Normally it takes years to prove a new vaccine is both
safe and effective before it can be used in the field. But with hundreds of
people dying a day in the worst ever outbreak of Ebola, there is no time to
wait.
In an effort to save lives, health authorities are
determined to roll out potential vaccines within months, dispensing with some
of the usual testing, and raising unprecedented ethical and practical questions,
Reuters reports.
"Nobody knows yet how we will do it. There are
lots of tough real-world deployment issues and nobody has the full answers
yet," said Adrian Hill, who is conducting safety trials on healthy
volunteers of an experimental Ebola shot developed by GlaxoSmithKline.
Hill, a professor and director at the Jenner Institute
at Britain's University of Oxford, says that if his results show no adverse
side-effects, GSK's new shot could used in people in West Africa by the end of
this year.
Even if a drug is shown to be safe, it takes longer to
prove it is effective - time that is simply not available when cases of Ebola
infection are doubling every few weeks and projected by the World Health
Organization to reach 20,000 by November.
Among questions that scientists are grappling with:
should an unproven vaccine be given to everybody, or just a few? Should it be
offered to healthcare workers first? The young before the old? Should it be
used first in Liberia where Ebola is spreading fastest, or Guinea where it is
closer to being under control?
Should people be told to assume it will protect them
from Ebola? Or should they take all the protective measures they would if they
hadn't been vaccinated? And if so, how will anyone know whether the vaccine
works?
GSK is one of several drug firms that have either
started or announced plans for human trials of candidate Ebola vaccines. Others
include Johnson & Johnson, NewLink, Inovio Pharmaceuticals and Profectus
Biosciences.
The WHO says it hopes to see small-scale use of the
first experimental Ebola vaccines in the West Africa outbreak by January next
year.
It has convened vaccine specialists, epidemiologists,
pharmaceutical companies and ethicists, for a meeting on Monday and Tuesday to
discuss the moral and practical issues.
"Normally safety is the absolutely paramount
thing when you're developing a new vaccine, but this time we're going to have
to take more risks," said Brian Greenwood, a professor at the London
School of Hygiene and Tropical Medicine who will take part in the WHO-led
meeting.
"Quite how we do that, and what risks we take,
hasn't really been thought through yet. That's what people are trying to figure
out."
TWO THINGS AT THE SAME TIME
The chaos caused by the epidemic itself makes it even
more difficult to deploy and track use of a new vaccine, said Hill.
"You're trying to do two things at the same time:
you're trying to evaluate a vaccine and deploy it - when normally you would
evaluate the vaccine first, by doing a randomised double blind controlled
trial, and then you'd deploy it if it was shown to be safe and effective."
Because Ebola virus is so deadly, those who receive a
trial vaccine must be told to take all other precautions and protect themselves
fully. This could make it harder for researchers to decipher whether the
protective clothing and safety protocols, or the new vaccine, is what kept them
safe.
Ebola vaccine
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Normally researchers testing a vaccine would give some
volunteers a placebo, or dummy, to create a "control" group to
compare against those who get the real drug. That seems unthinkable in a
situation where disease with a death rate of up to 90 percent is raging through
villages.
"Would it be ethical to do a trial where some
people don't get the vaccine because they are in the control group? Most people
think it wouldn't be - especially if you have reasonable evidence that the
vaccine might work," said Hill.
Jeremy Farrar, an infectious diseases expert and
director of the Wellcome Trust medical charity, said limited supplies of any
candidate vaccine could result in a form of natural control group being formed
anyway. Researchers can compare populations where the vaccine is available with
those where it isn't.
GSK has said it is aiming to have 10,000 doses of its
experimental shot by the end of the year, while Canada has given 800 vials of
the NewLink candidate vaccine to the WHO, expected to yield at least 1,500
doses.
Most experts interviewed by Reuters favour the idea of
the first doses going to frontline healthcare workers, since their exposure to
risk is so high. Researchers could then compare infection rates among health
workers who receive the vaccine to those working in regions still waiting for
it.
Peter Piot, a co-discoverer of the Ebola virus in 1976
and now director of the London School of Hygiene and Tropical Medicine said
that however complicated the ethics, reverting to the traditional years-long
process of testing vaccines, and withholding them from West Africa until then,
is not an option.
"It
may be that without a vaccine, we can't really stop this epidemic," he
said.
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