The cure is much worse than the soot
The cure is much worse than the soot
and
All injections with modRNA and LNP must be stopped and banned immediately
Explanation of the lack of antibody response to foreign glycoproteins.
We have always had difficulties in producing effective vaccines against infectious organisms that have glycoproteins on their surface. A glycoprotein consists of a protein with sugar molecules attached to cover part of its surface. We cannot make antibodies against sugar molecules or fats, but only against proteins.
This knowledge is old. Vaccine manufacturers have used various techniques to break down glycoproteins in order to inject viruses or bacteria with glycoproteins to make antibodies against the newly exposed inward-facing protein parts. This has rarely been successful, and the protection has not always been long-lasting, with often severe side effects from the vaccine.
Viruses such as the patented and thus man-made SARS-CoV-2, the natural viruses such as HIV, measles, RSV and avian flu, among others, have glycoproteins in their envelope proteins as the ultimate defense against the body's immune system, mainly antibodies.
Attempts to make protein vaccines against HIV since the discovery of the virus in the 1980s have failed to protect against infection by the virus, and these injections have caused severe side effects and even death. The same with RSV, measles and coronavirus.
This is because the viral spike protein is almost completely covered on the surface by sugar molecules, like tiles on a rooftop, and there are no protein parts exposed on the surface that antibodies can access. We must remember that antibodies are quite large in size and the sugar molecules are very dense.
If you break up the spike protein from, for example, the patented and thus human-engineered SARS-CoV-2 and inject it into a test subject, that person can form antibodies against certain parts of the inside of the spike protein and we get measurable and large amounts of antibodies against these inward-facing parts. But no antibodies against the sugar-coated outside.
These antibodies, despite measurably high levels, can not bind to the infectious virus inside, because the outside is covered with sugar molecules.
The antibodies have no protective effect on intact and therefore infectious virus particles. You risk getting sick from the infection because the antibodies cannot protect your body to attach to the viral recepton on the cell surface.
However, antibodies can bind to the inside of damaged virus particles. A damaged virus particle lacks infectivity.
Note that the artistic, artful and computer-generated images of the patented and thus human-engineered SARS-CoV-2 virus lack the clouds of sugar molecules that cover the outside of the spike proteins. If the sugar clouds were visualized or presented, then anyone could expose the fraud that the body could be able to form antibodies against the patented and thus man-made SARS-CoV-2 virus.
The body can produce very large amounts of antibodies against proteins that may have only a partial protective effect. This is called Antibody Dependent Enhancement [1] (ADE) when the body tries to defend itself with poorly functioning antibodies by producing more antibodies to try to compensate for poor efficacy.
It has been shown that the fragmented modRNA molecules can cause the cell to make parts of the spike protein, resulting in production of large amounts of completely undefined and unknown proteins.
The patented and thus man-made modRNA for the spike protein can remain for more than six months and produce more and more and more of the toxic, poisonous, hemagglutinating patented and thus man-made spike protein and fragments thereof. This results in even more production of poorly functioning antibodies and even more ADEs that can produce long protein complexes that look like worms in blood and lymph vessels.
In conclusion, the body cannot produce antibodies against viruses with glycoproteins on the outside of the virus.
A modRNA preparation cannot provide a protective effect against infection despite high antibody levels.
It produces the wrong antigens for the body to produce the wrong antibodies that are made and consumed and can form meter-long protein clots in blood and lymphatic vessels.
Then the body's immune system deteriorates within six months and these bioweapon injections increase the risk of severe illness and death caused by the patented and therefore man-made SARS-CoV-2.
The patented and therefore man-made modRNA is by definition a bioweapon and with sufficient knowledge in molecular biology, immunology and biochemistry we can immediately see that the cure is much worse than the soot:
All injections with modRNA and LNP must be stopped and banned immediately
Östervåla, June 2, 2024
Björn Hammarskjöld
Assistant Professor of Pediatrics at Strömstad Academy
Former consultant in pediatrics
Ph.D. in Biochemistry at Stockholm University (1971)
Molecular biologist
Virologist
References
Stephanie Seneff and Greg Nigh. Worse Than the Disease? Reviewing Some Possible Unintended Consequences of the mRNA Vaccines Against COVID-19. International Journal of Vaccine Theory, Practice, and Research 2(1), May 10, 2021. International Journal of Vaccine Theory, Practice, and Research 2(1), https://ijvtpr.com/index.php/IJVTPR/article/view/23