Kanegane Hirokazu
a Department of Child Health and Development, Graduate School of Medical and Dental Sciences , Tokyo Medical and Dental University (TMDU) , Tokyo , Japan.
Immunol Med. 2018 Dec;41(4):154-161. doi: 10.1080/25785826.2018.1556025. Epub 2019 Jan 11.
Recent advances in molecular biology have provided important insights into the genetic background of various inflammatory diseases. In particular, genome-wide association studies of inflammatory diseases have revealed genetic loci that play critical roles in the pathology of inflammation. Whole-exome and whole-genome sequencing analyses have also identified more than 300 causative genes for primary immunodeficiency diseases (PIDs). Some genetic loci that are associated with inflammatory diseases are mutated in PIDs, suggesting close relationships between inflammation and PIDs. Inflammatory diseases for which genetic associations have been described include inflammatory bowel disease (IBD), multiple sclerosis, rheumatoid arthritis, type 1 diabetes mellitus, and systemic lupus erythematosus. Herein, I discuss about the genetic interactions between IBD and PIDs.
分子生物学的最新进展为深入了解各种炎症性疾病的遗传背景提供了重要见解。特别是,炎症性疾病的全基因组关联研究已经揭示了在炎症病理过程中起关键作用的基因位点。全外显子组和全基因组测序分析也已经确定了300多个原发性免疫缺陷疾病(PID)的致病基因。一些与炎症性疾病相关的基因位点在PID中发生突变,这表明炎症与PID之间存在密切关系。已描述有遗传关联的炎症性疾病包括炎症性肠病(IBD)、多发性硬化症、类风湿性关节炎、1型糖尿病和系统性红斑狼疮。在此,我将讨论IBD与PID之间的遗传相互作用。