Jones-Hall Yava L, Grisham Matthew B
Department of Comparative Pathobiology, Purdue University, West Lafayette, IN 47906, United States.
Department of Immunology and Molecular Microbiology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, United States.
Pathophysiology. 2014 Nov;21(4):267-88. doi: 10.1016/j.pathophys.2014.05.002. Epub 2014 May 27.
Inflammatory bowel diseases (IBD) are chronic, relapsing conditions of multifactorial etiology. The two primary diseases of IBD are Crohn's disease (CD) and ulcerative colitis (UC). Both entities are hypothesized to occur in genetically susceptible individuals due to microbial alterations and environmental contributions. The exact etiopathogenesis, however, is not known for either disease. A variety of mouse models of CD and UC have been developed to investigate the pathogenesis of these diseases and evaluate treatment modalities. Broadly speaking, the mouse models can be divided into 4 categories: genetically engineered, immune manipulated, spontaneous and erosive/chemically induced. No one mouse model completely recapitulates the immunopathology of CD or UC, however each model possesses particular similarities to human IBD and offers advantageous for specific details of IBD pathogenesis. Here we discuss the more commonly used models in each category and critically evaluate how the immunopathology induced compares to CD or UC, as well as the advantages and disadvantages associated with each model.
炎症性肠病(IBD)是病因多因素的慢性复发性疾病。IBD的两种主要疾病是克罗恩病(CD)和溃疡性结肠炎(UC)。这两种疾病都被认为是由于微生物改变和环境因素,在遗传易感个体中发生。然而,这两种疾病的确切发病机制尚不清楚。已经开发了多种CD和UC的小鼠模型来研究这些疾病的发病机制并评估治疗方式。一般来说,小鼠模型可分为4类:基因工程模型、免疫调控模型、自发模型和侵蚀性/化学诱导模型。然而,没有一种小鼠模型能完全重现CD或UC的免疫病理学特征,不过每种模型都与人类IBD有特定的相似之处,并为IBD发病机制的特定细节提供了优势。在这里,我们讨论每一类中更常用的模型,并批判性地评估所诱导的免疫病理学与CD或UC的比较,以及与每个模型相关的优缺点。