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  • kovat 19 SARS CoV to the coronavirus no matter which name you've heard of the

  • virus and the pandemic it's caused impacting lives physically financially

  • and socially billions of people are social distancing and while we do our

  • part to combat the spread of the disease researchers are working endlessly to

  • produce a sustainable and reliable vaccine to finally end this crisis as

  • we've seen in the news there are teams globally working on vaccine solutions

  • and as of April 8th there are 115 vaccine candidates in varying stages of

  • research every day there seems to be a new development private companies like

  • moderna and inovio are making headlines as they're quickly progressing in the

  • first stages of the vaccine approval process a process that usually takes

  • years is being pushed in a matter of new months and that's the question with

  • urgency looming how viable are many of these fast vaccines and are we going to

  • have a vaccine solution within a year short answer a very apprehensive may be

  • so with everything by everybody in every place works perfectly could you

  • theoretically accomplish this in 18 months

  • I think it's optimistically 12 to 18 months under normal circumstances it

  • takes five to ten years to develop a vaccine it is a process designed to be

  • appropriately slow reflective evidence-based peer reviewed by other

  • scientists and then used in under normal circumstances taking vaccines from the

  • lab to licensing for public distribution not only takes time but money roughly 1

  • billion dollars worth or more but a large part of the acceleration of the

  • vaccines were hearing about have to do with an international organization that

  • launched in 2017 called the Coalition for epidemic preparedness innovations or

  • SETI the thing about these vaccines is that you need to have funding to move

  • from one stage to the next Zika disappeared so they took the money

  • away Ebola disappear so no money you have you have to get out

  • of that cycle so actually sepia merged because they

  • knew that this was a problem what would we do if something big came up and of

  • course it's a good thing they planned because something big did come up and

  • that's why Sethi had the funding available immediately to give to

  • organizations like Madera nikeyra back in ovo in Queensland and while the

  • funding helps to speed up the process the teams chosen by sepi also are

  • already ahead in their vaccine research teams either have experience with

  • previous outbreaks like MERS we're working on novel vaccine methods that

  • could significantly reduce the development timeline but before we get

  • carried away with how these new research platforms work we should know the

  • vaccine basics essentially a vaccine can be made in a few different ways we have

  • inactivated and live attenuated both known as whole pathogen vaccines subunit

  • vaccines including recombinant polysaccharide and conjugate vaccines

  • which are using a piece of the pathogen or the newer method of nucleic acid

  • vaccines using the DNA or RNA of the pathogen when injected into our body's

  • vaccines all aimed to mimic the infectious agent typically a vaccine is

  • often given with an adjuvant to boost the initial immune response after the

  • injection this response sounds the alarm in our body and begins the organization

  • of white blood cells like killer T cells and specific proteins called antibodies

  • killer T cells destroy the pathogen and the infected cells and the antibodies

  • neutralize the pathogen in SARS CoV to s case the antibodies head toward the

  • recognizable spike proteins on the outer shell of the corona virus and block the

  • proteins from connecting to the receptors of our cells this whole

  • process helps the body's immune system get trained by the vaccine and retain

  • the memory of the infection so that when a vaccinated person encounters a real

  • virus like SAR Co b2 they can quickly recover so basically your body comes up

  • with the preventative measures it needs to fight the pathogen we just need to

  • initiate that exposure in the old days we would just grind up the virus or the

  • bacteria and kill it with formalin or heat and inject it into animals and

  • sometimes that works sometimes it doesn't as we've

  • gotten more sophisticated now we can use molecular biology to either make these

  • tiny little proteins or to make particles that look like the virus or

  • you can make DNA or RNA vaccines all of these things have a potential to work so

  • which ones are set be focusing on well right now they have a number of funded

  • vaccine candidates in their portfolio but out of those funded platforms we're

  • hearing mostly about four of them to mRNA vaccines from moderna and cure back

  • one DNA vaccine from inovio and a protein vaccine from Australia's

  • University of Queensland there are no licensed DNA or RNA vaccines on the

  • other hand we believe that they can be made rapidly I mean I think you heard

  • inovio say that within three hours of seeing the sequence they had designed

  • the vaccine that they intended to take into humans it takes longer for protein

  • vaccine it takes longer for a whole inactivated virus vaccine that every

  • group is pursuing what it does best given the urgency of finding a vaccine

  • during this pandemic we're looking for new approaches like DNA and RNA vaccines

  • because they can be developed quickly however that doesn't mean that work on

  • other promising solutions stops as experts are advocating for a multi prong

  • approach when it comes to developing vaccines because we'll need as many

  • candidates as we can to pass the rigorous approval phases but what

  • exactly are these phases well for example once a viable coronavirus

  • vaccine candidate has been identified in preclinical studies they can move on to

  • the highly-anticipated phase one of the approval process space one studies

  • involve tens of people the moderna mRNA vaccine that's being

  • tested in the US will enroll forty five people and what you're doing there is

  • you're again looking to see does it produce an immune response and does it

  • appear to be safe now you only have tens of people so you won't see very much

  • once that hurdle is passed we can enter Phase two where the study enrolls

  • hundreds of patients now you're getting more refined in what doe

  • how to administer it how many doses you're looking again for immunogenicity

  • you might get some hints about effectiveness and you're looking for

  • safety and so phase two can actually be a fairly long time because you're

  • testing multiple things you're looking at your results because really the cost

  • of failure for large companies is huge that distance between phase 2 and phase

  • 3 is somewhat affectionately called the valley of death and the reason for it is

  • the vast majority of vaccines and drugs will not make it into or past phase 3

  • but let's say a corona virus vaccine it does pass if so it will go into phase 3

  • where thousands to tens of thousands of people are enrolled in a trial now what

  • you're looking at is efficacy does it actually work not just raising the

  • immune response but does it actually prevent disease from here the FDA

  • scrutinizes the data collected across all three phases if it all looks good

  • then they give the final approval on licensing and manufacturing whew we did

  • it it only took hundreds of hours of

  • vaccine development three major clinical trials and hundreds of thousands of

  • people plus a number of approval committees so by now you're probably

  • wondering how do we telescope something that is five to ten years into something

  • that may be 12 to 18 months so you do face two very close to Phase one maybe

  • overlapping it partially and then you see that you get the right protective

  • responses in the laboratory and rather than waiting until you've got all the

  • data to the very end of the trial you may wait a month to make sure that the

  • best responses are present and then based on those best responses either the

  • company or maybe sepi or a government will say okay fine let's move on to see

  • if this actually protects very quickly again if everything goes right and we

  • see no safety signals it would be possible it may be longer and so we're

  • going to have to get ready for co-ed 19 and living with it and figuring how to

  • work around it okay so best-case scenario we're looking

  • at 12 to 18 months before we have a viable

  • vaccine but even if this ambitious timeline is accomplished researchers

  • will need to find the means of being factoring it but there's some 8 billion

  • people on our planet but if they overcome all these challenges we'd be

  • looking at a vaccine that was developed at a historical speed one with the

  • potential to save millions of lives Kovan 19 is a huge subject one that's

  • impacted each and every one of us if there's another aspect of it that you

  • want to see us cover please let us know in the comments below and make sure to

  • subscribe to seeker to see how we follow this news thanks for watching and I'll

  • see you next time

kovat 19 SARS CoV to the coronavirus no matter which name you've heard of the

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