Persons who have been VACCINATED against COVID-19 are now subject to Antibody-Dependent Enhancement which is highly likely to . . . kill them.
This is the absolute worst-case scenario with any vaccine. People who took the vax should be quarantined and isolated immediately.
The “Journal of Infection” is a monthly peer-reviewed medical journal in the field of infectious disease, covering microbiology, epidemiology and clinical practice. Established in 1979, the journal was initially published quarterly by Academic Press. The first editor was Hillas Smith.
The Journal is the cutting-edge of information for Doctors specializing in Infectious Diseases. It is considered a “must read” each month by Infectious Disease Specialists.
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On August 9, The Journal of Infection published a peer-reviewed study titled:
Infection-enhancing anti-SARS-CoV-2 antibodies recognize both the original Wuhan/D614G strain and Delta variants. A potential risk for mass vaccination
This study revealed the terrifying news to the world:
- Antibody dependent enhancement (ADE) of infection is a safety concern for vaccine strategies. In a recent publication, Li et al. (Cell 184 :1-17, 2021) have reported that infection-enhancing antibodies directed against the N-terminal domain (NTD) of the SARS-CoV-2 spike protein facilitate virus infection in vitro, but not in vivo. However, this study was performed with the original Wuhan/D614G strain.
- Since the Covid-19 pandemic is now dominated with Delta variants, we analyzed the interaction of facilitating antibodies with the NTD of these variants.
- Using molecular modelling approaches, we show that enhancing antibodies have a higher affinity for Delta variants than for Wuhan/D614G NTDs. We show that enhancing antibodies reinforce the binding of the spike trimer to the host cell membrane by clamping the NTD to lipid raft microdomains.
- This stabilizing mechanism may facilitate the conformational change that induces the demasking of the receptor binding domain. As the NTD is also targeted by neutralizing antibodies, our data suggest that the balance between neutralizing and facilitating antibodies in vaccinated individuals is in favor of neutralization for the original Wuhan/D614G strain.
- However, in the case of the Delta variant, neutralizing antibodies have a decreased affinity for the spike protein, whereas facilitating antibodies display a strikingly increased affinity.
- Thus, ADE may be a concern for people receiving vaccines based on the original Wuhan strain spike sequence (either mRNA or viral vectors).
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Antibody Dependent Enhancement (ADE) is every virologists worst nightmare. It means the vaccine does the opposite of what was intended.
“In antibody-dependent enhancement, sub-optimal antibodies bind to both viruses and gamma receptors expressed on immune cells, then promoting infection of these cells.” In other words, your immune cells themselves BECOME infected and carry the virus.
Vaccinated antibodies will be a trojan horse that gives the virus entry into cells. ALL CELLS. The whole human body.
We will see massive sickness and death within the vaccinated. Boosters will likely make the situation even worse.
Quote: “ Thus, ADE may be a concern for people receiving vaccines based on the original Wuhan strain spike sequence (either mRNA or viral vectors).” Translation: The shot makes a subsequent Infection “strikingly” worse (their words) and everybody was vaxxed using the original strain.
By the way, given that ADE from MRNA in animal trials killed all of them, the word “concern” is a euphemism for “fucking scared.”
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Quote: “ the possibility of ADE should be further investigated as it may represent a potential risk for mass vaccination during the current Delta variant pandemic.” Further investigated. Yeah right… when? By whom? The same Quacks that gave us all this trouble in the first place?
Quote: “ Since the Covid-19 pandemic is now dominated with Delta variants.”
So … this is a “concern” for anyone taking the first shot (actually everyone) as mass vax is a risk for the Delta variant which is now the dominant variety.
The world now has the worst case scenario. We have it BECAUSE of the vaccine.
It is almost laughable that the study authors say a second, different vax should be developed. Well . . . . after most of the people who took Vax 1.0 are dead from ADE, do they really think anyone, anywhere, will trust them with Vax 2.0?
Below is a screen shot of the entire study in case someone decides to hide it. A direct link to the study on the original web site is HERE.
Bottom Line: People who got the vaccine, when they encounter the virus in real life, will not likely survive because their own immune system becomes infected and carries the disease absolutely everywhere in their body. The immune system itself becomes the actual viral carrier.
DO NOT TAKE THE VACCINE.
We’re Not Gonna Take It!
My understanding is that the mRNA ‘vaccine’ (they had to change the definition of vaccine to call it a vaccine) causes cells injected with an mRNA strand to produce proteins that elicit an immune response against a target virus. When the ‘vaccinated’ subject is exposed to the actual virus that their immune system has been trained to fight against, their immune system reacts as intended and destroys the virus. The problem is that in doing so, the immune system learns to recognize the mRNA injected cells eliciting the immune response as infected by that harmful virus. Cells that have this mRNA strand are then recognized by the immune system as having been infected by the harmful virus and killer t-cells kill all of the cells injected with the mRNA ‘vaccine’. After their own immune system kills all ‘vaccinated’ cells as infected, too few living cells remain and the ‘vaccinated’ suffer organ failure and die.
Incidentally, the means that they use to inject the mRNA strand into the human cells is with a chimpanzee virus. The virus is not able (almost certainly true, we hope) to replicate in the human body, so it does not spread (we pray) to the unvaccinated. The chimpanzee virus does what viruses do and injects its mRNA payload into the living cells that it is exposed to.
I don’t know whether this article is talking about the same issue as what I have read or not, but I suspect that it is. Part of the problem is that the articles that I read were on the web in early 2020, but have since been purged. I was researching the prospects of a vaccine being produced quickly thought that this would not happen using the mRNA technology. I was far more naïve a year ago.