In this interview, return guest Stephanie Seneff, Ph.D., a senior research scientist at MIT for over five decades,1 discusses her paper,2 “Innate Immune Suppression by SARS-CoV-2 mRNA Vaccinations: The Role of G-quadruplexes, Exosomes and MicroRNAs,” published in the June 2022 issue of Food and Chemical Toxicology.
The paper was co-written with Drs. Peter McCullough, Greg Nigh and Anthony Kyriakopoulos. In May 2021, Nigh and Seneff published a paper3 detailing the differences between the spike protein and the COVID jab spike protein.
In the “Innate Immune Suppression” paper, they and their other co-authors delve deep into the mechanisms of the COVID shots, showing how they suppress your innate immune system.
The paper caused quite a stir when it was first posted, prior to publication. A campaign was launched to have it retracted on the premise that it would discourage people from getting these life-saving shots — regardless of whether the mechanisms described were true or not.
Ultimately, the controversy led to the resignation of the editor of the journal. Many have also tried to discredit Seneff, and McCullough has since been stripped of his medical credentials.4
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G-quadruplexes (G4) are genomewide targets of transcriptional regulation, and as such as a novel target for drug design. The “G” in G4 stands for guanine, so G4 is DNA sequence of four guanines. It’s one of the four nucleotides — the basic code — in DNA, and it’s known to play an important role in diseases such as cancers and neurological disorders.5
As explained by Seneff, prions, when misfolded, build beta sheets and precipitate out of the cytoplasm, causing plaque to form. This plaque is a hallmark of several neurodegenerative diseases in animals and humans, such as Mad Cow disease, Creutzfeldt-Jakob disease, scrapie (which affects sheep) and chronic wasting disease in deer.
How the COVID Jab Can Induce Autoimmune Disease
As explained by Seneff, the mRNA in the jab is taken into your lymph system and spleen, germinal centers where antibodies are produced, and in order to produce the antibodies, these germinal centers release exosomes. This can help explain the phenomenon of “shedding,” but it also helps explain the immune destruction we see occurring. Seneff explains:
Mechanism of Action
Swiss researchers recently reported finding elevated troponin levels in 100% of COVID jabbed individuals, indicating everyone is suffering some degree of heart damage, even if they’re asymptomatic.6,7 Seneff explains the mechanism by which the COVID shot damages your heart.
The Role of MicroRNAs
Another piece of the puzzle is related to the role of microRNAs, which are embedded in the exosomes that travel to the tissues. MicroRNAs should not be confused with mRNA. They’re two different things. The microRNAs are short pieces of RNA, about 22 nucleotides long. Unlike mRNA, microRNA do not code for protein.
The mRNA in the jabs are designed to be extremely resilient. Normally, mRNA lasts a few hours, but the mRNA in the jabs stick around producing protein in cells for several months, at minimum primarily because of the substitution of the nucleotide uridine with pseudouridine.
Because the mRNA is so resilient, spleen cells have to try to cope with all the spike protein that they cannot stop making, and one way they do that is by pushing the spike protein out in the form of exosomes. Those exosomes also contain microRNAs. Indian researchers found two specific microRNAs in people who got the jab, and these microRNAs interfere with Type 1 interferon response.
Hypothesis to Explain Post-Jab Sudden Death
Seneff goes on to cite animal research from 2005, in which mice were exposed to a virus that causes myocarditis. They wanted to see what would happen if the mice were suffering from myocarditis and then got a shot of adrenaline. So, the mice were infected with the myocarditis-inducing virus, and then, 120 days later, they injected them with adrenaline.
The dose given killed 70% of them. Meanwhile, control mice that did not have myocarditis suffered no ill effect when injected with the same dose of adrenaline. The mice that died, died of heart failure. Basically, their hearts were too damaged to withstand the adrenaline rush. Today, we’re seeing a similar effect in athletes, who are dropping dead while exerting themselves.
Digging for other papers, Seneff found one that detailed the Type 1 interferon response in chromaffin cells, the cells that make adrenaline. Type 1 interferon inhibits and reduces their production of adrenaline.
Seneff’s theory is that the COVID jabs interferes with your body’s ability to respond to Type 1 interferon, thereby allowing too much adrenaline to be released. If your heart has been damaged by the spike protein, the outcome could be lethal, as we’ve seen.
At the same time, microthrombi (micro blood clots) are activated by the spike protein, which could have lethal effects, and endothelial cells (the cells lining your blood vessels) are also inflamed. So, there’s not just one mechanism by which the jabs could kill you.
Spike Protein Creates Incredibly Tough Blood Clots
According to Seneff, blood clots are also connected to the prion aspect. Many different proteins are amyloidogenic and can misfold, causing them to precipitate out, including proteins in your blood. Blood clots are tough to break down, and when you add spike protein into them, they become even tougher.
Seneff suspects the spike protein binds to fibrin, causing it then to misfold in a way that makes it very resistant to breaking down. The same thing happens with prion proteins. When they misfold, they create a gel that becomes denser over time, eventually becoming completely inaccessible to the water base.
This is why I recommend taking fibrinolytic enzymes like lumbrokinase (which is the most effective), serrapeptase and nattokinase, several times a day one hour before or two hours after a meal, if you’re struggling with long COVID, as they help break down the fibrin. To work, you have to take them between meals, on an empty stomach, or else they’ll just act as a digestive enzyme to break down food.
Another technique is to use a near-infrared sauna, which will help address the misfolding of proteins by encouraging autophagy, your body’s natural clean-out process.
The Role of Antibodies in Prion Disease
Antibodies may also play a role in the devastating side effects from the COVID jab. We know that prion protein is upregulated in cells that produce it under stress, and the COVID jab spike protein has been shown to cause cells to make more prion protein. One possibility is that antibodies to a particular part of the spike protein end up binding to the prion protein through molecular mimicry.
As explained by Seneff, researchers have discovered that if you produce antibodies to the C-terminal end of the prion protein, it can cause disease that looks a lot like prion disease but develops much faster.
As it turns out, the antibodies to the C-terminal end of the prion protein prevent the prion protein from going into the endoplasmic reticulum (ER), where it needs to go in order to do its job. Instead, the antibodies keep the prion in the cytoplasm.
Subsequently, the cell gets sick because of these antibodies. The late Luc Montagnier posted a case study with 26 people who developed symptoms of prion disease within the first month after their second vaccine. All died, many within three months of their diagnosis. All were dead within a year, from what was basically an extremely aggressive form of Creutzfeldt-Jakob disease (the human Mad Cow disease equivalent).
Seneff believes antibodies against the spike protein are to blame, because it didn’t happen until they got their second dose. Antibodies developed after that first dose, which primed the cells. Then, after the second dose the cells started making loads of spike protein again, which the antibodies bound to.
This exosome package then traveled up the vagus nerve to the brain, where neurons took them up. Seneff suspects this explains the disease process on those 26 patients.
COVID Jabs Impair Your Immune Function
To circle back to where we began, it seems the reason so many jabbed individuals are now contracting COVID and other infections, and are dying from them, is because Type 1 interferon is suppressed. That suppresses your immune function, making you more prone to contracting infections.
In the interview, Seneff also reviews how chronic exposure to glyphosate is a predisposing condition for bad COVID-19 outcomes, as glyphosate disrupts the immune system. For more details on that, please listen to the interview in its entirety. We also review how glycine supplementation can help displace glyphosate in your body, thereby limiting its damaging influence.
Sources and References
- 1 MIT Stephanie Seneff Bio
- 2 Food and Chemical Toxicology June 2022; 164: 113008
- 3 IJVTPR May 10, 2021: 2(1)
- 4 Rumble October 31, 2022
- 5 Cell Mol Life Science October 2021; 78(19-20): 6557-6583
- 6, 7 Daily Skeptic October 27, 2022
Dr. Joseph Mercola is the founder of Mercola.com. An osteopathic physician, best-selling author, and recipient of multiple awards in the field of natural health, his primary vision is to change the modern health paradigm by providing people with a valuable resource to help them take control of their health. This article was originally published on The Epoch Times.