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AAV-DJ is an engineered adeno-associated virus (AAV) capsid created through DNA shuffling and directed evolution of eight wild-type AAV serotypes (AAV1, 2, 4, 5, 8, 9, avian, and bovine). It is a hybrid vector, primarily a chimera of AAV2, AAV8, and AAV9, designed to exhibit superior liver transduction efficiency and resistance to neutralization by human antibodies (IVIG). Originally developed at Stanford University, it is widely used as a research tool and a platform for gene therapy delivery across various tissues, including the liver, retina, and central nervous system. The vector's unique capsid structure differs from AAV2 by 60 amino acids, providing enhanced tissue penetration and immune evasion properties.
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