Trevor Goodchild (@TrevorGoodchild)

K, here goes: The way your body destroys viral infections depends on an initial antibody response (normally produced via B-cells) "tagging" the virus as foreign so that killer white blood cells (T-cells/macrophages) from your immune system will recognize the antibody tags, kill virus-infected cells, absorb the viral particles, and destroy them. However, if the initial antibody "tags" are improperly formed it is possible that the immune cells will absorb the viral agent but be unable to destroy it (it's a complex sequential process that requires numerous receptors to access the antibody "tags"). So, for example, if you have received an experimental gene therapy that produces inferior antibodies rather than the normal ones unvaccinated people's B-cells produce, this is what can happen if you are exposed to even a slight variant of the initial virus you were "vaccinated" against. This is very, very bad because it means that the initial viral load you were infected with, however small, is now shielded within your own white blood cells. The virus will replicate freely. Your infected immune cells will circulate throughout your body. Eventually, the intracellular viral load will overwhelm the immune cells and cause them to rupture. And then you very rapidly go from relatively normal to critically ill and septic because this is happening on a massive scale, with a much larger viral load than you were initially exposed to suddenly overwhelming your defenses as the immune cells die, resulting in multiple organ systems shutting down at once. Survival rates from multi-system organ failure are dismal. This is why mRNA "vaccines" (gene therapy) were never approved prior to 2020. The animal studies kept showing this lethal effect. It's called "antibody-dependent enhancement". We're going to be hearing about it a lot.