I mistyped, it's
inactivated (barely a smidgen of meaning difference between the two words), and it's cultivated virus (or other pathogen, for non-viral diseases) that is
somehow 'killed' to be harmless. (In contrast with 'Live' which is weakened/attenuated.)
They can be 'whole virus' (though killed[1], perhaps by heat treatment or chemicals - I haven't checked what for the Sinopharm(s)) or 'split virus' where detergents actually fragment it to present as much (dismembered) virus-'body' to the immune system as possible. Either way, you'll get 'spike' resistance (natively) but probably loads of other responses that are useful.
Purify/concentrate the more useful components of a Split Virus soup and you get a 'subunit vaccine' (there are some of these in the fight against Covid, but not widely accepted). Spikes are sure to be in the mix, I imagine. I suppose you could even painstakingly construct such fragments outwith any original virus, but not sure this has been used for any of these "potentially millions of doses" treatments, as there's a lot of scaling issues.
Because anything not totally 'Live' is harder to discover as a Pathogen(-fragment) Of Interest, they tend to add further stuff to 'irritate' the immune system/wave and shout "Hey, look at us! We're invaders! Learn to fear us! *Ouch*"... This has been (minute amounts of) mercury, but it's
probably certainly something else these days. Not a heavy metal, even..?
The Sputnik, as with my own Oxford/AZ, uses a modified Adenovirus (chimp for AZ, not sure about Sputnik) which is non-replicating but contains "make bits of Covid" instructions that it can push into cells, let the cells make the bits and then present them to the immune system as per a concentrated split-soup (or nearly so) but more controllable once they have the AdV down pat. One disadvantage is that many people have adenovirus-exposure already so might be jumped on a
little too quickly. (That my fever kicked in after several hours might indicate it was response to the message, as finally read out, not the initial messenger. Based only on guesses, though.) What they (hope to) produce for immune-training will vary, but probably include spikes as priority. I'm not sure what stops the instructions being followed (once started) but must be related to standard DNA/(m|t)RNA shuffling. (It never gets into the genome, just mingles with the transferred instructions that came from there... I don't know as much about this as I should, but there must be a time-out/half-life to moderate any internally-slurved instruction not regularly given a repeated expression.)
Then DNA/RNA capsid vaccines do the same sort of thing as above but with a lipid-monolayer 'nanoparticle' container tailored to deliver just the blueprints into target cells, for them to distribute, without any virus in any traditional sense. Pfizer codes
I think just for the spikes, which
the body happily makes so long as (I think) they are still intact in the cell's endosomic organelles they get sucked into to start the work (again, never gets near your genes).
I'm sure there's more to know about each, but that's a less-than-summarised summary mostly from memory/extrapolation. Someone will doubtless be along to correct my schoolboy errors.
[1] A tricky word to use for a virus, that is not ever fully 'alive', but it seems to be the best to use.