Judicial Watch has uncovered a study by Pfizer/BioNTech that found the lipid nanoparticles (LNP's) used in its Covid-19 vaccine left the injection site in test animals and moved to various organs of the body, including the liver, adrenal glands, spleen and ovaries. The LNPs were found to be present in the body eight to 48 hours after an injection.
Judicial Watch also has records from Johnson & Johnson showing that for their Covid-19 vaccine, they relied on studies where vaccine DNA particles and injected virus particles were still present in test animals months later.
Biodistribution is a method of tracking where compounds like LNPs travel in an experimental animal or human subject.
Judicial Watch announced its findings after receiving 466 pages of records from the Department of Health and Human Services (HHS) regarding biodistribution studies and related data for the Covid-19 vaccines.
The watchdog group also received 663 pages of records from HHS regarding biodistribution studies and related data for Johnson and Johnson Covid-19 vaccines.
The Johnson & Johnson records also showed that as part of its submission to the FDA for approval of its Covid vaccine, the company they did not include studies of the spike protein encoded in its vaccine.
The data was obtained through a Freedom of Information Act (FOIA) lawsuit Judicial Watch filed after the Food and Drug Administration, the Centers for Disease Control and Prevention and the National Institute of Allergy and Infectious Disease failed to respond to a June 8, 2021, FOIA request for "[A]ccess to biodistribution studies and related data for the Pfizer, Moderna, and Johnson & Johnson vaccines used to treat and/or prevent SARS-CoV-2 and/or Covid-19."
These documents show why many Americans have concerns about whether the novel Covid-19 vaccines that were developed at such an accelerated pace were tested properly and thoroughly.Tom Fitton, Judicial Watch President
The following is from Judicial Watch
Key Findings from Pfizer Data:
- The Pfizer records include a report which was approved in February 2021, on the animal trials on the distribution of the Pfizer Covid vaccine in rat subjects, in a section titled "Safety Pharmacology," the report notes, "No safety pharmacology studies were conducted with BNT162b2 [the BioNTech vaccine] as they are not considered necessary for the development of vaccines according to the WHO guideline (WHO, 2005)." Similarly, under "Pharmacodynamic Drug Interactions," is "Nonclinical studies evaluating pharmacodynamic drug interactions with BNT162b2 were not conducted as they are generally not considered necessary to support development and licensure of vaccine products for infectious diseases (WHO, 2005)."
- This Pfizer report notes that when lipid nanoparticles (LNPs) "with a comparable composition," to that used in the Pfizer Covid vaccine were injected into rats, "Total recovery (% of injected dose) of LNP outside the injection site was greatest in the liver and was much less in the spleen, adrenal glands, and ovaries." ... "in summary" ... "the LNP distributes to the liver." In the detailed analysis, the report states, "Over 48 hours, the LNP distributed mainly to liver, adrenal glands, spleen and ovaries, with maximum concentrations observed at 8-48 hours post-dose. Total recovery (% of injected dose) of LNP, for combined male and female animals, outside of the injection site was greatest in the liver (up to 18%) ..."
- This same Pfizer/BioNTech study notes "No genotoxicity studies are planned for BNT162b2 [the Pfizer/BioNTech Covid vaccine] as the components of the vaccine constructs are lipids and RNA and are not expected to have genotoxic potential (WHO, 2005)." Similarly, "Carcinogenicity studies with BNT162b2 have not been conducted as the components of the vaccine construct are lipids and RNA and are not expected to have carcinogenic or tumorigenic potential."
- The conclusion of the study begins: "The nonclinical program demonstrates that BNT162b2 is immunogenic in mice, rats, and nonhuman primates, and the toxicity studies support the licensure of this vaccine." The report notes that "boost immunizations" were also being tested on the animals in the trial. Also, "Vaccine-related microscopic findings at the end of dosing for BNT162b2 were evident in injection sites and surrounding tissues, in the draining iliac lymph nodes, bone marrow, spleen, and liver."
- Also included in the Pfizer records is a report approved in January 2021, titled "Pharmacokinetics Tabulated Summary." A table in the report shows the biodistribution of lipid nanoparticles containing mRNA used in the vaccine using rats as the clinical trial subjects reports LNPs accumulating after 48 hours, especially in the lymph nodes, ovaries, small intestine and spleen.
- A summary of a study approved in November 2020, of LNP mRNA distribution in rats, sponsored by Acuitas Therapeutics, notes that the concentrations of the LNP mRNA saw "levels peaking in the plasma by 1-4 hours post-dose and distribution mainly into liver, adrenal glands, spleen and ovaries over 48 hours. Total recovery of radioactivity outside of the injection site was greatest in the liver, with much lower total recovery in spleen, and very little recovery in adrenals glands and ovaries. The mean plasma, blood and tissue concentrations and tissue distribution patterns were broadly similar between the sexes and ... did not associate with red blood cells."
- A September 2020 "Confidential" appendix to the clinical trial studies submitted for the Pfizer/BioNTech Covid vaccine (BNT162b2), titled "Justification for the absence of studies in CTD Module 4 (part of 2.4)" notes under "Safety Pharmacology" that "No safety pharmacology studies were conducted as they are not considered necessary according to the WHO guideline (WHO, 2005)."
- And under "Pharmacodynamic Drug Interactions," is written: "Nonclinical studies evaluating pharmacodynamic drug interactions were not conducted as they are not generally considered necessary to support development and licensure of vaccine products for infectious diseases (WHO, 2005)."
- Under the heading "Genotoxicity," is: "No genotoxicity studies are planned for BNT162b2 as the components of the vaccine constructs are lipids and RNA that are not expected to have genotoxic potential (WHO, 2005)."
Regarding "Carcinogenicity (including supportive toxicokinetics evaluations)" is written:
- Carcinogenicity studies with BNT162b2 have not been conducted as the components of the vaccine constructs are lipids and RNA that are not expected to have carcinogenic or tumorigenic potential. Carcinogenicity testing is generally not considered necessary to support the development and licensure of vaccine products for infectious diseases (WHO, 2005).
- In a "Confidential" Pfizer study approved in April 2020, looking at four Covid vaccine variants, the company tested a vaccine with an RNA strand "that self-amplifies upon entering the cell." It "encodes the Venezuelan equine encephalitis (VEE) virus RNA-dependent RNA polymerase (RDRP or replicase)."
- In the same Pfizer study, the authors note that, "Although liver function tests will be carefully monitored during the clinical development of these vaccines, BioNTech's prior clinical experience indicates that the distribution to the liver does not pose a safety concern."
Also, the Pfizer study authors note, "Based on previous nonclinical and clinical experience with the three RNA platforms, a beneficial safety profile is anticipated, and may include transient local reactions (such as swelling/edema or redness) and body temperature increases."
Key Findings from Johnson & Johnson Data:
- The Johnson & Johnson records include a 2007 study of the biodistribution of an intramuscular-administered adenovector-based viral vaccine using New Zealand white rabbits, which showed that the vaccine accumulated in "the spleen, iliac lymph node, and the muscle at the site of injection."
- A biodistribution table included as an appendix to the 2007 rabbit study showed that the vaccine DNA particles were still present in the iliac lymph nodes 91 days after injection.
- A chart of pharmacokinetics data from a November 2020 report of a study on "VAC31518 JNJ-78436735," the Johnson & Johnson vaccine, on rabbits shows collection of the injected virus particles in the spleen and iliac lymph nodes up to three months later, as well as particles found in the skin and muscle at the injection site.
- In a November 4, 2020, report submitted to the FDA regarding the Johnson & Johnson Covid vaccine, the authors discuss the 2007 New Zealand rabbit study in which adenovirus-vectored vaccine is trialed, but note that "No pharmacokinetic or biodistribution studies have been conducted with AD26.COV2.S specifically."
- The report notes that metabolism, excretion, and pharmacokinetic interactions with other drugs were not studied in this trial because they are "Not applicable to vaccines." It is also noted that "biodistribution studies have not been conducted with Ad26.COV2.S."
- A table in the report shows that the vaccine virus continued to appear in the rabbits' iliac lymph nodes 180 days after injection.
A June 2020 "Pharmacokinetics Written Summary for the Johnson & Johnson Covid-19 vaccines notes that:
- Ad26COVS1 (also known as VAC31518 or JNJ-78436735) is a monovalent, recombinant replication-incompetent adenovirus type 26 (Ad26) vectored vaccine encoding a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Spike protein.... No specific pharmacokinetic studies have been performed with Ad26COVS1. However, to assess distribution, persistence, and clearance of the Ad26 vector (platform), biodistribution studies were conducted in rabbits using two other Ad26-based vaccines encoding [redacted] and [redacted] antigens.... [T]he available biodistribution results are considered sufficient to inform on the biodistribution profile of Ad26COVS1, for which the same Ad26 vector backbone is used.
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Bill Andrews says
This Article ? What would be interesting Study in this articles different vaccines Lipids, is to see How Johnson and Johnson Vaccine against other vaccine makers in 5 out of 5 people, with a History of High Cholesterol levels with the Data mentioned above ??? Results ? Is these types of people data vary and or show a more elevated tumorigenic potential metabolic reactions with Higher Cholesterol Cell's activities in some people, and or causing future organ and High blood pressure future side effects in some people and or related Heart problems = ?? The unknown Medical data X Files ? Footnote: A live medical test rat is a good living metabolic vaccine cell test subject, but they don't have the more complex different Human genetics X > X-Y Chromosome activity...Examples: China people, Korean , African and so on ? I think some Covid long haulers themselves may end up with High blood pressure and or inflammation problems from getting the Virus in some people ...?
They use the enzyme Lucifer-ace also for tracking.