“People who had mild COVID-19 have long-lasting antibody protection, according to a study by researchers from Washington University School of Medicine in St. Louis. …..
“Last fall, there were reports that antibodies wane quickly after infection with the virus that causes COVID-19, and mainstream media interpreted that to mean that immunity was not long-lived,” said Ali Ellebedy, senior author of the study and an associate professor of pathology & immunology at Washington University.
“But that’s a misinterpretation of the data. It’s normal for antibody levels to go down after acute infection, but they don’t go down to zero; they plateau. Here, we found antibody-producing cells in people 11 months after first symptoms. These cells will live and produce antibodies for the rest of people’s lives. That’s strong evidence for long-lasting immunity,” he added.’
The research paper itself was published online in Nature on 24 May 2021 ( https://www.nature.com/articles/s41586-021-03647-4_reference.pdf )
My take on it.
If you were to ask a competent immunologist what happens normally in the advent of a viral infection, this is what you would have been told. These researchers are simply saying that SARS-CoV-2 has proved to be no different from what happens normally.
It is reasonable to ask why this was not the starting assumption for the formation of a public policy response. Eminent individuals certainly made that point at the time. Professor Cahill, if I recall correctly, was one.
It is reasonable to ask why this norm is still not informing public policy.
Again the question is Why?
And while we muse, the human immune system, perhaps our greatest personal asset, is under assault world-wide from a gene therapy injection program that is at best ill-conceived, and at worst malign. The human body is a lot smarter than any government. But it is not impregnable.
(This time I am providing more than a short statement, in the hope that it will be read in its entirety. See below for source acknowledgment.)
‘We Made a Big Mistake’ — COVID Vaccine Spike Protein Travels From Injection Site, Can Cause Organ Damage
Research obtained by a group of scientists shows the COVID vaccine spike protein can travel from the injection site and accumulate in organs and tissues including the spleen, bone marrow, the liver, adrenal glands and in “quite high concentrations” in the ovaries.
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.
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.”
Dr Byram Bridle, Associate Professor of Viral Immunology, University of Guelph, Ontario, Canada
as quoted by Megan Redshaw in The Defender, 3 June 2023
For original interview with Professor Bridle, see https://www.youtube.com/watch?v=Sis1Sddzbqk .
My take on it
The more we learn, the uglier this story gets.
And we the public learn about the ‘biodistribution’ of this widely promoted and yet life-threatening injection only because of expert enquiry to a foreign country (ie Japan), not through timely disclosure by the manufacturer.
The pretext for the ‘jab’ is to alleviate symptoms (not to stop infection or transmission). If you think about it, masking symptoms makes as much sense as removing the battery from a smoke detector. In the vast majority of cases*, infection is asymptomatic anyway; and in the very few cases* where symptoms are present and significant, they serve (in the hands of a qualified medical practitioner) to assist diagnosis and treatment.
In the past, much of the resistance to vaccines has been due to the inclusion of particular ingredients, including heavy metals, synthetic substances such as hydrogel, and foreign genetic material. If Professor Bridle and the other researchers that he cites are correct, we are now dealing with something far worse – an injected toxin replicating at the cellular level and circulating throughout the body, including across the blood:brain barrier.
Early on in life, we learn that people make mistakes. The sooner we admit them, the less damage is done.
What do you expect will happen next?
* The term ‘case’ has a specific meaning in medicine. The administration of a PCR test and a so-called ‘positive’ result, do not meet that criterion, as has been determined by eg the Lisbon Court of Appeal. (See my earlier post on this.)
“An explosive new study on the origins of COVID-19 pandemic claims researchers found ‘unique fingerprints’ in samples of the virus that they say could only have arisen from manipulation in a lab – supporting theories that it escaped from the Wuhan Institute of Virology in China.”
This article refers to a new 22-page paper authored by British Professor Angus Dalgleish and Norwegian scientist Dr. Birger Sørensen set to be published in the Quarterly Review of Biophysics Discovery.
My take on it
Does this qualify as News? In my own case, only because it refers to a new study.
More than a year ago eminent scientists were reporting that foreign insertions could be clearly identified in the native gene sequences. Dr Judy Mikovits, if I recall correctly, was one.
The original Gain of Function research (‘purposive manipulation’), the release of the virus and the endeavour by WRI to cover its tracks, are in my view very disappointing, but hardly “shocking allegations”. I wish they were.
According to the article, “the majority of experts have until recently staunchly denied the origins of COVID-19 were anything other than a natural infection leaping from animals to humans.”
Which takes me back to something my father said to me: ‘If ever you find yourself in the majority, get down on your knees and examine your conscience.’
A majority vote never made anything true. Pick your sources and your experts wisely.
Nor indeed do I accept that the majority of experts held the view claimed in the article. Certainly it has been the official narrative, as choreographed and jealously guarded by government, biocrats and the media. That barrier to the free flow of information has simply served to delay and frustrate the fruits of independent enquiry. This paper is just one evidence of that.
“Every scientist in the world knows that natural immunity is way better than vaccine immunity.”
Dr Peter McCullough, world leading cardiologist who testified last year in a Senate hearing to defend ‘alternative’ covid treatments HCQ and Ivermectin (which have been PROVEN to work, forcing many retractions including from the Lancet and the American Medical Association, most notably). Quoted by Martin Geddes on Telegram, 26 May 2021
My take on it
We must allow Dr McCullough some poetic licence. I don’t know that every scientist in the world agrees about anything.
That said, this core truth needs to be shouted from the rooftops – that natural immunity is effective, safe, and free. Vaccination is none of those things.
And those who really know this field of scientific endeavour, know that to be true.
For which reason, our innate immune system is to be revere, boosted and protected.
The experimental gene therapy (aka ‘the jab’) being promoted by politicians and biocrats as a policy response to Covid-19 is a direct, intentional and probably irreversible assault on that priceless asset.