Previously, Nigh and Seneff co-wrote an entire paper detailing the differences between the spike protein and the COVID jab spike protein. In a non-peer-reviewed research paper just this week published on the pre-print service authorea, they and their other co-authors delve deeply into the mechanisms of the COVID shots, showing how they absolutely, in no way, shape or form, are safe or effective. The shots actually suppress your innate immune system.
"I think McCullough is fantastic and I'm so happy to have him collaborate with me," Seneff says. "I really hope we will be able to find a journal that is willing to publish it. We may have to seek some kind of alternative media to get it published.On January 16, 2022, the pre-print service Authorea published this paper on its web site, assigning it a DOI, thus making it official.
It's really incredible the amount of censorship that's going on right now. I'm in a state of shock all the time. I just keep thinking it's not going to get any worse, and it's truly going to get better, and it just seems to keep on getting worse and worse.
I don't know where the end is. It's very discouraging ... Pharma has so much money behind [them] and they've got it all set up to make sure that nothing gets past them ...
We're hoping to put it up as a preprint, but ... remarkably, they can reject it at the level of preprint as well. We're working on that angle, but it's not easy. When you're writing something this radical, they really fight hard to keep it off the web."
Exceptionally Strong Safety Signals
As noted by Seneff, when you look at the various databases for adverse effects, you can see an exceptionally strong safety signal โ and the COVID shot developers know that. "The numbers are out of sight," Seneff says, and this goes for all levels of side effects, from mild to catastrophic.
Seneff has been looking at the cancer data, for example, and on average, there are twice as many reports of cancer following the COVID shots compared to all other vaccines combined over the last 31 years.
"It's just amazing, because it's overall two times [higher]. Breast cancer, for example, is three times [higher] for these vaccines in one year, as they are for all the other vaccines for 31 years. It's a hugely strong signal," Seneff says.The fact that the signal is that strong is even more remarkable when you consider that most people don't think the COVID shot could be a variable in their cancer emergence, so they never report it. "It puzzles me that they're willing to do such damage to the health of the whole population of the world. I don't understand that degree of evilness," Seneff says. Type-1 Interferon Disruption
"Lymphoma is also showing up much more frequently with these [COVID shots]. There's just an amazing signal there in VAERS [the U.S. Vaccine Adverse Events Reporting System]."
The shots suppress your innate immune system by inhibiting type-1 interferon. One of the first studies to tip off Seneff and McCullough to this was an Indian study, in which human cells grown in a culture were exposed to the DNA nanoparticles that instruct them to make SARS-CoV-2 spike protein, much like the COVID shots do.1
The cell strain is called HEK-293. These are cells that were taken from the kidneys of an aborted fetus in the 1980s and are frequently used in research. While taken from the kidneys, these cells have neuron-like properties. When programmed to make spike protein, these cells release that spike protein inside exosomes โ lipid nanoparticles inside which the spike protein is packaged.
Exosomes act as a communication network for cells. When a cell is under stress, it releases exosomes containing some of the molecules that are stressing it. So, in the case of the COVID shots, the exosomes contain spike protein and microRNA. MicroRNAs are signaling molecules that are able to influence cell function. They cause the cell to change its behavior or metabolism. Typically, they do this by suppressing certain enzymes.
The Indian study found two specific microRNAs inside the exosomes released by these neuron-like cells: miR-148a and miR-590. The researchers then exposed microglia (immune cells in your brain) to these exosomes. So, as explained by Seneff, you've got neurons in your brain producing spike protein, or taking up spike protein that is in circulation, and reacting to it by releasing exosomes.
The exosomes are then picked up by microglia, the immune cells in your brain. When the immune cells receive those exosomes, they turn on an inflammatory response. This is primarily a response to those microRNAs, the miR-148a and miR-590. Of course, you also have the toxic spike protein there.
Combined, they cause inflammation in the brain, which damages neurons. This inflammation, in turn, can contribute to a number of degenerative brain disorders. The lipid particles in the COVID shot, which contain the mRNA, are similar to exosomes, but not identical. They're also very similar to low-density lipid (LDL) particles.
"I think the exosomes are probably quite a bit smaller. The vaccine particles are bigger. They're more like an LDL particle. The vaccine particles have cholesterol in their membrane, and they have lipoprotein. So, they're made to look like an LDL particle.Seneff wrote an entire paper2 detailing the differences between the viral spike protein and the COVID jab spike protein, together with Greg Nigh, which was published in the International Journal of Vaccine Theory, Practice and Research in May 2021. It basically serves as a primer for understanding what we discuss here.
But then they throw in this cationic lipid, which is really, really toxic โ a synthetic cationic lipid that makes it positively charged. Experimentally, they've found that this lipid, when the particle is taken up by the cell, is released into the cytoplasm, [where] that mRNA then makes spike protein.
[The COVID shots] are very cleverly designed, both in terms of protecting the RNA from getting broken down, and in terms of making the RNA be very efficient at making spike protein. It's very different from the mRNA that the virus makes, even though it codes for the same protein."
Getting back to the Indian paper cited above, they found that the microglia ended up producing inflammation in the brain, and the two microRNAs were central in this process. The miR-148a and miR-590 were put into those exosomes with the spike protein, and these two microRNAs are able to significantly disrupt the type-1 interferon response in any cell, including immune cells.
Type-1 interferon also keeps latent viruses like herpes and varicella (which causes shingles) viruses in check, so if your interferon pathway is suppressed, these latent viruses can also start to emerge. The VAERS database reveals many who have been jabbed do report these kinds of infections. Suppressed interferon also raises your risk of cancer and cardiovascular disease.
Type-1 Interferon Response Is Crucial in Viral Infections
As explained by Seneff, the type-1 interferon response is absolutely crucial as the first-stage response to a viral infection. When a cell is invaded by a virus, it releases type-1 interferon alpha and type-1 interferon beta. They act as signaling molecules that tell the cell that it's been infected.
That, in turn, launches the immune response and gets it going early in the viral infection. It's been shown that people who end up with severe SARS-CoV-2 infection have a compromised type-1 interferon response. As noted by Seneff:
"It's ironic that the vaccines are being given to protect you from COVID, yet, they produce a situation where your immune cells are ill-equipped to fight SARS-CoV-2 if it gets into the cell. The trick is, the vaccine produces a tremendous antibody response, and that's typical of severe disease.Importantly, the antibody response you get from the COVID shot is exponentially higher than what you get from natural infection, and research has shown that the level of antibody response rises with disease severity. So, the shot basically mimics severe infection. In mild infection, you may not produce any antibodies at all, because the innate immune cells are strong enough to fight off the infection without them.
So, the [COVID shot] fools your immune system into thinking that you've had a severe case of COVID. It's really interesting that way, because it's gotten past the mucosal barrier of the lungs, it's gotten past the vascular barrier of the blood, into the muscle. Also, it's been disguised.
The RNA doesn't look like a virus RNA, it looks like a human RNA molecule. Part of the modifications [made to the mRNA in the jab] was to make it very sturdy, so it can't be broken down. It's also very good at making [spike] protein fast, which also has a problem because it leads to a lot of errors, which is another issue ...
The immune cells take up the nanoparticles and carry them through the lymph system into the spleen. Multiple studies have shown that it ends up in the spleen ... the ovaries, the liver, the bone marrow ... The spleen, of course, is very important for producing antibodies."
It's when your innate immune system is weak that you get into trouble, and part of that weakness is a suppressed type-1 interferon response. If your type-1 interferon response is deficient, your immune cells are not very capable of stopping the spread of the virus in your body.
According to Seneff, the reason type-1 interferon supplementation has not been recommended thus far is because you have to time it perfectly in order for the immune cascade to function properly. Type-1 interferon plays a definitive role only at the very earliest stage of the infection. Once you've entered a moderate or severe infection stage, it's too late to use it.
COVID Shots Confuse Your Immune System
As noted by Seneff, the COVID shots are so unnatural that your immune system doesn't quite know what to do anymore.
"My impression is that the immune cells don't know what the hell's going on. There's this toxic protein being produced in massive amounts by the immune cells. That's extremely unusual. There's no sign of any kind of viral infection because these RNAs look like human RNAs.There are also antibodies that enhance disease rather than fight it, and the level of these antibodies declines at a slower pace than the protective antibodies. So, after a number of months you end up with a NEGATIVE immune response. In other words, you're now more prone to infection than ever before. As explained by Seneff:
It's as if the human immune cells suddenly decided to make a really toxic protein, and make lots of it โ which is exactly what they're doing โ and the immune system is completely baffled by this. The immune cells have no clue what to do with it.
Of course, these immune cells that are overloaded with all this spike protein, they say, 'I've got to get rid of this stuff,' so they ship it out as these exosomes. The microRNAs [in the exosomes] think that the recipient cells are going to need those particular signaling molecules to help it do whatever it needs to do to cope with this toxic load.
So, you're spreading the spike protein around to the rest of the body, just to dissipate the toxicity you're coping with in the spleen, I think. Those exosomes are also very good for training antibodies. There was a nice paper that showed the exosomes being released [have] spike protein in their membrane, the exterior of the exosome.
It's quite cool that the spike protein is displayed there, because this allows the immune cells โ the B-cells and the T-cells that need to get up close and personal to it โ to figure out how to shape their antibodies. The antibodies get shaped to match the toxic protein that's exposed on the surface of the exosomes.
After something like 14 days of the second [jab], the exosomes induced an antibody response. [The researchers] felt the exosomes played a critical role in this extreme antibody response that was produced by the B-cells and the T-cells, the adaptive immune system.
But I think the way the vaccine works is that there's no game that you can choose other than to make antibodies. It's the only way you can fight this. It's a toxic protein that's being produced and released by these immune cells, and the only thing you can do to stop it is to make antibodies.
They try to make lots and lots of antibodies that will glue onto those toxic spike proteins and block them from being able to get in through the ACE2 receptor. That's the job of the antibodies. They do a good job of it, initially ... It's true that they do protect you from disease. Unfortunately, the antibody levels drop pretty dramatically, pretty quickly."
"There's a crossover point at which the enhancing antibodies can be stronger than the protective antibodies, and that's when you can get this antibody dependent enhancement (ADE) that people have seen in the past with [other] coronavirus vaccines. We're still trying to see if that's the case with [the COVID jabs]. There is some evidence here and there, but it's not [conclusive yet]."The Importance of Cytotoxic T-Cells
After the India study tipped off Seneff and McCullough to the interferon problem, they came across a Chinese study3 that tracked the effect of the COVID jab on the immune system over time. Here, they discovered that the infection caused an increase in CD8+ T-cells, important cytotoxic T-cells that actually remove infected cells.
As noted by Seneff, the CD8+ cells are an important part of the defense against SARS-CoV-2. Importantly, CD8+ T-cells were enhanced in response to natural infection, but not in response to the COVID shot. They too found type-1 interferon suppression post-jab. So, in the aftermath of the jab, not only is your first-line response depressed โ the type-1 interferon response โ but you're also missing the part of the immune response that cleans away infected cells.
The microRNA That Influences Myocarditis Risk
A third microRNA (mRNA) created by natural SARS-CoV-2 infection is miR-155, and it plays an important role in heart health. Early on in the pandemic, there were reports of COVID-19 causing heart problems.
Seneff suspects the miR-155-containing exosomes may also be present post-jab, and may play a role in the heart damage that's being reported. Specifically, miR-155 is associated with myocarditis. As mentioned earlier, microRNA suppresses certain proteins that then cause a complicated cascade response. When a particular protein that is a critical player gets suppressed by a microRNA, then a whole different cascade takes place.
Why Autoimmune Problems May Arise Post-Jab
The antibodies produced by the jab also have several short peptide sequences in them that have previously been found in several human cells that are related to autoimmune disease. Seneff explains:
"Kanduc has written a lot about this. She's an expert on these antibodies ... The [SARS-CoV-2] spike protein is very overlapped with human protein. That means when you build a really strong antibody response to the spike protein, those antibodies can get confused and they can attack a human protein that has a similar sequence.Neurological Problems in Women
That's a classic form of autoimmune disease. It's called molecular mimicry. There were many different proteins that matched. It was quite surprising ... It seems to be very well designed to induce autoimmune disease, if you produce antibodies to those sequences in the spike protein."
The shots are also tightly associated with neurological problems such as uncontrollable tremors and shaking. Curiously, this side effect disproportionally affects women. The mechanism here again involves the exosomes. Seneff explains:
"I feel there's a very strong signal for the idea, which I'm pushing, that you have those immune cells in the spleen making spike protein and releasing it in exosomes. It's been shown in studies on Parkinson's disease that those exosomes travel along nerve fibers.Sulfatide, an important lipid carrier, is the only sulfonated lipid in the human body. Your liver makes most of the sulfatide, which is then carried by your platelets (blood cells) to other areas in your body. The myelin sheath contains high amounts of sulfatide. It's part of what protects the myelin sheath. In demyelinating diseases, that sulfatide erodes, ultimately allowing the myelin to be attacked.4
They'll go along the splanchnic nerve, they'll hook up with the vagus nerve, they'll go up to the brain and get into all these different nerves in the brain. When you look at the VAERS database, you see tremendous signals for all kinds of things that suggest different nerves are being inflamed.
For example, there are 12,000 cases of tinnitus associated with the COVID-19 vaccine, and that's only what's reported. Tinnitus is a strong signal. Tinnitus is going to be inflammation of the auditory nerve. This means you have to go all the way from the spleen, up the vagus nerve, and then connect to the auditory nerve to cause tinnitus.
Then you have Bell's palsy, which is inflammation of the facial nerve. You have migraine headache. There are over 8,000 cases of migraine headache, which is linked to an inflammation of the trigeminal nerve.
It probably also goes, I suspect, along the nerve fibers of the spinal column, which may be causing some of these cases where they're finding paralysis. People have a lot of mobility issues connected with these vaccines.
I see the possibility of causing a lot of disturbances to the myelin sheath, and we talk about that in the paper. It involves, again, complex signaling. You can get to the myelin sheath problem through the type-1 interferon disruption.
That, again, involves something called interferon response factor 9 IRF9. This protein triggers the production of sulfatide in the liver, and this protein gets suppressed by these microRNAs that I mentioned earlier."
Seneff believes the COVID jab results in significant myelin damage, thanks to these inflammatory exosomes. This damage does not necessarily show up right away, although some jab recipients experience acutely devastating effects. It could take 10 years or more before a demyelinating disease sets in.
"I think we're going to see people getting these neurodegenerative diseases earlier and earlier in life than they used to," Seneff says, "and I think anybody who already has any of these diseases is going to have accelerated progression."We May Soon See an Explosion of Parkinson's Cases
Disturbingly, loss of smell and dysphagia, the inability to swallow, are both signs of Parkinson's disease, and both of these conditions are being reported post-jab by the thousands. So, in years to come, we could be looking at an explosion of Parkinson's.
"Parkinson's studies have shown that you can get pathogens in the gut that produce a prion-like protein, which is what the spike protein is. The immune cells then take it up and take it to the spleen. This, of course, causes stress.Health Problems We Can Expect to See More Of
A stressed immune cell in the spleen upregulates and produces more alpha-synuclein. Alpha-synuclein is a molecule that fights infection, and that's the molecule that misfolds in association with Parkinson's disease.
I'm fascinated with all of these molecules that are prion-like. There's the prion protein itself, which is associated with CJD, Creutzfeldt-Jakob disease, but then there's the alpha-synuclein and amyloid beta, there's TDP-43, which is associated with ALS.
All of those diseases are overrepresented in the VAERS database for the COVID shots, compared to all the other vaccines combined over 31 years. It's just completely out of line.
There are 58 cases of Alzheimer's in association with the COVID vaccines, and 13 in association with all the other vaccines over 31 years. That's several times more โ 58 versus 13.
CJD is also much more common. It's almost seven times as common in the COVID vaccine cases. CJD is a terrible disease. You get very crippled and die after a few years. That's the classic prion protein [disease]. It's extremely rare. Only 1 in 1 million gets CJD.
There was a person who contacted me from France whose wife got CJD just a few weeks after the second vaccine. He was absolutely convinced the vaccine caused it. There are actually 27 cases [of CJD] reported in VAERS for the COVID-19 vaccines, against only four cases over the entire history of all other vaccines combined."
In time, Seneff predicts we'll see a dramatic increase in infections and cancers of all types, autoimmune diseases, neurodegenerative diseases and reproductive issues. As mentioned, research has demonstrated that the spike protein accumulates in the spleen and women's ovaries.
Without doubt, inflammation in the ovaries is not a good thing. Men also report swollen testes, and that could be indicative of inflammation as well. Preliminary data show women who get the jab within the first 20 weeks of pregnancy have a miscarriage rate of 82% to 91%.5 There are also VAERS reports describing fetal damage. Of course, it could also impair future fertility.
As described earlier, some antibodies produced by the jab can react to human proteins. One protein that is similar to the spike protein that the antibodies attack is syncytin, which is essential for the fertilization of the egg. The concern is that the antibodies might attack and destroy syncytin, thereby disrupting and preventing implantation in the placenta.
Omicron โ A Blessing in Disguise?
The jabs also perpetuate COVID, with ever-new variants of the virus.
"In the first paper that Greg and I wrote, we predicted the vaccines would cause an increased emergence of variants of spike protein, altered versions of the virus, under the pressure of the vaccine," Seneff says.That blessing may be canceled out in those who have received multiple COVID jabs, however. Each dose erodes your immune response, such that it becomes increasingly compromised with each jab. Again, this has to do with the suppression of type-1 interferon, discussed earlier.
"Indeed, it looks to me like that's what's happening. But I'm really hopeful with Omicron, because Omicron looks like it's a milder virus, but incredibly infectious. It'll flash through the population and give everybody, essentially, a vaccine. It's kind of like a natural vaccine, I think.
[Research] showed that ... having had Omicron, you were protected, to some extent, from Delta. Delta's disappearing anyway, because Omicron is chasing it out. It's really great. I think Omicron is God's gift from heaven."
What Catalyzes Damage in Athletes?
More than 400 cases of serious heart problems and death have also been reported among professional athletes,6 who are some of the healthiest people on the planet. What mechanism can account for this phenomenon? How is it that the COVID jabs can cause enough damage to take out young people with optimized biology?
Seneff suspects that being fit might cause you to have more ACE2 receptors in the heart, and the S1 portion of the SARS-CoV-2 spike protein binds to the ACE2 receptor. She believes the spike protein is being delivered to the heart via exosomes, by way of the vagus nerve, and, again, the miR-155 exosome is associated with heart problems.7
Additionally, when the S1 spike protein binds to the ACE2 receptor,8 it disables the receptor. When you disable ACE2, you get an increase in ACE, which causes high blood pressure and elevates angiotensin 2. When angiotensin 2 is overexpressed, you can get intense inflammation in the heart. If you're engaging in intense exertion and your heart is inflamed, you can trigger cardiac arrest, which is what we see in many of these athlete cases. They're collapsing on the field.
G-Quadruplexes
Another focus of Seneff's and McCullough's paper is something called G4 or G-quadruplexes.
"G-quadruplexes are really fascinating, and I don't have a handle on them at all," Seneff says. "It's hard biology, even harder than a lot of the other stuff that I've been reading ...Summary
G4s are basically an arrangement of [guanines]. Guanines are one of the four nucleotides that make up DNA or RNA. Guanine is the G in the G4. What happens is that a sequence of nucleotides on a DNA or an RNA string can fold in on itself and form G-quadruplexes. It's four guanines, at different places on the protein, winding back around and sticking together.
There's a metal in the middle โ often potassium or calcium โ that helps to stabilize these G4s. The interesting thing about them is that they make the water around them structured. They make gelled water [aka exclusion zone (EZ) water] ...
Those G4s can form in the DNA, and that actually keeps it from becoming active. [The DNA] doesn't get converted into RNA, and it doesn't make protein if it has those G4s. Probably, the EZ water doesn't allow anything to get close. Think of it as being stuck in a gel.
There are a lot of G4s in the promoter regions of these DNA sequences, and there are lots of proteins that have these G4s in their promoter region. Interestingly, there are certain proteins that can unravel them. There are proteins that can bind to them and cause the G4 to undo, and that activates or allows the protein to be expressed.
It's a regulatory element that controls which proteins get to be expressed from the DNA. Many of the proteins that have these G4s in their promoter are cancer oncogenes. As long as they stay gelled, they're inactive, but if they become ungelled, they become active.
It turns out that prion proteins ... [are] made from RNA, and the RNA has these G4s. The protein can bind to the G4s in the RNA and both of them react. The theory is that the protein becomes prion-like. These prion proteins have two ways to be, one is safe and one is not safe, and the G4s increase the risk for prion protein misfolding.
The presence of those G4s, and the meeting with those G4s, increases the risk of misfolding in the prion-like configuration.9 The interesting thing about that is that spike protein is a prion-like protein. The RNA they built for the [COVID jab], they did something called codon optimization, which involved putting a lot more guanines into the RNA than [found] in the original [virus]. They enhanced the guanine.
Enhancing the guanine means increasing the number of G4s, which means increasing the risk of the spike protein misfolding into a prion like protein. I think that the G4s increase the risk, the danger of spike protein [acting] as a prion-like protein.
But we don't really know what the consequence of having all these G4 RNAs in the cytoplasm will be. We have massive numbers of these RNAs sitting there with their G4s. What is that going to do to the rest of the G4 regulatory process? We do not know. Nobody knows. Nobody has a clue."
To summarize the central point of Seneff's latest paper, the COVID jab causes alpha interferon suppression, which weakens your immune system. Indeed, regulators in the European Union are now warning that repeat COVID shots can weaken overall immunity.10
The primary mechanism is the impairment of alpha interferon response, which is essential for the proper activation of your innate immune system, your cellular immunity, mostly your T-cells and killer cells. When functioning properly, the cell launches the type-1 interferon response as soon as it's infected with a virus.
It triggers the immune cells to come in, kill the virus and remove the debris. This activates the humoral component of your immune system, the antibody production, which takes longer. (That's why they say you are not protected until 14 days after the injection.)
How is type-1 interferon suppressed by the jab? It's suppressed because type-1 interferon responds to viral RNA, and viral RNA is not present in the COVID shot. The RNA is modified to look like human RNA molecule, so the interferon pathway is not triggered. Worse, the interferon pathway is actively suppressed by the large number of spike proteins produced from the mRNA in the shot, and by the microRNAs in the exosomes released by the stressed immune cells.
Watch Dr. Seneff's interview here.
Sources and References:
- 1 Frontiers in Immunology April 14, 2021 DOI: 10.3389/fimmu.2021.656700
- 2 International Journal of Vaccine Theory, Practice and Research May 10, 2021; 2(1): 402-444
- 3 Cell Discovery 7, Article number: 99 (2021). October 26, 2021
- 4 J Lipid Res. 2012 Aug; 53(8): 1437-1450
- 5 Science, Public Health Policy, and the Law November 2021; 4: 130-143
- 6 Good Sciencing Athlete Deaths
- 7 European Journal of Heart Failure March 5, 2021
- 8 Frontiers in Immunology June 4, 2021
- 9 Nucleic Acids Res. 2014 Aug 18; 42(14): 9327-9333
- 10 Business Standard January 12, 2022
Reader Comments
BK
Most doctors are ignorant about the pernicious effects of oxalate in oxalate sensitive people. Here is a story from the Daily Mail from a physician who never considered the idea that oxalates in otherwise healthy foods could be causing severe ill health. Until, of course, it happened to her and her world was turned upside down: [Link]
BK
Who says Canadians cannot, PROTEST. This will be the biggest Freedom Convoy in history, bar non !! Meanwhile in the USA truckers are doing what ?
ps. PM Trudope called the truckers, terrorists. imagine that, eh...
[Link]
[Link]
as many as 150,000 Truckers headed to Ottawa,
[Link]
~ Gator
16. DiscussionThere has been an unwavering message about the safety and efficacy of mRNA vaccinations against SARSCoV-2 from the public health apparatus in the US and around the globe. The eefficacy is increasingly in doubt, as shown in a recent letter to the Lancet Regional Health by Gunter Kampf [215]. Kampf provided data showing that the vaccinated are now as likely as the unvaccinated to spread disease. He concluded: In this paper we call attention to three very important aspects of the safety pro file of these vaccinations.
First is the extensively documented subversion of innate immunity, primarily via suppression of IFN-a and its associated signaling cascade. This suppression will have a wide range of consequences, not the least of which include the reactivation of latent viral infections and the reduced ability to e effectively combat future infections.
Second is the dysregulation of the system for both preventing and detecting genetically driven malignant transformation within cells and the consequent potential for vaccination to promote those transformations.
Third, mRNA vaccination potentially disrupts intracellular communication carried out by exosomes, and induces cells taking up spike mRNA to produce high levels of spike-carrying exosomes, with potentially serious inflammatory consequences. Should any of these potentials be fully realized, the impact on billions of people around the world could be enormous and could contribute to both the short-term and long-term disease burden our health care system faces.
Given the current rapidly expanding awareness of the multiple roles of G4s in regulation of mRNA translation and clearance through stress granules, the increase in pG4s due to enrichment of GC content as a consequence of codon optimization has unknown but likely far-reaching consequences. Specific analytical evaluation of the safety of these constructs in vaccines is urgently needed, including mass spectrometry for identification of cryptic expression and immunoprecipitation studies to evaluate the potential for disturbance of or interference with the essential activities of RNA and DNA binding proteins.
17. Conclusions
It is imperative that worldwide administration of the mRNA vaccinations be stopped immediately until further studies are conducted to determine the extent of the potential pathological consequences outlined in this paper. It is not possible for these vaccinations to be considered part of a public health campaign without a detailed analysis of the human impact of the potential collateral damage. It is also imperative that VAERS and other monitoring system be optimized to detect signals related to the health consequences of mRNA vaccination we have outlined. We believe the upgraded VAERS monitoring system described in the Harvard Pilgrim Health Care, Inc. study, but unfortunately not supported by the CDC, would be a valuable start in this regard [208].
In the end, we are not exaggerating to say that billions of lives are at stake. We call on the public health institutions to demonstrate, with evidence, why the issues discussed in this paper are not relevant to public health, or to acknowledge that they are and to act accordingly. Until our public health institutions do what is right in this regard, we encourage all individuals to make their own health care decisions with this information as a contributing factor in those decisions.
Ken
But then they throw in this cationic lipid, which is really, really toxic โ a synthetic cationic lipid that makes it positively charged. Experimentally, they've found that this lipid, when the particle is taken up by the cell, is released into the cytoplasm, [where] that mRNA then makes spike protein. "
So, I've been researching this but I've made not conclusion as it's too complicated for my little brain.
Is having a thicker cell wall of LDL protective, as it (perhaps) provides (too) many layers to pass through. Or is a thick cell membranee of LDL more attractive? Lipophilic - attracting and magnetising other LDL particles into the cell membrane and ultimately pass and enter the cell?
Unless it just gets trapped in the cell membrane?
LDL and HDH have different physical characteristics as to how they place themselves on the cell membrane.. With the former standing upright and the latter crossing over (kind of). It appears to me that LDL is easier to pass through, as it does not cross over.
It will be a nice place to live when the current inhabitants are cleared from the surface.
Not fallen just wounded....Time for a Trucker Freedom Convoy down under !!
I have no free time to waste listening to him.
Reading his articles and seeing him in film productions, he never came across as really trustworthy person to me. My "female" and intuitive side speaking. I couldn't nail it before - but now.
In Ukraine there was a record holder for coronavirus vaccinations.
Aleksey Sukach travels the country receiving injections of various vaccines. In an interview with one of the Ukrainian TV channels, he talked about the reasons for such an unusual zeal.
The story, broadcast on Ukrainian television, says that the 29-year-old Ukrainian has already received 20 doses of the vaccine .
According to Sukach, he once managed to get 5 vaccinations in one day .
The man told the reporter that he came to Kharkov to get vaccinated because he wanted to walk around the city and get a ticket to a sanatorium.
โI thought Kharkiv would give me a ticket so that I can live there for at least a month, because there is better food and all. Because in Sumy, no matter how many documents I submitted, Sumy resists, refuses, "complains the hero of the story.
Sukach claims he feels good and declares his desire to be vaccinated more: he intends to receive three dozen vaccinations.
Note that the Ukrainian media already wrote about him in December, so the man had 15 injections.
Probably, a very determined Ukrainian will still be able to get what he wants
RC
as for adults, if you weren't a dirty child you better stock up on those supplements.