Exon skipping therapy for dystrophic epidermolysis bullosa
View Patent ↗The present invention also relates to an antisense oligonucleotide complementary to a nucleic acid sequence of COL7A1 gene that is necessary for correct splicing of one or more exons which encode amino acid sequence of type VII collagen implicated in dysfunction of a mutated type VII collagen wherein said exons are selected from the group consisting of exon 73, 74 or 80 of the COL7A1 gene. The present invention also relates to a method for the treatment of a patient suffering from Dystrophic Epidermolysis Bullosa caused by a dysfunction of a mutated type VII collagen, comprising the step of administering to said patient a least one antisense oligonucleotide according to the invention.
1. A method for restoring the function of a mutated type VII collagen comprising the step of preventing splicing of one or more exons which encode amino acid sequence of type VII collagen implicated in dysfunction of a mutated type VII collagen wherein said exons are selected from the group consisting of exon 73, 74 or 80 of the COL7A1 gene.
2. A synthetic antisense oligonucleotide complementary to a nucleic acid sequence of COL7A1 gene that is necessary for correct splicing of one or more exons which encode amino acid sequence of type VII collagen implicated in dysfunction of a mutated type VII collagen wherein said exons are selected from the group consisting of exon 73, 74 or 80of the COL7A1 gene, and wherein said antisense oligonucleotide is selected from the group consisting of sequences ESE73.3 (SEQ ID NO :1), ESE73.7 (SEQ ID NO :2), SA+ESE-74 (SEQ ID NO :3), SA+ESE-74 R2063W (SEQ ID NO :4), ESE-74.2+SD (SEQ ID NO :5), ESE-80.3(SEQ ID NO :6) and ESE80-3 Q2170X (SEQ ID NO :7), and wherein said antisense oligonucleotide prevents said splicing of said one or more exons into an mRNA transcript of said nucleic acid sequence of COL7A 1 gene.
3. The synthetic antisense oligonucleotide according to claim 2 which is inserted in a vector.
4. A pharmaceutical composition comprising at least one synthetic antisense oligonucelotide according to claim 2 .
5. A method of treating a patient suffering from Dystrophic Epidermolysis Bullosa comprising the step of
administering to the patient, in an amount sufficient to ameliorate symptoms of said Dystrophic Epidermolysis Bullosa, an antisense oligonucleotide complementary to a nucleic acid sequence of COL7A1 gene that is necessary for correct splicing of one or more exons which encode amino acid sequence of type VII collagen implicated in dysfunction of a mutated type VII collagen wherein said exons are selected from the group consisting of exon 73, 74 or 80of the COL7A1 gene.
6. The method of claim 5 , wherein said antisense oligonucleotide is selected from the group consisting of sequences ESE73.3 (SEQ ID NO :1), ESE73.7 (SEQ ID NO :2), SA+ESE-74 (SEQ ID NO :3), SA+ESE-74_R2063W (SEQ ID NO :4), ESE-74.2+SD (SEQ ID NO :5), ESE-80.3 (SEQ ID NO :6) and ESE80-3_Q2170X (SEQ ID NO :7).
7. The synthetic antisense oligonucleotide of claim 2 , wherein said synthetic antisense oligonucleotide is a type selected from the group consisting of oligodeoxyribonucleotide, oligoribonucleotide, morpholino, tricycle-DNA-antisense oligonucleotide, U7-mediated antisense oligonucleotide, peptide-conjugated antisense oligonucleotide and nanoparticle-complexed antisense oligonucleotide.