Alternative to mRNA injections that uses a protein injection plus a mucosal booster that prevents reinfection of any variant PLUS an alternative to the use of alum adjuvants
From this 85-minut interview here:
(100) Vaccine Developer DESTROYS COVID Narrative in Jaw-Dropping Interview (substack.com)
There is a broad ranging discussion about the “known to fail” mRNA and adenoviral vector platforms and an alternative vaccine that has been used on 8 million people in the middle east with no multiple infections of C19 variants.
Click through for link for the full interview.
Side not: it looks as if the UK’s vaccine guru resurrected the failed adenoviral vector platform ad worked with Oxford University to concoct a new failure called the Oxford/AstraZeneca “vaccine” that has proved so toxic that it was withdrawn from use in the EU after a few months – though remained the toxic injection of choice in India and continued to be administered for a long time in Canada and Australia, and available but not used until recently withdrawn in the UK.
Here she is Prof Sarah Gilbert: The woman who designed the Oxford vaccine - BBC News
Here is a link to Professor Nikolai Petrovsky website:
Also, here is a link to the potential replacement to a paper on another adjuvant that might replace aluminium/aluminium (alumiium) is used (as I understand it) in vaccines to provide an immune response that would not otherwise happen because our immune systems would destroy the contents of a vaccine before the vaccine could have the desired effect of “infecting” the body.
“In this work, we sought to address this issue through structural modifications in the agonists to enhance their adsorption capacity to the classic adjuvant alum.
We selected a potent TLR7-selective agonist, BBIQ (EC50 = 0.85 μM), and synthesized polyphenolic derivatives to assess their TLR7 agonistic activity and adjuvant potential alone or in combination with alum.”
I will leave it to the expert medics to comment in detail – though, no doubt, there is much to think about around T and B-cells, plus xheck this out abut an adjuvant that culd replace alum.
“Although the synthesized compounds were less active than resiquimod, the immunization data on combination with alum, specifically the IgG1, IgG2b and IgG2c responses, were superior in comparison to BBIQ as well as the reference standard resiquimod.
Compound 12b was 5-fold more potent (EC50 = 0.15 μM in TLR7) than BBIQ and induced double the IgG response to SARS-CoV-2 and hepatitis antigens. Similarly, compound 12c (EC50 = 0.31 μM in TLR7) was about 3-fold more potent than BBIQ and doubled the IgG levels.”
No mention of IgG4 in the paper, but the interview talks about how IgG4 is not an anti-viral antibody.
Dr McMillan’s interview has a full transcript. Here are his brief show notes for ease:
“In this eye-opening interview with Prof Nikolai Petrovsky, a prominent vaccine developer, he completely dismantles the COVID narrative, shedding light on key aspects that challenge the mainstream understanding of the pandemic.
Join us as we delve into the details that could change everything we thought we knew about COVID. Don't miss out on this jaw-dropping conversation that could revolutionize the way we view the current global situation.”
Listen to the end of the video for an interesting take on constant reinfection with a lower dose of initial injection that enable the body to turn a repeat infection as a “booster”!
Onwards!!!
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Uh....NO THANK YOU!
Do they call this new set up, "Killing Me Softly"?
Go to CDC dot gov and search "Symptoms of Covid-19". What pops up is an EXACT description of the common flu. If you think you can grow a cell culture in a Petri dish, stir some stuff around and then proclaim you have isolated a virus you have another think coming! During the Spanish flu researchers tried everything they could think of to infect healthy people in an effort to understand what was going on. They swabbed mucus from sick people and placed it in the eyes, ears noses and mouths of healthy people. NOT EVEN ONE person became sick. Viruses do not exist floating around in nature waiting to make you sick. They are created in and only exist INSIDE the body as a defense against something that's not right IN the body, like an acidic blood pH, due to exposure to the EMFs of 4G and 5G radiation and all of the other EMFs we are bombarded with every day. You cannot CATCH a virus. This is one of the biggest cover-ups in the world.