Tests of potential coronavirus vaccine spur growth of virus-fighting antibodies – USA TODAY

A potential vaccine for COVID-19 has been developed and tested successfully in mice, researchers reported Thursday.

"We'd like to get this into patients as soon as possible," said Andrea Gambotto, associate professor of surgery at the University of Pittsburgh School of Medicine and co-author of a paper announcing the vaccine in the journal EBioMedicine.

As far as reaching clinical trials,"we would like to thinka month, give or take. Maybe two months. We just started the process," said co-author Louis Falo, a professor and chairman of the Department of Dermatology at the University of Pittsburgh.

Thursday'sannouncement, more than three months into a pandemic that has killed 50,000 people and sickened almost 1 million worldwide, presents an urgent challenge to government regulators, who must weigh how much to speed up the vaccine approval process.

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Vaccinesoften take years to receive approval from the U.S. Food and Drug Administration. Yet on March 16, the first four healthy volunteersin Seattle received adifferent potential COVID-19 vaccine, made by a company called Moderna and administered in a small clinical trial at Kaiser Permanente Washington Health Research Institute.

Though the vaccine being tested in Seattle uses a new, faster but untested technology,the one developed in Pittsburgh employs the sametechnique used influ shots. The Pittsburgh vaccine uses lab-made viral proteinto builda person's immunity to the virus.

Tests in mice found that the vaccine spurred a wave of virus-fighting antibodies within two weeks.

"There are many, many vaccine candidates in various stages of testing," saidDavid O'Connor, professor at the University of Wisconsin School of Medicine and Public Health, who saw the published paper for the first time Thursday.

O'Connor saidshowing that a vaccine generates an immune response is"an important first step in determining which vaccines should move forward, but is only the first of many steps along the way to a useful vaccine. This paper shows some of this 'first step'data."

The potential COVID-19 vaccinefollows up on researchGambottoand Falo did in December 2003 when they were poisedto proceed to clinical trials with a vaccine for another coronavirus, Severe Acute Respiratory Syndrome. At the time, the journal Nature reported, "SARS vaccines speed toward clinic."

But the outbreak had already waned. The World Health Organization declared SARS contained in July 2003.

Funding for the SARS vaccine vanished.

"SARS CoV-2 is teaching us that it is important to react and (follow) all the way through," Gambottosaid. "Yes, it was a mistake not to test the vaccine back then."

Some scientists suggested that a vaccine for one coronavirus would probably have offered at least some protection from all of them.

The Pittsburghresearchers developed a vaccine to treat Arabian camels for another coronavirus, Middle East Respiratory Syndrome (MERS). Like SARS and COVID-19, MERS jumped from animals to people,infectingalmost 2,500 andkilling almost 860 since its discovery in 2012.

Gambotto saidtheyadapted techniques they had developed for previous coronavirusesto create one specifically designed for the virus that causesCOVID-19; theprocess of translating their work foruse onCOVID-19took the scientists 10 to 12 days. They collaboratedwith11 other scientists, including two from Erasmus Medical Center in Rotterdam, the Netherlands.

Gambotto and Falo said theirvaccine would be delivered to the upper armbut would not requirea shot from a needle asthe flu vaccine does.

The scientists developed a fingertip-sized patch that contains 400tiny needles, each just half a millimeter. The two scientistscompared the patch to a Band-Aid and said it would feel a lot like having Velcro pressed against the skin.

The needles, made from sugar and protein pieces, would penetrate the upper level of skin, absorb moisture from the skin and release molecules. The molecules would prompt the immune system to makeantibodies thatattack the virus.

The Pittsburgh researchers touted two advantages tothevaccine they call PittCoVacc.

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The vaccine does not have to be frozenwhen stored or transported; it can sit atroom temperature. That wouldmake the vaccine much cheaper to deliver to poorer countries.

Though the researchers could not say exactly how much a dose of the vaccine would cost, they estimated that the patchof needles used to deliver the vaccine would probably cost less than $10 apatch.

The technique employing the tiny needlesreleases a highly concentrated, much smaller amount of viral protein. The scientists said a single person would be able to make hundreds of vaccine patches a day.

The vaccine was developed without using the live virus that causes COVID-19. Scientists used DNA molecules made in the lab.

When released from the patch, the vaccineexploits the crucial part of the virus that latches onto human cells, the Spike protein.

The virus' Spike protein usually acts like a key opening up human cells and allowing the virus to invade. The vaccine acts a little like gum in a lock, preventing the key from working and keeping the virus from entering human cells.

Early in the pandemic, health officials took pains to stress that a vaccine would probably take18 months to develop, test and be ready for human use. Whether the first vaccines will take that long to reach people is not known, and many scientists greetnew reports such as the one from Pittsburgh with caution.

O'Connor, from the University of Wisconsin,stressed that vaccine makers have been forced by the urgency of fighting a pandemic to move when "there is much that we don't know about this virus." In particular, it's unknownhow long a person has immunity both natural immunity from having fought the virus and survivedand theimmunity inducedby vaccines.

"Dovaccines last for months? Years? An entire lifetime?" he asked.

Scientists have been working furiously to develop two possible treatment methods: the use of plasma from recovered COVID-19 patientsand drugs that have been found safe for use in people, such as the anti-malarial chloroquine.

Hospitals have begun using survivorplasmaon a compassionate, experimental basis.

Follow Mark Johnson on Twitter:@majohnso

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Tests of potential coronavirus vaccine spur growth of virus-fighting antibodies - USA TODAY