SARS-CoV-2 Vaccines and Neurodegenerative Diseases
part 2
by Stephanie Seneff, PhD, MIT Senior Researcher
This complete article with References is also available at:
Impaired Immune Response
Due to Over-vaccination
A characteristic of the elderly is an impaired ability to mount antibodies against new pathogenic threats, and this is reflected in a failure to generate protective antibodies in response to vaccination.
It has been demonstrated in experiments with mice that aged mice have an overabundance of long-lived memory (antigen-experienced) B cells, and this is paired with an inability to generate new B cells from progenitor cells in the bone marrow, as well as impairment in the process of refinement of the antibody response in germinal centers in the spleen and the associated class switching that produces effective IgG antibodies [43, 44].
A significant reduction in the number of naive follicular B cells, combined with an impaired ability to convert them into mature memory B cells leaves these aged mice highly vulnerable to new infections. It is likely that the same principle applies to humans.
A plausible conclusion is that aggressive vaccination campaigns accelerate the pace at which an individual’s immune system reaches an ”aged” status due to exuberant generation of memory B cells in response to the artificial stimuli induced by repeated vaccination.
It has now been confirmed that the S1 component of the spike protein shows up in the blood one day after the first mRNA vaccine and remains detectable for up to a month after vaccination, becoming cleared as IgA and IgG antibodies become available [45]. For immune compromised people, it likely stays in the blood much longer, exposing all the tissues -- the spleen, the heart, the brain, the gonads, etc. – to the toxic prion-like spike protein.
Today’s children are by far the most vaccinated generation in the history of humankind. If we decide in the near future to deliver a booster COVID-19 shot to them every year, as seems possible given the current climate of enthusiasm for these vaccines, are we inviting disaster for them in years to come? Will their immune system “age” must faster than that of previous generations, due to the exhaustion of the pool of progenitor B cells by all these vaccines?
Will they succumb to Parkinson’s disease or other debilitating prion-based neurodegenerative diseases much sooner and in much greater numbers than previous generations? This is an experiment that I hope we finally decide not to carry out.