Discover more from Alexander COVID News-Dr. Paul Elias Alexander's substack
COVID vaccine studies that show us clearly the devastating failure of the COVID vaccines (mRNA) that are non-sterilizing (do not stop infection or transmission) & actually bind & enhance infection
We underestimated the interplay between the virus & host immune system, this ecosystem, where the sub-optimal immune pressure from the non-neutralizing vaccinal antibodies drives variants
We have enhanced susceptibility (infection in the vaccinated) while also have reduced severe disease in the lower respiratory tract (deep in the lung). This is not a usual situation. Why?
These three show that the induced vaccinal antibodies (Abs) (non-neutralizing) bind to the virus’s spike and enhance the infectiousness of the virus to the vaccinated person. The infectious behavior of the virus cannot be accounted for by the virus itself. Properties intrinsic to the virus. We argue that infectiousness must be looked at from the view of the non-neutralizing Abs that bind and enhance infectiousness in the vaccinated. In short, the non-neutralizing Abs give the virus the property of increased infectiousness. Enhanced infectiousness.
Then additional researchers shows us why vaccinees are less vulnerable to severe disease in the lower lung, respiratory tract. Researchers show that the very same non-neutralizing Abs in the upper respiratory tract (URT) work in the lower respiratory tract (LRT) and prevents fusion of infected cells with non-infected cells that prevent the formation of syncytia and those syncytia is linked (correlated) to severe disease.
The ‘common’ denominator that is determining the infectiousness and severe nature of the virus is the non-neutralizing Abs. It binds in the URT and enhances infectiousness yet binds in the LRT and prevents severe disease. The concern is that this blocking of severe disease in the LRT may be overcome in time (lose their protective effect) and we run the risk if we continue with the non-neutralizing vaccines, of generating both infectious and severe lethal, virulent variants. I am trying to explain this complex issue so bear with me for its complex too for me;-)
These researchers showed us that with time, the sub-optimal immune pressure on viral infectiousness (the spike protein) was overcome by variants and Omicron emerged. The Omicron is now near completely resistant to the Abs generated against spike protein.
These researchers also showed us that there will be selection by the virus to overcome the sub-optimal pressure. The population is exerting immune pressure (sub-optimal) on virus virulence via non-neutralizing Abs. The virus became resistant to the neutralizing Abs and the non-neutralizing Abs grew in dominance and the non-neutralizing Abs at present, prevent transfection (drives severe disease) in the LRT.