The injected mRNA (or DNA, in the case of the Johnson & Johnson shot) instructs your body's cells to create millions of copies of the spike protein, the most pernicious constituent of the Covid-19-causing SARS-CoV-2 virus. The spike protein has been separated from the virus and studied in isolation. It is becoming apparent that it harms every tissue it comes in contact with. Though there are other harmful ingredients in the Covid-19 injections, the interaction of the spike protein with various bodily tissues is the primary biological mechanism of action that explains the wide variety of severe adverse event types being reported to VAERS as a result of the Covid-19 inoculations. What follows is an explanation of the literature on how the spike protein can damage the human body.
The Spike Protein can Cross the Blood-Brain Barrier and Cause Brain Inflammation:
The Spike Protein Can Cause Blood Clotting and Thrombosis:
The Spike Protein Causes Abnormal Cell Signaling Which May Cause Pathologies:
The Spike Protein May Induce Cancer Through Inhibition of Tumor Suppressing/DNA Repair Proteins:
The Spike Protein Has Prion Characteristics and Can Interact with Prion Proteins Involved in Neurodegenerative Diseases:
The Spike Protein May Harm Male Fertility:
The Spike Protein Rapidly Appears in the Blood:
The spike protein has been demonstrated to be in the blood plasma of 11 of 13 subjects. This means the injected mRNA or DNA entered cells and used them to produce the spike protein which then enters the bloodstream within twenty-four hours. Once in blood circulation, the spike protein can end up almost anywhere in the body.
The blood-brain barrier is a tightly-knit layer of cells that surrounds and protects the brain from things like the toxic substances we Americans are fond of consuming in our diets. This protection is vital as the brain is not as well equipped to handle toxic assault as the rest of the body. The spike protein, by itself, can cross the blood-brain barrier and, once there, can induce brain inflammation that can lead to a panoply of issues.
A prion is a protein that when it becomes misfolded, and therefore unable to function properly, tends to spread this misfolding issue to other like proteins (misfolded protein 'X' can cause other proteins 'X' to misfold) which then tend to form large aggregates of non-functioning protein. If the misfolding issue becomes large enough, it can destroy the cell in which it is occurring. The spike protein has characteristics of a prion protein. It has also been shown to interact with prion proteins known to be involved in the disease onset and progression of Alzheimer's, Parkinson's, and ALS. Thus, spike protein produced through Covid-19 "vaccination" may seed or exacerbate these neurodegenerative disorders.
The spike protein is fusogenic in nature; that is, it is the mechanism by which the SARS-CoV-2 virus fuses with and subsequently enters the host's cells. It is no stretch, therefore, to imagine spike protein-expressing cells fusing with other cells, particularly if the cells are in the blood. The molecular target with which the spike protein interacts is the ACE2 receptor. It has been demonstrated that the spike protein increases coagulation of blood platelets that express ACE2 to enhance thrombosis (the formation of a blood clot inside a blood vessel which obstructs the flow of blood). Thrombosis can be a severe problem and can cause death if the blood flow is sufficiently closed off to major organs. Another mechanism by which the spike protein can induce hypercoagulation is it impairs the breakdown of fibrinogen, a major structural constituent of a blood clot. Inhibition of fibrinogen destruction will enhance blood clot formation.
Cells that can produce ACE2 are found all over the body in various tissues. The normal function of ACE2 is to convert angiotensin II to angiotensin 1-7 which subsequently causes vasodilation to reduce blood pressure. However, when the spike protein interacts with ACE2 it can cause a signaling cascade which results in the ACE2-producing cell to do something it would not otherwise do. This aberrant spike protein-induced cell function can have significant negative heatlh ramifications.
The Spike Protein Alone can Interact with and Disrupt Heart Function:
The myriad reports of myocarditis and pericarditis post-"vaccination" can easily be a result of spike protein action at the heart. The above-mentioned cell signaling resultant from spike-ACE2 interactions can also occur through spike-CD147 receptor interplay and result in likewise detrimental consequences to cells surrounding the heart including increased migration and secretion of pro-inflammatory signaling molecules. The spike protein can also directly damage the heart by causing cardiomyocytes (heart cells) to shift into a diseased shape or induce malfunctioning electrical conductance which can then bring about improper contraction timing. One can see the danger in this, but, unfortunately, there is more. The spike protein by itself can cause heart dysfunction through hypertrophic remodeling (excess heart growth) and inflammation.
Antibodies Against the Spike Protein Can Cause Autoimmune Disorders:
The spike protein contains several peptides, which is a small string of amino acids that are identical to peptides in various other proteins that occur naturally in the human body. A problem arises when the immune system is trained to attack a peptide shared by the spike protein and another protein in the human body as the immune system begins to attack tissues expressing this protein of it's own body. This is the basic nature of autoimmunity. Antibodies mark targets which the immune system subsequently destroys. The peptides to which antibodies bind are called epitopes. The spike protein has over 300 peptides (potential epitopes) of 6 amino acids in length and over 25 that are 7 amino acids in length that are identical to human proteins. Thus, the Covid-19 so-called vaccinations have high potential to induce autoimmune disorders. Going further, it is possible that not only autoimmunity, but also a phenomenon known as pathogenic priming may result. This phenomenon occurs when antibodies against the SARS-CoV-2 spike protein actually enhance subsequent infections of the SARS-CoV-2 virus.
The spike protein has now been demonstrated to bind to and inhibit both p53 and BRCA1 proteins. These proteins are know as 'tumor suppressor' proteins for their ability to blunt cancer progression. Their molecular function is to sense and repair damage and/or mutation to DNA as these are a source of cancerous cell growth. So vital is the function of these proteins, that biology as we know it would not exist without them. The spike protein, once created by the cell, can enter the nucleus of the cell and interact with these vital proteins. This DNA repair mechanism is also involved in genetic recombination events that grant memory immune cells their ability to grant their host lifelong immunity to specific pathogens. More on this below.
The 'Vaccines' Now Have Negative Efficacy Which Implies They Are Inducing an Acquired Immunodeficiency Syndrome-like Response That Can Be Attributed To the Spike Protein:
Multiple studies are now showing the Covid-19 'vaccines' are producing negative efficacy which means the inoculated are more likely to be sickened by Covid-19 than those who are not inoculated. If the injections were merely saline solutions, one would expect an equal infection rate in both the vaxxed and unvaxxed. As that is not the case, it implies the injections are having a detrimental effect on the immune systems of the fully inoculated; it implies an acquired immunodeficiency syndrome (AIDS). Production of the spike protein in the body can produce the AIDS effect through multiple mechanisms. As mentioned in the section immediately above this, the spike protein can interfere with genetic recombination events critical to adaptive immunity. Multiple cell types that express the spike protein have been demonstrated to consume and destroy several varieties of immune cells. Lastly the Covid-19 shots have been demonstrated to retrain the immune responses in their recipients to reduce immunological potency against viruses, bacteria, fungi, and tumors. The injections are a recipe for AIDS.
Multiple cell types within the testes produce an abundance of the ACE2 receptor. As discussed in a different section on this page, spike protein interaction with ACE2 can produce pathological consequences in these unfortunate cells. Thus, inoculation-induced spike proteins present in the testes may induce aberrant cell functions which can negatively impact male reproductive capacity.