“Global Time Bomb” First case of postmortem study of patient vaccinated against SARS-CoV-2; “viral RNA found in every organ of the body”

viral RNA found in every organ of the body

By Hal Turner Radio

The first-ever autopsy of a person vaccinated against COVID-19, who tested negative 18 days later upon hospital admission but at 24 days after the VAX, has revealed viral RNA was found in almost every organ of the body.  The vaccine, while triggering an immune response, DID NOT STOP the virus from entering every organ in the body.

The viral RNA was found in virtually every organ in the body, which means the spike proteins as well.

There are antibodies (like the “vaccine” is supposed to create) but they’re irrelevant because, based on a study from Japan, we now know that the spike S1 protein is what does the damage.

We spoke to one Infectious Disease specialist from a hospital in New Jersey this morning.  We sent the actual autopsy findings to him and asked for his thoughts.

When he called back a while later, he was clearly shaken-up.   He told us “You cannot quote me by name, I will get fired by the hospital if you do.”   We agreed to conceal his identity.

He then told us:

“People think that only a MINORITY of people get adverse effects from the vaccine.

Based on this new research, it means that everyone – EVENTUALLY -will have adverse effects, because those spike proteins will be binding to ACE2 receptors everywhere in the body.  

That mRNA was supposed to stay in the injection site and it’s not.  That means the spike proteins created by the mRNA will be in every organ as well, and we now know it is the spike proteins that do the damage.

Worse, the viral RNA being found in every organ despite a vaccine, indicates either:

1) The vaccine doesn’t work at all, OR;

2) The virus is enjoying Antibody Dependent Enhancement (ADE), meaning it actually spreads FASTER in vaccinated people.

This is a GLOBAL TIMEBOMB.”

According to the published postmortem report, the vaccinated man was 86 years old and tested NEGATIVE for COVID-19 when first admitted to the hospital with severe gastro-intestinal trouble and difficulty breathing. Here is what the reports describes:

We report on an 86-year-old male resident of a retirement home who received vaccine against SARS-CoV-2. Past medical history included systemic arterial hypertension, chronic venous insufficiency, dementia and prostate carcinoma. On January 9, 2021, the man received lipid nanoparticle-formulated, nucleoside-modified RNA vaccine BNT162b2 in a 30 μg dose. On that day and in the following 2 weeks, he presented with no clinical symptoms (Table 1). On day 18, he was admitted to hospital for worsening diarrhea. Since he did not present with any clinical signs of COVID-19, isolation in a specific setting did not occur. Laboratory testing revealed hypochromic anemia and increased creatinine serum levels. Antigen test and polymerase chain reaction (PCR) for SARS-CoV-2 were negative.

The report of the postmortem makes clear tests showed “no morphological changes associated with COVID” in his organs. 

“Morphological” means structural.  COVID infection is now known to cause very specific structural changes to the places it infects.  THOSE CHANGES HAD NOT APPEARED in the vaccinated man before he died.

The now dead vaccinated man was in a room where another patient ultimately tested POSTIVE for COVID, and the report states they think the dead vaccinated man caught COVID after he was admitted, from the other patient in the same room.

So the damage to the organs of the now dead vaccine recipient, took place BEFORE he was infected with COVID by the other hospital room patient.

Worse, once the vaccinated man actually got COVID, it spread so fast within his body, he apparently never stood a chance.  Here are tissue images:

postmortem


The full postmortem report is published at ScienceDirect.com (HERE)

HAL TURNER COMMENTARY

I am not a Doctor or a Scientist so I cannot offer a competent medical analysis, but as a layman, from where I sit, this doesn’t look so good.

The Postmortem report says clearly “ These results indicate that the patient had already developed relevant immunogenicity through vaccination” yet he got infected by another patient at day 24 (after vax) upon being admitted to the hospital, and died 4 days later.

If one reads the entire article, the whole story is: Patient was given the vaccine, it got him hospitalized with ulcerative colitis due to blood clots, during his hospitalization he got infected by an asymptomatic hospital room mate, and died 4 days later.

My conclusion: the jab drove this elderly man to his end.

I might be wrong, but this is what I see from the postmortem report.

I have **not** taken the vax and I do not intend to take it.   

Throughout this entire COVID debacle, the one constant is that the disease has a 99.8% SURVIVAL rate.   To me, it’s not a pandemic.  To me it’s not even worth getting a vaccine; I think my immune system will handle it just fine.

Given all the adverse reactions to the vax, I now firmly conclude that getting the vax is a far more dangerous thing than getting the actual illness.

God gave me an immune system.  I think I will trust God on this.  After all, I truly believe I will not live one micro-second longer than God wants, and conversely, I will not die one micro-second sooner than God wants.

Faith is not “belief without proof”  it is “trust without reservation.”  I trust God.

SUDDEN DEATH of 32 YEAR OLD

This couple’s step-son, age 32, died from a heart attack 12 hours after getting the Johnson & Johnson Vaccine.  Coroner refuses to release reports; calls cause of death “inconclusive.”   A lot of these deaths are simply being covered up.   Here’s the family to tell you:

Shocking if true… pic.twitter.com/kd7E8LoGCC — Heidegger (@heidegger79) June 13, 2021

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Source: Hal Turner Radio

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Vaccinated people are walking biological time bombs and a THREAT to society

By RedNewspaper

People who are ignorant enough to be injected with an experimental vaccine that accelerates the generation of highly contagious super strains in their own bodies are walking biological time bombs and a threat to society.

The globalists know this, and consistent with their goals of global mass extermination, they are giving the most dangerous and most contagious people “vaccine passports” so they can freely roam across society, spreading their super strain viruses far and wide. Again, this is all by design.

The safest people are those who have strong innate immune systems and have already built antibodies against the coronavirus, without needing any medical intervention. This is easily accomplished in most people with the help of vitamin D, zinc, nutrition, restful sleep and avoidance of toxic foods and medications.

Yet the entire “science” industry refuses to recognize any role whatsoever for innate immunity, and antibodies that individuals create on their own are not recognized as serving any function whatsoever. For example, you can’t get an “antibody passport” from showing your own innate immunity, even though you have already defeated the pathogen thanks to your God-given immune system.

Modern “science” — if we dare even call it that — wants you to believe you have no immune system at all and that your body must be hijacked by mRNA vaccines in order to function. This is a gigantic, dangerous lie, and it is repeated by nearly every media outlet, medical journal and medical “authority” around the world (most of whom are working for the CCP to destroy Western nations, of course).

If lockdowns, quarantines and masks were to be required for anyone, it should be the vaccinated!

It’s the vaccinated people that are the most dangerous to society and the most likely to infect others with super strains which are already demonstrating complete immunity to existing vaccines. The vaccines, in other words, have already been rendered largely obsolete.

It’s only the innate human immune system that can handle the rapid mutations and defeat them in a few hours rather than waiting for 10+ months for the vaccine industry to roll out another “covid booster shot.”

The vaccine industry will be chasing these variants and mutant strains forever, in exactly the same way antibiotics are forever chasing superbugs in hospital settings. Yet today, the entire world is the super strain factory for the vaccine / bioweapons industry, and in truth, there’s something far more sinister at play here.

Fauci, the NIH and the CCP needed billions of humans to serve as bioweapons factories in order to accelerate their ultimate genocidal bioweapon

It turns out that Fauci, the NIH and the CCP didn’t actually succeed in building a deadly bioweapon that would wipe out humanity. The weapon they built — SARS-COV-2 — was intended merely to convince billions of people to take vaccines that would transform their own bodies into bioweapons factories so that the mutation development could then proceed globally.

In this way, the centralized bioweapons vaccine military complex was able to “decentralize” its bioweapons development program by releasing a relatively mild strain into the wild and following it up with a vaccine to accelerate the super strain adaptations. In effect, every human being who has taken the vaccine is now a walking bioweapons factory, churning out super strains and “shedding” them all over society with the help of their vaccine passports.

As cruise lines, sports arenas, airlines, universities and other organizations are now announcing “vaccinated only” policies for who they will allow to resume normal activities, they are creating “perfect storm” conditions for spreading the next global killer viral strain which will be the result of random mutations in a vaccinated person, not deliberate engineering in a genetic lab.

The real medical purpose of the vaccine is to wipe out the less lethal strains and provide viral adaptation pressures that accelerate the creation of more lethal strains.

This was all by design. They knew they couldn’t design the perfect weapon in the lab… they needed to put human beings to work as walking lab experiments. And that’s exactly what the vaccine accomplished.

Vaccinated people are dangerous to be around

Now, anyone who wants to survive the killer “super strain” wave that’s mutating right now in the bodies of the vaccinated must realize that staying away from vaccinated people may be a matter of life and death. It is the vaccinated who are the most dangerous and are therefore given the most access to society. In their own selfishness and scientific ignorance, these willing bioweapons volunteers are helping to carry out the greatest crime against humanity that could ever be imagined: A global plague, powered through decentralized, accelerated, adaptive genetic shaping that relies on billions of willing volunteers to serve as mutation labs.

The scale of this global medical experiment on live human subjects puts the entire Nazi regime to shame.

When the next death wave comes, of course, the media will blame the unvaccinated, even though the unvaccinated aren’t being allowed to go anywhere, increasingly. It is the vaccinated who will be killing themselves and others, which is why I say they are part of a “vaccine suicide cult.”

Source: Red News Paper

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Engineered ‘Nanobodies’ block SARS-CoV-2 from infecting human cells

Nanobody binding to spike
Researchers designed a three-part molecule (pink) that nestles into the coronavirus spike protein (blue), pinning it into a conformation that makes it unable to stick to ACE2, the receptor through which the virus gains entry into human cells. Top view and side view shown. Credit: Walter and Manglik Labs/UCSF/HHMI

Summary

Researchers have designed a molecule that sticks tightly to the coronavirus spike protein, preventing the virus from infecting cells. The molecule might someday be used in an aerosolized drug to treat or prevent COVID-19.

HHMI scientists are joining many of their colleagues worldwide in working to combat the new coronavirus. They’re developing diagnostic testing, understanding the virus’s basic biology, modeling the epidemiology, and developing potential therapies or vaccines. Over the next several weeks, we will be sharing stories of some of this work.

In the race to find drugs that halt the novel coronavirus, scientists are finding inspiration in unusual sources – like llamas.

A new lab-engineered molecule inactivates the machinery that the coronavirus, SARS-CoV-2, uses to infect cells. It’s modeled after the simple, compact antibodies found in some animals such as llamas, alpacas, and camels.

While the research is still preliminary, the team behind the advance hopes their molecule might someday be the key ingredient in an antiviral drug that could be delivered via nasal spray.

In just twelve weeks, we’ve found a molecule that’s a clinical lead,” says Howard Hughes Medical Institute Investigator Peter Walter, a biochemist at the University of California, San Francisco (UCSF), who co-led the work. The team described the advance August 17, 2020, in a preprint posted to bioRxiv.org.

Alongside vaccines, drugs that target SARS-CoV-2 are important tools for keeping the COVID-19 pandemic in check. Researchers have identified existing drugs that can be repurposed to treat symptoms of the virus and help quell severe infections. But a drug specifically designed to attack SARS-CoV-2 might be more effective at halting the virus in its tracks before it causes severe disease, Walter says. To make such drugs, he and others are designing custom antibodies.

Immune cells produce antibodies in response to infection, but it takes time for that response to develop. Lab-made antibodies could knock a virus out before it gains a foothold.

That’s where the llamas come in. Alpacas and llamas have a simpler version of the antibodies found in humans – only a tenth the size, with fewer components. These stripped-down antibodies, called “nanobodies,” are potentially powerful drug building blocks, says Aashish Manglik, a protein engineer at UCSF who co-led the study with Walter. “Because of their unique shape they can often fit deep inside the crevices of proteins.” They tend to be more stable than regular antibodies, too.

Manglik’s lab has developed large collections of these synthetic proteins as a resource for drug discovery. When the COVID-19 pandemic began, these collections were the perfect place to hunt for a molecule that could deactivate SARS-CoV-2, Walter says.

Michael Schoof, a graduate student in Walter’s lab, began mining Manglik’s nanobody collections en masse. The aim: Finding any nanobodies that would stick to the coronavirus spike protein, the key on the virus’s surface that lets it sneak into cells.

In a series of lab experiments, he and his colleagues winnowed down a pool of billions of different nanobodies to a few dozen that stuck strongly to the spike protein. Then, they engineered the most promising candidate, linking three copies of the same nanobody together into a chain.

That three-piece molecule wedged tightly against the virus spike protein, pinning it into a shape that prevented attachment to human cells. The researchers also discovered that the molecule is particularly sturdy. In test-tube experiments, a single nanobody fell off the spike protein within minutes. The team calculated that the three-piece version would be able to hold on for over a week without budging.

The work hasn’t yet been peer-reviewed, but Walter and Manglik are currently looking for partners who can produce and test the molecule for safety and efficacy in clinical trials. They hope the molecule could someday soon work as an aerosolized drug that would get directly to patients’ lungs.

Traditional antibody drugs are usually injected into the patient’s bloodstream – most antibodies fall apart when aerosolized by a nebulizer or a nasal spray, Walter says. Preliminary tests suggest that the new nanobody-based molecule is far hardier. The nanobodies kept their shape and function when sprayed, and withstood being freeze-dried and heated, too.

Aerosolized delivery of a nanobody drug “is an exciting possibility, but it hasn’t been demonstrated yet,” says Andrew Kruse, a biochemist at Harvard Medical School who has collaborated with Manglik’s team to build nanobody collections but wasn’t involved in the current study. “It would be very important to see how long an aerosol-delivered nanobody remains in the respiratory system,” he says.

Citation

Michael Schoof et al. “An ultra-potent synthetic nanobody neutralizes SARS-CoV-2 by locking Spike into an inactive conformation.” Posted on bioRxiv.org on August 17, 2020.

Source: hhmi  – Howard Hughes Medical Institute

Engineered llama antibodies neutralise COVID-19 virus

How llama blood could help fight coronavirus
How llama blood could help fight coronavirus

Antibodies derived from llamas have been shown to neutralise the SARS-CoV-2 virus in lab tests, UK researchers announced today.

The team involves researchers from Oxford University, the Rosalind Franklin Institute, Diamond Light Source and Public Health England. They hope the antibodies – known as nanobodies due to their small size – could eventually be developed as a treatment for patients with severe COVID-19. The peer reviewed findings are published in Nature Structural & Molecular Biology.Llamas, camels and alpacas naturally produce quantities of small antibodies with a simpler structure, that can be turned into nanobodies. The team engineered their new nanobodies using a collection of antibodies taken from llama blood cells. They have shown that the nanobodies bind tightly to the spike protein of the SARS-CoV-2 virus, blocking it from entering human cells and stopping infection.

Using advanced imaging with X-rays and electrons at Diamond Light Source and Oxford University, the team also identified that the nanobodies bind to the spike protein in a new and different way to other antibodies already discovered.

There is currently no cure or vaccine for COVID-19. However, transfusion of critically ill patients with serum from convalesced individuals, which contain human antibodies against the virus, has been shown to greatly improve clinical outcome. This process, known as passive immunisation, has been used for over 100 years, but it is not straightforward to identify the right individuals with the right antibodies and to give such a blood product safely. A lab-based product which can be made on demand would have considerable advantages and could be used earlier in the disease where it is likely to be more effective.

Professor James Naismith, Professor of Structural Biology at Oxford University  and Director of The Rosalind Franklin Institute, said,’These nanobodies have the potential to be used in a similar way to convalescent serum, effectively stopping progression of the virus in patients who are ill. We were able to combine one of the nanobodies with a human antibody and show the combination was even more powerful than either alone. Combinations are particularly useful since the virus has to change multiple things at the same time to escape; this is very hard for the virus to do. The nanobodies also have potential as a powerful diagnostic.’

Professor Ray Owens from Oxford University, who leads the nanobody program at the Franklin, said, ‘This research is a great example of team work in science, as we have created, analysed and tested the nanobodies in 12 weeks. This has seen the team carry out experiments in just a few days, that would typically take months to complete. We are hopeful that we can push this breakthrough on into pre-clinical trials.’

Professor David Stuart, from Diamond Light Source and Oxford University said, ‘The electron microscopy structures showed us that the three nanobodies can bind to the virus spike, essentially covering up the portions that the virus uses to enter human cells.’

The team started from a lab-based library of llama antibodies. They are now screening antibodies from Fifi, one of the ‘Franklin llamas’ based at the University of Reading, taken after she was immunised with harmless purified virus proteins. The team are investigating preliminary results which show that Fifi’s immune system has produced different antibodies from those already identified, which will enable cocktails of nanobodies to be tested against the virus.

Source:  Oxford University