Combat HIV via the CRISPR system
With permission from NPG |
The authors first transduced 293T cells with replication incompetent lentiviruses carrying a GFP as a target for CRISPR. Not surprisingly disruption of GFP was readily detectable in Cas9/gRNA expressing cells. Novelty here is that it seems Cas9 can target the pre-integration viral genome, i.e. the human chromosomal environment is not required for action (as assayed by non-integrating lentiviruses). This is quite plausible, since the original bacterial CRISPR system indeed inactivates viral and plasmid DNA sequences, which have not been integrated into the host. Interestingly, CRISPR was able to be active in a high copy number system, projecting its usefulness in transgene animal models, where multiple copies of the transgene is present.
Also not surprisingly CRISPR was able to target HIV viral sequences in 293T.CD4.CCR5 cells, latently infected human T cell lines and differentiated human pluripotent stem cells. However, primary human T-cells were conferred only partially resistant to HIV infection.
This study is in correlation with other studies demonstrating antiviral effect of CRISPR against hepatitis B virus, papillomavirus, herpes simplex virus. I'm not sure how these findings are translatable to human clinical trials.
Full text of the paper here: Liao HK, Gu Y, Diaz A, Marlett J, Takahashi Y, Li M, Suzuki K, Xu R, Hishida T, Chang CJ, Esteban CR, Young J, Izpisua Belmonte JC. Use of the CRISPR/Cas9
system as an intracellular defense against HIV-1 infection in human cells. Nat Commun. 2015 Mar 10;6:6413. doi: 10.1038/ncomms7413.
No comments:
Post a Comment