Iman Owliaee, Mehran Khaledian, Ali Shojaeian, Armin Khaghani Boroujeni
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引用次数: 0
Abstract
Arthropod-borne diseases (ABDs) refer to a group of viral pathogens that affect a wide range of vertebrate hosts, including humans and non-human primates. In addition to being transmitted by mosquitoes and ticks, arthropods can also spread pathogens that cause severe human diseases. On the other hand, extracellular vesicles (EVs) can serve as cross-placental drug delivery vehicles (DDVs) to the fetus and even as antigen-presenting cells (APCs). To this end, the current review aimed to examine the role of small EVs (sEVs) in the transmission and inhibition of arthropod-borne viruses, also known as arboviruses. First, a deeper understanding of the mechanistic aspects of how these vesicles function during insect-pathogen interactions is required. Next, scalability and yield optimization must be addressed while introducing EV-based therapeutics on an industrial scale in order to implement them effectively. Finally,it is recommended to consider that sEV-mediated transfer plays a crucial role in the spread of ABDs. This is because it transfers pathogenic agents between cells within vectors, resulting in subsequent transmission to hosts. Consequently, sEVs provide potential targets for the development of novel therapies that inhibit pathogen replication or reduce arthropod vector populations. Future research in this area should emphasize how these vesicles function within host-vector systems, using advanced imaging techniques - such as high-resolution microscopy (HRM) - and cost-effective methods, in order to produce sufficient quantities for large-scale implementation.
节肢动物传播的疾病(ABDs)指的是一组病毒病原体,它们会影响包括人类和非人灵长类动物在内的多种脊椎动物宿主。除了通过蚊子和蜱传播外,节肢动物还可以传播导致严重人类疾病的病原体。另一方面,细胞外囊泡(EVs)可作为胎儿的跨胎盘给药载体(DDVs),甚至可作为抗原递呈细胞(APCs)。为此,本综述旨在研究小EVs(sEVs)在节肢动物传播病毒(又称虫媒病毒)的传播和抑制中的作用。首先,需要更深入地了解这些囊泡在昆虫与病原体相互作用过程中的作用机理。其次,在工业规模上引入基于 EV 的疗法时,必须解决可扩展性和产量优化问题,以便有效实施这些疗法。最后,建议考虑到 sEV 介导的转移在 ABDs 传播中起着至关重要的作用。这是因为它能在载体内的细胞间转移病原体,导致随后向宿主传播。因此,sEV 为开发抑制病原体复制或减少节肢动物载体数量的新型疗法提供了潜在目标。该领域未来的研究应强调这些囊泡如何在宿主-载体系统中发挥作用,并采用先进的成像技术(如高分辨率显微镜(HRM))和具有成本效益的方法,以便生产足够数量的囊泡,供大规模应用。