Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Journal stats
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Journal stats
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
Neuraminidase-specific antibody responses are generated in naive and vaccinated newborn nonhuman primates following virus infection
Patrick K. Shultz, Kali F. Crofts, Beth C. Holbrook, Martha A. Alexander-Miller
Patrick K. Shultz, Kali F. Crofts, Beth C. Holbrook, Martha A. Alexander-Miller
View: Text | PDF
Research Article Immunology Vaccines

Neuraminidase-specific antibody responses are generated in naive and vaccinated newborn nonhuman primates following virus infection

  • Text
  • PDF
Abstract

Individuals younger than 6 months of age are at significant risk from influenza virus infection; however, there is currently no vaccine approved for this age group. Influenza virus neuraminidase (NA) has emerged as a potential additional target for vaccine strategies. In this study, we sought to understand the ability of newborns to mount an antibody response to NA. Here we employed a nonhuman primate model, given the similarities to humans in immune system and development. We measured antibody to NA following infection with an H1N1 virus or following vaccination and challenge. Administration of an inactivated virus vaccine was not capable of eliciting detectable NA-specific antibody, even in the presence of adjuvants previously shown to increase total virus-specific IgG. However, both naive and vaccinated newborns generated a NA-specific antibody response following virus infection. Interestingly, the presence of the vaccine-induced response did not prevent generation of systemic antibody to NA following challenge, although the respiratory response was reduced in a significant portion of newborns. These findings are the first, to our knowledge, to evaluate the newborn response to the influenza NA protein as well as the impact of previous vaccination on generation of these antibodies following virus infection.

Authors

Patrick K. Shultz, Kali F. Crofts, Beth C. Holbrook, Martha A. Alexander-Miller

×

Figure 1

Infant AGMs generate NA-specific antibodies with inhibitory activity following infection with influenza virus.

Options: View larger image (or click on image) Download as PowerPoint
Infant AGMs generate NA-specific antibodies with inhibitory activity fol...
Infant (6–10 days of age) and adult AGMs (6–9 years of age) were infected with PR8 (n = 4/group). The presence of total NA-specific IgG (A) and NAI antibody (B) was assessed on d14 p.i. (C) ELLA and ELISA values for antibody in plasma from individual animals. Total NA-specific IgG (D) and NAI antibody (E) in BAL were also measured. (F) ELLA and ELISA values for antibody in BAL from individual animals. Preinfection samples for the adult animals used in the study are shown. The naive newborn data were obtained from a separate cohort of age-matched animals, as we did not have preinfection samples available for testing. The dotted line shows the limit of detection (LOD) for the assay. Significance was assessed using an unpaired Student’s t test.

Copyright © 2026 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts