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Published on: September 6, 2019
Formula feeding skews immune cell composition toward adaptive immunity compared to breastfeeding
Yvonne Andersson1, Marie-Louise Hammarström, Bo Lönnerdal
1Department of Clinical Sciences, Pediatrics, Umeå University, Umeå SE-901 87, Sweden.
Insights
Infant feeding impacts immune cell development. Breastfeeding promotes steady immune cell composition, while formula feeding may delay innate immunity cell recruitment and enhance adaptive immunity cell maturation.
Area of Science:
- Immunology
- Pediatrics
- Nutrition
Background:
- The ontogeny of infant immune systems and the influence of feeding type remain incompletely understood.
- Early life nutrition significantly shapes immune system development and function.
Purpose of the Study:
- To analyze immune cell frequencies and composition in breastfed (BF) versus formula-fed (FF) infants.
- To compare the effects of different infant formulas on immune cell development.
Main Methods:
- Flow cytometry and immunoflow cytometry were used to analyze whole blood and peripheral blood mononuclear cells (PBMCs).
- Immune cell populations were assessed in exclusively BF infants and infants fed one of three different formulas at 1.5, 4, and 6 months of age.
Main Results:
- Breastfed infants showed increased neutrophils and stable lymphocyte proportions (CD4+ T cells, CD8+ T cells, B cells, NK cells, gammadelta T cells) from 1.5 to 6 months.
- Formula-fed infants had a decreased proportion of NK cells but increased naive CD4+ T cells and an elevated CD4/CD8 ratio compared to breastfed infants.
- No significant differences in immune cell composition were observed among the three formula groups.
Conclusions:
- Infant feeding type significantly influences immune cell ontogeny.
- Formula feeding is associated with delayed recruitment of innate immunity cells (NK cells) and accelerated maturation of adaptive immunity cells (naive CD4+ T cells) compared to breastfeeding.
Abstract:
The ontogeny of the immune system and the effect thereon by type of infant feeding is incompletely understood. We analyzed frequencies and composition of immune cells in blood of breastfed (BF) and formula-fed (FF) infants at 1.5, 4, and 6 mo of age. Three formulas with the same protein concentration but with varying levels of alpha-lactalbumin and caseinoglycomacropeptide were compared. Twenty-nine exclusively BF infants served as reference, and 17 infants in each formula group completed the study. Whole blood and PBMCs were analyzed by flow cytometry and immunoflow cytometry, respectively. Leukocyte count of BF infants increased with time due to increased frequency of neutrophils. Lymphocyte count was high at 1.5 mo and was unchanged over time, as were the relative proportions of CD4+ alphabetaT cells, CD8+ alphabetaT cells, B cells, NK cells, and gammadeltaT cells. Most CD45R0+CD3+ cells were HLA-DR- and hence memory cells. Compared with breastfeeding, formula feeding resulted in a significant decrease in proportion of NK cells, but a significant increase in naive CD4+ alphabetaT cells and an elevated CD4-to-CD8 ratio, that is, 3.3 in the combined FF groups compared with 2.6 in the BF group. No significant differences were found between the three groups of FF infants. In conclusion, blood cells of lymphoid lineage did not change significantly in frequencies or composition from 1.5 to 6 mo of age in BF infants. In contrast, FF infants displayed an ongoing maturation of adaptive immunity cells and a delayed recruitment of innate immunity cells as compared with BF infants.
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