Wednesday, 25th of July 2012 |
Presented by Katherine Dickman Dobbs (United States).
K. Dickman Dobbs1, C. Moloney2, E.R. Cooper2
1Boston Medical Center, Pediatrics, Boston, United States, 2Boston Medical Center, Pediatric Infectious Diseases, Boston, United States
Also accessible at http://pag.aids2012.org/abstracts.aspx?aid=1146
Background: Co-infection with hepatitis B virus (HBV) is an important cause of morbidity and mortality for HIV-infected patients. Compared to the HIV-uninfected population, children with HIV have shown lower rates of seroconversion after receiving the HBV vaccine series, varying from 20-78%, in comparison to 95-99%. Revaccination with double dose (DD) HBV vaccine has been shown to improve seroconversion rates in some populations, including those on hemodialysis and HIV-infected adults with high CD4 counts and relative viral suppression.
Methods: Our pediatric HIV clinic instituted a quality improvement measure in which patients who had not responded to initial standard dose vaccine series or subsequent booster doses (defined as HBsAb< 10 IU/L) were administered a three-dose series of DD HBV vaccine for age, at intervals of no less than 8 weeks. HBsAb levels were measured after first, second, and third DD. Baseline clinical characteristics were compared between responders and non-responders to the DD series.
Results: Sixty of 99 patients previously immunized with HBV (60.6%) were identified as having HBsAb levels < 10 IU/L after chart review. As of February 2012, 54 of these 60 have had one or more DD. The seroconversion rate after receiving one or more DD was 65.7%. As compared to non-responders, responders were younger (15.4 vs. 19.1 years, p=0.04), had lower average BMI (22.8 vs. 26.6 kg/m2, p=0.04), higher CD4 counts (766 vs. 487 cells/mm3, p=0.02), higher CD4 percentages (31.5% vs. 21.9%, p=0.004), and lower median viral loads (75 vs. 1491 copies/ml, p=0.05).
Conclusions: Revaccination using DD HBV vaccine improves seroconversion rates among HIV-infected children and adolescents with previous non-response to standard dose series. Investigation is needed to determine if this would be an effective first strategy, or if its success represents a booster effect suggesting past memory. Further study is needed for development of policy regarding immunization against HBV in HIV-infected children.
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