«COVID-19 mRNA vaccines direct host cells to manufacture prefusion-stabilized SARS-CoV-2 spike protein that retains its furin cleavage site andcarries two proline substitutions (K986P/V987P) in S2 that are not present in wild-type SARS-CoV-2 spike protein. This review examines two distinct forms of mRNA vaccine shedding: (i) molecular transcriptional shedding, involving the production, proteolytic fragmentation, persistence, and dissemination of vaccine-derived molecular products within vaccinated individuals through cellular division, extracellular release, and vesicular transport; and (ii) human-to-human shedding, involving the potential transfer of these products from vaccinated individuals to other individuals through biological secretions».
A new, exclusive study—authored by an expert in molecular biotechnology, John A. Catanzaro, CEO, co-founder, chairman, and Product Development Officer of Neo7Bioscience, the epidemiologist Nicholas Hulscher, and cardiologist Peter McCullough—confirms distinct types of concerning research regarding the dangers of Covid vaccines.
The study is published as a “preprint”—meaning it has yet to undergo peer review—but it effectively brings together startling findings already published in other, validated scientific research.
The Abstract of the Study published on Zenodo – link in the sources
In summary, here are the significant findings that confirm the extreme danger posed by mRNA genetic vaccines—a danger inherent in their very design:
The “double proline” insertion within the genetic code of the Covid vaccines, designed to make the Spike protein more resistant to the human immune system’s natural attempts to destroy it (as the immune system identifies it as a “foreign body” to be eliminated). This has resulted in the paradoxical and deleterious outcome of the toxic protein persisting in the blood of vaccinated individuals for over three years—a finding that confirms a major discovery first reported globally by the Italian bioimmunologist Mauro Mantovani.
The “diabolical Frankenstein molecule” N1-methylpseudouridine damage which can cause turbo-cancer
“Proteolytic fragmentation” occurring within the human body—highlighted in four studies by the Italian biochemist Gabriele Segalla—which can cause irreparable damage to human DNA, partly through the metabolic production of highly toxic substances that Pfizer failed to disclose in its official safety documentation.
The potential for this “artificially armored” Spike protein—engineered by the pharmaceutical industry—to be transmitted from vaccinated individuals to those who are unvaccinated.
The article was not published in in a little-known scientific journal, but in Zenodo, an open scientific repository for EU-funded research outputs from Horizon Europe, Euratom, and earlier Framework Programmes.
Horizon Europe is the European Commission’s primary research funding program, which includes the Graphene Flagship—an initiative that has funded studies on the potentially hazardous biomedical use of graphene oxide in pharmaceuticals, as well as in COVID-19 vaccines (the study by Delogu et al.).
The Persistence in Vaccinated Blood of the harmful Spike protein
Before analyzing the enormous significance of this research in detail, it should be noted that the groundbreaking studies by Italian scientists Mantovani and Segalla gained visibility in Italy only thanks to *Gospa News* and a few other alternative media outlets. In reality, these studies have been censored by the mainstream medical establishment—an establishment terrified of having to admit its complicity in a mass experiment involving mRNA vaccines, which has led to the extermination of human beings across the Western world. In these regions, such vaccines were even mandated by law, in line with a criminal project to globalize multiple vaccinations—a scheme launched by Bill Gates in 1999, right here in Italy.
«Evidence supporting internal molecular dissemination includes circulating spike protein, proteolytically released fragments, vaccine-derived mRNA, and spike-bearing extracellular vesicles capable of transporting molecular cargo beyond its original cellular source. Human studies document circulating S1 within 24 hours, spike-bearing exosomes by day 14, vaccine mRNA in plasma for up to 28 days,vaccine-derived spike peptides at 69–187 days, spike protein in monocytes at 852 days, circulating spike at 1,173 days, exosomal vaccine mRNA at 1,284 days, and spike protein alongside plasmid-associated DNA sequences in skin at 1,364 days».
This prolonged persistence of the Spike protein has been linked to a host of adverse reactions, including various forms of “turbo-cancer”—even affecting the heart, an organ historically and inherently free from cancerous pathologies.
The “diabolical Frankenstein molecule” N1-methylpseudouridine damage
However, the next phase of the research—authored by Catanzaro, Hulscher, and McCullough—focuses on the potential genetic damage inflicted upon the immune system by what we have termed a “diabolical Frankenstein molecule,” so named because it was chemically manipulated in a laboratory twice before being artificially incorporated into mRNA vaccines.
«N1-methylpseudouridine-associated +1 ribosomal frameshifting generates unintended translation products, expanding the repertoire of molecules potentially available for extracellular release. The proposed internal dissemination model incorporates two additional pathways: mitotic inheritance, whereby daughter cells may inherit an altered proteome following cellular division, and exosome-mediated communication, whereby molecular cargo may affect cells that never directly received vaccine mRNA. Experimental studies demonstrate spike-mediated interference with five interconnected molecular systems—coagulation, receptor–renin–angiotensin signaling, innate immune sensing, tumor-suppressor transcription, and vesicular interferon signaling. Together, these findings identify multiple pathways through which persistent vaccine-derived molecular products could disrupt cellular regulation, propagate abnormal signaling between cells, and potentially sustain downstream biological disturbances».
The devastating impact of the “diabolical molecule” N1-methylpseudouridine—for which its inventor Emmanuelle Marie Charpentier was awarded a Nobel Prize in Chemistry and inducted into the Pontifical Academy of Sciences rather than being sent to prison—has been clearly highlighted by the highly detailed and pioneering research of Canadian bioimmunologist Jessica Rose.
Human-to-human shedding of mRna vaccines Toxic Materials
And finally, here is the conclusion that transforms the transhumanist experiment involving mRNA genetic serums into a nightmarish tale—one so difficult to believe, were it not for its scientific detail…
«Regarding human-to-human shedding, vaccine-derived mRNA has been detected in trace, fragmented form within breast-milk extracellular vesicles, establishing its presence in a biological secretion transferred between individuals. Extracellular vesicles are also present in saliva, exhaled breath, sweat, semen, and other bodily secretions. Their capacity to protect molecular cargo, survive biological barriers, enter recipient cells, and deliver functional mRNA provides a biologically plausible pathway for wider interpersonal transfer. An observational study further reported associations between proximity to vaccinated individuals and menstrual irregularities among unvaccinated women. However, no published study has directly demonstrated transfer of vaccine-derived spike protein, mRNA, or plasmid-associated DNA between individuals through respiratory emissions, saliva, sweat, or other non-milk secretions, leaving a critical evidence gap concerning the extent and biological consequences of human-to-human shedding».
The study summary concludes by calling for further research—much of which has, in fact, already been conducted by Mantovani, Segalla, and others.
Unfortunately—and this is the only major flaw in the study—these Italian works, conducted by independent researchers, were not included in the researchers’ bibliography, as the Italian scientific community actively sought to obscure such contributions.
Their objective is to prevent the President of the Italian Republic, Sergio Mattarella—who signed the decrees mandating vaccination for various groups and for those over the age of 50, in clear violation of Article 32 of the Constitution—from facing impeachment, and to ensure that the officials of the Draghi administration, who implemented these measures, do not end up in prison indefinitely.
«Collectively, these findings support intracellular and intercellular dissemination of vaccine-derived molecular products, with evidence of persistence extending over multiple years. The convergence of proteolytic fragmentation, vesicular transport, and potential mitotic inheritance suggests mechanisms through which molecular products and their downstream signaling effects could extend beyond the original cells of production. Direct experimental studies are needed to establish the functional consequences of long-term persistence, determine whether these pathways sustain molecular disturbances across cellular generations, and establish whether biologically significant human-to-human transfer occurs through additional bodily secretions and, if so, its extent».
Below, you can read the analysis and reflections of one of the study’s authors, the renowned American epidemiologist Nicolas Hulscher.
Fabio Giuseppe Carlo Carisio – Gospa News founder and director
Hulscher: “New Paper Reveals How mRNA Vaccine Materials Could Spread From Vaccinated to Unvaccinated People”
by Nicolas Hulscher, MPH
All links to previous Gospa News inveatigations have been added in the aftermath
For years, people around the world have raised serious concerns about mRNA vaccine shedding—the possibility that vaccine-derived materials could spread beyond the individuals who received the injections. Despite years of public concern and debate, critical questions surrounding this possibility have remained unanswered.
We decided to examine the scientific evidence comprehensively, tracing what happens to vaccine-derived materials inside the body, how they spread between cells, and whether biological mechanisms exist that could allow these materials to pass from one person to another.
Drawing on published human investigations, molecular experiments, and research involving extracellular vesicles, we examined the existing evidence and identified two distinct forms of mRNA vaccine shedding:
1. Human-to-human shedding: The potential transfer of vaccine-derived materials from vaccinated individuals to other people through biological secretions.
1. Human-to-Human Shedding: Potential Transfer Between Individuals
Studies have detected vaccine-derived spike protein and mRNA on or within circulating exosomes multiple years after vaccination. Exosomes are microscopic, membrane-bound particles that protect and transport proteins, genetic material, and other biological cargo between cells.
Importantly, these same types of particles are naturally present in bodily secretions that may come into contact with other individuals:
Breast milk: Vaccine-derived mRNA has already been detected within exosomes in human breast milk. This documents the presence of vaccine genetic material in a secretion naturally transferred from vaccinated mothers to their infants.
Saliva: Exosomes are confirmed in human saliva, yet their potential carriage of vaccine-derived spike protein, mRNA, or plasmid-associated DNA remains untested.
Exhaled breath: Exosomes and other extracellular vesicles have been recovered from exhaled breath and breath condensate. Whether these particles carry vaccine-derived materials following mRNA vaccination has not been directly investigated.
Sweat: Extracellular vesicles have also been detected in human sweat, but their potential carriage of vaccine-derived molecular products remains untested.
Exosomes are not simply passive containers. Experimental research demonstrates that they can protect genetic material, enter recipient cells, and deliver molecular cargo capable of altering cellular activity.
These findings provide a plausible biological foundation for human-to-human transfer pathways beyond breast milk.
Adding to these concerns, an observational study involving thousands of respondents found associations between proximity to vaccinated individuals and menstrual irregularities among unvaccinated women.
Despite these observations, whether vaccine-derived spike protein, mRNA, or plasmid-associated DNA can transfer between individuals through saliva, exhaled breath, sweat, or other non-milk bodily secretions has never been directly tested.
2. Transcriptional Shedding: Internal Spread Throughout the Body
The second form of shedding examined in our paper involves the production, fragmentation, persistence, and dissemination of vaccine-derived molecular materials within the vaccinated individual.
Following mRNA vaccination, human cells manufacture SARS-CoV-2 spike protein. This protein can be broken into fragments through enzymatic processes, released into circulation, and transported through the body inside or on the surface of exosomes.
We examine two additional mechanisms that could extend this process.
Cell division (mitosis): When cells containing vaccine-derived proteins divide, their daughter cells may inherit portions of the altered cellular contents. This proposed mechanism could extend the presence and biological effects of vaccine-derived materials across successive generations of cells.
Cell-to-cell spread: Exosomes can transport spike-related materials and regulatory genetic cargo to distant cells that never directly received vaccine mRNA. Experimental studies involving spike-expressing cells demonstrate that exosomal cargo can alter signaling pathways in recipient cells.
Together, these mechanisms suggest a potentially self-reinforcing cycle of molecular dissemination and cellular signaling disruption:
Spike production → Protein fragmentation → Exosome release → Cellular signaling disruption → Further dissemination
As vaccine-derived materials spread between cells, they interfere with five interconnected biological systems: blood coagulation, innate immune sensing, tumor-suppressor signaling, cellular receptor regulation, and interferon signaling.
The possibility of sustained cellular disruption and human-to-human exposure of mRNA vaccine material demands immediate testing. In the meantime, a HALT to mRNA technology is warranted to protect innocent bystanders from potential shedding.
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