Methods and compositions for treatment of Gaucher Disease via modulation of C5a receptor
Disclosed are compositions and methods for the reduction of C5a mediated immune inflammation. The methods, in various aspects, may include the step of administering a C5aR antagonist to a subject in need of such treatment. In one aspect, the subject in need may have a lysosomal acid storage disease. Therapeutic kits and articles of manufacture are also disclosed.
1. A method of treating a lysosomal storage disease in an individual in need thereof, comprising administering a C5aR antagonist to said individual, said individual having one or more clinical signs selected from hepatosplenomegaly, anemia, thrombocytopenia, bone defects, or a combination thereof.
2. The method of claim 1 , said lysosomal storage disease being selected from globoid cell leukodystrophy, GM2 gangliosidosis, Niemann-Pick C, mucopolysaccharidoses, Fabry, Tay-Sachs, Sandhoff, Hypercholesterolemia, Gaucher's Disease, and combinations thereof.
3. The method according to claim 1 , said C5aR antagonist being administered in an amount sufficient to reduce inflammation in one or both of brain and lung tissue.
4. The method according to claim 1 , said C5aR antagonist being administered in an amount sufficient to reduce complement activation.
5. The method according to claim 1 , said C5aR antagonist being administered in an amount sufficient to reduce circulating levels of inflammatory cytokines and chemokines.
6. The method according, to claim 1 , said administering being carried out before, after, or during a second treatment, said second treatment being selected from gene therapy, substrate reduction therapy, enzyme replacement products, or a combination thereof.
7. The method of claim 1 , said lysosomal storage disease being Gaucher's disease.
8. The method of claim 6 , said second treatment being substrate reduction therapy comprising administration of one or more of eligustat and miglustat.
9. The method of claim 1 , said C5aR antagonist being an A8 Δ71-73 peptide.
10. The method of claim 9 , said lysosomal storage disease being selected from globoid cell leukodystrophy, GM2 gangliosidosis, Niemann-Pick C, mucopolysaccharidoses, Fabry, Tay-Sachs, Sandhoff, Hypercholesterolemia, Gaucher's Disease, and combinations thereof.
11. The method according to claim 9 , said A8 Δ71-73 peptide being administered in an amount sufficient to reduce complement activation.
12. The method according to claim 9 , said A8 Δ71-73 peptide being administered in an amount sufficient to reduce circulating levels of inflammatory cytokines and chemokines.
13. The method according to claim 9 , said A8 Δ71-73 peptide being administered in an amount sufficient to reduce inflammation in one or both of brain and lung tissue.
14. The method according to claim 9 , said administering being carried out before, after, or during a second treatment, said second treatment being selected from gene therapy, substrate reduction therapy, enzyme replacement products, or a combination thereof.
15. A method of treating Gaucher's disease in an individual in need. thereof, comprising administering an A8 Δ71-73 peptide to said individual, said individual having one or more clinical signs selected from hepatosplenomegaly anemia, thrombocytopenia, bone defects, or a combination thereof.
16. The method according to claim 15 , said A8 Δ71-73 peptide being administered in an amount sufficient to reduce complement activation.
17. The method according to claim 15 , said A8 Δ71-73 peptide being administered in an amount sufficient to reduce circulating levels of inflammatory cytokines and chemokines.
18. The method of claim 15 , said administering being carried out before, after, or during a second treatment, said second treatment being selected from gene therapy, substrate reduction therapy, enzyme replacement products, or a combination thereof.
19. The method according to claim 15 , said A8 Δ71-73 peptide being administered in an amount sufficient to reduce inflammation in one or both of brain and lung tissue.