摘要
目的探讨乙型肝炎病毒基因型和DNA载量与外膜大蛋白关系。方法采用荧光定量PCR方法、ELISA法和时间分辨免疫荧光分析法分别检测140例慢性乙型肝炎患者血清中HBV DNA、LHBs（Hepatitis B Virus Large Envelope Protein，LHBs）和HBV血清标志物，对HBV DNA阳性标本进行基因测序鉴定基因型，并进行相关性分析。结果HBV LHBs与HBV DNA阳性率在HBeAg阴性和阳性组中差异均无统计学意义（P〉0．05）；HBV LHBs吸光度A值与HBV DNA载量存在良好的相关性，相关系数为0．9267；乙型肝炎病毒B、C基因型间HBV-LHBs吸光度A值差异无统计学意义（P〉0．05）。结论血清LHBs水平与HBV DNA载量存在良好的相关性，能反映HBV感染者体内HBV复制程度，可作为判断HBV复制新的血清学指标；HBV LHBs的含量与HBV基因型无关。
Objective To explore the relation between hepatitis B virus DNA load and genotype with the level of large envelope protein. Methods Serum HBV DNA was quantitively detected by using real time polymerase chain reaction （RT-PCR）. The LHBs were detected by using enzyme linked immuno sorbent assay （ELISA） and HBV markers were detected by time differentiate immunofluorescence assay in 140 serum samples collected from chronic hepatitis B patients. The genotypes of HBV were identified by DNA sequencing; and analyze their relationship. Results There was no significant difference between positive rate of LHBs and that of HBV DNA in HBeAg negative and positive group（ P 〉 0.05）; The HBV LHBs absorbency was markedly correlated with the HBV DNA load（ R^2 = 0.9267）. The difference of HBV LHBs absorbency between HBV genotype B and C was not significant. Conclusions The close correlation between HBV LHBs absorbenee and HBV DNA load illustrated that he level of serum LHBs can be used to estimate the state of HBV replication; and there is no relationship between HBV LHBs absorbency and genotypes. So HBV LHBs may be used as a new serological marker to detect HBV replication.
出处
《中华实验和临床病毒学杂志》
CAS
CSCD
北大核心
2008年第5期348-350,共3页
Chinese Journal of Experimental and Clinical Virology
