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Oxford Covid Vaccine Among Those Developers Say Have Promising Initial Results

2020-07-21 10:15:43

LONDON — The race for a vaccine against the coronavirus intensified on Monday as three competing laboratories released promising results from early trials in humans.

Now comes the hard part: proving that any of the vaccines protects against the virus, and establishing how much immunity they provide — and for how long.

“What this means is that each of these vaccines is worth taking all the way through to a Phase III study,” said Dr. Peter Jay Hotez, a vaccine researcher at the Baylor College of Medicine. “That is it. All it means is ‘worth pursuing.’” Phase III trials test how well a drug works.

Two of the vaccine developers — the first, a partnership between Oxford University and the British-Swedish drug maker AstraZeneca; the second, the Chinese company CanSino Biologics — published their early results as peer-reviewed studies in The Lancet, a British medical journal.

More than 10,000 participants in Britain, Brazil and South Africa have already received doses. Another Phase III test involving 30,000 participants in the United States is set to begin next week, along with a parallel test of the Moderna vaccine.

The Oxford study released on Monday analyzed a few hundred participants who had received the vaccine in an earlier safety trial. Of those, only 10 received a booster shot, and they showed the most promising immune response.

“There is still a long way to go,” said Prof. Sarah Gilbert of Oxford, who is leading development of the vaccine.

The CanSino vaccine, tested in a trial of about 500 participants in China, appeared least likely to be effective, based on the early results released so far, scientists said. “Pretty weak compared to other vaccine candidates (to the extent that comparisons are possible),” Professor Moore noted in a summary of the results.

Both the Oxford and CanSino vaccines work by altering the genes of another common virus — the adenovirus — so that it harmlessly mimics the coronavirus and induces an immune response.

The Oxford vaccine exploits an adenovirus found in chimps; humans do not already have antibodies against it. The CanSino vaccine, on the other hand, travels on the back of a widespread adenovirus that causes the common cold in humans, and so pre-existing defenses against that adenovirus in many people appear to thwart the vaccine, scientists said.

The preliminary results released Monday by the Pfizer-BioNTech partnership, based on a trial with 60 participants in Germany at various dosage levels, appeared able to produce a strong immune response. The vaccine uses the same kind of specially engineered genetic material, mRNA, as the Moderna vaccine, and the early results from Pfizer-BioNTech may suggest an even stronger immune response, scientists said.

But the scientists cautioned that no response in a lab test guarantees that a vaccine will prevent a disease. And comparing the immune responses ascribed to the various vaccines is almost impossible because the reports are not standardized.

“It’s like judging a beautiful baby photo contest when every mom uses a different Instagram filter,” Professor Moore said.

What’s more, none of the trials has been able to measure results over more than a few weeks, raising questions about the longer term effects of the vaccines.

Professor Hotez argued that the eagerness of vaccine developers to promote such inconclusive results may actually undermine more immediate public health efforts to control the virus, like wearing masks and social distancing.

“All the hype makes it seem like a miracle is around the corner,” he said, “and that is just not the case. This is not going to be a quick fix. This is going to take years to sort out.”

Carl Zimmer contributed reporting.


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