CD38 modulating antibody
The present disclosure provides antibodies that bind to human CD38. In particular, the antibodies and antigen-binding portions thereof are defined by particular functional characteristics. The antibodies present features compatible for manufacturing and can be provided as fully human antibodies (e.g., fully human monoclonal antibodies or antigen-binding fragments) that can be useful for medical methods and compositions, in particular for treating cancer.
1 . An anti-CD38 antibody or antigen-binding fragment thereof, wherein the antibody or antigen-binding fragment thereof comprises:
a) the amino acid sequence of SEQ ID NO: 33 as heavy chain complementarity determining region 1;
b) the amino acid sequence of SEQ ID NO: 34 as heavy chain complementarity determining region 2;
c) the amino acid sequence of SEQ ID NO: 35 as heavy chain complementarity determining region 3;
d) the amino acid sequence of SEQ ID NO: 37 as light chain complementarity determining region 1;
e) the amino acid sequence of SEQ ID NO: 38 as light chain complementarity determining region 2; and
f) the amino acid sequence of SEQ ID NO: 39 as light chain complementarity determining region 3.
2 . The anti-CD38 antibody or antigen-binding fragment thereof according to claim 1 wherein the antibody or an antigen-binding fragment thereof is selected from the group consisting of:
a) an antibody or antigen binding fragment thereof comprising a variable heavy chain sequence having at least 95% sequence identity to SEQ ID NO: 36 and a variable light chain sequence having at least 95% sequence identity to SEQ ID NO: 40;
b) an antibody or antigen binding fragment thereof comprising a variable heavy chain sequence having at least 95% sequence identity to SEQ ID NO: 56 and a variable light chain sequence having at least 95% sequence identity to SEQ ID NO: 57; and
c) an antibody or antigen binding fragment thereof comprising a variable heavy chain sequence having at least 95% sequence identity to SEQ ID NO: 76 and a variable light chain sequence having at least 95% sequence identity to SEQ ID NO: 77.
3 . The anti-CD38 antibody or antigen-binding fragment thereof according to claim 1 , wherein the antibody or antigen-binding fragment thereof is a monoclonal antibody, a Fab fragment, a F(ab′)2 fragment, a single chain variable fragment (scFv), a scFv-Fc fragment, or a single chain antibody (scAb).
4 . The anti-CD38 antibody or antigen-binding fragment thereof according to claim 1 , wherein the antibody or antigen-binding fragment thereof is a rabbit, mouse, chimeric, humanized or fully human antigen-binding antibody.
5 . The anti-CD38 antibody or antigen-binding fragment thereof according to claim 1 , wherein the antibody is selected from the group consisting of IgG1, IgG2, IgG3, and IgG4 isotype antibodies.
6 . The anti-CD38 antibody or antigen-binding fragment thereof according to claim 1 , wherein the antibody or antigen-binding fragment thereof is comprised in a bispecific antibody, a multispecific antibody, or an immunoconjugate further comprising a therapeutic or diagnostic agent.
7 . The anti-CD38 antibody or antigen-binding fragment thereof according to claim 1 , wherein the antibody or antigen-binding fragment thereof binds the extracellular domain of human CD38.
8 . The antibody or an antigen-binding fragment thereof of according to claim 1 wherein the antibody or antigen-binding fragment thereof is afucosylated.
9 . An affinity matured variant of an antibody or antigen binding fragment thereof of claim 1 .
10 . A nucleic acid molecule encoding the antibody or antigen-binding fragment thereof of claim 1 .
11 . A nucleic acid vector comprising the nucleic acid molecule of claim 10 .
12 . A host cell comprising the nucleic acid vector of claim 11 .
13 . A method of producing an antibody or antigen binding fragment of claim 1 comprising culturing a host cell of claim 12 .
14 . A composition comprising an antibody or antigen-binding fragment thereof according to claim 1 .
15 . The composition of claim 14 that further comprises a pharmaceutically acceptable carrier or excipient.
16 . A method of treating cancer in a subject, comprising administering to the subject an effective amount of the composition of claim 15 .
17 . The method of claim 16 , wherein the antibody is for administration, simultaneously or sequentially in any order, with a second agent to the subject.
18 . The method of claim 16 wherein the subject has a solid tumour.
19 . The method of claim 16 wherein the subject has a haematological cancer.
20 . A method of preparing an anti-CD38 antibody comprising providing an antibody according to claim 1 , and subjecting the antibody to affinity maturation, wherein the anti-CD38 antibody produced has a greater affinity to CD38 than the parental antibody.
21 . A method of preparing a pharmaceutical composition comprising providing an antibody prepared according to a method of claim 20 and co-formulating the antibody with at least one or more pharmaceutically acceptable excipients.