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

Nat Commun. 2023 Dec 2;14(1):7976. doi: 10.1038/s41467-023-43758-2.

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.

MeSH terms

  • Gene Expression Profiling
  • Humans
  • Infant
  • Inflammation / metabolism
  • Interferons* / metabolism
  • Leukocytes, Mononuclear* / metabolism
  • Vaccination

Substances

  • Interferons