As noted above, immunology is a complex thing.
I used to have chronic Hepatitis B.
When people get a Hepatitis B viral infection, they develop two antigens - one which is a surface antigen, and one which is a core antigen. With these two antigens, the body fights the infection and people get better.
But some people only develop a partial immune system response - they only develop the surface antigen. Without the assistance of the core antigen, the body can only fight the HepB virus to a standstill, with the liver as a long-term battleground. Over time, this causes more and more liver damage leading to cirrhosis and raising the risks of hepatic cancer. This is chronic Hepatitis B. Oh, and the virus may mutate over this time which makes it harder for the body to control.
One of the primary causes of chronic Hepatitis B is maternal infection - the mother has chronic Hepatitis B, and the baby also gets exposed to the virus during birth. In this case, the undeveloped immune system of the child also does not develop core antigens and so chronic Hepatitis B develops.
I know I did not get Hepatitis B via this route - my mother never had Hepatitis B. So I was exposed at some other time (maybe what they call playground exposure to a classmates blood). But however I was exposed, my immune system was sufficiently inactive at the time so as to not develop core antigens.
30-40 years later, and I have mild fibrosis of the liver, and I am given anti-virals to control the virus. In general, this does not help clear the virus, it just maintains a very low viral load. I happened to move countries, and my new specialist put me forward for a stage 1 drug trial.
This trial drug was manufactured by a genetically engineered yeast that expressed the Hepatitis B core protein, so as to stimulate the immune system to produce the required core antigens - exactly like a vaccine. I had one immunologist clearly tell me at the start of the trial that he didn’t think that the approach would work, so I shouldn’t get too excited. From the results after 18 months of treatments, there was a suitable immunological response, but not one that was sufficiently large enough or remained long enough to produce a cure.
So I joined a new trial. In this trial, we were not only given the vaccine, but also an immune system modulator to extend the time the T-cells expressing the core antigen were active (PD-1 modulation).
And it worked for me. I had a flare in my liver enzymes that could have been an autoimmune hepatitis from the PD-1 modulator, but it wasn’t - it was all the infected liver cells dying as my now supercharged immune system cleared the virus, and I was eventually discharged, free of Hepatitis B.
But I was the only subject in that phase of the trial to have that response.
Was my immune system stronger at that time than the other subjects - I doubt it.
Did the PD-1 modulator tweak my immune system just in the right way - maybe.
I don’t know. What I do know is that I had an immune system that went from not handling a particular pathogen as a child, to fighting a holding action for 40 years, to (with a couple of nudges in the right direction) kicking that pathogen to the curb in a medically unique way.
I don’t think the trial researchers know (yet). I let them take all the data they needed (blood mostly - so many tubes of blood).
I know they are still running trials to discover better ways of using those tools to get better and more consistent results so they can develop something that cures a disease, and not just contains it.
So I think the fact is that at any one time, you might have the worlds strongest immune system against a particular pathogen. You might even be exposed to that pathogen.
But yesterday, tomorrow, next week - it’s a different story.