Eradication of these cells could lead to a cure for HIV infection. However, researchers have been hampered by their inability to identify them.
Now Gladstone researchers have found a way to identify and study latently infected cells in the laboratory. Their work is published in the April 15 issue of the European Molecular Biology Organization Journal.
"The latent pool is considered to be the barrier to eradication," said senior author Eric Verdin, MD, senior investigator at the Gladstone Institute of Virology and Immunology and UCSF professor of medicine. "Our work is geared toward finding a way to obliterate this latent pool, which would take us closer to actually finding a cure for AIDS."
Through genetic engineering, the researchers constructed a recombinant HIV strain carrying a green fluorescent protein. Using this marker, they identified a small fraction of infected cells in which the virus was latent. These cells represented less than one percent of the infected population and had eluded purification until this study.
"Before, the study of latent infection was restricted to the analysis of rare cells circulating in the blood of infected patients. As an experimental model to dissect the molecular basis of latency, these cells were very limiting," Verdin said. "We now have a laboratory model that we can use to delve deeply into what is going on."
During infection, the HIV genome integrates into the host cell's DNA. Transcription of the viral genome leads to production of virus. The Gladstone researchers found that, in latently infected cells, the HIV genome is integ
Contact: Daniel Oshiro
University of California - San Francisco