UNIR Health Sciences School & Medical Center, Madrid, Spain.
Department of Internal Medicine, Puerta de Hierro Research Institute & University Hospital, Madrid, Spain.
Liver Int. 2023 Aug;43 Suppl 1:108-115. doi: 10.1111/liv.15345. Epub 2022 Jun 30.
Hepatitis delta virus (HDV) is a defective agent that only infects individuals with hepatitis B virus (HBV). Around 5-10% of chronic hepatitis B patients worldwide are superinfected with HDV, which means 15-25 million people. Hepatitis delta is the most severe of all chronic viral hepatitis, leading to cirrhosis, liver cancer and/or transplantation in most patients. Despite it, many HDV patients remain undiagnosed. The only treatment available until recently was peginterferon alfa, with poor results and significant side effects. The recent approval of bulevirtide, a lipopeptide that blocks HBV/HDV entry, has revolutionized the field. Another drug, lonafarnib, already approved to treat progeria, is expected to be available soon as HDV therapy. Since there is no cell reservoir for the HDV RNA genome, hypothetically viral clearance could be achieved if complete blocking of viral replication occurs for a minimum time frame. This is what happens in hepatitis C using direct-acting antivirals, with the achievement of cure in nearly all treated patients. We envision the cure of hepatitis delta using combination antiviral therapy. Given that sexual and parenteral transmission routes are the most frequent for the acquisition of HBV and HDV, shared with HIV infection and HBV/HDV and HIV coinfection. The clinical outcome of hepatitis delta is worst in the HIV setting, with more frequent liver complications. Since most persons infected with HIV are on regular health care follow-up, we propose that HIV-HDV patients should be prioritized for moving forward new and potentially curative treatments for hepatitis delta.
丁型肝炎病毒(HDV)是一种缺陷型病毒,只能感染乙型肝炎病毒(HBV)感染者。全球约有 5-10%的慢性乙型肝炎患者会重叠感染 HDV,这意味着有 1500-2500 万人受到影响。丁型肝炎是所有慢性病毒性肝炎中最严重的一种,大多数患者会发展为肝硬化、肝癌和/或需要进行肝移植。尽管如此,许多 HDV 患者仍未被诊断出来。直到最近,唯一可用的治疗方法是聚乙二醇干扰素 alfa,但其治疗效果不佳,且有明显的副作用。最近批准的一种脂肽药物 bulevirtide,可阻断 HBV/HDV 进入细胞,这一药物的出现彻底改变了这一领域。另一种药物 lonafarnib,已被批准用于治疗早衰症,预计很快也将作为 HDV 治疗药物上市。由于 HDV RNA 基因组没有细胞储存库,因此如果能在最短的时间内完全阻断病毒复制,理论上就可以清除病毒。这在使用直接作用抗病毒药物治疗丙型肝炎时就是如此,几乎所有接受治疗的患者都能达到治愈。我们设想通过联合抗病毒治疗来治愈丁型肝炎。鉴于性传播和注射途径是乙型肝炎和 HDV 最常见的感染途径,与 HIV 感染和乙型肝炎/丙型肝炎和 HIV 合并感染相同。在 HIV 感染背景下,丁型肝炎的临床结局最差,肝脏并发症更常见。由于大多数感染 HIV 的人都在接受常规的医疗保健随访,因此我们建议应优先考虑对 HIV-HDV 患者进行新的、有潜在治愈作用的丁型肝炎治疗。