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使用相互作用组学区分单纯性鼻炎和伴哮喘的鼻炎。

Distinction between rhinitis alone and rhinitis with asthma using interactomics.

机构信息

6AM Data Mining, Barcelona, Spain.

Institute for Advanced Biosciences, UGA-INSERM U1209-CNRS UMR5309, Site Santé, Allée des Alpes, La Tronche, France.

出版信息

Sci Rep. 2023 Aug 12;13(1):13125. doi: 10.1038/s41598-023-39987-6.

Abstract

The concept of "one-airway-one-disease", coined over 20 years ago, may be an over-simplification of the links between allergic diseases. Genomic studies suggest that rhinitis alone and rhinitis with asthma are operated by distinct pathways. In this MeDALL (Mechanisms of the Development of Allergy) study, we leveraged the information of the human interactome to distinguish the molecular mechanisms associated with two phenotypes of allergic rhinitis: rhinitis alone and rhinitis in multimorbidity with asthma. We observed significant differences in the topology of the interactomes and in the pathways associated to each phenotype. In rhinitis alone, identified pathways included cell cycle, cytokine signalling, developmental biology, immune system, metabolism of proteins and signal transduction. In rhinitis and asthma multimorbidity, most pathways were related to signal transduction. The remaining few were related to cytokine signalling, immune system or developmental biology. Toll-like receptors and IL-17-mediated signalling were identified in rhinitis alone, while IL-33 was identified in rhinitis in multimorbidity. On the other hand, few pathways were associated with both phenotypes, most being associated with signal transduction pathways including estrogen-stimulated signalling. The only immune system pathway was FceRI-mediated MAPK activation. In conclusion, our findings suggest that rhinitis alone and rhinitis and asthma multimorbidity should be considered as two distinct diseases.

摘要

“一个气道一种疾病”的概念早在 20 多年前就已提出,但它可能过于简化了过敏疾病之间的联系。基因组研究表明,单独的鼻炎和伴有哮喘的鼻炎是由不同的途径引起的。在这项 MeDALL(过敏发生机制)研究中,我们利用人类相互作用组的信息来区分两种过敏性鼻炎表型(单独的鼻炎和伴有哮喘的鼻炎)的分子机制。我们观察到互作组的拓扑结构以及与每种表型相关的途径存在显著差异。在单独的鼻炎中,确定的途径包括细胞周期、细胞因子信号转导、发育生物学、免疫系统、蛋白质代谢和信号转导。在伴有哮喘的鼻炎多态性中,大多数途径与信号转导有关。其余的与细胞因子信号转导、免疫系统或发育生物学有关。在单独的鼻炎中发现了 Toll 样受体和 IL-17 介导的信号转导,而在伴有哮喘的鼻炎中发现了 IL-33。另一方面,很少有途径与两种表型都有关,大多数与信号转导途径有关,包括雌激素刺激信号。唯一的免疫系统途径是 FceRI 介导的 MAPK 激活。总之,我们的研究结果表明,单独的鼻炎和伴有哮喘的鼻炎应该被视为两种不同的疾病。

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