Methods and means for efficient skipping of exon 45 in Duchenne muscular dystrophy pre-mRNA
The invention relates to a method for inducing or promoting skipping of exon 45 of DMD pre-mRNA in a Duchenne Muscular Dystrophy patient, preferably in an isolated (muscle) cell, the method comprising providing an isolated muscle cell with a molecule that binds to a continuous stretch of at least 21 nucleotides within said exon. The invention further relates to such molecule used in the method.
1. A pharmaceutical composition comprising an antisense oligonucleotide and an excipient selected from the group consisting of polyethylenimine, and polypropylenimine, wherein said antisense oligonucleotide consists of the base sequence: 5′-UUUGCCGCUGCCCAAUGCCAUCCUG-3′ (SEQ ID: NO: 3), said oligonucleotide comprising a modification.
2. The pharmaceutical composition according to claim 1 , wherein the oligonucleotide comprises at least one nucleotide analogue or equivalent, wherein a nucleotide analogue or equivalent is defined as a residue having a modified base, and/or a modified backbone, and/or a non-natural internucleoside linkage, or a combination of these modifications.
3. The pharmaceutical composition according to claim 2 , wherein the nucleotide analogue has a modified base.
4. The pharmaceutical composition according to claim 2 , wherein the nucleotide analogue has a modified backbone.
5. The pharmaceutical composition according to claim 2 , wherein the nucleotide analogue comprises one or more sugar moieties that are mono-or disubstituted at the 2′, 3′ and/or 5′ position.
6. The pharmaceutical composition according to claim 5 , wherein said oligonucleotide comprises a 2′-O-substituted phosphorothioate antisense oligonucleotide.
7. The pharmaceutical composition according to claim 5 , wherein said oligonucleotide comprises a 2′-O-methyl ribose.
8. The pharmaceutical composition according to claim 6 , wherein all the sugar moieties are 2′-O-methyl substituted.
9. The pharmaceutical composition according to claim 4 , wherein the modified backbone is selected from the group consisting of a morpholino backbone, a carbamate backbone, a siloxane backbone, a sulfide backbone, a sulfoxide backbone, a sulfone backbone, a formacetyl backbone, a thioformacetyl backbone, a methyleneformacetyl backbone, a riboacetyl backbone, an alkene containing backbone, a sulfamate backbone, a sulfonate backbone, a sulfonamide backbone, a methyleneimino backbone, a methylenehydrazino backbone and an amide backbone.
10. The pharmaceutical composition according to claim 1 , wherein the oligonucleotide comprises phosphorodiamidate morpholino oligomer (PMO), peptide nucleic acid, and/or locked nucleic acid.
11. The pharmaceutical composition according to claim 1 , further comprising a molecule which is able to induce or promote skipping of exon 7, 44, 46, 51, 53, 59, or 67 of the pre-mRNA of the DMD gene of a patient.