COVID-19: 2 - WHERE ARE THE WINNERS AND WHERE ARE THE LOOSERS?

"Of all tyrannies, a tyranny exercised for the good of its victims may be the most oppressive".- C.S. Lewis

The latest litigation concerning damages and information about harmful effects of vaccines "against" viruses is reported here: https://www.globalresearch.ca/video-dr-anthony-fauci-on-the-2009-h1n1pandemic-the-2009-h1n1-vaccine-caused-brain-damage-in-children/5711540 . Mainstream media confirmation of the seriousness of the problem of virus interference alias vaccine-induced enhancement, which is misleadingly called "antibody-dependent enhancement" (to divert attention from vaccines) is given in Wikipedia here: https://en.wikipedia.org/wiki/Antibody-dependent_enhancement and here: https://en.wikipedia.org/wiki/Cytokine_storm .

And now the last important fact about the promised "COVID-19 vaccines". They are being botched in extreme haste and secrecy. Here is what is known about the two of them which Western mass-media advertise as "favorites" in the insane race for grabbing world-wide monopoly profits:

Moderna+B.Gates+NIH (USA)	AstraZeneca+B.Gates+Oxford University
Genetically modified (not specified) mRNA (cRNA) in some sort of liposome carrier, hence patentable, meaning monopoly superprofits (see pic below)	Common cold virus (Rhinovirus) with inserted COVID-19 spike protein gene, hence patentable, meaning monopoly superprofits (see pic below)
No animal testing, human testing already revealed health damage in 50 % of vaccinated!	No animal testing, human testing in South Africa and Brazil - corrupt governments
First mass vaccination campaign is planned to be carried out in West Africa - corrupt governments, no chances of persecuting the manufacturer for health damage to vaccinated	Plans of mass vaccination not yet publicized
World-wide mass-media PR and propaganda as "the only weapon against COVID-19"	World-wide mass-media PR and propaganda as "the only weapon against COVID-19"
Heavily subsidized by the US government	Heavily subsidized by the UK government

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I hope that everyone in democratic countries is free to draw his personal conclusion from the facts quoted above. Here is mine:

Nevertheless the governments around the world and especially the govt. of USA are irresponsibly squandering astronomical sums of money in a genuinely "helicopter" manner on useless and potentially dangerous vaccines "against COVID-19". All Big Pharma crooks get as much money as they wish. Let me quote recent news from here: https://www.cnbc.com/2020/07/22/us-government-taps-pfizer-to-produce-millions-of-doses-of-coronavirus-vaccine.html :

"The U.S. will pay Pfizer and biotech firm BioNTech $1.95 billion to produce and deliver 100 million doses of their Covid-19 vaccine if it proves safe and effective, the companies announced Wednesday. It was the largest such deal between the government and companies racing to develop a coronavirus vaccine. Under the agreement, the U.S. can acquire 500 million additional doses, the Department of Health and Human Services said. Germany-based BioNTech and Pfizer are jointly developing four potential vaccines. (...)

The companies previously said they expect to begin a large trial with up to 30,000 participants later this month, if they receive regulatory approval. Shares of Pfizer were 3.8% higher in early trading Wednesday and BioNTech stock was up 4%. The companies announced earlier this month preliminary data for vaccine candidate BNT162b1, the most advanced of their four potential vaccines. Researchers said the early-stage clinical trial showed the BNT162b1 vaccine produced some neutralizing antibodies, which researchers believe is necessary to build immunity to the virus."

Bloody hell! What does it mean - "SOME"??? And what about NON-neutralizing antibodies which can make infection VERY dangerous? But who cares? Let's read on: (...) "The deal was signed as part of Operation Warp Speed, the Trump administration's effort to accelerate development and production of vaccines and treatments to fight the coronavirus. (...)As part of the program, the government previously announced a $1.6 billion agreement with Novavax to accelerate development of its potential vaccine with the aim of delivering 100 million doses by January. The government also announced a $456 million investment in Johnson & Johnson's vaccine candidate in March, $486 million in support for Moderna's vaccine in April, and up to $1.2 billion in May for AstraZeneca's vaccine being developed with Oxford University. The U.S. government also awarded Emergent Biosolutions $628 million to expand domestic manufacturing capacity for a potential coronavirus vaccine and drugs to treat Covid-19." (End of quotation)

It is incredibly scandalous: Big Pharma Fat Cats get huge sums of money just for promises that one of them will deliver "a safe and effective vaccine", which is the equivalent of proverbial "pie in the sky"! The proper name for this "deal" is: corruption and rip-off. Profit-driven propaganda of vaccines by Mr. Bill Gates, Big Pharma and corrupt mass-media ignores the fundamental fact that vaccine-induced presence of specific antibodies, binding (agglutinating) in vitro antigens of SARS-Cov-2 virus does NOT mean that this enables the immune system of the vaccinated person to defeat SARS-Cov-2 infection. The cult of vaccines is a dangerous simplification, because the immune system of humans is very complicated and all its components must function in harmony to fend off viruses, bacteria, cancer cells and other pathogens.

Roughly speaking, our immune system consists of two parts which work together. The first one is called humoral immunity because its main (but not the only!) components are proteins and other biomolecules in extracellular fluids (blood and lymph), among them antibodies, the complement system and cytokines. It is the part of immune system which vaccination tries to exploit.

Humoral immunity exists thanks the ability (among other important functions) of B-cells (or B-lymphocytes) to proliferate a clone which mass-produces antibodies against the presented antigen in response to antigen presentation by macrophages (mediated by T-helper cells).

Antibodies, as mentioned before, differ in their function. Neutralizing antibodies activate the complement system which attacks and destroys the pathogen (microbe or virus). This is the short-cut functioning of the immune system which Mr. Bill Gates tries to falsely depict as the only way immunity works.

But immune system is much more complicated. All previous attempts to create vaccines against coronaviruses gave as results something that after injection produce mainly binding (non-neutralizing) antibodies which work in cooperation not with the complement, but with macrophages and other phagocytes, which require activation by the other part of immune system - the cell-mediated immunity. If phagocytes are not activated, as is obvious in case of coronavirus vaccines, vaccination is useless and obviously dangerous because of two things: first, non-neutralizing antibodies can induce vaccine-induced enhancement discussed earlier, and second, because of the side-effects of other vaccine components, of which the most dangerous are the so-called "adjuvants".

Whereas humoral immunity normally remains in good working condition at high age because it is based on B-cells which in mammals undergo maturation and differentiation in bone marrow, the cell-mediated immunity tends to weaken with growing age because it is based on T-cells which in mammals undergo maturation, differentiation and strict selection in thymus.

Thymus is a secretory organ which functions only in childhood and undergoes involution (atrophy) in puberty under the influence of sex hormones. There are many functional types of T-cells (or T-lymphocytes) which in their totality build the most important system of organism - the system of recognition "self-not self" which is formed in childhood by the selection of T-cells in thymus. The immune system is thus only a part of this more general system, which is demonstrated by the direct causal relation between disturbances of cell-mediated immunity and autoimmune diseases (recognizing "self" as "not self"), or cancer diseases (recognizing "not self" as "self").

It would be useful to watch this video ( https://www.youtube.com/watch?v=9E_UxnC_L2o ) to grasp in general the enormous complexity of the selection and maturation processes which T-cells undergo in thymus. But we have to concentrate now on cell-mediated immunity as a whole. Habitually it is defined as "an immune response that does not involve antibodies" (see e.g. https://en.wikipedia.org/wiki/Cell-mediated_immunity ) which is plainly wrong, because the immune system is one whole entity and there are many known and unknown interactions between the two parts of it, one of which are binding antibodies marking antigens for subsequent destruction by phagocytes.

The most important fact concerning COVID-19 is its danger to decrepit persons (i.e. the elderly and chronically ill), not those who are young and healthy. The obvious conclusion is that COVID-19 mortality is (provided there is no vaccine/viral induced "enhancement" of disease mentioned above) caused by the deficiency of cell-mediated immunity, particularly the T-cell insufficiency at high age which (see e.g. https://en.wikipedia.org/wiki/T_cell_deficiency ) "generally manifests as unusually severe common viral infections".

Therefore it is obvious that the vaccine-only monomaniacal approach (actually "business plan") of Mr. Bill Gates, Big Pharma and mass-media is badly wrong. The solution of COVID-19 problem lies in finding natural ways to boost cell-mediated immunity in order to give protection not only from viruses, but also from other pathogens and other diseases caused by the malfunctioning of immune system, such as cancer, HIV, diabetes mellitus type 1, multiple sclerosis, rheumatoid arthritis, and systemic lupus erythematosus. The victims of COVID-19 and all these diseases, as noted before, are predominantly the elderly, because the bottle-neck in functioning of their immune system is the insufficiency or weakness of cell-mediated immunity.

The tragic reality is: this direction of biomedical research is very poorly financed because it does not promise monopolistic super-profits which are now customarily made on vaccines and patented GM-organisms and GM-molecules (DNA and RNA). Nevertheless there were brilliant results of cancer research in this direction which have direct relevance to the problem of COVID-19 and other viral infections. I mean Prof. Nobuto Yamamoto's research of vitamin D-binding Gc protein-derived macrophage activating factor (GcMAF). Here are some references to his articles in cancer research journals:

Nobuto Yamamoto, Naofumi, Ushijima, and Yoshihiko Koga. Immunotherapy of HIV-infected patients with Gc protein-derived macrophage activating factor (GcMAF). Serum Gc protein (known as vitamin D3-binding protein) is the precursor. J Med Virol. Jan; 81(1):16-26. 2009.

Yamamoto N, Suyama H, Nakazato H, Yamamoto N-Y, Koga Y. 2008. Immunotherapy of metastatic colorectal cancer with vitamin D-binding protein-derived macrophage-activating factor, GcMAF. Cancer Immunol Immunother 57:1007–1016.

Yamamoto N, Suyama H, Yamamoto N-Y. 2008. Immunotherapy of prostate cancer with Gc protein-derived macrophage-activating factor, GcMAF. Translational Oncol 1:65–72. - http://www.transonc.com/pdf/manuscript/v01i02/neo08106.pdf

Yamamoto N, Suyama H, Yamamoto N-Y, Ushijima N. Immunotherapy of metastatic breast cancer patients with vitamin D-binding protein-derived macrophage-activating factor, (GcMAF). Int J Cancer 2008 Jan 15;122(2):461-7.

See also https://en.wikipedia.org/wiki/Vitamin_D-binding_protein .

We see here again one of the components of successful medical prevention and early-stage treatment of coronavirus diseases, including COVID-19, namely vitamin D... together with its protein carrier in blood (DBP) which turns out to have an important function in cell-mediated immunity, namely the activation of macrophages. It should be noted that vitamin D deficiency (avitaminosis) is one of the major causes of poor health among the elderly.

Macrophages are the most potent pathogen-fighting agents of cell-mediated immunity and therefore (so to say for safety reasons) need for their activation the vitamin D-binding protein (DBP) to be first converted into macrophage activating factor (GcMAF) by interaction with both B-cells and T-cells which are centrepieces of humoral and, correspondingly, cell-mediated parts of immune system. Unfortunately, many viruses possess an agent which prevents this conversion of DBP into GcMAF and therefore the activation of macrophages - the enzyme called n-acetylgalactosaminidase (nagalase). These interactions are in essence different enzymatic cleavages of the oligosaccharide attached to the threonine-420 residue of DBP:

Unfortunately I have to conclude this presentation with the sad message that successful treatment of cancer with injections of purified GcMAF by British GcMAF-enthusiasts Mr. David Noakes and Ms. Lyn Thyer was stopped by vicious scheming and litigation of Big Pharma.

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