Therapeutic vaccination in chronic hepatitis B
Autor: | Levent Erdem, Meral Akdogan, Fehmi Tabak, Selim Badur, Ali Mert, Gulsen Ozbay, Ersan Sander, Hakan Senturk, Resat Ozaras |
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Rok vydání: | 2002 |
Předmět: |
Adult
Male medicine.medical_specialty Hepatitis B virus Time Factors Adolescent medicine.medical_treatment Alpha interferon Interferon alpha-2 Gastroenterology Antiviral Agents Hepatitis B Chronic Chronic hepatitis Interferon Internal medicine medicine Humans Hepatitis B Vaccines Hepatitis B e Antigens Child Interferon alfa Aged Hepatitis B Surface Antigens Hepatology business.industry Interferon-alpha Alanine Transaminase Immunotherapy Middle Aged Recombinant Proteins Surgery Vaccination Treatment Outcome HBeAg Liver DNA Viral Drug Therapy Combination Female Viral disease business Biomarkers medicine.drug |
Zdroj: | Journal of gastroenterology and hepatology. 17(1) |
ISSN: | 0815-9319 |
Popis: | Aims: The aim was to test the efficacy of a pre-S2-containing vaccine (Genhevac-B) in chronic hepatitis B (CHB). Twenty-five naive patients (22 male, three female; median age 35; range: 6–69 years) with CHB were recruited. The inclusion criteria were: hepatitis B e antigen (HBeAg) positive or HBV-DNA detectable with liquid hybridization; alanine aminotransferase (ALT) is at least 1.5-fold the upper normal limit and histological evidence of chronic hepatitis. Methods: In the first period, all patients received monthly injections of 20, 40 and 60 μg of the vaccine. One month after the last injection, patients who still had HBV-DNA were divided into two randomly assigned groups. While the patients in the first group and the patients who lost HBV-DNA in the first period continued to receive monthly injections of 20 μg vaccine for a further 6 months, the patients in the second group received 9 MU interferon α-2b (Roferon-A), three times per week using the same method as for the first group. Patients were followed up after 12 months without treatment. Response was defined as the loss of HBV-DNA and normalization of ALT. Results: Six of the 25 patients lost HBV-DNA after 3 months. Nine of the remainder were randomly placed in the first group (vaccine-only) and 10 were placed in the second group (vaccine + interferon). End-of-treatment response was achieved, overall, 8/15 from the vaccine group and 6/10 from the combination. One patient from each group relapsed during the follow up. Overall, the sustained response (SR) rate was 46% (7/15) in the vaccine group, and 50% (5/10) in the combination group. Histological improvement was achieved in 6/7 SR with vaccine-only and all five with combination treatment, while 1/8 of failures of vaccine and 2/5 of failures of combination improved. Conclusions: It was concluded that Genhevac-B decreases serum HBV-DNA levels in the majority of patients with CHB and sustained clearance was achieved in some patients. Combination of interferon-α with Genhevac-B is effective for the vaccine failures and may increase sustained response compared to interferon-α alone. However, the mechanism of action is yet to be explained. |
Databáze: | OpenAIRE |
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