Sharma Saniya, Goel Sumit, Goyal Taru, Pilania Rakesh Kumar, Aggarwal Ridhima, Kaur Taranpreet, Dhaliwal Manpreet, Rawat Amit, Singh Surjit
Department of Pediatrics, Allergy Immunology Unit, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Expert Rev Clin Immunol. 2025 Jan;21(1):83-92. doi: 10.1080/1744666X.2024.2401105. Epub 2024 Sep 13.
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.
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.
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.
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。
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。
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。