As the member has pointed out, the bivalent vaccines, which have been recently authorized and recommended in Canada—from both Pfizer and Moderna—have been authorized based on antibody levels and neutralizing antibody titres.
That's not the same as clinical effectiveness, where we see in the real world how many cases of COVID-19 or particularly how many severe disease cases, hospitalizations and deaths are being prevented. However, we have seen in general, throughout the pandemic, a fairly strong correlation with neutralizing antibodies: Higher levels of antibodies can be protective against some of these outcomes. We don't have a correlative protection, so we don't know exactly what line in the sand you can draw to say you will prevent x number of cases with x level of antibodies, but there does seem to be a general trend of correlation that we are observing.
Those new vaccines have been authorized and recommended based on higher levels of antibodies against omicron strains, which is a good thing. As Dr. Tam noted in some of her opening responses, the direction so far that we're seeing in the variant environment is continuing toward omicron subvariants, so there's an advantage to having the immune system primed or boosted with omicron-containing vaccines.
While we see higher antibody levels in these products, we don't yet have the real-world evidence, and there's generally been a pattern throughout the pandemic of how this evidence comes to bear. We have research partners in provinces and territories in Canada who conduct vaccine effectiveness studies and monitoring, or the surveillance of how the vaccines perform once they're deployed. We know that the U.S. and the U.K. also have strongly based research groups that can issue those kinds of data and those estimates.
The general trend we've seen through the pandemic is that once the vaccines are deployed, somewhere between two and six months after the deployment we start seeing the real-world effectiveness data come in. We're on that track now that the bivalent vaccines are rolling out in Canada. We know that many millions of doses have been used in the U.S. as well, and also in the United Kingdom, so we do expect to see those vaccine effectiveness estimates start coming in.
I will note that the entire vaccine effectiveness monitoring landscape is becoming increasingly complex, because we now have multiple different vaccine products that people have had in terms of boosters. They've had different vaccine experiences through their primary series, and also we have different levels of infection from either pre-omicron variants or omicron variants. We have a very different mix of population in terms of who's been infected and who's had x number of boosters, so to actually try to calculate vaccine effectiveness is becoming harder and harder. It's probably not going to be a simple answer that it's x per cent, because it has to take into account whether it will be x per cent for people who have been previously infected or x per cent for people who have had x number of boosters. It's becoming more and more complex, but we are well established to be able to monitor this and see research estimates coming in over the coming months.
I will also note that this is very similar to how we conduct influenza vaccine programs, where we, as Dr. Tam noted, have strain substitutions and launch new products in the fall. Then the effectiveness monitoring comes in months after, and we see how the products perform in the real world. We're making some early assumptions based on the way the vaccines have been studied in the trials, and then we're deploying them and following up with the real-world effectiveness, which can feed back into policies and guidelines that can be updated, so it becomes a research or a knowledge cycle.
Thank you.