Redirecting antibody responses from egg-adapted epitopes following repeat vaccination with recombinant or cell culture-based versus egg-based influenza vaccines

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作者
Feng Liu
F. Liaini Gross
Sneha Joshi
Manjusha Gaglani
Allison L. Naleway
Kempapura Murthy
Holly C. Groom
Meredith G. Wesley
Laura J. Edwards
Lauren Grant
Sara S. Kim
Suryaprakash Sambhara
Shivaprakash Gangappa
Terrence Tumpey
Mark G. Thompson
Alicia M. Fry
Brendan Flannery
Fatimah S. Dawood
Min Z. Levine
机构
[1] Influenza Division,
[2] Centers for Disease Control and Prevention,undefined
[3] Baylor Scott & White Health,undefined
[4] Baylor College of Medicine,undefined
[5] Texas A & M University,undefined
[6] College of Medicine,undefined
[7] Kaiser Permanente Northwest Center for Health Research,undefined
[8] Abt Associates,undefined
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Repeat vaccination with egg-based influenza vaccines could preferentially boost antibodies targeting the egg-adapted epitopes and reduce immunogenicity to circulating viruses. In this randomized trial (Clinicaltrials.gov: NCT03722589), sera pre- and post-vaccination with quadrivalent inactivated egg-based (IIV4), cell culture-based (ccIIV4), and recombinant (RIV4) influenza vaccines were collected from healthcare personnel (18-64 years) in 2018−19 (N = 723) and 2019−20 (N = 684) influenza seasons. We performed an exploratory analysis. Vaccine egg-adapted changes had the most impact on A(H3N2) immunogenicity. In year 1, RIV4 induced higher neutralizing and total HA head binding antibodies to cell- A(H3N2) virus than ccIIV4 and IIV4. In year 2, among the 7 repeat vaccination arms (IIV4-IIV4, IIV4-ccIIV4, IIV4-RIV4, RIV4-ccIIV4, RIV4-RIV4, ccIIV4-ccIIV4 and ccIIV4-RIV4), repeat vaccination with either RIV4 or ccIIV4 further improved antibody responses to circulating viruses with decreased neutralizing antibody egg/cell ratio. RIV4 also had higher post-vaccination A(H1N1)pdm09 and A(H3N2) HA stalk antibodies in year 1, but there was no significant difference in HA stalk antibody fold rise among vaccine groups in either year 1 or year 2. Multiple seasons of non-egg-based vaccination may be needed to redirect antibody responses from immune memory to egg-adapted epitopes and re-focus the immune responses towards epitopes on the circulating viruses to improve vaccine effectiveness.
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