WHAT these liars REUSE TO OPENLY REVEAL
Antibody Dependent Enhancement:
“Exaggerated Immune Reaction” A major concern being voiced by scientists and physicians (including the ex-Pfizer head of respiratory research Dr. Michael Yeadon and the lung specialist and former head of the German public health department Dr. Wolfgang Wodarg) has to do with the potential for antibody-dependent enhancement (ADE), a phenomenon documented in humans, non-human primates, and ferrets in connection with the coronaviruses linked to SARS and MERS. In ADE, vaccines can cause antibodies present in a person’s body to act like a Trojan horse for wild viruses. In the case of individuals receiving COVID-19 vaccines, ADE could not only end up enhancing disease severity but could also lead to organ damage.
Of concern, COVID-19 vaccine trials are not designed to detect ADE. It is not known what proportion of the U.S. population might suffer pathogenic priming or ADE after receiving a COVID-19 vaccine, but the estimated 15 to 24 million Americans who already have an autoimmune disease could be particularly susceptible. The CDC has indicated that individuals with high-risk medical conditions — individuals excluded from the Phase I trials — are one of the proposed groups for early vaccination.
ANOTHER response could be either an acute inflammatory response or, later in life, the development of an autoimmune disease.
Spike proteins contain syncytin-homologous proteins, which are essential for the formation of the placenta. Vaccine against SARS-CoV-2 could trigger an immune reaction against syncytin-1. Such an immune reaction would cause infertility of indefinite duration in vaccinated women.
mRNA vaccines from Pfizer and Moderna contain polyethylene glycol (PEG). This coating hides the mRNA from our immune system, which ordinarily would kill any foreign material injected into the body. PEGylated lipid nanoparticles have been used in several drugs for years. Because of their effect on immune system balance, they have been shown to induce allergies and autoimmune diseases, according to several studies. Additionally, PEGylated lipid nanoparticles have been shown to trigger AUTO immune reactions, and cause damage to the liver.
PEG is not only a potential allergen, it is also a suspected carcinogen. Moderna’s 2018 corporate prospectus acknowledges that “there can be no assurance that our LNPs (lipid nanoparticles) will not have undesired effects,” including reactions that “could lead to significant adverse events.”
People with a history of severe allergic reactions were excluded from ALL clinical trials. Therefore, this life-threatening adverse safety signal did not appear in their clinical trial safety data __adverse immune responses include “probably underdiagnosed” life-threatening anaphylaxis. STUDIES Extrapolated to the U.S. population SUGGEST THAT 16.6 million may have antibody levels associated with adverse effects.
Moderna stated (p. 33):
[T]here can be no assurance that our LNPs will not have undesired effects. Our LNPs could contribute, in whole or in part, to one or more of the following: immune reactions, infusion reactions, complement reactions, opsonization reactions, reactions, antibody reactions . . . or reactions to the PEG from some lipids or PEG otherwise associated with the LNP. Certain aspects of our investigational medicines may induce immune reactions from either the mRNA or the lipid as well as adverse reactions within liver pathways or degradation of the mRNA or the LNP, any of which could lead to significant adverse events in one or more of our clinical trials.
ABOUT FDA APPROVED FETAL CELL LINES USED TO CULTURE THESE AND OTHER VACCINES:
Researchers harvested these cell lines from the eyeball of an 18-week-old human fetus aborted in 1985, and then rendered them immortal by making them cancerous … final vaccine products will contain this cellular debris and DNA fragments