WO2020172720A1 - Compositions and methods for treating oculopharyngeal muscular dystrophy (opmd) - Google Patents

Compositions and methods for treating oculopharyngeal muscular dystrophy (opmd) Download PDF

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WO2020172720A1
WO2020172720A1 PCT/AU2020/050182 AU2020050182W WO2020172720A1 WO 2020172720 A1 WO2020172720 A1 WO 2020172720A1 AU 2020050182 W AU2020050182 W AU 2020050182W WO 2020172720 A1 WO2020172720 A1 WO 2020172720A1
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seq
set forth
sequence set
sequence
shmir
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English (en)
French (fr)
Inventor
Vanessa STRINGS-UFOMBAH
David Suhy
Shih-Chu KAO
Petrus W. Roelvink
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Benitec Biopharma Pty Ltd
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Benitec Biopharma Pty Ltd
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Priority to JP2021549908A priority Critical patent/JP2022522166A/ja
Priority to BR112021017054A priority patent/BR112021017054A2/pt
Priority to MX2021010412A priority patent/MX2021010412A/es
Priority to US17/434,666 priority patent/US20220098614A1/en
Priority to KR1020217031046A priority patent/KR102959609B1/ko
Priority to SG11202108469XA priority patent/SG11202108469XA/en
Priority to CA3130221A priority patent/CA3130221A1/en
Priority to CN202511142034.9A priority patent/CN121160804A/zh
Application filed by Benitec Biopharma Pty Ltd filed Critical Benitec Biopharma Pty Ltd
Priority to AU2020229886A priority patent/AU2020229886B2/en
Priority to CN202080017400.7A priority patent/CN113631706A/zh
Priority to EP20762817.3A priority patent/EP3931317A4/en
Publication of WO2020172720A1 publication Critical patent/WO2020172720A1/en
Priority to IL285841A priority patent/IL285841A/en
Anticipated expiration legal-status Critical
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    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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Definitions

  • the viral capsid protein comprises mutations A42S, A67E, Q81R, K84D, A85S and Q105K with respect to the full length wild-type AAV serotype 8 capsid sequence set forth in SEQ ID NO: 93. In one example, the viral capsid protein comprises the amino acid sequence set forth in SEQ ID NO: 94.
  • a shmiR comprising an effector sequence set forth in SEQ ID NO: 19 and an effector complement sequence set forth in SEQ ID NO: 18;
  • each of the at least two nucleic acids within the ddRNAi construct may encode a shmiR comprising an effector sequence which is substantially complementary to a region of corresponding length in an RNA transcript set forth in one of SEQ ID NOs: 1, 2, 4, 7, 9, 10 and 13.
  • the at least two nucleic acids within the ddRNAi construct are selected from the group consisting of:
  • a first baculovirus vector comprising a nucleic acid molecule encoding an AAV viral capsid protein with the modified VP1 sequence as described herein;
  • the modified AAV9 VP1 sequence comprises a serine at position 1, a glutamic acid at position 26, an arginine at position 40, an aspartic acid at position 43, and a serine at position 44 relative to the AAV9 VP1 sequence set forth in SEQ ID NO: 87.
  • the modified AAV9 VP1 sequence may comprise the following modifications A1S, A26E, Q40R, K43D, and A44S relative to the sequence set forth in SEQ ID NO: 87.
  • the modified AAY9 YP1 sequence comprises the sequence set forth in SEQ ID NO: 88
  • Figure 3B shows silencing of PABPN1 expression (including expPABPN1) in TA muscles of A17 mice treated with the SR-construct. RNA was extracted from TA samples 14 weeks post SR-construct dosing.
  • SEQ ID NO: 2 RNA sequence for region within mRNA transcript corresponding to
  • SEQ ID NO: 5 RNA sequence for region within mRNA transcript corresponding to
  • SEQ ID NO: 12 RNA sequence for region within mRNA transcript corresponding to
  • SEQ ID NO: 70 DNA sequence for double construct version 1 coding for shmiR17 and shmiR13 under control of the muscle specific CK8 promoter and codon optimized PABPN1 under control of Spc512
  • SEQ ID NO: 87 Wildtype VP1 subsequence for AAV serotype 9, comprising the PLA2 domain and flanking sequence.
  • SEQ ID NO: 88 Modified VP1 subsequence for AAV serotype 9, comprising the PLA2 domain and flanking sequence.
  • duplex refers to regions in two complementary or substantially complementary nucleic acids (e.g ., RNAs), or in two complementary or substantially complementary regions of a single-stranded nucleic acid (e.g., RNA), that form base pairs with one another, either by Watson-Crick base pairing or any other manner that allows for a stabilized duplex between the nucleotide sequences that are complementary or substantially complementary. It will be understood by the skilled person that within a duplex region, 100% complementarity is not required; substantial complementarity is allowable. Substantial complementarity includes may include 79% or greater complementarity.
  • the dsRNA may be provided as a hairpin or stem loop structure, with a duplex region comprised of an effector sequence and effector complement sequence linked by at least 2 nucleotide sequence which is termed a stem loop.
  • a dsRNA is provided as a hairpin or stem loop structure it can be referred to as a "hairpin RNA” or “short hairpin RNAi agent” or “shRNA”.
  • Other dsRNA molecules provided in, or which give rise to, a hairpin or stem loop structure include primary miRNA transcripts (pri-miRNA) and precursor microRNA (pre- miRNA).
  • the effector sequence may be substantially complementary to a region of corresponding length in an RNA transcript comprising or consisting of the sequence set forth in any one of SEQ ID NOs: 1- 13 and contain 1 mismatch base relative thereto.
  • the effector sequence may be 100% complementary to a region of corresponding length in an RNA transcript comprising or consisting of the sequence set forth in any one of SEQ ID NOs: 1-13.
  • the ddRNAi construct comprises or consists of a DNA sequence set forth in SEQ ID NO: 62 and encodes a shmiR (shmiR9) comprising or consisting of the sequence set forth in SEQ ID NO: 49.
  • the ddRNAi construct comprises a nucleic acid comprising or consisting of a DNA sequence encoding shmiR11, and at least one other nucleic acid of the disclosure which encodes a shmiR targeting a region of a PABPN1 mRNA transcript.
  • exemplary nucleic acids encoding shmiR11 are described herein and shall be taken to apply mutatis mutandis to this example of the disclosure.
  • the ddRNAi construct encodes a plurality of shmiRs
  • at least one of the shmiRs comprises an effector sequence which is substantially complementary to a region of corresponding length in an RNA transcript comprising or consisting of the sequence set forth in SEQ ID NO: 2.
  • Suitable nucleic acids encoding a shmiR having an effector sequence which is substantially complementary to a region of corresponding length in an RNA transcript comprising or consisting of the sequence set forth in SEQ ID NO: 2 are described herein e.g., for shmiR3.
  • a nucleic acid with the PABPN1 construct encoding the functional PABPN1 protein is codon optimised such that its corresponding mRNA sequence is not recognised by the shmiR(s) encoded and expressed from the ddRNAi construct.
  • the functional PABPN1 protein encoded by the codon optimised nucleic acid sequence comprises the amino acid sequence set forth in SEQ ID NO: 74 i.e., the amino acid sequence of the wild- type human PABPN1 protein.
  • An exemplary ddRNAi construct encoding shmiR13 and shmiR17 for inclusion in a DNA construct of the disclosure comprises a nucleic acid comprising or consisting of a DNA sequence encoding a shmiR comprising an effector sequence set forth in SEQ ID NO: 31 and an effector complement sequence which is substantially complementary to the sequence set forth in SEQ ID NO: 31 e.g., an effector complement sequence set forth in SEQ ID NO: 30 (shmiR13), and a nucleic acid comprising or consisting of a DNA sequence encoding a shmiR comprising an effector sequence set forth in SEQ ID NO: 39 and an effector complement sequence which is substantially complementary to the sequence set forth in SEQ ID NO: 39 e.g., an effector complement sequence set forth in SEQ ID NO: 38 (shmiR17).
  • SR-construct The silence and replace construct (hereinafter “SR-construct”) was generated by subcloning DNA sequences encoding shmiR17 and shmiR13 (as described in Table 4) into the 3’ untranslated region of the optPABPN1 transcript in the pAAV2 vector backbone (pAAV-shmiR viral plasmid). Expression of both optPABPN1 and the two shmiRs in a single transcript is driven by the muscle specific promoter Spc512.
  • a schematic of the SR-construct is provided in Figure 1(A), Figure 1(B), and Figure 2.
  • AAV prepared in mammalian cells was compared to AAV prepared in insect cells as described above.
  • mammalian cells were infected in vitro with various titres of viruses and expression of processed shmiRs quantified using qRT PCR assays.
  • cells infected with AAV8 with unmodified wt VP1 prepared in mammalian cells produced readily detectable levels of shmiRs, whilst AAV8 with unmodified wt VP1 produced by baculovirus in insect cells produced little, if any, shmiRs.
  • AAV8 with modified VP1 produced by baculovirus in insect cells produced relatively high levels of shmiRs, indicating an increase in functionality of these AAVs as compare to the AAV8 with unmodified wt VP1 produced by baculovirus in insect cells.

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PCT/AU2020/050182 2019-02-28 2020-02-28 Compositions and methods for treating oculopharyngeal muscular dystrophy (opmd) Ceased WO2020172720A1 (en)

Priority Applications (12)

Application Number Priority Date Filing Date Title
CA3130221A CA3130221A1 (en) 2019-02-28 2020-02-28 Compositions and methods for treating oculopharyngeal muscular dystrophy (opmd)
MX2021010412A MX2021010412A (es) 2019-02-28 2020-02-28 Composiciones y metodos para tratar distrofia muscular oculofaringea (opmd).
US17/434,666 US20220098614A1 (en) 2019-02-28 2020-02-28 Compositions and Methods for Treating Oculopharyngeal Muscular Dystrophy (OPMD)
KR1020217031046A KR102959609B1 (ko) 2019-02-28 2020-02-28 안구인두 근이영양증 (opmd) 치료용 조성물 및 방법
SG11202108469XA SG11202108469XA (en) 2019-02-28 2020-02-28 Compositions and methods for treating oculopharyngeal muscular dystrophy (opmd)
CN202511142034.9A CN121160804A (zh) 2019-02-28 2020-02-28 用于治疗眼咽肌营养不良（opmd）的组合物和方法
AU2020229886A AU2020229886B2 (en) 2019-02-28 2020-02-28 Compositions and methods for treating oculopharyngeal muscular dystrophy (OPMD)
JP2021549908A JP2022522166A (ja) 2019-02-28 2020-02-28 眼咽頭型筋ジストロフィー（ｏｐｍｄ）を治療するための組成物及び方法
BR112021017054A BR112021017054A2 (pt) 2019-02-28 2020-02-28 Composições e métodos para o tratamento da distrofia muscular oculofaríngea (opmd)
CN202080017400.7A CN113631706A (zh) 2019-02-28 2020-02-28 用于治疗眼咽肌营养不良(opmd)的组合物和方法
EP20762817.3A EP3931317A4 (en) 2019-02-28 2020-02-28 COMPOSITIONS AND METHODS FOR TREATMENT OF OCULOPHARYNGEAL MUSCULAR DYSTROPHY (OPMD)
IL285841A IL285841A (en) 2019-02-28 2021-08-24 Compositions and methods for treating oculopharyngeal muscular dystrophy (opmd)

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WO2026011009A1 (en) * 2024-07-02 2026-01-08 Kate Therapeutics, Inc. Compositions and methods for muscle disorders

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Publication number Priority date Publication date Assignee Title
WO2025003978A1 (en) * 2023-06-28 2025-01-02 Benitec IP Holdings Inc. Device and methods for administering a therapeutic composition to the pharyngeal muscle
WO2026011009A1 (en) * 2024-07-02 2026-01-08 Kate Therapeutics, Inc. Compositions and methods for muscle disorders

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