Safety and immunogenicity of a modified process hepatitis B vaccine in healthy adults ≥50 years

التفاصيل البيبلوغرافية
العنوان: Safety and immunogenicity of a modified process hepatitis B vaccine in healthy adults ≥50 years
المؤلفون: Stephanie O. Klopfer, Christopher L. Gilbert, Prakash K. Bhuyan, Jason C. Martin, Florian Schödel
المصدر: Human vaccines. 7(12)
سنة النشر: 2011
مصطلحات موضوعية: Male, medicine.medical_specialty, HBsAg, Hepatitis B virus, Hepatitis B vaccine, medicine.medical_treatment, Immunology, medicine.disease_cause, law.invention, Randomized controlled trial, Adjuvants, Immunologic, Double-Blind Method, law, Internal medicine, medicine, Humans, Hepatitis B Vaccines, General Pharmacology, Toxicology and Pharmaceutics, Hepatitis B Antibodies, Immunization Schedule, Aged, Aged, 80 and over, Vaccines, Synthetic, Hepatitis B Surface Antigens, business.industry, Immunogenicity, virus diseases, Hepatitis B, Middle Aged, medicine.disease, Titer, Treatment Outcome, Female, business, Adjuvant
الوصف: Generating protective immune responses in older adults (particularly ≥65 y) remains challenging for vaccines in general. This study examined the immune response engendered in older adults by RECOMBIVAX HB™ manufactured using a modified adjuvant (modified-process hepatitis B vaccine; mpHBV), RECOMBIVAX-HB™, and ENGERIX-B™.Randomized, double-blind, multicenter study enrolled healthy, seronegative subjects (N=538) to receive mpHBV (10 µg hepatitis B surface antigen [HBsAg]), RECOMBIVAX-HB™ (10 µg HBsAg), or ENGERIX-B™ (20 µg HBsAg) at Day 1, Month 1, and Month 6. Prespecified analysis of subpopulations 50-64 y and ≥65 y was conducted. Serum antibody to HBsAg (anti-HBs) was measured Predose 1 and 1 mo Postdose 3.For subjects ≥50 y, seroprotection rates (SPR, anti-HBs titer ≥10 mIU/mL) were 75.7% (95% CI: 68.0,82.2) for mpHBV, 68.0% (95% CI: 59.8,75.5) for RECOMBIVAX HB™, and 84.0% (95% CI: 77.0,89.6) for ENGERIX-B™. For subjects 50-64 y, SPRs were 82.1% (95% CI: 73.8,88.7) for mpHBV, 77.4% (95% CI: 68.7,84.7) for RECOMBIVAX-HB™, and 88.5% (95% CI: 81.1,93.7) for ENGERIX-B™. For subjects ≥65 y, SPRs were 57.5% (95% CI: 40.9,73.0) for mpHBV, 34.4% (95% CI: 18.6,53.2) for RECOMBIVAX-HB™, and 67.7% (95% CI: 48.6,83.3) for ENGERIX-B™. There were 6 non-vaccine related serious adverse events reported.The majority of subjects ≥50 y old achieved seroprotection. The sub-population ≥65 y had lower vaccination responses than the 50-64 y sub-population. For subjects ≥65 y, mpHBV and ENGERIX-B™ groups achieved higher seroprotection rates than the RECOMBIVAX-HB group. The safety profile of mpHBV was consistent with the other groups.
تدمد: 1554-8619
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2df9d0709c2aea0912c6a8513aa3d20
https://pubmed.ncbi.nlm.nih.gov/22185811
رقم الانضمام: edsair.doi.dedup.....d2df9d0709c2aea0912c6a8513aa3d20
قاعدة البيانات: OpenAIRE