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Table 2 CRISPR/Cas systems for targeting proviral HIV-1 (In-vivo studies)

From: CRISPR/Cas9: a tool to eradicate HIV-1

CRISPR/Cas system

Organism

Target region

Delivery

Results

References

SaCas9

Tg26 mice

LTR and viral genes

AAV9 (Adeno-associated vector)

Deletion at the target sequences in all the tissue samples studied. Excision of target sequence, reduction of 80–90% gag and env RNA

Kaminski et al. [48]

SaCas9

Tg26 mice

NCr nude mouse

BLT mice

LTR and viral genes

AAV (Adeno-associated vector)

Deletions at target sequences in samples collected from spleen, liver and bone-marrow. Excision and reduction of HIV gene expression

Yin et al. [59]

SpCas9

NRG rats

LTR and gag

Lentivirus

Cleavage and excision of integrated provirus in between the target sites

Bella et al. [60]

SaCas9

Humanized Mice

(Engrafted with human CD34 + HSC)

LTR and gag

LASER ART therapy

 + 

AAV9 (Adeno-associated vector)

Effective decrease in viral load in dual treated mice compared to mice that were singularly treated with LASER ART or CRISPR alone

In two of the seven mice, the viral load was undetectable

Dash et al. [62]

SaCas9

Rhesus macaques

LTR and gag

AAV9 (Adeno-associated vector)

Significant reduction of viral DNA in the blood and tissues. Precise cleavage and excision in samples collected from infected lymph nodes, spleen, bone-marrow and brain

Mancuso et al. [61]