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Immunoglobulin A concentration is lower in mothers’ own milk and infant stool in infants who develop necrotising enterocolitis

Lookup NU author(s): Dr Claire Granger, Dr Andrea MasiORCiD, Professor Chris LambORCiD, Professor Nicholas EmbletonORCiD, Dr Lauren BeckORCiD, Dr Jeremy PalmerORCiD, Professor Christopher StewartORCiD, Professor Janet Berrington

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

© The Author(s), under exclusive licence to the International Pediatric Research Foundation, Inc 2025.Background: Immunoglobulin A (IgA) binding gut bacteria may modulate necrotising enterocolitis (NEC). In infants <32 weeks gestation exclusively receiving their mother’s own milk (MOM) who either did or did not develop NEC, we explored IgA concentration in MOM and infant stool. Methods: We quantified IgA and secretory IgA (sIgA) concentration by enzyme linked immunosorbent assay (ELISA). 41 NEC (median onset day 22) and 44 matched control infants, median gestation 25 weeks, contributed 202 MOM and 92 stool samples. Results: IgA and sIgA in MOM were significantly lower for the first three weeks in infants developing NEC compared to control infants (median IgA 499 μg/ml vs 1261 µg/ml, sIgA 481 µg/ml versus 1023 µg/ml, adjusted p < 0.001 between 0–6 and 7–13 days of life, adjusted p = 0.029 days 14–20). Stool IgA concentration before disease was also significantly lower in NEC infants compared with control infants (262 µg/ml versus 491 µg/ml, p = 0.045), but there was no statistical difference in sIgA. Conclusion: IgA and sIgA are lower in early MOM (before week 3 of life) received by infants who go on to develop NEC, reflected in lower stool IgA. Potential mechanisms require further elucidation. Targeted use of high IgA donor milk to preterm infants may be beneficial. Impact: This is the first published work that evaluates both milk and stool IgA and sIgA in control preterm infants and those developing NEC and has the benefit of samples taken before disease onset for some infants. In this study, IgA and sIgA are lower in early MOM (before week 3 of life) received by infants who go on to develop NEC, reflected in lower stool IgA. Targeted use of high IgA donor milk to preterm infants may be beneficial. Clinical practice in the interim should focus on maximising fresh MOM delivery to preterm babies.


Publication metadata

Author(s): Granger CL, Masi AC, Lamb CA, Embleton ND, Beck LC, Palmer JM, Stewart CJ, Berrington JE

Publication type: Article

Publication status: Published

Journal: Pediatric Research

Year: 2025

Pages: epub ahead of print

Online publication date: 03/12/2025

Acceptance date: 04/10/2025

Date deposited: 15/12/2025

ISSN (print): 0031-3998

ISSN (electronic): 1530-0447

Publisher: Springer Nature

URL: https://doi.org/10.1038/s41390-025-04570-4

DOI: 10.1038/s41390-025-04570-4

PubMed id: 41339769


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Funding

Funder referenceFunder name
Danone Early Life Nutrition
Human Milk Foundation (HMF)
Nestle Nutrition Institute
NIHR
Prolacta Biosciences

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