Does the spike protein from mRNA technology based COVID gene injection cause inflammation and immune activation? Yes, Khan et al. & Robles et al. present evidence e.g. inflammation of TLR2-Dependent
Does the spike protein from mRNA technology based COVID gene injection cause inflammation and immune activation? Yes, Khan et al. & Robles et al. present evidence e.g. inflammation of TLR2-Dependent
the video speaks in spanish but has English subtitles the President of COMUSAV Mexico Dr. Pedro Chavez Zavala, M.D.
"The first part of this experiment was preformed outdoors on "vaccinated" people, and it was done in this way so there would be no external influence of a bluetooth signal"
COMUSAV doctors also in, Switzerland Dr. h.c. Andrea Ludwig Kalcker talks about the shot inducing magnetism. Dr. h.c. Manuel Aparicio Alonso states "I sincerely could have never imagined that through an experimental inoculation would've been presence of nanotechnology, graphene, frequencies.", Professor Pablo Campra, Ph.D. "...he proved the presence of "graphene" in the vials", and Dr Pedro Chavez Zavala, M.D. proves "the inoculated emit frequencies".
It's the same video footage used in the "Final Days" video, watch for yourselves and decide,
In the new final days video by Stew Peters Karen Kingston Biotech Analyst and Med-Legal Advisor with over 25 years in the pharmaceutical, Medical Device, as Biotech Industries, and she has shown the capabilities and proven in the Patents of which I have copies of and looked in them on the pages she has shown on several interviews and paused each time to be sure where to find the info. In this movie at about the 38:45 mark is where she starts delving into the Moderna patents US 10, 703, 789 B2
and the "MODIFIED POLYNUCLEOTIDES FOR THE PRODUCTION OF SECRETED PROTEINS"
she states is one of the master patents for the mRNA so called vaccines and in the
( 57 ) ABSTRACT
A pharmaceutical composition which has a plurality of lipid nanoparticles that has a mean particle size of between 80 nm and 160 nm and contains a modified mRNA encoding a polypeptide . The lipid nanoparticles include a cationic lipid , a neutral lipid , a cholesterol , and a PEG lipid . The mRNA contains a 5 ' - cap , 5 ' - UTR , N1 - methyl - pseudouridine , a
3 ' - UTR , and a poly - A region with at least 100 nucleotides .
She says "what they are calling a "lipid" hosts cationic charges they host electromagnetic fields" She says "they are using the term "LIPID" instead of "Nonotechnology"," She then cites this site (my 1 free view for the month so keep it open and get a screen shot before closing)
" Without these lipid shells, there would be no mRNA vaccines for COVID-19"
"Fragile mRNA molecules used in COVID-19 vaccines can’t get into cells on their own. They owe their success to lipid nanoparticles that took decades to refine"
"The success of these COVID-19 vaccines is remarkable and was far from guaranteed. mRNA is incredibly delicate. Enzymes in the environment and in our bodies are quick to chop mRNA into pieces, making lab experiments difficult and the delivery of mRNA to our cells daunting. On top of that, mRNA strands are large and negatively charged and can’t simply waltz across the protective lipid membranes of cells. Many scientists thought the technology would never work." (We might like the names of all the scientists involved thank you very much)
"LNPs used in the COVID-19 vaccines contain just four ingredients: ionizable lipids whose positive charges bind to the negatively charged backbone of mRNA, pegylated lipids that help stabilize the particle, and phospholipids and cholesterol molecules that contribute to the particle’s structure. Thousands of these four components encapsulate mRNA, shield it from destructive enzymes, and shuttle it into cells, where the mRNA is unloaded and used to make proteins. Although the concept seems simple, perfecting it was far from straightforward."
"It is a tremendous vindication for everyone working in controlled drug delivery.
Robert Langer, chemical engineer, Massachusetts Institute of Technology"
"The devil is absolutely in the details as far as LNPs are concerned.
Giuseppe Ciaramella, former head of infectious diseases, Moderna"
"Cullis knew that adding positively charged lipids to the liposomes would help balance the negatively charged nucleic acids, but there was a problem. “There are no cationic lipids in nature,” Cullis says. “And we knew we couldn’t use permanently positively charged lipids because they are so damn toxic.” Those lipids would rip cell membranes apart, he adds."
"Pegylated lipids, in which polyethylene glycol (PEG) strands are attached to lipid heads, have several functions in a nanoparticle. PEG helps control the particle size during formulation, prevents the particles from aggregating in storage, and initially shields the particles from being detected by immune system proteins in the body, according to James Heyes, a former Protiva scientist. Heyes is now chief scientific officer of the LNP company Genevant Sciences—a firm with origins in Protiva.
But PEG also has liabilities. It prevents LNPs from binding to proteins that help shuttle them into cells. Because PEG extends particles’ life span in the body, the immune system has more time to spot the particles and start mounting an antibody response. And although PEG is found in many cosmetic, drug, and food products, scientists hypothesize that some people could develop antibodies to PEG and that giving those individuals an injection of PEG-coated nanoparticles could trigger an anaphylactic reaction."
"But PEG also has liabilities. It prevents LNPs from binding to proteins that help shuttle them into cells. Because PEG extends particles’ life span in the body, the immune system has more time to spot the particles and start mounting an antibody response." .... "And although PEG is found in many cosmetic, drug, and food products, scientists hypothesize that some people could develop antibodies to PEG and that giving those individuals an injection of PEG-coated nanoparticles could trigger an anaphylactic reaction." (Sound familiar?)
Then she sites the passage in section 219 of the above patent which is on page 129
"In another embodiement, the polymer-based self-assembled nanoparticles such as, but not limited to, micro-sponges, may be fully programmable nonoparticles." she says it's alarming "because they can be preporgammable as well as receive programs from an external source
TLR2 is indicated in Stills Disease. AOSD was once rare, at about 2 per million. Now it's becoming more common. Pfizer developed a spike protein vaccine in the late 80s. 1991 was when soldiers came down with Gulf War Syndrome. It was eventually attributed (after much denial & blame on exposure to war related chemicals) on the Anthrax vaccine. But, IMO, that was a cover up. Civilians also got sick at the same time with autoimmune inflammatory disorders. By blaming anthrax vaccine, they contained the fallout to military only. Pfizer dropped their spike protein vaccine research like a hot potato back then. Why?
What would be the purpose of a substance that can invade your cells? To promote healthier cells? There are NO drugs, NO vaccines and NO mRNA substances on the planet that can improve your health better than what your body can do.
Thank-you for finding what resources and articles you can to inform the public. It is important to keep this information out in the public domain. As a public, we should not have compliance to the game. Compliance is about keeping our mouths shut and not asking questions. It is about not saying no. It is about not telling people what you are learning.
Now for the part on the MAC addresses and I've found the video from the source, not just the parts in "Final Days" at
https://www.comusav.com/bluetruth/
the video speaks in spanish but has English subtitles the President of COMUSAV Mexico Dr. Pedro Chavez Zavala, M.D.
"The first part of this experiment was preformed outdoors on "vaccinated" people, and it was done in this way so there would be no external influence of a bluetooth signal"
COMUSAV doctors also in, Switzerland Dr. h.c. Andrea Ludwig Kalcker talks about the shot inducing magnetism. Dr. h.c. Manuel Aparicio Alonso states "I sincerely could have never imagined that through an experimental inoculation would've been presence of nanotechnology, graphene, frequencies.", Professor Pablo Campra, Ph.D. "...he proved the presence of "graphene" in the vials", and Dr Pedro Chavez Zavala, M.D. proves "the inoculated emit frequencies".
It's the same video footage used in the "Final Days" video, watch for yourselves and decide,
https://rumble.com/v2r004k-final-days-worldwide-premiere.html?mref=6zof&mrefc=2
In the new final days video by Stew Peters Karen Kingston Biotech Analyst and Med-Legal Advisor with over 25 years in the pharmaceutical, Medical Device, as Biotech Industries, and she has shown the capabilities and proven in the Patents of which I have copies of and looked in them on the pages she has shown on several interviews and paused each time to be sure where to find the info. In this movie at about the 38:45 mark is where she starts delving into the Moderna patents US 10, 703, 789 B2
https://assets.modernatx.com/m/197fe68e2047ca6a/original/US10703789.pdf
and the "MODIFIED POLYNUCLEOTIDES FOR THE PRODUCTION OF SECRETED PROTEINS"
she states is one of the master patents for the mRNA so called vaccines and in the
( 57 ) ABSTRACT
A pharmaceutical composition which has a plurality of lipid nanoparticles that has a mean particle size of between 80 nm and 160 nm and contains a modified mRNA encoding a polypeptide . The lipid nanoparticles include a cationic lipid , a neutral lipid , a cholesterol , and a PEG lipid . The mRNA contains a 5 ' - cap , 5 ' - UTR , N1 - methyl - pseudouridine , a
3 ' - UTR , and a poly - A region with at least 100 nucleotides .
She says "what they are calling a "lipid" hosts cationic charges they host electromagnetic fields" She says "they are using the term "LIPID" instead of "Nonotechnology"," She then cites this site (my 1 free view for the month so keep it open and get a screen shot before closing)
https://cen.acs.org/pharmaceuticals/drug-delivery/Without-lipid-shells-mRNA-vaccines/99/i8
" Without these lipid shells, there would be no mRNA vaccines for COVID-19"
"Fragile mRNA molecules used in COVID-19 vaccines can’t get into cells on their own. They owe their success to lipid nanoparticles that took decades to refine"
"The success of these COVID-19 vaccines is remarkable and was far from guaranteed. mRNA is incredibly delicate. Enzymes in the environment and in our bodies are quick to chop mRNA into pieces, making lab experiments difficult and the delivery of mRNA to our cells daunting. On top of that, mRNA strands are large and negatively charged and can’t simply waltz across the protective lipid membranes of cells. Many scientists thought the technology would never work." (We might like the names of all the scientists involved thank you very much)
"LNPs used in the COVID-19 vaccines contain just four ingredients: ionizable lipids whose positive charges bind to the negatively charged backbone of mRNA, pegylated lipids that help stabilize the particle, and phospholipids and cholesterol molecules that contribute to the particle’s structure. Thousands of these four components encapsulate mRNA, shield it from destructive enzymes, and shuttle it into cells, where the mRNA is unloaded and used to make proteins. Although the concept seems simple, perfecting it was far from straightforward."
"It is a tremendous vindication for everyone working in controlled drug delivery.
Robert Langer, chemical engineer, Massachusetts Institute of Technology"
"The devil is absolutely in the details as far as LNPs are concerned.
Giuseppe Ciaramella, former head of infectious diseases, Moderna"
"Cullis knew that adding positively charged lipids to the liposomes would help balance the negatively charged nucleic acids, but there was a problem. “There are no cationic lipids in nature,” Cullis says. “And we knew we couldn’t use permanently positively charged lipids because they are so damn toxic.” Those lipids would rip cell membranes apart, he adds."
"Pegylated lipids, in which polyethylene glycol (PEG) strands are attached to lipid heads, have several functions in a nanoparticle. PEG helps control the particle size during formulation, prevents the particles from aggregating in storage, and initially shields the particles from being detected by immune system proteins in the body, according to James Heyes, a former Protiva scientist. Heyes is now chief scientific officer of the LNP company Genevant Sciences—a firm with origins in Protiva.
But PEG also has liabilities. It prevents LNPs from binding to proteins that help shuttle them into cells. Because PEG extends particles’ life span in the body, the immune system has more time to spot the particles and start mounting an antibody response. And although PEG is found in many cosmetic, drug, and food products, scientists hypothesize that some people could develop antibodies to PEG and that giving those individuals an injection of PEG-coated nanoparticles could trigger an anaphylactic reaction."
"But PEG also has liabilities. It prevents LNPs from binding to proteins that help shuttle them into cells. Because PEG extends particles’ life span in the body, the immune system has more time to spot the particles and start mounting an antibody response." .... "And although PEG is found in many cosmetic, drug, and food products, scientists hypothesize that some people could develop antibodies to PEG and that giving those individuals an injection of PEG-coated nanoparticles could trigger an anaphylactic reaction." (Sound familiar?)
Then she sites the passage in section 219 of the above patent which is on page 129
"In another embodiement, the polymer-based self-assembled nanoparticles such as, but not limited to, micro-sponges, may be fully programmable nonoparticles." she says it's alarming "because they can be preporgammable as well as receive programs from an external source
TRUDEAU COMMITTED GENOCIDE https://rumble.com/v2868vw-the-university-of-british-columbia-exposed.html?fbclid=IwAR03t3VqCcK5bOPTjjI8-U2nF3P-jBLE2CANjQJxXmvg3BlJo5Z-Y8t0RjE
What is the Treatment suggested here. Example? Normal plain English?
Thx
UNITE WITH GOD AND LIKE MINDED FOR YOUR HEALTH NOW AND FUTURE
TLR2 is indicated in Stills Disease. AOSD was once rare, at about 2 per million. Now it's becoming more common. Pfizer developed a spike protein vaccine in the late 80s. 1991 was when soldiers came down with Gulf War Syndrome. It was eventually attributed (after much denial & blame on exposure to war related chemicals) on the Anthrax vaccine. But, IMO, that was a cover up. Civilians also got sick at the same time with autoimmune inflammatory disorders. By blaming anthrax vaccine, they contained the fallout to military only. Pfizer dropped their spike protein vaccine research like a hot potato back then. Why?
What would be the purpose of a substance that can invade your cells? To promote healthier cells? There are NO drugs, NO vaccines and NO mRNA substances on the planet that can improve your health better than what your body can do.
Thank-you for finding what resources and articles you can to inform the public. It is important to keep this information out in the public domain. As a public, we should not have compliance to the game. Compliance is about keeping our mouths shut and not asking questions. It is about not saying no. It is about not telling people what you are learning.
Is there a mammalian tissue that wouldn't be inflamed by being poked by a spear-like protein?