An Evaluation of the Efficacy of High-dose Hepatitis B Vaccine in Patients Using Biological Agents
Journal Title: Viral Hepatitis Journal - Year 2020, Vol 26, Issue 2
Abstract
Objectives: Hepatitis B virus (HBV) vaccination is efficient in the normal population, whereas lower humoral response rates in immunosuppressed patients. Biological agents used in the treatment of several diseases in recent years are a significant cause of immunosuppression in patients. In this study we aimed to evaluate the efficacy of double-dose HBV vaccination at months 0, 1, 2, and 6 in patients using biological agents. Materials and Methods: The patients who were using biological agents and seronegative for HBV received double-dose HBV vaccine (40 μg) on months 0, 1, 2 and 6, and response rates were assessed. Patients with anti-HBs titers >10 mIU/mL one month after completion of the vaccine plan were regarded as vaccineresponsive. Results: Eighty-four patients were evaluated. Forty patients (47.4%) were men and 44 (52.4%) were women. The mean age of the patients was 43.1±12.5 years. The most common underlying inflammatory rheumatic disease was ankylosing spondylitis at 51.2% (n=43). The most commonly used biological agent was adalimumab at 36.9% (n=31). Vaccine response was achieved in 85.7% (n=72) of the patients, while no response was achieved in 12 patients (14.3%). Sex, comorbidities, type of underlying inflammatory disease and biological agents had no effect on vaccine response. Conclusion: Administration of 40 μg HBV vaccine at months 0, 1, 2, and 6 to HBV seronegative patients using biological agents was found to be effective. This efficacy was found to be independent of the type of biological agent, the time of onset of the biological agent and the length of use of the biological agent.
Authors and Affiliations
Murat Aydın, Firdevs Aksoy, Zehra Yıldırım, İftihar Köksal
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