The Vaccine/Immunity Disconnect

I was sent the following from one of my friends, and am posting it because it contains valuable information you won’t find in the MSM or from the various colluding health authorities:

The Vaccine - Sentinel T-cell Disconnect

Following is opinion.

First, the practice of vaccinating those with a healthy Natural Immune System is inane, counter-productive, and potentially detrimental to the Natural Immune Systems. Those who have had and recovered from COVID-19, with or without symptoms, should be naturally immune thereafter. Further, as I understand, a blood test as used for some cancer patients whose immune systems have been attacked can give a good indication of an immune system’s health, e.g., one such a test includes:

Hematocrit determination (HCT),

Hemoglobin determination

Lymphocyte %

Lymphocyte Count:

Mean corpuscular hemoglobin concentration determination

Mean corpuscular hemoglobin determination (MCH)

Monocyte %

Monocyte Count:

Monocyte %

Platelet Count:

Red Blood Cell Count

Red Cell Distribution: (Size of Red Cells)

White Blood Cell Count

Vaccines are not designed to protect from variants or provide permanent immunity. In fact, the word immunity should seldom appear in the same sentence with the word vaccine. Short term protection, symptom reduction, and lower initial death count is not synonymous with immunity.

In the history of vaccines only one virus has ever been eradicated for humans , i.e., neutralized as a world risk - smallpox. Only one.

https://www.ncbi.nlm.nih.gov/books/NBK20370

[For the curious, The rinderpest virus has also been eradicated in ruminants (an even-toed ungulate mammal that chews the cud regurgitated from its rumen). That’s the only other success case.]

For anyone to assume or assert that “Vaccines protect against severe disease and death and are considered central to ending the pandemic,” is, in my opinion, naive or knowingly misleading by including, “...central to ending the pandemic”. That’s a whopper, particularly as our natural system is ignored and only one vaccine has been that successful.

Vaccines, by their nature, lack both long term and variant responsibilities. They are short term, designed with target specificity to protect against a ‘current’ threat, and are not designed for either long term or for variant responsibility. Variants will generally necessitate a ‘re-engineering / modification’ and vaccine re-release to combat serious variants.

Only the Natural Immune System (NIS) which has evolved over millions of years to insure the survival of the species , by protecting permanently against re-infection and all variants, can provide “immunity” - which by definition is long term. A person is either immune or is not immune to a specific virus / pathogen.

Incidentally, it has been found that some people are immune from COVID-19 who have not only never had COVID-19, but not even predecessor SARS. The Natural system is so effective long term that immunity from some unknown past time can be passed down through one’s genetic history into birth, called “Adoptive Immunity”.

Our NIS T-cells serve as sentinels and a killer function to pathogens which may re-appear in some related form. I read implications too often that vaccines and our NIS T-cells cooperate as if they were part of same system. However, vaccines do not appear to give full T-cell sentinel support, i.e., recognition of a variant.

In my opinion, we understand the logical functions of our NIS, but we do not fully understand the physical implementation of these logical functions. For instance, exactly how do the sentinels physically function? How do they ID exactly what determines a family variant, no matter how long past the original pathogen appearance?

As an example does the sentinel function capture key parameters of the antigen? Or perhaps is there some deep coded family signature, a virus family ID, yet not discovered in each antigen, meaningful only to the T sentinel, but which, therefore, is missing from vaccine wannabees?

Engineered vaccines, blind to such a key, or some other not yet discovered T-cell sentinel physical implementation technology, would fail the necessary code for T sentinel recognition and cooperation. Such appears to be the case from the evidence, i.e., there would be far more than one success case (smallpox) and not be the massive numbers of fully vaccinated falling prey to any virulent variant, and most certainly, no need for booster injections, hence history of failures to neutralize virulent variants would logically appear to make the case for the absolute disconnect between our vaccines, e.g., experimental COVID-19, and the NIS T-cell sentinel function required for variant recognition.

There can be no question that our world’s population is being misled by visions of “immunity” from any vaccine - other than for smallpox, certainly not COVID-19.

SKIP