Anti-CD33 and anti-CD7 combination treatment
This invention relates to the dual targeting of cell inhibiting agents to the cell surface receptors CD7 and CD33 in the treatment of hematological malignancy. In particular, the invention relates to cell inhibiting agents that bispecifically binds to CD33 and CD7 for use in the treatment of a CD7+CD33+ hematological malignancy. Such agents may comprise bispecific antibody drug conjugates.
1. A method of treating a CD7+CD33+ hematological malignancy by administering a cell inhibiting agent that bispecifically binds to CD33 and CD7, wherein said cell inhibiting agent comprises a cytotoxin linked to a bispecific antibody or antigen binding portion thereof, including a CD7 binding portion and a CD33 binding portion.
2. The method of treating the CD7+CD33+ hematological malignancy according to claim 1 , wherein said cell inhibiting agent is capable of inducing a CD33 and/or CD7 receptor mediated internalization of said cell inhibiting agent into a CD33+ and CD7+ cell.
3. The method of treating the CD7+CD33+ hematological malignancy according to claim 2 , wherein the CD33+ and CD7+ cell is an AML cell.
4. The method of treating the CD7+CD33+ hematological malignancy according to claim 1 , wherein said CD33 binding portion comprises an antigen binding fragment of an antibody.
5. The method of treating the CD7+CD33+ hematological malignancy according to claim 1 , wherein said CD7 binding portion comprises an antigen binding fragment of an antibody.
6. The method of treating the CD7+CD33+ hematological malignancy according to claim 1 , wherein said cell inhibiting agent further comprises a linking portion.
7. The method of treating the CD7+CD33+ hematological malignancy according to claim 1 , wherein said cytotoxin is selected from: i) a peptide toxin or ii) a chemical toxin.
8. The method of treating the CD7+CD33+ hematological malignancy according to claim 1 , wherein the cytotoxin is an auristatin.
9. The method of treating the CD7+CD33+ hematological malignancy according to claim 8 , wherein the auristatin is auristatin E, monomethylauristatin E, or monomethylauristatin F.