BOMBSHELL: A New Paper Confirms Presence of DNA in COVID-19 Shot Vials, Settles Issues Pertaining to DNA Quantification Methods, Shows Spike Persistence and Exosomal Shuttling

The following article should horrify every single person, whether “vaccinated” or not, because this latest peer-reviewed study proves that the conspiracy “theories” of anyone being subjected to these slow kill bioweapon “vaccines” has been:

  • genetically modified (large amounts of foreign DNA found in the “vaccine” vials integrate into the human genome )

  • permanently altered into walking spike protein factories
  • walking spike protein factories are shedding via exosomes all over both their fellow walking spike protein factories as well as the unvaccinated
  • the highly carcinogenic SV40 promotor that this Substack has been warning about for years is intentionally “contaminating” the Modified mRNA “vaccines”
  • the turbo cancer epidemic will continue to get progressively worse over time
  • disabilities and mortality will continue to get progressively worse over time
  • Etc. & etc. & etc.

These conspiracy facts are so profoundly terrifying, and so irrefutable that mass arrests are beyond long overdue.

A new paper confirms presence of DNA in COVID-19 shot vials, settles issues pertaining to DNA quantification methods, shows spike persistence and exosomal shuttling

And this was done in human cells…

JESSICA ROSE

Ulrike Kämmerer, Verena Schulz and Klaus Steger have just published what might be the paper of the century entitled: “BioNTech RNA-Based COVID-19 Injections Contain Large Amounts Of Residual DNA Including An SV40 Promoter/Enhancer Sequence”. It got through peer review on December 3, 2024 and it confirms much of what has already been evidenced and answers many questions lingering in the background.

Let’s unpack their results:

We demonstrate successful transfection of nucleoside-modified mRNA (modRNA) biologicals into HEK293 cells and show robust levels of spike proteins over several days of cell culture. Secretion into cell supernatants occurred predominantly via extracellular vesicles enriched for exosome markers. We further analyzed RNA and DNA contents of these vials and identified large amounts of DNA after RNase A digestion in all lots with concentrations ranging from 32.7 ng to 43.4 ng per clinical dose. This far exceeds the maximal acceptable concentration of 10 ng per clinical dose that has been set by international regulatory authorities. Gene analyses with selected PCR primer pairs proved that residual DNA represents not only fragments of the DNA matrices coding for the spike gene, but of all genes from the plasmid including the SV40 promoter/enhancer and the antibiotic resistance gene.

Spike protein expression in HEK293 cells after transfection with BNT162b2 biologicals is seen in green. This means the LNPs dump their payload successfully into human cells and this payload is translated into spike protein using the cell’s machinery (ribosomes) as per the design. The spike had a cytotoxic effect on cells (bad for cells = they die) and stuck around for at least 7 days (persistence). And that’s just when they stopped measuring. Spike got into the medium that the cells were in: it was released from the cells that were transfected. Spike can be cleaved from the membranes of cells, but, can also be exported in exosomes in full form (uncleaved).

Figure 1: Spike protein expression in HEK293 cells after transfection with BNT162b2 biologicals. Source: https://publichealthpolicyjournal.com/biontech-rna-based-covid-19-injections-contain-large-amounts-of-residual-dna-including-an-sv40-promoter-enhancer-sequence/ 

This is an incredibly important finding and has massive implications for shedding. Exosomes – which are like little information carriers between cells – are likely trafficking/shuttling spike to other cells in the in vivo setting. Based on these findings, there’s no reason to believe they wouldn’t be doing this.

The amount of RNA in the injected Pfizer product (30 ug) checks out. The “real” amount of DNA that they found after additionally treating with RNase to remove interfering signals from RNA exceeded EMA limits by 4-5 times.

Figure 2: RNA and DNA content of different BNT162b2 biologicals. Source: https://publichealthpolicyjournal.com/biontech-rna-based-covid-19-injections-contain-large-amounts-of-residual-dna-including-an-sv40-promoter-enhancer-sequence/
Figure 3: CRNA and DNA levels (following Triton-X-100 treatment) in the indicated vials of BioNTech lots before and after RNase A treatment. Source: https://publichealthpolicyjournal.com/biontech-rna-based-covid-19-injections-contain-large-amounts-of-residual-dna-including-an-sv40-promoter-enhancer-sequence/

 

All four Pfizer vials that they tested at a dilution of 1:10 showed strong signals for SV40 promoter/enhancer, neomycin cassette, ORI replicon, and spike protein (B: right), and all transfected HEK293 cells as well (B: left)!

Figure 4: Polymerase chain reaction (PCR) reveals residual DNA of the complete plasmid used in the modRNA production process. Source: https://publichealthpolicyjournal.com/biontech-rna-based-covid-19-injections-contain-large-amounts-of-residual-dna-including-an-sv40-promoter-enhancer-sequence/

 

They blew up the LNPs using Triton-X to get to the most DNA that they could (without having done this, a lot of the DNA is not available for measurement) and checked DNA levels using different 3 methods: Quant-iT PicoGreen dsDNA Assay (P), Qubit 1x dsDNA High Sensitivity Assay (Q), and AccuBlue dsDNA High Sensitivity Assay (A). This is WILDLY INCREDIBLE AND THOROUGH WORK. I hope people appreciate this and also that if the manufacturers and/or regulators this amount of work/checking, they sure didn’t show the public their findings.

Figure 5: DNA levels in the indicated vials of BioNTech batches before RNase A treatment, without and with Triton-X-100 treatment. Source: https://publichealthpolicyjournal.com/biontech-rna-based-covid-19-injections-contain-large-amounts-of-residual-dna-including-an-sv40-promoter-enhancer-sequence/

 

All in all, this paper is an excellent piece of work that confirms the presence of residual DNA that exceeds EMA limits many fold in all Pfizer COVID-19 modRNA-LNP product vials tested. Their methodology for ascertaining “real” DNA levels is second to none and they do account for RNA interference and eliminate this problem. They also got the most measurable DNA by treating the LNPs with Triton-X. I wish the manufacturers and regulators could say as much.

Perhaps the most disturbing ‘new’ finding is the release of spike into the cell media via exosomes. The authors write:

In case of an in-vivo situation, this would mean that the spike proteins are transported within exosomes to other tissues and organs via the blood stream and, consequently, taken up by the target cells. In fact, it has already been reported that spike proteins can be found in exosomes of vaccinated individuals.

This has massive implications for shedding and begs the questions:

Is this why there are so many people who feel the effects of someone else’s modRNA injection after spending a little time with them?

Are we all injected by proxy?

We need a moratorium on this platform (genetic material-LNP-based) and we need follow-up studies so that we can help people who are clearly suffering from what we can call spikeopathy. We basically need to figure a way out of this colossal mess. Together.


We need an outright ban of this entire deadly platform forever, and all of those higher-ups involved in this eugenics project must be arrested at once, not limited to the BigPharma C-Suites, but also their Intelligence Industrial Complex handlers who happen to own many of the C19 “vaccine” patents.

They always knew…

The greatest fear among vaccinologists is the creation of a vaccine that is not only ineffective, but which exacerbates disease. Unfortunately, CoV vaccines have a history of enhancing disease…”

 

This article was originally published by this Substack and is now revised.

 

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