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Assessment of enhanced influenza vaccination finds that FluAd conveys an advantage in mice and older adults

OBJECTIVES: Enhanced inactivated influenza vaccines (eIIV) aim to increase immunogenicity and protection compared with the widely used standard IIV (S‐IIV). METHODS: We tested four vaccines in parallel, FluZone high dose, FluBlok and FluAd versus S‐IIV in a randomised controlled trial of older adult...

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Autores principales: Kavian, Niloufar, Hachim, Asmaa, Li, Athena PY, Cohen, Carolyn A, Chin, Alex WH, Poon, Leo LM, Fang, Vicky J, Leung, Nancy HL, Cowling, Benjamin J, Valkenburg, Sophie A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997034/
https://www.ncbi.nlm.nih.gov/pubmed/32025302
http://dx.doi.org/10.1002/cti2.1107
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author Kavian, Niloufar
Hachim, Asmaa
Li, Athena PY
Cohen, Carolyn A
Chin, Alex WH
Poon, Leo LM
Fang, Vicky J
Leung, Nancy HL
Cowling, Benjamin J
Valkenburg, Sophie A
author_facet Kavian, Niloufar
Hachim, Asmaa
Li, Athena PY
Cohen, Carolyn A
Chin, Alex WH
Poon, Leo LM
Fang, Vicky J
Leung, Nancy HL
Cowling, Benjamin J
Valkenburg, Sophie A
author_sort Kavian, Niloufar
collection PubMed
description OBJECTIVES: Enhanced inactivated influenza vaccines (eIIV) aim to increase immunogenicity and protection compared with the widely used standard IIV (S‐IIV). METHODS: We tested four vaccines in parallel, FluZone high dose, FluBlok and FluAd versus S‐IIV in a randomised controlled trial of older adults and in a mouse infection model to assess immunogenicity, protection from lethal challenge and mechanisms of action. RESULTS: In older adults, FluAd vaccination stimulated a superior antibody profile, including H3‐HA antibodies that were elevated for up to 1 year after vaccination, higher avidity H3HA IgG and larger HA stem IgG responses. In a mouse model, FluAd also elicited an earlier and larger induction of HA stem antibodies with increased germinal centre responses and upregulation and long‐term expression of B‐cell switch transcription factors. Long‐term cross‐reactive memory responses were sustained by FluAd following lethal heterosubtypic influenza challenge, with reduced lung damage and viral loads, coinciding with increased T‐ and B‐cell recall. Advantages were also noted for the high‐dose FluZone vaccine in both humans and mice. CONCLUSION: The early, broadly reactive and long‐lived antibody response of FluAd indicates a potential advantage of this vaccine, particularly in years when there is a mismatch between the vaccine strain and the circulating strain of influenza viruses.
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spelling pubmed-69970342020-02-05 Assessment of enhanced influenza vaccination finds that FluAd conveys an advantage in mice and older adults Kavian, Niloufar Hachim, Asmaa Li, Athena PY Cohen, Carolyn A Chin, Alex WH Poon, Leo LM Fang, Vicky J Leung, Nancy HL Cowling, Benjamin J Valkenburg, Sophie A Clin Transl Immunology Original Article OBJECTIVES: Enhanced inactivated influenza vaccines (eIIV) aim to increase immunogenicity and protection compared with the widely used standard IIV (S‐IIV). METHODS: We tested four vaccines in parallel, FluZone high dose, FluBlok and FluAd versus S‐IIV in a randomised controlled trial of older adults and in a mouse infection model to assess immunogenicity, protection from lethal challenge and mechanisms of action. RESULTS: In older adults, FluAd vaccination stimulated a superior antibody profile, including H3‐HA antibodies that were elevated for up to 1 year after vaccination, higher avidity H3HA IgG and larger HA stem IgG responses. In a mouse model, FluAd also elicited an earlier and larger induction of HA stem antibodies with increased germinal centre responses and upregulation and long‐term expression of B‐cell switch transcription factors. Long‐term cross‐reactive memory responses were sustained by FluAd following lethal heterosubtypic influenza challenge, with reduced lung damage and viral loads, coinciding with increased T‐ and B‐cell recall. Advantages were also noted for the high‐dose FluZone vaccine in both humans and mice. CONCLUSION: The early, broadly reactive and long‐lived antibody response of FluAd indicates a potential advantage of this vaccine, particularly in years when there is a mismatch between the vaccine strain and the circulating strain of influenza viruses. John Wiley and Sons Inc. 2020-02-03 /pmc/articles/PMC6997034/ /pubmed/32025302 http://dx.doi.org/10.1002/cti2.1107 Text en © 2020 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Article
Kavian, Niloufar
Hachim, Asmaa
Li, Athena PY
Cohen, Carolyn A
Chin, Alex WH
Poon, Leo LM
Fang, Vicky J
Leung, Nancy HL
Cowling, Benjamin J
Valkenburg, Sophie A
Assessment of enhanced influenza vaccination finds that FluAd conveys an advantage in mice and older adults
title Assessment of enhanced influenza vaccination finds that FluAd conveys an advantage in mice and older adults
title_full Assessment of enhanced influenza vaccination finds that FluAd conveys an advantage in mice and older adults
title_fullStr Assessment of enhanced influenza vaccination finds that FluAd conveys an advantage in mice and older adults
title_full_unstemmed Assessment of enhanced influenza vaccination finds that FluAd conveys an advantage in mice and older adults
title_short Assessment of enhanced influenza vaccination finds that FluAd conveys an advantage in mice and older adults
title_sort assessment of enhanced influenza vaccination finds that fluad conveys an advantage in mice and older adults
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997034/
https://www.ncbi.nlm.nih.gov/pubmed/32025302
http://dx.doi.org/10.1002/cti2.1107
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