This OpEd will show that the present mainline “vaccines” being deployed against COVID-19 during the “pandemic” are ineffective in preventing viral infection and transmission, are harmful to the host, and enable the escape and propagation of viral mutants.
1. “Vaccine” Ineffectiveness
We live in a sea of viruses named the virome. We are continually exposed to these viruses; we can no more avoid them than we can avoid the oxygen in the air we breathe or the hydrogen in the water we drink. In fact, it is this continual interaction of the host with myriad viruses that potentially increases robustness and functionality of the host’s immune system.
Whether or not this exposure results in infection and serious disease depends on the pathogenicity of the virus and health of the host’s immune system. If the immune system is dysfunctional, it will be unable to fully neutralize any pathogenic virus. For the SARS-CoV-2 virus, the dysfunctional immune system will allow the virus to enter and replicate in cells and trigger a chain of events, ultimately leading to COVID-19.
The main source of SARS-CoV-2 viral entry is through inhalation, and somewhat less through ingestion. An effective vaccine would focus on cellular immunity in the respiratory and intestinal tract, in which secretory IgA is produced by “immune cells (lymphocytes) that are located directly underneath the mucous membranes that line the respiratory and intestinal tract. The antibodies produced by these lymphocytes are ejected through and to the surface of the linings. These antibodies are thus on site to meet air-borne viruses and they may be able to prevent viral binding and infection of the cells.
Unfortunately, the main inoculants used presently for COVID-19 focus on antibodies (IgG and circulating IgA) that occur in the bloodstream. “These antibodies protect the internal organs of the body from infectious agents that try to spread via the bloodstream.
Vaccines that are injected into the muscle – i.e., the interior of the body – will only induce IgG and circulating IgA, not secretory IgA. Such antibodies cannot and will not effectively protect the mucous membranes from infection by SARS-CoV-2. Thus, the observed “breakthrough infections” merely confirm the fundamental design flaws of the vaccines. Measurements of antibodies in the blood can never yield any information on the true status of immunity against infection of the respiratory tract.”
“a natural infection with SARS-CoV-2 (coronavirus) will in most individuals remain localized to the respiratory tract. The vaccines used presently “cause cells deep inside our body to express the viral spike protein, which they were never meant to do by nature. Any cell which expresses this foreign antigen on its surface will come under attack by the immune system, which will involve both IgG antibodies and cytotoxic T-lymphocytes. This may occur in any organ, but the damage will be most severe in vital organs. We are seeing now that the heart is affected in many young people, leading to myocarditis or even sudden cardiac arrest and death.”
In other words, we are dropping the wrong bomb on the wrong target at the wrong time!
2. “Vaccine” Harm to Host
“There are at least three types of toxicities associated with the inoculant. The spike protein resulting from the inoculant is extremely toxic….The LNP encapsulating shell has some extremely toxic components, such as polyethylene glycol, to which many people are sensitive…..and cationic lipids. The desired product of the inoculations, anti-spike protein antibodies, can react with tissues and cause myriad types of damage”
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https://trialsitenews.com/covid-19-vaccines-the-wrong-bomb-over-the-wrong-target-at-the-wrong-time/