Christie Laura Grace Profile picture
Dec 28 19 tweets 4 min read Read on X
1/🚨🚨CLNICAL TRIALS ARE IN PROCESS ON THE HARMS OF EXOGENOUS DNA ON CHILDREN!

"Exploration of the Activity of DNA Located Outside of Cellular Nucleus to Amplify Inflammation in Inflammatory Bowel Disease in Children Through Biological Pathway Cyclic GMP-AMP Synthase (cGAS)Image
2/Exploration of the Activity of DNA Located Outside of Cellular Nucleus to Amplify Inflammation in Inflammatory Bowel Disease in Children Through Biological Pathway Cyclic GMP-AMP Synthase (cGAS) - Stimulator of Interferon Genes (STING) (ROXANE)
3/ ID NCT05916274

Sponsor Centre Hospitalier Régional d'Orléans
Information provided by Centre Hospitalier Régional d'Orléans (Responsible Party)
Last Update Posted 2023-06-23ClinicalTrials.gov
clinicaltrials.gov/study/NCT05916…
4/ "Study Overview
Brief Summary
Frequency of Inflammatory Bowel Diseases in children (IBD)-Crohn's disease (CD), Ulcerative colitis (UC) is constantly increasing. Pediatric-onset IBD represent a different nosological entity (from adult IBD) because of their
5/ major inflammatory activity, their significant anatomical extent and their stenotic and/or fistulizing character sometimes from diagnosis. Intestinal lesions are due to dysregulation of the intestinal immune system but the cause is unknown.
6/The investigators hypothesize that extranuclear DNA participates in the amplification of the inflammatory response at the intestinal and blood levels during pediatric IBD through the cGAS-STING pathway.
7/ The investigators will analyse blood and fecal samples, and colonic biopsies issued from ill children and control participants on age of 6 to 17 years. The investigators think that this study will provide a better understanding of the mechanisms involved in pediatric IBD,
8/ assess the place of the cGAS-STING pathway, identify potential biomarkers of pediatric IBD and new potential therapeutic targets based in particular on the inhibition of the cGAS-STING pathway.
9/ Extracellular and extranuclear DNA (enDNA) play a major role in innate immunity by stimulating pro-inflammatory responses and activating type I interferon production. The pro-inflammatory action of enDNA is mediated by enzyme cGAS,
10/ protein STING, toll-like receptor 9 (TLR9), and the inflammasome complex NLRP3. The investigators hypothesize that enDNA participates in the amplification of the inflammatory response at the intestinal and blood levels during pediatric IBD through the cGAS-STING pathway.
11/ They also hypothesize that there are links between the cGAS-STING pathway and other pathways involved in pediatric IBD such as NOD2 and Autophagy. The investigators will analyse blood and fecal samples,
12/ and colonic biopsies issued from ill children and controls on age of 6 to 17 years. The investigators think that this study will provide a better understanding of the mechanisms involved in pediatric IBD, assess the place of the cGAS-STING pathway,
13/ identify potential biomarkers of pediatric IBD and new potential therapeutic targets based in particular on the inhibition of the cGAS-STING pathway."
clinicaltrials.gov/study/NCT05916…
14/ (above is directly from the study--below is commentary)

The DNA plasmid contamination that has been recently discovered in the RNA vaccines is ds DNA, that is double stranded DNA. It is also exogenous. Exogenous means from outside.Image
15/ The DNA plasmids that were used in process TWO of what is currently, and what has been given, to over half of the Earth's population, were not filtered out properly. An old rule regarding DNA is in place that does not account for the use of an LNP--a transfection agent.
16/ Transfection is the process of artificially introducing nucleic acids (DNA or RNA) into cells.
thermofisher.com/us/en/home/ref…
17/ the ds (double stranded) DNA plasmid contamination has the same type of structure of what is being studied in this clinical trial.
18/ These clinical trials (there are more) have unbelievable potential for implications regarding human exposure to exogenous DNA via contamination in vaccines.

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More from @_HeartofGrace_

Dec 27
1/🧵 🚨🚨🚨 💉
ds DNA Causes RAPID CLOT FORMATION in MICE in the
LINING of BLOOD VESSELS (arteries/veins/capillaries=vascular endothelium),
but ONLY in the presence of a
POSITIVELY (+) CHARGED LIPID TRANSFECTION AGENT.

RNA Vaccines contain ds DNA Contamination

A Study: Image
2/ THE STUDY:
"Double-stranded DNA induces a prothrombotic phenotype in the vascular endothelium"
Gaitzsch, E., Czermak, T., Ribeiro, A. et al. Double-stranded DNA induces a prothrombotic phenotype in the vascular endothelium. Sci Rep 7, 1112 (2017). doi.org/10.1038/s41598…Image
3/

The study investigates the prothrombotic (CLOT) effects of double-stranded DNA (dsDNA) in vascular endothelial cells.

Little is known (at the time of the study) about the pathophysiological relevance of dsDNA for the vascular endothelium. nature.com/articles/s4159…
Image
Read 29 tweets
Dec 26
1/ 🧵🚨
Plasmid DNA is a contaminant in 💉🦠🧬and is double stranded (ds) DNA: it contains CpG oligonucleotide (ODN).
A STUDY: Researchers found differences in cellular responses+ different gene responses to ds DNA and its effect on GENE MODIFICATION--transient transfection.Image
2/ The STUDY (HEAVY SCIENCE THREAD):
"Differential cellular responses to exogenous DNA in mammalian cells and its effect on oligonucleotide directed gene modification"
Igoucheva, O et al.
Gene therapy vol. 13,3 (2006): 266-75. doi:10.1038/sj.gt.3302643
sci-hub.se/10.1038/sj.gt.…
3/ Researchers wanted to know how cells respond to the presence of double-stranded DNA (dsDNA), and the influence that different dsDNA (different sizes/types) have on different cellular processes, and the impact on different genes. They found a variety of results.
Read 25 tweets
Dec 23
One only needs to know about zeta potential to know this would be false right out of the gate, based on photos.

Graphene Oxide is mentioned on an SOP to help elucidate (cryo-EM) the three dimensional structure of the spike protein, which occurred in the lab, after it was expressed in cells in the lab, recombinantly.

These photos are not of metal like structures.

These photos show blood cells stacked--this is a different concern.

Regarding a chain of 'metal like objects"-- graphene oxide would not do this in the blood. The reason, for starters, is zeta potential.

Graphene oxide can carry a net negative charge due to the presence of oxygen-containing functional groups on their surface.

The zeta potential of graphene oxide in blood depends on the specific functional groups, pH, and ionic strength of the blood.

A high negative zeta potential means a lot of dispersion and stability of graphene oxide as individual entities rather than forming large aggregates.

The negative charges on graphene oxide should lead to electrostatic repulsion between individual particles, preventing them from aggregating into long chains. This electrostatic repulsion will not permit this to occur.
If anything, they could undergo ion bridging, but it would not be so uniform or in a line like that. No.

These particles would not be in a chain as they are stating (the surgeons making these claims) in this study.

(IF it did happen, which it did not, these particles are not GO, but if it were to happen, in order to change the overall charge and the zeta potential, one would look at conducting covalent functionalization or the addition of specific biomolecules on to the graphene oxide itself. However, that did not occur here. And that is not GO in the blood they saw. It would have needed some changes to impact bioavailability and reduce toxicity. I only state this here to play devil's advocate and flip this on its head. There was metal contamination found that made the news, but this is not it. That was steel. And if that was steel, it would not look like that either in the blood.)

These people (researchers) did not know what they were looking at. And if things were "precipitating out" in the blood, these people (participants) would NOT have even been walking around.





ntdca.com/study-found-fo…
americanpharmaceuticalreview.com/Featured-Artic…
img.theepochtimes.com/assets/uploads…Image
Image
Image
Nope: "Study Found ‘Foreign Metal-Like Objects’ in 94 Percent of Sample Group"
ntdca.com/study-found-fo…
Image
"Smoking is one of the major factors of having coin stacking formation of Red Blood Cell or commonly known as RBC that can cause blood clots and can lead to stroke. Smokers tends have thicker, high count, and overlapping of RBC compared to non-smokers. Blood cell detection plays significant part in biomedical field."

.researchgate.net/figure/Coin-St…
Read 4 tweets
Dec 21
1/ 👀💉🧬🚨
Smaller DNA fragments (100-bp size and smaller), maintain significant mobility within the cytoplasmic compartment. They do not get chewed up as easily by endonucleases. They have a high chance of making it into the nucleus.

jbc.org/article/S0021-…

Image
2/ The study: Size-dependent DNA Mobility in Cytoplasm and Nucleus*
Gergely L. Lukacs Peter Haggie Olivier Seksek
D. Lechardeur Neal Freedman
A.S. Verkman Show footnotes
I: doi.org/10.1074/jbc.27…
Image
3/ The DNA plasmid contamination that multiple scientists have found exist in the RNA 💉🧬.
Dr. Buckhaults tracked the base pair length of the DNA plasmid contamination to be, on average, around 100 to 120 base pairs.
The size dependency of multiple studies of of dsDNA, Image
Read 25 tweets
Dec 18
1/ 💉🚨🧬PART TWO: How impurities in positively charged lipids inside an RNA/LNP 💉, covalently bond w/ DNA plasmid , allowing positively charged lipids to "hitch a ride" into the nucleus with the DNA (as an adduct) of cells, impacting histones (and maybe, aggressive cancer):
Image
2/ If the impurities in the positively charged ionizable lipids are covalently bonding with the DNA plasmid pieces in the LNP in the same way that has been proven with the RNA, covalently bonding and forming adducts, then it is highly plausible they will enter the nucleus in
3/ this state of being an adduct. It will depend on how many positively charged ionizable lipids are inside of the LNP. Once the positively charged lipid bonds to something, it does not get rid of its ability to bond again. The DNA plasmid pieces can enter the nucleus and
Read 25 tweets
Dec 18
1/ 🚨🧵🧬💉IMPURITIES in POSITIVELY CHARGED ionizable lipids in RNA/LNP💉w/ DNA plasmid contamination, are forming covalent bonds (adducts) w/RNA + DNA: can lead to: mutation, misfold, alteration of histones, aberrant proteins, DNA, damage glia + other mutations (oncogenic).
Image
2/ This is a thread on the study, which used RP-IP-HPLC that is called reverse phase ion pair HPLC to detect adducts which are forming--the impurities in the positively charged lipids are forming bonds with the RNA in this study.

3/ But there are key facotrs in this study that are able to be teased out, and applied elsewhere, when we look at the bigger picture from a macro view (zoom out)

The impurities in the positively charged lipids are committing what is called

ncbi.nlm.nih.gov/pmc/articles/P…
Image
Read 28 tweets

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