US2011311542A1PendingUtilityA1

Sp35 Antibodies and Uses Thereof

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Assignee: MI SHAPriority: Jul 8, 2005Filed: Jun 10, 2011Published: Dec 22, 2011
Est. expiryJul 8, 2025(expired)· nominal 20-yr term from priority
A61P 9/10A61P 43/00A61P 9/00A61P 25/28A61P 27/02A61P 25/00A61P 3/02A61P 25/04A61P 25/14A61P 25/16A61P 21/02C07K 16/18C12N 2310/14C07K 2317/76C12N 15/1138C12N 2310/111C07K 16/2803C07K 2317/75C07K 2317/55C07K 2317/24C07K 2317/21A61K 2039/505C07K 2317/33C07K 2319/30A61K 39/395C07K 16/28
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Claims

Abstract

Endogenous Sp35 is a negative regulator for neuronal survival, axon regeneration, oligodendrocyte differentiation and myelination (Negative Regulator). Molecules that block endogenous Sp35 function, such anti-Sp35 antibodies can be used as therapeutics for the treatment of neuron and oligodendrocyte dysfunction. The present invention provides antibodies specific for Sp35, and methods of using such antibodies as antagonists of endogenous Sp35 function. The invention further provides specific hybridoma and phage library-derived monoclonal antibodies, nucleic acids encoding these antibodies, and vectors and host cells comprising these antibodies. The invention further provides methods of promoting oligodendrocyte survival and myelination in a vertebrate, comprising administering to a vertebrate in need of such treatment an effective amount of an anti-Sp35 antibody

Claims

exact text as granted — not AI-modified
1 - 212 . (canceled) 
     
     
         213 . A binding molecule which is capable of binding to the protein according to amino acids 34 to 551 of SEQ ID NO:2, with a dissociation constant <1000 nM. 
     
     
         214 . The binding molecule according to  claim 213  which binds to one or more of the sequences chosen from the group consisting of amino acids 66-426, 138-161, 210-233, 234-257, 258-281, 417-424, or 412-493 of SEQ ID NO:2. 
     
     
         215 . The binding molecule according to  claim 213 , which is capable of disinhibiting spinal cord myelin at a concentration of less than 3 μg/ml. 
     
     
         216 . The binding molecule according to  claim 213 , which is capable of increasing mean neurite length. 
     
     
         217 . The binding molecule according to  claim 213 , which comprises at least one antigen binding site chosen from the group consisting of:
 a sequence which selected from the group consisting of SEQ ID NO:380 or SEQ ID NO:161, and;   a sequence which is selected from the group consisting of SEQ ID NO:381 or SEQ ID NO:276.   
     
     
         218 . The binding molecule according to  claim 213 , which is an antibody or a fragment thereof. 
     
     
         219 . The binding molecule according to  claim 218  in which the constant part or fragment thereof of the human heavy chain is of the γ4 type and the constant part or fragment thereof of the human light chain is of the κ type. 
     
     
         220 . The binding molecule according to  claim 218 , which is a human or chimeric or humanized monoclonal antibody. 
     
     
         221 . A polynucleotide encoding a binding molecule according to  claim 218 . 
     
     
         222 . An expression vector comprising one or more polynucleotides according to  claim 221 . 
     
     
         223 . An expression system comprising a polynucleotide according to  claim 221 , when said expression system or part thereof is present in a compatible host cell. 
     
     
         224 . An isolated host cell which comprises an expression system according to  claim 223 . 
     
     
         225 . A pharmaceutical composition comprising a binding molecule according to  claim 213  together with at least one pharmaceutically acceptable carrier or diluent. 
     
     
         226 . A method of treatment of diseases associated with the promotion of axonal regeneration comprising administering to a subject in need of such treatment an effective amount of a binding molecule according to  claim 213 .

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