I have been trying to understand and make sense of the information available out there on the new technology that is used as vaccines in hundreds of millions of people, with the intention to not only use it for immunization against SARS-CoV2, but against other viruses as well.
The source of the above image can be found here.
Full disclosure: I am not a scientist. My experience and knowledge in the field of biology is limited. I have a two year education to work in a laboratory that does biological research, but my main “work“ is in computers and programming.
So this above picture is already very helpful to understand the intended way the new “vaccines” are working. The LNPs deliver the mRNA to a host cell and that host cell produces the full spike protein and presents it on its cell membrane as well as that it produces exosomes covered with spike protein.
The only part shown from the immune system are dendritic cells and B-cells. And this already posts so many questions to me.
Where are the NK cells? Are they not part of the first line of defense, there, to facilitate and activate further cellular parts of the immune system? How do they react to a “host” cell, that presents a protein that actually belongs to a virus and is therefore foreign to the body?
There is an article from 2022 “Innate immunity: the first line of defense against SARS-CoV-2“ and basically I think we should be looking at everything this article describes and simply exchange “SARS-CoV-2“ with either BNT162b2 or Spikevax, as the Moderna version of the LNP/mRNA is called.
All we have ever heard in the media and from governmental agencies was how these vaccines create antibodies. We were never told what happens to those “host“ cells, which now all of a sudden have been capture by something I would call a pseudo-virus.
As far as I am aware, every cell in the human body has a function. Their “machinery” is geared towards fulfilling a certain purpose. I may be wrong, but I do not know of a cell that has “free capacity“ to just simply create proteins, which the cell itself cannot use and that detracts from the resources it needs to sustain itself and its function.
If that were the case, if the cells of our body could simply be used to produce foreign proteins without any detrimental effect, then surely the human species would have died out eons ago, when the first virus came along.
The above picture showing how the new “vaccines“ are simply “borrowing“ the machinery of a cell to produce spike protein leaves out a lot. The question about the innate immune system and its reaction to coopted cells I have already posed.
Another question becomes apparent when you combine findings from autopsies of individuals that died from severe COVID19. A look at their lungs reveals, that the virus and the immune systems reaction to the virus is not the only source of the damage to the tissue. And here is another article that to me seems very important.
In “Syncytia formation by SARS-CoV-2-infected cells“ one sentence stands out to me:
Expression of S without any other viral proteins triggers syncytia formation.
Here is another article that looks at syncytia formation during infection with SARS-CoV2. Adding another bad outcome from syncytia: Lymphopenia
The conclusions one can draw from this become even more terrifying, when you have seen the following table.
The above table is part of study 185350, which the FDA tried to keep from the public for 75 years.
So now we know, that since the 9th of November 2020 the Pfizer knew, that the vaccine would be detectable everywhere in your body, after 25 minutes. Even when given IM. We know that the LNPs do not discriminate between “host“ cells. They will meld with a cell they make contact with in the muscle in your arm, your heart, your liver, your kidney, your spleen, your brain, your bone marrow, your ovaries, your testies, your bladder, your adrenal glands, your pancreas, your lung, your skin, your prostate, your salivary glands, your spinal cord, your thyroid, your thymus, your uterus, etc.
Those host cells will start producing spike protein. A protein, that is foreign to the body, an actual part of a virus. Why have we not heard anything about the innate immune system response? Could it be, because of this?
The above slide has been taken from here. I take it, when the
Harvard Medical School creates a page with the title “How The Body Reacts To Viruses“ one can presume that they get things right.
I think what we are looking at here is a double whammy. First, the LNPs bring the mRNA for the spike to every corner of the body. From brain to bone marrow. There, the infected (they would like you to call this “new“ mechanism “transfection” but since they are injecting foreign mRNA into a cell I will stick to calling it infection) cells will start to produce spike protein. They will present these on their membrane and also start producing exosomes.
This first whammy means any cell that will show the foreign protein on their surface will become a potential target for your own immune system, especially your innate immune system, which will try to detect infected cells as soon as possible to curb the reproduction of a potential virus.
Already I think this is an absolute no go! How on earth did anyone think, that using a non-targeted vehicle to transport mRNA into whatever cell they get in contact with, knowing after study 185350, that this vehicle will get absolutely everywhere, that it would be a good choice?
With the knowledge of syncytia formation through spike protein alone it gets even worse. Not only are you going to loose whatever “host” cell was infected by the LNPs, either through stress or more directly through the killer cells of your immune system, and I am not cool with loosing brain cells, bone marrow cells or any other cell, thank you very much.
Now we have to consider that any cell that displays the spike protein on its surface can potentially form syncytia with other cells, if those cells are presenting ACE2 on their membrane! And yes, syncytia can be normal, when you are looking at muscle cells for instance, but even here, “wild“ syncytia formation is not a good thing. And it does not get better in any other organ, where these kinds of unusual cell formation will inhibit function of tissue and potentially can lead to more cells dying and localized inflammation.
And the list of tissue where cells exhibit ACE2 is not small and it contains one that is really bothersome. Endothelial cells.
These are the lining of every blood vessel in your body. And anytime that one of these gets to be a “host“ cell and produces spike protein, you have the chance of them being killed by your immune system as a single cell, or after they have fused with their neighboring endothelial cells that have ACE2 on their surface.
This will cause inflammatory processes in the wall of your blood vessel with all the bad potential outcomes, regardless of where that blood vessel is in your body. Even if you were lucky and it ends up in a fairly large blood vessel, you still have a risk of plaque forming and that can lead to thrombosis. Worse if this happens in a small blood vessel. Even worse still when this happens in your brain.
For me there are so many questions that just do not seem to have good answers, that the whole vaccination campaign with this new technology should have never been allowed to start in the first place. China and other countries were developing vaccines based on well known and well established technologies. Even the WHO gave the stamp of approval to some of the early vaccines from China. But the populations in Western countries were basically denied the choice of having a vaccine based on a true and tested technology.
And here is a last thought/question for you. What would you say, if someone were to find a way to deliver these LNPs with the mRNA in an aerosolized form and a higher concentration? People could breathe these in, unknowingly, and potentially develop all the damages we now see from the virus. Does that not sound like this technology could be easily weaponized, without having to fear the uncontrolled spread of a virus? Are we witnessing the creation of a new type of biological weapon, marketed as a vaccine against a virus?