Chris,
Your October 23, 2024, interview of Kevin McKernan was excellent – thank you.
The emergence of “turbo” cancers connected with the DS sponsored deployment of the Covid-shots seems to be much more than merely a difference in degree (prevalence) but is a difference in “kind”.
The drastic increase in the incidence of cancer and corresponding mortality post Covid-shot deployment – can be explained in part by dysregulation of the host immune system – both agonism and antagonism (overstimulation and suppression).
Covid-shot immune suppression compromises the ability of the human host immune system to fundamentally control and repress cancer – but it also compromises the host ability to fight infection – in particular reactivation of latent persistent viral infections - wherein the indicated viruses are oncogenic (cancer causing).
But the nature and scope of the emergent cancer signal post Covid-shot deployment – appears to be a new “animal” – aka a new type of disease - pathology and etiology that involves rapid emergence and progression of very aggressive lethal cancers – which I believe is potentially directly linked to SV40.
Wild-type SV40 is a simian (monkey origin) DNA polyomavirus that is a relatively small-sized virus – that came to fame because it was found to contaminate the polio virus (Salk and Sabine) that was deployed in the late 50’s and early 60’s and resulted in infection of humans and an apparent subsequent explosion of cancer rates.
SV40 is an oncogenic (cancer causing) virus – that is believed to integrate into the host cell genome and/or create latent persistent infection in human hosts. Note, human SV40 infection is not solely simply related to contaminated polio vaccines – and is known to cause human infection and human-to-human infection.
SV40 has very high DNA-code sequence homology with other well-known oncogenic polyomaviruses of human origin that include the BK (BKV) virus and JC virus (JCV).
An important but not publicized fact about SV40 is that there appear to be in existence non-wild-type SV40 strains created by government laboratories and government adjacent entities that have extreme gain-of-function - that are much more lethal from a cancer-causing perspective – and elements from the same appear to have been adopted and optimized for supposed “gene-therapy” applications by some in the private sector.
The emergent “turbo cancers” can potentially be explained in terms of reactivation and modification of latent persistent SV40 infection in human hosts – that is NOT via a typical reactivation that is induced by simple host immunosuppression.
SV40 virus has the ability to reactivate in an infected host via a “multiplicity reactivation” mechanism that when considered in conjunction with other latent persistent co-infections such as BKV or JCV that have high sequence homology AND THEN Covid-shots that contain certain Pfizer/Moderna gene-therapy elements – that is SV40 DNA – promotor, enhancer and origin-of-replication viral sequences - might explain the creation at the infected cellular level of new lethal highly active SV40 viral analogs that causes heretofore unknown “turbo cancer” disease.
A perhaps inadvertent consequence of Pfizer and Moderna including gene-therapy technology based on SV40 promoter, enhancer and/or origin-of-replication sequences in the bivalent-Covid-shots analyzed by Kevin McKernan – is that these sequences are introduced directly in active (undegraded) form via the lipid-nanoparticle technology into host cells such that these DNA sequences get used in a well-known SV40 multiplicity-reactivation process that results not in simply reactivated pathogenic SV40 virus – but rather results in creation of a gain-of-function highly active new SV40 virus strain that potentially causes the so-called emergent turbo-cancers.
The SV40 multiplicity-reactivation mechanism relates to a collection (multiplicity) of individually inactivated-degraded-attenuated SV40 virus elements (in a host) so as to reconstitute and recombine DNA sequences (in a host cell) so as to generate a live active pathogenic virus in an infected host. The multiplicity-reactivation mechanism is perhaps by some form of well-known in vivo homologous recombination mechanism or other mechanism – but the end result is the SV40 can reactivate by mixing and matching and collecting viral DNA sequence elements that co-exist in the infected host.
The speculation herein that perhaps is not considered generally yet – is that Covid-shots do two (2) important things – suppress the host immune system in hosts that may have latent persistent wild-type SV40 infection AND provide critically important new SV40 promoter, enhancer and core code sequences – that can result in the reactivation (endogenous creation) of a much more lethal modified pathogenic active highly oncogenic SV40 virus – via the multiplicity-reactivation mechanism.
It remains to be seen whether it will be ultimately shown that Covid-shot induced in vivo host gain-of-function by multiplicity-reactivation of latent-persistent SV40 infection to be the etiological agent causing some of the emergent turbo-cancers post-Covid-shot deployment.
A further factor to consider is whether latent-persistent co-infections in a host by other polyomaviruses that have very high sequence homology also contribute DNA code elements for a very lethal gain-of-function multiplicity-reactivation of SV40 in a host that has been given the Covid-shot(s).
The above is just my speculation about the potential link of SV40 to emergent turbo-cancers post Covid-shot deployment.
Again, thanks for your excellent interview.
pbd
