Science One in four who had Pfizer Covid jabs experienced unintended immune response - lol

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More than a quarter of people injected with mRNA Covid jabs suffered an unintended immune response created by a glitch in the way the vaccine was read by the body, a study has found.

No adverse effects were created by the error, data show, but Cambridge scientists found such vaccines were not perfect and sometimes led to nonsense proteins being made instead of the desired Covid “spike”, which mimics infection and leads to antibody production.

mRNA jabs, such as the ones created by Moderna and Pfizer, use a string of genetic material to tell the body to create a specific protein that safely imitates an infection.

Research in the field, spanning decades, had been slow work. It often stalled because RNA itself is often attacked by the body as a foreign invader.

But in 2023, the Nobel Prize for Medicine went to the pair of scientists who had spent years working to fix the problem. It was done by taking one of the RNA bases, uridine, and swapping in a very similar synthetic alternative.

This breakthrough allowed scientists to create proteins in the body without the immune system attacking the jab.

It allows for quick and precise vaccines that are highly effective and was the backbone of the Covid vaccine response.

Not a perfect fit​

It was thought the minor tweak to uridine caused no problems in cells, but a team of researchers at the University of Cambridge’s Medical Research Council (MRC) Toxicology Unit have now found when this partially synthetic code is read, the protein-making machine in the body sometimes struggles with the uridine analogues.

Because it is not a perfect fit for what is expected, there can be a momentary pause which causes the process to stutter and a letter in the code can get skipped, much like a bike slipping a gear.

This process, called frameshifting, throws out the way the code is interpreted as it relies on groups of three bases, known as codons, being read in the right order.

This issue, caused by the jab’s code, throws the process completely out of sync and the entire subsequent code becomes garbled.

In the case of the Covid jabs, the end result is a nonsensical and harmless protein, the team found, which the body attacks and leads to an immune system flare-up. The new study, published in Nature, found this occurred in around 25-30 per cent of people.

Rogue protein fear​

The vaccine is read well enough to create the strong protection against the coronavirus, the scientists say, but the frameshifting issue creates what was, until now, an unknown off-target effect.

The code relating to the Covid vaccines was harmless and no issues were created. However the team say that subsequent mRNA vaccines used for other diseases or infections could, in theory, lead to viable proteins being created that are active in the body.

In this scenario not only is the vaccine not making the right protein, it could lead to a rogue protein being produced.

There is no evidence of this occurring in the Covid jabs, the authors stress, and they say any trials on other mRNA therapeutics would detect any such problems in early stages.

Dr James Thaventhiran, senior author of the report, said: “Research has shown beyond doubt that mRNA vaccination against COVID-19 is safe. Billions of doses of the Moderna and Pfizer mRNA vaccines have been safely delivered, saving lives worldwide.”

The authors also found that there is an easy way to eradicate the frameshifting events which relies on changing the code of the mRNA drug to minimise the use of the problematic pseudo-uridine.

Replacing it with a natural base that when read as a trio still makes the correct amino acid is enough to stop the unwanted skips and therefore improve safety without sacrificing efficacy.

These findings were shared with medicines regulator MHRA around a year ago, the scientists say, and updated vaccines that use the improved form of mRNA are in the works for cancer jabs, and other therapeutics.

‘Revolutionary technology’​

“This technology is amazing and it’s going to be revolutionary as a new medicine platform for all sorts of things, but we’ve just made it a whole lot safer going forward,” Professor Anne Willis, co-senior study author and director of the MRC Toxicology Unit told reporters.

“Ribosomes are somehow sensing the modified RNAs, but the Covid vaccines are very, very safe and very, very efficacious.

“But there are decoding issues with this technology that can cause stalling and frameshifting and we can get cellular immunity to these peptides after vaccination.”

However, she adds it is very exciting that there is a way to fix the issue, which “massively de-risks this platform going forward”.

https://news.yahoo.com/more-one-four-had-mrna-171724613.html (Archive)
 
Celiac isn't really a disease that should send you to the ER in an ambulance. It's a slow burn disease with abdominal cramping, watery diarrhea, malabsorption and slow starvation. It also should go into complete remission with complete gluten avoidance.

I suppose abdominal cramping could be severe enough with gluten exposure to theoretically send you to the ER, but nothing should really be acute or life-threatening.

Anyone with repeated ambulance trips for celiac disease either has a poor understanding of what contains gluten or has something else going on.

Celiac isn't really a disease that should send you to the ER in an ambulance. It's a slow burn disease with abdominal cramping, watery diarrhea, malabsorption and slow starvation. It also should go into complete remission with complete gluten avoidance.

I suppose abdominal cramping could be severe enough with gluten exposure to theoretically send you to the ER, but nothing should really be acute or life-threatening.

Anyone with repeated ambulance trips for celiac disease either has a poor understanding of what contains gluten or has something else going on.

She says it's Celiac's and she -says- she avoids Gluten.

Her face got Flush, her heart rate was fast..and she got stomach aches and couldn't stand without getting dizy...and I was the guy in charge at the time so I said "Fuck it" and called 911 because she didn't get any better after 10 minutes of sitting down. I presume she has Celiac's + Some other Horseshit the doctors blame on Celiacs cause they are lazy faggots..but she trusts "THE SCIENCE" tm.
 
I'm taking the liberty of re-posting it since I luckily saved it before he DFE'd, since I thought it was such an informative post.
3. The deformed protein was recognized by the mouse immune system and destroyed, just like every
other damaged protein in the body. The body has an entire system for getting rid of crap proteins. The
mouse immune system attacked and digested the deformed protein exactly like it handled the correct
spike protein. There was no evidence that the deformed protein produced any detrimental effect on the
mice.

Thanks for the re-post. It was confusing trying to follow the reply trees post-nuke.

It was a decent summary and the user obviously had some background in the topic.

I think this point is where the point of contention is (I did not read the actual study, just their summary.)

The user did a good job explaining the way that the study authors demonstrated the frameshifting of the RNA reading and abnormal protein production while proving its link to the synthetic building block in the mRNA shot.

But simply handwaving it away by generically stating that it has no potential to harm mice or humans simply because "the immune system has a finely tuned system to handle abnormal proteins" is a big assumption.

And simply another example of the knee-jerk reaction to consider something safe because we wish it to be instead of objectively proving it through inquiry.

Edit: abnormal, not abdominal
 
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Imagine getting vaxxed for a virus that killed 5% of people over the age of 85. The vax for polio took TWO years of clinical trials, The disease that put you in an iron lung for the rest of your life, as a child. This one fast tracked in under six monthes.

Don't trust a vaccine for a virus that might make you feel like shit for a week, at worst. Untested, and doesn't even stop you from getting the illness. But no, I'm the crazy person. Unvaxxed, never got covid.
 
Imagine getting vaxxed for a virus that killed 5% of people over the age of 85. The vax for polio took TWO years of clinical trials, The disease that put you in an iron lung for the rest of your life, as a child. This one fast tracked in under six monthes.

Don't trust a vaccine for a virus that might make you feel like shit for a week, at worst. Untested, and doesn't even stop you from getting the illness. But no, I'm the crazy person. Unvaxxed, never got covid.
Who would have thought to qualify as an ubermensch required the ability to ask questions and say no sometimes?
 
He abandoned his account, so I don't know that his objection to it would mean very much.
Jesus christ. Manul was relatively reasonable before this and actually informative in a lot of threads. I don't really get why this would be his breaking point, pretty sure he'd already argued on covid shit plenty before and hadn't been this pro-vax side before, could be wrong.
 
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Archived tweet

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FWIW, I was fooling around on Twitter in my usual skeptic circles and came across this former LNP/RNA researcher who made similar comments as Manul.

I'm not familiar with her, but she does have some COVID skeptic stuff on her timeline.

Similar to Manul, her take seems to be that your average cell has robust systems in place to the any abnormally-folded proteins out of circulation.

Her concerns re: the frameshifting seems to be that it could create problems with normally-folded proteins on a meta level re: their interactions.

She also seems to be of the opinion that the reframing error would require a second fucked up mechanism caused by the mRNA platform to really make the coding error originally described more concerning.
 
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Here's the actual paper:



If they tell you that the random proteins produced by this are safe, they are fucking lying. These dickheads haven't characterized the proteins, they haven't tested the proteins, they don't have a single fucking clue what the malformed junk proteins will do.

If @Otterly were here, she'd have a field day with this. She knows Pfizer are faking their motherfucking western blots.

Pardon me, but this sounds really similar to the effects of Celiac disease.

The immune system detects the protein gluten as a foreign invader in the small intestine and attacks it. It's not a benign reaction. The attacks cause inflammation, illness, and damage to cilia (leading to nutrient deficiency in the long term) in Celiac disease sufferers. And that's just in the digestive system. I can't imagine what sort of effects people who have that sort of reaction in their entire body experience all caused by a vaccine they're told is "very, very, very safe for realzies, guys, pwease bewieve us."

The human immune system is a brutal son of a bitch. It summons armies of neutrophils that serve solely as kamikaze peroxide bombs, and since our actual cells are made of the same stuff as bacteria and viruses, they get inflamed and die too. The only thing holding it back from obliterating our own body is self-nonself discrimination, a process that is basically black magic even to immunologists. They know about MHC and how dendritic cells work, and they can't even fucking tell you exactly how the immune system knows what is human, what's strep, and what's virus, and why it forms antibodies against one but not the other. It's practically a black box.

Autoimmune diseases - as in loss of self-tolerance, like lupus and Celiac disease - are a complete bitch. Autoimmune diseases can be triggered by viruses, exposure to pollutants, chronic inflammation, all sorts of things. It is vastly preferable for someone to go their whole life without their immune system attacking their own organs, for obvious reasons.

Slight powerlevel, but I have a confession to make: I got the J&J clot shot back in 2021. It was either get shot or get lost, and I didn't want to lose my job. I followed some crackpot doctor's advice on Twitter and fasted for 48 hours- by fasting, your body would go into autophagy mode and eat the damaged proteins. I never got another shot since, and have moved to a new job that doesn't care if I'm vaxxed.

Am I going to die?

Have you had any obvious adverse symptoms? Have you had a troponin test? Blood count fine? No clots? No myocarditis? No massive aorta rupture?

You'll probably be okay. Hopefully. Fingers crossed.

The death rate from the vaccines, according to Denis Rancourt and company, is on the order of 0.02%. It's a vanishingly small chance, for an individual. However, since they dosed billions of people with this shit, in real-world terms, that 0.02% comes out to a literal vaccine holocaust with 17 million people dead.

Not only should all of the COVID-19 vaccines (which are actually untested gene therapy drugs masquerading as vaccines) be taken off the market immediately, their creators should be criminally charged for fraud and mass murder.

Fucking no shit this happened. These people need to prepare for it to get MUCH worse. And I'm sure the medical establishment will just stick their thumbs up their butts to say we don't know what the issue is....but your prolly just anxious so if you go to therapy you'll feel better.

Fuck forgive me for being MATI, just hits too fucking close to home with my immune response from the anthrax experimental clot shot. 15 years after health off a cliff. Docs can't figure it out.....8 years after symptoms first started...and 3 weeks ago get results back from immunologist, moderately positive for Inclusion Body Myositis.

That's the thing. Adverse effects could, quite literally, take years and years to show up. Subclinical myocarditis is no laughing matter. Someone could keel over several years later, not even realizing that their heart had mostly turned to scar tissue.

Lol remember when the prion angle was just drain todger conspiraposting two years ago? And now TPTB are admitting at least 25% of the Pfizer vax created misfolded proteins. Harmless ones, though! What a relief. If it were bad kind, millions of Americans would have signed their own death warrants.

That's when the vaccine successfully produces Spike, which is, itself, a fucking prion.




Meanwhile, "fact-checkers" say "don't worry, it's safe, it's fine, it's not a prion".

https://www.usatoday.com/story/news...cine-not-associated-prion-disease/7053007002/ - https://archive.md/1aAxq

@Manul Otocolobus thanks for the clear and detailed explanation of the study, I feel a bit less retarded now. I'm saving a copy of it.

Now I get that the OP article was clickbait and barely true to the original study, but in general, don't you agree that even if so far there doesn't seem to be strong proof of serious consequences, it was still shady as hell and reckless to release the vaxx so quick to the main public? The way I interpret these studies is that it's a matter of luck that so far no nasty consequences have been found, but there's still a lot that they haven't tested for definitively, as they say in the Nature paper itself. And meanwhile billions and billions have the spike Pfiz-tein (lol) flowing in their veins.

I'm going to give a quick rundown of my own.

This is how ribosomes work:



This is a codon table, showing each codon and its corresponding amino acids. Since there are fewer amino acids than codons, each amino acid has multiple codons that correspond to it.

The-codon-table-The-genetic-code-is-composed-of-four-different-letters-U-C-A-and-G (1).png

By way of analogy, let's say that we have a looping sequence ABCD. If I start reading at the second letter, it's BCDA. If I start reading at the third letter, it's CDAB. If I start reading at the fourth letter, it's DABC. See how I have four letters, but four completely different "products" depending on where I start reading? Genes and codons are very similar.

For instance, let's take a bit of the beginning of the SARS-CoV-2 Spike sequence, as RNA:

AUG-UUU-GUU-UUU-CUU-GUU-UUA-UUG-CCA-CUA-GUC-UCU-AGU-CAG-UGU-GUU-AAU-CUU-ACA-ACC-AGA

Look at the codon table and start reading. Methionine, phenylalanine, valine, et cetera.

But wait, what if I start reading at U, instead, and skip over the A at the beginning? This is a simplification; if we misread the start codon, then everything about the process will absolutely shit itself. But say that we did. How does it read now?

UGU-UUG-UUU-UUC-UUG-UUU-UAU-UGC-CAC-UAG-UCU-CUA-GUC-AGU-GUG-UUA-AUC-UUA-CAA-CCA

Huh. Cysteine, Leucine, Phenylalanine, wait a minute. It's completely different.

This is a frameshift.


They have no idea what the ultimate product is. They haven't characterized it, they haven't checked if it's toxic or immunogenic, they don't know a thing about it. All they know is that there are mystery products from pseudouridylated mRNA.

They can't say, with any authority, if it's safe to have in someone's cells or not. The hordes of fact-checkers coming out of the woodwork to insist that this is perfectly fine don't know a goddamn thing. Where is their experimental data? Totally absent.

Every single day Drain Todger is further vindicated...God what's it like to sperg out on the Internet and have everyone call you crazy only for medical articles to come out a week later reiterating everything you said almost verbatim? I imagine once or twice it's funny. By now I imagine the Drainy One as a crippling alcoholic who hates humanity.

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Quite a few of his posts are missing from this thread, so I checked @Manul Otocolobus. He quit and went to a cathedral hugbox. I should probably say he went back to one ...
Wait where and what
I put in a request and the mods were nicely restored his meltdown posts here. He abandoned his account, so I don't know that his objection to it would mean very much. Anyway thanks mods
They didn't get the first half of his bullshit btw.
@Drain Todger vindicated once again.
The issue people had back then was that his sources were as untested, if not moreso, than the vaccines itself.
Also the whole thing with his history.

I'm guessing it still is, but at this point the retards that started and perpetrated this fuckfest can defend themselves.
 
I'm increasingly convinced J&J's vaccine was effectively shut down because they dared to deliver to spec - a prototype vaccine based on a new but recently used technology that wasn't very good, but was useful enough on a short-term EUA basis to prevent severe illness and death in highly vulnerable people.
Canada approved a plant based COVID vaccine but it went out of business this year. It was called Medicago Covifenz and the WHO itself wanted nothing to do with it because it was made from tobacco leaves and had a bit of funding from cigarette companies. I think it would have been a good option for people who didn't want the mRNA vaccine, for whatever reason.
I imagine it didn't help them that the damn dirty Russians used the same viral vector approach for their own vaccine.
I do feel that was part of it, like how disgustingly polarized can a society be to marginalize a vaccine made with merely the same technology as a country they don't like?
Lol remember when the prion angle was just drain todger conspiraposting two years ago?
It still is.
Every single day Drain Todger is further vindicated
For his love of salty futa cock?
Why were some states mRNA-only and others weren't?
Some places have a more rural population and the JJ vax was better because it wasn't as hard to store.
IFUCKINGLOVESCIENCE redditors

is it all just fucking cats?
Ask @Cats
our scientific inquiries
More like sperging.
@Drain Todger HE CAN'T KEEP GETTING AWAY WITH THIS
This is the guy you anti-vax spergs are idolizing:
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Because viruses evolve to become less severe. If they kill their hosts, they don't spread and they die out. That's why the obnoxious-but-nonlethal cold is everywhere, while the Bubonic Plague isn't.

What they should've done for Covid is to isolate and treat any SEVERE cases, while letting people naturally develop immunity to the weaker strains. That's "Herd Immunity" and farmers have successfully done it with livestock for a long time.

And then if the vaccines don't actually prevent infection or transmission (like the "covid vaccines") and simply lessen the severity of the symptoms (again, like the "covid vaccines"), you have what's called a "leaky vaccine." Leaky vaccines are what lead to the clusterfuck in poultry populations known as Marek's Disease. It was once fairly benign, but made for some unsightly chickens, so they started vaxxing for it. All it did was mask the symptoms. As a result, Marek's was able to mutate into a much worse form that causes lymphoma throughout the infected bird's body. It is now 100% FATAL if contracted by an unvaccinated bird. Thus, all chickens are now vaccinated within a couple days of hatching, or even in ovo.

Maybe I'm crazy, but part of me thinks that's exactly what they wanted to happen. For the coof to mutate into something that's 100% deadly, requiring regular boooosters to keep you alive. A never-ending revenue stream that you can't refuse, because refusing would mean you die. A perfect control mechanism, as the government could simply withhold your next dose if you step out of line. So you keep doing exactly what they say, because otherwise you're not allowed to purchase the drug you need to stay alive.


I’m in Canada you condescending nitwit, I never said anything about VAERS.

I'm quoting you since Manul ragequit like a faggot, but this isn't really directed at interrogating you...
If VAERS is worthless like he claims, then why is it used by doctors all over the country to track trends? Why have other vaccines been pulled after just a few VAERS reports (to say nothing of the literally tens of thousands for the coof shots)? If it's so unimportant, why is it a federal offense under 18 U.S.C. § 1001 to file a false report?


You really should care, because it was that strict adherence to "The Science" which is what leads us all to this mery-go-fuck-you-all-round ride we're stuck in.

Science has no room at the dinner table without the guiding hand of morality to slap the shit out of it when it goes lets inject people with junk, it's okay because it's science!

The legions of Reddit Atheists have become so self-enlightened that they claim to have eschewed such primitive things as "religion" and "faith." But in reality, they've replaced God with The Science™ (also known as Soyence) in their new belief system. Published articles are scripture. The Experts™ are their clergy. Thinking for oneself is now heresy. Suffering adverse side effects is celebrated on the level of receiving stigmata ("OMG the Holy Vaccine turned my periods into a crime scene every month! Isn't Science™ amazing?! Praise be to Science™!"). And those who die from bad Science™ simply didn't believe hard enough, or it was something else other than the obvious that ACKSHYUALLY killed them.

Actual science appears nowhere in this system, as it would point out too many flaws in their thinking.


Unvaxxed, never got covid.

Unvaxxed, did get covid. Twice (although the evidence is circumstantial at best). If that's actually what I had, it was nothing to write home about.
 
It still is.
Unfortunately not.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380922/ - https://archive.md/e1H1G

Here we study the effect of isolated SARS-CoV-2 spike protein S1 subunit as potential inflammagen sui generis. Using scanning electron and fluorescence microscopy as well as mass spectrometry, we investigate the potential of this inflammagen to interact with platelets and fibrin(ogen) directly to cause blood hypercoagulation. Using platelet-poor plasma (PPP), we show that spike protein may interfere with blood flow. Mass spectrometry also showed that when spike protein S1 is added to healthy PPP, it results in structural changes to β and γ fibrin(ogen), complement 3, and prothrombin. These proteins were substantially resistant to trypsinization, in the presence of spike protein S1. Here we suggest that, in part, the presence of spike protein in circulation may contribute to the hypercoagulation in COVID-19 positive patients and may cause substantial impairment of fibrinolysis. Such lytic impairment may result in the persistent large microclots we have noted here and previously in plasma samples of COVID-19 patients. This observation may have important clinical relevance in the treatment of hypercoagulability in COVID-19 patients.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9551214/ - https://archive.md/VEMCl

SARS-CoV-2 ‘S1’ spike protein binds to the aggregation-prone glycosoaminoglycan heparin and heparin binding proteins (HBP) including amyloid-beta (Aβ) peptides, α-synuclein, tau and prion proteins and TDP-43 thus facilitating viral infection while accelerating the coalescence and aggregation of multiple pathological amyloidogenic proteins in the brain and CNS (Idrees and Kumar, 2021; Paiardi et al., 2022);

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7988450/ - https://archive.md/5nycC

In this study, we have investigated the interactions of SARS-CoV-2 S1 RBD to different amyloid forming proteins including Aβ, α-synuclein, tau, prions, and TAR DNA binding protein-43 (TDP-43). We also examine the binding of S1 RBD to heparin and their complex to the different amyloidogenic proteins present in the brain. The insights will help us in understanding the heparin binding induced increase in association of HBPs observed in neurodegeneration and also to prevent future outcomes of neurodegeneration by targeting this association process.

https://pubs.acs.org/doi/10.1021/jacs.2c03925 - https://archive.md/7rlM9

Full-length folded S-protein did not form amyloid fibrils, but amyloid-like fibrils with evident branching were formed during 24 h of S-protein coincubation with the protease neutrophil elastase (NE) in vitro. NE efficiently cleaved S-protein, rendering exposure of amyloidogenic segments and accumulation of the amyloidogenic peptide 194–203, part of the most amyloidogenic synthetic spike peptide. NE is overexpressed at inflamed sites of viral infection. Our data propose a molecular mechanism for potential amyloidogenesis of SARS-CoV-2 S-protein in humans facilitated by endoproteolysis. The prospective of S-protein amyloidogenesis in COVID-19 disease associated pathogenesis can be important in understanding the disease and long COVID-19.

https://www.researchgate.net/public...lared_a_few_days_after_a_COVID-19_vaccine_Jab - https://archive.md/C9Pzq

We highlight presence of Prion in the Spike proteins of original SARS-CoV2 as well as of all its successive variants and of all the vaccines built on this same sequence of the Spike SARS-CoV2 from Wuhan. Paradoxically, with a density of mutations 8 times greater than that of the rest of the spike, the possible harmfulness of this Prion region disappears completely in the Omicron variant. We are studying 26 Creutzfeld Jakob Diseases, in 2021, from an anamnestic point of view, centered on the chronological aspect of the evolution of this new prion disease, without being able to have an explanation of the etiopathogenic aspect of this new entity. We subsequently recall the usual history of this dreadfull subacute disease, and compare it with this new, extremely acute, prion disease, following closely vaccinations. In a few weeks, 26 cases of almost spontaneous emergence of suspected Creutzfeldt-Jakob disease have appeared in France, Europe and USA very soon after the injection of Pfizer, Moderna or AstraZeneka vaccines. To summarize, of the 26 cases analyzed, the first symptoms of CJD appeared on average 11.38 days after the injection of the COVID-19 "vaccine". Of these 26 cases, 20 had died at the time of writing this article while 6 were still alive. The 20 deaths occurred only 4.76 months after the injection. Among them, 8 of them lead to a sudden death (2.5 months). All this confirms the radically different nature of this new form of CJD, whereas the classic form requires several decades. On June 2022, last 5 patients had also died. Currently, only one of 26 patients survives.

https://kirschsubstack.com/p/proof-covid-vaccines-cause-prion - https://archive.md/PYrJc

And for CJD which is extremely rare (this is worldwide result over 30 years for all vaccines) we see 24 cases for COVID19, but pretty much zero over 30 years for all the other vaccines.

Do you have any idea how much of an absolute shitshow would ensue if it turned out that a significant number of people exposed to the Spike protein, from either the virus or vaccination, had their brains seeded with the scrapie form of Prion protein and had started incubating lethal Creutzfeldt-Jakob Disease?


If that is the case, then I hate to be the bearer of bad news, but we may yet see The Stand-level apocalyptic shit happening in this decade or the next, because of all this. I mean, just, absolute mountains of corpses.

I hope and pray this one particular blackpill is bullshit.
 
Similar to Manul, her take seems to be that your average cell has robust systems in place to the any abnormally-folded proteins out of circulation.

Her concerns re: the frameshifting seems to be that it could create problems with normally-folded proteins on a meta level re: their interactions.
Problem is: the spike protein is itself a foreign protein; the human intracellular disposal system for aberrant proteins cannot tell whether it is miscoded or not.

Her concern is moot because, again, the spike protein is not a human protein and does not work in tandem with other proteins (the way that kinesin does). The problem of "dominant negative" simply does not arise.
 
That's not all. This hasn't been widely reported, yet, but there's a mystery ORF in there that is very similar to spidroin.

https://anandamide.substack.com/p/intent-to-deceive - https://archive.md/pTk63

af152763-e72a-44cd-a8e2-10311b7ec7fb_1088x1460.png

Gee, I wonder why embalmers are pulling cell-free clots of solid protein out of dead bodies?

Oh, I don't need to wonder. I know why.

I don't know who that is.
Chise the Pine Marten, NIH employee (and 2022 NIH Director's Award recipient). One of the individuals who helped test and validate the potently pozzed furry juice you so happily took, of course.


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If you took the vax, it's all ogre. You may as well get the Chise plush to go on the mantel next to your Fauci bobblehead.



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