The Marvels of the HERV-K102 Virus-Anti-Virus Protection System of Humans Including Shed (Horizontal) Population Protection (and the Harms of Gene Therapy Shedding)
The Marvels of the HERV-K102 Virus-Anti-Virus Protection System of Humans Including Shed (Horizontal) Population Protection (and the Harms of Gene Therapy Shedding)
V.2 Evidence Consistent with Protective Shedding from those Vaccinated with Only One Dose While for Two Doses Shedding Putatively Promotes DEATH in the Unvaccinated (Updated April 11, 2024).
Please see new comment posted on X https://twitter.com/hervk102/status/1770827757674537343 on March 21, 2024 concerning differential impact of shedding on the unvaxed (no spike specific IgG4) versus the vaxed (with high levels of IgG4) and how vitamin D3 greater than 50 ng/ml can only protect those without IgG4 against all-cause mortality.
The CDC recognized long COVID in July 2021 as a new disease entity (https://www.cdc.gov/coronavirus/2019-ncov/long-term-effects/index.html?utm_source=substack&utm_medium=email) which was co-incidental with the projected maximal shedding related to increased C19 mortality (Image 5B) in the vaxed and unvaxed (for the UK population from ONS data). If morbidity is 33 times the rate of mortality, then Long COVID likely peaked around the same time. In other words, what I am saying is that Long COVID (and/or sudden death) may be moreso related to shedding from the recently vaccinated (affecting the vaxed and non-vaxed populations) and may have been particularly harmful with the emergence of the delta variant. Are the spike specific IgG1/3 from the upper respiratory tract being shed with the vaccinal spike mRNA that are captured in the exosomes (HERV-K102 particles) expressing spike at the surface which then targets the foamy macrophages in the new host (eg. sebocytes and tissue macrophages) explaining why shedding may be more dangerous with delta variant SARS-CoV-2 infection? I will summarize the exosome work in a new substack.
https://www.sciencedirect.com/science/article/pii/S0966842X17302123
Intentionally transmissible. They know what they’re doing
Great work, you are always bang on the money as far as I can tell as an enthusiastic amateur! You have taught me a lot so thankyou, and brilliant.
Very interested shedding transition between one-dose "vaccinated" and 2 dose "vaccinated", which I never would have suspected...
Now, what to do with that?
:-o
Please see new comment posted on X https://twitter.com/hervk102/status/1770827757674537343 on March 21, 2024 concerning differential impact of shedding on the unvaxed (no spike specific IgG4) versus the vaxed (with high levels of IgG4) and how vitamin D3 greater than 50 ng/ml can only protect those without IgG4 against all-cause mortality.
The CDC recognized long COVID in July 2021 as a new disease entity (https://www.cdc.gov/coronavirus/2019-ncov/long-term-effects/index.html?utm_source=substack&utm_medium=email) which was co-incidental with the projected maximal shedding related to increased C19 mortality (Image 5B) in the vaxed and unvaxed (for the UK population from ONS data). If morbidity is 33 times the rate of mortality, then Long COVID likely peaked around the same time. In other words, what I am saying is that Long COVID (and/or sudden death) may be moreso related to shedding from the recently vaccinated (affecting the vaxed and non-vaxed populations) and may have been particularly harmful with the emergence of the delta variant. Are the spike specific IgG1/3 from the upper respiratory tract being shed with the vaccinal spike mRNA that are captured in the exosomes (HERV-K102 particles) expressing spike at the surface which then targets the foamy macrophages in the new host (eg. sebocytes and tissue macrophages) explaining why shedding may be more dangerous with delta variant SARS-CoV-2 infection? I will summarize the exosome work in a new substack.