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Autoimmunity Resulting from Molecular Mimicry between COVID Vaccine and Human Proteins

I’ve been seeing this for two years, elevated d-dimers, blood clots, myocarditis, spontaneous colitis non-responsive to anti-biotics, sudden spontaneous bruising and bleeding after vaccination. Now, it all makes more sense.

In a recent study, researchers discovered molecular mimicry hotspots in the Spike protein and highlight two examples with very high autoimmune potential. This helps us understand the prolonged COVID-19 complications we’ve been seeing for the last two years. The spike protein shares similarities with 34 different human proteins in amino acid sequences in sets of sixes. These similarities stimulate high potential for autoimmune attack – causing the body’s immune system to attack its own organs with similar protein sequences.

These protein sequences are found in the thyroid, brain, nose, ear, skin, muscles, heart, blood, nerves, joints, intestines, and many more. In my office, I’ve seen over 50 patients with bleeding, bruising, rash, heart inflammation, intestinal inflammation, uterine and ovarian inflammation and abnormal menstrual changes spontaneously that I have never seen in 22 years of medical practice. All of these patients have had prolonged d-dimer levels elevated for 12-18 months post vaccination. These symptoms all started with in 4-8 weeks of vaccination as well.

The spike protein may also trigger Guillain-Barre syndrome, viral arthritis, immune thrombocytopenic purpura (bleeding), antiphospholipid syndrome, Kawasaki disease, systemic lupus erythematosus, and many others.

Two other recent studies here and here confirm that autoimmunity is the driver behind these post COVID vaccination symptoms. These two studies demonstrated that people who were vaccinated for COVID-19 had more antibodies against human tissues than people who were not infected and/or had natural infection.