The Niagara Falls Review

Take heart, we now know the light at the end of the COVID-19 tunnel is not a train

- Gwynne Dyer Gwynne Dyer’s new book is “Growing Pains: The Future of Democracy (and Work).”

All the usual caveats apply: don’t go out and celebrate, don’t let your guard down, it’s still going to be a long haul. This winter will be “hard,” warned Ugur Sahin, cofounder and CEO of BioNTech, the German company that announced the first effective COVID-19 vaccine only a week ago. It can’t be rolled out fast enough to reduce infections much in the current wave, he said.

The publicatio­n on Nov. 16 of positive results for a second vaccine, this time by the U.S. company Moderna, strengthen­ed the optimism. Clearly, this coronaviru­s can be beaten, and there are nine more potential COVID vaccines already in third-stage (final) human trials.

But again, the riders: there will be at least half a million more COVID deaths this winter — or over a million if people don’t observe the lockdowns and other restrictio­ns meant to contain the spread of the virus.

“What is absolutely essential,” said Sahin, “is that we get a high vaccinatio­n rate before autumn/ winter next year.” That’s when it could really be over.

And yet there is cause to celebrate, because of the 11 vaccine candidates that were already in thirdstage trials, both the front-runners are “messenger ribonuclei­c acid” (mRNA) vaccines, an entirely new approach that allows a much faster response to novel viral infections.

Traditiona­lly, new vaccines took around 10 years to be developed, tested and approved for general use. For the new mRNA vaccines, it has been 10 months.

After Chinese scientists posted the full genetic sequence of the COVID-19 virus online on Jan. 10, said Drew Weissman of the University of Pennsylvan­ia, “we were making RNA within a week or so.” Weissman then supplied that RNA to both BioNTech/Pfizer (Pfizer is a large American company that gives the German innovators U.S. distributi­on and regulatory clout) and Moderna.

RNA carries the genetic instructio­ns from the nucleus of the cell to build whatever protein is needed, and for the past decade researcher­s have been trying to fabricate ‘messenger’ RNA that could be inserted into human cells.

The mRNA would then use the cell’s own genetic machinery to make vaccines and other medically useful proteins.

By 2018 several companies had cracked the problem of getting the mRNA past the body’s immune defences.

With the full RNA sequence of the new coronaviru­s in their possession, all they had to do was choose which bit of the coronaviru­s RNA to use in the vaccine.

Obviously not the whole thing, or it would rebuild the entire virus in the cell.

Just a harmless segment of the virus’s RNA, copied millions of times by the vaccinated person’s cells, would alert the body’s immune system and train it to destroy any invading virus with that sequence. (They chose the “spike” that the virus uses to attach itself to the human cell.)

Several companies had mRNA vaccines ready for testing within two or three months, and the results have been spectacula­r.

BioNTech/Pfizer has just reported 95 per cent efficacy for its vaccine, and last weekend Moderna reported 94.5 per cent.

Yet another mRNA vaccine in third-phase trials could be even better, because it will be far cheaper than the BioNTech/Pfizer vaccine ($39 for two shots) or the Moderna jab ($74 for two shots) if it pans out.

At Imperial College in London, Robin Shattock’s team is working on a “self-amplifying RNA” vaccine that may require as little as onehundred­th of the amount of vaccine.

The mRNA technique may mean that future pandemics can be dealt with far more quickly. The vehicle is already available and waiting to carry the next vaccine.

Just “plug and play” for any future coronaviru­s, as one researcher put it. (We have had three new coronaviru­ses in the past two decades.)

Pfizer boss Albert Boura went even further: “It’s the greatest medical advance in the past 100 years.” Well, maybe, though a vote taken today would probably plump for antibiotic­s instead. But we are only beginning to see the potential of mRNA.

There are already trials underway for a wide variety of other illnesses: not just safer, more effective influenza, polio and HIV vaccines, but immunother­apies for cancer, heart conditions, cystic fibrosis and other systemic and congenital diseases.

There is a long, dark winter still ahead of us, no doubt, but miracles may await us over the horizon.

And we can now be sure that the light at the end of this particular tunnel is not an oncoming train.

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