Jikkyleaks drops a bombshell inside the blood brain barrier crater

Ignasz Semmelweisz

March 24, 2023

Recap – Bombshell number one

Remember when it was assumed that any vaccine injected into the deltoid muscle remained local to the injection site, was transported to the localised lymph nodes (typically armpit and neck region) and thereby resulted in an immune response developing? Remember when it was assumed by the manufacturers but not proven that unaspirated, “Safe and Effective” i.e. non-toxic Covid gene therapy doses injected into the deltoid acted in the same way?

Remember when Dr. Byram Bridle, Vaccinologist from University of Guelph, Canada, gave a primer on vaccination in the context of SARS-CoV-2 and laid out key, lay accessible knowledge and concerns in the field?  (See link for article)

Important excerpts:

Enter, stage right, Jikkyleaks, the most scientifically industrious white mouse known to mankind….

In short, Lipid NanoParticles have been seen to and designed to get to and through the placenta, into placental cells fundamental to pregnancy and foetal viability, implantation and development. Certain published claims that this has been done with “no toxicity” appear to be potentially false, with data proving the falsehood having been deliberately hidden or obfuscated within published research data using specific methods of data handling, classification and presentation. Some of this data from various research, including manufacturers, indicates that foetus loss increases – in one study doubling – in correlation with Covid vaccination i.e. there are major signals that LNPs cross the placenta, get into foetuses at all stages of development and can lead to foetal loss at various stages of pregnancy, despite Male et al claiming “no toxicity” and “no evidence of” toxicity. Some of the foetal losses occur so early that they are literally ignored and not counted as foetal losses in some of the research, which goes on to claim “no toxicity” by virtue of effectively having deliberately not looked for toxicity in certain foetuses….

Remember when governments and Pharma did all the necessary tests into the effects on human fertility of Covid gene therapies, BEFORE they were deployed in humans across the globe? No? That’s because they never did any human fertility testing.

(See link for article)


McKernan: DNA Contamination in Covid Shots #Plasmidgate

Kevin McKernan’s discovered genetic material contaminants and it’s off the charts

Important excerpts:

This article aims to provide:

  • a lay summary of the first (ongoing) research into the genetic content of Pfizer and Moderna Covid gene therapies….

The vectors contain mammalian promoters, bacterial origins of replication in addition to the neomycin and kanamycin resistance genes. Circular plasmids like this are used for stable transfection and continued expression of genes in mammalian cells with the strong SV40 promoter.

    1. The contaminant is therefore the plasmids, which have bacterial origins (their manufacture employed E. Coli), can replicate and interact in mammalian and bacterial cells, and are resistant to neomycin and kanamycin antibiotics (used in fighting gut infections).

A quick estimate… equates to 1 vector for every 3,000 mRNAs. The Pfizer vials have an order of magnitude higher rates of contamination. This is consistent with the fragment analysis having more off-target peaks.

    1. McKernan has found contaminants in Moderna and Pfizer monovalent and bivalent gene therapy samples.

    2. McKernan initially estimated the ratio of contamination to desired, specified mRNA active ingredient in the Moderna shot as 1 DNA molecule to 3000 RNA molecules, and flagged that the Pfizer samples are an order of magnitude beyond this contamination level (1:350).

This is unequivocal evidence that the contaminating vector sequence is double stranded DNA and not RNA.

    1. McKernan confirms that the genetic material contaminant is DNA, and therefore cannot be some form of corruption of the final active mRNA ingredient.

Important takeaway:

Alden et al “show that BNT162b2 mRNA is reverse transcribed intracellularly into DNA in as fast as 6 h upon BNT162b2 exposure,” which means that through LINE-1 Reverse Transcription, mRNA payload could integrate with human DNA in human liver cancer cells. That work was done in vitro, and did not directly mean that the result would certainly occur in vivo in normal human liver or other cells.

But McKernan’s finding of massive plasmid contamination (which exceeds EMA specifications by several orders of magnitude) leads him to suspect that LINE-1 RT may not be necessary for plasmid dsDNA to integrate with human host DNA.  Further, even if dsDNA RT and integration does not occur, McKernan flags concerns about potential endotoxin levels in the form of lipopolysaccharides (LPS), which are the component of the outer membrane of gram-negative bacteria released into circulation upon distribution of the intact bacteria and which can cause septic reactions with symptoms like fever, hypotension, nausea, shivering and shock with serious complications such as disseminated intravascular coagulation (DIC), endotoxin shock and adult respiratory distress syndrome (ARDS). 

An injectable healthcare product such as a vaccine or intravenous solution must be sterile or free of live bacteria, but the manufacturing process to kill any bacteria can result in release of LPS or endotoxin into the product. Just as with a bacterial infection or sepsis, if sufficient endotoxin gets into our blood stream or spinal fluid we can develop fever, shock, and organ failure. In extreme cases, it can even result in death.

Patients have no idea what they were injected with, what it will do to them over time, and why they were allowed to be placed in this horrible position.



Startling Evidence Suggests BioNTech & Pfizer Falsified Western Blots used to evaluate the protein expression of the mRNA in HEK cells which suggests a “smoking gun”.  Independent experts have also noted the duplication of the results to secure EUA status of the injections; however, mainstream media is asleep at the wheel and not reporting on this epic scandal known on social media as #Blotgate.


This evidence means, if proven, Pfizer’s indemnity status would no longer apply.

The scandal leaves many questions including:

  1. How did the “copy and paste” data sail through the radar of the regulators?

  2. How did the Journal of Pharmaceutical Sciences publish the same fraudulent looking data presented in a Pfizer-funded paper, written by Pfizer and BioNTech’s employees (Patel et al.)?

  3. What proteins are being expressed in human cells from the vaccinal modified mRNA, other than the SARS-CoV-2 spike protein?

  4. Why has no genomic sequence of the expressed protein of the mRNA vaccine ever been published?

Trial Site News previously broke the scandal of the leaked European Medicines Agency emails and confidential Pfizer/BioNTech related documents, with an in-depth analysis and a follow up report which shows that key regulators were fully aware of the drop in RNA integrity to 55% in commercial batches compared to 78% in clinical batches. On top of this, alarming concern arose of the possibility of translate proteins other than the intended spike protein to occur.  Recently, French biostatistician Christine Cotton published a report on Pfizer’s trials where she found:

  • The FDA initially did not plan on showing Pfizer’s clinical trial data for 75 years until a judge ordered it be released within 8 months.  80,000 pages were released publicly in June, 2022 thanks to a FOIA lawsuit by 80 public health officers and researchers formed an alliance to get the data.
  • This is where Cotton comes in.  She found many biases in the documents including:
    • Pfizer’s 95% efficacy claim simply doesn’t hold true.
    • When the anti-nucleocapsid serology is taken into account, which determines who had COVID and who didn’t during the “vaccine” trials, efficacy falls from 95-55%.
    • Pfizer hid data on waning immunity for months, as millions queued to get the jab.  


    • Pfizer data also shows that the clinical tests on monkeys showed efficacy would only last up to 3 months.
    • Pfizer chose not to even measure the length of efficacy after the second shot.
    • If antibodies had been measured after the 2nd dose, it would have been known as early as 12/2020 efficacy falls quickly and there wouldn’t have been a single agency that would have granted authorization for a product that is supposedly a “vaccine.”
    • A German newspaper reported on several deaths among trial participants that occurred shortly after the injection but were excluded from the trial data.
    • Cotton states that by not not choosing the right criteria and not taking the right measurements at the right time, as well as not reporting adverse effects, Pfizer was able to give their pre-determined outcome: the shots are safe and effective.
    • Pfizer engaged in data manipulation which is fraudulent.

A former employee of the Ventavia Research Group — which conducted some of the clinical trials for the Pfizer-BioNTech COVID-19 vaccine blew the whistle over a year ago over Pfizer’s falsifying trial data by unblinding patients, employing inadequately trained “vaccinators,” being slow to follow up on adverse events, and allowing workers to be overwhelmed by the volume of problems including mislabeled specimens – including blood specimens and nasal swabs.  Despite a federal judge in Texas dismissing the lawsuit the whistleblower promises an appeal and calls the ruling:

“…. a despicable & heinous betrayal of justice, a slap in the face to vaccine injured and whistleblowers, a blatant example of corruption, incompetence and cowardice, a declaration that the powerful are above the law.”  Brook Jackson

According to the whistleblower’s complaint, the three companies “deliberately withheld crucial information from the United States that calls the safety and efficacy of their vaccine into question,” and as a result, they defrauded the U.S. government which purchased the vaccines.

The $3 Trillion dollar false claims lawsuit drives home that Pfizer was contracted to deliver a safe and effective vaccine to prevent SARS-CoV-2 infection. The injection delivers neither.

Pfizer cuts deals with the feds and has created shell companies to take the rap for their misdeeds, with a criminal plea that has allowed them to remain unscathed.  Further, internal company documents show that Pfizer uses a multimillion-dollar medical education budget to pay hundreds of doctors as speakers and consultants to serve as public relations spokespeople.

It’s important to note that a common tactic used by Big Pharma is to gaslight those injured by pharmaceuticals by using the plausibility sham of “evidence-based medicine,” and then insisting there is no data linking the injury to the drug or vaccine; however, these injuries are observed in clinical trials but are simply covered up to create the illusion it is“safe and effective.”

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