Here's Jessica Rose, a computational biologist, on the topic:

https://jessicar.substack.com/p/a-new-paper-confirms-presence-of

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.

. . . 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)!

. . . This is WILDLY INCREDIBLE AND THOROUGH WORK. I hope people appreciate this and also that if the manufacturers and/or regulators [did] this amount of work/checking, they sure didn’t show the public their findings.

. . . 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.