Attention Bill Gates: ANY Platform That Tells Our Cells to Make Proteins is Dangerous

It must be understood that the experimental mRNA injections, willingly trumpeted as a means to end the highly propagandized COVID-19 pandemic, are indeed not vaccines. Loaded with toxic ingredients, including destructive lipid nanoparticles (LNPs), the mRNA jabs do not prevent infection or the spread of disease. Instead, these shots have one hazardous goal—to deliver a message to our cells to make proteins. These serum antibodies will never prevent infections; they can only react to them. Thus far, the vehicle used to carry out the delivery has been lipid nanoparticles, which is known to cross the blood-brain barrier and the placenta while contaminating DNA across the entire body. Though these dangers were first dubbed false and brushed under the rug, they are now proven true. So, determined to move forward, the deep state is promoting the next phase of its genetic medicine ruse in the form of a new delivery system, billing it as “safe and effective.”

Like clockwork, an article in Cell last September describes a new “safe and effective” way to deliver DNA and RNA using proteolipid vehicles (PLVs) instead of lipid nanoparticles. “Currently, AAV (adeno-associated virus) and LNPs are the main delivery platforms for genetic medicine,” wrote senior study author John Lewis, Ph.D. He added, “Both platforms have significantly advanced the field with approved therapies and vaccines for a variety of serious and often life-threatening diseases.” Again, the products are not vaccines. Also serving as the CEO of Entos Pharmaceuticals (the company funding his study), Lewis laid the case for how his Fusogenix™ PLV™ technology will develop cures and improve the lives of patients, declaring:

“Despite these advancements, gaps remain in the ability of current technologies to fully realize the potential of genetic medicines. We designed the FAST-PLV platform to bridge these gaps and deliver on the promise of genetic medicines that patients urgently need.”

However, the question persists: Do patients “urgently need” genetic medicines? Bill Gates and his partners in crime insist they do, but countless medical experts who are honest about the wrath of destruction caused by mRNA jabs undoubtedly disagree. Nonetheless, Gates isn’t giving up. A year ago, as part of the “ongoing collaboration” between Aegis Life and Entos Pharmaceuticals (Entos is the parent company of Aegis), the Bill & Melinda Gates Foundation invested $4.45 million to continue the development of “DNA-encoded therapeutic antibodies against infectious diseases” using the Fusogenix PLV platform. The investment follows an initial grant from the Gates Foundation to Aegis made in June 2023 to support their effort to develop DNA-encoded antibodies against infectious diseases. Determined to push ahead at all costs, it makes sense that Bill Gates is behind the sneaky shift from LNPs to a new “safe and effective” gene-damaging platform.

However, the concern remains. And here’s why. The dangerous mRNA platform—tainted in part by LNPs—is not at all remedied by the “safe and effective” FAST-PLV platform crafted to replace LNPs. Indeed, the dire situation is yet again overlooked. Significantly, concern remains because ANY platform that delivers a message to our cells to make proteins is dangerously unsafe. In June 2022, in a public submission to the CDC, Dr. Kevin Stillwagon, a retired airline captain with extensive research into mRNA technologies, spoke of the dangers of the mRNA path. He wrote that the only prevention of infection resides in the innate immune system, guarding the epithelial barrier between the outside and inside of the body without using serum antibodies.

On March 9, 2025, in an insightful and informative interview with Nicholas Hulscher, MPH, epidemiologist at the McCullough Foundation, Dr. Stillwagon explained the mechanics and risks of PLVs as a new delivery platform for genetic material. Stillwagon shared that, while without the “secondary toxic lipid nanoparticles found in previous mRNA technologies, PLVs spread widely throughout the body, potentially leading to widespread tissue destruction.” Dr. Stillwagon stressed that the lipids used in PLVs, including DOTAP, DODAP, and DOPE, are synthetically designed and toxic, with some even associated with cancer and fetal damage.

Moreover, as pointed out by Hulscher, with funding from the Gates Foundation, Entos Pharmaceuticals is conducting clinical trials using PLVs with plasmid DNA, raising concerns about genome integration and long-term health risks. On top of that, the PLV platform circumvents natural immune defenses, leading to likely cytotoxic T-cell destruction, micro hemorrhaging, micro clotting, and severe immune reactions. These outcomes are not safe and effective. Without question, the gene-damaging mRNA platform using PLV instead of LNPs remains just as dangerous and deadly and is not worthy of being introduced as safe and effective. Dr. Stillwagon pleads that the proper warnings are not being shared. But why would they be? Big Pharma currently owns the legacy media, and it funds and promotes the research of its own products. We hope that soon changes, because the truth is, there will always be catastrophic outcomes with mRNA technology. We should all be concerned and thankful to Dr. Stillwagon for his steadfast sharing of the truth about this dangerous mRNA technology. The HighWire reached out to Dr. Stillwagon regarding this latest scheme, and he shared the following critical message:

“What I want people to know is that delivering the message to have our cells make proteins is dangerous, regardless of the delivery mechanism. Cytotoxic t-cells are constantly monitoring the proteins being made by cells, and when they detect something foreign being made, they will either directly kill the cell or send an apoptotic signal to have the cell kill itself.

This works best at the epithelial barrier where infections normally happen. The cells that are starting to make viral proteins are taken out, and the cells get replaced with new ones quickly. This is what protects us from infections. But when you inject the message and deliver it to cells all through the body, you risk having Cytotoxic t-cells damage organ tissues, nerve tissues, and endothelial tissues that do not repair quickly. This is why we will always have vascular and neurological side effects with this technology.”