The Role of Extracellular Vesicles in Pandemic Viral Infections.
Woosung ShimAnjae LeeJung-Hyun LeePublished in: Journal of microbiology (Seoul, Korea) (2024)
Extracellular vesicles (EVs), of diverse origin and content, are membranous structures secreted by a broad range of cell types. Recent advances in molecular biology have highlighted the pivotal role of EVs in mediating intercellular communication, facilitated by their ability to transport a diverse range of biomolecules, including proteins, lipids, DNA, RNA and metabolites. A striking feature of EVs is their ability to exert dual effects during viral infections, involving both proviral and antiviral effects. This review explores the dual roles of EVs, particularly in the context of pandemic viruses such as HIV-1 and SARS-CoV-2. On the one hand, EVs can enhance viral replication and exacerbate pathogenesis by transferring viral components to susceptible cells. On the other hand, they have intrinsic antiviral properties, including activation of immune responses and direct inhibition of viral infection. By exploring these contrasting functions, our review emphasizes the complexity of EV-mediated interactions in viral pathogenesis and highlights their potential as targets for therapeutic intervention. The insights obtained from investigating EVs in the context of HIV-1 and SARS-CoV-2 provide a deeper understanding of viral mechanisms and pathologies, and offer a new perspective on managing and mitigating the impact of these global health challenges.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- immune response
- global health
- hiv infected
- human immunodeficiency virus
- hepatitis c virus
- hiv positive
- stem cells
- randomized controlled trial
- induced apoptosis
- hiv aids
- single molecule
- machine learning
- coronavirus disease
- bone marrow
- cell therapy
- mesenchymal stem cells
- single cell
- inflammatory response
- circulating tumor
- oxidative stress
- endoplasmic reticulum stress
- south africa
- cell cycle arrest
- dendritic cells
- cell free
- nucleic acid
- circulating tumor cells