great to see Bobby Kennedy Jnr here in the comments stating HHS, FDA, and CDC will convene an emergency review of this data and suspend the products in the meantime
I tried to read this but it’s way over my head. I know it’s important or you wouldn’t say “Please read this.” Maybe you could explain this like I’m 9 yo. TY
Ha ha! I save all of Jessica's writing in hopes that one day I will at least be able to put a few more pieces together!!! How fortunate are we to know of, and have access to, such brilliant minds that are able to unwind this snarly mess.
In short, this isn’t just another paper, it’s a trap. Kevin took away every excuse they had. No more “we didn’t know,” no more “the signal was too weak.” He used their own tools, did it better than they ever did, and showed the damage in full resolution. The contamination isn’t a theory anymore, it’s a crime scene. And now that it’s visible, they have to choose whether to lie about it or not. That’s the moment we’re in.
I have waited for this for so long. The only charge they can "prove" for conviction is perjury. Lied to congress, the people, the states, the nations and the world...willfully intentionally and consistently. They would naturally just spin off their malevolence as "Oopsie daisy, gee whiz, that caught us by surprise. We didn't know. Really, we didn't"
My part? To pray as have since the start of this plandemic, that the truth will be revealed no matter how despicable and horrifying. So grateful for the perseverance of so many gifted people.
"These data confirm that multiple Pfizer lots (FL8095 and GJ6665) contain contaminating plasmid DNA that is methylated compared to the residual DNA that may have existed in the PCR products from Process 1. This DNA is NOT FUNCTIONALLY INERT as claimed by the FDA. Activation of cGAS-STING may paradoxically induce an immune response against cancer but chronic activation may in fact lead to oncogenic processes. This is important to understand as we see Pharma parade out papers showing a single dose may reduce cancer with checkpoint inhibitors. This is a statistical game and you will not see this signal if you look at patients given 2+ doses."
You’ve shown that when regulators ignore methylation, they ignore the immune system’s native language. Dam and Dcm aren’t just relics of bacterial history, they are molecular flags that shout foreign DNA detected.
Your unmasking of Process 2 defects down to the linearization failures and G4 artifact disambiguation demonstrates a level of detail pharma QC won't ever dare touch.
I just saw this a short while ago and he did lose me on some of the more technical stuff, so would appreciate your tutelage on this, Jessica. You are so good at explaining these things to nonprofessionals.
Thank you. It is too deep for me. I understand the idea, but not the intricate details. One conclusion is unavoidable in my mind…. Yup, they can change human (and all living beings’) genes, make anyone or anything sick at will, but the cure for nail fungus or many other simple maladies remains strangely elusive. Something, somewhere is very wrong with the world of so called science. The bible describes it as “falsely called science.” I wonder why….
This paper shows the fingerprints and the weapon. It’s not just that there’s foreign DNA in these shots, it’s that he proved it can rewrite the script inside your cells, and regulators chose not to look. That’s not ignorance. That’s complicity. “Falsely so-called science,” indeed.
For the germ theory lovers only. Isn't it poisons your still making by rejiggering all the X's and O's? I would never trust anything from fizer or the HHS for that matter.
The big kahuna in the whole drug making/marketing process is that the FDA NEVER tests any drugs or vaccines and lets big pharma do all the trials and testing. The FDA depends on big pharma telling the low down truth. When revenues and profits are on the line, big pharma will cook the results to make a mud pie look like an elegant apple pie.
Every time someone gets too close to the truth, the chaos agents show up yelling ‘germ theory is a psyop!’ It’s not a revolution. It’s a distraction.
Yes, Pharma lies. That’s why Kevin is using independent sequencing to expose what they’re hiding in measurable, repeatable ways. If your answer to corruption is to reject biology itself, you’re not a threat to the system. You’re its decoy.
If your critique of Pfizer ends in ‘germ theory is fake,’ congratulations, you’ve become their best defense. This paper is about proving real harm with hard data, not abandoning the basics of how life works.
Thank you Kevin. Now if only some authority somewhere, anywhere would take the football and run. It seems that fear is rampant and they don’t want to get anywhere near it.
This explains a lot in terms of how humans can sense microbial DNA inside their cells that arise from an infection of a virus or DNA from bacteria ending up inside a cell; they sense the non-human methylation pattern in the viral or bacterial DNA.
Interferon seems indeed to be the driver of the anti-tumorogenic effect of SARS-CoV-2 mRNA vaccines observed in these experiments. The authors argue that higher-order/secondary structures of mRNA could be the driver of the interferon response and, as far as I could see, do not mention or discuss possible contamination with bacterial DNA with non-human methylation patterns. As I understand it, they used E. Coli to produce the mRNA vaccines used in their experiments. Maybe you are able to understand if their experimental set-up would introduce contamination with E. Coli DNA such that this could be a cause of the interferon response they observe?
As I understand it, these results where the mRNA vaccination results in anti-tumorgenic effects may then change if Grippin et al. had injected their animals repeatedly with a mRNA vaccine since chronic activation of the cCAS-STING pathway promotes tumorogensis.
What also if the person is already suffering from chronic activation of the cCAS-sting-interferon pathway? This would presumably create non-responders to the mRNA vaccine in terms of its anti-cancer effect, even with the first dose since the interferon pathway is already chronically activated.
Look for the Bombyx mori-silk fibroin codon that is potentially the cause of the biopolymer Calamari Not-Klotz
The Bombyx mori codon-optimized gene coding the SARS-CoV-2 S glycoprotein ectodomain (1-1208 amino acid residues) has been used in the production of subunit vaccines.
This codon-optimized sequence was synthesized and cloned into expression plasmids for use in the silkworm baculovirus expression vector system (BEVS) to produce the S protein in a trimeric state.
The use of codon optimization enhances the expression efficiency of the S protein in the silkworm system, contributing to the successful production of immunogenic subunit vaccines.
Additionally, the codon-optimized S protein was used in the development of nanoparticle vaccines, where it was fused with Helicobacter pylori ferritin to form self-assembling nanoparticles that induced protective immunity in mice.
These findings highlight the importance of codon optimization in improving the yield and immunogenicity of SARS-CoV-2 spike protein-based vaccines produced in Bombyx mori systems
The codon usage in Bombyx mori has been studied to optimize gene expression, particularly for transgenic applications. A compilation of the 14-base sequence context surrounding the ATG initiation codon from 50 B. mori genes revealed a consensus motif: (A/T)AN(A/T)ATCAAAatgN, which is associated with efficient translation.
This motif serves as a guide for enhancing recombinant protein production in transgenic silkworms. Additionally, the codon usage of the Cas9 protein was optimized specifically for B. mori to ensure high expression levels in genome editing experiments.
The complete sequence of the Bombyx mori fibroin heavy chain gene, which includes a highly repetitive and G-rich core, has been determined using a combination of shotgun and physical map-based sequencing strategies.
This gene's organization features 12 repetitive domains and 11 amorphous regions, with specific repetitive units (Ua and Ub) and conserved boundary elements that are critical for its structure and function
The silkworm, Bombyx mori, is used as a bioreactor for vaccine production, particularly through the baculovirus expression system. Recombinant baculoviruses, such as those derived from Bombyx mori nucleopolyhedrovirus (BmNPV), are engineered to display vaccine antigens on their surface. For instance, a recombinant BmNPV expressing the hemagglutinin (HA) protein of the H5N1 influenza virus was constructed and used to produce a vaccine candidate, with the HA protein displayed on the viral envelope surface.
This system allows for the large-scale production of recombinant proteins, including vaccine antigens, in silkworm pupae without the need for cell culture.
The codon usage of Bombyx mori is a critical factor in optimizing the expression of foreign genes in this system. Studies have shown that the context surrounding the ATG initiation codon significantly influences translation efficiency, and specific consensus motifs have been identified for optimal protein expression in different silkworm tissues.
For example, the consensus ATG-context motif (A/T)AN(A/T)ATCAAAatgN was found to enhance translation efficiency in BmN4 cells, although tissue-specific differences were observed, with the sericin 1 context showing the highest efficiency in middle and posterior silk glands.
Codon optimization of target genes, such as the hemolin protein from Bombyx mori, has also been performed to improve in vivo expression, resulting in a positive codon adaptation index (CAI) score.
This optimization is essential for maximizing the yield of recombinant proteins, including vaccine antigens, in transgenic silkworms.
Furthermore, the use of Bombyx mori as a host for recombinant protein production offers advantages such as cost-effectiveness and scalability. The purification of recombinant baculoviruses from silkworm larval hemolymph using techniques like size exclusion chromatography has been successfully demonstrated, enabling the production of high-titer virus stocks suitable for vaccine development.
The safety and immunogenicity of such vaccines have been evaluated in animal models, with studies showing that a BmNPV-based H5N1 vaccine induced neutralizing antibodies in monkeys and was well-tolerated at high doses.
These findings highlight the potential of Bombyx mori and its codon usage patterns as a platform for developing safe and effective vaccines.
Surely this is enough to prove fraud. Never mind the process 1 => Process 2 chicanery, the sponsors methodology given to the TGA, for example, to only PCR the Kan/R region plus this DNA remnant work you have pursued, utterly destroys the safe 'n effective lie.
Also, Kevin I received your message of thanks but I'm not on the app so I can't reply, so I'll say it here; no worries, glad to help out in whatever meagre way I could.
Ill have to check through these publications, but I thought that foreign plasmid DNA can stimulate cGAS–STING because it is DNA in the wrong cellular compartment…not because it contains Dam/Dcm methylation.
thank you Kevin,
great to see Bobby Kennedy Jnr here in the comments stating HHS, FDA, and CDC will convene an emergency review of this data and suspend the products in the meantime
.. oh, wait
I used to watch the Vinay Prasad show, the one place he never went on the jabs was DNA contamination.
Thanks for soldiering on for the truth. It matters.
I tried to read this but it’s way over my head. I know it’s important or you wouldn’t say “Please read this.” Maybe you could explain this like I’m 9 yo. TY
Ha ha! I save all of Jessica's writing in hopes that one day I will at least be able to put a few more pieces together!!! How fortunate are we to know of, and have access to, such brilliant minds that are able to unwind this snarly mess.
In short, this isn’t just another paper, it’s a trap. Kevin took away every excuse they had. No more “we didn’t know,” no more “the signal was too weak.” He used their own tools, did it better than they ever did, and showed the damage in full resolution. The contamination isn’t a theory anymore, it’s a crime scene. And now that it’s visible, they have to choose whether to lie about it or not. That’s the moment we’re in.
I have waited for this for so long. The only charge they can "prove" for conviction is perjury. Lied to congress, the people, the states, the nations and the world...willfully intentionally and consistently. They would naturally just spin off their malevolence as "Oopsie daisy, gee whiz, that caught us by surprise. We didn't know. Really, we didn't"
My part? To pray as have since the start of this plandemic, that the truth will be revealed no matter how despicable and horrifying. So grateful for the perseverance of so many gifted people.
To me, this is the tl;dr part:
"These data confirm that multiple Pfizer lots (FL8095 and GJ6665) contain contaminating plasmid DNA that is methylated compared to the residual DNA that may have existed in the PCR products from Process 1. This DNA is NOT FUNCTIONALLY INERT as claimed by the FDA. Activation of cGAS-STING may paradoxically induce an immune response against cancer but chronic activation may in fact lead to oncogenic processes. This is important to understand as we see Pharma parade out papers showing a single dose may reduce cancer with checkpoint inhibitors. This is a statistical game and you will not see this signal if you look at patients given 2+ doses."
Just read the beginning then scroll down to the argument conclusion which starts with the phrase: "Why are we obsessing ..."
I scan the whole thing and don't worry about what I can't understand. Lots of it is in plain English....at least 5% ha ha.
Just read the beginning then scroll down to the argument conclusion which starts with the phrase: "Why are we obsessing ..."
Good ‘ol FDA …not truthful at all 🤬. Thank u for your work 🙌🏼
You’ve shown that when regulators ignore methylation, they ignore the immune system’s native language. Dam and Dcm aren’t just relics of bacterial history, they are molecular flags that shout foreign DNA detected.
Your unmasking of Process 2 defects down to the linearization failures and G4 artifact disambiguation demonstrates a level of detail pharma QC won't ever dare touch.
Mistakes Were NOT Made ;-)
• https://margaretannaalice.substack.com/p/mistakes-were-not-made-an-anthem
I just saw this a short while ago and he did lose me on some of the more technical stuff, so would appreciate your tutelage on this, Jessica. You are so good at explaining these things to nonprofessionals.
Thank you. It is too deep for me. I understand the idea, but not the intricate details. One conclusion is unavoidable in my mind…. Yup, they can change human (and all living beings’) genes, make anyone or anything sick at will, but the cure for nail fungus or many other simple maladies remains strangely elusive. Something, somewhere is very wrong with the world of so called science. The bible describes it as “falsely called science.” I wonder why….
This paper shows the fingerprints and the weapon. It’s not just that there’s foreign DNA in these shots, it’s that he proved it can rewrite the script inside your cells, and regulators chose not to look. That’s not ignorance. That’s complicity. “Falsely so-called science,” indeed.
For the germ theory lovers only. Isn't it poisons your still making by rejiggering all the X's and O's? I would never trust anything from fizer or the HHS for that matter.
The big kahuna in the whole drug making/marketing process is that the FDA NEVER tests any drugs or vaccines and lets big pharma do all the trials and testing. The FDA depends on big pharma telling the low down truth. When revenues and profits are on the line, big pharma will cook the results to make a mud pie look like an elegant apple pie.
Every time someone gets too close to the truth, the chaos agents show up yelling ‘germ theory is a psyop!’ It’s not a revolution. It’s a distraction.
Yes, Pharma lies. That’s why Kevin is using independent sequencing to expose what they’re hiding in measurable, repeatable ways. If your answer to corruption is to reject biology itself, you’re not a threat to the system. You’re its decoy.
If your critique of Pfizer ends in ‘germ theory is fake,’ congratulations, you’ve become their best defense. This paper is about proving real harm with hard data, not abandoning the basics of how life works.
Thank you Kevin. Now if only some authority somewhere, anywhere would take the football and run. It seems that fear is rampant and they don’t want to get anywhere near it.
Thankou Kevin.
For an incredibly complex and highly detailed post, your explanations of each of the processes, steps and tests made it understandable.
This explains a lot in terms of how humans can sense microbial DNA inside their cells that arise from an infection of a virus or DNA from bacteria ending up inside a cell; they sense the non-human methylation pattern in the viral or bacterial DNA.
I found this paper titled "SARS-CoV-2 mRNA vaccines sensitize tumours to immune checkpoint blockade" by Grippin et al.: https://www.nature.com/articles/s41586-025-09655-y
Interferon seems indeed to be the driver of the anti-tumorogenic effect of SARS-CoV-2 mRNA vaccines observed in these experiments. The authors argue that higher-order/secondary structures of mRNA could be the driver of the interferon response and, as far as I could see, do not mention or discuss possible contamination with bacterial DNA with non-human methylation patterns. As I understand it, they used E. Coli to produce the mRNA vaccines used in their experiments. Maybe you are able to understand if their experimental set-up would introduce contamination with E. Coli DNA such that this could be a cause of the interferon response they observe?
As I understand it, these results where the mRNA vaccination results in anti-tumorgenic effects may then change if Grippin et al. had injected their animals repeatedly with a mRNA vaccine since chronic activation of the cCAS-STING pathway promotes tumorogensis.
What also if the person is already suffering from chronic activation of the cCAS-sting-interferon pathway? This would presumably create non-responders to the mRNA vaccine in terms of its anti-cancer effect, even with the first dose since the interferon pathway is already chronically activated.
Look for the Bombyx mori-silk fibroin codon that is potentially the cause of the biopolymer Calamari Not-Klotz
The Bombyx mori codon-optimized gene coding the SARS-CoV-2 S glycoprotein ectodomain (1-1208 amino acid residues) has been used in the production of subunit vaccines.
This codon-optimized sequence was synthesized and cloned into expression plasmids for use in the silkworm baculovirus expression vector system (BEVS) to produce the S protein in a trimeric state.
The use of codon optimization enhances the expression efficiency of the S protein in the silkworm system, contributing to the successful production of immunogenic subunit vaccines.
Additionally, the codon-optimized S protein was used in the development of nanoparticle vaccines, where it was fused with Helicobacter pylori ferritin to form self-assembling nanoparticles that induced protective immunity in mice.
These findings highlight the importance of codon optimization in improving the yield and immunogenicity of SARS-CoV-2 spike protein-based vaccines produced in Bombyx mori systems
The codon usage in Bombyx mori has been studied to optimize gene expression, particularly for transgenic applications. A compilation of the 14-base sequence context surrounding the ATG initiation codon from 50 B. mori genes revealed a consensus motif: (A/T)AN(A/T)ATCAAAatgN, which is associated with efficient translation.
This motif serves as a guide for enhancing recombinant protein production in transgenic silkworms. Additionally, the codon usage of the Cas9 protein was optimized specifically for B. mori to ensure high expression levels in genome editing experiments.
The complete sequence of the Bombyx mori fibroin heavy chain gene, which includes a highly repetitive and G-rich core, has been determined using a combination of shotgun and physical map-based sequencing strategies.
This gene's organization features 12 repetitive domains and 11 amorphous regions, with specific repetitive units (Ua and Ub) and conserved boundary elements that are critical for its structure and function
The silkworm, Bombyx mori, is used as a bioreactor for vaccine production, particularly through the baculovirus expression system. Recombinant baculoviruses, such as those derived from Bombyx mori nucleopolyhedrovirus (BmNPV), are engineered to display vaccine antigens on their surface. For instance, a recombinant BmNPV expressing the hemagglutinin (HA) protein of the H5N1 influenza virus was constructed and used to produce a vaccine candidate, with the HA protein displayed on the viral envelope surface.
This system allows for the large-scale production of recombinant proteins, including vaccine antigens, in silkworm pupae without the need for cell culture.
The codon usage of Bombyx mori is a critical factor in optimizing the expression of foreign genes in this system. Studies have shown that the context surrounding the ATG initiation codon significantly influences translation efficiency, and specific consensus motifs have been identified for optimal protein expression in different silkworm tissues.
For example, the consensus ATG-context motif (A/T)AN(A/T)ATCAAAatgN was found to enhance translation efficiency in BmN4 cells, although tissue-specific differences were observed, with the sericin 1 context showing the highest efficiency in middle and posterior silk glands.
Codon optimization of target genes, such as the hemolin protein from Bombyx mori, has also been performed to improve in vivo expression, resulting in a positive codon adaptation index (CAI) score.
This optimization is essential for maximizing the yield of recombinant proteins, including vaccine antigens, in transgenic silkworms.
Furthermore, the use of Bombyx mori as a host for recombinant protein production offers advantages such as cost-effectiveness and scalability. The purification of recombinant baculoviruses from silkworm larval hemolymph using techniques like size exclusion chromatography has been successfully demonstrated, enabling the production of high-titer virus stocks suitable for vaccine development.
The safety and immunogenicity of such vaccines have been evaluated in animal models, with studies showing that a BmNPV-based H5N1 vaccine induced neutralizing antibodies in monkeys and was well-tolerated at high doses.
These findings highlight the potential of Bombyx mori and its codon usage patterns as a platform for developing safe and effective vaccines.
Dr. Silvia Behrendt just released not only EMA's re-redacted documents but also for LNP-formulation: https://open.substack.com/pub/drsilviabehrendt751446/p/update-nov-25-ctd-comirnaty-new-disclosures?utm_source=share&utm_medium=android&r=31oy60
Surely this is enough to prove fraud. Never mind the process 1 => Process 2 chicanery, the sponsors methodology given to the TGA, for example, to only PCR the Kan/R region plus this DNA remnant work you have pursued, utterly destroys the safe 'n effective lie.
Also, Kevin I received your message of thanks but I'm not on the app so I can't reply, so I'll say it here; no worries, glad to help out in whatever meagre way I could.
Ill have to check through these publications, but I thought that foreign plasmid DNA can stimulate cGAS–STING because it is DNA in the wrong cellular compartment…not because it contains Dam/Dcm methylation.