Division of Hepatology, Department of Medicine II, Leipzig University Medical Center, Leipzig, Germany.
Ludwig Maximilians-University, Max von Pettenkofer-Institute for Hygiene and Clinical Microbiology, Munich, Germany.
J Hepatol. 2021 Feb;74(2):283-292. doi: 10.1016/j.jhep.2020.08.039. Epub 2020 Sep 12.
BACKGROUND & AIMS: During treatment of chronic HBV infections, loss or seroconversion of the HBV surface antigen (HBsAg) is considered a functional cure. HBsAg consists of the large (LHBs), middle (MHBs), and small surface protein (SHBs) and their relative proportions correlate strongly with disease stage. Our aim was to assess the association between HBsAg composition and functional cure during treatment.
A total of 83 patients were retrospectively analyzed. HBsAg loss was achieved by 17/64 patients during nucleos(t)ide analogue (NA) treatment and 3/19 patients following treatment with pegylated interferon-alfa2a (PEG-IFN) for 48 weeks. Sixty-three patients without HBsAg loss were matched as controls. LHBs, MHBs and SHBs were quantified in sera collected before and during treatment.
Before treatment, median MHBs levels were significantly lower in patients with subsequent HBsAg loss than in those without (p = 0.005). During treatment, MHBs and LHBs proportions showed a fast decline in patients with HBsAg loss, but not in patients with HBV e antigen seroconversion only or patients without serologic response. MHBs became undetectable by month 6 of NA treatment in all patients with HBsAg loss, which occurred on average 12.8 ± 8.7 (0-52) months before loss of total HBsAg. Receiver-operating characteristic analyses revealed that the proportion of MHBs was the best early predictor of HBsAg loss before NA treatment (AUC = 0.726, p = 0.019). In patients achieving HBsAg loss with PEG-IFN, the proportions of MHBs and LHBs showed similar kinetics.
Quantification of HBsAg proteins shows promise as a novel tool to predict early treatment response. These assessments may help optimize individual antiviral treatment, increasing the rates of functional cure in chronically HBV-infected patients.
The hepatitis B surface antigen (HBsAg) is a key serum marker for viral replication. Loss of HBsAg is considered stable remission, which can be achieved with antiviral treatments. We have investigated whether the ratios of the different components of HBsAg, namely the large (LHBs) and medium (MHBs) HBsAg during different treatments are associated with the occurrence of HBsAg loss. We found that LHBs and MHBs decrease earlier than total HBsAg before HBsAg loss and we propose LHBs and MHBs as promising novel biomarker candidates for predicting cure of HBV infection.
在慢性乙型肝炎病毒(HBV)感染的治疗过程中,HBV 表面抗原(HBsAg)的丢失或血清转换被认为是一种功能性治愈。HBsAg 由大(LHBs)、中(MHBs)和小表面蛋白(SHBs)组成,其相对比例与疾病阶段密切相关。我们的目的是评估 HBsAg 组成与治疗过程中功能性治愈之间的关系。
对 83 例患者进行回顾性分析。核苷(酸)类似物(NA)治疗后,17/64 例患者发生 HBsAg 丢失,聚乙二醇干扰素-α2a(PEG-IFN)治疗 48 周后,3/19 例患者发生 HBsAg 丢失。未发生 HBsAg 丢失的 63 例患者作为对照。在治疗前和治疗期间收集血清,定量检测 LHBs、MHBs 和 SHBs。
治疗前,与未发生 HBsAg 丢失的患者相比,随后发生 HBsAg 丢失的患者 MHBs 水平显著降低(p=0.005)。治疗期间,HBsAg 丢失患者的 MHBs 和 LHBs 比例迅速下降,但仅发生 HBV e 抗原血清转换或无血清学应答的患者则没有这种情况。所有 HBsAg 丢失的患者在 NA 治疗的第 6 个月时 MHBs 均无法检测到,这平均发生在总 HBsAg 丢失前 12.8±8.7(0-52)个月。受试者工作特征曲线分析显示,MHBs 比例是预测 NA 治疗前 HBsAg 丢失的最佳早期预测指标(AUC=0.726,p=0.019)。在接受 PEG-IFN 治疗实现 HBsAg 丢失的患者中,MHBs 和 LHBs 的比例显示出相似的动力学变化。
HBsAg 蛋白的定量分析有望成为一种预测早期治疗反应的新工具。这些评估可能有助于优化个体抗病毒治疗,提高慢性 HBV 感染患者的功能性治愈率。
注:以上译文仅为示例,可能存在不够准确的地方,具体内容请以英文原文为准。