The antegens used to create the immune response in the mRNA vaccine are the RNA code (not the DNA code) for the Spike Protein (the highly defined antigen). The COVID-19 uses that Spike to fuse into the cell wall and deliver its RNA message to the cell ribosomes, which are protein factories, that will create new COVID-19 viruses.
What the mRNA does is use that RNA blueprint (”fractions thereof administered”) to be read (translation) by the ribosomes to create the proteins that make up those spikes on the virus’s outer wall. Once these proteins are created, it will present segments of these proteins on the surface of the host cell’s membrane where they bind to the MHC-1 and MHC-2 complex molecules. This is a process to make sure that the ribosome’s normal production of proteins is true to its instructions. If not, it triggers an immune response. It is here on the MHC-1 and MHC-2 recepters,that the Spike Protein is biochemically evaluated: is it true or false. If it is false the process of creating antibodies, cytoxic T-cells, and and memory cells occurs. The false (foreign) protein is destroyed.
Up to this time, vaccines have only been able to produce the antibodies and memory cells. The mRNA vaccine has been able to create cytoxic T-cells for the antigen (the Spike Protein segment) on the MHC-2 complex molecules. When attracted to that antigen it will destroy the entire cell if infected by the virus. That is very useful. The host cell may have began to create new viruses. Cytoxic T-cells will take those cells out. Also, Cytoxic T-cells ends the Spike Protein translation process for that cell.
When the COVID-19 enters the body, these programmed immune cells attack the spikes that it uses to invade the cell. They have been programmed to destroy those proteins that make up the spike. In doing that, they have performed the function that any vaccine was designed to do.
In fact, the Johnson and Johnson uses the older method, a modified adenovirus to inject the Spike Protein into the cell where the cell’s ribosomes recreate the proteins where segments are bond to the MHC-1 complex molecules. That initiates the process for creating the antibody and memory cells.
Both these mechanism for creating immunity fit the definition of a vaccine.
I know it was a labor of love to find the legal definition for a vaccine. I understand the mechanism of these vaccines enough to understand their immunity function. I hope you now know it too.
jonrick46,
Sadly, you’re intentionally wrong.
Since the Covid-19 virus was not available in isolated form when the gene therapies were developed (Covid-19 has still not been isolated), the therapies were designed to respond to viruses similar, but not the same as Covid-19.
For this reason, a person with the vaccine will develop different antibodies than a person who actually had Covid-19.
This is a problem - it means that there are unknowns that could potentially cause severe problems, like ADE. People may be triggered by other viruses to over produce this antibody. Far too much was unknown but hey, they can call it a vaccine and get protection from liability so what’s to stop them?
The Vaccine companies have defined their Covid-19 as gene therapies in their own marketing information. Fauci has stressed a tiny portion of the true nature of these gene therapies by explaining to the public that you’d still be able to transmit the virus to others, you’d still be able to get the illness yourself, but it’s hoped that the vaccine will reduce the severity of the disease.
So when are we to believe vaccine companies? When they tell us their latest product lacks the basic properties of vaccines, by definition as well as by their marketing, should we accuse them of lying and say those gene therapies really WILL stop transmission and infection?
Your description of how the gene therapies work is best case scenario when in fact VAERS is filling up with the consequences of forcing experimental gene therapies on the public.
It’s a shame, too, ‘cause you tried so hard to make it sound legitimate.