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Published on: September 7, 2022
Stereotypic Immune System Development in Newborn Children
Axel Olin1, Ewa Henckel2, Yang Chen1
1Science for Life Laboratory, Department of Women's and Children's Health, Karolinska Institutet, 17121 Solna, Sweden.
Insights
Early life immune system development in newborns shows significant changes within the first three months. Microbial interactions drive this immune trajectory, but gut dysbiosis can impede it.
Area of Science:
- Immunology
- Neonatal Research
- Microbiome Studies
Background:
- Early life exposures significantly influence immune-mediated diseases.
- Infants are highly susceptible to infections, necessitating studies on early immune development.
- Existing research often uses animal models or cord blood, which don't capture postnatal environmental influences.
Purpose of the Study:
- To longitudinally analyze immune system development in newborns during the first three months of life.
- To identify changes in immune cell populations and plasma proteins after birth.
- To understand the factors influencing infant immune trajectories.
Main Methods:
- Longitudinal blood sampling (up to 4 times) from 100 newborns over their first 3 months.
- Mass cytometry analysis of 58 immune cell populations.
- Immunoassay analysis of 267 plasma proteins.
Main Results:
- Observed drastic, stereotypic immune system changes not predictable from cord blood data.
- Identified distinct immune profiles at birth for preterm and term infants that converge over time.
- Found evidence suggesting microbial interactions drive immune development, with gut dysbiosis as a potential hindrance.
Conclusions:
- Newborn immune development follows a predictable pattern influenced by postnatal exposures.
- Microbial factors, particularly gut bacteria, play a crucial role in shaping infant immunity.
- Early gut dysbiosis may negatively impact the trajectory of immune system maturation.
Abstract:
Epidemiological data suggest that early life exposures are key determinants of immune-mediated disease later in life. Young children are also particularly susceptible to infections, warranting more analyses of immune system development early in life. Such analyses mostly have been performed in mouse models or human cord blood samples, but these cannot account for the complex environmental exposures influencing human newborns after birth. Here, we performed longitudinal analyses in 100 newborn children, sampled up to 4 times during their first 3 months of life. From 100 μL of blood, we analyze the development of 58 immune cell populations by mass cytometry and 267 plasma proteins by immunoassays, uncovering drastic changes not predictable from cord blood measurements but following a stereotypic pattern. Preterm and term children differ at birth but converge onto a shared trajectory, seemingly driven by microbial interactions and hampered by early gut bacterial dysbiosis.
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