CRISPR/Cas9-mediated glycolate oxidase disruption is an efficacious and safe treatment for primary hyperoxaluria type I.
Nerea ZabaletaMiren BarberiaCristina Martín HiguerasNatalia Zapata-LinaresIsabel BetancorSaray RodriguezRebeca Martinez-TurrillasLaura TorellaAfrica ValesCristina OlagüeAmaia Vilas-ZornozaLaura Castro-LabradorDavid Lara-AstiasoFelipe ProsperEduardo SalidoGloria Gonzalez-AseguinolazaJuan Roberto Rodriguez-MadozPublished in: Nature communications (2018)
CRISPR/Cas9 technology offers novel approaches for the development of new therapies for many unmet clinical needs, including a significant number of inherited monogenic diseases. However, in vivo correction of disease-causing genes is still inefficient, especially for those diseases without selective advantage for corrected cells. We reasoned that substrate reduction therapies (SRT) targeting non-essential enzymes could provide an attractive alternative. Here we evaluate the therapeutic efficacy of an in vivo CRISPR/Cas9-mediated SRT to treat primary hyperoxaluria type I (PH1), a rare inborn dysfunction in glyoxylate metabolism that results in excessive hepatic oxalate production causing end-stage renal disease. A single systemic administration of an AAV8-CRISPR/Cas9 vector targeting glycolate oxidase, prevents oxalate overproduction and kidney damage, with no signs of toxicity in Agxt1-/- mice. Our results reveal that CRISPR/Cas9-mediated SRT represents a promising therapeutic option for PH1 that can be potentially applied to other metabolic diseases caused by the accumulation of toxic metabolites.
Keyphrases
- crispr cas
- genome editing
- end stage renal disease
- chronic kidney disease
- oxidative stress
- peritoneal dialysis
- induced apoptosis
- genome wide
- cancer therapy
- gene expression
- ms ms
- type diabetes
- single cell
- adipose tissue
- body mass index
- dna methylation
- metabolic syndrome
- combination therapy
- cell cycle arrest
- transcription factor
- endoplasmic reticulum stress
- weight gain
- smoking cessation
- replacement therapy
- cell proliferation
- structural basis