scholarly journals Dane particles-associated hepatitis B core antigen in patients with HBsAg-positive chronic hepatitis

1978 ◽  
Vol 75 (5) ◽  
pp. 864-868 ◽  
Author(s):  
E. Sagnelli ◽  
S.J. Vernace ◽  
F. Paronetto
1982 ◽  
Vol 28 (2) ◽  
pp. 351-353 ◽  
Author(s):  
E Sagnelli ◽  
C Pereira ◽  
G Triolo ◽  
S Vernace ◽  
F Paronetto

Abstract Serum hepatitis B core antigen (HBcAg) is an important marker of hepatitis B virus replication. We describe an easy, sensitive radioimmunoassay for determination of HBcAg in detergent-treated serum pellets containing Dane particles. Components of a commercial kits for anti-core determination are used, and HBcAG is measured by competitive inhibition of binding of 125I-labeled antibodies to HBcAg with HBcAg-coated beads. We assayed of HBcAG in the sera of 49 patients with hepatitis B surface antigen (HBsAg)-positive chronic hepatitis, 50 patients with HBsAg-negative chronic hepatitis, and 30 healthy volunteers. HBcAg was detected in 41% of patients with HBsAg-positive chronic hepatitis but not in patients with HBsAg-negative chronic hepatitis. Hepatitis Be antigen (an antigen closely associated with the core of Dane particles) determined in the same sera by radioimmunoassay, was not detected in 50% of HBcAg-positive sera.


2021 ◽  
pp. 135965352110598
Author(s):  
Yu-Qing Fang ◽  
Xiao-Yan Xu ◽  
Feng-Qin Hou ◽  
Wei Jia

Background Few models to predict antiviral response of peginterferon were used in hepatitis B e antigen (HBeAg)-positive chronic hepatitis B patients and the prediction efficacy was unsatisfied. Quantitative antibody to hepatitis B core antigen (anti-HBc) is a new predictor of treatment response. We aimed to develop a new model to identify HBeAg-positive Chinese patients who were more likely to respond to peginterferon. Methods Data from 140 peginterferon recipients with HBeAg-positive were applied with generalized additive models and multiple logistic regression analysis to develop a baseline scoring system to predict serological response (SR: HBeAg loss and HBeAg seroconversion 24 weeks post-treatment) and combined response (CR: SR plus serum HBV DNA levels <2000 IU/mL 24 weeks post-treatment). Results Anti-HBc levels, alanine aminotransferase ratio, and HBeAg were retained in the final model. The new model scored from 0 to 3. Among patients with scores of 0, 1, or ≥2, SR was achieved in 6.45% (2/31), 13.21% (7/51), and 55.36% (31/56), respectively, and CR in 3.23% (1/31), 9.43% (5/53), and 25.00% (14/56), respectively. Our model has a higher AUROC for SR comparing to Chan’s (Z = 2.77 > 1.96, p < 0.05) and Lampertico’s (Z = 2.06 > 1.96, p < 0.05) model. The negative predictive value for SR and CR were both 100% in patients with score 0 and hepatitis B surface antigen ≥20,000 IU/mL at week 12. Conclusions Patients with higher scores at baseline were more likely to respond to peginterferon. This new model may predict the treatment response.


Kanzo ◽  
1985 ◽  
Vol 26 (6) ◽  
pp. 689-695
Author(s):  
Mitsuo SUGA ◽  
Yoshikazu AKAHONAI ◽  
Haruyasu YOSHIZAKI ◽  
Tetsuo OHSHIMA ◽  
Akira YACHI

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