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

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 heterogenei...

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Detalles Bibliográficos
Autores principales: Nouri, Nima, Cao, Raquel Giacomelli, Bunsow, Eleonora, Nehar-Belaid, Djamel, Marches, Radu, Xu, Zhaohui, Smith, Bennett, Heinonen, Santtu, Mertz, Sara, Leber, Amy, Smits, Gaby, van der Klis, Fiona, Mejías, Asunción, Banchereau, Jacques, Pascual, Virginia, Ramilo, Octavio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693608/
https://www.ncbi.nlm.nih.gov/pubmed/38042900
http://dx.doi.org/10.1038/s41467-023-43758-2
Descripción
Sumario: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(hi) 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(hi) 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.