iScience
Volume 24, Issue 9, 24 September 2021, 102970
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Article
Endoplasmic reticulum stress response and bile acid signatures associate with multi-strain seroresponsiveness during elderly influenza vaccination

https://doi.org/10.1016/j.isci.2021.102970Get rights and content
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Highlights

  • Seroprotected elderly had heterogeneous titre responses to all three influenza strains

  • Multi-strain responses are linked to distinct transcriptomic and bile acid profiles

  • XBP-1 related pathways are specifically enriched in complete responders

  • XBP-1 upregulation is better preserved in vaccinated complete responders

Summary

The elderly are an important target for influenza vaccination, and the determination of factors that underlie immune responsiveness is clinically valuable. We evaluated the immune and metabolic profiles of 205 elderly Singaporeans administered with Vaxigrip. Despite high seroprotection rates, we observed heterogeneity in the response. We stratified the cohort into complete (CR) or incomplete responders (IR), where IR exhibited signs of accelerated T cell aging. We found a higher upregulation of genes associated with the B-cell endoplasmic-reticulum stress response in CR, where XBP-1 acts as a key upstream regulator. B-cells from IR were incapable of matching the level of XBP-1 upregulation observed in CR after inducing ER stress with tunicamycin in vitro. Metabolic signatures also distinguished CR and IR – as CR presented with a greater diversity of bile acids. Our findings suggest that the ER-stress pathway activation could improve influenza vaccination in the elderly.

Subject areas

Immunology
Virology
Clinical microbiology
Cell biology

Data and code availability

  • The microarray data is available on Gene Expression Omnibus (NCBI) under the accession number GSE107990.

  • This paper does not report original code.

  • Any additional information required to reanalyze the data reported in this paper is available from the lead contact upon request.

Cited by (0)

5

These authors contributed equally

6

These authors contributed equally

7

Senior authors

8

Lead contact