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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.

DOI:10.1038/s41598-023-39987-6
PMID:37573373
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10423213/
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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Sci Rep. 2023 Aug 12;13(1):13125. doi: 10.1038/s41598-023-39987-6.
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本文引用的文献

1
Signaling and functions of interleukin-33 in immune regulation and diseases.白细胞介素-33在免疫调节及疾病中的信号传导与功能
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Rhinitis associated with asthma is distinct from rhinitis alone: The ARIA-MeDALL hypothesis.哮喘相关鼻炎与单纯鼻炎不同:ARIA-MeDALL 假说。
Allergy. 2023 May;78(5):1169-1203. doi: 10.1111/all.15679. Epub 2023 Apr 10.
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Epithelial cell alarmin cytokines: Frontline mediators of the asthma inflammatory response.
上皮细胞警报素细胞因子:哮喘炎症反应的一线介质。
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Blockade of CBX4-mediated β-catenin SUMOylation attenuates airway epithelial barrier dysfunction in asthma.阻断CBX4介导的β-连环蛋白SUMO化可减轻哮喘中的气道上皮屏障功能障碍。
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DAVID: a web server for functional enrichment analysis and functional annotation of gene lists (2021 update).DAVID:一个用于基因列表功能富集分析和功能注释的网络服务器(2021 更新)。
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The IntAct database: efficient access to fine-grained molecular interaction data.IntAct 数据库:高效访问细粒度分子相互作用数据。
Nucleic Acids Res. 2022 Jan 7;50(D1):D648-D653. doi: 10.1093/nar/gkab1006.
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FGF/FGFR signaling: From lung development to respiratory diseases.FGF/FGFR 信号通路:从肺发育到呼吸疾病。
Cytokine Growth Factor Rev. 2021 Dec;62:94-104. doi: 10.1016/j.cytogfr.2021.09.002. Epub 2021 Sep 20.
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Viruses, SUMO, and immunity: the interplay between viruses and the host SUMOylation system.病毒、SUMO 与免疫:病毒与宿主 SUMO 化系统的相互作用。
J Neurovirol. 2021 Aug;27(4):531-541. doi: 10.1007/s13365-021-00995-9. Epub 2021 Aug 3.
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A positive feedback loop reinforces the allergic immune response in human peanut allergy.正反馈循环增强了人类花生过敏中的过敏免疫反应。
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