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Dr. Doug Corrigan

Apr 17 • 12 tweets • 3 min read

1/I warned about Antibody Dependent Cellular Cytotoxicity (ADCC) many months ago, and this recent paper demonstrates that antibodies from the jab’d are much more potent at eliciting a Natural Killer response against Spike expressing cells than are antibodies from an infection.

2/ In ADCC, any cell expressing the Spike protein will be targeted for destruction by Natural Killer Cells. Any cells that take up LNP encapsulated mRNA will express Spike and will be destroyed by cytotoxic enzymes release by NK cells.

3/This is one reason why the rate of adverse events goes up with subsequent doses, as ADCC is an antibody-dependent process. According to this paper, vaccinal antibodies are particularly well-suited for activating NK cells — much more so than antibodies from a natural infection.

4/ Reference —> onlinelibrary.wiley.com/doi/abs/10.100…

https://twitter.com/sciencewdrdoug/status/1451178916056604679

5/Original thread 6 months ago —>

https://twitter.com/sciencewdrdoug/status/1451178916056604679

6/ Note: Do not confuse this with Antibody Enhancement (ADE), which is an entirely different process altogether.

6/To be even more clear, biodistribution studies (in rats) show that mRNA/LNPs locate to just about every tissue in the body (to one degree or another). They can even cross the blood brain barrier. They are not simply localized to the deltoid muscle and surrounding lymph nodes.

7/Why does this matter? Because any tissue that takes up the mRNA will express Spike protein. Spike protein acts like a beacon to the primed immune system. Antibodies bind to Spike, the antibodies then tether to Natural Killer cells, and then NK cells destroy that cell.

8/This is why the adverse reaction matrix is so large and diverse. It depends on the stochastic nature of where the LNPs travel in a given person’s body, which is varied and person specific.

9/This will be true for any vector that delivers instructions to your cell (either DNA or mRNA) to synthesize the antigen of interest. By turning your cells into the “vaccine factory,”
your cells are now the enemy. With every booster, your cells become the enemy again.

10/ In a traditional vaccine, this is not the case (because the antigen is produced in a vaccine plant and remains external to your cells upon injection). It was absolutely moronic and insane to employ such a strategy whereby your cells are hijacked to synthesize the antigen.

11/ If you want to learn more about what the Spike protein can do to our body, listen to episode 1 of my podcast—> anchor.fm/ScienceWithDrD…

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More from @ScienceWDrDoug

Dr. Doug Corrigan

@ScienceWDrDoug

Apr 1

1/The 4th jab was approved. Let’s do the math: 15mos/4 jabs = avg. of 3.75 months/jab.

What would you call something that you need to take every 3.75 months to work? Last time I checked, our immune system normally has a memory of longer than 3.75 months.

Why such frequency?

2/ Circulating Spike protein has been demonstrated for up to 4
months after the jab. This number is very close to the window of efficacy presumably provided by the jab.

3/ Hypothesis - the effects of the jab are not *mainly* due to the immune response. By what mechanism could such a phenomenon occur?

Read 7 tweets

Dr. Doug Corrigan

@ScienceWDrDoug

Mar 27

1/ 3-8 months after initial diagnosis of myocarditis in teenagers post jab, a large majority are still persistently showing abnormal markers (GLS and LGE) associated with a worse prognosis of present and future heart function. This is despite improvement in other cardiac markers.

2/ “The presence of LGE is an indicator of cardiac injury and fibrosis and has been strongly associated with worse prognosis in patients with classical acute myocarditis.”

3/“LGE is a predictor of all cause death, cardiovascular death, cardiac transplant, rehospitalization, recurrent acute myocarditis and requirement for mechanical circulatory support”

Read 10 tweets

Dr. Doug Corrigan

@ScienceWDrDoug

Mar 26

1/Remember this study from Denmark? It shows negative vaccine efficacy after the antibodies wane, which means an increased rate of infection if you’re jabbed. Data from other countries shows the same trend. Why? Is this evidence that the jab is impairing the immune system?

2/ Data from the UK shows higher rates of infection (rate per 100,000) with increased number of jabs.

3/ medrxiv.org/content/10.110…

Read 5 tweets

Dr. Doug Corrigan

@ScienceWDrDoug

Mar 14

1/ Repeated over-stimulation by the same antigen can reprogram T-cells (via TCR revision) to become autoantibody inducing cells, leading to autoimmune conditions, like Systemic Lupus Erythematosus (SLE) - as demonstrated in this mouse model.

2/ This mechanism for potentially causing unintended autoimmune disorders should not be overlooked when considering the safety of repeated doses of the same antigen, such as the proposed and developing regiment of the current mRNA jab program.

3/ ncbi.nlm.nih.gov/labs/pmc/artic…

Read 8 tweets

Dr. Doug Corrigan

@ScienceWDrDoug

Mar 12

1/ Why do jabbed people still become infected and transmit the virus? As this recent Science paper shows, jabbed people are lacking IgA/IgG mucosal immunity. They also show that mucosal immunity is substantially gained only after a jabbed person has a natural infection.

2/ The authors conclude: “We also speculate that the extraordinarily high antibody titers observed in vaccinated individuals who develop breakthrough infections may lead to subsequent long-term protection in those individuals.”

3/ Translation: The only way a jabbed person can gain long lasting & sterilizing immunity that prevents further infection and transmission is to become naturally infected.

Read 6 tweets