Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 16 min ago
PreprintCC BY-NCbioRxiv

Distinct Longitudinal Antibody Responses Following Primary Influenza Infection or Vaccination in Infants: A Prospective Birth Cohort Study

2 more authors
  1. 1Emory University

Abstract

The longitudinal effects of initial influenza exposure on the magnitude, persistence, and antigen specificity of antibody responses during infancy remain incompletely understood. We investigated humoral antibody responses following primary influenza infection or seasonal vaccination in a prospective US birth cohort with weekly respiratory surveillance for influenza infection. Influenza-specific serum IgG binding to H1 and H3 haemagglutinin (HA) antigens, HA inhibition (HAI), and live-virus neutralizing antibody responses were assessed longitudinally. To minimize influence of maternally derived antibodies, analyses of primary exposure responses were restricted to infants for whom influenza-specific maternal antibodies had declined below the assay detection limit before exposure. Antibody responses were compared following primary infection and vaccination and examined after subsequent annual vaccination. We found that maternal influenza-specific IgG declined rapidly during early infancy. Among infants without detectable pre-exposure influenza-specific antibodies, primary influenza infection was associated with greater post-exposure antibody responses and less measurable decline over follow-up than primary vaccination. These groups differed in age, calendar season, and exposure characteristics, limiting direct attribution of these differences to route of exposure. In infants with previous influenza infection followed by vaccination, responses after subsequent vaccination initially showed greater binding to the previously infecting subtype among the tested HA antigens. With repeated vaccination, responses became more distributed across the tested antigens. Our findings reveal differences in the magnitude, persistence, and antigen specificity of antibody responses according to the nature and sequence of influenza exposure. By prospectively capturing early-life exposures, this study provides longitudinal evidence linking exposure history to subsequent humoral antibody responses.

Related

  1. Intranasal adenovirus type 5 influenza vaccination enhances milk antibody responses and passive transfer to neonatal ferrets
    L. S. Stafford, P. Baker, M. Moyer +10
    bioRxivPreprintCC BYFull textMicrobiologybioRxiv
  2. Distinct transcriptional states of draining lymph node T cells following influenza vaccination in individuals with underrepresented ancestries
    S. Kim, J. Siu, T. Chan +17
    bioRxivPreprintCC BYFull textImmunologybioRxiv
  3. Effects of a multistrain probiotic formulation on immune response and microbiome modulation following influenza vaccination in adults: a randomised, triple-blind, placebo-controlled trial
    Malwina Naghibi, Eric Climent Sanz, Andrea Rodenes-Gavidia +8
    Frontiers in ImmunologyPeer-reviewedCC BY 4.0ImmunologyCrossref
  4. Optimized Epitope-Flanking Sequences Enhance Antigen Presentation and T-Cell Responses Following mRNA Vaccination.
    Marie-Pierre Hardy, Gabriel Ouellet-Lavallée, Catherine Thériault +9
    CellsPeer-reviewedCC BYFull textImmunologyEurope PMC
  5. Genome-wide association study reveals putative genetic determinants of longitudinal immune responses to avian influenza and Newcastle disease in chickens
    Haile Berihulay, Wei Luo, Ainong Lao +9
    Genetics Selection EvolutionPeer-reviewedCC BY 4.0Full textGenetics & genomicsHAL
BibTeX
@misc{joshi2026distinct,
  title = {{Distinct Longitudinal Antibody Responses Following Primary Influenza Infection or Vaccination in Infants: A Prospective Birth Cohort Study}},
  author = {D. Joshi and S. Kumar and V. I. Zarnitsyna and A. R. Burrell and C. Rolhfs and S. Danzy and T. P. Charles and F. A. Mbadugha and L. Xu and D. C. Payne and J. Kohlmeier and A. C. Lowen and M. Allen Staat and J. Wrammert},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.28.755012},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.28.755012v1},
  note = {CC BY-NC},
}
RIS
TY  - UNPB
TI  - Distinct Longitudinal Antibody Responses Following Primary Influenza Infection or Vaccination in Infants: A Prospective Birth Cohort Study
AU  - D. Joshi
AU  - S. Kumar
AU  - V. I. Zarnitsyna
AU  - A. R. Burrell
AU  - C. Rolhfs
AU  - S. Danzy
AU  - T. P. Charles
AU  - F. A. Mbadugha
AU  - L. Xu
AU  - D. C. Payne
AU  - J. Kohlmeier
AU  - A. C. Lowen
AU  - M. Allen Staat
AU  - J. Wrammert
PY  - 2026
DA  - 2026/09/28
PB  - bioRxiv
DO  - 10.64898/2026.09.28.755012
UR  - https://www.biorxiv.org/content/10.64898/2026.09.28.755012v1
AB  - The longitudinal effects of initial influenza exposure on the magnitude, persistence, and antigen specificity of antibody responses during infancy remain incompletely understood. We investigated humoral antibody responses following primary influenza infection or seasonal vaccination in a prospective US birth cohort with weekly respiratory surveillance for influenza infection. Influenza-specific serum IgG binding to H1 and H3 haemagglutinin (HA) antigens, HA inhibition (HAI), and live-virus neutralizing antibody responses were assessed longitudinally. To minimize influence of maternally derived antibodies, analyses of primary exposure responses were restricted to infants for whom influenza-specific maternal antibodies had declined below the assay detection limit before exposure. Antibody responses were compared following primary infection and vaccination and examined after subsequent annual vaccination. We found that maternal influenza-specific IgG declined rapidly during early infancy. Among infants without detectable pre-exposure influenza-specific antibodies, primary influenza infection was associated with greater post-exposure antibody responses and less measurable decline over follow-up than primary vaccination. These groups differed in age, calendar season, and exposure characteristics, limiting direct attribution of these differences to route of exposure. In infants with previous influenza infection followed by vaccination, responses after subsequent vaccination initially showed greater binding to the previously infecting subtype among the tested HA antigens. With repeated vaccination, responses became more distributed across the tested antigens. Our findings reveal differences in the magnitude, persistence, and antigen specificity of antibody responses according to the nature and sequence of influenza exposure. By prospectively capturing early-life exposures, this study provides longitudinal evidence linking exposure history to subsequent humoral antibody responses.
ER  -