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单细胞RNA测序:一种揭示川崎病单细胞水平先天性和适应性免疫反应失调的新兴工具。

Single-cell RNA sequencing: an emerging tool revealing dysregulated innate and adaptive immune response at single cell level in Kawasaki disease.

作者信息

Sharma Saniya, Goel Sumit, Goyal Taru, Pilania Rakesh Kumar, Aggarwal Ridhima, Kaur Taranpreet, Dhaliwal Manpreet, Rawat Amit, Singh Surjit

机构信息

Department of Pediatrics, Allergy Immunology Unit, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Expert Rev Clin Immunol. 2025 Jan;21(1):83-92. doi: 10.1080/1744666X.2024.2401105. Epub 2024 Sep 13.

DOI:10.1080/1744666X.2024.2401105
PMID:39230194
Abstract

INTRODUCTION

Kawasaki disease [KD] is a systemic disorder characterized by acute febrile illness due to widespread medium-vessel vasculitis, mainly affecting children. Despite the ongoing advanced research into the disease pathophysiology and molecular mechanisms, the exact etiopathogenesis of KD is still an enigma. Recently, single-cell RNA sequencing [scRNA-seq], has been utilized to elucidate the pathophysiology of KD at a resolution higher than that of previous methods.

AREA COVERED

In the present article, we re-emphasize the pivotal role of this high-resolution technique, scRNA-seq, in the characterization of immune cell transcriptomic profile and signaling/response pathways in KD and explore the diagnostic, prognostic, and therapeutic potential of this new technique in KD. Using combinations of the search phrases 'KD, scRNA-seq, CAA, childhood vasculitis' a literature search was carried out on Scopus, Google Scholar, and PubMed until the beginning of 2024.

EXPERT OPINION

scRNA-seq presents a transformative tool for dissecting KD at the cellular level. By revealing rare cell populations, gene expression alterations, and disease-specific pathways, scRNA-seq aids in understanding the intricacies of KD pathogenesis. This review will provide new insights into pathogenesis of KD and the field of applications of scRNA-seq in personalized therapeutics for KD in the future.

摘要

引言

川崎病(KD)是一种全身性疾病,其特征为因广泛的中血管血管炎引起的急性发热性疾病,主要影响儿童。尽管对该疾病的病理生理学和分子机制的研究不断深入,但KD的确切病因仍不清楚。最近,单细胞RNA测序(scRNA-seq)已被用于以高于以往方法的分辨率阐明KD的病理生理学。

涵盖领域

在本文中,我们再次强调这种高分辨率技术scRNA-seq在表征KD免疫细胞转录组谱和信号/反应途径方面的关键作用,并探讨这种新技术在KD中的诊断、预后和治疗潜力。使用“KD、scRNA-seq、CAA、儿童血管炎”等搜索词组合,在Scopus、谷歌学术和PubMed上进行了文献检索,直至2024年初。

专家观点

scRNA-seq是一种在细胞水平剖析KD的变革性工具。通过揭示罕见细胞群体、基因表达改变和疾病特异性途径,scRNA-seq有助于理解KD发病机制的复杂性。本综述将为KD的发病机制以及scRNA-seq在未来KD个性化治疗中的应用领域提供新的见解。

相似文献

1
Single-cell RNA sequencing: an emerging tool revealing dysregulated innate and adaptive immune response at single cell level in Kawasaki disease.单细胞RNA测序:一种揭示川崎病单细胞水平先天性和适应性免疫反应失调的新兴工具。
Expert Rev Clin Immunol. 2025 Jan;21(1):83-92. doi: 10.1080/1744666X.2024.2401105. Epub 2024 Sep 13.
2
Integration of scRNA-Seq and bulk RNA-Seq uncover perturbed immune cell types and pathways of Kawasaki disease.单细胞 RNA-Seq 和批量 RNA-Seq 的整合揭示了川崎病中失调的免疫细胞类型和途径。
Front Immunol. 2023 Sep 28;14:1259353. doi: 10.3389/fimmu.2023.1259353. eCollection 2023.
3
Single cell RNA-seq resolution revealed CCR1/SELL/XAF CD14 monocytes mediated vascular endothelial cell injuries in Kawasaki disease and COVID-19.单细胞 RNA 测序分辨率揭示了 CCR1/SELL/XAF CD14 单核细胞在川崎病和 COVID-19 中介导的血管内皮细胞损伤。
Biochim Biophys Acta Mol Basis Dis. 2023 Jun;1869(5):166707. doi: 10.1016/j.bbadis.2023.166707. Epub 2023 Mar 29.
4
Identification of novel metabolism-related biomarkers of Kawasaki disease by integrating single-cell RNA sequencing analysis and machine learning algorithms.通过整合单细胞RNA测序分析和机器学习算法鉴定川崎病新的代谢相关生物标志物。
Front Immunol. 2025 Apr 10;16:1541939. doi: 10.3389/fimmu.2025.1541939. eCollection 2025.
5
CD14 monocytes: the immune communication hub in early vasculitis symptoms of Kawasaki disease.CD14单核细胞:川崎病早期血管炎症状中的免疫通讯枢纽。
Front Immunol. 2025 Mar 26;16:1557231. doi: 10.3389/fimmu.2025.1557231. eCollection 2025.
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The mechanism underlying B-cell developmental dysfunction in Kawasaki disease based on single-cell transcriptomic sequencing.基于单细胞转录组测序的川崎病 B 细胞发育功能障碍的机制。
Front Immunol. 2024 Oct 23;15:1438640. doi: 10.3389/fimmu.2024.1438640. eCollection 2024.
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Single-cell RNA sequencing of peripheral blood mononuclear cells from acute Kawasaki disease patients.急性川崎病患者外周血单个核细胞的单细胞 RNA 测序。
Nat Commun. 2021 Sep 14;12(1):5444. doi: 10.1038/s41467-021-25771-5.
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RNAseq-based transcriptomics of treatment-naïve multi-inflammatory syndrome in children (MIS-C) demonstrates predominant activation of matrisome, innate and humoral immune pathways.基于 RNA 测序的治疗初发儿童多系统炎症综合征(MIS-C)的转录组学研究表明,基质、先天和体液免疫途径的激活占主导地位。
Rheumatol Int. 2024 Aug;44(8):1445-1454. doi: 10.1007/s00296-023-05478-0. Epub 2023 Oct 12.
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scRNA+TCR-seq reveals the pivotal role of dual receptor T lymphocytes in the pathogenesis of Kawasaki disease and during IVIG treatment.单细胞 RNA+T 细胞受体测序揭示双受体 T 淋巴细胞在川崎病发病机制及免疫球蛋白 IV 治疗中的关键作用。
Front Immunol. 2024 Oct 3;15:1457687. doi: 10.3389/fimmu.2024.1457687. eCollection 2024.
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Utilizing single-cell RNA sequencing for analyzing the characteristics of PBMC in patients with Kawasaki disease.利用单细胞 RNA 测序分析川崎病患者 PBMC 的特征。
BMC Pediatr. 2021 Jun 14;21(1):277. doi: 10.1186/s12887-021-02754-5.

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Proteomic insights into molecular alterations associated with Kawasaki disease in children.儿童川崎病相关分子改变的蛋白质组学见解
Ital J Pediatr. 2025 Feb 21;51(1):56. doi: 10.1186/s13052-025-01853-8.