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French
Therapeutic AIDS Vaccine Shows Promise in Early Testing
By Sabin Russell, San Francisco Chronicle
French
researchers reported [this week] that an AIDS vaccine designed to
treat the disease, rather than prevent it, has scored an initial
success by suppressing the virus for up to a year among a small
group of patients who tried it.
Although
the technique is cumbersome and costly, the experiment published
in an online version of the British journal Nature Medicine
is being touted as "the first demonstration of an efficient
therapeutic
vaccine
against AIDS."
The
vaccine was tested in Brazil on 18 volunteers who were already infected
with HIV, the virus that causes AIDS, but who were not yet taking
any antiviral drugs. After four months, the level of HIV in their
bloodstreams had been reduced an average of 80 percent.
By
the end of one year, eight patients in the group had maintained
a 90 percent reduction in virus particles in their bloodstream.
Four of those patients had virus levels so low that they were comparable
to so-called "long- term non-progressors," a rare cohort
of people infected with HIV who never seem to get sick.
Unlike
a conventional vaccine, this one cannot block infection from occurring.
However, if the French technique could be perfected, it has the
potential to keep some HIV-infected patients healthy without their
having to take the three-drug "cocktails" of toxic antiviral
drugs.
Instead,
a series of injections, perhaps once a year, would keep their chronic
infections in check.
The
lead investigators in the French study are Drs. Jean-Marie Andrieu
and Wei Lu of the Institute of Research for Vaccines and Immunotherapies
for Cancer and AIDS, in Paris.
In
an interview, Andrieu estimated that the cost of the annual therapy
could be $4,000 to $8,000, less than a year's course of antiviral
drugs. He said the only side effect of the therapy was a swelling
of the lymph nodes, which caused no pain. The swelling was, in fact,
an indicator that the vaccine was marshalling the body's immune
system properly to ward off the AIDS virus.
No
new patients have been enrolled in the experiment, but Andrieu said
future research will attempt to understand "why it works in
some people, and not in others.''
Although
the experiment falls short of a breakthrough against AIDS, it represents
a rare piece of good news in the field of vaccine research, which
has been marked in recent years by a string of setbacks.
UCSF
Doctor Sees Cause for Hope
"This
is just a preliminary study, but it is encouraging,'' said virologist
Dr. Jay Levy of the UCSF AIDS Research Institute. Levy did not participate
in the research but is familiar with its findings.
Further
studies are needed, Levy said, to learn exactly why the vaccine
worked better than other, similar versions. A critically important
step would be to determine whether the vaccine also reduced the
amount of virus in sexual fluids. If it did so, a population of
HIV infected individuals treated with the therapeutic vaccine would
be less likely to transmit the virus to others. "The purpose
of a real vaccine is to protect a population. This would have that
advantage,'' Levy said.
At
present, however, the vaccine is difficult to produce, and impractical
to deliver to large numbers of people. This therapeutic vaccine
is essentially custom-made for each patient who takes it.
To
make a dose of vaccine, the French doctors extract from each HIV-
infected patient a sample of dendritic cells -- starfish-shaped
white blood cells that play a special role in the human immune system.
They also take a sample of the virus from the infected blood of
each patient.
In
the laboratory, they separately grow uninfected dendritic cells
and a batch of the virus itself. The virus is eventually killed
and mixed in with the dendritic cells, whose special function then
becomes vital.
The
dendritic cells consume the virus, breaking it into pieces and displaying
the parts on their surfaces like grisly trophies.
Doctors
then inject the dendritic cells back into each patient.
Lymph
nodes receive the message inside
the body, the dendritic cells migrate to the lymph nodes, carrying
their message of an invading microbe to resting banks of "killer"
white blood cells. The broken bits of HIV on the dendritic cell's
surface help to program these killer cells to recognize the virus
-- like bloodhounds given a scent to chase. Once activated, they
will seek out and destroy any cell in the human body that is infected
by HIV.
It
is a system of "cellular immunity" that the body routinely
uses to protect itself. The AIDS virus, for reasons not fully understood,
has managed to hijack the process. Dendritic cells are, in fact,
one of the favored targets of living HIV, and once it ferries HIV
to the lymph nodes, it then infects other white blood cells, making
more copies of itself, and eventually depleting the cells.
The
French laboratory intervention, by mixing dendritic cells outside
the body with killed HIV, seems to restore their proper defensive
role when they are returned to the body.
It
is this focus on dendritic cells, and the use of a whole, killed
virus, that distinguishes the French effort from other attempts
to make a therapeutic vaccine.
Any
optimism about the French experiment must be tempered with caution.
The history of AIDS vaccine research is littered with failure. An
attempt by British and Kenyan scientists to use this concept of
cellular immunity to make a preventive vaccine was abandoned in
August after a trial in Nairobi showed it did not stir up a strong
enough response to protect against HIV.
Laboratory
experiments with a similar vaccine that showed great promise in
monkeys have slowed after further studies showed the virus was able
to mutate into a vaccine-resistant strain.
12/01/04
Source
S
Russell. French vaccine fuels hope in AIDS treatment. San Francisco
Chronicle. November 29, 2004.
Reference
Wei Lu and others. Therapeutic
dendritic-cell vaccine for chronic HIV-1 infection. Nature
Medicine. Published online November 28, 2004.
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