patrick.net

charlie303 says

And how do you know the debunkers are right?

Haha, that's the crux of this entire event. Very little truth is being shared. Critical thinking is your only weapon/shield.

'It's a complete and utter waste of time.' - Prof. Angus Dalgleish on the PM's Omicron booster plan

https://www.youtube.com/watch?v=AKHYkHTRTnM&source=patrick.net


Authority figures are slowly waking up to the fact that something is not right and that the vaccine is causing the problems but they have not yet realized that we are at War. interesting to see the narrative slowly failing overtime

i think this message is diametrically opposed to science. By exerting narrow immunoligical pressure on the virus, you, in fact, enhance the emergence of new variants.

WineHorror1 says

Very little truth is being shared. Critical thinking is your only weapon/shield.

I hate critical thinking. It really puts a crimp in my insane thinking time.

Sergio Aguero: Barcelona's former Man City striker retires https://www.bbc.co.uk/sport/football/59660727?source=patrick.net

The 33-year-old sobbed while announcing the news on Wednesday, fewer than six months after joining Barcelona.
The former Manchester City striker was taken to hospital on 30 October after experiencing "chest discomfort" during a 1-1 draw with Alaves.
"The decision I have made, I have taken it for my health," said Aguero.

...

Aguero, who ends his career with 427 goals in 786 games, took time to compose himself after crying at the start of the event and added: "This conference is to communicate that I have decided to stop playing football. It's a very difficult moment.
"When they did the first physical test on me in the clinic, the medical staff called me to tell me there was a very big possibility that I wouldn't be able to keep playing. From that point I was processing it all but it wasn't easy. One of the doctors told me straight up, 'that's enough'.

....

FuckCCP89 says

took time to compose himself after crying at the start of the event and added: "This conference is to communicate that I have decided to stop playing football. It's a very difficult moment.

Dude needs to grow a pair. Make sure you spend and invest your money wisely and you'll be fine. Careers end. Nothing to cry about. Be happy you're alive after taking that shit even with complications. Other people have had it worse.

I just received a group email from my sister in law. She sent the news that my 29 year old niece has contracted Covid. "Luckily", she wrote, "she just got her booster two weeks ago so it should not be that bad".

I don't argue with my SiL since the great "White Privilege is not racist" debate at the family reunion a couple of years ago. You can't wake the woke.

I fear for the future of our children.

FAUXI: BELIEVES INJECTIONS SHOULD BE 'REQUIREMENTS' AS OPPOSED TO 'MANDATES'

https://www.westernjournal.com/cdc-officials-consider-pulling-restricting-covid-vaccine-due-dangerous-side-effects/?source=patrick.net

CDC Officials Consider Pulling or Restricting COVID Vaccine Due to Dangerous Side Effects

https://www.yahoo.com/news/fauci-pushes-word-apos-mandates-171643598.html?source=patrick.net

Fauci pushes new word for 'mandates,' admits changing 'fully vaccinated' definition 'certainly on the table'

https://healthimpactnews.com/2021/the-cdc-caught-in-their-own-lies-the-unvaccinated-in-the-u-s-for-covid-19-is-millions-more-than-originally-reported/?source=patrick.net

The CDC Caught in their Own Lies: The Unvaccinated in the U.S. for COVID-19 is “Millions” More than Originally Reported

Onvacation says

You can't wake the woke.

Great summary! I will remember that one.

Onvacation says

FAUXI: BELIEVES INJECTIONS SHOULD BE 'REQUIREMENTS' AS OPPOSED TO 'MANDATES'

I want to punch that fucker so hard. He's a little boy too, so I'd have to be careful not to kill him. Sooooooo fucking condescending. Little piece of shit.

WookieMan says

Onvacation says

FAUXI: BELIEVES INJECTIONS SHOULD BE 'REQUIREMENTS' AS OPPOSED TO 'MANDATES'

I want to punch that fucker so hard. He's a little boy too, so I'd have to be careful not to kill him. Sooooooo fucking condescending. Little piece of shit.

Jus kick him in the crotch.

Geert:‍

Dear John,

I think that after this, I am going to keep quiet (in terms of articles) for a little while.
I am beyond worried about mass vax against Omicron.
I cannot emphasize enough how a complete lack of understanding of viral evolution is now dominating the scene.

The article is about one page. Could you please do me a favor and review it? Txs!!

‍John:‍

Is it truly our last chance? Or will the cycle repeat itself, cause waves of severe disease/death with new vaccines rolled out, then further mutation resulting in another escape strain from those vaccines, thereby resetting back to innate immunity again, and on and on?‍

‍Geert:‍

Remember: ‘Continued mass vaccination will only push the evolutionary capacity of SARS-CoV-2 Spike protein beyond the Omicron version’ – allosteric mutations and ADE, remember?

It’s ADE that is going to tip the balance in the wrong and irreversible direction. ADE in vaccinees will provide the virus with exceptional virulence and make it resemble Marek in unvaccinated…this means natural selection against all those whose innate immunity got messed up.‍

‍John:‍

Ah ok now I believe understand... Enough mutation in RBD of S specifically allows for the “reset” because there is no longer binding/recognition by previous antibodies. Allosteric mutation on the other hand results in binding of previous antibodies, but no longer blocking entrance via ACE2 and potentially allowing infection of other immune cells (macrophages etc) via Fc receptors. Is that right?‍

‍Geert:‍

The only correction, John, is that the altered binding site does not need to be an Fc receptor on macrophages. It can basically bind to other domains on permissive host cells. As we already know, SC-2 is not strictly bound to entering the cell via Ace-2 (although this is still the preferred receptor). A cell has many surface determinants that could serve as a receptor for an altered binding site…‍

‍John:‍

Yes, I do remember you talking about the alternative receptor sites.
And this could have happened with another subvariant of Delta... But now that Omicron appears to be rapidly taking over, it would likely happen with an Omicron sublineage?
I’m curious if there is a way of calculating probability of an allosteric mutation leading to this outcome versus the probability of another set of mutations in RBD leading to another Omicron-style variant down the road?‍

‍Geert:‍

Computational biology is not my strength!

Anyway, it’s reasonable to postulate that when one administers a vaccine that induces Abs to all of the mutated neutralizing epitopes at once (which we never did with the Wuhan-based vaccines as they were already facing variants right from start), one will drive natural selection of mutants that have a dramatic impact on that life-threatening ‘attack’. I am convinced that this is only going to be possible via a substantial antigenic SHIFT (instead of drift) and that it will need to involve allosteric mutations to basically bypass the current RBD which has now (i.e., upon anti-Omicron vax) fallen prey to a multitude of effective neutralizing Abs. I don’t think there is any probability that further changes in RBD could occur fast enough to bypass Omicron vaccine-induced Abs as there is always a fitness cost to pay for a mutation and it takes time to overcome the ‘valley of fitness cost’. As you will appreciate, all of the mathematical models used so far, even the most sophisticated ones, have miserably failed. That’s because they’re only as good as the assumptions are…‍

‍John:‍

Wonderful explanation - thank you.

I just assumed the "antigenic shift" necessary to bind other receptor sites (from allosteric mutations or otherwise) would require a MUCH larger fitness cost than that which is necessary to rework RBD once again (similar to what happened with Omicron) - I guess that wouldn't be the case?
‍
I would think modifying the "key" (changes to RBD) but still binding to the same "lock" (ACE2) would be much easier than selecting a new lock altogether!
Or, perhaps you're stating that one of these other receptor sites that's already in use (albeit relatively inconsequential) by SARS-CoV-2 then becomes the preferred point of entry?

Sorry for the drawn-out mental exercise. Perhaps it will help you in crafting future statements that may address this!‍

‍Geert:‍

Txs, John, for your feedback. The fitness cost is pretty high if you want to implement changes within a narrow domain (RBD) that is also subject to physicochemical/ steric constraints for binding to a specific receptor (Ace-2). On the contrary, any mutation that enhances binding to another cell surface determinant (that is already in use, at least to some extent) will not be facing these constraints as it doesn’t need to deal with any of the (previously) neutralizing Abs (those can just bind as before).

That’s why I am beyond fearful that the catastrophe (ADE) could occur very fast after mass vax with anti-Omicron starts.

Makes sense?
If not, do let me know!‍

‍John:‍

Makes sense! I was unaware that there were already other sites that SARS-CoV-2 latches onto... So I thought those recepting binders would have to evolve "from scratch". Now that I know they already exist, and just have to be improved upon, this makes complete sense!‍

‍Geert:‍

Yes! So, indeed, the requirements for receptor-mediated entry of CoVs are not very stringent!‍

‍John:‍

I still have few other quick questions.

Why would this "immune reset" with Omicron result in mild/moderate disease initially (due to innate immunity being "reactivated") when the original Wuhan outbreak started off bad right off the bat... Is this because of some level of pre-existing "herd immunity" and innate immune training to SC2?‍

‍Geert:‍

Omicron should not be a problem for the unvax’ed whose innate immunity got meanwhile well trained. Older vax’ed age groups have revealed lower case rates (according to PHE) than younger age groups which suggests enhanced affinity of innate Abs (must have been acquired prior to vaccination). Younger vax’ed age groups have high titers of naïve Abs. When set free, those can easily deal with variants (that’s why no youngsters or children got the disease at the beginning of the pandemic). Of course, there are still the people with underlying diseases, most of whom have been jabbed. They cannot rely on their innate Abs and yes, I expect a relatively high case fatality rate in those (unless treated) but of very short duration as a steep incline of infectivity (due to high level of infectiousness) would be followed by a steep decline (due to massive elimination of the virus by a large cohort of +/- simultaneously asymptomatically/ mildly infected individuals.‍

‍John:‍

This clears that up great - thank you.
Next question: Why the assumption that a new host entry mechanism would result in significantly more severe disease than that which was the case with ACE2? I understand how traditional ADE (via Fc receptors) can amplify disease... But this would simply be a new entry site, not an additional added mechanism, correct?‍

‍Geert:‍

Omicron would still have the same entry site (Ace-2) as neutralizing Abs don’t bind. It’s only when allosteric mutations occur (new variant) that vaccinal Abs raised against Omicron S-based vaccine will bind to RBD (no longer capable of mediating viral entry) of this new variant and cause ADE. So severity depends on ADE not on mechanism of cell entry.‍

‍John:‍

‘…vaccinal Abs raised against Omicron S-based vaccine…’ Still a bit confused on this part. So an allosteric mutation would potentially prevent the virus from entering cells via ACE2 altogether, but Omicron S-based vaccinal antibodies would still bind to it (just no longer neutralizing)?‍

‍Geert:‍

Correct.‍

‍John:‍

So the virus would then infect immune cells specifically? (That's why I was curious why the FcyR receptor wouldn't be involved?)‍

‍Geert:‍

I’ve not been taking a deep dive into the mechanistic details of ADE. However, what I can say is that non-neutralizing Abs that bind with high affinity to the virus will precipitate its entry into host cells. I am not sure this mechanism (exclusively) occurs through FcyR on macrophages/ dendritic cells. Of course, these receptors are expressed on those cells and they bind of course to immunoglobulins. But I do not rule out that coating of virus particles with immunoglobulins that don’t neutralize, could suffice to cause non-receptor-mediated viral entry into host cells….. Anyway, the outcome of all this is enhanced/ exacerbated pathogenicity…‍

‍Thank you Geert and John.

https://www.voiceforscienceandsolidarity.org/scientific-blog/q-a-06-geert-and-johns-email-exchange-of-thought-and-ideas-about-the-omicron-articles

https://djhjmedia.com/rich/japanese-study-says-young-people-are-40-times-as-likely-to-die-from-vaccines-than-from-covid/?source=patrick.net

Japanese Study Says Young People Are 40 Times More Likely To Die From Vaccines Than From COVID

https://boriquagato.substack.com/p/what-fresh-hell-is-this/comments?source=patrick.net

https://jamescintolo.substack.com/p/new-bombshell-myocarditis-study-out?r=xgj7l&utm_campaign=patrick.net&utm_medium=patrick.net&utm_source=patrick.net

https://www.thegatewaypundit.com/2021/12/oxford-study-shocker-1-100-vaccinated-individuals-admitted-hospital-died-arrhythmia-study-period/

"OXFORD STUDY SHOCKER: 1 in 100 Vaccinated Individuals Were Admitted to Hospital or Died with Arrhythmia During Study Period"

joshuatrio says

"OXFORD STUDY SHOCKER: 1 in 100 Vaccinated Individuals Were Admitted to Hospital or Died with Arrhythmia During Study Period"

Lol. That's like 90% more than would die from a Covid infection. I shouldn't laugh as my most of my adult family has gotten vaccinated including the wife. The side effects have been more troublesome from the vaccine than her breakthrough case of Covid. You'll be called conspiracy theorist, but I'm telling everyone I can not to touch this shit. Our own government still hasn't approved vaccines, yet pumps it via press conferences and media daily.

Definitive breakdown on the corruption and fraud involved in the Pfizer Inoculation testing and approvals from the Canadian Covid Care Alliance:
https://rumble.com/vqx3kb-the-pfizer-inoculations-do-more-harm-than-good.html?source=patrick.net
Pfister is an Ongoing Criminal Enterprise and should be prosecuted under the RICO statutes.

Only 48%???





Then again, it doesn't add up to 100% and has a huge margin of error.