/sci/ - Science & Math

https://www.medrxiv.org/content/10.1101/2021.05.03.21256520v1
The mRNA-based BNT162b2 vaccine from Pfizer/BioNTech was the first registered COVID-19 vaccine and has been shown to be up to 95% effective in preventing SARS-CoV-2 infections. Little is known about the broad effects of the new class of mRNA vaccines especially whether they have combined effects on innate and adaptive immune responses
Here we confirmed that BNT162b2 vaccination of healthy individuals induced effective humoral and cellular immunity against several SARS-CoV-2 variants. Interestingly however the BNT162b2 vaccine also modulated the production of inflammatory cytokines by innate immune cells upon stimulation with both specific (SARS-CoV-2) and non-specific (viral, fungal &bacterial) stimuli. The response of innate immune cells to TLR4 and TLR7/8 ligands was lower after BNT162b2 vaccination while fungi-induced cytokine responses were stronger. In conclusion the mRNA BNT162b2 vaccine induces complex functional reprogramming of innate immune responses which should be considered in the development and use of this new class of vaccines.

In other words, the immune system becomes depressed against viruses and bacteria and intensifies against fungi. Plus, once you create an adaptive immune response, the body tends to rely on it over innate immunity. So, for example, when a person who is vaccinated encounters a current variant, their immune system will respond with antibodies generated from the original Wuhan strain. Unfortunately these are not a good match. So the immune system will pump out a bunch of antibodies that fail to bind properly to the virus while suppressing IgM and killer T cells. This will allow the virus to continue replicating

Take deferoxamine instead to combat COVID
COVID through endolysosomal deacidification causes iron disbiosys within the brain via release of hepcidin through downregulation of FPN1 and upregulation of DMT1. Iron-induced ROS is responsible for COVID brain damage

https://www.medrxiv.org/content/10.1101/2021.05.03.21256520v1
The mRNA-based BNT162b2 vaccine from Pfizer/BioNTech was the first registered COVID-19 vaccine and has been shown to be up to 95% effective in preventing SARS-CoV-2 infections. Little is known about the broad effects of the new class of mRNA vaccines especially whether they have combined effects on innate and adaptive immune responses. Here we confirmed that BNT162b2 vaccination of healthy individuals induced effective humoral and cellular immunity against several SARS-CoV-2 variants. Interestingly however the BNT162b2 vaccine also modulated the production of inflammatory cytokines by innate immune cells upon stimulation with both specific (SARS-CoV-2) and non-specific (viral, fungal &bacterial) stimuli. The response of innate immune cells to TLR4 and TLR7/8 ligands was lower after BNT162b2 vaccination while fungi-induced cytokine responses were stronger. In conclusion the mRNA BNT162b2 vaccine induces complex functional reprogramming of innate immune responses which should be considered in the development and use of this new class of vaccines.

In other words, the immune system becomes depressed against viruses and bacteria and intensifies against fungi. Plus, once you create an adaptive immune response, the body tends to rely on it over innate immunity. So, for example, when a person who is vaccinated encounters a current variant, their immune system will respond with antibodies generated from the original Wuhan strain. Unfortunately these are not a good match. So the immune system will pump out a bunch of antibodies that fail to bind properly to the virus while suppressing IgM and killer T cells. This will allow the virus to continue replicating

Take deferoxamine instead to combat COVID
COVID through endolysosomal deacidification causes iron disbiosys within the brain via release of hepcidin through downregulation of FPN1 and upregulation of DMT1. Iron-induced ROS is responsible for COVID brain damage

https://www.medrxiv.org/content/10.1101/2021.05.03.21256520v1
The mRNA-based BNT162b2 vaccine from Pfizer/BioNTech was the first registered COVID-19 vaccine and has been shown to be up to 95% effective in preventing SARS-CoV-2 infections. Little is known about the broad effects of the new class of mRNA vaccines, especially whether they have combined effects on innate and adaptive immune responses. Here we confirmed that BNT162b2 vaccination of healthy individuals induced effective humoral and cellular immunity against several SARS-CoV-2 variants. Interestingly, however, the BNT162b2 vaccine also modulated the production of inflammatory cytokines by innate immune cells upon stimulation with both specific (SARS-CoV-2) and non-specific (viral, fungal and bacterial) stimuli. The response of innate immune cells to TLR4 and TLR7/8 ligands was lower after BNT162b2 vaccination, while fungi-induced cytokine responses were stronger. In conclusion, the mRNA BNT162b2 vaccine induces complex functional reprogramming of innate immune responses, which should be considered in the development and use of this new class of vaccines.

In other words, the immune system becomes depressed against viruses and bacteria, and intensifies against fungus. In addition, once you create an adaptive immune response, the body tends to rely on it over innate immunity. So, for example, when a person who is vaccinated encounters a current variant, their immune system will respond with antibodies generated from the original Wuhan strain. Unfortunately these are not a good match. So the immune system will pump out a bunch of antibodies that fail to bind properly to the virus, while suppressing IgM and killer T cells. This will allow the virus to continue replicating.

>>14652123
> I just wanted to say I highly appreciate your research. You are definitely onto something, and I say that after having skimmed through many of the studies you have posted.

Thanks!
> the well has been poisoned too much already.

We've come far in the past week and I see all of the support, the threads on deferoxamine made by so many different imposters it feels kind of appropriate to say that we've created a reality where there's people that impersonate me and almost blindly go through all efforts to share my research I believe we're past the point of contention. There's about 12 of us and we report amazing improvements in our heath and cognition. My memory is as good as you might possibly imagine and improvements in all cognitive domains including hearing and eyesight.My reaction time is significantly better, I don't experience sadness or anxiety whatsoever. If i can summarize everything in one sentence we just feel life more!

I can say its everything I've gotten from researching for 8 years its insane how its possible for me to learn as much as i now know like the back of my hand.

I hope its been entertaining. The imposters have little credibility and people see through that.

>>14594499
>How do we fix the concept of money so it works with us instead of against us?

>Be western governments
>Give monopolistic privilege to multinational corporations
>Enforce subsidies on oil and food production
>create inefficiencies in the market that perpetuate established monopolies
>tax the populace and perpetuate fractional reserve banking to promote the accumulation of wealth into said monopolistic corporations
>dont enforce antitrust laws
>dont evoke medicare for all
>dont enact prescription drug pricing reforms
>Have a global pandemic from mismanaged government resources towards maintaining economic activity at all costs
>Great reset
>give blank checks to multinational drug companies
>Vaccines remain intellectual property of drug companies
>variants come out of poor countries without sufficient access to vaccines
>Covid becomes endemic
>Scientists and politicians race for a solution
>Find a drug that treats most metabolic and neurological disorders
>make it cheap
>mass awakening
>IQ explosion
>singularity