Christie Laura Grace Profile picture
May 24 25 tweets 5 min read Read on X
1/ 💉🚨 Hypothetical: Rapid Onset of Paralysis after COVID 19 Vaccination: potential cause: cGAS-STING "hyper" Activation a WITH INCREASED activation due to physioolgical differences in teenager compared to adult.
This thread will discuss upsetting scenario.
(Heavy science) Image
2/ Emerging role of STING signalling in CNS injury: inflammation, autophagy, necroptosis, ferroptosis and pyroptosis

jneuroinflammation.biomedcentral.com/articles/10.11…
Image
3/ Scenario: teen is given covid vaccine mRNA based, may or may not have NDA plasmid contamination, or other contamination.

DNA plasmid, spike protein, and bacteria are all known to activate cGAs STING pathway.

This pathway can be hyperactivated
4/ of in one or more areas it is bombarded repeatedly with virus (spike), dsDNA (double stranded DNA, like DNA Plasmid), bacteria, and can also become dysregulated if STING 3 variant is there, a mutation, other TMEM173 variant, etc. nature.com/articles/s4143…
Image
5/ Scenario: young teen, gets covid vaccine. spike protein (and or DNA plasmid or other contaminant) bombards cGAs STING pathway (STING variant may be present/and or mutation in STING):
Mechanism of cGAS-STING Activation and Hyperactivation
1. cGAS-STING Pathway:
6/ cGAS: Detects plasmid DNA/spike and produces cyclic GMP-AMP (cGAMP).

STING (Stimulator of Interferon Genes): Activated by cGAMP, leading to the production of type I interferons and other pro-inflammatory cytokines.
7/ This will lead to chronic activation and positive forward/Feedback loop and hyperactivation of this pathway.

Continuous presence of DNA plasmid pieces in the cytosol due to their repeated introduction or inefficient clearance/with spike protein.
8/ this results in sustained activation of the cGAS-STING pathway, resulting in a chronic inflammatory state.

This generates more cells that are nearby to become involved due to paracrine diffusion. ncbi.nlm.nih.gov/pmc/articles/P…
9/ Persistent inflammation causes continuous tissue damage, releasing more cellular debris and DNA, further activating the cGAS-STING pathway. The cells that are getting attacked by the body's own immune system release their OWN DNA , and this activates cGAS again, and the
10/ body comes back in and attacks a second time, and begins a LOOP of attack, a cycle, and it continues (many other threads on this starting back in October).
11/ then the neuroinflammation begins of the brain and central nervous system.

High levels of inflammatory cytokines can cross the blood-brain barrier (BBB), leading to inflammation in the central nervous system (CNS).
12/ Chronic inflammation can activate microglia (the brain's resident immune cells), causing them to release neurotoxic substances.
This is all a cascade occurring from the cGAS STING pathway being activated, and becoming dysregulated as it is activated.
13/ cGAS is supposed to protect us.

Demyelination and neuronal damage now starts to occur. Nerves are now being damaged, and neurons in the brain are being attacked by the body's immune system.
14/ Chronic inflammation might trigger an autoimmune response against neural tissues, leading to demyelination (loss of the protective myelin sheath around nerves) and neuronal damage.
15/ this prolonged inflammation and immune attack can result in axonal injury, disrupting neural communication--the communication with the brain to other parts of the body--like the arms and legs.
Inflammatory myelopathy might begin.
16/ : Inflammation of the spinal cord (myelitis) can cause damage to the neural pathways responsible for motor control--this is muscle control.

Them in the case of paralysis. severe inflammation can lead to swelling or compression of the spinal cord,
17/ impairing neural transmission.
Inflammatory damage to peripheral nerves can result in neuropathy, affecting muscle function and leading to weakness or paralysis.

I am so sorry.
18/ If occurring over a couple of weeks:
Early Symptoms:
Weakness including Initial weakness in limbs, difficulty walking, or muscle fatigue.
Numbness, tingling, or pain in affected areas.
19/ Progressive loss of motor control, leading to difficulty with movement and coordination.
Complete loss of voluntary muscle function in affected regions, potentially leading to paraplegia or quadriplegia depending on the extent of spinal cord or nerve involvement.
20/ reason for teens to suffer from stronger damage is stronger immune response due to age. Adolescents may have a more robust immune response, which could result in an exaggerated reaction to the presence of DNA plasmid and spike protein with contaminants and/or sting variant
21/ younger nervous system. Puberty involves significant hormonal changes, which could modulate immune responses and contribute to a more intense inflammatory reaction.
22/ What happened:
The persistent presence of DNA plasmids and or spike with STING variation maintains the activation of the cGAS-STING pathway, causing a cytokine storm with high levels of inflammatory mediators in the bloodstream.
23/ Pro-inflammatory cytokines cross the blood-brain barrier, leading to inflammation within the central nervous system (CNS). Microglia (resident immune cells in the brain and spinal cord) become activated and start releasing neurotoxic substances.
24/ Inflammation spreads to the spinal cord (myelitis), causing swelling, edema, and damage to neural tissues, attack the myelin sheath, leading to demyelination, disrupting neural signal transmission.

And then, axonal damage and permanent damage to the central nervous system
25/ paralysis

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More from @_HeartofGrace_

May 24
1/ 💉🚨🚨🚨MYOCARDITIS:
Inflammation and damage to the heart by DNA plasmid contamination and spike--activation of the cGAS STING pathway causes damage including MYOCARDITIS after COVID "VACCINATION"
Transfection of the cardiomyocyte

(layman's explanation at the end) Image
2/ (quick review--the cardiomyocyte is not the easiest thing to get a lipid nanoparticle into. It is protected. But the LNP is not stable, even on the best of days, it can break down, and it has issues. The lipids are inflammatory--positive, negative, neutral, all of them. ) Image
3/ A ratio of ionizable lipids to RNA/DNA, in a 20:1 ratio does not do the greatest job of transfecting the cardiomyocyte, however, when the ratio of positively charged lipids to negatively charged RNA (or DNA) is at a molar ratio of 10 to 1, you are


Image
Read 25 tweets
May 24
1/ 🚨💉COVID 19 "VACCINES" CAUSING MULTI SYSTEM ORGAN DAMAGE AND FAILURE through (hyper) ACTIVATION/DYSREGULATION of cGAS STING pathway
by interacting with DNA PLASMID contamination, SPIKE PROTEIN, and BACTERIAL CONTAMINATION.

(variants of STING (SNP) and mutation of STING) Image
2/ This could occur over the course of 24-72 hours, or over weeks, or TWO MONTHS.

The person receives a mRNA COVID VACCINE and is exposed to DNA plasmid pieces encapsulated within lipid nanoparticles, and there is expression of spike protein, and possible bacteria (LPS).
3/ The LNP facilitate the entry of the DNA plasmids into cells, where they activate the cGAS-STING pathway.
Initial symptoms might include mild flu-like symptoms such as fever, fatigue, and malaise due to the initial immune response and cytokine release. Image
Read 26 tweets
May 23
🚨💉HOW MOST OF THE DISEASES WE ARE SEEING ARE ACTIVATED BY THAT PROTEIN BELOW, WHICH IS THE STING PROTEIN, AND PART OF cGAS STING pathway as a result of the COVID VACCINES.
(multiple myeloma is even included here)
That protein below--that is STING. Even scientists liked that tweet who thought it was spike, WITH PhDs, and MDs. THAT is not the SPIKE!

and SPIIKE can activate STING, and guess what? The SAME smalll molecule will help reverse the disease course in SPIKE/COVID/VIRAL/AUTOIMMUNE/CANCER

.

I was slapping my head into the desk in frustration witnessing the people saying they are MD or PhD momlecular bio and thinking that is spike. Does that look like spike? NOOOOOO!

THIS is what is behind most of the injuries. Zeta is part of the clot formation with charge, of course. Both positive and negative charges can cause clots and remodeling of the vascular.

But that picture below is NOT the spike. That is STING. And STING is part of cGAS STING.
This pathway is activated by the spike protein, bacteria, and DNA, including plasmid DNA. And it can become dysregulated. And when it does, a few things can happen.

However, I asked the question that fell again on deaf ears, how do two people, two males in fact, aged 18, same city, same food, same diet, same sports team, same batch of jab--one gets myocarditis, and one does not?

Well, there are four variants of STING and then mutations within those 4 variants. The variants are linked YES, to RACE.
And here is what I did not want to type, because, it could be taken "the wrong way" .

"Genetic variants involved in the cGAS-STING pathway to predict outcome in patients (pts) with metastatic colorectal cancer (mCRC): Data from FIRE-3 and TRIBE trials."

Even in cancer, it is KNOWN that STING is involved, and a major player. And if this is not spoken about, especially by doctors who are working in cancer and genetics, then THAT is a huge problem. STING drives cancer.
DYSREGULATED STING is a DRIVER OF CANCER!!!

That is what I was writing my paper about, the combination of auto immune, cancer, myocarditis, ADD, and neurodegenerative, is driven by cGAS STING. It recognizes spike protein, DNA plasmid, and bacteria. But again, this pathway is meant to protect us.
So, we have four variants of STING, the pathway that activates the immune system to come into an area.
Four.
STING Type I: African
STING Type II: East Asian
STING Type III: European (WHITE/CAUCASIAN) and Middle Eastern
STING IV: Indigenous of the Americas

The variations are different due to a single nucleotide polymorphism, or SNP.

STING type III is rs11554776 also known as p.rg71Leu.

Guess what STING III has issues with that the other variants do not experience to such a degree?
Autoimmune dysregulation.


Genetic variations in cGAS STING, incliuding type III, are associated with autoimmune disease, inflammatory disorders, and CANCER. STING dysregulation can DRIVE CANCER--the inflammation is caused in the area by dysregulation of cGAS STING, and the immune system comes back in to the area so hard, it CAYUSES MUTATIONS ITSELF--DRIVING MUTATION and mestasis. No sv40 needed. This is FACT and do you know why?




Because a small molecule was developed and is in clinical trial right now for colon cancer, and it is KNOCKING COLON TUMORS BACK INTO THEIR SEATS by over 80% by targeting STING.

And that same small molecule is working diABZI analogue, diABZI-4!!!!
STING agonist diABZI enhances the cytotoxicity of T cell towards cancer cells




cGAS STING when dysregulated can drive:
myocarditis, stroke, AIDP. GB, other autoimmune, pancreatic cancer, lung cancer, breast cancer. melanoma. colorectal, and more.
Then we have mutations of STING that are involved such as:
V154M: valine to methionine change mutation at position 154 will drive hyperactivation possible of cGAS STING to positive forward loop to drive autoimmune and sever autoinflammation.
R284s: arginine to serine at position 284 of STING can lead to autoimmune AND impaired viral response.
R71H: mutation is amino acid change
arginine to histidine ar position 71 of STING. Will activate SLE and AGS, and other autoimmune.
N153S: asparagine to serine at position 153 of STING protein will cause autoimmune AND INTERFERONopathies.

Population prevalence (genetic prevalence):
V154M=1/1000
R284S: 1/10000
R71H: 1/1000
N153S= 1/1000
Math: 0.0031 .31% of population.
Vasculitis is linked to SNP variation in STING.

However, flooding cGAS without mutation can also cause positive forward feedback loop to hyperactive genes to go into hyperdrive expression of genes in immune activation. Turning off STING is not possible. That is why small molecule inhibitors are being developed to attack STING. They have also been show to "deactivate" spike protein activation of STING in study.

cGAS sting is also activated by spike and exogenous DNA like plasmid DNA and can cause alzheimers, parkinsons, and ALS.

The other receptors people talk about are downstream from STING.

Chronic inflammation by over activation of cGAS STING in people who have type III and who have another mutation, are at higher risk, of auto immune, auto inflammatory, AND if they already have a polyp, and inflammation, cGAS can cause instability to drive more mutations, without integration, and without SV40. Without insertional mutagensis.

Other ways cGAS is involved:
rheumatoid arthritis
sjogren's
vascultitis
AGS
Systemic Sclerosis
Multi organ failure (did someone you know die of a vaccine inury by multi organ failure????)
Inflammatory Myopathy
Prostate Cancer
COPD can also get worse
AASD
Myocarditis
MULTIPLE MYELOMA
Also, cGAs CAN be implicated in blood clots too by immune cell activation and endothelial cells engaging in expression of pro coagulant factors, causing DVT, PE, and Myocardial Infarction.

take all of this, write a paper, slap your name on it while simultaneously defaming me behind your fake name account, and go keep throwing daggers on twitter, while tellling me I do not know what I am talking about.

Once again, you want to take any study from what I have posted in all of those threads? Go bananas.
But sh!t on me whilst doing it? Wow.
that is some chutzpah
Now what is the molar ratio needed to transfect the cardiomyocyte of nucleic acids to positively charged lipids in an LNP?

It's 10 to 1. That is your ratio.

ncbi.nlm.nih.gov/pmc/articles/P…
ascopubs.org/doi/10.1200/JC…
nature.com/articles/s4157…
frontiersin.org/journals/immun…
embopress.org/doi/full/10.15…
nature.com/articles/s4141…
ncbi.nlm.nih.gov/pmc/articles/P…
Image
2/ Hyperactivation of cGAS STING and positive forward feedback loop can drive AAD. Plasmid DNA contamination, spike protein, or even bacteria can do this.
Read 8 tweets
May 9
💉Stone me 40 ways from Sunday, and kick me for saying this, but SV40, insertional mutagenesis, and DNA mutation are not the reasons for the bulk of the injuries out there. The kinetic charge potentials of the LNP are absolutely impacting bio distribution, clot formation, and how certain cells are transfected, and how other cells, will almost never be, transfected.
While horrifying in their concerns, and probably accurate, current injuries, even if vastly different, most likely, are attributed, to this (and if it takes writing it all in a paper and submitting it to a journal, for scientists to do the proper testing, then game on):Image
Image
for those who need a bit more context in a graph
(please excuse the crudeness of it) Image
@StphaneGuay5
parles-tu anglais ? Voudriez-vous discuter, s'il vous plait ? mon français n'est pas tres bon. merci
Read 4 tweets
May 3
1/ 🚨🧬💉SPERM UPTAKE of PLASMID DNA--USE of LIPIDS vs ELECTROPORATION DURING the SPERM GROWTH CYCLE:
(73-75 days for sperm to mature)
Electroporation: "shocking holes" into cells.
Lipid=LIPOFECTAMINE.
Both methods used in study to get DNA into sperm cells
LIPIDS worked BETTER Image
2/ The STUDY: Comparative Efficiency for in vitro Transfection of Goat Undifferentiated Spermatogonia Using Lipofectamine Reagents and Electroporation
DOI

doi.org/10.2147/SCCAA.…
dovepress.com/comparative-ef…
3/ goats were castrated, and the testes were transported on ice to ILRI laboratory
(ouch)

Lipofectamine 2000 (Invitrogen by Life Technologies, Renfrew, United Kingdom) and Lipofectamine Stem (Invitrogen by Life Technologies, Renfrew, UK) reagents were used for transfection.
Read 15 tweets
Apr 30
1/🧵For those who like berries and seeds: The miracle berry. It changes how we taste food--metallic/sour things will taste sweet for about an hour after consuming, just one.
It helps those going through chemo with taste of food and diabetics.
The FDA, in the 70s, squashed it. Image
2/ I've been eating these things for over 20 years. I'm not diabetic and haven't been through chemo. I was introduced to this berry at a "fruit tripping party". We ate a berry, then ate grapefruit, lemons, limes--anything I ate that was sour/spicy--was now a sweet confection. Image
3/ grapefruit tastes like sweet candy. Same with lemons. Radishes dunked in hot sauce tasted like crunchy honey. A wedge of granny smith apple with pungent cheese on top with cinnamon tasted like sweet apple cake. Use your imagination. Sour now tastes sweet. Spicy tastes sweet. Image
Read 20 tweets

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