The Incredible Roaming Covid Spikes! By Mrs Vera West
Here is more information for your consideration about the coronavirus spike proteins, which according to new research can travel from the site of injection, I take it the shoulder, but in the good old days, it was the butt if my memory serves me somewhat well, The problem is what happens when the spike protein starts circulating in the body, if it does? Clearly the best thing to do now is like the origin of Covid-19, to shut down all debate, imprison all recalcitrant scientists, and sing “don’t worry, be happy.” That should solve the problem, yes sir!
“COVID vaccine researchers had previously assumed mRNA COVID vaccines would behave like traditional vaccines. The vaccine’s spike protein — responsible for infection and its most severe symptoms — would remain mostly in the injection site at the shoulder muscle or local lymph nodes.
But new research obtained by a group of scientists contradicts that theory, a Canadian cancer vaccine researcher said last week.
“We made a big mistake. We didn’t realize it until now,” said Byram Bridle, a viral immunologist and associate professor at University of Guelph, Ontario. “We thought the spike protein was a great target antigen, we never knew the spike protein itself was a toxin and was a pathogenic protein. So by vaccinating people we are inadvertently inoculating them with a toxin.”
Bridle, who was awarded a $230,000 grant by the Canadian government last year for research on COVID vaccine development, said he and a group of international scientists filed a request for information from the Japanese regulatory agency to get access to Pfizer’s “biodistribution study.”
Biodistribution studies are used to determine where an injected compound travels in the body, and which tissues or organs it accumulates in.
“It’s the first time ever scientists have been privy to seeing where these messenger RNA [mRNA] vaccines go after vaccination,” Bridle said in an interview with Alex Pierson where he first disclosed the data. “Is it a safe assumption that it stays in the shoulder muscle? The short answer is: absolutely not. It’s very disconcerting.”
The Sars-CoV-2 has a spike protein on its surface. That spike protein is what allows it to infect our bodies, Bridle explained. “That is why we have been using the spike protein in our vaccines,” Bridle said. “The vaccines we’re using get the cells in our bodies to manufacture that protein. If we can mount an immune response against that protein, in theory we could prevent this virus from infecting the body. That is the theory behind the vaccine.”
“However, when studying the severe COVID-19, […] heart problems, lots of problems with the cardiovascular system, bleeding and clotting, are all associated with COVID-19,” he added. “In doing that research, what has been discovered by the scientific community, the spike protein on its own is almost entirely responsible for the damage to the cardiovascular system, if it gets into circulation.”
When the purified spike protein is injected into the blood of research animals, they experience damage to the cardiovascular system and the protein can cross the blood-brain barrier and cause damage to the brain, Bridle explained.
The biodistribution study obtained by Bridle shows the COVID spike protein gets into the blood where it circulates for several days post-vaccination and then accumulates in organs and tissues including the spleen, bone marrow, the liver, adrenal glands and in “quite high concentrations” in the ovaries.
“We have known for a long time that the spike protein is a pathogenic protein, Bridle said. “It is a toxin. It can cause damage in our body if it gets into circulation.”
A large number of studies have shown the most severe effects of SARS-CoV-2, the virus that causes COVID, such as blood clotting and bleeding, are due to the effects of the spike protein of the virus itself.
A recent study in Clinical and Infectious Diseases led by researchers at Brigham and Women’s Hospital and the Harvard Medical School measured longitudinal plasma samples collected from 13 recipients of the Moderna vaccine 1 and 29 days after the first dose and 1-28 days after the second dose.
Out of these individuals, 11 had detectable levels of SARS-CoV-2 protein in blood plasma as early as one day after the first vaccine dose, including three who had detectable levels of spike protein. A “subunit” protein called S1, part of the spike protein, was also detected.
Spike protein was detected an average of 15 days after the first injection, and one patient had spike protein detectable on day 29 –– one day after a second vaccine dose –– which disappeared two days later.
The results showed S1 antigen production after the initial vaccination can be detected by day one and is present beyond the injection site and the associated regional lymph nodes.
Assuming an average adult blood volume of approximately 5 liters, this corresponds to peak levels of approximately 0.3 micrograms of circulating free antigen for a vaccine designed only to express membrane-anchored antigen.
In a study published in Nature Neuroscience, lab animals injected with purified spike protein into their bloodstream developed cardiovascular problems. The spike protein also crossed the blood-brain barrier and caused damage to the brain.
It was a grave mistake to believe the spike protein would not escape into the blood circulation, according to Bridle. “Now, we have clear-cut evidence that the vaccines that make the cells in our deltoid muscles manufacture this protein — that the vaccine itself, plus the protein — gets into blood circulation,” he said.
Bridle said the scientific community has discovered the spike protein, on its own, is almost entirely responsible for the damage to the cardiovascular system, if it gets into circulation.
Once in circulation, the spike protein can attach to specific ACE2 receptors that are on blood platelets and the cells that line blood vessels, Bridle said. “When that happens it can do one of two things. It can either cause platelets to clump, and that can lead to clotting — that’s exactly why we’ve been seeing clotting disorders associated with these vaccines. It can also lead to bleeding,” he added.
Both clotting and bleeding are associated with vaccine-induced thrombotic thrombocytopenia (VITT). Bridle also said the spike protein in circulation would explain recently reported heart problems in vaccinated teens.
Stephanie Seneff, senior research scientists at Massachusetts Institute of Technology, said it is now clear vaccine content is being delivered to the spleen and the glands, including the ovaries and the adrenal glands, and is being shed into the medium and then eventually reaches the bloodstream causing systemic damage.
“ACE2 receptors are common in the heart and brain,” she added. “And this is how the spike protein causes cardiovascular and cognitive problems.”
Dr. J. Patrick Whelan, a pediatric rheumatologist, warned the U.S. Food and Drug Administration (FDA) in December, mRNA vaccines could cause microvascular injury to the brain, heart, liver and kidneys in ways not assessed in safety trials.
In a public submission, Whelan sought to alert the FDA to the potential for vaccines designed to create immunity to the SARS-CoV-2 spike protein to instead cause injuries.
Whelan was concerned the mRNA vaccine technology utilized by Pfizer and Moderna had “the potential to cause microvascular injury (inflammation and small blood clots called microthrombi) to the brain, heart, liver and kidneys in ways that were not assessed in the safety trials.”
https://www.nature.com/articles/s41593-020-00771-8
Abstract
It is unclear whether severe acute respiratory syndrome coronavirus 2, which causes coronavirus disease 2019, can enter the brain. Severe acute respiratory syndrome coronavirus 2 binds to cells via the S1 subunit of its spike protein. We show that intravenously injected radioiodinated S1 (I-S1) readily crossed the blood–brain barrier in male mice, was taken up by brain regions and entered the parenchymal brain space. I-S1 was also taken up by the lung, spleen, kidney and liver. Intranasally administered I-S1 also entered the brain, although at levels roughly ten times lower than after intravenous administration. APOE genotype and sex did not affect whole-brain I-S1 uptake but had variable effects on uptake by the olfactory bulb, liver, spleen and kidney. I-S1 uptake in the hippocampus and olfactory bulb was reduced by lipopolysaccharide-induced inflammation. Mechanistic studies indicated that I-S1 crosses the blood–brain barrier by adsorptive transcytosis and that murine angiotensin-converting enzyme 2 is involved in brain and lung uptake, but not in kidney, liver or spleen uptake.
https://www.naturalnews.com/2021-06-03-spike-proteins-engineered-to-cross-blood-brain-barrier.html
“A study from Nature Neuroscience finds the S1 spike protein of SARS-CoV-2 crosses the blood–brain barrier in mice and can cause damage to the cardiovascular and central nervous systems. The spike protein is readily cleared from the blood and taken up by peripheral tissues. SARS-CoV-2 RNA was recovered from cerebrospinal fluid, proving it can cross the blood–brain barrier.
The study shows that these new spike proteins have been engineered to exploit angiotensin-converting enzyme 2 (ACE2), allowing for increased intake of spike proteins into the lungs and specifically to the brain. This is why a real case of SARS-CoV-2 can cause symptoms in the central nervous system, include changes to taste and smell, headaches, twitching, seizures, confusion, vision impairment, nerve pain, dizziness, impaired consciousness, nausea, hemiplegia, ataxia, stroke and cerebral hemorrhage.
So why are people going along with these new “vaccines” — if they turn their own cells into spike protein factories?
Intravenous administration of spike proteins concentrates in the brain TEN times greater than nasal exposure
The engineered SARS-CoV-2 spike protein binds to human cells using its S1 sub-unit. The researchers reveal that the S1 sub-unit was readily taken up in the parenchymal brain space, the hippocampus, the olfactory bulb, and was measured in eleven regions of the brain. When the spike proteins were administered intravenously, they concentrated in the brain TEN TIMES greater than when administered intranasally!
These are the same spike proteins that human cells are forced to translate, synthesize and replicate using the genetic instructions provided by new mRNA vaccines and adenovirus-vectored vaccines. The lab-engineered spike protein that is being mass produced in human cells is not only subverting the natural genetic template of protein synthesis, but it is also inundating the brain with foreign TOXINS.
The research finds that spike proteins readily cross the blood-brain barrier through a process called adsorptive transcytosis. Transcytosis is a type of trans-cellular transport in which various macro-molecules are transported across the interior of a cell. Adsorptive-mediated transcytosis provides a means for brain delivery of medicines across the blood-brain barrier.
Why are the spike proteins designed to readily adsorb across the blood brain barrier? Could this mode of action be intended to deliver other medicines and chemicals, genetic instructions or autoimmune attacks to the brain cells? Is this the real reason for encephalitis and brain hemorrhage following both infection and vaccination? What are the ramifications of spike proteins accumulating in the brain? Will recently vaccinated persons suffer acute or permanent brain damage from these experimental injections?
The research also showed that inflammation increases spike protein uptake in the brain and lungs. When the animals were induced with inflammation, the intravenously-administered spike proteins entered the brain more readily. People who eat a plant-based, anti-inflammatory diet are more equipped to survive spike protein attacks to the brain.
Engineering coronavirus spike proteins for human experimentation and vaccine development
Naturally-occurring coronaviruses were first identified in the mid-1960s. They are named after the crown-like spikes on their surface. These viruses are prevalent in animals; however, four coronaviruses are known to infect humans, including 229E, NL63, OC43, HKU1. All of these strains cause mild, cold-like symptoms in humans.
In the twenty-first century, scientists have been studying and engineering the coronavirus spike protein. Scientists can splice genes into the coronavirus spike protein, allowing natural selection to rapidly mutate the spike protein in the lab, one gene at a time. This serial passage technique hides any trace of human interference, but the advanced attachment properties of the resulting virus are a dead give-way that the virus was manipulated in a lab. This controversial gain-of-function research was banned in the US in 2004, but continued to take place in the US and abroad — as long as the research was conducted to invent new vaccines. Today, new experimental vaccines are being unleashed, as the outbreaks occur in real time.
Since coronavirus gain-of-function research began, three new coronaviruses have emerged, causing severe illness in humans. SARS-CoV-1 was first identified in China in 2003; MERS-CoV was first identified in Saudi Arabia in 2012; and today’s SARS-CoV-2, was first identified in Wuhan, nearby the Wuhan Institute of Virology in China.
Beijing researchers affiliated with the Academy of Military Medical Science published a study in June 2020, explaining the methods they used to modify coronavirus spike proteins to exploit human lung cells. The researchers equipped mice with the ACE2 receptor from human lung cells. By exploiting the ACE2 receptor, the spike protein is engineered to attack the brain and lungs of humans. The damage of this laboratory-leak vaccine experiment will only continue as new vaccine experiments go live on the population, translating spike proteins in human cells and attacking human brains into the unforeseeable future.”
https://www.naturalnews.com/2021-06-03-canadian-researcher-covid-vaccine-spike-proteins-death.html
“Terrifying” new research has found that the spike proteins contained in and manufactured by Wuhan coronavirus (Covid-19) “vaccines” are directly responsible for cardiovascular injury and death.
Dr. Byram W. Bridle, Ph.D. says the he and several colleagues gained access to a first-of-its-kind “biodistribution” study out of Japan showing that even when injected in muscle tissue in the arm, the mRNA (messenger RNA) injections from Moderna and Pfizer-BioNTech cause the production of spike proteins that more often than not get into the bloodstream and cause deadly blood clots, heart and brain damage, and infertility.
“The spike protein on its own is almost entirely responsible for the damage to the cardiovascular system,” Bridle warned during a recent radio interview.
“The spike protein gets into the blood, circulates through the blood in individuals over several days post-vaccination,” Bridle further explained. “It accumulates in a number of tissues such as the spleen, the bone marrow, the liver, the adrenal glands, the ovaries.”
In the study, 13 healthcare workers were given injections of Moderna’s shot for the Chinese Virus, resulting in 11 of them having detectable spike protein in their blood. This, Bridle says, only further solidifies the fact that the vaccine spike proteins are pathogenic proteins that are toxic to the body.
“It can cause damage in our body if it gets into circulation,” Bridle warned about the vaccine spike protein.
“Now we have clear-cut evidence that the vaccines that make the cells in our deltoid muscles manufacture this protein – the vaccine itself plus the protein gets into blood circulation. When in circulation, the spike proteins bind to the receptors that are on our platelets, and the cells that line our blood vessels. When that happens, it can either cause platelets to clump, which can lead to clotting … it can also lead to bleeding, and the heart is involved.”
Even worse is the fact that after being injected into muscle tissue, mRNA-induced spike proteins also have the potential to cross the blood-brain barrier and cause neurological damage. This is why in many of the fatal cases of blood clots the damage is observed in the brain.
While there may be a handful of researchers out there who actually had good intentions when coming up with the idea of injecting deadly spike proteins into the body, the whole thing was still “a big mistake,” Bridle says.
“We didn’t realize it until now,” he contends about the process. “We thought the spike protein was a great target antigen, we never knew the spike protein itself was a toxin and was a pathogenic protein. So by vaccinating people we are inadvertently inoculating them with a toxin.”
Bridle and a group of scientists received a $230,000 grant last year from the government to research Chinese Virus injections. With this, they were able to obtain data on the shots showing that the spike proteins they contain or produce are almost solely responsible for all the cardiovascular damage being observed in patients after they receive their injections.”
Yes, but could it not be argued that Covid-19 is so deadly and has killed off so many people, like a new Black Death, that these sorts of concerns are just academic? It is not going to stop me getting my promised 16 vaccines a day. Maybe tomorrow. Or, the next day. No, I have to go shopping then for masks and toilet paper. But, I will get around to it, maybe quicker if some incentive could be given, such as chocolates! At my advanced age, blood clots in my brain would only improve things!
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