SARS-CoV-2 Spike Protein Takes the Gloves Off and Causes Chronic Inflammation
Studies show the NLRP3 Inflammasome response is unleashed by the Spike protein. It's around for 4 months. Aberrant NLRP3 inflammasome response leads to chronic illness and death. What you can do.
I enjoy doing research, but I hate it when the evidence is so depressing. Thank goodness for Dr. Levy. You’ll see why at the end.
This is the study that set me off:
Long-lived macrophage reprogramming drives spike protein-mediated inflammasome activation in COVID-19 https://www.embopress.org/doi/full/10.15252/emmm.202114150
The NLRP3 Inflammasome Response
The NLRP3 Inflammasome response is one of the myriad normal responses by which mammalian immune systems activate against viral infection. It’s supposed to be a short-term response than shuts down after the pathogen is defeated.
Good news: Spike protein primes the NLRP3 Inflammasome.
During infection, the NLRP3 Inflammasome response does its jobs.
Very bad news: Spike protein primes the NLRP3 Inflammasome, is systemic, and is found 4 months following injection.
After injection (and during Long-Haul COVID (LHC)), the NLRP3 Inflammasome response and must be doing chronic, systemic damage.
Spike Not Localized
The spike protein is not localized but is, per this Harvard study, systemic following injection
Circulating Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Vaccine Antigen Detected in the Plasma of mRNA-1273 Vaccine Recipients https://academic.oup.com/cid/advance-article/doi/10.1093/cid/ciab465/6279075
It is around for a lot longer than the virus:
While this Ogata study found the antigen up to15 days in 3/15 patients (20%),
This study found it in circulating exosomes up to 4 months(!)
Exosomes Cutting Edge: Circulating Exosomes with COVID Spike Protein Are Induced by BNT162b2 (Pfizer-BioNTech) Vaccination prior to Development of Antibodies: A Novel Mechanism for Immune Activation by mRNA Vaccines https://pubmed.ncbi.nlm.nih.gov/34654691/
Boosters Mean Repeated Chronic Inflammation
With never-ending boosters, we’re going to see chronic illness in the vaccinated at rates that are undeniable. None of it will be attributed to the vaccine.
More boosters means more chronic illness and death. Science tells us we can expect increased cancer, neurodegenerative disease, and a host of sublethal inflammation-mediated symptoms.
Here is a sample of articles that tell us this is necessarily so.
Aberrant NLRP3 Inflammasome Activation Ignites the Fire of Inflammation in Neuromuscular Diseases https://pubmed.ncbi.nlm.nih.gov/34199845/
NLRP3 Inflammasome Activation in Cancer: A Double-Edged Sword
https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC7360837/
Inflammasomes: An Emerging Mechanism Translating Environmental Toxicant Exposure Into Neuroinflammation in Parkinson’s Disease https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC6659017/
Be aware of SARS-CoV-2 spike protein: There is more than meets the eye https://pubmed.ncbi.nlm.nih.gov/34100279/
What You Can Do
Ok, so what’s the solution?
(1) Remove all other sources of toxins in your life. Thoroughly and urgently. You cannot afford these toxins. (I offer Environmental Toxicology in the Fall - email info@ipak-edu.org subject line “EnvTox” if you’d like me to offer access as pay-per-view (no instructor).
(2) Sign up for my new course in immunology. We start in the second week of January.
(3) And/Or sign up for Dr. Brownstein’s new course Wholistic Approaches to Human Health. (3) Read this article by Dr. Levy. Tell him Dr. Jack says hi.
(4) Read this article by Dr. Levy - Canceling the Spike Protein Striking Visual Evidence Editorial by Thomas E. Levy, MD, JD http://orthomolecular.org/resources/omns/v17n24.shtml
(5) Fund the IPAK Spike Protein Oncogenic Potential Study (new in 2022) VISIT HERE.
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Amazing to think (and kind of obvious) that something as fundamental as our sleep/wake cycles may make all the difference to NLRP3. Dark during the night, light during the day. Melatonin and vitamin D both have a strong modulatory effect on NLRP3. Turn off the TV...get some sleep...get some sun.
I had to go read the study to clarify if the findings suggest that post-infection NLRP3 inflammatory pathways were chronically active - "unleashed" as you put it. It seems just that recovered CD14+ cells are primed to form inflammasomes upon reencounter with spike, whereas naive donor CD14+ cells do not react to spike. So, only a concern for "long-haulers" and for the vaccinated as you said.