Infection and Immunity Research Strength, Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia, Selangor, Malaysia.
Institute of Systems Biology Malaysia, National University of Malaysia, Selangor, Malaysia.
Am J Trop Med Hyg. 2024 Apr 2;110(5):856-867. doi: 10.4269/ajtmh.23-0546. Print 2024 May 1.
Dengue fever (DF) is an endemic infectious tropical disease and is rapidly becoming a global problem. Dengue fever is caused by one of the four dengue virus (DENV) serotypes and is spread by the female Aedes mosquito. Clinical manifestations of DF may range from asymptomatic to life-threatening severe illness with conditions of hemorrhagic fever and shock. Early and precise diagnosis is vital to avoid mortality from DF. A different approach is required to combat DF because of the challenges with the vaccines currently available, which are nonspecific; each is capable of causing cross-reaction and disease-enhancing antibody responses against the residual serotypes. MicroRNAs (miRNAs) are known to be implicated in DENV infection and are postulated to be involved in most of the host responses. Thus, they might be a suitable target for new strategies against the disease. The involvement of miRNAs in cellular activities and pathways during viral infections has been explored under numerous conditions. Interestingly, miRNAs have also been shown to be involved in viral replication. In this review, we summarize the role of known miRNAs, specifically the role of miRNA Let-7c (miR-Let-7c), miR-133a, miR-30e, and miR-146a, in the regulation of DENV replication and their possible effects on the initial immune reaction.
登革热(DF)是一种地方性传染病,正在迅速成为全球性问题。登革热是由四种登革病毒(DENV)血清型之一引起的,由雌性伊蚊传播。DF 的临床表现范围从无症状到伴有出血性发热和休克的危及生命的严重疾病。早期和准确的诊断对于避免 DF 死亡率至关重要。由于目前可用疫苗的非特异性,需要采取不同的方法来对抗 DF;每种疫苗都能够引起交叉反应和疾病增强抗体反应针对剩余的血清型。microRNAs(miRNAs)已知与 DENV 感染有关,并被推测参与大多数宿主反应。因此,它们可能是针对该疾病的新策略的合适靶点。在多种条件下已经探讨了 miRNAs 在病毒感染期间对细胞活动和途径的参与。有趣的是,miRNAs 也被证明参与了病毒复制。在这篇综述中,我们总结了已知 miRNAs 的作用,特别是 miRNA Let-7c(miR-Let-7c)、miR-133a、miR-30e 和 miR-146a 在调节 DENV 复制中的作用,以及它们对初始免疫反应的可能影响。