Botswana Guardian

How SARS- CoV- 2 causes Covid- 19

- Howard Armistead

Viruses are incredibly small and a bit mysterious. They can cause debilitati­ng disease, death, and pandemics that threaten both families and national economies. The word virus comes from the Latin word vir, meaning poison. Viruses cannot reproduce on their own and can only do so by infecting cells. There are thousands of plant and animal viruses, but not all those that infect humans threaten our lives. According to the book A World of Viruses, the average person has about one hundred different viruses living inside them, mostly in peaceful coexistenc­e with their own cells.

Peacefully coexisting viruses have existed in humans for ages. However, when novel viruses initially jump the species barrier into humans from chimpanzee­s, birds, bats, or other animals; then a microbiolo­gical war ensures with viruses commandeer­ing our cells to produce copies of themselves and raiding our cellular resources.

Researcher­s work diligently to understand a disease and how a virus works so they can design therapies to treat it. Within a year of its discovery scientists developed a theory explaining how HIV causes AIDS that seemed to fit the facts. It was simple. The HIV virus infects T- helper cells, also known as CD4 cells. Then viral replicatio­n produces thousands of viral copies in those cells until they burst and die. That releases viruses to infect more cells. Today the common understand­ing remains that HIV causes AIDS by killing CD4 cells. Surprising­ly, that overly simplistic, early hypothesis is logically impossible.

On the 20th anniversar­y of the discovery of AIDS, in his keynote address at the first “scientific” conference on AIDS in Buenos Aires, Argentina, Dr David Ho explained that the way everyone thought and taught that HIV causes AIDS could not possibly be true because HIV only infects one percent of CD4 cells. “HIV cannot kill all CD4 cells if it only infects 1percent of them. Something else must be happening.” That statement was shocking. One of the premiere AIDS researcher­s in the world, Dr Ho who had developed the protease inhibitors drugs that stopped the dying, was telling the most imminent gathering of internatio­nal scientists that the common knowledge they thought was true was not. In one speech Dr Ho completely shattered the existing theoretica­l paradigm of AIDS causation. However, he did not propose an alternativ­e.

If HIV did not cause AIDS by killing CD4 cells, what was the other thing that “must be happening”? In my essay “How HIV Causes AIDS” I provided a logical scientific explanatio­n. HIV does not cause AIDS by killing CD4 cells. Rather it does so by gradually reducing the production of new CD4 cells. My theory fits the scientific facts much

Omore closely than the original explanatio­n that was obviously a premature hypothesis.

A fter years of research surveying the scientific literature about HIV and other viruses and reading numerous books on virology and immunology, when the 2014 Ebola epidemic erupted in West Africa, I knew exactly what could reduce the high mortality rate. Something that had already proved effective against Marburg virus, HIV, and deadly Hantavirus, and according to the Lancet medical journal should help against most RNA viruses – selenium. The Liberian Ministry of Health requested me to bring selenium to Monrovia to test. There Dr Jerry Brown treated his patients at the ELWA- ll Ebola treatment unit with 1.2 grams of selenium added to the prevailing standard- of- care. Adding selenium reduced the Ebola mortality rate by 46.8 percent compared to the standard- of- care alone. During the 2014- 2016 epidemic no other medicine proved nearly as effective. When Covid- 19 emerged in January 2020, I noted many similariti­es, but also its difference­s from Ebola virus disease. If selenium worked so effectivel­y against numerous other RNA viral diseases, theoretica­lly it should show tremendous benefit against Covid too.

There is a long list of symptoms of Covid- 19. Not everyone experience­s the same set. But most suffer the most common ones. Covid progresses through several stages commencing with a brief asymptomat­ic phase, followed by cold- like symptoms, then flu- like symptoms, progressin­g to pneumonia, oxygen deprivatio­n requiring supplement­al oxygen, then ventilatio­n, and finally a critical stage characteri­zed by a cytokine storm, sepsis, organ failure, and death. Like Ebola, Covid involves generalize­d blood- clotting, technicall­y known as DIC – disseminat­ed intravascu­lar coagulatio­n. Although we peg Ebola as haemorrhag­ic fever – a disease of bleeding – like Covid, initially it causes massive internal blood clotting. A cornerston­e of Covid- 19 is the extensive oxidative damage done to lung alveoli cells that oxygenate blood, and the capillarie­s in the lungs that carry oxygen. ne reason Covid is so devastatin­g is that unlike influenza or HIV, it affects many different structures in the body. That is because it enters cells using the ACE2 receptor, a receptor found on the surface of many cell types. One easily could list twenty or more symptoms of Covid and its frequent aftermath, long- Covid. That would provide a general picture of the course of the disease, but it would not reveal the underlying mechanisms of how the virus causes those symptoms. For that one must dig deeper to what is taking place in the immune system and inside infected cells where the virus replicates. Once there, you realize this is a very smart virus. Smarter than many who are dedicated to fighting it. That is why we are losing the treatment war. As with HIV, if the theoretica­l paradigm is incorrect, we miss a key piece of the scientific puzzle, and with it the potential to improve life- saving therapy. The virus wins. Humanity loses.

Antioxidan­ts are naturally occurring enzymes in each cell that prevent oxygen free radicals from damaging structures in those cells. They are essential for cellular and human health. Without sufficient cellular antioxidan­ts, cells get sick and eventually so does a person. The most important antioxidan­t in the body is glutathion­e- peroxidase ( GPx), the “universal” antioxidan­t that is in every cell of the body. The functional part of GPx consists of a seleniumco­ntain protein. Without enough of the essential trace element selenium, antioxidan­ts cannot be formed.

A virus infects a cell and seizes its factory- like protein production machinery located in its nucleus. Then it diverts the chemical resources of that cell to produce its own viral proteins according to the blueprint laid out in its viral genetic code. According to scientists both HIV and Ebola geneticall­y encode selenium containing proteins for their protective, envelop sheathing. Biologists refer to selenium as the “universall­y protective element”. Viruses secure their own protection by stealing that protective element from our cells, primarily from our antioxidan­ts where much of the cell’s selenium is found. Destructio­n of our cellular antioxidan­ts by SARS- 2 damages oxygen exchanging alveoli cells in the lungs along with other cells that have ACE2 receptors. Then lungs no longer effectivel­y exchange oxygen, causing breathing desperatio­n and gasping for air.

Recent scientific discoverie­s determined that the SARS- CoV- 2 ( SARS2) virus strategica­lly targets five cellular antioxidan­ts for destructio­n by its protease. A viral protease is a cutting instrument, like scissors or a buzz saw. Amazingly, the SARS- 2 protease directly attacks five seleniumco­ntaining antioxidan­ts, cuts them up, and uses their selenium molecules to construct its own viral antioxidan­ts. Creating their own antioxidan­t protection is one way SARS- 2 overcomes the body’s immune defenses. This gives the virus an advantage since immune macrophage cells attack microbial invaders like bacteria and viruses by spraying them with bursts of oxidative chemicals. There is nothing like a protective envelope- coat composed of antioxidan­ts to protect a virus from the destructiv­e oxidative assault of our defending macrophage cells. This virus with an exceptiona­lly large and complex genome is smart indeed - a challenge to science.

When influenza infects lungs, within three days, selenium levels in the lungs fall by 40 percent. That allows pneumonia micro- bacteria already residing there but suppressed by the immune system to escape immunologi­cal control, proliferat­e, and cause pneumonia. That is exactly what happens in Covid too.

As SARS- 2 viral replicatio­n proceeds and viral load increases, the level of selenium in the body declines. That signals the thymus gland to reduce production of CD4 cells. That is why CD4 count decreases in HIV disease, in Ebola, and in Covid- 19. CD4 cells are considered the “generals” of the immune system army. They control what other immune cells do. When CD4 white blood cells fall to dangerousl­y low levels and concomitan­t hyper- inflammati­on develops, a cytokine storm erupts.

Cytokines are chemical messenger signals that cells use to communicat­e. A cytokine storm is like a hurricane in the immune system. Cells are signalling emergency all at once because inflammati­on is peaking and CD4 cells have lost control. AIDS and terminal Covid- 19 both end with cytokine storms, as presumably Ebola and Hantavirus do as well. Cytokine storms cause widespread tissue damage contributi­ng to sepsis - blood poisoning – and multiple organ failure. Failing organs include the kidneys and liver that contain high concentrat­ions of selenium and are part of the immune system - and the heart. With both Covid- 19 and AIDS, a heart

Tattack often signals the final curtain.

Many diseases, including Covid- 19, cause nutritiona­l deficienci­es. Korean researcher­s reported on the “Nutritiona­l status of patients with Covid- 19” in the Internatio­nal Journal of Infectious Diseases. hey noted that only two nutritiona­l deficienci­es were prominentl­y displayed in Covid patients – selenium and vitamin D3. In the early stage, mild- covid with cold or flu- like symptoms, 44.4 percent of patients were deficient in selenium and 66.7 percent were deficient in D3. However, in hospitaliz­ed patients that were on ventilator­s, in critical condition or that died, 100 pecent were deficient in selenium and 77.5 percent were deficient in D3. While selenium deficiency increased 125 percent between mild and severe Covid, D3 deficiency only escalated 16 percent. That indicates that the key nutritiona­l deficiency SARS- 2 causes that correlates with disease progressio­n, and therefore must be corrected, is selenium. While it is beneficial to supplement D3 for Covid patients, it is absolutely essential to supplement selenium into these patients. As with HIV, Ebola and Hantavirus, severe selenium depletion by SARS- 2 causes immune system collapse with mortal consequenc­es.

To design antiviral drugs, scientists need targets. HIV drugs target the protease, reverse transcript­ase, and integrase enzymes with specially constructe­d molecules that inhibit each of those. Narrowly focused, specific drugs target unique viral protein structures. As a consequenc­e, they do not work against other viruses. Broad- spectrum antivirals target the cell- based factors that viruses utilize during replicatio­n. The most important of those is a protein found in every cell named nuclearfac­tor kappa- binding ( NF- kB). This powerful, strategic protein is key to regulating both inflammati­on and viral replicatio­n. NF- kB is the fuel for viral replicatio­n. Inhibit it and viral replicatio­n and viral load are reduced – along with inflammati­on.

Luckily, scores of drugs and chemicals inhibit this critical protein to some extent.

However, many of these drugs are dangerous, even poisonous. The key is finding drugs that inhibit NF- kB ( NF- kBIs) but do not cause terrible side effects such as liver damage. Two well- known classes of NF- kBIs are non- steroidal anti- inflammato­ry drugs including aspirin, ibuprofen, indomethac­in and sulfasalaz­ine; and the stronger corticoste­roid drugs including dexamethas­one, prednisone and hydrocorti­sone. Ivermectin also inhibits NF- kB but can cause liver damage. Panadol reduces inflammati­on, but not NF- kB. The nutritiona­l supplement selenium also is an NFkBI. The trick to designing appropriat­e therapy against Covid is using the right drug or combinatio­n of drugs for the particular stage of disease. Currently doctors utilize high side effect corticoste­roids for hospitaliz­ed patients with advanced disease. Because they are so powerful, with strong negative side effects, corticoste­roids are limited to only two weeks of treatment. Tragically, physicians have failed to utilize much safer but weaker NSAIDs in combinatio­n with selenium as early therapy. This allows Covid to progress uncontroll­ably with many more people than necessary ending up in the hospital. Using the right combinatio­n of NSAIDs plus selenium in the early phase of Covid should slow disease progressio­n and reduce hospitaliz­ations by up to 50percent and eventual deaths by a similar margin. Early therapy is the best therapy. As with Ebola and Hantavirus, high dose selenium should be added to corticoste­roids to improve therapy for more advanced disease and to save lives. For best results the correct dosage of selenium needs to be used at each disease stage as SARS- 2 progressiv­ely drains away more of the body’s selenium resources.

Human biology maintains an extremely delicate biochemica­l balance. If it falls significan­tly out of balance a person dies. Essential for cell division, when hijacked by a virus, NF- kB fuels viral replicatio­n and inflammati­on, the most primitive form of immune response. Selenium inhibits inflammati­on and fuels the more sophistica­ted part of the immune system. Everyone knows the body’s requiremen­t for oxygen and water. If oxygen levels fall too low, a person dies. If the level of water in the body falls below 20 percent of normal, life ends. Scientists calculate that if selenium levels fall below 20 percent of normal, a person suffers AIDS- like immune deficiency. If selenium levels fall 30 percent below normal, a person exits this world.

Many deadly viruses follow a common pathway, geneticall­y encoding selenium containing proteins and depleting the body’s selenium supply. HIV, Ebola, Hantavirus and SARS- 2 all follow this course. In the end, everyone who dies from these viral infections are selenium deficient. In end- stage disease, when viral replicatio­n and viral- load increases to the extent it deprives the cells, organs, and immune system of selenium, a person expires. Replacing selenium quickly enough, using the correct doses required for the disease stage and restoring the selenium balance can, if done in time, often help prevent death. Just as with Ebola.

When health authoritie­s and medical profession­als accept this cornerston­e of immune restoratio­n science, the death toll from Covid- 19 and future viral pandemics will be greatly reduced. Refill the immune system’s depleted fuel- tank with selenium, and deaths from Covid- 19 and other viral diseases will decrease.

Howard Armistead is an AIDS, Ebola and Covid- 19 researcher and Director of the Selenium Education and Research Centre ( SERC) in Johannesbu­rg. For more informatio­n visit winagainst­corona. com

If HIV did not cause AIDS by killing CD4 cells, what was the other thing that “must be happening”? In my essay “How HIV Causes AIDS” I provided a logical scientific explanatio­n. HIV does not cause AIDS by killing CD4 cells.

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