Innate immune suppression by SARS-CoV-2 mRNA vaccinations
Stephanie Seneff, Greg Nigh, [...], and Peter A. McCullough
Y'know death don't have no mercy in this land
Death don't have no mercy in this land, in this land
Come to your house, you know he don't take long
Look in bed this morning, children find your mother gone.
I said death don't have no mercy in this land.
Death will leave you standing and crying in this land,
Death will leave you standing and crying in this land, in this land, yeah!
Whoa! come to your house, why' know he don't stay long,
Why' look in bed this morning,
Children you find that your brothers and sisters are gone.
I said death don't have no mercy in this land.
Death will go in any family in this land.
Death will go in any family in this land.
Come to your house, you know he don't take long.
Look in the bed on the morning, children find that your family's gone.
I said death don't have no mercy in this land.
Death will leave you standing and crying in this land,
In this land. whoa! come to your house,
Why' know it don't stay long, why' look in bed this morning,
Children find that your brothers and sisters are gone.
I said death don't, death don't have no mercy in this land.
The mRNA SARS-CoV-2 vaccines were brought to market in response to the public health crises of Covid-19. The utilization of mRNA vaccines in the context of infectious disease has no precedent. The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein. However, the immune response to the vaccine is very different from that to a SARS-CoV-2 infection. In this paper, we present evidence that vaccination induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance. These disturbances potentially have a causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell's palsy, liver disease, impaired adaptive immunity, impaired DNA damage response and tumorigenesis. We show evidence from the VAERS database supporting our hypothesis.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012513/