Humanized L243 antibodies

Patent metadata

Field	Value
Publication number	US-8992917-B2
Application number	US-201314080231-A
Country	US
Kind code	B2
Filing date	Nov 14, 2013
Priority date	Mar 3, 2005
Publication date	Mar 31, 2015
Grant date	Mar 31, 2015

Abstract

Humanized antibodies are provided that specifically bind HLA-DR. The antibodies recognize the epitope recognized by the murine monoclonal antibody L243. Processes for preparing such antibodies, pharmaceutical compositions containing such antibodies, and clinical therapeutic and diagnostic, as well as research-related uses for such antibodies, are provided.

First claim

What is claimed is:

1. A method of treating a B-cell leukemia comprising:
a) obtaining a humanized L243 antibody or antigen-binding fragment thereof, comprising heavy chain variable domain complementarity determining region (CDR) sequences CDR1 (NYGMN, residues 31 to 35 of SEQ ID NO: 4), CDR2 (WINTYTREPTYADDFKG, residues 50 to 66 of SEQ ID NO:4), and CDR3 (DITAVVPTGFDY, residues 99 to 110 of SEQ ID NO:4) and heavy chain framework residues F27, K38, K46, A68 and F91 and light chain variable domain CDR sequences CDR1 (RASENIYSNLA, residues 24 to 34 of SEQ ID NO:2), CDR2 (AASNLAD, residues 50 to 56 of SEQ ID NO:2), and CDR3 (QHFWTTPWA, residues 89 to 98 of SEQ ID NO:2) and light chain framework residues R37, K39, V48 and F49, wherein the remainder of the humanized L243 antibody framework region and constant region sequences are from one or more human antibodies; and
b) administering the humanized L243 antibody or fragment thereof to a subject with an HLA-DR positive B-cell leukemia,

wherein the leukemia is selected from the group consisting of acute lymphocytic leukemia (ALL), chronic lymphocytic leukemia (CLL) and hairy cell leukemia.

2. The method of claim 1 , wherein the humanized L243 antibody or fragment thereof comprises human IgG4 constant region sequences and wherein the humanized L243 antibody or fragment thereof comprises a Ser241Pro point mutation in the hinge region of the antibody or fragment thereof.

3. The method of claim 1 , wherein the humanized L243 antibody has a lower dissociation constant for HLA-DR + cells than the murine L243 antibody.

4. The method of claim 1 , wherein the humanized L243 antibody or antigen-binding fragment thereof is a naked antibody or fragment thereof.

5. The method of claim 4 , further comprising administering at least one therapeutic agent to the subject.

6. The method of claim 5 , wherein the therapeutic agent is selected from the group consisting of antibodies, antibody fragments, drugs, chemotherapeutic agents, toxins, hormones, hormone antagonists, immunomodulators and cytokines.

7. The method of claim 6 , wherein the chemotherapeutic agent is a taxane, a nitrogen mustard, an ethylenimine, an alkyl sulfonate, a nitrosourea, a triazene, a folic acid analog, a pyrimidine analog, a purine analog, an antibiotic, a platinum coordination complex, a COX-2 inhibitor, an apoptotic agent, a substituted urea, a methyl hydrazine, a steroid, a progestin, an estrogen, an antiestrogen, an androgen, actinomycin, azaribine, anastrozole, azacytidine, bleomycin, bryostatin-1, busulfan, carmustine, celecoxib, chlorambucil, cisplatinum, irinotecan (CPT-11), carboplatin, cladribine, cyclophosphamide, cytarabine, dacarbazine, docetaxel, dacarbazine, dactinomycin, daunorubicin, dexamethasone, diethylstilbestrol, doxorubicin, ethinyl estradiol, estramustine, etoposide, floxuridine, fludarabine, flutamide, 5-fluorouracil, fluoxymesterone, gemcitabine, hydroxyprogesterone caproate, hydroxyurea, idarubicin, ifosfamide, L-asparaginase, leucovorin, lomustine, mechlorethamine, medroprogesterone acetate, megestrol acetate, melphalan, mercaptopurine, methotrexate, mitoxantrone, mitomycin, mitotane, oxaliplatin, phenyl butyrate, prednisone, procarbazine, paclitaxel, pentostatin, semustine, streptozocin, SN-38, tamoxifen, taxanes, testosterone propionate, thalidomide, thioguanine, teniposide, topotecan, uracil mustard, vinblastine, vinorelbine or vincristine.

8. The method of claim 6 , wherein the therapeutic agent is a second antibody or antigen-binding fragment thereof that binds to a tumor-associated antigen.

9. The method of claim 8 , wherein the tumor-associated antigen is selected from the group consisting of A3, BrE3-antigen, CD1, CD1a, CD3, CD5, CD15, CD19, CD20, CD21, CD22, CD23, CD25, CD30, CD45, CD74, CD79a, CD80, HLA-DR, NCA95, NCA90, HCG, CEA (CEACAM-5), CEACAM-6, CSAp, EGFR, EGP-1, EGP-2, Ep-CAM, Ba 733, HER2/neu, hypoxia inducible factor (HIF), KC4-antigen, KS-1 antigen, KS1-4, Le-Y, macrophage inhibition factor (MIF), MAGE, MUC1, MUC2, MUC3, MUC4, MUC16, PAM-4-antigen, PSA, PSMA, RS5, S100, TAG-72, p53, tenascin, IL-6, IL-8, insulin growth factor-1 (IGF-1), Tn antigen, tumor necrosis antigens, VEGF, 17-1A-antigen, an angiogenesis marker, ED-B fibronectin, an oncogene marker, an oncogene product, HM1.24, VEGF, ILGF, placental growth factor and carbonic anhydrase IX.

10. The method of claim 1 , wherein the humanized L243 antibody or antigen-binding fragment thereof is conjugated to at least one therapeutic or diagnostic agent.

11. The method of claim 10 , wherein the therapeutic agent is selected from the group consisting of antibodies, antibody fragments, drugs, chemotherapeutic agents, toxins, enzymes, nucleases, hormones, hormone antagonists, immunomodulators, cytokines, chelators, boron compounds, photoactive agents, dyes and radioisotopes.

12. The method of claim 1 , wherein the humanized L243 antibody or antigen-binding fragment thereof is administered intravenously, subcutaneously, or intramuscularly at a dose of between 20 and 2000 mg.

13. The method claim 1 , wherein the humanized L243 antibody or antigen-binding fragment thereof is conjugated to one or more lipids, polymeric carriers, micelles, nanoparticles, or a combination thereof.

14. The method of claim 11 , wherein the chemotherapeutic agent is selected from the group consisting of a taxane, a nitrogen mustard, an ethylenimine, an alkyl sulfonate, a nitrosourea, a triazene, a folic acid analog, a pyrimidine analog, a purine analog, an antibiotic, a platinum coordination complex, a COX-2 inhibitor, an apoptotic agent, a substituted urea, a methyl hydrazine, a steroid, a progestin, an estrogen, an antiestrogen, an androgen, actinomycin, azaribine, anastrozole, azacytidine, bleomycin, bryostatin-1, busulfan, carmustine, celecoxib, chlorambucil, cisplatinum, irinotecan (CPT-11), carboplatinum, cladribine, cyclophosphamide, cytarabine, dacarbazine, docetaxel, dacarbazine, dactinomycin, daunorubicin, dexamethasone, diethylstilbestrol, doxorubicin, ethinyl estradiol, estramustine, etoposide, floxuridine, fludarabine, flutamide, 5-fluorouracil, fluoxymesterone, gemcitabine, hydroxyprogesterone caproate, hydroxyurea, idarubicin, ifosfamide, L-asparaginase, leucovorin, lomustine, mechlorethamine, medroprogesterone acetate, megestrol acetate, melphalan, mercaptopurine, methotrexate, mitoxantrone, mitomycin, mitotane, oxaliplatin, phenyl butyrate, prednisone, procarbazine, paclitaxel, pentostatin, semustine, streptozocin, SN-38, tamoxifen, taxanes, testosterone propionate, thalidomide, thioguanine, teniposide, topotecan, uracil mustard, vinblastine, vinorelbine and vincristine.

15. The method of claim 11 , wherein the toxin is selected from the group consisting of ricin, abrin, ribonuclease, DNase I, Staphylococcal enterotoxin-A, pokeweed antiviral protein, gelonin, diphtheria toxin, Pseudomonas exotoxin and Pseudomonas endotoxin.

16. The method of claim 11 , wherein the immunomodulator is selected from the group consisting of a cytokine, a stem cell growth factor, a lymphotoxin, a tumor necrosis factor (TNF), TNF-α, a hematopoietic factor, an interleukin, IL-1, IL-2, IL-3, IL-6, IL-10, IL-12, IL-18, IL-21, a colony stimulating factor, G-CSF, GM-CSF, interferon-α, -β or -γ, erythropoietin and thrombopoietin.

17. The method of claim 11 , wherein the cytokine is interferon-α, interferon-β, interferon-γ or GM-CSF.

18. The method of claim 11 , wherein the radioisotope is selected from the group consisting of In-111, Lu-177, Bi-212, Bi-213, At-211, Cu-62, Cu-64, Cu-67, Y-90, I-125, I-131, P-3

Assignees

• Immunomedics Inc

Inventors

• Goldenberg David M
• Hansen Hans J
• Qu Zhengxing
• Chang Chien-Hsing

Classifications

• A61P35/02

  specific for leukemia · CPC title

• A61P37/00

  Drugs for immunological or allergic disorders · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• A61P37/06

  Immunosuppressants, e.g. drugs for graft rejection · CPC title

• A61P37/02

  Immunomodulators · CPC title