US researchers say the vaccine offered protection to 13 of 24 rhesus macaques treated in the experiment.
In 12 of the monkeys, the vaccine was still effective 12 months later.
They claim the work, published in the journal Nature, could "significantly contribute" to the development of an effective HIV/Aids vaccine.
The researchers gave 24 healthy rhesus macaques a vaccine
containing a genetically modified form of the virus, rhesus
cytomegalovirus (CMV).
In 13 of the monkeys, the vaccine appeared to offer
protection against simian immunodeficiency virus (SIV), the monkey
equivalent of HIV. Of these 13, 12 monkeys were still protected one year
on.
The researchers say the vaccine works by stimulating the
production of a particular type of blood cell, called "effector memory
T-cells", which can remain vigilant in the body long after an infection
has abated.
Lead author Professor Louis J Picker, of the Vaccine and Gene
Therapy Institute in Oregon, compares these cells to armed soldiers at
the ready.
"There are soldiers that are back at the base with their
rifles in the shed, and then you have the guys out in the field," he
told the BBC.
There was also evidence, he said, that the vaccine all but
eradicated traces of SIV in the monkeys, something which he said was
"unprecedented" in HIV vaccine research.
Safety concerns
Researchers in the field welcomed the study, but said safety
issues would need to be addressed before similar approaches could be
tried in humans.
"I'm excited by the science because it really does
demonstrate that it may be possible to eradicate the HIV virus by a
strong immune response," said Professor Sir Andrew McMichael of Oxford
University.
"But at the same time I'm scratching my head how to take this approach into humans."
Professor McMichael said HIV arose from a type of SIV found in
chimpanzees, so the animal model used in the study was a good one. The
problem, he said, was the potential safety and regulatory issues with
introducing CMV into humans, even though many of us already carry the
virus.
"CMV is not totally benign, it does cause a number of
diseases. If you're giving people something you're not going to be able
to get rid of should it cause problems, then that's quite a difficult
risk to manage."
Professor Robin Shattock of Imperial College, London, agreed safety would be key.
"The breakthrough here is in using a viral-delivered vaccine
that persists - essentially using an engineered virus to thwart a
pathogenic virus. The tricky part will be showing it is safe and
effective in humans."
Professor Picker responded by saying such issues would be
addressed in forthcoming work, pointing out that early forms of the
smallpox vaccine also carried health risks to humans. Read more
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