High affinity anti-prostate stem cell antigen (PSCA) antibodies for cancer targeting and detection
The present invention provides novel high affinity antibodies and fragments thereof that bind to the cancer antigen PSCA. The antibodies of the present invention may be used for cancer diagnosis, prognosis, treatment, visualization, and the like. The present invention also provides methods for the detection, visualization, and treatment of various cancers expressing PSCA.
1. An antigen binding protein construct that binds to human prostate stem cell antigen (PSCA) comprising an antigen binding domain comprising a heavy chain variable domain comprising the complementarity determining regions (CDRs) of the heavy chain variable domain of SEQ ID NO: 7 and a light chain variable domain comprising the CDRs of the light chain variable domain of SEQ ID NO: 7.
2. The antigen binding protein construct of claim 1 , wherein said antigen binding domain comprises a light chain variable domain comprising the light chain variable domain of SEQ ID NO: 7.
3. The antigen binding protein construct of claim 1 , wherein said antigen binding domain comprises a heavy chain variable domain comprising the heavy chain variable domain of SEQ ID NO: 7.
4. The antigen binding protein construct of claim 1 , wherein the construct is a minibody.
5. The antigen binding protein construct of claim 4 , wherein said minibody comprises an amino acid sequence that is at least 95% identical to SEQ ID NO: 12.
6. The antigen binding protein construct of claim 5 , wherein said minibody comprises the amino acid sequence of SEQ ID NO: 12.
7. The antigen binding protein construct of claim 1 , wherein the construct is a diabody.
8. The antigen binding protein construct of claim 1 , wherein the construct is a humanized antibody.
9. The antigen binding protein construct of claim 1 , wherein the construct is an affinity matured antibody.
10. The antigen binding protein construct of claim 1 , wherein the construct is conjugated to a therapeutic agent.
11. The antigen binding protein construct of claim 10 , wherein the therapeutic agent is a cytotoxic agent.
12. The antigen binding protein construct of claim 11 , wherein the cytotoxic agent is selected from a group consisting of ricin, ricin A-chain, doxorubicin, daunotubicin, paclitaxel, ethiduim bromide, mitomycin, etoposide, tenoposide, vincristine, vinblastine, colchicine, dihydroxy anthracin dione, actinomycin D, diphteria toxin, Pseudomonas, exotoxin (PE) A, PE40, abrin, arbrin A chain, modeccin A chain, alpha-sarcin, gelonin mitogellin, retstrictocin, phenomycin, enomycin, curicin, crotin, calicheamicin, sapaonaria officinalis inhibitor, maytansinoids, and glucocorticoidricin.
13. The antigen binding protein construct of claim 10 , wherein the therapeutic agent is a radioactive isotope.
14. The antigen binding protein construct of claim 13 , wherein the radioactive isotope is 212 Bi, 131 I, 111 In, 90 Y or 186 Re.
15. The antigen binding protein construct of claim 1 , wherein the construct is linked to an anti-cancer pro-drug activating enzyme capable of converting a pro-drug to its active form.
16. The antigen binding protein construct of claim 1 , which is labeled with a detectable marker.
17. The antigen binding protein construct of claim 16 , wherein the detectable marker is a radioisotope, a fluorescent compound, a bioluminescent compound, a chemiluminescent compound, a metal chelator or an enzyme.
18. The antigen binding protein construct of claim 16 , wherein the detectable marker is 124 I, 86 Y, 18 F, or 94 Tc.
19. A pharmaceutical composition comprising the antigen binding protein construct of claim 1 and a pharmaceutically acceptable excipient, carrier, or stabilizer.
20. The composition of claim 19 , which is formulated as an aqueous solution or a lyophilized solid.
21. A polynucleotide encoding the antigen binding protein construct of claim 1 .
22. A method for inhibiting the growth of a prostate, pancreatic or bladder cancer cell expressing PSCA, said method comprising contacting said cancer cell with an antigen binding protein construct of claim 1 , wherein said antigen binding protein construct is conjugated to an effector moiety that is effective to inhibit the growth of said cancer cell.
23. The method of claim 22 , further comprising administering to the cancer cell a chemotherapeutic agent.
24. The method of claim 22 , further comprising administering radiation therapy to the cancer cell.
25. A method for killing a prostate, pancreatic or bladder cancer cell expressing PSCA, said method comprising contacting said cancer cell with an antigen binding protein construct of claim 1 , wherein said antigen binding protein construct is conjugated to an effector moiety that is effective to kill said cancer cell.
26. A method for treating a prostate, pancreatic or bladder cancer expressing PSCA in a patient, said method comprising administering to said patient an antigen binding protein construct of claim 1 , wherein said antigen binding protein construct is conjugated to an effector moiety that is effective to inhibit the growth of said cancer.
27. The method of claim 26 , further comprising administering to the patient hormone ablation therapy or hormone antagonist therapy.
28. The method of claim 26 , wherein the antigen binding protein construct is administered intravenously, intraperitoneally, intramuscularly, intratumorally, or intradermally.
29. A method for imaging prostate, pancreatic or bladder cancer cells expressing PSCA in a patient, said method comprising administering to said patient an antigen binding protein construct of claim 1 , wherein said antigen binding protein construct is conjugated to a detectable moiety, and detecting the presence and location of the antigen binding protein construct within the patient's body.
30. The method of claim 29 , wherein imaging is performed using a method selected from the group consisting of magnetic resonance imaging (MRI), nuclear magnetic resonance (NMR), computerized axial tomography (CAT) scan, cooled charged coupled device (CCD) camera optical imaging, bioluminescent optical imaging, position emission tomography (PET), single photon emission computed tomography, and microPET.
31. A method for detecting a cancerous cell expressing PSCA, said method comprising contacting a sample comprising cells with an antigen binding protein construct of claim 1 and detecting any complex of a cancerous cell expressing PSCA and said antigen binding protein construct that forms.
32. An antibody that binds to human prostate stem cell antigen (PSCA) comprising an antigen binding domain comprising a heavy chain variable domain comprising the complementarity determining regions (CDRs) of the heavy chain variable domain of SEQ ID NO: 7 and a light chain variable domain comprising the CDRs of the light chain variable domain of SEQ ID NO: 7.
33. The antibody of claim 32 , wherein said antibody is a minibody, a diabody, a scFv or a scFv-Fc.