Evidence shows that C-19 is a designed bioweapon that has a toxic structure replicated in vaccines.
We have reported that C-19 was created in a lab, and we have two arguments. The first scientific recipe for the lab creation of C-19 was described in the 2018 grant app to the US DARPA given by scientists who directly collaborated with the Zheng-Li Shi of the Wuhan Institute of Virology.
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The research proposal explicitly stated that bat coronaviruses, collected in southern China by the WIV, would be isolated and genetically sequenced, particularly the spike proteins.
The spike proteins demonstrated a high risk for infection would be artificially combined with other bat coronaviruses backbones, producing entirely new and potentially dangerous coronaviruses.
The second fact in the DARPA grant app was the artificial insertion of furin polybasic cleavage sites, short sequences of amino acids.
According to TGP, the enzyme furin ‘’is ubiquitous in the human body, found in multiple organ systems including lungs, heart, kidneys, brain and blood vessels.’’
The PRRA sequence is C-19 doesn’t exist in hundreds of close bat coronaviruses relatives from C-19 emerged.
The 2018 DARPA research app proposed inserting furin polybasic cleavage sites like PRRA into low-risk bat coronaviruses and testing the lab-created viruses’ ability to infect human cells.
DARPA rejected the app because it involved the dangerous gain of function experiments creating viruses.
We have to mention that the section of the C-19 genetic code that creates the PR segment of the PRRA is very rare.
One scientific article emphasized the C-19 furin polybasic cleavage site, and its structures may be toxic.
‘’ The approximately 20 amino acids surrounding COVID-19’s furin polybasic cleavage site possess sequence and structural elements comparable to those of Staphylococcal enterotoxin B (SEB).
SEB acts as a “superantigen” and immune system activator stimulating the release of large amounts of cytokines, often called “cytokine storm,” and capable of producing multi-organ hyper inflammation similar to toxic shock syndrome.
The authors also state that COVID-19 mutations strengthen its “superantigen” character.’’ The article added.
Caution is warranted regarding C-19 mandates, which initiate spike protein synthesis inside humans and replicate the toxic structures.
“dramatically increase inflammation on the endothelium and T cell infiltration of cardiac muscle and may account for the observations of increased thrombosis, cardiomyopathy, and other vascular events following vaccination.” The article said.
We also have to mention that Moderna, a biotechnology company, holds a patent filed on February 7, 2017, explaining protein cleavage sites and including a complimentary genetic sequence.