Humanized antibodies against CD269 (BCMA)
A method of treating a medical disorder associated with the presence of pathogenic B cells expressing B cell maturation antigen (BCMA), the method comprising administering to a subject an isolated antibody or antibody fragment comprising specific VH and VL domain complementary determining region (CDR) sequences, wherein the antibody or fragment thereof specifically binds an epitope of the extracellular domain of CD269 (BCMA).
1. A method of treating a human subject to trigger cytotoxicity in pathogenic B cells expressing B cell maturation antigen (BCMA) or pathogenic plasma cells expressing BCMA, the method comprising administering to the subject an antibody fragment comprising:
(a) a VH domain that comprises:
CDR1 sequence RYWIS (SEQ ID NO: 18) or RYWES (SEQ ID NO. 19);
CDR2 sequence EINPNSSTINYAPSLKDK (SEQ ID NO: 20) or EINPSSSTINYAPSLKDK (SEQ ID NO: 21); and
CDR3 sequence SLYYDYGDAYDYW (SEQ ID NO. 22); and
(b) a VL domain that comprises:
CDR1 sequence KASQSVX 1 X 2 NVA (SEQ ID NO. 23), wherein X 1 X 2 is ES;
CDR2 sequence SASLRFS (SEQ ID NO 24); and
CDR3 sequence QQYNNYPLTFG (SEQ ID NO. 25),
wherein said antibody or antibody fragment binds an epitope of the extracellular domain of CD269 (BCMA).
2. The method of claim 1 , wherein the administering is effective to treat a cancer of plasma cells or a cancer of B lymphocytes.
3. The method of claim 1 , wherein the subject has an autoimmune disease associated with autoreactive plasma cells and/or autoreactive memory B cells.
4. The method of claim 2 , wherein said cancer of B lymphocytes is Hodgkin's disease.
5. The method of claim 2 , wherein said cancer of plasma cells is multiple myeloma, plasmacytoma, Waldenström macroglobulinemia or plasma cell leukemia.
6. The method of claim 1 , wherein the subject has an inflammatory autoimmune disease.
7. The method of claim 6 , wherein the inflammatory autoimmune disease is systemic lupus erythematosus (SLE) or rheumatic arthritis.
8. The method of claim 1 , wherein the antibody or antibody fragment is in an antibody-drug conjugate (ADC) comprising the antibody or antibody fragment conjugated to a therapeutic agent.
9. The method of claim 1 , wherein the antibody or antibody fragment comprises a VH domain that comprises the sequence of SEQ ID NO. 6, SEQ ID NO. 7, SEQ ID NO. 8 or SEQ ID NO. 9.
10. The method of claim 1 , wherein the VL domain comprises the sequence of SEQ ID NO. 14.
11. The method of claim 1 , wherein the antibody binds an epitope of the N-terminus of CD269, wherein the epitope consists of amino acids 13, 15, 16, 17, 18, 19, 20, 22, 23, 26, 27 or 32 of SEQ ID NO: 39.
12. The method of claim 1 , wherein the antibody binding to CD269 (BCMA) disrupts BAFF-CD269 and/or APRIL-CD269 interaction.
13. The method of claim 1 , wherein the antibody is glycosylated.
14. The method of claim 13 , wherein the antibody comprises the sequence of SEQ ID NO: 29, and wherein the antibody comprises a glycan that is an N-linked oligosaccharide chain at Asn297 of the heavy chain consisting of the sequence of SEQ ID NO: 29.
15. The method of claim 1 , wherein the antibody or antibody fragment is administered to the subject together with a pharmaceutically acceptable carrier.
16. The method of claim 1 , wherein the VH domain has at least 80% sequence identity to the sequence of SEQ ID NO: 6, SEQ ID NO: 7, SEQ ID NO: 8 or SEQ ID NO: 9 and wherein the CDR sequences are those recited in claim 1 .
17. The method of claim 1 , wherein the VH domain has at least 90% sequence identity to the sequence of SEQ ID NO; 6, SEQ ID NO: 7, SEQ ID NO: 8 or SEQ ID NO: 9 and wherein the CDR sequences are those recited in claim 1 .