AIDS is a particularly difficult infection to treat because it actually infiltrates, and becomes part of, the patient’s own DNA. It’s not easy to edit our own genetic blueprint. But we have new techniques…
In 2019, researchers at Temple University and the University of Nebraska found that using Crispr to delete those regions eliminated HIV from the genomes of rats and mice. A year later, the Temple group also showed that the approach safely removed viral DNA from macaques with SIV, the monkey version of HIV…
The Excision trial will eventually enroll nine participants and test three dosage amounts to determine which is most effective.
Layperson-friendly article: https://arstechnica.com/science/2022/10/a-bold-effort-to-cure-hiv-using-crispr/.
Detailed report: https://www.nature.com/articles/s41467-020-19821-7.
By the way, CRISPR techniques (CRISPR stands for Clustered Regularly Interspaced Short Palindromic Repeats) are something we learned by studying bacteria, which can be attacked by viruses. They evolved a way to recognize and destroy viral genetic codes, a crude immune system. Researchers first discovered the repeats in 1987 (see Wikipedia), and studied these for years, eventually resulting in a Nobel Chemistry Prize in 2020 for Emmanuelle Charpentier and Jennifer Doudna.
