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Can Interferon Therapy Change the Natural Course of Hepatitis Delta Infection?: a Clinical and Pathological Study.干扰素治疗能否改变乙型肝炎 delta 感染的自然病程?:一项临床和病理学研究。
Antimicrob Agents Chemother. 2022 Jan 18;66(1):e0158621. doi: 10.1128/AAC.01586-21. Epub 2021 Oct 25.
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Efficacy of interferon treatment for patients with chronic hepatitis C: comparison of response in cirrhotics, fibrotics, or nonfibrotics.干扰素治疗慢性丙型肝炎患者的疗效:肝硬化患者、纤维化患者或非纤维化患者的反应比较。
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本文引用的文献

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Durable virological response and functional cure of chronic hepatitis D after long-term peginterferon therapy.长期聚乙二醇干扰素治疗后慢性丁型肝炎的持久病毒学应答和功能性治愈。
Aliment Pharmacol Ther. 2021 Jul;54(2):176-182. doi: 10.1111/apt.16408. Epub 2021 May 28.
2
The global prevalence of hepatitis D virus infection: Systematic review and meta-analysis.全球丁型肝炎病毒感染的流行情况:系统评价和荟萃分析。
J Hepatol. 2020 Sep;73(3):523-532. doi: 10.1016/j.jhep.2020.04.008. Epub 2020 Apr 23.
3
Hepatitis B surface antigen seroclearance: Immune mechanisms, clinical impact, importance for drug development.乙肝表面抗原血清学清除:免疫机制、临床影响、对药物开发的重要性。
J Hepatol. 2020 Aug;73(2):409-422. doi: 10.1016/j.jhep.2020.04.013. Epub 2020 Apr 22.
4
Long-Term Study of Hepatitis Delta Virus Infection at Secondary Care Centers: The Impact of Viremia on Liver-Related Outcomes.长期在二级护理中心进行的乙型肝炎病毒感染研究:病毒血症对肝脏相关转归的影响。
Hepatology. 2020 Oct;72(4):1177-1190. doi: 10.1002/hep.31214. Epub 2020 Sep 24.
5
New epidemiology of hepatitis delta.丁型肝炎的新流行病学
Liver Int. 2020 Feb;40 Suppl 1:48-53. doi: 10.1111/liv.14357.
6
Interferon Treatment Duration in Patients With Chronic Delta Hepatitis and its Effect on the Natural Course of the Disease.慢性 Delta 肝炎患者的干扰素治疗持续时间及其对疾病自然病程的影响。
J Infect Dis. 2018 Mar 28;217(8):1184-1192. doi: 10.1093/infdis/jix656.
7
Late HDV RNA relapse after peginterferon alpha-based therapy of chronic hepatitis delta.聚乙二醇干扰素α治疗慢性丁型肝炎后晚期 HDV RNA 复发。
Hepatology. 2014 Jul;60(1):87-97. doi: 10.1002/hep.27102.
8
Prevalence and clinical course of hepatitis delta infection in Greece: a 13-year prospective study.希腊的庚型肝炎病毒感染的流行情况和临床病程:一项 13 年的前瞻性研究。
J Hepatol. 2013 Nov;59(5):949-56. doi: 10.1016/j.jhep.2013.07.005. Epub 2013 Jul 10.
9
Efficacy of pegylated interferon-α treatment for 24 months in chronic delta hepatitis and predictors of response.聚乙二醇化干扰素-α治疗慢性丁型肝炎24个月的疗效及反应预测因素
Antivir Ther. 2013;18(4):561-6. doi: 10.3851/IMP2381. Epub 2012 Sep 14.
10
Treatment of chronic delta hepatitis.慢性 delta 肝炎的治疗。
Semin Liver Dis. 2012 Aug;32(3):237-44. doi: 10.1055/s-0032-1323629. Epub 2012 Aug 29.

干扰素治疗能否改变乙型肝炎 delta 感染的自然病程?:一项临床和病理学研究。

Can Interferon Therapy Change the Natural Course of Hepatitis Delta Infection?: a Clinical and Pathological Study.

机构信息

Istanbul Universitygrid.9601.e-Cerrahpasa, Cerrahpasa Medical School, Department of Internal Medicine, Section of Gastroenterology, Istanbul, Turkey.

Diyarbakir State Hospital, Diyarbakir, Turkey.

出版信息

Antimicrob Agents Chemother. 2022 Jan 18;66(1):e0158621. doi: 10.1128/AAC.01586-21. Epub 2021 Oct 25.

DOI:10.1128/AAC.01586-21
PMID:34694876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8765312/
Abstract

Chronic delta hepatitis (CDH) has a worse outcome than other types of viral hepatitis. High-dose, long-term alpha interferon (IFN-α) is the approved treatment and may ameliorate the course of infection. We evaluated long-term histological outcomes of CDH patients treated with IFN-α. Patients with histologically proved noncirrhotic CDH who were treated with high-dose IFN-α for at least 1 year were classified as cirrhotic or noncirrhotic at the end of treatment. Noncirrhotic patients also had posttreatment liver biopsies. Patients were designated histologically responsive or nonresponsive on the basis of fibrosis status. Histological, virological, and biochemical courses were analyzed. Forty-eight patients were treated with IFN-α (conventional and/or pegylated) for a median of 24 months with a posttreatment follow-up of 5 years. During the follow-up, cirrhosis developed in 24 patients, 5 of whom were decompensated. There was no difference between pre- and posttreatment fibrosis scores for 24 noncirrhotic patients at the end of follow-up. Among patients, 13% ( = 6) had decreased, 21% ( = 10) had steady, and 16% ( = 8) had increased fibrosis scores. Persistent viral response (PVR) was achieved in 16 patients (33%). Twenty percent of the entire group was histologically responsive (decreasing or steady fibrosis scores with improved necroinflammatory scores), while nearly 80% had histological progression/cirrhosis. PVR was significantly associated with histological response. The long-term natural course of patients who were treated with high dose IFN-α for at least 1 year was evaluated clinically and histologically. Despite the association of PVR with histological response, IFN-α treatment did not change the natural course of CDH; clinical and histological progression continued in two-thirds of the cases despite treatment.

摘要

慢性 delta 肝炎 (CDH) 的预后比其他类型的病毒性肝炎更差。高剂量、长期的α干扰素 (IFN-α) 是批准的治疗方法,可能改善感染过程。我们评估了接受 IFN-α治疗的 CDH 患者的长期组织学结果。经组织学证实为非肝硬化 CDH 的患者,接受高剂量 IFN-α治疗至少 1 年,在治疗结束时分为肝硬化或非肝硬化。非肝硬化患者还进行了治疗后肝活检。根据纤维化状态将患者指定为组织学反应或无反应。分析了组织学、病毒学和生化过程。48 例患者接受 IFN-α(常规和/或聚乙二醇化)治疗,中位数为 24 个月,治疗后随访 5 年。在随访期间,24 例患者发展为肝硬化,其中 5 例失代偿。在随访结束时,24 例非肝硬化患者的治疗前后纤维化评分无差异。在患者中,13%(=6)的纤维化评分降低,21%(=10)的纤维化评分稳定,16%(=8)的纤维化评分增加。16 例患者(33%)获得持续病毒应答(PVR)。整个组中有 20%的患者具有组织学反应(纤维化评分降低或稳定,坏死性炎症评分改善),而近 80%的患者具有组织学进展/肝硬化。PVR 与组织学反应显著相关。用高剂量 IFN-α治疗至少 1 年的患者的长期自然病程进行了临床和组织学评估。尽管 PVR 与组织学反应相关,但 IFN-α治疗并未改变 CDH 的自然病程;尽管治疗,但三分之二的病例仍出现临床和组织学进展。