The review describes viral and non-viral vectors as delivery modalities used in preclinical AF gene-therapy studies.
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viral and non-viral vectors
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Evidence Snippets
This review summarizes recent preclinical studies using viral and non-viral vectors
significantly expanding the therapeutic landscape using viral and non-viral vectors
In this review, we will discuss the most commonly used tools for the delivery of genetic material in the CNS, including viral and non-viral vectors; their main applications; their advantages and disadvantages.
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The therapeutic landscape described in the source uses viral and non-viral vectors.
using viral and non-viral vectors
Challenges in atrial targeting, immune control, and durable expression are barriers to atrial fibrillation gene-therapy translation.
Recent preclinical atrial fibrillation gene-therapy studies include viral vectors, non-viral vectors, atrial-specific delivery strategies, and targets involving ion channels, fibrosis, and oxidative stress.
Gene therapy is a promising approach to modulate molecular drivers of atrial fibrillation.
No atrial fibrillation gene therapy has FDA approval.
Gene therapy is presented as an attractive option for CNS disorders because it enables delivery of genetic material encoding therapeutic molecules.