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

Nouri, Nima; Cao, Raquel Giacomelli; Bunsow, Eleonora; Nehar-Belaid, Djamel; Marches, Radu; Xu, Zhaohui; Smith, Bennett; Heinonen, Santtu et al. · Nat Commun · 2023

basic_science · Level V

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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 ISG<sup>hi</sup> 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+ ISG<sup>hi</sup> 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.

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