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用卵清蛋白对棕色挪威大鼠和三种小鼠品系进行口腔致敏实验。

Examination of oral sensitization with ovalbumin in Brown Norway rats and three strains of mice.

作者信息

Akiyama H, Teshima R, Sakushima J I, Okunuki H, Goda Y, Sawada J I, Toyoda M

机构信息

Division of Foods, National Institute of Health Sciences, 1-18-1, Kamiyoga, Setagaya-ku, Tokyo 158-8501, Japan.

出版信息

Immunol Lett. 2001 Aug 1;78(1):1-5. doi: 10.1016/s0165-2478(01)00229-2.

DOI:10.1016/s0165-2478(01)00229-2
PMID:11470144
Abstract

We studied the conditions needed to sensitize animals to the oral feeding of food allergens, without induction of tolerance, in order to investigate the allergenicity of orally ingested food proteins. Brown Norway (BN) rats were sensitized by daily OVA (ovalbumin)-gavage or by drinking OVA containing water ad libitum and the ASA (active systemic anaphylaxis) response, as the immediate hypersensitivity response to antigen stimulation after oral sensitization, was examined. The oral administration of OVA by gavage produced a higher OVA-specific IgE response and an increase in serum histamine after antigen challenge, as compared to those produced by drinking water. Next, we examined the effect of murine age, the oral feeding technique and the oral feeding dose on sensitization using BALB/c, B10A and ASK mice. Twenty-week-old mice showed the strongest OVA-specific IgE and IgG1 responses and ASA-associated serum histamine contents increased with gavage in the three different age groups of BALB/c mice. Administering 0.1 mg of OVA by gavage daily for 9 weeks appeared to induce a higher response than administering 1 mg of OVA, in terms of OVA-specific IgE and IgG1 antibody responses and ASA responses. Among the three strains of mice, B10A mice exhibited the highest response in terms of OVA-specific IgE and IgG1 antibody and ASA responses. These findings suggested BN rats and B10A mice were suitable models for oral sensitization with antigen protein and that oral sensitization in mice requires low dose, intermittent antigen intakes.

摘要

我们研究了使动物对口服食物过敏原敏感而不诱导耐受所需的条件,以调查口服摄入的食物蛋白的致敏性。通过每日卵清蛋白(OVA)灌胃或随意饮用含OVA的水使棕色挪威(BN)大鼠致敏,并检测作为口服致敏后对抗原刺激的速发型超敏反应的主动全身过敏反应(ASA)。与饮水相比,通过灌胃口服OVA在抗原攻击后产生了更高的OVA特异性IgE反应和血清组胺增加。接下来,我们使用BALB/c、B10A和ASK小鼠研究了小鼠年龄、口服喂养技术和口服喂养剂量对致敏的影响。在BALB/c小鼠的三个不同年龄组中,20周龄的小鼠表现出最强的OVA特异性IgE和IgG1反应,并且随着灌胃,与ASA相关的血清组胺含量增加。就OVA特异性IgE和IgG1抗体反应以及ASA反应而言,每天通过灌胃给予0.1mg OVA持续9周似乎比给予1mg OVA诱导更高的反应。在这三种小鼠品系中,B10A小鼠在OVA特异性IgE和IgG1抗体以及ASA反应方面表现出最高的反应。这些发现表明BN大鼠和B10A小鼠是用于抗原蛋白口服致敏的合适模型,并且小鼠口服致敏需要低剂量、间歇性的抗原摄入。

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Immunol Lett. 2001 Aug 1;78(1):1-5. doi: 10.1016/s0165-2478(01)00229-2.
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