Two problems?
The 70% threshold depends how infectious the virus is in a completely non immune population. ...It corresponds to an R0 around 2.6 as originally claimed for covid. If the real R0 is much higher than this, then you need much more. If R0 was 10, then you need 90% immune to bring that downe to an observed R of 1.0. I think the best explanation how this epidemic has evolved ia real Ro higher than this, which however did not find us completely non immune. There is proven cross immunity with other corona viruses (AKA 'colds'), and also with sars and mers where these borke out in -er-.... the pacific region where covid has been more easily controlled.
Cross immunity is more accurately called cross reactivity. The problem with the word immunity is that it is not binary. And cross reactivity in fact does not even necessarily infer cross protection.
For example, cross-reactivity can also destructively interfere, where immune response to one pathogen lowers the response to a different pathogen.
Which does a better job will only be discovered in the field, and especially as new variants come along we will see if natural or vaccine immunityb holds up better against them.
So far, the vaccines have won that battle.
Of course, the british government for one is determined to eradicate all unvaccinated peope, so we will never know if natural immunity works better than vaccinated. It will all be claimed as the benefit of being vaccinated when clearly it
is not.
Yes, in what I presume is the misguided aim of (at least occasionally) attempting to minimize the death count, they have vaccinated people. Go figure.
Well actually they do infect and then presumably lead to the death of body cells. Thats deliberate. It is somewhat different to what I understand as the traditional approach where you inject a dead virus and there is simply a response to eradicate from the blood what was injected. The vaccines do take over body cells to amplify the effect of just the injected virus components.
I actually said the vaccines cannot commandeer host cells and reproduce, and you cannot get long covid from the vaccines. As a result, the amount of body cells that are destroyed is significant lower.
But as you mention it,
the definition of infection is the invasion of bodily tissue by pathogenic microorganisms that proliferate, resulting in tissue injury that can progress to disease. And thus, the
vaccines cannot infect.
The mRNA and adenovirus platform vaccines don't take over body cells. They can't infect you. They can't make you sick. In both cases they contain portions of the spike, so they can't enter your cells and interfere with your DNA.
The california study suggested actually some research has said this isnt true. I guess as you say the reason why the spike would be preserved is because its exact formulation is critical to its success in entering cells. But that doesnt mean no change is possible, only that its difficult to do. But on the other hand, faced with a huge antibody response to this spike, there is also huge adaptive pressure upon the virus to change the spike as it has become a critical area of failure.
Okay, so like other coronaviruses, SARS-CoV-2 use a spike glycoprotein on the envelope to bind to their cellular receptors (ACE2). This binding triggers a cascade of events that leads to the fusion between cell and viral membranes, facilitating cell entry. Within the spike, there are two key subunits - S1 and S2 - that mediate for cell attachment and membrane fusion respectively. There is a short domain within the S1 subunit containing two glycosylation sites. These secrete short fragments of receptor binding domain that bind to the ACE2 receptor.
So, its not so much a concern that portions of the spike mutates. Its more the case that the ACE2 binding subunit, by nature, is highly conserved as the binding of the viral RBD on its S-domain is an essential step for membrane fusion and entry into target host cells. It is only at that stage can the S2 domain transition from its pre-fusion state to its stable post-fusion state.
It is true that the delta variant has a couple of S1 mutations which enable it to bind better to ACE2 whilst also helping it avoid immune system recognition. But
the Delta spike evades neutralizing antibodies triggered by both infection and vaccination. The likely explanation for the increased spread of Delta variant in India (where seroprevalence can be higher than 70%) is natural infection immune evasion, i.e., the ability to spread in a population in which a substantial portion of individuals has pre-existing immune responses against SARS-CoV-2. This is certainly the case in certain resource-poor communities across India.
Thus far, the two-dose vaccination protocol has held against Delta in preventing moderate to severe illness - much more effectively than natural infection. It was always anticipated that vaccine tweaks for boosters might be necessary to cover variants (much like the annual 'flu vaccines). To date, we haven't needed these yet.
Being double-vaccinated by an mRNA vaccine still provides the best protection against the Delta variant, irrespective of whether you have contracted the Alpha/Beta variants or not. In fact, having contracted it naturally plus subsequent vaccinations gives an even stronger response to the vaccines, and thus subsequent infections. There is little downside to the mRNA vaccinations.
Thus.. it may be better to use a diffuse approach in vaccine or natural immnity, because if you use a target one it risk creating this huge pressure for the virus to change exacty there. Sciens has made an assumtion about how best to make a vaccine, which might simply be wrong. This is quite possible the first real field trial. IT IS the first full scale trial of either of these new vaccine delivery systems.
Science makes guesses, called hypothesis, which are logical assumption based on available evidence. The next part of science validates these guesses, through empirical testing, and uses this evidence to mature and explain the hypothesis by way of a thesis.
None of the big pharmaceutical companies go about injecting people with these vaccines without having a highly detailed understanding at the cellular level of how exactly they function.
No, they are. Really, they are!
All of the public health bodies globally
genuinely are of the converse opinion to yours.
They claim massive success based upon massive generation of specific antibody. In the field results in the UK are not nearly so good. Its quite interesting reading some of the posts on here from the US, where much greater vaccine success is being claimed, but mostly not against the Indian/delta strain. Which is a kinda important caveat since covid has mutated its spike, which is what it isnt supposed to be able to do.
Who said SARS-CoV-2 isn't "supposed" to be able to mutate its spike? There have been over 4,000 mutations have been detected in its spike protein alone. Accepting this, the spike is still highly conserved.
"They" claimed success based on preventing people from contracting moderate to severe disease and in preventing hospitalisations.
Also, they don't claim success based on generation of a specific antibody. You don't appear to understand how vaccines are licensed. Eliciting the immune response of a specific antibody alone would fall fair short of the meeting the burden of proof, and certainly wouldn't qualify a vaccine for emergency use. You have to prove the vaccine does *something* (i.e., generate an immune response - in the case of vaccines, antibodies plus T-cell responses), *and* that the immune response is efficacious (i.e., keeps people out of hospital), *and* that any potential side effects are captured, and that said side effects, if present, are outweighed by the benefit of taking the vaccine.
I haven't seen any "field results" from the UK that are bad. On the contrary, the vaccines have worked incredibly. You can see in the UK that they have strongly attenuated the link between infection and hospitalisation. In the US, it appears to be a disease of the unvaccinated (with the caveat that the US numbers were wildly inaccurate during Trump and undercounting, and presumably have swung the other way somewhat with Biden with overcounting)...
Whilst the UK case numbers are screwy at the moment (the 5-day dip is not entirely surprising, and likely explained by a combination of the Euros ending, schools finishing, and the general muddle in British testing anyway and any political interference or messing that has gone on -- I am convinced British case numbers are under-counted at the moment), it will be very interesting to see what happens over the next 2 weeks as the removal of all restrictions leads to a subsequent uptick or whether hospitalisations remain stable.
If they do remain stable, we may well be starting to move from pandemic to endemic, which would be terrific. However, there is still plenty left to be explained in the pursuit of ensuring we do no harm. For example, Israel was ahead of the UK on vaccination and yet it has had to reverse some of its reopening.