Orgel Kelly, Kulis Michael
Department of Pediatrics, Division of Allergy, Immunology, and Rheumatology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Methods Mol Biol. 2018;1799:39-47. doi: 10.1007/978-1-4939-7896-0_4.
Animal models of disease enable the study of the pathology, biomarkers, and treatments for the disease being studied. These models become particularly useful in the study of diseases, such as peanut allergy, that currently have no FDA-approved therapy options. Here, we describe a mouse model of peanut allergy using a peanut extract and cholera toxin that can be applied to both BALB/c and C3H/HeJ mouse strains. Sensitization is induced through the gastrointestinal tract resulting in elevated levels of peanut-specific IgE and anaphylaxis upon challenge with peanut proteins. This model has been used to study the cells and molecules involved in the development of peanut allergy and to evaluate novel immunotherapy approaches and the underlying mechanisms of immunotherapy. Potential utilities of this model are numerous and may include studies on microbial influences on peanut allergy and discovery of biomarkers of anaphylaxis.
疾病动物模型有助于研究所研究疾病的病理学、生物标志物和治疗方法。这些模型在研究目前尚无FDA批准治疗方案的疾病(如花生过敏)时特别有用。在此,我们描述一种使用花生提取物和霍乱毒素的花生过敏小鼠模型,该模型可应用于BALB/c和C3H/HeJ小鼠品系。通过胃肠道诱导致敏,导致花生特异性IgE水平升高,并在接触花生蛋白时引发过敏反应。该模型已用于研究参与花生过敏发展的细胞和分子,并评估新型免疫治疗方法及其免疫治疗的潜在机制。该模型的潜在用途众多,可能包括研究微生物对花生过敏的影响以及发现过敏反应的生物标志物。