可少的抗HBV药物,因为它是实现功能性HBV治愈的唯一药物。

    存在Peg-IFNα作为治疗乙肝病毒的有效性的宿主和病毒预测因子(基线和治疗中)。这些预测因子的组合进一步确定了反应最有利的患者。

    新型HBV标记HBcrAg和HBV RNA最近被确定为Peg-IFNα治疗的有前途的预测因素。

    在已经接受稳定NUC治疗的患者中,“附加”或“切换至” Peg-IFNα的策略明显增加了治疗反应。建议在应用这些策略之前仔细考虑其优缺点。

    医生应使用所描述的预测因素考虑患者的各个方面,以获得最佳治疗策略和反应,并确定最可能对Peg-IFNα反应的患者。

利益声明

黄洁夫为罗氏,Sysmex,吉利德科学公司,PharmaEssentia担任顾问,并获得了百时美施贵宝,Abbvie,Sysmex,吉利德科学公司,PharmaEssentia,默克公司的酬金。于明龙获得了雅培,BMS,吉利德和默克公司的研究支持(拨款);曾担任Abbvie,Abbott,Ascletis,BMS,Gilead,Merck和Roche的顾问,还曾担任Abbvie,Abbott,BMS,Gilead,Merck和IPSEN的发言人。除了与本文讨论的主题或材料有经济利益或与之有财务冲突的任何组织或实体,作者没有任何其他关联或财务往来关系
作者: newchinabok    时间: 2020-12-20 11:57

PEG-IFNα仍然是必不可少的抗HBV药物,因为它是实现功能性HBV治愈的唯一药物。


这句话说到现实处了




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