Hemagglutinin- and neuraminidase-targeting antibody responses after receipt of egg-based inactivated or recombinant influenza vaccines among adults aged 18-64 years.

VaccineOct 27, 2026 (epub)

Vasiliy P Mishin, Mira C Patel, Rongyuan Gao et al.

✦ AI-curated · Sources linked

In 30 seconds

This randomized trial compared hemagglutinin (HA)- and neuraminidase (NA)-targeting antibody responses after 2022–2023 recombinant influenza vaccine (RIV) or standard-dose inactivated influenza vaccine (SD-IIV) in adults aged 18–64 years. RIV recipients had two-fold higher anti-HA responses to cell-based type A and B/Yamagata viruses; the difference for B/Victoria was not statistically significant. SD-IIV did not produce a rise in NA-inhibiting antibodies to mammalian cell-grown viruses, although responses to egg-grown NA antigens increased. The findings highlight that measured antibody responses depend on the virus substrate used in testing.

Key findings

  • Anti-HA responses to cell-based type A and B/Yamagata viruses were two-fold higher with RIV than SD-IIV.
  • SD-IIV recipients showed no rise in NA-inhibiting antibodies to mammalian cell-grown viruses.
  • After SD-IIV, ≥ 4-fold rises in ELLA GMTs occurred for egg-prepared N1 in 13% and N2 in 37% of recipients.
  • Neutralizing antibodies waned faster than HI antibodies to most vaccine viruses.

Why it matters

The study shows that vaccine-associated antibody findings can differ according to whether test antigens are egg- or cell-grown, particularly for NA. This matters when interpreting immunogenicity studies and comparing vaccine responses: assays using egg-grown antigens may capture responses that are not evident against mammalian cell-grown viruses. HA and NA measurements therefore provide complementary information about humoral responses.

What to keep in mind

The antibody analyses were conducted in a subgroup of trial participants, and the reported outcomes are immunologic measures rather than clinical influenza outcomes.

Source

Published in Vaccine. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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