IP Library Granted Patent US 10,815,306
Granted Patent B2
US 10,815,306 · App. 16/308,113 · Granted Oct 27, 2020

Humanized and chimeric monoclonal antibodies to CD81

Inventors: Shoshana Levy (Stanford, CA); Aurelien Marabelle (Sceaux, FR); Ranjani Rajapaksa (Mountain View, CA); Felipe Vences-Catalan (Stanford, CA); Chiung-Chi Kuo (Stanford, CA); Jie Liu (Palo Alto, CA); Ronald Levy (Stanford, CA)
Assignee: The Board of Trustees of the Leland Stanford Junior University
C07K16/2896A61P35/00A61P35/04A61K2039/505C07K2317/24C07K2317/41C07K2317/52C07K2317/565C07K2317/732C07K2317/734
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Quick Facts
Patent No.
US 10,815,306
App. No.
16/308,113
Granted
Oct 27, 2020
Kind
B2
Abstract

Humanized or chimeric anti-CD81 (cluster of differentiation 81) monoclonal antibodies are provided. The antibodies bind to human CD81, and find use in various therapeutic methods, including without limitation the reduction or prevention of tumor metastasis. Further provided are heavy chain and light chain variable region sequences as well as associated complementarity-determining region (CDR) sequences.

Claims (11)

1. An isolated chimeric or humanized antibody that specifically binds to human CD81, and comprises a variable heavy region with CDR1, CDR2 and CDR3 from SEQ ID NO:1, and a variable light region with CRD1, CDR2 and CDR3 from SEQ ID NO:4.

2. The antibody of claim 1 , wherein the heavy chain variable region comprises the amino acid sequence set forth in SEQ ID NO:1, 2 or 3.

3. The antibody of claim 2 , wherein the variable heavy region further comprises a human Fc.

4. The antibody of claim 3 , wherein the human Fc is an IgG.

5. The antibody of claim 4 , wherein the IgG provides for high ADCC activity.

6. The antibody of claim 3 , wherein the Fc region engineered for enhanced ADCC activity.

7. The antibody of claim 6 , wherein the Fc region comprises glyco-engineered carbohydrate side chains.

8. The antibody of claim 6 , wherein the Fc region comprises amino acid substitutions that enhance binding to FcγRIIIA.

9. The antibody of claim 1 , wherein the light chain variable region comprises the amino acid sequence set forth in SEQ ID NO:4, 5 or 6.

10. The antibody of claim 1 , further comprising amino terminal amino acid residues linked by cleavable linkers.

11. A method of reducing breast cancer or lymphoma metastasis in a human subject in need thereof, the method comprising the step of administering to a subject a therapeutically effective amount of an isolated chimeric or humanized antibody that specifically birds to human CD81, and comprises a variable heavy region with CDR1, CDR2 and CDR3 from SEQ ID NO:1, and a variable light region with CDR1, CDR2 and CDR3 from SEQ ID NO;4.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jun 8, 2022
From: STANFORD UNIVERSITY
To: UNITED STATES GOVERNMENT
Reel/Frame 060392/0641 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 13, 2018
From: LEVY, SHOSHANA; MARABELLE, AURELIEN; RAJAPAKSA, RANJANI; VENCES-CATALAN, FELIPE; KUO, CHIUNG-CHI; LIU, JIE; LEVY, RONALD
To: THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY
Reel/Frame 047770/0414 →
Continuity (2)
Provisional Application 62351054 · Jun 16, 2016
Related Publication 20190177425A1 · Jun 13, 2019