Discipline of Virology, School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban 4000, South Africa.
National Health Laboratory Service, Inkosi Albert Luthuli Central Hospital, Durban 4091, South Africa.
Viruses. 2022 Apr 10;14(4):788. doi: 10.3390/v14040788.
To understand the problem of persistent Hepatitis B virus (HBV) viraemia in HIV/HBV co-infected patients on HBV-active antiretroviral therapy (ART), we assessed the rate of HBV virological response in patients on HBV-active ART in KwaZulu-Natal, South Africa, and analysed factors associated with persistent HBV viraemia. One hundred and fifty eligible participants with a chronic HBV diagnosis, with or without HIV coinfection, were enrolled and followed up after 6 months. The HBV pol gene was sequenced by next-generation sequencing and mutations were determined using the Stanford HBVseq database. Logistic regression analysis was used to assess factors associated with HBV viraemia at 6-month follow-up. The mean duration of HBV-active ART was 24 months. Thirty-seven of one hundred and six (35%) participants receiving HBV-active ART for longer than 6 months had virological failure. Advanced immunosuppression with CD4+ cell counts <200 cells/μL was independently associated with persistent HBV viraemia, aOR 5.276 (95% CI 1.575−17.670) p = 0.007. A high proportion of patients on HBV-active ART are unsuppressed, which will ultimately have an impact on global elimination goals. Better monitoring should be implemented, especially in HIV-coinfected patients with low CD4+ cell counts and followed by early HBV drug-resistance testing.
为了了解在接受乙型肝炎病毒(HBV)活性抗逆转录病毒治疗(ART)的 HIV/HBV 合并感染患者中持续存在 HBV 病毒血症的问题,我们评估了南非夸祖鲁-纳塔尔省接受 HBV 活性 ART 的患者的 HBV 病毒学应答率,并分析了与持续 HBV 病毒血症相关的因素。我们招募了 150 名符合条件的慢性 HBV 诊断患者,无论是否合并 HIV 感染,在 6 个月后进行随访。通过下一代测序对 HBV pol 基因进行测序,并使用斯坦福 HBVseq 数据库确定突变。使用逻辑回归分析评估与 6 个月随访时 HBV 血症相关的因素。HBV 活性 ART 的平均持续时间为 24 个月。106 名接受 HBV 活性 ART 治疗超过 6 个月的患者中,有 37 名(35%)发生病毒学失败。CD4+细胞计数<200 个/μL 的严重免疫抑制与持续 HBV 病毒血症独立相关,比值比(aOR)为 5.276(95%置信区间 [CI] 1.575-17.670),p = 0.007。相当一部分接受 HBV 活性 ART 的患者未得到抑制,这最终将对全球消除目标产生影响。应实施更好的监测,特别是在 CD4+细胞计数低的 HIV 合并感染患者中,并在早期进行 HBV 耐药性检测。