Washington: Two COVID-19 vaccines might be nearing the finish line, but scientists caution it's critical that enough people volunteer to help finish studying other candidates in the US and around the world.
Moderna Inc and competitor Pfizer Inc recently announced preliminary results showing their vaccines appear more than 90% effective, at least for short-term protection against COVID-19.
If those early results hold up and US regulators agree the shots are safe, emergency use of small, rationed supplies could start in late December. Other countries with contracts for early doses would undertake their own reviews.
But multiple vaccines will be needed to meet global demand and help end the pandemic, raising concern that studies that still need to sign up thousands of volunteers could run short if people wait for an already OK'd option instead.
We don't want to see that happen, said Dr. James Cutrell, an infectious disease expert at UT Southwestern Medical Centre in Dallas.
Supplies aside, other COVID-19 vaccines under development may work differently in different populations, and "we likely will benefit from having a menu of vaccine options, Cutrell said.
We still need volunteers, stressed National Institutes of Health Director Francis Collins, urging Americans to sign up.
Additionally, participants in the Moderna and Pfizer studies who originally got dummy shots would almost certainly be offered the real vaccine if the US Food and Drug Administration allows emergency use. But no one knows how long protection would last, meaning those studies also must continue to track recipients somehow.
It's one thing to be effective two months after your last vaccination and another thing to be effective a year later said Dr. Jesse Goodman of Georgetown University, a former director of the FDA's vaccine division. It's going to be really important to complete these clinical trials and the trials of the other vaccines so we can make comparisons.
The promising Moderna and Pfizer news bode well for some of their competitors, said Dr. Anthony Fauci, the US government's top infectious disease expert whose team at NIH helped develop the Moderna candidate.
Those shots target the spike protein that studs the surface of the coronavirus, and the early results prove that's enough to generate a protective response, Fauci said. Conceptually this looks good for other spike-focused vaccines made in different ways.
Here's a scorecard of the frontrunners in the global vaccine race:
GENETIC CODE VACCINES
The Moderna-NIH vaccine and the candidate developed by Pfizer and its German partner BioNTech aren't made with the coronavirus itself, meaning there's no chance anyone could catch it from the shots.
Instead, the vaccines are made with a brand-new technology that injects a piece of genetic code for the spike protein. That messenger RNA, or mRNA, instructs the body to make some harmless spike protein, enough to prime the immune system to react if it later encounters the real virus.
There are no licensed mRNA vaccines for people, so scientists had no idea if or how well the COVID-19 candidates might work.
Both manufacturers are working to scale up production in factories in the US and Europe. They can't simply partner with other vaccine companies to take on some of the work because the technology is so different than the way most of today's shots are made.
It is not a very easy or quick swap, said Moderna CEO Stephane Bancel.
TROJAN HORSE VACCINES
A different way to target the spike protein: Use another, harmless virus to carry the spike gene into the body. Once again, the body produces some spike protein and primes the immune system.
Britain's Oxford University and AstraZeneca are making their version of this viral vector vaccine with a cold virus, or adenovirus, that normally infects chimpanzees. Studies of tens of thousands of people are underway in the UK, US, and several other countries.
Johnson & Johnson is using a human adenovirus for its version and is the only option in advanced US testing aiming to show if a single dose rather than two would be enough.
China's government authorized the emergency use of CanSino Biologics' adenovirus shots in the military ahead of any final testing. Russia likewise began offering an adenovirus vaccine ahead of late-stage tests.
PROTEIN VACCINES
Novavax makes its vaccine candidate by growing harmless copies of the coronavirus spike protein in the laboratory and packaging them into virus-sized nanoparticles.
There are protein-based vaccines against other diseases, so it's not as novel technology as some of its competitors. Novavax has begun a large final-stage study in Britain and is set soon to begin another in the US.
KILLED VACCINES
Spike-focused vaccines aren't the only option. Making vaccines by growing a disease-causing virus and then killing it is a tried-and-true approach it's the way Jonas Salk's famed polio shots were made.
China has three so-called inactivated COVID-19 vaccine candidates in final testing in several countries and has allowed emergency use in some people ahead of the results. An Indian company is testing its own inactivated candidate.
Safely brewing and then killing the virus takes longer than newer technologies. But inactivated vaccines give the body a sneak peek at the germ itself rather than just that single spike protein.
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New Delhi (PTI): A Delhi court has sentenced Haryana gangster Vikas Gulia and his associate to life imprisonment under MCOCA provisions, but refused the death penalty saying the offences did not fall under the category of 'rarest of the rare cases'.
Additional Sessions Judge Vandana Jain sentenced Gulia and Dhirpal alias Kana to rigorous imprisonment for life under Section 3 (punishment for organised crime) of the Maharashtra Control of Organised Crime Act (MCOCA).
In an order dated December 13, the judge said, "Death sentence can only be awarded in 'rarest of the rare cases' wherein the murder is committed in an extremely inhumane, barbarous, grotesque or dastardly manner as to arouse umbrage of the community at large."
The judge said that on weighing the aggravating and mitigating circumstances, it could be concluded that the present case did not fall under the category, and so, the death penalty could not be imposed upon the convicts.
"Thus, both the convicts are sentenced to undergo rigorous imprisonment for life and to pay a fine of Rs 3 lakh each, for committing the offence under Section 3 of MCOCA," she said.
The public prosecutor, seeking the death penalty for both the accused, submitted that they were involved in several unlawful activities while they were on bail in other cases.
He argued that the accused had shown no respect for the law and acted without any fear of legal consequences, and therefore did not deserve any leniency from the court.
The court noted that both convicts were involved in offences of murder, attempt to murder, extortion, robbery, house trespass, and criminal intimidation. Besides, they had misused the liberty of interim bail granted to them by absconding.
It said, "The terror of the convicts was such that it created fear psychosis in the mind of the general public, and they lost complete faith in the law enforcement agencies and chose to accede to the illegal demands of convicts. Despite suffering losses, they could not gather the courage to depose against them."
The court noted that Gulia was involved in at least 18 criminal cases, while Dhirpal had links to 10 serious offences.
It underlined that MCOCA had been enacted "keeping in view the fact that organised crime had come up as a serious threat to society, as it knew no territorial boundaries and is fuelled by illegal wealth generated by committing the offence of extortion, contract killings, kidnapping for ransom, collection of protection money, murder, etc."
Both accused persons had been convicted on December 10 in a case registered at Najafgarh police station. The police filed a chargesheet under Section 3 (punishment for organised crime) and 4 (punishment for possessing unaccountable wealth on behalf of member of organised crime syndicate) of MCOCA.
