Microbiologist Explains COVID Jab Effects

13 He that answereth a matter before he heareth it, it is folly and shame unto him. ~ Proverbs 18:13 KJV

First Signs of What Scientists Fear Most About the mRNA Jabs

Disturbingly, the first indications are appearing of the most dreaded effect from the COVID-19 experimental vaccines. Scientists warned, but few people listened. The condition doctors are witnessing in India and likely Israel should be a red flag to anyone thinking of rolling up a sleeve.

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Analysis by Dr. Joseph Mercola / Fact Checked

August 22, 2021

 Effects Of The Covid-19 Jab: Microbiologist Dr. Sucharit Bhakdi Interviewed by Dr. Joseph Mercola (bitchute.com)

STORY AT-A-GLANCE

• The FDA can only grant emergency use authorization for a pandemic drug or vaccine if there’s no safe and effective preexisting treatment or alternative. Since there are several such alternatives, the FDA is legally required to revoke the emergency authorization for these shots
• While the COVID injections have been characterized as being somewhere around 95% effective against SARS-CoV-2 infection, this is the relative risk reduction, which tells you very little about its usefulness. The absolute risk reduction is only around 1% for all currently available COVID shots
• Antibody-dependent enhancement (ADE) refers to a condition where the vaccination augments your risk of serious infection. We are now starting to see evidence that ADE is occurring in the vaccinated population
• One of the most common side effects of the COVID shots is abnormal blood clotting, which can result in strokes and heart attacks
• Even microclots that don’t completely block the blood vessel can have serious ramifications. You can check for presence of microclots by performing a D-dimer blood test. If your D-dimer is elevated, you have clotting somewhere in your body

In this interview, German microbiologist Dr. Sucharit Bhakdi sifts through the facts and fictions of the coronavirus pandemic. Together with Karina Reiss, Ph.D., he’s written two books on this subject, starting with “Corona False Alarm? Facts and Figures,” published in October 2020, followed by “Corona Unmasked: New Facts and Figures.”

The second book is currently only available in German, but you can download a free chapter of “Corona Unmasked” in English on FiveDoves.com (You can also read it below).

Bhakdi’s Medical Credentials

Bhakdi graduated from medical school in Germany in 1970. After a year of clinical work, he joined the Max Planck Institute of Immunobiology, where he remained for four years as a post-doc.

There, he also began researching immunology. Eventually, he ended up chairing the department of medical, microbiology and hygiene at the University of Mainz, where he worked for 22 years until his retirement nine years ago. During that time, Bhakdi also worked on vaccine development, and says he’s “certainly pro-vax with regards to the vaccinations that work and that are meaningful.”

Much of his research focused on what’s called the complement system. When activated, the complement system ends up working in such a way that it destroys rather than aids your cells. Interestingly enough, SARS-CoV-2 uses this very system to its advantage, turning your immune system toward a path of self-destruction.

The same self-destructive path also appears to be activated by the COVID shots, which is part of why Bhakdi believes they are the greatest threat humanity has ever faced. “It is our duty to aggressively inform people about the dangers that they are subjecting themselves and their loved ones to by this ‘vaccination,’” he says.

How Effective Are the COVID Shots?

While the COVID injections have been characterized as being somewhere around 95% effective against SARS-CoV-2 infection, this claim is the product of statistical obfuscation. In short, they’ve conflated relative risk reduction and absolute risk reduction. The absolute risk reduction is actually right around 1% for all currently available COVID shots.¹

In “Outcome Reporting Bias in COVID-19 mRNA Vaccine Clinical Trials”² Ron Brown, Ph.D. calculates the absolute risk reduction for Pfizer’s and Moderna’s injections, based on their own clinical trial data, so that they can be compared to the relative risk reduction reported by these companies. Here’s a summary of his findings:

• Pfizer/BioNTech vaccine BNT162b2 — Relative risk reduction: 95.1%. Absolute risk reduction: 0.7%
• Moderna vaccine mRNA-1273 — Relative risk reduction: 94.1%. Absolute risk reduction 1.1%

In a July 1, 2021, commentary in The Lancet Microbe,³ Piero Olliaro, Els Torreele and Michel Vaillant also argue for the use of absolute risk reduction when discussing vaccine efficacy with the public. They too went through the calculations, coming up with the following:

• Pfizer/BioNTech — Relative risk reduction: 95%. Absolute risk reduction: 0.84%
• Moderna — Relative risk reduction: 94%. Absolute risk reduction: 1.2%
• Gamaleya (Sputnic V) — Relative risk reduction: 91%. Absolute risk reduction: 0.93%
• Johnson & Johnson — Relative risk reduction: 67%. Absolute risk reduction: 1.2%
• AstraZeneca/Oxford — Relative risk reduction: 67%. Absolute risk reduction: 1.3%

What Kind of Protection Do the COVID Shots Provide?

Aside from providing insignificant protection in terms of your absolute risk reduction, it’s important to realize that they do not provide immunity. All they can do is reduce the severity of the symptoms of infection. According to Bhakdi, they fail even at this.

“They showed absolutely zero [benefit in the clinical trials],” he says. “This is the ridiculousness. People don’t understand that they’re being fooled and have been fooled all along. Let’s take the one of these Pfizer trials: 20,000 healthy people were vaccinated and another 20,000 people were not vaccinated.

And then they observed, over a period of 12 weeks or so, how many cases they found in the vaccinated group and how many cases they found the non-vaccinated. What they found was that less than 1% of the vaccinated group got COVID-19 and less than 1% in the non-vaccinated group also got COVID-19.

The difference was 0.8 to 0.1%, which is nothing, considering the fact that they were not even looking at severe cases. They were looking at people with a positive PCR test — which as we all now know is worthless — plus one symptom, which could be cough or fever.

That is not a severe case of COVID-19. Any vaccination that is going to get authorized must be shown to protect against severe illness and death, and this has definitely not been shown. So, forget authorization. It can’t be authorized, not by any normal means.

Now [the COVID injections do not have] full authorization, it’s an emergency authorization, which again is absolute bullshit, since we know the infection fatality rate of this disease or virus is not greater than that of seasonal flu. John Ioannidis has published these numbers, which have never been contested by anyone in the world and cannot be contested.

If you are under 70 years of age and have no severe preexisting illness, you can hardly die [from SARS-CoV-2 infection]. So, there is no fatality rate that can be reduced.

And for people who are elderly and have preexisting illness, as we know from Dr. Peter McCullough and his colleagues’ work, there are very good means and medicines to treat this virus so that the fatality rates go down another 70 to 80%, which means there is no ground for emergency use whatsoever.

This means the FDA should be able to be forced to retract this emergency use authorization — unless they are in league with whoever wants to do this.”

I neglected to follow-up on his comment about 40,000 people being equally divided between the injection and no injection groups in the COVID injection trials. A few months ago, they actually abandoned the non-injection arm of the trial, so no there is no control group anymore.

The justification was that the injection was too important to deny it to the control group. It’s just another sneaky way to skirt around reporting all the adverse effects occurring in the injection group.

That said, it’s worth repeating that the FDA can only grant emergency use authorization for a pandemic drug or vaccine if there’s no safe and effective preexisting treatment or alternative. Since there are several such alternatives, the FDA is legally required to revoke the emergency authorization for these shots.

Evidence of Increased Infection Risk After Injection

Presently, the Centers for Disease Control and Prevention claims some 95% of SARS-CoV-2 infections resulting in hospitalization are occurring among the unvaccinated. This too is a statistical fiction, as they’re using data from January through June 2021, when most of the American public were unvaccinated.

Looking at more recent data, we’re finding that the majority of severe cases and hospitalizations are actually occurring among those that received the COVID jab. Unfortunately, as noted by Bhakdi:

“It’s all manipulated. And, if someone wants to manipulate something and are in a position to then propagate it, you have no chance of analyzing it and telling people because we have no voice in this affair. When we stand up and tell people this, they just turn around and say that’s not the truth.”

Disturbingly, we’re now starting to see the first indications of antibody-dependent enhancement (ADE), which many scientists were concerned about from the very beginning. India, for example, where 10% of the population has been “vaccinated,” is now seeing very severe cases of COVID-19. Bhakdi says:

“What we’re witnessing in India and probably also in Israel is the immune dependent enhancement of disease … It’s bound to happen. So, the people who are getting vaccinated now have to be fearful of the next wave of genuine infections, whether it’s [SARS-CoV-2 variants] or any other coronaviruses, because they’re all related and they will all be subject to immune dependent enhancement, obviously.”

Antibody-dependent enhancement (ADE), or paradoxical immune enhancement (PIE) refers to a condition where the vaccination results in the complete opposite of what you’re looking for. Rather than protect against the infection, the vaccine augments and worsens the infection.

ADE can occur through more than one mechanism, and Bhakdi is of the opinion that the enhancement is primarily due to over-reactive killer lymphocytes and secondary complement activation, both of which cause severe damage.

Antibodies Versus Lymphocytes

Bhakdi explains:

“There are two major arms of defense against viral infection. One is the antibodies that, if they are present, may prevent the virus from entering your cells. These are so-called neutralizing antibodies, which the vaccination is supposed to [produce].

But the antibodies are not at the place that they are needed, which is on the surface of the airway epithelium. They are in the blood, but not at the surface of the epithelium where the virus arrives. The second arm of immune defense then comes into play, and these are the lymphocytes.

There are different types of lymphocytes and I will simplify matters by saying the important lymphocytes are the so-called killer lymphocytes that sense whenever a virus product is being produced in the cell. They will then destroy the cells that harbor the virus and thus the factory is closed and you get well again.

That is the mechanism for how we can survive viral infections of the lung, and this happens all the time. So, the lymphocytes, in contrast to the antibodies, recognize many, many, many parts of the proteins. So, if a virus changes a little bit, it doesn’t matter, because the waste products that are recognized by the killer lymphocytes remain very similar.

That is why all of us, and this is now known, all of us have memory lymphocytes in our lymph nodes and lymphoid organs that are trained to recognize these coronaviruses. And whether or not a mutant is there, it doesn’t really matter, because they will recognize a mutant or variant.”

According to Bhakdi, coronaviruses can only undergo point mutations, meaning only one nucleotide at a time can be changed. The influenza virus, meanwhile, can undergo more radical mutations. For example, a flu virus can completely change its spike protein by swapping spike proteins with another virus that is simultaneously present.

This sort of shift is not possible with coronaviruses. Therefore, you will never have leaps in antigenic changes either for antibodies or for T-cell killer lymphocytes. That’s why the background immunity that evolves during the lifetime of a human being is very broad and solid.

Natural Immunity Is Far Superior to Vaccine-Induced Immunity

One of the most egregious nullifications of medical scientific truth is the claim that COVID “vaccination” confers superior protection compared than the natural immunity you get after you’ve been exposed to the virus and recover. The reality is that natural immunity is infinitely more superior to the vaccine-induced protection you get from these shots, which is both narrow and temporary.

The COVID shot produces antibodies against just one of the viral proteins, the spike protein, whereas natural immunity produces antibodies against all parts of the virus, plus memory T cells. As noted by Bhakdi:

“The very fact that the World Health Organization has changed the definition of herd immunity … is such a scandal. I’m at a loss of words to describe how ridiculous I find this all, that this is being accepted by our colleagues. How can the physicians and scientists of the world bear to listen to all this nonsense?”

How the COVID Shot Causes Damage

As explained by Bhakdi, when you get a COVID shot, genetic instructions are being injected into your deltoid muscle. Muscle drains into your lymph nodes, which in turn can enter your bloodstream. There may also be direct translocation from the muscle into smaller blood vessels.

Animal data submitted by Pfizer to Japanese authorities show the mRNA appeared within the blood within one or two hours of injection. The rapidity of it suggests the nano particles are translocated from the muscle directly into the blood, bypassing the lymph nodes.

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“Even microclots that don’t completely block the blood vessel can have serious ramifications. You can check for presence of microclots by performing a D-dimer blood test. If your D-dimer is elevated, you have clotting somewhere in your body.”

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Once inside your bloodstream, the genetic instructions are delivered to the cells available, namely your endothelial cells. These are the cells that line your blood vessels. These cells then start producing spike protein, as per the mRNA instructions. As the name implies, the spike protein looks like a sharp spike protruding from the cell wall, into the bloodstream.

Since they are not supposed to be there, your killer lymphocytes rush to the area, thinking the cells are infected. The killer lymphocytes attack the cells, which causes damage to the cell wall. This damage, in turn, provokes clot formation. We’re now seeing evidence that COVID shots are causing all manner of clotting issues, from microsized clots to massive clots stretching a foot or more in length.

Of course, when a large enough clot occurs in the heart, you end up with a heart attack. In the brain, you end up with stroke. But even microclots that don’t completely block the blood vessel can have serious ramifications. You can check for presence of microclots by performing a D-dimer blood test. If your D-dimer is elevated, you have clotting somewhere in your body.

How Vaccine-Induced Antibodies Can Cause Harm

But that’s not all. The anti-spike protein antibodies can also be harmful. Bhakdi explains:

“The other thing that has now emerged is just as frightening [as the clotting problem]. One to two weeks after the first jab, you start making antibodies in large amounts.

Now, when the second jab is done, and the spike proteins starts to project from the walls of your vessels into your bloodstream, it is not only met by the killer lymphocytes, but now the antibodies are also there and the antibodies activate [the] complement [system].

That was my first field of research. The first cascade system is the clotting system. Turn it on and the blood will clot. If you turn on the complement system with the antibodies that bind to your vessel wall, then this complement system will start creating holes in the vessel wall.

And you see these patients who have bleeding in the skin. Ask, where does that come from? Well, if you go around riddling your vessels with holes, you [get bleeding]. If the holes riddle vessels of the liver, or the pancreas or the brain, then the blood will seep through the vessels into the tissues …

[The COVID injections] are in your bloodstream for at least a week, and they will seep into any organ. And when those [organ] cells then start to make the spike protein themselves, then the killer lymphocytes will also seek and destroy them [in that organ, creating more damage and subsequent clotting].

What we are witnessing is one of the most fascinating experiments that could lead to massive autoimmune disease. When this will happen, God knows. And what this will lead to, God knows.”

COVID Jab May Trigger Latent Viruses and Cancer

The COVID jabs can also decimate your lymph nodes, as your lymph nodes are full of lymphocytes and other immune cells. Some of the lymphocytes will die immediately upon contact, causing inflammation.

Cells that don’t die and take up the mRNA and start producing spike protein will be recognized as virus producers and get attacked by the complement system. It essentially creates a war between some immune cells against other immune cells. As a result of this attack, your lymph nodes swell and become painful.

This is a serious problem, as the lymphocytes in your lymph nodes are lifelong sentinels that keep latent infection such as shingles under control. When they malfunction or are destroyed, these latent viruses can activate. This is why we’re seeing reports of shingles, lupus, herpes, Epstein-Barr, tuberculosis and other infections emerge as a side effect of the shots. Of course, certain cancers can also be affected.

“As we all know, tumors are forming every day in our bodies, but those tumor cells are recognized by our lymphocytes and then they’re snuffed out,” Bhakdi says. “So, I am worried sick that the world is being goaded into taking something into the body that is going to change the whole face of medicine.”

Informed Consent Is Virtually Impossible

After giving this issue a great deal of thought, Bhakdi is convinced that the COVID injection campaign must be stopped.

“Gene-based vaccines are an absolute danger to mankind and their use at present violates the Nuremberg codex, such that everyone who is propagating their use should be put before tribunal,” Bhakdi says.

“Especially the vaccination of children is something that is so criminal that I have no words to express my horror … We are horribly worried that there’s going to be an impact on fertility. And this will be seen in years or decades from now. And this is potentially one of the greatest crimes, simply one of the greatest crimes imaginable …

As we all know, it is laid down by the Nuremberg codex that in case experiments are to be conducted in humans, this can only be performed with informed consent.

Informed consent means that the person to be vaccinated has to be informed about all the risks, the risk benefit ratios, the potential dangers and what is known about side effects. This cannot be done with children, because children are not in the position to understand it.

Therefore, they cannot give informed consent. Therefore, they cannot be vaccinated. If anyone does that, he should be set before a tribunal. If grownups have been informed and want to get the shot, that’s all right. But don’t force anyone to get the shot. It has to be by informed consent only.”

Of course, informed consent is also virtually impossible even for adults, as they’re only given one side of the story. All side effects and risks are censored virtually everywhere and discussions about them are banned. The U.S. government is even pushing to criminalize discussion about COVID injection risks.

Where Do We Go From Here?

If you’ve already gotten one or two shots, there’s nothing you can do about that. Certainly, do not get a booster, as each booster is undoubtedly going to magnify the damage.

“In the end, I predict that we’re going to see mass illnesses and deaths among people who normally would have wonderful lives ahead of them,” Bhakdi says. The question on people’s minds is, can anything be done to reverse the damage from these shots? As yet, we do not know.

However, if you have received one or more shots and develop symptoms of an infection, Bhakdi recommends treatment with hydroxychloroquine and/or ivermectin, such as the Zelenko protocol,⁴ and the MATH+ protocols,⁵ which have proven their effectiveness. It’s important to realize you may actually be more prone to serious infection, not less.

Nebulized hydrogen peroxide can also be used for prevention and treatment of COVID-19, as detailed in Dr. David Brownstein’s case paper⁶ and Dr. Thomas Levy’s free e-book, “Rapid Virus Recovery.” Whichever treatment protocol you use, make sure you begin treatment as soon as possible, ideally at first onset of symptoms.

Sources and References

• ¹ The BMJ Opinion November 26, 2020
• ² Medicina 2021; 57: 199
• ³ The Lancet Microbe July 1, 2021; 2(7): E279-E280
• ⁴ Zelenko protocol
• ⁵ Covid19criticalcare.com
• ⁶ Science, Public Health Policy and The Law July 2020; 1: 4-22 (PDF)

Luis Vega (16 May 2021)
“CORONA UNMASKED – Free Chapter Download Dr. Bhakdi”

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CORONA UNMASKED
FREE CHAPTER DOWNLOAD
Dr. Sucharit Bhakdi
by Luis B. Vega
vegapost@hotmail.com
http://www.PostScripts.org
The purpose of this post is to make the General Public aware of a fee chapter to download and read from a book exposing the COVID Cover-Up by Dr. Sucharit Bhakdi. He was born Sucharit Punyaratabandhu in Washington, D.C. He is a retired Thai-German Microbiologist. Bhakdi is a prominent exponent which believes, based on his research that the COVID-19 pandemic is a hoax. Like many other censored and de-platformed and discredited Virologists and Scientist who are Experts in this field, they are seen as being counter to the ‘Official Scientific Consensus’. He is warning of the dire consequences of millions taking the COVID-19 mRNA shots as they will encounter numerous complications and even mass-death to eventually follow.
He was a Professor at the University of Mainz, where from 1991 to 2012 he was Head of the Institute of Medical Microbiology and Hygiene. Bhakdi’s parents were Thai Diplomats. Bhakdi’s Mother studied at Johns Hopkins University in Baltimore. Bhakdi studied at the Universities of Bonn, Gießen, Mainz and Copenhagen, and at the Max Planck Institute of Immunobiology and Epigenetics in Freiburg.
He studied Medicine at the University of Bonn from 1963 to 1970, during part of which (from 1966 to 1970) he was a scholarship holder of the German Academic Exchange Service. Bhakdi worked for a while as a Private Assistant to the Internal Medicine Specialist Walter Siegenthaler. In February 1971 he received his Doctorate in medicine. From 1972 to 1978, he studied at the Max Planck Institute for Immunobiology in Freiburg on scholarships from the Max Planck Society at the Max Planck Institute of Immunobiology in Freiburg and the Alexander von Humboldt Foundation.
He worked at the University of Copenhagen for a year before moving to the Institute of Medical Microbiology at the Justus Liebig University in Gießen, where he worked from 1977 to 1990. Bhakdi was appointed C2 professor at Gießen in 1982. He spent a further year in Copenhagen and became C3 Professor of Medical Microbiology (at Gießen again) in 1987 before being appointed to the University of Mainz in 1990. From 1991 he headed the Institute of Medical Microbiology and Hygiene as a C4 professor.
Prior to his retirement, Bhakdi produced scientific work in fields such as Bacteriology and Atherosclerosis and published multiple Scientific Articles in these areas. Awards he received include the Order of Merit of Rhineland-Palatinate.(1)
Bhakdi has written several books now on the dangers of the COVID-19 shots that proposes are not ‘vaccines’ but Gene-Therapy and will have dire consequences. He has publicly released the following free chapter to download in English and in German from his book, Corona Unmasked.

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This chapter is a preliminary part of the forthcoming book “Corona Unmasked“ and is made available by the authors for free download for private use only. To be ordered from the publisher, a bookshop or online.
All rights reserved.
The authors and the publisher have prepared this work with the utmost care. Nevertheless, any liability of the publisher or the authors is excluded.
Cover: Carolyn Magerle
Foto: iStockphoto/Nastco
German ISBN: 978-3-99060-231-7
© 2021 Goldegg Verlag GmbH, Berlin & Vienna http://www.goldegg-verlag.com
THE VACCINATION CRAZE
This is a pre-publication of a chapter that will be finalized in the forthcoming book «Corona Unmasked« by Sucharit Bhakdi and Karina Reiss.

Will good things come only to those who wait?
Until now, most of the public has accepted and sup-ported the development of vaccines without doubt and hesitation. And rightly so, since vaccinations can save lives. But no vaccination will ever be perfect and free of side effects. Useful vaccines must meet two important requirements: 1. the vaccine must offer protection against a serious or even life-threatening disease; 2. its side effects must be within tolerable and acceptable limits.
On balance, the benefit must be much greater than the risk. Sounds logical, doesn’t it? And it is true. Who would get vaccinated against a common cold if this meant taking an incalculable risk of severe side effects? Furthermore, not every vaccination has to be useful for every person. Living in Germany, we do not need a vaccination against yellow fever, since it does not occur here.
We already know that COVID-19 puts a clearly de-fined group of people at risk – namely, those over 70 with serious preexisting conditions. For these people, vaccination against SARS-CoV-2 might possibly make sense. Of course, before such vaccinations could begin, the vaccine‘s efficacy and potential dangers would need to be examined very carefully. However, the clinical studies conducted thus far have excluded precisely this group of patients, so that efficacy and risks remained unknown before the roll-out of the vaccine.

Does the »killer coronavirus« justify exceptions?
In mid-October 2020, the President of the Robert Koch-Institute (RKI), Lothar Wieler, told the Phoenix television station: “We all assume that vaccines will be approved next year. We don’t know yet exactly how they will work, how well they will work, what they will do; but I’m very optimistic that there will be vaccines.” He was right about everything. The vaccines are here, and they are being given en masse – yet we don’t know if they work, how well they work, or what they do. That is why these vaccines have not been given regular approval by the EU, but only a “conditional approval” for emergency use (1). In the next 2 years, it will be reviewed whether their benefits outweigh the risks. Every person who gets vaccinated now is part of this huge experiment. But, of course, without any liability! Because with vaccinations under emergency rules, the manufacturers make no guarantees whatsoever – in case of serious reactions, or even in case of death, they are free from any liability.
Especially for completely novel, gene-based vaccines such as the mRNA vaccines against SARS-CoV-2, a careful study of the possible risks would be particularly important, because according to the current state of scientific knowledge, a variety of severe side effects are conceivable.
It is thus all the more astonishing that meaningful studies on the efficacy and safety of these novel vaccines do not exist at all – but at the same time, these same vaccines have already been preordered by European governments for the population in huge quantities. Nor were such studies feasible within the short time available. Three pharmaceutical companies were at the fore-front of the mad race for the highly lucrative emergency approval: AstraZeneca with its DNA vector vaccine based on an adenovirus, and Biontech/Pfizer as well as Moderna with their mRNA vaccines. On December 21, 2020, the EU Commission approved the Biontech/Pfizer vaccine, followed shortly thereafter on January 6 by approval of the Moderna vaccine; and on January 29, AstraZeneca received EU approval, too. While careful clinical testing of a new vaccine was previously known to take at least 7–10 years, the whole process has now been shortened to mere months. Could reliable data be on the table in such a short time, so that the public could weigh risk versus benefit? Of course not.
Nevertheless, everything was accepted and bought sight unseen by the authorities in Europe. In contrast, the Indian health authorities said NO to the Biontech/Pfizer vaccine because the safety of the population was not guaranteed (2).

Do current vaccines protect against severe SARS-CoV-2 infection?
As a matter of fact, a protective effect against severe and possibly life-threatening COVID-19 disease could not be shown in monkey models with any of the vaccines (3–5). All of these trials faced the same crucial problem: infected monkeys never became severely ill, either with or without vaccination (6). The monkeys can model infection, but they cannot model the dangerous form of the disease.

What do the human trials say?
Mainstream media jubilantly spread the press releases of the companies without ever asking any critical questions. Thus, from the media we learn that the protection afforded by the vaccines is simply great – with Biontech/Pfizer the level of protection is even 95 per-cent! That sounds great – bring on the vaccination!

But how do these numbers come about, knowing that healthy people very rarely get life-threatening COVID-19?
In fact, among the 40,000+ test subjects of the Biontech/Pfizer study (7), just 170 COVID-19 “cases” occurred (about 0.4%). Of these, 8 occurred among the vaccinated (1x severe), whereas 162 in the unvaccinated control group. The 8 cases in the first group equal 5% of the 162 in the second – therefore, 95% protection!?
Considering this small number of cases overall, the evidence must be described as plainly ridiculous from a scientific point of view. Moreover: how did this study define a “COVID-19 case” in the first place? Aha: symptoms like cough, cold, hoarseness and a positive RT-PCR test, which is extremely unreliable, as everyone knows by now. So, what we have here is a vaccination that might possibly prevent cough, cold, hoarseness in 0.7% of the vaccinated. For this breathtaking achievement, hundreds of vaccinated people had to accept severe side effects, some of which led to hospitalization.
The situation is no better for the other vaccine manufacturers. Accordingly, Professor Peter Doshi, writing in the prestigious British Journal of Medicine (8), complains: “None of the studies currently underway are designed to detect a reduction in severe outcomes in terms of hospitalization, admission to intensive care units, or death.”
How great is the benefit of vaccination, especially for the group most at risk from the infection? No one knows. Thereby, the justification for the conditional approval is the demonstrated prevention of serious or even deadly events. The conditional approvals for all gene-based vaccines were thus made without any basis whatsoever. The human trial continues, and everyone who is now enthusiastic about being vaccinated is taking part.

Does the vaccine prevent infection and thus the spread of the viruses?
A widely proclaimed goal of vaccination is not only to prevent COVID-19 disease in the vaccinated persons, but also to prevent the spread of the virus in the population. Already in kindergartens and elementary schools, children are taught that they could unknowingly kill their grandparents because they carry the viruses without being sick themselves. To prevent this, everyone should be vaccinated, including the children. Does this make sense – can a vaccination prevent an infection at all?
Let us start with the first question: does it make sense to try to prevent the spread of viruses that are of little danger to most people in order to supposedly protect a risk group?
First, some basics. Did you know that 90% of Germans carry herpes viruses around without realizing it (9)? The viruses only become noticeable when the immune system is weakened, for example during other infectious diseases, fever, or stress. Strictly speaking, we all carry an astonishing number of possible pathogens on and inside our bodies – yet we are healthy. Coronaviruses have also been known to be carried around by people for decades without causing symptoms. In the past, these people were called “healthy,” and nobody paid any attention to them. Today, they are deemed “asymptomatically infected” and therefore highly dangerous. However, we now know that the same is true for SARS-CoV-2: people without acute symptoms will not spread the severe disease COVID-19 in public (10– 12).
When we do develop symptoms, this is a sign that the viruses have found a chance to become active, and also that our immune system has entered the battle. If there is no cough, cold, hoarseness, etc., it means that our body is keeping the viruses at bay from the start. The viral load that a person can release into the out-side world without symptoms is too small to endanger other people in public. Therefore, the plan to vaccinate the entire population is a delusional and insane under-taking.
Let us turn to question 2: could the vaccines prevent the spread of SARS-CoV-2 viruses at all? The RKI states that this question is completely unresolved so far (13). To find out, one would have to examine whether
1-vaccinated people can still get an infection and whether 2-in this case, the amount of virus present is sufficient to infect others. AstraZeneca alone made headlines with the news that vaccinated people were significantly less contagious. However, on closer inspection, it is blindingly obvious that once more no data exist to draw this conclusion. The study in question only looked at part 1 of the question: how many more people get an infection after being vaccinated. How was this checked?
The only criterion was positive RT-PCR tests (14). Now even the WHO says that the PCR test alone is not enough to diagnose an infection (15). So, what is the unsubstantiated claim worth that the spread of infection was massively reduced by the AstraZeneca vaccine? NOTHING.
Anyone who has the slightest idea about infections and immune defense also knows that the mechanistic concept for the SARS-CoV-2 vaccination which is presented to the public is amateurish and naive from the start. The antibodies induced by the vaccination will circulate for the most part in the bloodstream. For an analogy, readers may imagine that they themselves are such antibodies, sitting together in the living room – which represents a blood vessel of the lungs.
Now the virus comes to the house – not bothering to ring the bell, it just grabs the door handle and steps into the hallway: the lung cell. How could you possibly stop it from doing so, while sitting in the living room? You can’t.
Antibodies can basically only help prevent the further spread of an intruder through the bloodstream. But that is not the primary protection against an attack from the air against the lungs. And that is precisely why there is no truly effective vaccine protection against respiratory infections, including influenza.

If the benefits of vaccinations are more than questionable, what about the risks?
We read in the mainstream media: mRNA vaccines are not new after all. That is true, but they have NEVER been used on humans to fight a viral infection. And humans have never been inoculated with recombinant viral genes, in the form of either DNA or mRNA.
Accordingly, the vaccinations were under a dark cloud from the outset. With all three gene-based vaccines, disturbing immediate side effects were noted – but carefully hidden from general awareness: severe swelling and pain at the injection site, high fever and chills, severe headache, limb and muscle pain throughout the body, diarrhea, nausea, vomiting. Many vaccinated people were so sick that they were unable to work. In the AstraZeneca study, the side effects were so bad that the study protocol had to be changed halfway through: in the later stages, study participants received high doses of the pain- and fever-relieving drug acetaminophen in order to make the vaccination reasonably tolerable (16). Such changes of protocol in the middle of a study are actually not permitted at all. Why was an exception made here?
But that is not all. The AstraZeneca study was interrupted in July and September 2020 because of the occurrence in vaccinees of an extremely rare autoimmune disease, which affects the spinal cord (17). “Transverse myelitis” is associated with paralysis and normally occurs at the very low frequency of approximately 3 per 1 million population, every year. It is surprising, then, that 2 such cases occurred among a relatively small number of vaccinated individuals. AstraZeneca announced days later: calm down people, the first test person had incipient multiple sclerosis, the second case was purely an unfortunate coincidence. The show will go on! And so, it did – AstraZeneca continued to forge ahead. But not only AstraZeneca – so did everyone else. The Biontech/Pfizer vaccine caused acute facial paralysis in 4 participants, and Moderna vaccine in 2, without the cause having been clarified (18). The prevailing attitude was, apparently: Why bother with such details if the race is on to save the world’s population from ruin, for better or worse ?
Comparable events occurred with competitors Moderna and Biontech/Pfizer. With both vaccines, volunteers suffered similarly severe general side effects. This sentence might be moved up to the discussion of general febrile reactions to the AstraZeneca vaccine.
Such a variety of immediate side effects has never been observed with any other vaccination. In America, when comparing the number of reported side effects of different vaccines over the 2 last years, the COVID-19 vaccine already comes out on top, although it was approved only in December 2020 (19).

Is the mRNA vaccine dangerous?
“No” is the answer that is spread everywhere. This is because 1) the vaccine introduces into our body only the information for a small part of the virus, for the so-called spike protein, which means that there is no intact virus that could propagate, and 2) the vaccine only imitates what Nature, too, would do. Intact viruses also release their genetic material into our cells when they attack, turning our cells into virus factories. So, no problem there at all, right?
Far from it. A natural respiratory infection typically affects only the respiratory tract itself. If, at worst, cell death occurs, the damage is local and can be repaired relatively easily.
With a vaccine, however, the viral genetic information is injected into the muscle. Many believe that the packaged viral genes remain at the site of injection – that is, within in the muscle. The genes would be taken up by cells at the site, which is where most “virus factories” would be created. Side effects such as swelling, redness and pain at the injection site would be expected because of this, but they would remain relatively harmless and go away after a few days.
What a fatal mistake!
The virus genes in the Moderna and Biontech/Pfizer vaccines are packaged in so-called nanoparticles – which can be thought of as tiny packages, not made of paper, but of fatlike substances. This protects the con-tents and makes it easier for them to be absorbed by the cells of our body. The packaging itself causes a risk of severe allergic reactions that is many times higher than with conventional vaccines (20). It is thus not without reason that people with allergies are now being warned not to get vaccinated – life-threatening reactions (anaphylactic shock) could be triggered. In fact, such dangerous side effects did occur in some vaccination volunteers, who required emergency treatment. In addition, nanoparticles can have numerous other harmful effects because they can interfere with the function of our blood cells and clotting system (21).
But it gets infinitely worse. It is part of basic medical knowledge that all soluble substances injected into muscle tissue enter the bloodstream and are distributed throughout the body within a very short time. This is precisely why substances that are supposed to act immediately are injected into the muscles.
It is known that the injected gene packets also enter the bloodstream (22). Which cell types will take them up, process them, and then produce the virus protein?
The answer to this is not known with certainty. We are now witnessing large-scale experiments on humans. This is absolutely irresponsible, especially since there was reason for caution from the beginning. The potential dangers from the “packaging” were already known. More significantly, however, alarming antibody-dependent enhancement – in this case, the antibodies do not prevent uptake of the virus into cells, but rather enhance it – has been observed in animal studies on SARS and other coronaviruses (23, 24). In the decades-long, yet futile effort to develop vaccines against SARS or MERS, this enhancement effect was repeated-ly observed, as one among problem among many others (25). With this in mind, should not animal studies have been conducted to clearly rule out this effect for SARS-CoV-2? Physicians who do not alert those willing to be vaccinated to the risk that vaccination could make the disease worse, not better, are in violation of their duty to inform (26).
And more seriously, could the inoculation of viral genes trigger other novel immune-related enhancement effects? Shouldn’t such very elementary things have been considered and tested beforehand?
As a reminder, lymphocytes have a long-term memory – they remember what the «molecular garbage« looks like that is produced in Coronavirus infections. And corona garbage looks pretty much the same no matter which member of the virus family it is derived from. All humans have had training rounds with coronaviruses, and thus they have lymphocytes that will re-cognize SARS-CoV-2 garbage. People without in-depth knowledge might counter that these cross-reactive killer lymphocytes were detected in only 40–70% of old blood samples, and they reacted only weakly against SARS-CoV-2 (27, 28). However, it is known that only a small proportion of all lymphocytes are in the blood at any given time. The others are just taking a break and resting in the lymphoid organs (including the lymph nodes).
Here, we note an exciting finding: In April 2020, Swedish researchers reported that they had discovered something truly remarkable. Activated and combat-ready T lymphocytes were found in the blood of all people (100%) infected with SARS-CoV-2, regardless of the severity of the disease (29).

This finding is a clear, unmistakable warning.
For context: during an initial confrontation of the immune system with a virus, the lymphocyte response will be sluggish. Rapid, strong reactions such as that documented by the Swedish team reveal that forewarned troops are already at the ready and can be mobilized on short notice. They will swarm out of the lymphoid organs to fight the enemy. Their main task: ex-termination of the virus factories – death to the body’s own cells that produce the virus particles.
And now back to the new reality: the large-scale experiment on humans. The injected gene packets are taken up locally in muscle cells, but a large part reaches first the local lymph nodes and, after passing through these, the bloodstream. The lymph nodes are where the immune cell team resides. When the viral gene is taken up by any cell there, production of the spike protein gets underway. The corona killer lymphocyte next door wakes up and springs into action – the brotherly battle begins! Lymph node swelling. Pain. The lymphocytes psyche each other up and then emerge from the lymph nodes to seek out more enemies.
Yes – over there – the muscle cells! There they are!!! Attack!!! At the injection site redness, swelling, bad pain.
But now the nightmare.
This is because the substances with small molecules – for example, blood sugar – can easily seep out of the blood into the tissue, whereas large molecules such as proteins cannot. For them, the vessel walls are tight thanks to the lining with a cell layer – the endothelial cells.

What are the gene packages like – large or small?
Right – compared to blood sugar, they certainly are large. Therefore, once they enter the bloodstream, they will remain in the closed network of vascular tubes just like the blood cells. A small part of them is taken up by white blood cells. Presumably, however, most of the virus factories will be established in the endothelial cells, that is, in the innermost cell layer of the blood vessels themselves.
This would happen mainly where the blood flows slowly – within the smallest and smallest vessels – because the gene packages can be taken up particularly efficiently by the cells there (30).
The endothelial cells then produce the viral spike protein and place the waste at the door – on the side that faces the bloodstream, where killer lymphocytes are on patrol. This time, the fight is one-sided. The endothelial cells have no defense.
What happens then can only be guessed at. Injury to the vascular lining usually leads to the formation of blood clots. This would likely happen in countless vessels in countless places in the body. If it happens in the placenta, severe damage to the child in the womb could result. Shudder.
Is there evidence that something like this is taking place? Yes, there is talk of rare blood disorders in which a possible link to vaccination would have to be investigated (31). Strikingly, there are reports of patients in whom a sharp drop in blood platelets (thrombocytes) was observed. This would fit the hypothesis put for-ward here, because platelets are activated and used up at the sites of blood clot formation.
Could you check if the assumption is correct? Yes. Laboratory findings provide immediate information on whether blood clotting is underway. Autopsies could clarify whether clots have formed in the small vessels. And in the meantime, consideration could be given to whether anticoagulants should be administered to patients as a preventive measure. The administration of cortisone preparations to dampen lymphocyte activity might also be worth considering.
There currently is a continuous stream of reports on deaths happening worldwide in close temporal connection with the vaccination. Officially it is said, of course, that the vaccination has nothing to do with these deaths. It is almost all older people with numerous preexisting conditions, who would have soon departed this world anyway. If that should be actually so, probably no thinking and sympathetic humans can fathom why these poor people still had to be inoculated with a poorly characterized vaccine such a short time before their natural deaths.

What could cause death in a frail person hours or days after vaccination?

Several effects are conceivable. Stress from the vaccination itself; allergic reactions. Autoimmune attack. Lymphocytes are also operational in old age. In elderly people with preexisting disease, the attack on the virus factories could be the straw that breaks the camel’s back.
It becomes somewhat more complicated when a simultaneous infection with the SARS-CoV-2 also comes into play. In several nursing homes, there have apparently been COVID-19 outbreaks just in the days after residents were vaccinated. Funny, funny – up until that point, there had been hardly any cases in the entire area, and all hygiene measures had been followed. There were outbreaks even after the second injection of the vaccine (32,33), a clear and expected indication that vaccination does not protect against infection.
I think here one must distinguish between patients with and without preexisting latent infections – it is conceivable (though unlikely) that those without infection are protected, whereas those with the infection are killed.
What is more, it seems that particularly the vaccinated are dying. Is this perhaps the immune-related exacerbation of diseases we have reason to fear? Not caused by antibodies, but by activated killer lymphocytes? And couldn’t this happen at any time to anyone vaccinated – tomorrow, the next day, next week, next fall? Because lymphocytes have an elephant’s memory. And they recognize something that looks similar in all coronaviruses: the molecular garbage that is produced by the virus-infected cells. That is, the lymphocyte-induced exacerbation of disease progression could arguably occur with any infection with a related virus. In any “successfully” vaccinated person – young or old – and at any time in the near or distant future.

Conclusion
Gene-based vaccines received emergency approval at lightning speed to combat a virus that is no more dangerous than influenza (34). There is now clear evidence that people can become severely ill and die from these vaccinations. No real-world benefit of vaccination has ever been shown. Until reliable and convincing data are available, this high-risk human experiment must not be allowed to continue.
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References
(1)              www.ema.europa.eu/en/documents/product-informati-on/comirnaty-epar-product-information_de.pdf
(2)              https://m.dw.com/en/india-pfizer-withdraws-covid-vac-cine-application-for-emergency-use/a-56462616
(3)              https://www.biorxiv.org/content/10.1101/2020.12.11.421008v1
(4)              https://www.nejm.org/doi/full/10.1056/NEJ-Moa2024671
(5)              https://www.nature.com/articles/s41586–020–2608-y
(6)              https://science.sciencemag.org/content/368/6494/1012.%20long
(7)              https://www.nejm.org/doi/full/10.1056/%20NEJMoa2034577?query=featured_home
(8)              https://www.bmj.com/content/371/bmj.m4037
(9)              https://www.bmbf.de/de/90-prozent-der-deutschen-tra-gen-die-herpes-simplex-viren-vom-typ-1-in-sich-4310.%20html
(10)            https://pubmed.ncbi.nlm.nih.gov/32453686/
(11)            https://www.nature.com/articles/s41467%20020%20%2019802-w
(12)            https://www.nature.com/articles/s41591–020–1046–6
(13)            https://www.rki.de/DE/Home/homepage_node.html
(14)            https://papers.ssrn.com/sol3/papers.cfm?abstract_%20id=3777268
(15)            https://www.who.int/news/item/20–01–2021-who-in-formation-notice-for-ivd-users-2020–05
(16)            https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7445431/
(17)            https://www.aerztezeitung.de/Nachrichten/Astra-Zeneca-stoppt-Corona-Impfstudien-412708.html
(18)            https://www.rki.de/DE/Content/Infekt/Impfen/Mate-rialien/Downloads-COVID-19/Aufklaerungsbogen-de.%20pdf?__blob=publicationFile
(19)            https://wonder.cdc.gov/
(20)            https://www.nejm.org/doi/full/10.1056/NEJM-ra2035343
(21)            https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829615/
(22)            https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383180/
(23)            https://jvi.asm.org/content/85/20/10582
(24)            https://www.jstage.jst.go.jp/article/jvms/60/1/60_1_49/_article
(25)            https://jbiomedsci.biomedcentral.com/articles/10.1186/s12929–020–00695–2
(26)            https://onlinelibrary.wiley.com/doi/10.1111/ijcp.13795
(27)            https://www.researchsquare.com/article/rs-35331/v1
(28)            https://doi.org/10.1016/j.cell.2020.05.015
(29)            http://dx.doi.org/10.1016/j.cell.2020.08.017
(30)            https://onlinelibrary.wiley.com/doi/abs/10.1002/adma.201906274
(31)            https://www.nytimes.com/2021/02/08/health/immu-ne-thrombocytopenia-covid-vaccine-blood.html
(32)            https://www.br.de/nachrichten/deutschland-welt/ge-impfte-altenheim-bewohner-positiv-auf-corona-varian-te-getestet,SOLqrXv
(33)            https://www.welt.de/vermischtes/article225923129/Landkreis-Osnabrueck-Trotz-zweiter-Impfung-Ausbruch-von-Corona-Variante-in-Altenheim.html
(34)            https://www.who.int/bulletin/online_first/%20BLT.20.265892.pdf
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GERMAN VERSION:
Bhakdi, Sucharit/Reiss, Karina
Corona unmasked
Neue Zahlen, Daten, Hintergründe
Taschenbuch, 160 Seiten
ISBN 978-3-99060-231-7
Erscheint April 2021
Preis: 15,– Euro
http://www.goldegg-verlag.com

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Main Sources
goldegg-verlag.com
https://www.goldegg-verlag.com/goldegg-verlag/wp-content/uploads/corona_unmasked_engl_leseprobe.pdf

(1) Wikipedia.com