Preprint: "The SARS-CoV-2 Delta variant is poised to acquire complete resistance to vaccines"
When it escapes, vaccine-induced antibodies to legacy spike will enhance infectiousness.
A pre-print by researchers at Osaka University in Japan studies the specifics of Delta immune-escape adaptations, and brings more ominous news: The Delta strains now circulating have obvious vaccine-escape adaptations. In some ways, these adaptations have enhanced the potential infectiousness of Delta. But this potential has not yet been realised, because the Delta spike protein has not fully escaped. When that escape does happen, antibodies against legacy spike elicited by the BioNTech/Pfizer vaccines will probably enhance Delta’s transmissibility.
To understand how this can be true, we must take a closer look at spike:
The pink/magenta region at the top is the ACE2 receptor binding domain, or RBD. The RBD interacts with the ACE2 protein expressed by cells in our lungs. Think of it as a key that SARS-2 uses to enter your cells. The vaccines elicit anti-RBD antibodies that interfere with ACE2 interactions. It’s the equivalent of changing your locks, and now Delta has been forced to try a different key: It has two distinctive RBD mutations, but these mutations are not unique to Delta. We also find them in other variants, which are less successful than Delta, so it looks like they’re not crucial to Delta’s success.
The preprint researchers note, however, that Delta appears to have special, unique enhancements to the N-terminal domain (NTD), which is the blue area on the upper left of this spike diagram. “This suggests,” they say, “that mutations in the NTD may play a key role in the high infectivity of the Delta variant.”
Our vaccines elicit antibodies against both of these domains, but so far most attention has been directed against anti-RBD antibodies. Researchers, however, have shown that antibodies against the (blue) NTD play an equally crucial role, and that the wrong anti-NTD antibodies change the configuration of the RBD and actually enhance its capacity to bind to ACE2. Here a simple schematic from another article by the Osaka researchers:
Basically, SARS-2 virions have receptor binding domains that are not fully optimised always and everywhere for binding to ACE2. The right kinds of antibodies, however, can force the NTD and then the RBD into a more ideal configuration and enhance infectiousness, as you see on the right side of this image.
Your immune system, in other words, deploys a variety of antibodies against the NTD. Some of them neutralise it. These are the ones you want. Others, however, merely force NTD and thereby RBD into a more infectious configuration. These are the ones you don’t want. The enhancing antibodies aren’t a problem if you also have neutralising antibodies against NTD and RBD to counteract any advantage.
Back to the preprint. The authors ask how our vaccine antibodies against legacy spike hold up to the new and improved Delta NTD:
We analyzed … 16 anti-NTD neutralizing antibodies, and found that none of the anti-NTD neutralizing antibodies could recognize Delta spike … In contrast, when we analyzed the binding of the anti-NTD infectivity-enhancing antibodoies … eight out of ten anti-NTD enhancing antibodies bound to Delta spike at levels comparable with wild-type spike …
The situation, then, is precisely this: The vaccines gave billions of people antibodies to legacy spike proteins, including anti-NTD neutralising antibodies and anti-NTD enhancing antibodies. Delta is evolving to escape the neutralising antibodies, but not the enhancing antibodies. Which is what you would expect. We have sown antibodies against one viral protein in the lungs of half of mankind, and that protein has now evolved slight modifications to use those antibodies to its advantage where it can, and to escape the rest.
Remember, we are still talking about a single domain in the complex spike protein: There are other antibodies to RBD that still disadvantage Delta. The net effect is still that all of these antibodies, added together – particularly those against the RBD – hurt rather than help.
There are, however, Delta strains with key escape RBD mutations. The authors of this preprint find that four such mutations, already out there in various Delta sub-strains, are sufficient for Delta to evade the anti-RBD antibodies more or less completely.
In sum: Beneath the surface, Delta has evolved to use anti-NTD antibodies, like those elicited by BioNTech/Pfizer vaccines, to enhance its infectiousness. So far we have not seen any effect, because the BioNTech/Pfizer vaccines still elicit anti-RBD antibodies that hurt Delta on balance. But, all the mutations necessary to escape these crucial anti-RBD antibodies exist. All that remains is for a single Delta strain to pick up the right combination of them, and BioNTech/Pfizer antibodies will provide “weak neutralization only at the highest concentration”. Otherwise, they will enhance infectiousness.
UPDATE: Some objections about the in vitro approach of the study authors by Brian Mowrey (who writes Unglossed) in comments here. While I don’t share all of his reservations, he’s right that the significance of these findings for the broader immune response of the vaccinated to potential future Delta escape strains is unclear.
It’s all irrelevant because human immune systems hardly respond to spike. Instead our immune system generates antibodies and cytotoxic T-cells against stable parts of SARS-CoV-2. There seems to be a near obsession with circulating IgG antibodies, when immunological experience teaches that, for respiratory viruses, antibodies in blood play a secondary role in host defence.
Secreted IgA antibodies are a different matter but almost no one studies these.
What has been studied in depth is the repertoire of cytotoxic T-lymphocytes. No question, cross-immunity from beating somewhat related viruses leaves most of us with some cross-protection. It’s possible that ADE will make infection worse, but I’m not concerned about these breathy pieces telling us the sky is falling. It’s not.
The exit is simple except the elites are interested in mass depopulation. That exit is to halt mass PCR testing & lift all restrictions. Within weeks the position would be indistinguishable from any other autumn.
Remember, there are around 200 other respiratory viruses. In almost no case can illness be unequivocally ascribed to a specific virus. It’s just lies to misuse the PCR mass testing system. Helps no one.
Years ago I worked as graduate student. Our lab introduced single amino acid mutations to evaluate for change in bacterial toxin configuration and activity. It was amazing how such a small change could result in a wide variety of outcomes, sometimes that being enhanced toxin activity. Protein folding is a sort of molecular ballet.
I seriously doubt anyone considered the caveats of protein folding before they took the jab.
Within nature there seems to be a sort of purity. Like that of fire, it burns away the refuse of virtue signaling and lays waste to the fear of dying. Nature has all the time it needs to prove its might.