Unveiling Pfizer’s plasmid: Potential risks and regulatory oversight failures

• Pfizer’s vaccine contains three human DNA fragments: ?-globin (blood), AES/TLE5 (immune) and MT-RNR1 (neurological).
• Plasmids can integrate into human genomes, carrying these DNA fragments.
• Independent reviews and Pfizer’s own 5.3.6 report show blood, immune and neurological injuries cluster post-vaccination.
• Fragments regulate blood, immune and neurological systems, matching injury clusters.
• Integration of plasmid DNA fragments may drive the injuries documented.
• Grounds to halt the vaccine and launch an immediate investigation.

Pfizer’s COVID-19 vaccine has been under increasing scrutiny following revelations that it contains human DNA fragments capable of integrating into the human genome. These fragments are embedded in the vaccine’s plasmid, which is integral to its manufacturing process. Independent reviews and Pfizer’s own data show injuries concentrated in blood, immune and neurological systems. The alignment between the plasmid’s DNA fragments and the injury clusters raises significant concerns about the vaccine’s safety. This article examines the evidence, explores the implications and calls for immediate action.

Plasmid DNA and its design

By definition, plasmids are integration-competent DNA molecules, used in genetic engineering to insert sequences into host genomes. Pfizer’s vaccine plasmid contains three human DNA fragments: ?-globin (blood), AES/TLE5 (immune) and MT-RNR1 (neurological). These fragments are not idle additives; they are active regulatory sequences that can influence gene expression. The ?-globin fragment regulates blood and cardiovascular functions, AES/TLE5 controls immune pathways, and MT-RNR1 is linked to neurological and mitochondrial functions. These sequences are not inert; they can potentially integrate into the human genome, altering gene regulation.

Serious adverse events: The data speaks

Pfizer’s own data, compiled in their confidential 5.3.6 pharmacovigilance report, provides alarming evidence. After analyzing 42,086 case reports and 158,893 adverse events in the first three months of the vaccine rollout, the report highlighted the following clusters of serious adverse events (SAEs):

• Neurological disorders: 25,957 nervous system events, including seizures, Guillain-Barré, multiple sclerosis relapses, encephalopathy, neuropathies and facial paralysis.
• Immune/autoimmune disorders: 1,050 cases, including hypersensitivity, myocarditis, pericarditis, autoimmune flares and cytokine storms.
• Blood/hematological disorders: 932 cases, including immune thrombocytopenia, hemorrhage, clotting events, petechiae and deep vein thrombosis.

These categories are not random; they align perfectly with the systems controlled by the human DNA fragments in the plasmid: blood, immune and neurological. The alignment between the plasmid’s design and the injury clusters is too precise to be coincidental, suggesting a potential connection between the two.

Evidence of plasmid integration

Independent studies have provided evidence that plasmids can integrate into human DNA. A 2023 study in Nature Scientific Reports demonstrated that when linear DNA fragments were introduced into human cells, 1–20% of cells stably integrated these fragments into their genomes. More critically, a 2024 preprint study by Kevin McKernan found that plasmid DNA from Pfizer’s vaccine did integrate into the genome of human cancer cell lines, and in November 2024, Dr. Phillip Buckhaults confirmed integration into non-cancerous human epithelial stem cells. These findings indicate that the integration of plasmid DNA into human cells is not just a theoretical risk but a demonstrated biological reality.

Call for immediate action

The alignment between the DNA fragments in Pfizer’s plasmid and the injury clusters reported in their safety data is alarming. Independent reviews in 2022 and 2024 have also concluded that the most serious adverse events are clustered in blood, immune and neurological systems. This exact match raises the possibility that the design of Pfizer’s vaccine itself may be contributing to the injuries. The implications of plasmid integration into human DNA are profound and call for immediate action.

The alignment between the plasmid’s design and the injury clusters is too precise to be coincidence, suggesting that the integration of these human DNA fragments may be driving the documented injuries. Pfizer’s own data and the plasmid design point to a direct connection between the human DNA fragments in the vaccine and the blood, immune and neurological injuries dominating the safety signal.

Urgent need for action

The evidence underscores the potential risks associated with mRNA vaccines that use plasmids carrying human DNA. The alignment between the plasmid’s design and injury clusters, coupled with documented integration studies, demands immediate action. Pfizer should halt the vaccine’s distribution until these risks are fully understood and addressed. Regulators must launch a comprehensive investigation into the use of human DNA fragments in vaccine plasmids and their potential impacts on human health. The global health community must prioritize transparency and rigorous oversight to prevent further risks to public health.

Sources for this article include:

Substack.com

JonFleetwood.Substack.com

ThePeoplesVoice.tv