Abstract | BACKGROUND: METHODS AND PRINCIPAL FINDINGS: Two hundred forty two HBeAg-positive chronic hepatitis B patients were immunized with six injections of either 30 microg YIC, 60 microg of YIC or alum adjuvant as placebo at four-week intervals under code. HBV markers and HBV DNA were monitored during immunization and 24 weeks after the completion of immunization. The primary endpoint was defined as loss of HBeAg, or presence of anti-HBe antibody or suppression of HBV DNA, while the secondary endpoint was both HBeAg seroconversion and suppression of HBV DNA. Statistical significance was not reached in primary endpoints four weeks after the end of treatment among three groups, however, at the end of follow-up, HBeAg sero-conversion rate was 21.8% (17/78) and 9% (7/78) in the 60 microg YIC and placebo groups respectively (p = 0.03), with 95% confidence intervals at 1.5% to 24.1%. Using generalized estimating equations (GEEs) model, a significant difference of group effects was found between 60 microg YIC and the placebo groups in terms of the primary endpoint. Eleven serious adverse events occurred, which were 5.1%, 3.6%, and 5.0% in the placebo, 30 microg YIC and 60 microg YIC groups respectively (p>0.05). CONCLUSIONS: Though statistical differences in the preset primary and secondary endpoints among the three groups were not reached, a late and promising HBeAg seroconversion effect was shown in the 60 microg YIC immunized regimen. By increasing the number of patients and injections, the therapeutic efficacy of YIC in chronic hepatitis B patients will be further evaluated. TRIAL REGISTRATION: ChiCTR.org ChiCTR-TRC-00000022.
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Authors | Dao-Zhen Xu, Kai Zhao, Li-Min Guo, Lan-Juan Li, Qing Xie, Hong Ren, Ji-Ming Zhang, Min Xu, Hui-Fen Wang, Wen-Xiang Huang, Wen-Xiang Wang, Xue-Fan Bai, Jun-Qi Niu, Pei Liu, Xin-Yue Chen, Xin-Liang Shen, Zheng-Hong Yuan, Xuan-Yi Wang, Yu-Mei Wen |
Journal | PloS one
(PLoS One)
Vol. 3
Issue 7
Pg. e2565
(Jul 02 2008)
ISSN: 1932-6203 [Electronic] United States |
PMID | 18596958
(Publication Type: Clinical Trial, Phase II, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antigen-Antibody Complex
- DNA, Viral
- Hepatitis B Vaccines
- YIC vaccine
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Topics |
- Adolescent
- Adult
- Aged
- Antigen-Antibody Complex
(therapeutic use)
- DNA, Viral
(metabolism)
- Hepatitis B Vaccines
(immunology, therapeutic use)
- Hepatitis B, Chronic
(drug therapy, immunology)
- Humans
- Kinetics
- Middle Aged
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