Thermet Alexandre, Buronfosse Thierry, Werle-Lapostolle Bettina, Chevallier Michele, Pradat Pierre, Trepo Christian, Zoulim Fabien, Cova Lucyna
Université Lyon 1, IFR62, F-69008 Lyon, France.
INSERM, Unit 871, F-69424 Lyon, France.
J Gen Virol. 2008 May;89(Pt 5):1192-1201. doi: 10.1099/vir.0.83583-0.
This study used a duck hepatitis B virus (DHBV) model to evaluate whether a novel DNA vaccination protocol alone or associated with antiviral (lamivudine) treatment was able to clear the intrahepatic covalently closed, circular viral DNA (cccDNA) pool responsible for persistence of infection. DHBV carriers received DNA vaccine (on weeks 6, 10, 13, 14, 28 and 35) targeting the large envelope and/or core proteins alone or combined with lamivudine treatment (on weeks 1-8) or lamivudine monotherapy. After 10 months of follow-up, a dramatic decrease in viraemia and liver DHBV cccDNA (below 0.08 cccDNA copies per cell) was observed in 9/30 ducks (30 %) receiving DNA mono- or combination therapy, compared with 0/12 (0 %) from lamivudine monotherapy or the control groups, suggesting a significant antiviral effect of DNA immunization. However, association with the drug did not significantly improve DHBV DNA vaccine efficacy (33 % cccDNA clearance for the combination vs 27 % for DNA monotherapy), probably due to the low antiviral potency of lamivudine in the duck model. Seroconversion to anti-preS was observed in 6/9 (67 %) ducks showing cccDNA clearance, compared with 1/28 (3.6 %) without clearance, suggesting a significant correlation (P<0.001) between humoral response restoration and cccDNA elimination. Importantly, an early (weeks 10-12) drop in viraemia was observed in seroconverted animals, and virus replication did not rebound following the cessation of immunotherapy, indicating a sustained effect. This study provides the first evidence that therapeutic DNA vaccination is able to enhance hepadnaviral cccDNA clearance, which is tightly associated with a break in humoral immune tolerance. These results also highlight the importance of antiviral drug potency and an effective DNA immunization protocol for the design of therapeutic vaccines against chronic hepatitis B.
本研究采用鸭乙型肝炎病毒(DHBV)模型,以评估单独使用一种新型DNA疫苗接种方案或联合抗病毒(拉米夫定)治疗能否清除导致感染持续存在的肝内共价闭合环状病毒DNA(cccDNA)库。DHBV携带者单独接受针对大包膜和/或核心蛋白的DNA疫苗接种(在第6、10、13、14、28和35周),或与拉米夫定治疗(在第1 - 8周)联合使用,或接受拉米夫定单药治疗。经过10个月的随访,在接受DNA单药或联合治疗的9/30只鸭子(30%)中观察到病毒血症和肝脏DHBV cccDNA显著下降(低于每细胞0.08个cccDNA拷贝),相比之下,拉米夫定单药治疗组或对照组的12只鸭子中无一例(0%)出现这种情况,这表明DNA免疫具有显著的抗病毒作用。然而,与药物联合使用并未显著提高DHBV DNA疫苗的疗效(联合治疗组cccDNA清除率为33%,DNA单药治疗组为27%),这可能是由于拉米夫定在鸭模型中的抗病毒效力较低。在显示cccDNA清除的9只鸭子中有6只(67%)出现抗前S血清转化,而未清除的28只鸭子中有1只(3.6%)出现血清转化,这表明体液免疫反应恢复与cccDNA清除之间存在显著相关性(P<0.001)。重要的是,在血清转化的动物中观察到病毒血症在早期(第10 - 12周)下降,并且在免疫治疗停止后病毒复制没有反弹,这表明具有持续效应。本研究提供了首个证据,即治疗性DNA疫苗接种能够增强嗜肝DNA病毒cccDNA的清除,这与体液免疫耐受的打破密切相关。这些结果还突出了抗病毒药物效力和有效的DNA免疫接种方案对于设计慢性乙型肝炎治疗性疫苗的重要性。