Sangamo Therapeutics Announces Nature Medicine Publication Detailing the Activity of Disease Allele-Selective Zinc Finger Proteins in Preclinical Models of Huntington’s Disease
The publication describes research by Sangamo and collaborators at the
Huntington’s disease is a progressive, fatal, neurodegenerative disorder caused by a dominant mutation involving the expansion of a CAG trinucleotide repeat in exon 1 of the HTT gene. Fully penetrant disease alleles of mutant HTT have more than 39 CAG repeats, but most HD patients have one healthy wild-type copy of HTT with less than 22 CAG repeats. Led by first author
“Ever since the mutation that causes Huntington’s Disease was identified in 1993, the ultimate goal for HD research has been to develop a therapy that could directly target the mutant CAG repeat while avoiding the wild-type form given its important role in many cellular functions,” said
Data from preclinical in vivo studies using different HD mouse models demonstrated improvements in a range of molecular, histopathological, electrophysiological, and other functional endpoints following treatment with Sangamo’s ZFP-TFs. In neurons cultured from the zQ175 mouse model (~188 CAG repeats) of HD, recombinant AAV delivery of ZFP-TFs to primary neurons resulted in reduction of mutant HTT mRNA and HTT protein by more than 98% with no reduction of wild-type HTT. In vivo, toxic aggregates of the mutant HTT protein were reduced by greater than 99%. Moreover, the well-characterized zQ175 electrophysiological deficits in the brain were fully reversed following ZFP treatment. Functional restoration of neuronal biomarkers was also demonstrated by several measures, including the use of PET imaging ligands in living mice. This outcome has the potential to be translated for use as an efficacy marker in clinical trials. The results were confirmed and extended in an additional mouse model of HD, in which treatment with ZFP-TFs led to the repression of mutant HTT protein and significant improvement in motor function.
Finally, extensive in vivo tolerability assessments showed no evidence of a neuroinflammatory response or changes in behavior or locomotor function in mice treated with ZFP-TFs out to 15 months of age. This suggests that the long-term striatal expression of ZFP-TFs is generally well-tolerated in mice.
“These studies present the first direct demonstration of disease allele-selective transcriptional repression at the mutated Huntingtingene locus. While several HTT-lowering therapies are advancing into the clinic, they all rely on indirect approaches that do not directly target the mutation. Moreover, these strategies either lower both mutant and normal HTT or employ allele-targeting that is limited to a subgroup of patients, in some cases requiring multiple intrathecal injections over a patient’s lifetime,” said
About Huntington’s Disease
Huntington’s disease (HD) is an inherited neurodegenerative disease that typically presents in adults aged between 30 and 50. HD is caused by a mutation in one of the alleles of the huntingtin gene (HTT), leaving only one functional or healthy copy of HTT in the cell. The mutated HTT produces the mutant HTT protein, leading to profound neuronal loss and progressive deterioration of motor, psychiatric, and cognitive abilities. There are currently no disease-modifying therapies available for HD.
About Sangamo’s Gene Regulation Platform
Sangamo's zinc finger protein transcription factor (ZFP-TF) gene regulation technology is designed to either selectively repress (down-regulate) or activate (up-regulate) the expression of a specific gene or gene allele following a single administration. This technology enables targeting of a broad range of diseases requiring regulation of endogenous gene expression and differs from other approaches such as gene therapy or zinc finger nuclease-mediated (ZFN) genome editing, which are designed to replace or correct a missing or mutated gene or DNA sequence.
Sangamo is developing ZFP-TFs as a novel therapeutic approach for diseases of the central nervous system (CNS). Sangamo has a collaboration with Pfizer, deploying the ZFP-TF gene regulation approach to repress the expression of the mutated C9ORF72 gene allele linked to genetic forms of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (
This press release contains forward-looking statements based on Sangamo's current expectations. These forward-looking statements include, without limitation, statements relating to the therapeutic potential of Sangamo's ZFP-TF gene regulation platform for the treatment of CNS diseases, including the potential of Sangamo’s ZFP-TF gene regulation platform as a novel disease modifying therapeutic approach for the treatment of HD; the potential for Sangamo's ZFP-TF approach to represent an allele-selective treatment that could possibly require a one-time administration; the potential for HD mouse model preclinical data to translate into the clinic; the potential for preclinical studies to be IND-enabling; and other statements that are not historical fact. These statements are not guarantees of future performance and are subject to certain risks, uncertainties and assumptions that are difficult to predict. Factors that could cause actual results to differ include, but are not limited to, risks and uncertainties related to: early preclinical data, including the risk that the early preclinical data may not warrant regulatory approvals to conduct any human clinical trials, and may not be representative of the results of any such human clinical trials; whether ZFP-TFs will produce any beneficial therapeutic effect in humans; Sangamo's reliance on Takeda, its other partners and other third-parties to further develop its technology; Sangamo's ability to develop commercially viable products; and the potential for technological developments by Sangamo's competitors that will obviate Sangamo's ZFP-TF technology. These risks and uncertainties are described more fully in Sangamo's Quarterly Report on Form 10-Q for the quarter ended
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