If you look around on the Internet, you’ll find that anyone who suggests these vaccines are a form of gene therapy is immediately censored. The fact-checkers, our timeline’s equivalent of bureaucrats of the Ministry of Truth, are also eager to debunk the assertion that the vaccines are a form of gene therapy. And so when you look it up, you’ll immediately find yourself exposed to a massive lie of omission. Because what do they tell you?
That’s the lie of omission right there. You can argue about whether Moderna and Pfizer’s mRNA vaccines should be considered gene therapy, as the mRNA should be transiently expressed. But what are we missing here? We’re missing two of the four vaccines that we are receiving in the Western world. You can argue that the mRNA vaccines are not a form of gene therapy because the mRNA is probably not permanently integrated into your genome. However, billions of people around the world have now received a dose of two other vaccines manufactured by Janssen and Astrazeneca.
Notice how the fact-checkers NEVER mention the Adenovirus vector vaccines when they try to debunk the “gene therapy” claim. They don’t mention it, because these vaccines are designed as gene therapy. There’s not a word mentioned about these Adenovirus vector vaccines in the article I linked to above. It is an admission by omission.
The whole point of using an Adenovirus vector is to cause permanent genetic alterations to your body. And if we’re doing that to someone who has an otherwise deadly metabolic disease due to a genetic mutation, you won’t hear me complain. But they have given these vaccines to hundreds of millions of young healthy people worldwide.
We have now seen 2.5 billion doses of the Astrazeneca vaccine distributed worldwide. In addition to this, there are hundreds of millions of people, who have received the Janssen vaccine. In Russia, millions of people are receiving the Sputnik vaccine, which also uses an Adenovirus vector.
What do these vaccines have in common? They are replication defective Adenovirus vector vaccines. An Adenovirus is a DNA virus that will enter your cells, to deliver DNA that the cell will then go on to express. The Adeno viruses that they use in these vaccines are missing certain genes, which should generally prohibit them from going on to make new copies of themselves that can infect more cells. However, they succeed in initially entering your cells and delivering the genetic payload.
What these vaccines are designed to do is to deliver DNA that produces copies of the Spike protein into your cells. Whereas mRNA expression should be temporary, these Adenovirus vector vaccines are designed to permanently make your body express the DNA deliver to your cells.
Adenoviral vectors persist in vivo and maintain activated CD8+ T cells: implications for their use as vaccines
CD8+ T cell-numbers rapidly expand and then contract after exposure to their cognate antigen. Here we show that the sustained frequencies of transgene product-specific CD8+ T cells elicited by replication-defective adenovirus vectors are linked to persistence of low levels of transcriptionally active adenovirus vector genomes at the site of inoculation, in liver, and lymphatic tissues. Continuously produced small amounts of antigen maintain fully active effector CD8+ T cells, while also allowing for their differentiation into central memory cells. The long-term persistence of adenoviral vectors may be highly advantageous for their use as vaccines against pathogens for which T-cell–mediated protection requires both fully activated T cells for immediate control of virus-infected cells and central memory CD8+ T cells that, because of their higher proliferative capacity, may be suited best to eliminate cells infected by pathogens that escaped the initial wave of effector T cells.
Further down we read:
To formally demonstrate whether the E1-deleted Ad vector genome persists, tissues of mice were tested for presence of vector sequences 4, 30, 90, and 360 days after intramuscular immunization with an AdC68 vector by a nested real-time PCR (Figure 2A).19 Vector sequences could not be detected from most tissues such as ovaries, muscle distant from the inoculation site, lung, heart, brain, stomach, nasal associated lymphoid tissue, or trachea (not shown). Four days after vaccination with an AdC68 vector, transgene sequences could be detected in liver, spleen, and the inoculated muscle. By days 30 and 90, vector sequences remained detectable in most animals in these tissues but gradually declined 102 to 103-fold. After 1 year, relative copy numbers in liver and the injected muscles were comparable with those seen on day 90, whereas a further decline was seen in spleens.
These Adenovirus vectors are designed to make your own tissues express the DNA forever. The only reason the expression declines over time, is because your own immune system will seek out these cells to destroy them. If you received one of the Adenovirus vector vaccines, there is a continual effort ongoing in your body by your immune system to get rid of all the cells that were reprogrammed to produce the toxic spike protein. However, it seems that your body is unable to get rid of these cells from the muscle and the liver.
Besides the simple fact that you don’t want your immune system to attack your own tissues, the spike protein is toxic. Your own body is now chronically producing this toxic protein that is released into the bloodstream. The spike protein damages your hematopoietic stem cells. These stem cells are responsible for producing your white blood cells.
If you have received one of the Adenovirus vector vaccines then it means you have been injected with a genetically manipulated virus, that is intended to introduce foreign genetic material into your cells that persists for as long as the cells themselves survive. This genetic material produces a toxic protein that is capable of damaging the stem cells that are responsible for producing your white blood cells.
This is what these vaccines are designed to do. The whole technique they’re using is meant to get your body to continually produce small amounts of this toxic protein, so that your immune system will continually mount a sustained immune response against this toxic protein. That’s why they only have to give you one dose, whereas with the mRNA vaccines they give you two doses.
They can’t even give you two doses of the Adenovirus vector vaccines, because it won’t even properly work anymore. Your immune system is immediately on high alert for the Adenovirus material and will do whatever it can to prevent these viruses from entering your cells again. It only works the first time, because your immune system is not yet prepared for what they’re doing. Notice how all the boosters people are given are based on mRNA. Nobody who received an Adenovirus vector vaccine receives a booster based on an Adenovirus vector vaccine.
And if you weren’t aware yet, the Spike protein of the actual virus changes over time. But right now, your own cells are still producing a version of the Spike protein that is completely different from the version found in Omicron. Your immune system is being prepared to defend against a version of the Spike protein that no longer exists, because your own cells were reprogrammed to produce a version of the Spike protein that no longer exists.
And worth noting too is that they don’t just make your cells produce the regular plain Wuhan spike protein. They introduced changes into the genome, to produce a version of the Spike protein that is stabilized in the conformation that allows it to bind to the ACE2 receptor. Affinity of this stabilized version of the Spike protein to the ACE2 receptor appears to be higher than that of the natural spike protein.
Your T cells are now continually forced to attack any of the cells they encounter that express this spike protein. Persistent infections are known to lead to T cell exhaustion, these adenovirus vector vaccines may very well cause the same issue in some people, we just don’t know right now. It’s not normal for a vaccine to produce an immune response that declines this dramatically within a few months. Keep in mind, the reason the vaccines cease to work is not just because the virus itself changes, there is also some issue related to the immune response itself rapidly declining. Why does the immune response decline so rapidly? We don’t know.
Gene therapy is difficult and full of risks. Gene therapies with retroviruses caused leukemia. Gene therapies with adenoviruses were thought to be pretty safe initially, but now it’s clear that these also cause changes that lead to cancer. In mice, the adenovirus gene therapies have been known to lead to liver cancer. The adenovirus DNA causes changes that encourages the cells to divide themselves. In human children, we encounter adenovirus DNA in most brain tumors.
Nobody can tell you whether these Adenovirus vector vaccines are going to be causing cancer years down the line. It’s a risk that is impossible to quantify, but it’s an experiment that has now been carried out with hundreds of millions of young people around the world. Hundreds of millions of people have been subjected to gene therapy, not to cure a disease, but in an effort to protect them against a virus that might infect them, only for the attempt to protect them against the virus to fail.
This is the most reckless experiment in human history.