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- W3204395522 endingPage "1585" @default.
- W3204395522 startingPage "1585" @default.
- W3204395522 abstract "Adenoviruses represent exceptional candidates for wide-ranging therapeutic applications, from vectors for gene therapy to oncolytics for cancer treatments. The first ever commercial gene therapy medicine was based on a recombinant adenovirus vector, while most recently, adenoviral vectors have proven critical as vaccine platforms in effectively controlling the global coronavirus pandemic. Here, we discuss factors involved in adenovirus cell binding, entry, and trafficking; how they influence efficiency of adenovirus-based vectors; and how they can be manipulated to enhance efficacy of genetically modified adenoviral variants. We focus particularly on endocytosis and how different adenovirus serotypes employ different endocytic pathways to gain cell entry, and thus, have different intracellular trafficking pathways that subsequently trigger different host antiviral responses. In the context of gene therapy, the final goal of the adenovirus vector is to efficiently deliver therapeutic transgenes into the target cell nucleus, thus allowing its functional expression. Aberrant or inefficient endocytosis can impede this goal, therefore, it should be considered when designing and constructing adenovirus-based vectors." @default.
- W3204395522 created "2021-10-11" @default.
- W3204395522 creator A5004835580 @default.
- W3204395522 creator A5023772881 @default.
- W3204395522 creator A5050457268 @default.
- W3204395522 creator A5055952307 @default.
- W3204395522 creator A5073241309 @default.
- W3204395522 creator A5077500117 @default.
- W3204395522 date "2021-09-29" @default.
- W3204395522 modified "2023-10-18" @default.
- W3204395522 title "The Revolving Door of Adenovirus Cell Entry: Not All Pathways Are Equal" @default.
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