4.7 Article

Metabolomic and transcriptomic signatures of influenza vaccine response in healthy young and older adults

Journal

AGING CELL
Volume 21, Issue 9, Pages -

Publisher

WILEY
DOI: 10.1111/acel.13682

Keywords

immune response; influenza; metabolomics; systems biology; systems vaccinology; transcriptomics; vaccine

Funding

  1. National Institutes of Health [K24 AG042489, U19 AI089992, U19 GR101641]

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A study on the metabolic changes and molecular markers associated with influenza vaccine response in different age groups provides insights for the development of effective vaccines. The research found age-related differences in metabolic baselines and identified specific metabolites and genes indicative of immune response to vaccination.
Seasonal influenza causes mild to severe respiratory infections and significant morbidity, especially in older adults. Transcriptomic analysis in populations across multiple flu seasons has provided insights into the molecular determinants of vaccine response. Still, the metabolic changes that underlie the immune response to influenza vaccination remain poorly characterized. We performed untargeted metabolomics to analyze plasma metabolites in a cohort of younger and older subjects before and after influenza vaccination to identify vaccine-induced molecular signatures. Metabolomic and transcriptomic data were combined to define networks of gene and metabolic signatures indicative of high and low antibody response in these individuals. We observed age-related differences in metabolic baselines and signatures of antibody response to influenza vaccination and the abundance of alpha-linolenic and linoleic acids, sterol esters, fatty-acylcarnitines, and triacylglycerol metabolism. We identified a metabolomic signature associated with age-dependent vaccine response, finding increased tryptophan and decreased polyunsaturated fatty acids (PUFAs) in young high responders (HRs), while fatty acid synthesis and cholesteryl esters accumulated in older HRs. Integrated metabolomic and transcriptomic analysis shows that depletion of PUFAs, which are building blocks for prostaglandins and other lipid immunomodulators, in young HR subjects at Day 28 is related to a robust immune response to influenza vaccination. Increased glycerophospholipid levels were associated with an inflammatory response in older HRs to flu vaccination. This multi-omics approach uncovered age-related molecular markers associated with influenza vaccine response and provides insight into vaccine-induced metabolic responses that may help guide development of more effective influenza vaccines.

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