Microsphere entrapped bee-venom phospholipase A2 retains specific IgE binding capacity:: a possible use for oral specific immunotherapy

被引:10
作者
Guérin, V [1 ]
Dubarry, M
Robic, D
Brachet, F
Rautureau, M
André, C
Bourbouze, R
Tomé, D
机构
[1] Inst Natl Agron Paris Grignon, Unite INRA Biol & Nutr Humaine, Paris, France
[2] Univ Paris 05, CNRS, UMR 8015, Fac Sci Pharmaceut & Biol, F-75270 Paris, France
[3] Lab Stallergenes SA, Antony, France
关键词
microspheres; IgE binding capacity; poly(D; L-lactide-co-glycolide); bee-venom phospholipase A2; allergen;
D O I
10.1080/02652040210162612
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The only specific treatments of allergy are long and exacting desensitization by subcutaneous injections of the allergens. While oral administration of allergens could greatly facilitate these treatments, effective delivery systems are needed to prevent allergen degradation in the gastrointestinal tract and to enable their uptake by Peyer's patches. The potential for bee-venom phospholipase A2 (PLA2) to be used in such oral immunotherapy was tested. For this purpose, PLA2 potential alterations were analysed when encapsulated into poly(D,L-lactide-co-glycolide) microspheres by double emulsion solvent evaporation. It was shown that microencapsulation had only limited effects on the integrity of the entrapped PLA2, which retained its fully specific murine IgE binding capacity. Thus, PLA2 loaded microspheres could represent a potential delivery system for bee venom allergy-specific oral immunotherapy.
引用
收藏
页码:761 / 765
页数:5
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