There is a Plausible Epigenetic Molecular Mechanism in Biology Whereby the Vaccinated May Affect the Health Status of the Unvaccinated
The third major substantiating factor behind identifying the potential harm the vaccinated may have on the unvaccinated concerns the discovery of so-called
horizontal information transfer within biological systems mediated by extracellular vesicles (EVs),
which include a virus-like phenomenon known as microvessicle shedding and/or exosome-mediated transfer of nucleic acids.
This falls within the category of epigenetics, which the apologists and shills for the mRNA vaccines' purported safety and efficacy conveniently ignore in order to make their claim that was debunked in 1970 with the discovery of the enzyme reverse transcriptase.
Reverse transcriptase is able to transcribe RNA to DNA, essentially destroying the fundamental dogma of molecular biology, namely, the undirectional flow of information from the cell nucleus to mRNA to protein can not be reversed.
This dogma is still being used half-a-century later to make the false claim that the only health risk a genetically modified vaccine has worth discussing is the possibility that it may affect the structure or function of nuclear, protein-coding genes.
We've even seen, through the discovery of exosomes, that the Weismann barrier has been penetrated, and somatic cells can communicate heritable information to the germline cells in what amounts to real-time, essentially devalidating the risk models presently used by vaccine manufacturers and regulators which do not account for the power epigenetic processes have to amplify the unintended adverse effects of genetically modified technologies and interventions.
While mRNA vaccines are designed using genetically modified processes not dependent on live cell substrates, thereby precluding conventional problems with shedding associated with first generation vaccines like the MMR, it is possible that they do, in fact, contribute to microvessicle shedding, which represents an even greater, more persistent threat than live-cell vaccine shedding when it comes to the persistent biological impact the vaccinated can have on the un-vaccinated.
Microvessicles, which range in size between 0.1–1.0 μm are a type of extracellular vesicle (EVs), that are secreted by many different cell types within the body, both in times of health and disease, and are known to reflect the antigenic content of the cell of origin.
They have stunningly similar characteristics to viruses.
For instance, like SARS-COV-2, microvessicles have a lipid bilayer formed from the budding off from host cell membranes, and they can incorporate and reproduce aspects of a vaccinated or infected cells’ immunogenicity, such as including functional mRNA, viral proteins, and other nucleic acids capable of profoundly altering the structure and function of the cells to which they are transmitted.
For instance, it is theoretically feasible that a vaccine recipient’s cells expressing COVID-19 spike protein as a result of transfection with mRNA from a Covid-19 vaccine may secrete microvesicles containing components "originally alien to the cell, such as proteins and nucleic acids that are transiently or constitutively expressed via plasmid or viral vector.
These microvessicles, like viruses, and other extracellular vessicles known as exosomes, can be transmitted to other individuals (inter-individual transmission) through both normal or diseased physiological processes.
Extracellular exosomes have even been found to transfer nucleic acids cross kingdoms (plant > animal, fungal > bacterial), affecting the phenotypal expression of the target species.
Therefore, it is plausible that microvessicles can transmit mRNA from a recently vaccinated individual to those within close proximity, and therefore could, in fact, “shed” mRNA and related biomolecules induced from the mRNA vaccination process to non-vaccinated individuals, inducing symptoms similar to those experienced by the vaccinated.
Indeed, microvessicles may have a profound affect on the immune status of those who both produce them, and are exposed to them.
A recent study concluded that research “strongly suggests that MVs may function as strong regulator of both innate and adaptive immune systems.
Microvessicles and exosomes have also been researched and developed as vaccine candidates, further indicating that they are already being looked at by the scientific community as potential vectors of immunogenicity and carriers of viral-like and disease-modulating if not also disease-promoting bio-information.
Given the plausible mechanism through which a COVID-19 vaccine recipient’s body produces vaccine antigen (e.g. spike protein), and can package and transmit these antigens through viral-like microvessicles (and perhaps also exosomes) to others, Leila Centner’s statement “it appears that those who have received the injections may be transmitting something from their bodies to those with whom they come in contact,” has a plausible mechanism of action.
Especially considering the afforementioned fact that Pfizer's study protocol itself acknowledges that an unknown factor or mechanism may cause the unvaccinated to be adversely affected by the vaccinated.
Centner Academy, a private school in Miami, has made international headlines for directing its employees who have not yet received the experimental COVID-19 vaccine to wait until the end of the school year, as a precautionary step to protect the health of their school community, given both...
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