WEBVTT - How Were COVID-19 mRNA Vaccines Released So Quickly?

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<v Speaker 1>Welcome to Brainstuff, a production of iHeart Radio, Hey brainstuffe

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<v Speaker 1>Lauren Bogobam here. For decades, researchers have dreamed about harnessing

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<v Speaker 1>the power of genetic technology to prevent or treat a

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<v Speaker 1>range of diseases. A synthetic version of a molecule in

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<v Speaker 1>the human body known as messenger ribonucleic acid or m

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<v Speaker 1>RNA held that promise. Just how to make it work

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<v Speaker 1>presented daunting challenges that much of the science community thought

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<v Speaker 1>was a mountain too hide a climb, But a handful

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<v Speaker 1>of researchers didn't give up. They spent years trying to

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<v Speaker 1>solve the mystery of m RNA. Then, just like a

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<v Speaker 1>made for TV movie, but very much real, they cracked

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<v Speaker 1>the code just in time to save the world from

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<v Speaker 1>the deadly novel coronavirus. M RNA vaccines work by delivering

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<v Speaker 1>instructions to cells that empower those cells to produce antigens,

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<v Speaker 1>which are molecules that prompt and i'm une system response

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<v Speaker 1>in your body, which includes your immune system creating antibodies

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<v Speaker 1>that can identify and fight an invader like the coronavirus.

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<v Speaker 1>But let's unpack all of that to understand mr Anda

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<v Speaker 1>vaccine technology and how it's being used to protect us

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<v Speaker 1>from COVID nineteen. We need to talk about proteins. Proteins

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<v Speaker 1>are often referred to as the building blocks of life.

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<v Speaker 1>They're posential for the structure, function, and regulation of the

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<v Speaker 1>body's tissues and organs. Every cell in your body contains

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<v Speaker 1>tens of thousands of distinct proteins, each of which is

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<v Speaker 1>made up of several types of amino acids that attached

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<v Speaker 1>to each other to create chains of varying lengths that

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<v Speaker 1>fold into various shapes. Proteins shape has a great deal

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<v Speaker 1>to do with its function. Some proteins regulate specific processes

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<v Speaker 1>within a cell, like growth, development, metabolism, and reproduction. Some

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<v Speaker 1>proteins act as biological atalysts to help the body build muscle,

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<v Speaker 1>destroy toxins, and break down food particles during digestion. Other

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<v Speaker 1>proteins are antibodies that let the immune system fight infections

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<v Speaker 1>and clear out harmful pathogens. The cells are assigned their

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<v Speaker 1>amino acid sequences and thus told the function of their

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<v Speaker 1>proteins via the body's messenger RNA or mRNA. You can

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<v Speaker 1>think of this process like a spy mission. mRNA hands

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<v Speaker 1>the cell instructions to make a certain protein. Once the

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<v Speaker 1>cell makes its protein, the cell destroys the instructions and

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<v Speaker 1>then goes to work manufacturing that specific protein. A few

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<v Speaker 1>researchers began to wonder what if science could develop a

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<v Speaker 1>synthetic mRNA with a specific coding sequence that could be

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<v Speaker 1>delivered to the body and instruct cells to create any

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<v Speaker 1>type of protein, growth agents to repair damaged tissues, enzymes

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<v Speaker 1>to cure rear diseases, or antibodies to protect at infection.

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<v Speaker 1>In n A group of University of Wisconsin researchers actually

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<v Speaker 1>succeeded in making synthetic mRNA and tested it in laboratory mice. Unfortunately,

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<v Speaker 1>that synthetic mRNA was identified by the mice's immune systems

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<v Speaker 1>as an invader and was destroyed before ever reaching the

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<v Speaker 1>target cell to deliver the coded message. Many in the

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<v Speaker 1>scientific world saw this as a fatal flaw and turned

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<v Speaker 1>their attentions elsewhere, but two researchers at the University of

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<v Speaker 1>Pennsylvania set out to find a way to make mRNA

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<v Speaker 1>more stable. In two thousand five, after a decade of

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<v Speaker 1>painstaking research, they discovered that they could use tiny balls

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<v Speaker 1>of fat called lipid nanoparticles or LPNs to protect the

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<v Speaker 1>synthetic mRNA. This gave the fragile molecule stealth like qualities

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<v Speaker 1>that enabled it to escape the immune systems radar. With

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<v Speaker 1>this tool in hand, more research followed. In twenty in

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<v Speaker 1>the Cambridge, Massachusetts based pharmaceutical and biotechnology company Maderna Incorporated

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<v Speaker 1>was founded to focus specifically on mr anda vaccine technologies.

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<v Speaker 1>The name Maderna comes from combining the words modified and RNA.

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<v Speaker 1>And Meanwhile, back in two thousand eight, German based bio

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<v Speaker 1>n Tech short for Biopharmaceutical New Technologies, had been founded

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<v Speaker 1>to develop pharmaceutical cancer immunotherapy candidates using mRNA technology. In

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<v Speaker 1>the company partnered with US based Visor Incorporated to develop

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<v Speaker 1>mRNA based flu vaccines, and then the world was hit

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<v Speaker 1>by a pandemic. Researchers everywhere began directing all their efforts

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<v Speaker 1>toward developing a vaccine for the novel coronavirus. And all

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<v Speaker 1>of this research that had come before is part of

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<v Speaker 1>how mRNA vaccines got approved so fast. Let's talk about viruses.

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<v Speaker 1>Viruses cannot reproduce on their own. They need to infect

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<v Speaker 1>a host cell in a creature's body to begin the

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<v Speaker 1>process which can make the creature sick. A for an

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<v Speaker 1>mRNA vaccine for COVID nineteen to work, researchers needed to

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<v Speaker 1>know which protein the virus was using to attack host cells,

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<v Speaker 1>and for that they needed to crack COVID nineteen's genetic code.

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<v Speaker 1>This process was simplified because the virus that causes COVID

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<v Speaker 1>nineteen was similar to two other coronaviruses that had previously

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<v Speaker 1>infected humans, mers and stars. By December thirty one, twenty nineteen,

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<v Speaker 1>when China first reported pneumonia like infections from some kind

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<v Speaker 1>of virus or group of similar viruses, Chinese researchers were

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<v Speaker 1>already working to map the virus is genetic code. About

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<v Speaker 1>two weeks later, on January twelve, they released the gene

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<v Speaker 1>sequence data. This gave researchers everywhere the ammunition to start

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<v Speaker 1>on a vaccine. For the article, this episode is based

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<v Speaker 1>on How Stuff Works Folk with Paul Geptford, m D,

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<v Speaker 1>Professor of medicine at the University of Alabama at Birmingham

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<v Speaker 1>and an expert in vaccine design. He said, we knew

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<v Speaker 1>that the spike protein was the Achilles heel. M RNA

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<v Speaker 1>vaccines are amenable to very rapid development. We got kind

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<v Speaker 1>of lucky from that aspect. A week later, Maderna and

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<v Speaker 1>Fightser made their vaccines. The companies were then able to

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<v Speaker 1>propel ahead of drug companies developing traditional vaccines and move

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<v Speaker 1>quickly into animal testing, and shortly thereafter human trials began.

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<v Speaker 1>Both the Maderna and Fightser bio n tech vaccines are

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<v Speaker 1>performing surprisingly well, and studies have shown that a full

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<v Speaker 1>double dose of Fiser's or Maderna's vaccine provides and protection

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<v Speaker 1>against the original virus, respectively. Yet barely half of all

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<v Speaker 1>Americans are fully vaccinated. Getfort said. One of the reasons

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<v Speaker 1>for vaccine hesitancy is that people have this misunderstanding that

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<v Speaker 1>mrn A covid vaccines were developed so quickly and that

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<v Speaker 1>in doing so we skipped safety evaluation, which is not

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<v Speaker 1>true at all. This vaccine has been tested on incredible

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<v Speaker 1>numbers of people, and it actually underwent the normal safety

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<v Speaker 1>testing of any products, and now that it's under emergency

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<v Speaker 1>use authorization, we have millions more safety data, actually more

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<v Speaker 1>than any other product that we've had for a vaccine.

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<v Speaker 1>These mr ANDA vaccines work so well because they induce

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<v Speaker 1>multiple arms of defense in the immune system, Giptford explained.

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<v Speaker 1>They induce the neutralization of antibodies, which I think of

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<v Speaker 1>as spears because they can knock out the virus before

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<v Speaker 1>you even get infected. They induce functional antibodies, which utilize

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<v Speaker 1>cells to be more effective, and they induce T cell responses,

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<v Speaker 1>both helper and killer cell responses, which are extremely important.

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<v Speaker 1>T cells help prevent severe disease and death. Traditional evact

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<v Speaker 1>scenes also create neutralizing antibodies and induce antibody responses, but

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<v Speaker 1>aren't as good inducing T cell responses. So what does

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<v Speaker 1>the future hold for mRNA technology. This is likely just

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<v Speaker 1>the beginning. Back in two, clinical trials were already underway

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<v Speaker 1>to test mRNA vaccines against several infectious diseases, including HIV, influenza, zica,

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<v Speaker 1>and rabies. Other research is testing whether m RNA technology

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<v Speaker 1>could prevent cancer from recurring. It turns out that mRNA

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<v Speaker 1>vaccines can target almost any pathogen as long as you

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<v Speaker 1>code for the right protein to stimulate the right immune response.

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<v Speaker 1>That means scientists the diseases like malaria, tuberculosis, hepatitis B,

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<v Speaker 1>and cystic fibrosis could all be prevented in the future

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<v Speaker 1>with mRNA vaccines. Getfort said, these vaccines are remarkable even

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<v Speaker 1>an older adults. They work really, really well, which is

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<v Speaker 1>unusual for most any vaccine that we have, so that's

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<v Speaker 1>just remarkable. Today's episode is based on the article will

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<v Speaker 1>m RNA technology transform medicine beyond COVID nineteen on how

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<v Speaker 1>stuff Works dot Com, written by Jennifer Walker. Journey brain

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<v Speaker 1>Stuff is production of I Heart Radio in partnership with

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<v Speaker 1>HowStuffWorks dot Com and is produced by Tyler Clang. Four

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<v Speaker 1>more podcasts from my heart Radio visit the heart Radio app,

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