Anti-PD-L1 cancer immunotherapy antibodies
Inventors
Li, Chiang J. • UNNIRAMAN, SHYAM • BADER, HANNAH • JHA, MITHILESH
Assignees
1globe Biomedical Co Ltd Aka Qiangxin Institute Of Technology • 1Globe Biomedical Co Ltd • 1Globe Health Institute LLC
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Abstract
Provided are compositions and methods relating to or derived from anti-PD-L1 antibodies with ADCC and/or CDC activities. More specifically, provided are fully human antibodies that bind PD-L1, PD-L1-binding antibody fragments, derivatives of such antibodies, and PD-L1-binding polypeptides comprising such fragments.
Core Innovation
The invention is directed to an antigen-binding polypeptide that binds to a human PD-L1 epitope. The polypeptide comprises a heavy chain variable domain and a light chain variable domain containing respective PD-L1-specific sequences defined as sequence pairings selected from SEQ ID NO: 18 with SEQ ID NO: 20, SEQ ID NO: 42 with SEQ ID NO: 44, or SEQ ID NO: 34 with SEQ ID NO: 36.
The described subject matter further encompasses antigen-binding polypeptides configured as fully human antibodies and including a human constant region. In these embodiments, the human constant region comprises ADCC and/or CDC activities, linking PD-L1 epitope binding to effector functions. The polypeptides are also provided in antigen-binding formats and sequence embodiments such as fragments and derivatives.
In addition to the antigen-binding polypeptide, the invention provides nucleic acids encoding the polypeptide, including DNA or RNA encoding embodiments, and mammalian expression systems for producing the polypeptide. The document also provides pharmaceutical compositions comprising a pharmaceutically acceptable excipient, carrier or diluent with the antigen-binding polypeptide, and therapeutic treatment and prophylaxis methods for human subjects using these compositions for cancers characterized by detectable PD-L1 expression in tumor cells.
Claims Coverage
The independent claims cover antigen-binding polypeptides that bind to a human PD-L1 epitope, defined by specific heavy-chain/light-chain variable domain sequence pairings, and a method of treating a human subject with cancer using a pharmaceutical composition containing such polypeptides. The inventive features are anchored by three alternative SEQ ID NO pairing sets plus the treatment administration context with those same SEQ ID-based polypeptides.
PD-L1 epitope binding via defined variable-domain sequence pairings
An antigen-binding polypeptide that binds to a human PD-L1 epitope, comprising a heavy chain variable domain and a light chain variable domain having respective PD-L1-specific sequences, wherein the respective PD-L1-specific sequences consist of a sequence pairing selected from the group consisting of SEQ ID NO: 18 and SEQ ID NO: 20, SEQ ID NO: 42 and SEQ ID NO: 44, and SEQ ID NO: 34 and SEQ ID NO: 36.
Treating a human subject with cancer by administering a PD-L1-binding pharmaceutical composition
A method of treating a human subject in need thereof for a cancer therapeutically, comprising administering a therapeutically effective amount of a pharmaceutical composition comprising a pharmaceutically acceptable excipient, carrier or diluent, and an antigen-binding polypeptide that binds to a human PD-L1 epitope, wherein the polypeptide comprises a heavy chain variable domain and a light chain variable domain defined by the same SEQ ID NO pairings.
Overall, the independent-claim scope is centered on PD-L1 epitope-binding antigen-binding polypeptides whose heavy and light chain variable domains are defined by specified SEQ ID NO pairings. A further independent claim covers therapeutic treatment of a human subject with cancer by administering a pharmaceutical composition containing such PD-L1-binding polypeptides.
Stated Advantages
Not explicitly described in patent.
Documented Applications
Treatment and prophylaxis for cancers characterized by detectable PD-L1 expression in tumor cells.
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