AstraZeneca said it was investigating whether the patient’s reported side effect is connected with the vaccine.
But is this a setback for the development of the vaccine and what happens next?
The vaccine – called ChAdOx1 nCoV-19 – uses a weakened version of a common cold virus (adenovirus) which causes infections in chimpanzees.
It has been genetically changed so it is impossible for it to grow in humans.
It is hoped the vaccine will make the body recognise and develop an immune response to the spike protein – recognisable in images of the virus – that will help stop Covid-19 from entering human cells and therefore prevent infection.
AstraZeneca issued a statement saying the late-stage studies of the vaccine had been paused while the company investigates whether the patient’s reported side effect was connected with the vaccine.
A spokeswoman said the pause was part of a standard review process which occurs in trials if there is a “potentially unexplained illness” reported in any trial subject, and that the subject’s illness could also be coincidental.
No details about the patient suffering the potential side effect, or the nature of the reaction, were given.
But The New York Times has reported that the patient had been diagnosed with transverse myelitis, an inflammatory syndrome that affects the spinal cord often sparked by viral infections.
AstraZeneca said it had voluntarily paused vaccination to allow review of safety data by an independent committee to take place.
Wellcome Trust director and Sage member Professor Sir Jeremy Farrar told BBC Radio 4’s Today programme that such an occurrence is quite common but each one must be taken seriously.
He said an independent investigation would look at whether the illness in the trial volunteer is related to the vaccine or placebo and, if not, then the trial can restart safely.
Prof Farrar added that it is inevitable that some of the 30,000 to 40,000 people given the vaccine will have illnesses unrelated to it.
Temporary holds of large medical studies are not uncommon, and looking into any unexpected reactions is a mandatory part of safety testing.
There was a pause earlier in the summer and that was resolved without a problem
It was not immediately clear how long AstraZeneca’s pause would last.
Health Secretary Matt Hancock said the Oxford vaccine trial had been paused earlier in the year.
He said: “There was a pause earlier in the summer and that was resolved without a problem.”
The vaccine is being trialled in tens of thousands of volunteers in the UK, South Africa, Brazil and the US.
It is expected that there will be up to 50,000 participants globally, the University of Oxford has said.
This trial aims to assess how well people across a broad range of ages could be protected from Covid-19.
Results from the late-stage trials are anticipated later this year, the university has said.
The results of the clinical trials, published in The Lancet in July, indicate that the vaccine candidate has triggered two responses in the immune system.
The first is that it stimulates the immune system to produce antibodies – proteins produced by the blood in response to antigens which are harmful substances that come from outside the body, such as from viruses or bacteria – and that it also causes the body to produce T-cells.
Oxford’s Covid-19 vaccine produces a good immune response, reveals new study.
Teams at @VaccineTrials and @OxfordVacGroup have found there were no safety concerns, and the vaccine stimulated strong immune responses: https://t.co/krqRzXMh7B pic.twitter.com/Svd3MhCXWZ— University of Oxford (@UniofOxford) July 20, 2020
If the non-specific immune cells which respond to any invader instantly cannot tackle it, the T-cells come into play.
These cells attack the virus directly.
With questions remaining about the duration of the antibody response to Covid-19, research suggests T-cells have a more important role in offering protection against the disease.
