Farncombe Family Digestive Health Research Institute, Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Gastroenterology. 2024 Jun;167(1):34-50. doi: 10.1053/j.gastro.2024.01.030. Epub 2024 Jan 28.
Celiac disease (CeD) is a chronic autoimmune condition driven by gluten ingestion in genetically predisposed individuals, resulting in inflammatory lesions in the proximal small intestine. Although the presence of specific HLA-linked haplotypes and gluten consumption are necessary for disease development, they alone do not account for the variable onset of CeD in susceptible individuals. This review explores the multifaceted role of non-host factors in CeD development, including dietary and microbial influences. We discuss clinical associations and observations highlighting the impact of these factors on disease onset and severity. Furthermore, we discuss studies in CeD-relevant animal models that offer mechanistic insights into how diet, the microbiome, and enteric infections modulate CeD pathogenesis. Finally, we address the clinical implications and therapeutic potential of understanding these cofactors offering a promising avenue for preventive and therapeutic interventions in CeD management.
乳糜泻(CeD)是一种由遗传易感性个体摄入麸质引起的慢性自身免疫性疾病,导致近端小肠炎症性病变。尽管特定的 HLA 连锁单倍型和麸质摄入是疾病发展的必要条件,但它们本身并不能解释易感性个体中 CeD 的可变发病。本综述探讨了非宿主因素在 CeD 发展中的多方面作用,包括饮食和微生物的影响。我们讨论了突出这些因素对疾病发病和严重程度影响的临床关联和观察结果。此外,我们还讨论了 CeD 相关动物模型中的研究,这些研究为饮食、微生物组和肠内感染如何调节 CeD 发病机制提供了机制上的见解。最后,我们讨论了理解这些协同因素的临床意义和治疗潜力,为 CeD 管理中的预防和治疗干预提供了有希望的途径。