Failure of therapeutic vaccination using hepatitis B surface antigen vaccine in the immunotolerant phase of children with chronic hepatitis B infection

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Küçük Resim

Tarih

2003

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia

Erişim Hakkı

info:eu-repo/semantics/closedAccess

Özet

Summary Aim: The aim of this study was to investigate the efficacy of specific hepatitis B virus (HBV) vaccination as active immunotherapy in treating chronic hepatitis B (CHB) infection during the immune-tolerant phase in children with normal aminotransferase levels and high viral load. Methods: Fifty-one immunotolerant patients were randomly and prospectively recruited into two groups. Group 1 included 23 patients that were vaccinated with three standard injections of the GenHevac B vaccine in the deltoid or quadricep muscle, initially, and at 30 days and 60 days, for specific immunization. Group 2 contained 28 patients who did not receive any medication or vaccination and were recruited as the control group. Post-vaccination evaluation was performed at 6 months from the first injection and at the end of the 12th month by serological and virological analyses. A response criterion to therapy was defined as loss of HBV-DNA in serum and hepatitis B early antigen (HBeAg) seroconversion (loss of HBeAg, development of antibody to HBeAg (anti-HBe)). Results: The mean alanine aminotransferase (ALT) value in group 1 at the beginning of the vaccination was 33.6 ± 8.1 IU/L; this changed to 31.7 ± 9.0 IU/L at 6 months after first injection and 29.2 ± 7.1 IU/L at the end of 12 months (P > 0.05). In this group, mean HBV-DNA load at the starting point of the vaccination was 3709 ± 1126 pg/mL; this value changed to 3569 ± 726 pg/mL at the sixth month and 3295 ± 832 pg/mL at the 12th month (P > 0.05). In group 2, the mean ALT values at the beginning of therapy, and at the 6th and 12th month were 32 ± 8 IU/L, 31.8 ± 8 IU/L, and 29.7 ± 7 IU/L, respectively (P > 0.05), and the mean viral load of HBV-DNA values were 3827 ± 1375 pg/mL, 3498 ± 886 pg/mL, and 3059 ± 731 pg/mL, respectively (P > 0.05). The load of HBV DNA of all patients in both groups was greater than 2000 pg/mL. There was no statistically significant difference in the mean ALT values and mean viral load of HBV DNA (P > 0.05) between group 1 and group 2 at the end of the 6th and 12th months. Except for one each patient in each group, hepatitis B surface antigen (HBsAg) and HBeAg clearance or antibody to HBsAg (anti-HBs) and anti-HBe seroconversion were not observed during the follow-up period (P > 0.05). Conclusion: In this study, comparison of vaccinated and unvaccinated groups of immunotolerant children with CHB infection showed no difference in the clearance of HBV DNA and seroconversion of HBeAg to anti-HBe. Different immunization protocols should be considered for future investigations in the immunotolerant phase of children with CHB infection.

Açıklama

Anahtar Kelimeler

Children, Chronic hepatitis B, Immunotolerant period, Therapy, Vaccine

Kaynak

Journal of Gastroenterology and Hepatology

WoS Q Değeri

Q3

Scopus Q Değeri

Q1

Cilt

18

Sayı

2

Künye

Dikici, B., Boşnak, M., Uçmak, H., Atlı, A., Ece, A., Haspolat, Y. K. ve diğerleri. (2003). Failure of therapeutic vaccination using hepatitis B surface antigen vaccine in the immunotolerant phase of children with chronic hepatitis B infection. Journal of Gastroenterology and Hepatology, 18(2), 218-222.