Did you read the Salk Institute study? The jabs don’t stimulate your immune system one bit. They tell your cells to create spike proteins, which is the virus protein. Then your body is supposed to defeat these proteins (the so called immune response) The problem is the spike protein by itself does a lot of damage to the human body. So having a couple million spike protein factories in your body is not a good thing.
They injected mice with only the spike protein and they all had symptoms that we are seeing in the people who have died from the jabs. The mice did not have Covid as they were not injected with covid only the spike proteins.
How to you weasel outta that study Amigo?
Link the study; let’s look at it and see what it actually says.
Thank you for linking what you were talking about. Let’s review:
“The jabs don’t stimulate your immune system one bit.”
At no point does anything in your link or any of the links therein say this. Numerous carefully controlled studies going all the way back to March 2020 demonstrate that the S protein is an antigen which stimulates lymphocytes, dendritic cells, macrophages, etc. Just as the S protein of the original SARS 2003 virus did. Just as the S protein of the MERS 2012 virus did. The other primary antigen yielding strong immune system reaction is the nucleocapsid protein or N protein.
“They tell your cells to create spike proteins, which is the virus protein. Then your body is supposed to defeat these proteins (the so called immune response)”
Mostly accurate here. The S protein is one of several viral proteins, including the M protein and the N protein.
“The problem is the spike protein by itself does a lot of damage to the human body.”
This is where we get to your link. Let’s start with one of the first lines in your link:
“Now, a major new study shows that the virus spike proteins (which behave very differently than those safely encoded by vaccines) also play a key role in the disease itself.”
Second, let’s look at a line toward the end of the study linked in your link:
“This conclusion suggests that vaccination-generated antibody and/or exogenous antibody against S protein not only protects the host from SARS-CoV-2 infectivity but also inhibits S protein-imposed endothelial injury.”
So your link says the vaccines are safe and the study they link to says the vaccines do even more to protect not only against the virus itself, but the S protein the study is concerned with. Your own link says vaccination is safe and effective.
“How to you weasel outta that study Amigo?”
I was going to ask you the same thing.
Here’s the real rub: you’re going to tell me that the SARS-CoV-2 virus isn’t a problem and that nearly everyone survives it. But that virus contains not only S proteins, but also self-amplifying RNA which leads to Billions of copies of that virus (and all its spike proteins) replicating all over your body. In the next breath, you claim the spike protein is hugely dangerous and any contact with it is a serious risk. But you can’t have it both ways: either the virus is no big deal (and so are its S proteins), or the S proteins are a problem. And if the S proteins are a problem, I have to ask: would you rather have a short-lived (~3 days) vaccine making a few million copies of just the S protein, or uncontrolled viral replicating making tens of billions of S proteins?
Here’s another interesting bit that I actually didn’t know about:
“In the Moderna, Pfizer/BioNTech, J&J, and Novavax vaccines, the Spike protein has some proline mutations introduced to try to hold it in its “prefusion” conformation, rather than the shape it adopts when it binds to ACE2. So that should cut down even more on the ability of the Spike protein produced by these vaccines to bind and produce the effects noted in the recent papers.”
https://blogs.sciencemag.org/pipeline/archives/2021/05/04/spike-protein-behavior
Do you have the link to that study so I can read it too?
As for the spike protein doing damage in the body, that is what your immune system does to any foreign proteins that get loose in the body. Your digestive system is continuously bringing in all kinds of substances into the body. The job of the innate immune system is to fight harmful substances and germs that enter the body, for instance through the skin or digestive system.
The lipid nanoparticle that encloses the mRNA vaccine is specially designed to fuse onto a cell wall membrane of cells that have MHC molecules that play an important role in the presentation of foreign antigens, which is a critical step in the activation of T cells and thus an important mechanism of the adaptive immune system.
The process goes as follows: The lipid nanoparticle fuse on the cell wall where it releases the RNA Messenger into the cell, where the host cell’s ribosomes read the RNA instruction and translates it into the protein that is the exact copy of the C-viruis Spike Protein. These proteins are then presented on the surface of the host cell's membrane where they bind to the MHC-1 and MHC-2 complex molecules. Once in contact with these MHC molecules there is generated an interaction between these foreign proteins with the T helper cells. This interaction triggers the T helper cells to produce cytokines (interlukens) and memory cells. The interlukens attracts B-cells that produce plasma cells which act to produce antibodies that will bind on the C-virus's Spike protein, whenever present, neutralize it and destroy it. It is not known how long these specially programmed antibodies stay in the body. The memory cells will produce T-cells that are programmed to produce antibodies that will also attack any future C-virus’s Spike Proteins present in the body.
Proteins on the host MHC-2 complex molecule attract cytoxic T-cells that release destructive molecules which destroys the host cell, thus ending the translation of more Spike Proteins. Since there are billions of cells in the body, a few sacrificial host cells will not make a difference.