Cargando…
Multiplexed tat-Targeting CRISPR-Cas9 Protects T Cells from Acute HIV-1 Infection with Inhibition of Viral Escape
HIV-1 cure strategy by means of proviral knock-out using CRISPR-Cas9 has been hampered by the emergence of viral resistance against the targeting guide RNA (gRNA). Here, we proposed multiple, concentrated gRNA attacks against HIV-1 regulatory genes to block viral escape. The T cell line were transdu...
Autores principales: | Ophinni, Youdiil, Miki, Sayaka, Hayashi, Yoshitake, Kameoka, Masanori |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693572/ https://www.ncbi.nlm.nih.gov/pubmed/33126728 http://dx.doi.org/10.3390/v12111223 |
Ejemplares similares
-
CRISPR/Cas9 system targeting regulatory genes of HIV-1 inhibits viral replication in infected T-cell cultures
por: Ophinni, Youdiil, et al.
Publicado: (2018) -
The Impact of HIV-1 Genetic Diversity on CRISPR-Cas9 Antiviral Activity and Viral Escape
por: Darcis, Gilles, et al.
Publicado: (2019) -
Suicidal ideation, psychopathology and associated factors among HIV-infected adults in Indonesia
por: Ophinni, Youdiil, et al.
Publicado: (2020) -
Correction to: Suicidal ideation, psychopathology and associated factors among HIV-infected adults in Indonesia
por: Ophinni, Youdiil, et al.
Publicado: (2020) -
A combinational CRISPR/Cas9 gene-editing approach can halt HIV replication and prevent viral escape
por: Lebbink, Robert Jan, et al.
Publicado: (2017)