METHODS FOR TREATING CONDITIONS ASSOCIATED WITH MASP-2 DEPENDENT COMPLEMENT ACTIVATION
In one aspect, the invention provides methods of inhibiting the effects of MASP-2-dependent complement activation in a living subject. The methods comprise the step of administering, to a subject in need thereof, an amount of a MASP-2 inhibitory agent effective to inhibit MASP-2-dependent complement activation. In some embodiments, the MASP-2 inhibitory agent inhibits cellular injury associated with MASP-2-mediated alternative complement pathway activation, while leaving the classical (C1q-dependent) pathway component of the immune system intact. In another aspect, the invention provides compositions for inhibiting the effects of lectin-dependent complement activation, comprising a therapeutically effective amount of a MASP-2 inhibitory agent and a pharmaceutically acceptable carrier.
1 . A method of reducing or preventing the severity of tissue damage from cerebral ischemia reperfusion injury in a subject that has recently had, is having, or is at risk for having a cerebral ischemia reperfusion injury comprising administering to the subject an amount of a composition comprising a MASP-2 inhibitory monoclonal antibody effective to reduce MASP-2-dependent complement activation by greater than 50% and thereby reduce or prevent the severity of tissue damage from the cerebral ischemia reperfusion injury in the subject, wherein the MASP-2 inhibitory monoclonal antibody specifically binds to a polypeptide comprising SEQ ID NO:6 and selectively inhibits MASP-2 dependent complement activation without substantially inhibiting C1 q-dependent complement activation.
2 . The method of claim 1 , wherein the MASP-2 inhibitory agent specifically binds to a polypeptide comprising SEQ ID NO:6 with an affinity of at least 10 times greater than it binds to a different polypeptide in the complement system.
3 . The method of claim 1 , wherein the monoclonal antibody or fragment thereof is selected from the group consisting of a recombinant antibody, a chimeric antibody, a humanized antibody and a human antibody.
4 . The method of claim 1 , wherein the monoclonal antibody has reduced effector function.
5 . The method of claim 1 , wherein the subject exhibits one or more symptoms indicating the onset of a stroke, wherein the one or more symptoms are selected from the group consisting of: (1) alterations in consciousness; (2) headache; (3) aphasia; (4) facial weakness or asymmetry; (5) uncoordination, weakness, paralysis, or sensory loss of one or more limbs; (6) ataxia; (7) visual loss; and (8) intense vertigo, double vision, unilateral hearing loss, nausea, vomiting and/or photophobia.
6 . The method of claim 1 , wherein the subject at risk for suffering from a cerebral ischemia reperfusion injury has one or more of the following risk factors: high blood pressure, atrial fibrillation, high cholesterol, diabetes, atherosclerosis, obesity, previous stroke or transient ischemic attack (TIA), fibromuscular dysplasia, or patent foramen ovale.
7 . The method of claim 1 , wherein the subject at risk for suffering from a cerebral ischemia reperfusion injury has had a therapeutic intervention selected from the group consisting of a coronary artery bypass graft surgery, a coronary angioplasty surgery, a transplant surgery and a cardiopulmonary bypass surgery.
8 . A method of reducing or preventing the neurological deficit in a subject that has recently had, is having, or is at risk for having an acute ischemic stroke or a transient ischemic attack comprising administering to the subject an amount of a composition comprising a MASP-2 inhibitory monoclonal antibody effective to reduce MASP-2-dependent complement activation by greater than 50% and thereby reduce or prevent the neurological deficit from the ischemic stroke or transient ischemic attack in the subject, wherein the MASP-2 inhibitory monoclonal antibody specifically binds to a polypeptide comprising SEQ ID NO:6 and selectively inhibits MASP-2 dependent complement activation without substantially inhibiting C1q-dependent complement activation.
9 . The method of claim 8 , wherein the composition is administered to the subject at a time immediately after to about 24 hours from the onset of the acute ischemic stroke or the transient ischemic attack.
10 . The method of claim 8 , wherein the composition is administered to the subject by at least one of intra-arterial, intravenous, intrathecal, intracranial, intramuscular or subcutaneous administration.
11 . The method of claim 8 , wherein the MASP-2 inhibitory agent specifically binds to a polypeptide comprising SEQ ID NO:6 with an affinity of at least 10 times greater than it binds to a different polypeptide in the complement system.
12 . The method of claim 8 , wherein the monoclonal antibody or fragment thereof is selected from the group consisting of a recombinant antibody, a chimeric antibody, a humanized antibody and a human antibody.
13 . The method of claim 8 , wherein the monoclonal antibody has reduced effector function.
14 . The method of claim 8 , wherein the subject exhibits one or more symptoms indicating the onset of a stroke, wherein the one or more symptoms are selected from the group consisting of: (1) alterations in consciousness; (2) headache; (3) aphasia; (4) facial weakness or asymmetry; (5) uncoordination, weakness, paralysis, or sensory loss of one or more limbs; (6) ataxia; (7) visual loss; and (8) intense vertigo, double vision, unilateral hearing loss, nausea, vomiting and/or photophobia.
15 . The method of claim 8 , wherein the subject has one or more of the following risk factors for having an acute ischemic stroke or a transient ischemic attack: high blood pressure, atrial fibrillation, high cholesterol, diabetes, atherosclerosis, obesity, previous stroke or transient ischemic attack (TIA), fibromuscular dysplasia, or patent foramen ovale.
16 . The method of claim 8 , wherein the subject at risk for having an acute ischemic stroke or a transient ischemic attack has had a therapeutic intervention selected from the group consisting of a coronary artery bypass graft surgery, a coronary angioplasty surgery, a transplant surgery and a cardiopulmonary bypass surgery.