A baby girl in Mississippi who was born with HIV has been
cured after very early treatment with standard HIV drugs, U.S. researchers
reported on Sunday, in a potentially ground-breaking case that could offer
insights on how to eradicate HIV infection in its youngest victims.
Dr. Deborah Persaud |
The child’s story is the first account of an infant
achieving a so-called functional cure, a rare event in which a person achieves
remission without the need for drugs and standard blood tests show no signs
that the virus is making copies of itself.
More testing needs to be done to see if the treatment would
have the same effect on other children, but the results could change the way
high-risk babies are treated and possibly lead to a cure for children with HIV,
the virus that causes AIDS.
“This is a proof of concept that HIV can be potentially curable
in infants,” said Dr. Deborah Persaud, a virologist at Johns Hopkins University
in Baltimore, who presented the findings at the Conference on Retroviruses and
Opportunistic Infections in Atlanta.
The child’s story is different from the now famous case of
Timothy Ray Brown, the so-called “Berlin patient,” whose HIV infection was
completely eradicated through an elaborate treatment for leukemia in 2007 that
involved the destruction of his immune system and a stem cell transplant from a
donor with a rare genetic mutation that resists HIV infection.
“We believe this is our Timothy Brown case to spur research
interest toward a cure for HIV infection in children,” Persaud said at a news
conference.
Instead of Brown’s costly treatment, however, the case of the
Mississippi baby, who was not identified, involved the use of a cocktail of
widely available drugs already used to treat HIV infection in infants.
When the baby girl was born in a rural hospital in July
2010, her mother had just tested positive for HIV infection. Because her mother
had not received any prenatal HIV treatment, doctors knew the child was at high
risk of infection. They transferred her to the University of Mississippi
Medical Center in Jackson, where she came under the care of Dr. Hannah Gay, a
pediatric HIV specialist.
Because of her risk, Dr. Gay put the infant on a cocktail of
three HIV-fighting drugs – zidovudine (also known as AZT), lamivudine, and
nevirapine – when she was just 30 hours old. Two blood tests done within the
first 48 hours of the child’s life confirmed her infection and she was kept on
the full treatment regimen, Persaud told reporters at the conference.
In more typical pregnancies, when an HIV-infected mother has
been given drugs to reduce the risk of transmission to her child, the baby
would only have been given a single drug, nevirapine.
Researchers believe use of the more aggressive
antiretroviral treatment when the child was just days old likely resulted in
her cure by keeping the virus from forming hard-to-treat pools of cells known
as viral reservoirs, which lie dormant and out of the reach of standard
medications. These reservoirs rekindle HIV infection in patients who stop
therapy, and they are the reason most HIV-infected individuals need lifelong
treatment to keep the infection at bay.
10-MONTH GAP
After starting on treatment, the baby’s immune system
responded and tests showed diminishing levels of the virus until it was
undetectable 29 days after birth. The baby received regular treatment for 18
months, but then stopped coming to appointments for a period of about 10
months, when her mother said she was not given any treatment. The doctors did
not say why the mother stopped coming.
When the child came back under the care of Dr. Gay, she
ordered standard blood tests to see how the child was faring before resuming
antiviral therapy.
What she found was surprising. The first blood test did not
turn up any detectible levels of HIV. Neither did the second. And tests for
HIV-specific antibodies, the standard clinical indicator of HIV infection, also
remained negative.
“At that point, I knew I was dealing with a very unusual
case,” Dr. Gay said.
Baffled, Dr. Gay turned to her friend and longtime
colleague, Dr. Katherine Luzuriaga of the University of Massachusetts, and she
and Persaud did a series of sophisticated lab tests on the child’s blood.
The first looked for silent reservoirs of the virus where it
remains dormant but can replicate if activated. That is detected in a type of
immune cell known as a CD4 T-cell. After culturing the child’s cells, they
found no sign of the virus.
Then, the team looked for HIV DNA, which indicates that the
virus has integrated itself into the genetic material of the infected person.
This test turned up such low levels that it was just above the limit of the
test’s ability to detect it.
The third test looked for bits of genetic material known as
viral RNA. They only found a single copy of viral RNA in one of the two tests
they ran.
Because there is no detectible virus in the child’s blood,
the team has advised that she not be given antiretroviral therapy, whose goal
is to block the virus from replicating in the blood. Instead, she will be
monitored closely.
There are no samples that can be used by other researchers
to confirm the findings, which may lead skeptics to challenge how the doctors
know for sure that the child was infected.
Persaud said the team is trying to use the tiny scraps of
viral genetic material they have been able to gather from the child to compare
with the mother’s infection, to confirm that the child’s infection came from
her mother. But, she stressed, the baby had tested positive in two separate
blood tests, and there had been evidence of the virus replicating in her blood,
which are standard methods of confirming HIV infection.
ADDITIONAL RESEARCH
Dr. Anthony Fauci, director of the National Institutes of
Allergy and Infectious Diseases, said although tools to prevent transmission of
HIV to infants are available, many children are born infected. “With this case,
it appears we may have not only a positive outcome for the particular child,
but also a promising lead for additional research toward curing other
children,” he said.
Dr. Rowena Johnston, vice president and director of research
for amfAR, The Foundation for AIDS Research, which helped fund the study, said
the fact that the cure was achieved by antiretroviral therapy alone makes it
“imperative that we learn more about a newborn’s immune system, how it differs
from an adult’s and what factors made it possible for the child to be cured.”
Because the child’s treatment was stopped, the doctors were
able to determine that this child had been cured, raising questions about
whether other children who received early treatment and have undetectable viral
loads may also be cured without their doctors knowing it.
But the doctors warned parents not to be tempted to take
their children off treatment to see if the virus comes back. Normally, when
patients stop taking their medications, the virus comes roaring back, and
treatment interruptions increase the risk that the virus will develop drug
resistance.
“We don’t want that,” Dr. Gay said. “Patients who are on
successful therapy need to stay on their successful therapy until we figure out
a whole lot more about what was going on with this child and what we can do for
others in the future.”
The researchers are trying to find biomarkers that would
offer a rationale to consider stopping therapy within the context of a clinical
trial. If they can learn what caused the child to clear her virus, they hope to
replicate that in other babies, and eventually learn to routinely cure
infections.
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