Protease-digested egg-white products induce oral tolerance in mice but elicit little IgE production upon epicutaneous exposure

Protease-digested egg-white products induce oral tolerance in mice but elicit little IgE production upon epicutaneous exposure
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蛋白酶消化的蛋清产品可诱导小鼠口服耐受,但经皮暴露后几乎不会产生 IgE

DOI:
10.1016/j.alit.2022.03.006
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发表时间:
2022
影响因子:
6.8
通讯作者:
Matsumoto Kenji
Matsumoto Kenji
中科院分区:
医学2区
文献类型:
--
作者:
Yamada Ayako;Hasegawa Takanori;Fujieda Mikiya;Morita Hideaki;Matsumoto Kenji

文献摘要

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背景:早期食物引入诱导耐受,但表皮暴露,特别是通过湿疹病变,促进IgE致敏。为了安全有效地一级预防鸡蛋过敏,我们检查了几种蛋白酶消化的蛋清(EW)产品的三种特性:1)诱导口服耐受性,防止IgE致敏,2)弱的IgE结合,即使在IgE致敏的小鼠中也可以预防过敏反应,以及3)即使与发炎的皮肤接触,表皮IgE致敏作用也很小。方法:在最佳条件下用多种蛋白酶消化加热的EW。首先,三周龄的BALB/c雌性小鼠灌胃给予EW或每种蛋白酶消化的EW产品,然后腹腔内注射卵清蛋白(OVA)或卵类粘蛋白(OVM)与明矾。测定血清OVA和OVM特异性IgE滴度。其次,用OVA/OVM致敏6周龄小鼠,并在腹腔内施用EW或每种蛋白酶消化的EW后测量直肠温度。第三,将EW或每种蛋白酶消化的EW产品施用于胶带剥离的皮肤,每周3天,持续3周。结果:口服胃蛋白酶消化的EW产品(PDEW)和Thermoase PC 10 F消化的EW产品(TDEW)可显著抑制OVA/OVM特异性IgE的产生。两种产品均未引起OVA/OVM致敏小鼠体温下降(过敏反应)。血清OVA-/OVM特异性IgE水平显着降低小鼠epicuphilis暴露于PDEW或TDEW比EW暴露mice.Conclusions:两种蛋白酶消化的EW显示出潜在的最佳EW产品,为早期引进鸡蛋过敏的一级预防。
Background: Early food introduction induces tolerance, but epicutaneous exposure, especially via eczema lesions, promotes IgE sensitization. Aiming for safe and effective primary prevention of egg allergy, we examined several protease-digested egg-white (EW) products for three properties: 1) induction of oral tolerance that prevents IgE sensitization, 2) weak IgE binding that can prevent allergic reactions even in IgE-sensitized mice, and 3) minimal epicutaneous IgE sensitization even when in contact with inflamed skin.Methods: Heated EW was digested with several proteases under optimal conditions. First, three-week-old BALB/c female mice were intragastrically administered EW or each protease-digested EW product, followed by intraperitoneal ovalbumin (OVA) or ovomucoid (OVM) injection with alum. Serum OVA-and OVM-specific IgE titers were measured. Second, six-week-old mice were sensitized with OVA/OVM, and the rectal temperature was measured after intraperitoneal administration of EW or each protease-digested EW. Third, EW or each protease-digested EW product was applied to the tape-stripped skin for 3 days/week for 3 weeks. Serum OVA-and OVM-specific IgE titers were measured.Results: Orally administered pepsin-digested EW product (PDEW) and Thermoase PC10F-digested EW product (TDEW) significantly suppressed OVA-/OVM-specific IgE production. Neither product elicited a body temperature decline (anaphylaxis) in OVA-/OVM-sensitized mice. Serum OVA-/OVM-specific IgE levels were significantly lower in mice epicutaneously exposed to PDEW or TDEW than in EW-exposed mice.Conclusions: Two protease-digested EWs showed potential as optimal EW products for early introduction for primary prevention of egg allergy.