Comment from Dr. Marian Laderoute

See attached file(s). Overview: The spike mRNA gene therapy products should never be used for vaccination. Aside from the direct autoimmunity (requiring the immune system to eat various 'transfected' cells of the host), and the largely unknown risk of genetic modification regardless of whether the host was innoculated, the biggest problem stems from the fact the spike mRNA clot shots cause the high production of IgG1 and IgG3 spike antibodies in the upper respiratory tract (URT). This is highly problematic as these isotypes bind complement and when transmitted with SARS-CoV-2 virions or worse shed spike commandeered HERV-K102 particles that have been covered in spike protein due to the Pfizer-BioNTech LNPS (targeting to the URT), these antigen-antibody complexes upon reaching the microcirculation deep in the lungs, set off complement binding, which becomes coagulation and thrombosis, and vasculitis. There are two types of abnormal clots, the white fibrous clots that form casts which generate the non-COVID-19 deaths (often after the second dose: at day 0-2 due to shedding from the vaccinator; at day 15-30 and slightly less at day 31-60 due to shedding at the workplace and home, and finally the deaths after 60 days. Note that shedding (bioweaponized HERV-K102) is only from the Pfizer-BioNTech LNPs (due to contamination with spike protein and/or high endotoxin levels) while both Moderna and Pfizer-BioNTech create the bioweaponized SARS-CoV-2. The death rate from bioweaponized SARS-CoV-2 is about 1/100 [Bowe B et al, 2022]. The death rate from shedding is about 1/118 [Levi R et al., medRxiv, April 29, 2025]. The 60 day window after the 2nd dose likely is due to trained immunity releasing IRF-1 which upregulates PD-L1 (CD274) on the vascular endothelium which lasts for the 2 months. Note, that high testosterone blocks the upregulation of PD-L1 on vascular endothelium thereby explaining the excess clotting risk (and sudden deaths) in younger males. It can be estimated from VAERS data that perhaps only 10% of the deaths reported to VAERS are ordinary SARS-CoV-2 infections (such as transmitted from the unvaccinated). This means the use of the spike mRNA gene therapy technology has switched the susceptible from the old and sick to all ages (although the elders are still at higher risk of death from any cause) and renders any immunity (innate or adaptive) useless against the transmission of disease which now involves clots/vasculitis and/or myocarditis. In other words the mRNA technology destroys the meaning of immunity against the transmission of disease. Billions were spent, lives ruined only to render AMERICANS non-immune to the new transmission of two bioweapons. By continuing to vaccinate the elderly, this continues to launch bioweapons against the entire community. Products that create transmissible bioweapons must be banned in humans and all animals including clinical trials.