Department of Microbiology, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.
Department of Tropical Pediatrics, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Pathog Glob Health. 2023 Feb;117(1):76-84. doi: 10.1080/20477724.2022.2088465. Epub 2022 Jun 16.
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.
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。