Self-Amplifying mRNA Part 2
How close are they to rolling them out?
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Synopsis
In Self-Amplifying mRNA (sa-mRNA): Part 2, we will look into the current status of these new sa-mRNA "vaccines". We will link to the major companies involved in their production, as well as the countries that have already approved their use. This is not in the distant future. This is happening RIGHT NOW.
However, first let’s delve a bit deeper into how sa-mRNA "vaccines" work and the "logic" that lies behind them.
RdRP Backbones in sa-mRNA "Vaccines"
As mentioned in Part 1, Self-Amplifying mRNA "Vaccines" use a stripped-down viral sequence, containing only the RdRP complex, also called "Replicon". All of the other genetic proteins that make up that particular virus have been removed, to which the desired singular antigenic protein (e.g., SARS-2 Spike protein) will be attached to be replicated multiple times. As mentioned in Part 1, the logic of this is to reduce the quantity of actual mRNA "vaccine" formula solution that is required to achieve the same effect as the current mRNA injections/boosters. With long-term replication of the antigen, boosters would be negated. These viral antigens would continue to be replicated, just like the actual RNA virus, until the body’s immune system confronts and kills the infected cells. And since the LNP "shell" they are contained within can merge with ALL cells, including those across the "Blood-Brain Barrier", it suggests that every cell will be under attack by our immune system.
The fact that they are using an RdRP complex from one virus to produce the singular viral protein supports Baric’s assertions that RdRP acts the same for ALL RNA viruses. They are, essentially, the same RdRP complex. And as we’ve seen from Baric and Zelenko’s research and human implementation, Zinc + Zinc Ionophores (HCQ, EGCG, Quercetin, etc.) will inhibit/block that RdRP in the initial stages of an infection. This logically implies that those same RdRP inhibiting protocols/drugs will ALSO block the RdRP of the sa-mRNA "vaccines", effectively neutralizing them completely.
Get your Vaccine Passport with a “wink, wink, nudge, nudge”.
Yes, that sounds a bit flippant on my part, but for those who implement the RdRP inhibiting protocol, or drugs PRIOR, during the injection, and likely for a few weeks after receiving their future mandated sa-mRNA injection, it very well mean ultimate freedom. Those who require a "vaccine" in order to work, go to school, or travel not only will know that they’ve ‘defeated’ these RdRP-based gene-therapies/vaccines. More importantly though, they will be armed with the knowledge of how to combat a real RNA viral infection from a wild RNA virus.
People will receive their required ‘proof of vaccination’ card, or QR code on their phones, that provides the evidence that you received your shot. But they know that they’ve neutralized their ability to function, or to cause potential adverse effects to your immune system, or your body (remember that IgG4 issue we touched upon in Part 1)
How would Big Pharma react to this? Could they continue to demonize EARLY RdRP inhibiting treatments for infected patients? Not really, I opine, since that would immediately raise the obvious question as to why they DENIED such early treatment to the world in the first place against the actual RNA virus? It would become a global scandal, governments might fall, and heads might roll, literally. It would mean, ultimately the justifiable death of their RNA viral “vaccine” money machine, financed by the taxes of common individuals. The world would finally know why they quashed the Baric-based, Zelenko Protocol, as well as Ivermectin in 2020, at the cost of millions of lives and the careers of dedicated, innovative physicians who implemented EARLY treatment.
Do you really think that they would want to take that risk?
Treatment
I HAVE A DREAM!!!
With these science-based revelations, might we even see a post-WWII-style medical Nuremberg Tribunal, where the perpetrators of this global viral holocaust, and resulting censorship of known EARLY treatments will face legal accountability for their greed and lies? The very same people that we trusted to guard the global health of humanity, but sold their souls in order to transfer debt-financed money into their pockets. Globalist elites bent upon obtaining power and control over humanity through their use of RNA viral pandemic terrorism. Yet, they are no different from the Nazi physicians who experimented on concentration camp prisoners. In fact, they turned the entire world into a concentration camp upon which to conduct their experiments. Is it just about control through fear? Or does it suggest that Bill Gates' words about reducing population through vaccination are indeed as sinister as they sounded when he first spoke those words at a TedX presentation? Will he be forced to disappear like Dr. Mengele, or will he face a criminal court, be convicted, and sentenced?
As I said.. I HAVE A DREAM!!
However, there remain a few questions we need to address first, as well as the current players in the sa-mRNA industry and their status.
Were mRNA and sa-mRNA “vaccines” blended as a test experiment?
Since both mRNA and sa-mRNA “vaccines” use similar LNP delivery means into the cell, exactly how can we be certain that selected batches of the mRNA “vaccine” formulas weren’t mixed with sa-mRNA? They have already tested sa-mRNA ‘vaccines’ against SARS-2. Both produce the SAME synthetic mRNA Spike protein, and that can be tested for. But how would we be able to discern the difference between Syn-Spike produced by mRNA, and that produced by sa-mRNA processes? Supposedly, they can detect different RdRP, and other viral proteins using PCR-RT testing.
Given that researchers have evidence of extended Syn-Spike protein evident in long-haul Covid patients, is it possible that Pfizer and/or Moderna mRNA shots were co-mingled with the newer sa-mRNA ‘vaccines’ to produce the same syn-Spike protein? How would we know, when all of the ingredients are considered ‘proprietary’, with no requirement to disclose them? And researchers would have to know about such a possibility, to motivate them to conduct the appropriate tests, right?
“There have been very few studies assessing the biodistribution and persistence of SARS-CoV-2 mRNA vaccines in humans. Using human axillary lymph node biopsies, spike protein and vaccine mRNA were reported to persist up to 60 days from vaccination with either BNT162b2 or mRNA-1273 as detected by immunohistochemistry and in-situ hybridization18.”
This seems an appropriate question to be considered, and could go far in explaining the long-term presence of Syn-Spike months afterwards. The Pfizer and Modern mRNA only produce (supposedly) one syn-Spike protein. But those sa-RNA ‘vaccines’ can keep replicating them for a long period of time, by their very design. After all, this is exactly what sa-mRNA “vaccines” are supposed to do, right? Create long-term antigenic proteins that “train” our immune systems.
All we have are the hollow words of Big Pharma to rely upon. We can trust them, right? However, if this could be proven, it would directly imply that the Operation: Warp Speed “vaccine program was actually a cover story for wide-spread testing of sa-MRNA “vaccines” without our informed consent.
WHO ARE THE PLAYERS?
Right now, I would opine that there is one leading player in sa-mRNA. Arcturus Therapeutics was started in 2013 and headquartered in San Diego, California. Their sa-mRNA “vaccine” is known as ARCT-154 That link will show they’ve ALREADY tested it versus current mRNA “vaccines” for SARS-2 "syn-Spike” protein!! It’s in the current April, 2024 Lancet Journal.
But their Joint Venture (JV) facility in Japan was completed in July, 2023, and is ALREADY complete and ready to begin making ARCT-154. Sounds like they were pretty confident in their Phase 3 trials, right? And Japan has ALREADY approved its use. The Joint Venture in Japan is capable producing enough sa-mRNA for 1 BILLION doses.
“The vaccine is dosed at 5mcg per shot. Given Arcalis’ annual capacity of 5kg of drug substance per year, the company can make mRNA substance for up to 1 billion doses of the shot, the Arcturus spokesperson said.”
That is, indeed, HIGH CONFIDENCE, correct? No need for long-term testing for adverse side effects being seen in the current mRNA injections, right?
YOU ARE GOING TO USE A VIRAL ENCEPHALITIS VIRAL RdRP COMPLEX?!!
ARCT-154 uses the RdRP backbone of an Equine Encephalitis Virus!! My goodness.. I guess a common influenza virus wouldn’t have sufficed, right? Why not use the RdRP the actual SARS-2 virus? What could possibly go wrong in using a Viral Encephalitis viral RdRP backbone, right?
But yet, that is what ARCT-154 uses as it’s RdRP complex:
“The ARCT-154 study vaccine consists of sa-mRNA encapsulated in lipid nanoparticles. The RNA comprises a replicon based upon Venezuela equine encephalitis virus (VEEV) in which RNA coding for the VEEV structural proteins has been replaced.” (Bottom of Page 6).
Again, I ask.. Why the VEEV virus, of all of the ones they could choose from? After all, they are attaching a SARS-2 spike, or other viral, protein to it, so why VEEV as the RdRP backbone?
What are the symptoms of VEEV in humans?
“Severe encephalitis in humans is less frequent with VEEV than with EEEV and WEEV with a low fatality rate, though neurological sequelae are fairly common. Pregnant women are also at an increased risk of having abortions with VEEV infection.”
Encephalitis is, basically, it is inflammation of the brain. And it leads to all kinds of nasty ramifications, like dizziness, partial paralysis, seizures, hallucinations, memory loss, and even death. Sounds wonderful doesn’t it?
I don’t know.. must just be a coincidence, right? I mean, I don’t want to be spreading conspiracy theories, or anything, right? It just strikes me as rather odd that VEEV is what they chose for the RdRP in the Arcturus sa-mRNA “vaccine”. The one of which their JV in Japan is gearing up to make 1 Billion doses per year.
LNP crosses blood brain barrier and they are about to inject us with a vaccine that contains the RdRP complex of the VEEV virus? Are they INSANE??!! Might they “accidentally” mix some of the active VEEV virus into those injections? I report. You decide for yourselves.
Given the ongoing concerns that the Spike protein represents a Prion and its being attached to an VEEV RdRP backbone, maybe its the prelude to the long-awaited Zombie Apocalypse? (wink, wink, nudge, nudge 😁 ).
What CAN BE SAID is that sa-mRNA “vaccines” have been in development since at least 1999 as a cancer “vaccine” Here is a decent link to examine the history of sa-mRNA “vaccine” development. That represents a HUGE investment, one they are already on the brink of rolling out. But one that EARLY treatment RdRP inhibitor would ultimately NEUTRALIZE, derailing the entire sa-mRNA program.
Have they already tested them? As mentioned above, Japan has recently approved their use based upon clinical trials of 19,000 subjects in Vietnam.
Self-Amplifying mRNA “vaccines” are already here, being tested, and can be NEUTRALIZED with RdRP inhibitors like the Zelenko Protocol and/or combined with Ivermectin.
Again, you just learned the secret, in my humble opinion, as to WHY EARLY TREATMENT, based upon the eminent Ralph Baric’s RdRP inhibiting research was suppressed. You now have compelling evidence that it HAD TO BE suppressed in order to NOT undermine years of research, and millions of dollars of investment based upon a $20 dollar Zinc + HCQ Zelenko Protocol. And if you’re particular “frugal”, you can utilize a natural Zinc Ionophore, such as EGCG, or Quercetin to replace the prescription only HCQ. That could bring the cost down to less than $5, or less.
There has been major investment in sa-mRNA technology, and they are manufacturing plants in place to manufacture it in large quantities. These investments are not spontaneous. They take time and planning.
Ask yourself now.. WHY in the hell do they require that kind of production capacity for a country, Japan, with a, declining, population of 125 million people??!!
And in Vietnam, Arcturus is also setting up an sa-mRNA manufacturing facility:
“Arcturus investigational COVID-19 vaccines utilize Arcturus’ self-transcribing and replicating (STARR) mRNA technology, and the STARR mRNA is delivered with Arcturus’s lipid-mediated delivery system called LUNAR delivery system.”
Additionally, sa-mRNA “vaccines” have been tested in laboratory mice against the deadly H5N1 Avian RNA virus (52% mortality in some 900 “natural human cases), while Ferrets were protected against H1N1.
So what’s the problem with sa-mRNA “vaccines”? They tested them on 19,000 unsuspecting Vietnamese subjects, with apparently few major adverse effects, right? We shouldn’t be concerned that they had to go to a Communist ruled country to do their human testing, right?
IgG4, the “tolerating antibody”:
In recent months, there has been increasing evidence that with every booster shot of the current mRNA vaccines, it results in an increase in IgG4 antibody production. IgG4 is an antibody produced to “calm” the immune system down when confronted with non-lethal invaders such as pollen (allergies), and other non-replicative invaders. Since the Synthetic Spike protein that is produced is just one singular protein that embeds itself into the cellular membrane, rather than forming a complete virus/virion that escapes from the cell (budding) into our bloodstreams, is it possible that IgG4 is being produced because our immunity is recognizing these embedded Spike protein as a non-threatening part of our physiology? I can only ask the question. This gentleman can provide a better explanation of IgG4 than I can.
And this video related to “Turbo-Cancers”.
p53 protein interference
The p53 protein is incorporated within the DNA of the human body to deal with damaged DNA that result in tumors/cancer). When DNA is damaged, due to oxidative stresses, or other factors, its cellular division can go unchecked/unrestrained, creating tumors. p53 acts to bind that damaged DNA, preventing it’s cellular division, until it can either be repaired, or a molecular “signal” is transmitted ordering the destruction of the cell. This represents the body’s primary mechanism for self-defense against unfettered cellular division and growth (tumors).
There have been recent revelations that the Spike protein interferes with the p53 “Guardian of the Genome” protein. Thus, we must ask the question of whether there is a connection to the IgG4 issue as well. The author of the above link, Dr. Wafik S. El-Deiry, of Brown University, is one of the leading scientists on the function of p53, so his findings are not to be taken lightly:
"We examined the interaction between SARS-CoV-2 spike, p53, and MDM2 (E3 ligase, which mediates p53 degradation) in cancer cells using an immunoprecipitation assay. We observed that the SARS-CoV-2 spike protein interrupts p53-MDM2 protein interaction but did not detect SARS-CoV-2 spike bound with the p53 protein in the cancer cells. We further observed that the SARS-CoV-2 spike suppresses p53 transcriptional activity in cancer cells, including after nutlin exposure of wild-type p53, and spike S2-expressing tumor cells. It inhibits chemotherapy-induced p53 gene activation of p21(WAF1)."
So the logical deduction to be recognized is that if “wild” Spike protein disrupts the normal p53 function, what effect could long-term production of synthetic Spike from mRNA, or sa-mRNA vaccines have?
A recent revelation that I discovered is that this incredibly vital p53 protein is ACTIVATED BY ZINC. If you are Zinc deficient, p53 doesn’t work properly:
“A large percentage of transcription factors require zinc to bind DNA. In this review, we discuss what makes p53 unique among zinc-dependent transcription factors. The conformation of p53 is unusually malleable: p53 binds zinc extremely tightly when folded, but is intrinsically unstable in the absence of zinc at 37°C. Whether the wild-type protein folds in the cell is largely determined by the concentration of available zinc. Consequently, zinc dysregulation in the cell as well as a large percentage of tumorigenic p53 mutations can cause p53 to lose zinc, misfold, and forfeit its tumor suppressing activity.”
Don’t be Zinc Deficient
I hope the reader can now fully grasp the critical importance of Zinc, both as an antiviral “bullet”, and also it’s critical function in activating the p53 protein that helps prevent the development of cancer.
It is my impression that if “wild Spike” results in such deleterious effects on p53, and IgG4, we must infer that the mRNA jabs are just as capable of causing even greater physiological insults upon our bodies. And if the current mRNA vaccines which only produce one copy of the Syn-Spike protein can create these reactions, what will be the case when they have Self-Amplifying mRNA making MULTIPLE copies, for an unknown period of time? Will IgG4 antibody production increase even more? Will more p53 function be disrupted, leading to greater susceptibility for “Turbo-Cancers”?
These are all questions that need to be considered, IMO.
What have we learned?
I pray the reader now understands the significance of why EARLY treatment protocols HAD TO BE SUPPRESSED? Big Pharma stands to lose BILLIONS of dollars if their new sa-mRNA “vaccines are NEUTRALIZED by Zinc + HCQ, or even natural Ionophores like EGCG, or Quercetin and/or Ivermectin!! “Vaccines” that have been in the R&D pipeline for over 20 years!
That knowledge of what we can do to neutralize them through EARLY treatment/prophylaxis represents action we ALL can take to prevent harm from the next round of “mandated” sa-mRNA “vaccines”!!!
When these sa-mRNA “vaccines” are forced upon us, we have the ability to apply EARLY treatment to neutralize them. HOWEVER, the potential deleterious effects of the LNP that encapsulate them remain a mystery yet to be fully revealed. So bear that in mind.
Ensure that you remain Zinc sufficient according to your age and risk profile. But given the toxicity of excess Zinc in the body over a longer duration, DO NOT OVERDO your Zinc supplementation. 15mg of ELEMENTAL Zinc is considered the normal requirement for adults. And Zinc Sulfate only contains 21% elemental Zinc, which translates into 50mg tablets.
As we sum up this story, the most obvious point is that a compelling argument can be made that Big Pharma SACRIFICED millions of people TO DIE around the planet from SARS-2. It’s quite plausible that demonization of EARLY treatment, RdRP inhibitors, was to protect these sa-mRNA vaccines into which they had poured so much time and money over the past decades (Arcturus, for example, was founded in 2013). It requires a lot of money to ramp up these kinds of facilities. And, of course, these EARLY treatment protocols, with the exception of Ivermectin, were BASED UPON the research pioneered by their chief “Wonder Boy”, Dr. Ralph Baric. And his research was tested for the first time in humans by Dr. Vladimir “Zev” Zelenko (Zelenko Protocol).
Note": As I was recently researching and writing this article, I happened across this video posted a year ago, from noted cadilogist/lawyer Dr. Richard Fleming, who provided a very extensive and informative discussion of mRNA and sa-mRNA vaccine issues. You might want to watch it.
RdRP inhibiting EARLY treatment protocols, based upon Ralph Baric’s 2010 Zinc + Ionophores (HCQ, EGCG, Quercetin.. etc) research, as well as Ivermectin, had to be suppressed because they threatened to throw a MONKEY WRENCH into their Self-Amplifying mRNA vaccine “machinery”.
And if those EARLY treatment protocols would disrupt sa-mRNA RdRP functionality, it IMPLICITLY SIGNIFIES that such protocols work against “live” RNA viruses as well, just as Baric demonstrated “in vivo” and Zelenko and others proved in human beings.
That strongly implies that THEY KNEW RdRP inhibiting EARLY treatments were EFFECTIVE. And if the world learned about them, it would undermine, if not nullify, the entire reason for the Big Pharma vaccine industry to exist (at least for RNA viruses) and with it, their profits, as well as the tool for globalist control over the world’s population. They would no longer be able to use viral pandemics as a fear-mongering device to induce compliance by the world population.
And companies like Arcturus Therapeutics will see their business model completely unravel when confronted with the reality of RdRP inhibiting EARLY treatment options. And with it, the loss of a profit motive for the WHO treaty that is about to be finalized this month, rendering unto it, ultimate sovereign control over global pandemic response.
