It is widely believed that cow's milk proteins ingested by the mother, in particular beta-lactoglobulin (beta-LG), can pass into breast milk and thus sensitize predisposed infants. However, studies to evaluate bovine beta-LG in human milk have given conflicting results. The aim of this study was to analyse the correlation between the amount of cow's milk in the mother's diet and the presence of bovine beta-LG in breast milk. Human milk samples from 14 healthy non-atopic women on diets with different cow's milk contents were examined. The total concentration of bovine beta-LG or beta-LG immuno-like proteins (beta-LGIP) was determined by enzyme-linked immunosorbent assay (ELISA). Two separation procedures utilizing ELISA plates and an affinity chromatography column were set up to identify the human whey components recognized by the anti-beta-LG antibodies. beta-LGIP reactivities of milk from three groups on different diets were not significantly different. After splitting the antigen-antibody complexes, three main protein components, human lactoferrin, human beta-casein and human alpha-lactalbumin, were identified. This study would suggest that, at least in healthy subjects, false-positive results in ELISA determinations of bovine beta-LG in human milk might be due to cross-reactions between polyclonal antibodies and different protein antigens.

Human milk proteins may interfere in ELISA measurements of bovine beta-lactoglobulin in human milk.

BERTINO, Enrico;FABRIS, Claudio;MARTINO, Silvana;CARDAROPOLI, Simona;
1996-01-01

Abstract

It is widely believed that cow's milk proteins ingested by the mother, in particular beta-lactoglobulin (beta-LG), can pass into breast milk and thus sensitize predisposed infants. However, studies to evaluate bovine beta-LG in human milk have given conflicting results. The aim of this study was to analyse the correlation between the amount of cow's milk in the mother's diet and the presence of bovine beta-LG in breast milk. Human milk samples from 14 healthy non-atopic women on diets with different cow's milk contents were examined. The total concentration of bovine beta-LG or beta-LG immuno-like proteins (beta-LGIP) was determined by enzyme-linked immunosorbent assay (ELISA). Two separation procedures utilizing ELISA plates and an affinity chromatography column were set up to identify the human whey components recognized by the anti-beta-LG antibodies. beta-LGIP reactivities of milk from three groups on different diets were not significantly different. After splitting the antigen-antibody complexes, three main protein components, human lactoferrin, human beta-casein and human alpha-lactalbumin, were identified. This study would suggest that, at least in healthy subjects, false-positive results in ELISA determinations of bovine beta-LG in human milk might be due to cross-reactions between polyclonal antibodies and different protein antigens.
1996
85(5)
543
549
Bertino E; Prandi GM; Fabris C; Cavaletto M; Martino S; Cardaropoli S; Calderone V; Conti A.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/31733
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