produced promising results, U.S. scientists said, raising hopes that protection from the deadly disease may be on the horizon.
All 20 healthy adults who
received the vaccine in a trial run by researchers from the National
Institutes of Health in Maryland produced an immune response and
developed anti-Ebola antibodies, the NIH said Wednesday.
None suffered serious side effects, although two people developed a brief fever within a day of vaccination.
The vaccine is being
developed by the NIH's National Institute of Allergy and Infectious
Diseases and British pharmaceutical giant GlaxoSmithKline. The process
has been fast-tracked in light of the current catastrophic Ebola
outbreak in West Africa, which has claimed more than 5,000 lives.
"Based on these positive
results from the first human trial of this candidate vaccine, we are
continuing our accelerated plan for larger trials to determine if the
vaccine is efficacious in preventing Ebola infection," said Anthony
Fauci, director of the National Institute of Allergy and Infectious
Diseases.
In this trial, genetic
material from two strains of the Ebola virus, Sudan and Zaire, was
delivered using a chimpanzee cold virus that does not harm humans. The
vaccine does not contain the Ebola virus and cannot cause a person to be
infected with Ebola, the NIH said. The current outbreak involves the
Zaire strain.
Blood tested
The adults, volunteers
ages 18 to 50, were split into two groups. Half received an
intramuscular injection of vaccine at a lower dose and 10 received the
same vaccine at a higher dose, the NIH said.
Researchers tested the
volunteers' blood at two weeks and four weeks after vaccination to
determine if anti-Ebola antibodies had been produced.
All 20 volunteers
developed such antibodies within four weeks of receiving the vaccine,
with levels higher in those who were given the higher-dose vaccine.
The researchers also
looked to see if the vaccine prompted production of immune system cells
called T cells, after a previous study on primates using the same
vaccine suggested they may also help to protect from the disease.
They found that many of
the volunteers did produce T cells, including CD8 T cells, which may
play a crucial role in protecting against infection by Ebola viruses.
Four weeks after
vaccination, the CD8 T cells were found in two volunteers who received
the lower-dose vaccine and in seven who had the higher dose, the NIH
said.
The two volunteers who briefly developed a fever had received the higher-dose vaccine.
Unanswered questions
Professor Andrew Easton,
a leading virologist at Britain's Warwick University, told CNN that the
trial was an "essential first step" toward a vaccine to prevent Ebola
and justifies some optimism.
However, there are still some unanswered questions, he said.
"We know from some of
the preliminary work that went on in animal studies previously that the
antibodies that are generated in response to the vaccine don't last as
long as we would like -- there was a clear reduction over a fairly long
period of time, about 10 months," he said.
"So it's possible that
that might be a problem in humans, but the reality is we won't know
until it's actually been tested in humans.
"We can hope that it
will provide a longer-term protection. If it doesn't, at least it gives
us some level of protection over a window, which could be enormously
valuable in protecting people from outbreaks at the time the outbreaks
occur."
Other approaches are
being looked at too, he said, and will also benefit from the World
Health Organization's decision this summer to allow some processes to be
fast-tracked.
Source:CNN

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