Moderna's director Dr. Moncef Slaoui to oversee the White House's operation Warp Speed initiative
New Coronavirus Vaccine Candidate Shows Promise In Early, Limited Trial
Here is the reality of our circumstances. We should by now have the best health in people that has ever been available on planet earth with what we know about nutrition and sanitation. Nutrition and sanitation were always the key fundamental foundation for good health. This has always been known and is beyond comprehension with what is going on here with this corporate priest class of scientists. Why for example are infertility rates skyrocketing? Would that have anything to do with people pissing out glyphosate? These psychopaths running these big pharmaceutical military-connected mafia entities, who think GMOs are just great for you and who want to force vaccines on you, are nothing more than the marketing arm of a relentless onslaught with a dangerous agenda that could give a shit about your health.
News update for 20 May 2020 by Robert Kennedy Jr: CATASTROPHE: 20% Of Human Test Subjects Severely Injured From Gates-Fauci Coronavirus Vaccine By Moderna
The reason why the health and nutrition industry has practically been driven under ground is to force people into the private sector where vaccines and GMO foods pressed out of stainless steel industrial vats await you. That's what the pharmaceutical-military industrial complex wants: layer after layer of bureaucracy to prevent you from sitting down with your doctor, and the two of you try and figure out what the f*ck is wrong with you and fixing it. Science has been turned into a very dark and "evil" religion and Bill Gates & Co. are the face of this greedy religion. According to Bill, you are going to "go to zero."
Bill's Simplistic Formula: CO2--->Temperature Increase--->Negative Effects - The Joke Is On You - "P" Has To Go To Zero - Bill Wants To Turn You On Or Off By Remote - High Tech Vaccines and GMOs On the Way
Italian Politician Demand Bill Gates Arrest For Crimes Against Humanity
Taken at its face value: Flu Vaccine Increases Coronavirus Risk 36% Says Military Study
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Source: Life Site
EXCLUSIVE: Virus researchers uncover new evidence implying COVID-19 was created in a lab
Preliminary study results suggest virus was produced in lab cultures using human cells.
May 16, 2020 | By Matthew Cullinan Hoffman
A clinical support technician extracts viruses from swab samples so that the genetic structure of a virus can be analysed and identified in the coronavirus testing laboratory at Glasgow Royal Infirmary, on February 19, 2020 in Glasgow, Scotland.
May 16, 2020 (LifeSiteNews) – A team of Australian scientists has produced new evidence that the novel coronavirus that causes COVID-19 is optimized for penetration into human cells rather than animal cells, undermining the theory that the virus randomly evolved in an animal subject before passing into human beings, and suggesting instead that it was developed in a laboratory.
The study, which has not yet been peer reviewed, provides new but not yet conclusive evidence favoring the theory that the novel coronavirus originated not in a food market as has been claimed, but rather in a laboratory, presumably one operated by the Wuhan Institute of Virology in Wuhan, China, the city in which the first outbreak of COVID-19 occurred in December of 2019.
The lead researcher on the team says that the results represent either "a remarkable coincidence or a sign of human intervention" in the creation of the virus.
The authors of the study, led by vaccine researcher Nikolai Petrovsky of Flinders University in Australia, used a version of the novel coronavirus collected in the earliest days of the outbreak and applied computer models to test its capacity to bind to certain cell receptor enzymes, called "ACE2," that allow the virus to infect human and animal cells to varying degrees of efficacy.
They tested the propensity of the COVID-19 virus's spike protein, which it uses to enter cells, to bind to the human type of ACE2 as well as to many different animal versions of ACE2, and found that the novel coronavirus most powerfully binds with human ACE2, and with variously lesser degrees of effectiveness with animal versions of the receptor.
According to the study's authors, this implies that the virus that causes COVID-19 did not come from an animal intermediary, but became specialized for human cell penetration by living previously in human cells, quite possibly in a laboratory.
The authors write that "this finding is particularly surprising as, typically, a virus would be expected to have highest affinity for the receptor in its original host species, e.g. bat, with a lower initial binding affinity for the receptor of any new host, e.g. humans. However, in this case, the affinity of SARS-CoV-2 is higher for humans than for the putative original host species, bats, or for any potential intermediary host species."
As a consequence, they add, a "possibility which still cannot be excluded is that SARSCoV-2 was created by a recombination event that occurred inadvertently or consciously in a laboratory handling coronaviruses, with the new virus then accidentally released into the local human population."
Please go to Life Site to read the entire article.
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By F. William Engdahl | 18 May 2020
Image Credit: Maryland GovPics: Emma Walmsley and Moncef Slaoui, December 2016. License: Creative Commons Attribution 2.0 Generic with conditions https://cutt.ly/NyTn9OD
The US White House has appointed a coronavirus "Vaccine Czar" from Big Pharma to oversee something dubbed Operation Warp Speed. The goal is to create and produce 300 million doses of a new vaccine to supposedly immunize the entire US population by year-end against COVID-19. To be sure that Big Pharma companies give their all to the medical Manhattan Project, they have been fully indemnified by the US government against liabilities should vaccine recipients die or develop serious disease as a result of the rushed vaccine. The FDA and NIH have waived standard pre-testing on animals in the situation. The US military, according to recent remarks by the US President, is being trained to administer the yet-to-be unveiled vaccine in record time. Surely nothing could go wrong here?
Warp speed is a term out of the sci-fi Star Trek media, defined as a speed faster than the speed of light. In recent weeks billions of dollars have been pledged from governments, from the Bill and Melinda Gates Foundation and others to fast-track a vaccine as well as test medical treatments to combat the VODIV19 illness said to originate from a novel coronavirus first discovered late 2019 in Wuhan China. This rush to create a "miracle" vaccine is ominous and suggests some hidden agenda.
The Conflicted Czar
Washington's Operation Warp Speed is reportedly the brainchild of Presidential Adviser and son-in-law Jared Kushner. It is being formally run by the Health and Human Services Secretary Alex Azar and Defense Secretary Mark Esper who will work with a new Vaccine Czar. The Vaccine Czar selected for Kushner's Operation Warp Speed is former GlaxoSmithKline Chairman of its Vaccines Division, Morrocan-born US citizen, Dr. Moncef Slaoui. From 2006 through 2017 Slaoui was Chairman of Global R&D and Vaccines at GlaxoSmithKline and sat on the company's Executive team and Board of Directors.
While at GSK Slaoui headed the development of Cervarix. Its Cervarix HPV cervical cancer vaccine was reported tied to multiple deaths or severe crippling effects in many recipients. A 2017 WHO monitoring report revealed that serious adverse effects from Moncef Slaoui's HPV vaccine included complex regional pain syndrome (CRPS), postural orthostatic tachycardia syndrome (POTS) and chronic fatigue syndrome (CFS) that "exceeds any other vaccine." That is not reassuring in terms of the new Czar of a rushed coronavirus vaccine.
In 2015 the Indian Supreme Court investigated charges that young Indian village girls died after being given Cervarix from Slaoui's GSK. It was done in illegal vaccine "human guinea pig" tests of the HPV vaccine where neither the girls nor their parents were told what it was. The study was reportedly funded by the Bill and Melinda Gates Foundation.
In 2012 while Slaoui headed GSK global R&D and vaccine development, and sat on the GSK board, the company was fined $3 billion by the US Department of Justice, the largest ever fine against a pharmaceutical company. Among the charges was that GlaxoSmithKline deliberately withheld alarming safety data for its major-selling diabetes drug, Advandia, from the US FDA. After Advandia quietly vanished from the product list of GSK.
Slaoui also has ties to the projects of the Bill & Melinda Gates Foundation. He sat on the board of the Gates-funded International AIDS Vaccine Initiative. The IAVI was initiated in 1994 at a Rockefeller Foundation conference and is backed among others by the Gates Foundation, by the US Department of Defense and by Tony Fauci's National Institute of Allergy and Infectious Diseases.
At a May 15 White House press conference where the President introduced Slaoui as the head of the crash vaccine project, Slaoui stated, "Mr. President, I have very recently seen early data from a clinical trial with a coronavirus vaccine. These data make me feel even more confident that we will be able to deliver a few hundred million doses of vaccine by the end of 2020."
Though he did not say, he was clearly referring to Moderna and its mRNA gene-edited vaccine, the first US vaccine authorized to enter Phase I human trials after the US government gave the company a staggering $483 million of funding to fast-track the COVID-19 vaccine.
Vaccine Czar Slaoui is well-placed with regard to Moderna. After leaving GSK from 2017 until he joined the Trump Operation Warp Speed, Slaoui was on the Moderna Board of Directors. He also still holds $10 million worth of Moderna stock options, options likely to soar in value as the Warp Speed zooms forward. This would suggest a glaring conflict of interest with Czar Slaoui, but that's only the start of this saga, where millions of lives are potentially at threat from a novel inadequately-tested or proven genetically edited vaccine.
Moderna and Slaoui
At this point the leading US Government candidate for winning the "warp speed" race to roll out a COVID-19 vaccine is Slaoui's Moderna Inc. in Cambridge, Massachusetts. That's surely a coincidence?
Moderna claims that between January 11, when they got the DNA sequence of the virus from China, and January 13–in just two days–working together with Anthony Fauci's National Institute of Allergies and Infectious Diseases (NIAID) of NIH, they managed to finalize the sequence for mRNA1273 vaccine against the novel coronavirus. At that point Fauci announced unprecedented plans to run human Phase I trials of the vaccine without prior animal studies. The FDA waived animal pretest requirements. The Moderna mRNA1273 tests were funded by the Gates Foundation-funded Coalition for Epidemic Preparedness Innovations (CEPI).
Please go to F. William Engdahl's website to read the entire article.
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Source: Irene Caesar
SARS-CoV-19 is the Resurrected, SARS-Camouflaged, GOF HIV Airborne, 100-Anniversary Deadliest H1N1 Spanish Flu Pandemics of 2019-2020
May 17, 2020 | By Irene Caesar
WARNING TO THE US INTELLIGENCE СOMMUNITY. ILLICIT ISRAELI WAR AGAINST UNITED STATES THROUGH THE MOSSAD SHILLS IN CIA
SARS-2 (COVID-19) pandemic is a camouflaged — resurrected and recombinant — 1918 flu virus (H1N1) that caused the deadliest pandemic in the history of humankind ("Spanish Flu" killed an estimated 50 million people worldwide, including an estimated 675,000 people in the United States). The aggressive virulence factors (sustained human to human transmission), characteristic of 1918 virus, were specifically extracted from the 1918 virus and combined with various forms of human influenza and coronavirus. The 2009 H1N1 pandemic and COVID-19 pandemic (1918 virus camouflaged as "Coronavirus") were meant to "celebrate" the 10th "anniversary" and the 100-year "anniversary" of the 1918 pandemic respectively.
It is established that the emergence of the 1957 H2N2 and 1968 H3N2 influenza A pandemic viruses was caused by the RECOMBINATION where new avian genome segments were imported into the backbone of 1918-descended H1N1 viruses (137), as well as the 2003 emergence of the pathogenic Fujian H3N2 influenza strain by interclade reassortment. Source:
Webby, R. J., and R. G. Webster. 2001. Emergence of influenza A viruses. Philos. Trans. R. Soc. Lond. B 3561817-1828
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2546865/
This means that the 1918 flu virus (H1N1) samples were carefully preserved and kept all these years, whatever CDC says about its recent digging out from the Alaska permafrost.
"Avian" or "swine" or “dogs” (coronavirus) specifics of the pandemics is explained by the biomaterial, in which the 1918 virus is grown. Coronavirus was specifically used to conceal that the SARS-1 and SARS-2 (COVID-19) pandemics were simply the heavily recombinant 1918 virus. I emphasize, specifically the 1918 virus had provided the sustained human to human transmission, i.e., high virulence of SARS-CoV-19 virus. This is called "GAIN OF FUNCTION" (GOF). The recombinant (man-made) nature of all the recent pandemics explains why CDC has "pre-pandemic vaccines". Of course, if you make viruses (Pathogen) yourself, you have the vaccine (Antigen) automatically.
"The 2019 novel coronavirus, or "SARS-CoV-2", was discovered because of Wuhan virus pneumonia cases in 2019, and was named by the World Health Organization on January 12, 2020. It belongs to the beta genera of the Coronaviridae family, together with SARS coronavirus in 2003 and MERS coronavirus in 2012. The alignment between SARS-CoV-2 and 2003 SARS CoV has about 70% sequence (some say 86%) similarity and 40% sequence similarity with MERS CoV. The coronavirus genome encodes a spike protein, an envelope protein, a membrane protein, and a nucleoprotein. Among them, spike protein is the most important surface membrane protein of coronavirus." (source: https://sars-cov-2.creative-biolabs.com/sars-cov-2-2019-ncov-spike-protein-elisa-kit-329.htm). Remark: 70% sequence similarity and 40% sequence with SARS-1 and MERS is a proof of itself for the intentional "accelerated virus evolution". "SARS-CoV-2 has all the same genetic equipment as the original SARS-CoV, which caused a global outbreak in 2003, but with around 6,000 mutations sprinkled around in the usual places where coronaviruses change. Think whole milk versus skim milk." Source:
https://www.snopes.com/news/2020/04/02/what-the-coronavirus-does-to-your-body-that-makes-it-so-deadly/
In the SARS-CoV-1 outbreak, the first Coronavirus virus, that was synthesized by CDC, was inefficiently transmitted by most infected people, so that, quarantine allowed the epidemic to be stopped before the virus could become fully established in humans. Now, its variation in the SARS-CoV-2, the second Coronavirus was artificially made to gain the ability to spread "efficiently". The fairytale that this virus had "emerged naturally" is laughable, because the second version of SARS-CoV had suddenly emerged with GOF – GAIN OF FUNCTION. Evidently, somebody in CDC had worked hard to make the virus "spread more efficiently". See:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2546865/#r137
This statement is confirmed by Dr. Fang Li of the Minnesota University in the important paper on the artificially GAINED OF FUNCTION SARS-CoV-1, analyzed below.
"Gain of Function" was objected by French scientist Dr. Simon Wain-Hobson of Pasteur Institute in Paris in 2014. He pointed that GOF is clearly the DURC = "Dual-Use Research of Concern", i.e., the bioweapons:
https://www.ncbi.nlm.nih.gov/pubmed/25077136
In October 2014 the administration of US President Barack Obama banned GOF research on influenza, SARS, and MERS. Concerns over so-called “gain-of-function” (GOF) studies that make pathogens more potent or likely to spread in people erupted in 2011, when Kawaoka’s team and Ron Fouchier’s lab at Erasmus Medical Center in Rotterdam, the Netherlands, announced that they had modified the H5N1 bird flu virus to enable it to spread between ferrets (that is, to cross the barrier between species). The ban was lifted on December 19 2017, according to Science:
https://www.sciencemag.org/news/2017/12/nih-lifts-3-year-ban-funding-risky-virus-studies
Importantly, there should be "an intermediate host" for the Coronavirus to hop from snakes or bats to humans. Notably, the paper published by the US Federal government-funded researchers in the Nature Medicine on November 15, 2015 had proven that only the CHIMERIC SARS-like virus out of the surface spike protein of a coronavirus found in horseshoe bats, called SHC014, and the backbone of a SARS virus that could be grown in mice, CERTAINLY WITH OTHER ADDITIONS, can infect humans. See: "A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence" by Vineet D Menachery, Boyd L Yount Jr, Kari Debbink, Sudhakar Agnihothram, Lisa E Gralinski, Jessica A Plante, Rachel L Graham, Trevor Scobey, Xing-Yi Ge, Eric F Donaldson, Scott H Randell, Antonio Lanzavecchia, Wayne A Marasco, Zhengli-Li Shi & Ralph S Baric. The research was jointly done by the University of North Carolina at Chapel Hill, USA; the Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts, USA; and the Chinese Academy of Sciences, Wuhan, China:
https://www.nature.com/articles/nm.3985.pdf?origin=ppub
https://www.nature.com/news/engineered-bat-virus-stirs-debate-over-risky-research-1.18787
Notably, "these certain other additions' were made earlier, now forgotten in the public eye. In the paper "Structural Analysis of Major Species Barriers between Humans and Palm Civets for Severe Acute Respiratory Syndrome Coronavirus Infections" by Fang Li, published in J Virol. 2008 Jul, it is claimed that (1) "The major species barriers between humans and civets for SARS-CoV infections are the specific interactions between a defined receptor-binding domain (RBD) on a viral spike protein and its host receptor, angiotensin-converting enzyme 2 (ACE2); (2) to cross this inter-species barrier, "a chimeric ACE2 bearing the critical N-terminal helix from civet and the remaining peptidase domain from human was constructed, and it was shown that this construct has the same receptor activity as civet ACE2". (3) Furthermore, “crystal structures of the chimeric ACE2 complexed with RBDs from various human and civet SARS-CoV strains were synthesized”. This means that the CROSS-SPECIES LINK was artificially synthesized to transmit SARS-CoV from a civet to a human. While a civet was a link from a bat to a human. Dr. Fang Li says that "the major species barrier for the transmission of SARS-CoV from a civet to a human WAS IN NATURE the INCOMPATIBILITY between four ACE2 residues (residues 31, 35, 38, and 353) in humans and two RBD residues (residues 479 and 487) in civets. That is why the NATURALLY-OCCURRING civet (animal) SARS-CoV virus was prevented from infecting humans due to "incompatible salt bridges at the hydrophobic virus/receptor interface". Dr. Fang Li claims that after his manipulations with the SARS-CoV virus of civets, he was a success of trespassing this incompatibility "by eliminating unfavorable free charges at the interface through stepwise mutations at positions 479 and 487". As the result, Dr. Fang Li says, the SARS-CoV virus of civets had gained "the sustained infectivity for human cells". The newly SYNTHESIZED GOF SARS-CoV was submitted to the Protein Data Bank under accession numbers 3D0G (complex of chimeric ACE2 and hTor02 RBD), 3D0H (complex of chimeric ACE2 and cSz02 RBD), and 3D0I (complex of chimeric ACE2 and cGd05 RBD). Dr. Fang Li works for the Department of Pharmacology at the University of Minnesota Medical School, Minneapolis, Minnesota. Though the data on the Gained of Function SARS-CoV was filed by the University of Minnesota in July 2008 after the epidemic of SARS in 2002-2003, we can definitely claim that this 2002-2003 pandemic was itself a synthesized GOF binary biological warfare, though that time, the SARS-CoV-1 did not have enough human to human virulence. This was precisely corrected by the joint forces at the University of Minnesota. And, do, Dr. Fang Li says that SARS-CoV-1 had "reemerged in Guangdong in 2003 to 2004, with four sporadic infections, no fatalities, and no subsequent human-to-human transmission. SARS has been absent in humans ever since". This makes it clear that if not for the University of Minnesota efforts to keep SARS-CoV-1 highly virulent in the human-to-human transmission, we would not have gotten the present SARS-CoV-2 pandemic:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2446986/
Dr. Fang Li is a front man for Dr. Stephen C. Harrison who evidently wanted to stay in shadows for this controversial research. The research on the GAINED IN FUNCTION SARS-CoV-1 by Dr. Fang Li was funded by NIH (US National Institute of Health) grant CA-13202 to Stephen C. Harrison of Harvard. Dr. Stephen C. Harrison is the director of the Center for Molecular and Cellular Dynamics of Harvard Medical School, head of the Laboratory of Molecular Medicine at Boston Children’s Hospital, and investigator of the Howard Hughes Medical Institute. Remarkably, Stephen C. Harrison led the Structural Biology team at the Center for HIV/AIDS Vaccine Immunology (CHAVI) when it received National Institute of Allergy and Infectious Diseases (NIAID) funding of around $300 million to design and test the HIV vaccine. As is seen below, the HIV inserts play the major role in the GAINED OF FUNCTION SARS-CoV-2.
The research by Fang Li proves that there can be no direct transmission of SARS-CoV between bats and humans without an intermediate host. The argument that the closely related viruses in human can be a bridge for the SARS-CoV transmission from bats to humans does not hold, according to Dr. Fang Li research.
The Wuhan lab worked with the CLOSEST known relative of SARS-CoV-2, which is a bat coronavirus called RaTG13. The evolutionary virologist Edward Holmes, of the Charles Perkins Center and the Marie Bashir Institute for Infectious Diseases and Biosecurity at the University of Sydney, said in a statement from the Australian Media Center that “the level of genome sequence divergence between SARS-CoV-2 and RaTG13 is equivalent to an average of 50 years (and at least 20 years) of evolutionary change." That means that in the wild, it would take about 50 years for these viruses to evolve to be as different as they are. Thus, we have a clear "accelerated virus evolution". Nikolai Petrovsky of the College of Medicine and Public Health at Flinders claims that Bat coronaviruses can be cultured in lab dishes with cells that have the human ACE2 receptor, so that, over time, the virus will gain adaptations that let it efficiently bind to human receptors. Source:
https://www.msn.com/en-us/health/medical/does-the-novel-coronavirus-have-any-links-to-a-high-security-lab-in-wuhan/ar-BB12QiM3
For recombination to occur, the two divergent viruses are made to infect the same organism simultaneously. So, SARS-CoV-2 has HIV inserts. The genetic mosaicism exists not only between divergent viruses, but also between viruses and bacteria. Thus, there certainly can be the recombination between the influenza virus H1N1 1918 and the SARS-CoV-2. That is why the Flu Vaccine Increases Coronavirus Risk 36% Says Military:
Flu Vaccine Increases Coronavirus Risk 36% Says Military Study
https://www.sciencedirect.com/science/article/pii/S0264410X19313647?via%3Dihub
And, in fact, CDC had published in its Volume 26, Number 6—June 2020 (retrieved on May 15th, 2020) the Research Letter "Co-infection with SARS-CoV-2 and Influenza A Virus in Patient with Pneumonia, China” by Xiaojing Wu, Ying Cai, Xu Huang, Xin Yu, Li Zhao, Fan Wang, Quanguo Li, Sichao Gu, Teng Xu, Yongjun Li, Binghuai Lu, and Qingyuan Zhan of China-Japan Friendship Hospital, Beijing; The Sixth Medical Center of PLA General Hospital, Beijing; Weifang No. 2 People's Hospital, Weifang; Vision Medicals Co., Ltd., Guangzhou, all in China:
https://wwwnc.cdc.gov/eid/article/26/6/20-0299_article
Please go to Irene Caesar to read the entire article.
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Related:
EXPERT REACTION: Did COVID-19 come from a lab in Wuhan?
Outcry- Prosecute Corona-Con War Criminals!!
The Rest of the Liability Story
Beware the Pentagon's Pandemic Profiteers
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