Therefore, the formulation has the potential to prevent and treat the serious conditions caused by pathogenic antibodies during a COVID-19 infection. In addition, the formulation has potential to prevent and treat the adverse reactions of COVID-19 vaccines because the vaccines can induce similar antibodies, including pathogenic antibodies. The formulation will be helpful in increasing the safety of the vaccines without reducing the vaccine’s efficacy.
LOL, You are right OP, a jab to protect you from the other jab.
In a recent study, we reported that certain anti-spike antibodies of COVID-19 and SARS-CoV viruses can have a pathogenic effect through binding to sick lung epithelium cells and misleading immune responses to attack self-cells. We termed this new pathogenic mechanism “Antibody Dependent Auto-Attack” (ADAA). This study explores a drug candidate for prevention and treatment of such ADAA-based diseases. The drug candidate is a formulation comprising N-acetylneuraminic acid methyl ester (NANA-Me), an analog of N-acetylneuraminic acid. NANA-Me acts through a unique mechanism of action (MOA) which is repairment of the missing sialic acid on sick lung epithelium cells. This MOA can block the antibodies’ binding to sick cells, which are vulnerable to pathogenic antibodies. Our in vivo data showed that the formulation significantly reduced the sickness and deaths caused by pathogenic anti-spike antibodies. Therefore, the formulation has the potential to prevent and treat the serious conditions caused by pathogenic antibodies during a COVID-19 infection. In addition, the formulation has potential to prevent and treat the adverse reactions of COVID-19 vaccines because the vaccines can induce similar antibodies, including pathogenic antibodies. The formulation will be helpful in increasing the safety of the vaccines without reducing the vaccine’s efficacy. Compared to existing antiviral drugs, the formulation has a unique MOA of targeting receptors, broad spectrum of indications, excellent safety profile, resistance to mutations, and can be easily produced.
"In a recent study, we reported that certain anti-spike antibodies of COVID-19 and SARS-CoV viruses can have a pathogenic effect through binding to sick lung epithelium cells and misleading immune responses to attack self-cells. We termed this new pathogenic mechanism “Antibody Dependent Auto-Attack” (ADAA)."
Isn't that similar to what happened to all the animals in the mRNA studies through the years? 🤔
Not the same, what you're referring to is ADE: antibody dependent enhancement.
ADE in a nutshell is where the programmed immune response by the mRNA "vaccine" is inadequate and your antibodies bind to the virus but don't kill it.
Our cell walls have a complex chemical gating system, but when those walls detect our own body's cells (like the antibodies attached to the corona viruses), the drawbridge gets lowered allowing the corona virus to swarm into the cell and hijack/kill it. The result is an organism that's now incredibly vulnerable to the virus that the vaccine was ostensibly supposed to fight. This is one of the many reasons why it's important for all the Leftards out there to understand that this "vaccine" is very different in that it's not using weakened or dead virus in the injection.
Past vaccines of course have used weakened or dead virus and consequently, the immune response is IDENTICAL to actually encountering the live virus.
What they're referring to in this paper is the phenomenon of cytokine storms (inflammation) that's set off by the damn spike protein in this "vaccine". Inflammation destroys tissue and that's particularly bad when the inflammation is occurring in cardiac tissue (as we've seen with many young men after the jab) or brain tissue (or any organ for that matter).
All this talk about antibodies, why is noone talking about T-cells? They are responsible for clearing virus infected cells. They do this by checking the MHC1 molecules, present on every cell in the body. All cells produce proteins, and every last one of these proteins are transported to and presented on the MHC. This includes faulty cancer proteins, viral proteins, and spikeproteins produced by vaccine mRNA. What do all the experts think happens to the cells that take up the mRNA and produce spikeproteins?
Translation:
You took the free "vax"... and now, in order to stay alive, you need to take repeated doses of the new drug we are developing.
It won't be free.
The other ones weren't free either.
It also likely wont be covered by ins.
Just like the street dealers, first hit free to get you hooked.
LOL, You are right OP, a jab to protect you from the other jab.
All Chinese authors
Yeah, cause that will make the over 50% of us Americans not fully vaxxed rush out and get one =(. They are stupid.
In a recent study, we reported that certain anti-spike antibodies of COVID-19 and SARS-CoV viruses can have a pathogenic effect through binding to sick lung epithelium cells and misleading immune responses to attack self-cells. We termed this new pathogenic mechanism “Antibody Dependent Auto-Attack” (ADAA). This study explores a drug candidate for prevention and treatment of such ADAA-based diseases. The drug candidate is a formulation comprising N-acetylneuraminic acid methyl ester (NANA-Me), an analog of N-acetylneuraminic acid. NANA-Me acts through a unique mechanism of action (MOA) which is repairment of the missing sialic acid on sick lung epithelium cells. This MOA can block the antibodies’ binding to sick cells, which are vulnerable to pathogenic antibodies. Our in vivo data showed that the formulation significantly reduced the sickness and deaths caused by pathogenic anti-spike antibodies. Therefore, the formulation has the potential to prevent and treat the serious conditions caused by pathogenic antibodies during a COVID-19 infection. In addition, the formulation has potential to prevent and treat the adverse reactions of COVID-19 vaccines because the vaccines can induce similar antibodies, including pathogenic antibodies. The formulation will be helpful in increasing the safety of the vaccines without reducing the vaccine’s efficacy. Compared to existing antiviral drugs, the formulation has a unique MOA of targeting receptors, broad spectrum of indications, excellent safety profile, resistance to mutations, and can be easily produced.
This is too funny. All this shit or.... you get sick and let you body handle it, shocking I know.
So let me get this straight. The science that I'm reading in this paper says that the vax kills people. Unambiguously.
But the LSM says the science says it is safe and effective?
The current vaxxes are bio weapons. They are developing a vaccine to counter the current bio weapon.
There I made it make more sense now.
"In a recent study, we reported that certain anti-spike antibodies of COVID-19 and SARS-CoV viruses can have a pathogenic effect through binding to sick lung epithelium cells and misleading immune responses to attack self-cells. We termed this new pathogenic mechanism “Antibody Dependent Auto-Attack” (ADAA)."
Isn't that similar to what happened to all the animals in the mRNA studies through the years? 🤔
Not the same, what you're referring to is ADE: antibody dependent enhancement.
ADE in a nutshell is where the programmed immune response by the mRNA "vaccine" is inadequate and your antibodies bind to the virus but don't kill it.
Our cell walls have a complex chemical gating system, but when those walls detect our own body's cells (like the antibodies attached to the corona viruses), the drawbridge gets lowered allowing the corona virus to swarm into the cell and hijack/kill it. The result is an organism that's now incredibly vulnerable to the virus that the vaccine was ostensibly supposed to fight. This is one of the many reasons why it's important for all the Leftards out there to understand that this "vaccine" is very different in that it's not using weakened or dead virus in the injection.
Past vaccines of course have used weakened or dead virus and consequently, the immune response is IDENTICAL to actually encountering the live virus.
What they're referring to in this paper is the phenomenon of cytokine storms (inflammation) that's set off by the damn spike protein in this "vaccine". Inflammation destroys tissue and that's particularly bad when the inflammation is occurring in cardiac tissue (as we've seen with many young men after the jab) or brain tissue (or any organ for that matter).
and millions of dumb fucks will run right out and get it.
I'll wait for "Vaccine: Endgame" to come out before getting too invested in the series.
I already have the cure for the vaccine. DON’T TAKE IT!!!!!
All this talk about antibodies, why is noone talking about T-cells? They are responsible for clearing virus infected cells. They do this by checking the MHC1 molecules, present on every cell in the body. All cells produce proteins, and every last one of these proteins are transported to and presented on the MHC. This includes faulty cancer proteins, viral proteins, and spikeproteins produced by vaccine mRNA. What do all the experts think happens to the cells that take up the mRNA and produce spikeproteins?
lol