Video: Self-Amplifying RNA Shots ( sa-RNA ) Next Generation of RNA Vaccine Tech is Here
Big Pharma developing a more potent form of experimental gene therapy technology
that will be sold to the public as life-saving 'vaccines.'
What Distinguishes saRNA From modRNA?
The term “self-amplifying” is self-explanatory: saRNA replicates itself repeatedly, which is not natural, as natural mRNA is always (without exception) transcribed from DNA (this is called the “central dogma of molecular biology”).Compared to modRNA, a small amount of saRNA results in an increased amount of produced antigen; one shot of saRNA-based injection may be enough to generate sufficient antibodies against a virus.
Both saRNA and modRNA represent the blueprint for a viral protein, which, after entering our cells, will be produced by our cell machinery (i.e., ribosomes).
Unlike modRNA, saRNA does not contain methyl-pseudouridines, but uridines. Why? Since saRNA self-replicates and synthetic methyl-pseudouridines are not available in our cells, saRNA must rely on natural uridines that exist in our cells. Our cells will produce foreign proteins using their own cell machinery and their own natural resources—the main reason these cells finally become exhausted.
However, this causes a significant problem: mRNA is highly unstable and, therefore, has only a short lifespan—too short for our immune system to produce sufficient antibodies. The solution to this problem is the second difference between modRNA and saRNA.
Unlike modRNA, saRNA contains an additional sequence for the replicase, as destroyed (by RNases) saRNA must be replaced by new saRNA.
As natural mRNA will never self-replicate, saRNA definitely represents a genetically modified RNA (modRNA).
Why the Change to saRNA?
saRNA is the political solution: the same amount (or even more) of antigen in only one shot! The public will likely be told that due to the regular mutations of the virus, yearly adapted boosters will continue to be necessary.saRNA Injections Will Not Solve the Problems With modRNA Injections
As we discovered with modRNA, the spike protein is poisonous to our bodies. We know that modRNA results in the production of more spike protein than would be available during a natural infection, and we know that repeated boosters cause immune tolerance.Compared to modRNA, a small amount of saRNA results in an increased amount of produced antigen.
Another Dubious Step Forward: From Linear to Circular saRNA
As RNA-degrading enzymes (RNases) are known to act from both ends of linear RNA, scientists tried to prevent these enzymes from doing their natural duty—degrading mRNAs that are no longer needed—and created circular RNA. This resulted in increased stability and translation efficiency, followed by the production of an increased amount of the desired antigen.Long-Term Presentation of an Antigen Is Known to Cause Immune Tolerance
After getting vaccinated, our bodies generate antibodies, mostly immunoglobulin G (IgG), including IgG1 and IgG4.RNA-Based Injections Are Recognized as Gene Therapy Products
Incomprehensibly, RNA-based injections for protecting against infectious diseases were named “vaccines,” which allowed exclusion from the strict regulations for gene therapy products (GTPs). Again, this happened without providing the public with any scientific justification.- The contaminating DNA results from Pfizer-BioNTech’s change in the manufacturing process after finishing the BNT162b2 (Comirnaty) Clinical Trial C4591001. Initially (Process 1), Pfizer-BioNTech modRNA was produced by in-vitro transcription from synthetic DNA and amplified by PCR (polymerase chain reaction). However, to scale up manufacturing (see rapid responses to this BMJ study), modRNA encoding DNA was cloned into bacterial plasmids (Process 2). Put simply, the clinical trial was run on process-1 lots, but the world’s populations received process-2 lots.
- Detailed sequence analyses revealed that the plasmid-DNA in the Pfizer-BioNTech and Moderna COVID-19 shots contain a 72-base pair sequence of the Simian Virus-40 (SV40) promoter, which is well-known to enhance transport of the plasmid DNA into the nucleus.
- RNA-based “vaccine” technology goes against the central idea of evolution over the past millions of years. While injected modRNA and saRNA produce antigens without stopping, in fact, the short lifespan of natural messenger RNA (mRNA) is a prerequisite for healthy and specific cell functions. (The short lifespan of mRNA allows our cells to adapt as quickly as possible to changing circumstances and avoid the production of unnecessary proteins.)
- A premise of RNA-based “vaccine” technology—that all of our body cells have to produce a foreign viral protein—goes against fundamental biological principles, like distinguishing between our own cells and foreign invaders, and will result in our immune system attacking our own cells.
- RNA can be reverse-transcribed into DNA even without the presence of (the enzyme) reverse transcriptase (i.e., by LINE1 elements present in our genome/DNA). Contaminating DNA (in RNA-based vaccines) is the rule rather than the exception. As both RNA and DNA can be integrated into the human genome, the so-called “vaccines” based on RNA technology are actually gene therapy products.
It is in no way justifiable to subject RNA-based GTPs for medical use to strict controls but to exclude RNA-based GTPs, called vaccines, from these regulations even though they are intended for most of the human population. Even in an emergency, no one should be forced to be injected with any substance—least of all by politicians.
What Did COVID-19 Teach Us About Science, Politics, and Society?
For many years, scientists dreamed of manipulating human “software”—that is, DNA or RNA. Ethically, manipulating DNA has always been taboo. In retrospect, COVID-19 may represent the dawn of RNA-based “vaccines” and the end of the taboo against manipulating human DNA.Remember: When questions are allowed, it is science; when they are not, it is propaganda.
So-called “experts” selected by politicians told us that we must be vaccinated to be able to fight a new respiratory virus. This contradicts the science of the human immune system. Our immune systems are dynamic and can clear a virus they have never encountered; they can also develop cross-immunity to identify variants even if the virus mutates. However, since RNA-based vaccines will produce a single antigen, our immune system is deprived of the possibility of developing cross-immunity against virus variants. This applies, in particular, to respiratory viruses exhibiting a high mutation rate. In the long run, this will lead to an increase in both the frequency and the severity of infectious diseases. Thus, politicians interested in protecting the population against future infections would be well-advised to offer health programs that strengthen the immune system before seasonal infections.
Scientists haven’t the faintest idea of how to direct modRNA or saRNA to a specific cell type or how to stop the translation of administered RNA. However, they continue to study how the stability of injected RNA and the amount of generated antigen can be further increased. The current development of RNA-based vaccine technology reminds one of the poem “The Sorcerer’s Apprentice,” which German poet Johann Wolfgang von Goethe wrote over 200 years ago:
“The spirits, whom I’ve careless raised, are spellbound to my power not.”
