Bispecific antibodies for use in the treatment of hematological malignancies
The present invention relates to novel methods for the treatment of hematological malignancies. In particular, the invention relates to the treatment of hematological malignancies using antibodies comprising a first binding moiety that is able to bind human CD1d and a second binding moiety that is able to bind the human Vγ9Vδ2-TCR.
1. A method of treating Chronic Lymphocytic Leukemia (CLL), Multiple Myeloma (MM), or Acute Myeloid Leukemia (AML) in a subject in need thereof comprising administering an antibody comprising
(a) a first binding moiety that is able to bind human CD1d and comprises a complementarity determining region (CDR)1 comprising the amino acid sequence of SEQ ID NO: 34, a CDR2 comprising the amino acid sequence of SEQ ID NO: 35, and a CDR3 sequences comprising the amino acid sequence of SEQ ID NO: 36; and
(b) a second binding moiety that is able to bind the human Vγ9Vδ2-TCR and comprises the amino acid sequence of SEQ ID NO: 162.
2. The method of claim 1 , further comprising administering a compound capable of upregulating CD1d expression.
3. The method of claim 2 , further comprising administering an EZH2 inhibitor.
4. The method of claim 1 , further comprising administration of an aminobisphosphonate.
5. The method of claim 1 , wherein the subject is above 65 years of age.
6. The method of claim 1 , wherein the first and/or second binding moiety is a single domain antibody.
7. The method of claim 1 , wherein the antibody is able to activate iNKT cells.
8. The method of claim 1 , wherein the antibody is able to reduce Vδ1 T cell activation.
9. The method of claim 1 , wherein the first binding moiety comprises SEQ ID NO: 161.
10. The method of claim 1 , wherein the antibody is able to bind Vδ2.
11. The method of claim 1 , wherein the antibody comprises the sequence set forth in SEQ ID NO: 164.
12. The method of claim 1 , wherein the antibody further comprises a tumor targeting moiety.
13. The method of claim 2 , wherein the compound capable of upregulating CD1d expression is all-trans retinoic acid.