Cambridge University kicks off vaccine race to fight all coronaviruses
London: The University of Cambridge on Wednesday confirmed plans to begin trials of a potential new vaccine not only against COVID-19 but all coronaviruses that may spill over from animals to humans in the future.
The new vaccine candidate, DIOS-CoVax2, uses banks of genetic sequences of all known coronaviruses, including those from bats, believed to be the natural hosts of many relatives of human coronaviruses.
A vaccine that clears all trials can then be delivered pain-free without a needle into the skin through a spring-powered jet injection.
Our approach involves 3D computer modelling of the SARS-CoV-2 [Covid-19] virus' structure. It uses information on the virus itself as well as its relatives SARS, MERS and other coronaviruses carried by animals that threaten to spill-over' to humans again to cause future human epidemics, said Professor Jonathan Heeney, head of the Laboratory of Viral Zoonotics at the University of Cambridge, and founder of DIOSynVax a Cambridge spin-out company.
We're looking for chinks in its armour, crucial pieces of the virus that we can use to construct the vaccine to direct the immune response in the right direction. Ultimately we aim to make a vaccine that will not only protect from SARS-CoV-2, but also other related coronaviruses that may spill over from animals to humans, he said.
Prof Heeney said his team's strategy involves targeting those domains of the virus' structure that are absolutely critical for docking with a cell, while avoiding the parts that could make things worse.
What we end up with is a mimic, a synthetic part of the virus minus those non-essential elements that could trigger a bad immune response, he added.
His team have developed libraries of computer-generated antigen structures encoded by synthetic genes that can train the human immune system to target key regions of the virus and to produce beneficial anti-viral responses.
These immune responses include neutralising antibodies, which block virus infection, and T-cells, which remove virus-infected cells.
This so-called laser-specific computer generated approach is able to help avoid the adverse hyper-inflammatory immune responses that can be triggered by recognition of the wrong parts on the coronavirus' surface.
Most research groups have used established approaches to vaccine development because of the urgent need to tackle the pandemic. We all hope the current clinical trials have a positive outcome, but even successful vaccines are likely to have their limitations they may be unsuitable for vulnerable people, and we do not know how long their effects will last for, for example, said Dr Rebecca Kinsley, Chief Operating Officer of DIOSynVax and a postdoctoral researcher at the University of Cambridge.
Our approach using synthetic DNA to deliver custom designed, immune selected vaccine antigens is revolutionary and is ideal for complex viruses such as coronavirus. If successful, it will result in a vaccine that should be safe for widespread use and that can be manufactured and distributed at low cost, she said.
DIOS-CoVax2, which hopes to go into human trials by later this year, is the latest vaccine candidate to be backed by the UK government with 1.9 million pounds in funding as part of a collaboration between DIOSynVax, which is contributing an additional 400,000 pounds to the trial, the University of Cambridge and the University Hospital Southampton NHS Foundation Trust.
The team say their proposed new vaccine can be freeze-dried as a powder and is therefore heat stable, meaning that it does not need to be cold-stored. This makes transport and storage much more straightforward, particularly important in low and middle income countries, and it can be delivered through PharmaJet Tropis intradermal Needle-free Injection System, which delivers the vaccine in less than a 1/10th of a second jet injection.
Professor Saul Faust, Director of the NIHR Southampton Clinical Research Facility, said: It is especially exciting that the clinical trial will test giving the vaccine through people's skin using a device without any needles as together with stable DNA vaccine technology this could be a major breakthrough in being able to give a future vaccine to huge numbers of people across the world.
The news comes as the University of Oxford revealed that its trials of a potential vaccine against COVID-19 being developed with AstraZeneca could be put before regulators this year if scientists are able to gather enough data.
The Oxford vaccine, as it is commonly known, showed early promise in the first human trial when it produced an immune response, underlining its position as one of the leading candidates in the race to help vaccinate humans against the deadly novel coronavirus.
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US VP JD Vance says Lebanon not part of ceasefire, calls it ‘misunderstanding’
Budapest/Washington: US Vice President J D Vance has said that Lebanon was never included in the ceasefire understanding with Iran, describing the confusion as a “legitimate misunderstanding”.
Speaking to reporters before departing from Hungary, Vance said, “I think the Iranians thought that the ceasefire included Lebanon and it just didn’t. We never made that promise.”
He stressed that the United States had not included Lebanon in the scope of the ceasefire at any stage.
His remarks come amid continued Israeli strikes in Lebanon, where more than 200 people were reported killed, even as ceasefire talks between Iran and the US move forward.
Vance said Israel had “offered … to check themselves a little bit in Lebanon because they want to make sure that our negotiation is successful”.
He warned that if Iran allows the situation in Lebanon to affect the negotiations, it could derail the talks.
“If Iran wants to let this negotiation fall apart in a conflict where they were getting hammered over Lebanon, which has nothing to do with them and which the United States never once said was part of the ceasefire, that’s ultimately their choice,” he said.
