ULB Center for Diabetes Research, Medical Faculty, Université Libre de Bruxelles (ULB), Brussels, Belgium.
Interuniversity Institute of Bioinformatics in Brussels, Université Libre de Bruxelles-Vrije Universiteit Brussel, Brussels, Belgium.
Sci Adv. 2021 Jan 6;7(2). doi: 10.1126/sciadv.abd7600. Print 2021 Jan.
Autoimmune diseases are typically studied with a focus on the immune system, and less attention is paid to responses of target tissues exposed to the immune assault. We presently evaluated, based on available RNA sequencing data, whether inflammation induces similar molecular signatures at the target tissues in type 1 diabetes, systemic lupus erythematosus, multiple sclerosis, and rheumatoid arthritis. We identified confluent signatures, many related to interferon signaling, indicating pathways that may be targeted for therapy, and observed a high (>80%) expression of candidate genes for the different diseases at the target tissue level. These observations suggest that future research on autoimmune diseases should focus on both the immune system and the target tissues, and on their dialog. Discovering similar disease-specific signatures may allow the identification of key pathways that could be targeted for therapy, including the repurposing of drugs already in clinical use for other diseases.
自身免疫性疾病通常主要研究免疫系统,而对暴露于免疫攻击的靶组织的反应关注较少。我们目前根据现有 RNA 测序数据评估了炎症是否会在 1 型糖尿病、系统性红斑狼疮、多发性硬化症和类风湿关节炎的靶组织中引起类似的分子特征。我们发现了趋同的特征,许多与干扰素信号有关,这表明可能有针对治疗的途径,并且在靶组织水平上观察到不同疾病的候选基因的高(>80%)表达。这些观察结果表明,未来对自身免疫性疾病的研究应该既关注免疫系统和靶组织,又关注它们之间的对话。发现类似的疾病特异性特征可能允许确定可以针对治疗的关键途径,包括重新利用已经用于其他疾病的临床药物。