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微小 RNA 作为结核病的免疫调节剂和生物标志物。

MicroRNAs as immune regulators and biomarkers in tuberculosis.

机构信息

Department of Biology, School of Life Sciences, Chongqing University, Chongqing, China.

Department of Zoology, Molecular Physiology Division, Faculty of Science, Beni-Suef University, Beni-Suef, Egypt.

出版信息

Front Immunol. 2022 Oct 27;13:1027472. doi: 10.3389/fimmu.2022.1027472. eCollection 2022.

DOI:10.3389/fimmu.2022.1027472
PMID:36389769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9647078/
Abstract

Tuberculosis (TB), which is caused by (Mtb), is one of the most lethal infectious disease worldwide, and it greatly affects human health. Some diagnostic and therapeutic methods are available to effectively prevent and treat TB; however, only a few systematic studies have described the roles of microRNAs (miRNAs) in TB. Combining multiple clinical datasets and previous studies on Mtb and miRNAs, we state that pathogens can exploit interactions between miRNAs and other biomolecules to avoid host mechanisms of immune-mediated clearance and survive in host cells for a long time. During the interaction between Mtb and host cells, miRNA expression levels are altered, resulting in the changes in the miRNA-mediated regulation of host cell metabolism, inflammatory responses, apoptosis, and autophagy. In addition, differential miRNA expression can be used to distinguish healthy individuals, patients with TB, and patients with latent TB. This review summarizes the roles of miRNAs in immune regulation and their application as biomarkers in TB. These findings could provide new opportunities for the diagnosis and treatment of TB.

摘要

结核病(TB)是由结核分枝杆菌(Mtb)引起的,是全球最致命的传染病之一,严重影响人类健康。目前已有一些诊断和治疗方法可有效预防和治疗结核病,但仅有少数系统性研究描述了 microRNAs(miRNAs)在结核病中的作用。我们结合多个临床数据集和以前关于 Mtb 和 miRNAs 的研究,指出病原体可以利用 miRNAs 与其他生物分子之间的相互作用来逃避宿主的免疫清除机制,并在宿主细胞中长期存活。在 Mtb 与宿主细胞的相互作用过程中,miRNA 的表达水平发生改变,导致 miRNA 介导的宿主细胞代谢、炎症反应、细胞凋亡和自噬的调控发生变化。此外,差异表达的 miRNA 可用于区分健康个体、结核病患者和潜伏性结核病患者。本综述总结了 miRNAs 在免疫调节中的作用及其作为结核病生物标志物的应用。这些发现为结核病的诊断和治疗提供了新的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4cf/9647078/59e3ca721f90/fimmu-13-1027472-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4cf/9647078/fd604ef4aefa/fimmu-13-1027472-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4cf/9647078/813d6a3b40a7/fimmu-13-1027472-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4cf/9647078/ac7c5866e856/fimmu-13-1027472-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4cf/9647078/59e3ca721f90/fimmu-13-1027472-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4cf/9647078/fd604ef4aefa/fimmu-13-1027472-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4cf/9647078/813d6a3b40a7/fimmu-13-1027472-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4cf/9647078/ac7c5866e856/fimmu-13-1027472-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4cf/9647078/59e3ca721f90/fimmu-13-1027472-g004.jpg

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Microbiol Spectr. 2022 Jun 29;10(3):e0262521. doi: 10.1128/spectrum.02625-21. Epub 2022 Apr 18.
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Nat Microbiol. 2022 Apr;7(4):497-507. doi: 10.1038/s41564-022-01080-5. Epub 2022 Apr 1.
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High miRNA-378 expression has high diagnostic values for pulmonary tuberculosis and predicts adverse outcomes.
A set of plasmatic microRNA related to innate immune response highly predicts the onset of immune reconstitution inflammatory syndrome in tuberculosis co-infected HIV individuals (ANRS-12358 study).
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Front Immunol. 2025 Jun 20;16:1603338. doi: 10.3389/fimmu.2025.1603338. eCollection 2025.
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miRNA Differential Expression Profile Analysis and Identification of Potential Key Genes in Active Tuberculosis.活动性肺结核中miRNA差异表达谱分析及潜在关键基因的鉴定
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