US2012027758A1PendingUtilityA1
Use of anti-cd100 antibodies
Est. expiryJan 31, 2023(expired)· nominal 20-yr term from priority
A61P 37/06A61P 31/14A61P 35/02A61P 43/00A61P 37/00A61K 2039/505A61P 25/28C07K 16/2803A61P 25/00A61P 29/00A61P 25/02
40
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Claims
Abstract
The invention relates to the use a BD16 and/or BB18 anti-CD100 antibody or of a chimeric or humanized or human form thereof, or a fragment thereof, for the therapy or diagnosis of a central nervous system disorder, more particularly a myelin disorder or a disease that affects oligodendrocytes, such as multiple sclerosis or HTLV-1 associated myelopathy or peripheral myelinating cells.
Claims
exact text as granted — not AI-modified1 . A method for treating a neuroinflammatory disorder in a subject, said method comprising administering an effective amount of an anti-CD100 antibody or an antigen-binding fragment thereof to said subject, wherein said anti-CD100 antibody or an antigen-binding fragment thereof blocks the interaction of soluble CD100 with plexin B1 receptor.
2 . The method of claim 1 , wherein said neuroinflammatory disorder is a central nervous system (CNS) inflammatory disorder.
3 . The method of claim 1 , wherein said neuroinflammatory disorder is a peripheral nervous system (PNS) inflammatory disorder.
4 . The method of claim 1 , wherein said subject has a high level of soluble CD100 in a biological sample taken from said subject when compared to a control subject.
5 . The method of claim 4 , wherein said biological sample is cerebral spinal fluid (CSF) or blood.
6 . The method of claim 1 , wherein said neuroinflammatory disorder is a myelin disorder or a disease that affects oligodendrocytes
7 . The method of claim 1 , wherein said neuroinflammatory disorder is a disease that affects myelinating peripheral cells.
8 . The method of claim 1 , wherein said neuroinflammatory disorder is selected from the group consisting of an oligodendroglioma, leucodystrophy, Guillain-Barrésyndrome, Alexander disease, Canavan disease, Krabbe disease, Pelizaeus-Merzbacher disease, Zellweger disease, Refsum disease, CACH disease, X-linked adrenoleucodystrophy, adrenoleucodystrophy, adrenomyeloneuropathy, leucodystrophies of undetermined origin, HTLV-1 associated myelopathy, multiple sclerosis, and polyradiculoneuritis.
9 . The method of claim 8 , wherein said neuroinflammatory disorder is HTLV-1 associated myelopathy.
10 . The method of claim 8 , wherein said neuroinflammatory disorder is polyradiculoneuritis.
11 . The method of claim 8 , wherein said neuroinflammatory disorder is multiple sclerosis.
12 . The method of claim 1 , wherein said neuroinflammatory disorder is a post-trauma myelin disorder of the central or peripheral nervous system.
13 . The method of claim 1 , wherein said anti-CD100 antibody is a chimeric, humanized, or human antibody.
14 . A method for protecting neural progenitor cells or oligodendrocytes from cell death, said method comprising administering to a subject an effective amount of an anti-CD100 antibody or an antigen-binding fragment thereof, and wherein said anti-CD100 antibody or an antigen-binding fragment thereof blocks the interaction of soluble CD100 with plexin B1 receptor.
15 . The method of claim 14 , wherein said subject has a high level of soluble CD100 in a biological sample taken from said subject in comparison to a control subject.
16 . The method of claim 15 , wherein said biological sample is cerebral spinal fluid (CSF) or blood.
17 . The method of claim 14 , wherein said anti-CD100 antibody is a chimeric, humanized, or human antibody.Join the waitlist — get patent alerts
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