Liu Mo-Han, Chen Qin-Yan, Harrison Tim J, Li Guo-Jian, Li Hai, Wang Xue-Yan, Ju Yu, Yang Jin-Ye, Fang Zhong-Liao
Department of Microbiology, School of Preclinical Medicine, Guangxi Medical University, Nanning, Guangxi, China.
Guangxi Zhuang Autonomous Region Center for Disease Prevention and Control, Nanning, Guangxi, China.
J Med Virol. 2015 Aug;87(8):1351-60. doi: 10.1002/jmv.24186. Epub 2015 Apr 16.
Despite several studies regarding the correlation between serum HBsAg titers and viral loads, the association remains uncertain. Eighty-nine individuals were selected randomly from a Chinese cohort of 2,258 subjects infected persistently with hepatitis B virus (HBV) for cross-sectional and longitudinal analysis. Viral loads of mutant HBV are lower than those of wild type HBV. The serum HBsAg titers correlate positively with viral loads in both HBeAg positive and negative subjects (r = 0.449, P = 0.013; r = 0.300, P = 0.018, respectively). No correlation between serum HBsAg titer and viral loads was found in any of the four phases of chronic HBV infection. The serum HBsAg titers correlate positively with viral loads in the group with wild type sequences of the PreS/S, basal core promoter (BCP), and preC regions of HBV(r = 0.502, P = 0.040). However, the correlation was not seen in the group with mutations in these regions (r = 0.165, P = 0.257). The correlation between HBsAg titers and viral loads was seen in individuals with wild type PreS/S sequences but not in the subgroup with BCP double mutations or PreC stop mutation, although their sequences in the preS/S regions were wild type. All these findings were confirmed by the longitudinal analysis. In conclusion, the correlation between serum HBsAg levels and viral loads may not differ between HBeAg positive and negative individuals but may depend on wild-type or mutated genomic sequences. Therefore, HBsAg quantitation may be used as a surrogate for viral loads in only wild-type HBV infections.
尽管有多项关于血清乙肝表面抗原(HBsAg)滴度与病毒载量之间相关性的研究,但这种关联仍不明确。从一个包含2258名持续感染乙型肝炎病毒(HBV)的中国队列中随机选取89名个体进行横断面和纵向分析。突变型HBV的病毒载量低于野生型HBV。在HBeAg阳性和阴性受试者中,血清HBsAg滴度均与病毒载量呈正相关(分别为r = 0.449,P = 0.013;r = 0.300,P = 0.018)。在慢性HBV感染的四个阶段中,均未发现血清HBsAg滴度与病毒载量之间存在相关性。在HBV的前S/S、核心启动子(BCP)和前C区具有野生型序列的组中,血清HBsAg滴度与病毒载量呈正相关(r = 0.502,P = 0.040)。然而,在这些区域发生突变的组中未观察到这种相关性(r = 0.165,P = 0.257)。在具有野生型前S/S序列的个体中可观察到HBsAg滴度与病毒载量之间的相关性,但在具有BCP双突变或前C区终止突变的亚组中未观察到,尽管这些亚组在前S/S区域的序列为野生型。所有这些发现均通过纵向分析得到证实。总之,血清HBsAg水平与病毒载量之间的相关性在HBeAg阳性和阴性个体之间可能并无差异,但可能取决于野生型或突变的基因组序列。因此,HBsAg定量仅可作为野生型HBV感染中病毒载量的替代指标。