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Modified Vaccinia Ankara: The Future of Vaccines πŸ’‰

MVA's impact on vaccine safety and effectiveness.

πŸ‘‹ Hey, this is a πŸ”’ Premium-only issueπŸ”’. To get full access πŸ‘‡πŸ»

Hey, I found something interesting about vaccines. There's a modified virus called Modified Vaccinia Ankara (MVA), which is super safe because it can’t replicate in human cells.

Researchers are using it to develop vaccines for HIV, flu, and some cancers. It triggers a strong immune response without causing the disease.

Although there are challenges like existing immunity from old smallpox vaccines, scientists are finding solutions. Overall, MVA shows great promise for improving public health. Thought you'd find this fascinating!

Why Is MVA a Potential Vaccine Vector?

The field of vaccine research has been transformed by the invention of recombinant DNA technology, and MVA is one particularly promising vector.

MVA was first created by Anton Mayr in Germany in the late 1950s from Chorioallantois Vaccinia virus Ankara (CVA) after being attenuated in chicken embryo fibroblasts(CEF) through more than 500 passages.

The extensive passaging of MVA in CEF cultures led to significant deletions in its genome and numerous mutations, impacting most known virulence and immune evasion factors of vaccinia virus (VACV).

As a result, MVA replication is highly restricted to avian cells, and the virus cannot produce infectious progeny in most mammalian cells.

Between 1968 and 1985, the Bavarian State Vaccine Institute produced MVA as a human smallpox vaccine. MVA is a weakened strain of the vaccinia virus used in vaccines known as MVA-BN.

These vaccines, branded as Imvanex in the EU, Imvamune in Canada, and Jynneos in the US, protect against smallpox and mpox, and are known for having fewer side effects compared to other poxvirus-derived smallpox vaccines.

As a third-generation smallpox vaccine, MVA's significant advantage lies in its inability to reproduce complete virions in human cells.

The MVA life cycle is blocked at the virion assembly stage, resulting in the formation of immature virus particles that are not released from infected cells.

Additionally, MVA is employed as an experimental viral vector for vaccines against various non-poxvirus diseases by incorporating antigen genes into its genome.

Because of its special quality, MVA provides a secure and efficient foundation for creating vaccines to prevent a variety of illnesses.

Advancement & Attenuation

Initially, the vaccinia virus, known as the Ankara strain, was passed down several times in order to decrease its potency.

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