Coupling AAV-mediated promoterless gene targeting to SaCas9 nuclease to efficiently correct liver metabolic diseases

JCI Insight. 2019 Jun 18;5(15):e128863. doi: 10.1172/jci.insight.128863.

Abstract

Non-integrative AAV-mediated gene therapy in the liver is effective in adult patients, but faces limitations in pediatric settings due to episomal DNA loss during hepatocyte proliferation. Gene targeting is a promising approach by permanently modifying the genome. We previously rescued neonatal lethality in Crigler-Najjar mice by inserting a promoterless human uridine glucuronosyl transferase A1 (UGT1A1) cDNA in exon 14 of the albumin gene, without the use of nucleases. To increase recombination rate and therapeutic efficacy, here we used CRISPR/SaCas9. Neonatal mice were transduced with two AAVs: one expressing the SaCas9 and sgRNA, and one containing a promoterless cDNA flanked by albumin homology regions. Targeting efficiency increased ~26-fold with an eGFP reporter cDNA, reaching up to 24% of eGFP-positive hepatocytes. Next, we fully corrected the diseased phenotype of Crigler-Najjar mice by targeting the hUGT1A1 cDNA. Treated mice had normal plasma bilirubin up to 10 months after administration, hUGT1A1 protein levels were ~6-fold higher than in WT liver, with a 90-fold increase in recombination rate. Liver histology, inflammatory markers, and plasma albumin were normal in treated mice, with no off-targets in predicted sites. Thus, the improved efficacy and reassuring safety profile support the potential application of the proposed approach to other liver diseases.

Keywords: Gene therapy; Genetics; Hepatology; Monogenic diseases; Mouse models.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Bilirubin
  • CRISPR-Cas Systems
  • Clustered Regularly Interspaced Short Palindromic Repeats
  • DNA, Complementary
  • Disease Models, Animal
  • Female
  • Gene Targeting / methods*
  • Gene Transfer Techniques
  • Genetic Therapy / methods*
  • Genetic Vectors
  • Glucuronosyltransferase / genetics*
  • Glucuronosyltransferase / metabolism
  • HEK293 Cells
  • Hepatocytes / metabolism
  • Humans
  • Liver / metabolism*
  • Liver / pathology
  • Male
  • Metabolic Diseases / genetics*
  • Metabolic Diseases / metabolism
  • Metabolic Diseases / pathology
  • Metabolic Diseases / therapy*
  • Mice
  • Mice, Knockout
  • NIH 3T3 Cells
  • Serum Albumin
  • Therapeutic Uses

Substances

  • DNA, Complementary
  • Serum Albumin
  • Therapeutic Uses
  • UGT1A1 enzyme
  • Glucuronosyltransferase
  • Bilirubin