“We do not believe any group of men adequate enough or wise enough to operate without scrutiny or without criticism. We know that the only way to avoid error is to detect it, that the only way to detect it is to be free to inquire. We know that in secrecy error undetected will flourish and subvert.” –J. Robert Oppenheimer
TL;DR – The spike protein not only contains a special sequence that allows it into the cell nucleus – it also has an ability to bring its own spike mRNA sequence with it. Both features appear to be unique among coronaviruses. The features explain genomic incorporation found for both the virus and the vaccines. The special key and the mRNA shepherding can be considered to be defects in any spike vaccine that has them.
Also, NONE of the “bigs” are talking about this, but it is HUGE, if only people will read the paper.
By sheer luck, I was alerted to this new development ASAP on Twitter.
A follower of mine, who I had followed back, posted on Twitter the link to a paper with this title:
Nuclear translocation of spike mRNA and protein is a novel feature of SARS-CoV-2
I immediately realized what this was about.
It’s about how the SARS-CoV-2 (COVID) virus spike protein and its mRNA get into the cell nucleus – an extremely important point which WSB has been hitting on over and over. It’s very important, because THAT is how “genomic incorporation” happens. And genomic incorporation is what HIV does – what retroviruses do. They “get into” the DNA and leave cookies, so to speak.
Sometimes, they leave enough cookies, that the whole virus comes back out, fully functional, and ready to infect. Sometimes, they only leave enough junk in the DNA to cause some damage. Sometimes, they leave enough to change us – and that is why human DNA is filled with “viral leftovers”.
In principle, mRNA technology should NOT do this. We were TOLD that mRNA technology could not do this. But somebody LIED TO US. And not only that – NOBODY – from Bill Gates on down – ever apologized to us about lying, or even about just “being mistaken”.
We’ll get to that later.
You will recall that there are two papers I love to mention.
One is the “Jaenisch paper”, which describes how the SARS-CoV-2 virus manages to get some of its genetic instructions for the spike protein into the DNA of cells.
The other is the “De Marinis paper”, which describes how the Pfizer vaccine did the same thing to human liver cells in vitro – meaning that in an experiment using cells in culture, the Pfizer vaccine got its mRNA sequences into the DNA genetic material of human liver cells, and it did so in a matter of minutes.
McCullough got in a lot of trouble with Twitter for posting this, even though it was utterly true. Now we know that the government was trying to shut it down. They likely used the technicality of McCullough’s very VALID speculation (stated as speculation and concern), which turned out to be correct, IMSO.
These papers explain ALMOST everything. When I saw the Jaenisch paper, I predicted that we would see the De Marinis paper. MEANING – when I saw that the virus could get mRNA into the DNA, I predicted that the vaccine might get its mRNA into the DNA, too. And yes, I was right. Clearly others thought the same thing, and decided to investigate.
Now, after the De Marinis paper, it seemed very obvious to me that one did not need any kind of special conditions or reverse transcription promoters to get the vaccine mRNA to incorporate.
That bothered me, and I suspected, at the time, that MAYBE – just maybe – the spike protein ITSELF was somehow causing genomic incorporation – that it functioned as a kind of reverse transcription promoter.
Well, it sure looks like that is the case.
According to the discoveries revealed in the new paper, which I have taken to calling the “Mehedi paper”, there is a special sequence in the spike protein that acts like a “key to the nucleus” – and this sequence is found in NO other coronavirus spike protein.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes severe pathophysiology in vulnerable older populations and appears to be highly pathogenic and more transmissible than other coronaviruses. The spike (S) protein appears to be a major pathogenic factor that contributes to the unique pathogenesis of SARS-CoV-2. Although the S protein is a surface transmembrane type 1 glycoprotein, it has been predicted to be translocated into the nucleus due to the novel nuclear localization signal (NLS) “PRRARSV,” which is absent from the S protein of other coronaviruses. Indeed, S proteins translocate into the nucleus in SARS-CoV-2-infected cells. S mRNAs also translocate into the nucleus. S mRNA colocalizes with S protein, aiding the nuclear translocation of S mRNA. While nuclear translocation of nucleoprotein (N) has been shown in many coronaviruses, the nuclear translocation of both S mRNA and S protein reveals a novel feature of SARS-CoV-2.
Let me put that in plainer English.
COVID-19 really hurts old people and seems to be both deadlier and easier to catch than other coronaviruses. The spike protein seems to be why. Although the spike protein is a surface protein that normally would not do this, it might be predicted to get into the cell nucleus because it has a special sequence “PRRARSV,” a known key to the nucleus which appears in no other coronavirus. Sure enough, the COVID spike protein gets into the nucleus of infected cells. What’s more, the mRNA for COVID spike protein also gets into the nucleus. What happens is that the spike mRNA collects near the spike protein, which helps it get in. While a different protein called the “nucleoprotein” of many coronaviruses is known to get into the nucleus of cells, the penetration of the cell nucleus by BOTH the spike protein AND the mRNA for it, seems to be a unique new feature of the SARS-CoV-2 virus.
Once you read it in plain English, it’s much more mind-blowing.
Now – I really recommend that you read the rest of the paper, but it’s really just technical details about what was mentioned in the abstract. Those details can help you gauge the expectedness or unexpectedness of things, but I have tried to do that as best as I could in the translation.
At this point, you should have all kinds of questions.
could this defect of the vaccines have been predicted?
should it have been predicted?
did the Chinese know this when they sent us the sequence?
did we know it when we got the sequence?
would NOT using the full spike protein have prevented this?
if so, why did we use the full spike protein anyway?
would the “forbidden” Winfried Stöcker RBD vaccine have avoided this?
if so, why was his vaccine suppressed by the German government?
does this affect the Peter Hotez vaccine, Corbevax?
if not, why didn’t his vaccine get promoted through the process quicker?
is nuclear penetration a common problem with mRNA technology?
how did this “key” get into the sequence? Naturally or not?
could “directed evolution” of the spike have yielded this?
why wasn’t this clear from the moment we got the sequence?
did people know this and hide the information?
were key people like Bill Gates (their side) and Robert Malone (our side) aware of this possibility?
The last question is a gift to WSB and her virologist friend. I am by default a defender of Dr. Malone, but WSB and her friend are long-time skeptics of the technology, and thus of Dr. Malone. In all fairness, I think we have to ask EVERYBODY the same questions.
Did people KNOW that mRNA technology had this vulnerability?
Does this look any more like an engineered bioweapon, designed to get into the nucleus?
Was this thing made by nature, by people, or by somebody with more advanced technology?
What is the purpose of getting into the nucleus, if it is designed to do that?
That should be enough. I will leave some links to prior comments I have made, in an appendix, hopefully added later.
Thank you.
W
John Fink and James Coburn discuss case in a scene from the film ‘The Carey Treatment’, 1972. (Photo by Metro-Goldwyn-Mayer/Getty Images)
U.S. President Donald Trump and first lady Melania Trump arrive for the 96th annual National Christmas Tree Lighting ceremony near the White House in Washington, U.S., November 28, 2018. REUTERS/Jim Young – RC1E6EA87210
AND our beautiful REALFLOTUS.
Get your rest, Trumpy Bear! You’re going back to the White House!!!
I think this statement is one of the best political speeches ever! Thank you, Trumpismine, for alerting us to this gem!
Please Stand By For A Brief Interruption…..
*SNUCK – A Special Wolfie’s Wheatie’s Word of the Day
Is it “snuck” or is it “sneaked”? DA WOOF was raised on “snuck”, more than likely because of his young hillbilly associates.
The Merriam-Webster Dictionary has a wonderful discussion of this point.
The original past tense of sneak was sneaked, following the pattern of other regular verbs. However, in the 19th century snuck started appearing, and is now the more common version for the past tense of “sneak.” Most irregular verbs become regular over time, but sneak has become irregular, and no other word like sneak (peek, creak, etc.) follows a similar pattern.
We shall return to our roots and use “snuck” as often as possible, but “sneaked” where it sounds better, like “sneaked a peek”.
We now return you to our regular programming.
The Business At Hand
This Stormwatch Monday Open Thread remains open – VERY OPEN – a place for everybody to post whatever they feel they would like to tell the White Hats, and the rest of the MAGA/KAG/KMAG world (with KMAG being a bit of both).
And indeed, it’s Monday…again.
But we WILL get through it, NO PROBLEM.
The Rules
Boilerplate, more or less, but worth reading again and again, if only for the minor changes, and to stay out of moderation.
The bottom line is Free Speech. Theories and ideas you don’t agree with must be WELCOME here, and you must be part of that welcoming. But you do NOT need to be part of any agreement.
I want to make TWO POINTS today.
POINT 1 – No Political Correctness (of Any Kind)
We shall endeavor to keep all forms of political correctness OUT of this place.
Even a hypothetical MAGA PC.
The idea that some things cannot be said “because MAGA” or “because Trump” is a non-starter. Don’t even.
THAT is a path back to BUSHISM and RINOism.
The utter banishment of PC is how we make sure that ALL “non-establishment voices” can be heard.
Political correctness always starts off with “we’re just asking you to be nice”, or, “we all believe this, don’t we?”, but it always ends up in censorship, because that is where it was ALWAYS HEADED.
You can use LOGIC, REASON, RELIGION, SCIENCE, and any other form of honest quarrel, even as simple as saying “I don’t like that”, but NOT political correctness.
PC is the most insidious infringement of free speech to ever exist.
And PC is not just a leftist thing.
A classic example from history is “You can’t criticize a sitting President during wartime.”
Where in the hell did THAT come from?
I would think that wartime is THE MOST IMPORTANT TIME for there to be criticism – even from people I absolutely can’t STAND (and I did like the Dixie Chicks, even when they were stupid as hell!)
Nope.
No idea, discussed honestly, truthfully, and with the agreed level of civility, is “beyond the pale”.
This site does not exist to protect certain ideas from examination. It exists to shine light into EVERY nook and cranny.
Thus, please don’t demand that certain topics or ideas be “off limits”, or declare that they are justifying of incivility.
Point 2 – Ignoring Those Who Disagree In Automatic Ways
People who disagree with your comments are simply part of this place, because of FREE SPEECH. You just have to put up with it. All viewpoints are subject to being countered in a civil fashion.
“Civil” does not necessarily mean that you will not be annoyed or frustrated by the reply or replies.
Feel free to offer to “agree to disagree”.
Now there are some people who don’t want to “agree to disagree”. They feel a kind of necessity to speak their mind – to state ALL disagreements, and to continue ad infinitum. Often this is religious, where the person believes that failure to disagree is a dereliction of moral responsibility.
This can get frustrating, if you feel that you HAVE TO RESPOND.
Because you DON’T HAVE TO RESPOND.
The best medicine for ad infinitum disagreements, even in moral duty, is to IGNORE THE REPLY. And I mean don’t respond in ANY way.
Do not demand that the other person “henceforth ignore what you say”, because that’s not part of free speech. YOU ignoring THEM is.
Trust me – when people see that you are not responding to somebody who “gets in the last word no matter what”, they are NOT thinking thatthis person “won the argument”. They think you have better things to do. AND YOU DO.
SO….. [ENGAGE BOILERPLATE…..]
We must endeavor to persevere to love our frenemies – even here.
Those who cannot deal with this easy requirement will be forced to jump the hoops of moderation, so that specific comments impugning other posters and violating the minimal rules can be sorted out and tossed in the trash.
In Wheatie’s words, “We’re on the same side here so let’s not engage in friendly fire.”
That includes the life skill of just ignoring certain other posters.
We do have a site – The U Tree – where civility is not a requirement. Interestingly, people don’t really go there much. Nevertheless, if you find yourself in an “argument” that can’t really stay civil, please feel free to “take it to the U Tree”. The U Tree is also a good place to report any technical difficulties, if you’re unable to report them here. Please post your comment there on one of Wolf’s posts, or in reply to one of Wolf’s comments, to make sure he sees it (though it may take a few hours).
We also have a backup site, called The Q Tree as well, which is really The Q Tree 579486807. You might call it “Second Tree”. The URL for that site is https://theqtree579486807.wordpress.com/. If this site (theqtree.com) ever goes down, please reassemble at the Second Tree.
If the Second Tree goes down, please go to The U Tree, or to our Gab Group, which is located at https://gab.com/groups/4178.
We also have some “old rules” and important guidelines, outlined here, in a very early post, on our first New Year’s Day, in 2019. The main point is not to make violent threats against people, which then have to be taken seriously by law enforcement, and which can be used as a PRETEXT by enemies of this site.
In the words of Wheatie, “Let’s not give the odious Internet Censors a reason to shut down this precious haven that Wolf has created for us.”
A Moment of Prayer
Our policy on extreme religious freedom on this site is discussed HERE. Please feel free to pray and praise God anytime and anywhere.
Thus, please pray for our real President, the one who actually won the election.
You may also pray for our enemies, even Pantifa, who need a good prison ministry.
BREAKING: Garrett Smith arrested today with a "pipe-type explosive device" near a rally in support of J6 defendant Jeremy Brown
Smith was wearing all black and had a helmet in his backpack decorated with what appears to be the antifa "Three Arrows" symbol pic.twitter.com/bQcSLFovmV
For your listening enjoyment, and general encouragement, we continue Wheatie’s tradition of fine music videos, shipped fresh from the seas of information by our intrepid authors.
First – a little “commercial” music from a certain airline.
Well – one thing leads to another. A bit of island-hopping, and then back to Hawaii…..
OK – that’s enough of that. Give me some of that LUCINDA CHICK that Smiley turned me onto! Let’s try the same song LIVE.
Now just add some ELVIS COSTELLO, who shows up with everybody.
OK – let’s see who else we can hook up Elvis with…..
OK. Maybe a good transition.
Call To Battle
Our beloved country is under Occupation by hostile forces.
Daily outrage and epic phuckery abound.
We can give in to despair…or we can be defiant and fight back in any way that we can.
Yup. MASS, GRAVITY, TIME and CONSEQUENCES THEREOF are most definitely a thing.
Joe Biden didn’t win.
And we will keep saying Joe Biden didn’t win until we get His Fraudulency out of our White House.
The Ethical Skeptic’s Elevator Pitch
You will recall LAST FRIDAY’S POST in which one of the topics was entitled:
This segment of the daily open covered a wonderful post (more like a “blog paper”) by The Ethical Skeptic, in which it is postulated (and to my satisfaction, demonstrated) that the Omicron variant is of a separate lineage from the Wuhan release and descendants thereof.
I had commented on The Ethical Skeptic’s post, that if he formulated an “elevator pitch” for his paper, I would trumpet it to the world.
WELL, HE DID!
Here is his “elevator pitch”, as well as the context.
WOO-HOO!!!
I got an “elevator pitch” from The Ethical Skeptic!!!
“When one examines the complete 144-slot genetic profile of the SARS-CoV-2 Omicron variant, it becomes clear that its lineage is a full two years older than even the first Covid virus in Wuhan, China. Not only did this ancestor of Omicron cause an outbreak across the world in 2018 and 2019, that was mistaken as an 8-fold higher rate of flu across the Asia-Pacific-Africa for those years, but its genetics reveal a robust history of lab mouse serial passes and lab-edited alleles. This proving that its 2018 release as a less-deadly immunity-builder prophylactic virus, and the subsequent release of the more-deadly Wuhan variant two years later, both originated from a weapons-grade bio-lab in China.
China set up a red herring for the world to ‘discover’ at the Wuhan Institute of Virology and its local seafood wet market, suggesting an unfortunate but understandable accident was being thinly concealed. Now, the problem for China is, that unlike all the other variants, Omicron stuck around for some reason, and is now spilling the beans on the whole sordid affair.”
TES
Now, let me repeat that in five pieces, with commentary in between.
But first, let me remind you, that this elevator pitch is NOT an abstract or a summary of the blog post. It is a small “explainer and convincer” that gives you the GIST of the proposition – enough to make you GET IT.
If you have just a few seconds to convince somebody that something needs attention, you need an “elevator pitch” – as in “I got on the elevator with the head of research, and finished my proposal right as she got off on her floor.”
Here we go!
When one examines the complete 144-slot genetic profile of the SARS-CoV-2 Omicron variant, it becomes clear that its lineage is a full two years older than even the first Covid virus in Wuhan, China.
In my opinion, it has been clear that EVERYBODY is surprised by the genetic divergence of Omicron from the original Wuhan strain, as well as all the other descendants thereof. How in the HECK did that happen?
Well, it gets worse. It turns out that Omicron or its close ancestors have been around since about the time we first started looking at SARS-CoV-2.
It is NEARLY IMPOSSIBLE that this virus is a product of mutation of Wuhan.
Something stinks.
Well, what TES has done, is to look closely at the genetics, and come up with a VERY plausible explanation of them, which ALSO explains many other interesting facts – particularly in the 2018-2019 timeframe.
Not only did this ancestor of Omicron cause an outbreak across the world in 2018 and 2019, that was mistaken as an 8-fold higher rate of flu across the Asia-Pacific-Africa for those years, but its genetics reveal a robust history of lab mouse serial passes and lab-edited alleles.
This matches up with many facts from 2018 and 2019, as well as my belief that China was actively engaged in some kind of shenanigans with the SARS outbreak of 2003.
China, in my opinion, has not only been LEARNING from secret and public accidental viral releases – it has been engineering many intentional releases for DECADES.
I think now is a good time to accept the following.
NOTHING that the CCP says should be believed or disbelieved. What they say is irrelevant, except as evidence of possible deception, criminality, and lies.Treat CCP or proxy statements as evidence from criminals – nothing more.
Here is a perfect example of Chinese scientific disinformation and Sun Tzu subterfuge.
LEARN from the ChiComs.
Chinese scientists (who may or may not believe what they are saying, because of omnipresent CCP infiltration, influence, control, and monitoring of all Chinese scientists) submitted – almost exactly 1 month after TES posted his work – a paper that is essentially COVER-UP of the evidence of mouse genetics in the lineage of Omicron which was revealed by TES.
The first link explains the paper in layman’s terms. The second link is to the paper itself.
What’s really SMART about this ChiCom “fix” is that they’re using Didier Raoult’s work concerning minks as a pretext here. This is a VERY typical Chinese science-spy suck-up technique.
Had I not worked with a bunch of Chinese and Russian spies for decades, being completely on guard for their bullshit, and yet having fallen for it a few times in spite of that experience and suspicion, I would not appreciate just how EXTREMELY GOOD they are at doing this stuff.
They will WEAR YOU DOWN WITH THE SUGAR and then SLIDE THE KNIFE IN when you can’t possibly see it.
And I ain’t sayin’ CIA CHICKS are bad, either, if you know what I mean.
What can I say? This is just like the horrible Zhang paper “proving” masks “work”, which was then used by American Democrat politicians to justify their mask policies used in their electoral coup of Trump.
Science is no longer free of OMNIPRESENT DECEPTION. Treat it accordingly.
I simply cannot emphasize this enough.
The CCP has no respect for “global” science. NONE. They use it – abuse it – and destroy it – all in the name of holding power. All those who trust the CCP, or the people it manipulates and influences – including many American governmental and organizational leaders – are going to get BURNED.
Likewise, if you automatically treat the science that CCP touches as “real”, be prepared to stumble.
This proving that its 2018 release as a less-deadly immunity-builder prophylactic virus, and the subsequent release of the more-deadly Wuhan variant two years later, both originated from a weapons-grade bio-lab in China.
The beauty of this explanation is not only that it explains the genetics, but that it explains many facts which we observed. TES has a good run-down, but in general, the “pre-COVID almost-COVID bugs” that people observed WERE IN FACT SOMETHING.
I think the real question is how much HELP China got on “our side”.
This is straight out of modern Chinese warfare – to strike an enemy in such a way that the enemy does not even understand THAT they have been struck. By using a prior release as a vaccine, the Chinese avoided all blame for a second release on their own soil.
This is brilliant warfare.
This fully comports with a tactic that the ChiComs absolutely love – which is to publicly “anticipate” a warfare capability that they ALREADY OWN AND USE IN BATTLE.
You will notice that by later in 2021, a few of those infamous “Chinese colonels” began to engage in a kind of “wolf warrior braggadocio” over the idea that China had won a great biological warfare victory over the West, by virtue of their superior “response” to COVID-19, and thus that biological warfare needed to be a key part of *FUTURE* Chinese war-fighting strategy.
Do NOT be fooled by this.
What this means is that China is already using biological warfare – and has been for some time. When Chinese colonels do this stuff, it is a psychological operation.
China set up a red herring for the world to ‘discover’ at the Wuhan Institute of Virology and its local seafood wet market, suggesting an unfortunate but understandable accident was being thinly concealed.
Again, the TES proposition explains so much about the multi-layer Chinese release cover-up, and all the subsequent, pre-calculated, pre-arranged back-pedaling.
First, there was bat soup.
Then there was no bat soup, but plenty of blame of racism. Clearly the work of the racist but infinitely self-hoaxing CCP.
Then I think it went to pangolins, and that was where I just started rolling my eyes. Smart people started believing blood samples (H/T Linda).
The Red Cross said it was definitely in America in December 2019.
Until somebody else proved October 2019.
And then the Italians proved it was prevalent in Europe in September 2019.
Again, the TES theory is perfect, explaining how the earlier “protective” viruses did a “long march” across Asia, thereby protecting China in a “mid-term practice run” of sorts – working out all the bugs, so to speak.
It just fits too well. Sorry, China.
AND – of course – this explains why the CIA and Twitter and the cut-out group “DRASTIC” created a double-down on a lab escape, conveniently proffered by a media that pilloried Trump for the same ideas, but realized that their “concession” would get Trump’s supporters to buy into a late release accident, to prevent them from seizing upon the highly explanatory idea of a two-stage release operation.
REALLY. They’re so easy to understand now.
Now, the problem for China is, that unlike all the other variants, Omicron stuck around for some reason, and is now spilling the beans on the whole sordid affair.
So – I have to ask – what is “some reason”?
Auberginebelieves that the Omicron mildness is by White Hat design, and I almost have to agree.
Or perhaps there’s a bit of “AND” logic here.
Wouldn’t it be hilarious if the American military identified Omicron precursors in old blood samples, realized the actual viral timelines, realized that Omicron was a “remnant” of the Chinese pre-Wuhan “vaccine strain”, and essentially RE-DEPLOYED THE CHINESE VACCINE STRAIN as Omicron, in some fashion, at some time?
What this means is that instead of finding and using a racially selective bioweapon, which will inevitably be achieved and used by these racist CCP goons, but is still *possibly* a bit out of reach, the ChiComs worked with what they had on hand – a chronologically and geographically and immunologically selective BINARY bioweapon.
And yet – well – it’s blowing back a bit now. In more ways than one.
Interesting times just got more interesting.
Corbevax – The “Good” Vaccine That Sneaked Past The Criminals
I’ve already been pimping this crap online and IRL, and I have offered some opinions already, but now I’m ready to give you all a real run-down on it.
Here is my latest “pimp job” on The Gateway Pundit, on an article about some poor Israeli teenage girl who got killed by ONE INJECTION of the “clot shot”…..
WOLFM00N 2m
Any pro-vax out there who are even thinking of vaccinating your kids – WAIT FOR CORBEVAX.
no mRNA or cDNA
no full spike protein
no nanolipid technology
no Pfizer, Moderna, Wuhan or China involved
non-profit, developed by Texas vaccine expert Dr. Peter Hotez
professor of pediatrics at Baylor (yes – a pediatrician)
patent-free – anybody can make it
made in India (right now) – very cheap
Google “corbevax hotez” and get more information. This is an RBD subunit protein antigen vaccine – meaning it works around almost every WRONG THING that was done on purpose in the current vaccines in order to PUSH technology. This is an old-school vaccine.
If you’re hesitant, wait for a few months of results. The Phase III trial was good (zero serious side effects), but we all know better – a million doses have to go out before you really know how safe these things are.
IMO, the only safer vaccine would be this exact same type by nasal delivery.
SO – TMI – information overload for sure.
What did I say? Some safer vaccine?
YES – let’s start from the beginning now.
First, a hat tip to TheseTruths for a link to some OANN coverage of this new vaccine.
OAN Newsroom UPDATED 10:26 AM PT – Wednesday, January 5, 2022
Texas scientists rolled out a new COVID-19 vaccine, saying it’s patent-free and can be produced by any manufacturer in any country. The vaccine, called Corbevax, was developed by the Texas Children’s Hospital and Baylor College of Medicine.
It has successfully passed human trials as safe and effective. The new treatment is based off protein-based technology that has been used in other vaccines for decades and it does not use MRNA.
India has already authorized production of 100 million doses per month of the new vaccine. Meanwhile, Texas scientists say not-for-profit vaccines will help defeat COVID-19 quicker.
“We, about 10 years ago, started making coronavirus vaccines and the irony is that all of our processes are used with that in mind,” explained Professor Peter Hotez, M.D. Baylor College of Medicine. “We build in low cost processes from the beginning because our health economist that we’ve collaborated with have always said if you don’t make it for under a few dollars a dose, you might as well not make it at all. So that’s all we know how to do, is make low cost vaccines.”
The irony here is rich. You can already tell by the price – this is the UBUNTU (Linux) of coronavirus vaccines. And yet, it has somehow managed to get the blessings of organizations owned by BILL GATES.
Yes, Hotez had to let Pfizer and Moderna go first, but I still find it amazing that Hotez got this vaccine past the wicked Bill Gates during his own lifetime.
Almost makes me wonder if Hotez got some help from his anti-vaxx enemies, putting pressure on the various CLOT SHOTS.
Hmmmmmm……
Yes, Professor Hotez actually DESPISES Sharyl Attkisson over the autism issue, and used to savage her on Twitter. Not sure if he’s blocked her, but I would not be surprised.
AND YET – well – just listen to him.
You heard him. The only leftist buzzword that Hotez left out was “sustainability”. It’s very clear that he knows how to do the university PC bullshit walk, and yet – this guy may end up saving millions of “Deplorable” lives, with a “plain Jane” vaccine that could actually have BENEFITS exceeding RISKS.
Let’s look at more coverage.
Here is a fluff piece written by HOTEZ HIMSELF and his colleague, Maria Elena Bottazzi, in good old super-wokester SCI-AM.
Maria Elena Bottazzi is co-director of the Texas Children’s Hospital Center for Vaccine Development. She is also a professor of pediatrics and molecular virology and microbiology at Baylor College of Medicine and associate dean of its National School of Tropical Medicine.
I must STRONGLY recommend reading the ENTIRE ARTICLE, which is short and easy to understand.
It is absolutely DRIPPING with VAXZI NARRATIVE and PC BUZZWORDS – and yet one gets the sense that the entire project is planned, positioned, and poised to BRING DOWN THE CLOT SHOTS. Or perhaps just to race right past them, as they self-destruct.
FTA (buzzwords and key points emphasized BY ME):
Two years into the pandemic, CORBEVAX is the first COVID vaccine designed specifically for global health. It is a milestone for global vaccine equity, something we believe will overcome vaccine hesitancy, and serves as a blueprint for how to develop a potent vaccine for pandemic use in the absence of substantial public funding.
The vaccine prototype was first developed by scientists at Texas Children’s CVD and Baylor before it was licensed, with no patents or strings attached, to Biological E. Limited (BioE).
The central government of India has already ordered 300 million doses. And BioE, the company manufacturing the vaccine, plans to produce 100 million or more doses per month starting in February. Approximately 150 million doses have already been produced and are ready to roll out. In addition to what the company is supplying to India, BioE plans to deliver more than one billion additional doses to other countries.
What this means is that CORBEVAX will soon vaccinate more people than vaccine doses donated so far by the U.S. government or any other G7 country.
This new COVID vaccine has several distinct features that make it particularly suitable for use in resource-poor settings: it is safe, effective and can be locally produced at very high quantities. CORBEVAX is easy to store and inexpensive. We hope it will be used in low- and middle-income countries in Africa, Asia and Latin America, where vaccine availability has generally been abysmal.
CORBEVAX is made using technology that has been employed worldwide for decades, meaning that manufacturing processes are generally already well-known and won’t require a steep learning curve like the one needed for the scale-up of new technologies such as mRNA, adenovirus and protein particle vaccines.
CORBEVAX is made through microbial fermentation in yeast, similar to the process used to produce the recombinant hepatitis B vaccine that many resource-poor countries make and employ. This will allow for local manufacturing of COVID vaccines similar to CORBEVAX. Texas Children’s CVD and Baylor have already licensed the COVID vaccine technology to companies in Indonesia and Bangladesh and have licensed it for production in African countries such as Botswana. Such vaccine technology and licensing agreements, together with co-development partners, represent the ideal example of how COVID vaccines can and should be produced locally and widely in countries in the Global South.
Like the recombinant hepatitis B vaccine that comes from the same technology, CORBEVAX has an excellent safety profile. In a phase 3 trial conducted in India, CORBEVAX produced mainly mild adverse events, making it perhaps one of the safest COVID-19 vaccines in use.
When compared with doses of the AstraZeneca–University of Oxford vaccine manufactured by the Serum Institute of India, CORBEVAX also produced a higher amount of neutralizing antibodies against the Delta and Beta variants of SARS-CoV-2, the virus that causes COVID (We expect to have Omicron data soon.) And it provided more durable and lasting protection. The vaccine neutralized variants of concern in laboratory animal studies and was highly protective in two nonhuman primate challenge trials. The trial results are being prepared for submission to a peer-reviewed journal.
As a recombinant protein vaccine developed from the receptor biding domain of the spike protein on the virus’s surface, combined with Dynavax Technologies’ CpG 1018 adjuvant with alum, the Texas Children’s CVD COVID vaccine can be stored using simple refrigeration. And like the hepatitis B vaccine, this COVID vaccine has one of the lowest costs of any available to date. No patents have been filed on the vaccine technology, and Texas Children’s CVD is assisting and co-developing the vaccine alongside BE and other vaccine producers in the Global South, which helps keep the cost low.
There is a research paper cited in the text, from Hotez and company, which shows that this is strong recombinant tech – it is NOT a rushed product.
Genetic modification to design a stable yeast-expressed recombinant SARS-CoV-2 receptor binding domain as a COVID-19 vaccine candidate
Now you all may remember me talking about a German vaccinologist named Winfried Stoecker, who tried to develop and promote a very similar RBD vaccine – and who was shut down immediately by Angie The Dung Cow and her Green Shirts.
In my opinion, this guy is like a “reality” version of the angry white faux-tranny Titania McGrath – a troll so perfect that it has to be real, or reality so SPOT-ON that it becomes a troll.
Peter Hotez is so authentically in compliance with the narrative, that he holds power over the hypocrites who force it on everybody else.
Thus, Bill Gates and Anthony Fauci are forced to go along with their own narrative, by this bow-tie bozo – this three-mask martinet of mandate over-compliance.
Don’t worry – this move away from the clot shot serves the agenda of Gates and Fauci, by covering their rear ends when the heat is on. The super-villains are not stupid, and did not rise to their levels of control by allowing guys like Hotez to be anything but a “parachute” of sorts, if their private jets catch fire.
Still, how did Hotez pull it off?
In my opinion, going to INDIA was the key move. India understands the precarious position they are in, thanks to CHINA JOE in the White House. India telling Pfizer to talk to the hand, and also backing off on trumpeting the virtues of ivermectin, are BOTH in my opinion connected to an exit via the Hotez vaccine.
HOTEZ had to know that INDIA was his key to getting HIS VACCINE produced.
INDIA had to know that HOTEZ was capable of bailing them out from the CLOT SHOT.
INDIA understood that HOTEZ was donating them a money-maker to gain leverage on the CLOT SHOT.
HOTEZ understood that INDIA needed an easy break to steal influence from CHINA.
Both HOTEZ and INDIA knew that BILL GATES, CHINA and BIDEN were weakened by CLOT SHOT blowback, and were not in a position to keep the murderous ruse of the CLOT SHOT going.
The HOTEZ VACCINE could be delayed at first, but it could not be stopped, because CLOT SHOT problems would eventually make it impossible to delay or stop any other reasonable vaccines.
All in all, a beautiful chess game of scientific leverage.
So who wins?
In my opinion – GOD.
Matthew 18:6
But if anyone causes one of these little ones who believe in Me to stumble, it would be better for him to have a large millstone hung around his neck and to be drowned in the depths of the sea.
Peter Hotez is very clear about the pediatric possibility of this vaccine. No matter what, I think he REALLY wants to help kids. If his vaccine isn’t “Clot Shot, Jr.”, then I think he may just do that.
We anticipate people will readily accept CORBEVAX and similar recombinant protein COVID vaccines, including for pediatric use. And clinical trials in children are also underway in India. Parents may even be more willing to accept CORBEVAX than vaccines made with a newer technology. If there was ever a COVID vaccine that might triumph over vaccine hesitancy and refusal, we believe this could be the one.
Is this vaccine better than simply catching the disease? We’ll see.
After what Pfizer, Moderna, Fauci, Gates and Biden have done, I trust NATURE more than vaccines. But I also “trust” some vaccines more than others.
I HOPE that THIS one – Corbevax – may be the new “gold standard” of coronavirus vaccine safety.
In the process of finding this video – passing over videos about – well – you can guess – I found THIS one, from Australia. The title is misleading – designed to get clicks and subscribers.
It’s worth watching to see the good and the bad of the Australian spring this last October.
We knew it was a snake when we let it in. Now, we all have to kick it out.
In which I argue that WE are the new cell culture for an uncontrolled gain of function experiment, that only WE can end.
It took me a while to figure out WHY they insisted on using the FULL SPIKE PROTEIN for these damn vaccines. This question has bugged me from the very beginning, and it got worse and worse as more and more spike protein side effects piled up.
Thankfully, sleeping late on the morning of 9/12/ 21, I had a DREAM which finally helped me see the answer.
It wasn’t exactly Kekulé’s dream, but it served the same purpose – to accept what I had not yet been able to fully see and accept.
Now, normally I would not mention that ANY of this came from a dream. There is no faster way to lose credibility, than to say “it came from a dream” – other than saying the answer came from the voice of God. But the truth of the matter is that I often find that UNRESOLVED QUESTIONS form what might be called “motifs” in my dreams, and sometimes I actually get some kind of resolution FROM the dreams.
If I tried to explain the dream itself, it would be almost meaningless to you. Things shift and change in dreams. Stone becomes brick becomes concrete and then vanishes. Stairs appear and disappear. People are there and people are gone, to be replaced by different people. One location changes smoothly into another location.
All of THAT is a jumble. This dream was a real doozy, too. Crazy! But in the dream I kept trying to resolve something – actually TWO things – which were composed of collections of ideas. These two things were like little, linear, diagrammatic collections of jewelry boxes, and it was impossible for me to SAY anything useful about the two collections, and how they related to each other, without actually interacting with them and looking into the jewelry boxes in some fashion or another, and in doing so, the collections were no longer separated and isolated from what might be called “everything else”.
It was IMPOSSIBLE for me, in the dream, to separate these things from “everything else”, if I wanted to know anything about their reality.
When I woke up, I realized the point of the dream.
The point of the dream was that the two things – IN REALITY – were both connected not only to each other, but to everything else. The point of the dream was that I needed to look at how the two things EACH interacted with everything else, to see how they were TRULY related to each other.
Not how they were SUPPOSED to be related to each other, but how they are ACTUALLY related to each other.
And THEN – in the “generality” of that moment – I realized that this “model”, if you will, applied to the COVID-19 VIRUSES (one collection) and the mRNA VACCINES (the second collection). And in THAT moment, I stopped looking at them as ANTAGONISTIC things, just because a LIAR named Fauci says they are antagonistic, but instead as SIMILAR and COMPLEMENTARY things.
As genetic material.
THAT is when “IT” hit me.
I woke up fully, and realized the following.
The VIRUSES and the VACCINES are DESIGNED to interact with each other in the realm of “everything else”, that being us humans. They are NOT designed to interact in the way we are being told. They are designed to interact in the way that they ACTUALLY DO interact.
Let me give you a simple representation of this relationship.
Consider a square. Color the top side GREEN – that represents “everything else”, not as it “should” be, but as it REALLY IS. Every point on that line segment is part of the world, relating to other points in the ways that they REALLY DO, in a “green” way. It’s ALL GREEN.
Now make the bottom two CORNER POINTS the two collections. Connect those points to the top of the square by green lines – the left and right sides of the square. Again, this is how they REALLY connect.
We are being TOLD that the bottom side of the square is RED.
Why should we believe that? What if it’s NOT red? What if it’s GREEN? What if there is a simpler GREEN ANSWER?
And IMMEDIATELY I knew what the GREEN ANSWER WAS.
The mRNA “vaccines” encoding a spike protein are designed to do in HUMANS containing the virus exactly the same thing that similarly added spike protein mRNA does in CELL CULTURES containing the virus. They are designed to CHANGE THE VIRUS – to make it GAIN FUNCTION. ALL that is needed to create the new virus is an otherwise identical injection with a NEW CODE that GAINS FUNCTION.
In other words, genetic vaccines offer an opportunity to smoothly regulate the rate and direction of evolution of the virus, without humanity knowing it. And they do it IN THE ANIMAL HOST INTENDED.
This solved many mysteries, which I will explain shortly.
This told me that there is ZERO need to go off and create a new variant in a lab. All one has to do is to change the code of the vaccine mRNA, and PRESTO – a new variant is introduced “in the wild”, with almost no chance of getting caught.
At this point, many of you are doing a WTF, so let me back up and explain this again.
What science does to “create a new virus” in the laboratory, from RNA or DNA, is to “somehow” (COUGH, COUGH, COUGH) get the RNA or DNA that they want to get into the NEW VIRUS, into laboratory cell cultures that are making OLD VIRUS. They need to get it into the cells, pretty much like they get the vaccine mRNA into our cells, using nanotech or virus vectors. THEN, the “old virus process” slips the “new genetic instructions” into the old protein shell, but as the virus spreads and multiplies, IF there is any “gain of function”, then the NEW INSTRUCTIONS in the NEW protein shell will WIN, and the result will be THE NEW VIRUS with GAIN OF FUNCTION.
Nobody really wants to spell out all the details of gain of function techniques in public, just like they don’t want to give the directions of how to make high explosives to terrorists. But THAT KNOWLEDGE IS OUT THERE, and we know roughly HOW THEY DO IT.
Honestly, it’s a bit like plant grafting, only instead of being largely in the Z DIRECTION (up), it’s in the T DIRECTION (time). You GRAFT new instructions into an old virus, until the new virus TAKES.
What they have done here is to create a PLATFORM for genetic change. Eventually it will be used to change US, but for the moment, they are clearly using it to CHANGE THE VIRUS (which is used to help change us, albeit somewhat indirectly).
Now – I said that this solved many mysteries. I’m going to list them here.
Why the full spike protein in the vaccines, despite its toxicity, and the greater likely safety of vaccines based on smaller subunits like the RBD?
Because the full spike is the main part of the virus that they’ve been changing, and which “gains function”. To get a new virus with a new spike, you have to change the instructions for the spike that get encoded in the virus. Also because you want to include the genetic instructions for ONE OR MORE FULL PIECES of the virus, if not the entire virus. That depends on exactly how the virus builds. We know (the Jaenisch paper) that the virus uploads fragments of its own RNA into the genomic DNA of the host, which come back out and are transcribed to RNA, so it will presumably do the same to pieces of the vaccine when both are present. Viruses that build from the vaccine spike variants will tend to WIN if they have gained function.
Why mRNA vaccines, despite the obvious safety advantages of protein vaccines?
Because protein is GENETICALLY SAFE – and that is NOT what they want. If the human population is now the experimental platform for virus gain-of-function experimentation, then only by being able to inject us with mRNA or DNA will viruses be able to be swiftly and decisively modified IN VIVO.
Short answer – they are not trying to change OUR genes yet – but they ARE trying to change viruses IN US. In vivo. And not in a way for our own good.
Why did they fight so hard against short-protein subunit vaccines like those from Winfried Stöcker and Sorrento?
Because if those vaccines are clearly superior to genetic vaccines due to safety or efficacy, then the conspirators will LOSE THEIR PLATFORM for genetic modification of viruses IN VIVO in the human population. Thus, these likely safer subunit and PROTEIN vaccines encountered delay after delay, and roadblock after roadblock, and in the case of the Stöcker vaccine, threats of arrest and legal trouble.
Why is Ralph Baric now doing work on chimeric mRNA vaccines that include LONGER mRNA encoding MULTIPLE proteins from SARS-CoV-2?
Because this approach toward longer and more mRNA leads closer to what they need to do – to inject us with the complete instructions for modified viruses – basically as what are called “virus-like particles” (VLPs), or by using viral vectors. These are “Fauci-compliant” in that they are “all about more and more antibodies”, and thus follow Fauci’s “antibody hypnosis” act, but clearly they will have more and more side effects, possibly including ADE.
As you can see, the vaccines are “less and less about natural immunity”, less and less about individual health, and more and more about experimentation and sociobiological engineering.
What does this have to do with Judy Mikovits?
Judy is one of the few people who have honestly explained the GAMES that the Faucists are playing with gain of function.
https://www.youtube.com/watch?v=0B17QQTr6xY
She explained that what these people have done – in complete violation of the CONTROLS that were placed on genetic engineering back in the 1970s – is to FORCE VIRUSES to “take” in human cells, allegedly in order to “see if they can or cannot take in human cells”. They are basically saying “we have to try hard to change the liquid to make the liquid catch fire, to see if it’s flammable”. This is a special kind of dishonesty.
There are MANY ways to make a virus “gain function”, but one of the FIRST and SIMPLEST is to just use tricks to make it change enough on its own, to eventually “take” in human cell culture.
It’s a lot like Nancy Pelosi and Obamacare – “you have to pass it to see what’s in it”. That is a special kind of cynical dishonesty, IMO.
But NOW they have actually HIDDEN gain of function research in PLAIN SIGHT. In us. Thanks to genetic vaccines.
Why did Adam Schiff go after Natural News and get them deplatformed?
Because the greatest danger to their plan is that humans will reject the future of human genetic modification IN VIVO. Natural News and their movement are a focal point of organized opposition. The Democrats KNEW this was coming, and they wanted the opposition out of the way.
This is also why so much work goes into discrediting these people.
But if the vaccine is for the SAME spike protein as in the virus, then how is THAT gain of function?
It’s NOT. It is ONLY if the vaccine contains DIFFERENT genetic material, DIFFERENT instructions, that any possibility for CHANGING the virus ensues.
Now tell me how you are going to go into EVERY vaccine that is given ANYWHERE in the world, and make sure that the mRNA doesn’t encode a new variant?
You can’t. That’s the evil genius of this plot.
If I want to introduce a variant ANYWHERE, all I have to do is give out a vaccine at the target location, where my vaccine looks just like the official stuff – or maybe even IS official stuff – but mine contains whatever genetic data is needed for a new virus, inside the same old nanotechnology.
You see – WE. HUMANS. OURSELVES. ARE. NOW. THE. GAIN-OF-FUNCTION. PLATFORM.
Pretty slick, if you ask me.
Could this platform be used for ADE as an intended effect?
Yes – because the variant that challenges prior antibodies is controlled by whoever launches the variant – and if that person or group is the same one controlling the vaccines, then TOUGH LUCK. And the ADE could be pinpointed in space and time, pretty much like Stalin’s Holmodor against the middle class in Ukraine. This platform of viral control can be used to control people at the individual, family, local, regional, state, national, continental, and global levels.
If we stop using these vaccines, will the variants stop?
They might stop. It will become much harder for the variants to appear, whether they are natural, and arise from vaccine evolutionary pressure, or are man-made, and require the vaccines for delivery.
Some of the best early opinions, IMO, thought that the initial genetic drift of SARS-CoV-2 was sufficiently small, that a single vaccination would cover all likely variants. While I’m not highly confident in that thought any more, I think it indicates that drift would be small, were it not for the vaccine.
So which is the plot – the virus or the vaccine?
AND logic – it’s BOTH OF THEM – the message of the dream. And it’s BOTH OF THEM in the SAME context that it would be in HUMAN CELLS. We are just “human cells on the hoof”.
The virus is out – and now they can change it “in the wild” thanks to GENETIC VACCINES – the greatest cover for genetic experimentation on viruses and humans that was ever conceived.
So how do we stop this plot?
Easy. We utterly reject genetic vaccines as a RISKY PLATFORM FOR TREATING VIRAL DISEASE, because they can be used to manipulate the disease and the diseased. The risks are not just individual – they are SOCIETAL as well. So we make them highly illegal. To get there, we use CIVIL DISOBEDIENCE FIRST. We REFUSE genetic vaccines.
For those who want vaccines, we go to old-school, time-tested, PLOT-SCUTTLING, protein vaccines. And all VOLUNTARY.
We don’t call this a RELIGIOUS objection. We are honest and call it a MORAL OBJECTION. If, however, your CHURCH OR SYNAGOGUE takes up the sword of abolition, and adheres to the morality of rejecting genetic vaccines, e.g., as considering them a form of “tempting the devil”, then you CAN validly call it a religious objection, too.
However, as an ETHICAL objection, like the objection to SLAVERY, all humans can take part.
Make no mistake – we are now in a literal HUMAN GAIN OF FUNCTION EXPERIMENT, using the whole human population as test subjects, and genetic vaccines as the obvious GOF vector.
The only way to STOP THE EXPERIMENT COLD, is to STOP USING GENETIC VACCINES.
Simple. Don’t let the snake in. Or if you HAVE let it in, kick it out!!!
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