Scientists have removed HIV from human immune cells using a new gene-editing technique

Using the much-touted CRISPR/Cas9 gene editing method, 科学家证明了他们如何从人类免疫细胞DNA中编辑出HIV, and in doing so, can prevent the reinfection of unedited cells too.

If you haven’t heard of the CRISPR/Cas9 gene-editing technique before, get ready to hear a whole lot more about it in 2016, because it’s set to revolutionise how we investigate and treat the root causes of genetic disease. It allows scientists to narrow in on a specific gene, and cut-and-paste parts of the DNA to change its function.
CRISPR/Cas9 is what researchers in the UK have recently gotten approval to use on human embryos so they can figure out how to improve IVF success rates and reduce miscarriages, and it’s what Chinese scientists were caught using in 2015 to tweak human embryos on the down-low.

Earlier this year, scientists started using CRISPR/Cas9 to successfully treat a genetic diseaseDuchenne muscular dystrophyin living mammals for the first time, and now it’s showing real potential as a possible treatment for HIV in the future.

The technique works by guiding ‘scissor-likeproteins to targeted sections of DNA within a cell, and then prompting them to alter or ‘editthem in some way. CRISPR refers to a specific repeating sequence of DNA extracted from a prokaryotea single-celled organism such as bacteriawhich pairs up with an RNA-guided enzyme called Cas9.

So basically, if you want to edit the DNA of a virus within a human cell, you need a bacterium to go in, encounter the virus, and produce a strand of RNA that’s identical to the sequence of the virtual DNA.

This ‘guide RNAwill then latch onto the Cas9 enzyme, and together they’ll search for the matching virus. Once they locate it, the Cas9 gets to cutting and destroying it.

Using this technique, researchers from Temple University managed to eliminate HIV-1 DNA from T cell genomes in human lab cultures, and when these cells were later exposed to the virus, they were protected from reinfection.



While gene-editing techniques have been trialled before when it comes to HIV, this is the first time that scientists have figure out how to prevent further infections, which is crucial to the success of a treatment that offers better protection than our current antiretroviral drugs. Once you stop taking these drugs, the HIV starts overloading the T-cells again.

Antiretroviral drugs are very good at controlling HIV infection,” “But patients on antiretroviral therapy who stop taking the drugs suffer a rapid rebound in HIV replication.

There’s still a lot more work to be done in getting this technique ready for something more advanced than human cells in a petri dishparticularly when it comes to perfect accuracy for the ‘cuttingprocessbut it’s an exciting first step.


分类: 干细胞治疗