The Important Differences Between Innate and Adaptive Immunity for Pandemics
Testimony from an Expert Witness
The adaptive immune response to a pathogen never seen before is not very useful. It typically takes 2 to 3 weeks for its full activation whereas the pathogen could have killed the host long before this. That is where the innate immune system, “the first responders” comes in.
Actually innate immunity effectors are also “the front line of defense”. Sebocytes are foamy macrophages constitutively producing and releasing the CRITICAL HERV-K102 particles by lysis in sebaceous glands. Sebaceous glands are in the skin and all mucosal surfaces.
Unfortunately, IgG antibodies to the spike protein, a product of the adaptive immune system can cause i) the selection of immune escape variants and ii) ADE which serves only to interfere with innate immunity in the foamy macrophages. Several lines of evidence suggest the HERV-K102 Protector System is critical for the host to fight and recover from emerging or pandemic viruses including HIV-1 and SARS-CoV-2 [Laderoute MP. submitted]. Both of these ongoing pandemics involve enveloped RNA viruses. (I will explain what is meant by enveloped in this context, later).
Explanation of “Enveloped RNA Viruses” HIV-1 and SARS-CoV-2
When a virus or any pathogen infects a cell, it induces the expression of HERV-K102 envelope at the cell surface, which serves to the innate immune system as a marker of cells for destruction. Enveloped viruses are those that bud through the cell surface like HIV-1 and SARS-CoV-2. When they bud their virions pick up whatever is on the cell surface, in this case, HERV-K102 envelope. Now HERV-K102 envelope antibodies can neutralize and clear the HIV-1 or SARS-CoV-2 particles.
The neutralizing IgG antibodies to spike protein also can clear or remove SARS-CoV-2 particles but the growth of already mutated variants will be favored, and before long a new strain is selected. Antibodies that still can bind the new variants, will cause the entry of SARS-CoV-2 into the protector foamy macrophages. Once inside the macrophage, the forces of evil will take over to cause disease progression, as explained below.
Consistent with the notion that innate immunity protects against SARS-CoV-2 while adaptive immunity doesn’t (due to IgG antibodies to spike protein) is the ONS UK data compiled above. The only month where the all-cause mortality rate ratio was below 1 was February 2021 when 96 % of the immunized had only received one dose (see below) proving innate immunity provided protection but not adaptive.
The 50+ age group are at highest risk of SARS-CoV-2 Deaths.
Using two separate algorithms from the UK ONS mortality data, it can be estimated that the inoculation of the COVID-19 vaccine (ever vaccinated) in the 50+ Canadian population may have been associated with a minimum of 250,000 deaths (227,358 - 278913) although surely this is an underestimation. This is because the algorithm is from the UK population up to May 31, 2022 and at most the UK population had been exposed to 3 shots. By March 26, 2023, almost 4 million Canadians had 5 shots (where it is known each shot is sequentially more deadly).
It is not reassuring that public health officials did not understand or willfully ignored the major differences between innate and adaptive immunity and how dangerous the IgG antibodies to spike protein produced by the COVID-19 vaccines really were … due to ADE.
Here is the full powerpoint written for submission to the National Citizens Inquiry as testimony from an expert witness.
Thankyou Marian, this is an excellent presentation. Are the slides from a formal presentation you have done somewhere? For those of us who do not have biology background and want to understand more it would be great to see this expanded upon.
Thank you.