Full Form of AAV

Full formMedical & Health
AAVstands for

Adeno-Associated Virus

What is AAV?

Adeno-Associated Virus (AAV) is a small, non-enveloped virus belonging to the Parvoviridae family, widely recognized for its role as a delivery vector in gene therapy. In the Indian context, AAV is pivotal in biomedical research and clinical trials targeting genetic disorders such as hemophilia, Leber congenital amaurosis, and Duchenne muscular dystrophy. Unlike wild-type parvoviruses, recombinant AAV (rAAV) has been engineered to carry therapeutic genes without causing disease, making it a safe and efficient tool. It is used in laboratory settings, biotech companies, and academic institutions like the National Institute of Immunology and the Centre for Stem Cell Research. For students preparing for exams like NEET, CSIR NET, and GATE in biotechnology, understanding AAV vectors is essential because they are a cornerstone of modern gene editing and regenerative medicine. AAV's ability to infect both dividing and non-dividing cells, along with its low immunogenicity, has made it a preferred choice for in-vivo gene therapy, and India is actively contributing to AAV-based clinical trials through initiatives like the Indian Council of Medical Research.

AAV का फुल फॉर्म

एडिनो-संबद्ध वायरस

Example

Indian researchers at an IISc lab successfully delivered a corrective gene using an AAV vector to restore vision in mouse models of retinal degeneration.

AAV — frequently asked questions

What is the full form of AAV?
The full form of AAV is Adeno-Associated Virus.
What is AAV used for in gene therapy?
AAV is used as a delivery vector to carry therapeutic genes into patient cells, enabling treatment of genetic disorders like hemophilia and inherited blindness.
Is AAV safe for human gene therapy?
Yes, recombinant AAV is considered safe because it does not integrate into the host genome and causes a minimal immune response, making it suitable for clinical trials in India and worldwide.
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