Author
Listed:
- Nima Nouri
(The Jackson Laboratory for Genomic Medicine
Precision Medicine and Computational Biology, Sanofi)
- Raquel Giacomelli Cao
(Abigail Wexner Research Institute at Nationwide Children’s Hospital
Nationwide Children’s Hospital, and The Ohio State University College of Medicine)
- Eleonora Bunsow
(Abigail Wexner Research Institute at Nationwide Children’s Hospital)
- Djamel Nehar-Belaid
(The Jackson Laboratory for Genomic Medicine)
- Radu Marches
(The Jackson Laboratory for Genomic Medicine)
- Zhaohui Xu
(Abigail Wexner Research Institute at Nationwide Children’s Hospital
St. Jude Children’s Research Hospital)
- Bennett Smith
(Abigail Wexner Research Institute at Nationwide Children’s Hospital)
- Santtu Heinonen
(Abigail Wexner Research Institute at Nationwide Children’s Hospital
Helsinki University Hospital and University of Helsinki)
- Sara Mertz
(Abigail Wexner Research Institute at Nationwide Children’s Hospital)
- Amy Leber
(Nationwide Children’s Hospital)
- Gaby Smits
(National Institute for Public Health and the Environment (RIVM))
- Fiona Klis
(National Institute for Public Health and the Environment (RIVM))
- Asunción Mejías
(Abigail Wexner Research Institute at Nationwide Children’s Hospital
Nationwide Children’s Hospital, and The Ohio State University College of Medicine
St. Jude Children’s Research Hospital)
- Jacques Banchereau
(The Jackson Laboratory for Genomic Medicine
Immunai)
- Virginia Pascual
(Weill Cornell Medicine)
- Octavio Ramilo
(Abigail Wexner Research Institute at Nationwide Children’s Hospital
Nationwide Children’s Hospital, and The Ohio State University College of Medicine
St. Jude Children’s Research Hospital)
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.
Suggested Citation
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 Klis & Asunción M, 2023.
"Young infants display heterogeneous serological responses and extensive but reversible transcriptional changes following initial immunizations,"
Nature Communications, Nature, vol. 14(1), pages 1-16, December.
Handle:
RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43758-2
DOI: 10.1038/s41467-023-43758-2
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