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Developing antisense oligonucleotides for a TECPR2 mutation-induced, ultra-rare neurological disorder using patient-derived cellular models.
Williams, Luis A; Gerber, David J; Elder, Amy; Tseng, Wei Chou; Baru, Valeriya; Delaney-Busch, Nathaniel; Ambrosi, Christina; Mahimkar, Gauri; Joshi, Vaibhav; Shah, Himali; Harikrishnan, Karthiayani; Upadhyay, Hansini; Rajendran, Sakthi H; Dhandapani, Aishwarya; Meier, Joshua; Ryan, Steven J; Lewarch, Caitlin; Black, Lauren; Douville, Julie; Cinquino, Stefania; Legakis, Helen; Nalbach, Karsten; Behrends, Christian; Sato, Ai; Galluzzi, Lorenzo; Yu, Timothy W; Brown, Duncan; Agrawal, Sudhir; Margulies, David; Kopin, Alan; Dempsey, Graham T.
Afiliação
  • Williams LA; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Gerber DJ; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Elder A; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Tseng WC; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Baru V; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Delaney-Busch N; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Ambrosi C; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Mahimkar G; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Joshi V; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Shah H; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Harikrishnan K; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Upadhyay H; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Rajendran SH; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Dhandapani A; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Meier J; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Ryan SJ; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Lewarch C; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Black L; Charles River Laboratories, Montreal, QC, Canada.
  • Douville J; Charles River Laboratories, Montreal, QC, Canada.
  • Cinquino S; Charles River Laboratories, Montreal, QC, Canada.
  • Legakis H; Charles River Laboratories, Montreal, QC, Canada.
  • Nalbach K; Munich Cluster for Systems Neurology, Ludwig-Maximilians-Universität München, Germany.
  • Behrends C; Munich Cluster for Systems Neurology, Ludwig-Maximilians-Universität München, Germany.
  • Sato A; Department of Radiation Oncology, Weill Cornell Medical College, New York, NY, USA.
  • Galluzzi L; Department of Radiation Oncology, Weill Cornell Medical College, New York, NY, USA.
  • Yu TW; Boston Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA.
  • Brown D; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Agrawal S; University of Massachusetts Medical School, Department of Medicine, Worcester, MA 01655, USA.
  • Margulies D; Arnay Sciences LLC, Shrewsbury, MA 01545, USA.
  • Kopin A; Q-State Biosciences, 179 Sidney Street, Cambridge, MA 02139, USA.
  • Dempsey GT; Tufts University School of Medicine, Boston, MA, USA.
Mol Ther Nucleic Acids ; 29: 189-203, 2022 Sep 13.
Article em En | MEDLINE | ID: mdl-35860385
Mutations in the TECPR2 gene are the cause of an ultra-rare neurological disorder characterized by intellectual disability, impaired speech, motor delay, and hypotonia evolving to spasticity, central sleep apnea, and premature death (SPG49 or HSAN9; OMIM: 615031). Little is known about the biological function of TECPR2, and there are currently no available disease-modifying therapies for this disease. Here we describe implementation of an antisense oligonucleotide (ASO) exon-skipping strategy targeting TECPR2 c.1319delT (p.Leu440Argfs∗19), a pathogenic variant that results in a premature stop codon within TECPR2 exon 8. We used patient-derived fibroblasts and induced pluripotent stem cell (iPSC)-derived neurons homozygous for the p.Leu440Argfs∗19 mutation to model the disease in vitro. Both patient-derived fibroblasts and neurons showed lack of TECPR2 protein expression. We designed and screened ASOs targeting sequences across the TECPR2 exon 8 region to identify molecules that induce exon 8 skipping and thereby remove the premature stop signal. TECPR2 exon 8 skipping restored in-frame expression of a TECPR2 protein variant (TECPR2ΔEx8) containing 1,300 of 1,411 amino acids. Optimization of ASO sequences generated a lead candidate (ASO-005-02) with ∼27 nM potency in patient-derived fibroblasts. To examine potential functional rescue induced by ASO-005-02, we used iPSC-derived neurons to analyze the neuronal localization of TECPR2ΔEx8 and showed that this form of TECPR2 retains the distinct, punctate neuronal expression pattern of full-length TECPR2. Finally, ASO-005-02 had an acceptable tolerability profile in vivo following a single 20-mg intrathecal dose in cynomolgus monkeys, showing some transient non-adverse behavioral effects with no correlating histopathology. Broad distribution of ASO-005-02 and induction of TECPR2 exon 8 skipping was detected in multiple central nervous system (CNS) tissues, supporting the potential utility of this therapeutic strategy for a subset of patients suffering from this rare disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article