Targeting complement factor H for treatment of diseases
View Patent ↗The invention provides a CR2-FH molecule comprising a CR2 portion comprising CR2 protein or a fragment thereof and a FH portion comprising a factor H protein or a fragment thereof, and pharmaceutical compositions comprising a CR2-FH molecule. Also provided are methods of using the compositions for treatment diseases in which the alternative complement pathway is implicated, such as age-related macular degeneration, rheumatoid arthritis, and ischemia reperfusion.
1. A complement receptor 2 (CR2)-factor H (FH) molecule comprising:
a) a CR2 portion comprising a CR2 or a fragment thereof, and
b) a FH portion comprising a FH or a fragment thereof, said FH or fragment thereof comprising at least the first four N-terminal short consensus repeat (SCR) domains of FH;
wherein the CR2 portion of the CR2-FH molecule is capable of binding to a CR2 ligand, and wherein the FH portion of the CR2-FH molecule is capable of inhibiting complement activation of the alternative pathway.
2. The CR2-FH molecule of claim 1 , wherein the CR2 portion comprises at least the first two N-terminal SCR domains of CR2.
3. The CR2-FH molecule of claim 1 , wherein the CR2 portion comprises at least the first four N-terminal SCR domains of CR2.
4. The CR2-FH molecule of claim 1 , wherein the FH portion comprises at least the first five N-terminal SCR domains of FH.
5. The CR2-FH molecule of claim 1 , wherein the CR2-FH molecule comprises two or more FH portions, wherein the two or more FH portions each comprise a FH or fragment thereof comprising at least the first four N-terminal SCR domains of FH.
6. The CR2-FH molecule of claim 1 , wherein the CR2 portion comprises the first four N-terminal SCR domains of CR2 and the FH portion comprises the first five N-terminal SCR domains of FH.
7. The CR2-FH molecule of claim 6 , wherein the CR2 portion comprises amino acids 23 to 271 of SEQ ID NO:1 and the FH portion comprises amino acids 21 to 320 of SEQ ID NO:2.
8. The CR2-FH molecule of claim 1 , wherein the CR2-FH molecule is a fusion protein.
9. A polynucleotide encoding the fusion protein of claim 8 .
10. A vector encoding the polynucleotide of claim 9 .
11. A host cell comprising the polynucleotide of claim 10 .
12. A pharmaceutical composition comprising a CR2-FH molecule of claim 1 and a pharmaceutically acceptable carrier.
13. The composition of claim 12 , wherein the composition is suitable for intraocular, intravenous, intraarterial, sub-cutaneous, intratracheal, or inhalational administration.
14. A method of treating a disease in which the alternative complement pathway is implicated in an individual, comprising administering to the individual an effective amount of a pharmaceutical composition of claim 12 .
15. The method of claim 14 , wherein the disease in which the alternative complement pathway is implicated is any of macular degeneration, rheumatoid arthritis, ischemia reperfusion, organ transplant rejection, membranoproliferative glomerulonephritis, type II (MPGN II), hemolytic uremic syndrome (HUS), and lupus nephritis.
16. The method of claim 15 , wherein the disease in which the alternative complement pathway is implicated is age-related macular degeneration.
17. The method of claim 15 , wherein the disease in which the alternative complement pathway is implicated is ischemia reperfusion.
18. The method of claim 15 , wherein the disease in which alternative complement pathway is implicated is organ transplant rejection.
19. The method of claim 15 , wherein the HUS is factor H-related.
20. A method of treating an individual having a disease in which the alternative complement pathway is implicated, wherein the disease is characterized by symptoms comprising microangiopathic hemolytic anemia, thrombocytopenia, and acute renal failure, the method comprising administering to the individual an effective amount of a pharmaceutical composition of claim 12 .