Methods of treating stroke and traumatic brain injury using humanized AQC2 anti-VLA-1 antibodies
View Patent ↗Methods and compositions for treating stroke are disclosed.
1. A method of treating a traumatic brain injury (TBI) in a subject, the method comprising administering to the subject a humanized AQC2 anti-VLA-1 (Very Late Activation Antigen-I) antibody, or an antigen-binding fragment thereof, wherein the anti-VLA-1 antibody, or antigen-binding fragment thereof, is first administered within 48 hours of the TBI, and wherein the anti-VLA-1 antibody, or antigen-binding fragment thereof, reduces infarct size in a hemisphere affected by the TBI, such that the percentage of the hemisphere infarcted is 40% or less, and wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is administered at a dosage from 0.1 mg/kg per day to 5 mg/kg per day.
2. The method of claim 1 , wherein the TBI is a contusion, bruise, laceration or hematoma.
3. The method of claim 1 , wherein the administering step reduces the infarct size by at least 10% in the hemisphere affected by the TBI, as compared to an infarct size in an untreated subject.
4. The method of claim 1 , wherein the administering step reduces the infarct size by at least 20% in the hemisphere affected by the TBI, as compared to an infarct size in an untreated subject.
5. The method of claim 1 , wherein the administering step reduces edema, such that the size of the hemisphere affected by the TBI is increased by no more than 10% following the TBI.
6. A method of treating a stroke in a subject, the method comprising administering to the subject a humanized AQC2 anti-VLA-1 (Very Late Activation Antigen-1) antibody, or an antigen-binding fragment thereof, wherein the anti-VLA-1 antibody, or antigen-binding fragment thereof, is first administered within 48 hours of the stroke, and wherein the anti-VLA-1 antibody, or antigen-binding fragment thereof, reduces infarct size in a hemisphere affected by the stroke, such that the percentage of the hemisphere infarcted is 40% or less, and wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is administered at a dosage from 0.1 mg/kg per day to 5 mg/kg per day.
7. The method of claim 6 , wherein the humanized AQC2 anti-VLA-1 antibody, or antigen-binding fragment thereof, is produced by a hybridoma having ATCC Deposit No. PTA3275.
8. The method of claim 6 , wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is effective to improve neurologic function.
9. The method of claim 6 , wherein the stroke is an ischemic stroke.
10. The method of claim 6 , wherein the stroke is an hemorrhagic stroke.
11. The method of claim 6 , wherein the subject is a mammal.
12. The method of claim 11 , wherein the subject is a human.
13. The method of claim 6 , wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is administered intravenously or parenterally.
14. The method of claim 6 , wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is administered at least twice within 7 days after the stroke.
15. The method of claim 6 , wherein the administering step reduces the infarct size by at least 10% in the hemisphere affected by the stroke, as compared to an infarct size in an untreated subject.
16. The method of claim 6 , wherein the administering step reduces the infarct size by at least 20% in the hemisphere affected by the stroke, as compared to an infarct size in an untreated subject.
17. The method of claim 6 , wherein the administering step reduces edema, such that the size of the hemisphere affected by the stroke is increased by no more than 10% following the stroke.
18. The method of claim 6 , wherein the anti-VLA-1 antibody or antigen-binding fragment thereof is administered in combination with another therapeutic agent.
19. The method of claim 18 , wherein the other therapeutic agent is selected from the group consisting of an antiplatelet agent, a thrombolytic enzyme, an aggregation inhibitor, a glycoprotein IIb/IIIa inhibitor, a glycosaminoglycan, a thrombin inhibitor, an anticoagulant, heparin, coumarin, tPA, GCSF, streptokinase, urokinase, Ancrod, acetylsalicyclic acid, melatonin, and a caspase inhibitor.