A team of Japanese researchers analyzed blood transfusions taken from
individuals who were previously inoculated with COVID-19 vaccines. The
researchers found that experimental COVID-19 vaccines destroy the continuity and biochemistry of human blood
in six key areas. The vaccine damage is so significant; the
contaminated blood can further damage unvaccinated and vaccinated people
who receive blood transfusions or organ transplants from the
vaccinated. The researchers published a pre-print paper on their findings and make suggestions for specific tests, testing methods and regulations to help deal with these risks.
Now the researchers are sounding the alarm about serious risks
associated with using blood from people inoculated with COVID-19
vaccines. They are calling on the global medical community to put an end
to these products.
“The health injuries caused by genetic vaccination
are already extremely serious, and it is high time that countries and
relevant organizations take concrete steps together to identify the
risks and to control and resolve them,” the researchers wrote.
Six areas of blood contamination caused by COVID-19 vaccines
There are six key areas of blood contamination from vaccinated blood that researchers are concerned about:
One: Spike protein contamination
All covid-19 vaccines are designed to hijack the normal protein
synthesis of the cell and transcribe foreign spike proteins that are
modeled after the original SARS-CoV-2 bioweapon. The vaccine
manufacturers originally promised that the spike protein would be
quickly neutralized in the deltoid muscles; however, researchers have
documented the persistence of the spike proteins in the blood and their
accumulation in distal organs. Therefore, these spike proteins have
exhibited various toxicities, including cardio-toxic effects on red
blood cells, platelet aggregation and amyloid formation. Blood products
derived from these vaccines should be purified to remove all spike
protein cardio-toxins.
Two: Amyloid aggregates and microthrombi formed by spike proteins
In some cases, the human immune system does not neutralize the spike
proteins that are generated by the COVID-19 vaccines. This allows the
spike protein to persist and cause further adverse reactions. These
reactions may include the formation of amyloid aggregates and
microthrombi. Once these amyloid aggregates are formed, they are not
easily cleared and pose further health issues throughout the body. To
ensure that blood products and organ transplants are safe, these amyloid
aggregates must also be cleared from the contaminated blood.
Low levels of immunoglobulins
Multiple doses of COVID-19 vaccines prime the human immune system for failure through antibody dependent enhancement.
Blood donated from heavily-vaccinated individuals may provide
inadequate levels of immunity to common infections due to immune
imprinting or class switch to IgG4. In these cases, a blood donor with
an impaired immune system may spread sub-clinical infectious disease to
the blood recipient. Healthcare professionals must now use caution to
prevent infection and further harm to immune-compromised individuals due
to tainted blood transfusions and organs derived from vaccinated
individuals.
Lipid nanoparticles and pseudouridinated mRNA
The mRNA vaccines use lipid nanoparticles (LNPs) and pseudouridinated
mRNA that can linger in the blood long after injection. Healthcare
professionals must be cautious when using blood from recently vaccinated
individuals. A sufficient deferral period should be observed after
vaccination to ensure that blood recipients are not receiving
transfusions that still contain lipid nanoparticles. The LNPs are
inflammatory and may cause thrombogenic reactions.
Moreover, the pseudouridinated mRNA, encapsulated by the LNPs, may
cause runaway spike protein synthesis in random areas of the body.
Aggregated red blood cells
A contaminated blood product may contain aggregated red blood cells
or platelets. This is one of the side effects of the spike protein. If
these aren’t removed before a transfusion, a blood or organ recipient
could suffer blood clots and other cardiovascular events.
Memory B cells generating IgG4
The long-term exposure to specific antigens (the vaccine’s spike
protein) can cause immunoglobulins to become IgG4 antibodies.
Furthermore, this overexposure to an identical antigen can force some B
cells to differentiate into memory B cells that circulate in the body
for a sustained period. The influx of IgG4-positive plasma cells can
cause chronic inflammation. This can cause immune dysfunction over a
longer period of time.
The COVID-19 vaccines not only
harm the recipient, but they can also transfer problems to blood and
organ recipients. Individuals who once vaccinated for the “good of all”
have only tainted the blood supply of the human race — putting
vulnerable people in harm’s way.
(Article by Lance D Johnson republished from NaturalNews.com)
Click this link for the original source of this article.
Author: Planet Today
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