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Breast milk IgA to foods has different epitope specificity than serum IgA—Evidence for entero‐mammary link for food‐specific IgA?
Author(s) -
Seppo A. E.,
Savilahti E. M.,
Berin M. C.,
Sampson H. A.,
Järvinen K. M.
Publication year - 2017
Publication title -
clinical and experimental allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 154
eISSN - 1365-2222
pISSN - 0954-7894
DOI - 10.1111/cea.12945
Subject(s) - epitope , antibody , immunogenicity , immunology , breast milk , colostrum , biology , milk allergy , casein , food allergy , allergy , immunoglobulin e , biochemistry
Summary Background We have previously shown that maternal cow's milk ( CM ) elimination results in downregulation of CM ‐specific IgA antibody levels in BM , but not in serum, suggesting that an entero‐mammary link may exist for food‐specific antibody‐secreting cells. Objective We sought to investigate whether food‐specific IgA epitope profiles differ intra‐individually between mother's serum and BM . We also examined how infants’ food epitope‐specific IgA develops in early infancy and the relationship of IgA epitope recognition with development of cow's milk allergy ( CMA ). Methods We measured specific IgA to a series of overlapping peptides in major CM allergens (α s1 ‐, α s2 ‐, β‐ and κ‐caseins and β‐lactoglobulin) in paired maternal and infant serum as well as BM samples in 31 mother‐infant dyads within the first 15 post‐partum months utilizing peptide microarray. Results There was significant discordance in epitope specificity between BM and maternal sera ranging from only 13% of sample pairs sharing at least one epitope in α s1 ‐casein to 73% in κ‐casein. Epitope‐specific IgA was detectable in infants’ sera starting at less than 3 months of age. Sera of mothers with a CMA infant had increased binding of epitope‐specific IgA to CM proteins compared to those with a non‐ CMA infant. Conclusion & Clinical Relevance These findings support the concept that mother's milk has a distinct antifood antibody repertoire when compared to the antibody repertoire of the peripheral blood. Increased binding of serum epitope‐specific IgA to CM in mothers of infants with CMA may reflect inherited systemic immunogenicity of CM proteins in these families, although specific IgA in breast milk was not proportionally up‐regulated.

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