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mSystems. 2020 Sep 15;5(5):e00724-20. doi: 10.1128/mSystems.00724-20.
2
Dengue hemorrhagic fever - A systemic literature review of current perspectives on pathogenesis, prevention and control.登革出血热——关于发病机制、预防与控制的当前观点的系统性文献综述
J Microbiol Immunol Infect. 2020 Dec;53(6):963-978. doi: 10.1016/j.jmii.2020.03.007. Epub 2020 Mar 26.
3
Serum miR-126-3p level is down-regulated in sepsis patients.脓毒症患者血清miR-126-3p水平下调。
Int J Clin Exp Pathol. 2018 May 1;11(5):2605-2612. eCollection 2018.
4
Role of microRNAs in antiviral responses to dengue infection.miRNAs 在抗登革病毒感染的抗病毒反应中的作用。
J Biomed Sci. 2020 Jan 3;27(1):4. doi: 10.1186/s12929-019-0614-x.
5
Dengue haemorrhagic fever: a job done via exosomes?登革出血热:通过外泌体完成的工作?
Emerg Microbes Infect. 2019;8(1):1626-1635. doi: 10.1080/22221751.2019.1685913.
6
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Biomed Pharmacother. 2019 Jul;115:108761. doi: 10.1016/j.biopha.2019.108761. Epub 2019 May 14.
7
Association between circulating microRNA-126 expression level and tumour necrosis factor alpha in healthy smokers.健康吸烟者循环 microRNA-126 表达水平与肿瘤坏死因子α的关系。
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Infect Genet Evol. 2017 Dec;56:99-110. doi: 10.1016/j.meegid.2017.11.009. Epub 2017 Nov 10.
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Decreased serum microRNA-21 level is associated with obesity in healthy and type 2 diabetic subjects.血清 microRNA-21 水平降低与健康人群和 2 型糖尿病患者的肥胖有关。
Arch Physiol Biochem. 2018 Oct;124(4):300-305. doi: 10.1080/13813455.2017.1396349. Epub 2017 Nov 7.
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MiR-126 and miR-126* regulate shear-resistant firm leukocyte adhesion to human brain endothelium.miR-126 和 miR-126* 调节抗剪切力的牢固白细胞黏附至人脑内皮细胞。
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登革热感染泰国儿科患者外周血循环 hsa-miR-126-3p 的表达。

The expression of circulating hsa-miR-126-3p in dengue-infected Thai pediatric patients.

机构信息

Department of Microbiology, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.

Department of Tropical Pediatrics, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.

出版信息

Pathog Glob Health. 2023 Feb;117(1):76-84. doi: 10.1080/20477724.2022.2088465. Epub 2022 Jun 16.

DOI:10.1080/20477724.2022.2088465
PMID:35708203
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9848246/
Abstract

Circulating hsa-miRNA-126 (CmiR-126) has been reported to involve in the pathogenesis of many infectious diseases including dengue virus infection. However, no prior study has been conducted to describe more details in dengue-infected pediatric patients. This study aimed to describe CmiR-126-3p in dengue-infected pediatric patients during the febrile and convalescent phases. Additionally, the correlations between CmiR-126-3p and other relevant clinical laboratory factors were investigated. Sixty paired-serum specimens collected during febrile and convalescent phases were retrieved from patients with dengue fever (DF) (n = 30) and dengue hemorrhagic fever (DHF) (n = 30). Thirty paired-serum specimens collected from non-dengue acute febrile illness patients (AFI) were included as the control group. CmiR-126-3p was determined using reverse transcription quantitative real-time polymerase-chain reaction (RT-qPCR). Relative miRNA expression was calculated as 2 using CmiR-16-5p for data normalization. CmiR-126-3p expression during febrile and convalescent phases in dengue-infected patients was significantly lower than AFI ( < 0.05). However, miRNA levels were not different ( > 0.05) compared between DF and DHF and between primary and secondary infection. CmiR-126-3p levels in DF in the convalescent were significantly higher than in the febrile phase ( = 0.025). No association between CmiR-126-3p and hematocrit, WBC level, platelet count, WBC differential count or dengue viral load was observed ( > 0.05). The data suggest that hsa-miR-126-3p involved in pathogenesis of dengue infection and may be a promising early and late biomarker for DENV infection. However, hsa-miR-126-3p alone cannot be used as a predictor for dengue severity.

摘要

循环 hsa-miRNA-126(CmiR-126)已被报道参与许多传染病的发病机制,包括登革热病毒感染。然而,以前没有研究描述登革热感染的儿科患者中更详细的情况。本研究旨在描述登革热感染的儿科患者在发热和恢复期的 CmiR-126-3p。此外,还研究了 CmiR-126-3p 与其他相关临床实验室因素之间的相关性。从登革热(DF)(n=30)和登革出血热(DHF)(n=30)患者的发热和恢复期采集了 60 对血清标本,从非登革热急性发热性疾病(AFI)患者(n=30)采集了 30 对血清标本作为对照组。使用逆转录定量实时聚合酶链反应(RT-qPCR)测定 CmiR-126-3p。使用 CmiR-16-5p 进行数据归一化,相对 miRNA 表达计算为 2。登革热感染患者发热和恢复期的 CmiR-126-3p 表达明显低于 AFI(<0.05)。然而,DF 和 DHF 之间以及原发性和继发性感染之间的 miRNA 水平没有差异(>0.05)。DF 恢复期的 CmiR-126-3p 水平明显高于发热期(=0.025)。CmiR-126-3p 水平与血细胞比容、白细胞计数、血小板计数、白细胞分类计数或登革热病毒载量之间无相关性(>0.05)。数据表明,hsa-miR-126-3p 参与登革热感染的发病机制,可能是 DENV 感染的有前途的早期和晚期生物标志物。然而,hsa-miR-126-3p 本身不能用作登革热严重程度的预测指标。