One for the gifted scientific researchers – EV’s, not the electricity guzzlers, but extracellular vesicles in the context of self propagating mRNA “vaccines”

From here (h/t Ranger71):

Leplicons can infect and multiply between cells through extracellular vesicles: From a paper published in viruses|Hiroshi Arakawa (note.com)

We have this statement:

“The authors' experiments clearly show that replicons themselves can infect cells through extracellular vesicles because they do not use viruses.

This study is crucial because it proves that leplicon RNA, which does not have a viral protein that binds to cellular receptors, can propagate between cells and multiply in infected cells. There is concern that the same mechanism of action works in the replicon vaccine.”

Having said that, here is the context:

“The replicon vaccine (self-amplifying RNA vaccine), which is scheduled to be administered in Japan from the fall of this year as a new coronavirus vaccine for Japan, is a self-propagating mRNA vaccine, which is a gene preparation that has an RNA replication gene in addition to an antigen gene. The genome of the replicon vaccine is made by removing the protein that binds to the cell receptor from the original RNA virus and replacing it with the antigen protein of the vaccine, so to speak, it has a structure like a virus without a shell.”

And here’s a little more context:

(100) Terrible threat of an airborne “inoculation” of a man-made self-spreading mutating virus being developed – funded by Congress and DARPA (substack.com)

“The theory is that you chop a bit off the end of a virus, and it will act as a parasite to attack the actual deadly virus you are targeting AND will evolve in the same way as the targeted virus mutates.”

Back to the research study that answers the key question.

“So, can a replicon vaccine that does not have a protein that transmits such cells infect cells?”

The answer appears to be “yes”, and the self-propagating “vaccines” are not as safe as they are billed to be.

“… it cannot be ruled out that infectious virus particles may be contaminated with the prepared EVs. In this study, cells containing subgenomic replicons derived from Japan encephalitis virus and dengue virus and not producing replicating competent viruses were used as EV donors. The EV contained in the culture supernatant of these cells has been shown to be able to transfer the replicon genome to other cells of various types.”

Over to the smart people in the big boy/girl pants!

The WHO fabrication of Disease X may be the next intentional lab leak and dispersal of H5N1 by the sellers of “vaccines”. It may be that Tedros thinks that “climate change” will generate a disease – and so CO2 levels must be reduced to prevent climate change (yeah, I know, he is as much a quack climatologist as he is a quack medic and so is the rest of the chicken littles preaching that crap) – or it may be a manufactured pandemic (with a “pandemic” defined by morons who consider words to be violence and must be countered with the redefinition of all words to suit their own evil purposes).

I am worried about the rise in Dengue fever. Indeed, Dengue is mentioned in the paper along with a few other diseases.

The real Public Health Emergency of International Concern has NOT ben declared. That emergency is of course the damage caused by the injection of 5.6 billion with toxic chemicals that change human DNA/human genome. Perhaps this is manifesting through the conversion of human organs into cartilage via fibrous white blood clotting. Who knows. The detection and destruction of these clots would seem to be a matter of more than a little urgency – and a real emergency, requiring all the diagnostic and treatment facilities associated with a global pandemic. A pandemic of the vaccinated – which should be extended to sufferers from all vaccine injuries.

An entire field of medicine – treatment of vaccine damage. Specializing in developing mechanisms of action that reverse it in each damaged organ – including the organ of the skin.

Onwards!!!

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