Humanized antibodies against CD269 (BCMA)
The invention relates to humanized antibodies or antibody fragments that bind CD269 (BCMA), thereby disrupting the interaction between CD269 and its native ligands (BAFF and APRIL), and their use in the treatment of plasma cell-mediated diseases such as multiple myeloma and autoimmune diseases.
1. An antibody or antibody fragment, comprising:
a VH domain and a VL domain, wherein the VH domain comprises:
the CDR1 sequence RYWIS (SEQ ID NO: 18) or RYWFS (SEQ ID NO. 19);
the CDR2 sequence EINPNSSTINYAPSLKDK (SEQ ID NO: 20) or EINPSSSTINYAPSLKDK (SEQ ID NO: 21); and
the CDR3 sequence SLYYDYGDAYDYW (SEQ ID NO. 22),
and wherein the VL domain comprises:
the CDR1 sequence KASQSVESNVA (SEQ ID NO: 23, wherein X 1 X 2 is ES);
the CDR2 sequence SASLRFS (SEQ ID NO. 24); and
the CDR3 sequence QQYNNYPLTFG (SEQ ID NO. 25),
wherein said antibody or fragment thereof specifically binds an epitope of the extracellular domain of CD269 (BCMA).
2. The antibody or antibody fragment of claim 1 , comprising 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.
3. The antibody or antibody fragment of claim 1 , comprising a VL domain that comprises the sequence of SEQ ID NO. 14.
4. The antibody or antibody fragment 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.
5. The antibody or antibody fragment of claim 1 , wherein the antibody binding to CD269 (BCMA) disrupts BAFF-CD269 and/or APRIL-CD269 interaction.
6. The antibody or antibody fragment of claim 1 , wherein the antibody is glycosylated.
7. The antibody or antibody fragment of claim 6 , 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.
8. An antibody-drug conjugate (ADC) comprising the antibody or antibody fragment of claim 1 conjugated to a therapeutic agent.
9. A pharmaceutical composition comprising the antibody or antibody fragment of claim 1 , together with a pharmaceutically acceptable carrier.
10. The antibody or antibody fragment of claim 1 , comprising a VH domain with 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 a VL domain with at least 80% sequence identity to the sequence of SEQ ID NO: 14, wherein the CDR sequences are those recited in claim 1 .
11. The antibody or antibody fragment of claim 1 , comprising a VH domain with 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 a VL domain with at least 90% sequence identity to the sequence of SEQ ID NO: 14, wherein the CDR sequences are those recited in claim 1 .