Was there early evidence by Föhse et al. (Seneff) that Pfizer mRNA technology based vaccine against COVID reprograms both adaptive & innate immune responses? Yes! Response of innate immune cells to

by Paul Alexander

toll-like receptors (TLR 4 & TLR 7 & 8) TLR4 and TLR7/8 ligands was suppressed after Pfizer BNT162b2 vaccination; vaccine induces complex functional reprogramming of innate immune responses

‘The BNT162b2 vaccine also modulated the production of inflammatory cytokines by innate immune cells upon stimulation with both specific (SARS-CoV-2) and non-specific (viral, fungal and bacterial) stimuli.

The response of innate immune cells to TLR4 and TLR7/8 ligands was lower after BNT162b2 vaccination, while fungi-induced cytokine responses were stronger. In conclusion, the mRNA BNT162b2 vaccine induces complex functional reprogramming of innate immune responses, which should be considered in the development and use of this new class of vaccines.’


See Seneff and McCullough:

‘present the evidence that vaccination, unlike natural infection, induces a profound impairment in type I interferon signaling, which has diverse adverse consequences to human health. We explain the mechanism by which immune cells release into the circulation large quantities 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 are shown to have a potentially direct causal link to neurodegenerative disease, myocarditis, immune thrombocytopenia, Bell’s palsy, liver disease, impaired adaptive immunity, increased tumorigenesis, and DNA damage.’