US2003032073A1PendingUtilityA1
Method for diagnosis and therapy of Hodgkin's lymphomas
Priority: Dec 20, 1996Filed: Jan 23, 2002Published: Feb 13, 2003
Est. expiryDec 20, 2016(expired)· nominal 20-yr term from priority
A61P 35/00C07K 16/2884G01N 33/6878G01N 33/5759
41
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Claims
Abstract
The invention relates to a method for diagnosing and treating Hodgkin's lymphomas (lymphogranulomatosis) which is based on the expression of the variant exon v10 of the CD44 gene as a molecular marker or target. There is a significant correlation between v10 expression and the stage and prognosis of the disease. In a preferred embodiment, v10-specific antibody molecules are used to measure the expression of the exon in samples. In another preferred embodiment, radiolabelled v10-specific antibodies are used to treat Hodgkin's lymphomas.
Claims
exact text as granted — not AI-modified1 . Method of diagnosing or treating Hodgkin's lymphomas (lymphogranulomatosis), characterised in that this method is based on the expression of the variable exon v10 of the gene CD44 as molecular marker.
2 . Method according to claim 1 , characterised in that it is based on the binding of an antibody molecule to an epitope which is coded by the variable exon v10 of the gene CD44.
3 . Method according to claim 2 , characterised in that an antibody molecule is used which recognises the amino acid sequence according to SEQ ID NO. 2.
4 . Method according to one of claims 1 to 3 , characterised in that the antibody molecule is a monoclonal antibody, an Fab- or F(ab′) 2 -fragment of an immunoglobulin, a recombinantly produced antibody, a recombinantly produced chimeric, humanised antibody or single chain antibody (scFv).
5 . Use of an antibody molecule which is specific to an epitope which is coded by the variant exon v10 of the CD44 gene, in a method according to one of claims 1 to 4 .
6 . Use of an antibody molecule which is specific for an epitope within the amino acid sequence coded by the variable exon v10 of the CD44 gene, for treating Hodgkin's lymphomas (lymphogranulomatosis).
7 . Use according to claim 6 , characterised in that the antibody molecule binds to the amino acid sequence according to SEQ ID NO. 2.
8 . Use according to one of claims 6 and 7 , characterised in that the antibody molecule is a monoclonal antibody, a Fab- or F(ab′) 2 -fragment of an immunoglobulin, a recombinantly produced antibody, a recombinantly produced chimeric or humanised antibody, or single chain antibody (scFv).
9 . Use according to one of claims 6 to 8 , characterised in that the antibody molecule is linked to a radioactive isotope, a radioactive compound, an enzyme, a toxin, a cytostatic, a prodrug, a cytokine or another immunomodulatory polypeptide.
10 . Use of an antibody molecule which is specific for an epitope within the amino acid sequence coded by the variable exon v10 of the CD44 gene, for preparing a pharmaceutical composition for diagnosing and/or treating tumoral diseases.
11 . Use according to claim 10 , characterised in that the tumoral disease is a Hodgkin's lymphoma (lymphogranulomatosis).
12 . Use according to claim 10 or 11 , characterised in that the antibody molecule binds to the amino acid sequence according to SEQ ID NO. 2.
13 . Antibody molecule which is specific for an epitope within the amino acid sequence coded by the variable exon v10 of the CD44 gene, for pharmaceutical use.
14 . Antibody molecule according to claim 14 , characterised in that it binds to the amino acid sequence according to SEQ ID NO. 2.
15 . Antibody molecule according to claim 13 or 14 , characterised in that it is a monoclonal antibody, a Fab- or F(ab′) 2 -fragment of an immunoglobulin, a recombinantly produced antibody, a recombinantly produced chimeric or humanised antibody or single chain antibody (scFv).
16 . Antibody molecule according to one of claims 13 to 15 , characterised in that it is linked to a radioactive isotope, a radioactive compound, an enzyme, a toxin, a cytostatic, a prodrug, a cytokine or another immunomodulatory polypeptide.Join the waitlist — get patent alerts
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