Decoding the success of the pfizer vaccine - the statesman
Decoding the success of the pfizer vaccine - the statesman"
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Preliminary data from the Pfizer/ BioNTech COVID-19 vaccine trial suggests it provides 90 per cent efficacy at preventing the disease. At the very least, this news will result in a large
sigh of relief across the vaccine community. It signifies a breakthrough – it’s the first announcement that a vaccine can protect against SARS-CoV-2 infection in humans. This shows it can be
done. But how well it can be done is still a big question that no one has the answer to. These results are promising, but there’s a lot more we now need to confirm. Advertisement The 90 per
cent efficacy is a strong result, but we should remember that this is an interim analysis, based on 94 cases of disease that have occurred across those receiving either the vaccine or a
placebo. Pfizer has noted in its trial protocol that it needs at least 164 cases of disease to occur across the study to reliably assess the vaccine’s efficacy. Advertisement If subsequent
cases occur more frequently among those who have had the vaccine rather than the placebo, then this efficacy figure will fall. So, we don’t yet know if this number is truly reflective of the
vaccine’s protective ability – meaning crucially, we need to get to the end of the trial. But if this is the case, why announce these interim results now? An interim analysis of trial data
like this isn’t uncommon, particularly in phase 3 vaccine trials, as it’s not unusual for trials to fail during testing. Therefore, you need to determine as soon as you can, with as much
robustness as you can, whether pursuing the trial is worthwhile. Continuing when things are futile is a waste of resources – and in some cases unethical. The only way to see whether
continuing is the right option is for the trial’s independent data and safety monitoring board to look at some or all of the results. For Covid19, where time is a major constraint, many
efforts have been made to incorporate interim analysis into studies in a way that provides an answer, with some confidence, in as timely a manner as possible. This interim review was
therefore planned at the start of the trial and has fulfilled its purpose. It is a very positive signal that the trial needs to continue – even if the actual data from the review leaves us
with many questions. One key thing these interim results don’t tell us is how long protection lasts. Participants in this phase 3 trial received two doses of the vaccine, and measurement of
its efficacy was taken seven days after the second dose was given. This is likely around the height of the initial immune response. It will be really important to understand how durable this
initial protection is after this point. A pessimist would hope for retaining efficacy for at least three months. An optimist would hope for retaining high levels of protection for a number
of years. However, being realistic, this mRNA-based vaccine platform is new, and so we’ll need time to understand if and when the initial response starts to wane. We also need to understand
if this vaccine and others in development can induce good memory responses from the immune system that will provide protection for years to come. It’s also important to identify the exact
immune response that is mediating protection – what are called the “correlates of protection”. Is it a particular type of antibody or T cell that’s involved, and what is the threshold amount
of these needed to protect an individual? With this knowledge, future trials can focus on measuring the quantity of these immune markers in individuals to better assess whether vaccines are
working. One other important thing we need to know is whether the vaccine completely prevents people from getting infected with any virus at all, or if it simply makes people more effective
at fighting the virus off if they do succumb to some infection. This will govern whether the vaccine prevents only disease or can prevent viral transmission as well. All we know at the
moment is that it has reduced symptomatic cases by 90 per cent. Though it doesn’t have the full picture, the US FDA has said it will consider authorising the vaccine for emergency use –
ahead of full approval – once the trial has collected two months’ worth of safety data on half of the participants. Pfizer expects to have this available by the third week of November. The
trial will also continue for many months to come – in order to reach that reliability threshold of 164 cases of disease – and there will be further follow-ups looking at the vaccine’s safety
and the immune responses and protection it elicits in different groups of participants. This should give further transparent information and confidence on how well this vaccine works and in
which populations. If the vaccine’s safety and efficacy are looking good, it will then be submitted to regulatory agencies for full approval. The highest risk groups will then be first in
line for immunisation. In the UK, this will likely include care home residents and workers, health and social care workers, and people over 80, assuming the vaccine is shown to be safe and
effective in these groups. In Europe, prioritised groups include healthcare and essential workers, those vulnerable to the disease and socioeconomically disadvantaged people. But even if
approved, big challenges remain. Pfizer expects to have 50 million doses ready this year, enough to immunise 25 million people, and 1.3 billion by the end of 2021. Given the size of the
world’s population – and the fact the vaccine requires two doses – universal coverage is a long way away. The other vaccines in development therefore remain just as important. We will need
more than one vaccine for global coverage, and to ensure we have the right one for each age and health cohort. Overall, these results should be celebrated, but with the realisation that this
is only one step in the journey. We still have a long way to go in getting the world back to normal – but the compass is pointing in the right direction. The writer is Senior Lecturer in
Biochemistry and Cell Biology, University College Cork. This article was published on www.theconversation.com Advertisement
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