DEAR KAG: 20220225 – The Pub is OPEN / COVID-19 Vaccine Interference With AIDS and Syphilis Tests / Moscow Mule Revisited / Failure of Socialized Science and Peer Review Exposed in a JAMA-Published Ivermectin Study

The Pub is OPEN!

And we’re finally serving a NORMAL DRINK tonight. Even though it’s a SECOND ROUND.

STAY TUNED…..

While our beloved REAL bartender takes a needed break of unknown duration, we continue to ENDEAVOR TO PERSEVERE.

and what time of year is it now???


Christmas Spirit

We continue our WAAAAAY too-long celebration of Christmas by noting that some of our neighbors STILL have their lights and decorations up.

We saw a nice red Christmas bow laying in somebody’s yard by their driveway.

We ourselves just got rid of our tree.

And TODAY is the 25th of the month. That’s VERY “Christmassy”.

So yeah. Given that there are a few days weeks months AFTER Christmas where it’s STILL Christmas, that means we have a few more weeks left. Riiiiiiight?

Sure! So have some hot CHRISTMAS chocolate!

And now, the rules of the pub.


HOUSE RULES

God bless us, every one! Tiny Tim had such a beautiful soul. He hadn’t a mean bone in his body…unlike most of us. But in keeping with Christmas, we promise to honor Wolf’s rules and keep Scrooge at bay. The Utree is where the Ghost of Christmas Present will conduct you should you need to rattle some chains. Another option, should all hell break loose is here.

Now, back to business.


AMEN!

Free the January Brothers!


Current Art On The Wall

We’re just gonna segue into the next item with our selection, if that’s OK.

This gets a bit “planetary”…..

Venus and Mercury Instructing Cupid
Christiaan Huygens, Saturn, and Something
Raindrops on Titan
https://owlcation.com/stem/Huygens-Mission-on-Titan
LINK: https://www.instagram.com/p/BAOVsasAXhl/

Mercury, the old cure for grandgore.

COVID-19 Vaccine Interference With AIDS and Syphilis Tests

Earlier this week, RAC brought a news item from CTH, which really got me thinking:

This had to do with a CDC alert…..

LINK: https://www.cdc.gov/std/FDA-alert-12-20-2021.pdf

…..which was based off of an FDA alert (sketchy link)…..

…..which actually links back to a different CDC alert (even sketchier link)…..

WHATEVER.

Here is that final CDC alert. Only the top 3 paragraphs are important here.

Let me quote the text of those first 3 paragraphs for Zoe. I will make BOLD what is important.


Dear Partners in Prevention,

December 20, 2021

I’m writing to share the U.S. Food and Drug Administration (FDA) alert sent to clinical laboratory staff and health care providers about a syphilis test. The alert reports that false reactivity, or “false-positive,” Rapid Plasma Reagin (RPR; non-treponemal) test results, when using the Bio-Rad Laboratories BioPlex 2200 Syphilis Total & RPR kit, can occur in some people who received a COVID-19 vaccine and includes recommendations for addressing these potential false positives.

Historically, false-reactive RPR test results have been observed in people with systemic infections unrelated to syphilis, such as tuberculosis, rickettsial diseases, and endocarditis. False-reactive RPR testing also has been previously observed following immunization (specifically following smallpox vaccine). False reactivity with RPR can also occur during pregnancy.

Per CDC’s 2021 STI Treatment Guidelines, reactive RPR results should always be confirmed with treponemal testing (e.g., Treponema pallidum particle agglutination, TP-PA). This is, in part, because of the above-mentioned issue: false-positive nontreponemal test results can be associated with multiple medical conditions and factors unrelated to syphilis. According to FDA’s alert, treponemal testing for syphilis does not appear to be impacted by this issue.


Allow me to translate.

It turns out that “being vaccinated for COVID-19” throws off an ANTIBODY-BASED SYPHILIS TEST, and can give false positives.

The reason is that these are a sort of antibodies against substances released from cells attacked by certain diseases and conditions. Thus, they’re not exclusively the downstream product of syphilis.

Normally, certain diseases, certain vaccines, and pregnancy can all throw off this more rapid but less conclusive syphilis test, and that is part of the reason why people are supposed to follow up this easier test, with a test that looks for the actual organism which causes syphilis.

Thus, we have added one more cause for the test to be thrown off.

This is not the same as the HIV test that was thrown off by a particular Australian vaccine, because the antigen in the vaccine actually contained an HIV protein (gp41) as part of the vaccine, and created antibodies against HIV. I talked about that last week. That was a much more direct test interference, easily expected.


Saved From The Frankenvax

How a Psycho Vaccine Marrying the Infamous COVID Spike Protein to HIV’s Neurotoxic gp41 Was [Allegedly] Canned by a Mere Testing SNAFU How Australia Dodged The First Mad Vax Bullet of the WEF Scamdemic / Plannedemic Darwin Award Vaccine Featured Insane Merger of HIV and COVID But Failed Due to Buggering of AIDS Tests, NOT …


What I find interesting is that one of the things that normally sets off the syphilis test is endocarditis.

Endocarditis, which is inflammation of the inner surfaces of the heart, is one of the three main heart inflammations, thus being pretty damned close to myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the outer sac), both of which have very prominent correlations to the jabs.

So while this means that – NO – the shots are not giving people syphilis – the shots ARE basically acting like an illness, and very much like a known cardiac illness.

You were warned.


Now – while I was researching syphilis, I became interested in the treatment with compounds of mercury.

Traditional mercury-based pastes were used in cures. Whilst this was partially effective, the toxic side effects of the mercury probably outweighed any advantages.

This is actually a HUGE understatement.

It turned out that arsenic was considerably better.

The first effective treatment for syphilis was arsphenamine, discovered by Sahachiro Hata in 1909, during a survey of hundreds of newly synthesized organic arsenical compounds led by Paul Ehrlich. It was manufactured and marketed from 1910 under the trade name Salvarsan by Hoechst AG.[88] This organoarsenic compound was the first modern chemotherapeutic agent.

It wasn’t too long after that success, that penicillin took over as the real cure for syphilis.

I will come back to MERCURY in a future post, because I found something quite amazing in its history.


But if you look ONE COLUMN TO THE LEFT and TWO ROWS UP…..


COPPER is also bacteriostatic and algicidal – and at concentrations below where it is a health risk. And THAT leads back to a DRINK that Grandmaintexas introduced us to……


Moscow Mule Revisited

Based upon my reading of Grandma’s post on the subject, the Moscow Mule simply is not a proper Moscow Mule unless it is served in copper vessels.

The health effects of COPPER are about as debatable as the effects of mercury – although, in general, copper is much less toxic, so when it’s being “not good for you”, it’s a lot less “not good for you” than lead. At the same time, copper is much MORE toxic to things like algae, fungi, plant roots, and other “pests”, than it is to us, and that is why it is found among the gardening pesticides in hardware stores. The antimicrobial activity of copper is extremely well-documented, but appears to be complex. Simply having copper in the household or workplace environment seems to have health benefits – and this was particularly noted back in the days of less sanitary environments. Water passing through copper fixtures tended not to spread disease.

We tend to forget about OLD SCIENCE, so we can’t put new things into good perspective.

LEAD and other CHEMICAL ADVANCES saved us from the horrible BIOLOGICAL diseases and maladies of the uncivilized life.

Did they have chemical consequences? Yes. The TRICK is REMEMBERING AND ADMITTING OLD RISKS AND BENEFITS while also DISCOVERING AND ADMITTING NEW RISKS AND BENEFITS, then BALANCING HONESTLY with the PROPER PRIORITIES which put PEOPLE FIRST.

It is VERY easy to see where CDC went off the rails with the COVID-19 vaccines, being unable to admit old benefits (of lasting immunity to caught and treated diseases), while also being unable to admit new risks (of vaccines using untested and immature technologies).

Likewise, looking back, it is easy to see that basic sanitation – not vaccination – REALLY conquered diseases. Vaccines came in, mopped up, and took all the credit, by design, because bad people realized that vaccines in the hands of a technological elite, combined with an ignorant populace they can essentially murder and experiment on at will, allow them to basically FARM HUMANITY.

Sorry, Bill Gates. We understand your social engineering of us. We know your M.O. We know your real intentions. Including for the “people of color” you pretend to care about.

You will note that, in general, the further down the periodic table one goes, the more toxic the metals. Surprisingly, the second-lightest one – beryllium – is quite toxic, but even lightweight aluminum simply isn’t all that bad, in the big picture (but you’ve got to keep it on the OUTSIDE). In contrast, if you get down and heavy there with mercury, thallium and lead, or even as far down the table as cadmium and indium, the metals can be quite toxic.

Lead used to be used for plumbing – enough to lend its name to the profession. Copper then took over – before plastic began to displace copper. Nevertheless, copper is still highly valued for plumbing, as well as for electrical wiring.

As noted above, copper in drinking water is an interesting beast. Lead and copper in drinking water are controlled by the EPA under something called the Lead and Copper Rule, or LCR. Note that the linked document, which talks about the most recent “upgrade” to the rule, is over 400 pages. Yeah – there is a MESS of goofiness outside the actual rule there. Most of the concern is about lead, which is now highly restricted. Here is all that is said about copper’s toxicity in the linked explainer:

Acute copper exposure causes gastrointestinal distress. Chronic exposure to copper is particularly a concern for people with Wilson’s disease because they are prone to copper accumulation in body tissue, which can lead to liver damage, neurological, and/or psychiatric symptoms. For a more detailed explanation of the health effects associated with copper see Appendix E of the final rule Economic Analysis (USEPA, 2020). EPA did not propose revisions to the copper requirements; thus, the final rule does not revise the copper requirements.

Copper is basically off the hook at 1.3 ppm or below. That number has not been upgraded. Why is that level important? In my opinion, it’s because copper is bacteriostatic and algicidal in practice at between 0.1 and 1.0 ppm. Thus, one can SAFELY DRINK water which is being purified against microorganisms with copper.

And THAT would include the Moscow Mule, depending upon how long it sits.

I refer you now to an excellent article, which relies on a breathless scaremongering headline, but actually DOES provide a balanced set of viewpoints on both the DANGERS and BENEFITS of dietary copper.

Sipping This Popular Cocktail Is a “Health Hazard,” Experts Say

AFTER 27 MINUTES, YOU MAY BE AT RISK OF HEAVY METAL POISONING.

LINK: https://bestlifeonline.com/moscow-mule-copper-news/

ARCHIVE: https://archive.fo/6YT3X

First of all, copper isn’t really a “heavy metal” IMO, but whatever. It’s heavier than some.

You will note, after reading at the link, that you have to drink a ton of Moscow Mules, or a few that have sat around for a very long time, to MAYBE get sickened by them.

In general, avoid drinking acidic things that have been in contact with copper for a long time, and you will be OK.

Remember – most household water has sat around in copper pipes for quite a while at neutral pH, and it’s simply not toxic (due to copper). You DO get less lead if you flush your water 30 seconds before getting drinking water, but again – we’re talking about levels that would make Romans, Victorians, and even people from 70 years ago howl with laughter at our prissy over-concern – even knowing the science.

Perspective is very important – as you are about to see in a beautiful example of the failure of modern science, thanks to CCP socialism infecting both global science and science publishing.


Failure of Socialized Science and Peer Review Exposed in a JAMA-Published Ivermectin Study

The fact that Pierre Kory now calls JAMA “PHAMA” is a nice short way of saying that medicine has been utterly taken over by the pharmaceutical industry, and IMO set back several thousand years. Hippocrates would be HORRIFIED by what has happened to medicine – and I say that as somebody OUTSIDE medicine, and a lot closer to the pharmaceutical industry.

IMO it’s too late to save the pharmaceutical industry from scandalous criminal survival – but it’s not too late to save the profession of medicine from utter moral death. And thus, you will be treated to my following scientific opinion.


Steve Kirsch doesn’t play defense. He saw how JAMA (the Journal of the American Medical Association) completely FUMBLED an ivermectin paper, and how Pierre Kory picked it up off the ground, taking complete control, but more or less just standing there, lamenting the bad refs and horrible cheating. So Kirsch did the only thing he does. He grabbed the ball from Kory and ran it back for a touchdown.

“New JAMA paper show Ivermectin blows the COVID vaccines out of the water”

This is an utter reversal of the conclusion of the paper.

All because some guy in the stands named “Massimaux” spotted the free ball and yelled “FUMBLE!!!”

If you understand science, and science publishing, then you will see that what Kirsch did here was BRUTAL. And I’m gonna show you where all the bruises and black eyes are.

I almost feel sorry for JAMA, but not enough to miss this opportunity to LEAP ONTO THE DOGPILE and give AMA’s hare-brained PC leadership a good WEDGIE.

Don’t worry about the AMA. They’re protected by Pfizer, Biden, and the media. And just like any good mafia arrangement, as long as AMA keeps saying the right things, and not saying the wrong things, everything is gonna be OK.

Everything but science. But that’s OK, too.

We’ll take care of things. Just like we did here.


Here is the Kirsch gab that grabbed my attention.


Repeating for Zoe, as well as our silicon friends…..

Steve Kirsch
@stkirsch
·

New JAMA paper show Ivermectin blows the COVID vaccines out of the water 

https://stevekirsch.substack.com/p/new-jama-paper-show-ivermectin-blows?r=o7iqo&utm_campaign=post&utm_medium=web

New JAMA paper show Ivermectin blows the COVID vaccines out of the water

Whoops! How embarrassing! The CDC gave you bad advice. If you want to survive COVID, you should use the drug they said to avoid, and avoid the drug they said to…

stevekirsch.substack.com

View Link Feed

2,589 likes
208 comments
1,670 reposts
42 quotes


Now, as soon as I saw this, I was going….

“Wait a second. I thought there was some paper just out that Alex Berenson said was basically the end of ivermectin, although scientifically, I know that’s pretty much impossible. I know there is SOME explanation for why this paper (which I have not read yet) has to be deviating in some way from the MANY papers that show limited but solid efficacy – and especially against DEATH – just like HCQ. But this CANNOT be the same paper. No way! Kirsch would not be saying this unless the results were stunningly IN FAVOR of ivermectin, and there is no WAY that some authors with a NEGATIVE-LEANING study would be……. I mean….. WHAT THE HELL????”

SO – I just stopped to see what in the hell paper Kirsch was talking about.

YUP.

This is the SAME PAPER.

ARTICLE: https://jamanetwork.com/journals/jamainternalmedicine/fullarticle/2789362

SUPPLEMENTARY: https://cdn.jamanetwork.com/ama/content_public/journal/intemed/0/ioi220006supp2_prod_1644957301.65433.pdf

This is the SAME PAPER that caused Alex Berenson to issue TWO articles:

Ivermectin fails

To the ivermectin fanatics

Now we’ve discussed (in the comments on this site) Berenson’s very weird attack on Robert Malone when they appeared together on Fox News, which didn’t make sense THEN, but which does NOW – and I will explain that momentarily. But first, back to Kirsch.

Kirsch explains that – YES – this paper states in BOTH its abstract and its conclusion the following:

“The study findings do not support the use of ivermectin for patients with COVID-19.”

However, that is NOT what the data says.

Certainly not to everybody.

Certainly not to me.

In other words, DIFFERENT scientists (like Kirsch, Kory, me, and an anonymous Twitter poster names Massimaux, who found the key issue) have looked at the data, and see something quite different.

Kory goes into a rather long analysis of the whole war against ivermectin, but Kirsch digs into Kory’s article and then finds and elucidates the key nugget – discovered by Massimaux – that just ends the arguments.

It helps to read this in Kirsch’s article, but if you’re going to be lazy, I’ll explain here.

Here is Massimaux’s tweet:

Look at the bottom line in the two tables and compare. Not only is ivermectin CLEARLY better than the vaccine at preventing death – the significance of the result is significantly greater.

If the efficacy of ivermectin against death is not true, then very little else in the study is true.

This data says that ivermectin is exactly what we’ve been saying it is. It’s not a miracle cure, but it WORKS – particularly in preventing DEATH – its only real purpose. That result is IN THE PAPER. It is IN THE DATA. And if the authors want to argue that it’s not in the data, because it’s not significant enough, then nothing ELSE is in the data, because most everything else is even LESS significant.

Now it’s very important to realize that this nice little pair of tables FROM THE DATA is not due to the original authors – it’s due to a POST-PUBLICATION “peer review” by somebody who looked at the very same data, and PROVED using the authors’ own data that they were WRONG to say that the data didn’t support use of ivermectin.

So why did the authors tack on that wrong statement?

Did the EDITORS make them tack on that statement?
Did the AUTHORS tack it on to get the paper to publish?
Or is the “peer bias” against ivermectin, mostly due to the media, SO STRONG that scientists didn’t even look through their own data to see a conclusion they didn’t want to see?

Or is it a combination of ALL of these?

It is clearly in the data that ivermectin is three times as effective as the vaccines in preventing death. Even more importantly, if you add in what is known OUTSIDE the paper in question – namely the adverse effects of the vaccine and the safety of ivermectin, then it’s a no-brainer to NOT take the vaccine and to just use ivermectin. And Kirsch explains THAT rather nicely.

The data LITERALLY justify our position.

This was my hunch all along, and as vaccine side effects loomed larger and larger, and ivermectin proved to be rather shockingly harmless, even at antiviral doses comparable to large-animal systemic antiparasitic doses. All ivermectin had to do was prevent death to some moderate extent, and it was a no-brainer that people should take it.

To conclude anything else, based on the data, is murderous folly, in my opinion.

When I was a young lad – a mere student – but also one who WROTE PAPERS (because I had a great professor who TRAINED US to be full-blooded scientists), we EXPECTED to be CRITICIZED in peer review by people exactly like Steve Kirsch, Pierre Kory, and myself. We expected that others would look at data and see it completely differently.

And we would then have to ACKNOWLEDGE the alternative interpretations, or convince the editors that the criticism was not even worth acknowledging (a VERY rare occurrence in any legitimately contested field).

My lab had PRACTICE criticizing other people’s work – and we expected it in return. I personally found quite a few errors in the literature. Most were small – mostly problems of the writing – but some were huge and affected the science. Sometimes the big errors would only partially alter the author’s conclusions, but other times they had a significant impact.

However, I have to admit that I never ran into data which PROVED THE OPPOSITE of the authors’ main conclusion – even if only to the critic – and THAT is what we have here.

PEER REVIEW is designed to subject a paper to (hopefully at least TWO) critical readers who will very likely DEMAND improvements. Those improvements often mean acknowledging DIFFERENT views of the data as being possible and maybe even reasonable.

That kind of QUALITY peer review was VERY OBVIOUSLY not done here.

What we have RIGHT HERE is a demonstration that HERD REVIEW is much more important than PEER REVIEW.

PEER REVIEW is subject to BIAS. It is subject to SUBVERSION and GAMING.

I go back to the Zhang mask paper, for crying out loud.

To me, this will always remain a horrifying example of “fitting the data to the theory”, rather than looking to see what the data says. You can just look at this graph and see the crime.

I lay this stuff SQUARELY at the feet of SOCIALISM, which has politicized science and removed control of science from the people of science themselves, investing much of it in a media which WILL NOT question government narratives. People raised under socialism who become “go-alongers” – and so SOME degree that is everybody – stop questioning things that need to be questioned.

I have WATCHED and I have SEEN how WEF and CCP corruption have degraded science everywhere.

They’re not going to fix this stuff – at least not yet.

But until then, know this:

Ivermectin WORKS, and it was just proven by people who said it doesn’t work.

Thanks to HERD REVIEW.

One last point.

Why did Alex Berenson not see this?

IMO, it’s because Berenson is simply not a scientist – he’s an investigative journalist. Thus, his virtue-signaling attack on Malone was meant to show “journalistic balance”, NOT that he himself had deeply researched the history of the topic, in which case he (Berenson) would have likely said “Yes, Malone really is the most foundational of the founding fathers of the tech.”

But let’s not blame Alex too hard. THE AUTHORS OF THIS STUDY – that’s right – the authors themselves – didn’t see it, either.

See what I’ve always said? Real science is contentious.

But it has a good heart.

It wants the TRUTH.


ENJOY THE SHOW.

Thank you all for being here. Have a great weekend.

W

Saved From The Frankenvax

How a Psycho Vaccine Marrying the Infamous COVID Spike Protein to HIV’s Neurotoxic gp41 Was [Allegedly] Canned by a Mere Testing SNAFU


How Australia Dodged The First Mad Vax Bullet of the WEF Scamdemic / Plannedemic

How Science Monetization and Corruption Has Broken All Vaccine Safety Mechanisms and Made Sneaky Liars Out of Scientists


Mood Music


Intro – Prepare To Be Shocked

This is one of the craziest stories your either never heard, or barely heard. I am certain of the following. Nobody ever spelled out to you how NUTS this failed vaccine really was. This absolutely bonkers vaccine, that was almost used on all Australians.

AND MAY STILL BE.

The fact that nobody even followed this story, shows that the captured corporate media is absolutely not doing its job. Either THAT, or their job is to help deceive us.

And you know where my money is on that.

Surely, in the past, both journalists and scientists might have said something to the effect of “Hey – marrying a cardiovascular pathogenic bat virus spike protein and a neurotoxic AIDS protein in a vaccine to prevent a cold seems a little weird.”

BUT NO. NOT NOW.

And yet, some of us, few as we might be, might still have some questions.

We assume – ASSUME – as in ASS / U / ME – that all people in all of science are acting in all of our best interests all the time.

I have been completely broken of this spell, and I can tell you – what I can see now is not pretty.

I need to prepare you for what I’m about to tell you.


State of Corruption of Vaccine Science

First, a fantastic interview of Dr. Robert Malone by Tucker Carlson. It’s very folksy and long – a bit over an hour – but it will absolutely cure you of any idea that science in 2022 has not been almost totally corrupted by money, power, and SECRET AGENDAS.

This guy Malone is as close to a Moderna insider / honest outsider as you’re gonna get, and he clearly sees the dirty play from the Moderna point of view.

Hat tips to FG&C and GA/FL for keeping this video in play. Gail has been pumping this video, too. EVERYBODY need to watch this.

LINK: https://rumble.com/vuo2uu-dr.-robert-malone-on-tucker-carlson-today-feb-10-2022.html

In fact, I suspect that there is some relationship between this interview dropping that the following “factoid”.

Indeed, let’s just save that tweet as an image, in case Twitter decides Jack is becoming too much of a liability.

One of the biggest BOOMS dropped in the video, IMO, is the fact that Robert Malone WARNED the FDA about the toxicity of the spike protein, and they SHRUGGED IT OFF.

Yes. Malone gave them documentation, as asked, and they came back to him and said everything was OK. And THAT is when he started to think something was very wrong.

We’re about to do it AGAIN – only I’m not the first – I’m just rediscovering an obvious “why the heck are they doing THAT” point.

But we’ll get to that in a minute. We need to broaden our list of corrupt suspects.

You see, corporate “science” isn’t the only bad actor here. What about governments that conspire with the corporations to “mandate” their products for a mutual PAYOFF?

It turns out that both Justin Trudeau and the Canadian government have a very large incentive in mandating the broken, dubious, and just plain BAD Moderna and Pfizer “vaccines”.

LINK: https://rumble.com/vupkuv-breaking-criminal-canadian-monopoly-dr.-david-martin-exposes-why-trudeau-wo.html

When you realize that Justin Trudeau is not only following his mandate madness for WEFfian ideological reasons, and for Papa Fidel power, but also for CASTRO CASH, you understand what’s REALLY going on.

SO – now that you realize THESE PEOPLE care more about other things, than they care about us, the following will make more sense.


The Frankenvax That Almost Was

So just today, FG&C posted THIS TWEET which made me go WTF…..

Basically, an Australian COVID vaccine that falsely triggers AIDS / HIV tests was recalled. The vaccine was NOT sent out for use by the public, because it gave people positive AIDS tests.

GREAT, but…..

  • WHY did the vaccine do this? And by the way….
  • Didn’t this happen BEFORE – like over a year ago?
  • I could have SWORN this happened before.
  • Is this OLD NEWS or a DIFFERENT VACCINE?
  • Or did they bring the SAME vaccine BACK?
  • Or even worse….. AND logic…..

You see, I remember something just like this bit of news, over a year ago. It was some vaccine from an Australian university that accidentally triggered AIDS tests.

Well, when I looked closer at this, it turned out to be THE SAME NEWS. Meaning that this recent tweet was just OLD NEWS.

HOWEVER – I happen to know a lot more now, a year later, so I dug DEEPER and FOUND MORE.

And now I want to explain to you, exactly what is going on.

Because this monster AIN’T DEAD.


VolksWackcine 451

Let’s begin by looking at the actual announcement that all this news came from. The paragraph in BOLD is the critical one. If you’re going to TL;DR past all the rest, read THAT paragraph.


Update on The University of Queensland COVID-19 vaccine

11 Dec 2020

Friday, 11th December, 2020: The University of Queensland (UQ) and CSL today announce that the Phase 1 trial of the UQ-CSL v451 COVID-19 vaccine has shown that it elicits a robust response towards the virus and has a strong safety profile. There were no serious adverse events or safety concerns reported in the 216 trial participants. However, following consultation with the Australian Government, CSL will not progress the vaccine candidate to Phase 2/3 clinical trials.

The University of Queensland commenced a Phase 1 trial of their COVID-19 vaccine candidate – v451 – in July 2020, to assess safety and immunogenicity in healthy volunteers. CSL was working towards taking responsibility for the Phase 2/3 clinical trial and large-scale manufacture of the vaccine, upon completion of successful trials.

The Phase 1 data also showed the generation of antibodies directed towards fragments of a protein (gp41), which is a component used to stabilise the vaccine. Trial participants were fully informed of the possibility of a partial immune response to this component, but it was unexpected that the levels induced would interfere with certain HIV tests.

There is no possibility the vaccine causes infection, and routine follow up tests confirmed there is no HIV virus present.

With advice from experts, CSL and UQ have worked through the implications that this issue presents to rolling out the vaccine into broad populations. It is generally agreed that significant changes would need to be made to well-established HIV testing procedures in the healthcare setting to accommodate rollout of this vaccine. Therefore, CSL and the Australian Government have agreed vaccine development will not proceed to Phase 2/3 trials.

The Phase 1 trial will continue, where further analysis of the data will show how long the antibodies persist, with studies so far showing that levels are already falling. The University of Queensland plans to submit the full data for peer review publication.

UQ Vice-Chancellor, Professor Deborah Terry, said while the outcome was disappointing, she was immensely proud of the UQ team who had shouldered a heavy burden of responsibility while the world watched on. “I also want to thank our many partners, our donors – including the Federal and Queensland Government – and of course the 216 Queenslanders who so willingly volunteered for the Phase 1 trials.”

UQ vaccine co-lead, Professor Paul Young, said that although it was possible to re-engineer the vaccine, the team did not have the luxury of time needed. “Doing so would set back development by another 12 or so months, and while this is a tough decision to take, the urgent need for a vaccine has to be everyone’s priority.”

“I said at the start of vaccine development that there were no guarantees, but what is really encouraging is that the core technology approach we used has passed the major clinical test. It is a safe and well-tolerated vaccine, producing the strong virus-neutralising effect that we were hoping to see.

So we will continue to push forward and we are confident that with further work the Molecular Clamp technology will be a robust platform for future vaccine development here in Australia and to meet future biosecurity needs.

Dr Andrew Nash, Chief Scientific Officer for CSL said “This outcome highlights the risk of failure associated with early vaccine development, and the rigorous assessment involved in making decisions as to what discoveries advance.”

“This project has only been made possible by the innovative science developed by world-class scientists at The University of Queensland and the strong collaboration between our organisations, and many others, over the last 10 months. CSL and Seqirus are committed to continuing our work to protect the Australian population against COVID-19. Manufacture of approximately 30 million doses of the Oxford/AstraZeneca vaccine candidate is underway, with first doses planned for release to Australia early next year. In addition, CSL has agreed at the request of the Australian Government to manufacture an additional 20 million doses.”

UQ and CSL acknowledge the support of the Coalition for Epidemic Preparedness Innovations (CEPI) in partnering to enable the rapid development of the vaccine candidate through clinical trials.

– ENDS –

LINK: https://www.csl.com/news/2020/20201211-update-on-the-university-of-queensland-covid-19-vaccine


WOLF AGAIN.

So what they’re saying is that this vaccine – which uses the HIV protein gp41 – sets off HIV tests. And THAT made the test unacceptable to move forward. The remaining phase II and phase III trials were cancelled, while the phase I trials continued to finish collecting data.

And WHILE they say that the phase I testing showed that the vaccine was safe and effective, if you look more closely, they only tested it on 216 people.

We KNOW from the Moderna and Pfizer tests, that even after HUGE phase II and phase III trials, using thousands or tens of thousands of participants, there are serious side effects that are STILL not discovered until actual roll-out to the public, when millions receive the shot.

And that does NOT include long-term effects. We know NOW that this determination can be critical in many cases.

And one more point for the record. As you can see by the statement at the end of the press release, this vaccine was supported by the Bill Gates organization CEPI.

Yeah, that CEPI, and THAT Bill Gates.

Like I say, CEPI is how Gates gets TWO VOTES, and GAVI is how he gets THREE.

So the bottom line – this vaccine was killed because it set off AIDS tests.

But let’s dig a little deeper into that.


So What’s With HIV and the COVID Vaccines?

When I first heard about this particular Australian vaccine (UQ-CSL v451, or v451 hereafter) triggering HIV tests, my immediate thought was that this might be proof that the Indian researchers were CORRECT – that the spike protein really contained those four inserts from HIV, and that THIS was setting off tests for HIV.

Later, I heard that – no – there was actually some segment of HIV protein being used in the v451 vaccine INTENTIONALLY. Thus, the whole problem seemed stupid, the use of the HIV protein seemed short-sighted, and I promptly forgot about it. No smoking gun – just a stink bomb.

However, a year’s time changed all that.

Think how different the perspective is now.

  • virus almost certainly came out of a biowarfare lab in China with PLA/NIH ties
  • Fauci, Dazsak and minions now known to have LIED about origins
  • Fauci gang also lied when pooh-poohing the Indian HIV insert hypothesis
  • mRNA vaccines seem to be producing immune deficiency, a.k.a. “VAIDS”
  • there are working hypotheses now which explain immune deficiency
  • Fauci’s history with HIV mirrors current history with COVID – lies and hidden agenda
  • Fauci seems to be obsessed with immunodeficiency and vaccines
  • Fauci promoted bad killer drugs as treatments in both cases (AZT, remdesivir)
  • Fauci seems to have an agenda clearly counter to truth as we know it, and is likely serving something beyond the increasing “fake” science which the public believes is operant in the world, but which is very likely a “reduced set” intended to deceive us

Thus, with all that WEIRD background, it NOW seems a bit “par for the course” that somebody in that world would want to bring HIV into the COVID equation.

But is that a good idea?

Now – before I go talking about why this might be a BAD idea, I want to give you plenty of references as to why they SAY it was a good idea.

Let’s start with a good explanation of why the false positives occurred. This article includes a lot of information on the v451 vaccine itself.

LINK: https://theconversation.com/how-did-the-university-of-queensland-csl-vaccine-fail-due-to-false-positive-hiv-tests-a-vaccine-expert-explains-151911

ARCHIVE: https://archive.fo/duxjK

The article mentions, without too much detail, that the HIV protein is part of a “molecular clamp” – a trimeric molecular “holder” of spike protein molecules. This holder allows three molecules of any attached spike-type protein to stay locked into a rigid, parallel conformation, which will remain in the desirable pre-fusion (with a cell) configuration, and not change into the useless post-fusion configuration.

The article also links to a scientific paper on the technology:

LINK: https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC7672035/


Front Immunol. 2020; 11: 592370. Published online 2020 Nov 4. doi: 10.3389/fimmu.2020.592370 PMCID: PMC7672035 PMID: 33250897

Rapid Response Subunit Vaccine Design in the Absence of Structural Information

Danushka K. Wijesundara, 1 , 2 Michael S. Avumegah, 1 , 2 Julia Lackenby, 1 , 2 Naphak Modhiran, 1 , 3 Ariel Isaacs, 1 Paul R. Young, 1 , 2 , 3 Daniel Watterson, 1 , 2 , 3 , * and Keith J. Chappell 1 , 2 , 3 , *

ABSTRACT

Prior to 2020, the threat of a novel viral pandemic was omnipresent but largely ignored. Just 12 months prior to the Coronavirus disease 2019 (COVID-19) pandemic our team received funding from the Coalition for Epidemic Preparedness Innovations (CEPI) to establish and validate a rapid response pipeline for subunit vaccine development based on our proprietary Molecular Clamp platform. Throughout the course of 2019 we conducted two mock tests of our system for rapid antigen production against two potential, emerging viral pathogens, Achimota paramyxovirus and Wenzhou mammarenavirus. For each virus we expressed a small panel of recombinant variants of the membrane fusion protein and screened for expression level, product homogeneity, and the presence of the expected trimeric pre-fusion conformation. Lessons learned from this exercise paved the way for our response to COVID-19, for which our candidate antigen is currently in phase I clinical trial.


Here is part of a really good graphic from the paper.

You can see how it’s possible to produce a spike protein with the “molecular clamp” attached, and then simply let this recombinant construction TRIMERIZE (form a triple, side to side) around the three molecular clamps, and thereby stabilize the three spike protein molecules next to each other.

This is a bit like a “motif” within an actual virus, where spike proteins, sticking out next to each other, protect each other’s sides. THAT is the basic idea of this thing.

Remember how Novavax assembles a bunch of spikes via modified ass ends into a kind of antigenic cloved apple, to create a kind of fake virus? Same very basic principle.

Indeed, the molecular clamp is even a bit like TWO motifs, since gp41 serves a somewhat similar purpose in the HIV virus, being the root of a stalk to an attack mechanism.

HIV-1 fusion process. It involves both subunits of the envelope spike complex. Notably, gp41 is shown in green with its transmembrane region buried in the virion membrane, both segments of heptad repeats (CHR closer to the virus and NHR closer to the host cell) before and after conformational changes, and the N-terminal end of the ectodomain in gray. In the last two panels pointed out by the red arrows, gp41 is observed following penetration of the host cell and following a conformational change resulting in the six-helix bundle which brings the viral and cell membranes into close proximity.

So – in a very real sense – this whole “vaccine” thingie is a literal marriage of HIV and coronavirus – the simplest possible one.

And they didn’t tell you ANY of this shit – did they?

So all of that WORKS, but the problem is that antibodies don’t just form to the attached spike protein – they ALSO form to the “molecular clamp”, meaning to the gp41 protein.

And what does that mean?


An AIDS Vaccine in Disguise?

The people who made the v451 vaccine say they didn’t expect there to be so much antibody response to the gp41 parts of the vaccine, thus triggering HIV tests.

You know what?

I don’t believe them.

I think they were gaslighting us all along.

Part of this is due to the fact that I’ve seen gp41 named numerous times as a potential basis for subunit vaccines against HIV. In fact, in one reference, I saw it named as THE BEST HOPE for an AIDS vaccine.

They didn’t mention that? LOL. OH, REALLY.

So WHY would anybody be using gp41 as part of an antigen, and not expect it to generate antibodies?

In fact, one might almost look at this v451 vaccine and regard it as an HIV vaccine, with spike proteins tacked onto gp41 as a kind of “nasty adjuvant” to initiate the immune response to the HIV protein.

Seriously – which is the real target here – COVID or HIV? Or BOTH?

This looks to me like a perfect example of…..

WAIT FOR IT….

“REVERSO”.

But let’s just set that aside for now, and pretend that the thing which COULD be a vaccine for EITHER ONE of the two things they stuck in it, is REALLY a vaccine for the fakey-fake cold that we don’t need a vaccine for, and NOT a vaccine for the sexual disease that stands in the way of Luciferian scum creating their polyamorous sexual paradise of literal epic random phuckery.

OMG, these people have just lied, and lied, and lied again. And they will KEEP lying.

But we’ll pretend they’re not lying, for just a little while longer.

So if we have an actual COVID vaccine here…..

…..is it a good idea to include the HIV gp41 protein subunit?

Well, after what we’ve seen with the spike protein, I was thinking maybe it wouldn’t be.

And it turns out, I wasn’t the first person who thought of this.


Doorless Carp’s Suspicious Cat In A Box

When I went looking for the toxicity of the gp41 protein, one of the first things that came up was some guy or gal who appears to have been actively suppressed on Twitter, eventually banned to Gab, and whose substack article on the topic has only two likes – ONE OF THEM MINE.

Doesn’t mean the article’s not important. And I think it’s about to get a few more hits.


LINK: https://doorlesscarp953.substack.com/p/update-on-the-university-of-queensland

Update on The University of Queensland COVID-19 vaccine. “..trial did not give trial participants HIV”, just a neurotoxic glycoprotein

11 Dec 2020

DoorlessCarp Feb 11

This is a wonderful article that is simply SKEPTICAL of the entire “it was pulled because of triggering AIDS tests” reasoning.

DoorlessCarp read the same press release I cited above, and pokes and prods it from the point of view of somebody who knows a heck of a lot about HIV and AIDS, and doesn’t buy what (s)he’s reading in that press release. Something doesn’t sniff right to “them”, and “they” spell out the issues.

I will attempt to summarize DoorlessCarp’s concerns (noted as “DLC” hereafter).

First, DLC admits to actually being led to the problem by one of those Fake News “straw man fact checks”, which attempt to either “debunk” facts or mislead scandals by setting up an adjacent strawman and knocking it down. OBSERVE.

“Fact check: An Australian vaccine trial did not give trial participants HIV”

https://www.reuters.com/article/uk-factcheck-hiv-idUSKBN28R2WT

LOL. No. The truth they’re protecting is that the “COVID vaccine” gave them HIV antibodies, and it was very likely the whole point.

To quote DLC about the Aussie vaccine researchers: “I wouldn’t let these clowns dispense aspirin, let alone design fast tracked vaccines.

DLC then makes this statement, noting that there is a curious skew between the reality of HIV testing and the idea that there is some kind of a problem here.

Interesting rapid response to the effect that antibody only HIV tests have long since been debunked as a diagnostic tool on their own due to cross reactivity from other antibodies. They don’t tell you anything useful.

DLC then quotes extensively from this letter which explains why HIV testing via antibodies is actually a rather horrible mishmash of false positives and negatives, ultimately requiring a clinical diagnosis and “validation by lifestyle facts”.

Which leads to the next section, which I quote:

So what was the real reason for pulling the Australian trial, was it the gp41 toxicity?

The antibody problem raises more questions than it answers as spike S2 has homology to P24, GP41 and GP120.

This is dark stuff, P24 has been ported straight across from HIVs capsid to the spike protein. Here’s the proof, at least as far as what specific antibodies are telling us, which don’t lie:

What is p24 antigen?

“One distinctive HIV antigen is a viral protein called p24, a structural protein that makes up most of the HIV viral core, or ‘capsid’. High levels of p24 are present in the blood serum of newly infected individuals during the short period between infection and seroconversion, making p24 antigen assays useful in diagnosing primary HIV infection.”

https://www.aidsmap.com/about-hiv/faq/what-p24-antigen

This section makes the following points:

  • suspects the real reason for pulling the vaccine was the toxicity of gp41
  • notes that the spike protein already has potentially dangerous homologies to three HIV proteins, p24, gp41 and gp120
  • p24 is basically the nucleocapsid protein of HIV
  • p24 tends to be detected early in the AIDS process, before antibodies to it form

DLC then cites several papers demonstrating that there is already a lot of understanding of antibody cross-talk between the SARS-CoV-2 spike protein and either (1) original SARS-CoV proteins, and (2) HIV-1 proteins.

In the latter case, there is specific interaction with gp41.

References given:

The SARS CoV-2 spike directed non-neutralizing polyclonal antibodies cross-react with Human immunodeficiency virus (HIV-1) gp41 (Dec. 2021)

https://www.sciencedirect.com/science/article/pii/S1567576921008237?via%3Dihub

Cros-reactivity of SARS-CoV-2 with HIV chemiluminescent assay leading to false-positive results (2020)

https://jcp.bmj.com/content/74/9/614#request-permissions

DLC then lays the hammer down on the fact that gp41 is responsible for the dementia of AIDS.

I’m including the whole thing here.

Pathology:

Accumulation of β-Amyloid Precursor Protein in Axons Correlates with CNS Expression of SIV gp41 (2002)

“In this study, a strong association (p = 0.005) was identified between elevated axonal β-APP levels and the amount of SIV gp41 present in white matter, implicating HIV/SIV gp41 as a mediator of axonal damage.

https://academic.oup.com/jnen/article/61/1/85/2916415

For those who don’t know, beta amyloid is associated with several degenerative neurological disorders:

Amyloid-β and Parkinson’s disease (2018)

https://pubmed.ncbi.nlm.nih.gov/30377818/

Beta-amyloid 42 accumulation in the lumbar spinal cord motor neurons of amyotrophic lateral sclerosis patients (2004)

https://www.sciencedirect.com/science/article/abs/pii/S0969996105000276?via%3Dihub

Alzheimer’s Disease and the β-Amyloid Peptide (2010)

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2813509/

They knew this way back in 1999:

Mechanisms and Structural Determinants of HIV-1 Coat Protein, gp41-Induced Neurotoxicity (1999)

Abstract

Of the individuals with human immunodeficiency virus type 1 (HIV-1) infection, 20–30% will develop the neurological complication of HIV-associated dementia (HAD). The mechanisms underlying HAD are unknown; however, indirect immunologically mediated mechanisms are theorized to play a role. Recently, the HIV-1 coat protein gp41 has been implicated as a major mediator of HAD through induction of neurocytokines and subsequent neuronal cell death. Using primary mixed cortical cultures from neuronal nitric oxide synthase (NOS) null (nNOS−/−) mice and immunological NOS null (iNOS−/−) mice, we establish iNOS-derived NO as a major mediator of gp41 neurotoxicity. Neurotoxicity elicited by gp41 is markedly attenuated in iNOS−/− cultures compared with wild-type and nNOS−/− cultures. The NOS inhibitor l-nitroarginine methyl ester is neuroprotective in wild-type and nNOS−/− cultures, confirming the role of iNOS-derived NO in gp41 neurotoxicity. Confirming that iNOS−/− cultures lack iNOS, gp41 did not induce iNOS in iNOS−/− cultures, but it markedly induced iNOS in wild-type and nNOS−/− cultures. We elucidate the region of gp41 that is critical for iNOS induction and neuronal cell death by monitoring iNOS induction with overlapping peptides spanning gp41. We show that the N-terminal region of gp41, which we designate as the neurotoxic domain, induces iNOS protein activity and iNOS-dependent neurotoxicity at picomolar concentrations in a manner similar to recombinant gp41 protein. Our experiments suggest that gp41 is eliciting the induction of iNOS through potential cell surface receptors or binding sites because the induction of iNOS is dose dependent and saturable and occurs at physiologically relevant concentrations. These data confirm that the induction of iNOS by gp41 and the production of NO are primary mediators of neuronal damage and identify a neurotoxic domain of gp41 that may play an important role in HAD.

Keywords: HIV-1, HIV-associated dementia, neurotoxicity, gp41, immunological nitric oxide synthase, nitric oxide

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782354/

DLC’s concluding remark:

“Off to Moderna we go”

Insist that love drive the clown car – Pam Grout

Yeah, I kinda get this sentiment.

And I quote again:

I wouldn’t let these clowns dispense aspirin, let alone design fast tracked vaccines.

Is gp41 a danger? It may well be. And nobody is asking the question, because (IMO) the neural pathogenic initiator that gp41 is, was passed off as a “molecular clamp” instead of the REAL ANTIGEN.

If they’re going to resurrect this weirdo COVID-HIV vaccine – and YES, they’re thinking about it – then there needs to be some examination FIRST of what the HELL is going on.


So What The Heck Is Going On Here?

When I was a young lad in the old days of science, there was lying, misrepresentation, and thievery, but it was on a much smaller scale.

We used to joke very cynically, back in the ’70’s, that every natural product being synthesized in a laboratory cured cancer, because we all knew that was not true.

We knew that these substances were really being synthesized merely because the molecules were a synthetic challenge, and a way for professors to make a name for themselves in synthetic chemistry. Almost NONE of these substances would EVER be used to treat cancer, and most would wash out very soon upon investigation. Almost none of them would ever even LEAD to a useful cancer drug. But LYING about their importance was how people got money for their labs. Every structurally interesting new molecule was always the next savior – until it wasn’t.

I used to think that the people giving out the money were fools about this, but not any more. I am beginning to think that the “givers” have always been just as corrupt as the “takers” – they’re just the “insiders” who turn on the spigots for their fellow “outsiders”.

I have no reason to think that vaccines are any different.

I think that a false crisis was used as a massive MONEY-BOMB – a global pile-on of the giddiest and most corrupt kind.

Probably the biggest one in 20 years.

I think that an AIDS vaccine was passed off as a COVID vaccine, by plausibly passing off the natural function of the HIV subunit as a new tool for other things, because – well – it IS such a new tool – just like every new interesting molecule MIGHT actually be some amazing new drug that cures cancer.

They lie skillfully, and they lie with truth, and it’s almost impossible to PROVE that the secondary “oh by the way” was actually the primary motivation.

We have changed from white lies that everybody understood WERE lies, to much more devious lies where scientists engage in fooling not just the public, but even other scientists.

I do think we have to wake up now. We can no longer afford the luxury of pretending not to know.

If I have to thank Joe Biden and his puppetmasters, including his “handler” Obama, for anything, it is for WAKING ME UP with these stupid mandates.

Nothing worked so well, to show us that the NEW WORLD ORDER is a direct threat to humanity, and needs to be stopped.

Science can be good again. But it must never, ever, abandon TRUTH.

And here we are.

W