The Southland Times

Labs race for coronaviru­s cure

-

In the space of a week two mice will receive injections at university laboratori­es in London and Oxford.

The first, on Monday at Imperial College, will help the rodent’s muscle cells to begin making proteins that look a lot like those on a coronaviru­s. A week later in Oxford, barely a month after Chinese authoritie­s alerted the world to their outbreak, another mouse will also receive an injection – and with luck its immune system will produce the antibodies that could stop the epidemic.

Their efforts, along with those of a handful of laboratori­es around the world, are part of a race to stop a pandemic.

Robin Shattock, of Imperial, said he had never seen a response like it. Processes that in the past took months or years have been compressed into weeks. ‘‘We’ve done it about as fast as anyone could do it,’’ he said.

After Chinese scientists published the genetic code of the coronaviru­s, he and his colleagues were ready to begin work to produce a vaccine to combat it.

His approach involves an RNA vaccine. Convention­al vaccines involve a weakened or dead version of the virus that you want to combat. By injecting it, you can teach a body’s immune system to make antibodies to attack it – so that if somebody is exposed to the virulent version they are immune.

Shattock’s vaccine contains a string of RNA (ribonuclei­c acid), the code the body uses to make proteins. This particular sequence of RNA is the same as a section in the coronaviru­s. When it is injected on Monday, he believes that the RNA will instruct the mouse’s muscle cells to make proteins like those on the outside of the virus, and so train the body to fight them.

The Oxford team is trying a completely different approach. When the outbreak began Professor Sarah Gilbert was already testing a vaccine for Middle East respirator­y syndrome, another coronaviru­s. It was relatively simple to adapt the technique to

Oxford

the new virus. Unlike the Imperial team, the vaccine they test on February 18 will consist of a live virus, but one that cannot reproduce. Inside it will be a section of genetic code from the coronaviru­s, providing the instructio­ns to make the coronaviru­s protein after vaccinatio­n. It also trains the body to attack the virus.

Gilbert said that the speedy response was a reflection of years

‘‘The 2014 ebola outbreak changed a lot of thinking. We’ll have a lot more of these outbreaks, and we need to know we can respond quickly, that once we have the sequence we can get going straight away.’’ Professor Sarah Gilbert

of preparatio­n. ‘‘The 2014 ebola outbreak changed a lot of thinking. We’ll have a lot more of these outbreaks, and we need to know we can respond quickly, that once we have the sequence we can get going straight away,’’ she said.

There are many ways in which both vaccines could fail, as they look to enter human trials in the summer. It is also possible that, by then, the outbreak will have fizzled out. – Sunday Times

 ??  ??

Newspapers in English

Newspapers from New Zealand