Extracting CD4 T cells from 12 patients, researchers from the University of Pennsylvania, the Albert Einstein College of Medicine, and Sangamo BioSciences used a zinc-finger nuclease to disable the CCR5 gene, and reinfused the immune cells—of which 11 percent to 28 percent were modified at the CCR5 gene—into the patients. HIV was at undetectable levels in one of the treated patients, and in all 6 patients who stopped their regimen of antiretroviral drugs, modified T cells declined significantly less than untreated cells. This suggested that the gene editing protected the immune cells from HIV invasion. “It’s a great strategy,” Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, who was not involved in the research, told The New York Times. “It’s exciting, interesting, elegant science. But a lot of ‘ifs’ need to be addressed before you can say ‘Wow, this could really work.’”
In other news, a nine-month-old baby in Southern California who was born with the virus appears to be HIV-free after receiving antiretroviral treatment since she was four hours old. Pediatrician Audra Deveikis gave the infant a cocktail of three drugs—AZT, 3TC, and nevirapine—at high doses typically used for treating the virus. “Of course I had worries,” Deveikis said in an interview at a Boston conference where she broke the news. “But the mother’s disease was not under control, and I had to weigh the risk of transmission against the toxicity of the meds.”
The “Long Beach baby,” as she is being called, is the second case of an HIV-positive baby becoming HIV negative after early administration of antiretrovirals. Last March, researchers reported that a baby in Mississippi was given powerful HIV medications within 30 hours of birth. That child is now three years old and is HIV free.