Dual specific immunotoxin for brain tumor therapy
We tested the in vitro and in vivo efficacy of a recombinant bispecific immunotoxin that recognizes both EGFRwt and tumor-specific EGFRvIII receptors. A single chain antibody was cloned from a hybridoma and fused to toxin, carrying a C-terminal peptide which increases retention within cells. The binding affinity and specificity of the recombinant bispecific immunotoxin for the EGFRwt and the EGFRvIII proteins was measured. In vitro cytotoxicity was measured. In vivo activity of the recombinant bispecific immunotoxin was evaluated in subcutaneous models and compared to that of an established monospecific immunotoxin. In our preclinical studies, the bispecific recombinant immunotoxin, exhibited significant potential for treating brain tumors.
1. A method of treating a tumor in a human, comprising:
administering to the human a single chain variable region antibody which binds with a binding affinity that is at least 5×10 8 M −1 as measured by surface plasmon resonance to both (a) EGFR found on normal human cells and (b) EGFR variant III mutant, wherein the single chain variable region antibody is cloned from a hybridoma producing monoclonal antibody D2C7, wherein the single chain variable region antibody is covalently linked to a cytotoxic agent which is a form of Pseudomonas exotoxin A, whereby tumor cells are killed.
2. The method of claim 1 wherein the tumor is a squamous cell head and neck tumor.
3. The method of claim 1 wherein the tumor is a brain tumor.
4. The method of claim 1 wherein the tumor is a breast tumor.
5. The method of claim 1 wherein the tumor is a glioblastoma multiforme.
6. The method of claim 1 wherein the tumor is an astrocytoma.
7. The method of claim 1 wherein the tumor contains an EGFRvIII allele.
8. The method of claim 1 wherein the single chain variable region antibody is administered directly to the central nervous system.
9. The method of claim 1 wherein the single chain variable region antibody is administered directly to the brain.
10. The method of claim 1 wherein the single chain variable region antibody is administered directly to a surgically-created tumor resection cavity.
11. The method of claim 1 wherein the single chain variable region antibody is administered directly to a natural tumor cyst.
12. The method of claim 1 wherein the single chain variable region antibody is administered directly to tumor parenchyma.
13. The method of claim 1 wherein the cytotoxic agent is produced as a fusion protein with the single chain variable region antibody.
14. The method of claim 1 wherein the cytotoxic agent further comprises a KDEL peptide.
15. The method of claim 1 wherein the single chain variable region antibody comprises a VH sequence having SEQ ID NO: 1.
16. The method of claim 1 wherein the single chain variable region antibody comprises a VL sequence having SEQ ID NO: 2.
17. The method of claim 1 wherein the single chain variable region antibody comprises CDR1, CDR2, and CDR3 regions having SEQ ID NOs: 3-8.