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Differences in Regulatory Mechanisms Induced by β-Lactoglobulin and κ-Casein in Cow’s Milk Allergy Mouse Model–In Vivo and Ex Vivo Studies

The presence of various proteins, including modified ones, in food which exhibit diverse immunogenic and sensitizing properties increases the difficulty of predicting host immune responses. Still, there is a lack of sufficiently reliable and comparable data and research models describing allergens i...

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Autores principales: Złotkowska, Dagmara, Stachurska, Emilia, Fuc, Ewa, Wróblewska, Barbara, Mikołajczyk, Anita, Wasilewska, Ewa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911159/
https://www.ncbi.nlm.nih.gov/pubmed/33503831
http://dx.doi.org/10.3390/nu13020349
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author Złotkowska, Dagmara
Stachurska, Emilia
Fuc, Ewa
Wróblewska, Barbara
Mikołajczyk, Anita
Wasilewska, Ewa
author_facet Złotkowska, Dagmara
Stachurska, Emilia
Fuc, Ewa
Wróblewska, Barbara
Mikołajczyk, Anita
Wasilewska, Ewa
author_sort Złotkowska, Dagmara
collection PubMed
description The presence of various proteins, including modified ones, in food which exhibit diverse immunogenic and sensitizing properties increases the difficulty of predicting host immune responses. Still, there is a lack of sufficiently reliable and comparable data and research models describing allergens in dietary matrices. The aim of the study was to estimate the immunomodulatory effects of β-lactoglobulin (β-lg) in comparison to those elicited by κ-casein (κ-CN), in vivo and ex vivo, using naïve splenocytes and a mouse sensitization model. Our results revealed that the humoral and cellular responses triggered by β-lg and κ-CN were of diverse magnitudes and showed different dynamics in the induction of control mechanisms. β-Lg turned out to be more immunogenic and induced a more dominant Th1 response than κ-CN, which triggered a significantly higher IgE response. For both proteins, CD4(+) lymphocyte profiles correlated with CD4(+)CD25(+) and CD4(+)CD25(+)Foxp3(+) T cells induction and interleukin 10 secretion, but β-lg induced more CD4(+)CD25(+)Foxp3(-) Tregs. Moreover, ex vivo studies showed the risk of interaction of immune responses to different milk proteins, which may exacerbate allergy, especially the one caused by β-lg. In conclusion, the applied model of in vivo and ex vivo exposure to β-lg and κ-CN showed significant differences in immunoreactivity of the tested proteins (κ-CN demonstrated stronger allergenic potential than β-lg), and may be useful for the estimation of allergenic potential of various food proteins, including those modified in technological processes.
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spelling pubmed-79111592021-02-28 Differences in Regulatory Mechanisms Induced by β-Lactoglobulin and κ-Casein in Cow’s Milk Allergy Mouse Model–In Vivo and Ex Vivo Studies Złotkowska, Dagmara Stachurska, Emilia Fuc, Ewa Wróblewska, Barbara Mikołajczyk, Anita Wasilewska, Ewa Nutrients Article The presence of various proteins, including modified ones, in food which exhibit diverse immunogenic and sensitizing properties increases the difficulty of predicting host immune responses. Still, there is a lack of sufficiently reliable and comparable data and research models describing allergens in dietary matrices. The aim of the study was to estimate the immunomodulatory effects of β-lactoglobulin (β-lg) in comparison to those elicited by κ-casein (κ-CN), in vivo and ex vivo, using naïve splenocytes and a mouse sensitization model. Our results revealed that the humoral and cellular responses triggered by β-lg and κ-CN were of diverse magnitudes and showed different dynamics in the induction of control mechanisms. β-Lg turned out to be more immunogenic and induced a more dominant Th1 response than κ-CN, which triggered a significantly higher IgE response. For both proteins, CD4(+) lymphocyte profiles correlated with CD4(+)CD25(+) and CD4(+)CD25(+)Foxp3(+) T cells induction and interleukin 10 secretion, but β-lg induced more CD4(+)CD25(+)Foxp3(-) Tregs. Moreover, ex vivo studies showed the risk of interaction of immune responses to different milk proteins, which may exacerbate allergy, especially the one caused by β-lg. In conclusion, the applied model of in vivo and ex vivo exposure to β-lg and κ-CN showed significant differences in immunoreactivity of the tested proteins (κ-CN demonstrated stronger allergenic potential than β-lg), and may be useful for the estimation of allergenic potential of various food proteins, including those modified in technological processes. MDPI 2021-01-25 /pmc/articles/PMC7911159/ /pubmed/33503831 http://dx.doi.org/10.3390/nu13020349 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Złotkowska, Dagmara
Stachurska, Emilia
Fuc, Ewa
Wróblewska, Barbara
Mikołajczyk, Anita
Wasilewska, Ewa
Differences in Regulatory Mechanisms Induced by β-Lactoglobulin and κ-Casein in Cow’s Milk Allergy Mouse Model–In Vivo and Ex Vivo Studies
title Differences in Regulatory Mechanisms Induced by β-Lactoglobulin and κ-Casein in Cow’s Milk Allergy Mouse Model–In Vivo and Ex Vivo Studies
title_full Differences in Regulatory Mechanisms Induced by β-Lactoglobulin and κ-Casein in Cow’s Milk Allergy Mouse Model–In Vivo and Ex Vivo Studies
title_fullStr Differences in Regulatory Mechanisms Induced by β-Lactoglobulin and κ-Casein in Cow’s Milk Allergy Mouse Model–In Vivo and Ex Vivo Studies
title_full_unstemmed Differences in Regulatory Mechanisms Induced by β-Lactoglobulin and κ-Casein in Cow’s Milk Allergy Mouse Model–In Vivo and Ex Vivo Studies
title_short Differences in Regulatory Mechanisms Induced by β-Lactoglobulin and κ-Casein in Cow’s Milk Allergy Mouse Model–In Vivo and Ex Vivo Studies
title_sort differences in regulatory mechanisms induced by β-lactoglobulin and κ-casein in cow’s milk allergy mouse model–in vivo and ex vivo studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7911159/
https://www.ncbi.nlm.nih.gov/pubmed/33503831
http://dx.doi.org/10.3390/nu13020349
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