I know what you mean is "not dormant and doing something for months/years", but at the same time, if it can initiate a modification of immune response, it can do "other things".
I believe we must take the utmost of care at this juncture, and make sure assurances are not construed as in a poor light.
So, even if producing the proteins turns out to be somewhat harmful long term, it cannot possibly be as harmful as the whole virus.
Assuming that covid infection is inevtable without a vaccine, we really have a choice between getting a little bit of mRNA injected into our cells, and a ton of mRNA injected.
https://www.sciencedaily.com/releases/2016/03/160322100714.h...
The extent to which a molecule is active in your body is only slightly correlated with toxicity. There is zero reason why a fragile molecule can't cause damage before it breaks down.
This is how ended up with thalidomide. They tested it in pregnant lab rats, but the window for birth defects is incredibly short in rats. So everything checked out.
In drug development you can't assume anything without data to back it up.
The FDA at this point certainly doesn't have the ability to analyze that either, so the best we have is a theoretical understanding.
Are there any notable helpers or adjuvants or preservatives?