The Times - UK (2020-07-21)

(Antfer) #1

10 2GM Tuesday July 21 2020 | the times


News


The government has secured at least
90 million doses of potential Covid-
vaccines from overseas companies in
an attempt to spread its risk between
different technologies.
The agreements with German,
American and French pharmaceutical
firms were part of a flurry of announce-
ments which also included plans to sign
up 500,000 British volunteers to take
part in future vaccine trials and a deal to
secure a million doses of an antibody
treatment from AstraZeneca, the Brit-
ish drugmaker.
The new deals represent a bet on
three technologies. They include
30 million doses of an “RNA vaccine”
being developed by Biontech and Pfiz-
er. This involves injecting a small piece
of genetic code into muscle cells, which
then produce coronavirus proteins.
A second deal announced yesterday
morning would allow the purchase of
60 million doses of a vaccine from Val-
neva, a French company that uses an
inactivated form of coronavirus to train
the immune system.
This comes on top of an earlier agree-
ment with AstraZeneca to supply
100 million doses of the Oxford Uni-
versity vaccine, which uses a safe virus
to deliver the code for making a corona-
virus protein.
Both the Oxford and the Biontech
vaccine could be available sooner than
Valneva’s offering, possibly by the end
of the year, but are more experimental.
The decision to place orders for
several types of vaccine reflects the un-
certainty that any of them will work.
Kate Bingham, chairwoman of the
UK Vaccine Taskforce, said the inten-
tion was to have a broad portfolio, in the
hope that one approach succeeded, and
then to use that to vaccinate key work-
ers and the vulnerable. “You’ve got two
of the more advanced vaccine modali-
ties — they are the least well-under-
stood,” she said. “And there’s the boring
one, the inactivated virus, which is bet-
ter understood but less sexy. If you’re
betting you would bet on the boring


ones, not the hairy scary sexy ones. But
we can’t not make an investment in the
hairy scary sexy ones in case they pan
out.” Given the promising early results
of the Oxford vaccine, they were hope-
ful for a positive early result, she said.
If the Valneva vaccine, which has not
yet entered human trials, is shown to be
safe and effective, the government has

pledged to back the manufacture of
another 40 million doses, probably at
its factory in Livingston, Scotland.
Many would be distributed abroad.
Alok Sharma, the business secretary,
said: “We are doing everything we can
to ensure the British public get access to
a safe and effective coronavirus vaccine
as soon as possible. This new partner-

Quarter of


Britons may


decline to


have vaccine


Kat Lay Health Correspondent

More than a quarter of Britons might
refuse to have a Covid-19 vaccine even
if one passes all trials.
Some 14 per cent of people in a poll
said that they would not want to be
vaccinated against coronavirus “if a
high quality vaccine were available”,
with a further 13 per cent “unsure” if
they would have the jab.
There are concerns over anti-
vaccination sentiment, with fears that
misinformation is spreading online.
The poll, carried out by ORB
International, surveyed 2,065 people
across the UK last week.
Women were more likely than men
to say they would refuse a vaccine, at 16
per cent compared with 12 per cent.
People aged 65 or over were least
likely to be against Covid-
vaccination, at 9 per cent, compared
with 22 per cent of those aged between
25 and 34.
Paul Hunter, professor of medicine at
the University of East Anglia, told the

The runners


Type Adenovirus vector,
moderately
experimental

Timeline Finished phase
1 trials, phase 2/3 under
way, aiming for full
results by year’s end

Mechanism The Oxford
team think it is enough
to show your immune
system a single bit of the
virus: the spikes on its
outside. The virus uses
these spikes to infect us
and our immune system
learns to destroy them
but on their own they
are harmless. The

Oxford vaccine is a way
of making these spikes
inside you. The vaccine
is itself a virus but one
that cannot reproduce in
humans. Inside this
benign virus is a sliver of
something less benign: a
section of genetic code
from the coronavirus
providing instructions to
make the spike.
After vaccination, your
body starts producing
these spikes and training
the immune system to
spot them. When it sees
them attached to the
coronavirus itself it
should know what to do.

Oxford University Biontech-Pfizer


Type mRNA, very
experimental

Timeline Finished
phase 1 trials, aiming for
full results by year end

Mechanism For
vaccinologists this is not
only the most
experimental vaccine
but also the most
exciting. It is a wholly
new technology, similar
to that also being tested
by the Imperial College
team, based on a piece
of genetic code called
mRNA. Inside our bodies
mRNA is the last step in

making proteins. It
converts DNA
instructions into the
molecules used to
power our bodies. The
trick is to use this
process for the vaccine’s
own ends. The mRNA
that Biontech is injecting
makes a protein seen on
the outside of the
coronavirus: a protein
spike. The hope is that
our cells will gobble up
the mRNA, turn into
spike factories and
churn them out, training
the body to spot the real
thing. Nothing like this
has been done before.

Valneva


Type Inactivated full
virus, standard tech

Timeline Not in human
trials until the end of the
year, full results by
mid-2021 at the earliest

Mechanism Valneva’s
vaccine is, from an
immunological
perspective, the most
boring. It is far closer to
the sort of vaccine that
you will have learnt
about at school than the
sort scientists now
consider cutting edge.
The French company is
making a deactivated

version of the
coronavirus, set to be
manufactured in
Scotland. It is a little like
a car without an engine.
What they inject will
look like coronavirus. It
will have the bodywork
of coronavirus but, like
an engineless car, it
won’t go. Your immune
system will, it is hoped,
make antibodies that
latch on to the spikes on
the outside, and T-cells
that can chomp on to
cells infected by it. When
the real thing revs it can
defeat it before it has
time to get going.

Coronavirus Chimpanzee virus Antibody

Gene

Inactivated virus used to transport the genetic
code for a coronavirus spike into the body,
where it is then manufactured, provoking an
immune response

Cell

Genetic code for a coronavirus spike is transported
straight into body’s cells, which start producing
copies

Antibody

Genetic
code

Live virus is inactivated and injected
into body, teaching the immune
system what to recognise

Inactivated
virus

Coronavirus

The Tory and Labour leaders focused

News Coronavirus


Bets are placed on 190m doses,


Rhys Blakely Science Correspondent
Tom Whipple Science Editor


ship with some of the world’s foremost
pharmaceutical and vaccine compa-
nies will ensure the UK has the best
chance possible of securing a vaccine
that protects those most at risk.”
Yesterday’s announcements re-
flected a belief, however, that the
pandemic still has a long way to run. An
NHS Covid-19 vaccine research
registry was also launched. The online
service should allow members of the
public to register their interest and be
contacted to participate in clinical
studies. The aim is to get 500,
volunteers signed up by October — but
they will only be a useful resource if
significant viral transmission remains.
Professor Chris Whitty, the chief
medical officer for England, said:
“Thanks to Covid-19 patients’ willing-
ness to take part in treatment studies,
we’ve been able to identify treatments
that work and ones that don’t, which
has improved patient care worldwide.
Now that there are several promising
vaccines on the horizon, we need to call
again on the generosity of the public to
help find out which potential vaccines
are the most effective. Please go to the
website and consider volunteering.”
As part of a wider £131 million invest-
ment by the government, support has
also been given to Imperial College
London to develop their vaccine candi-
date, which started human studies in
June. The government has also reached
an agreement “in principle” to buy a
million doses of a treatment containing
laboratory-made Covid-19 antibodies
from AstraZeneca. This could be used
by people for whom vaccines are not
suitable, such as cancer patients whose
immune systems are compromised.
Without any guarantee that any
one vaccine will work, talks are being
held internationally to find ways to
pool the risk between nations, and
ensure equitable access for at-risk
groups. The government has pledged
£250 million to the Coalition for
Epidemic Preparedness Innovations, a
global group working to ensure that
treatments and vaccines are available
around the world.
Drugmaker’s shares boom, pages 38-

Analysis


W


hen the
first
vaccine
is shown
to work against
coronavirus, the world
will demand
eight billion doses
(Tom Whipple writes).
To understand what
that means, consider
this warning from
Peter Piot, director of
the London School of
Hygiene and Tropical
Medicine: the world
does not even have
that many glass vials,
let alone the vaccine
doses to put in them.
That is why Britain
has secured access to
90 million doses of
vaccines that might
not work. This is to
add to our early
purchase of a similar
number of doses of
the Oxford vaccine,
another that, despite
promising phase 1
results yesterday,
might also not work.
It is great news that
Oxford has developed
an immune response,
but all vaccines are
long shots. The reason
for these early
purchases is simple.
When — if — the

vaccines are proven to
work we will be ready
to go. At that point
these vaccines — two
of which we cannot
make at scale on
British soil — will be
the most in-demand
pharmaceutical
product in history.
And there is no
guarantee that we will
get them. So rather
than buying them
after they have
succeeded in trials,
we buy them before,
as a bet.
The three vaccines
Britain has bought
range from the
experimental to the
bog-standard.
Biontech-Pfizer’s is
cutting edge. Oxford’s
is still new
technology, but with
an approach shown to
work in the past. In
including Valneva’s
offering, an
inactivated version of
the virus, the
government is
accepting that in the
vaccine race the
tortoise of tried and
true methods might
beat the hare of the
speedy but flashy
alternatives.

Until we put these
vaccines into people,
and then expose them
naturally to the virus,
we have no idea
whether they will
work.
No vaccine has
been shown to beat
this coronavirus. In a
year’s time the world
hopes one will. We
must hope that one of
Britain’s purchases
pays off. If it doesn’t,
we will have to rely on
other countries.
That is why talks
are also under way to
make international
spread bets, to pool
risk before and pool
results after.
It may be that one
of the vaccines
Britain has bought
stops the virus. If so,
we will vaccinate our
elderly and
vulnerable; and we
may well donate what
remains to other
countries. To give
away vaccines we can
use might be
politically difficult but
it will be easier than
finding that none of
ours works and that
no one is prepared to
help.
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