Since the COVID-19 pandemic swept across the world more than two years ago, more than 4.5 billion people worldwide have become fully vaccinated against it. Now more and more people are concerned that the spike proteins used in the vaccines and present in the virus are the cause of long COVID syndrome.
The spike protein, also known as the S protein, is the largest structural protein in the SARS-CoV-2 virus, which causes COVID-19. It’s a signature structure that protrudes from the surface of the virus, creating the crown-like shape that coronaviruses get their name from. Corona is Latin for “crown” or “wreath.”
8 Ways Spike Protein Harms the Body
During more than two years of the COVID-19 pandemic, many studies have analyzed the effects of the spike protein from different aspects and have discovered that it’s harmful to the human body in several ways, including:1. Damaging the lung cells (including the pulmonary alveoli and pulmonary endothelial cells). 2. Damaging the mitochondria and DNA structures. 3. Damaging cardiovascular cells. 4. Increasing the risk of blood clots. 5. Damaging brain cells. 6. Promoting inflammation. 7. Suppressing immunity. 8. Increasing the risk of cancer.We'll go into the details of each of these points.
S Proteins Can Affect Multiple Organs
When the virus enters the human body, the spike proteins will affect multiple organs in different ways. Studies have shown that many organ cells can be affected by spike proteins, such as those in the heart, brain, and cardiovascular system. In addition, a paper published in 2021 in the bioRxiv preprint repository states that S proteins cause:- the Type 1 catalytic receptors in the kidneys to increase in kidney cell tissues, and these types of receptors can become hosts for the virus, making the kidneys more susceptible to viral infection.
- cells in the small intestine to stimulate a large amount of L-SIGN (liver/lymph node-specific intracellular adhesion molecules-3 grabbing non-integrin) receptors to defend against pathogens. However, this causes a reaction that eventually makes the small intestine more susceptible to viral infection. A similar situation can also occur in other organs, such as the kidneys and duodenum (the first section of the small intestine).
- the amount of DC-SIGN (Dendritic Cell-Specific Intercellular adhesion molecule-3-Grabbing Non-integrin) receptors in the lungs to increase, which may cause inflammatory symptoms in the lungs.
When spike proteins are present in the human body, the pulmonary alveolar cell walls in the lungs will begin to thicken and solidify, and lung functions will decline. The pulmonary alveoli are the tiny, balloon-shaped air sacs that expand and shrink in our lungs as we breathe.
Spike Proteins Damage Mitochondria, Possibly Causing Long COVID
Under normal circumstances, mitochondria in cells are tubular cellular power stations responsible for synthesizing energy.When the spike proteins stimulate our pulmonary alveolar cells or endothelial cells (which line our blood vessels and lymphatic vessels), the mitochondrial structure will change dramatically and become heavily fragmented, and the number of tubular mitochondria will be greatly reduced. As the cells in the alveoli or endothelial tissues become damaged, they no longer produce energy efficiently, which is likely to cause the cells to enter a state of premature decline and death.
Scientists have hypothesized that long COVID may be caused by this damage to the mitochondria. One of the major symptoms of this chronic form of COVID-19 is fatigue. This may be because of the fact that the cellular mitochondria are damaged or dying, resulting in a lack of energy at the most essential level of our body.
Damage to the Cardiovascular System and Blood Clots
The cardiac and the myocardial systems of the heart contain a very important type of cell: the pericardial cells, which are outside the endothelial cells of blood vessels and are usually combined with endothelial cells to help blood vessels transmit different signals.A study published in Clinical Science discovered that when the SARS-CoV-2 virus enters the body, spike proteins will bind to the CD147 receptors on the surface of the pericardial cells, making them more likely to shed from the surface of the endothelial cells. This will affect some of the functions of the endothelial cells and accelerate the death of the vascular wall cells.
In addition, spike proteins themselves can directly stimulate pericardial cells to produce more pro-inflammatory factors that can damage the myocardium and cause blood clots.
Spike proteins can also induce thrombosis, which is when blood clots block veins. Another experiment published in the BioRxiv preprint repository investigated how platelets would change after being stimulated by spike proteins.
Spike Proteins Impair Immunity
When the human body is infected by a coronavirus such as COVID-19, the immune system recognizes the spike protein as an invader and the innate immune system and acquired immune system get to work. Cytokines are released to signal the area to defend. In short, the impact of spike proteins on the immune systems is comprehensive. This is also shown in a paper published in the journal Leukemia.For instance, there are 11 types of toll-like receptors in the innate immune system, and the seventh type of these toll-like receptors can recognize the RNA of single-stranded viruses. The mRNA (messenger RNA) that enters the body after COVID-19 infection or vaccination is also single-stranded, and immune cells will recognize the virus’s RNA and attack it. In the presence of spike proteins, the toll-like receptor expression quantity may increase in response to the viral attack and complementary immune cells may release more interferons in response to different viral variants.
Do Vaccine Spike Proteins Stay in the Body?
As we know, the COVID-19 vaccines have incorporated an expression mechanism for the viral spike proteins that triggers our immune systems to respond to the virus. But the question remains: How long do the spike proteins from the vaccines remain in the body?The spike proteins are divided into two parts: S1 and S2, with S1 remaining in the blood and S2 bound to the cell membranes.
A study published in Clinical Infectious Diseases discovered that the S1 proteins would appear in humans soon after the first dose of the Moderna vaccine, and that some people would still have intact spike proteins two weeks after the first dose of the vaccine.
The finding that intact spike proteins were still present in people two weeks after vaccination was beyond expectations.
Another study published in the Journal of Immunology found that S2 proteins could still be detected four months after the second dose of the Pfizer vaccine.
However, the harm of spike proteins is related to their amount. The aforementioned side effects are all based on in vitro studies and animal models, and the relatively serious damage occurred only when the amount of spike proteins was large.
How to Get Spike Proteins Out of the Body
If someone develops Long COVID-19 syndrome after infection or vaccination, they may wonder what medicines can be used to expel the spike proteins and relieve their symptoms. The World Council for Health (WCH) has made several recommendations for nutrients and medications.- Vitamin C
- Vitamin D
- Omega 3
- Quercetin
- Melatonin
- Zinc
- Aspirin
- Antihistamines
- Steroids
- Colchicine
- Mast cell stabilizers
- Ivermectin
3. Plant Extracts- Selfheal extract
- Pine needle extract
- Dandelion leaf extract
- Rheum emodin
Some of these ingredients, such as the shikimic acid contained in pine needles, have antioxidant properties that can reduce oxidized free radicals in the body and provide a detoxifying effect.
The above-suggested medicines aren’t cures, but they can help boost the body’s immunity and balance the body’s immune mechanism, which is helpful in the overall fight against the virus.
It’s important to emphasize that everyone’s situation is different. So talk to your physician before taking the medications recommended by the WCH to make sure they’re suitable.
https://www.biorxiv.org/content/10.1101/2021.07.07.451411v1.full.pdf
https://www.ahajournals.org/doi/epub/10.1161/CIRCRESAHA.121.318902
https://pubmed.ncbi.nlm.nih.gov/34807265/
https://www.nature.com/articles/s41375-021-01332-z
https://www.biorxiv.org/content/10.1101/2021.12.14.472668v2.full.pdf
https://academic.oup.com/cid/article/74/4/715/6279075
https://www.jimmunol.org/content/207/10/2405
