This research has brought hope to cure the disease of the century.(Photo: Shutterstock / vchal.)
The team conducted experiments on three groups of mice:
With the first group, the scientists managed the gene while blocking the ability of HIV-1 to work and reducing the expression of RNA by viral genes by up to 95% compared to previous studies.
In the second group, the EcoHIV virus is easily spread, multiplying rapidly. During an acute infection, the HIV virus will actively regenerate. For mice infected with EcoHIV, when scientists used CRISPR / Cas9 gene editing technology , 96% of the mice 's viruses were removed, successfully preventing replication and spread of the EcoHIV virus. This demonstrates the ability of the HIV-1 virus to be removed by the CRISPR / Cas9 system.
With the third group after only one treatment with CRISPR / Cas9, latent virus in the tissues and organs of mice was completely removed.
This is the first time scientists have succeeded in completely eliminating the HIV virus in living animals and in the future they will conduct experiments on primates and eventually human clinical trials.
CRISPR-Cas9 is a popular genetic modification method. A protein called Cas9 derived from bacteria is used as a tool to make precise changes to the genomes of living cells.
CRISPR-Cas9 has a blade-like function to cut DNA while the rest is RNA that puts a scalpel to the right nucleotide (structural unit of DNA) for cutting. As a result, scientists can inject artificial genes to specific regions of DNA and cut them accurately. CRISPR has been used to "neutralize" genes and remove small fragments of broken DNA.
Previously, CRISPR has been used by scientists to modify genes that cause HBB hemolytic anemia or là thalassemia.