Healthbeat
August 1, 2008 1:35 PM

BY: LEIGH ANN STUART




Scientists discovered that by sabotaging the gene that creates chemokine (C-C motif) receptor 5, a surface protein to which HIV bonds, the HIV virus is essentially unable to enter its targeted cell.

The gene is altered using a “zinc-finger nuclease,” comprised of a zinc-finger component that binds exclusively to genetic material found in the CCR5 gene, and a “nuclease” section that essentially castrates the gene, rendering it incapable of ever making CCR5 again – thus effectively rendering the cells HIV infection immune.
Researchers tested their theory by treating mice with the zinc-finger nuclease, then infecting the animals with HIV. Findings after six weeks, compared to a control group, indicated a 10-fold suppression of the HIV virus and a five-fold increase in circulating T-cells, usually ravaged by HIV.

The developing scientists hope to test their method in human patients by the end of this year.

“[The new technology] prevents women from having a painful, scary procedure while they are awake and substitutes an equally effective injection performed while they are sedated or asleep,” said Woltering in a June 24 LSUHSC press release.

 The next step toward FDA approval of the technology will be a Phase II clinical trial to be conducted at University Medical Center in Lafayette.