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Factors associated with Humoral Immune Response in Older Adults who Received Egg-free Influenza Vaccine
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1 16 2023
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Source: Vaccine. 41(3):862-869
Details:
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Alternative Title:Vaccine
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Personal Author:
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Description:Background:
Immune responses to influenza vaccination tend to be lower among older, frequently vaccinated adults. Use of egg-free influenza vaccines is increasing, but limited data exist on factors associated with their immunogenicity in older adults.
Methods:
Community-dwelling older adults ≥56 years of age were enrolled in a prospective, observational study of immunogenicity of 2018–2019 influenza vaccine. Hemagglutination inhibition (HAI) antibody titers were measured pre-vaccination (Day 0) and four weeks after vaccination (Day 28) to calculate geometric mean titers, seropositivity (HAI titers ≥1:40), seroconversion (four-fold rise in HAI titer with post-vaccination titer ≥1:40) and geometric mean fold rise (GMFR). Linear regression models assessed the association of predictors of GMFR for each vaccine antigen.
Results:
Among 91 participants who received egg-free influenza vaccines, 84 (92.3%) received quadrivalent recombinant influenza vaccine (RIV4, Flublok, Sanofi Pasteur), and 7 (7.7%) received quadrivalent cell culture-based influenza vaccine (ccIIV4, Flucelvax, Seqirus). Pre-vaccination seropositivity was 52.8% for A(H1N1), 94.5% for A(H3N2), 61.5% for B/Colorado and 48.4% for B/Phuket. Seroconversion by antigen ranged from 16.5% for A(H1N1) and B/Colorado to 37.4% for A(H3N2); 40 participants failed to seroconvert to any antigen. Factors independently associated with higher GMFR in multivariable models included lower pre-vaccination HAI antibody titer for A(H1N1), B/Colorado and B/Phuket, and younger age for A(H1N1).
Conclusion:
Overall pre-vaccination seropositivity was high and just over half of the cohort seroconverted to ≥1 vaccine antigen. Antibody responses were highest among participants with lower pre-vaccination titers. Among older adults with high pre-existing antibody titers, approaches to improve immune responses are needed.
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Source:
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Pubmed ID:36543682
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Pubmed Central ID:PMC9850444
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Funding:
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Volume:41
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Issue:3
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