Publishing in the Sept. 2005 issue of the Journal of Virology, the researchers show that HIV in the temporal lobe mutates at a rate 100 times faster than in other parts of the body, triggering white blood cells to continually swarm to attack the infection. The associated overcrowding and inflammation appear to cause the dementia.

Earlier studies had suggested that the build-up of white blood cells could lead to HIV-related dementia, but this is the first study to track the probable mechanism.

The findings could lead to new treatments that target HIV-infected white blood cells, perhaps one day countering the brain wasting that will affect as many as 15 percent of the nearly 40 million people around the world who are infected with the virus.

The study is a collaboration among researchers at the University of California at Irvine, the University of Florida at Gainesville, Gene Johnson, Inc., of St. Augustine, Fla., the University of California at San Francisco (UCSF) and the University of Oxford in the United Kingdom.

One of the critical tools behind the discovery is HIVBase, a genetic data-storage and -analysis tool with which the researchers tracked the rapidly evolving viruses. Gene Johnson developed the tool with the support of an NSF Small Business Innovation Research award.

According to co-author Susanna Lamers of Gene Johnson and UCSF, the results strengthen an earlier hypothesis by Kenneth Williams of Harvard University and William Hickey of Dartmouth Medical School. They had suggested that the continual build-up of white blood cells in the brain could lead to HIV-associated dementia.

"In our work," says Lamers, "we conducted a thorough examination of HIV genetic sequences and were able to prove that the researchers' concept was a good expla
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Contact: Josh Chamot
jchamot@nsf.gov
703-292-7730
National Science Foundation
29-Sep-2005