do let us know should HHS Secretary Bobby Kennedy Jnr send a team to confer with you on your latest findings .. which should be understood as impacting the national security of all nations
Again I was only an English Literature major. I don't talk science but would love to have this put into simple language for us dimwits. I think you are wonderful and you are performing work very few could understand. Love and Thanks.
When Pfizer and Moderna make their COVID shots, they copy the spike RNA from a circular piece of DNA (a plasmid). Some of this DNA gets stuck extremely tightly to the newly made RNA, forming “hybrid” pairs that are almost impossible to pull apart with normal cleanup tools.
-- Why the usual cleanup step failed
The companies use an enzyme called DNase1 to chew up leftover DNA at the end of production. This enzyme (mostly, but not always) works fine on loose DNA, but it cannot touch the DNA that is glued to the RNA in these hybrids. As a result, a lot of DNA—protected inside the hybrids—stays in the final product and gets wrapped inside the lipid nanoparticles with the RNA, and delivered inside of cells.
-- What the new lab tests showed
Kevin, Jessica and Charles treated vaxxine samples with special enzymes that can break the hybrids. When they did, huge amounts of hidden DNA appeared, including the SV40 promoter sequence in Pfizer shots (a piece of DNA known to interfere with cancer-protecting proteins). Regulators had only tested the easy-to-reach DNA, so they never saw the protected pieces that remained (.. or did they?).
Dumb question here, but what exactly does the "SV40 promoter sequence" promote, and why is it in the Pfizer shots. I have heard that it helps DNA enter the nucleus of a cell, but I would think that is a bad thing as, in theory, it increases the chances of genome modification.
Not a dumb question at all Beyowulf760 - this is the single most concerning part of the whole story.
The SV40 promoter is a short DNA sequence borrowed from Simian Virus 40 (a monkey virus that can cause cancer in animals). In molecular biology it is used as an extremely strong “on-switch” that forces mammalian cells to make huge amounts of whatever protein the attached gene codes for. It is one of the most powerful promoters we have, which is why labs love it.
Pfizer included it in the bacterial plasmid they used to mass-produce the spike DNA template (Process 2). It sits in the “backbone” of the plasmid and drives the antibiotic-resistance gene so the bacteria can be selected on kanamycin plates, and it also doubles as a high-copy replication origin. It’s a standard off-the-shelf trick in biotech, but it means every billion doses of Pfizer contain billions of copies of this sequence.
Moderna’s plasmid design simply doesn’t have it, so their shots don’t have this particular piece, but still contains all the other crap synthetic DNA Jessica, Kevin, and Charles have been nailing down.
The part that worries people (and the reason it keeps coming up) is that this exact SV40 promoter fragment acts as a nuclear targeting sequence (as in the ‘nucleus’ of our cells).
When DNA that contains it gets into a cell, cellular proteins recognise the sequence and actively shuttle that Pfizer’s synthetic DNA into the nucleus far more efficiently than they would shuttle ordinary DNA.
Once it’s in the nucleus there is a real chance of integration into the genome. If the fragment inserts upstream of an oncogene, the powerful SV40 promoter can drive uncontrolled cell growth – a NOT theoretical cancer risk.
This is why the old SV40-contaminated polio vaccines (1955–1963) still spark so much debate - mesotheliomas and brain tumours appeared at higher-than-expected rates in people who received those batches, and the virus causes tumours in rodents by very similar insertional/promoter mechanisms. Indeed, listen to Professor Angus Dalgliesh who tells the world how his cancer research team used SV40 sequences all the time for purposefully inducing cancers rapidly in lab rats, so they could test their anti-cancer treatments. Labs the world over do the same thing.
So yes, having a known oncogenic promoter that also moonlights as a “please deliver me to the nucleus” tag in a product injected into billions of arms is … not ideal. Regulators say the amounts are tiny and “within limits,”(*cough* BS) but the new (and old) papers show the limits were measured incorrectly because the DNA was hidden in RNA–DNA hybrids, so the real residual amounts (and therefore the real risk) are higher than any regulator wants to admit – doing so means taking responsibility for millions/billions adversely impacted, plus trillions of dollars in liability payouts.
Another concern - separate from integration - is that any foreign DNA floating in the cytoplasm (even tiny fragments that never reach the nucleus) is detected by the cell’s cGAS-STING sensor, an alarm system evolved to spot viral DNA. When triggered, it unleashes a powerful inflammatory response (type I interferons, NF-(k)B, etc.).
Persistent or repeated activation of cGAS-STING is now known to drive chronic inflammation and, in multiple studies, to promote tumour progression and metastasis downstream (aka, cancers) - essentially turning an anti-viral defence pathway into a cancer-facilitating one when it won’t switch off.
So the SV40 promoter isn’t the only problem; the sheer presence of plasmid DNA itself (from Pfizer and Moderna) is proinflammatory in a way regulators never accounted for, and again, do not want to account for .. that liability issue again.
I am very very grateful that you took the time to write such and excellent and complete explanation. For laypeople like myself this really helps to flesh out our understanding of what is happening, even if it is simply terrifying! I am sure many people will benefit from this information you have so kindly provided. After all it is hard to fight if we don't understand and can't put into words what we are fighting for.
Thank you for having the courage and integrity to write about the unprecedented injuries from the mRNA COVID shots.
The Biggest Lie of the "COVID vaccine propaganda" is that the mRNA COVID shots are vaccines.
People need to understand the truth that the "COVID vaccines" are modified mRNA-LNP gene "therapy" transfection products.
And that even if there was no E.coli DNA plasmid "contamination" with no carcinogenic SV-40 promotor sequence, even if they had not deceptively injected shots into the public that were made by Process 2, even if the spike protein was not pathogenic...these mRNA transfection injections would have still injured and killed people.
The mRNA transfection platform itself is irreparably flawed & inherently dangerous and the platform itself IS the primary problem.
The mechanism of action (using mRNA instructions to turn one’s own cells into foreign non-self “spike protein factories”) IS the primary mechanism of harm.
For those who are seeking an understanding as to why the injuries from these mRNA transfection injections are so widespread and can greatly vary from person to person:
The modified mRNA-LNP transfection injections genetically instruct one's own cells to become "factories" for the production of foreign non-self proteins...
This triggers an immune system attack response, starting with the Killer T-Lymphocyte cells which will target and destroy one's formerly healthy cells, ANYWHERE in the body, that are now expressing non-self proteins...starting a cascade of damage at the deepest biological/cellular level.
Due to the biodistribution properties of the (toxic & inflammatory) lipid nanoparticles, the encased (designed to be long-lasting) n1-methyl pseudouridine modified mRNA can go anywhere in the body, including crossing the blood-brain and placental barriers...The LNP "delivery vehicles" traveled to different parts of the body in different people.
Expressing any foreign protein is fatal to the cell doing the expressing. The reason is, our bodies are protected by being able to distinguish ourselves from things that shouldn't be there. Anything non-self will trigger immune destruction of the cells & tissues involved.
Some people will express lots of foreign proteins in vulnerable locations. Others express less in less vulnerable areas.
The location of expression defines the adverse event: if you get foreign protein expression in your heart cells, you could get myocarditis & experience cardiac arrest; if the expression is in your brain, spinal cord, or peripheral nervous system, you could get one or more of a variety of neurological conditions; if in your eye, possible blindness; if in your ovaries, possible infertility; if in the placenta, possible miscarriage, stillbirth, or birth defects; if in the endothelial cells that line your blood vessels, possible vascular &/or microvascular injuries like clots/microclots or the long white fibrous clots, leading to strokes, heart attacks, or pulmonary embolisms…
If the expression of foreign proteins is in your own immune cells, you could experience immune dysfunction, dysregulation, & suppression including repeated infections, immune tolerance of a pathogenic foreign protein due to antibody subclass switch to IgG4 & increased IgG4-related diseases, T cell exhaustion, interference with & suppression of innate immunity, persistent systemic inflammation, dysregulation of toll-like receptors and reduced cancer surveillance or the suppression of tumor-suppressing immune system activities & cell-signaling (increasing your risk of fast-growing and aggressive cancers)…
And more…
Pathology reports, including from autopsies, have revealed & confirmed the Killer T Lymphocyte infiltration & destruction of cells, oftentimes in vital organs.
There's no limit to the horrible consequences of injecting into your body something that triggers your own immune system to attack & kill your own formerly healthy cells & tissues.
The public “health” agencies, the COVID “authorities”, & the “mainstream” media fraudulently marketed these experimental mRNA gene “therapy” transfection products as “safe & effective vaccines”. Trusting people thought that they were being presented with the choice (or the mandate) as to whether or not to take a “safe & effective vaccine”…But that was/is a deceptively false “choice”…
The COVID-19 mRNA shots are NOT safe, they are NOT effective, and they are NOT vaccines.
These modified mRNA-LNP gene “therapy” transfection injections never would have passed proper safety studies required for gene therapy products. Safety studies (including biodistribution, immunogenicity, immunotoxicity, genotoxicity, carcinogenicity, reproductive toxicity, shedding, long-term effects, & more) that were bypassed because of the fraudulent mislabeling as “vaccines”. (And because of the EUA & “countermeasure” designations under the Project BioShield Act & PREP Act in the United States).
The danger is NOT limited to just getting more COVID “boosters”. ANY mRNA (or DNA) gene “therapy” product that transfects your cells and instructs those cells to produce foreign non-self proteins (ANY non-self protein) will trigger an immune system attack response against your own cells & tissues (the role of the Killer T-cells is to monitor ALL the cells of the body, ready to destroy/kill any that express foreign, non-self proteins). This makes EVERY mRNA-based (or DNA-based) transfection product harmful by design.
This entirely predictable immune response to one's own cells being instructed to create & express non-self proteins (ANY non-self protein) can trigger autoimmune responses, & then T-cell exhaustion, immune system dysfunction & possible immune collapse...regardless of whether or not the foreign protein is toxic itself (or whether or not there are carcinogenic DNA "contaminants" within the injected product).
Self vs. Non-self...Basic fundamental Immunology 101...
EVERY SINGLE DOCTOR or medical professional should have been able to recognize the immunological dangers of these mRNA transfection shots...
"While the pharmaceutical industry rushes to expand mRNA use for its speed and profit, a fundamental immunological principle is being overlooked: Any cell that produces a foreign protein is marked for destruction by the immune system.
This isn't theoretical. Clear histopathological evidence from biopsies and autopsies confirms the vaccine's genetic material does not stay at the injection site. It enters systemic circulation and spreads uncontrollably throughout the body, including to vital organs like the brain and heart.
Once there, the body's own cells are forced to produce the foreign antigen, triggering an immune attack on its own tissues."
The undermining of this basic foundational principle of human immunity made the IMMUNOLOGICAL CATASTROPHE of the modified mRNA-LNP gene "therapy" transfection injections entirely predictable...(and I am not a doctor nor am I in the medical field).
And they can shed on others, making them dangerous and injurious for those who said "Hell NO!" as well...
These transfection injection bioweapons NEVER should have been injected into a single human being...
It is not enough for there to be no mandates...
Tragically, because more people do not understand that this is not about "choice", this is not about the ability to tell others what to do or not...
Because more people are not standing up and demanding that these "traditional" modified mRNA-LNP transfection injections be pulled from the market, the next "evolution" is moving forward (the self amplifying mRNA transfection technology platform)...
Vioxx, 1976 Swine flu shot, Thalidomide, DES, DDT, etc...etc...ALL removed from the market after having previously been approved for use in the USA, or Europe, or wherever...yet now some people are acting like removing a product from the market is unprecedented...
Dangerous, injurious, deadly products must be pulled from the market!!! You do NOT give uninformed or misinformed people the "choice" to use such products.
Especially when their uninformed "consent" leads to them taking a product that sheds and poses a legitimate danger to the health of those being shed on.
Shedding from these transfection injection bioweapons IS an extremely serious concern, with some people being affected more than others...
NO ONE should have ever had the “choice” of taking these gene “therapy” transfection injections because the modified mRNA-LNP genetic transfection technology platform is fundamentally flawed & dangerous by design.
I cannot say it enough: It is NOT enough for there to be no mandates.
I will say again: These transfection injection bioweapons NEVER should have been injected into a single human being.
And as Dr. Sansone has correctly asserted, bioweapons are ALREADY illegal!!
Thank you! These extra explanations, yours and the one above, are so beneficial!
And this whole debacle is so frustrating. From an outsider perspective, there is too much money to be made in playing games with the building blocks of life, and too little emphasis on not doing permanent damage to the human gene pool, to continue this (idiocy). Feeding greed is now the purpose of "science."
Humans survived with far better rapport with the planet and its other inhabitants before the rise of civilization(s) and this one seems hell-bent on maiming and murdering its way to ultimate destruction.
Excellent summary in a way that many can understand. How wonderful. Jessica is a force of nature , and her tireless actions to uncover what has happened alongside other heroes is nothing short of miraculous! May God bless all of them. Thank you for your comments… it made things much more clear. Eileen
SV40 (simian virus 40) is a cancer promoter. it was in the original polio vaccines; as part of the manufacturing process, they cultured the vaccine in monkey kidneys and the mass vaccination campaign may have resulted in the uptick in population level cancer afterwards.
then again, i'm also not a scientist. just a long time broadway costume maker and costume director of a major international arts festival who was fired after 40 years because i wouldn't take the covid shot.
so if i've said anything wrong here, i hope someone more qualified will correct me
Wow; that's appalling that you were fired because of your refusal of the Covid shot. I'm just a lay journalist, and, as I said above, I have had to clamber up a vertiginous learning curve in writing about Covid vaccine injury and the possible lab origin of SARS-CoV-2. I will write something about these new discoveries, and Julian's explanations really help. Here is one of my previous articles: https://changingtimes.media/2024/12/06/experts-warn-of-cancer-risk-as-dna-contamination-is-found-in-mrna-covid-19-vaccines/ You seem to me to have understood the situation very well.
i have been a medical skeptic since childhood so my distrust of conventional medicine goes WAY back. i'm 72 and have never had a mammogram or a colonoscopy. interestingly, my last tetanus shot was in 1980 as a condition of the contract for the job that i was eventually fired from because of the covid vaccine which i was NEVER going to take. the 2nd year (1981) when i went to my doctor for another tetanus shot because the contract required it, my family doctor refused. he said "if you get a tetanus shot every year, you'll get tetanus!" i never had another one. for years afterward, i just signed the contract and ignored that clause. then they started taking my presence for granted and forgot to give me a contract for a decade or more. then one year, they wouldn't pay me unless i signed a contract. they had outsourced the payroll to a company which spooked me. i hate bureaucracies. i reminded the festival that they hadn't given me a contract and when they did, i read it carefully and refused to sign it until they removed the language about the tetanus shot. so they shouldn't have been too surprised when i refused to take a covid shot.
i read lots of medical books and have always gone to alternative doctors. even on medicare, i go to doctors who don't take insurance and pay out of pocket for the kind of care i want. fortunately i don't require much care and if i get hit by a car or something where i need conventional medicine, i use medicare.
On my documentation at Radio France International they wrote something like 'still refusing to have a tetanus shot". I was lucky that, when the Covid shots came in, I was working alone/independently. I ended up illegal in India, though, but that's a whole other story that is still messing up my life.
See Lex Acker on Substack. He did a nice forensic accounting assessment in B.C., Canada, and showed that about 10% of the health and government employees were "disemployed" [my term!] as a result of declining their clot-shots in 2021.
The performing arts unions were the worst offenders of the cvid/injection hoax. I am a member of two. They took that holier than thou ball and ran with it. Far longer than most, I think. Sad.
I hope you have found other means of satisfying income while continuing your art.
i've never been a member of a union; in fact i opened my own costume shop after i had to leave a job in a top union shop because i wouldn't join. i assumed we would never do broadway work because of my principles but our work was so good that we did "union" work all the time! my boyfriend is a long time member of local 1.
the unions totally discredited themselves during the pandemic. they have one function which is to protect the labor of their members- not the vaccinated only members, not the democrat only voting members, but ALL their members.
Hey Dear Beyo…”SV40” is a virus contaminate from the polio virus from the 1950s. Everyone who got the polio shot and sugar cube as a young child is contaminated with the SV40 virus, which is another way to speak of fast track tumors and other immune deficiencies. None of the scientists looked for viruses on the monkey kidneys where the polio vaccine was grown from. When this SV40 virus problem , a fast track for immune issues was discovered, it was hidden from the general public. “Dr Mary’s Monkey “ is a scary, sad, and true book to read; which addresses this trespass,( with an astonishing amount of footnotes). Dr Mary was ready to tell the whole world about this problem.The author of this book’s father knew Dr Mary personally. Dad told his reporter son, on his death bed,to never research Dr Mary’s death because the people responsible for her death would also kill him…So grateful to this disobedient son and his investigative skills. Richard Nixon was told in the 1950s about this SV40 problem; one of the first things he did as president in 1968 was to declare “war on cancer”…because he already knew the levels of cancer were rising as SV40 settled in to all the vaccinated human bodies. It is not only our food that is killing us…”Devils chessboard” is another fabulous read about the Dulles brothers and the CIA… investigative journalism from the 1940,50,and 60s…Stay well and Stay Curious 💜…BTW…this was a great question…💥
Really good book, "Dr. Mary's Monkey." Sad but worthwhile read. Thanks for more of the backstory on it.
I also read Edward Hooper's "The River" at the same time, and Duesberg's "Inventing the AIDS Virus" shortly after. The three books combine to give an interesting perspective of medical research in the very recent past.
To learn more about Dr. Mary and the monkeys' watch this wonderful piece from CHD with Dr. Suzanne Humphries. She's goes pretty deep into the story. Fascinating.
No, the hybrids do not stay locked together forever once they’re inside your cells - and that’s actually the worrying part.
The lipid nanoparticle (the fatty bubble that carries everything into the cell) pops open pretty quickly in the cytoplasm and dumps its cargo.
At that point the RNA–DNA hybrid is naked and floating around inside the cell, and cells hate RNA–DNA hybrids.
Our cells have a dedicated enzyme called RNase H whose whole job is to spot these hybrids and immediately chew up the RNA strand. When it does that, the DNA strand is suddenly set free as plain single-stranded DNA.
Once the DNA is loose in the cytoplasm:
-- It can trigger the cGAS-STING alarm system (chronic inflammation – leading to - possible cancer-promoting effects over time).
-- It has a much better chance of being shuttled into the nucleus (especially if it has the SV40 promoter tag).
-- It becomes available for integration events or reverse transcription .. both activities are well documented, with the reverse transcription being known for at least 40 years (I wrote a paper on just this: https://ijvtpr.com/index.php/IJVTPR/article/view/83).
So the hybrid is basically a Trojan horse: it protects the DNA on the journey in, then the cell itself unwraps the package and hands you the naked synthetic DNA once it’s safely past all the defences.
Please, please, please, laymen terms for the average dimwit. I sell complex products and my success has always been anchored in simple relatable explanations. Explain it for a child to understand…
With all the maiming and deaths , including fetuses, it should have been off the market ASAP. However, the ACOG still wants every pregnant woman jabbed . Nefarious intent IMO
They can barely claim they did not know of complication considering the trial they ran and stopped due to injuries . https://clinicaltrials.gov/study/NCT04754594?tab=history&a=24#version-content-panel Panel 19 Placebo 1.3 % vs Vaccinated 5.1 % AESI = Adverse event of special Interest . As i understand it , if one more baby would have been harmed the trial would have counted as failure and set precedent . Just the amount of listed Study Design / Status feels like it got altered to suit the wanted outcome but failed despite of it . So they stopped it , problem evaded .
Geert says that when he worked at Glaxo years ago the quality control was taken very seriously to keep DNA out of the vaccines. Was Pfizer's incompetence deliberate for population control or was it unintentional? Petula Clark turned 93 today. I hope she is unjabbed.
Thanks-glad I instinctively knew the controls had changed-this was my first “red flag” warning when I heard the vax jab was ready to stab people in “minutes” not “years”!!
This should surprise nobody because these were never like vaccines beyond similarity of syringe delivery. They are made with the same process used for ALL biologics and the contaminants are expected which is why biologics undergo expensive filtering and purification.
Another name for the process of producing the mRNA TRANSFECTION products is Gain of Function which are CRISPR clones grown in E.coli the decades old bench tool worth priced as petrie dish commodity but turned to cash cow with IP reset as "novel vaccine" treatments.
It should be embarrassing six years into this Covidian fraud knowing that bodies NEVER tolerate non-self proteins and that ANY protein transfected was criminal medical insanity on par with lobotomy another deadly Nobel Prize winning human experiment.
Even the New York Times reported the deadly effects of TRANSFECTION in 1999 with the Biotech Death of Jesse Gelsinger because immune systems kill non-self proteins. When the truth of this crime against humanity is more broadly recognized you folks who pretended to be advocating for an informed public while burying truth will be seen as traitors to humanity.
1) can you now finally prove the fraud that will void the liability protection granted by the EUA? this would allow the vaccine injured to sue the drug companies themselves and not seek compensation from the government (over burdened tax payer).
a flurry of lawsuits would make the mRNA products less profitable and therefore less appealing. it seems RFKjr is having to proceed very carefully in getting the mRNA products off the market. they are, after all, Trump's signature achievement. but if they were less profitable, the companies would abandon them, in true free market fashion.
2) can you find an enzyme that will dissolve/digest the spike protein and maybe act as a therapy to help the vaccine injured? i think there are a lot of very damaged people out there and i fear that as time passes, the harms will accrue.
Barnes has been litigating the Brooks (Pfizer whitleblower) case for about 4 years. It's maddening. Clear case of fraud but it's stuck in the court. The DOJ got involved and tried to shut it down. The corruption is massive.
Carolyn, we know that the new people in HHS, like Hoag, Prasad, Retsef, MaKary and RFK Jr spoke out publicly on social media against these shots. So,I believe the very powerful are shutting down any investigation.
Next useful experiment that you and Charles Rixey might like to try in Kevin's lab, would be to use Kevin's patented Endotoxin removal magnetic beads and see if the Endotoxin stuck to the Pfizer and Moderna nRNA and residual Plasmid DNA can be levered off, to give enhanced access to the enzymes DNase1 and/or DNase-XT.
Even more fun might be the study of cord blood from women vaxxed during pregnancy, to see if the spike dNA has been transfected into the foetal (infant's) WBCs.
Continue the SLOW roll. Don’t mention that we knew ALL this in 2021. Transfection; see Jesse Gelsinger. Don’t note that the plasmid issue is a known problem with “biologics”. And repeat over and over that this slew of reactions are mysterious even though in labs monkeys (because they’re so expensive) are rarely transfected because it is KNOWN the animal will die soon after. Lastly keep secret many were likely given placebos.
If the pharmaceutical companies had not been given liability protection for these products, would this contamination have occurred in the first place? Cutting corners in these instances would surely have to be regarded as criminal negligence.
Why not call this what it is - transfection. SV40 or no SV40 would intramuscular injection of a novel substance to augment immune system was not and is not a good idea. Stat Mews as far back as ‘15 told us reason Moderna was struggling to progress through pre-clinical trials, was because animals were dying.
How come you and your cadre of MAHA grifters refuse to critique all the useless NPIs like masking, distancing, virtual learning, isolation of elderly? Or deadly hospital protocols like use of high flow oxygen (unsupervised), depriving anti-biotics for bacterial pneumonia, liberal use of end of life drugs as well as Remdesivir. All this for a “deadly virus”we knew had an IFRnof less than 1 given Diamond Princess data?
You and the rest of the DARPA/NIH actors are setting us up for a new and improved mRNA transfection along with personalized gene therapy marketed as “personalized medicine”.
Pete, I’m injured too as are untold numbers of others and those whose doctors who are clueless to the causal depth of the injuries caused by these shots.
thank you Dr Rose, Kevin, and Charles
do let us know should HHS Secretary Bobby Kennedy Jnr send a team to confer with you on your latest findings .. which should be understood as impacting the national security of all nations
yes, and obviously RFK, Jr was copied on the memo as shown in image here!
He has no excuse not to acknowledge this officially and have scientists in the FDA orgs do so on stage with all cameras running. . .
Ron Johnson should do the same.
Prosecutions MUST be advanced.
Those propagating this horror on humanity must PAY.
Again I was only an English Literature major. I don't talk science but would love to have this put into simple language for us dimwits. I think you are wonderful and you are performing work very few could understand. Love and Thanks.
Kathleen,
-- How DNA ends up in the mRNA vaccines
When Pfizer and Moderna make their COVID shots, they copy the spike RNA from a circular piece of DNA (a plasmid). Some of this DNA gets stuck extremely tightly to the newly made RNA, forming “hybrid” pairs that are almost impossible to pull apart with normal cleanup tools.
-- Why the usual cleanup step failed
The companies use an enzyme called DNase1 to chew up leftover DNA at the end of production. This enzyme (mostly, but not always) works fine on loose DNA, but it cannot touch the DNA that is glued to the RNA in these hybrids. As a result, a lot of DNA—protected inside the hybrids—stays in the final product and gets wrapped inside the lipid nanoparticles with the RNA, and delivered inside of cells.
-- What the new lab tests showed
Kevin, Jessica and Charles treated vaxxine samples with special enzymes that can break the hybrids. When they did, huge amounts of hidden DNA appeared, including the SV40 promoter sequence in Pfizer shots (a piece of DNA known to interfere with cancer-protecting proteins). Regulators had only tested the easy-to-reach DNA, so they never saw the protected pieces that remained (.. or did they?).
.. trust this helps
THANK YOU! Yes...I get it now. They hid the real murder weapon in the hopes we couldn't figure it out. Horrifying stuff. Demonic even.
Dumb question here, but what exactly does the "SV40 promoter sequence" promote, and why is it in the Pfizer shots. I have heard that it helps DNA enter the nucleus of a cell, but I would think that is a bad thing as, in theory, it increases the chances of genome modification.
Not a dumb question at all Beyowulf760 - this is the single most concerning part of the whole story.
The SV40 promoter is a short DNA sequence borrowed from Simian Virus 40 (a monkey virus that can cause cancer in animals). In molecular biology it is used as an extremely strong “on-switch” that forces mammalian cells to make huge amounts of whatever protein the attached gene codes for. It is one of the most powerful promoters we have, which is why labs love it.
Pfizer included it in the bacterial plasmid they used to mass-produce the spike DNA template (Process 2). It sits in the “backbone” of the plasmid and drives the antibiotic-resistance gene so the bacteria can be selected on kanamycin plates, and it also doubles as a high-copy replication origin. It’s a standard off-the-shelf trick in biotech, but it means every billion doses of Pfizer contain billions of copies of this sequence.
Moderna’s plasmid design simply doesn’t have it, so their shots don’t have this particular piece, but still contains all the other crap synthetic DNA Jessica, Kevin, and Charles have been nailing down.
The part that worries people (and the reason it keeps coming up) is that this exact SV40 promoter fragment acts as a nuclear targeting sequence (as in the ‘nucleus’ of our cells).
When DNA that contains it gets into a cell, cellular proteins recognise the sequence and actively shuttle that Pfizer’s synthetic DNA into the nucleus far more efficiently than they would shuttle ordinary DNA.
Once it’s in the nucleus there is a real chance of integration into the genome. If the fragment inserts upstream of an oncogene, the powerful SV40 promoter can drive uncontrolled cell growth – a NOT theoretical cancer risk.
This is why the old SV40-contaminated polio vaccines (1955–1963) still spark so much debate - mesotheliomas and brain tumours appeared at higher-than-expected rates in people who received those batches, and the virus causes tumours in rodents by very similar insertional/promoter mechanisms. Indeed, listen to Professor Angus Dalgliesh who tells the world how his cancer research team used SV40 sequences all the time for purposefully inducing cancers rapidly in lab rats, so they could test their anti-cancer treatments. Labs the world over do the same thing.
So yes, having a known oncogenic promoter that also moonlights as a “please deliver me to the nucleus” tag in a product injected into billions of arms is … not ideal. Regulators say the amounts are tiny and “within limits,”(*cough* BS) but the new (and old) papers show the limits were measured incorrectly because the DNA was hidden in RNA–DNA hybrids, so the real residual amounts (and therefore the real risk) are higher than any regulator wants to admit – doing so means taking responsibility for millions/billions adversely impacted, plus trillions of dollars in liability payouts.
Another concern - separate from integration - is that any foreign DNA floating in the cytoplasm (even tiny fragments that never reach the nucleus) is detected by the cell’s cGAS-STING sensor, an alarm system evolved to spot viral DNA. When triggered, it unleashes a powerful inflammatory response (type I interferons, NF-(k)B, etc.).
Persistent or repeated activation of cGAS-STING is now known to drive chronic inflammation and, in multiple studies, to promote tumour progression and metastasis downstream (aka, cancers) - essentially turning an anti-viral defence pathway into a cancer-facilitating one when it won’t switch off.
So the SV40 promoter isn’t the only problem; the sheer presence of plasmid DNA itself (from Pfizer and Moderna) is proinflammatory in a way regulators never accounted for, and again, do not want to account for .. that liability issue again.
I am very very grateful that you took the time to write such and excellent and complete explanation. For laypeople like myself this really helps to flesh out our understanding of what is happening, even if it is simply terrifying! I am sure many people will benefit from this information you have so kindly provided. After all it is hard to fight if we don't understand and can't put into words what we are fighting for.
I am also very grateful to Julian. As a lay journalist I have had to clamber up a vertiginous learning curve in writing about Covid vaccine injury and the possible lab origin of SARS-CoV-2. I will write something about these new discoveries, and Julian's explanations really help. Here is one of my previous articles: https://changingtimes.media/2024/12/06/experts-warn-of-cancer-risk-as-dna-contamination-is-found-in-mrna-covid-19-vaccines/
Thank you for having the courage and integrity to write about the unprecedented injuries from the mRNA COVID shots.
The Biggest Lie of the "COVID vaccine propaganda" is that the mRNA COVID shots are vaccines.
People need to understand the truth that the "COVID vaccines" are modified mRNA-LNP gene "therapy" transfection products.
And that even if there was no E.coli DNA plasmid "contamination" with no carcinogenic SV-40 promotor sequence, even if they had not deceptively injected shots into the public that were made by Process 2, even if the spike protein was not pathogenic...these mRNA transfection injections would have still injured and killed people.
The mRNA transfection platform itself is irreparably flawed & inherently dangerous and the platform itself IS the primary problem.
The mechanism of action (using mRNA instructions to turn one’s own cells into foreign non-self “spike protein factories”) IS the primary mechanism of harm.
For those who are seeking an understanding as to why the injuries from these mRNA transfection injections are so widespread and can greatly vary from person to person:
The modified mRNA-LNP transfection injections genetically instruct one's own cells to become "factories" for the production of foreign non-self proteins...
This triggers an immune system attack response, starting with the Killer T-Lymphocyte cells which will target and destroy one's formerly healthy cells, ANYWHERE in the body, that are now expressing non-self proteins...starting a cascade of damage at the deepest biological/cellular level.
Due to the biodistribution properties of the (toxic & inflammatory) lipid nanoparticles, the encased (designed to be long-lasting) n1-methyl pseudouridine modified mRNA can go anywhere in the body, including crossing the blood-brain and placental barriers...The LNP "delivery vehicles" traveled to different parts of the body in different people.
Expressing any foreign protein is fatal to the cell doing the expressing. The reason is, our bodies are protected by being able to distinguish ourselves from things that shouldn't be there. Anything non-self will trigger immune destruction of the cells & tissues involved.
Some people will express lots of foreign proteins in vulnerable locations. Others express less in less vulnerable areas.
The location of expression defines the adverse event: if you get foreign protein expression in your heart cells, you could get myocarditis & experience cardiac arrest; if the expression is in your brain, spinal cord, or peripheral nervous system, you could get one or more of a variety of neurological conditions; if in your eye, possible blindness; if in your ovaries, possible infertility; if in the placenta, possible miscarriage, stillbirth, or birth defects; if in the endothelial cells that line your blood vessels, possible vascular &/or microvascular injuries like clots/microclots or the long white fibrous clots, leading to strokes, heart attacks, or pulmonary embolisms…
If the expression of foreign proteins is in your own immune cells, you could experience immune dysfunction, dysregulation, & suppression including repeated infections, immune tolerance of a pathogenic foreign protein due to antibody subclass switch to IgG4 & increased IgG4-related diseases, T cell exhaustion, interference with & suppression of innate immunity, persistent systemic inflammation, dysregulation of toll-like receptors and reduced cancer surveillance or the suppression of tumor-suppressing immune system activities & cell-signaling (increasing your risk of fast-growing and aggressive cancers)…
And more…
Pathology reports, including from autopsies, have revealed & confirmed the Killer T Lymphocyte infiltration & destruction of cells, oftentimes in vital organs.
There's no limit to the horrible consequences of injecting into your body something that triggers your own immune system to attack & kill your own formerly healthy cells & tissues.
The public “health” agencies, the COVID “authorities”, & the “mainstream” media fraudulently marketed these experimental mRNA gene “therapy” transfection products as “safe & effective vaccines”. Trusting people thought that they were being presented with the choice (or the mandate) as to whether or not to take a “safe & effective vaccine”…But that was/is a deceptively false “choice”…
The COVID-19 mRNA shots are NOT safe, they are NOT effective, and they are NOT vaccines.
These modified mRNA-LNP gene “therapy” transfection injections never would have passed proper safety studies required for gene therapy products. Safety studies (including biodistribution, immunogenicity, immunotoxicity, genotoxicity, carcinogenicity, reproductive toxicity, shedding, long-term effects, & more) that were bypassed because of the fraudulent mislabeling as “vaccines”. (And because of the EUA & “countermeasure” designations under the Project BioShield Act & PREP Act in the United States).
The danger is NOT limited to just getting more COVID “boosters”. ANY mRNA (or DNA) gene “therapy” product that transfects your cells and instructs those cells to produce foreign non-self proteins (ANY non-self protein) will trigger an immune system attack response against your own cells & tissues (the role of the Killer T-cells is to monitor ALL the cells of the body, ready to destroy/kill any that express foreign, non-self proteins). This makes EVERY mRNA-based (or DNA-based) transfection product harmful by design.
This entirely predictable immune response to one's own cells being instructed to create & express non-self proteins (ANY non-self protein) can trigger autoimmune responses, & then T-cell exhaustion, immune system dysfunction & possible immune collapse...regardless of whether or not the foreign protein is toxic itself (or whether or not there are carcinogenic DNA "contaminants" within the injected product).
Self vs. Non-self...Basic fundamental Immunology 101...
EVERY SINGLE DOCTOR or medical professional should have been able to recognize the immunological dangers of these mRNA transfection shots...
https://entwine.substack.com/p/the-platform-is-deadly
https://robertchandler.substack.com/p/vaccinated-dead-kruger-lang-morz
https://x.com/newstart_2024/status/1981375686251069797
"While the pharmaceutical industry rushes to expand mRNA use for its speed and profit, a fundamental immunological principle is being overlooked: Any cell that produces a foreign protein is marked for destruction by the immune system.
This isn't theoretical. Clear histopathological evidence from biopsies and autopsies confirms the vaccine's genetic material does not stay at the injection site. It enters systemic circulation and spreads uncontrollably throughout the body, including to vital organs like the brain and heart.
Once there, the body's own cells are forced to produce the foreign antigen, triggering an immune attack on its own tissues."
The undermining of this basic foundational principle of human immunity made the IMMUNOLOGICAL CATASTROPHE of the modified mRNA-LNP gene "therapy" transfection injections entirely predictable...(and I am not a doctor nor am I in the medical field).
And they can shed on others, making them dangerous and injurious for those who said "Hell NO!" as well...
These transfection injection bioweapons NEVER should have been injected into a single human being...
It is not enough for there to be no mandates...
Tragically, because more people do not understand that this is not about "choice", this is not about the ability to tell others what to do or not...
Because more people are not standing up and demanding that these "traditional" modified mRNA-LNP transfection injections be pulled from the market, the next "evolution" is moving forward (the self amplifying mRNA transfection technology platform)...
https://www.drtrozzi.news/p/world-council-for-health-the-dangers
Vioxx, 1976 Swine flu shot, Thalidomide, DES, DDT, etc...etc...ALL removed from the market after having previously been approved for use in the USA, or Europe, or wherever...yet now some people are acting like removing a product from the market is unprecedented...
Dangerous, injurious, deadly products must be pulled from the market!!! You do NOT give uninformed or misinformed people the "choice" to use such products.
Especially when their uninformed "consent" leads to them taking a product that sheds and poses a legitimate danger to the health of those being shed on.
Shedding from these transfection injection bioweapons IS an extremely serious concern, with some people being affected more than others...
https://www.midwesterndoctor.com/p/what-weve-learned-from-a-year-of
https://pierrekorymedicalmusings.com/p/shedding-of-covid-mrna-vaccine-components
(This is part 1 of a 9 part series - other parts linked at the end of the part 1 article)...
AND...if all of this is not already horrific enough, there are legitimate concerns that the blood supply is contaminated:
https://x.com/Safe_Blood3/status/1942237297035899370
https://vesavanhatupa.substack.com/p/a-call-to-action-lets-end-the-silence
https://laurakasner.substack.com/p/the-devil-was-hard-at-work-trying
https://laurakasner.substack.com/p/results-of-the-2024-worldwide-embalmer
NO ONE should have ever had the “choice” of taking these gene “therapy” transfection injections because the modified mRNA-LNP genetic transfection technology platform is fundamentally flawed & dangerous by design.
I cannot say it enough: It is NOT enough for there to be no mandates.
I will say again: These transfection injection bioweapons NEVER should have been injected into a single human being.
And as Dr. Sansone has correctly asserted, bioweapons are ALREADY illegal!!
https://www.josephsansone.com/p/breaking-news-ain-tribunal-order
Atrocities have been committed...these were/are crimes against humanity.
Meant to put the Substack link to that article: https://changingtimes.substack.com/p/experts-warn-of-cancer-risk-as-dna
Thank you! These extra explanations, yours and the one above, are so beneficial!
And this whole debacle is so frustrating. From an outsider perspective, there is too much money to be made in playing games with the building blocks of life, and too little emphasis on not doing permanent damage to the human gene pool, to continue this (idiocy). Feeding greed is now the purpose of "science."
Humans survived with far better rapport with the planet and its other inhabitants before the rise of civilization(s) and this one seems hell-bent on maiming and murdering its way to ultimate destruction.
I am very appreciative of your comments. I am also a civilian when it comes to this science, though I have read a lot over the last 5 years.
Excellent summary in a way that many can understand. How wonderful. Jessica is a force of nature , and her tireless actions to uncover what has happened alongside other heroes is nothing short of miraculous! May God bless all of them. Thank you for your comments… it made things much more clear. Eileen
SV40 (simian virus 40) is a cancer promoter. it was in the original polio vaccines; as part of the manufacturing process, they cultured the vaccine in monkey kidneys and the mass vaccination campaign may have resulted in the uptick in population level cancer afterwards.
then again, i'm also not a scientist. just a long time broadway costume maker and costume director of a major international arts festival who was fired after 40 years because i wouldn't take the covid shot.
so if i've said anything wrong here, i hope someone more qualified will correct me
Wow; that's appalling that you were fired because of your refusal of the Covid shot. I'm just a lay journalist, and, as I said above, I have had to clamber up a vertiginous learning curve in writing about Covid vaccine injury and the possible lab origin of SARS-CoV-2. I will write something about these new discoveries, and Julian's explanations really help. Here is one of my previous articles: https://changingtimes.media/2024/12/06/experts-warn-of-cancer-risk-as-dna-contamination-is-found-in-mrna-covid-19-vaccines/ You seem to me to have understood the situation very well.
i have been a medical skeptic since childhood so my distrust of conventional medicine goes WAY back. i'm 72 and have never had a mammogram or a colonoscopy. interestingly, my last tetanus shot was in 1980 as a condition of the contract for the job that i was eventually fired from because of the covid vaccine which i was NEVER going to take. the 2nd year (1981) when i went to my doctor for another tetanus shot because the contract required it, my family doctor refused. he said "if you get a tetanus shot every year, you'll get tetanus!" i never had another one. for years afterward, i just signed the contract and ignored that clause. then they started taking my presence for granted and forgot to give me a contract for a decade or more. then one year, they wouldn't pay me unless i signed a contract. they had outsourced the payroll to a company which spooked me. i hate bureaucracies. i reminded the festival that they hadn't given me a contract and when they did, i read it carefully and refused to sign it until they removed the language about the tetanus shot. so they shouldn't have been too surprised when i refused to take a covid shot.
i read lots of medical books and have always gone to alternative doctors. even on medicare, i go to doctors who don't take insurance and pay out of pocket for the kind of care i want. fortunately i don't require much care and if i get hit by a car or something where i need conventional medicine, i use medicare.
On my documentation at Radio France International they wrote something like 'still refusing to have a tetanus shot". I was lucky that, when the Covid shots came in, I was working alone/independently. I ended up illegal in India, though, but that's a whole other story that is still messing up my life.
See Lex Acker on Substack. He did a nice forensic accounting assessment in B.C., Canada, and showed that about 10% of the health and government employees were "disemployed" [my term!] as a result of declining their clot-shots in 2021.
OK!
vertiginous. . . great word.
Jeff Childers(Coffee & Covid) likes a similar word: oleaginous(often used to describe people like gov of Ca)
Yeah man, keep 'em coming.
The performing arts unions were the worst offenders of the cvid/injection hoax. I am a member of two. They took that holier than thou ball and ran with it. Far longer than most, I think. Sad.
I hope you have found other means of satisfying income while continuing your art.
i've never been a member of a union; in fact i opened my own costume shop after i had to leave a job in a top union shop because i wouldn't join. i assumed we would never do broadway work because of my principles but our work was so good that we did "union" work all the time! my boyfriend is a long time member of local 1.
the unions totally discredited themselves during the pandemic. they have one function which is to protect the labor of their members- not the vaccinated only members, not the democrat only voting members, but ALL their members.
they failed spectacularly!
Thank-you!
Hey Dear Beyo…”SV40” is a virus contaminate from the polio virus from the 1950s. Everyone who got the polio shot and sugar cube as a young child is contaminated with the SV40 virus, which is another way to speak of fast track tumors and other immune deficiencies. None of the scientists looked for viruses on the monkey kidneys where the polio vaccine was grown from. When this SV40 virus problem , a fast track for immune issues was discovered, it was hidden from the general public. “Dr Mary’s Monkey “ is a scary, sad, and true book to read; which addresses this trespass,( with an astonishing amount of footnotes). Dr Mary was ready to tell the whole world about this problem.The author of this book’s father knew Dr Mary personally. Dad told his reporter son, on his death bed,to never research Dr Mary’s death because the people responsible for her death would also kill him…So grateful to this disobedient son and his investigative skills. Richard Nixon was told in the 1950s about this SV40 problem; one of the first things he did as president in 1968 was to declare “war on cancer”…because he already knew the levels of cancer were rising as SV40 settled in to all the vaccinated human bodies. It is not only our food that is killing us…”Devils chessboard” is another fabulous read about the Dulles brothers and the CIA… investigative journalism from the 1940,50,and 60s…Stay well and Stay Curious 💜…BTW…this was a great question…💥
Really good book, "Dr. Mary's Monkey." Sad but worthwhile read. Thanks for more of the backstory on it.
I also read Edward Hooper's "The River" at the same time, and Duesberg's "Inventing the AIDS Virus" shortly after. The three books combine to give an interesting perspective of medical research in the very recent past.
Thank-you!
To learn more about Dr. Mary and the monkeys' watch this wonderful piece from CHD with Dr. Suzanne Humphries. She's goes pretty deep into the story. Fascinating.
This is a very recent interview.
https://live.childrenshealthdefense.org/chd-tv/shows/good-morning-chd/deadly-secrets--monkey-business/
If you don’t break the hybrids does it stay encapsulated forever ergo may not be a problem?
Excellent question Vivien,
No, the hybrids do not stay locked together forever once they’re inside your cells - and that’s actually the worrying part.
The lipid nanoparticle (the fatty bubble that carries everything into the cell) pops open pretty quickly in the cytoplasm and dumps its cargo.
At that point the RNA–DNA hybrid is naked and floating around inside the cell, and cells hate RNA–DNA hybrids.
Our cells have a dedicated enzyme called RNase H whose whole job is to spot these hybrids and immediately chew up the RNA strand. When it does that, the DNA strand is suddenly set free as plain single-stranded DNA.
Once the DNA is loose in the cytoplasm:
-- It can trigger the cGAS-STING alarm system (chronic inflammation – leading to - possible cancer-promoting effects over time).
-- It has a much better chance of being shuttled into the nucleus (especially if it has the SV40 promoter tag).
-- It becomes available for integration events or reverse transcription .. both activities are well documented, with the reverse transcription being known for at least 40 years (I wrote a paper on just this: https://ijvtpr.com/index.php/IJVTPR/article/view/83).
So the hybrid is basically a Trojan horse: it protects the DNA on the journey in, then the cell itself unwraps the package and hands you the naked synthetic DNA once it’s safely past all the defences.
Wonder if TLRs recognize hybrids?
Please, please, please, laymen terms for the average dimwit. I sell complex products and my success has always been anchored in simple relatable explanations. Explain it for a child to understand…
Thank you Julian. You sound more like a molecular biologist than a lawyer, you must be way above average intelligence. I’m impressed.
With all the maiming and deaths , including fetuses, it should have been off the market ASAP. However, the ACOG still wants every pregnant woman jabbed . Nefarious intent IMO
They can barely claim they did not know of complication considering the trial they ran and stopped due to injuries . https://clinicaltrials.gov/study/NCT04754594?tab=history&a=24#version-content-panel Panel 19 Placebo 1.3 % vs Vaccinated 5.1 % AESI = Adverse event of special Interest . As i understand it , if one more baby would have been harmed the trial would have counted as failure and set precedent . Just the amount of listed Study Design / Status feels like it got altered to suit the wanted outcome but failed despite of it . So they stopped it , problem evaded .
Geert says that when he worked at Glaxo years ago the quality control was taken very seriously to keep DNA out of the vaccines. Was Pfizer's incompetence deliberate for population control or was it unintentional? Petula Clark turned 93 today. I hope she is unjabbed.
I would also like know if it was QC incompetence or deliberate incompetence? Plausible deniability seems to be a common practice to cover up a crime.
Thanks-glad I instinctively knew the controls had changed-this was my first “red flag” warning when I heard the vax jab was ready to stab people in “minutes” not “years”!!
did you see this?
https://voiceforscienceandsolidarity.substack.com/p/quality-fraud-instead-of-quality?utm_source=substack&publication_id=555295&post_id=178999095&utm_medium=email&utm_content=share&utm_campaign=email-share&triggerShare=true&isFreemail=true&r=634q5&triedRedirect=true
Love Petula!!
This should surprise nobody because these were never like vaccines beyond similarity of syringe delivery. They are made with the same process used for ALL biologics and the contaminants are expected which is why biologics undergo expensive filtering and purification.
Another name for the process of producing the mRNA TRANSFECTION products is Gain of Function which are CRISPR clones grown in E.coli the decades old bench tool worth priced as petrie dish commodity but turned to cash cow with IP reset as "novel vaccine" treatments.
https://web.archive.org/web/20161206155142/http://www.gryphonscientific.com/wp-content/uploads/2016/04/Risk-and-Benefit-Analysis-of-Gain-of-Function-Research-Final-Report.pdf
It should be embarrassing six years into this Covidian fraud knowing that bodies NEVER tolerate non-self proteins and that ANY protein transfected was criminal medical insanity on par with lobotomy another deadly Nobel Prize winning human experiment.
Even the New York Times reported the deadly effects of TRANSFECTION in 1999 with the Biotech Death of Jesse Gelsinger because immune systems kill non-self proteins. When the truth of this crime against humanity is more broadly recognized you folks who pretended to be advocating for an informed public while burying truth will be seen as traitors to humanity.
\https://web.archive.org/web/20121025034826/https://www.nytimes.com/1999/11/28/magazine/the-biotech-death-of-jesse-gelsinger.html
i want to know 2 things:
1) can you now finally prove the fraud that will void the liability protection granted by the EUA? this would allow the vaccine injured to sue the drug companies themselves and not seek compensation from the government (over burdened tax payer).
a flurry of lawsuits would make the mRNA products less profitable and therefore less appealing. it seems RFKjr is having to proceed very carefully in getting the mRNA products off the market. they are, after all, Trump's signature achievement. but if they were less profitable, the companies would abandon them, in true free market fashion.
2) can you find an enzyme that will dissolve/digest the spike protein and maybe act as a therapy to help the vaccine injured? i think there are a lot of very damaged people out there and i fear that as time passes, the harms will accrue.
thank you for your good work
I have not yet found a lawyer who wants to have the EUA retrospectively revoked because Pfizer lied. That was known in early 2021.
https://geoffpain.substack.com/p/pfizer-lied-about-endotoxin-to-get
surely Aaron Siri or Robert Barnes have the clout and the desire to see liability protections revoked
Sadly they are too busy to interact with me directly.
Aaron Siri could have benefited when working with persecuted US Military.
https://geoffpain.substack.com/p/fda-controlled-high-school-student
Barnes has been litigating the Brooks (Pfizer whitleblower) case for about 4 years. It's maddening. Clear case of fraud but it's stuck in the court. The DOJ got involved and tried to shut it down. The corruption is massive.
Carolyn, we know that the new people in HHS, like Hoag, Prasad, Retsef, MaKary and RFK Jr spoke out publicly on social media against these shots. So,I believe the very powerful are shutting down any investigation.
Next useful experiment that you and Charles Rixey might like to try in Kevin's lab, would be to use Kevin's patented Endotoxin removal magnetic beads and see if the Endotoxin stuck to the Pfizer and Moderna nRNA and residual Plasmid DNA can be levered off, to give enhanced access to the enzymes DNase1 and/or DNase-XT.
More about Kevin's Endotoxin Removal Patent here:
https://geoffpain.substack.com/p/production-of-the-pfizer-biontech
Even more fun might be the study of cord blood from women vaxxed during pregnancy, to see if the spike dNA has been transfected into the foetal (infant's) WBCs.
I have a feeling it would come up positive. They need to cover all angles. Fertility, immunity, cancer, encephalitis. Perfect.
Ok.... where do we go from here? What's the plan moving forward?
Continue the SLOW roll. Don’t mention that we knew ALL this in 2021. Transfection; see Jesse Gelsinger. Don’t note that the plasmid issue is a known problem with “biologics”. And repeat over and over that this slew of reactions are mysterious even though in labs monkeys (because they’re so expensive) are rarely transfected because it is KNOWN the animal will die soon after. Lastly keep secret many were likely given placebos.
SLOW RIDE!
I don’t think the people who made these death jabs are stupid. So I have to then believe it was intentional.
me too.
💉Excellent detective work, thanks so much.
If the pharmaceutical companies had not been given liability protection for these products, would this contamination have occurred in the first place? Cutting corners in these instances would surely have to be regarded as criminal negligence.
David, and the race to be first to get the lucrative contracts from all countries.
Great article 🙏🏻
i just cleaned up my explanation: it was really quite bad previously!
Thank you for this post. Keep up the great work. The pharmaceutical companies and the Federal Regulators all need to be held accountable.
Why not call this what it is - transfection. SV40 or no SV40 would intramuscular injection of a novel substance to augment immune system was not and is not a good idea. Stat Mews as far back as ‘15 told us reason Moderna was struggling to progress through pre-clinical trials, was because animals were dying.
How come you and your cadre of MAHA grifters refuse to critique all the useless NPIs like masking, distancing, virtual learning, isolation of elderly? Or deadly hospital protocols like use of high flow oxygen (unsupervised), depriving anti-biotics for bacterial pneumonia, liberal use of end of life drugs as well as Remdesivir. All this for a “deadly virus”we knew had an IFRnof less than 1 given Diamond Princess data?
You and the rest of the DARPA/NIH actors are setting us up for a new and improved mRNA transfection along with personalized gene therapy marketed as “personalized medicine”.
You are so brilliant! Thank you for doing this valuable research.
As I've said in the past "what would we do without you" but what now for the vaccine injured?
Pete, I’m injured too as are untold numbers of others and those whose doctors who are clueless to the causal depth of the injuries caused by these shots.
I find this to be, on Pfizer and Moderna’s part, they either didn’t care, because they were so sloppy or they did it on purpose pick one of the two!