Hu Jie-Li, Huang Ai-Long
Key Laboratory of Molecular Biology on Infectious Diseases, Ministry of Education, Chongqing Medical University, Chongqing 400016, China.
Microorganisms. 2023 Feb 27;11(3):600. doi: 10.3390/microorganisms11030600.
Eradication of cccDNA is an ideal goal of chronic hepatitis B (CHB) therapy. Understanding the changes in the cccDNA pool during therapy provides a basis for developing CHB treatment strategies. On the other hand, the shift in the balance of the cccDNA pool following therapies allowed researchers to investigate the dynamics of cccDNA. Central to the description of cccDNA dynamics is a parameter called cccDNA half-life. CccDNA half-life is not an intrinsic property of cccDNA molecules, but a description of an observed phenomenon characterized by cccDNA pool decline. Since cccDNA has to be in the nuclei of host cells to function, the half-life of cccDNA is determined by the state and destiny of the host cells. The major factors that drive cccDNA decay include noncytopathic effects and hepatocyte turnover (death and division). In some cases, the determining factor is not the half-life of cccDNA itself, but rather the half-life of the hepatocyte. The main purpose of this review is to analyze the major factors affecting cccDNA half-life and determine the areas requiring further study. In addition, the discrepancy in cccDNA half-life between short-term and long-term nucleot(s)ide analog (NUC) therapy was reported. Hypotheses were proposed to explain the multi-phasic decline of cccDNA during NUC therapy, and a framework based on cccDNA dynamics was suggested for the consideration of various anti-HBV strategies.
清除共价闭合环状DNA(cccDNA)是慢性乙型肝炎(CHB)治疗的理想目标。了解治疗期间cccDNA库的变化为制定CHB治疗策略提供了依据。另一方面,治疗后cccDNA库平衡的变化使研究人员能够研究cccDNA的动态变化。描述cccDNA动态变化的核心参数是cccDNA半衰期。cccDNA半衰期不是cccDNA分子的固有属性,而是对以cccDNA库下降为特征的观察到的现象的描述。由于cccDNA必须存在于宿主细胞核中才能发挥作用,因此cccDNA的半衰期由宿主细胞的状态和命运决定。驱动cccDNA衰变的主要因素包括非细胞病变效应和肝细胞更新(死亡和分裂)。在某些情况下,决定因素不是cccDNA本身的半衰期,而是肝细胞的半衰期。本综述的主要目的是分析影响cccDNA半衰期的主要因素,并确定需要进一步研究的领域。此外,还报道了短期和长期核苷(酸)类似物(NUC)治疗之间cccDNA半衰期的差异。提出了假设来解释NUC治疗期间cccDNA的多相下降,并提出了一个基于cccDNA动态变化的框架,以供考虑各种抗HBV策略。