Anti-CD20 glycoantibodies and uses thereof
AssigneeAcademia Sinica
InventorsChi-Huey Wong, Chung-Yi Wu, Ming-Hung Tsai
Life of this patent
Estimating the term…
Abstract
The present disclosure relates to a novel class of anti-CD20 monoclonal antibodies comprising a homogeneous population of anti-CD20 IgG molecules having the same N-glycan on each of Fc. The antibodies of the invention can be produced from anti-CD20 monoclonal antibodies by Fc glycoengineering. Importantly, the antibodies of the invention have improved therapeutic values with increased ADCC activity and increased Fc receptor binding affinity compared to the corresponding monoclonal antibodies that have not been glycoengineered.
Claims9
A method comprising treating or improving treatment of a patient for a cancer selected from the group consisting of B cell lymphomas, NHL, precursor B cell lymphoblastic leukemia/lymphoma and mature B cell neoplasms, B cell chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL), B cell prolymphocytic leukemia, lymphoplasmacytic lymphoma, mantle cell lymphoma (MCL), follicular lymphoma (FL), low-grade, intermediate-grade and high-grade (FL), cutaneous follicle center lymphoma, marginal zone B cell lymphoma, MALT type marginal zone B cell lymphoma, nodal marginal zone B cell lymphoma, splenic type marginal zone B cell lymphoma, hairy cell leukemia, diffuse large B cell lymphoma, Burkitt's lymphoma, plasmacytoma, plasma cell myeloma, post-transplant lymphoproliferative disorder, Waldenstrom's macroglobulinemia, and anaplastic large-cell lymphoma (ALCL), wherein the patient is in need of such treatment, wherein the method comprises increasing antibody-dependent cellular cytotoxicity (ADCC) activity in the patient by administering to the patient an effective amount of a composition comprising an isolated homogeneous population of anti-CD20 IgG molecules, wherein the anti-CD20 IgG molecules have been glycoengineered and have the same N-glycan on each of the Fc region;
- wherein:
- the N-glycan is free of core fucose;
- the N-glycan is
- Sia2(α2-6)Gal2 GlcNAc2Man3GlcNAc2,
- wherein the glycoengineered anti-CD20 IgG molecules have increased ADCC activity compared to the corresponding monoclonal antibodies that have not been glycoengineered;
- and
- wherein the anti-CD20 IgG molecule comprises a heavy chain having the amino acid sequence set forth in SEQ ID NO:
- 1, and a light chain having the amino acid sequence set forth in SEQ ID NO:
- 2 or wherein the anti-CD20 IgG molecule comprises a light chain sequence and a heavy chain sequence of rituximab.
Dependencies are inferred from the claim text.