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Immunogenicity and safety of concomitant MF59-adjuvanted influenza vaccine and 23-valent pneumococcal polysaccharide vaccine administration in older adults
Institution:1. HealthPartners Institute for Education and Research, Minneapolis, MN, United States;2. Department of Obstetrics and Gynecology, Yale University, New Haven, CT, United States;3. Center for Health Research, Kaiser Permanente Northwest, Portland, OR, United States;4. Vaccine Study Center, Kaiser Permanente of Northern California, Oakland, CA, United States;5. Kaiser Permanente of Southern California, Pasadena, CA, United States;6. Kaiser Permanente Institute for Health Research, Denver, CO, United States;7. Denver Health Community Health Services, Denver, United States;8. Immunization Safety Office, Division of Healthcare Quality and Promotion, Centers for Disease Control and Prevention, Atlanta, GA, United States;1. Department of Internal Medicine, Clinical Immunology Unit, University of Genova, Genova, Italy;2. Department of Health Sciences, Vaccines and Clinical Trials Unit, University of Genova, Genova, Italy
Abstract:BackgroundConcomitant administration of influenza and pneumococcal vaccines facilitates their uptake by older adults; however, data on immunogenicity and safety of concomitant administration of adjuvanted trivalent inactivated influenza vaccine (aIIV3) and 23-valent pneumococcal polysaccharide vaccine (PPSV23) have not been reported.MethodsSubjects aged ≥65 years (N = 224) were randomized 1:1:1:1 to receive MF59-aIIV3 alone, MF59-aIIV3 + PPSV23 in contralateral arms, MF59-aIIV3 + PPSV23 in the same arm or PPSV23 alone (Clinical Trial Number – NCT02225327). Hemagglutination inhibition assay and multiplex opsonophagocytic killing assay were used to compare immunogenicity after single or concomitant vaccination.ResultsAll groups met immunogenicity criteria for the influenza vaccine in older adults with similar seroconversion rates and geometric mean fold-increases, irrespective of concomitant vaccinations and injection site. For each pneumococcal serotype, opsonic index (OI) increased markedly after the PPSV23 vaccination, irrespective of the concomitant influenza vaccine. All subjects showed an OI  8 for serotypes 6B, 18C and 19A post-vaccination, with a suggestion that the ipsilateral concomitant vaccination might be associated with higher OIs for some antigens. Local and systemic adverse events were more common in subjects receiving PPSV23 compared to those receiving aIIV3 alone.ConclusionsNo interference was observed with antibody responses to influenza or pneumococcal antigens when aIIV3 and PPSV23 were administered concomitantly.
Keywords:Influenza vaccine  Pneumococcal polysaccharide vaccine  MF59  Emulsion adjuvant
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