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Published on: August 12, 2020
Breastfeeding and Neonatal Age Influence Neutrophil-Driven Ontogeny of Blood Cell Populations in the First Week of
Sebastiano Montante1, Rym Ben-Othman2,3, Nelly Amenyogbe2,4
1BC Cancer Agency, 675 West 10th Avenue, Vancouver V5Z 1G1, BC, Canada.
Insights
Newborns exhibit conserved white blood cell (WBC) changes, influenced by breastfeeding and vaccination. This early immune development offers a window for interventions to shape lifelong immune health.
Area of Science:
- Human immunology
- Neonatal immune development
- Comparative cohort studies
Background:
- The first week of life is critical for immune system adaptation, impacting lifelong health.
- Early life immune development trajectories are not well understood.
- Standardized phenotyping is needed to map immune changes in newborns.
Purpose of the Study:
- To characterize peripheral white blood cell (WBC) population dynamics in newborns.
- To identify factors influencing early immune development trajectories.
- To explore potential windows for immune-modulating interventions.
Main Methods:
- High-throughput, standardized flow cytometry phenotyping of WBCs from 796 newborns across two cohorts.
- Unbiased automated gating analysis of peripheral blood samples collected at birth and Days 1, 3, or 7.
- Comparative analysis of immune cell composition across different time points and populations.
Main Results:
- Newborn WBC composition follows conserved developmental patterns across diverse environments.
- Innate myeloid compartment shows the most significant changes in the first week of life.
- Breastfeeding and neonatal vaccination correlate with neutrophil and monocyte count alterations.
Conclusions:
- Newborn immune development follows a common trajectory, potentially influenced by breastfeeding timing.
- Early life immune patterns may offer protection against infections.
- These findings highlight a critical window for interventions to shape neonatal immune ontogeny.
Abstract:
The first few days of life are characterized by rapid external and internal changes that require substantial immune system adaptations. Despite growing evidence of the impact of this period on lifelong immune health, this period remains largely uncharted. To identify factors that may impact the trajectory of immune development, we conducted stringently standardized, high-throughput phenotyping of peripheral white blood cell (WBC) populations from 796 newborns across two distinct cohorts (The Gambia, West Africa; Papua New Guinea, Melanesia) in the framework of a Human Immunology Project Consortium (HIPC) study. Samples were collected twice from each newborn during the first week of life, first at Day of Life 0 (at birth) and then subsequently at Day of Life 1, 3, or 7 depending on the randomization group the newborn belongs to. The subsequent analysis was conducted at an unprecedented level of detail using flow cytometry and an unbiased automated gating algorithm. The results showed that WBC composition in peripheral blood changes along patterns highly conserved across populations and environments. Changes across days of life were most pronounced in the innate myeloid compartment. Breastfeeding, and at a smaller scale neonatal vaccination, were associated with changes in peripheral blood neutrophil and monocyte cell counts. Our results suggest a common trajectory of immune development in newborns and possible association with timing of breastfeeding initiation, which may contribute to immune-mediated protection from infection in early life. These data begin to outline a specific window of opportunity for interventions that could deliberately direct WBC composition, and with that, immune trajectory and thus ontogeny in early life. This trial is registered with NCT03246230.
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