More bad news for COVID gene injection vaccine with Substantial Neutralization Escape by SARS-CoV-2 Omicron Variants BQ.1.1 & XBB.1 (Miller); immune imprinting, fixation, immune escape, antigenic sin

These findings suggest that the BQ.1.1 and XBB.1 variants may reduce the efficacy of current mRNA vaccines; clear evidence of vital immune escape/evasion, immune prejudicing, original antigenic sin

See Figure 1, Frames B, C, & D for before and after boosting for the neutralizing antibody titers for BQ 1.1, and XBB 1.1. Look at WA 1/2020 and the impact of boosting.

All of a sudden we have this flurry of research papers showing immune evasion from BQ and XBB sub-variants/clades. It is clear. The booster has failed. Yet we warned them, McCullough, Vanden Bossche, Risch, Yeadon, Tenenbaum, Oskoui, Ladapo, Cole, myself etc. What did we know that they did not? Even a Grade 11 biology student could have told them and knew this would happen. Are they that inept?

Five devastating aspects of the COVID gene injection today (mRNA & DNA platforms):

i)There are significant adverse effects from the COVID gene injection (mRNA & DNA platforms) e.g. bleeding, blood clotting, myocarditis, paralysis, anaphylaxis etc. including death

ii)There is clear evidence that the COVID gene injection (mRNA & DNA platforms) drives original antigenic sin, viral immune escape, and immune fixation, priming; We are seeing clear evidence of original antigenic sin (I call the sin ‘mortal’ given there is no reversal of the initial primed response), viral immune escape, immune tolerance, immune fixation/prejudicing/imprinting. There is also the risk of antibody-dependent enhancement of infection (and of disease) and pathogenic priming (https://pubmed.ncbi.nlm.nih.gov/32292901/).

iii)There is substantial risk that the antigen-specific ‘high-affinity’ vaccine induced antibodies subvert and sideline, outcompete the broadly protective lower-affinity innate antibodies of the naïve innate immune system of the young child that needs training and education as the maternal antibodies wane. This sets the child up for auto-immune disease as the training to recognize ‘self’ from ‘non-self’ (& nuances self-like, self-mimicking) components in the child is subverted (this involves sub-optimal training of the natural killer cells (NK))

iv)The sub-optimal non-neutralizing vaccinal antibodies in the teeth of a pandemic when there is constant elevated infectious pressure drives natural selection (selective) pressure to select for more infectious sub-variants and a potentially more lethal virulent one

v)The vaccine induced antibodies are giving the virus infectivity properties it prior did not have, causing the vaccinated to become infected, with increased illness, hospitalization, and death; the vaccinated no longer could contribute to herd immunity and are transmitting virus to other vaccinated as well as unvaccinated persons; See Fantini et al (Infection-enhancing anti-SARS-CoV-2 antibodies recognize both the original Wuhan/D614G strain and Delta variants. A potential risk for mass vaccination?): https://pubmed.ncbi.nlm.nih.gov/34384810/)

SOURCE for Miller et al:

https://pubmed.ncbi.nlm.nih.gov/36652339/

‘Our data show that the BQ.1.1 and XBB.1 variants escaped neutralizing antibodies substantially more effectively than the BA.5 variant by factors of 7 and 17, respectively, after monovalent mRNA boosting and by factors of 7 and 21, respectively, after bivalent mRNA boosting. The neutralizing antibody titers to BQ.1.1 and XBB.1 were dramatically lower than titers to the WA1/2020 strain by factors of 53 and 127, respectively, in the monovalent booster cohort and by factors of 80 and 232, respectively, in the bivalent booster cohort. These findings suggest that the BQ.1.1 and XBB.1 variants may reduce the efficacy of current mRNA vaccines’