By inoculating the host with a sub-optimal vaccine and applying such a vaccine for large-scale immunization programs (e.g., across all age groups), the risk of viral immune escape can only be increased. By placing widespread immune pressure on spike protein (mass vaccination with S-based vaccines!) of a virus that exerts high infectious pressure (dominant circulation of more infectious variants), mass vaccination during a pandemic of more infectious variants is adding fuel to the fire in that it enables the population to exert more and more pressure on viral infectiousness (as S spike protein is responsible for viral infectiousness). Consequently, stakeholders of these campaigns have gravely underestimated and discounted the evolutionary capacity of the virus to naturally select highly infectious variants and adapt them to an environment of high but suboptimal population-level immune pressure. Widespread rising levels of non-sterilizing immunity provides more infectious variants with a fitness advantage they would not normally have during the evolution of a natural pandemic (i.e., in the absence of massive S-directed immune pressure). As vaccination of large cohorts of the population provides a breeding ground for more infectious variants, the latter will now expand in prevalence and become dominant.
The purpose of this brief op-ed is therefore to warn the very same public health decision makers who implemented this flawed vaccine program using imperfect non-sterilizing vaccines that if they continue, they run the risk of driving the emergence of highly infectious variants that may eventually lead to more frequent and more pronounced pathogenicity. It is reasonable to assume that coronaviruses (CoVs) are amenable to escaping from all neutralizing antibodies by promoting variants capable of using alternative receptors on the surface of permissive host cells. As this would not affect epitopes recognized by previously neutralizing antibodies, antibody-opsonized virions would be suspicious of causing enhanced/ exacerbated pathogenicity. This is a very dangerous situation, particularly so if we move to vaccinate our children who do not need these vaccines and bring a near statistical zero risk of severe outcome to the table. The vaccines offer all risk and no benefit to children. Childern have the gift of innate immunity; it is very powerful and usually serves them as their first line of immune defense. Why subvert this?
We warn again that mass vaccination as it is occurring now with these vaccines can potentially accelerate development of further variants as well as antibody-dependent enhancement (ADE) of disease. “Previous respiratory syncytial virus and dengue virus vaccine studies revealed human clinical safety risks related to ADE, resulting in failed vaccine trials.” We point to the seminal work by Read et al. (about Marek’s disease) that imperfect vaccination can enhance the transmission of highly virulent pathogens. We thus state emphatically here that it is very misguided of public health, the CDC, and NIH, to discount the impact of the mass vaccination and to disregard the role of the vaccinated populations in the transmission of COVID virus, both to the vaccinated and the vulnerable unvaccinated persons. We argue that the vaccinated has a role potentially equal, if not superior, in the transmission of COVID virus to that of the unvaccinated. This argument is based on the published data out of Israel, the UK, the US, and elsewhere. The fully vaccinated must be considered a source of transmission, and while it is no fault of their own and they must not be stigmatized just as the unvaccinated must not be stigmatized, it is a consequence of a combination of immune pressure, infectious pressure, and the mass vaccine program during the midst of a pandemic with massive circulating pathogen. The evidence is strong that the fully vaccinated can become infected, colonize, and transmit the virus—particularly heavy loads of virus. This opens the door for an unvaccinated person with a fully intact functional immune system to be potentially overwhelmed by a massive viral load from the vaccinated. The vaccine has failed against Delta; disregarding the vaccinated as a source of pathogen and spread could be catastrophic. We point to the following more recently published evidence and call on decision makers to urgently consider this data and adjust their control measures. You will not be able to avoid infection or disease by staying away from vaccinees. What counts instead is improving your immune defense: first, by declining the shot and, second, by improving innate immunity (via a healthy lifestyle, nutrition. etc.). What is the key evidence that underpins this warning? How do we know that the vaccine has failed against the Delta and there is a real serious problem? We argue that continued mass vaccination will only push the evolutionary capacity of SARS-CoV-2 Spike protein beyond the Omicron version. As examples, Gazit et al., Acharya et al., Riemersma et al., Chemaitelly et al., Subramanian and Kumar, Chau et al., Shitrit et al., Hetemaki et al., Levin et al., Rosenberg et al., Suthar et al., Nordström et al., Yahi et al., Goldberg et al., Singanayagam et al., Keehner et al., Juthani et al., Embi et al. at the CDC , Eyre et al., Levine-Tiefenbrun et al., Puranki et al., Saade et al., Canaday et al., Israel et al., Salvatore et al., Eyran et al., Andeweg et al., and Di Fusco et al. have shown us that the vaccinated can become infected, can harbour the virus, and can potentially transmit it. We are looking at not only potentially more infectious variants, but more lethal ones due to these sub-optimal non-sterilizing vaccines. This is a huge problem, and Kampf as well as Masre et al. (alternative receptors for SARS‐CoV‐2 viral entry into host cell) provides us further warnings. Kampf echoes a key warning of ours: “It appears to be grossly negligent to ignore the vaccinated population as a possible and relevant source of transmission when deciding about public health control measures.” It is very likely that the vaccinated do transmit. They can harbour elevated viral loads and thus can potentially spread the virus to the vaccinated and unvaccinated. We now have consistent credible reports (as above) of no significant difference in PCR cycle count threshold values between vaccinated and unvaccinated, asymptomatic and symptomatic groups infected with SARS-CoV-2 Delta, no difference in viral loads when comparing unvaccinated individuals to those who have vaccine “breakthrough” infections, and waning efficacy (antibody responses and T cell immunity) by the fourth to sixth months. The vaccinated are showing on average much more virus in their nose than the infected unvaccinated. Alarmingly, secondary transmission in nosocomial outbreaks is occurring from nurses with symptomatic infections in spite of the use of personal protective equipment and masks. Also of concern is the finding in the UK data (reports 42, 43, 44, 45, 46, 47) of elevated infection in the vaccinated and depressed N antibody levels in persons who acquire infection following 2 doses of vaccination. Because of the evidence presented above and a simultaneous consideration of the adverse events and deaths reported to the CDC’s VAERS database, we cannot support this mass vaccination. The COVID vaccines are proven to be too ineffective and unsafe at this time to warrant support for mass vaccination. This must be stopped and not even vulnerable persons should be vaccinated with these vaccines; definitely they should not be given to our children. For the latter, the costs are unacceptable. As mentioned above, these sub-optimal non-sterilizing vaccines would damage and subvert the potent polyspecific innate immune system response in children that is their first line of immunological defense and which serves them so well in fighting SARS-CoV-2, including all its variants (specific high-affinity vaccinal antibodies could outcompete polyspecific low-affinity innate antibodies). This could not only potentially create asymptomatic super-spreaders of highly infectious variants, but also, alarmingly, leave children highly vulnerable to other viruses and pathogens due to their subverted ‘first line of defense’ innate immune system. None of these defense mechanisms can be replaced by the vaccinal antibodies from which the virus is now increasingly escaping. To close, we are bypassing fully capable and sterilizing innate immune systems in our populations (and also natural adaptive/acquired immune systems) and eroding them by inducing non-sterilizing immune responses with an ever-decreasing capacity to recognize the target pathogen (antigen). This can have catastrophic consequences for populations and humanity. This deserves very serious consideration as we move forward. Moreover, repeated natural boosting due to high rates of viral re-exposure (circulation of highly infectious variants) will prevent vaccinal antibody titers from declining and is, therefore, at risk of continually suppressing the innate immune system, which could have devastating consequences for both adults and children. It is our opinion that a hard stop to this vaccine program is the only path forward, with an equally acute pivot to the use of chemoprophylaxis antivirals as well as for treatment of the infected. These current COVID vaccines are proving to be too unsafe with rapidly waning immunity to justify use. President Trump must come forward and speak out against the vaccine of young persons and children. We need his leadership in this for OWS under him spawned these vaccines. Meanwhile, ostracizing, stigmatizing, and attacking unvaccinated persons (including the COVID-recovered) is not only morally wrong and unethical, it has no credible medical or scientific basis. Read more at: LifeSiteNews.comThey are screwing with the weather maps: SUN is BAD!
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