Medical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA, USA.
Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA, USA.
J Viral Hepat. 2021 Apr;28(4):621-629. doi: 10.1111/jvh.13461. Epub 2021 Jan 23.
It is unknown how past and active hepatitis B virus (HBV) infection affect immunorecovery and mortality in people with HIV who initiate tenofovir-based antiretroviral therapy (ART). Using data collected between 2008 and 2015, we studied people with HIV in sub-Saharan Africa initiating immediate ART in the Temprano randomized control trial. We classified participants into HBV groups at ART initiation: hepatitis B surface antigen (HBsAg)-positive with HBV DNA ≥ 2,000 IU/ml; HBsAg-positive with HBV DNA < 2,000 IU/ml; isolated HBcAb-positive; resolved infection (HBsAb-positive/HBcAb-positive); and HBV non-immune/vaccinated (HBcAb-negative). We compared square-root CD4-cell count increases using mixed-effect, non-linear regression adjusted for age, sex, baseline CD4 cell count, and HIV RNA. We compared all-cause mortality using Bayesian parametric survival regression. Among 879 participants, 24 (2.7%) had HBsAg with high HBV DNA, 76 (8.6%) HBsAg with low HBV DNA, 325 (37.0%) isolated anti-HBcAb, 226 (25.7%) resolved HBV infection and 228 (25.9%) HBV non-immune/vaccinated. We found no significant difference in CD4 cell increases between HBV-infection groups after adjustment (p = 0.16). Participants with HBsAg and high HBV DNA had the highest incidence of all-cause mortality (1.9/100 person-years, 95% Credibile Interval [CrI] = 1.0-3.4). By comparison, incidence rates of mortality were reduced by 57% (95%CrI = -79%, -13%), 60% (95%CrI = -82%, -12%) and 66% (95%CrI = -84%, -23%) in those who had isolated anti-HBcAb-positive, resolved HBV infection and HBV non-immune/vaccinated, respectively. In conclusion, individuals with HIV and past HBV infection or isolated anti-HBcAb-positive serology, much like HBV non-immune/vaccinated, experience lower mortality than those with HBsAg and high HBV DNA. Additional HBV-related management would not be necessary for these individuals.
目前尚不清楚既往和现症乙型肝炎病毒(HBV)感染如何影响开始替诺福韦为基础的抗逆转录病毒治疗(ART)的 HIV 感染者的免疫重建和死亡率。我们利用 2008 年至 2015 年间收集的数据,在撒哈拉以南非洲 Temprano 随机对照试验中研究了开始即刻 ART 的 HIV 感染者。我们在开始 ART 时将参与者分为 HBV 组:HBsAg 阳性伴 HBV DNA≥2000IU/ml;HBsAg 阳性伴 HBV DNA<2000IU/ml;单独 HBcAb 阳性;已清除感染(HBsAb 阳性/抗-HBc 阳性);HBV 无免疫/未接种(HBcAb 阴性)。我们使用混合效应、非线性回归比较了调整年龄、性别、基线 CD4 细胞计数和 HIV RNA 后的平方根 CD4 细胞计数增加。我们使用贝叶斯参数生存回归比较了全因死亡率。在 879 名参与者中,24 名(2.7%)HBsAg 伴高 HBV DNA,76 名(8.6%)HBsAg 伴低 HBV DNA,325 名(37.0%)单独 HBcAb 阳性,226 名(25.7%)已清除 HBV 感染,228 名(25.9%)HBV 无免疫/未接种。调整后,HBV 感染组的 CD4 细胞增加无显著差异(p=0.16)。HBsAg 伴高 HBV DNA 者的全因死亡率最高(1.9/100 人年,95%可信区间 [CrI]为 1.0-3.4)。相比之下,单独 HBcAb 阳性、已清除 HBV 感染和 HBV 无免疫/未接种者的死亡率分别降低了 57%(95%CrI 为-79%,-13%)、60%(95%CrI 为-82%,-12%)和 66%(95%CrI 为-84%,-23%)。总之,与 HBsAg 伴高 HBV DNA 相比,既往 HBV 感染或单独 HBcAb 阳性血清学者,以及 HBV 无免疫/未接种者,死亡率更低。这些人不需要进行额外的 HBV 相关治疗。