Study on combined treatment of PEG IFN α-2a and recombinant hepatitis B vaccine in CHB patients with HBeAg positive
10.3760/cma.j.issn.1003-9279.2014.03.019
- VernacularTitle:聚乙二醇干扰素α-2a联合基因重组酵母乙肝疫苗治疗HBeAg阳性CHB的疗效观察
- Author:
Junping WANG
1
;
Ka ZHANG
;
Xiaoan YANG
;
Haixia SUN
;
Qihuan XU
Author Information
1. 527200,广东省罗定市人民医院感染科
- Keywords:
Hepatitis B;
Interferons;
Hepatitis B vaccines
- From:
Chinese Journal of Experimental and Clinical Virology
2014;28(3):216-218
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the efficacy of combined treatment of PEG IFNα-2a and recombinant hepatitis B vaccine in CHB patients with HBeAg positive.Methods 75 CHB patients with HBeAg positive were enrolled into this study.45 patients received the monotherapy of pegylated IFNα-2a (group A),and 30 patients were treated with PEG IFNα-2a combined with recombinant hepatitis B vaccine (group B).The two groups were compared clinical features,such as ALT,HBsAg levels and HBeAg seroconversion rates,HBV DNA suppression,at different time point(At 0,24,48,72 week).Results At week 0,levels of aminotransferases,HBsAg and HBV DNA were not statistically significant between the two groups(P >0.05).But the level of HBeAg in group B was much more than that in group A.This diversity show statistical significance(P < 0.05).During week 24 to week 48,rates of aminotransferases normalization HBsAg seroconversion HBeAg seroconversion,and HBV DNA suppression were also not statistically significant between group A and B (P > 0.05).At the 72 week of follow up,levels of aminotransferases,HBeAg seroconversion rate and HBsAg levels were not statistically significant among the two groups (P >0.05),but the negative conversion rate of HBV DNA drop in group B was much more than that in group A,the difference was statistically significant (P =0.032).Conclusion The combined treatment of PEG IFNα-2a and recombinant hepatitis B vaccine in CHB patients with HBeAg positive can improve the negative conversion rate of HBV DNA 72 weeks after the end of the 48 week of treatment,but wasn't associated with HBeAg seroconversion and HBsAg levels.