adeno associated viral vectors (aav)

How are these challenges being addressed?

Researchers are actively working on overcoming the limitations of AAV vectors:
1. Capsid modification: Engineering capsids to evade the immune system and enhance tissue-specific targeting.
2. Use of novel serotypes: Exploring different AAV serotypes or creating hybrid vectors to bypass pre-existing immunity.
3. Optimizing production: Developing more efficient production methods and purification techniques to scale up AAV vector availability.

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