Endotoxin induced Interleukin 18 identified as a useful marker for Jab induced Myocarditis and 2,374 other Injuries
Recent paper compared Multisystem Inflammatory Syndrome in Children, Myocarditis from causes other than Covid19, associated with Covid19 infection and Covid19 Jabbing found IL18 useful for the latter.
First a big thanks to my friend Dr Sabine Stebel (Dr Bine) for alerting the news about a recent open access paper in Nature by Maatz and coworkers that compared Multisystem Inflammatory Syndrome in Children, Myocarditis from causes other than Covid19, Myocarditis associated with Covid19 infection and Myocarditis from Covid19 Jabbing which found IL18 useful as a marker for the latter.1 2
Here is the top of Maatz et al Extended Data Figure 1 that shows the Heart tissue biopsy samples. Note the Needle.
Part of the caption:
a) Images of Hematoxylin eosin- (HE), CD3-, and CD68-stained and
b) of CD4- and CD8- stained EMB sections. Representative images from each group are shown. Stainings on EMB sections were performed for all patients (Non-COVID-19: n = 8, Post-COVID-19: n = 10, Post-Vaccination: n = 4, MISC: n = 2).
c) Size of human left ventricular endomyocardial cardiac biopsies (EMBs) for snRNA-seq. The image shows different EMB tissue sizes and their weight before nuclei isolation in a 5 cm dish on ice.
Note the CD68 staining that is diagnostic for Endotoxin.3
The Maatz paper also discusses CD4 to CD8 cell ratios.45
The Maatz paper was written by authors from Germany, Canada, UK, USA.
The fundng and conflicts of interest were declared:
This project was made possible, in part, by the Chan Zuckerberg Foundation (2019-202666) to N.H., M.N., C.E.S., J.G.S. and S.A.T.; the Leducq Foundation (16CVD03) to N.H., C.E.S. and J.G.S.; the British Heart Foundation and Deutsches Zentrum für Herz-Kreislauf-Forschung (BHF/DZHK: SP/19/1/34461) to N.H., M.N. and S.A.T.; the German Center for Cardiovascular Research (DZHK) (Personify program) to C.T.; and German Research Foundation (DFG) SFB-1470 to N.H. (project B03), C.T. (project B02) and S.V.L. (project A07). N.H. was supported by a European Research Council advanced grant under the European Unionʼs Horizon 2020 Research and Innovation Program (AdG788970). S.K. received support from the DZHK, Partner Site Berlin. S.K. was supported by an unrestricted research grant by Philips Healthcare and partially funded by DFG SFB-1470-B06. G.O. was funded by the Canadian Institutes of Health Research and the Heart and Stroke Foundation and was a member of the Canadian Long COVID Web. C.E.S. received partial support from the Howard Hughes Medical Institute, and J.G.S. received partial support from the National Heart, Lung, and Blood Institute (HL080494).
Competing interests
The following authors report competing interests. C.E.S. and J.G.S. (Maze, BridgeBio and Bristol Myers Squibb); board of directors: C.E.S. (Burroughs Wellcome Fund US and Merck). In the past 3 years, S.A.T. has consulted or been a member of scientific advisory boards at GlaxoSmithKline, Qiagen, ForeSite Labs and Element Biosciences and is an equity holder of Transition Bio and EnsoCell Therapeutics. All companies were not involved in any aspect of the study’s experimental design, execution and analyses or in the preparation of the manuscript. B.H. (together with Joshua M. Hare) is inventor on a granted patent application (application number EP2152916A1, European Patent Office) filed by the University of Miami that uses RNA for diagnosis of myocarditis. This patent application does not cover specific aspects of this paper.
The Patent is interesting reading, see for example the Zinc Finger Proteins.6
Dr Bine’s reference 11 was to a 2025 paper7 by German researchers with close links to Novartis, Amgen and Swedish Orphan Biovitrum (SOBI) which provides this graphical abstract.
Kessel and coworkers state, warning of Endotoxin initiated Hyperinflammation during GMO CAR T cell therapy8
Chimeric antigen receptor (CAR) T cell therapy of solid cancer remains below expectations; adding cytokine help through IL-18 has shown remarkable efficacy in first clinical trials.
As IL-18 is also a powerful driver of hyperinflammatory conditions, we discuss to what extent unleashing IL-18 is a double-edged sword in CAR T cell therapies.
That in turn took me to a 2019 paper from researchers in Germany and USA on Interleukin 18.9
Verweyen et al. found that IL-18 expression from Human monocytes and animal models is “orchestrated by synergistic Toll-like receptor and type I IFN signaling”.
Their focus was on Macrophage Activation Syndrome (MACS).10
Interleukin 18 caused by Endotoxin
The US Government Comparative Toxicogenomics Database (CTD) entry for Interleukin 18 shows the numerous synonyms. Please click to enlarge and see that Endotoxin (Lipopolysaccharides) dominates the bar graph of interacting chemicals.
CTD provides 133 line entries with effects of Endotoxin (LPS) with references to the peer reviewed literature.11 Note 22 entries for E coli O55-B5.12
2,375 Diseases linked to Interleukin 18
The CTD shows a neat summary of Disease linked to this Endotoxin induced protein and there has been a small amount of human curation marked in Blue.
Perhaps Robert F Kennedy Jr. can increase CTD staffing levels and not let Jab developer Elon Musk sack the people capable of joining the dots in Jab injury?
Wikipedia gives a useful quick overview of IL18.13
Thread on X
I started a thread on X which is proving quite popular despite Elon Musk actively suppressing it.14
One of the older posts I found contained this lovely picture, that I traced back to a free paper by Martin Heil in Mexico.15
Would readers like me to add a list of 2,375 Diseases linked to Interleukin 18 ?
Henrike Maatz, Eric L Lindberg, Eleonora Adami, Natalia López-Anguita, Alvaro Perdomo-Sabogal, Lucía Cocera Ortega, Giannino Patone, Daniel Reichart , Anna Myronova, Sabine Schmidt, Ahmed Elsanhoury, Oliver Klein, Uwe Kühl, Emanuel Wyler, Markus Landthaler, Schayan Yousefian, Simon Haas, Florian Kurth, Sarah A Teichmann, Gavin Y Oudit, Hendrik Milting, Michela Noseda, Jonathan G Seidman, Christine E Seidman, Bettina Heidecker, Leif E Sander, Birgit Sawitzki, Karin Klingel, Patrick Doeblin, Sebastian Kelle, Sophie Van Linthout, Norbert Hubner, Carsten Tschöpe. 2025. The cellular and molecular cardiac tissue responses in human inflammatory cardiomyopathies after SARS-CoV-2 infection and COVID-19 vaccination. https://www.nature.com/articles/s44161-025-00612-6
CD68 Diseases caused by Endotoxin in Jabs
Myocarditis and Pericarditis are caused by upregulation of CD68 cells by Endotoxin in Covid19 jabs, as explained in an earlier article.
Endotoxin replacing PEG in Lipid Nanoparticles increases CD8 T Killer cells
In 2016 researchers at Harvard designed Lipid Nanoparticles with a slightly negative Zeta potential to transfect dendritic cells, macrophages, and neutrophils, which we know are the primary targets of the mRNA jabs.
CD4/CD8 Ratio is altered by Endotoxin in Covid19 Jabs
I discussed the CD4/CD8 ratio in an earlier post this year.
Joshua M. Hare and Bettina Heidecker. Filed 1 May 2008, Granted 20 April 2016. A transcriptomic biomarker of myocarditis. https://patents.google.com/patent/EP2152916A1/en
Christoph Kessel, Claudia Rossig and Hinrich Abken. 2025. Weal and woe of interleukin-18 in the T cell therapy of cancer. Journal for Immunotherapy of Cancer. 13(1):e010545. https://jitc.bmj.com/content/13/1/e010545
https://en.wikipedia.org/wiki/CAR_T_cell
Emely Verweyen, Dirk Holzinger, Toni Weinhage, Claas Hinze, Helmut Wittkowski, Peter Pickkers, Sabrin Albeituni, Katherine Verbist, Kim E Nichols, Grant Schulert , Alexei Grom, Dirk Foell, Christoph Kessel. 2025. Synergistic Signaling of TLR and IFNα/β Facilitates Escape of IL-18 Expression from Endotoxin Tolerance. https://www.atsjournals.org/doi/10.1164/rccm.201903-0659OC
https://en.wikipedia.org/wiki/Macrophage_activation_syndrome
https://ctdbase.org/detail.go?type=gene&acc=3606&view=ixn&chemAcc=D008070
https://ctdbase.org/detail.go?type=gene&acc=3606&view=ixn&chemAcc=C482199
https://en.wikipedia.org/wiki/Interleukin_18
https://x.com/FluoridePoison/status/1897860727744217230
Martin Heil. 2022. Self-DNA driven inflammation in COVID-19 and after mRNA-based vaccination: lessons for non-COVID-19 pathologies. https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2023.1259879/full