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Reduced immunogenicity of BNT162b2 booster vaccination in combination with a tetravalent influenza vaccination: results of a prospective cohort study in 838 health workers.
Radner, Helga; Sieghart, Daniela; Jorda, Anselm; Fedrizzi, Clemens; Hasenöhrl, Timothy; Zdravkovic, Andrej; Redlberger-Fritz, Monika; Puchammer-Stoeckl, Elisabeth; Anderle, Karolina; Bergmann, Felix; Firbas, Christa; Jordakieva, Galateja; Wagner, Barbara; Haslacher, Helmuth; Perkmann, Thomas; Heinz, Leonhard X; Bonelli, Michael; Crevenna, Richard; Aletaha, Daniel; Zeitlinger, Markus.
Afiliación
  • Radner H; Department of Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
  • Sieghart D; Department of Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
  • Jorda A; Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Fedrizzi C; Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Hasenöhrl T; Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University of Vienna, Vienna, Austria.
  • Zdravkovic A; Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University of Vienna, Vienna, Austria.
  • Redlberger-Fritz M; Center of Virology, Medical University of Vienna, Vienna, Austria.
  • Puchammer-Stoeckl E; Center of Virology, Medical University of Vienna, Vienna, Austria.
  • Anderle K; Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Bergmann F; Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Firbas C; Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.
  • Jordakieva G; Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University of Vienna, Vienna, Austria.
  • Wagner B; Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University of Vienna, Vienna, Austria.
  • Haslacher H; Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
  • Perkmann T; Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
  • Heinz LX; Department of Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
  • Bonelli M; Department of Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
  • Crevenna R; Department of Physical Medicine, Rehabilitation and Occupational Medicine, Medical University of Vienna, Vienna, Austria.
  • Aletaha D; Department of Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
  • Zeitlinger M; Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria. Electronic address: Markus.zeitlinger@meduniwien.ac.at.
Clin Microbiol Infect ; 29(5): 635-641, 2023 May.
Article en En | MEDLINE | ID: mdl-36509374
OBJECTIVE: To investigate the immunogenicity and safety of BNT162b2 booster vaccination with and without a tetravalent influenza vaccine. METHODS: A prospective, open-label cohort study on immunogenicity and safety of COVID-19 booster vaccination with or without a tetravalent influenza vaccine was performed. Eight hundred thirty-eight health care workers were included in the following study arms: BNT162b2 booster-only, influenza-vaccine-only or combination of both. Levels of antibodies against SARS-CoV-2 spike receptor binding domain, and haemagglutinin inhibition tested for four different influenza strains (A(H1N1)pdm09, A(H3N2), B/Victoria, B/Yamagata) were measured at the time of vaccination and 4 weeks later. RESULTS: After 4 weeks, median (interquartile range) levels of antibodies against the receptor binding domain of the viral spike (S) protein and relative change from baseline were high in individuals who received BNTb162b2 booster vaccination only (absolute: 16 600 [10 980-24 360] vs. 12 630 [8198-18 750] BAU/mL [p < 0.0001]; relative increase: 49% [23.6-95.3] vs. 40% [21.9-80.6] [p 0.048]; booster-only n = 521 vs. combination-arm n = 229 respectively). Results were confirmed after matching for sex, age, body mass index, baseline antibody levels and vaccine compound received for primary immunization (absolute: 13 930 [10 610-22 760] vs. 12 520 [8710-17 940]; [p 0.031]; relative increase: 55.7% [27.8-98.5] vs. 42.2% [22.9-74.5]; p 0.045). Adverse events were almost identical in the booster-only and the combination-arm, but numerically low in the influenza arm (525/536 [97.9%] vs. 235/240 [97.9%] vs. 26/33 [78.8 %]). DISCUSSION: Although no safety concerns occurred, our study provides evidence on reduced immunogenicity of a BNT162b2 booster vaccination in combination with a tetravalent influenza vaccine. Further studies investigating new influenza variants as well as potential differences vaccine effectiveness are needed.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vacunas contra la Influenza / Gripe Humana / Subtipo H1N1 del Virus de la Influenza A / COVID-19 Tipo de estudio: Etiology_studies / Observational_studies Límite: Humans Idioma: En Revista: Clin Microbiol Infect Asunto de la revista: DOENCAS TRANSMISSIVEIS / MICROBIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Austria Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vacunas contra la Influenza / Gripe Humana / Subtipo H1N1 del Virus de la Influenza A / COVID-19 Tipo de estudio: Etiology_studies / Observational_studies Límite: Humans Idioma: En Revista: Clin Microbiol Infect Asunto de la revista: DOENCAS TRANSMISSIVEIS / MICROBIOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: Austria Pais de publicación: Reino Unido