Myostatin inhibition for enhancing muscle and/or improving muscle function
Abstract
The present invention relates to methods for inhibitiing myostatin, a regulator of muscle mass, for muscle enhancement (including inducing hypertrophy and/or hyperplasia) as well as improving muscle function (including decreasing atrophy and/or increasing endurance, force and/or strength). Some of the methods involve delivering genes to cells using gene delivery or other delivery techniques known in the art in order to inhibit myostatin. Examples of genes to be delivered are genes encoding proteins such as Follistatin, Follistatin-related gene-1 (FLRG-1), growth differentiation factor associated protein-1 (GASP-1) and myostatin precursor propeptide. The genes can be delivered using, for example, a recombinant Adeno-associated virus (rAAV), lentivirus or equine-associated virus capable of infecting the cells. Following introduction, the genes are expressed in the cell body of the infected cell and the encoded proteins are secreted systemically. In other methods of the invention, expression of proteins such as activin IIb and myostatin is inhibited by oligonucleotide techniques to effect muscle enhancement. All the methods have applications in the treatment of musculoskeletal and neurodegenerative disorders among others, as well as enhancing muscle in livestock.
Claims
exact text as granted — not AI-modified1 . A method of delivering a myostatin inhibitor to an animal in need thereof, comprising the step of intravenously administering to the animal a composition comprising one or more infectious encapsidated rAAVs, each comprising a recombinant AAV genome comprising at least one AAV inverted terminal repeat flanking a polynucleotide encoding a myostatin inhibitor, wherein the genome lacks AAV rep and cap DNA
2 . The method of claim 1 wherein the polynucleotide encodes a myostatin inhibitor protein and is operatively linked to transcriptional control DNA.
3 . The method of claim 1 wherein the polynucleotide encodes a myostatin inhibitor RNA.
4 - 12 . (canceled)
13 . The method of claim 1 wherein the musculoskeletal disease is a muscular dystrophy or inclusion body myositis (IBM).
14 . The method of claim 13 wherein the muscular dystrophy is Duchenne muscular dystrophy.
15 - 17 . (canceled)
18 . The method of claim 1 wherein the neurodegenerative disease is Amyotrophic Lateral Sclerosis, multiple sclerosis or spinal muscular atrophy.
19 - 21 . (canceled)
22 . The method of claim 2 wherein the myostatin inhibitor protein is follistatin, follistatin-related gene (FLRG), myostatin precursor propeptide or growth differentiation factor associated protein-1 (GASP-1).
23 - 25 . (canceled)
26 - 29 . (canceled)
30 . The method of claim 22 wherein the myostatin inhibitor protein binds to the myostatin receptor activin IIb.
31 - 34 . (canceled)
35 . A packaging cell producing an infectious encapsidated rAAV comprising a recombinant AAV genome comprising at least one AAV inverted terminal repeat flanking a polynucleotide encoding a myostatin inhibitor , wherein the genome lacks AAV rep and cap DNA.
36 . A composition comprising one or more infectious encapsidated rAAVs, each comprising a recombinant AAV genome comprising at least one AAV inverted terminal repeat flanking a polynucleotide encoding a myostatin inhibitor , wherein the genome lacks AAV rep and cap DNA.
37 . The composition of claim 36 wherein the polynucleotide encodes a myostatin inhibitor protein and is operatively linked to transcriptional control DNA.
38 . The composition of claim 36 wherein the myostatin inhibitor protein is follistatin, follistatin-related gene (FLRG), myostatin precursor propeptide or growth differentiation factor associated protein-1 (GASP-1).
39 - 42 . (canceled)
43 . The composition of claim 38 wherein the myostatin inhibitor protein binds to the myostatin receptor activin IIb.
44 . The composition of claim 36 wherein the polynucleotide encodes a myostatin inhibitor RNA.
45 - 46 . (canceled)Join the waitlist — get patent alerts
Track US2017151348A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.