Hypothesis of Auto-Immune Disease Part-5 Of 8

Hypothesis of Auto-Immune Disease Part-5 Of 8

AIDS:


IS THE DISRUPTION THAT ALLOWS THE AIDS VIRUS TO GET A TOE HOLD THE EXTENDED LONG TERM REACTION OF THE 2ND STAGE STRESS RESPONSE TO THE CELL STARVATION, BROUGHT ON BY THE OXALIC AND PHYTIC ACIDS BLOCKING THE NUTRITIONAL DELIVERY SYSTEM?

TRANSMISSION DISRUPTION:

The initial disruption that would allow the easier transmission of the AIDS virus would be the disruption in the storage of glycogen creating an insufficient supply. This disruption is created when the low ATP trigger kicks in and stops the storage of glycogen. Glycogen is the substance that the vagina needs to maintain a large storage of in order to produce the mucosa. In the mucosa upon decomposition glycogen produces organic acids that create a low pH environment that serves to retard microbial and bacterial growth.

T4 CELL DISRUPTION:

As the stress continues from the nutrient depletion, the body goes into the General adaptation syndrome in the long-term resistance reaction 2nd stage stress response. As the controlled ranges are reset the Cortisol secretion becomes excessive (discussed in the Stress response). When homeostasis cannot be achieved due to the two acids then the negative feedback system that keeps the immune response in check is disrupted.

The immune system cannot achieve its goal so it cannot be switched-off. Initially the IL-1 stimulates a powerful immune response to the stressors. IL-1 stimulates secretion of ACTH which stimulates production of Cortisol. And the Cortisol suppresses further production of IL-1...

Thus the IL-1 becomes deficient. IL-1 must be present to costimulate the CD4 displaying helper T cells, without this stimulation the T cells cannot be activated an remain in a state of inactivity called anergy. In a state of anergy the T4 cells does not proliferate and differentiate cloning itself to form more highly specialized cells. Since the macrophages are inhibited from secreting IL-1, the T4 cells cannot be costimulated to secret cytokines such as IL-2, gamma-interferon, IL-4, and transforming growth factor beta (TGF-B)…IL-2 is needed for all immune responses and it is the prime trigger for T cell proliferation.

It also serves as a costimulator of resting helper Tor catatonic T cells, and it enhances activation and proliferation of T cells, B cells, and natural killer cells. IL-2 serves as a Positive feedback system .IL-2 acts in a paracrine {cure all} manner by binding to neighboring Th, Tc or B cells and serves as a costimulator to activate them when they bind to an antigen.

This disruption continues on much farther but it makes my point, on how the HIV can gain entry and cancers and toxins etc and seemingly the immune system is not activated are in major disarray. Well, it seems to me that it is! Because the body is in the 2nd stage long-term stress response and so the normal immune functions are inhibited. The deficient nutrients activate the stress response causing excessive cortisol which inhibits IL-1, and when the IL-1 is inhibited it cannot co stimulate the helper T cells to stimulate the cytokines, and the cytokines cannot stimulate the activity of monocytes, neutrophil and macrophages, IL-2, etc.

AIDS DISRUPTIONS:

Aids lowers the victim's immunity. CD4 molecules on the T4 cells allow the HIV entry. Slowly the T4 cell population is destroyed, as the cells become infected and die. The result is a progressive collapse of the immune system. The cytokines, monocytes, neutrophils, macrophages and non-specific defense mechanisms are depressed. ..

More Immune Disruptions:

CANCER:

IS CANCER SIMPLY THE CELLS' RESPONSE TO THEIR CELLULAR METABOLISM BEING ROBBED, AND THE CELLS PERCEIVING THIS AS A VIRUS HAVING TAKEN OVER..

A virus destroys a cell by taking over its cellular metabolism mechanism. So when the cell becomes so deficient that it can no longer perform its normal functions, it perceives a virus has infected it and so to protect the surrounding cells, it releases interferon which activates the inflammatory response. It also triggers a metabolism shift that inhibits the production of iron, zinc and other nutrients.

It also activates increased synthesizes of proteins by the other cells to disrupt the atmosphere in which the virus would thrive. The increased activation of protein synthesize, would seem to me, to be over-ridding the instructions encoded on the surrounding cells' DNA. Alteration of the DNA code means the cell has become damaged, and at this point cancerous changes are liable to occur. So the cells must go through cell death to make way for new cells and remove the damaged ones. The clotting factors that are suppose to trap released germs in these destructive processes, is disrupted by the deficient calcium, which plays a major role in the clotting process.

So germs are not contained for the white blood cells to remove. This battle of trying to capture and destroy the escaping germs and taking care of all the damaged and dying cells takes a considerable toll on the white blood cells (neutrophil). In an excessive vigorous prolonged battle that is actively going on, the white blood cells can begin to spill their garbage disposing enzymes (lysosomal), into the surrounding areas. These garbage disposals (lysosomes) are already weakened by the lack of sufficient oxygen created by the declining iron, which causes them to become fragile and rupture and burst.

The abnormal release of these enzymes does not only destroy the white blood cells, and the dying cells but also surrounding cells. This process can lead to pus and abscesses because the inflammatory responses that functions to remove this debris are inhibited by the excessive cortisol being released in the 2nd stage stress response, which has been activated by disruption in the nutritional delivery pathway.

The prolonged battle can cause normal human tissues to become cancerous. I feel, the greater amount of the nutritional deficiency, would translate into a greater number of white blood cells being released into the blood, which is called leukocytosis. These disruptions in my opinion could be contributing to the development of cancer and leukemia… Then add on the disruption in the immune response listed under AIDS and it seems to me this has created the breeding grounds for cancer…

Immunological surveillance disruption: The IL-1 stress related disruption in the activation of the cytotoxic T cells and macrophages and natural killer cells would open the chances up for a person to contract virus related cancers…Removal of the hindrance the original stressors the acid blockage, that leads to the stress response would allow the IL-2 to return to the activation process of the cytotoxic T cells and neutral killer cell causing them to return to the lymphokine-activated killer (LAK) cells naturally and without tumor immunotherapy or cytokine therapy, or antibody therapy, it would seem…

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