Patent Application
20220025040
The present invention relates generally to the field of molecular biology and medicine. More particularly, the invention provides monoclonal antibodies and antigen-binding fragments that bind to CEACAM1 and therapeutic compositions thereof, as well as methods of using such antibodies, including the inhibition of homophilic and heterophilic interactions with CEACAM1, and methods for treating cancer and infectious diseases.
Carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) is a member of the carcinoembryonic antigen (CEA) family of immunoglobulin (Ig) like transmembrane glycoproteins. CEACAM family members are involved in cell-cell recognition and modulate cellular processes that range from the shaping of tissue architecture and neovascularization to the regulation of insulin homeostasis and T cell proliferation.
Various cellular activities have been attributed to the CEACAM1 protein, including roles in the differentiation and arrangement of tissue three-dimensional structure, angiogenesis, apoptosis, tumor suppression, metastasis, and the modulation of innate and adaptive immune responses. Further, several cell types express CEACAM1, including tumor cells, T cells, natural killer (NK) cells, and certain macrophages.
For instance, high CEACAM1 expression occurs in a variety of cancers such as melanoma, colorectal, gastric, pancreatic, bladder, and thyroid cancer and is associated with worse tumor progression, metastasis and poor clinical prognosis. Non-small cell lung cancers (NSCLC), for example, with high CEACAM1 expression exhibit high microvessel density, distant metastases, and shorter median overall survival and progression free survival. CEACAM1 expression has also been strongly correlated with distant metastasis of pancreatic adenocarcinoma. CEACAM1 expression on tumors promotes CEACAM1-mediated inhibition of T and NK cells. Consequently, inhibiting CEACAM1 activity can inhibit tumor cell metastasis and the formation of a cancer stem cell niche.
CEACAM1 is also expressed in certain immune system cells and plays a role in immune suppression and immune cell exhaustion. High CEACAM1 expression on tumor infiltrating lymphocytes (TILs) and other tumor infiltrating immune cells from gastric, lung, melanoma, colorectal cancer and glioma, for example, is associated with a poor prognosis. On T cells, CEACAM1 expression is mostly excluded from resting (naïve) T cells, while the protein is expressed at high levels on activated T cells. CEACAM1-L is the dominant isoform expressed in most T cells and acts as an inhibitory receptor downregulating T cell activation and suppressing T cell functions. As such, inhibition of CEACAM1 on T-cells can recover T cell activity and increase anti-tumor responses.
CEACAM1 is further expressed on NK cells, which are lymphocytes involved in innate immunity, participating in early control of viral infection and immune-surveillance of tumors. When NK cells encounter cells that express major histocompatibility complex (MHC) class I, an immune response against these cells is prevented by inhibitory signals through receptor-ligand interactions. However, when encountering cells in which MHC class I is downregulated, such as in virus-infected cells or cancer cells, NK cells are activated by the lack of inhibitory signals, which makes the “diseased” cells prone to NK cell-mediated killing. When CEACAM1 is present on the surface of both NK and melanoma cells, the CEACAM1:CEACAM1 interactions lead to an inhibition of NK-mediated killing, independent of MHC class I expression. As such, disruption of this homophilic CEACAM1 interaction can be beneficial for restoring the NK-mediated immune response.
CEACAM1 expression on subsets of macrophages is further associated with fibrosis in the tumor microenvironment. CEACAM1 also regulates other stromal cells in the tumor microenvironment such as the vascular endothelium. Therefore, inhibiting interactions of CEACAM1 with its binding partners can further inhibit fibrosis and angiogenesis.
CEACAM1 also mediates intercellular adhesion via the extracellular portion of CEACAM1 containing a IgV-like N-domain, which is involved in homophilic (CEACAM1:CEACAM1) and heterophilic interactions (e.g. with CEA, CEACAM5, CEACAM8, T cell-immunoglobulin and mucin-domain containing 3 (TIM-3) protein, Helicobacter pylori adhesin HopQ, Neisseria gonorrhoeae/meningitidis opacity proteins (OPA), Moraxella sp. Opa-like protein OlpA, Haemophilus influenzae outer membrane protein (OMP) P1, Haemophilus aegyptius OMP P1, Candida albicans, and influenza viruses such as H5N1). TIM-3 was identified as a Th1 specific cell surface protein that is expressed on activated T cells, subsets of dendritic cells and macrophages and NK cells. TIM-3 is an activation-induced inhibitory molecule that has been implicated in tolerance, and shown to induce T cell exhaustion in chronic viral infections and cancer. CEACAM1, which is also expressed on activated T cells, has been shown to interact with TIM-3, and this interaction is important for TIM-3-mediated T cell inhibition.
As indicated above, CEACAM1 also serves as cellular receptor on the apical membrane of mucosal cells for a variety of Gram-negative bacterial pathogens associated with the human mucosa, as well as with fungal pathogens such as Candida albicans. For instance, N. gonorrhoeae, N. meningitidis, Moraxella catarrhalis, H. influenza, H. aegyptius and pathogenic Escherichia coli strains possess well-characterized CEACAM11-binding adhesins. CEACAM1 engagement with bacterial adhesins triggers endocytosis of the bacteria into epithelial cells and transcytosis of microorganisms through intact epithelial layers, thus allowing the microorganisms to exploit CEACAM1 during mucosal colonization. Additionally, CEACAM1 has been implicated in infection with influenza virus H5N1 and with filial nematodes such as Wucheria bancrofti.
Provided herein are antibodies and antigen-binding fragments thereof that bind to CEACAM1 and that block the interaction of CEACAM1 with one or more binding partners. Also provided are therapeutic compositions of such antibodies and antigen-binding fragments thereof, as well as methods of using these antibodies. By blocking the interaction of CEACAM1 with one or more binding partners, the antibodies and antigen-binding fragments thereof are useful for reducing, inhibiting, and/or reversing T cell tolerance and/or for enhancing T cell expansion. The CEACAM1 antibodies and antigen-binding fragments thereof are further useful for treating cancer, for reducing tumor growth, for reducing tumor metastasis, and/or for reducing cancer stemness in a subject in need thereof. The CEACAM1 antibodies and antigen-binding fragments thereof are also useful for treating patients that are resistant to checkpoint therapy. Further provided are methods of using the CEACAM1 antibodies and antigen-binding fragments thereof for reducing colonization of mammalian epithelia with bacteria expressing bacterial adhesins or Candida albicans or for reducing replication of an influenza virus or the release of pro-inflammatory cytokines or chemokines associated with influenza virus infection.
In one aspect, the invention relates to an antibody, or antigen-binding fragment thereof, which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein each of the heavy chain and the light chain variable regions comprises a CDR1, CDR2, and CDR3, and wherein:
In one embodiment, the invention relates to an antibody, or antigen-binding fragment thereof, which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein each of the heavy chain and the light chain variable regions comprises a CDR1, CDR2, and CDR3, and wherein:
In one embodiment, the invention relates to an antibody, or antigen-binding fragment thereof, which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein each of the heavy chain and the light chain variable regions comprises a CDR1, CDR2, and CDR3, and wherein:
In one embodiment, the invention relates to an antibody, or antigen-binding fragment thereof, which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein each of the heavy chain and the light chain variable regions comprises a CDR1, CDR2, and CDR3, and wherein
In one embodiment, the invention relates to an antibody, or antigen-binding fragment thereof, which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein each of the heavy chain and the light chain variable regions comprises a CDR1, CDR2, and CDR3, and wherein
In one aspect, the invention provides an antibody or antigen-binding fragment thereof, which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein the sequence of the heavy chain variable region comprises a sequence that is at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% identical to the heavy chain variable region amino acid sequence of SEQ ID NO:13, and wherein the sequence of the light chain variable region comprises a sequence that is at least 90% identical to a light chain variable region amino acid sequence selected from the group consisting of SEQ ID NO:14, SEQ ID NO:15, and SEQ ID NO: 16.
In one embodiment, the invention provides an antibody or antigen-binding fragment thereof, which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein the sequence of the heavy chain variable region comprises SEQ ID NO:13, and wherein the sequence of the light chain variable region comprises a sequence selected from the group consisting of SEQ ID NO:14, SEQ ID NO:15, and SEQ ID NO:16.
In another embodiment, the invention provides an antibody or antigen-binding fragment thereof which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein the sequence of the heavy chain variable region comprises SEQ ID NO:13, and wherein the sequence of the light chain variable region comprises SEQ ID NO:14.
In another embodiment, the invention provides an antibody or antigen-binding fragment thereof which binds to CEACAM1, wherein the sequence of the heavy chain variable region comprises SEQ ID NO:13, and wherein the sequence of the light chain variable region comprises SEQ ID NO:15.
In one aspect, the invention provides an antibody or antigen-binding fragment thereof which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region; wherein the sequence of the heavy chain variable region comprises a sequence that is at least 85% identical to the heavy chain variable region amino acid sequence of SEQ ID NO:13;
In one aspect, the invention provides an antibody or antigen-binding fragment thereof which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region,
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided by the invention is a chimeric antibody, a CDR-grafted antibody, or a humanized antibody or antigen-binding fragment thereof.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided by the invention is a multispecific or a bispecific antibody or antigen-binding fragment thereof. In one embodiment, the antibody or antigen-binding fragment is a bispecific antibody comprising a complementary region that binds binds to PD-1 or PD-L1.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided by the invention is an scFv, Fv, Fab′, Fab, F(ab′)2, or diabody.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided by the invention has isotype IgG4.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided by the invention contains a S241P substitution in the constant region of the heavy chain.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided by the invention is deglycosylated.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided by the invention is lacking a C-terminal lysine in the heavy chain.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided by the invention is conjugated to one ore more of a cytotoxin, a fluorescent label, and/or an imaging agent.
In another aspect, the invention provides CEACAM1 antibodies and antigen-binding fragments thereof that are characterized by the epitopes on CEACAM1 that they bind to. As described, such antibodies include, but are not limited to, the CEACAM1 antibodies and antigen-binding fragments thereof described by their structural features herein, including CDR motifs, CDR sequences, and heavy and light variable chain sequences. In some embodiments, the invention provides CEACAM1 antibodies and antigen-binding fragments thereof that bind to residues in the IgV-like N-domain of CEACAM1. In another embodiment, the antibodies and antigen-binding fragments thereof provided herein also bind selectively to CEACAM1 over one or more CEACAM family members. In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof does not exhibit significant binding to other CEACAM family members including to CEACAM3, CEACAM5, CEACAM6 and/or CEACAM8. In some embodiments, the invention provides CEACAM1 antibodies and antigen-binding fragments that bind an epitope on the N-domain of CEACAM1 that overlaps or at least partially overlaps with the CEACAM1:CEACAM1 dimer interface, thereby blocking CEACAM1 homophilic interactions. In some embodiments, the invention provides CEACAM1 antibodies and antigen-binding fragments that bind to CEACAM1 residues that are located in the binding site on CEACAM1 for heterologous interaction partners, including but not limited to, other CEACAM family members, TIM family members, bacterial adhesins (such as HopQ, OPA, OMP P1 and/or OlpA), Candida albicans, influenza viruses (such as H5N1) and/or filial nematodes such as Wucheria bancrofti.
In one embodiment, the contemplated CEACAM1 antibody or antigen-binding fragment thereof binds to the same epitope as an antibody or antigen-binding fragment with a heavy chain variable region and a light variable chain region, wherein the sequence of the heavy chain variable region comprises SEQ ID NO:13 and wherein the sequence of the light chain variable region comprises SEQ ID NO:14.
In one aspect, the contemplated CEACAM1 antibody or antigen-binding fragment thereof binds to the IgV-like N-domain of CEACAM1 and binds to an epitope comprising one or more residues selected from the group consisting of residues F29, Y34, D40, G41, N42, T56, Q89, S93, D94, N97, and E99 of SEQ ID NO:17. In one embodiment, the epitope further comprises residue Q44 of SEQ ID NO:17. In one embodiment, the epitope further comprises one or more residues selected from the group consisting of residues S32, Q44, A49, 191, L95, and V96 of SEQ ID NO:17.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof binds to the IgV-like N-domain domain of CEACAM1.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof does not bind to one of more of CEACAM3, CEACAM5, CEACAM6, and CEACAM 8.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof binds at least partially binds to the binding site on CEACAM1 for TIM3.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof at least partially binds to the binding site on CEACAM1 for CEACAM1 during homodimerization.
In one aspect, the invention provides antibodies or antigen-binding fragments thereof which bind to CEACAM and which bind partially or fully to the binding site on CEACAM1 for bacterial adhesins including, but not limited to Helicobacter pylori adhesin HopQ, Neisseria gonorrhoeae Opa, Neisseria meningitidis Opa, Haemophilus influenza OMP P1, Haemophilus aegyptius OMP P1, and/or Moraxella sp. Opa-like protein OlpA. In one aspect, the CEACAM1 antibody or antigen-binding fragments thereof binds to an epitope comprising one or more residues selected from the group consisting of residues F29, Y34, N42, Q89, and N97 of SEQ ID NO:17.
In one aspect, the CEACAM1 antibody or antigen-binding fragment thereof binds to an epitope comprising one or more residues selected from the group consisting of residues Y34, G41, N42, Q44, Q89, S93, D94, V96, and N97 of SEQ ID NO:17. In one embodiment, the the epitope further comprises residues F29, S32, D40, A49, T56, I91, L95, and E99 of SEQ ID NO:17.
In one embodiment, the invention provides for nucleic acid molecules encoding the CEACAM1 antibodies or antigen-binding fragments thereof described herein, as well as vectors comprising such nucleic acid molecules. Also provided are cells comprising a vector encoding the CEACAM1 antibodies or antigen-binding fragments thereof described herein as well as cells expressing the CEACAM1 antibodies or antigen-binding fragments thereof described herein. Provided herein is further a chimeric antigen receptor T-cells comprising the CDRs of any of the antibodies or antigen-binding fragments disclosed herein.
In one embodiment, the invention provides compositions comprising the antibodies or antigen-binding fragments thereof described herein and a pharmaceutically acceptable excipient.
In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for inhibiting binding of CEACAM1 its interaction partners and/or for reducing CEACAM1 activity, the method comprising contacting CEACAM1 with a CEACAM1 antibody or antigen-binding fragment thereof described herein. For instance, embodiments of the inventions are useful for inhibiting the interaction between CEACAM1 and a member of the CEACAM family. In one embodiment, the CEACAM family member is CEACAM3, CEACAM5, CEACAM6, or CEACAM8. In some embodiments, the CEACAM family member is CEACAM1 itself.
In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for inhibiting binding of CEACAM1 to a member of the TIM family, the method comprising contacting CEACAM1 with a CEACAM1 antibody or antigen-binding fragment thereof described herein. In some embodiments, the TIM family member is TIM-3.
In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for inhibiting binding of CEACAM1 to bacterial adhesins, the method comprising contacting CEACAM1 with a CEACAM1 antibody or antigen-binding fragment thereof described herein. In some embodiments, the bacterial adhesin is Helicobacter pylori adhesin HopQ, Neisseria gonorrhoeae Opa, Neisseria meningitidis Opa, Haemophilus influenza OMP P1, Haemophilus aegyptius OMP P1, or Moraxella sp. adhesin OlpA. In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for inhibiting binding of CEACAM1 to Candida albicans, the method comprising contacting CEACAM1 with a CEACAM1 antibody or antigen-binding fragment thereof described herein. In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for inhibiting binding of CEACAM1 to an influenza virus, the method comprising contacting CEACAM1 with a CEACAM1 antibody or antigen-binding fragment thereof described herein. In one embodiment, the influenza virus is H5N1.
In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for reducing colonization of mammalian epithelia with bacteria expressing bacterial adhesins, the method comprising contacting CEACAM1 with a CEACAM1 antibody or antigen-binding fragment thereof described herein. In some embodiments, the bacterial adhesin is Helicobacter pylori adhesin HopQ, Neisseria meningitidis Opa, Haemophilus influenza OMP P1, Haemophilus aegyptius OMP P1, or Moraxella sp. adhesin OlpA.
In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for reducing colonization of mammalian epithelia with Candida albicans, the method comprising contacting CEACAM1 with a CEACAM1 antibody or antigen-binding fragment thereof described herein.
In one embodiment, the invention provides methods of reducing replication of an influenza virus, the method comprising contacting CEACAM1 with a CEACAM1 antibody or antigen-binding fragment thereof described herein. In one embodiment, the invention provides methods of of reducing the release of pro-inflammatory cytokines or chemokines associated with an infection with an influenza virus, the method comprising contacting a cell population comprising epithelial cells with a CEACAM1 antibody or antigen-binding fragment thereof described herein. In some embodiments, the influenza virus is H5N1.
In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for reducing T cell tolerance, and/or for enhancing T cell expansion or activation. These methods are useful for in vitro and in vivo applications.
In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for reducing T cell tolerance and/or enhancing T cell expansion in a subject in need thereof, the method comprising administering to the subject an effective amount of the antibody or antigen-binding fragment thereof. In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for treating cancer in a subject in need thereof, the method comprising administering to the subject an effective amount of the antibody or antigen-binding fragment thereof. In some embodiments, the cancer is glioma, glioblastoma, thymoma, mesothelioma, sarcoma, uterine carcinosarcoma, chromophobe renal cell carcinoma, adenoid cystic carcinoma, acute myeloid leukemia, melanoma, uveal melanoma, papillary renal cell carcinoma, clear cell renal cell carcinoma, chloangiocarcinoma, lung adenocarcinoma, diffuse large B-cell lymphoma, pheochromocytoma and paraganglioma, pancreatic cancer, thyroid cancer, lung cancer, colorectal cancer, squamous cancer, breast cancer, prostate cancer, bladder cancer, gastric cancer, testicular germ cell cancer, ovarian cancer, head and neck cancer, uterine cancer, cervical cancer, or liver cancer. In embodiments, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for reducing tumor growth, reducing tumor metastasis, reducing tumor-associated fibrosis, and/or reducing cancer stemness in a subject in need thereof by administering to the subject an effective amount of the antibody or antigen-binding fragment. In some embodiments, the invention provides methods that further comprise administering a checkpoint inhibitor. In certain embodiments, the checkpoint inhibitor is a CTLA-4, a PD-1, a PD-L1, and a PD-L2 inhibitor. In some embodiments, the invention provides methods that further comprise administering one or more of an inhibitor of LAG3, TIGIT, LAP, Podoplanin, Protein C receptor, ICOS, GITR, CD226 or CD160. In some embodiments, the invention provides methods that further comprise administering a TIM-3 inhibitor. In some embodiments, the inhibitor is administered concurrently or consecutively with the antibody or antigen-binding fragment. In some embodiments, the inhibitor is administered separately or as a mixture with the antibody or antigen-binding fragment.
In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for reducing colonization of a subject's epithelia with bacteria expressing bacterial adhesins in a subject in need thereof, the method comprising administering to the subject an effective amount of the CEACAM1 antibodies or antigen-binding fragments thereof described herein. In some embodiments, the bacterial adhesin is Helicobacter pylori adhesin HopQ, Neisseria meningitidis Opa, Haemophilus influenza OMP P1, Haemophilus aegyptius OMP P1, or Moraxella sp. OlpA.
In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for reducing colonization of a subject's epithelia with Candida albicans in a subject in need thereof, the method comprising administering to the subject an effective amount of the CEACAM1 antibodies or antigen-binding fragments thereof described herein.
In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for reducing replication of an influenza virus in a subject in need thereof, the method comprising administering to the subject an effective amount of the CEACAM1 antibodies or antigen-binding fragments thereof described herein. In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for reducing the release of pro-inflammatory cytokines or chemokines associated with an infection with an influenza virus in a subject in need thereof, the method comprising administering to the subject an effective amount of the CEACAM1 antibodies or antigen-binding fragments thereof described herein. In some embodiments, the influenza virus in H5N1.
In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for treating a subject that does not respond to therapy with a checkpoint inhibitor therapy (primary resistance), as well as patients that initially respond to treatment, but later become resistant to checkpoint inhibitor blockade (secondary or acquired resistance). Such methods for treating comprise administering to said subject the CEACAM1 antibodies or antigen-binding fragments thereof described herein. In some embodiments, the subject has acquired resistance to therapy with one or more of a PD-1 inhibitor, a PD-L1 inhibitor, and a CTLA-4 inhibitor. Resistant cancer may also be referred to as refractory cancer.
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application published with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
Antibodies
The term “antibody” is used in the broadest sense and includes monoclonal antibodies (including full length or intact monoclonal antibodies), polyclonal antibodies, multivalent antibodies, multispecific antibodies (e.g., bispecific antibodies), antibody fragments, and antigen-binding portions thereof (e.g., paratopes, CDRs), so long as they exhibit the desired biological activity and specificity.
As used herein, “antibody variable domain” refers to the portions of the light and heavy chains of antibody molecules that include amino acid sequences of Complementarity Determining Regions (CDRs; i.e., CDR1, CDR2, and CDR3), and Framework Regions (FRs). VH refers to the variable domain of the heavy chain. VL refers to the variable domain of the light chain. The amino acid positions assigned to CDRs and FRs may be defined according to Kabat or according to Chothia. The term “framework regions” (FR) refers to those variable domain residues other than the CDR residues.
As used herein, the term “Complementarity Determining Regions” (CDRs) refers to portions of an antibody variable domain that are (typically) involved in antigen binding. Each variable domain typically has three CDR regions identified as CDR1, CDR2 and CDR3. Each CDR can comprise amino acid residues from a CDR as defined by e.g. Kabat (i.e., about residues 24-34 (L1), 50-56 (L2) and 89-97 (L3) in the light chain variable domain and 31-35 (H1), 50-65 (H2) and 95-102 (H3) in the heavy chain variable domain (Kabat et al., Sequences of Proteins of Immunological Interest, 5th Ed. Public Health Service, National Institutes of Health, Bethesda, Md. (1987, 1991)). Each CDR can also comprise amino acid residues from a “hypervariable loop” (i.e., about residues 26-32 (LI), 50-52 (L2) and 91-96 (L3) in the light chain variable domain and 26-32 (H1), 53-55 (H2) and 96-101 (H3) in the heavy chain variable domain (Chothia & Lesk 196 J. Mol. Biol. 901 (1987)). In some instances, a CDR can include amino acids from both a CDR region defined according to Kabat and a hypervariable loop. The Kabat residue designations do not always correspond directly with the linear numbering of the amino acid residues (primary amino acid sequence). The actual linear amino acid sequence may contain fewer or additional amino acids than in the strict Kabat numbering corresponding to a shortening of, or insertion into, a structural component, whether framework or CDR, of the basic variable domain structure. The correct Kabat numbering of residues may be determined for a given antibody or antigen-binding fragment thereof by alignment of residues of homology in the sequence of the antibody or antigen-binding fragment thereof with a “standard” Kabat numbered sequence. An example of how the Kabat numbering relates to the primary amino acid sequence of an antibody can be seen in
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided herein comprises six CDRs, wherein:
In another embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided herein comprises six CDRs, wherein:
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof comprises six CDRs, wherein:
As shown in the Examples below, affinity maturation of CDR1H, CDR3H and CDR3L of a humanized, aglycosylated CEACAM1 antibody led to variants that conferred substantial improvements in CEACAM1 binding affinity. Inspection of the variants that were obtained and comparison of these variants with the variability introduced into the affinity maturation libraries indicates certain CDR positions at which amino acids remained relatively unchanged and other CDR positions at which variation could be introduced, resulting in improved binding.
In one aspect, the invention provides CEACAM1 antibodies or antigen-binding fragments thereof that comprise a CDR1H, wherein the CDR1H comprises residues 31-35 of the CEACAM1 antibody (Kabat definition, corresponds, e.g., to residues 31 to 35 in the primary amino acid sequence of the heavy variable chain of SEQ ID NO:19, see
Alternatively, CDR1H can be defined using the IMGT definition, wherein CDR1H comprises residues 26-33 of the CEACAM1 antibody (corresponds, e.g., to residues 26 to 33 in the primary amino acid sequence of the heavy variable chain of SEQ ID NO:19, see
In one embodiment, CDR1H (Kabat definition) of the CEACAM1 antibody or antigen-binding fragment thereof comprises sequence SHGMS (SEQ ID NO: 9).
In some embodiments, CDR1H (IMGT definition) comprises sequence GFIFSHG (SEQ ID NO: 21).
In one aspect, the invention provides CEACAM1 antibodies or antigen-binding fragments thereof that comprise a CDR1H region, wherein the CDR1H comprises residues 26-35 of the CEACAM1 antibody (Kabat definition, corresponds, e.g., to residues 26 to 35 in the primary amino acid sequence of the heavy variable chain of SEQ ID NO:19, see
In one embodiment, the CDR1H region comprises sequence GFIFSSHGMS (SEQ ID NO: 23).
In one aspect, the invention provides CEACAM1 antibodies or antigen-binding fragments thereof that comprise a CDR3H, wherein the CDR3H comprises residues 95-102 (Kabat definition, corresponds, e.g., to residues 99 to 110 in the primary amino acid sequence of the heavy variable chain of SEQ ID NO:19, see
In one embodiment, CDR3H comprises residues 95-102 (Kabat definition, corresponds, e.g., to residues 99 to 110 in the primary amino acid sequence of the heavy variable chain of SEQ ID NO:19, see
In one embodiment, CDR3H comprises sequence HDFDYFPYWFAH (SEQ ID NO:10).
In one aspect, the invention provides CEACAM1 antibodies or antigen-binding fragments thereof that comprise a CDR3H region, wherein the CDR3H region comprises residues 94-102 (Kabat definition, corresponds, e.g., to residues 98 to 110 in the primary amino acid sequence of the heavy variable chain of SEQ ID NO:19, see
In one aspect, the CDR3H region comprises sequence RHDFDYFPYWFAH (SEQ ID NO:25).
In one aspect, the invention provides CEACAM1 antibodies or antigen-binding fragments thereof that comprise a CDR3L, wherein the CDR3L comprises residues 89-97 (Kabat definition, corresponds, e.g., to residues 88 to 96 in the primary amino acid sequence of the heavy variable chain of SEQ ID NO:14, see
In one embodiment, CDR3L comprises residues 89-97 (Kabat definition, corresponds, e.g., to residues 88 to 96 in the primary amino acid sequence of the heavy variable chain of SEQ ID NO:14, see
In one embodiment, CDR3L comprises sequence QQWSSNPPT (SEQ ID NO:11) or sequence QQWTSNPPT (SEQ ID NO:12).
In one aspect, the invention relates to an antibody, or antigen-binding fragment thereof, which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein each of the heavy chain and the light chain variable regions comprises a CDR1, CDR2, and CDR3, and wherein:
wherein
In one aspect, the invention relates to an antibody, or antigen-binding fragment thereof, which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein each of the heavy chain and the light chain variable regions comprises a CDR1, CDR2, and CDR3, and wherein:
wherein
In one aspect, the invention relates to an antibody, or antigen-binding fragment thereof, which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein each of the heavy chain and the light chain variable regions comprises a CDR1, CDR2, and CDR3, and wherein:
In one aspect, the invention provides CEACAM1 antibodies or antigen-binding fragments thereof, the CEACAM1 antibodies or antigen-binding fragments thereof comprising a heavy chain variable region and a light chain variable region, wherein the chain variable region comprises a CDR1H, CDR2H, and CDR3H (Kabat definitions), wherein the light chain variable region comprises a CDR1L, CDR2L, and CDR3L (Kabat definitions), and wherein:
the sequence of CDR1H comprises the sequence X1HX2X3S (SEQ ID NO:1), the sequence of CDR2H comprises the sequence TISSGGTYTYYPDSVKG (SEQ ID NO:2),
the sequence of CDR3H comprises the sequence HX4X5DYX6PX7WFAX8(SEQ ID NO:3),
the sequence of CDR1L comprises the sequence RANSAVSYMY (SEQ ID NO:4),
the sequence of CDR2L comprises the sequence LTSNRAT (SEQ ID NO:5), and
the sequence of CDR3L comprises the sequence QQX9X10X11X12PX13T (SEQ ID NO:6).
X1-X18 have been previously defined.
In one embodiment, the invention relates to an antibody, or antigen-binding fragment thereof, which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region, wherein each of the heavy chain and the light chain variable regions comprises a CDR1, CDR2, and CDR3, and wherein:
In one embodiment, the CEACAM1 antibodies or antigen-binding fragments thereof comprise a heavy chain variable region and a light chain variable region, wherein the chain variable region comprises a CDR1H, CDR2H, and CDR3H (Kabat definitions), wherein the light chain variable region comprises a CDR1L, CDR2L, and CDR3L (Kabat definitions), and wherein:
According to certain embodiments, the contemplated antibodies and antigen-binding fragments thereof also feature humanized frameworks for reduced immunogenicity. In certain embodiments, the CDRs of the contemplated antibody or antigen-binding fragment thereof are located in frameworks obtained from a human antibody or antigen-binding fragment thereof. In other embodiments, surface-exposed framework residues of the contemplated antibody or antigen-binding fragment thereof are replaced with framework residues of a human antibody or antigen-binding fragment thereof. The CDRs may also be located in murine or humanized frameworks linked to human constant regions (i.e., chimeric antibodies). In a preferred embodiment, the CDRs of a contemplated antibody or antigen-binding fragment thereof are located in frameworks that are a composite of two or more human antibodies. In such embodiments, the contemplated antibodies or antigen-binding fragments thereof comprise two or more sequence segments (“composites”) derived from V-regions of unrelated human antibodies that are selected to maintain monoclonal antibody sequences important for antigen binding of the starting precursor anti-human CEACAM1 monoclonal antibody, and which have all been filtered for the presence of potential T cell epitopes using “in silico tools” (Holgate & Baker, IDrugs. 2009 April; 12(4):233-7). The close fit of human sequence segments with all sections of the starting antibody V regions and the elimination of CD4+ T cell epitopes prior to synthesis of the antibody or antigen-binding fragment thereof allow this technology to circumvent immunogenicity while maintaining optimal affinity and specificity through the prior analysis of sequences necessary for antigen-specificity (Holgate & Baker, 2009).
Also provided herein variable heavy chain and variable light chain sequences as well as pairing thereof that are similar, but not identical to the variable heavy chain and variable light chains disclosed in SEQ ID NOs:13-16 and pairings thereof.
In some embodiments, the CEACAM1 antibody or antigen-binding fragment thereof comprises a variable heavy chain amino acid sequence comprising SEQ ID NO:13.
In some embodiments, the antibody or antigen-binding fragment thereof comprises a variable light chain amino acid sequence comprising SEQ ID NO:16. In other embodiments, the antibody or antigen-binding fragment thereof comprises a variable light chain amino acid sequence comprising SEQ ID NO:14. In other embodiments, the antibody or antigen-binding fragment thereof comprises a variable light chain amino acid sequence comprising SEQ ID NO: 15.
In some embodiments, the CEACAM1 antibody or antigen-binding fragment thereof comprises a variable heavy chain amino acid sequence comprising SEQ ID NO:13 and a variable light chain amino acid sequence comprising SEQ ID NO:14.
In some embodiments, the CEACAM1 antibody or antigen-binding fragment thereof comprises a variable heavy chain amino acid sequence comprising SEQ ID NO:13 and a variable light chain amino acid sequence comprising SEQ ID NO:15.
In some embodiments, the CEACAM1 antibody or antigen-binding fragment thereof comprises a variable heavy chain amino acid sequence comprising SEQ ID NO:13 and a variable light chain amino acid sequence comprising SEQ ID NO:16.
As used herein, the term “identity” refers to sequence identity between two nucleic acid molecules or polypeptides. Identity can be determined by comparing a position in each sequence which may be aligned for purposes of comparison. For example, when a position in the compared nucleotide sequence is occupied by the same base, then the molecules are identical at that position. A degree identity between nucleic acid or amino acid sequences is a function of the number of identical or matching nucleotides or amino acids at shared positions. For example, polypeptides having at least 85%, 90%, 95%, 98%, or 99% identity to specific polypeptides described herein and preferably exhibiting substantially the same functions, as well as polynucleotides encoding such polypeptides, are contemplated. Methods and computer programs for determining both sequence identity and similarity are publicly available, including, but not limited to, the GCG program package (Devereux et al., Nucleic Acids Research 12: 387, 1984), BLASTP, BLASTN, FASTA (Altschul et al., J. Mol. Biol. 215:403 (1990), and the ALIGN program (version 2.0). The well-known Smith Waterman algorithm may also be used to determine similarity. The BLAST program is publicly available from NCBI and other sources (BLAST Manual, Altschul, et al., NCBI NLM NIH, Bethesda, Md. 20894; BLAST 2.0 at http://www.ncbi.nlm.nih.gov/blast/). In comparing sequences, these methods account for various substitutions, deletions, and other modifications.
In another aspect, the CEACAM1 antibody or antigen-binding fragment thereof comprises
In another aspect, the CEACAM1 antibody or antigen-binding fragment thereof comprises
In another aspect, the CEACAM1 antibody or antigen-binding fragment thereof comprises
In one aspect, the invention provides an antibody or antigen-binding fragment thereof which binds to CEACAM1, wherein the antibody or antigen-binding fragment comprises a heavy chain variable region and a light chain variable region;
In another aspect, the CEACAM1 antibody or antigen-binding fragment thereof comprises
In another aspect, the CEACAM1 antibody or antigen-binding fragment thereof comprises
In another aspect, the CEACAM1 antibody or antigen-binding fragment thereof comprises
In another aspect, the CEACAM1 antibody or antigen-binding fragment thereof comprises
In another aspect, the CEACAM1 antibody or antigen-binding fragment thereof comprises
In another aspect, the CEACAM1 antibody or antigen-binding fragment thereof comprises
It will be evident that any of the frameworks described herein can be utilized in combination with any of the CDRs and CDR motifs described herein. In some embodiments, the CEACAM1 antibody or antigen-binding fragment thereof utilizes a framework described in
Table 1.
In some embodiments of the aspects described herein, amino acid sequence modification(s) of the antibodies or antigen-binding fragments thereof that bind to CEACAM1 described herein are contemplated. Amino acid sequence variants of the antibody or antigen-binding fragment thereof are prepared by introducing appropriate nucleotide changes into the nucleic acid encoding the antibody or antigen-binding fragment thereof, or by peptide synthesis. Such modifications include, for example, deletions from, and/or insertions into and/or substitutions of, residues within the amino acid sequences of the antibody or antigen-binding fragment thereof. Any combination of deletion, insertion, and substitution is made to arrive at the final construct, provided that the final construct possesses the desired characteristics, e.g., binding specificity, inhibition of biological activity.
One type of variant is a conservative amino acid substitution variant. These variants have at least one amino acid residue in the antibody or antigen-binding fragment thereof replaced by a different residue that has similar side chain properties. Amino acids can be grouped according to similarities in the properties of their side chains (see Lehninger, BIOCHEMISTRY (2nd ed., Worth Publishers, New York, 1975):
(1) non-polar: Ala (A), Val (V), Leu (L), Ile (I), Pro (P), Phe (F), Trp (W), Met (M);
(2) uncharged polar: Gly (G), Ser (S), Thr (T), Cys (C), Tyr (Y), Asn (N), Gln (Q);
(3) acidic: Asp (D), Glu (E);
(4) basic: Lys (K), Arg (R), His (H).
As such, a non-limiting example for a conservative amino acid substitution is one that replaces a non-polar amino acid with another non-polar amino acid.
Alternatively, naturally occurring residues can be divided into groups based on common side-chain properties:
(1) hydrophobic: Ala (A), Val (V), Leu (L), Ile (I), Met (M);
(2) neutral hydrophilic: Ser (S), Thr (T), Cys (C), Asn (N), Gln (Q);
(3) acidic: Asp (D), Glu (E);
(4) basic: Lys (K), Arg (R), His (H);
(5) residues that influence chain orientation: Gly (G), Pro (P);
(6) aromatic: Phe (F), Trp (W), Tyr (Y).
As such, a non-limiting example for a conservative amino acid substitution is one that replaces a hydrophobic amino acid with another hydrophobic amino acid.
Further contemplated are amino acid sequence insertions, which can include amino- and/or carboxyl-terminal fusions ranging in length from one residue to polypeptides containing a hundred or more residues, as well as intrasequence insertions of single or multiple amino acid residues. Examples of terminal insertions include an antibody or antigen-binding fragment thereof with an N-terminal methionyl residue or the antibody or antigen-binding fragment thereof fused to a cytotoxic polypeptide. Other insertional variants of the antibody or antigen-binding fragment thereof include the fusion to the N- or C-terminus of the antibody or antigen-binding fragment thereof to an enzyme or a polypeptide which increases the serum half-life of the antibody or antigen-binding fragment thereof, such as, for example, biotin.
Any cysteine residue not involved in maintaining the proper conformation of the antibodies or antigen-binding fragments thereof that bind to CEACAM1 also can be substituted, for example with a serine or an alanine, to improve the oxidative stability of the molecule and prevent aberrant crosslinking.
Conversely, cysteine bond(s) can be added to the antibody or antigen-binding fragment thereof to improve its stability (particularly where the antibody or antigen-binding fragment thereof is an antibody fragment such as an Fv fragment).
In some embodiments, the antibodies or antigen-binding fragments thereof describes have amino acid alterations that alter the original glycosylation pattern of the antibody or antigen-binding fragment thereof. By “altering the original glycosylation pattern” is meant deleting one or more carbohydrate moieties found in the antibody or antigen-binding fragment thereof, and/or adding one or more glycosylation sites that are not present in the antibody or antigen-binding fragment thereof. Glycosylation of antibodies is typically either N-linked or O-linked. N-linked refers to the attachment of the carbohydrate moiety to the side chain of an asparagine residue. The tripeptide sequences asparagine-X-serine and asparagine-X-threonine, wherein X is any amino acid except proline, are the recognition sequences for enzymatic attachment of the carbohydrate moiety to the asparagine side chain. Thus, the presence of either of these tripeptide sequences in a polypeptide creates a potential glycosylation site. O-linked glycosylation refers to the attachment of one of the sugars N-aceylgalactosamine, galactose, or xylose to a hydroxyamino acid, most commonly serine or threonine, although 5-hydroxyproline or 5-hydroxylysine can also be used. Addition of glycosylation sites to the antibodies or antigen-binding fragments thereof that bind to CEACAM1 is accomplished by altering the amino acid sequence such that it contains one or more of the above-described tripeptide sequences (for N-linked glycosylation sites). The alteration can also be made by the addition of, or substitution by, one or more serine or threonine residues to the sequence of the original antibody or antigen-binding fragment thereof (for O-linked glycosylation sites).
In some embodiments, the CEACAM1 antibodies or antigen-binding fragments thereof provided herein are deglycosylated or aglycosylated. In some embodiments, the contemplated CEACAM1 antibody or antigen-binding fragment thereof lacks a C-terminal lysine in the heavy chain and/or contains a S241P substitution in the constant region of the heavy chain. In some embodiments, the CEACAM1 antibody or antigen-binding fragment thereof lacks a glycosylation site in the CDR1 of the variable light chain. In some embodiments, the CEACAM1 antibody or antigen-binding fragment thereof lacks an N-X-S/T consensus sequence in the CDR1 of the variable light chain. In some embodiments, the CEACAM1 antibody or antigen-binding fragment thereof has a mutation in CDR residues 26 and/or 29 (Kabat numbering) of the CDR1 of the variable light chain. Where the antibody or antigen-binding fragment thereof comprises an Fc region, the carbohydrate(s) attached thereto can be altered. For example, antibodies with a mature carbohydrate structure that lacks fucose attached to an Fc region of the antibody or antigen-binding fragment thereof are described. See, e.g., U.S. Patent Pubs. No. 2003/0157108; No. 2004/0093621. Antibodies with a bisecting N-acetylglucosamine (GlcNAc) in the carbohydrate attached to an Fc region of the antibody or antigen-binding fragment thereof are referenced in WO 03/011878; U.S. Pat. No. 6,602,684. Antibodies with at least one galactose residue in the oligosaccharide attached to an Fc region of the antibody or antigen-binding fragment thereof are reported in WO 97/30087. See also WO 98/58964; WO 99/22764 concerning antibodies with altered carbohydrate attached to the Fc region thereof.
In some embodiments, it can be desirable to modify the antibodies or antigen-binding fragment thereof that bind to CEACAM1 described herein with respect to effector function, e.g., so as to enhance antigen-dependent cell-mediated cyotoxicity (ADCC) and/or complement dependent cytotoxicity (CDC) of the antibody or antigen-binding fragment thereof. This can be achieved by introducing one or more amino acid substitutions in an Fc region of the antibody or antigen-binding fragment thereof. Alternatively or additionally, one or more cysteine residues can be introduced in the Fc region, thereby allowing interchain disulfide bond formation in this region. The homodimeric antibody or antigen-binding fragment thereof thus generated can have improved internalization capability and/or increased complement-mediated cell killing and antibody-dependent cellular cytotoxicity (ADCC). See Caron et al., 176 J. Exp. Med. 1191 (1992); Shopes, 148 J. Immunol. 2918 (1992). Homodimeric antibodies with enhanced anti-tumor activity can also be prepared using heterobifunctional cross-linkers as described in Wolff et al., 53 Cancer Res. 2560 (1993). Alternatively, an antibody or antigen-binding fragment thereof can be engineered which has dual Fc regions and can thereby have enhanced complement lysis and ADCC capabilities. See Stevenson et al., 3 Anti-Cancer Drug Design 219 (1989).
For example, WO 00/42072 describes antibodies with improved ADCC function in the presence of human effector cells, where the antibodies comprise amino acid substitutions in the Fc region thereof. Preferably, the antibody or antigen-binding fragment thereof with improved ADCC comprises substitutions at positions 298, 333, and/or 334 of the Fc region (Eu numbering of residues). Typically, the altered Fc region is a human IgG1 Fc region comprising or consisting of substitutions at one, two or three of these positions. Such substitutions are optionally combined with substitution(s) which increase C1q binding and/or CDC. Substitutions include an Asn297Ala mutation in IgG1 Fc.
Antibodies with altered C1q binding and/or complement dependent cytotoxicity (CDC) are described in WO 99/51642, U.S. Pat. Nos. 6,194,551, 6,242,195, 6,528,624, and 6,538,124. The antibodies comprise an amino acid substitution at one or more of amino acid positions 270, 322, 326, 327, 329, 313, 333 and/or 334 of the Fc region thereof (Eu numbering of residues).
Antibodies with improved binding to the neonatal Fc receptor (FcRn), and increased half-lives, are described in WO 00/42072 and U.S. Patent Pub. No. 2005/0014934. These antibodies comprise an Fc region with one or more substitutions therein which improve binding of the Fc region to CEACAM1. For example, the Fc region can have substitutions at one or more of positions 238, 250, 256, 265, 272, 286, 303, 305, 307, 311, 312, 314, 317, 340, 356, 360, 362, 376, 378, 380, 382, 413, 424, 428 or 434 (Eu numbering of residues). The preferred Fc region-comprising an antibody variant with improved CEACAM1 binding comprises amino acid substitutions at one, two or three of positions 307, 380 and 434 of the Fc region thereof (Eu numbering of residues). In one embodiment, the antibody or antigen-binding fragment thereof has 307/434 mutations. Engineered antibodies that bind to CEACAM1 with three or more (e.g., four) functional antigen binding sites are also contemplated. See, e.g., U.S. Patent Pub. No. US 2002/0004587.
Antibody Fragments and Types
In some embodiments of the aspects described herein, the CEACAM1 antibody fragment is a Fab fragment, which comprises or consist essentially a variable (VL) and constant (CL) domain of the light chain and a variable domain (VH) and the first constant domain (CH1) of the heavy chain.
In some embodiments of the aspects described herein, the CEACAM1 antibody fragment is a Fab′ fragment, which refers to a Fab fragment having one or more cysteine residues at the C-terminus of the CH1 domain.
In some embodiments of the aspects described herein, the CEACAM1 antibody fragment is an Fd fragment comprising or consisting essentially of VH and CH1 domains.
In some embodiments of the aspects described herein, the CEACAM1 antibody portion is an Fd′ fragment comprising VH and CH1 domains and one or more cysteine residues at the C-terminus of the CH1 domain.
Single-chain Fv or scFv antibody fragments comprise or consist essentially of the VH and VL domains of antibody, such that these domains are present in a single polypeptide chain. Generally, an Fv polypeptide further comprises a polypeptide linker between the VH and VL domains, which allows the scFv to form the desired structure for antigen binding. See, for example, Pluckthun, 113 Pharmacology Monoclonal Antibodies 269 (Rosenburg & Moore, eds., Springer-Verlag, New York, 1994). Accordingly, in some embodiments of the aspects described herein, the CEACAM1 antibody fragment is a Fv fragment comprising or consisting essentially of the VL and VH domains of a single arm of an antibody.
In some embodiments of the aspects described herein, the CEACAM1 antibody portion is a diabody comprising two antigen binding sites, comprising a heavy chain variable domain (VH) connected to a light chain variable domain (VL) in the same polypeptide chain.
In some embodiments of the aspects described herein, the CEACAM1 antibody portion is a dAb fragment comprising or consisting essentially of a VH domain.
In some embodiments of the aspects described herein, the CEACAM1 antibody portion is a F(ab′)2 fragment, which comprises a bivalent fragment comprising two Fab′ fragments linked by a disulfide bridge at the hinge region.
Linear antibodies refers to the antibodies as described in Zapata et al., Protein Engin., 8(10):1057-1062 (1995). Briefly, these antibodies comprise a pair of tandem Fd segments (VH-CH1-VH-CH1), which, together with complementary light chain polypeptides, form a pair of antigen binding regions. Linear antibodies can be bispecific or monospecific. In some embodiments of the aspects described herein, the CEACAM1 antibody fragment is a linear antibody comprising a pair of tandem Fd segments (VH-CH1-VH-CH1) which, together with complementary light chain polypeptides, form a pair of antigen binding regions.
Various techniques have been developed and are available for the production of antibody fragments. Traditionally, these fragments were derived via proteolytic digestion of intact antibodies. See, e.g., Morimoto et al., 24 J. Biochem. Biophys. Meths. 107 (1992); Brennan et al., 229 Science 81 (1985). However, these fragments can now be produced directly by recombinant host cells. For example, antibody fragments can be isolated from the antibody phage libraries discussed herein. Alternatively, Fab′-SH fragments can be directly recovered from E. coli and chemically coupled to form F(ab′)2 fragments (Carter et al., 1992). According to another approach, F(ab′)2 fragments can be isolated directly from recombinant host cell culture. Other techniques for the production of antibody fragments will be apparent to the skilled practitioner. In other embodiments, the antibody fragment of choice is a single chain Fv fragment (scFv). See, for example, WO 93/16185.
In one embodiment, the antibody is a bispecific antibody comprising a complementary region that binds to CEACAM1 and a complementary region that binds to PD-1.
In one embodiment, the antibody is a bispecific antibody comprising a complementary region that binds to CEACAM1 and a complementary region that binds to PD-L1.
Contemplated antibodies or antigen-binding fragments may have all types of constant regions, including IgM, IgG, IgD, and IgE, and any isotype, including IgG1, IgG2, IgG3, and IgG4. In one embodiment, the human isotype IgG1 is used. In another embodiment, the human isotype IgG4 is used. Light chain constant regions can be λ or κ. The antibody or antigen-binding fragment thereof may comprise sequences from more than one class or isotype.
Also disclosed herein are chimeric antigen receptor T-cells (CAR T-cells) that bind to CEACAM In one embodiment, one or more of the CDRs of an anti-CEACAM antibody disclosed herein are grafted onto a chimeric antigen receptor (CAR) on a T-cell Such a genetically modified T-cell utilizes the CAR, also known as a chimeric T cell receptor, to target antigens expressed on tumor cells in a human leukocyte antigen-independent manner.
Antibody Binding
The human CEACAM1 gene produces 11 isoforms by alternative splicing. Each isoform has one variable (V)-like Ig domain at the amino (N) end of the protein. With the exception of CEACAM1-1L and CEACAM1-1S isoforms, the various isoforms also have 2 or 3 constant C2-like Ig domains. Eight CEACAM1 isoforms are anchored to the cellular membrane via a transmembrane domain and three CEACAM1 isoforms (CEACAM1-4C1, -3 and -3C2) lack the transmembrane domain and are secreted. Two isoforms (CEACAM1-3AL and -3AS) have an Alu family repeat sequence (A) between the constant C2-like Ig domains and the transmembrane domain. The transmembrane CEACAM1 isoforms also possess a long (L) or short (S) cytoplasmic domain determined by inclusion or exclusion of CEACAM1 exon 7 in the message. The CEACAM1 L cytoplasmic domain has two ITIM motifs, which are unique to CEACAM1 among the CEACAM family members. In one aspect, the invention provides CEACAM1 antibodies or antigen-binding fragments thereof, including the antibodies described herein by their structural characteristics, that bind to the extracellular, variable (V)-like Ig domain at the amino (N) end of the protein (N-domain) of CEACAM1, a domain that is common to all isoforms of CEACAM1, including CEACAM1 isoforms 1L, 1S, 3L, 3S, 4L, 4S, 3A1, 3AS, 3, 4C1, and 4C2. In some embodiments, the provided antibodies and antigen-binding fragments thereof bind to human CEACAM1. In some embodiments, the provided antibodies and antigen-binding fragments thereof bind to mammalian CEACAM1. The sequence of the full-length form of CEACAM1 (NCBI Reference Sequence NP_001703.2; UNIPROT ID P13688) is provided as SEQ ID NO:26 (signal sequence: residues 1-34 of SEQ ID NO:26; Ig-V N domain: residues 35-142 of SEQ ID NO:26. The mature form of CEACAM1 (without signal sequence) is provided as SEQ ID NO:17.
As used herein, “binding” of an antibody or antigen binding fragment thereof to CEACAM1, an epitope on CEACAM1, or, in certain embodiments described below, particular residues on CEACAM1, includes the selective interaction of the antibody or antigen binding fragment thereof with CEACAM1. Binding therefore includes, e.g., primary and secondary interactions including hydrogen bonds, ionic interactions, salt bridges, as well as hydrophilic and hydrophobic interactions.
In certain embodiments, the CEACAM1 antibodies or antigen-binding fragments thereof described herein bind to CEACAM1 with a KD of 10−5 to 10−12 mol/l, 10−6 to 10−12 mol/l, 10−7 to 10−12 mol/l, 10−8 to 10−12 mol/l, 10−9 to 10−12 mol/l, 10−10 to 10−12 mol/l, or 10−11 to 10−12 mol/l. In other embodiments, the CEACAM1 antibodies or antigen-binding fragments thereof described herein bind to CEACAM1 with a KD of 10−5 to 10−11 mol/l, 10−6 to 10−11 mol/l, 10−7 to 10−11 mol/l, 10−8 to 10−11 mol/l, 10−9 to 10−11 mol/l, or 10−10 to 10−11 mol/l. In other embodiments, the CEACAM1 antibodies or antigen-binding fragments thereof described herein bind to CEACAM1 with a KD of 10−5 to 10−10 mol/l, 10−6 to 10−10 mol/l, 10−9 to 10−10 mol/l, 10−8 to 10−10 mol/l, or 10−9 to 10−10 mol/l. In other embodiments, the CEACAM1 antibodies or antigen-binding fragments thereof described herein bind to CEACAM1 with a KD of 10−5 to 10−8 mol/l, 10−6 to 10−8 mol/l, or 10−7 to 10−8 mol/l.
The term “specificity” herein refers to the ability of an antibody or antigen-binding fragment thereof, such as an anti-CEACAM1 antibody or antigen-binding fragment thereof, to recognize an epitope within CEACAM1, while only having little or no detectable reactivity with other portions of CEACAM1. Specificity can be relatively determined by competition assays or by epitope identification/characterization techniques described herein or their equivalents known in the art.
As used herein, an “epitope” can be formed both from contiguous amino acids, or noncontiguous amino acids juxtaposed by tertiary folding of a protein. Epitopes formed from contiguous amino acids are typically retained on exposure to denaturing solvents, whereas epitopes formed by tertiary folding are typically lost on treatment with denaturing solvents. An epitope typically includes at least 3, and more usually, at least 5, about 9, or about 8-10 amino acids in a particular spatial conformation. An “epitope” includes the unit of structure conventionally bound by an immunoglobulin VH/VLpair. Epitopes define the minimum binding site for an antibody or antigen-binding fragment thereof, and thus represent the target of specificity of an antibody or antigen-binding fragment thereof. In the case of a single domain antibody, an epitope represents the unit of structure bound by a variable domain in isolation.
In a particular embodiment, the contemplated antibody or antigen-binding fragment specifically binds to the same epitope as antibody CP08H03/Vk8 S29A. In another embodiment, the contemplated antibody or antigen-binding fragment binds to the same epitope as CP08H03/CP08F05.
In one aspect, the invention provides antibodies and antigen-binding fragments thereof, including the antibodies described herein by their structural characteristics, wherein the antibodies and antigen-binding fragments thereof specifically bind to at least part of the homophilic binding domain on CEACAM1 (i.e. in portion of the CEACAM1 protein that is involved in formation of a CEACAM1:CEACAM1 homodimer), thereby blocking CEACAM1 homophilic interactions. In certain embodiments, the provided antibody or antigen-binding fragment thereof specifically binds to one or more of CEACAM1 residues that are contained in the CC′ and FG loops of CEACAM1 and that include a YQQN pocket at the CEACAM1:CEACAM1 dimer interface (i.e., Y34, Q44, Q89, N97 of SEQ ID NO:17), see Huang et al., Nature. 2015 Jan. 15; 517(7534):386-90.
As used herein, a “blocking” antibody or an antibody “antagonist” is one that inhibits or reduces biological activity of the antigen to which it binds. For example, in some embodiments, a CEACAM1 antagonist antibody or antigen-binding fragment thereof binds CEACAM1 and inhibits activity of CEACAM1 and/or binding of CEACAM1 to heterologous binding partners such as other CEACAM proteins or TIM-3. Inhibition of activity and inhibition of binding includes partial inhibition. Methods for the identification of CEACAM1 antibodies that block CEACAM1 homophilic and heterophilic interactions are described herein and are known to the ones skilled in the art. For instance, competing, cross-blocking, and cross-blocked antibodies can be identified using any suitable method known in the art, including competition ELISAs or BIACORE® assays where binding of the competing or cross-blocking antibody to human CEACAM1 prevents the binding of an antibody disclosed herein or vice versa.
In one embodiment, the heavy chain of the contemplated antibody or antigen-binding fragment thereof specifically binds to CEACAM1 at residues F29, Y34, T56, Q89, S93, and/or D94 of SEQ ID NO:17. In another embodiment, the heavy chain of the contemplated antibody or antigen-binding fragment thereof further specifically binds to CEACAM1 at residues S32, Q44, A49, and/or 191 of SEQ ID NO:17.
In one embodiment, the light chain of the contemplated antibody or antigen-binding fragment thereof specifically binds to CEACAM1 at residues D40, G41, N42, N97, and/or E99 of SEQ ID NO:17. In another embodiment, the light chain of the contemplated antibody or antigen-binding fragment thereof further specifically binds to CEACAM1 at residues L95, and/or V96 of SEQ ID NO:17.
In another embodiment, the CEACAM1 antibody or antigen-binding fragment thereof specifically binds to CEACAM1 at residues F29, Y34, D40, G41, N42, T56, Q89, S93, D94, N97, and/or E99 of SEQ ID NO:17. In another preferred embodiment, the CEACAM1 antibody or antigen-binding fragment thereof further specifically binds to CEACAM1 at residues S32, Q44, A49, 191, L95, and/or V96 of SEQ ID NO:17.
In another embodiment, the CEACAM1 antibody or antigen-binding fragment thereof specifically binds to CEACAM1 at residues F29, Y34, D40, G41, N42, T56, Q89, S93, D94, N97, and E99 of SEQ ID NO:17.
In another embodiment, the CEACAM1 antibody or antigen-binding fragment specifically binds to CEACAM1 at residues F29, 532, Y34, D40, G41, N42, Q44, A49, T56, Q89, I91, S93, D94, L95, V96, N97, and E99 of SEQ ID NO:17.
In certain embodiments, not all CDRs are directly involved in binding to the antigen. In one embodiment, four out of six CDRs of the CEACAM1 antibody or antigen-binding fragment thereof make contact with the antigen. In one embodiment, five out of six CDRs of the CEACAM1 antibody or antigen-binding fragment thereof make contact with the antigen. In one embodiment, six out of six CDRs of the CEACAM1 antibody or antigen-binding fragment thereof make contact with the antigen. In one embodiment, CDR2H, CDR3H, CDR1L, CDR2L, and CDR3L of the CEACAM1 antibody or antigen-binding fragment thereof are directly involved in binding to the antigen.
In one embodiment, the antibodies and antigen-binding fragments thereof provided herein specifically bind to an epitope of CEACAM1 located on the N-domain of CEACAM1. In one embodiment, the antibody or antigen-binding fragment thereof specifically binds a CEACAM1 epitope comprising one or more CEACAM1 residues selected from F29, S32, D40, A49, and T56 of SEQ ID NO:17. In a further embodiment, the CEACAM1 antibody specifically binds a CEACAM1 epitope comprising residues F29, S32, D40, A49, T56, and 191 of SEQ ID NO:17.
In one embodiment, the antibodies and antigen-binding fragments thereof provided herein specifically bind to an epitope of CEACAM1 located on the N-domain of CEACAM1. In one embodiment, the antibody or antigen-binding fragment thereof specifically binds a CEACAM1 epitope comprising one or more CEACAM1 residues selected from S32, D40, A49, and 191 of SEQ ID NO:17. In a further embodiment, the CEACAM1 antibody specifically binds a CEACAM1 epitope comprising residues S32, D40, A49, and 191 of SEQ ID NO:17.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided herein binds to CEACAM1, wherein
CDR2H residue Y57 binds to CEACAM1 at residue F29,
CDR2H residue Y59 binds to CEACAM1 at residue S93,
CDR3H residue D102 binds to CEACAM1 at residue T56,
CDR3H residue Y103 binds to CEACAM1 at residues Y34 and/or Q89,
CDR3H residue F104 binds to CEACAM1 at residue F29,
CDR3H residue Y106 binds to CEACAM1 at residue D94,
CDR1L residue S30 binds to CEACAM1 at residue E99,
CDR1L residue Y31 binds to CEACAM1 at residue N97,
CDR2L residue S51 binds to CEACAM1 at residue D40, and/or
CDR2L residue N52 binds to CEACAM1 at residues G41 and/or N42.
Numbering of CDR residues is based on the primary amino acid sequence of the antibody, see
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided herein binds to CEACAM1, wherein
CDR2H residue Y57 binds to CEACAM1 at residue F29,
CDR2H residue Y59 binds to CEACAM1 at residue S93,
CDR3H residue D102 binds to CEACAM1 at residue T56,
CDR3H residue Y103 binds to CEACAM1 at residues S32, Y34, Q44, and/or Q89,
CDR3H residue F104 binds to CEACAM1 at residues F29 and/or A49,
CDR3H residue P105 binds to CEACAM1 at residue 191,
CDR3H residue Y106 binds to CEACAM1 at residue D94,
CDR1L residue S30 binds to CEACAM1 at residue E99,
CDR1L residue Y31 binds to CEACAM1 at residue N97,
CDR2L residue S51 binds to CEACAM1 at residue D40,
CDR2L residue N52 binds to CEACAM1 at residues G41 and/or N42,
CDR3L residue S91 binds to CEACAM1 at residue L95, and/or
CDR3L residue S92 binds to CEACAM1 at residue V96.
Numbering of residues is based on the primary amino acid sequence of the antibody, see
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof provided herein binds to CEACAM1, wherein
CDR2H residue Y57 binds to CEACAM1 at residue F29,
CDR2H residue Y59 binds to CEACAM1 at residue S93,
CDR3H residue D102 binds to CEACAM1 at residue T56,
CDR3H residue Y103 binds to CEACAM1 at residues S32, Y34, Q44, and Q89,
CDR3H residue F104 binds to CEACAM1 at residues F29 and A49,
CDR3H residue P105 binds to CEACAM1 at residue 191,
CDR3H residue Y106 binds to CEACAM1 at residue D94,
CDR1L residue S30 binds to CEACAM1 at residue E99,
CDR1L residue Y31 binds to CEACAM1 at residue N97,
CDR2L residue S51 binds to CEACAM1 at residue D40,
CDR2L residue N52 binds to CEACAM1 at residues G41 and N42,
CDR3L residue S91 binds to CEACAM1 at residue L95, and
CDR3L residue S92 binds to CEACAM1 at residue V96.
Numbering of residues is based on the primary amino acid sequence of the antibody, see
CEACAM family members are expressed widely expressed on a variety of cell types (especially leukocytes), affecting a magnitude of cellular functions. For instance, CEACAM1 is expressed on epithelial cells, endothelial cells, lymphocytes, and myeloid cells, CEACAM3 is expressed on granulocytes and neutrophils, CEACAM5 expressed on epithelial cells, and CEACAM6 is expressed on epithelial cells and granulocytes. However, the N-domain of CEACAM1 is about 90% similar to the N-domains of CEACAM family members 3, 5, and 6, making it difficult to target CEACAM1 selectively.
Despite the high similarity of N-domains among CEACAM family members, in some embodiments, antibodies or antigen-binding fragments thereof provided herein, including the antibodies described herein by their structural characteristics, are selective for CEACAM1. By selectively targeting CEACAM1, embodiments of the invention may avoid undesired interfering e.g. with the broad activating function of CEACAM3.
The terms “selective” and “selectivity” herein refer to the preferential binding of an antibody or antigen-binding fragment thereof (i.e., a CEACAM1 antibody or antigen-binding fragment thereof), for a particular region, target, or peptide; typically a region or epitope in CEACAM1, as opposed to one or more other biological molecules, including other CEACAM family members.
In some embodiments, the contemplated CEACAM1 antibody or antigen-binding fragment thereof does not exhibit significant binding to CEACAM3, CEACAM5, CEACAM6 and/or CEACAM8. In some embodiments, the contemplated CEACAM1 antibody or antigen-binding fragment thereof does not exhibit detectable binding to CEACAM3, CEACAM5, CEACAM6 and/or CEACAM8. In some embodiments, the contemplated CEACAM1 antibody or antigen-binding fragment thereof binds CEACAM1 with an affinity that is at least 10 times, such as at least 100 times, and at least 1000 times, and up to 10,000 times or more stronger than the affinity with which the contemplated CEACAM1 antibody or antigen-binding fragment thereof binds to another target or polypeptide.
As used herein, “affinity”, represented by the equilibrium constant for the dissociation (KD) of an antigen with an antigen-binding protein, is a measure of the binding strength between an antigenic determinant and an antigen-binding site on the antigen-binding protein, such as an antibody or antibody fragment thereof. The smaller the value of the KD, the stronger the binding strength between an antigenic determinant and the antigen-binding molecule. Alternatively, the affinity can also be expressed as the affinity constant (KA), which is 1/KD). As will be clear to the skilled person, affinity can be determined in a manner known per se, depending on the specific antigen of interest.
In one aspect, the invention provides antibodies and antigen-binding fragments thereof, including the antibodies described herein by their structural characteristics, wherein the antibodies and antigen-binding fragments thereof specifically bind to at least part of the binding site on CEACAM1 for one or more other members of the CEACAM family, thereby blocking CEACAM1 interactions with the one or more other members of the CEACAM family. These CEACAM family members include, but are not limited to, CEACAM3, CEACAM5, CEACAM6, and CEACAM8 (Ramani et al, Anal. Biochem. Jan. 15, 2012; 420(2); 127-38; Scheffrahn et al, J. Immunol. May 15, 2002; 168(10); 5139-46).
In one aspect, the invention provides antibodies and antigen-binding fragments thereof, including the antibodies described herein by their structural characteristics, wherein the antibodies and antigen-binding fragments thereof specifically bind to at least part of the binding site on CEACAM1 for a member of the TIM family, thereby blocking CEACAM1 interaction with the TIM family member. In some embodiments, this TIM family member is TIM-1, TIM-3, or TIM-4. In some embodiments, the CEACAM1 antibody or antigen-binding fragment thereof specifically binds to one or more of CEACAM1 residues Y34, G41, N42, Q44, Q89, S93, D94, V96, and/or N97 of SEQ ID NO:17, residues which have been indicated to be involved in CEACAM1 binding to TIM-3 (Huang et al., Nature. 2015 Jan. 15; 517(7534):386-90).
In one aspect, the invention provides antibodies and antigen-binding fragments thereof, including the antibodies described herein by their structural characteristics, wherein the antibodies and antigen-binding fragments thereof specifically bind to at least part of the binding site on CEACAM1 for a bacterial adhesive surface protein (adhesin), thereby blocking the interaction between CEACAM1 and the adhesin. In certain embodiments, the adhesin is expressed on the surface of a CEACAM1-binding pathogenic bacterium including, but not limited to, Escherichia coli, particularly Diffusively Adhering Escherichia coli (DAEC), Neisseria gonorrhoeae, N. meningitidis, commensal Neisseria, Moraxella catarrhalis, Haemophilus influenza, Haemophilus aegyptius, Helicobacter pylori, and/or Salmonella sp.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and HopQ expressed on the surface of Helicobacter pylori. In one embodiment, the CEACAM1 antibody or antigen-binding fragment specifically binds to one or more of CEACAM1 residues F29, Y34, N42, Q89, and N97, which have been predicted to be involved in CEACAM1 binding to HopQ.
In another embodiment, the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and an opacity-associated (Opa) adhesin protein expressed on the surface of Neisseria sp, including, but not limited to, Opa52, Opa65, Opa68, Opa70, Opa72, Opa73, Opa74, and Opa75. In one embodiment, the CEACAM1 antibody or antigen-binding fragment specifically binds to one or more of CEACAM1 residues Q44 and A49, which have been predicted to be involved in CEACAM1 binding to neisserial Opa proteins.
In another embodiment, the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and Opa-like protein OlpA expressed on the surface of Moraxella sp.
In one embodiment, the the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and Haemophilus influenza OMP P1. In one embodiment, the CEACAM1 antibody or antigen-binding fragment specifically binds to one or more of CEACAM1 residues Q44 and A49, which have been predicted to be involved in CEACAM1 binding to Haemophilus influenza OMP P1.
In another embodiment, the the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and Haemophilus aegyptius OMP P1. In one embodiment, the CEACAM1 antibody or antigen-binding fragment specifically binds to CEACAM1 residue F29, which has been predicted to be involved in CEACAM1 binding to Haemophilus aegyptius OMP P1.
In another embodiment, the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and C. albicans.
In another embodiment, the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and an influenza virus, including but not limited to H5N1.
In another embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for inhibiting binding of CEACAM1 to a filial nematode, the method comprising contacting CEACAM1 with a CEACAM1 antibody or antigen-binding fragment thereof described herein. In one embodiment, the filial nematode is Wucheria bancrofti.
Antibody Conjugates
In some embodiments of the aspects described herein, the antibody or antigen-binding fragment thereof that bind to CEACAM1 are conjugated to a functional moiety. Examples of useful functional moieties include, but are not limited to, a blocking moiety, a detectable moiety, a diagnostic moiety, a targeting, and a therapeutic moiety.
Exemplary blocking moieties include moieties of sufficient steric bulk and/or charge such that reduced glycosylation occurs, for example, by blocking the ability of a glycosidase to glycosylate the antibody or antigen-binding fragment thereof. The blocking moiety may additionally or alternatively, reduce effector function, for example, by inhibiting the ability of the Fc region to bind a receptor or complement protein. Preferred blocking moieties include cysteine adducts and PEG moieties.
In a preferred embodiment, the blocking moiety is a cysteine, preferably a cysteine that has associated with a free cysteine, e.g., during or subsequent to the translation of the Fc containing polypeptide, e.g., in cell culture. Other blocking cysteine adducts include cystine, mixed disulfide adducts, or disulfide linkages.
In another preferred embodiment, the blocking moiety is a polyalkylene glycol moiety, for example, a PEG moiety and preferably a PEG-maleimide moiety. Preferred pegylation moieties (or related polymers) can be, for example, polyethylene glycol (“PEG”), polypropylene glycol (“PPG”), polyoxyethylated glycerol (“POG”) and other polyoxyethylated polyols, polyvinyl alcohol (“PVA”) and other polyalkylene oxides, polyoxyethylated sorbitol, or polyoxyethylated glucose. The polymer can be a homopolymer, a random or block copolymer, a terpolymer based on the monomers listed above, straight chain or branched, substituted or unsubstituted as long as it has at least one active sulfone moiety. The polymeric portion can be of any length or molecular weight but these characteristics can affect the biological properties. Polymer average molecular weights particularly useful for decreasing clearance rates in pharmaceutical applications are in the range of 2,000 to 35,000 Daltons. In addition, if two groups are linked to the polymer, one at each end, the length of the polymer can impact upon the effective distance, and other spatial relationships, between the two groups. Thus, one skilled in the art can vary the length of the polymer to optimize or confer the desired biological activity. PEG is useful in biological applications for several reasons. PEG typically is clear, colorless, odorless, soluble in water, stable to heat, inert to many chemical agents, does not hydrolyze, and is nontoxic. Pegylation can improve pharmacokinetic performance of a molecule by increasing the molecule's apparent molecular weight. The increased apparent molecular weight reduces the rate of clearance from the body following subcutaneous or systemic administration. In many cases, pegylation can decrease antigenicity and immunogenicity. In addition, pegylation can increase the solubility of a biologically-active molecule.
Examples of detectable moieties which are useful in the methods and antibodies and antigen-binding fragments thereof contemplated by the invention include fluorescent moieties or labels, imaging agents, radioisotopic moieties, radiopaque moieties, and the like, e.g. detectable labels such as biotin, fluorophores, chromophores, spin resonance probes, or radiolabels. Exemplary fluorophores include fluorescent dyes (e.g. fluorescein, rhodamine, and the like) and other luminescent molecules (e.g. luminal). A fluorophore may be environmentally-sensitive such that its fluorescence changes if it is located close to one or more residues in the modified protein that undergo structural changes upon binding a substrate (e.g. dansyl probes). Exemplary radiolabels include small molecules containing atoms with one or more low sensitivity nuclei (13C, 15N, 2H, 125, 123I, 99Tc, 43K, 52Fe, 67Ga, 68Ga, 111In and the like). Other useful moieties are known in the art.
Examples of diagnostic moieties which are useful in the methods and antibodies and antigen-binding fragments thereof contemplated by the invention include detectable moieties suitable for revealing the presence of a disease or disorder. Typically a diagnostic moiety allows for determining the presence, absence, or level of a molecule, for example, a target peptide, protein, or proteins, that is associated with a disease or disorder. Such diagnostics are also suitable for prognosing and/or diagnosing a disease or disorder and its progression.
Examples of therapeutic moieties which are useful in the methods and antibodies and antigen-binding fragments thereof contemplated by the invention include, for example, anti-inflammatory agents, anti-cancer agents, anti-neurodegenerative agents, anti-infective agents, or generally a therapeutic. The functional moiety may also have one or more of the above-mentioned functions.
Exemplary therapeutic moieties include radionuclides with high-energy ionizing radiation that are capable of causing multiple strand breaks in nuclear DNA, and therefore suitable for inducing cell death (e.g., of a cancer). Exemplary high-energy radionuclides include: 90Y, 125I, 131I, 123I, 111In, 105Rh, 153Sm, 67Cu, 67Ga, 166Ho, 177Lu, 186Re and 188Re. These isotopes typically produce high-energy α- or β-particles which have a short path length. Such radionuclides kill cells to which they are in close proximity, for example neoplastic cells to which the conjugate has attached or has entered. They have little or no effect on non-localized cells and are essentially non-immunogenic.
Exemplary therapeutic moieties also include cytotoxic agents such as cytostatics (e.g. alkylating agents, DNA synthesis inhibitors, DNA-intercalators or cross-linkers, or DNA-RNA transcription regulators), enzyme inhibitors, gene regulators, cytotoxic nucleosides, tubulin binding agents, hormones and hormone antagonists, anti-angiogenesis agents, and the like.
Exemplary therapeutic moieties also include alkylating agents such as the anthracycline family of drugs (e.g., adriamycin, carminomycin, cyclosporin-A, chloroquine, methopterin, mithramycin, porfiromycin, streptonigrin, anthracenediones, and aziridines). In another embodiment, the chemotherapeutic moiety is a cytostatic agent such as a DNA synthesis inhibitor. Examples of DNA synthesis inhibitors include, but are not limited to, methotrexate and dichloromethotrexate, 3-amino-1,2,4-benzotriazine 1,4-dioxide, aminopterin, cytosine β-D-arabinofuranoside, 5-fluoro-5′-deoxyuridine, 5-fluorouracil, ganciclovir, hydroxyurea, actinomycin-D, and mitomycin C. Exemplary DNA-intercalators or cross-linkers include, but are not limited to, bleomycin, carboplatin, carmustine, chlorambucil, cyclophosphamide, cis-diammineplatinum(II) dichloride (cisplatin), melphalan, mitoxantrone, and oxaliplatin.
Exemplary therapeutic moieties also include transcription regulators such as actinomycin D, daunorubicin, doxorubicin, homoharringtonine, and idarubicin. Other exemplary cytostatic agents that are compatible with the present invention include ansamycin benzoquinones, quinonoid derivatives (e.g. quinolones, genistein, bactacyclin), busulfan, ifosfamide, mechlorethamine, triaziquone, diaziquone, carbazilquinone, indoloquinone EO9, diaziridinyl-benzoquinone methyl DZQ, triethylenephosphoramide, and nitrosourea compounds (e.g. carmustine, lomustine, semustine).
Exemplary therapeutic moieties also include cytotoxic nucleosides such as, for example, adenosine arabinoside, cytarabine, cytosine arabinoside, 5-fluorouracil, fludarabine, floxuridine, ftorafur, and 6-mercaptopurine; tubulin binding agents such as taxoids (e.g. paclitaxel, docetaxel, taxane), nocodazole, rhizoxin, dolastatins (e.g. Dolastatin-10, -11, or -15), colchicine and colchicinoids (e.g. ZD6126), combretastatins (e.g. Combretastatin A-4, AVE-6032), and vinca alkaloids (e.g. vinblastine, vincristine, vindesine, and vinorelbine (navelbine)); anti-angiogenesis compounds such as Angiostatin K1-3, DL-α-difluoromethyl-ornithine, endostatin, fumagillin, genistein, minocycline, staurosporine, and (±)-thalidomide.
Exemplary therapeutic moieties also include hormones and hormone antagonists, such as corticosteroids (e.g. prednisone), progestins (e.g. hydroxyprogesterone or medroprogesterone), estrogens, (e.g. diethylstilbestrol), antiestrogens (e.g. tamoxifen), androgens (e.g. testosterone), aromatase inhibitors (e.g. aminogluthetimide), 17-(allylamino)-17-demethoxygeldanamycin, 4-amino-1,8-naphthalimide, apigenin, brefeldin A, cimetidine, dichloromethylene-diphosphonic acid, leuprolide (leuprorelin), luteinizing hormone-releasing hormone, pifithrin-α, rapamycin, sex hormone-binding globulin, and thapsigargin.
Exemplary therapeutic moieties also include enzyme inhibitors such as, S(+)-camptothecin, curcumin, (−)-deguelin, 5,6-dichlorobenz-imidazole 1-β-D-ribofuranoside, etoposide, formestane, fostriecin, hispidin, 2-imino-1-imidazolidineacetic acid (cyclocreatine), mevinolin, trichostatin A, tyrphostin AG 34, and tyrphostin AG 879.
Exemplary therapeutic moieties also include gene regulators such as 5-aza-2′-deoxycytidine, 5-azacytidine, cholecalciferol (vitamin D3), 4-hydroxytamoxifen, melatonin, mifepristone, raloxifene, trans-retinal (vitamin A aldehydes), retinoic acid, vitamin A acid, 9-cis-retinoic acid, 13-cis-retinoic acid, retinol (vitamin A), tamoxifen, and troglitazone.
Exemplary therapeutic moieties also include cytotoxic agents such as, for example, the pteridine family of drugs, diynenes, and the podophyllotoxins. Particularly useful members of those classes include, for example, methopterin, podophyllotoxin, or podophyllotoxin derivatives such as etoposide or etoposide phosphate, leurosidine, vindesine, leurosine and the like.
Still other cytotoxins that are compatible with the teachings herein include auristatins (e.g. auristatin E and monomethylauristan E), calicheamicin, gramicidin D, maytansanoids (e.g. maytansine), neocarzinostatin, topotecan, taxanes, cytochalasin B, ethidium bromide, emetine, tenoposide, colchicin, dihydroxy anthracindione, mitoxantrone, procaine, tetracaine, lidocaine, propranolol, puromycin, and analogs or homologs thereof.
Techniques for conjugating such therapeutic moiety to antibodies are well known, see, e.g., Amon et al., “Monoclonal Antibodies For Immunotargeting Of Drugs In Cancer Therapy”, in Monoclonal Antibodies And Cancer Therapy, Reisfeld et al. (eds.), pp. 243-56 (Alan R. Liss, Inc. 1985); Hellstrom et al., “Antibodies For Drug Delivery”, in Controlled Drug Delivery (2nd Ed.), Robinson et al. (eds.), pp. 623-53 (Marcel Dekker, Inc. 1987); Thorpe, “Antibody Carriers Of Cytotoxic Agents In Cancer Therapy: A Review”, in Monoclonal Antibodies '84: Biological And Clinical Applications, Pinchera et al. (eds.), pp. 475-506 (1985); “Analysis, Results, And Future Prospective Of The Therapeutic Use Of Radiolabeled Antibody In Cancer Therapy”, in Monoclonal Antibodies For Cancer Detection And Therapy, Baldwin et al. (eds.), pp. 303-16 (Academic Press 1985), and Thorpe et al., “The Preparation And Cytotoxic Properties Of Antibody-Toxin Conjugates”, Immunol. Rev., 62:119-58 (1982).
To increase the half-life of the antibodies or polypeptide containing the amino acid sequences described herein, one can attach a salvage receptor binding epitope to the antibody or antigen-binding fragment thereof (especially an antibody fragment), as described, e.g., in U.S. Pat. No. 5,739,277. The term “salvage receptor binding epitope” may refer to an epitope of the Fc region of an IgG molecule (e.g., IgG1, IgG2, IgG3, or IgG4) that is responsible for increasing the in vivo serum half-life of the IgG molecule (e.g., Ghetie et al., 18 Ann. Rev. Immunol. 739 (2000). Antibodies with substitutions in an Fc region thereof and increased serum half-lives are also described in WO 00/42072, WO 02/060919; Shields et al., 276 J. Biol. Chem. 6591 (2001); Hinton, 279 J. Biol. Chem. 6213-6216 (2004). For example, a nucleic acid molecule encoding the salvage receptor binding epitope can be linked in frame to a nucleic acid encoding a polypeptide sequence described herein so that the fusion protein expressed by the engineered nucleic acid molecule comprises the salvage receptor binding epitope and a polypeptide sequence described herein. In another embodiment, the serum half-life can also be increased, for example, by attaching other polypeptide sequences. For example, antibodies or antigen-binding fragments thereof useful in the methods of the invention can be attached to serum albumin or a portion of serum albumin that binds to the CEACAM1 receptor or a serum albumin binding peptide so that serum albumin binds to the antibody or antigen-binding fragment thereof, e.g., such polypeptide sequences are disclosed in WO 01/45746. In one embodiment, the half-life of a Fab is increased by these methods. See also, Dennis et al., 277 J. Biol. Chem. 35035 (2002), for additional serum albumin binding peptide sequences
Other types of functional moieties are known in the art and can be readily used in the methods and compositions of the present invention based on the teachings contained herein.
Nucleic Acids
Also provided herein are nucleic acids encoding CEACAM1 antibodies and antigen-binding fragments thereof, as well as vectors, host cells, and expression systems. The term “nucleic acid” as used herein refers to a polymeric form of nucleotides of any length, either ribonucleotides or desoxyribonucleotides. Thus, this term includes, but is not limited to, single-, double- or multi-stranded DNA or RNA, genomic DNA, cDNA, DNA-RNA hybrids, or a polymer comprising purine and pyrimidine bases, or other natural, chemically or biochemically modified, non-natural, or derivatized nucleotide bases.
The nucleic acids encoding CEACAM1 antibodies and antigen-binding fragments thereof may be, e.g., DNA, cDNA, RNA, synthetically produced DNA or RNA, or a recombinantly produced chimeric nucleic acid molecule comprising any of those polynucleotides either alone or in combination. For example, provided is an expression vector comprising a polynucleotide sequence encoding a CEACAM1 antibody or antigen-binding fragment thereof described herein operably linked to expression control sequences suitable for expression in a eukaryotic and/or prokaryotic host cell.
The term “vector” refers to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked. A “vector” includes, but is not limited to, a viral vector, a plasmid, a RNA vector or a linear or circular DNA or RNA molecule which may consists of a chromosomal, non-chromosomal, semi-synthetic or synthetic nucleic acids. In some embodiments, the employed vectors are those capable of autonomous replication (episomal vector) and/or expression of nucleic acids to which they are linked (expression vectors). Large numbers of suitable vectors are known to those of skill in the art and commercially available. Viral vectors include retrovirus, adenovirus, parvovirus (e.g., adeno associated viruses, AAV), coronavirus, negative strand RNA viruses such as orthomyxovirus (e.g., influenza virus), rhabdovirus (e. g., rabies and vesicular stomatitis virus), paramyxovirus (e.g., measles and Sendai), positive strand RNA viruses such as picornavirus and alphavirus, and double-stranded DNA viruses including adenovirus, herpesvirus (e.g., Herpes Simplex virus types 1 and 2, Epstein-Barr virus, cytomegalovirus), and poxvirus (e.g., vaccinia, fowlpox and canarypox). Other viruses include Norwalk virus, togavirus, flavivirus, reoviruses, papovavirus, hepadnavirus, and hepatitis virus, for example. Examples of retroviruses include: avian leukosis-sarcoma, mammalian C-type, B-type viruses, D type viruses, HTLV-BLV group, lentivirus, and spumavirus.
A variety of expression vectors have been developed for the efficient synthesis of antibodies and antigen-binding fragments thereof in prokaryotic cells such as bacteria and in eukaryotic systems, including but not limited to yeast and mammalian cell culture systems have been developed. The vectors can comprise segments of chromosomal, non-chromosomal and synthetic DNA sequences. Also provided are cells comprising expression vectors for the expression of the contemplated CEACAM1 antibodies or antigen-binding fragments thereof.
Antibody Preparation and Expression Systems
The antibodies or antigen-binding fragments thereof of the invention are typically produced by recombinant expression. Nucleic acids encoding light and heavy chain variable regions, optionally linked to constant regions, are inserted into expression vectors. The light and heavy chains can be cloned in the same or different expression vectors. The DNA segments encoding immunoglobulin chains are operably linked to control sequences in the expression vector(s) that ensure the expression of immunoglobulin polypeptides. Expression control sequences include, but are not limited to, promoters (e.g., naturally-associated or heterologous promoters), signal sequences, enhancer elements, and transcription termination sequences. Preferably, the expression control sequences are eukaryotic promoter systems in vectors capable of transforming or transfecting eukaryotic host cells. Once the vector has been incorporated into the appropriate host, the host is maintained under conditions suitable for high level expression of the nucleotide sequences, and the collection and purification of the cross-reacting antibodies.
These expression vectors are typically replicable in the host organisms either as episomes or as an integral part of the host chromosomal DNA. Commonly, expression vectors contain selection markers (e.g., ampicillin-resistance, hygromycin-resistance, tetracycline resistance or neomycin resistance) to permit detection of those cells transformed with the desired DNA sequences (see, e.g., Itakura et al., U.S. Pat. No. 4,704,362).
The expression of the antibodies and antigen-binding fragments contemplated by the invention can occur in either prokaryotic or eukaryotic cells. Suitable hosts include bacterial or eukaryotic hosts, including yeast, insects, fungi, bird and mammalian cells either in vivo, or in situ, or host cells of mammalian, insect, bird or yeast origin. The mammalian cell or tissue can be of human, primate, hamster, rabbit, rodent, cow, pig, sheep, horse, goat, dog or cat origin, but any other mammalian cell may be used.
E. coli is one prokaryotic host particularly useful for cloning the polynucleotides (e.g., DNA sequences) of the present invention. Other microbial hosts suitable for use include bacilli, such as Bacillus subtilus, and other enterobacteriaceae, such as Salmonella, Serratia, and various Pseudomonas species.
Other microbes, such as yeast, are also useful for expression. Saccharomyces and Pichia are exemplary yeast hosts, with suitable vectors having expression control sequences (e.g., promoters), an origin of replication, termination sequences and the like as desired. Typical promoters include 3-phosphoglycerate kinase and other glycolytic enzymes. Inducible yeast promoters include, among others, promoters from alcohol dehydrogenase, isocytochrome C, and enzymes responsible for methanol, maltose, and galactose utilization.
Further, by use of, for example, the yeast ubiquitin hydrolase system, in vivo synthesis of ubiquitin-transmembrane polypeptide fusion proteins can be accomplished. The fusion proteins so produced can be processed in vivo or purified and processed in vitro, allowing synthesis of a CEACAM1 antibody or antigen-binding fragment thereof of the present invention with a specified amino terminus sequence. Moreover, problems associated with retention of initiation codon-derived methionine residues in direct yeast (or bacterial) expression maybe avoided. Sabin et al., 7 Bio/Technol. 705 (1989); Miller et al., 7 Bio/Technol. 698 (1989).
Any of a series of yeast gene expression systems incorporating promoter and termination elements from the actively expressed genes coding for glycolytic enzymes produced in large quantities when yeast are grown in mediums rich in glucose can be utilized to obtain recombinant CEACAM1 antibodies or peptides of the present invention. Known glycolytic genes can also provide very efficient transcriptional control signals. For example, the promoter and terminator signals of the phosphoglycerate kinase gene can be utilized.
Production of CEACAM1 antibodies or antigen-binding fragments thereof in insects can be achieved. For example, by infecting the insect host with a baculovirus engineered to express a transmembrane polypeptide by methods known to those of skill. See Ausubel et al., 1987, 1993.
In addition to microorganisms, mammalian tissue culture may also be used to express and produce the antibodies or antigen-binding fragments thereof of the present invention (e.g., polynucleotides encoding immunoglobulins or fragments thereof). See Winnacker, From Genes to Clones, VCH Publishers, N.Y., N.Y. (1987). Eukaryotic cells are actually preferred, because a number of suitable host cell lines capable of secreting heterologous proteins (e.g., intact immunoglobulins) have been developed in the art, and include CHO cell lines, various COS cell lines, HeLa cells, 293 cells, myeloma cell lines, transformed B-cells, and hybridomas. Expression vectors for these cells can include expression control sequences, such as an origin of replication, a promoter, and an enhancer (Queen et al., Immunol. Rev. 89:49 (1986)), and necessary processing information sites, such as ribosome binding sites, RNA splice sites, polyadenylation sites, and transcriptional terminator sequences. Preferred expression control sequences are promoters derived from immunoglobulin genes, SV40, adenovirus, bovine papilloma virus, cytomegalovirus and the like. See Co et al., J. Immunol. 148:1149 (1992).
Alternatively, nucleotide sequences encoding antibodies or antigen-binding fragments thereof can be incorporated in transgenes for introduction into the genome of a transgenic animal and subsequent expression in the milk of the transgenic animal (see, e.g., Deboer et al., U.S. Pat. No. 5,741,957, Rosen, U.S. Pat. No. 5,304,489, and Meade et al., U.S. Pat. No. 5,849,992). Suitable transgenes include coding sequences for light and/or heavy chains in operable linkage with a promoter and enhancer from a mammary gland specific gene, such as casein or beta lactoglobulin.
Additionally, plants have emerged as a convenient, safe and economical alternative main-stream expression systems for recombinant antibody production, which are based on large scale culture of microbes or animal cells. Antibodies or antigen-binding fragments thereof can be expressed in plant cell culture, or plants grown conventionally. The expression in plants may be systemic, limited to sub-cellular plastids, or limited to seeds (endosperms). See, e.g., U.S. Patent Pub. No. 2003/0167531; U.S. Pat. Nos. 6,080,560 and 6,512,162; and WO 0129242. Several plant-derived antibodies have reached advanced stages of development, including clinical trials (see, e.g., Biolex, NC).
The vectors containing the polynucleotide sequences of interest (e.g., the heavy and light chain encoding sequences and expression control sequences) can be transferred into the host cell by well-known methods, which vary depending on the type of cellular host. For example, calcium chloride transfection is commonly utilized for prokaryotic cells, whereas calcium phosphate treatment, electroporation, lipofection, biolistics or viral-based transfection may be used for other cellular hosts. (See generally Sambrook et al., Molecular Cloning: A Laboratory Manual (Cold Spring Harbor Press, 2nd ed., 1989). Other methods used to transform mammalian cells include the use of polybrene, protoplast fusion, liposomes, electroporation, and microinjection (see generally, Sambrook et al., supra). For production of transgenic animals, transgenes can be microinjected into fertilized oocytes, or can be incorporated into the genome of embryonic stem cells, and the nuclei of such cells transferred into enucleated oocytes.
The antibodies and antigen-binding fragments thereof of the invention can be expressed using a single vector or two vectors. When the antibody heavy and light chains are cloned on separate expression vectors, the vectors are co-transfected to obtain expression and assembly of intact immunoglobulins. Once expressed, the whole antibodies, their dimers, individual light and heavy chains, or other immunoglobulin forms of the present invention can be purified according to standard procedures of the art, including ammonium sulfate precipitation, affinity columns, column chromatography, HPLC purification, gel electrophoresis and the like (see generally Scopes, Protein Purification (Springer-Verlag, N.Y., (1982)). Substantially pure immunoglobulins of at least about 90 to 95% homogeneity are preferred, and 98 to 99% or more homogeneity most preferred, for pharmaceutical uses.
Methods for Modulating CEACAM1 Activity
In one aspect, the invention provides methods of using the antibodies and antigen-binding fragments thereof described herein for decreasing the interaction between CEACAM1 and another member of the CEACAM family, including, but not limited to, CEACAM1, CEACAM3, CEACAM5, CEACAM6, and CEACAM8. In some embodiments, the antibody or antigen-binding fragment thereof disrupts the homophilic interaction between CEACAM1 monomers.
In another aspect, the invention provides methods of using the antibodies and antigen-binding fragments thereof of the invention for decreasing the interaction between CEACAM1 and a member of the TIM family, including but not limited to TIM-1, TIM-3, and TIM4-4. In some embodiments, the antibody or antigen-binding fragment thereof disrupts the heterophilic interaction between CEACAM1 and TIM-3. Disruption of the interaction between CEACAM1 and TIM-3 by using the antibodies and antigen-binding fragments thereof contemplated by the invention may reverse CEACAM1 inhibitory functions while maintain TIM-3 activating functions.
The embodiments of the invention are useful for reducing immunosuppression, e.g., T cell tolerance. By “reducing” is meant the ability to cause an overall decrease of about 20% or greater, 30% or greater, 40% or greater, 45% or greater, 50% or greater, of 55% or greater, of 60% or greater, of 65% or greater, of 70% or greater, or 75%, 80%, 85%, 90%, 95%, or greater, as compared to a control that is not treated. Immunosuppression can be mediated by immune inhibitory receptors expressed on the surface of an immune cell, and their interactions with their ligands. For example, cytotoxic CD8 T cells can enter a state of “functional exhaustion,” or “unresponsiveness” whereby they express inhibitory receptors that prevent antigen-specific responses, such as proliferation and cytokine production. Accordingly, by inhibiting the activity and/or expression of such inhibitory receptors, an immune response to a cancer or tumor that is suppressed, inhibited, or unresponsive, can be enhanced or uninhibited. Such enhancements or reversal of inhibition of the immune response can lead to greater T cell activity, responsiveness, and/or ability or receptiveness with regards to activation.
Methods of measuring T cell activity are known in the art. By way of non-limiting example, T cell tolerance can be induced by contacting T cells with recall antigen, anti-CD3 in the absence of costimulation, and/or ionomycin. Levels of, e.g., IL-27, LDH-A, RAB10, and/or ZAP70 (both intracellular or secreted) can be monitored, for example, to determine the extent of T cell tolerogenesis (with levels of IL-2, interferon-γ and TNF correlating with increased T cell tolerance). The response of cells pre-treated with, e.g. ionomycin, to an antigen can also be measured in order to determine the extent of T cell tolerance in a cell or population of cells, e.g., by monitoring the level of secreted and/or intracellular IL-2 and/or TNF-α (see, e.g., Macian et al. Cell 2002 109:719-731). Other characteristics of T cells having undergone adaptive tolerance include increased levels of Fyn and ZAP-70/Syk, Cbl-b, GRAIL, Ikaros, CREM (cAMP response element modulator), B lymphocyte-induced maturation protein-1 (Blimp-1), PD1, CD5, and SHP2; increased phosphorylation of ZAP-70/Syk, LAT, PLCy1/2, ERK, PKC-Θ/IKBA; increased activation of intracellular calcium levels; decreased histone acetylation or hypoacetylation and/or increased CpG methylation at the IL-2 locus. Thus, in some embodiments, one or more of any of these parameters can be assayed to determine whether the antibodies or antigen-binding fragments thereof disclosed herein that inhibit CEACAM1 decrease immune tolerance. Reduction of T cell tolerance can also be assessed by examination of tumor infiltrating lymphocytes or T lymphocytes within lymph nodes that drain from an established tumor. Such T cells exhibit features of “exhaustion” through expression of cell surface molecules such as PD1, TIM-3 or LAG-3, for example, and decreased secretion of cytokines such as interferon-γ. Accordingly, evidence that T cell tolerance has been reduced in the presence of a CEACAM1 antibodies or antigen-binding fragments thereof includes, e.g., increased quantities of T cells with (a) antigen specificity for tumor associated antigens (e.g., as determined by major histocompatibility complex class I or class II tetramers which contain tumor associated peptides) and (b) the capability of secreting high levels of interferon-γ and cytolytic effector molecules such as granzyme-B, relative to that observed in the absence of the inhibitory agent.
The CEACAM1 antibodies and antigen-binding fragments thereof are further useful for enhancing T cell expansion, activation, and proliferation.
In another aspect, the invention provides methods of using the antibodies and antigen-binding fragments thereof of the invention for decreasing the interaction between CEACAM1 and bacterial adhesins. In some embodiments, the antibodies and antigen-binding fragments thereof of the invention are effective in reducing and/or preventing the colonization of mammalian epithelia. In some embodiments, the adhesins are expressed by Escherichia coli, particularly Diffusively Adhering Escherichia coli (DAEC), Neisseria gonorrhoeae, N. meningitidis, commensal Neisseria, Moraxella catarrhalis, Haemophilus influenza, Haemophilus aegyptius, Helicobacter pylori, and/or Salmonella sp. In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and HopQ expressed on the surface of Helicobacter pylori. In another embodiment, the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and opacity-associated (Opa) adhesin proteins expressed on the surface of Neisseria sp. In another embodiment, the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and OMP adhesin proteins expressed on the surface of Haemophilus sp.
In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and C. albicans. In one embodiment, the CEACAM1 antibody or antigen-binding fragment thereof disrupts the interaction between CEACAM1 and influenza virus, including but not limited to H5N1. In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for inhibiting binding of CEACAM1 to a filial nematode. In one embodiment, the filial nematode is Wucheria bancrofti.
Methods of Treatment
In one aspect, the invention provides for CEACAM1 antibodies and antigen-binding fragments thereof that are also useful for the treatment of subjects in need thereof.
In the methods described herein, a therapeutically effective amount of an antibody or antigen-binding portions thereof set forth herein is administered to a mammal in need thereof. Although antibodies or antigen-binding portions thereof set forth herein are particularly useful for administration to humans, they may be administered to other mammals as well. The term “mammal” as used herein is intended to include, but is not limited to, humans, laboratory animals, domestic pets and farm animals. “Therapeutically effective amount” means an amount of antibody or antigen-binding portions thereof set forth herein that, when administered to a mammal, is effective in producing the desired therapeutic effect.
In some aspects, the antibody or antigen-binding fragment thereof binds to CEACAM1 expressed by an exhausted T cell or natural killer (NK) cells, thereby recovering T cell and NK cell activity and leading to increased anti-tumor responses. In other aspects, the antibody or antigen-binding fragment thereof binds to CEACAM1 expressed by a tumor cell, thereby inhibiting tumor cell metastasis and the formation of a cancer stem cell niche. In yet another aspects, the antibody or antigen-binding fragment thereof binds to CEACAM1 expressed by macrophage associated with fibrosis in the tumor environment thereby inhibiting fibrosis. In another aspects, the antibody or antigen-binding fragment thereof binds to CEACAM1 expressed by other stromal cells in the tumor microenvironment such as vascular endothelium cells, thereby inhibiting angiogenesis.
As such, also provided herein are methods of treating a subject having a cancer or tumor and/or reducing tumor growth, comprising administering an effective amount of a CEACAM1-antibody or antigen-binding fragment thereof provided herein. “Reducing” includes inhibiting and/or reversing and can refer to, for example, the symptoms of the disorder being treated, the presence or size of metastases or micrometastases, the size of the primary tumor, the presence or the size of the dormant tumor.
The term “cancer” refers to or describes the physiological condition in mammals that is typically characterized by unregulated cell growth. Included in this definition are benign and malignant cancers, as well as dormant tumors or micrometastases. Accordingly, the term “cancer” as used herein refers to an uncontrolled growth of cells, which interferes with the normal functioning of the bodily organs and systems, including cancer stem cells and tumor vascular niches. A subject that has a cancer is a subject having objectively measurable cancer cells present in the subject's body. Included in this definition are benign and malignant cancers, as well as dormant tumors or micrometastases. Cancers that migrate from their original location and seed vital organs can eventually lead to the death of the subject through the functional deterioration of the affected organs. Hematopoietic cancers, such as leukemia, are able to out-compete the normal hematopoietic compartments in a subject, thereby leading to hematopoietic failure (in the form of anemia, thrombocytopenia and neutropenia) ultimately causing death.
By “subject” is meant a mammal, including, but not limited to, a human or non-human mammal, such as a bovine, equine, canine, ovine, or feline, etc. Individuals and patients are also subjects herein.
The terms “treat,” “treated,” “treating,” or “treatment” as used herein refer to therapeutic treatment, wherein the object is to slow down (lessen) an undesired physiological condition, disorder or disease, or to obtain beneficial or desired clinical results. For the purposes of this invention, beneficial or desired clinical results include, but are not limited to, alleviation of symptoms; diminishment of the extent of the condition, disorder or disease; stabilization (i.e., not worsening) of the state of the condition, disorder or disease; delay in onset or slowing of the progression of the condition, disorder or disease; amelioration of the condition, disorder or disease state; and remission (whether partial or total), whether detectable or undetectable, or enhancement or improvement of the condition, disorder or disease. Treatment includes eliciting a clinically significant response without excessive levels of side effects. Treatment also includes prolonging survival as compared to expected survival if not receiving treatment. The terms “prevent”, “prevention”, and the like refer to acting prior to overt disease or disorder onset, to prevent the disease or disorder from developing or to minimize the extent of the disease or disorder, or slow its course of development.
The embodiments of the invention may be used for treating metastasis, which relates to the spreading of cancer from its primary site to other places in the body. Cancer cells can break away from a primary tumor, penetrate into lymphatic and blood vessels, circulate through the bloodstream, and grow in a distant focus (metastasize) in normal tissues elsewhere in the body. Metastasis can be local or distant. Metastasis is a sequential process, contingent on tumor cells breaking off from the primary tumor, traveling through the bloodstream, and stopping at a distant site. At the new site, the cells establish a blood supply and can grow to form a life-threatening mass. Both stimulatory and inhibitory molecular pathways within the tumor cell regulate this behavior, and interactions between the tumor cell and host cells in the distant site are also significant. Metastases are most often detected through the sole or combined use of magnetic resonance imaging (MRI) scans, computed tomography (CT) scans, blood and platelet counts, liver function studies, chest X-rays and bone scans in addition to the monitoring of specific symptoms.
Also contemplated are methods of reducing cancer stemness comprising the administration of the CEACAM1 antibodies or antigen-binding fragments thereof disclosed herein. Cancer stemness may refer to the ability of a cell to self-renew and to generate an additional, phenotypically distinct cell type. Cancer stem cells (CSCs) are cancer cells that exhibit stem-cell like properties. CSCs often exhibit at least one hallmark of cancer, and is capable of generating at least one additional, phenotypically distinct cell type. Furthermore, cancer stem cells are capable of both asymmetric and symmetric replication. It is appreciated that a cancer stem cell may result from differentiated cancer cells that acquire stemness traits and/or stem cells that acquire phenotypes associated with cancer cells. Alternatively, cancer stem cells can reconstitute non-stromal cell types within a tumor.
CEACAM1 is expressed by many tumor types and CEACAM1 may regulate the growth and metastatic behavior of the tumor. In another embodiment, CEACAM1 inhibition will decrease tumor growth and metastasis.
CEACAM1 expression on subsets of macrophages is associated with fibrosis during carcinogenesis. In a further embodiment, CEACAM1 inhibition will decrease tumor-associated fibrosis.
Cancers that may be treated by the compositions and methods contemplated by the invention include tumors that are not vascularized, or not yet substantially vascularized, as well as vascularized tumors. The cancers may comprise nonsolid tumors (such as hematological tumors, for example, leukemias and lymphomas) or may comprise solid tumors. Types of cancers to be treated include, but are not limited to benign and malignant tumors, and malignancies e.g., sarcomas, carcinomas, and melanomas. Adult tumors/cancers and pediatric tumors/cancers are also included. Examples of cancer include but are not limited to, carcinoma, lymphoma, blastoma, sarcoma, and leukemia. More particular examples of such cancers include, but are not limited to, basal cell carcinoma, biliary tract cancer; bladder cancer; bone cancer; brain and CNS cancer; breast cancer; cancer of the peritoneum; cervical cancer; choriocarcinoma; colon and rectum cancer; connective tissue cancer; cancer of the digestive system; endometrial cancer; esophageal cancer; eye cancer; cancer of the head and neck; gastric cancer (including gastrointestinal cancer); glioblastoma; hepatic carcinoma; hepatoma; intra-epithelial neoplasm; kidney or renal cancer; larynx cancer; leukemia; liver cancer; lung cancer (e.g., small-cell lung cancer, non-small cell lung cancer, adenocarcinoma of the lung, and squamous carcinoma of the lung); lymphoma including Hodgkin's and non-Hodgkin's lymphoma; melanoma; myeloma; neuroblastoma; oral cavity cancer (e.g., lip, tongue, mouth, and pharynx); ovarian cancer; pancreatic cancer; prostate cancer; retinoblastoma; rhabdomyosarcoma; rectal cancer; cancer of the respiratory system; salivary gland carcinoma; sarcoma; skin cancer; squamous cell cancer; stomach cancer; testicular cancer; thyroid cancer; uterine or endometrial cancer; cancer of the urinary system; vulval cancer; as well as other carcinomas and sarcomas; as well as B-cell lymphoma (including low grade/follicular non-Hodgkin's lymphoma (NHL); small lymphocytic (SL) NHL; intermediate grade/follicular NHL; intermediate grade diffuse NHL; high grade immunoblastic NHL; high grade lymphoblastic NHL; high grade small non-cleaved cell NHL; bulky disease NHL; mantle cell lymphoma; AIDS-related lymphoma; and Waldenstrom's Macroglobulinemia); chronic lymphocytic leukemia (CLL); acute lymphoblastic leukemia (ALL); Hairy cell leukemia; chronic myeloblastic leukemia; and post-transplant lymphoproliferative disorder (PTLD), as well as abnormal vascular proliferation associated with phakomatoses, edema (such as that associated with brain tumors), and Meigs' syndrome. A patient can have more than one type of cancer.
The efficacy of the treatment methods for cancer comprising therapeutic formulations of the compositions comprising the antibodies and antigen-binding fragments thereof described herein can be measured by various endpoints commonly used in evaluating cancer treatments, including but not limited to, tumor regression, tumor weight or size shrinkage, time to progression, duration of survival, progression free survival, overall response rate, duration of response, and quality of life. In the case of cancers, the therapeutically effective amount of the recombinant CEACAM1-antibody or antigen-binding fragment thereof can reduce the number of cancer cells; reduce the tumor size; inhibit (i.e., slow to some extent and preferably stop) cancer cell infiltration into peripheral organs; inhibit (i.e., slow to some extent and preferably stop) tumor metastasis; inhibit, to some extent, tumor growth; and/or relieve to some extent one or more of the symptoms associated with the disorder. In cases where a patient has more than one type of cancer, the therapeutically effective amount of the recombinant CEACAM1-antibody or antigen-binding fragment thereof is an amount effective in treating at least one of the cancers. To the extent the recombinant CEACAM1-antibody or antigen binding-fragment thereof acts to prevent growth and/or kill existing cancer cells, it can be cytostatic and/or cytotoxic. For cancer therapy, efficacy in vivo can, for example, be measured by assessing the duration of survival, duration of progression free survival (PFS), the response rates (RR), duration of response, and/or quality of life.
Checkpoint proteins interact with specific ligands that send a signal into the T cell and switch off or inhibit T cell function. By expressing high levels of checkpoint proteins on their surface, cancer cells can control the function of T cells that enter the tumor microenvironment, thus suppressing the anticancer immune response. The immune checkpoint protein Programmed Death-1 (PD-1) is a key immune checkpoint receptor expressed by activated T and B cells and mediates immunosuppression. PD-1 is a member of the CD28 family of receptors, which includes CD28, CTLA-4, ICOS, PD-1, and BTLA. Two cell surface glycoprotein ligands for PD-1 have been identified, Programmed Death Ligand-1 (PD-L1) and Programmed Death Ligand-2 (PD-L2), that are expressed on antigen-presenting cells as well as many human cancers and have been shown to downregulate T cell activation and cytokine secretion upon binding to PD-1 (Freeman et al., 2000; Latchman et al., 2001). Inhibition of the PD-1/PD-L1 interaction can promote potent antitumor activity. Examples of PD-1 inhibitors include, but are not limited to, Pembrolizumab (MK-3475), Nivolumab (MDX-1106), Cemiplimab-rwlc (REGN2810), Pidilizumab (CT-011), Spartalizumab (PDR001), tislelizumab (BGB-A317), PF-06801591, AK105, BCD-100, BI 754091, JS001, LZM009, MEDIO680, MGA012, Sym021, TSR-042. Examples of PD-L1 inhibitors include, but are not limited to, Atezolizumab (MPDL3280A), Durvalumab (MEDI4736), Avelumab (MSB0010718C), BGB-A333, CK-301, CS1001, FAZ053, KN035, MDX-1105, MSB2311, SHR-1316.
However, there is a significant population of cancer patients receiving checkpoint inhibitor therapy that (1) fail to respond to this type of therapy (innate or primary resistance) or that (2) initially respond but eventually develop disease progression (secondary or acquired resistance). Resistant cancer may also be referred to as refractory cancer. As shown in the Examples below, tumor associated cells isolated from patients with acquired resistance to PD-1/PD-L1 inhibitors upregulate CEACAM1 expression relative tumor associated cells isolated from naïve patients, that had not been exposed to PD-1 inhibitors. When CEACAM1 is expressed in the setting of acquired resistance, the CEACAM1 bearing cells are more like likely to be effector memory rather than central memory cells, consistent with a reduction of an anti-cancer response in the resistant patients.
As such, also provided herein are methods of using CEACAM1 antibodies and antigen-binding fragments thereof, including, but not limited to the specific CEACAM1 antibodies and antigen-binding fragments thereof provided herein, for the treatment of patients with resistance to checkpoint inhibitors such as inhibitors of PD-1, PD-L1, and/or CTLA-4. In some embodiments, the CEACAM1 antibody used in the treatment of patients with resistance to inhibitors of PD-1, PD-L1, and/or CTLA-4 is CP08H03/Vk8 S29A or CP08H03/CP08F05. In some embodiments, the resistance is innate or primary resistance. In some embodiments, the resistance is secondary or acquired resistance. In some embodiments, the administered CEACAM1 antibodies, including, but not limited to the CEACAM1 antibodies and antigen-binding fragments thereof provided herein, reverse T cell exhaustion in patients resistant to checkpoint inhibitor therapy. Any cancer exhibiting PD-1, PDL-1 and/or CTLA-4 resistance is suitable for treatment with the methods of the invention. In some embodiments, the CEACAM1 antibody or antigen-binding fragment is administered to a patient that has not previously receive checkpoint inhibitor therapy.
In another aspect, the invention provides for the use of the CEACAM1 antibodies and antigen-binding fragments provided herein in the treatment of patients with resistance to therapy with other checkpoint inhibitors, including but not limited to, inhibitors of PD-L2, B7-H3, B7-H4, BTLA, HVEM, GAL9, LAG3, TIM-3, VISTA, KIR, 2B4 (belongs to the CD2 family of molecules and is expressed on all NK, γδ, and memory CD8+ (αβ) T cells), CD160 (also referred to as BY55), CGEN-15049, CHK1 and CHK2 kinases, A2aR and various B-7 family ligands (including, but are not limited to, B7-1, B7-2, B7-DC, B7-H1, B7-H2, B7-H3, B7-H4, B7-H5, B7-H6 and B7-H7).
In another aspect, the invention provides methods of using the CEACAM1 antibodies and antigen-binding fragments thereof disclosed herein for the treatment of a subject in need of reducing and/or preventing the colonization of mammalian epithelia with Candida albicans and/or bacteria expressing bacterial adhesins (including, but not limited to, Escherichia coli, particularly Diffusively Adhering Escherichia coli (DAEC), Neisseria gonorrhoeae, N. meningitidis, commensal Neisseria, Moraxella catarrhalis, Haemophilus influenza, Haemophilus aegyptius, Helicobacter pylori, and/or Salmonella sp,). In another aspect, the invention provides methods of using the CEACAM1 antibodies and antigen-binding fragments thereof disclosed herein for reducing replication of an influenza virus and/or for reducing the release of pro-inflammatory cytokines or chemokines associated with an infection with an influenza virus. In some embodiments, the influenza virus is H5N1. In another aspect, the invention provides methods of using the CEACAM1 antibodies and antigen-binding fragments thereof disclosed herein for the treatment of a subject in need of reducing and/or preventing the infection with a filial nematode such as Wucheria bancrofti. In another aspect, the invention provides methods of using the CEACAM1 antibodies and antigen-binding fragments thereof disclosed herein for the treatment of a subject in need of reducing and/or preventing the development of lymphedema and/or hydrocele associated with an infection with a filial nematode such as Wucheria bancrofti. In one embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for reducing invasion of a subject's lymphatic system with a filarial worm in a subject in need thereof. In one embodiment, the filial nematode is Wucheria bancrofti. A subject may be infected with more than one of a bacterium expressing a bacterial adhesin, Candida albicans, an influenza virus and/or a filial nematode.
In another embodiment, the invention provides methods of using the CEACAM1 antibodies or antigen-binding fragments thereof described herein for reducing the invasion of a subject's lymphatic system with cancer cells in a subject in need thereof.
Screening Methods
Provided herein are also methods of identifying patent populations who are likely to respond to treatment with the CEACAM1 antibodies and antibody-fragments provided herein, including but not limited to, CP08H03/Vk8 S29A and CP08H03/CP08F05.
In some embodiments, a cancer patient is screened for CEACAM1 expression on certain cell types, including T cells, NK cells, tumor cells, or other cells in the tumor microenvironment such as macrophages. In some embodiments, cancer patients that show an increased expression of CEACAM1 on certain cell types as compared to a control are selected for treatment with the CEACAM1 antibodies and antibody-fragments provided herein. A “control” level of CEACAM1 expression can refer to the level of CEACAM1 expression in one or more individuals to do not have cancer. The level may be measured on an individual-by-individual basis, or on an aggregate basis such as an average. In some embodiments, the control level of CEACAM1 expression from the same individual whose condition is being monitored, but is obtained at a different time. In certain embodiments, a “control” level can refer to a level obtained from the same patient at an earlier time, e.g., weeks, months, or years earlier. In some embodiment, the control level is obtained from a patient before the patient received any cancer therapy. In some embodiment, the control level is obtained from a patient before the patient received treatment with a checkpoint inhibitor.
In some embodiments, CEACAM1 expression is determined for patients resistant to checkpoint inhibitor therapy, including, but not limited to therapy with PD-1/PD-L1/CTLA-4 inhibitors. In some embodiments, patients that are resistant to checkpoint inhibitor therapy and that show an increased expression of CEACAM1 on certain cell types as compared to a control are selected for treatment with the CEACAM1 antibodies and antibody-fragments provided herein, including but not limited to, CP08H03/Vκ8 S29A and CP08H03/CP08F05.
In some embodiments, a patient is assayed for an allelic variant of human CEACAM1. Based on which allelic variant of human CEACAM1 the patient expresses, more or less anti-CEACAM1 antibody may be administered to the patient as compared to a patient expressing the wildtype variant of CEACAM1. In some embodiments, the patient is assayed for the presence of a Y34C, a Q44L, and/or a Q89H allelic variant of CEACAM1. In some embodiments, a patient that is found to express a Y34C, a Q44L, and/or a Q89H allelic variant of CEACAM1 is administered a higher and/or a more frequent dose of an anti-CEACAM1 antibody as compared to a patient expressing the wildtype variant of CEACAM1.
Pharmaceutical Compositions
In another aspect, the present invention provides pharmaceutically acceptable compositions that comprise a therapeutically effective amount of a CEACAM1 antibody or antigen-binding fragment thereof is described herein formulated together with one or more pharmaceutically acceptable excipients.
The dosage of active agent(s) may vary, depending on the reason for use, the individual subject, and the mode of administration. The dosage may be adjusted based on the subject's weight, the age and health of the subject, and tolerance for the compound(s) or composition. For example, depending on the disease, for an antibody or antigen-binding fragment thereof, this may require 0.1, 1.0, 3.0, 6.0, or 10.0 mg/Kg. For an IgG having a molecular mass of 150,000 g/mole (two binding sites), these doses correspond to approximately 18 nM, 180 nM, 540 nM, 1.08 μM, and 1.8 μM of binding sites for a 5 L blood volume.
The active agent and excipient(s) may be formulated into compositions and dosage forms according to methods known in the art. The pharmaceutical compositions of the present invention may be specially formulated in solid or liquid form, including those adapted for parenteral administration, for example, by subcutaneous, intratumoral, intramuscular or intravenous injection as, for example, a sterile solution or suspension.
Therapeutic compositions comprising antibodies or antigen-binding fragments thereof that bind to CEACAM1 may formulated with one or more pharmaceutically-acceptable excipients, which can be a pharmaceutically-acceptable material, composition or vehicle, such as a liquid or solid filler, diluent, carrier, manufacturing aid (e.g., lubricant, talc magnesium, calcium or zinc stearate, or steric acid), solvent or encapsulating material, involved in carrying or transporting the therapeutic compound for administration to the subject, bulking agent, salt, surfactant and/or a preservative. Some examples of materials which can serve as pharmaceutically-acceptable excipients include: sugars, such as lactose, glucose and sucrose; starches, such as corn starch and potato starch; cellulose and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; gelatin; talc; waxes; oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; glycols, such as ethylene glycol and propylene glycol; polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; esters, such as ethyl oleate and ethyl laurate; agar; buffering agents; water; isotonic saline; pH buffered solutions; and other non-toxic compatible substances employed in pharmaceutical formulations.
A bulking agent is a compound which adds mass to a pharmaceutical formulation and contributes to the physical structure of the formulation in lyophilized form. Suitable bulking agents according to the present invention include mannitol, glycine, polyethylene glycol and sorbitol.
The use of a surfactant can reduce aggregation of the reconstituted protein and/or reduce the formation of particulates in the reconstituted formulation. The amount of surfactant added is such that it reduces aggregation of the reconstituted protein and minimizes the formation of particulates after reconstitution. Suitable surfactants according to the present invention include polysorbates (e.g. polysorbates 20 or 80); poloxamers (e.g. poloxamer 188); Triton; sodium dodecyl sulfate (SDS); sodium laurel sulfate; sodium octyl glycoside; lauryl-, myristyl-, linoleyl-, or stearyl-sulfobetaine; lauryl-, myristyl-, linoleyl- or stearyl-sarcosine; linoleyl-, myristyl-, or cetyl-betaine; lauroamidopropyl-, cocamidopropyl-, linoleamidopropyl-, myristamidopropyl-, palmidopropyl-, or isostearamidopropyl-betaine (e.g. lauroamidopropyl); myristamidopropyl-, palmidopropyl-, or isostearamidopropyl-dimethylamine; sodium methyl cocoyl-, or disodium methyl oleyl-taurate; and polyethyl glycol, polypropyl glycol, and copolymers of ethylene and propylene glycol (e.g. Pluronics, PF68, etc.).
Preservatives may be used in formulations of invention. Suitable preservatives for use in the formulation of the invention include octadecyldimethylbenzyl ammonium chloride, hexamethonium chloride, benzalkonium chloride (a mixture of alkylbenzyl-dimethylammonium chlorides in which the alkyl groups are long-chain compounds), and benzethonium chloride. Other types of preservatives include aromatic alcohols such as phenol, butyl and benzyl alcohol, alkyl parabens such as methyl or propyl paraben, catechol, resorcinol, cyclohexanol, 3-pentanol, and m-cresol. Other suitable excipients can be found in standard pharmaceutical texts, e.g. in “Remington's Pharmaceutical Sciences”, The Science and Practice of Pharmacy, 19th Ed. Mack Publishing Company, Easton, Pa., (1995).
The compositions comprising an antibody or antigen-binding fragment thereof and a pharmaceutically acceptable carrier may comprise the CEACAM1 antibodies or antigen-binding portions thereof set forth herein at various concentrations. For example, the compositions may comprise an antibody or antigen-binding fragment thereof at 10 mg/ml to 200 mg/ml, 25 mg/ml to 130 mg/ml, 50 mg/ml to 125 mg/ml, 75 mg/ml to 110 mg/ml, or 80 mg/ml to 100 mg/ml. The compositions also may comprise an antibody or antigen-binding fragment thereof at about 10 mg/ml, 20 mg/ml, 30 mg/ml, 40 mg/ml, 50 mg/ml, 60 mg/ml, 70 mg/ml, 80 mg/ml, 90 mg/ml, 100 mg/ml, 110 mg/ml, 120 mg/ml, 130 mg/ml, 140 mg/ml, or 150 mg/ml.
In some embodiments, the compositions comprising the antibody or antigen-binding fragment thereof and the pharmaceutically acceptable carrier are lyophilized and provided in a composition for reconstitution prior to administration.
Methods of Administration
Therapeutic compositions comprising the contemplated antibody or antigen-binding fragment thereof may be administered in any convenient manner, including by injection, transfusion, implantation or transplantation. The compositions described herein may be administered to a patient subcutaneously, intradermally, intratumorally, intranodally, intramedullary, intramuscularly, intracranially, by intravenous or intralymphatic injection, or intraperitoneally. In one embodiment, the cell compositions of the present invention are preferably administered by intravenous injection.
In certain embodiments, the antibody or antigen-binding fragment thereof is administered to the mammal by intravenous infusion, i.e., introduction of the antibody or antigen-binding fragment thereof into the vein of a mammal over a certain period of time. In certain embodiments, the period of time is about 5 minutes, about 10 minutes, about 30 minutes, about 1 hour, about 2 hours, about 4 hours, or about 8 hours.
In certain embodiments, a dose of a compound or a composition is administered to a subject every day, every other day, every couple of days, every third day, once a week, twice a week, three times a week, once every two weeks, or once a month. In other embodiments, two, three or four doses of a compound or a composition is administered to a subject every day, every couple of days, every third day, once a week, once every two weeks or once a month. In some embodiments, a dose(s) of a compound or a composition is administered for 2 days, 3 days, 5 days, 7 days, 14 days, 21 days or 28 days. In certain embodiments, a dose of a compound or a composition is administered for 1 month, 1.5 months, 2 months, 2.5 months, 3 months, 4 months, 5 months, 6 months or more.
Combination Therapies
In one aspect, the invention provides CEACAM1 antibodies or antigen-binding fragments thereof that are administered with an additional therapeutic agent. Such additional agents include, but are not limited to, cytotoxic agents, chemotherapeutic agents, growth inhibitory agents, anti-inflammatory agents, anti-cancer agents, anti-neurodegenerative agents, and anti-infective agents. Agents that are used in such combination therapies may fall into one or more of the preceding categories. The administration of the antibody or antigen-binding fragment thereof and the additional therapeutic agent may be concurrently or consecutively. The administration of the antibody or antigen-binding fragment thereof and the additional therapeutic agent may be separately or as a mixture. Further, the methods of treatment contemplated by the invention can relate to a treatment in combination with one or more cancer therapies selected from the group of antibody therapy, chemotherapy, cytokine therapy, dendritic cell therapy, gene therapy, hormone therapy, laser light therapy, and radiation therapy.
Exemplary additional therapeutic agents also include radionuclides with high-energy ionizing radiation that are capable of causing multiple strand breaks in nuclear DNA, and therefore suitable for inducing cell death (e.g., of a cancer). Exemplary high-energy radionuclides include: 90Y, 125I, 131I, 123I, 111In, 105Rh, 153Sm, 67Cu, 67Ga, 166Ho, 177Lu, 186Re and 188Re. These isotopes typically produce high energy α- or β-particles which have a short path length. Such radionuclides kill cells to which they are in close proximity, for example neoplastic cells to which the conjugate has attached or has entered. They have little or no effect on non-localized cells and are essentially non-immunogenic.
Exemplary additional therapeutic agents also include cytotoxic agents such as cytostatics (e.g. alkylating agents, DNA synthesis inhibitors, DNA-intercalators or cross-linkers, or DNA-RNA transcription regulators), enzyme inhibitors, gene regulators, cytotoxic nucleosides, tubulin binding agents, hormones and hormone antagonists, anti-angiogenesis agents, and the like.
Exemplary additional therapeutic agents also include alkylating agents such as the anthracycline family of drugs (e.g. adriamycin, carminomycin, cyclosporin-A, chloroquine, methopterin, mithramycin, porfiromycin, streptonigrin, anthracenediones, and aziridines). In another embodiment, the chemotherapeutic moiety is a cytostatic agent such as a DNA synthesis inhibitor. Examples of DNA synthesis inhibitors include, but are not limited to, methotrexate and dichloromethotrexate, 3-amino-1,2,4-benzotriazine 1,4-dioxide, aminopterin, cytosine β-D-arabinofuranoside, 5-fluoro-5′-deoxyuridine, 5-fluorouracil, ganciclovir, hydroxyurea, actinomycin-D, and mitomycin C. Exemplary DNA-intercalators or cross-linkers include, but are not limited to, bleomycin, carboplatin, carmustine, chlorambucil, cyclophosphamide, cis-diammineplatinum(II) dichloride (cisplatin), melphalan, mitoxantrone, and oxaliplatin.
Exemplary additional therapeutic agents also include transcription regulators such as actinomycin D, daunorubicin, doxorubicin, homoharringtonine, and idarubicin. Other exemplary cytostatic agents that are compatible with the present invention include ansamycin benzoquinones, quinonoid derivatives (e.g. quinolones, genistein, bactacyclin), busulfan, ifosfamide, mechlorethamine, triaziquone, diaziquone, carbazilquinone, indoloquinone E09, diaziridinyl-benzoquinone methyl DZQ, triethylenephosphoramide, and nitrosourea compounds (e.g. carmustine, lomustine, semustine).
Exemplary additional therapeutic agents also include cytotoxic nucleosides such as, for example, adenosine arabinoside, cytarabine, cytosine arabinoside, 5-fluorouracil, fludarabine, floxuridine, ftorafur, and 6-mercaptopurine; tubulin binding agents such as taxoids (e.g. paclitaxel, docetaxel, taxane), nocodazole, rhizoxin, dolastatins (e.g., Dolastatin-10, -11, or -15), colchicine and colchicinoids (e.g., ZD6126), combretastatins (e.g., Combretastatin A-4, AVE-6032), and vinca alkaloids (e.g., vinblastine, vincristine, vindesine, and vinorelbine (navelbine)); anti-angiogenesis compounds such as Angiostatin K1-3, DL-α-difluoromethyl-ornithine, endostatin, fumagillin, genistein, minocycline, staurosporine, and (±)-thalidomide.
Exemplary additional therapeutic agents also include hormones and hormone antagonists, such as corticosteroids (e.g., prednisone), progestins (e.g., hydroxyprogesterone or medroprogesterone), estrogens, (e.g., diethylstilbestrol), antiestrogens (e.g., tamoxifen), androgens (e.g., testosterone), aromatase inhibitors (e.g., aminogluthetimide), 17-(allylamino)-17-demethoxygeldanamycin, 4-amino-1,8-naphthalimide, apigenin, brefeldin A, cimetidine, dichloromethylene-diphosphonic acid, leuprolide (leuprorelin), luteinizing hormone-releasing hormone, pifithrin-α, rapamycin, sex hormone-binding globulin, and thapsigargin.
Exemplary additional therapeutic agents also include enzyme inhibitors such as, S(+)-camptothecin, curcumin, (−)-deguelin, 5,6-dichlorobenz-imidazole 1-β-D-ribofuranoside, etoposide, formestane, fostriecin, hispidin, 2-imino-1-imidazolidineacetic acid (cyclocreatine), mevinolin, trichostatin A, tyrphostin AG 34, and tyrphostin AG 879.
Exemplary additional therapeutic agents also include gene regulators such as 5-aza-2′-deoxycytidine, 5-azacytidine, cholecalciferol (vitamin D3), 4-hydroxytamoxifen, melatonin, mifepristone, raloxifene, trans-retinal (vitamin A aldehydes), retinoic acid, vitamin A acid, 9-cis-retinoic acid, 13-cis-retinoic acid, retinol (vitamin A), tamoxifen, and troglitazone.
Exemplary additional therapeutic agents also include cytotoxic agents such as, for example, the pteridine family of drugs, diynenes, and the podophyllotoxins. Particularly useful members of those classes include, for example, methopterin, podophyllotoxin, or podophyllotoxin derivatives such as etoposide or etoposide phosphate, leurosidine, vindesine, leurosine and the like.
Still other additional therapeutic agents that are compatible with the teachings herein include auristatins (e.g. auristatin E and monomethylauristan E), calicheamicin, gramicidin D, maytansanoids (e.g. maytansine), neocarzinostatin, topotecan, taxanes, cytochalasin B, ethidium bromide, emetine, tenoposide, colchicin, dihydroxy anthracindione, mitoxantrone, procaine, tetracaine, lidocaine, propranolol, puromycin, and analogs or homologs thereof.
In one embodiment, the CEACAM antibody or antigen-binding fragment thereof is administered in combination with an agent that is a checkpoint inhibitor. Such inhibitors may include small molecule inhibitors or may include antibodies, or antigen binding fragments thereof, that bind to and block or inhibit immune checkpoint receptors or antibodies that bind to and block or inhibit immune checkpoint receptor ligands. Illustrative checkpoint molecules that may be targeted for blocking or inhibition include, but are not limited to, CTLA-4, PDL1, PDL2, PD1, B7-H3, B7-H4, BTLA, HVEM, GAL9, LAG3, TIM-3, VISTA, KIR, 2B4 (belongs to the CD2 family of molecules and is expressed on all NK, γδ, and memory CD8+ (αβ) T cells), CD160 (also referred to as BY55), CGEN-15049, CHK1 and CHK2 kinases, A2aR and various B-7 family ligands. B7 family ligands include, but are not limited to, B7-1, B7-2, B7-DC, B7-H1, B7-H2, B7-H3, B7-H4, B7-H5, B7-H6 and B7-H7. Checkpoint inhibitors include antibodies, or antigen binding fragments thereof, other binding proteins, biologic therapeutics or small molecules, that bind to and block or inhibit the activity of one or more of CTLA-4, PDL1, PDL2, PD1, BTLA, HVEM, TIM-3, GAL9, LAG3, VISTA, KIR, 2B4, CD160 and CGEN-15049. Illustrative immune checkpoint inhibitors include Tremelimumab (CTLA-4 blocking antibody), anti-OX40, and Yervoy/ipilimumab (anti-CTLA-4 checkpoint inhibitor), as well as the PD-1 and PD-L1 inhibitors described above. Checkpoint protein ligands include, but are not limited to PD-L1, PD-L2, B7-H3, B7-H4, CD28, CD86 and TIM-3.
In some embodiments, the CEACAM1 antibodies and antigen-binding fragments thereof described herein are administered with a TIGIT, LAP, Podoplanin, Protein C receptor, ICOS, GITR, CD226 or a CD160 inhibiting agent.
In some embodiments, the CEACAM1 antibodies and antigen-binding fragments thereof described herein are administered with a CTLA-4, a PD-1, a PD-L1, or a PD-L2 inhibiting agent. In some embodiments, the CEACAM1 antibodies and antigen-binding fragments thereof described herein are administered with a TIM-3 inhibiting agent.
It is to be understood that this invention is not limited to the particular molecules, compositions, methodologies, or protocols described, as these may vary. Any methods and materials similar or equivalent to those described herein can be used in the practice or testing of embodiments of the present invention. It is further to be understood that the disclosure of the invention in this specification includes all possible combinations of such particular features. For example, where a particular feature is disclosed in the context of a particular aspect or embodiment of the invention, or a particular claim, that feature can also be used, to the extent possible, in combination with and/or in the context of other particular aspects and embodiments of the invention, and in the invention generally.
Where reference is made herein to a method comprising two or more defined steps, the defined steps can be carried out in any order or simultaneously (except where the context excludes that possibility), and the method can include one or more other steps which are carried out before any of the defined steps, between two of the defined steps, or after all the defined steps (except where the context excludes those possibilities).
All other referenced patents and applications are incorporated herein by reference in their entirety. Furthermore, where a definition or use of a term in a reference, which is incorporated by reference herein is inconsistent or contrary to the definition of that term provided herein, the definition of that term provided herein applies and the definition of that term in the reference does not apply.
To facilitate a better understanding of the present invention, the following examples of specific embodiments are given. The following examples should not be read to limit or define the entire scope of the invention.
1. Generation of Humanized Antibody Variants
Design of Composite Human Antibody Variable Region Sequences and Expression of Antibodies
First, structural models of the parental, murine CEACAM1 antibody's V regions were produced using Swiss PDB and analyzed in order to identify potential “constraining” amino acids in the V regions that were likely to contribute to the binding properties of the antibody. For regions outside of, and flanking the CDRs, a wide selection of human sequence segments were identified as possible components of the novel humanized V regions.
Based upon the structural analysis, a large preliminary set of sequence segments that could be used to create humanized CEACAM antibody variants were selected and analyzed using iTope™ technology for in silico analysis of peptide binding to human MHC class II alleles (Perry et al, 2008. Drugs RD 9(6):385-396), and using the TCED™ of known antibody sequence-related T cell epitopes (Bryson et al 2010, Biodrugs 21 (1):1-8). Sequence segments that were identified as significant non-human germline binders to human MHC class II or that scored significant hits against the TCED™ were discarded. This analysis resulted in a reduced set of segments, and combinations of these were again analyzed, as above, to ensure that the junctions between segments did not contain potential T cell epitopes. Selected sequence segments were assembled into complete V region sequences that were devoid of significant T cell epitopes. The heavy and light chains chosen for gene synthesis, expression in mammalian cells, and testing for activity are listed in
Table 1. Some of the heavy and light chains in
Table 1 contained variations at positions to be considered part of a CDR according to the Kabat CDR definition, but not according to the IMGT CDR definition.
Next, the VH and Vκ sequences of the parental, murine CEACAM1 antibody and the humanized CEACAM antibody variants were synthesized with flanking restriction enzyme sites for cloning into the pANT expression vector system for IgG4 (S241P) heavy and x light chain (
Thirty-nine heavy and light chain pairings were transiently transfected into HEK EBNA adherent cells using a PEI transfection method and incubated for 5-7 days post-transfection. These 39 pairings included three controls: (1) the chimeric antibody VH0/Vκ0 (consisting of the murine VH region (VH0) fused to the constant heavy region of human IgG4, and the murine Vκ region (Vκ0) fused to the constant light region of human IgG4); (2) the pairing of the chimeric VH heavy chain (VH0) with the light chain variant Vκ1; and (3) the pairing of the VH1 heavy chain with the chimeric Vκ light chain variant (Vκ0). The other 36 were combinations of the composite IgG4 VH and the Vκ variants: VH1 was paired with Vκ1 through Vκ12, VH2 was paired with Vκ1 through Vκ12, VH3 was paired with Vκ1 through Vκ6, and VH4 was paired with Vκ1 through Vκ6.
Antibodies were purified from cell culture supernatants on Protein A sepharose columns, buffer exchanged into PBS pH 7.4 and quantified by OD 280 nm using an extinction coefficient based on the predicted amino acid sequence. 1 μg of each antibody was analyzed by SDS-PAGE and bands corresponding to the profile of a typical antibody were observed. The size of the light chain and the presence of a faint band at 25 kDa indicates that the glycosylation motif identified in the light chain is substantially utilized.
Competition ELISA Analysis of Humanized Variants Binding to CEACAM1
The binding of the purified antibodies to human CEACAM1 was assessed in a competition ELISA assay. Nunc Immuno MaxiSorp 96 well flat bottom microtitre plates were pre-coated with 1 μg/ml of GST-CEACAM1 in 1×PBS, overnight at 4° C. The following day the plates were blocked for 1 hour at room temperature (“RT”) with 2% BSA/PBS before washing 3× with PBST pH 7.4. A 3-fold dilution series of the chimeric antibody chimeric antibody VH0/Vκ0, an irrelevant IgG4 antibody, and the humanized CEACAM1 antibodies from 100 μg/ml to 0.07 or 0.002 μg/ml were pre-mixed with a constant concentration of parental murine antibody (0.45 μg/ml final concentration), added to the plate and incubated for 1 hour at room temperature. Following 3×PBST washes, the binding of the parental murine CEACAM1 antibody was detected with an anti-mouse-HRP and TMB substrate. The reaction was stopped with 3 M HCl, absorbance read at 450 nm on a Dynex Technologies MRX TC II plate reader and the binding curves plotted. The binding of the humanized CEACAM antibody variants to CEACAM1 was compared to the chimeric antibody (VH0/Vκ0), which was included on each plate. Twelve of the 36 humanized CEACAM antibody variants showed no binding to CEACAM1 (those including Vκ3, Vκ4, and Vκ5). Variants that bound CEACAM1 showed a range of relative IC50 values from 0.9 to 5.2 compared to the chimeric antibody VH0/Vκ0. Data are summarized in Table 2.
V
H
1/Vκ2
1.8
V
H
1/Vκ7
1.6
V
H
1/Vκ8
1.7
V
H
1/Vκ9
1.5
V
H
1/Vκ10
1.6
V
H
1/Vκ12
1.4
V
H
2/Vκ7
1.3
V
H
2/Vκ8
1.6
V
H
2/Vκ9
1.7
V
H
2/Vκ10
1.4
V
H
2/Vκ11
1.4
V
H
2/Vκ12
1.5
Kinetic Analysis of Humanized Variants Binding to CEACAM1
As an alternative approach to assess the binding of the 36 antibody combinations and the three control antibodies to CEACAM1, a kinetic analysis was performed on a Biacore T200 (serial no. 1909913) running Biacore T200 Evaluation Software V2.0.1 (Uppsala, Sweden). All experiments were run at 25° C. with HBS-P+ running buffer (pH 7.4) (GE Healthcare, cat. no. BR100671). All kinetic experiments were performed using His-tagged CEACAM1 as the analyte. For all experiments, antibodies were immobilized onto a Series S Protein A sensor chip surface. For kinetic experiments, the amount of immobilized/captured ligand was limited to avoid mass transfer effects at the surface of the chip with the surface ideally having an analyte binding level (Rmax) of 50-150 RUs. Using a MW of 45 kDa for the CEACAM1 analyte, 150 kDa for the antibody ligand (estimated value for IgG), 50 RU for Rmax and the stoichiometry (Sm) as 2 due to the ability of each antibody to bind 2 target molecules, a target response level of ˜75 RUs was set for capture of all the sample antibodies.
Single cycle analysis of the 36 antibody combinations and the three control antibodies was performed on purified antibodies (Vκ1 to Vκ6 variants) or on the supernatants of the transiently transfected HEK EBNA cells (Vκ7 to Vκ12 variants). In some instances, where supernatant was not available, purified chimeric antibody VH0/Vκ0 was spiked into HEK EBNA culture medium to use as a positive control. Antibodies were diluted in HBS-P+ to a concentration of 1 μg/ml (as determined by an IgG quantitation ELISA). At the start of each cycle, antibodies were loaded onto Fc2, Fc3 and Fc4 of a protein A chip and IgG captured at a flow rate of 8 μl/min to give an RU of ˜75. The surface was then allowed to stabilize. Single cycle kinetic data was obtained at a flow rate of 50 l/min to minimize any potential mass transfer effects. Multiple repeats of the chimeric antibody VH0/Vκ0 were performed to check the stability of the surface and analyte over the kinetic cycles. The signal from the reference channel Fc1 (no antibody) was subtracted from that of Fc2, Fc3 and Fc4 to correct for differences in non-specific binding to a reference surface. A 5 point 2-fold dilution range from 3.125 to 50 nM CEACAM1 without regeneration between each concentration was used. The association phase for the 5 injections of increasing concentrations of CEACAM1 was monitored for 100 seconds and a single dissociation phase was measured for 150 seconds following the last injection of CEACAM1. Regeneration of the Protein A surface was conducted using 2 injections of 10 mM glycine-HCl pH 1.5 followed by a stabilization period of 500 seconds. The signal from each antibody blank run (no CEACAM1) was subtracted to correct for differences in surface stability. Single cycle kinetics
Table 3) demonstrated that 24 humanized variants bound to CEACAM1 while 12 variants did not bind. The light chains of Vκ3, Vκ5 and Vκ6 abolished CEACAM1 binding when combined with any humanized heavy chain. These data are consistent with the competition ELISA data (Table 2).
V
H
1/Vκ2
Purified
134
3.2
V
H
1/Vκ7
S/N
109
2.6
V
H
1/Vκ9
S/N
142
3.4
V
H
1/Vκ10
S/N
146
3.5
V
H
1/Vκ12
S/N
143
3.5
V
H
2/Vκ7
S/N
152
3.7
V
H
2/Vκ8
S/N
125
3.0
V
H
2/Vκ9
S/N
110
2.7
V
H
2/Vκ10
S/N
131
3.2
V
H
2/Vκ11
S/N
122
3.0
V
H
2/Vκ12
S/N
145
3.5
Of the 24 antibodies that bound to CEACAM1, the antibody variants that showed binding within 2-fold of the chimeric antibody VH0/Vκ0 with relative IC50s ranging from 0.9 to 1.8 were taken forward for multi-cycle kinetics analysis using Biacore: VH1/Vκ2, VH1/Vκ7, VH1/Vκ8, VH1/Vκ9, VH1/Vκ10, VH1/Vκ12, VH2/Vκ7, VH2/Vκ8, VH2/Vκ9, VH2/Vκ10, VH2/Vκ11 and VH2/Vκ12 (see Table 2 and
Table 3, highlighted in bold).
For multi-cycle kinetic analysis, purified antibody was immobilized at a protein concentration of 1 μg/ml in HBS-P+. At the start of each cycle, antibody was captured on Protein A to give an RU of ˜75 and the surface allowed to stabilize. Kinetic data was obtained at a flow rate of 80 μl/min to minimize any potential mass transfer effects. Multiple repeats of the blank (no CEACAM1) and a repeat of a single concentration of the analyte were programmed into the kinetic run in order to check the stability of both the surface and analyte over the kinetic cycles. For kinetic analysis, a 2-fold dilution range was selected from either 200 to 3.125 nM or 100 to 1.5625 nM CEACAM1. The association phase of CEACAM1 was monitored for 50 or 150 seconds and the dissociation phase was measured for 100 seconds. Regeneration of the Protein A surface was conducted using two injections of 10 mM glycine-HCL pH 1.5 at the end of each cycle.
The signal from the reference channel Fc1 was subtracted from that of Fc2, Fc3 and Fc4 to correct for differences in non-specific binding to a reference surface, a global Rmax parameter was used in the 1-to-1 binding model. The relative KD compared to VH1/Vκ0 was calculated by dividing the KD of the humanized CEACAM antibody variants by that of the chimeric antibody VH0/Vκ0 on the same chip. The kinetic parameters measured for the interaction of CEACAM1 with humanized CEACAM antibody variants are shown in Table 4. A summary of the averaged relative KD obtained for the 12 antibody combinations analyzed using multi cycle kinetics can be found in Table 5.
Selectivity Analysis of Humanized Variants Binding to CEACAM1
Binding selectivity for CEACAM1 was tested for the 24 humanized antibody variants that bound to CEACAM1 (see
Table 3), as well as the chimeric control antibody VH0/Vκ0, by flow cytometry on HeLa cells transfected with CEACAM1, 3, 5, 6 and 8. As shown in
2. Removal of N-Linked/HEK-Derived Glycosylation
Sequence analysis revealed a potential N-linked glycosylation motif in the original mouse hybridoma light chain CDR1. CDR1L of the parental, murine antibody contains an N-X-S/T consensus sequence (N26 and S29 according to Kabat numbering, correspond to residues 26 and 28 in the primary amino acid sequence of the light variable chain, see
Competition ELISA experiments (see Table 6), multi-cycle kinetic analysis (see Table 7), and selectivity analysis (see Table 8) were performed to confirm binding of the mutant chimerics to CEACAM1. Compared to antibody mutant N26Q, antibody mutant S29A (Kabat numbering scheme) exhibited higher expression levels and KD more similar to the un-mutated antibody (see
Table 9), while maintaining a high selectivity for CEACAM1. As such, the S29A mutation (Kabat numbering scheme) was incorporated into the CEACAM1 lead antibodies during further development.
V
H
0/Vκ0 S29A
7.25
1.05
0.84
3. Affinity Maturation of the Aglycosylated CEACAM1 Antibody VH1/Vκ8 S29A
Phage vector construction and testing of binding of parent VH1 Vκ8 S29A scFv
For the affinity maturation of one of the lead antibodies, VH1/Vκ8, genes encoding the VH1 and Vκ8 were constructed and converted to a scFv format using overlapping PCR where the heavy chain was linked to the light chain via a 15 amino acid (G4S)3 linker. CDR1L residue S29 is numbered according to the Kabat numbering scheme and corresponds to residue 28 in the primary amino acid sequence of the light variable chain (
Mutagenesis and Library Construction
For the construction of an affinity maturation library, specific amino acids within the CDR1H, CDR3H and CDR3L of the aglycosylated, humanized antibody VH1/Vκ8 S29A were targeted for “hotspot” mutagenesis using semi-randomized codons. Sequence positions were analyzed for likely contact residues and ranked in order within each block. This information was used together with the amino acid preferences at any given position within the CDR3 and the crystal structure of the parental murine antibody. Where possible, priority was given to the highest ranked contact residue within each block.
Four different libraries were generated: one library for the mutation of CDR1H (HC), two libraries for the mutation of CDR3H, and one library for the mutation of CDR3L (see
CDR1H was identified as being five amino acids (S31 to S35) in length (Kabat definition, corresponds to residues 31-35 of the primary amino acid sequence of the heavy variable chain, see
CDR3H was identified as being 12 amino acids in length (H95-Y102 according to Kabat definition, corresponds to residues 99-110 of the primary amino acid sequence of the heavy variable chain, see
CDR3L was identified as being 9 amino acids (Q89-T97) (according to Kabat definition, corresponds to residues 88 to 96 of the primary amino acid sequence of the light variable chain, see
An overview of library construction is shown in
For the CDR3L library, randomization of the CDR3L was carried out by performing two PCRs. In the first PCR, a randomized 3′ primer and a VH FW1 specific 5′ primer containing a Sfi I restriction site were used to amplify the majority of the scFv gene and introduce mutations into the Vκ CDR3. The second PCR added the remainder of the scFv and appended a restriction site (Not I) for subcloning of the fragment.
For the VH libraries, the PCR for the VH repertoire was carried out by performing two PCRs using two templates containing portions of the full-length parent scFv. Initially, the VH was amplified with the randomized 5′ library primer and a 3′ primer specific for the Vκ light chain FW4. In a separate PCR, the remainder of the VH was amplified with a 5′ primer based in the heavy chain FW1 region plus a 3′ primer that was complementary to a portion of the VH CDR randomized primer. The full length VH CDR randomized scFv libraries were then constructed by annealing of the two amplified fragments and re-amplification of the scFv by PCR with primers that appended two restriction sites (either Sfi I or Not I) for subcloning of the fragment.
To assess the diversity of the generated libraries, purified, amplified DNA for all four libraries was then digested using Sfi I and Not I and ligated into the similarly cut phagemid vector (pANT43). Ligated DNA was precipitated, resuspended in nuclease-free water and transformed by electroporation into freshly prepared electrocompetent TG1 cells. The following day, colonies were counted, plates scraped and glycerol stocks prepared. Libraries were electroporated multiple times in order to sufficiently cover the theoretical library diversity. In all cases, a coverage of 4.0-fold or greater was obtained. Individual colonies from each of the four libraries were sequenced to confirm that the appropriate CDR block had been mutated.
Bacteria from each library were inoculated into 150 ml 2TYCG (2%) cultures using inocula at least 10× the observed library diversity. The cultures were grown to mid-log phase (OD600nm≈0.5-0.6) and the total number of cells estimated (based on an OD600nm of 1 5×108 cells/ml). Helper phage were added and incubated for 1 hour, then centrifuged, resuspended in 2TYCK media and grown overnight at 30° C. The following day, phage were harvested by recovering the culture supernatant by centrifugation followed by precipitation using 4/10th× volume of chilled 20% PEG/2.5 M NaCl. After 1 hour incubation on ice, precipitated phage were recovered by centrifugation and the pellet resuspended in 1×PBS pH 7.4. The supernatant was re-centrifuged to remove any cellular debris, following which the supernatant was re-precipitated as described above. The precipitated phage were resuspended in 1×PBS pH 7.4 and filter sterilized. To increase the chances of obtaining scFvs with increased affinity, multivalent hyperphage M13 K07ΔpIII helper phage were used at a multiplicity of infection of 20 for library rescue due to the relatively low affinity of the starting antibody. Following the first round of selection, monovalent M13K07 helper phage at a multiplicity of infection of 10 were used as a result of an expected enrichment of antigen binders.
Affinity Improved Phage Selection
Two separate selection strategies were implemented to increase the probability of obtaining affinity improved phage. CEACAM1 was used throughout the selections either biotinylated (for soluble selections) or unbiotinylated (for solid phase panning). Soluble selections (Campaign 1) or solid phase panning selections (Campaign 2) were used at round 1 in the different selection cascades to enrich for functional binding phage and diversity. Deselection using the closely related family members CEACAM5 and CEACAM6 was performed by separate panning of each protein at 1 μg/ml in order to try and reduce cross reactivity. This was performed twice during each campaign, either by deselecting prior to any rounds of selection and prior to round 2 (Campaign 1) or prior to both the second and third rounds of selection (Campaign 2). For both campaigns the four libraries were kept separate at all stages.
For soluble selections, each of the libraries were pre-blocked with PBSB following which the phage was incubated with decreasing concentrations of biotinylated CEACAM1 antigen for up to three hours. Following incubation, streptavidin paramagnetic beads (pre-blocked as above) were added to each selection and rotated turning end-over-end for 15 minutes. Streptavidin-antigen-phage complexes were washed using increasing numbers of washes with PBST at each successive round of selection followed by a PBS wash, capturing with a magnet between each step. Phage were eluted from the beads by the addition of 50 mM HCl following which the solution was neutralized by the addition of 1 M Tris-HCl pH 9.0.
Solid-phase panning selections and all deselections were performed on Nunc Immuno MaxiSorp 96 well flat bottom microtitre plates coated with antigen overnight at 4° C. then blocked with PBSB. For deselections, pre-blocked phage was incubated with CEACAM5 followed by CEACAM6 before unbound phage were removed and used for subsequent selections. For CEACAM1 panning selections pre-blocked phage were incubated with 8 μg/ml antigen before plates were washed with 3×PBST and 2×PBS. Bound phage were eluted with 50 mM HCl as with the soluble selection. For both soluble and panning selections, eluted phage were added to mid-log E. coli TG1 and allowed to infect the cells for 1 hour at 37° C. before plating out on 2TYCG (2%) plates and growing overnight at 37° C. The following day, colonies were picked for screening or, alternatively, plates were scraped, and the phage rescued as described above. An overview of the different selection strategies used is shown in
Expression and Initial Testing of scFv
Soluble scFv were initially expressed and tested as crude periplasmic extracts. Individual colonies were picked into 1 ml 2TYCG (0.1%) media and grown by shaking at 37° C. for 5 hours. Cultures were induced by adding IPTG to a final concentration of 1 mM and then grown overnight, with shaking, at 30° C. The following day, cultures were centrifuged and the supernatant discarded. Bacterial pellets were resuspended in Tris(hydroxymethyl)methyl-2-aminoethanesulfonic acid (TES) buffer pH 7.4 and incubated on ice for 30 minutes. The cells were then centrifuged and the supernatant discarded. The pellet was resuspended in ice cold 5 mM MgSO4. The plate was then centrifuged and the scFv-containing supernatant transferred to a fresh plate for assay.
Periplasmic extracts of colonies from different rounds of selection were screened in a single point binding assay for their ability to bind GST-CEACAM1. The parental scFv (VH1/Vκ8 S29A) and an irrelevant scFv were included on each assay plate for comparison. Periplasmic extracts were blocked by diluting 1:1 with PBSB before incubating for 1 hour at room temperature on a Nunc Immuno MaxiSorp 96 well flat bottom microtitre plate pre-coated with GST-CEACAM1 at 1.0 μg/ml. Plates were subsequently washed and the binding of scFv was detected with an anti-HIS6-TRP antibody and TMB substrate. The reaction was stopped with 1 M HCl, absorbance read at 450 nm on a Dynex Technologies MRX TC II plate reader and the binding data plotted.
Improved clones were identified on the basis of activity in the binding ELISA relative to the parental scFv VH1/Vκ8 S29A (which contains the mouse CDRs) and the irrelevant scFv assayed on the same plate. Greater than 4400 periplasmic extracts were analyzed and 34 leads with binding at least 1.5 greater than parent in two separate experiments were sequenced and unique clones identified. Examination of the sequences obtained showed that in several positions the parental amino acid was found but was encoded by a different codon from the parent. This indicates that selection had occurred as expected but that the parent amino acid was the preferred amino acid at this position. Based upon this sequence analysis, 19 unique CDR1H, three CDR3H block 1, three CDR3H block 2 and 9 unique CDR3L clones were taken forward for large scale scFv expression. A summary of the 34 leads that were selected for further analysis as purified scFvs is shown in Table 10, together with the CDR mutations of these mutants.
Table 11, Table 12, and Table 13 highlight the conservation/variability of affinity matured CDRs in scFv variant leads identified using the GST-CEACAM1 binding ELISA.
EFTFSDHAMS
FPAWFAL
FPYWFAH
FPAWFAF
KHPPDYF
$Numbering of residues based on Kabat numbering scheme.
$Numbering of residues based on Kabat numbering scheme.
#Not part of the CDR according to Kabat definition. Residue was included in mutagenesis to allow for more diversity in the germline residue anchoring the CDR.
$Numbering of residues based on Kabat numbering scheme.
#Residue was not mutated during affinity maturation.
Large Scale ScFv Expression and Purification
Selected clones were expressed, purified and quantified in order to accurately test the scFv by binding ELISA. Briefly, individual colonies were picked into 15 ml 2TYCG (20%) media and grown overnight by shaking at 30° C. The starter culture was used to inoculate 500 ml 2TYCG (0.10%) and grown at 30° C. until OD600 nm=−0.8. Cultures were induced by adding TPTG to a final concentration of 1 mM and then grown overnight with shaking at 30° C. The following day, cultures were centrifuged and the supernatant discarded. The bacterial pellets were resuspended in 15 ml TES and incubated on ice for 15 minutes. 22.5 ml of TES (diluted 1 in 5 in cold water) was then added and incubated on ice for a further 30 minutes. The cells were then centrifuged and the scFv-containing supernatant transferred to a fresh tube, following which MgCl2, NaCl and imidazole were added to final concentrations of 1 mM, 300 mM and 20 mM respectively to reduce non-specific binding. Ni-agarose beads were added and scFv allowed to bind by incubating with rotation at 4° C. for 2 hours. Beads were pelleted by centrifugation and washed twice with wash buffer (25 mM Tris pH 7.4, 300 mM NaCl, 20 mM imidazole) before scFv were eluted from the beads using elution buffer (25 mM Tris pH 7.4, 300 mM NaCl, 400 mM imidazole). Samples were quantified by measuring the OD 280 nm and using an extinction coefficient based on the predicted amino acid sequences. Approximately 1 μg of each scFv was analyzed by SDS-PAGE. Bands corresponding to the profiles of typical scFv were observed.
Assessment of scFv Binding to GST-CEACAM1 as Determined by ELISA
The binding of affinity matured purified scFv to human CEACAM1 was analyzed using GST-CEACAM1. A Nunc Immuno MaxiSorp 96 well flat bottom microtitre plate was pre-coated with 1.0 μg/ml GST-CEACAM1 overnight at 4° C. The following day a two-fold dilution series of VH1/Vκ8 S29A parent scFv or test scFv (50 μg/ml to 0.8 μg/ml) in PBSB was incubated for 2 hours at RT on pre-coated ELISA plates. The binding of scFv was detected with an anti-HIS6-TRP antibody and TMB substrate. The reaction was stopped with 3 M HCl, absorbance read at 450 nm on a Dynex Technologies MRX TC II plate reader and the binding curves plotted. Example binding assay data is shown in
Construction and testing of affinity matured whole antibodies
Reformatting of scFvs to Whole IgG
The 34 variants identified by scFv screening were PCR amplified using primers that introduced flanking restriction enzyme sites for cloning into a IgG4 S241P pANTVhG4 vector and x light chain pANTVK vector. 25 affinity matured VH variants were subcloned into the IgG4 S241P pANTVhG4 vector using Mlu I and Hind III restriction sites. Similarly, 9 affinity matured Vκ sequences were subcloned into the κ light chain pANTVK vector using BssH II and BamH I restriction sites. All constructs were confirmed by sequencing.
For expression, the 25 lead humanized affinity matured IgG4 VH variants were combined with the parent humanized, aglycosylated light chain (Vκ8 S29A). The 9 lead humanized affinity matured κ light chains were combined with the parent humanized heavy chain (VH1). These combinations were transiently transfected into HEK EBNA adherent cells (in 6-well plates using a PEI transfection method. Five to seven days post-transfection, the supernatants were harvested, quantified by ELISA and filtered for Biacore single-cycle kinetics analysis.
Single-Cycle Kinetics Analysis of Humanized and Affinity Matured Lead IgGs Binding to CEACAM1
In order to assess the binding of the humanized, affinity matured reformatted lead IgGs, single-cycle kinetics analysis was performed on crude supernatants using a Biacore T200 running Biacore T200 Control Software V2.0.1 and Biacore T200 Evaluation Software V3.0. Antibodies were diluted in HBS-P+ to a final concentration of 0.5 μg/ml. At the start of each cycle, antibodies were loaded onto Fc2, Fc3 and Fc4 of the Protein A chip. IgGs were captured at a flow rate of 10 μl/min to give an immobilisation level (RL) of ˜100 RU (a level calculated to obtain a Rmax of ˜ 50-150 RU once the analyte is bound). The surface was then allowed to stabilize. Single-cycle kinetics data was obtained with CEACAM1 as the analyte at a flow rate of 80 l/min to minimize any potential mass transfer effects. Multiple repeats with the parent (VH1/Vκ8 S29A) antibody were performed to check the stability of the surface and analyte over the kinetic cycles. The signal from the reference channel Fc1 (no antibody) was subtracted from that of Fc2, Fc3 and Fc4 to correct for differences in non-specific binding to the reference surface. A three point, two-fold dilution range from 70 nM to 280 nM CEACAM1 without regeneration between each concentration was used. The signal from each antibody blank run (no CEACAM1) was subtracted to correct for differences in surface stability. The association phase for the three injections of increasing concentrations of CEACAM1 was monitored for 80 seconds each time and a single dissociation phase was measured for 150 seconds following the last injection of CEACAM1. Regeneration of the Protein A surface was conducted using two injections of 10 mM glycine-HCL pH 1.5 followed by a stabilization period of 250 seconds.
Single-cycle kinetic constants (
Table 14) demonstrated that all but one humanized, affinity matured antibody bound to CEACAM1.
CP09C02
2.0 × 10
5
1.7 × 10
−2
8.8 × 10
−8
7.1
CP09B03
1.5 × 10
5
3.9 × 10
−2
2.6 × 10
−7
2.4
CP09E05
1.2 × 10
5
3.7 × 10
−2
3.2 × 10
−7
1.4
CP08G09
4.7 × 10
5
4.9 × 10
−2
1.1 × 10
−7
5.9
CP08D02
4.3 × 10
5
4.3 × 10
−2
1.0 × 10
−7
6.2
CP08F05
4.0 × 10
5
1.1 × 10
−1
2.8 × 10
−7
2.2
CP08E05
2.4 × 10
5
3.4 × 10
−2
1.4 × 10
−7
4.4
CP08E01
3.3 × 10
5
5.4 × 10
−2
1.7 × 10
−7
3.7
CP08H03
1.8 × 10
5
7.6 × 10
−3
4.5 × 10
−8
13.7
8.7 × 104
Eight humanized and affinity matured heavy and light chain variants were identified that demonstrated relative KDs>two-fold compared to parent (highlighted in bold in
Table 14). These included three VH variants (CP08H03, CP09B03 and CP09C02) and five κ light chain variants (CP08E01, CP08E05, CP08F05, CP08D02, and CP08G09).
CP09C02 (which originated from the CDR1H library) contained an additional point mutation in CDR3H B1 (D96G), which most likely had been introduced through PCR at the library construction stage (see section “Example 1, 1. Generation of humanized antibody variants”). Therefore, an additional heavy chain clone CP09E05 was also taken forward as it was identified as having only this single point mutation in VH CDR3 B1 and thus could potentially help to identify which region was involved in the observed affinity gain. The four VH and five Vκ variants were subsequently taken forward to determine whether there could be improved effects from recombining affinity matured heavy and light chains.
Expression of Combined Lead Heavy and Light Chain Antibodies
Each of the four humanized affinity matured IgG4 VH variants (CP08H03, CP09B03, CP09C02, and CP09E05) identified following expression with parent light chain were combined with the five lead humanized affinity matured κ light chains (CP08E01, CP08E05, CP08F05, CP08D02, and CP08G09) (i.e. a total of 20 pairings, see Table 15). As controls, the humanized affinity matured IgG4 VH variants were combined with the parent light chain (Vκ8 S29A) and the five lead humanized affinity matured κ light chains were combined with the parent heavy chain (VH1) (i.e. a total of 10 control antibodies, see Table 15). As described above, combinations were transiently transfected into HEK EBNA adherent cells in 6-well plates using a PEI transfection method and incubated for 5-7 days post-transfection. The supernatants were harvested, quantified by ELISA and filtered for single-cycle kinetics analysis on the Biacore.
Single-Cycle Kinetics Analysis of Combined Lead Heavy and Light Chain Antibodies
Single-cycle kinetics using transient HEK supernatant was performed as described previously. The fitted data for the single-cycle kinetics are shown
Table 16. Fifteen heavy and light chain combinations had relative KDs at least two-fold better than parent. Of these, six combinations (CP08H03/CP08EO5, CP08H03/CP08F05, CP08H03/Vκ8 S29A, CP09B03/CP08E05, CP09C02/CP08E05, and CP09C02/CP08F05) achieved KDs greater than four-fold better than parent (highlighted in bold in
Table 16). These six variants were taken forward for larger scale production and Protein A purification for further analysis. Single-cycle kinetics also revealed that three variants were found to be non-functional when combined.
CP08H03/CP08E05
7.1 × 10
4
8.5 × 10
−3
1.2 × 10
−7
4.6
CP08H03/CP08F05
7.0 × 10
4
7.4 × 10
−3
1.1 × 10
−7
5.2
CP08H03/Vκ8 S29A
6.5 × 10
4
8.5 × 10
−3
1.3 × 10
−7
4.2
CP09B03/CP08E05
1.1 × 10
5
1.0 × 10
−2
9.7 × 10
−8
5.7
CP09C02/CP08E05
9.6 × 10
4
7.5 × 10
−2
7.8 × 10
−8
7.1
CP09C02/CP08F05
1.1 × 10
5
1.1 × 10
−2
1.0 × 10
−7
5.5
Recombination of Four Affinity Maturated Heavy Chain CDRs to Create Six Additional Heavy Chain Variants
The six combinations with greater than four-fold improvements comprised three unique heavy chains with mutations in four different VH CDRs: CP08H03 (CDRH3 B32); CP091B03 (CDR1H) and CP09C02 (CDR3H B2 and a single mutation in CDR3H B1 which is also uniquely present in CP08E05), see Table 17. In order to determine whether further improvements could be gained, recombinations of the four mutated VH CDRs were performed (Table 18). Using scFv specific primers individual VH CDRs were recombined using pull through PCR and subsequently cloned into IgG4 S241P heavy chain expression vectors using Mlu I and Hind III restriction sites to generate six new VH variants (8H3_9B3, 8H3_9C2, 8H3_9E5, 9B3_9E5, 8H3_9C2(CDR1) and 9B3_9E5_8H3).
EFTFSDHAMS
FPYWFAH
FPYWFAH
EFTFSDHAMS
FPYWFAH
FPYWFAH
EFTFSDHAMS
FPYWFAH
FPYWFAH
Expression of recombined VH CDR1 and CDR3 heavy chains with lead light chains:
The six recombined VH CDR1 and CDR3 variants (see Table 18) were combined with the (1) parent light chain (Vκ8 S29A), (2) light chain CP08E05, or (3) light chain CP08F05. The latter two light chains previously gave an improved effect when combined with affinity matured heavy chains (see
Table 16). The resulting 18 combinations are summarized in Table 19. These combinations were transiently transfected in 6-well plates into HEK EBNA adherent cells using a PEI transfection method and incubated for 5-7 days post-transfection. The supernatants were harvested, quantified by ELISA and filtered for single-cycle kinetics analysis on the Biacore.
Single-Cycle Kinetics Analysis of Recombined VH with Lead VL Antibodies:
Single-cycle kinetics using transient HEK supernatant was performed as described previously. The fitted data for the single-cycle kinetics are shown Table 20.
Eight variants were found to have relative KDs greater than four-fold compared to parent. Of these, five achieved KDs greater than six-fold better than the parent (bold in Table 20). Five antibodies, 8H3_9B3/CP08E05, 8H3_9B3/CP08F05, 8H3_9B3/Vκ8 S29A, 8H3_9C2/CP08F05 and 9B3_9E5/CP08E05, were taken forward for larger scale production and Protein A purification for further analysis.
8H3
—
9B3/CP08E05
9.3 × 10
4
7.2 × 10
−3
7.7 × 10
−8
7.3
8H3
—
9B3/CP08F05
9.0 × 10
4
6.3 × 10
−3
7.0 × 10
−8
8
8H3
—
9B3/Vκ8 S29A
9.0 × 10
4
6.9 × 10
−3
7.7 × 10
−8
7.2
8H3
—
9C2/CP08F05
6.6 × 10
4
6.1 × 10
−3
9.3 × 10
−8
6
9B3
—
9E5/CP08E05
1.2 × 10
5
7.8 × 10
−3
6.7 × 10
−8
8.3
Expression, Purification and Testing of Lead Antibodies
The six most improved combined variants (CP08H03/CP08EO5, CP08H03/CP08F05, CP08H03/Vκ8 S29A, CP09B03/CP08EO5, CP09C02/CP08E05, and CP09C02/CP08F05, highlighted in bold in
Table 16) together with the five most improved VH CDR1 and VH CDR3 recombined variants (8H3_9B3/CP08E05, 8H3_9B3/CP08F05, 8H3_9B3/Vκ8 S29A, 8H3_9C2/CP08F05, and 9B3_9E5/CP08E05, highlighted in bold in Table 20) were transiently transfected into HEK EBNA adherent cells in triple flasks using the PEI method and incubated for 5-7 days post-transfection. Antibodies were purified from cell culture supernatants on Protein A sepharose columns, buffer exchanged into PBS pH 7.2 and quantified by OD280nm using an extinction coefficient based on the predicted amino acid sequence. 2 μg of each antibody was analyzed by SDS-PAGE and bands corresponding to the profile of a typical antibody were observed.
Single-Cycle Kinetics Analysis of Purified Lead Humanized and Affinity Matured Antibodies (Using Purified Proteins)
Single-cycle kinetics was performed as described above using purified antibodies instead of HEK supernatants. The fitted data for the single-cycle kinetics are shown in Table 21. Expression levels for the individual mutants are provided in Table 22.
All 11 lead variants bound >four-fold better than the parent antibody (see Table 21). Data obtained using purified IgG was consistent with data previously obtained using supernatants.
Removal of potential CD4+ T Cell Epitopes
The sequences of the 11 lead antibodies (see Table 21) were analyzed using iTope™ technology for in silico analysis of peptide binding to human MHC class II alleles (Perry et al 2008), and using the TCED™ of known antibody sequence-related T cell epitopes (Bryson et al 2010) to ensure that no significant T cell epitopes had been introduced during the affinity maturation process. The CDR1 mutation (G26E, CDR definition according to IMGT) found in the heavy chain of CP09C02 is associated with the introduction of a promiscuous high epitope not observed in the parent sequence (see Table 21).
Selectivity Analysis of Lead Antibodies
An initial selectivity analysis of several lead antibodies indicated that antibodies with a phenylalanine (F) at CDR3H position 104 showed on average an increased selectivity for CEACAM1 as compared to antibodies with a aspartic acid (D) at CDR3H position 104 (
Multi-Cycle Kinetic Analysis
Variants CP08H03/Vκ8 S29A and CP08H03/CP08F05 were further analyzed using multi-cycle kinetics analysis, using a Biacore T200 instrument running Biacore T200 Evaluation Software V3.0.1. The purified antibodies were diluted to a concentration of 1 g/ml in HBS-P+. At the start of each cycle, each antibody was captured on the Protein A surface to give an RL of ˜100 RU. Following capture, the surface was allowed to stabilize. Kinetic data was obtained using a flow rate of 80 l/min to minimize any potential mass transfer effects. Multiple repeats of the blank (no CEACAM1) and a repeat of a single concentration of the analyte were programmed into the kinetic run in order to check the stability of both the surface and analyte over the kinetic cycles. For kinetic analysis, a two-fold dilution range was selected from 100 to 1.56 nM CEACAM1. The association phase of CEACAM1 was monitored for 150 seconds and the dissociation phase was measured for 150 seconds. Regeneration of the Protein A surface was conducted using two injections of 10 mM glycine-HCL pH 1.5 at the end of each cycle.
The signal from the reference channel Fc1 was subtracted from that of Fc2, Fc3 and Fc4 to correct for differences in non-specific binding to a reference surface, and a global Rmax parameter was used in the 1-to-1 binding model. The relative KD compared to Parent (VH1/Vκ8 S29A) was calculated by dividing the KD of the affinity matured composite human antibody variants by that of the Parent on the same chip. The kinetic parameters measured for the interaction of CEACAM1 with affinity matured CEACAM1 antibody variants CP08H03/Vκ8 S29A and CP08H03/CP08F05 are shown in Table 23. Both affinity matured CEACAM1 antibody variants demonstrated affinity improvements of >four-fold compared to VH1/Vκ8 S29A parent.
To further assess the binding selectivity of CEACAM1 antibodies VH0/Vκ0, CP08H03/Vκ8 S29A, CP08H03/CP08F05 CEACAM1 over other proteins, binding affinities to CEACAM1, CEACAM3, CEACAM5, and CEACAM6 were compared using single-cycle kinetics analysis performed as described above. Single cycle kinetics was conducted using CEACAM concentrations from 280 nM to 70 nM. Antibodies were loaded onto the chip at the following concentrations (taking into account the varying analyte MWs):100 RU for CEACAM1, 375 RU for CEACAM3, 71.4 RU for CEACAM5, and 150 RU for CEACAM6. No significant binding of the three CEACAM1 antibodies, CP08H03/Vκ8 S29A, CP08H03/CP08F05, and VH0/Vκ0, was observed for CEACAM3, CEACAM5, and CEACAM6 (see
These results were consistent with data obtained by measuring antibody specificity with an ELISA. For the ELISA experiments, a 96 well plate was coated with CEACAM1 at either 0.5 or 1.0 μg/ml. Non-specific binding was blocked with 2% BSA/Dulbecco's PBS. A 1:3 dilution series of CP08H03/Vκ8 S29A, CP08H03/CP08F05, or VH0/Vκ0 (50 μg/mL starting concentration) was prepared in 2% BSA/PBS. 100 μL of the sample was added to the pre-coated plate and incubated for 1 h at RT. Anti-human Igκ chain—Peroxidase secondary antibody (AP502P) used to detect the CEACAM antibodies. Plates were developed with TMB and stopped with 3M HCl. Results were analyzed by subtracting the background. Essentially no binding of the three CEACAM1 antibodies, CP08H03/Vκ8 S29A, CP08H03/CP08F05, and VH0/Vκ0 to CEACAM3, CEACAM5, or CEACAM6 was observed (see
This high degree of selectivity can be observed despite the fact that the N-domains of different CEACAM share high degrees of homology: The N-domains of CEACAM1 and CEACAM3 are 88% identical, the N-domains of CEACAM1 and CEACAM5 are 89% identical, and N-domains of CEACAM1 and CEACAM6 are 90% identical, as indicated by a percent identity matrix created using Clustal2.1 (see
To determine which residues on CEACAM1 are involved in binding to certain CEACAM1 antibodies contemplated by the invention, single point mutations were introduced into FLAG-tagged CEACAM1. Each FLAG-tagged CEACAM1 mutant was transfected into 293T cells. 48 hours after transfection, CEACAM1 proteins were subjected to Western blotting. CEACAM1 antibodies VH0/Vκ0 (chimeric antibody), VH1/Vκ8, VH2/Vκ4, VH3/Vκ1, and VH4/Vκ1 were used as the antibody for detection. Mutation of CEACAM1 residues Y34, V39, G41, N42, R43, Q44, G47, and Q89, which are part of the CEACAM1 GFCC′ face, lead to reduced binding of CEACAM1 to the CEACAM1 antibodies, indicating that these CEACAM1 residues may be involved in binding (see
To more precisely map the binding interface between CEACAM1 and CP08H03/Vκ8 S29A, the crystal structure of human CEACAM1 in complex with a CP08H03/Vκ8 S29A Fab fragment was determined.
CEACAM1 was expressed from E. coli transformed with a pET21D-based plasmid expressing a tagless version of CEACAM1. The protein was refolded in an arginine-containing buffer, and purified. The Fab fragment was prepared by digestion of the antibody, after concentrating to ˜18 mg/ml, using immobilized papain resin and then purified by protein A affinity and gel filtration chromatography. Purified CEACAM1 and Fab were mixed at a 1:1 molar ratio prior to crystallization screening. Initial crystallization hits of the CEACAM1:Fab complex were identified and subsequently optimized. Diffraction quality crystals were grown at room temperature in a condition containing 18-20% PEG 6000, 50 mM potassium dihydrogen phosphate, 20 mM Tris pH 7.0, and 1% 0-octylglucoside. SDS-PAGE analysis and silver staining of a washed crystal was used to verify crystallization of the complex. X-ray data from numerous crystals were collected from beamline NE-CAT 24-ID-E at the Advanced Photon Source of Argonne National Laboratory. The best data from two non-twinned isomorphous crystals were merged to produce a highly redundant dataset at 3.3 Å for structure determination and refinement. The structure of the complex was solved by molecular replacement and refined to final R and Rfree values of 24.9% and 32.8%, respectively.
The structure of the CEACAM1:CP08H03/Vκ8 S29A Fab complex was determined to 3.3 Å resolution. The CP08H03/Vκ8 S29A Fab binds to CEACAM1 in a 1:1 stoichiometric ratio (see
#Numbering of residues based on Kabat numbering scheme.
#Numbering of residues based on Kabat numbering scheme.
With reference to an existing structure of the CEACAM1 dimer (
In the Fab light chain, residues in CDR1, CDR2, and CDR3 (
The interacting surfaces have a shape complementarity of 0.5, and complex formation buries 1607 A2 of total solvent accessible surface. No interactions are seen between the antigen and the Fab heavy chain CDR1.
Alignments of human CEACAM family members indicated that CEACAM3, 5, 6, 7, and 8 all contain a valine residue at position 49, while human CEACAM1 contains an alanine in this location. In addition, human CEACAM5 contains histidine at position 89. The polymorphisms in hCEACAM-1 at these residues include Ala49Val (rs8l 10904) and Gln89His (rs8111468). To further examine the selective nature of CEACAM1 antibody CP08H03/Vκ8 S29A, a human CEACAM1 A49V/Q89H mutant was expressed and purified as described above. Note that a natural human allelic variant of human CEACAM1 exists which convert Q89 to H89 as described in Huang et al., Nature. 2015 Jan. 15; 517(7534):386-90. A structure of the CEACAM1 A49V/Q89H mutant was determined to 1.7 Å resolution and compared to the CEACAM1 wildtype:CP08H03/Vκ8 S29A Fab complex. As discussed above, CDR3H residue F104 of CP08H03/Vκ8 S29A makes contact with residue F29 in wildtype CEACAM1 (see
The ability of the CEACAM1 antibodies to block CEACAM1 homodimerization was tested. CEACAM1-CEACAM1 competition ELISA studies were done in triplicates to determine ability of the CP08H03/Vκ8 S29A antibody (concentration range 0-1000 nM) to inhibit human CEACAM1 IgV domain tagless protein (1 μg/ml) and human CEACAM1-GST protein (37.5 μg/ml) binding. In addition, IgG4 antibody was used as a control (0-1000 nM). Goat polyclonal anti-GST-HSP antibody from Abcam (1:2000) was used and assays were developed by addition of TMB solution (Life technologies). OD values were read at 450 nm on a plate reader. Data was plotted in a Graphpad and best-fit IC-50 values were determined.
CEACAM1 antibody CP08H03/Vκ8 S29A was shown to block CEACAM1:CEACAM1 homophilic interactions (see
The ability of the CEACAM1 antibodies to reduce the binding of CEACAM1 to TIM-3 was examined. CEACAM1/TIM-3 competition ELISA studies were done in triplicates to determine ability of CP08H03/Vκ8 S29A antibody (concentration range 0-300 nM) to inhibit human TIM-3 IgV domain tagless protein (3 μg/ml) and human CEACAM1-GST protein (37.5 μg/ml) binding. In addition, human IgG4 antibody was used as a control (0-1000 nM). Goat polyclonal anti-GST-HSP antibody from Abcam (1:2000) was used and assays were developed by addition of TMB solution (Life technologies). OD values were read at 450 nm on a plate reader. Data was plotted in a Graphpad and best-fit IC-50 values were determined. As shown in
The ability of CEACAM antibodies CP08H03/Vκ8 S29A and CP08H03/CP08F05 to induce T cell proliferation was investigated in humanized NOD scid gamma mice (NSG mice). See
No antibody-dependent cell-mediated cytotoxicity (ADCC) was observed in any of the groups tested (see
To assess the ability of CEACAM1 antibodies to reduce tumor growth, 1×106 MALME-3M (human melanoma) were injected subcutaneously into 7-8 week old male NSG (NOD.Cg-Prkdcscid Il2rgtm1Wj1/SzJ) mice with 5×106 human PBMC. The MALME-3M (BRAFV600E) cell line was established in 1975 from a metastatic site (lung) from a 43-year-old Caucasian male with metastatic melanoma. On days 7-9, it was confirmed that all mice exhibited a reconstituted T cell population (see
The human melanoma cell lines MALME-3M were kindly provided by Dr. Nicole Beauchemin (McGill University, Montreal, Canada). MALME-3M were established in year of 1975 from a metastatic site (lung) in a 43-year-old Caucasian male with metastatic melanoma with BRAFV600E. 2×10{circumflex over ( )}7 MALME-3M were subcutaneously (s.c.) injection into NOD.Cg-Prkdcscid Il2rgtm1Wj1/SzJ (NSG) mice. After a 30 min period of acclimation, freshly isolated human PBMCs (1×10{circumflex over ( )}8) were then transferred via intraperitoneal (i.p.) injection into the tumor-bearing NSG mice. 7- to 9-days post PBMC injection, NSG animals were examined for human immune cell implantation by tail-bleeding. 10, 13, 17, 20, and 24 days post human cell injection the tumor-bearing humanized NSG mice received a total of five doses of the indicated concentrations of CEACAM1 antibody or isotype control antibody via i.p. injection. Upon study termination (34 days post human cell injection), mice were sacrificed and surgical dissection performed.
CEACAM1 antibody CP08H03/Vκ8 S29A was effective in reducing tumor growth at various concentrations and proliferation (see
CEACAM1 is expressed on a significant portion of TILs derived from naïve or anti-PD-1 and/or anti-CTLA-4 therapy resistant melanoma patients; with CEACAM1 expression levels being greater than the expression levels of PD-1 or TIM-3 (see
As expected, there was a relative decrease in central memory (Tem) relative to effector memory (Tem) cells among the CD8+ T cells in patients resistant to anti-PD-1 and/or anti-CTLA-4 therapy as compared to patients that had no previous exposure to anti-PD-1 and/or anti-CTLA-4 therapy, consistent with a reduction of an anti-cancer response in the resistant patients (see
To assess the ability of CEACAM1 antibodies to reverse T cell exhaustion in patients that are resistant to treatment with checkpoint inhibitors such as PD-1/PD-L1 and CTLA-4 inhibitors, PBMCs and tumor associated cells were isolated from a melanoma patient with secondary resistance to Pembrolizumab (PD-1 inhibitor), Ipilimumab (CTLA-4 inhibitor)+Nivolumab (PD-1 inhibitor) and Dabrafenib (B-Raf inhibitor)+Trametinib (MEK inhibitor) and Stage IV disease. Tumor associated cells and PBMC were stained for CEACAM1, PD1 or TIM-3 and proportion of CD8+ and CD4+ T cells denoted (see
The properties of antibody CP08H03/Vκ8 S29A were compared to anti-CEACAM1 antibody CM-24 (WO2015/166484). Unlike CEACAM1 antibody CP08H03/Vκ8 S29A disclosed herein, CM-24 (i) binds to CEACAM1 away from the dimer interface based upon modeling, (ii) exhibits cross-reactivity with CEACAM3 and CEACAM5, (iii) shows a limited ability to reverse T cell tolerance in TILs, and (iv) functions as an agonistic, rather than antagonistic antibody in mouse models of metastatic melanoma.
CP08H03/Vκ8 S29A is selective for CEACAM1 and did not show significant binding to CEACAM3, CEACAM5, CEACAM6, or CEACAM8. CM-24 on the other hand showed significant cross-reactivity with CEACAM3 and CEACAM5 at higher antibody concentrations (
Further, CM-24 showed a limited ability to reserve T cell tolerance in tumor associated cells. Incubation of tumor associated cells with antibody CP08H03/Vκ8 S29A lead to a more extensive reversal of T cell tolerance over a range of antibody concentrations as compared to CM-24 in naïve Merkel cell carcinoma tumor cells (
In a metastic melanoma model (see
HopQ is expressed on the surface of Helicobacter pylori, a bacterium that specifically colonizes the human gastric epithelium and is the major causative agent for ulcer disease and gastric cancer development. The HopQ-CEACAM1 interaction has been suggested to promote gastric colonization and Hp-induced pathologies, for example by enabling translocation bacterial virulence factors into host cells and enhancing the release of pro-inflammatory mediators.
Published crystal structure data (PDB IDs 6AW2, 6GBH, 6GBG, see Bonsor, D, et. al. EMBO J. 2018 Jul. 2; 37(13) and Moonens K et al. EMBO J. 2018 Jul. 2; 37(13)) indicate that the GFCC′ loop of CEACAM1 is involved in binding to HopQ and that CEACAM1 residues F29, Y34, N42, Q89, and N97 make various hydrogen bonded and hydrophobic interactions with HopQ residues (see
The ability of CEACAM1 antibody CP08H03/Vκ8 S29A to promote long-term survival of tumor-bearing mammals was investigated using a mouse melanoma model.
106 MALME-3M (human melanoma) cells, along with 5×106 human PBMC (from HLA-A2 matched donors) were injected subcutaneously into NSG mice. At day 10, the tumor tumors had reached 2-2.5 mm3, and the mice were randomized (n=4/group). Anti-CEACAM1 antibody CP08H03/Vκ8 S29A or a control human IgG4 antibody, respectively, were administered intraperitonally on days 10, 13, 17, 20, and 24. Survival was monitored for 104 days, at which point the surviving animal that exhibited vigorous clinical activity was sacrificed (arrow).
As shown in
The ability of CEACAM1 antibody CP08H03/Vκ8 S29A to increase the immune response in tumors derived from melanoma patients who were naïve or who exhibited secondary resistance to immunotherapy was examined using isolated tumor specimens.
In one example, the isolated tumor specimen from a patient with secondary resistance was disrupted by mechanical dissociation and the dissociated cells treated for 4 days in culture medium with either CP08H03/Vκ8 S29A or a hIgG4 control antibody (2 μg/ml) in the presence of 2 μg/ml anti-CD3 and 40 units/ml recombinant IL-2. The cells were then examined by mass cytometry using the following antibodies to detect a variety of intracellular factors associated with immune responses to tumors in CD8+ T cells using standard techniques: IFNγ (clone B27; 168Er), IL-17A (clone N49-653; 164Dy), IL-17F (clone SHLR17; 166Er); granzyme B (clone GB 11; 171Yb); Perforin (clone B-D48; 175Lu); MIP1beta (clone D21-1351; 150Nd); TNFalpha (clone Mab11; 152Sm), CD3 (clone UCHT1; 170Er); CD8 (clone RPA78; 146Nd); intercalator (103Rh).
As shown in
In another example, the tumors specimens associated with two melanoma patients with either no prior treatment (subject 189) or with secondary resistance to immunotherapy (subject 185) were disrupted by mechanical dissociation (Miltenyi). 8×105/ml dissociated tumor cells were placed in a culture dish. Freshly isolated tumor dissociated cells were exposed to only 2 μg/ml CP08H03/Vκ8 S29A or human IgG4 isotype control antibody. After 96 hours, the supernatants were removed and ELISA analysis was performed in triplicate for detection of the presence of interferon-gamma.
As shown in
In summary, these data demonstrate that anti-CEACAM1 antibodies and fragments thereof disclosed herein are useful for treating naïve cancer patients and those with secondary resistance to immunotherapy.
Overview of Sequences
While the foregoing written description of the invention enables one of ordinary skill to make and use what is considered presently to be the best mode thereof, those of ordinary skill will understand and appreciate the existence of variations, combinations, and equivalents of the specific embodiments, methods, and examples herein.
This invention was made with government support under NIH DK51362 awarded by the National Institutes of Health. The government has certain rights in the invention.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2019/065212 | 12/9/2019 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62776877 | Dec 2018 | US |
