International [U.S COVID Vaccine News] CDC to Lift COVID-19 Testing Requirement for international Travelers

nothing more than one of dozens if not hundreds of schemes in which we bankrupt canada for the benefit of the chinese elite.

The hardest lesson learned are the best lessons - hopefully.

Look on the bright side though, the table has turned and a Canadian company is now raking in the dough for licensing their early-stage mRNA tech to China, just because the CCP can't bring themselves to back-pedal and use the Pfizer-BioNTech shots to boost their inferior vaccines after spending months spreading fake news on it.

With the Canadian vaccine candidate still in the pipeline, the CCP may be more open to co-op it as a "homegrown shot" rather than the well-known names in the market that are now synonymous with the West's success, especially in comparison with China's Sinopharm and Sinovac.

----

Chinese Firm Licenses Canada mRNA Vaccine Tech in $500 Million Deal
Bloomberg News | September 13, 2021

Chinese biopharma firm Everest Medicines Ltd. will license an mRNA Covid-19 vaccine from Canada’s Providence Therapeutics Holdings Inc., as companies try to bring the most effective inoculation platform into China despite its apparent resistance to western shots.

Everest will gain rights to Providence’s vaccine in Greater China and countries including Indonesia, Singapore, and Thailand, it said in a statement Monday. It will pay $100 million cash upfront for access to the vaccines and mRNA technology, and up to $100 million in profit-sharing, the statement said. The deal includes another payment of up to $300 million in stock if further products are developed using Providence’s mRNA technology platform.

While almost 1 billion people have been fully vaccinated in China, the country is still lacking an mRNA shot, with most of the population inoculated with inactivated vaccines from Sinopharm Group Co. and Sinovac Biotech Ltd., which studies have found to be less effective. A deal by Fosun Pharmaceutical Group Co. to sell BioNTech SE’s mRNA shot in mainland China has yet to be approved by regulators, suggesting it may not be easy to bring in a foreign mRNA vaccine, partly because of political sensitivities.

If approved, the Everest-Providence vaccine will likely be used as a booster shot in China given most of the population has been vaccinated, Everest Chief Executive Officer Kerry Blanchard said in an interview. In other Asian nation’s within Everest’s remit, there’s still the need for primary vaccination, he said.

“That’s still a large group of people,” Blanchard said. “I think it’s a reasonable assumption that most adults will likely need a booster at some point, and the older you are, the more rapidly the immunity wanes. People will need to have at least one booster.”

Everest’s full technology transfer of the Providence shot means the Chinese firm would have a bigger stake in the vaccine, which may potentially help its chances to be considered as a Chinese vaccine, compared to Fosun Pharma which would only manufacture and distribute the BioNTech jab.

Given the vaccine has only just completed Phase-1 trials in Canada, it’s difficult to put a timeline on the shot’s development, which depends on the enrollment of patients, execution of the trials, and flexibility of the regulatory system. But a phase III trial will likely start this year or early next year, he said.

Homegrown Shot
While there’s little knowledge on how much protection the vaccine will provide against the virus, Blanchard said the immunogenicity and the neutralization are “as good or better than Pfizer and Moderna” against the original strain of the virus and its variants.

The delay in approving the BioNTech-Pfizer shot has stoked speculation China’s government is trying to avoid acknowledging that local shots may be less effective than Western ones.

“We believe that a locally manufactured vaccine is the right approach, and that’s the approach we’ll pursue,” Blanchard said. “I do believe our ability to do full technology transfer into China is important.”

https://www.bloomberg.com/news/arti...-canada-mrna-vaccine-tech-in-500-million-deal
 
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Sounds like greedy Moderna might not get a lending hand so easily from the U.S government next time.

Moderna vs. U.S. National Institutes of Health:
COVID-19 vaccine patent dispute headed to court

By Julie Steenhuysen | Nov 10, 2021

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CHICAGO, Nov 10 (Reuters) - U.S. National Institutes of Health scientists played "a major role" in developing Moderna Inc's COVID-19 vaccine and the agency intends to defend its claim as co-owner of patents on the shot, NIH Director Dr. Francis Collins told Reuters on Wednesday.

In a story first reported by the New York Times on Tuesday, Moderna excluded three NIH scientists as co-inventors of a central patent for the company's multibillion-dollar COVID-19 vaccine in its application filed in July.

"I think Moderna has made a serious mistake here in not providing the kind of co-inventorship credit to people who played a major role in the development of the vaccine that they're now making a fair amount of money off of," Collins said in an interview ahead of the Reuters Total Health conference, which will run virtually from Nov. 15-18.

Moderna expects 2021 sales of $15 billion to $18 billion from the COVID-19 vaccine - its first and only commercial product - and up to $22 billion next year.

In a statement emailed to Reuters, Moderna acknowledged that scientists at NIH's National Institute of Allergy and Infectious Diseases (NIAID) played a "substantial role" in developing Moderna's messenger RNA (mRNA) vaccine, but the company said it disagrees with the agency's patent claims.

Collins said the NIH has been trying to resolve the patent conflict with Moderna amicably for some time and has failed.

"But we are not done. Clearly this is something that legal authorities are going to have to figure out," he said.

NIH has asserted that three of its scientists - Dr. John Mascola, Dr. Barney Graham and Dr. Kizzmekia Corbett - helped design the genetic sequence used in Moderna's vaccine and should be named on the patent application. Graham has since retired and Corbett is now working at Harvard.

"It's not a good idea to file a patent when you leave out important inventors, and so this is going to get sorted as people look harder at this," Collins told Reuters.

"I did not expect that to be the outcome from what had been a very friendly, collaborative effort between scientists at NIH and Moderna over many years."

In its statement, Moderna said, "We do not agree that NIAID scientists co-invented claims to the mRNA-1273 sequence itself. Only Moderna’s scientists came up with the sequence for the mRNA used in our vaccine."

Moderna said the company has acknowledged NIH scientists in other patent applications, such as those related to dosing. But for the core patent, Moderna is only required to list Moderna scientists as inventors of the sequence under the strict rules of U.S. patent law, it said.

"We are grateful for our collaboration with NIH scientists, value their contributions, and remain focused on working together to help patients," the company added.

https://www.reuters.com/business/he...ute-headed-court-us-nih-head-says-2021-11-10/
 
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Why Moderna won't share rights to the COVID-19 vaccine with the government that paid for its development
By Ana Santos Rutschman, Assistant Professor of Law, Saint Louis University | November 18, 2021​

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The U.S. government funded a significant portion of the R&D behind the Moderna vaccine
A quiet monthslong legal fight between the U.S. National Institutes of Health and drugmaker Moderna over COVID-19 vaccine patents recently burst into public view. The outcome of the battle has important implications, not only for efforts to contain the pandemic but more broadly for drugs and vaccines that could be critical for future public health crises.

Moderna recently offered to share ownership of its main patent with the government to resolve the dispute. Whether or not this is enough to satisfy the government’s claims, I believe the dispute points to serious problems in the ways U.S. companies bring drugs and vaccines to market.

In my view, the dispute is a reminder of the many problems embedded in how vaccines are made and delivered in the U.S. And it shows that when taxpayers fund basic research of a drug, they deserve more of the control – and rewards – when that drug succeeds.
https://news.yahoo.com/why-moderna-wont-share-rights-201648779.html
 
Moderna offers NIH co-ownership of COVID vaccine patent amid dispute with government
BY ALEXANDER TIN |NOVEMBER 15, 2021​

The National Institutes of Health said Monday it has engaged Moderna in "good faith discussions" to resolve a monthslong dispute over the company's patent application that advocates say could impact global production of the shots.

Moderna is offering to share ownership of its COVID-19 vaccine patent with the U.S. government to resolve the dispute, the vaccine maker said, and would allow the Biden administration to "license the patents as they see fit."

An NIH spokesperson declined Monday to comment directly on Moderna's offer, citing "ongoing discussions."

The company claims it had no choice under the "strict rules" of American patent law to list only its own scientists "as the inventors on these claims."

But the National Institute of Allergy and Infectious Diseases disagrees.

A spokesperson for the government research arm - housed within the NIH - said that "its own thorough review" had determined that scientists Kizzmekia Corbett, Barney Graham, and John Mascola also deserved to be named as inventors.

"Moderna has made a serious mistake here in not providing the kind of co-inventorship credit to people who played a major role in the development of the vaccine that they are now making a fair amount of money off of," NIH Director Dr. Francis Collins told Reuters last week.

"Omitting NIH inventors from the principal patent application deprives NIH of a co-ownership interest in that application and the patent that will eventually issue from it," said an NIAID spokesperson.

Public Citizen, a government watchdog group, penned a letter this month to the NIH urging the agency "to publicly reclaim the foundational role" it played in developing the shots, criticizing a July patent filing by Moderna claiming it had "reached the good-faith determination" that the NIH's scientists "did not co-invent the mRNAs" in their application.

The New York Times first reported on Public Citizen's discovery.

"The U.S. government has done so much for Moderna and yet asked for so little in return, consistently. There is an urgent need for the U.S. government to reassert more control over how this vaccine is priced and produced," said Zain Rizvi, Public Citizen's research director.

The Government Accountability Office recently estimated that the NIH has earned $2 billion in royalties since 1991 over licensing patents for FDA-approved drugs.

Moderna announced this month it had earned $10.7 billion from COVID-19 vaccine sales in 2021 through September. Under the Trump administration early in the pandemic, Operation Warp Speed, the accelerated government effort to develop a COVID-19 vaccine, pledged to cover up to $483 million of costs to accelerate development and manufacturing of the vaccine.

Beyond the money the federal government could earn from the patent, Rizvi said the Biden administration could leverage a license with co-inventorship to allow developing countries to ramp up production of the shots and prepare for future pandemics without strings attached.

"Moderna says it offered to allow that NIH to be a co-owner on some of the patent applications. But it did not say what it demanded from the NIH, if anything, in return. Was this a unilateral offer?" said Rizvi.

Who invented Moderna's vaccine?
Early in 2020, the NIAID's Vaccine Research Center helmed by Graham was already working on vaccines for other diseases with Moderna when the agency says its scientists pivoted to ramping up research into a new virus that had been raising alarm overseas.

Having long worked with scientists in a lab led by Jason McLellan at the University of Texas at Austin on research into similar kinds of viruses, the university says the NIH's scientists were able to accelerate their development of genetic sequences that could be delivered in mRNA vaccines, which train the body to spot and fend off a signature spike protein on SARS-CoV-2.

"The work of Dr. Barney Graham and Kizzmekia Corbett and others stabilized the pre-fusion spike protein which is used in virtually all, with few exceptions, of the vaccines that are now successful," NIAID Director Dr. Anthony Fauci told a House of Representatives hearing in April.

Corbett, Graham, and McLellan are among the scientists listed on a patent first filed on February 11, 2020 for a COVID-19 vaccine stemming from that work. An NIAID spokesperson said Moderna uses its "stabilized spike protein technology in its vaccine."

Both Moderna and NIH scientists are also listed together on another patent filing from May of 2020, regarding "methods of use" for mRNA vaccines to address COVID. The NIAID spokesperson described it as a "minor patent application."

"Virtually everything that comes out of the government's research labs is a non-exclusive licensing agreement, so that it doesn't get blocked by any particular company," Graham told The Financial Times in April, saying the government could "use the leverage of the public funding to solve public health issues."

Early press releases by Moderna acknowledged the work with Graham's team, describing their mRNA-1273 vaccine as using a spike protein "designed by Moderna in collaboration with NIAID."

But Moderna has also sought to separate the development of its vaccine from the NIH's research, saying that the mRNA sequence in the company's vaccine "was selected exclusively by Moderna scientists using Moderna's technology, and without input of NIAID scientists."

The company says the NIH's scientists were "not even aware of the mRNA sequence" used in its vaccines until after Moderna had filed its patent request, which dates to as early as late January.

The February filing by the NIH's scientists was further evidence that "the same thing cannot be claimed to be invented twice by the same people working with two different collaborators," Moderna said.

"The Moderna team worked in Boston while the NIH team worked outside of D.C. and we then compared notes," Moderna's CEO Stéphane Bancel told the "I Am Bio" podcast last year, saying it was "encouraging" that the two groups of scientists "independently came to exactly the same antigen" for the vaccine.

Graham and McLellan both declined to comment for this article.

In an interview published Wednesday by The Grio, Corbett said she had "decided that it is not my place to really say anything."

"Patent disputes and all of those things, I like to say, I leave it to the institutions and the attorneys to really figure that out. I sleep at night knowing that lives have been saved and knowing that the science that I put blood, sweat, and tons of tears into is saving those lives," added Corbett.

https://www.cbsnews.com/news/moderna-covid-vaccine-patent-dispute-national-institutes-health/
 
There's a serious conflict of interest going on between Pfizer and FDA.

Wait what? FDA wants 55 years to process FOIA request over vaccine data
https://www.reuters.com/legal/gover...ss-foia-request-over-vaccine-data-2021-11-18/
(Reuters) - Freedom of Information Act requests are rarely speedy, but when a group of scientists asked the federal government to share the data it relied upon in licensing Pfizer’s COVID-19 vaccine, the response went beyond typical bureaucratic foot-dragging.

As in 55 years beyond.

That’s how long the Food & Drug Administration in court papers this week proposes it should be given to review and release the trove of vaccine-related documents responsive to the request. If a federal judge in Texas agrees, plaintiffs Public Health and Medical Professionals for Transparency can expect to see the full record in 2076.

The 1967 FOIA law requires federal agencies to respond to information requests within 20 business days. However, the time it takes to actually get the documents “will vary depending on the complexity of the request and any backlog of requests already pending at the agency,” according to the government’s central FOIA website.

Justice Department lawyers representing the FDA note in court papers that the plaintiffs are seeking a huge amount of vaccine-related material – about 329,000 pages.



How did the FDA approve the Pfizer Vaccine in under 3 months?
 
Novavax asks EU drug regulator to OK its COVID vaccine
By The Associated Press | November 17, 2021

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The European Union's drug regulator said it received an application from Novavax to authorize the American biotechnology company's coronavirus vaccine, a request that could significantly boost the continent’s vaccine supplies if it's granted.

In a statement on Wednesday, the European Medicines Agency said it had begun evaluating data submitted by Novavax for its two-dose vaccine. An expedited review process could produce a decision within weeks “if the data submitted are sufficiently robust and complete to show the efficacy, safety and quality of the vaccine,” the agency said.

Novavax’s COVID-19 vaccine is made using a different technology than others currently on the market, including those made by AstraZeneca and Johnson & Johnson, and the messenger RNA vaccines produced by Moderna and Pfizer-BioNTech.

Novavax's shot is made with lab-grown copies of the spike protein that coats the coronavirus, which then trigger an immune response.

In June, Maryland-based Novavax announced the vaccine had proven about 90% effective against symptomatic COVID-19 in a study of nearly 30,000 people in the United States and Mexico. It also worked against variants circulating in those countries at the time, the company said.

The company said side effects were mild and included tenderness at the injection site, headache, aches and pains, and fatigue.

To date, the European Medicines Agency has authorized the vaccines made by Pfizer-BioNTech, Moderna, AstraZeneca and Johnson & Johnson. It is currently reviewing vaccines made by China's Sinovac and France's Sanofi Pasteur, as well as Russia's Sputnik V.

Novavax said previously it would prioritize getting clearance in developing countries because its vaccine is easier to transport; Indonesia gave the green light earlier this month. The vaccine is pending authorization by the World Health Organization and countries that include the United Kingdom, Australia and Canada.

Europe, which had more than two thirds of the COVID-19 cases confirmed worldwide in the last week, is currently the epicenter of the pandemic. National authorities are considering reimposing lockdown restrictions and working to speed up immunization efforts.

In October, Novavax addressed concerns that a lack of raw materials and other issues had slowed production of its vaccine. The company said it planned to “achieve a capacity of 150 million doses per month by the end of the fourth quarter” through partnerships with Serum Institute of India, SK Bioscience in South Korea and Takeda in Japan, among others.

https://abcnews.go.com/Business/wireStory/novavax-asks-eu-drug-regulator-covid-vaccine-81227184
 
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Fact check: Wife of Pfizer CEO alive and well, not "dead from COVID-19 vaccine"
The claim: The wife of Pfizer's CEO died from COVID-19 vaccine complications

Misinformation about the COVID-19 vaccines continues to spread online, stoking fear about rare or nonexistent side effects. Now, an article claims those fears were realized for the family of a Pfizer executive.

"Myriam Bourla – the wife of Pfizer CEO Albert Bourla – has died from complications from the COVID-19 vaccine early Wednesday, according to her doctor," reads a Nov. 10 story from Canadian website the Conservative Beaver.

The article goes on to say she "passed away in the emergency room at New York-Presbyterian Lawrence Hospital after being brought in by paramedics."

The post received more than 1,900 interactions on Facebook within three days, according to the social media analytics tool CrowdTangle. USA TODAY has previously debunked false claims from the Conservative Beaver, including an article that wrongly claimed Albert Bourla had been arrested for fraud related to the COVID-19 vaccine.

This article is bogus, too.

Myriam Bourla has been seen publicly since the Conservative Beaver claimed she died, and news of her alleged death was not published in any major newspaper. A Pfizer spokesperson confirmed she is "alive and well." The COVID-19 vaccines do not cause death.

USA TODAY reached out to the Conservative Beaver for comment.

Pfizer debunks claim
The article claiming Myriam Bourla died was published Nov. 10. But a day later, Albert Bourla shared a photo on Twitter of the pair attending the Atlantic Council's Distinguished Leadership Awards.

USA TODAY could find no obituaries or other evidence indicating Myriam Bourla has died. Other independent fact-checking organizations have debunked the claim.

Amy Rose, a spokesperson for Pfizer, confirmed Myriam Bourla is "alive and well."

"It is unconscionable that a person posing as a journalist would spread such lies about our CEO and his family with the goal of undermining confidence in a vaccine that has been given to hundreds of millions of people worldwide," Rose said.

As USA TODAY has previously reported, the COVID-19 vaccines are not linked to death.

The Centers for Disease Control and Prevention says the vaccines are "safe and effective" and that they have undergone the "most intensive safety monitoring in U.S. history." Spokesperson Martha Sharan previously told USA TODAY “statements that imply that deaths following vaccination equate to deaths caused by vaccination are scientifically inaccurate, misleading, and simply irresponsible.”

“Vaccines are one of the tools that are going to help the U.S. get back to normal life,” she said.

Our rating: False

Based on our research, we rate FALSE the claim that the wife of Pfizer's CEO died from COVID-19 vaccine complications. Myriam Bourla has been seen publicly since the Conservative Beaver claimed she died, and news of her alleged death was not published in any major newspaper. A spokesperson confirmed she is "alive and well."

https://amp.usatoday.com/amp/8591125002
 
In about 2 week, actual data will reveal whether the new Omicron mutation from South Africa is a legitimate concern like India's Delta, or just a mild dud like California's Epsilon.

Keep calm and let science take its course.

Will Covid variant omicron need a new vaccine? Time and data will tell
By Jon Schuppe | Nov 26. 2021



The discovery of another coronavirus variant has raised new concerns about the ability of existing vaccines to protect against the mutating virus — and whether they’ll need to be updated.

The answer isn’t clear yet.

That’s because the new variant — named omicron and labeled a “variant of concern” by the World Health Organization on Friday because of its high level of mutations — has been spreading for only a couple of weeks. It was first reported in southern Africa, where it showed signs of rapid transmission.

The variant has also demonstrated a greater ability than others in dodging prior immunity, either in vaccinated people or those who’d been infected by the coronavirus before, according to researchers in South Africa. Several countries, including the U.S., said they would restrict travel from South Africa and seven other countries because of concerns over the omicron variant.

But it remains to be seen whether omicron poses a greater risk of hospitalization or death, including among vaccinated people. That data won’t be available for another two weeks or so, said Jinal Bhiman, principal medical scientist at the National Institute for Communicable Diseases in South Africa, which was the first country to report the new variant to the World Health Organization.

If existing vaccines don’t offer the same level of protection against serious infection, that may spur vaccine-makers to tweak their products, Bhiman said.

“An increase would be a sign that we may have to come up with something new,” Bhiman said.

Vaccine-makers aren’t waiting around.

Several companies said Friday they are already researching the new variant to see if it eludes immunity from their vaccinations. Developing new batches to test against would take several weeks, the companies said.

Moderna said it was testing existing boosters to see if they could be used against the omicron variant.

Pfizer, which developed a vaccine with BioNTech, said in a statement that if a “vaccine-escape” variant emerges, the two companies would be able to develop and produce a “tailor-made vaccine” in about 100 days.

Vaccine-makers have been able to avoid doing that against prior variants, including the delta variant, which spread across the world this year and remains the predominant strain in the United States. Existing vaccines turned out to be effective in protecting against serious infection by the delta variant.

That may turn out to be the case with the omicron variant, too.

“It could be that we don’t need to update the vaccinations,” David Kennedy, who studies the evolution of infectious diseases at Pennsylvania State University, said.

The omicron variant has raised legitimate worries based on a limited amount of data from South Africa and elsewhere, Kennedy said. “It’s enough to make me think we should watch this and be concerned but not enough to make me panic — yet,” he said.

Historically, vaccinations aren’t significantly undermined by evolving viruses, Kennedy said. With omicron, a key factor will be conclusive data showing whether serious infections of vaccinated people increase significantly, he said.

Deepti Gurdasani, clinical epidemiologist at Queen Mary University of London, said it was smart to be preparing for updated vaccines. But those efforts are most effective if the world manages to also contain the virus’s spread.

“It’s possible that Pfizer might come up with this vaccine in three or four months’ time and by the time it becomes available, there’s a new globally dominant variant,” Gurdasani said. “So vaccine development and re-engineering has to go hand in hand with efforts to contain transmission, which is the only way that we’re going to be able to get on top of the virus adaptation.”

https://www.nbcnews.com/news/amp/rcna6819
 
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In about 2 week, actual data will reveal whether the new Omicron mutation from South Africa is a legitimate concern like India's Delta, or just a mild dud like California's Epsilon.

Keep calm and let science take its course.

Will Covid variant omicron need a new vaccine? Time and data will tell
By Jon Schuppe | Nov 26. 2021



https://www.nbcnews.com/news/amp/rcna6819

It’s pretty clear. This new certain is a bastard offspring of the incurable AIDS and Covid. These same pharma you are saying are based on accurate science have failed for decades to cure AIDS/HIV.

we are doomed and it’s all over.

CovAids-19 was the final boss

https://www.bloomberg.com/news/arti...-covid-19-variant-circulating-in-south-africa
 
When All Else Fails, Bring Out the Masks


https://www.americanthinker.com/articles/2021/11/when_all_else_fails_bring_out_the_masks.html

excerpt:

.....Will this simply be another rinse and repeat cycle, endless booster shoots, masks, and social distancing in response to each new COVID variant or seasonal surge? We now have the South African or Omicron variant, described by scientists as “horrific” or “the worst variant they’d seen.” Travel restrictions are already popping up in Europe and will soon be implemented in the U.S., although with an inexplicable delay based on Dr. Fauci’s recommendation, despite this being called an emergency. There will be no criticism from corporate media claiming that travel bans are racist and xenophobic, unlike when President Trump instituted such bans.

Clearly COVID isn’t going away any time soon and it’s time for an all hands on deck approach, not limited to vaccines and masks, but prophylaxis, early treatment, acknowledgement of natural immunity, and potential therapeutics, including the off-label medications mocked by the media and medical establishment. Playing politics while people get sick and die is not following the science.

Will new mask mandates make any difference or simply add to everyone’s holiday angst over supply chain disruptions and runaway inflation? At least masks will hide the many sad faces of those just trying to live their lives under ever increasing rules, restrictions, and mandates as we head into what traditionally has been a season of hope and joy.
 
South African scientists explore vaccines’ effectiveness against Omicron
By Ian Sample | 29 Nov 2021

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Scientists in South Africa have begun crucial work to assess how well Covid vaccines hold up against the Omicron variant that has been detected in more than a dozen countries since it was formally reported last week.

The variant carries dozens of mutations that are expected to change how the virus behaves, including its ability to cause infection and how well it can hide from immune defences primed by vaccines or previous infection with an older variant.

Antibodies protect against viruses by gumming them up and preventing them from infecting human cells. To do so, they must recognise particular parts of the virus. Most Covid antibodies latch on to one of three sites on the virus, but all are mutated in Omicron, meaning antibodies produced by vaccines or past infection may be significantly less effective.

Prof Penny Moore at the University of the Witwatersrand and the National Institute for Communicable Disease in South Africa said “pseudoviruses” – harmless, non-replicating viruses used to model coronavirus variants – will be engineered to carry Omicron’s mutations. These will then be exposed to antibody-carrying blood plasma from vaccinated people and those who have recovered from Covid infection to see if they neutralise the virus.

Her lab will assess the protection provided by the Oxford/AstraZeneca, Pfizer/BioNtech and Johnson & Johnson vaccines, while tests on plasma from recovered patients will help to shed light on the risk of reinfection with Omicron. Early reports from South Africa suggest that reinfections are more common with Omicron than the Delta variant, but far more data is needed to be sure.

Moore’s results, which could be available in the next two weeks, are expected to provide some of the first laboratory evidence on whether existing vaccines are sufficient to keep Omicron at bay, or whether manufacturers will need to produce an updated vaccine. But with Omicron carrying so many mutations, making the pseudoviruses is not straightforward. “It will take some time to introduce so many mutations,” Moore said.

Further work on vaccine protection is under way at the African Health Research Institute in Durban where Prof Alex Sigal, a virologist, is growing batches of live Omicron from people who became infected in the recent surge in Gauteng in South Africa. Once he has enough to work with, the variant will be tested against blood plasma from vaccinated people and those with some natural immunity after a Covid infection.

South African scientists were the first to report the Omicron variant to the World Health Organization on 24 November. At the time, the first known infection was on 9 November, but earlier infections may come to light as countries conduct thorough searches for cases, chiefly among travellers who recently returned from the region.

The work in South Africa is part of an urgent global effort to understand the threat posed by Omicron. Ravi Gupta, professor of clinical microbiology at the University of Cambridge, hopes to join the effort soon, first with pseudoviruses and then with live Omicron. Further experiments, he said, will look at how well synthetic antibody treatments deal with the variant. The therapies are crucial for patients who are not able to mount their own immune response to the virus.

Several vaccine manufacturers have also launched studies into how well the jabs protect against Omicron. AstraZeneca is analysing infections and vaccination status in people in Botswana and Eswatini on the borders of South Africa. Meanwhile, a spokesperson for Pfizer said the company hoped to have initial results from its own antibody studies “in the coming weeks”.

If the variant largely evades vaccines, both Moderna and Pfizer claim they can produce a new, tailor-made vaccine in about 100 days, subject to approval by regulators.

https://amp.theguardian.com/world/2...xplore-vaccines-effectiveness-against-omicron
 
What I believe:

Leaky vaccines create vaccine resistant variants. The mutations of the virus that survive after mutation will be only the ones resistant to the vaccine, especially when the "immunity" conferred is only to a small portion of the virus, like a spike protein. Also, many doctors have come forward stating that you cant create immunity to a respiratory virus through an intramuscular injection; that the method of administration would have to protect from respiratory and mucosal spread, like with a nasal spray.

Under this scenario:

Vaccination is pointless until we have a substance that confers immunity to a larger portion of the virus and it is administered via an appropriate method.

What the media is telling me:

Vaccine resistant variants are created by the unvaccinated. So unless the world is 100% vaccinated, we are going to keep having mutations and vaccine resistant variants.

Also what the media is telling me:

Big pharma and the Gates' blocked even Astrazenica from releasing the intellectual property for their vaccine to poorer countries in favor of having a voluntary donation program "COVAX," that has been completely unsuccessful as Africa is only 7% vaccinated.

Under this scenario:

Vaccination is basically pointless because Africa will keep turning out variants as fast as pharma keeps churning out new, untested vaccines. Its like big pharma's wet dream: They keep blaming Africa for new variants while not vaccinating them, then sell all of their new vaccines every three months to all the rich countries on earth with no legal liability and no end in sight.

EDIT: Even under their own logic, (which I disagree with) they are basically using Africa as a petri dish to grow new variants while using the rest of the world as a drugstore to sell new injections.
 
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Lol, 'be calm and let science take its course.

FFS, that's how things got like this.

Science without ethics is predatory, to some degree
 
South African doctor who first spotted the Covid omicron variant says symptoms seem 'mild' so far
By Holly Ellyatt | Nov 29 2021



Covid symptoms linked to the new omicron variant have been described as "extremely mild" by the South African doctor who first raised the alarm over the new strain.

Dr. Angelique Coetzee, chair of the South African Medical Association, told the BBC on Sunday that she started to see patients around Nov.18 presenting with "unusual symptoms" that differed slightly from those associated with the delta variant, which is the most virulent strain of the virus to date and globally dominant.

"It actually started with a male patient who's around the age of 33 ... and he said to me that he's just [been] extremely tired for the past few days and he's got these body aches and pains with a bit of a headache," she told the BBC.

The patient didn't have a sore throat, she said, but more of a "scratchy throat" but no cough or loss of taste or smell — symptoms that have been associated with previous strains of the coronavirus.

Coetzee said she tested the male patient for Covid, and he was positive, as was his family, and then said she saw more patients that day presenting with the same kinds of symptoms that differed from the delta variant.

This prompted her to raise the alarm with South Africa's vaccine advisory committee, of which she is a member.

Other patients Coetzee had seen so far with the omicron variant had also experienced what she described as "extremely mild" symptoms, and she added that her colleagues had noted similar cases.

"What we are seeing clinically in South Africa — and remember I'm at the epicenter of this where I'm practicing — is extremely mild, for us [these are] mild cases. We haven't admitted anyone, I've spoken to other colleagues of mine and they give the same picture."

Investigations ongoing

The WHO has said it will take weeks to understand how the variant may affect diagnostics, therapeutics and vaccines.

Coetzee's initial observations are only based on a very small number of cases and experts are worried about omicron's large number of mutations. Preliminary evidence suggests the strain has an increased risk of reinfection, according to the WHO.

Early data suggests that the variant is spreading in South Africa more rapidly than previous strains did and that the variant, known formally as B.1.1.529, could be starting to trigger a new wave of infections, according to analysis by the Financial Times.

It could take a while to fully understand what specific symptoms, if any, are attributable to the new omicron variant on a wider scale.

Covid symptoms have changed since the virus first emerged in China in late 2019. The "alpha" and "delta" variants, first discovered in the U.K. and India, respectively, were seen to cause different symptoms, for example, with the latter causing more headaches, sore throat, runny nose and fever.

The U.S. CDC has highlighted the variety of Covid symptoms that have been reported, noting "anyone can have mild to severe symptoms" that may appear two to 14 days after exposure to the virus.

On the list of symptoms from the CDC are fever or chills, a cough, fatigue, shortness of breath or difficulty breathing, muscle or body aches, headache, new loss of taste or smell, sore throat, congestion or a runny nose, nausea or vomiting and diarrhea.

Unnecessary panic?

A swath of countries has now temporarily banned travel from several southern African countries where the variant has been found, a move slammed as a "knee-jerk, draconian" reaction by South Africa's health minister on Friday.

Asked by the BBC's Andrew Marr whether countries like the U.S., U.K., Israel and EU were "panicking unnecessarily," Coetzee stressed that the omicron variant had already likely spread to those nations.

"I think you already have it there in your country without even knowing it so I would say at this stage, definitely. Two weeks on, maybe we will say something different," she added.

Margaret Harris, spokesperson for the WHO, told CNBC on Monday that "we have South Africa to thank" for raising the alarm over the new variant, which has already been found in the U.K., France, Israel, Belgium, the Netherlands, Germany, Italy, Australia, Canada and Hong Kong, but not yet in the U.S.

Harris said the organization didn't like to see travel restrictions but understood that countries needed to take precautions based on their own epidemiological situations and risk-based analysis of the current data.

The U.N. health agency said Monday that the delta variant is still responsible for most of the current infections globally and, as such, was still its biggest concern.

"Over 99% of cases around the world are due to the delta variant and more deaths are occurring in the unvaccinated," WHO Chief Scientist Dr. Soumya Swaminathan told CNBC's "Squawk Box Asia" on Monday.

"I think that's our priority while we wait to find out more about [the omicron] variant."

Whether fresh restrictions and lockdowns might have to be introduced to counteract this new variant remain to be seen, experts say.

"The big issue and the big uncertainty is how severe illness will be with this new variant. There are signs from South Africa that, maybe, the illness is less severe than with delta but we don't really know if that is the case, and if it is, why that's happening," Paul Hunter, professor of medicine at the Norwich School of Medicine at the University of East Anglia, told CNBC on Monday.

"Maybe that's because it's reinfecting people who have already got some degree of immunity," he added. "If it generally is causing mild disease and if, as I suspect, the booster campaign will go a long way to still reduce hospitalizations and deaths, hopefully we won't have to live under restrictions again."

https://www.cnbc.com/amp/2021/11/29/omicron-covid-variant-symptoms-heres-what-we-know-so-far.html
 
South African doctor who first spotted the Covid omicron variant says symptoms seem 'mild' so far
By Holly Ellyatt | Nov 29 2021



Covid symptoms linked to the new omicron variant have been described as "extremely mild" by the South African doctor who first raised the alarm over the new strain.

Dr. Angelique Coetzee, chair of the South African Medical Association, told the BBC on Sunday that she started to see patients around Nov.18 presenting with "unusual symptoms" that differed slightly from those associated with the delta variant, which is the most virulent strain of the virus to date and globally dominant.

"It actually started with a male patient who's around the age of 33 ... and he said to me that he's just [been] extremely tired for the past few days and he's got these body aches and pains with a bit of a headache," she told the BBC.

The patient didn't have a sore throat, she said, but more of a "scratchy throat" but no cough or loss of taste or smell — symptoms that have been associated with previous strains of the coronavirus.

Coetzee said she tested the male patient for Covid, and he was positive, as was his family, and then said she saw more patients that day presenting with the same kinds of symptoms that differed from the delta variant.

This prompted her to raise the alarm with South Africa's vaccine advisory committee, of which she is a member.

Other patients Coetzee had seen so far with the omicron variant had also experienced what she described as "extremely mild" symptoms, and she added that her colleagues had noted similar cases.

"What we are seeing clinically in South Africa — and remember I'm at the epicenter of this where I'm practicing — is extremely mild, for us [these are] mild cases. We haven't admitted anyone, I've spoken to other colleagues of mine and they give the same picture."

Investigations ongoing

The WHO has said it will take weeks to understand how the variant may affect diagnostics, therapeutics and vaccines.

Coetzee's initial observations are only based on a very small number of cases and experts are worried about omicron's large number of mutations. Preliminary evidence suggests the strain has an increased risk of reinfection, according to the WHO.

Early data suggests that the variant is spreading in South Africa more rapidly than previous strains did and that the variant, known formally as B.1.1.529, could be starting to trigger a new wave of infections, according to analysis by the Financial Times.

It could take a while to fully understand what specific symptoms, if any, are attributable to the new omicron variant on a wider scale.

Covid symptoms have changed since the virus first emerged in China in late 2019. The "alpha" and "delta" variants, first discovered in the U.K. and India, respectively, were seen to cause different symptoms, for example, with the latter causing more headaches, sore throat, runny nose and fever.

The U.S. CDC has highlighted the variety of Covid symptoms that have been reported, noting "anyone can have mild to severe symptoms" that may appear two to 14 days after exposure to the virus.

On the list of symptoms from the CDC are fever or chills, a cough, fatigue, shortness of breath or difficulty breathing, muscle or body aches, headache, new loss of taste or smell, sore throat, congestion or a runny nose, nausea or vomiting and diarrhea.

Unnecessary panic?

A swath of countries has now temporarily banned travel from several southern African countries where the variant has been found, a move slammed as a "knee-jerk, draconian" reaction by South Africa's health minister on Friday.

Asked by the BBC's Andrew Marr whether countries like the U.S., U.K., Israel and EU were "panicking unnecessarily," Coetzee stressed that the omicron variant had already likely spread to those nations.

"I think you already have it there in your country without even knowing it so I would say at this stage, definitely. Two weeks on, maybe we will say something different," she added.

Margaret Harris, spokesperson for the WHO, told CNBC on Monday that "we have South Africa to thank" for raising the alarm over the new variant, which has already been found in the U.K., France, Israel, Belgium, the Netherlands, Germany, Italy, Australia, Canada and Hong Kong, but not yet in the U.S.

Harris said the organization didn't like to see travel restrictions but understood that countries needed to take precautions based on their own epidemiological situations and risk-based analysis of the current data.

The U.N. health agency said Monday that the delta variant is still responsible for most of the current infections globally and, as such, was still its biggest concern.

"Over 99% of cases around the world are due to the delta variant and more deaths are occurring in the unvaccinated," WHO Chief Scientist Dr. Soumya Swaminathan told CNBC's "Squawk Box Asia" on Monday.

"I think that's our priority while we wait to find out more about [the omicron] variant."

Whether fresh restrictions and lockdowns might have to be introduced to counteract this new variant remain to be seen, experts say.

"The big issue and the big uncertainty is how severe illness will be with this new variant. There are signs from South Africa that, maybe, the illness is less severe than with delta but we don't really know if that is the case, and if it is, why that's happening," Paul Hunter, professor of medicine at the Norwich School of Medicine at the University of East Anglia, told CNBC on Monday.

"Maybe that's because it's reinfecting people who have already got some degree of immunity," he added. "If it generally is causing mild disease and if, as I suspect, the booster campaign will go a long way to still reduce hospitalizations and deaths, hopefully we won't have to live under restrictions again."

https://www.cnbc.com/amp/2021/11/29/omicron-covid-variant-symptoms-heres-what-we-know-so-far.html

One can only hope, but we need more data
 
What I believe:

Leaky vaccines create vaccine resistant variants. The mutations of the virus that survive after mutation will be only the ones resistant to the vaccine, especially when the "immunity" conferred is only to a small portion of the virus, like a spike protein. Also, many doctors have come forward stating that you cant create immunity to a respiratory virus through an intramuscular injection; that the method of administration would have to protect from respiratory and mucosal spread, like with a nasal spray.

I dont think you have any of this right really.

Firstly look at where these variants have been first detected: low/no vaccinated areas. Secondly, transmissibility seems to be prioritised for dominance of a Covid variant over immune evasion. [see D->G 614 substitution in early 2020 & then Delta]. The covid spike is also actually a pretty huge antigen target and even in an infection, almost all of the neutralising antibody response is directed towards it.

Its also not true that immunity cant be obtained from an injection [measles?]; recall early into the vaccination roll-out that high efficacy against infection was being reported in real-world observations. Infection may grant a better localised immune response but injection will also provide systemic circulation of antibodies that can go where needed -including stimulation of IgA antibodies found at mucosal surfaces:
Antibody Responses to SARS-CoV-2 mRNA Vaccines Are Detectable in Saliva

The scenario you outline i think better describes drug resistance rather than vaccine resistance, and this article covers the difference in more detail:
Why does drug resistance readily evolve but vaccine resistance does not?
 
Bro are we going to be wearing masks the rest of our lives? Wtf
 
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