In the video1
above, Dr. Steven E. Greer interviews microbiologist Kevin McKernan — a
former researcher and team leader for the MIT Human Genome project2 — and Dr. Sucharit Bhakdi about the DNA contamination McKernan’s team has found in the Pfizer and Moderna mRNA shots.
As it turns out, spike protein and the mRNA are not the only hazards
of these injections. McKernan’s team have also discovered simian virus
40 (SV40) promoters that, for decades, have been suspected of causing
cancer in humans, including mesotheliomas, lymphomas and cancers of the
brain and bone.3 The findings4,5,6,7 were posted on OSF Preprints in early April 2023. As explained in the abstract:8
“Several methods were deployed to assess the nucleic
acid composition of four expired vials of the Moderna and Pfizer
bivalent mRNA vaccines. Two vials from each vendor were evaluated ...
Multiple assays support DNA contamination that exceeds the European
Medicines Agency (EMA) 330ng/mg requirement and the FDAs 10ng/dose
requirements ...”
As noted by Greer,9
this means that governments and drug companies “have misled the world
to a far greater extent than previously known.” If these findings are
correct, it would also mean that “the so-called ‘vaccines’ are actually
altering the human genome and causing permanent production of the deadly
spike protein,” and this internal production of spike protein would, in
turn, “trigger the immune system to attack its own cells,” Greer says.
In the interview, McKernan explains
how the DNA contaminants found in the COVID jabs can result in the
genetic modification of the human genome, and Bhakti reviews how and why
the shots can trigger autoimmune diseases.
Background: What Is SV40?
In 2002, the Lancet published10
evidence linking polio vaccines contaminated with SV40 to Non-Hodgkin's
lymphoma. According to the authors, the vaccine may be responsible for
up to half the 55,000 Non-Hodgkin's lymphoma cases diagnosed each year.
How did this simian (monkey) virus get into the human population?
According to the late Dr. Maurice Hilleman, a leading vaccine developer,
Merck inadvertently unleashed the virus via their polio vaccine.11
It’s unclear exactly when SV40 was eliminated from the polio vaccine.
The timing also varies from country to country. For example,
SV40-contaminated polio vaccines were administered in Italy as recently
as 1999.12
As reported in a Lancet book review of “The Virus and the Vaccine:
The True Story of a Cancer-Causing Money Virus, Contaminated Polio
Vaccine and the Millions of Americans Exposed”:13
“By 1960, scientists and vaccine manufacturers knew
that monkey kidneys were sewers of simian viruses. Such contamination
often spoiled cultures, including those of an NIH researcher named
Bernice Eddy, who worked on vaccine safety ... Her discovery ...
threatened one of the USA's most important public-health programs ...
Eddy tried to get word out to colleagues but was
muzzled and stripped of her vaccine regulatory duties and her laboratory
... [Two] Merck researchers, Ben Sweet and Maurice Hilleman, soon
identified the rhesus virus later named SV40 — the carcinogenic agent
that had eluded Eddy.
In 1963, U.S. authorities decided to switch to
African green monkeys, which are not natural hosts of SV40, to produce
polio vaccine. In the mid-1970s, after limited epidemiological studies,
authorities concluded that although SV40 caused cancer in hamsters, it
didn't seem to do so in people.
Fast forward to the 1990s: Michele Carbone, then at
NIH, was working on how SV40 induces cancers in animals. One of these
was mesothelioma, a rare cancer of the pleura thought in people to be
caused mainly by asbestos. The orthodoxy held that SV40 didn't cause
human cancers.
Emboldened by a 1992 NEJM paper that found DNA
‘footprints’ of SV40 in childhood brain tumors, Carbone tested human
mesothelioma tumor biopsies at the National Cancer Institute: 60%
contained SV40 DNA. In most, the monkey virus was active and producing
proteins.
He published his results in Oncogene in May, 1994,
but the NIH declined to publicize them ... Carbone ... moved to
Loyola University. There he discovered how SV40 disables tumor
suppressor genes in human mesothelioma, and published his results in
Nature Medicine in July, 1997. Studies in Italy, Germany, and the USA
also showed associations between SV40 and human cancers.”
mRNA COVID Jabs Contaminated With Double-Stranded DNA
With that background, let’s get back to McKernan’s findings, which in
addition to the featured video are also discussed in Daniel Horowitz’s
podcast above. In short, his team discovered elevated levels of
double-stranded DNA plasmids, including SV40 promoters (DNA sequence
that is essential for gene expression) that are known to trigger cancer
development when encountering an oncogene (a gene that has the potential
to cause cancer).
The level of contamination varies depending on the platform used to
measure it, but no matter which method is used, the level of DNA
contamination is significantly higher than the regulatory limits in both
Europe and the U.S., McKernan says. The highest level of DNA
contamination found was 30%, which is rather astounding.
As explained by McKernan, when using a typical PCR test, you’ll be
considered positive if the test detects the SARS-CoV-2 virus using a
cycle threshold (CT) of about 40. In comparison, the DNA contamination
is detected at CTs below 20.
That means the contamination is a million-fold greater than the
amount of virus you’d need to have in order to test positive for COVID.
“So, there’s an enormous difference here with regards to the amount of
material that’s in there,” McKernan says.
In his Substack article,14
he also points out that people who argue that double-stranded DNA and
viral RNA is a false equivalency because viral RNA is replication
competent, are wrong.
“The majority of the sgRNA you are detecting in a nasal swab in your nose is NOT REPLICATION COMPETENT as shown in Jaafar et al.15 It is just an RNA fragment that should have lower longevity in your cells than dsDNA contaminating fragments,” he writes.
In that Substack article, McKernan has also copied a 2009 study
discussing how DNA in vaccines can cause cancer and highlighted the most
relevant parts. It’s a helpful resource if you want to learn more.
Quality Control Is Sorely Lacking
As for how SV40 promoters ended up in the mRNA shots, it appears to
be related to poor quality control during the manufacturing process,
although it’s unclear where in the development SV40 might have sneaked
in. Quality control deficiencies may also be responsible for the high
rate of anaphylactic reactions we’ve been seeing. McKernan tells Greer:
“It's in both Moderna and Pfizer. We looked at the
bivalent vaccines for both Moderna and Pfizer and only the monovalent
vaccines for Pfizer because we didn't have access to monovalent vaccines
for Moderna. In all three cases, the vaccines contain double-stranded
DNA contamination.
If you sequence that DNA, you'll find that it matches
what looks to be an expression vector that's used to make the RNA ...
Whenever we see DNA contamination, like from plasmids, ending up in any
injectable, the first thing people think about is whether there's any E.
coli endotoxin present because that creates anaphylaxis for the
injected.
And, of course ... there's a lot of anaphylaxis going
on, not only on TV but in the VAERS database. You can see people get
injected with this and drop. That could be the background from this E.
coli process of manufacturing the DNA ...”
Regulatory Agencies Knew There Was a Contamination Problem
In a May 20, 2023, Substack article,16
McKernan points out that Pfizer itself submitted evidence to the
European Medicines Agency (EMA) showing sampled lots contained vast
differences in the levels of double-stranded DNA contamination.
The arbitrary limit for dsDNA that the EMA came up with was 330
nanograms per milligram (ng/mg). Data submitted to the EMA by Pfizer
shows sampled lots had anywhere from 1 ng/mg to 815 ng/mg of DNA.
McKernan adds:17
“This limit likely did not consider the potency of
this dsDNA contamination if it was packaged in an LNP [lipid
nanoparticle]. Packaged dsDNA is more potent as a gene therapy. We now
know this DNA is packaged and transfection ready.18 Even lower limits should be applied if the DNA is packaged in transfection ready LNPs ...
Even with Pfizer being able to cherry pick the data
they provided to the EMA for 10 lots, they see a 1 to 815ng/mg variance.
If you were to expand this study to 100 or 1000 lots, you’d likely see
another order or two of magnitude variance.”
Double-Stranded DNA May Integrate Into Your Genome
The presence of double-stranded DNA also brings up another major concern, and that is the possibility of genomic integration.
“At least on the Pfizer side of things, it has what's
known as an SV40 promoter. This is an oncogenic virus piece. It's not
the entire virus. However, the small piece is known to drive very
aggressive gene expression.
And the concern that people, even at the FDA, have
noted in the past whenever injecting double-stranded DNA, is that these
things can integrate into the genome,” McKernan says.
While McKernan’s paper does not present evidence of genome
integration, it does point out that it’s possible, especially in the
presence of SV40 promoters:19
“There has been a healthy debate about the capacity
for SARs-CoV-2 to integrate into the human genome ... This work has
inspired questions regarding the capacity for the mRNA vaccines to also
genome integrate. Such an event would require LINE-1 driven reverse
transcription of the mRNA into DNA as described by Alden et al.
dsDNA [double-stranded DNA] contamination of sequence
encoding the spike protein wouldn’t require LINE-1 for Reverse
Transcription and the presence of an SV40 nuclear localization signal in
Pfizer’s vaccine vector would further increase the odds of
integration.”
Manifold Risks
That said, even if genetic modification does not occur, the fact that
you’re getting foreign DNA into your cells poses a risk in and of
itself, McKernan says. For example, partial expression could occur, or
it might interfere with other transcription translations that are
already in the cell.
Bhakti also points out that the SV40 promoters do not need to be
present in the nucleus of the cell for problems to occur. Cytoplasmic
transfection can, in and of itself, allow for genetic manipulation,
because the nucleus disassembles and exchanges cellular components with
the cytosol during cell division.
In addition to having DNA floating around and causing potential
problems, the RNA in the COVID jab is also modified to resist breakdown.
“So, we have TWO versions of the spike protein floating around that can
persist longer than anticipated,” McKernan says, and the spike protein,
of course, is the most toxic part of the virus that can cause your body
to attack itself.
Both McKernan and Bhakti are adamant that ALL mRNA “vaccines” must be
immediately stopped, whether for human or animal use, due to the
magnitude of the risks involved.
‘Alarming Problems’
In the video above,20
Yusuke Murakami, a professor at Tokyo University, expresses alarm over
the finding of SV40 promoters in the COVID jabs. The interview is in
Japanese but has English subtitles. I’ve included it because I think he
does a good job of putting the problem into layman’s terms:
“The Pfizer vaccine has a staggering problem,” Murakami says. “This
figure is an enlarged view of Pfizer's vaccine sequence. As you can
see, the Pfizer vaccine sequence contains part of the SV40 sequence
here. This sequence is known as a promoter.
Roughly speaking, the promoter causes increased
expression of the gene. The problem is that the sequence is present in a
well-known carcinogenic virus. The question is why such a sequence that
is derived from a cancer virus is present in Pfizer's vaccine.
There should be absolutely no need for such a
carcinogenic virus sequence in the vaccine. This sequence is totally
unnecessary for producing the mRNA vaccine. It is a problem that such a
sequence is solidly contained in the vaccine.
This is not the only problem. If a sequence like this
is present in the DNA, the DNA is easily migrated to the nucleus. So it
means that the DNA can easily enter the genome. This is such an
alarming problem.
It is essential to remove the sequence. However,
Pfizer produced the vaccine without removing the sequence. That is
outrageously malicious. This kind of promoter sequence is completely
unnecessary for the production of the mRNA vaccine. In fact, SV40 is a
promoter of cancer viruses.”
Resources for Those Injured by the COVID Jab
The more we learn about the COVID jabs, the worse they appear. While
they suck as vaccines, they’re truly masterful bioweapons, as they’re
capable of destroying health in any number of ways, through myriad
mechanisms.
If you got one or more jabs and are now reconsidering, first and
foremost, never ever take another COVID booster, another mRNA gene
therapy shot or regular vaccine. You need to end the assault on your
body. Even if you haven’t experienced any obvious side effects, your
health may still be impacted long-term, so don’t take any more shots.
If you’re suffering from side effects, your first order of business
is to eliminate the spike protein that your body is producing. Two
remedies that can do this are hydroxychloroquine and ivermectin. Both of
these drugs bind and facilitate the removal of spike protein.
The Front Line COVID-19 Critical Care Alliance (FLCCC) has developed a post-vaccine treatment protocol called I-RECOVER.
Since the protocol is continuously updated as more data become
available, your best bet is to download the latest version straight from
the FLCCC website at covid19criticalcare.com21 (hyperlink to the correct page provided above).
For additional suggestions, check out the World Health Council’s spike protein detox guide,22
which focuses on natural substances like herbs, supplements and teas.
To combat neurotoxic effects of spike protein, a March 2022 review paper23 suggests using luteolin and quercetin. Time-restricted eating (TRE) and/or sauna therapy can also help eliminate toxic proteins by stimulating autophagy.