This finding identifies yet another hurdle to finding effective therapies to clear the viral reservoir and ultimately cure HIV.
April 25, 2017
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Defective copies of HIV that are integrated into long-living immune
cells distract the immune system, complicating the effort to track down
and kill viable copies of the virus. This finding identifies yet another
hurdle to finding effective therapies to clear the viral reservoir and
ultimately cure HIV.
When HIV infects an immune cell,
the virus integrates its genetic materials into the cell’s own DNA,
yielding what is known as an HIV provirus. However, the majority of
proviruses cannot produce new, intact copies of HIV because of flaws in
the reproduction process. Consequently, until recently,
researchers believed that proviruses amounted to a biological dead end
and that cells latently infected (meaning they are not replicating and
are therefore invisible to standard HIV treatment) with defective
provirus could not prompt a repopulation of the virus in the body.
Publishing
their findings in Cell Host & Microbe, scientists studied memory
CD4 cells drawn from HIV-positive individuals as well as reconstructed
defective proviruses drawn from people with HIV. Latently infected
memory CD4 cells, which can live a very long time, are a major component
of the viral reservoir, the presence of which frustrates attempts to
cure the virus.
The investigators concluded that the
presence of the defective proviruses promotes the survival of the
overall HIV infection by serving as a decoy. The immune system,
recognizing the viral proteins that serve as signs of infection in the
cells infected with defective proviruses, wastes resources attacking
those cells.
In its effort to seek out and destroy
proviruses, the immune system is confronted with a needle-in-a-haystack
effort because people with HIV have about 1,000 times more defective
proviruses than viable ones, and the immune system apparently cannot
detect the difference between them.
This decoy effect
also complicates the effort to measure the viral reservoir because most
current tests also cannot distinguish between defective and viable
provirus.
To read a press release about the study, click here.
To read the study abstract, click here.
Read more articles from POZ, here.
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