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首页> 外文期刊>Journal of Clinical Microbiology >Hepatitis B Virus Core-Related Antigens as Markers for Monitoring Chronic Hepatitis B Infection
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Hepatitis B Virus Core-Related Antigens as Markers for Monitoring Chronic Hepatitis B Infection

机译:乙型肝炎病毒核心相关抗原可作为监测慢性乙型肝炎感染的标志物

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A sensitive chemiluminescence enzyme immunoassay has been developed for hepatitis B virus (HBV) core-related antigen (HBcrAg) detection. We aimed to investigate the usefulness of HBcrAg measurement for monitoring chronic hepatitis B disease. HBcrAg levels were measured by a chemiluminescence enzyme immunoassay in 54 untreated patients and 39 patients treated with either entecavir or lamivudine. The HBcrAg concentration correlated positively with the levels of serum HBV DNA (r = 0.820), intrahepatic total HBV DNA (r = 0.700), and covalently closed circular DNA (cccDNA) (r = 0.664; for all, P values were <0.001). A higher HBcrAg concentration was associated with a greater proportion of hepatitis B core antigen immunostaining. Although the differences were not statistically significant, patients with higher Knodell necroinflammation and fibrosis scores tended to have higher serum HBcrAg concentration levels. In the treated patients, the logarithmic reduction in HBcrAg at week 48 correlated positively with the logarithmic reduction of serum HBV DNA, intrahepatic total HBV DNA, and cccDNA. Of the 31 patients with undetectable serum HBV DNA (<300 copies/ml) at the end of treatment, 20 (65%) still had detectable HBcrAg. A greater reduction in posttreatment HBcrAg concentration was associated with histological improvement and a decrease in hepatitis B core antigen immunostaining. HBcrAg concentrations of <40,000 kU/ml at baseline and <200 kU/ml at week 24 were associated with a higher chance of having undetectable HBV DNA at week 48. In conclusion, serum HBcrAg levels correlated with HBV virological markers and reflected the chronic hepatitis B disease activity in the liver.
机译:已经开发出一种灵敏的化学发光酶免疫测定法,用于检测乙型肝炎病毒(HBV)核心相关抗原(HBcrAg)。我们旨在调查HBcrAg测量对监测慢性乙型肝炎的有用性。通过化学发光酶免疫法对54例未经治疗的患者和39例接受恩替卡韦或拉米夫定治疗的患者的HBcrAg水平进行了测定。 HBcrAg浓度与血清HBV DNA( r = 0.820),肝内总HBV DNA( r = 0.700)和共价闭合环状DNA(cccDNA)呈正相关。 ( r = 0.664;对于所有 P 值,其<0.001)。较高的HBcrAg浓度与更大比例的乙型肝炎核心抗原免疫染色有关。尽管差异无统计学意义,但Knodell坏死性炎症和纤维化评分较高的患者倾向于具有较高的血清HBcrAg浓度水平。在接受治疗的患者中,第48周时HBcrAg的对数减少与血清HBV DNA,肝内总HBV DNA和cccDNA的对数减少呈正相关。在治疗结束时有31例血清HBV DNA检测不到(<300拷贝/ ml)的患者中,有20例(65%)仍具有可检测的HBcrAg。治疗后HBcrAg浓度的更大降低与组织学改善和乙型肝炎核心抗原免疫染色降低有关。基线时HBcrAg浓度<40,000 kU / ml,第24周<200 kU / ml与HBV DNA在48周时检出的可能性更高。总之,血清HBcrAg水平与HBV病毒学标志物相关,反映了慢性肝炎乙肝疾病活动。

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