What does AAV mean in LABORATORY


Adeno Associated Virus, or AAV, is a virus that, while known to cause disease in humans and animals, can also be used for great therapeutic purposes. Originally discovered in the 1960s, AAV has been extensively studied for decades and has recently become a popular vector for gene therapy. With its ability to be adapted to specific cells and target diseases, AAV offers promise in the field of medicine.

AAV

AAV meaning in Laboratory in Medical

AAV mostly used in an acronym Laboratory in Category Medical that means Adeno Associated Virus

Shorthand: AAV,
Full Form: Adeno Associated Virus

For more information of "Adeno Associated Virus", see the section below.

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What is AAV?

AAV stands for Adeno Associated Virus. It is a type of virus from the Parvoviridae family that infects both humans and animals. Types of AAV can affect different types of cells, including epithelial cells like those found in the respiratory tract or those related to cardiovascular system functions. It is not replication-competent, meaning it cannot reproduce on its own without help from another virus such as adenovirus or herpesvirus. Therefore, AAV must be modified to become useful for medical applications such as gene therapy.

Use in Medicine

AAV has been extensively studied and used in recent years due to its potential therapeutic benefits. Since it cannot reproduce on its own, scientists have worked to develop various methods that allow them to modify the virus into a beneficial form so that it may be used as an effective vehicle for gene therapy. For example, AAV can be adapted with specific sequences of DNA so that they bind to certain types of cells and target certain diseases with new forms of treatment. In this way, scientists can use AAV as vectors for delivering therapeutic genes directly into cells with precision targeting capability. This may offer treatments for genetic disorders which are currently difficult or impossible to treat due to their complexities or lack of efficacy with conventional methods.

Essential Questions and Answers on Adeno Associated Virus in "MEDICAL»LABORATORY"

What is Adeno-Associated Virus (AAV)?

Adeno-Associated Virus (AAV) is a small, nonpathogenic virus that is capable of transferring genetic material into cells. It is an attractive vector for gene therapy applications due to its lack of pathogenicity and ability to specifically target certain cell types.

What is the size range of AAV?

The Size range of AAV is 20-25 nm in diameter and 4.7kb in length.

How does AAV interrupt with human cells?

AAV enters human cells by binding to heparin sulfate receptor and then releases viral genome into the nucleus for expression.

What kinds of applications can be used with AAV?

Adeno-associated virus has been used in a variety of gene therapy protocols, including delivery of therapeutic genes to treat cancer, cystic fibrosis, HIV/AIDS, heart diseases and other inherited disorders.

Does AAV interact with other viruses?

Yes, AAV can form hybrid viruses when packaged with other viral genomes such as adenovirus, herpes simplex virus or lentivirus.

Is it possible to create recombinant vectors using AAV?

Yes, recombinant vectors derived from AAV can be produced using site-directed mutagenesis or homologous recombination.

Are there any limitations to using AAV for gene transfer?

Yes, the main limitation is that since the packaging capacity for the vector capsids is limited at around 5kb, this means large transgene expression cassettes cannot be used for gene replacement therapy applications. Additionally, pre-existing immunity may reduce transcriptional efficiency in some cases.

What are the benefits of using AAV over other viral delivery systems?

The advantages of using Adeno-Associated Virus (AAV) include its low toxicity profile and high efficiency transduction capability when delivered via direct injection or systemic administration routes. Additionally, it has low immunogenicity which makes it an attractive option for long term gene delivery systems compared to other viral vectors such as adenovirus or lentivirus.

Is there a risk of integrating into one's own genome when using AAV vector?

No, studies have shown that integration is rare (<0.001%) when using properly manufactured recombinant adeno-associated virus as a vector for gene transfer.

Final Words:
Adeno Associated Virus (AAV) is a virus from the Parvoviridae family with potential therapeutic applications due its ability to be modified genetically so that it binds specifically to certain cell types and target diseases precisely. While most people associate viruses with illness and harm, researchers have put considerable effort into developing ways of manipulating these viruses so that they may improve health outcomes rather than cause damage as pathogens would normally do. As current research progresses with this approach towards medical advancement, it will hopefully lead us closer towards providing more effective forms of treatments against genetic disorders.

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