It’s embarrassing to watch the TGA tie itself up in knots and contradict itself over the safety of the vaccine.
The mRNA vaccine is designed to attack your own cells because the antigen sits on the cell membrane. The T-cell which responds to the vaccine antigen can’t separate your cell from the spike protein. It kills both and the TGA has already admitted as much in the past conceding myocarditis is an autoimmune response.
The spike proteins are not rapidly degraded as numerous studies have shown they last in the body for up to 60 days.
But more importantly the mRNA is designed to last much longer and produce more proteins.
This means the body produces a much larger concentration of the toxic spike protein than what the virus would have delivered.
And I quote from one study:
“Later studies documented similar effects for 5-methylcytidine and 2-thiouridine and observed that modified mRNAs produced 10- to 100-fold more protein compared with unmodified mRNAs. Recently, N1-methylpseudouridine (m1Ψ), the modification used in the current mRNA SARS-CoV-2 vaccines, was found to possess superior characteristics to Ψ; m1Ψ elicited less immunogenicity and increased protein production by more than an order of magnitude relative to Ψ.”
And another on the Poly-A tail increases the duration.
“Whether for the mRNA vaccine from Pfizer/BioNtech® laboratories or that of Moderna®, the two mRNA sequences end in a Poly(A) tail. The purpose of this addition is to increase the stability of the mRNA in biological medium and also to allow the recruitment of the ribosome, in order to initiate an efficient translation.
After translation, the mRNA can be reused several times, but when this happens, it also loses part of the Adenines of its Poly(A) tail, as enzymatic degradation begins there, which only ensures a transient protection against this degradation. When this tail is too degraded, the mRNA is no longer functional and is destroyed. The poly(A) tail stabilizes mRNA and boosts protein translation, and the length of the poly(A) tail is proportional to translation efficiency. It is a critical factor in determining the longevity of mRNA molecules.”
Long story short – the TGA continues to lie.
Quotes from:
https://pmc.ncbi.nlm.nih.gov/articles/PMC9376333/
https://pmc.ncbi.nlm.nih.gov/articles/PMC9864138/#:~:text=Whether%20for%20the%20mRNA%20vaccine,to%20initiate%20an%20efficient%20translation
Community Affairs Legislation Committee
07/11/2024
Estimates
HEALTH AND AGED CARE PORTFOLIO
Therapeutic Goods Administration
Senator RENNICK: I’ll just touch on Professor Langham’s comment about spike protein. I have a study here that says that the use of the synthetic nucleotide methylpseudouridine produced 10 to 100 times more spike protein than the natural uridine nucleoside. Given these spike proteins are often chopped up as peptides and put on the cell membrane and then presented out to the immune system, wouldn’t the corresponding autoimmune response from the T cells have the potential to damage body organs?
Prof. Langham : Thanks for the question, Senator Rennick. The purpose of providing antigen is to generate a response specific to that antigen, not to the body itself. The spike proteins that are generated and produced are rapidly degraded.
Senator RENNICK: You say they’re rapidly degraded, but the poly-A tail was increased from 30 adenine nucleotides to over 100, which increased its duration. There have been studies that showed the spike protein remains in the body for up to 60 days, so how can you say that it rapidly degrades?
Prof. Langham : I’m not aware of the specific research paper that you are quoting but I do know of the studies that have demonstrated detection of parts of a spike protein that are in the body. They are often done in very small populations where the process can’t be validated or, alternatively, are done in patients with other medical conditions.
Dr Kerr : The poly-A tail is actually on the mRNAs, not on the protein.
Senator RENNICK: That’s right, so the mRNA will last longer—will produce spike proteins for longer. If the mRNA survives three or four days, that’s longer than breaking down, and those lipids last longer as well.
Dr Kerr: As Professor Langham said, the purpose of having the protein there is to generate the immune response. You get a stronger immune response if you have more protein there.
Senator RENNICK: Yes. But we’ve also been told in this committee that myocarditis was an autoimmune response to the vaccine as well, so it does obviously cause a certain level of damage. Anyway, that’s okay. I want to move on to the next question.
CHAIR: Dr Kerr, did you want to respond to that?
Dr Kerr: No, I can leave it there.
