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A Randomized Controlled Phase IIb Trial of Antigen-Antibody Immunogenic Complex Therapeutic Vaccine in Chronic Hepatitis B Patients
BACKGROUND: The safety of the immune complexes composed of yeast-derived hepatitis B surface antigen (HBsAg) and antibodies (abbreviated as YIC) among healthy adults and chronic hepatitis B patients has been proved in phase I and phase IIa trial. A larger number of patients for study of dosage and e...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2430617/ https://www.ncbi.nlm.nih.gov/pubmed/18596958 http://dx.doi.org/10.1371/journal.pone.0002565 |
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author | Xu, Dao-Zhen Zhao, Kai Guo, Li-Min Chen, Xin-Yue Wang, Hui-Fen Zhang, Ji-Ming Xie, Qin Ren, Hong Wang, Wen-Xiang Li, Lan-Juan Xu, Min Liu, Pei Niu, Jun-Qi Bai, Xue-Fan Shen, Xin-Liang Yuan, Zheng-Hong Wang, Xuan-Yi Wen, Yu-Mei |
author_facet | Xu, Dao-Zhen Zhao, Kai Guo, Li-Min Chen, Xin-Yue Wang, Hui-Fen Zhang, Ji-Ming Xie, Qin Ren, Hong Wang, Wen-Xiang Li, Lan-Juan Xu, Min Liu, Pei Niu, Jun-Qi Bai, Xue-Fan Shen, Xin-Liang Yuan, Zheng-Hong Wang, Xuan-Yi Wen, Yu-Mei |
author_sort | Xu, Dao-Zhen |
collection | PubMed |
description | BACKGROUND: The safety of the immune complexes composed of yeast-derived hepatitis B surface antigen (HBsAg) and antibodies (abbreviated as YIC) among healthy adults and chronic hepatitis B patients has been proved in phase I and phase IIa trial. A larger number of patients for study of dosage and efficacy are therefore needed. METHODS AND PRINCIPAL FINDINGS: Two hundred forty two HBeAg-positive chronic hepatitis B patients were immunized with six injections of either 30 µg YIC, 60 µg 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 µg 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 µg 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 µg YIC and 60 µg 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 µg 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 |
format | Text |
id | pubmed-2430617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-24306172008-07-02 A Randomized Controlled Phase IIb Trial of Antigen-Antibody Immunogenic Complex Therapeutic Vaccine in Chronic Hepatitis B Patients Xu, Dao-Zhen Zhao, Kai Guo, Li-Min Chen, Xin-Yue Wang, Hui-Fen Zhang, Ji-Ming Xie, Qin Ren, Hong Wang, Wen-Xiang Li, Lan-Juan Xu, Min Liu, Pei Niu, Jun-Qi Bai, Xue-Fan Shen, Xin-Liang Yuan, Zheng-Hong Wang, Xuan-Yi Wen, Yu-Mei PLoS One Research Article BACKGROUND: The safety of the immune complexes composed of yeast-derived hepatitis B surface antigen (HBsAg) and antibodies (abbreviated as YIC) among healthy adults and chronic hepatitis B patients has been proved in phase I and phase IIa trial. A larger number of patients for study of dosage and efficacy are therefore needed. METHODS AND PRINCIPAL FINDINGS: Two hundred forty two HBeAg-positive chronic hepatitis B patients were immunized with six injections of either 30 µg YIC, 60 µg 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 µg 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 µg 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 µg YIC and 60 µg 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 µg 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 Public Library of Science 2008-07-02 /pmc/articles/PMC2430617/ /pubmed/18596958 http://dx.doi.org/10.1371/journal.pone.0002565 Text en Xu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Xu, Dao-Zhen Zhao, Kai Guo, Li-Min Chen, Xin-Yue Wang, Hui-Fen Zhang, Ji-Ming Xie, Qin Ren, Hong Wang, Wen-Xiang Li, Lan-Juan Xu, Min Liu, Pei Niu, Jun-Qi Bai, Xue-Fan Shen, Xin-Liang Yuan, Zheng-Hong Wang, Xuan-Yi Wen, Yu-Mei A Randomized Controlled Phase IIb Trial of Antigen-Antibody Immunogenic Complex Therapeutic Vaccine in Chronic Hepatitis B Patients |
title | A Randomized Controlled Phase IIb Trial of Antigen-Antibody Immunogenic Complex Therapeutic Vaccine in Chronic Hepatitis B Patients |
title_full | A Randomized Controlled Phase IIb Trial of Antigen-Antibody Immunogenic Complex Therapeutic Vaccine in Chronic Hepatitis B Patients |
title_fullStr | A Randomized Controlled Phase IIb Trial of Antigen-Antibody Immunogenic Complex Therapeutic Vaccine in Chronic Hepatitis B Patients |
title_full_unstemmed | A Randomized Controlled Phase IIb Trial of Antigen-Antibody Immunogenic Complex Therapeutic Vaccine in Chronic Hepatitis B Patients |
title_short | A Randomized Controlled Phase IIb Trial of Antigen-Antibody Immunogenic Complex Therapeutic Vaccine in Chronic Hepatitis B Patients |
title_sort | randomized controlled phase iib trial of antigen-antibody immunogenic complex therapeutic vaccine in chronic hepatitis b patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2430617/ https://www.ncbi.nlm.nih.gov/pubmed/18596958 http://dx.doi.org/10.1371/journal.pone.0002565 |
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