A troubling new medical report is drawing urgent attention from scientists and vaccine safety advocates after a renowned neuroscientist revealed the presence of dangerous prion-like clots in the blood of a toddler born to a woman who received the Pfizer COVID-19 mRNA vaccine during pregnancy.
The findings, which center on the discovery of amyloid fibrils—misfolded proteins linked to deadly neurological diseases—were released by Dr. Kevin McCairn, a systems neuroscientist with over 25 years of experience in modeling neurodegenerative conditions.
His report marks what may be the first known instance of amyloid fibrils found in the blood of a child exposed to mRNA technology in utero.
The child was born prematurely at 35 weeks, just one week after the mother’s second dose of Pfizer’s BNT162b2 mRNA vaccine, the Gateway Pundit reports.
According to McCairn’s report, the child had no vital signs at birth and required immediate resuscitation.
Over the following three years, the toddler experienced repeated immune system dysfunctions and required several surgeries, including a tonsillectomy and treatments for persistent middle ear infections.
These health challenges prompted closer investigation.
McCairn’s team conducted a series of blood tests using advanced imaging techniques such as Thioflavin T staining and scanning electron microscopy (SEM).
They detected fibrous structures with clear amyloid characteristics—markers of pathological protein misfolding, which have been associated with systemic inflammation and abnormal clotting.
“It has been widely claimed that spike protein and mRNA clear rapidly from both maternal and fetal systems,” McCairn noted. “However, this assertion is not supported by accumulating empirical data.”
McCairn cited the 2025 Yale Post-Vaccine Syndrome study, which identified spike protein circulating in some individuals up to 700 days after vaccination.
He also referenced a 2023 study by Yonker et al., which found spike protein present in adolescents weeks or even months after injection.
These results contradict early public health claims that vaccine components leave the body quickly, GP notes.
Additionally, the assumption that the placenta blocks vaccine transmission has also come under scrutiny.
In 2023, Swingle et al. demonstrated that lipid nanoparticles (LNPs) could reach the placenta in vivo.
A year later, Safford et al. found that certain LNPs optimized for elasticity enhanced distribution to the maternal-fetal interface—offering direct evidence that mRNA and its delivery systems can cross into fetal circulation.
Critics of mRNA technology have long warned about prion-like behavior of spike proteins.
McCairn emphasized that amyloid fibrils can persist even after a single exposure through a self-perpetuating process called autocatalysis.
“Inflammatory cytokines, cellular stress, and exposure to amyloidogenic peptides can perpetuate misfolding cascades long after the original exposure has ended,” he explained. “This view ignores well-characterized prion-like behaviors.”
McCairn concluded that while postnatal exposure to environmental spike protein cannot be fully ruled out, the proximity of the birth crisis to the mother’s vaccination suggests a vaccine-induced cause.
He warned that environmental spike exposure would likely worsen any pre-existing amyloid condition rather than initiate it.
“These findings call into question the original pharmacokinetic modeling used during vaccine approval phases,” he said. “The precautionary principle must be applied when considering continued mRNA use in pregnancy.”
The report is being hailed by some in the scientific community as a potential turning point in the debate over maternal vaccine safety.
McCairn has called for a full halt to mRNA vaccination in expectant mothers until more comprehensive safety data is made publicly available.
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Author: Gloriel Howard
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