What makes AAV a great viral vector? The short answer is that it has many unique features. In this blog article, learn about what the Adeno-associated virus (AAV) is, how it affects the body and how you can use it for medical treatments.
Adeno-associated viral vector (AAV) is a gene therapy vector that carries therapeutic genes directly into cells. The vectors are designed to bypass the immune system and enter the cells without being destroyed. To know more about AAV, you can also visit https://www.bosterbio.com/services/aav-packaging-service.
This makes AAV a popular choice for gene therapy applications in which the patient’s immune system must be suppressed.
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One of the key advantages of using AAV is that it is relatively easy to create custom vectors. This means that researchers can quickly identify and address any potential problems with a particular AAV vector. In addition, AAV vectors are capable of entering multiple cell types, making them optimal for treating a wide range of diseases.
Despite these advantages, there are some limitations to using AAV vectors. For example, they are not well-suited for treatments that require long-term expression or delivery into specific tissues.
Additionally, they can only carry a limited number of genes, which may make them unsuitable for certain applications. Overall, however, the advantages of using AAV vectors make them an important option in the development of gene therapies.