The Defender | 25 Mar 2022
Swedish researchers showed the mRNA from the Pfizer COVID-19 vaccine can be reverse-transcribed into DNA in human liver cells in vitro, but more research is needed to determine if this transcribed vaccine-derived DNA can integrate into human genomic DNA.
- There have been large numbers of adverse events associated with the Pfizer-BioNTech mRNA vaccine, or BNT162b2.
- RNA vaccines are appealing because they can be developed quickly compared to vaccines that use other technologies.
- However, with this novel technology, we don’t know all the potential risks, such as the possibility of genetic modification of the genomic DNA.
- This study from Lund University showed BNT162b2 enters human liver cells in vitro and is reverse-transcribed into DNA within six hours.
- The study did not assess whether the DNA reverse-transcribed from BNT162b2 is integrated into human genomic DNA.
- The investigators recommended further research to determine if the reverse-transcribed DNA derived from BTN162b2 can integrate into human genomic DNA, because this could cause adverse events.
Researchers from Lund University in Sweden published a study showing the mRNA from the Pfizer-BioNTech COVID-19 vaccine (BNT162b2) can be reverse-transcribed into DNA in human liver cells in vitro (outside the living body).
Transcription is the normal process by which mammalian cells use DNA to synthesize a molecule of RNA, before translating the RNA into protein. Reverse-transcription is when the cells use RNA molecules to synthesize DNA.
Some articles and social media posts interpreted the Lund study to mean that if the BNT162b2-derived DNA is reverse-transcribed, it can then integrate into the genomic DNA within the cell nucleus, and thus change human DNA.
However, this interpretation is incorrect. What the study actually showed is that mRNA from the Pfizer vaccine can be reverse-transcribed into DNA fragments within the cells of a human liver cell line in vitro.
In other words, the researchers witnessed the reverse-transcription process in a lab, outside the human body — they did not observe the reverse-transcription in a human who received the vaccine.
The authors concluded further studies are needed to investigate whether BNT162b2-derived DNA can integrate into human chromosomes.
The authors are right — scientists should conduct these studies.
Why? Because if vaccine-derived mRNA can be reverse-transcribed into DNA, and then integrate into the chromosomal DNA in a given cell, it’s possible this cell would be able to keep making the spike protein indefinitely. If that were to happen, and the spike protein continued to “present” on the cell’s surface, the immune system would target those cells for destruction, which could lead to organ damage.
Moreover, this DNA would be replicated each time the cell divides, giving rise to an entire cell line that is potentially capable of generating spike protein.
Another potential concern is this: If the BNT162b2-derived DNA can become integrated into human genomic DNA, this could cause genetic modification of the germline, meaning the DNA within egg or sperm cells. If this were to occur, the genetic modification could be inherited.
Pfizer’s preclinical data from animal studies showed that small amounts of BNT162b2 end up in the ovaries and testes after injection.
If BNT162b2 DNA became integrated into an important gene in an egg or sperm cell, and disrupted the expression of that gene, that could be catastrophic for the resulting embryo.
Worse, if the DNA coding the spike protein remained intact and expressed, that would likely be lethal to an embryo.
The BNT162b2-derived DNA could also become integrated into a non-coding region (a region of DNA that does not code for a protein), and not cause issues. The key is to determine if this is a possibility, and if it is, what is the risk?
Plenty of evidence of Pfizer vaccine adverse events
Multiple sources of data — including the Vaccine Adverse Event Reporting System (VAERS) database, data released by a German health insurance company, a recent survey conducted by Israel’s Ministry of Health, and the Pfizer phase 3 trial — indicate a high number of adverse events associated with Pfizer’s COVID vaccine.
The Lund paper lists 12 papers on adverse events.
A court-ordered document released in November 2021 by the U.S. Food and Drug Administration (FDA) revealed 1,232 deaths occurred in recipients of Pfizer’s shot during the first three months of the vaccine’s rollout.
The 1,232 deaths were a subset of 42,086 case reports listing 158,893 adverse events during those three months.
In light of the clear evidence of harm and death associated with the rollout of BNT162b2, it is imperative to reassess claims made to the public by the FDA, the U.S. Centers for Disease Control and Prevention (CDC) and other health authorities that BNT162b2 is “safe and effective.”
The contribution of this paper from Lund University is preliminary work to investigate a possible mechanism for how adverse events associated with Pfizer’s vaccine could be occurring for extended periods after inoculation.
COVID-19 vaccine development: background
Before diving into the Lund paper itself, let’s look back at the race to develop COVID vaccines.
After the World Health Organization in March 2020 declared COVID-19, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a global pandemic, the race was on to develop vaccines.
Health officials told the public vaccines were the only way to end the pandemic. A flurry of research on vaccines using a range of technologies ensued.
The established approaches were replication-defective recombinant adenoviral vector vaccines (pursued by Johnson & Johnson (Janssen), AstraZeneca, Sputnik V and CanSino), and inactivated virus vaccines (investigated by Sinopharm, Bharat Biotech and Sinovac).
Pfizer-BioNTech and Moderna chose to use a recent innovation: mRNA vaccines.
Viruses are fascinating beings at the threshold of what we consider living and non-living. They are submicroscopic, so tiny that we cannot see them with a microscope.
Viruses contain genetic material (DNA or RNA) inside a protein coat. They have no metabolism and can reproduce only by hijacking a host cell’s protein-synthesis and DNA-replication abilities.
Viruses appear completely inactive, tiny bits of protein with genetic material inside, floating passively around — until they encounter a potential host cell. Then the virus can infect the cell, hijack the cell’s machinery and make more copies of itself.
In the process, they may kill the host cell.
Humans are eukaryotes, meaning our cells contain a nucleus. Our cells are composed of the nucleus, the cytoplasm, and a cell membrane. Our DNA lives within the nucleus.
The “Central Dogma” of genetics is that DNA gets transcribed into messenger RNA (mRNA), which is then translated into protein. Much of our bodies are made of protein, which is encoded by our DNA.
The job of the mRNA is to take the information from the DNA out of the nucleus and into the cytoplasm, where the cell’s ribosomes then turn that information into proteins.
When a virus infects a cell, it uses the cell’s transcription and translation abilities to replicate itself. The host cell acts like a diligent factory that churns out new viruses, composed of viral DNA or RNA, packaged in the viral protein coat.
The purpose of a vaccine is to try to teach the body’s immune system to recognize a pathogen and protect the body, without actually being infected with the pathogen.
With viruses, this is accomplished by exposing the cells to all or parts of the virus’ protein coat, and convincing the body’s immune system that this bit of protein is harmful and so warrants mounting an immune response and subsequent immunity.
mRNA-based vaccines are a recent innovation, thrust into the limelight during the pandemic. The first report on the successful use of mRNA to produce protein in animals was published in 1990, when mRNA was injected into mice and protein production was detected.
To make mRNA vaccine technology a viable option, researchers had to find a way to protect the mRNA from RNAse and deliver it into the cell. RNAse, found everywhere including inside and outside the human body, destroys RNA. Several vehicles for RNA were researched.
The authors of a November 2021 study, “BNT162b2 safety and efficacy,” published in the New England Journal of Medicine (NEJM), described BNT162b2 as lipid nanoparticle (LNP)-encapsulated, meaning the LNP capsule protects the RNA from RNAse.
The BNT162b2 RNA is nucleoside-modified RNA (modRNA) and encodes the full-length of SARS-CoV-2 spike protein.
The way the Pfizer vaccine works is a bit like the RNA-based SARS-CoV-2 virus itself. Unlike a virus, the RNA in an LNP-encapsulated vaccine is encapsulated in fat rather than in protein.
Once in the cell, in the case of BNT162b2, the vaccine produces only the spike protein, versus using the cells’ organelles to manufacture new whole viruses (composed of genetic material and protein coats) — the way a real virus would.
Thus, instead of exposing the host to the SARS-CoV-2’s entire protein coat, BNT162b2 exposes the host only to the spike protein.
One of the strengths of this novel approach is that vaccines can be developed relatively quickly because all that is needed to get started is the viral genetic sequence.
According to the authors of the NEJM study, the development of BNT162b2 began on Jan. 10, 2020, when the SARS-CoV-2 genetic sequence was released. Eleven months later, the FDA granted the vaccine Emergency Use Authorization.
Another advantage of mRNA vaccines, according to Pardi et al, 2018, is safety: “mRNA is a non-infectious, non-integrating platform, there is no potential risk of infection or insertional mutagenesis. Additionally, mRNA is degraded by normal cellular processes,” which means the molecule does not persist in the body.
However, human cells are capable of reverse-transcribing mRNA into DNA. This is the exception to the “Central Dogma” of genetics, which says information flows only one way in mammalian cells, from DNA to RNA to protein.
The Lund paper investigated whether BNT162b2 could be reverse-transcribed by human liver cells themselves, with their own native mechanism.