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Development of New Strategies Using Extracellular Vesicles Loaded with Exogenous Nucleic Acid
Gene therapy is a therapeutic strategy of delivering foreign genetic material (encoding for an important protein) into a patient’s target cell to replace a defective gene. Nucleic acids are embedded within the adeno-associated virus (AAVs) vectors; however, preexisting immunity to AAVs remains a sig...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7464422/ https://www.ncbi.nlm.nih.gov/pubmed/32722622 http://dx.doi.org/10.3390/pharmaceutics12080705 |