Thursday, June 22, 2023



SARS-CoV-2 Mass Vaccination Likely Accelerates Viral Mutation—Time to Upgrade COVID-19 Vaccines?

The lead scientist at Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, Saint-Petersburg, Russia, and an expert infectious disease modeler at University Medical Center, Utrecht, Julius Center, Epidemiology & Health Economics in the Netherlands combined their intellectual prowess to investigate SARS-CoV-2 immune selection pressures, ultimately producing an important, published analysis titled “Evolutionary implications of SARS-COV-2 vaccination for the future design of vaccination strategies.” Mass vaccination was the “pillar of the public health response to the COVID-19 pandemic.”

But critics such as Geert Vanden Bossche, a TrialSite contributor, warned that mass vaccination might trigger mass evolutionary pressures, thus accelerating pathogen mutations. The Belgian virologist was summarily dismissed by mainstream science and its media channels as an overreacting crank. However, here, an intellectually gifted duo based in Russia and Holland raise the specter that based on their modeling “mass vaccination might accelerate SARS-CoV-2 evolution in antibody-binding regions compared to natural infection at the population level.”

In what should be a must read for decision makers in vaccination, the authors both review the most important factors shaping vaccination strategies during the COVID-19 crisis, while also probing the implications of SARS-CoV-2 vaccination on virus evolution in light of accumulated knowledge and in the context of viral evolutionary theory.

Their analysis raises the specter of a reality involving the evolution of rapidly mutating antibody-binding regions. Finally, the pair acknowledge the need for their own assumptions to be validated, while also pointing to the need for the research necessary to design potential future advancements in both vaccination and broader vaccination strategy.

The basis for mass vaccination

The formidable pair introduce the reader to vaccination strategies in the context of COVID-19, educating that primary tools employed during the pandemic were predictions based on robust epidemiological models tailored to the available data. Called “dynamic transmission models” or “infectious disease models”, they were used to simulate the transmission of a virus across a specific population, introducing and evaluating potential software simulated control measures.

It was, after all, transmission models for the virus, including mutation and how vaccination would respond, that were used to develop vaccination schemes during COVID-19: many national strategies were based on these models.

Key assumptions

Embracing material evidence of robust genetic variation in antibody-binding regions of SARS-CoV-2, the authors both capitalize on the similarity involving both the envelope proteins of SARS-CoV-2 as well as influenza, the pair make a key assumption: “That immune selection pressure acting on these regions” of both COVID-19 and the flu are comparable.

The authors, hardening their data including assumptions, analyze and discuss implications for SARS-CoV-2 evolution based on a mathematical model developed initially for influenza. The duo, if their analyses are accurate, most certainly impacts the future design of SARS-CoV-2 vaccination strategies.

While mass vaccination helped reduce morbidity and mortality, in many cases, that was a temporal public health gain, due to the combination of both an evolving pathogen and what TrialSite has argued are limitations with the initial vaccination products (e.g., durability, breadth challenges, lack of sterilizing powers, etc.).

Chinks in the mass vaccination armor?

Both Rouzine and Ganna raise the specter of limitation to the current mass vaccination approach. They raise the critical concern that “vaccination can also have implications for SARS-CoV-2 evolution in antibody-binding regions, located in the spike protein that is targeted by the available vaccines. SARS-CoV-2 perpetually evolves due to its escape from the immune response in individuals induced by both natural infection and vaccination.”

In fact, the authors remind the reader that irrespective of vaccination, when it comes to a pathogen like SARS-Cov-2 accumulating mutations in T-cell epitopes and antibody-binding regions powers selection pressure to escape natural immunity.

The authors demonstrate via modeling that mass vaccination can in fact, increase this inherent pressure, thus accelerating SARS-CoV-2 evolution in spike epitopes when compared to natural infection. The authors model this, thus conveying the distinct possibility that the arguments of Vanden Bossche have some merit.

Future research

The authors’ time and effort into this investigation evidence ongoing concern. “If SARS-CoV-2 continues to cause the substantial burden of severe disease in vulnerable individuals, we should either design a type of vaccine that does not carry any potential danger of accelerating virus evolution in epitopes but is still effective against severe disease or find other methods of reducing virus circulation.”

Rouzine and Ganna introduce several research pathways to consider for ongoing investigation into better options. Will apex research institutes, national public health agencies and major centers of biomedical research be receptive?

Summary

While the authors contribute their customary kudos to the current response to COVID-19 mass vaccination scheme, completely bypassing the topic of serious safety signals, they acknowledge that the pathogen that caused the COVID-19 pandemic continues to evolve, escaping in many cases from both natural and vaccine-induced immunity.

Demonstrating the distinct possibility that mass vaccination schemes in the context of the SARS-CoV-2 pathogen may serve to accelerate its evolution in rapidly mutating antibody-binding regions when comparing to natural infection, Rouzine and Ganna point out that their conclusion rests upon fundamental assumptions, including A) that the immune selection pressure exerted on antibody-binding regions of SARS-CoV-2 are in fact similar to those of influenza and B) on existing multi-locus models of influenza evolution.

Capitalizing on similarities between the envelope proteins of both SARS-CoV-2 and influenza in antibody epitopes, they further acknowledge that their model’s assumptions must be tested and potentially hardened. But in these author’s favor—they’ve proven to be correct with influenza—they have a serious track record.

Emphasizing what are limitations with the current COVID-19 mass vaccination approach, the authors carefully warn public health leaders that the role of mass vaccination on SARS-CoV-2 evolution “should be acknowledged for future vaccination strategies that target most at-risk populations, especially if vaccination campaigns will cover a substantial part of the population.”

Key considerations in the next round of COVID-19 vaccine development: “Mutations in immunologically relevant genomic regions, viral recombination, virulence and fitness evolution.”

The authors conclude by validating the current approach as likely the best considering all the factors involved (emergency pandemic, etc.).

*************************************************

Covid heartburn on Twitter

It’s incredible how soft some people are on social media. And I’m not even talking about overly political people right now. A mass exodus of scientists and medical professionals appears to be leaving Twitter because they can’t handle the trolls. Do they know of these fantastic features called the “mute” and “block” buttons that drown out the clowns? Some are annoying, but if they’re asking questions and looking for a debate, you can choose to or not to engage with them. Those with too much time on their hands focusing only on ad hominem attacks should be blocked. It’s not complicated.

Conservative women, especially, have been subjected to heinous harassment by progressives, who are, at their core—just miserable people. Incapable of accepting differing views and the people who hold them for some reason. They have an addiction to harassing people to cower to their political opinions. While not religious, left-wingers do carry the same evangelist zeal, stunningly intolerant that some people think differently than they do. We’re supposedly on the "wrong side of history"—how often have you heard that phrase— and they can’t sleep at night knowing everyone doesn’t think alike under the authoritarian ethos of progressivism.

And yet, scientists decide to leave the battlefield because some no-name trolls decide to call out these people about vaccines. Galileo was tortured and didn’t bend. Eppur si muove has lost its meaning. The fireworks began when Dr. Peter Hotez appeared on Joe Rogan’s podcast (via Axios):

A feud broke out on Twitter over the weekend between popular podcaster Joe Rogan and prominent vaccine researcher Peter Hotez, with the podcaster challenging the scientist to a debate about vaccines in an online skirmish that drew fire from a few billionaires.

Why it matters: The incident — which ultimately resulted in individuals approaching the scientist outside his home — highlighted the potential risks for researchers and medical professionals using the platform, which saw a rise in hate speech after its acquisition by billionaire Elon Musk.

[…]

The Twitter battle over the weekend started after Rogan hosted Democratic presidential candidate Robert F. Kennedy Jr. on his show for three hours, spending much of the time talking about anti-vaccine views.

In response, Hotez, part of a Nobel Prize-nominated team that created an affordable, patent-free COVID vaccine for use in poorer countries, retweeted a Vice article with the headline "Spotify Has Stopped Even Sort of Trying to Stem Joe Rogan's Vaccine Misinformation."

The show spread "nonsense," Hotez tweeted.

That prompted a challenge from Rogan to Hotez: "Peter, if you claim what RFKjr is saying is 'misinformation' I am offering you $100,000.00 to the charity of your choice if you're willing to debate him on my show with no time limit."

What happened next: Rogan's challenge sparked an internet pile-on against Hotez, accusing him of being a "pharma shill," as well as a back-and-forth between some of Twitter's most influential, including Musk and billionaire investor Mark Cuban.

[…]

What they're saying: Twitter is "no longer a tool that's accelerating science. On the contrary," said Michael Mina, chief science officer at eMed and a pediatric immunologist who regularly used Twitter during the pandemic to talk about COVID. He still uses Twitter, but sparingly, and expects he'll leave completely within the next six months, he said.

"It allowed me to effectively and efficiently sift through the noise of this massive explosion of new publishers and journals and papers that were published," Mina told Axios.

[…]

In comments to Axios as well as online, scientists and medical researchers have said they're increasingly finding it difficult to find relevant information on Twitter. A recent study found Twitter's new algorithms are amplifying anger more since Musk took over the platform.

Hotez told Axios he's seen a clear shift in anti-vaccine views as part of a well-organized, well-financed anti-science movement, and that's playing out on the platform.

Of course, Axios finds a way to thread a swipe at Elon Musk’s takeover of Twitter. There are ways to moderate your communities, as mentioned above. The publications added that scientists are posting elsewhere, like Substack. Still, the fires of outrage over vaccines could be addressed if the medical community owned up to the misinformation about the COVID vaccine and the pandemic. We were told to get the shot, take off the mask. The efficacy rates were touted as the main selling points. And then the vaccinated got COVID during the Omicron wave.

There have been shiploads of people dying from cardiovascular episodes, many under 44. And now, we’ve learned that those who have contracted and survived infection had an antibody response that was just as good as those vaccinated with two doses of the mRNA vaccine. The reality of the vaccine is that it might prevent death, but there’s no protection against infection. It’s very much like the flu shot, which has an efficacy of less than 60 percent, but it does increase the odds of you not dying from the virus that kills tens of thousands of Americans every winter.

But that fact dilutes the panic and fear the COVID regime sold to us for months over a virus with a 99-plus percent survival rate. People got vaccinated and still contracted COVID, with some dying from infection, especially older Americans. And now, with boosters, we’re learning that it weakens the immune system. Until these philosopher kings admit they blew it on COVID, expect more angry folks to confront them.

The online shenanigans still pale compared to what Galileo and other scientists of his era endured when presenting their scientific findings. Imagine being tortured for suggesting the Earth revolves around the sun. He stood firm while today’s Dr. Hotez mulls leaving because it’s too heated on Twitter. Yikes.

********************************************************

Also see my other blogs. Main ones below:

http://edwatch.blogspot.com (EDUCATION WATCH)

http://antigreen.blogspot.com (GREENIE WATCH)

http://pcwatch.blogspot.com (POLITICAL CORRECTNESS WATCH)

http://australian-politics.blogspot.com (AUSTRALIAN POLITICS)

http://snorphty.blogspot.com (TONGUE-TIED)

https://immigwatch.blogspot.com (IMMIGRATION WATCH)

https://awesternheart.blogspot.com (THE PSYCHOLOGIST)

http://jonjayray.com/blogall.html More blogs

***************************************************

No comments: