Class switch towards non-inflammatory IgG4 antibodies after vaccination
science.org
science.org
With most vaccines on the market, the effect of vaccination according to the recommended schedule is tested for real: actual disease outcomes are studied and the vaccine schedule is determined accordingly. For example, people who get both measles vaccine doses largely don’t get measles (and largely is quantified). People who get two doses of the chickenpox vaccine don’t get chickenpox [0].
With the Covid vaccines, for some reason public health authorities are okay with flying blind. The effect of, say, bivalent boosters on their recipients’ blood neutralizing viruses and virus-like imitation viruses are studied in the lab (but even the studies of this effect by the vaccine makers are barely public and seem to consist mostly of press releases). Studies on actual infections rates seem to be almost completely absent.
And now we have this study, which at least gives a plausible mechanism by which repeated mRNA vaccination could fail to improve actual immunity or maybe even reduce it.
What we need is a real study of whether vaccine recipients on different schedules get sick and how sick. And these need to be well designed, ongoing, and public.
For what it’s worth, IgG4 production is observed in allergy patients receiving immunotherapy, which consists essentially of very frequent repeated vaccination against allergens.
[0] The chickenpox vaccine is incredibly effective against chickenpox — it makes any of the Covid vaccines look pathetic. But, to be fair, the effect of chickenpox vaccination on shingles seems to only slowly coming in to focus by real studies. But to give the FDA credit, figuring this out takes multi-decade studies.
The worst part is with politicians who are okay with forcing the general public to trust the sight of these blind public health authorities.
Numerous studies have been presented to ACIP over the last few years covering asymptomatic infections, symptomatic infections, and hospitalizations. From the 2021 meeting covering Pfizer-BioNTech, there were 5, [1] 17 [2], and 13 [3] of these studies, respectively. There are similar sets for Moderna [4]. From what I've seen of the ACIP meetings, those are the results they focused on the most.
I don't have much knowledge of medical research but I don't see how this could possibly be "completely absent". Would love to hear more about what's missing from these and the dozens of other studies which have been done since.
1: https://www.cdc.gov/vaccines/acip/recs/grade/covid-19-pfizer...
2: https://www.cdc.gov/vaccines/acip/recs/grade/covid-19-pfizer...
3: https://www.cdc.gov/vaccines/acip/recs/grade/covid-19-pfizer...
4: https://www.cdc.gov/vaccines/acip/recs/grade/covid-19-pfizer...
https://www.cdc.gov/vaccines/acip/recs/grade/covid-19-bivale...
Which seems to be entirely lacking in efficacy data. MMWR just has immunogenicity and speculation, too:
Basically, is it "good" news, "bad" news, or just, news ?
(To clarify in case that's what caused the downvotes : I'm not writing "bad" news because I think vaccines are "bad". If we really need to get boosted once a year, so be it - but it would arguably be a worse outcome than "not needing it")
"Further investigations are needed to clarify the precise immunological mechanisms driving this response and to evaluate whether an IgG4-driven antibody response affects subsequent viral infections and booster vaccinations. This is not only relevant for potential future vaccine campaigns against SARS-CoV-2, but also for new mRNA-based vaccine developments against other pathogens."
However, it's also "news", because the hypothesis that getting boosted could make you _more_ sick is pretty, well, say, novel.
(Hypothesis still to be confirmed, I get it, but if I understand the other comments correctly,that's the jist of it ?)
Also, in médecine, pretty much anything that goes into the direction of "more sick people" is, well, "bad" news ? Again, maybe there is a silver lining here, and I don't know enough about the topic.
Or maybe it's just a "Burn After Reading" thing.
"I guess we learned not to do it again" ? (except, no, we'll have to do it again, and FSM knows what would have happened if...)
> "seasonal flu vaccination almost doubled the risk of infection with pandemic flu":
https://www.cbc.ca/news/health/flu-vaccine-paradox-adds-to-p...
> "Canadian researchers noticed in the early weeks of the pandemic that people who got a flu shot for the 2008-2009 winter seemed to be more likely to get infected with the pandemic virus than people who hadn't received a flu shot."
> The ferrets in the vaccine group became significantly sicker than the other animals, though all recovered. "The findings that we show are consistent with the increased risk that we saw in the human studies," Ms. Skowronski said.
https://www.theglobeandmail.com/life/health-and-fitness/heal...
Let's focus on three types of antibodies - the things your immune system creates in response to a foreign object in your body - for this story:
1) IgM - this is created in your mucosal membranes when you breathe in something foreign. In the context of COVID, we'd expect to find IgM antibodies in people exposed to the virus because the mucosal membranes of the respiratory systems are the first places exposed to a respiratory virus.
2) IgG3 - this is created in your blood and is the main killer of a foreign object. This is what you think of when your immune system is fighting a virus. It also drives the inflammation which is what you generally recognize as the "flu-like symptoms".
3) IgG4 - this is created in response to what we recognize as allergens. For example, if you breathe in a bunch of pollen in the spring, you may have an IgG3 response and feel terrible. Or you body may recognize that that foreign object really isn't a big deal. In this case it will create IgG4 which basically tells your body to ignore the object until it's cleared. It's kind of the opposite of IgG3: rather than ramping up inflammation to fight the object, it's ramps it down and just says "nothing to see here" so you don't waste resources fighting something harmless.
What they found is that vaxxed and boosted people have a ton of IgG4 floating around and little to no IgM and IgG3.
So what does that mean? Here's where people are going to get spun up because we have to create hypotheses and test them. But even stating some hypotheses will cause the political machine to get mad.
1) IgM is really good at stopping viruses early. From this we'd expect that unvaxxed people exposed to COVID to be more resistant to future infections because the first exposure will create IgM and the virus will be stopped/attenuated in the nose. I don't know the state of the research on this, but it's a hypothesis to test.
2) IgG4 is a bad thing in the context of a replicating virus. If you have IgG4, it's telling your body to ignore the virus because it's "just an allergen". That's fine for pollen which will be cleared out of your system, but it's bad for a replicating virus because it can replicate unfettered. The hypothesis to test here is if people who are more vaxxed have more (re)infections of COVID. Another thought is that the infection may never go away and flare up occasionally (long COVID?). Again, I don't know the research, we need to test these hypotheses to understand it.
But it is one piece of the puzzle and a plausible explanation for this (https://www.medrxiv.org/content/10.1101/2022.12.17.22283625v...) where we see a nearly linear increase in vaccine doses and COVID infection. Again, these are just hypotheses and we need to test them without getting political about the vaccine.
This may also be a plausible explanation for COVID related OAS (Original Antigenic Sin) and ADE (Antibody Dependent Enhancement) that some researchers claim they see.
At a minimum we can say that the more vaxxed and boosted a person is, the more "non-standard" (compared to other vaccines) their immune response is, and that's worth further investigation.
When someone inevitably spins it as "they sold you vaccines that will let you catch the disease _more_ often, we told you so, subscribe to my podcast / buy my book / vote for me / etc...", what is the counterargument ? That we need more data to confirm ? That there can be other factors causing the reinfections ?
At this point, I'm looking forward for someone saying "it's more complicated than that", which is not a great sign :/
In non-emergency cases, we have some random people that follow the right path and that message gets amplified and we find a solution. In this case, that didn't happen (or maybe I should say "hasn't yet happened"). We are seeing with the latest twitter files that some people who were more right then wrong were silenced. The bias towards a more right answer was taken away. Why were they silenced? Could be something as simple a trying to make an easy message "anything that promotes vaccine hesitancy is bad" because good people truly believed that the vaccine would get out of it and they didn't want any confusion.
Back to your comment about "worst case scenario." Yes this is bad, if the vaccine (and in particular the boosters) are actually destroying the immune system, we have a problem. Typically we would have tested this for a long time to see this effect (which is not unknown in the immunology community) but for some reason "we didn't have the time" and we rushed it into millions (billions?) of people. That is bad. Can it get worse? Yes! What if the latent IgG4-enabled virus evolves in vaccinated people and we get another outbreak of a worse virus?
You can probably imagine more bad scenarios. I was a co-author on a paper about significant more (1000x) pregnancy and fertility adverse events after the COVID vaccine compared to the flu vaccine. So we're talking generational effects!
Anyway, not to be too doom and gloom here, but I think you're right "it's more complicated than that" and "we need more data" we just need to collect everything we can, make hypotheses, test them, and learn. That requires lots of open communication.
Extra info: earlier this summer I started to put together a figure to illustrate the "entropy of ignorance" It's outdated, I've learned more since then, but this was my best understanding this summer. You can see how it's easy to have a bad decision keep compounding into more bad decisions. And they can easily happen randomly, it doesn't take nefarious reasons.
Well, in all fairness, the "some reason"s were thousands people dying _every day_ in western countries, overloading health systems. Anyone playing the "let's wait two more years, just to be sure" card had a _very_ hard sell.
To follow your analogy, this is probably a situation where there is vastly more wrong decisions to make, and the right ones require the benefits of 20/20 insight, which, well, GPT-42, maybe ?
To roughly quote a former PM from that period: "my job these days is to arbitrage between bad decisions".
This is were the scientific method of searching for the truth clashes with the politics of managing a human society. Not a particularly new debate, I suppose...
For "laughs" : I almost wish we'd go the complete opposite road next time, keeping the vaxxes in the lab as long a possible, just to see the opposition parties everywhere spread conspiracy theories about the "secret vaccine that the government does not want you to take", etc... Just, for a change.
Wow, that's heavily biased. "Create a culture of fear and weakness -> Enforce useless mask-mandates"? That's extremely biased (and ignorant in itself).
Also, it does not follow potential ramifications of some major decision, for example, "lockdown -> no" ends there, failing to illustrate outcomes when observing current spread rates, mutation rates, and death rates of a virus.
Like, the mRNA vaccines are basically doing the first few steps of what the real virus does: attaching to ACE2 receptors with Spike and producing viral proteins from mRNA. It's hard for me to see where the immune system could get led down a different path.
First, let's look at what happens when you're exposed to a respiratory virus. It gets stuck in your mucus membranes and your immune system starts finding matches. Your immune system starts making antibodies that match parts of the virus. There are hundreds of different fragments (epitopes) that your immune system could look for as a "fingerprint". Of those hundreds, your immune system probably picks dozens or so. That means that a later (mutated) infection will likely have overlap with at least one of those and you'll have a quicker response. This also mostly happens in the mucus membranes and IgM gets involved before anything else gets turned on.
A traditional vaccine uses either a dead or live attenuated whole (or at least a large chunk) of the virus. And that's why we typically have success. There are still lots of epitopes and our immune system picks a few to react to. And your immune system will pick different matches than mine, that gives us a broad spectrum herd immunity because we all react to a different part of the virus, and small mutations never get a chance to win.
With this vaccine we did two things wrong.
1 - We picked one protein, the spike protein, as the only match for the immune system. So the immune system only reacts to one match. That means rather than spreading out and trying a broad approach, the immune system gets hyper focused on only one match. From the immune system's perspective, it only has one thing do to so it starts to over focus on one thing. From the population's perspective, we all react to the same thing, that means there's tons of evoluationary pressure for the virus to mutate away from that one protein and it has a free pass in the entire population (Omicron?)
2 - The second factor is the the delivery mechanism. Normally we use something like an adenovirus to deliver the (attenuated/dead) virus to the cells. What we do is simply inject a whole virus, the immune system sees it and starts the response. This isn't as good as a typical infection because IgM never gets involved, but it works good enough. Here with the mRNA vector, we're injecting the instructions to generate the spike protein and then our cells generate the spike protein which are then attacked (and killed) by the immune system. That's a good story and sounds like really cool science fiction. But there are problems with this
2a - Rather than killing an injected adenovirus, your immune system is killing your own cells that have been hijacked to express spike protein. Granted, you have trillions of cells, that's fine. But there are some cells that don't reproduce and you have all of the ones you're ever going to have (e.g. cardiac muscle). The mRNA was supposed to stay at the injection site, but that was shown very early to not be the case. It can go anywhere, and there's a Japanese study that shows that it tends to collect in cardiac muscle, testes, and ovaries. Don't know why.
2b - Your body doesn't really want mRNA floating around in the blood. We have an enzyme creatively named mRNAase that eats up any mRNA that just floats around (like when a normal cell dies and explodes). So to protect the mRNA good enough to get into your cells we did two things, wrap it in a lipid nanoparticle (little fat bubble). Some people are freaked out about that. I don't know enough to comment on the safety of those. The other thing we did is the scary thing: we used changed some of the bases in the mRNA.
DNA has ATCG as it's bases. RNA uses AUCG. The U is uradine. In nature, sometimes (in very small quantities) the uradine is slightly different, and we call that pseudouradine (I'll use P here, but they really use phi as the symbol). It behaves like uradine, but it looks different. It's harder to break down mRNA with P than U, but it's usually in such small quantities that it doesn't matter.
To make mRNA more stable (and resistant to mRNAase), we made the mRNA delivery with much much more P (I forget the numbers, but very high compared to nature). So what's the problem with that? The way this whole thing is supposed to work: Transfect a human cell with mRNA. mRNA makes Spike. Immune system learns about Spike and kills that cell. That cell explodes (apoptosis) and the contents get cleaned up. Any new infections of Spike are primed to be killed by the immune system. But if that mRNA is pseusourdinated, then it doesn't broken down by the mRNAase and it goes on to transfect a new cell and the cycle continues.
So we have constant production of more spike by our own cells, that both keeps the immune system on alert (this can be driving the IgG4 story) and it also means that our immune system keeps attacking our own cells (autoimmunity).
The way it was described to me is that the mRNA was supposed to be like a log falling in the forest, it would naturally rot and get cleaned up. But we manufactured a fiberglass log that looks in all ways like the natural one, but it doesn't rot.
Long post, sorry.
tl;dr - Natural infection means IgM does most of the work. Traditional vaccine trains the immune system on the whole virus. This vaccine trains the immune system on a single protein in a way that causes it to hyperfocus and kill your own cells and keep your immune system on alert.
The concern here is if the worse-case scenario turns out to be true: that the mRNA-based vaccines, and especially the boosters, end up training the immune system to tolerate the infection rather than clear it. That would mean a significant fraction of the population are at risk of outcomes ranging from persistent COVID to death, and becoming breeding grounds for more variants in the process.
Hopefully further research rules out that scenario.
If you mean “might” instead of “would probably”, then maybe I’d agree that you’re on the right track.
> I don’t think I could have had it any worse.
You’re alive and you haven’t described severe disability lasting at least a year, so this part is just not correct.
Being healthy and young reduces the risk of severe outcomes, but not to zero.
There was a clear indication from the data in Israel that nothing was working as it was advertised in Europe. Now high profile publications are coming out that confirm some of the worst fears, so who knows maybe at some point these people will have to take some accountability.
Also, in general you don't want your immune system to be more aggressive/destructive than necessary when you consider having to rebuild tissue afterwards, which also might include more risks the older you get.
In the case if an infection not seeming life-threatening to your body, a softening of the overall reaction might actually just be the right path to persue. The question is whether we want that in this case or whether we want to further move that towards a more protective optimum in the future with these insights.
For the "I knew it" and "we should have waited" discussion, I personally prefer an early protection, even with a lower reaction, that still keeps me from being hospitalized over being nakedly exposed like we were in the early days of that pandemic. We might have forgotten about this with the current "mild" Omicron variant.
I would love to see the study include severe breakthrough infections, if there are any, to see if the dampening effect and antibody distribution would be different in these cases.
Source? And why are the non-mRNA vax not showing this effect?
> that still keeps me from being hospitalized over being nakedly exposed like we were in the early days of that pandemic
Unless you were elderly (over 60 or 65) or have comorbidities, it should have at least been a choice to take it or not take it. Instead we got mandates and sold the dream of the vax ending the pandemic.
So, what about it? Is this effect powerful enough to be helpful?
But did you mean "strains that are not using the spike protein anymore to enter cells"?
In which case, why do you think it would be harder to tackle than the original virus?
In my opinion, the same work (developing again mRNA vaccines etc) could also apply to any other receptor, couldn't they?
Yes, new mRNA vaccines could be produced and distributed, thereby generating even more tolerance as this article shows and making things even worse for people's immune systems if so. The point is these vaccines are generating resistance to the virus but at the same time, unlike traditional ones, they are making the immune systems tolerant of the virus. The infection is incompletely suppressed, symptoms are mild or imperceptible, but the virus is getting passed on despite being partly suppressed.
The emergence of new strains is favored when there is a large medium (the reservoir population of people, tolerant but infected and shedding) where the virus can proliferate (thus plenty of viral code copying, where mutations happen) and where there is selective pressure (i.e., an advantage to the new strain such as being able to enter cells even more effectively because of the lack of interference compared to the current strain) for a mutated virus to thrive.
It would be harder to tackle because it would be even more infective than the current strain (given the tolerance that has been introduced in the population) but at the same time more aggressive (because more cells being entered would mean more damage to the body) and maybe with different kinds of damage (because it could trigger autoimmune responses, they say, although I'm not sure how that argument goes).
I'm not an expert on this so I cannot elaborate further, but that's the idea as far as I grasp it. We'll see, I guess.