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川崎病诊断的未来:液体活检可能是关键。

The Future of Kawasaki Disease Diagnosis: Liquid Biopsy May Hold the Key.

机构信息

Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore.

School of Medicine, Royal College of Surgeons in Ireland, D02 YN77 Dublin, Ireland.

出版信息

Int J Mol Sci. 2024 Jul 24;25(15):8062. doi: 10.3390/ijms25158062.

DOI:10.3390/ijms25158062
PMID:39125631
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11311979/
Abstract

Kawasaki disease (KD) is a febrile illness characterised by systemic inflammation of small- and medium-sized blood vessels, which commonly occurs in young children. Although self-limiting, there is a risk of developing coronary artery lesions as the disease progresses, with delay in diagnosis and treatment. Unfortunately, the diagnosis of KD continues to remain a clinical dilemma. Thus, this article not only summarises the key research gaps associated with KD, but also evaluates the possibility of using circulating endothelial injury biomarkers, such as circulating endothelial cells, endothelial microparticles and vascular endothelial cell-free DNA, as diagnostic and prognostic tools for KD: a "liquid biopsy" approach. The challenges of translating liquid biopsies to use in KD and the opportunities for improvement in its diagnosis and management that such translation may provide are discussed. The use of endothelial damage markers, which are easily obtained via blood collection, as diagnostic tools is promising, and we hope this will be translated to clinical applications in the near future.

摘要

川崎病(KD)是一种以小、中血管全身性炎症为特征的发热性疾病,常见于幼儿。虽然川崎病具有自限性,但随着疾病的进展,仍有发生冠状动脉病变的风险,如果诊断和治疗不及时,这种风险会更高。不幸的是,川崎病的诊断仍然是一个临床难题。因此,本文不仅总结了与川崎病相关的关键研究空白,还评估了循环内皮损伤生物标志物(如循环内皮细胞、内皮微颗粒和血管内皮细胞游离 DNA)作为川崎病诊断和预后工具的可能性:一种“液体活检”方法。本文讨论了将液体活检转化为川崎病应用的挑战,以及这种转化可能为川崎病的诊断和治疗带来的改进机会。使用通过血液采集即可轻易获得的内皮损伤标志物作为诊断工具具有广阔的前景,我们希望这将在不久的将来转化为临床应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/018d/11311979/e6fbd49a373e/ijms-25-08062-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/018d/11311979/ca4693803a48/ijms-25-08062-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/018d/11311979/ceb357bacd64/ijms-25-08062-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/018d/11311979/e6fbd49a373e/ijms-25-08062-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/018d/11311979/ca4693803a48/ijms-25-08062-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/018d/11311979/aa99c3bf80c9/ijms-25-08062-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/018d/11311979/aa2cead68cf9/ijms-25-08062-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/018d/11311979/ceb357bacd64/ijms-25-08062-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/018d/11311979/e6fbd49a373e/ijms-25-08062-g005.jpg

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本文引用的文献

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The DNA methylome of human vascular endothelium and its use in liquid biopsies.人类血管内皮的 DNA 甲基组及其在液体活检中的应用。
Med. 2023 Apr 14;4(4):263-281.e4. doi: 10.1016/j.medj.2023.03.006.
2
MicroRNAs in Kawasaki disease: An update on diagnosis, therapy and monitoring.川崎病相关 microRNAs:诊断、治疗和监测的新进展。
Front Immunol. 2022 Oct 24;13:1016575. doi: 10.3389/fimmu.2022.1016575. eCollection 2022.
3
Circulating Endothelial Cells: A New Possible Marker of Endothelial Damage in Kawasaki Disease, Multisystem Inflammatory Syndrome in Children and Acute SARS-CoV-2 Infection.
循环内皮细胞:川崎病、儿童多系统炎症综合征和急性 SARS-CoV-2 感染中内皮损伤的新的可能标志物。
Int J Mol Sci. 2022 Sep 3;23(17):10106. doi: 10.3390/ijms231710106.
4
Molecular mechanisms of endothelial dysfunction in Kawasaki-disease-associated vasculitis.川崎病相关血管炎中内皮功能障碍的分子机制
Front Cardiovasc Med. 2022 Aug 8;9:981010. doi: 10.3389/fcvm.2022.981010. eCollection 2022.
5
Platelet-derived microRNA-223 attenuates TNF-α induced monocytes adhesion to arterial endothelium by targeting ICAM-1 in Kawasaki disease.血小板衍生的 microRNA-223 通过靶向 ICAM-1 减轻川崎病 TNF-α 诱导的单核细胞黏附至动脉内皮。
Front Immunol. 2022 Aug 2;13:922868. doi: 10.3389/fimmu.2022.922868. eCollection 2022.
6
Liquid biopsy: a step closer to transform diagnosis, prognosis and future of cancer treatments.液体活检:癌症诊疗的变革更近一步。
Mol Cancer. 2022 Mar 18;21(1):79. doi: 10.1186/s12943-022-01543-7.
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Adv Genet. 2021;108:81-145. doi: 10.1016/bs.adgen.2021.08.003. Epub 2021 Oct 7.
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