WEBVTT - Inside the Race to Develop a Coronavirus Vaccine

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<v Speaker 1>It's Monday, April six. I'm Oscar Ramires from the Daily

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<v Speaker 1>Dive podcast in Los Angeles, and this is your daily

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<v Speaker 1>coronavirus update while we brace ourselves to make it through

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<v Speaker 1>this time. Right now, the scientific community around the world

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<v Speaker 1>is in a race to develop a vaccine for COVID nineteen.

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<v Speaker 1>There are currently at least forty three different vaccines and

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<v Speaker 1>development around the world, but the process remains slow. Well,

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<v Speaker 1>many things have changed about how to develop vaccines, such

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<v Speaker 1>as being able to target the DNA and RNA of

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<v Speaker 1>the viruses in quick fashion, the rest of the process,

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<v Speaker 1>testing in humans and also manufacturing for wide use, remains

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<v Speaker 1>very slow. That is why we might still be a

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<v Speaker 1>year away from an effective vaccine some months. Supermannian contributor

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<v Speaker 1>to The Guardian long Reads, joins us for the work

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<v Speaker 1>behind the race to develop a coronavirus vaccine. Thanks for

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<v Speaker 1>joining us a month happy. I wanted to continue talking

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<v Speaker 1>about coronavirus COVID nineteen, and one of the things that

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<v Speaker 1>everybody is racing for to get completed is a vaccine.

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<v Speaker 1>We've been told for a while now, since this whole

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<v Speaker 1>pandemic started, that it was going to take twelve to

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<v Speaker 1>eighteen months something like that to really get an effective vaccine.

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<v Speaker 1>And because it just takes a long time, the human trials,

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<v Speaker 1>the studying of it takes a long time. What has

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<v Speaker 1>changed is actually being able to get vaccine candidates. Uh,

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<v Speaker 1>that's changed, and it's much much quicker than it's been

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<v Speaker 1>in the past. Currently, there's at least forty three COVID

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<v Speaker 1>nineteen vaccines in development around the world, and everybody is

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<v Speaker 1>racing to to do this. There's one vaccine that was

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<v Speaker 1>made in sixty three days by the American biotech firm

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<v Speaker 1>nay More Moderna, and they're actually doing human trials already

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<v Speaker 1>though started on March sixteen. So some tell us a

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<v Speaker 1>little bit about the vaccine making process and and and

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<v Speaker 1>how it's changed over the years as well well. So

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<v Speaker 1>the vaccine, you know, the principle of vaccination hasn't changed

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<v Speaker 1>at all, right, I've any idea is to get um

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<v Speaker 1>your immune system to record eyes a virus or a

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<v Speaker 1>bacteria without actually making you sick. So what they used

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<v Speaker 1>to do earlier was they used to weaken a virus

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<v Speaker 1>or a bacteria and they would introduce that into your

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<v Speaker 1>body and your immune system would recognize it and it

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<v Speaker 1>would generate all these antibodies that tend to stay in

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<v Speaker 1>your system, so the body learns to fight this germ.

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<v Speaker 1>And then when you actually get infected with a full

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<v Speaker 1>strength strain of this pathogen, your body can fight it off.

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<v Speaker 1>It has all these antibodies and t sales and you

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<v Speaker 1>can fight these pathogens. So that's how they used to

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<v Speaker 1>do it earlier, and that was the case for you know,

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<v Speaker 1>most of the twentieth century. They would take these viruses

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<v Speaker 1>of these bacteria and they would put them in cell cultures,

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<v Speaker 1>tissue cultures and labs, and they would try to weaken

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<v Speaker 1>these trains. And sometimes it was a really tricky process

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<v Speaker 1>to do. I mean, it's very difficult if you aren't

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<v Speaker 1>quite um, you know, in possession of the kind of

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<v Speaker 1>sensitive equipment that we have right now. The first step

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<v Speaker 1>forward from that was when scientists realized that, look, you

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<v Speaker 1>don't have to put the entire via it us into

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<v Speaker 1>a body. You can just put a part of the

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<v Speaker 1>virus or a part of the bacteria into the body

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<v Speaker 1>and the antibodies will still be generated. So they would

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<v Speaker 1>take like some molecules of a particular toxin that a

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<v Speaker 1>bacteria would release, or they would take a part of

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<v Speaker 1>the shell on the outside that the bacteria or the

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<v Speaker 1>virus have, and they would introduce these molecules into our bodies.

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<v Speaker 1>And that's you know, already sort of thousands of times

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<v Speaker 1>smaller than the bacteria or the virus itself, which are tiny.

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<v Speaker 1>And then what's happened over the last few years, and really,

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<v Speaker 1>I mean, you know, this has been development for a while,

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<v Speaker 1>but genetic technology has only come up to a particular

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<v Speaker 1>speed and efficiency and power over the last few years.

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<v Speaker 1>Is that instead of making these molecules, you know, the

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<v Speaker 1>toxin or the protein shell or the outside, instead of

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<v Speaker 1>making them in labs or in factories, what scientists have

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<v Speaker 1>learned to do is to take short snatches of the

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<v Speaker 1>genetic material of the bacteria or the IRUs itself, which

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<v Speaker 1>you know, has the instructions coded to produce these toxins

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<v Speaker 1>or these protein shells and so on, and put the

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<v Speaker 1>genetic material directly into a body, into a vaccine, and

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<v Speaker 1>use ourselves, our bodies as factories for making these molecules.

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<v Speaker 1>So you've gone from introducing the whole pathogen to introducing

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<v Speaker 1>a part of the pathogen, to now introducing the genetic

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<v Speaker 1>material that codes for a part of the pathogen, so

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<v Speaker 1>you're just putting the gene you know, you're synthesizing these

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<v Speaker 1>genes outside in a lab and you're putting those genes

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<v Speaker 1>into your body. Now I should mention that this last bit,

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<v Speaker 1>the vaccines that use DNA or RNA, these genetic material vaccines,

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<v Speaker 1>you know, these are completely unproven. You know, they've they've

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<v Speaker 1>been sort of tested in labs, um there's been a

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<v Speaker 1>couple of human trials, but we haven't ever had a

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<v Speaker 1>real world vaccine out there that works on this principle yet.

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<v Speaker 1>So it's really fast to do, but we still don't

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<v Speaker 1>know whether it's and work, if it will go through

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<v Speaker 1>human trials and succeed and get out on the market

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<v Speaker 1>for all of us to use. And that's one of

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<v Speaker 1>the interesting parts about this is that, as you were

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<v Speaker 1>mentioning beforehand, UH scientists had to use parts of the

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<v Speaker 1>actual virus they were dealing with that organism there. And

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<v Speaker 1>now a lot of this stuff is being done on

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<v Speaker 1>computer modeling. You know. After China release the full genome

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<v Speaker 1>of the coronavirus of COVID nineteen, scientists were immediately getting

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<v Speaker 1>onto it to start seeing what they can do, what

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<v Speaker 1>they could use to try to make effective vaccines for it.

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<v Speaker 1>That's right. I mean, I think, like because sequencing the

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<v Speaker 1>genome of a small organism like a bacteria aut virus

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<v Speaker 1>is now so quick. You know, they have that, They

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<v Speaker 1>had that online and like mid January, and as I

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<v Speaker 1>say in my story, I mean that's sort of like

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<v Speaker 1>a startup stol for all these scientists everywhere to look

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<v Speaker 1>at the genome and try to understand what parts of

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<v Speaker 1>this virus, uh they might want to introduce them to

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<v Speaker 1>our body, and what parts of the genome code for

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<v Speaker 1>those sections of the virus, the sub units of the virus,

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<v Speaker 1>and so really that that's the you know, that's the

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<v Speaker 1>powerhouse beginning to this entire process. And then, as you

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<v Speaker 1>say quite rightly, I mean a lot of the work

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<v Speaker 1>happens in computers right up until they actually synthesize these genes.

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<v Speaker 1>Everything is happening online. All this modeling is happening with software,

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<v Speaker 1>and then they get these genes back and then they

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<v Speaker 1>start to deal with real world testing on mice and

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<v Speaker 1>other animals. And this is the part that takes obviously

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<v Speaker 1>the longest part. Now, I mean we're just talking about

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<v Speaker 1>how quickly now they can get this candidates, they can

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<v Speaker 1>figure something out. But the real world testing, the human trials,

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<v Speaker 1>and then the manufacturing of this this is the slow part.

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<v Speaker 1>So when people say, hey, twelve to eighty months, this

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<v Speaker 1>is the bulk of the time right there. Yeah, I mean,

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<v Speaker 1>you know, both of these things are slow. So human

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<v Speaker 1>trials can only proceed at the lay at the rate

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<v Speaker 1>of human physiology. Right. We can't speed our systems up

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<v Speaker 1>to react quicker or slower to give scientists results, So

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<v Speaker 1>it has to go just as slow as as it

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<v Speaker 1>can go. Um. But but the problem also is human

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<v Speaker 1>physiology is so complicated. Uh, we can test these vaccines

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<v Speaker 1>as much as we want on computers or in mice,

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<v Speaker 1>but when it comes to putting something into a human body,

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<v Speaker 1>it's impossible to predict the kind of side effects it

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<v Speaker 1>will have, what kind of dosage will work, whether it

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<v Speaker 1>will work at all. You know, it's impossible to predict

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<v Speaker 1>all of this stuff. So that takes takes time. And

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<v Speaker 1>then the second part of it is just sort of

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<v Speaker 1>economics in a sense. It's business. Uh, you need a

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<v Speaker 1>big drug company with the equipment and factories and so

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<v Speaker 1>on to manufacture these huge doses of vaccines, but very

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<v Speaker 1>Often companies don't want to touch vaccines unless they're sure

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<v Speaker 1>there's like a profit margin in there for them. So

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<v Speaker 1>if they you know, if we come through human trials

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<v Speaker 1>for this vaccine, say by January next year, let's assume

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<v Speaker 1>I don't know if that's the right time scale, but

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<v Speaker 1>you know, by that time, coronavirus everywhere around the world

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<v Speaker 1>might have shrunk, the pandemic won't quite be as virulent

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<v Speaker 1>as it is now, and so companies at that point

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<v Speaker 1>might look at us and say, well, you know, we

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<v Speaker 1>don't want to touch this as a product. I mean,

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<v Speaker 1>there's not many people who need to be vaccinated. Most

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<v Speaker 1>of the world has immunity to it. So what's going

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<v Speaker 1>to happen? Then we have no way of knowing. So

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<v Speaker 1>there's so many moving parts in both how complex human

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<v Speaker 1>physiology is and in the economics of this. That's why

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<v Speaker 1>it's going to take twelve to eighteen months if we're lucky,

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<v Speaker 1>for a vaccine to be out on the market. And

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<v Speaker 1>we know that's true because it's happened before. There were

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<v Speaker 1>vaccines in the process for stars when that was going around,

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<v Speaker 1>and because you know, by the time they were getting

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<v Speaker 1>around to getting something that was viable. Everything had calmed

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<v Speaker 1>down with stars, so funding for that stuff dried up

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<v Speaker 1>very quickly. So I think this I'm I'm hoping this

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<v Speaker 1>might be a different case because there's a lot more

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<v Speaker 1>eyes on this. You know, it's this whole big thing

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<v Speaker 1>that everybody's kind of paying attention to, so hopefully it's different.

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<v Speaker 1>But you know, we've gone through this process before. Um

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<v Speaker 1>you know, some of the experts have said that for

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<v Speaker 1>the cost of this vaccine to produce and manufacture enough

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<v Speaker 1>to maybe be the pandemic, it could be about three

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<v Speaker 1>billion dollars. But you know, as you mentioned, everything is

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<v Speaker 1>constantly changing with all of this. For this story, you

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<v Speaker 1>you actually spoke to a Canadian pathologist. His name is

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<v Speaker 1>Jonathan Heeney. He works with a company who's also working

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<v Speaker 1>on a possible vaccine. What can you tell us about

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<v Speaker 1>their work and you know what you're learning from them? Well,

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<v Speaker 1>so um perious company, which is called deal sin Vax,

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<v Speaker 1>is based here in Cambridge, England, where I live. And

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<v Speaker 1>you know, it's just the strangeness of the world right

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<v Speaker 1>now that they're about a twelve minute bicycle right from

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<v Speaker 1>where I live, and I was unable to visit because

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<v Speaker 1>you know, he can't take the risk of outsiders coming

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<v Speaker 1>in possibly carrying a virus and infecting his stuff, infecting him.

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<v Speaker 1>So we had to speak on zoom on like video conference,

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<v Speaker 1>even though he's so close to what I live. And they,

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<v Speaker 1>you know, like a lot of other UH labs and

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<v Speaker 1>universities and you know, companies around the world. They started

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<v Speaker 1>work as soon as genomal published in January twelve or

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<v Speaker 1>just after. UM. What they're doing is kind of different.

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<v Speaker 1>I think it's more ambitious. UH. They're trying to build

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<v Speaker 1>this vaccine that will not just work against this coronavirus

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<v Speaker 1>disease COVID nineteen, but also against you know, many members

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<v Speaker 1>of the family of coronaviruses. You know, so sours for example,

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<v Speaker 1>was caused by a coronavirus as well. And so their

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<v Speaker 1>idea is to get this vaccine, UH, to replicate within

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<v Speaker 1>us the production of common parts of all these viruses.

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<v Speaker 1>So every virus has something called a spike protein on

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<v Speaker 1>the outside of the shell, so they'll make maybe you know,

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<v Speaker 1>the vaccine will come into the human body and it

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<v Speaker 1>will make a part of the spike protein that is

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<v Speaker 1>common across all these coronaviruses. Maybe it'll make two or

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<v Speaker 1>three out of four other sections of the same viruses.

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<v Speaker 1>So there's two or three or four common elements floating around.

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<v Speaker 1>And the theory is that the antibodies that our body

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<v Speaker 1>releases will then be able to eventually work against all

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<v Speaker 1>of these coronaviruses. And this is his thing, right, he

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<v Speaker 1>needs things. He has a platform where he uh he's

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<v Speaker 1>done this for philo viruses, so um West Nile virus

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<v Speaker 1>for example, that diseases called caused by a fire of

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<v Speaker 1>philo virus, and he has a platform for that. He's

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<v Speaker 1>working on a universal flu vaccine which will hopefully work

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<v Speaker 1>against every kind of flu out there. So that's his

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<v Speaker 1>that's his big m o. And uh, you know, I mean,

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<v Speaker 1>as I said, as he says, it's early days. They're

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<v Speaker 1>still doing trials on mice. Uh. And he you know,

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<v Speaker 1>he says quite um, quite clearly that the vaccine field

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<v Speaker 1>has his graveyard full of dead vaccine candidates. So he's

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<v Speaker 1>quite realistic about his chances. But it's a it's an

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<v Speaker 1>ambitious thing to try for. And I I had a

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<v Speaker 1>great time talking to him. Yeah, I mean, it's amazing.

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<v Speaker 1>And at the same time, you know, you mentioned the

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<v Speaker 1>article talking to a bunch of people. Excuse me, you

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<v Speaker 1>mentioned the article talking to a bunch of people. We

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<v Speaker 1>have to avoid overpromising because if there ever was something

0:11:57.360 --> 0:11:59.520
<v Speaker 1>to go wrong and accident with these vaccines, that's why

0:11:59.559 --> 0:12:02.120
<v Speaker 1>we needed take the time to do the clinical trials

0:12:02.120 --> 0:12:04.040
<v Speaker 1>and really get all the data. You know, it could

0:12:04.080 --> 0:12:05.920
<v Speaker 1>turn people off to getting it, you know, if there's

0:12:06.000 --> 0:12:09.079
<v Speaker 1>something that goes wrong. You know, while it might help

0:12:09.200 --> 0:12:12.800
<v Speaker 1>to avert COVID nineteen or other coronaviruses, people might not

0:12:12.880 --> 0:12:15.839
<v Speaker 1>want it after that. So it's a very tricky situation.

0:12:15.880 --> 0:12:17.880
<v Speaker 1>And I know the United States has fast tracked a

0:12:17.920 --> 0:12:19.599
<v Speaker 1>lot of things. We're doing a lot of trials and

0:12:19.640 --> 0:12:21.600
<v Speaker 1>you're trying to do it very quickly, but we've got

0:12:21.600 --> 0:12:24.520
<v Speaker 1>to take the time to get it right some months.

0:12:24.559 --> 0:12:27.680
<v Speaker 1>Supermanian contributor to The Guardian long Reads. Thank you very

0:12:27.760 --> 0:12:32.920
<v Speaker 1>much for joining us. Thanks Oscar, I'm Oscar Ramirez, and

0:12:32.960 --> 0:12:35.959
<v Speaker 1>this has been your daily coronavirus update. Don't forget that.

0:12:36.080 --> 0:12:37.960
<v Speaker 1>For today's big news stories, you can check me out

0:12:38.000 --> 0:12:41.000
<v Speaker 1>on the Daily Dive podcast every Monday through Friday. So

0:12:41.080 --> 0:12:43.360
<v Speaker 1>follow us on I Heart Radio or wherever you get

0:12:43.400 --> 0:12:44.119
<v Speaker 1>your podcasts.