Methods and materials for identifying and treating membranous nephropathy
US-2024353404-A1 · Oct 24, 2024 · US
US9550835B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9550835-B2 |
| Application number | US-201214240057-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 23, 2012 |
| Priority date | Aug 23, 2011 |
| Publication date | Jan 24, 2017 |
| Grant date | Jan 24, 2017 |
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As a result of producing anti-DDR1 antibodies and conducting extensive studies on the antitumor activity thereof, antibodies that bind to the stalk domain in the amino acid sequence of human DDR1 were found to have a potent activity even when used alone compared to antibodies that bind to other domains. It was also found that the antibodies have one or more activities selected from the group consisting of: (i) an activity to suppress cell proliferation, (ii) an activity to inhibit cell migration, (iii) an activity to inhibit phosphorylation of DDR1 in cells, (iv) an activity to be taken up into cells, (v) an activity to decrease the expression level of DDR1 in cells, and (vi) an activity to decrease the expression level of TGF-β in cells.
Opening claim text (preview).
The invention claimed is: 1. An antibody that binds to the stalk domain of Discoidin Domain Receptor 1 (DDR1) (SEQ ID NO:4) and not to the discoidin domain of DDR1 (SEQ ID NO:3). 2. The antibody according to claim 1 that is a chimeric antibody or humanized antibody. 3. The antibody according to claim 1 that is a minibody. 4. The antibody according to claim 1 that is linked with a cytotoxic agent. 5. A monoclonal antibody produced by a hybridoma deposited under any one of Accession Nos. FERM BP-11399, FERM BP-11398, and FERM BP-11397. 6. A humanized antibody, wherein the antibody is a humanized version of a monoclonal antibody produced by a hybridoma deposited under any one of Accession Nos. FERM BP-11399, FERM BP-11398, and FERM BP-11397. 7. An antibody that binds to the stalk domain of DDR1 (SEQ ID NO:4), wherein the antibody comprises six CDRs identical to heavy chain CDR1, CDR2, and CDR3 and light chain CDR1, CDR2, and CDR3, respectively, of a monoclonal antibody produced by a hybridoma deposited under any one of Accession Nos. FERM BP-11399, FERM BP-11398, and FERM BP-11397. 8. The antibody of claim 1 , wherein the antibody has the same epitope specificity as a monoclonal antibody produced by a hybridoma deposited under any one of Accession Nos. FERM BP-11399, FERM BP-11398, and FERM BP-11397. 9. An antibody that binds to the stalk domain of DDR1 (SEQ ID NO:4) and is produced by a host cell expressing cDNAs encoding antibody heavy and light chains identical to heavy and light chains of a monoclonal antibody produced by a hybridoma deposited under any one of Accession Nos. FERM BP-11399, FERM BP-11398, and FERM BP-11397. 10. An antibody that binds to the stalk domain of DDR1 (SEQ ID NO: 4), said antibody comprising light and heavy chain variable domain amino acid sequences identical to those of a monoclonal antibody produced by a hybridoma deposited under any one of Accession Nos. FERM BP-11399, FERM BP-11398, and FERM BP-11397. 11. An antibody that binds to the stalk domain of DDR1 (SEQ ID NO: 4), said antibody comprising light and heavy chains identical to the light and heavy chains of a monoclonal antibody produced by a hybridoma deposited under any one of Accession Nos. FERM BP-11399, FERM BP-11398, and FERM BP-11397.
against enzymes · CPC title
Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues · CPC title
Lung · CPC title
against the lectin superfamily, e.g. CD23, CD72 · CPC title
Antagonist effect on antigen, e.g. neutralization or inhibition of binding · CPC title
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