Anti-BTN3A antibodies and their use in treating cancer or infectious disorders
The present invention relates to humanized antibodies that specifically bind to human BTN3A and their use in treating cancer and infectious disorders.
1. A method of treating cancer in a subject in need thereof, comprising administering a therapeutically effective amount of an anti-BTN3A antibody comprising a variable heavy chain polypeptide VH of SEQ ID NO:1 and a variable light chain polypeptide VL of SEQ ID NO:2 or SEQ ID NO: 3.
2. The method of claim 1 , wherein said anti-BTN3A antibody is administered in combination with an anti-PD1 or anti-PD-L1 antibody.
3. The method of claim 1 , wherein said anti-BTN3A antibody binds to human BTN3A1 polypeptide with a KD of 5 nM or less as measured by surface plasmon resonance.
4. The method of claim 1 , wherein said anti-BTN3A antibody induces the activation of Vγ9Vδ2-T cells in co-culture with BTN3A expressing cells, with an EC 50 of 1 μg/ml or below, as measured in a degranulation assay.
5. The method of claim 1 , wherein said anti-BTN3A antibody is administered in combination with IL-2 or IL-15 or their derivatives.
6. The method of claim 1 , wherein said anti-BTN3A antibody comprises a mutant or chemically modified IgG1 constant region, wherein said mutant or chemically modified IgG1 constant region confers no or decreased binding to Fcγ receptors when compared to a corresponding antibody with wild type IgG1 isotype constant region.
7. The method of claim 6 , wherein said mutant IgG1 constant region is IgG1 triple mutant L247F, L248E and P350S.
8. The method of claim 1 , wherein said anti-BTN3A antibody comprises a heavy chain of SEQ ID NO:4 and a light chain of SEQ ID NO:6.
9. The method of claim 1 , wherein said anti-BTN3A antibody is administered in combination with an anti-PD1 antibody selected from the group consisting of nivolumab, pembrolizumab, avelumab, durvalumab, cemiplimab, and atezolizumab.
10. The method of claim 1 , wherein said anti-BTN3A antibody is administered in combination with pembrolizumab.
11. The method of claim 1 , wherein said cancer is a non-hematological cancer.
12. The method of claim 1 , wherein said method comprises administering a therapeutically efficient amount of an anti-BTN3A antibody having a heavy chain of SEQ ID NO:4 and a light chain of SEQ ID NO:6, and wherein said cancer is a non-hematological cancer.
13. The method of claim 1 , wherein said method comprises administering a therapeutically efficient amount of an anti-BTN3A antibody having a heavy chain of SEQ ID NO:4 and a light chain of SEQ ID NO:6, in combination with an anti-PD1 antibody, and wherein said cancer is a non-hematological cancer.
14. The method of claim 1 , wherein said method comprises administering a therapeutically efficient amount of an anti-BTN3A antibody having a heavy chain of SEQ ID NO:4 and a light chain of SEQ ID NO:6, in combination with pembrolizumab, and wherein said cancer is a non-hematological cancer.