IP Library Granted Patent US 10,550,195
Granted Patent B2
US 10,550,195 · App. 15/321,684 · Granted Feb 4, 2020

Tumor selective macropinocytosis-dependent rapidly internalizing antibodies

Inventor: Bin Liu (San Francisco, CA)
Assignee: The Regents of the University of California
C07K16/30A61K45/06A61K49/00C07K16/005C07K16/3069C07K2317/21C07K2317/32C07K2317/73C07K2317/77C40B40/10
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Quick Facts
Patent No.
US 10,550,195
App. No.
15/321,684
Granted
Feb 4, 2020
Kind
B2
Abstract

Methods are provided for identifying and selecting antibodies that are internalized into cells via the macropinocytosis pathway. Additionally antibodies that are internalized via this pathway are provided as well as immunoconjugates comprising such antibodies.

Claims (25)

1. An isolated antibody that is internalized into a cell via a macropinocytosis pathway, wherein:

said antibody comprises VH CDR1, VH CDR2,VH CDR3, VL CDR1, VL CDR2, and VL CDR3 of HCA-F1 (represented by SEQ ID NOs: 2 and 6); or

said antibody comprises VH CDR1, VH CDR2, VH CDR3, VL CDR1, VL CDR2, and VL CDR3 of HCA-F2 (represented by SEQ ID NOs: 3 and 7).

2. The antibody of claim 1 , wherein said antibody comprises VH CDR1, VH CDR2,VH CDR3, VL CDR1, VL CDR2, and VL CDR3 of HCA-F1 (represented by SEQ ID NOs: 2 and 6).

3. The antibody of claim 1 , wherein said antibody comprises VH CDR1, VH CDR2,VH CDR3, VL CDR1, VL CDR2, and VL CDR3 of HCA-F2(represented by SEQ ID NOs: 3 and 7).

4. The antibody of claim 1 , wherein said antibody is an antibody selected from the group consisting of an intact immunoglobulin, a Fab, a (Fab′) 2 , an scFv, and an (ScFv′) 2 .

5. The antibody of claim 1 , wherein said antibody comprises the VH domain (SEQ ID NO:2) and the VL domain of HCA-F1 (SEQ ID NO:6).

6. The antibody of claim 1 , wherein said antibody comprises the VH domain (SEQ ID NO:3) and the VL domain of HCA-F2 (SEQ ID NO:7).

7. An immunoconjugate comprising an antibody of claim 1 attached to an effector wherein said effector is selected from the group consisting of a second antibody, a detectable label, a cytotoxin or cytostatic agent, a liposome containing a drug, a radionuclide, a drug, a prodrug, a viral particle, a cytokine, a chelate, and an siRNA.

8. A pharmaceutical formulation said formulation comprising:

a pharmaceutically acceptable excipient and an composition comprising an antibody of claim 1 .

9. The antibody of claim 4 , wherein said antibody is an intact immunoglobulin.

10. The antibody of claim 9 , wherein said antibody is an IgG or an IgA.

11. The immunoconjugate of claim 7 , wherein said antibody is attached to a moiety selected from the group consisting of an siRNA, a cytotoxic protein, and a cytotoxic and/or cytostatic drug.

12. The immunoconjugate of claim 11 , wherein said antibody is attached directly or through a linker to one or more of the following:

said cytotoxic or cytostatic drug

a lipid or liposome complexed with and/or containing said cytotoxic or cytostatic drug;

a polymeric drug carrier comprising said cytotoxic or cytostatic drug; and

a nanoparticle drug carrier comprising said cytotoxic or cytostatic.

13. The immunoconjugate of claim 12 , wherein said drug is an anti-cancer drug.

14. The immunoconjugate of claim 13 , wherein said drug is selected from the group consisting of a tubulin inhibitor, a DNA interacting agent, and a pathway or enzyme inhibitor.

15. The immunoconjugate of claim 14 , wherein said drug is selected from the group consisting of auristatin, 1,-(2-chloroethyl)-3-cyclohexyl-lnitrosourea, 1,3-bis(2-chloroethyl)-1-nitosourea (BCNU), 5- fluorouracil, 5-trifluoromethyl-2′-deoxyuridine, 6-mercaptopurine, 6-thioguanine (6-TG), abraxane, abraxane, actinomycin D, anastrozole, azathioprine, belotecan, bendamustine, busulfan, camptothecin, camptothecin derivative, capecitabine, capecitabine, carboplatin, carboplatin, carmustine, chlorambucil, chloromethine, cisplatin, cladribine, colchicine, combretastatin, cyclophosphamide, cytosine Arabinoside, dacarbazine (DTIC), daunorubicin citrate, docetaxel, dolastatin, doxorubicin, epirubicin, erlotinib, etoposide, exemestane, flourouracil (5-FU), floxuridine (5-fluoro-2), fludarabine phosphate, fotemustine, gemcitabine, goserelin acetate, hexamethylmelamine, ifosfamide, imatinib mesylate, interferon, irinotecan, ixabepilone, larotaxel, letrozole, lomustine, mannosulfan, megestroltamoxifen, melphalan, methotrexate, methyl (CCNU), mitoxantrone, mTOR/PI3K inhibitor, nedaplatin, neosar, nimustine, ortataxel, oxaliplatin, paclitaxel, pamidronate disodium, pemetrexed, pentostatin, prednimustine, procarbazine HCL, raltitrexed, ranimustine, retinoic acid, a retinoic acid derivative, ribonucleotide reductase inhibitor (RNR), rubitecan, satraplatin, semustine, sorafinib, streptozocin, sunitinib, tamoxifen, taxol, temozolomide, teniposide (VM-26), tesetaxel, thiotepa, thioTEPA, topotecan, topotecan HCL, toremifene, trastuzumab, treosulfan, triaziquone, triethylene melamine, triplatin tetranitrate, trofosfamide, uramustine, vinblastine, vincristine, vindesine sulphate, vinflunine, vinorelbine tartrate, and zoledronic acid.

16. The immunoconjugate of claim 14 , wherein said drug is an auristatin is selected from the group consisting of Auristatin E (AE), Monomethylauristatin E (MMAE), Auristatin F (MMAF), vcMMAE, and vcMMAF.

17. The immunoconjugate of claim 16 , wherein said drug is monomethyl auristatin F.

18. The immunoconjugate of claim 13 , wherein said drug is conjugated to said antibody via a maleimidocaproyl-valine-citrulline-p-aminobenzyloxycarbonyl (MC-cPAB) linker.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 6, 2017
From: LIU, BIN
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 042613/0835 →
CONFIRMATORY LICENSE Recorded Jan 23, 2017
From: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 041061/0673 →
Continuity (2)
Provisional Application 62023689 · Jul 11, 2014
Related Publication 20170137532A1 · May 18, 2017
Cited By (1)
US 12,492,490