Are Covid-19 Vaccines Promoting the Formation of Stealth Adapted Variant Coronaviruses?

Public Health officials seem to not realize the probable role of Covid-19 vaccines in hastening the creation of stealth adapted coronaviruses. Indeed, they’ve already still not accepted arsenic intoxication widespread human infections with stealth adapted monkey-derived viruses. These viruses were inadvertently introduced into humans from polio vaccines. This occurred as being the consequence of using polio vaccines grown inside the cultured kidney cells of cytomegalovirus infected monkeys.

A faulty assumption could be that the current Covid-19 vaccines provide immunity which is comparable to that surrounding natural infections. This is clearly less than. First, the vaccine has by intramuscular injections, whereas natural infections occur through respiratory mucosa. Intramuscular injections aren’t particularly effective in stimulating enhancing mucosal immunoglobulin A (IgA) antibodies or resident cytotoxic T lymphocytes (CTL). The lowered volume of vaccine induced mucosal immunity signifies that upon experience SARS-CoV-2 virus, a proportion of vaccinated individuals will more than likely acquire a persisting, subclinical infection which is restricted towards the superficial respiratory mucosa. Public Health authorities allude to the present possibility by insisting that people who are immunized should continue wearing masks. The persisting low-level infections will, however, supply the opportunity for that emergence of virus variants. Some of these is often more infectious, and some will be better capable to evade vaccine evoked immunity and, therefore, be widespread through the body.

The second major difference between the vaccine and natural infection is FDA’s allowance in the use of just one virus component inside the vaccine, namely the spike protein. It is much easier for virus modification, or perhaps deletion, of just one component as opposed to for concurrent changes to occur within the multiple antigens targeted by immunity to natural infections. Deletion on the spike protein may be possible since coronaviruses have other method of entering into cells. The virus will then more easily undergo changes inside remaining genes that code for your relatively few virus components typically targeted by cellular immunity.

The persistence of subclinical infections due to relative absence of mucosal immunity achieved by intramuscular injections along with the systemic immune response being limited by only the spike protein, oftentimes leads more rapidly than will natural infection, on the formation of stealth adapted coronaviruses. A corollary on this premise is usually that the English, South African, and Brazillian variants probably started in individual participants in the Covid-19 vaccine trials conducted in each from the countries. With wider vaccine use, more variants, including stealth adapted coronaviruses, need to be expected.

Stealth adaptation has another very concerning feature. It is the incorporation more genetic sequences that happen to be probably required for your virus to regain infectivity. The added sequences may appear from the cellular genome and on the genomes of other microbes. This has, as an example, allowed polio vaccine derived stealth adapted viruses to get monkey cellular sequences into humans.

The mental faculties are particularly vulnerable to symptomatic illnesses brought on by stealth adapted viruses. These viruses is usually cultured from patients using the chronic fatigue syndrome (CFS) plus from children with autism. The Long Covid syndrome has lots of clinical features that resembles CFS. Until proven otherwise, the Long Covid syndrome is highly recommended as a viral illness together with the potential of human to human transmission, including when pregnant. It is critical to begin culturing blood samples from patients with all the Long Covid syndrome as well as sequence any resulting viruses.

Although the cellular body’s defense mechanisms will normally not build relationships with stealth adapted viruses they are able to still be suppressed with the alternative cellular energy (ACE) pathway. This pathways has likely preceded photosynthesis in plants along with the obtaining of one’s energy by all life forms through the metabolism of food. In humans and animals, the mental faculties are probably the major receiver on the life-force energy with the ACE pathway. The attracted energy might be transferred towards the body’s fluids where it truly is expressed being an added kinetic activity. The energy is termed KELEA, an abbreviation for Kinetic Energy Limiting Electrostatic Attraction. KELEA will also be added to water, which will then be termed KELEA excellerated water. Wearable pouches containing this water and inhaling nebulized mists through the water are evaluated as simple ways of enhancing the ACE pathway. These approaches can seemingly suppress both conventional and stealth adapted virus illnesses.