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Immunogenicity of adjuvanted versus high-dose inactivated influenza vaccines in older adults: a randomized clinical trial

BACKGROUND: Adjuvanted inactivated influenza vaccine (aIIV) and high-dose inactivated influenza vaccine (HD-IIV) are U.S.-licensed for adults aged ≥ 65 years. This study compared serum hemagglutination inhibition (HAI) antibody titers for the A(H3N2) and A(H1N1)pdm09 and B strains after trivalent aI...

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Autores principales: Schmader, Kenneth E., Liu, Christine K., Flannery, Brendan, Rountree, Wes, Auerbach, Heidi, Barnett, Elizabeth D., Schlaudecker, Elizabeth P., Todd, Christopher A., Poniewierski, Marek, Staat, Mary A., Harrington, Theresa, Li, Rongxia, Broder, Karen R., Walter, Emmanuel B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314373/
https://www.ncbi.nlm.nih.gov/pubmed/37393237
http://dx.doi.org/10.1186/s12979-023-00355-7
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author Schmader, Kenneth E.
Liu, Christine K.
Flannery, Brendan
Rountree, Wes
Auerbach, Heidi
Barnett, Elizabeth D.
Schlaudecker, Elizabeth P.
Todd, Christopher A.
Poniewierski, Marek
Staat, Mary A.
Harrington, Theresa
Li, Rongxia
Broder, Karen R.
Walter, Emmanuel B.
author_facet Schmader, Kenneth E.
Liu, Christine K.
Flannery, Brendan
Rountree, Wes
Auerbach, Heidi
Barnett, Elizabeth D.
Schlaudecker, Elizabeth P.
Todd, Christopher A.
Poniewierski, Marek
Staat, Mary A.
Harrington, Theresa
Li, Rongxia
Broder, Karen R.
Walter, Emmanuel B.
author_sort Schmader, Kenneth E.
collection PubMed
description BACKGROUND: Adjuvanted inactivated influenza vaccine (aIIV) and high-dose inactivated influenza vaccine (HD-IIV) are U.S.-licensed for adults aged ≥ 65 years. This study compared serum hemagglutination inhibition (HAI) antibody titers for the A(H3N2) and A(H1N1)pdm09 and B strains after trivalent aIIV3 and trivalent HD-IIV3 in an older adult population. RESULTS: The immunogenicity population included 342 participants who received aIIV3 and 338 participants who received HD-IIV3. The proportion of participants that seroconverted to A(H3N2) vaccine strains after allV3 (112 participants [32.8%]) was inferior to the proportion of participants that seroconverted after HD-IIV3 (130 participants [38.5%]) at day 29 after vaccination (difference, − 5.8%; 95%CI, − 12.9% to 1.4%). There were no significant differences between the vaccine groups in percent seroconversion to A(H1N1)pdm09 or B vaccine strains, in percent seropositivity for any of the strains, or in post-vaccination GMT for the A(H1N1)pdm09 strain. The GMTs for the post-vaccination A(H3N2) and B strains were higher after HD-IIV than after aIIV3. CONCLUSIONS: Overall immune responses were similar after aIIV3 and HD-IIV3. For the primary outcome, the aIIV3 seroconversion rate for H3N2 did not meet noninferiority criteria compared with HD-IIV3, but the HD-IIV3 seroconversion rate was not statistically superior to the aIIV3 seroconversion rate. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03183908. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12979-023-00355-7.
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spelling pubmed-103143732023-07-02 Immunogenicity of adjuvanted versus high-dose inactivated influenza vaccines in older adults: a randomized clinical trial Schmader, Kenneth E. Liu, Christine K. Flannery, Brendan Rountree, Wes Auerbach, Heidi Barnett, Elizabeth D. Schlaudecker, Elizabeth P. Todd, Christopher A. Poniewierski, Marek Staat, Mary A. Harrington, Theresa Li, Rongxia Broder, Karen R. Walter, Emmanuel B. Immun Ageing Research BACKGROUND: Adjuvanted inactivated influenza vaccine (aIIV) and high-dose inactivated influenza vaccine (HD-IIV) are U.S.-licensed for adults aged ≥ 65 years. This study compared serum hemagglutination inhibition (HAI) antibody titers for the A(H3N2) and A(H1N1)pdm09 and B strains after trivalent aIIV3 and trivalent HD-IIV3 in an older adult population. RESULTS: The immunogenicity population included 342 participants who received aIIV3 and 338 participants who received HD-IIV3. The proportion of participants that seroconverted to A(H3N2) vaccine strains after allV3 (112 participants [32.8%]) was inferior to the proportion of participants that seroconverted after HD-IIV3 (130 participants [38.5%]) at day 29 after vaccination (difference, − 5.8%; 95%CI, − 12.9% to 1.4%). There were no significant differences between the vaccine groups in percent seroconversion to A(H1N1)pdm09 or B vaccine strains, in percent seropositivity for any of the strains, or in post-vaccination GMT for the A(H1N1)pdm09 strain. The GMTs for the post-vaccination A(H3N2) and B strains were higher after HD-IIV than after aIIV3. CONCLUSIONS: Overall immune responses were similar after aIIV3 and HD-IIV3. For the primary outcome, the aIIV3 seroconversion rate for H3N2 did not meet noninferiority criteria compared with HD-IIV3, but the HD-IIV3 seroconversion rate was not statistically superior to the aIIV3 seroconversion rate. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT03183908. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12979-023-00355-7. BioMed Central 2023-07-01 /pmc/articles/PMC10314373/ /pubmed/37393237 http://dx.doi.org/10.1186/s12979-023-00355-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Schmader, Kenneth E.
Liu, Christine K.
Flannery, Brendan
Rountree, Wes
Auerbach, Heidi
Barnett, Elizabeth D.
Schlaudecker, Elizabeth P.
Todd, Christopher A.
Poniewierski, Marek
Staat, Mary A.
Harrington, Theresa
Li, Rongxia
Broder, Karen R.
Walter, Emmanuel B.
Immunogenicity of adjuvanted versus high-dose inactivated influenza vaccines in older adults: a randomized clinical trial
title Immunogenicity of adjuvanted versus high-dose inactivated influenza vaccines in older adults: a randomized clinical trial
title_full Immunogenicity of adjuvanted versus high-dose inactivated influenza vaccines in older adults: a randomized clinical trial
title_fullStr Immunogenicity of adjuvanted versus high-dose inactivated influenza vaccines in older adults: a randomized clinical trial
title_full_unstemmed Immunogenicity of adjuvanted versus high-dose inactivated influenza vaccines in older adults: a randomized clinical trial
title_short Immunogenicity of adjuvanted versus high-dose inactivated influenza vaccines in older adults: a randomized clinical trial
title_sort immunogenicity of adjuvanted versus high-dose inactivated influenza vaccines in older adults: a randomized clinical trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314373/
https://www.ncbi.nlm.nih.gov/pubmed/37393237
http://dx.doi.org/10.1186/s12979-023-00355-7
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