Differential gene expression in peripheral blood mononuclear cells from children immunized with inactivated influenza

John F Alcorn1, Raghunandan Avula2, Anish B Chakka2

  • 1Department of Pediatrics, University of Pittsburgh , Pittsburgh, PA, USA.

Insights

Influenza vaccination in children triggers dynamic immune responses, with gene expression changes varying by age and prior vaccination history. These transcriptomic shifts reveal insights into innate inflammation, cellular processes, and immune cell maturation following vaccination.

Area of Science:

  • Immunology
  • Transcriptomics
  • Vaccinology

Background:

  • The immune response to inactivated influenza vaccines is complex and influenced by host factors.
  • Understanding post-vaccination molecular changes in children is crucial for assessing vaccine efficacy and safety.

Purpose of the Study:

  • To identify and characterize transcriptomic alterations in peripheral blood mononuclear cells (PBMCs) of children after inactivated influenza vaccination.
  • To investigate how age and prior vaccine history impact these molecular responses.

Main Methods:

  • Blood samples were collected from children before and 3 or 7 days after receiving the 2016-2017 quadrivalent inactivated influenza vaccine.
  • RNA sequencing was performed on PBMCs to analyze gene expression.
  • Differential gene expression analysis was conducted, comparing time points and stratifying by age and vaccine history.

Main Results:

  • A significant number of differentially expressed genes (DEGs) were observed at both 3 and 7 days post-vaccination.
  • Early (Day 3) changes were dominated by innate inflammation and apoptosis pathways, while later (Day 7) changes involved cellular processes and immunoglobulin gene expression.
  • Older children showed increased inflammatory gene expression at Day 3. Prior vaccination history modulated responses, including decreased phagosome and dendritic cell maturation.

Conclusions:

  • Post-inactivated influenza vaccination transcriptomic responses in children are dynamic and significantly influenced by the timing of sample collection, age, and previous vaccination status.
  • These findings provide a temporal molecular map of the immune response to influenza vaccination in pediatric populations.

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