Scientists have issued a warning urging hospitals not to accept blood donations from people who have received the COVID-19 vaccine due to the presence of toxic and inorganic compounds in their blood.
Japanese scientists published a paper warning of the risks of using COVID-19-vaccinated blood for transfusions.
They are now calling on medical professionals to completely ban the vaccinated from donating blood.
“The health injuries caused by genetic vaccination are already extremely serious, and it is high time that countries and relevant organisations take concrete steps together to identify the risks and to control and resolve them,” they said.
The news comes amid reports of so-called genetic vaccines resulting in many suffering from thrombosis and subsequent cardiovascular damage, as well as diseases involving all organs and systems.
According to the paper, the risks associated with blood transfusions from vaccine recipients, including those who have received mRNA vaccines, could be catastrophic.
The researchers added, “It should also be stressed that the issues discussed here pertain to all organ transplants, including bone marrow transplants, and not just blood products.”
Table 1 of the paper outlines the six major concerns with blood products derived from gene vaccine recipients, Expose News reported.
See Below:
- Spike protein contamination
The spike protein, which is the antigen of SARS-CoV-2 and genetic vaccines, has already been found to have various toxicities, including effects on red blood cells and platelet aggregation, amyloid formation, and neurotoxicity. It is essential to recognise that the spike protein itself is toxic to humans. It has also been reported that the spike protein can cross the blood-brain barrier. Therefore, it is essential to remove the spike protein derived from the gene vaccine itself from blood products.
- Contamination with amyloid aggregates and microthrombi formed by spike proteins
It is not yet clear how the amyloid aggregates and microthrombi formed by the spike proteins develop into visible thrombi. However, once formed, amyloid aggregates may not be readily cleared and therefore need to be removed from blood products. These amyloid aggregates have also been shown to be toxic.
- Events attributable to decreased donor immune system and immune abnormalities due to immune imprinting or class switch to IgG4, etc. resulting from multiple doses of genetic vaccines
When the immune function of a donor is impaired by gene vaccination, there is a risk that the donor has some (subclinical) infectious disease or is infected with a pathogenic virus and has developed viremia or other conditions, even if the donor has no subjective symptoms. For this reason, healthcare professionals who perform surgical procedures, including blood sampling and organ transplantation, as well as using blood products, should manage the blood of genetic vaccine recipients with care to prevent infection through blood. It will also be necessary to inform all healthcare professionals of these risks.
- Lipid nanoparticles (“LNPs”) and pseudouridinated mRNA (mRNA vaccines only)
In the case of mRNA vaccines, LNPs and pseudouridinated mRNA may remain in the blood of recipients if blood is collected without a sufficient deferral period after gene vaccination. LNPs are highly inflammatory and have been found to be thrombogenic themselves, posing a risk to transfusion recipients. LNPs themselves have potent adjuvant activity and are at risk of inducing Adjuvant-Induced Autoimmune Syndrome (“ASIA syndrome”). An additional risk is that if the pseudouridinated mRNA is incorporated into the recipient’s blood while still packaged in LNPs, additional spike protein may be produced in the recipient’s body.
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- Contamination with aggregated red blood cells or platelets
The spike protein causes red blood cells and platelets to aggregate and therefore these aggregates will be carried into the recipient’s blood unless they are removed from the blood product.
- Memory B cells producing IgG4 and IgG4 produced from them
Large amounts (serum concentration typically above 1.25–1.4 g/L) of non-inflammatory IgG4-positive plasma cells can cause chronic inflammation such as fibroinflammatory disease.
IgG4 is an antibody and is the acronym for immunoglobulin G4. Earlier in the paper, the authors wrote that “long-term exposure to a specific identical antigen (in this case, spike protein) causes immunoglobulins to become IgG4 and some of the B cells [or lymphocytes] that produce them are likely to differentiate into memory B cells that survive in the body for a sustained period, the immune dysfunction of genetic vaccine recipients is expected to be prolonged (Table 1, point 3 & 6). More details on these points are expected to be revealed in the future.”
The researchers also make suggestions for specific tests, testing methods and regulations to deal with these risks.
In their conclusion, the authors wrote:
The impact of these genetic vaccines on blood products and the actual damage caused by them are unknown at present. Therefore, in order to avoid these risks and prevent further expansion of blood contamination and complication of the situation, we strongly request that the vaccination campaign using genetic vaccines be suspended and that a harm–benefit assessment be carried out as early as possible.
As we have repeatedly stated, the health injuries caused by genetic vaccination are already extremely serious, and it is high time that countries and relevant organisations take concrete steps together to identify the risks and to control and resolve them. Concerns regarding Transfusions of Blood Products Derived from Genetic Vaccine Recipients and Proposals for Specific Measures, Jun Ueda, Hideyuki Motohashi, Yuriko Hirai, Kenji Yamamoto, Yasufumi Murakami, Masanori Fukushima, Akinori Fujisawa, Non-peer reviewed version published 15 March 2024
