Micronutritional supplementation with a holoBLG‐based FSMP (food for special medical purposes)‐lozenge alleviates allergic symptoms in BALB/c mice: Imitating the protective farm effect

含片 脱颗粒 免疫球蛋白E 免疫系统 免疫学 抗原 化学 食物过敏 药理学 医学 过敏 生物化学 受体 抗体 历史 考古
作者
Sheriene Moussa Afify,Andreas Regner,Luis F. Pacios,Bart R. Blokhuis,Sebastian Jensen,Frank A. Redegeld,Isabella Pali‐Schöll,Karin Hufnagl,Rodolfo Bianchini,Sonja Guethoff,Matthias Krämer,Alessandro Fiocchi,Zdeněk Dvořák,Erika Jensen‐Jarolim,Franziska Roth‐Walter
出处
期刊:Clinical & Experimental Allergy [Wiley]
卷期号:52 (3): 426-441 被引量:23
标识
DOI:10.1111/cea.14050
摘要

Abstract Background Previously, the protective farm effect was imitated using the whey protein beta‐lactoglobulin (BLG) that is spiked with iron‐flavonoid complexes. Here, we formulated for clinical translation a lozenge as food for special medical purposes (FSMP) using catechin‐iron complexes as ligands for BLG. The lozenge was tested in vitro and in a therapeutical BALB/c mice model. Methods Binding of iron‐catechin into BLG was confirmed by spectroscopy and docking calculations. Serum IgE binding of children allergic or tolerating milk was assessed to loaded (holo‐) versus empty (apo‐) BLG and for human mast cell degranulation. BLG and Bet v 1 double‐sensitized mice were orally treated with the holoBLG or placebo lozenge, and immunologically analysed after systemic allergen challenge. Human PBMCs of pollen allergic subjects were flow cytometrically assessed after stimulation with apoBLG or holoBLG using catechin‐iron complexes as ligands. Results One major IgE and T cell epitope were masked by catechin‐iron complexes, which impaired IgE binding of milk‐allergic children and degranulation of mast cells. In mice, only supplementation with the holoBLG lozenge reduced clinical reactivity to BLG and Bet v 1, promoted Tregs, and suppressed antigen presentation. In allergic subjects, stimulation of PBMCs with holoBLG led to a significant increase of intracellular iron in circulating CD14+ cells with significantly lower expression of HLADR and CD86 compared to their stimulation with apoBLG. Conclusion The FSMP lozenge targeted antigen presenting cells and dampened immune activation in human immune cells and allergic mice in an antigen‐non‐specific manner, thereby conferring immune resilience against allergic symptoms.
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