Department of Pediatrics, University of North Carolina School of Medicine, Chapel Hill, NC; University of North Carolina Food Allergy Initiative, Chapel Hill, NC.
Department of Genetics, University of North Carolina School of Medicine, Chapel Hill, NC.
J Allergy Clin Immunol. 2019 Mar;143(3):1027-1037.e7. doi: 10.1016/j.jaci.2018.10.009. Epub 2018 Oct 19.
Improved animal models are needed to understand the genetic and environmental factors that contribute to food allergy.
We sought to assess food allergy phenotypes in a genetically diverse collection of mice.
We selected 16 Collaborative Cross (CC) mouse strains, as well as the classic inbred C57BL/6J, C3H/HeJ, and BALB/cJ strains, for screening. Female mice were sensitized to peanut intragastrically with or without cholera toxin and then challenged with peanut by means of oral gavage or intraperitoneal injection and assessed for anaphylaxis. Peanut-specific immunoglobulins, T-cell cytokines, regulatory T cells, mast cells, and basophils were quantified.
Eleven of the 16 CC strains had allergic reactions to intraperitoneal peanut challenge, whereas only CC027/GeniUnc mice reproducibly experienced severe symptoms after oral food challenge (OFC). CC027/GeniUnc, C3H/HeJ, and C57BL/6J mice all mounted a T2 response against peanut, leading to production of IL-4 and IgE, but only the CC027/GeniUnc mice reacted to OFC. Orally induced anaphylaxis in CC027/GeniUnc mice was correlated with serum levels of Ara h 2 in circulation but not with allergen-specific IgE or mucosal mast cell protease 1 levels, indicating systemic allergen absorption is important for anaphylaxis through the gastrointestinal tract. Furthermore, CC027/GeniUnc, but not C3H/HeJ or BALB/cJ, mice can be sensitized in the absence of cholera toxin and react on OFC to peanut.
We have identified and characterized CC027/GeniUnc mice as a strain that is genetically susceptible to peanut allergy and prone to severe reactions after OFC. More broadly, these findings demonstrate the untapped potential of the CC population in developing novel models for allergy research.
为了深入了解导致食物过敏的遗传和环境因素,我们需要建立更完善的动物模型。
我们旨在评估基因多样化的小鼠群体中的食物过敏表型。
我们选择了 16 种 CC(Collaborative Cross)小鼠品系,以及经典近交系 C57BL/6J、C3H/HeJ 和 BALB/cJ 品系进行筛选。雌性小鼠通过胃内给予花生和霍乱毒素进行致敏,然后通过口服灌胃或腹腔注射进行花生激发,并评估过敏反应。定量检测花生特异性免疫球蛋白、T 细胞细胞因子、调节性 T 细胞、肥大细胞和嗜碱性粒细胞。
在 16 种 CC 品系中,有 11 种品系对腹腔内花生挑战有过敏反应,而只有 CC027/GeniUnc 小鼠在口服食物挑战(OFC)后会反复出现严重症状。CC027/GeniUnc、C3H/HeJ 和 C57BL/6J 小鼠均对花生产生了 T2 反应,导致产生 IL-4 和 IgE,但只有 CC027/GeniUnc 小鼠对 OFC 有反应。CC027/GeniUnc 小鼠口服诱导的过敏反应与循环中 Ara h 2 的血清水平相关,但与过敏原特异性 IgE 或黏膜肥大细胞蛋白酶 1 水平无关,这表明胃肠道吸收的全身性过敏原对过敏反应很重要。此外,CC027/GeniUnc 但不是 C3H/HeJ 或 BALB/cJ 小鼠,在没有霍乱毒素的情况下也可以致敏,并对 OFC 中的花生产生反应。
我们已经鉴定并描述了 CC027/GeniUnc 作为一种对花生过敏易感且在 OFC 后易发生严重反应的品系。更广泛地说,这些发现证明了 CC 群体在开发过敏研究新模型方面具有尚未开发的潜力。