Researchers may have answered a bedeviling chicken-or-egg question about the persistence of HIV during antiretroviral treatment.
April 24, 2017
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Researchers may have finally answered a bedeviling chicken-or-egg
question about the relationship between the persistence of HIV in the
body during antiretroviral (ARV) treatment and the virus-related immune
system activation and inflammation that also continues while people are
on ARVs. This finding likely adds further weight to the urgency of
diagnosing and treating HIV as soon as possible following infection.
HIV
hides its genetic material in cells or locations in the body that
remain out of reach of ARVs. This result of this overall effect is known
as the viral reservoir, the existence of which prevents standard HIV
treatment from curing the virus.
Publishing their
findings in PLOS Pathogens, researchers from the AIDS Clinical Trials
Group (ACTG) studied 101 people with HIV who had plasma and blood-cell
samples taken before they started ARVs, one and four years after
beginning HIV treatment, and once more between years six and 15 of
treatment. All the participants achieved a viral load considered
undetectable by standard laboratory measures and maintained this level
of viral suppression for an average of seven years, with some doing so
for more than a decade.
The participants experienced
the steepest decline in measures of HIV’s genetic material (detected
with highly sensitive tests) during their first four years on ARVs;
afterward, they still experienced a decline, albeit at a slower pace.
Looking
at the samples taken before the participants started ARVs, the
researchers identified a correlation between levels of HIV and
indicators of immune system activation and inflammation.
However, this
association ceased after the individuals started treatment for the
virus. More specifically, the low levels of HIV found in the samples
taken while people were on ARVs did not seem to influence the levels of
immune system activation and inflammation during that time.
The
investigators ultimately concluded that the levels of both immune
system activation and HIV in the pretreatment samples predicted the
levels of persistence of the virus and immune activation seen in the
samples taken when the participants were on ARVs.
“Our
findings suggest that damage to the immune system that occurs before
people are started on [HIV] treatment leads to continued immune
activation, even though the medicines are keeping the virus in check,”
the study’s lead author, Rajesh Gandhi, MD, of the Massachusetts General
Hospital Division of Infectious Diseases, said in a press release.
“This suggests that diagnosing HIV and starting antiretroviral therapy
as soon as possible may prevent the elevated immune activation that can
lead to health problems, such as heart disease. The results also suggest
that new strategies focused on reducing immune activation may need to
be added to novel interventions designed to reduce and eventually
eliminate HIV.”
To read the study, click here.
To read a press release about the study, click here.
Read more articles from POZ, here.
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