Persistence of Spike Protein Induces a State of Chronic Disease (Parallels to Asbestos): The Essence of Long COVID
A study published March 4th definitively proves Spike Protein presence in COVID vaccine recipients who developed PASC.
I have hypothesized and written extensively that Long COVID is, in essence, Spike Protein persistence. This persistence induces chronic damage and inflammation resulting in a unique state of chronic disease. A study published March 4th essentially proved that Spike Protein administration alone, without prior COVID infection may induce PASC – or Long COVID.
The researchers found that the inflammatory profile and presence of S1 protein were similar to those suffering from Long COVID.
Using two algorithms (severity score and long hauler index) previously derived from these biomarkers10, we found that post-vaccination PASC-like symptoms were associated with an inflammatory profile with statistically significant elevations in CCL5, sCD40L, IL-6, and IL-8. Further these patients were classified as PASC using a single classifier and PASC with inflammation using a dual classifier. Elevated IL-8 was a unique marker in postvaccination individuals with PASC-like symptoms. We recently found a statistically significant correlation between decreased IL-8 and improvement in the NYHA cardiac symptom score in PASC following treatment with a CCR5 antagonist and statin. Because of the similarities between PASC and patients with post-vaccination PASC-like symptoms, we examined whether S1 protein persistence might also occur in patients with postvaccination PASC-like symptoms. We demonstrated a statistically significant elevation of S1 protein containing non-classical monocytes (NCM) and in S1-containing intermediate monocytes (IM) in post-vaccination PASC-like patients compared to normal controls.
The presence of Spike remaining in monocytes post vaccination may explain the mechanism that leads to many of the observed sudden cardiac deaths. It also explains another mechanism for what I have long maintained as SPED (Spike Protein Endothelial Disease).
Stress and exercise mobilize non-classical monocytes including up to 4-fold with exercise. The interaction between fractalkine and CX3CR1 has been involved in the pathogenesis of atherosclerosis, vasculitis, vasculopathies, and inflammatory brain disorders and could also be contributing to vascular endotheliitis in postvaccination individuals with PASC-like symptoms.
Persistence of S1 Spike Protein in CD16+ Monocytes up to 245 Days in SARS-CoV-2 Negative Post COVID-19 Vaccination Individuals with Post-Acute Sequalae of COVID-19 (PASC)-Like Symptoms
https://www.medrxiv.org/content/10.1101/2024.03.24.24304286v1.full.pdf
This clearly debunks the forthcoming Australian study claiming that Long COVID is nothing but a common post-viral syndrome. It is not. The whole point is that the Spike Protein is like Asbestos. It causes constant inflammation and damage. What’s worse, the Spike has access to the entire body. Please note the precise similarity.
Inhaled asbestos fibers become entrapped in the lung, and some migrate through the lymphatics to the pleura. The deposition of asbestos in the lung and pleura causes chronic inflammation that may lead to lung fibrosis and reactive mesothelial hyperplasia; it is around these areas that MM and lung cancer develop.
Programmed necrosis induced by asbestos in human mesothelial cells causes high-mobility group box 1 protein release and resultant inflammation
https://www.pnas.org/doi/full/10.1073/pnas.1006542107#
I have written about how the Spike is a source of Chronic Inflammation and Injury.
THE SPIKE PROTEIN AS SOURCE OF CONSTANT INJURY AND CHRONIC INFLAMMATION
https://wmcresearch.org/the-spike-protein-as-source-of-constant-injury-and-chronic-inflammation/
And, how the Spike Protein vaccines “bypass” the respiratory system to directly attack organs via the Endothelium.
Spike Protein Persistence: The Essence of Long COVID and a Danger to All: mRNA Therapy as Respiratory BYPASS
https://wmcresearch.substack.com/p/spike-protein-persistence-the-essence
What could the end result of this be? A situation exactly the same as HIV. However, instead of keeping HIV viral levels low, you will need to keep Spike Protein levels low. Of course, this goes hand in hand with the lifespan reducing complications that ANY level of HIV (or Spike Protein) induce.
I will continue to study, report and find solutions which may treat an neutralize the damage caused by the Spike Protein of SARS-CoV-2 and the virus itself.
Spot on! Great analogy of mRNA gene therapy and asbestosis.
Unfortunately, in a 90% metabolically impaired, 85% mRNA therapied, alcohol and sugar binging, glyphosate and rancid seed oil loaded, ... population with chronically inflamed individuals there's a perfect storm brewing.
We recently saw a female friend (post-menopausal vaxxed & boosted) with all her fingernails blackened (melanonychia.) In reply to our obvious concern, she replied that her doctor had just calmed her fears with, "It's a normal post-covid response." No investigation of viral or bacterial or other causal mechanisms!
It's interesting that asbestosis leads to clubbing of the fingers.
The Salk institute published a study a few years ago showing that the spike protein alone was pathogenic. I naively thought the publication of this study would shut down the Covid “vaccination” campaign all those years ago. What a crazy place we are in now. You can still line up for a shot that forces your body to make unknown amounts of spike protein with no known mechanism to shut it down (except an autoimmune reaction). And the CDC is still pushing them in infants, pregnant women and children. It’s just such a nightmare.