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Article: Immunogenicity of standard, high-dose, MF59-adjuvanted, and recombinant-HA seasonal influenza vaccination in older adults

TitleImmunogenicity of standard, high-dose, MF59-adjuvanted, and recombinant-HA seasonal influenza vaccination in older adults
Authors
Issue Date2021
PublisherNature Research: Fully Open Access Journals. The Journal's web site is located at http://www.nature.com/npjvaccines/
Citation
NPJ Vaccines, 2021, v. 6 n. 1, p. article no. 25 How to Cite?
AbstractThe vaccine efficacy of standard-dose seasonal inactivated influenza vaccines (S-IIV) can be improved by the use of vaccines with higher antigen content or adjuvants. We conducted a randomized controlled trial in older adults to compare cellular and antibody responses of S-IIV versus enhanced vaccines (eIIV): MF59-adjuvanted (A-eIIV), high-dose (H-eIIV), and recombinant-hemagglutinin (HA) (R-eIIV). All vaccines induced comparable H3-HA-specific IgG and elevated antibody-dependent cellular cytotoxicity (ADCC) activity at day 30 post vaccination. H3-HA-specific ADCC responses were greatest following H-eIIV. Only A-eIIV increased H3-HA-IgG avidity, HA-stalk IgG and ADCC activity. eIIVs also increased polyfunctional CD4+ and CD8+ T cell responses, while cellular immune responses were skewed toward single-cytokine-producing T cells among S-IIV subjects. Our study provides further immunological evidence for the preferential use of eIIVs in older adults as each vaccine platform had an advantage over the standard-dose vaccine in terms of NK cell activation, HA-stalk antibodies, and T cell responses.
Persistent Identifierhttp://hdl.handle.net/10722/297206
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLI, APY-
dc.contributor.authorCohen, CA-
dc.contributor.authorLeung, NHL-
dc.contributor.authorFang, VJ-
dc.contributor.authorGangappa, S-
dc.contributor.authorSambhara, S-
dc.contributor.authorLevine, MZ-
dc.contributor.authorIuliano, AD-
dc.contributor.authorPerera, RAPM-
dc.contributor.authorIp, DKM-
dc.contributor.authorPeiris, JSM-
dc.contributor.authorThompson, MG-
dc.contributor.authorCowling, BJ-
dc.contributor.authorDoak, SAV-
dc.date.accessioned2021-03-08T07:15:40Z-
dc.date.available2021-03-08T07:15:40Z-
dc.date.issued2021-
dc.identifier.citationNPJ Vaccines, 2021, v. 6 n. 1, p. article no. 25-
dc.identifier.urihttp://hdl.handle.net/10722/297206-
dc.description.abstractThe vaccine efficacy of standard-dose seasonal inactivated influenza vaccines (S-IIV) can be improved by the use of vaccines with higher antigen content or adjuvants. We conducted a randomized controlled trial in older adults to compare cellular and antibody responses of S-IIV versus enhanced vaccines (eIIV): MF59-adjuvanted (A-eIIV), high-dose (H-eIIV), and recombinant-hemagglutinin (HA) (R-eIIV). All vaccines induced comparable H3-HA-specific IgG and elevated antibody-dependent cellular cytotoxicity (ADCC) activity at day 30 post vaccination. H3-HA-specific ADCC responses were greatest following H-eIIV. Only A-eIIV increased H3-HA-IgG avidity, HA-stalk IgG and ADCC activity. eIIVs also increased polyfunctional CD4+ and CD8+ T cell responses, while cellular immune responses were skewed toward single-cytokine-producing T cells among S-IIV subjects. Our study provides further immunological evidence for the preferential use of eIIVs in older adults as each vaccine platform had an advantage over the standard-dose vaccine in terms of NK cell activation, HA-stalk antibodies, and T cell responses.-
dc.languageeng-
dc.publisherNature Research: Fully Open Access Journals. The Journal's web site is located at http://www.nature.com/npjvaccines/-
dc.relation.ispartofNPJ Vaccines-
dc.rightsNPJ Vaccines. Copyright © Nature Research: Fully Open Access Journals.-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleImmunogenicity of standard, high-dose, MF59-adjuvanted, and recombinant-HA seasonal influenza vaccination in older adults-
dc.typeArticle-
dc.identifier.emailLeung, NHL: nanleung@connect.hku.hk-
dc.identifier.emailPerera, RAPM: mahenp@hku.hk-
dc.identifier.emailIp, DKM: dkmip@hku.hk-
dc.identifier.emailPeiris, JSM: malik@hkucc.hku.hk-
dc.identifier.emailCowling, BJ: bcowling@hku.hk-
dc.identifier.emailDoak, SAV: sophiev@hku.hk-
dc.identifier.authorityLeung, NHL=rp02637-
dc.identifier.authorityPerera, RAPM=rp02500-
dc.identifier.authorityIp, DKM=rp00256-
dc.identifier.authorityPeiris, JSM=rp00410-
dc.identifier.authorityCowling, BJ=rp01326-
dc.identifier.authorityDoak, SAV=rp02141-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/s41541-021-00289-5-
dc.identifier.pmid33594050-
dc.identifier.pmcidPMC7886864-
dc.identifier.scopuseid_2-s2.0-85100942614-
dc.identifier.hkuros321564-
dc.identifier.volume6-
dc.identifier.issue1-
dc.identifier.spagearticle no. 25-
dc.identifier.epagearticle no. 25-
dc.identifier.eissn2059-0105-
dc.identifier.isiWOS:000618864100001-
dc.publisher.placeUnited Kingdom-

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