Further evidence CDC lied, Part 2 Australian peer reviewed study, vaccine disperses rapidly from the injection site and can be found in nearly all parts of the body
Further evidence CDC lied, Part 2 Australian peer reviewed study, vaccine disperses rapidly from the injection site and can be found in nearly all parts of the body
First of all, many thanks to Steve Kirsch for presenting this study and all that he does.
From COVID-19 vaccines – An Australian Review.
“Initial information
The mRNA vaccines were supposed to remain at the injection site and be taken up by the lymphatic system. This assumption proved to be wrong. During an autopsy of a vaccinated person that had died after mRNA vaccination it was found that the vaccine disperses rapidly from the injection site and can be found in nearly all parts of the body [1]. The mRNA is enveloped in liquid nano particles (LNP) containing a mixture of phospholipids, cholesterol, PEGylated lipids and cationic or ionizable lipids [2]. Research has shown that such nanoparticles can cross the blood-brain barrier [3] and the blood-placenta barrier [4], so it came as no surprise that the European Medicines Agency assessment report for the Moderna vaccine on page 47 (https://www.ema.europa.eu/en/documents/ assessment-report/spikevax-previously-covid-19-vaccinemoderna-epar-public-assessment-report_en.pdf) also noted that mRNA could be detected in the brain following intramuscular administration at about 2% of the level found in plasma. In 2021 researchers from Japan reported a disproportionately high mortality due to cerebral venous sinus thrombosis and intracranial haemorrhage. Despite not being able to prove a causal link with vaccines, as no autopsies were performed, they still believed that a link with vaccination is possible and further analysis is warranted [5].
It was furthermore stated that the mRNA will degrade quickly. Normally, mRNA breaks down within a few minutes to hours, however, the mRNA in these vaccines is nucleoside-modified to reduce potential innate immune recognition [6, 7] and it has been shown that production of the spike protein in some vaccines is kept up for an extraordinarily long time. A study by Röltgen et al. [8] found that the vaccine mRNA persists in the body up to 60 days, with 60 days being the end point of their study. It is thus unknown and impossible to define how much of the spike protein is actually produced in the vaccinated. It is a standard requirement for vaccine producers to define the amount of antigen in each injection. For a “so called “vaccine that is using the human body as the production facility there is no possible quantification of antigen. This is highly variable and dependant on the amount and stability of nanoparticles in the injection, age and fitness of the vaccinee, their immune status and the injection technique – if a blood vessel is directly injected, the nanoparticles will travel in minutes to all major organs including the brain. It is therefore impossible to assess how much spike protein any individual vaccinee produces following an inoculation. In summary, it is unknown where exactly the vaccine travels once it is injected, and how much spike protein is produced in which (and how many) cells.
Prominent cardiologist Dr Peter McCullough stated that the spike protein - a cytotoxin solely responsible for the severity of the respiratory infection - makes the use of it as immunizing agent dangerous. The spike protein in itself can produce COVID- 19 symptoms as shown in animal experiments. The S1 subunit of the SARS-CoV-2 spike protein when injected into transgenic mice overexpressing human ACE-2 caused a COVID-19 like response (a decline in body weight, dramatically increased white blood cells and protein concentrations in bronchoalveolar lavage fluid (BALF), upregulation of multiple inflammatory cytokines in BALF and serum, histological evidence of lung injury, and activation of signal transducer and activator of transcription 3 (STAT3) and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathways in the lung [9].
It was further shown that the spike protein S1 subunit, when added to red blood cells in vitro, could induce clotting by binding fibrinogen and ACE2 on platelets, thus triggering their aggregation [10]. The S protein also increases human cell syncytium formation, removes lipids from model membranes and interferes with the capacity of high-density lipoprotein to exchange lipids [11, 12]. Another in silico study showed that the spike protein S2 subunit specifically interacts with BRCA-1/2 and 53BP1 [13]. BRCA1 is frequently mutated in breast cancer in women and prostate cancer in men, while 53BP1 is a well-established tumor suppressor protein.
Why has the CDC continued to propagate the following lie?
“How mRNA Vaccines work.
First, mRNA COVID-19 vaccines are given in the upper arm muscle or upper thigh, depending on the age of who is getting vaccinated.
After vaccination, the mRNA will enter the muscle cells. Once inside, they use the cells’ machinery to produce a harmless piece of what is called the spike protein. The spike protein is found on the surface of the virus that causes COVID-19. After the protein piece is made, our cells break down the mRNA and remove it, leaving the body as waste.