Chen Y L, Simons F E, Peng Z
Section of Allergy and Clinical Immunology, Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, Canada.
Int Arch Allergy Immunol. 1998 Aug;116(4):269-77. doi: 10.1159/000023955.
To date, there are no ideal animal models for study of natural sensitization leading to IgE- and lymphocyte-mediated hypersensitivities. We established such a model in which four BALB/c mice were each sensitized by exposure to at least 16 mosquito Aedes aegypti bites, twice a week for 4 weeks. Four non-exposed control mice were also studied. Mosquito A. aegypti head and thorax extract, saliva, and two recombinant salivary allergens (rAed a 1 and rAed a 2) were used in vitro as antigens. Intradermal tests were performed. Serum mosquito antigen-specific IgG, IgG1, IgG2a, and total IgE were measured by ELISA; specific IgE was measured by passive cutaneous anaphylaxis (PCA). IgE responses to each antigen in the saliva were analyzed using Western blotting. Spleen lymphocyte proliferation assays were performed to determine the cell-mediated hypersensitivity response. Antigen-induced IL-4 and IFN-gamma production in the spleen lymphocytes were evaluated using ELISA. After 4 weeks, all 4 mosquito-sensitized mice developed a positive immediate wheal 20 min after skin tests with mosquito antigens, and a positive delayed papule 24 h later, while control mice did not. Also, the sensitized mice had a positive PCA response, which correlated significantly with total IgE levels (r = 0.84, p<0.05), confirming the presence of antigen-specific IgE, while none of control mice had a positive response. Antigen-specific IgG1, but not IgG2a, was increased in the sensitized mice (p<0.01). Western blotting showed that 5 of the 8 antigens which elicited mouse IgE responses, including 2 major antigens, also elicited human IgE responses. The mean lymphocyte proliferation response to mosquito antigens also elicited human IgE responses. The mean lymphocyte proliferation response to mosquito antigens was significantly increased in the sensitized mice (p<0.05). IL-4 production was significantly increased and IFN-gamma production was decreased, further suggesting that a Th2 immune response predominates despite the development of the delayed skin reaction. This new model of natural sensitization without using an adjuvant is potentially useful for the study of other allergic disorders as well as mosquito allergy.
迄今为止,尚无用于研究导致IgE和淋巴细胞介导的超敏反应的自然致敏作用的理想动物模型。我们建立了这样一种模型,其中4只BALB/c小鼠每周两次、每次至少接受16次埃及伊蚊叮咬,持续4周以进行致敏。还对4只未暴露的对照小鼠进行了研究。体外使用埃及伊蚊头部和胸部提取物、唾液以及两种重组唾液变应原(rAed a 1和rAed a 2)作为抗原。进行了皮内试验。通过酶联免疫吸附测定(ELISA)测量血清中蚊子抗原特异性IgG、IgG1、IgG2a和总IgE;通过被动皮肤过敏反应(PCA)测量特异性IgE。使用蛋白质印迹法分析对唾液中每种抗原的IgE反应。进行脾淋巴细胞增殖试验以确定细胞介导的超敏反应。使用ELISA评估脾淋巴细胞中抗原诱导的白细胞介素-4(IL-4)和γ-干扰素(IFN-γ)的产生。4周后,所有4只经蚊子致敏的小鼠在用蚊子抗原进行皮肤试验后20分钟出现阳性即刻风团,24小时后出现阳性迟发性丘疹,而对照小鼠则未出现。此外,致敏小鼠有阳性PCA反应,与总IgE水平显著相关(r = 0.84,p<0.05),证实存在抗原特异性IgE,而对照小鼠均无阳性反应。致敏小鼠中抗原特异性IgG1升高,但IgG2a未升高(p<0.01)。蛋白质印迹法显示,在引发小鼠IgE反应的8种抗原中,有5种(包括2种主要抗原)也引发人类IgE反应。对蚊子抗原的平均淋巴细胞增殖反应也引发人类IgE反应。致敏小鼠中对蚊子抗原的平均淋巴细胞增殖反应显著增加(p<0.05)。IL-4产生显著增加而IFN-γ产生减少,进一步表明尽管出现了迟发性皮肤反应,但仍以Th2免疫反应为主导。这种不使用佐剂的自然致敏新模型可能对研究其他过敏性疾病以及蚊子过敏也有用。