Drew Weissman Endotoxin induced Interleukin-6 Legacy
Knowing that his mRNA LNP jabs massively increased Endotoxin Interleukin-6 damage and death, he promoted Interleukin-6 receptor antagonists Tocilizumab and Sarilumab in Covid19 patients.
In my recent article I pointed to a new patent application by Drew Weissman and colleagues in which it was revealed that mRNA LNP jabs massively increased Endotoxin Interleukin-6 damage and death.1
And I pointed to a huge literature2 of 114,582 peer-reviewed papers covering Interleukin-6 when searching PubMed using that term and 197,744 peer-reviewed papers searching on the abbreviation IL-6.
On the US Government Comparative Toxicogenomics Database (CTD) we find a useful Human Curated Chart of IL-6 induced Diseases. They list 2,990 Diseases caused by IL-6.
CTD also displays the plethora of IL-6 synonyms and this chart clearly shows Endotoxin as the dominant cause of increased expression of this deadly Cytokine.
Searching PubMed for Weissman Interleukin 6 yields 26 papers. So perhaps we can look at that sample. Not all Weissman references match Drew.
A free paper by Weissman and very many co-authors pops up in which he and coworkers promoted Interleukin-6 receptor antagonists Tocilizumab3 and Sarilumab4 in Covid19 patients.5
Deaths from Tocilizumab
To 30 June 2024, US FAERS shows 7,064 Deaths from Tocilizumab.
Death rate is 80,230 per million case reports.
In Australia there have been 30 Deaths from 2,378 cases where it was the single suspected drug, which is a Death rate is 12,615 per million case reports, pehaps due to lower reporting rates to TGA DAEN.
Deaths from Sarilumab
To 30 June 2024, US FAERS shows 849 Deaths from Sarilumab.
Death rate is 56,789 per million case reports.
More papers from Weissman
I will list them now and expand commentary later.
In 1993 Weissman, Poli, Bousseau and Anthony Fauci looked at reducing Cytokine Storm in HIV infection and replication.6
In 1994 Weissman, Poli and Anthony Fauci published a paper showing that Interleukin 10 reduced the inflammation caused by HIV forming IL-6 in human cells.7
In 2013 Weissman investigated IL-6 in relation to HIV.8
Also in 2013 Weissman reported on the use of pseudouridine-modified mRNA to reduce IL-6 generated by mmune reaction.9
In 2016 Weissman looked ar rising systemic Interleukin 6 in Tuberculosis victims.10
At the height of mass jabbing, Weissman submitted a paper11 that announced that LNPs in combination with Inflammation caused by Endotoxin or other conditon are inflammatory. It was Received 10 November 2020; Received in revised form 14 November 2021; Accepted 19 December 2021. Why delay for 13 months?
Part of the Abstract reveals why:
Herein, we induce an acute-inflammation model in mice with lipopolysaccharide (LPS = Endotoxin) intratracheally (IT), 1 mg kg−1, or intravenously (IV), 2 mg kg−1, and then IV administer modmRNA-LNP, 0.32 mg kg−1, after 4 h, and screen for inflammatory markers, such as pro-inflammatory cytokines. ModmRNA-LNP at this dose caused no significant elevation of cytokine levels in naive mice.
In contrast, shortly after LPS immune stimulation, modmRNA-LNP enhanced inflammatory cytokine responses, Interleukin-6 (IL-6) in serum and Macrophage Inflammatory Protein 2 (MIP-2) in liver significantly. Our report identifies this phenomenon as inflammation exacerbation (IE), which was proven to be specific to the LNP, acting independent of mRNA cargo, and was demonstrated to be time- and dose-dependent.
Macrophage depletion as well as TLR3 −/− and TLR4−/− knockout mouse studies revealed macrophages were the immune cells involved or responsible for IE.
In November 2021 Weissman and coworkers announced that LNPs are inflammatory.12
December 2022 saw a paper on long-term outcomes.13
In this bayesian adaptive randomized clinical platform trial that included 4869 critically ill patients with COVID-19, the probability was high that IL-6 receptor antagonists and antiplatelet agents improved survival at 6 months (posterior probabilities of superiority of >99.9% and 95.0%, respectively). Long-term outcomes were not improved with therapeutic anticoagulation (11.5%), convalescent plasma (54.7%), or lopinavir-ritonavir (31.9%) and were worsened with hydroxychloroquine (posterior probability of harm, 96.8%). Corticosteroids did not improve long-term outcomes, although enrollment had been terminated early in response to external evidence.
Question for Dear Readers
Would you like me to add the 2,990 Diseases caused by IL-6 listed by the US Government CTD?
https://en.wikipedia.org/wiki/Tocilizumab
https://en.wikipedia.org/wiki/Sarilumab
Anthony C. Gordon, Paul R. Mouncey, Farah Al-Beidh, Kathryn M. Rowan, Alistair D. Nichol, Ph.D., Yaseen M. Arabi, Djillali Annane, Abi Beane, Wilma van Bentum-Puijk, Lindsay R. Berry, Zahra Bhimani, Marc J.M. Bonten, M.D., Charlotte A. Bradbury, Frank M. Brunkhorst, Adrian Buzgau, Allen C. Cheng, Michelle A. Detry, Eamon J. Duffy, Lise J. Estcourt, Mark Fitzgerald, Herman Goossens, Rashan Haniffa, Alisa M. Higgins, Thomas E. Hills, Christopher M. Horvat, Francois Lamontagne, Patrick R. Lawler, Helen L. Leavis, Kelsey M. Linstrum, Edward Litton, M.D., Elizabeth Lorenzi, John C. Marshall, Florian B. Mayr, Daniel F. McAuley, Anna McGlothlin, Shay P. McGuinness, Bryan J. McVerry, Stephanie K. Montgomery, Susan C. Morpeth, Srinivas Murthy, Katrina Orr, Rachael L. Parke, Jane C. Parker, Asad E. Patanwala, Ville Pettilä, Emma Rademaker, Marlene S. Santos, Christina T. Saunders, Christopher W. Seymour, Manu Shankar-Hari, Wendy I. Sligl, Alexis F. Turgeon, Anne M. Turner, Frank L. van de Veerdonk, Ryan Zarychanski, Cameron Green, Roger J. Lewis, Derek C. Angus, M.D., Colin J. McArthur, Scott Berry, Steve A. Webb, and Lennie P.G. Derde. 2021. Interleukin-6 Receptor Antagonists in Critically Ill Patients with Covid-19. https://www.nejm.org/doi/10.1056/NEJMoa2100433
D Weissman, G Poli, A Bousseau, A S Fauci. 1993. A platelet-activating factor antagonist, RP 55778, inhibits cytokine-dependent induction of human immunodeficiency virus expression in chronically infected promonocytic cells. https://www.pnas.org/doi/10.1073/pnas.90.6.2537
D Weissman, G Poli, A S Fauci. 1994. Interleukin 10 Blocks HIV Replication in Macrophages by Inhibiting the Autocrine Loop of Tumor Necrosis Factor α and Interleukin 6 Induction of Virus. https://www.liebertpub.com/doi/10.1089/aid.1994.10.1199
Shruthi Ravimohan, Neo Tamuhla, Andrew P Steenhoff, Rona Letlhogile, Didimalang Kgomotso Makutu, Kebatshabile Nfanyana, Tumelo Rantleru, Ann Tierney, Kelebogile Nkakana, Adam B Schwartz, Robert Gross, Rob Roy Macgregor, Scarlett L Bellamy, Ian Frank, Drew Weissman, Gregory P Bisson. 2013. Early Immunologic Failure is Associated With Early Mortality Among Advanced HIV–Infected Adults Initiating Antiretroviral Therapy With Active Tuberculosis. https://academic.oup.com/jid/article/208/11/1784/851327
Gábor Boros, Edit Miko, Hiromi Muramatsu, Drew Weissman, Eszter Emri, Dávid Rózsa, Georgina Nagy, Attila Juhász, István Juhász, Gijsbertus van der Horst, Irén Horkay, Éva Remenyik, Katalin Karikó, Gabriella Emri. 2013. Transfection of pseudouridine-modified mRNA encoding CPD-photolyase leads to repair of DNA damage in human keratinocytes: a new approach with future therapeutic potential. https://www.sciencedirect.com/science/article/abs/pii/S1011134413002182
Shruthi Ravimohan, Neo Tamuhla, Kebatshabile Nfanyana, Andrew P. Steenhoff, Rona Letlhogile, Ian Frank, Rob Roy MacGregor, Robert Gross, Drew Weissman, and Gregory P. Bisson. 2016. Robust Reconstitution of Tuberculosis-Specific Polyfunctional CD4+ T-Cell Responses and Rising Systemic Interleukin 6 in Paradoxical Tuberculosis-Associated Immune Reconstitution Inflammatory Syndrome. https://academic.oup.com/cid/article/62/6/795/2463019
Hamideh Parhiz, Jacob S. Brenner, Priyal N. Patel, Tyler E. Papp, Hamna Shahnawaz, Qin Li, Ruiqi Shi, Marco E. Zamora, Amir Yadegari, Oscar A. Marcos-Contreras, Ambika Natesan, Norbert Pardi, Vladimir V. Shuvaev, Raisa Kiseleva, Jacob W. Myerson, Thomas Uhler, Rachel S. Riley, Xuexiang Han, Michael J. Mitchell, Kieu Lam, James Heyes, Drew Weissman, Vladimir R. Muzykantov. 2020 -2021. Added to pre-existing inflammation, mRNA-lipid nanoparticles induce inflammation exacerbation (IE). https://www.sciencedirect.com/science/article/pii/S0168365921006805
Mohamad-Gabriel Alameh, Istvan Tombacz, Emily Bettini, Katlyn Lederer, Sonia Ndeupen, Chutamath Sittplangkoon, Joel R. Wilmore, Brian T. Gaudette, Ousamah Y. Soliman, Matthew Pine, Philip Hicks, Tomaz B. Manzoni, James J. Knox, John L. Johnson, Dorottya Laczko´, Hiromi Muramatsu, Benjamin Davis, Wenzhao Meng, Aaron M. Rosenfeld, Shirin Strohmeier, Paulo J.C. Lin, Barbara L. Mui, Ying K. Tam, Katalin Kariko´ Alain Jacquet, Florian Krammer, Paul Bates, Michael P. Cancro, Drew Weissman, Eline T. Luning Prak, David Allman,5 Botond Z. Igyarto´, Michela Locci, and Norbert Pardi. November 2021. Lipid nanoparticles enhance the efficacy of mRNA and protein subunit vaccines by inducing robust T follicular helper cell and humoral responses. https://www.cell.com/immunity/fulltext/S1074-7613(21)00490-8
Alisa M. Higgins, Lindsay R. Berry, Elizabeth Lorenzi, Srinivas Murthy, Zoe McQuilten, Paul R. Mouncey, Farah Al-Beidh, Djillali Annane, MD, Yaseen M. Arabi, Abi Beane, Wilma van Bentum-Puijk, Zahra Bhimani, Marc J. M. Bonten, MD, Charlotte A. Bradbury, Frank M. Brunkhorst, Aiden Burrell, Adrian Buzgau, Meredith Buxton; Walton N. Charles, Matthew Cove, Michelle A. Detry, Lise J. Estcourt, Elizabeth O. Fagbodun, Mark Fitzgerald, Timothy D. Girard, Ewan C. Goligher, Herman Goossens, Rashan Haniffa, Thomas Hills, Christopher M. Horvat, David T. Huang, MD, Nao Ichihara, Francois Lamontagne, John C. Marshall, Daniel F. McAuley, Anna McGlothlin, Shay P. McGuinness, Bryan J. McVerry, Matthew D. Neal, Alistair D. Nichol, Rachael L. Parke, Jane C. Parker, Karen Parry-Billings, Sam E. C. Peters, Luis F. Reyes, Kathryn M. Rowan, Hiroki Saito, Marlene S. Santos, Christina T. Saunders, Ary Serpa-Neto, Christopher W. Seymour, Manu Shankar-Hari, Lucy M. Stronach, Alexis F. Turgeon, Anne M. Turner, Frank L. van de Veerdonk, Ryan Zarychanski, Cameron Green, Roger J. Lewis, Derek C. Angus, Colin J. McArthur, Scott Berry, Lennie P. G. Derde, MD, Anthony C. Gordon, MBBS, Steve A. Webb, Patrick R. Lawler. December 2022. Long-term (180-Day) Outcomes in Critically Ill Patients With COVID-19 in the REMAP-CAP Randomized Clinical Trial. https://jamanetwork.com/journals/jama/fullarticle/2799870
Thank you for your great research in bringing this information to public attention. How are we to make informed decisions without the appropriate information. Of course, that’s the whole point, isn’t it?
Respectfully, I would say anyone with high IL-6, such as myself, has such due to a toxicant, whether that be the toxic mRNA shots, or in my case, due to toxic mold/mycotoxin exposure. Specifically, as to toxic mold/mycotoxin exposure, approximately 25% of the population - perhaps even more, lack the genes to properly detoxify, and Dr. Gupta of Australia has opined that 20% of the population has a health condition due to toxic mold/mycotoxin exposure. After doing much research, I have found that everything from cancer, to Alzheimer's, to arthritis, to mental disorder, to endocrine disorder, to cardiac condition can result from toxic mold/mycotoxin exposure. Combine that with these novel shots, people leaving their homes less so those in water-damaged homes are further sickened and it's no wonder the death rate is skyrocketing as well as the rate of other so-called diseases. Never would I get chemotherapy. It's crazy LDN isn't used more to treat high inflammation, which is far safer and has fewer side effects than chemotherapy. Better yet, natural things such as turmeric also treat inflammation.
I wonder if these deadly drugs you discuss here are the same monoclonal antibody treatments the likes of Dr. McCullough presented as beneficial, which by the way, in large part are made from fetal tissue, much like many harmful and deadly shots. Also, how the heck were they using Sarilumab/Kevzara when the drug manufacturer previously said the drug wasn't helpful for COVID? https://www.bostonglobe.com/2020/09/01/business/sanofi-halts-tests-arthritis-drug-treating-covid-19/ It is mind-boggling why this drug in particular is allowed to be used for anything at all.