It marks another breakthrough in the race to develop a vaccine to prevent Covid-19, after jabs made by Moderna and Pfizer and BioNTech were both revealed to be around 95 per cent effective within the past week.

Oxford’s results are from an earlier stage of testing so cannot estimate how well the vaccine protects against Covid, but are still a positive step. Detailed results about how well it works are expected within weeks, the university said.

The research showed that people in all age groups developed antibodies – virus-destroying substances made by the immune system – within 28 days of their first dose of the vaccine, and these were boosted further after the second dose.

Britain has pre-ordered 100million doses of Oxford’s jab, which is being made with pharmaceutical firm AstraZeneca, so if it works and can be manufactured fast enough it could be used to protect the majority of the UK’s population. 

Oxford University scientists published the results of their second-phase trial of the jab in medical journal The Lancet this morning, showing that it appears to work in adults of all ages

Volunteers in the trial demonstrated similar immune responses across all three age groups – they had been split into 18-55, 56 to 69, and 70-plus. 

Health officials in the UK have suggested that vaccines for younger adults and children are lower priority, and that vaccinating the over-50s and people with serious health conditions would cover the vast majority of people likely to die.

Professor Deborah Dunn-Walters, chair of the British Society for Immunology, described the announcement as ‘positive’.

‘The vaccine appears to be well tolerated in all age groups, with older individuals reporting fewer side-effects.’

‘One clue to this from the current study is that older people reacted less to the vaccine – fewer fevers, less injection site pain and swelling – but encouragingly, the immune responses in the older patients were indistinguishable from those in younger patients. 

And Dr Michael Tildesley, a Warwick University epidemiologist who advises SAGE, said the vaccine could be a ‘game changer’.

He told BBC Breakfast the number of doses acquired by the Government could push the UK towards ‘that magic herd immunity’

Volunteers in the study were split into two groups and either received two doses of the real vaccine candidate or a placebo meningitis vaccine. 

Dr Maheshi Ramasamy, investigator in the Oxford Vaccine Group and a consultant doctor, said: ‘Older adults are a priority group for Covid-19 vaccination, because they are at increased risk of severe disease, but we know that they tend to have poorer vaccine responses.

‘The next step will be to see if this translates into protection from the disease itself.’

Britain’s drug regulator yesterday confirmed it is waiting for Pfizer to send over the full results of its final Covid-19 vaccine trial so it can consider approving it as the first ever coronavirus jab.

The US company, most famous for making Viagra, announced it would submit the necessary data to regulators in America and the UK ‘within days’, bolstering hopes that Britain could embark on its major Army-backed operation to vaccinate millions of people from as soon as December 1. 

UK drug regulator the MHRA has been doing a ‘rolling review’ of the vaccine and could, as a result, complete the approval process within a matter of days of receiving the application from Pfizer and BioNTech, a German firm involved in making the jab. 

Dr June Raine, the MHRA’s chief executive, said: ‘The results reported by Pfizer today are very encouraging and add to their announcement from last week. 

‘We look forward to receiving the full results of the trials as soon as possible, after which we will rigorously assess the evidence of safety and effectiveness of the vaccine.’

Britain has already pre-ordered 40million doses of the vaccine and could be set to get 10m of those next month, with the NHS gearing up start dishing it out within a fortnight. Professor Stephen Powis, NHS England’s medical director, today said the health service was ‘working incredibly hard’ to prepare.

Pfizer and BioNTech’s final trial results showed that only eight people out more than 20,000 who got the vaccine caught coronavirus, compared to 162 who were given a fake jab. A total of 10 people got severe Covid-19, one of whom had been given the real vaccine.

An independent safety committee ‘has not reported any serious safety concerns related to the vaccine’ since the final stage trial began in July, Pfizer said. Side effects were limited – the most common was fatigue, which 3.8 per cent of people got, and headaches (2 per cent).

The announcement is an improvement on Pfizer’s early estimate that the vaccine was 90 per cent effective, and comes just days after rival firm Moderna claimed its own jab was 94.5 per cent effective, which sparked fears the UK had hitched its wagon to the wrong project because No10 hadn’t bought any doses.

Pfizer and BioNTech yesterday said the final results of their clinical trial suggested their vaccine was 95 per cent effective, just days after Moderna claimed its own jab showed efficacy of 94.5 per cent.

Today’s Lancet study also found the vaccine, being developed with AstraZeneca, was less likely to cause local reactions at the injection site and symptoms on the day of vaccination in older adults than in the younger group.

The authors note some limitations to their study, including that the participants in the oldest age group had an average age of 73-74 and few underlying health conditions, so they may not be representative of the general older population, including those living in residential care settings or aged over 80.

The Oxford findings come after Pfizer and BioNTech announced that their vaccine candidate has shown 95 per cent efficacy, with a 94 per cent effectiveness in those aged 65 and over.

Forty million doses of that vaccine have been bought by the UK, with rollout potentially starting in early December if the jab is given the green light by regulators.

Earlier in the week US biotech firm Moderna released data suggesting its vaccine is almost almost 95 per cent effective.

WHAT DO WE KNOW ABOUT OXFORD’S VACCINE? 

When will it be ready? 

The results are expected imminently. Drugs giant AstraZeneca, which owns the rights to the vaccine, said in November it ‘anticipated’ data on the effectiveness of the experimental jab in quarter four — by the end of the year.  

Once the data is ready, it will then be examined by the healthcare regulator MHRA, who will then decide if it can be rolled-out for use in the wider community.

The NHS is geared up to administer a Covid-19 vaccine as soon as December, if one is proven to work, health officials have promised.  

Kate Bingham, head of the UK’s vaccines taskforce, said on November 4 it was possible a jab would be ready ‘before the end of the year’. 

When will you be able to get one? 

Despite the fact the Government have secured a deal for 100million doses, only about four million would actually be available by the end of the year, Ms Bingham has revealed. This would cover just two million people.

The first wave of vaccines would not be good enough to allow society to immediately return to normal, Ms Bingham said. 

A priority list for vaccination in the UK has been drawn up officials, putting care home residents and workers, those over the age of 80 and healthcare workers at the front of the queue, encompassing at least six million people.

Will it be successful? 

In July, interim results from the ongoing Phase I and Phase II trials were published in The Lancet, showing the vaccine generated a robust immune responses against the SARS-CoV-2 virus. Health Secretary Matt Hancock said it was ‘very encouraging news’.

Crucially, nobody suffered any bad side effects. Some people developed headaches, tiredness and pain in their arm after they were given the jab, but scientists claimed none of the side effects were severe. 

Experts say the news that one coronavirus vaccine works bodes well for others, even if they use different technology.

All vaccines, regardless of their method, have been developed to target the ‘spike protein’ of the coronavirus – just one of many proteins that form its makeup that is found on the outside of the particle.

After news that the Pfizer/BioNTech jab was ’90 per cent effective’ broke on November 11, the deputy chief medical officer Professor Jonathan Van-Tam said it was good news for other future vaccines.

Sarah Gilbert, a professor of vaccinology who has been leading the Oxford team, has been vocal about her confidence in the vaccine. In an interview with The Times before trials began, she said she was ’80 per cent’ confident of its success, ‘based on other things that we have done with this type of vaccine’. 

What obstacles have the team faced? 

Trials were paused three times to investigate serious events in volunteers. 

On two occasions, in July and September, trial participants had developed symptoms that were feared to have been caused by the jab. And one man in Brazil died of Covid-19 in October— but was reported to have been given the placebo jab.  

In each event, independent reviewers judged it was safe to continue the jab experiments after they were stopped for several days.

Chief executive of AstraZeneca Pascal Soriot dismissed concerns that pauses in the scientific trials due to investigations of volunteers falling ill had delayed the progression in a company webcast on November 5. 

Scientists feared that because transmission levels of Covid-19 dropped in the summer, it would drag the study out for much longer than hoped. Researchers have to wait until 100 or more people get the virus before they can stop the trial and look at the results.  

Considering ministers first hoped for the Oxford jab to be ready by September, this may have had an impact. 

How does it work? 

The vaccine is known as a ‘recombinant viral vector vaccine’. It is made using a piece of the virus, often weakened and incapable of causing disease itself. 

Researchers place genetic material from the coronavirus into another virus that’s been modified. In this case, a common cold virus (adenovirus) from chimpanzees. It has been genetically changed so that it is impossible for it to grow in humans.  

They will then inject the virus into a human, hoping to produce an immune response against SARS-CoV-2. 

If the vaccines can successfully mimic the spikes inside a person’s bloodstream, and stimulate the immune system to create special antibodies to attack it, this could train the body to destroy the real coronavirus if they get infected with it in future. 

Is it safe?

Probably, based on the initial results of trials. But this won’t become clear until the vaccine completes stage three clinical trials. It won’t be rolled out unless it is proven to be safe. 

Even though it has been made at lightning speed – it’s gone through the stages of vaccine development that usually take five years in just four months – Professor Gilbert said that none of the normal safety steps had been missed out. 

Chimpanzee adenoviral vectors are a very well-studied vaccine type, having been used safely in thousands of subjects. 

How has it been tested?

Some 1,100 British people were involved in the Phase 1 trial. Phase II enrolled around 11,000 adults and children across the UK.  

More than 50,000 people worldwide will take part in Phase III trials, scientists involved have said. Half will be given the real vaccine candidate, while others will receive a placebo.

In September AstraZeneca said the jab had been given to 18,000 people across the world so far.

Who made the vaccine and who owns it?

Clinical teams at the Oxford University’s Jenner Institute and Oxford Vaccine Group began developing the ChAdOx1 nCoV-19 vaccine in January. 

After they partnered up with pharmaceutical giant AstraZeneca in May, the jab was named AZD1222. 

The intellectual rights to its vaccine are owned by the University of Oxford and a spin-out company called Vaccitech. 

How does it compare to other vaccines?  

The Oxford vaccine is the same as that being produced by Janssen, which is also a recombinant vector vaccine using a human adenovirus. GSK/Sanofi’s works in a similar way, but with the addition of an adjuvant – which can give the immune system a boost.

But jabs produced by Pfizer/BioNTech and Moderna – the first to have results published this month – are known as messenger RNA (mRNA) vaccines. 

They insert genetic code from the virus into the body to prompt it to make the spike proteins. This provokes the immune system to make antibodies. This experimental technology has never previously been proven in humans. 

A team at Imperial College London is also among those developing an RNA vaccine candidate. It will try to transport the RNA inside liquid droplets injected into the bloodstream.

Which other countries have secured doses?

France, Germany, Italy and the Netherlands have secured 400million doses. Australia has secured doses for its population of 25million people. The US has secured 100million doses. The Serum Institute of India has also secured a billion doses. AstraZeneca has said that doses will be handed out equitably.

How much does it cost?

The vaccine may cost as little as £2.23 per dose, which compares to the estimated £15 per dose of Pfizer/BioNTech.

AstraZeneca has said it will not profit from the it, but may earn extra royalties if the coronavirus becomes an endemic infection like flu. The US has spent $1.2 billion (£930million) securing doses, meaning they are worth $4 (£3.10) each.

This content was originally published here.