Immunomodulating properties of protein hydrolysates for application in cow's milk allergy

被引:36
作者
Kiewiet, M. B. G. [1 ]
Gros, M. [2 ]
van Neerven, R. J. J. [2 ]
Faas, M. M. [1 ]
de Vos, P. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol & Med Biol, Immunoendocrinol,Div Med Biol, NL-9713 GZ Groningen, Netherlands
[2] FrieslandCampina, Amersfoort, Netherlands
关键词
epithelial barrier; food allergy; hydrolysates; Th1; Th2; balance; Toll-like receptor; T-CELLS; INTESTINAL BARRIER; CASEIN HYDROLYSATE; BIOACTIVE PEPTIDES; ATOPIC-DERMATITIS; VIBRIO-CHOLERAE; ORAL TOLERANCE; WHEY; PREVENTION; BACTERIA;
D O I
10.1111/pai.12354
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Cow's milk proteins cause allergic symptoms in 2-3% of all infants. In these individuals, the tolerogenic state of the intestinal immune system is broken, which can lead to sensitization against antigens and eventually to allergic responses. Although a true treatment for food allergy is not available, symptoms can be avoided by providing the infants with hydrolyzed proteins. Hydrolyzed proteins are proteins that are enzymatically degraded. They lack typical allergenic IgE-binding epitopes but are also thought to play a pertinent role in other mechanisms inducing hypoallergenic effects. This review discusses the mechanisms and evidence for immunomodulating properties of cow's milk hydrolysates. Hydrolysates are found to strengthen the epithelial barrier, modulate T-cell differentiation, and decrease inflammation. Some studies suggest a role for hydrolysates in manipulating pathogen recognition receptors signaling as underlying mechanism. Peptides from hydrolysates have been shown to bind to TLR2 and TLR4 and influence cytokine production in epithelial cells and macrophages. Current insight suggests that hydrolysates may actively participate in modulating the immune responses in subjects with cow's milk allergy and those at risk to develop cow's milk allergy. However, more research is required to design effective and reproducible means to develop targeting strategies to modulate the immune response.
引用
收藏
页码:206 / 217
页数:12
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