Nature Communications (Dec 2023)

Young infants display heterogeneous serological responses and extensive but reversible transcriptional changes following initial immunizations

  • Nima Nouri,
  • Raquel Giacomelli Cao,
  • Eleonora Bunsow,
  • Djamel Nehar-Belaid,
  • Radu Marches,
  • Zhaohui Xu,
  • Bennett Smith,
  • Santtu Heinonen,
  • Sara Mertz,
  • Amy Leber,
  • Gaby Smits,
  • Fiona van der Klis,
  • Asunción Mejías,
  • Jacques Banchereau,
  • Virginia Pascual,
  • Octavio Ramilo

DOI
https://doi.org/10.1038/s41467-023-43758-2
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 16

Abstract

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Abstract Infants necessitate vaccinations to prevent life-threatening infections. Our understanding of the infant immune responses to routine vaccines remains limited. We analyzed two cohorts of 2-month-old infants before vaccination, one week, and one-month post-vaccination. We report remarkable heterogeneity but limited antibody responses to the different antigens. Whole-blood transcriptome analysis in an initial cohort showed marked overexpression of interferon-stimulated genes (ISGs) and to a lesser extent of inflammation-genes at day 7, which normalized one month post-vaccination. Single-cell RNA sequencing in peripheral blood mononuclear cells from a second cohort identified at baseline a predominantly naive immune landscape including ISGhi cells. On day 7, increased expression of interferon-, inflammation-, and cytotoxicity-related genes were observed in most immune cells, that reverted one month post-vaccination, when a CD8+ ISGhi and cytotoxic cluster and B cells expanded. Antibody responses were associated with baseline frequencies of plasma cells, B-cells, and monocytes, and induction of ISGs at day 7.