Positive Developments on the HIV Front

A gene-editing protocol shows promise, and a second baby who was started on antiretroviral drugs soon after birth appears to be virus-free a year later.

Written byBob Grant
| 2 min read

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A T cell (blue) covered in HIV (yellow)WIKIMEDIA, NIHThis week was filled with good news about treating HIV. On Thursday (March 6), researchers reported in the New England Journal of Medicine that a gene-editing method that modifies patients’ own immune cells to make some of them lack CCR5, a surface protein critical to HIV’s entry into cells, was safe to use in humans and may even reduce viral load in some HIV patients.

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, ...

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  • From 2017 to 2022, Bob Grant was Editor in Chief of The Scientist, where he started in 2007 as a Staff Writer. Before joining the team, he worked as a reporter at Audubon and earned a master’s degree in science journalism from New York University. In his previous life, he pursued a career in science, getting a bachelor’s degree in wildlife biology from Montana State University and a master’s degree in marine biology from the College of Charleston in South Carolina. Bob edited Reading Frames and other sections of the magazine.

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