Patent Application
20210277128
The Sequence Listing associated with this application is provided in text format in lieu of a paper copy, and is hereby incorporated by reference into the specification. The name of the text file containing the Sequence Listing is Sequence Listing_ST25_0003 PCT2.txt. The text file is about 227 KB, was created on Dec. 18, 2015, and is being submitted electronically via EFS-Web.
The present disclosure generally relates to the technical field of antibody therapeutic agents, and more particularly relates to bispecific tetravalent antibodies against two different members of EGFR family.
Overexpression and/or deregulation of members of the ErbB/HER receptor family such as EGFR, HER2, HER3, HER4 have been shown to play an important role in tumorigenesis in cancers. Mutation and amplification of EGFR or HER2 produce aberrant growth signal which activates downstream signaling pathway contributing to tumorigenesis. Therapeutic antibodies and small-molecule inhibitors directed against EGFR and HER2 have been approved for use in the treatment of cancer (Arteaga et al., Nature Reviews Clinical Oncology 9 16-32, January 2012). Monoclonal antibodies against members of EGFR family such as EGFR and HER2, have demonstrated good clinical responses in colon cancer (Price et al., The Lancet Oncology 15(6), Pages 569-579, May 2014), squamous cell carcinoma of head and neck (Cohen, Cancer Treatment Reviews 40 (2014) 567-577), breast and gastric cancers (Arteaga et al., Nature Reviews Clinical Oncology 9 16-32, January 2012). Several therapeutic anti-EGFR antibodies, including cetuximab, panitumumab and nimotuzumab are approved therapeutics for several cancers including metastatic colorectal cancer, head and neck squamous cell carcinoma and glioma (Price and Cohen, Curr Treat Options Oncol. 2012 March; 13(1):35-46; Bode et al., Expert Opin Biol Ther. 2012 December; 12(12):1649-59). Unfortunately, many tumors that initially respond to these therapeutic agents eventually progress due to an acquired resistance to the agents (Jackman et al. J Clin Oncol 2010; 28:357-60). Therefore, there exists a need for better cancer therapeutics.
The disclosure provides bispecific tetravalent antibodies. The bispecific tetravalent antibodies may include an immunoglobulin G (IgG) moiety with two heavy chains and two light chains, and two scFv moieties being covalently connected to either C or N terminals of the heavy or light chains. The IgG moiety may have a binding specificity to a first member of EGFR family. The scFv moiety may have a binding specificity to a second member of the EGFR family. The IgG moiety and two scFv moieties are covalently connected to be functional as a bispecific tetravalent antibody. The objectives and advantages of the disclosure will become apparent from the following detailed description of preferred embodiments thereof in connection with the accompanying drawings.
Preferred embodiments according to the present disclosure will now be described with reference to the FIGs, in which like reference numerals denote like elements.
The present disclosure This disclosure provides bispecific tetravalent antibodies with superior therapeutic properties or efficacies over the currently known anti-EGFR antibodies. In one embodiment, the antibodies target two members of EGFR family including, without limitation, EFFR and HER3. The bispecific tetravalent antibodies may inhibit both EGFR and HER3 mediated signaling simultaneously therefore overcome resistance in EGFR inhibitor or monoclonal antibody treatment.
It must be noted that as used herein and in the appended claims, the singular forms “a”, “and”, and “the” in Throughout this specification and claims, the word “comprise,” or variations such as “comprises” or “comprising,” will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers include plural referents unless the context clearly dictates otherwise.
“Antibody fragments” comprise a portion of an intact antibody, preferably the antigen-binding or variable region of the intact antibody. Examples of antibody fragments include Fv, Fab, Fab′, F(ab′)2, Fab′-SH; diabodies; linear antibodies (see U.S. Pat. No. 5,641,870, Example 2; Zapata et al., Protein Eng. 8(10): 1057-1062 (1995)); single-chain antibody molecules (e.g. scFv). While in the present description, and throughout the specification, reference is made to antibodies and various properties of antibodies, the same disclosure also applies to functional antibody fragments, e.g. dual action Fab fragments.
In one aspect, the bispecific tetravalent antibodies may include an immunoglobulin G (IgG) moiety with two heavy chains and two light chains, and two scFv moieties being covalently connected to either C or N terminals of the heavy or light chains. The IgG moiety may have a binding specificity to a first member of EGFR family. The scFv moiety may have a binding specificity to a second member of the EGFR family. The IgG moiety may provide stability to the scFv moiety. The bispecific tetravalent antibody may block signalling for both AKT and MAPK/ERK pathways and may mediate antibody dependent cell-mediated cytotoxicity (ADCC) towards cells expressing either one or both antigens. In one embodiment, the bispecific tetravalent antibody is capable of binding both antigens simultaneously. In some embodiments, the bispecific tetravalent antibody provides stronger tumour inhibition in proliferation assays in vitro and in vivo than the mono-specific antibody parental control or combination of the mono-specific antibody parental controls.
In one embodiment, the disclosure provides a bispecific tetravalent antibody having two IgG1 heavy chains, two kappa light chains, and two single chain Fv (scFv) domains. The two IgG1 heavy chains and kappa light chains form an IgG moiety with a binding specificity to a first member of the EGFR family. The two scFv domains have a binding specificity to a second member of the EGFR family, and each scFv domain is connected to the C-terminus of either of the IgG1 heavy chains by a connector with an amino acid sequence (gly-gly-gly-gly-ser)n, also known as (G4S)n, to provide a IgG1-connector connection. n is an integral of at least 1. For example, n may be 2, 3, 4, 5, 6, 7, 8, 9, 10, or 17. Each scFv domain has a structure order of N terminus-variable heavy-linker-variable light-C terminus. The linker may have an amino acid sequence of (gly-gly-gly-gly-ser)m, also known as (G4S)m. m may be an integral of at least 2 or at least 3. For example, m may be 3, 4, 5, 6, 11, or 12. In some embodiments, at least one or both of the IgG1 heavy chains are humanized or human. In some embodiments, at least one or both of the kappa light chains are humanized or human.
The EGFR family members may include EGFR, HER2, HER3, a fragment or a derivative thereof. In some embodiments, the first member of the EGFR family may be EGFR, HER2, a fragment or a derivative thereof. In some embodiments, the second member of the EGFR family may be HER3, a fragment or a derivative thereof. In one embodiment, the IgG moiety may have a binding specificity for HER3. In one embodiment, the scFv domains may have a binding specificity for EGFR. In one embodiment, the IgG moiety may have a binding specificity for HER3, and the scFv domains may have a binding specificity for EGFR. In one embodiment, the IgG moiety may have a binding specificity for EGFR. In one embodiment, the scFv domains may have a binding specificity for HER3. In one embodiment, the IgG moiety may a binding specificity for EGFR, and the scFv domains may have a binding specificity for HER3.
In some embodiments, the C terminus of one or both of the IgG1 heavy chains misses an amino acid residue. For example, the lysine reside may be deleted from the C terminus of the IgG1 chain before the connector is fused onto the C-terminus. The deletion of the lysine residue makes the IgG1-connector connection resistant to protease activity.
In some embodiments, one or both of the IgG1 heavy chains contain two mutations in the CH3 domain. For example, the two mutations may be reversion to the common residues in human CH3 domain.
In some embodiments, the IgG1 heavy chains may an amino acid sequences of or with at least 95%, 98% or 99% similarity to SEQ ID NO 7, 15, 23, 31, 39, 47, and 127. In some embodiments, the IgG1 heavy chain, connector, and scFv domain may have an amino acid sequence of or with at least 95%, 98% or 99% similarity to SEQ ID NO 56, 66, 76, 86, 98, 108, 118, and 136. In some embodiments, the kappa light chains may have an amino acid sequence of or with at least 95%, 98% or 99% similarity to SEQ ID NO 3, 11, 19, 27, 35, 43, 51, 61, 71, 81, 92, 103, 113, 123, and 131. In some embodiments, the variable light chain may an amino acid sequence of or with at least 95%, 98% or 99% similarity to SEQ ID NO 4, 12, 20, 28, 36, 44, 52, 62, 72, 82, 93, 104, 114, 124, and 132. In some embodiment, the variable heavy chain may have an amino acid sequence of or with at least 95%, 98% or 99% similarity to SEQ ID NO 8, 16, 24, 32, 40, 48, 57, 67, 77, 87, 99, 109, 119, 128, and 137.
In some embodiments, the IgG moiety has a binding specificity for HER3, and the scFv domains have a binding specificity for EGFR. In one embodiment, the IgG1 heavy chain, connector, and scFv domain have an amino acid sequence of SEQ ID NO 56, and the kappa light chain has an amino acid sequence of SEQ ID NO 51. In one embodiment, the IgG1 heavy chain, connector, and scFv domain have an amino acid sequence of SEQ ID NO 76, and the kappa light chain has an amino acid sequence of SEQ ID NO 71. In one embodiment, the IgG1 heavy chain, connector, and scFv domain have an amino acid sequence of SEQ ID NO 108, and the kappa light chain has an amino acid sequence of SEQ ID NO 103.
In some embodiments, the IgG moiety has a binding specificity for EGFR, and the scFv domains have a binding specificity for HER3. In one embodiment, the IgG1 heavy chain, connector, and scFv domain have an amino acid sequence of SEQ ID NO 66, and the kappa light chain has an amino acid sequence of SEQ ID NO 61. In one embodiment, the IgG1 heavy chain, connector, and scFv domain have an amino acid sequence of SEQ ID NO 86, and the kappa light chain has an amino acid sequence of SEQ ID NO 81. In one embodiment, the IgG1 heavy chain, connector, and scFv domain have an amino acid sequence of SEQ ID NO 98, and the kappa light chain has an amino acid sequence of SEQ ID NO 92. In one embodiment, the IgG1 heavy chain, connector, and scFv domain have an amino acid sequence of SEQ ID NO 118, and the kappa light chain has an amino acid sequence of SEQ ID NO 113. In one embodiment, the IgG1 heavy chain, connector, and scFv domain have an amino acid sequence of SEQ ID NO 136, and the kappa light chain has an amino acid sequence of SEQ ID NO 131.
The bispecific tetravalent antibodies have the activity of inhibiting cancer cell growth. In certain embodiments, an antibody of the invention has a dissociation constant (Kd) of ≤80 nM, ≤50 nM, ≤30 nM, ≤20 nM, ≤10 nM, or ≤0.1 nM for its target EGRF or HER3. The antibody may bind to both targets simultaneously. In some embodiments, the antibody binds to EGRF and HER3 with a Kd less than 50 nM. In some embodiments, the antibody binds to EGRF and/or HER3 with a Kd less than 40, 30, 25, 20, 19, 18 or 10 nM. In one embodiment, the antibody binds to EGRF with a Kd less than 30 nM and binds to HER3 with a Kd less than 30 nM. In one embodiment, the antibody binds to EGRF with a Kd less than 50 nM and binds to HER3 with a Kd less than 50 nM simultaneously.
In another aspect, the disclosure provides isolated nucleic acids encoding the bispecific tetravalent antibodies or its sub-component disclosed herein. The sub-component may be the IgG1 heavy chain, the kappa light chain, the variable light chain, or the variable heavy chain.
In a further aspect, the disclosure provides expression vectors having the isolated nucleic acids encoding the bispecific tetravalent antibody or its sub-component disclosed herein. The vectors may be expressible in a host cell. The host cell may be prokaryotic or eukaryotic.
In a further aspect, the disclosure provides host cells having the isolated nucleic acids encoding the bispecific tetravalent antibodies disclosed herein or the expression vectors including such nucleic acid sequences.
In a further aspect, the disclosure provides methods for producing bispecific tetravalent antibodies. In one embodiment, the method may include culturing the above-described host cells so that the antibody is produced.
In a further aspect, the disclosure provides immunoconjugates including the bispecific tetravalent antibodies described herein and a cytotoxic agent.
In a further aspect, the disclosure provides pharmaceutical compositions. The pharmaceutical composition may include the bispecific tetravalent antibodies or the immunoconjugates described herein and a pharmaceutically acceptable carrier. In some embodiments, the composition may further include radioisotope, radionuclide, a toxin, a therapeutic agent, a chemotherapeutic agent or a combination thereof.
In a further aspect, the disclosure provides methods of treating a subject with a cancer. In one embodiment, the method includes the step of administering to the subject an effective amount of a bispecific tetravalent antibody described herein. The cancer may include cells expressing at least two members of EGFR family including, for example, EGFR, HER2, HER3, a fragment or a derivative thereof. The cancer may be breast cancer, colorectal cancer, pancreatic cancer, head and neck cancer, melanoma, ovarian cancer, prostate cancer, and non-small lung cell cancer, glioma, esophageal cancer, nasopharyngeal cancer, anal cancer, rectal cancer, gastric cancer, bladder cancer, cervical cancer and brain cancer.
In one embodiment, the method may further include co-administering an effective amount of a therapeutic agent. The therapeutic agent may be, for example, an antibody, a chemotherapy agent, a cytotoxic agent, an enzyme, or a combination thereof. In some embodiments, the therapeutic agent may be an anti-estrogen agent, a receptor tyrosine inhibitor, or a combination thereof. In some embodiments, the therapeutic agent may be biologics. In one embodiment, the therapeutic agent may be a checkpoint inhibitor. In some embodiments, the therapeutic agent may include PD1, PDL1, CTLA4, 4-1BB, OX40, GITR, TIM3, LAG3, TIGIT, CD40, CD27, HVEM, BTLA, VISTA, B7H4, a derivative, a conjugate, or a fragment thereof. In some embodiments, the therapeutic agent may be capecitabine, cisplatin, trastuzumab, fulvestrant, tamoxifen, letrozole, exemestane, anastrozole, aminoglutethimide, testolactone, vorozole, formestane, fadrozole, letrozole, erlotinib, lafatinib, dasatinib, gefitinib, imatinib, pazopinib, lapatinib, sunitinib, nilotinib, sorafenib, nab-palitaxel, or a derivative thereof. In some embodiments, the subject in need of such treatment is a human.
In one embodiment, the disclosure provides methods for treating a subject by administering to the subject an effective amount of the bispecific tetravalent antibody to inhibit a biological activity of a HER receptor.
In one embodiment, the disclosure provides solutions having an effective concentration of the bispecific tetravalent antibody. In one embodiment, the solution is blood plasma in a subject.
A diagram of the general structure of IgG is shown in
A diagram of the representative structure of the bispecific tetravalent antibodies according to some embodiments is shown in
In addition, a control molecule 1C4 (also designated as SI-1C4) was used in some of the studies. 1C4 is a bispecific antibody against EGFR and HER3 built on the two-in-one platform described by Schaefer et. al., 2011 (Schaefer et al., Cancer Cell. 2011 Oct. 18; 20(4):472-86). IC4 has a similar structure to a monoclonal antibody. The molecule can bind to either EGFR or HER3 on each Fab arm, but cannot engage both targets simultaneously on each Fab arm.
Variable light chain, variable heavy chain and single chain Fv (scFv) DNA fragments were generated by gene synthesis through an outside vendor. Human Gamma-1 heavy chain and human kappa light chain DNA fragments were generated by gene synthesis through an outside vendor. The fragments were assembled together by DNA ligation using restriction sites and cloned into a vector that is designed for transient expression in mammalian cells. The vector contains a strong CMV-derived promoter, and other upstream and downstream elements required for transient expression. The resulting IgG expression plasmids were verified as containing the expected DNA sequences by DNA sequencing.
Transient expression of the antibody constructs was achieved using transfection of suspension-adapted HEK293F cells with linear PEI as described elsewhere (see CSH Protocols; 2008; doi:10.1101/pdb.prot4977). Antibodies were purified from the resulting transfection supernatants using protein affinity chromatography and size exclusion chromatography if needed. Protein quality is analysed by Superdex 200 column. Protein used for all the assays have a purity of greater than 90%.
The bispecific antibody may be used for the treatment of cancer types with EGFR and HER3 co-expressions, including without limitation colon cancer, head and neck squamous cell carcinoma, lung cancer, glioma, pancreatic cancer, nasopharyngeal cancer and other cancer types.
The bispecific antibody is of tetravalent dual specificity. The example antibody may include an IgG and two scFv, which provides two different binding specificities compared to mono-specific antibody IgG. The IgG component provides stability and improved serum half-life over other bispecific antibodies that used only scFv such as BiTE technology (Lutterbuese et al., Proceedings of the National Academy of Sciences of the United States of America 107.28 (2010): 12605-12610. PMC. Web. 2 Dec. 2014) and others (for example, U.S. Pat. No. 7,332,585B2). It is also capable of mediating ADCC while those without Fc component cannot (for example, U.S. Pat. No. 7,332,585B2). The tetravalent dual specificity nature provides the bispecific antibody a simultaneous binding capability over some other bispecific antibodies, which may only bind one antigen at a time (Schanzer et al, Antimicrob. Agents Chemother. 2011, 55(5):2369; EP272942A1).
For the convenient of narration, the sequences of or related to the bispecific antibodies are summarized in TABLE 1 herein below.
While The following examples are provided by way of illustration only and not by way of limitation. Those of skill in the art will readily recognize a variety of non-critical parameters that could be changed or modified to yield essentially the same or similar results.
SI-1X4.2 is a modification of SI-1X4 molecule and contained 5 amino acid changes as follows: V71A, T75S, N76S, A93T and S107T using the Kabat numbering system. Some of these changes especially positions 75, 76 and 93 potentially made interaction with antigen even though these are not in the CDR loops and are essential for binding and activity.
Monomeric EGFR extracellular domain binding was measured in a biolayer interferometry (BLI) binding assay on a BLItz instrument (ForteBio, Inc.). 25 μg/mL of SI-1C3, SI-1C4, SI-1C6, SI-1X1, SI-1X2, SI-1X5, and SI-1X6 were diluted in PBS and captured on anti-hulgG Fc BLItz biosensor tips for 120 seconds. Tips were washed for 30 seconds in PBS and moved to an EGFR (ProSpec Bio, PKA-344) sample for binding at 588 nM. Binding of EGFR ECD to the tips was recorded as biolayer interferometry signals (Δnm) over an association time of 120 seconds. Tips were moved to PBS and dissociation was observed for 240 seconds (*SI-1C6 dissociation time of only 120 seconds observed).
Since SI-1C3 and SI-1X2 share their EGFR binding domain displayed as a Fab, their binding profiles are similar and stronger than the scFv form displayed on SI-1X1 (
Bispecific binding to EGFR and Her3 extracellular domains was measured in a biolayer interferometry (BLI) binding assay on a BLItz instrument (ForteBio, Inc.). 200 nM of SI-1C1, SI-1C3, SI-1C4, SI-1C6, SI-1X1, SI-1X2, SI-1X3, SI-1X4, SI-1X5, and SI-1X6 were diluted in 1X Kinetics Buffer (ForteBio, Inc.) and captured on anti-hulgG Fc BLItz biosensor tips for 120 seconds. Tips were washed in KB for 30 seconds and moved to an EGFR sample (ProSpec Bio, PKA-344) for binding at 200 nM. Binding of EGFR ECD to the tips was recorded as biolayer interferometry signals (Δnm) over an association time of 120 seconds. Tips were moved to KB and dissociation was observed for 60 seconds. The process was repeated with Her3 ECD sample (Sino Biological, 10201-H08H-10) at 200 nM for 120 seconds and a similar dissociation step of 60 seconds in KB.
As observed earlier, SI-1X3 and SI-1X4 were unable to bind a monomeric form of EGFR in a BLI assay (
ELISA was performed using dimeric EGFR ECD reagent, SI-2C1, fused to rabbit Fc created in house. EGFR was coated onto Maxisorp immunoplates (Nunc) at 3 μg/mL in PBS at 4° C. overnight. Plates were blocked in PBS with 3% BSA and 0.05% Tween20 for 2 hours at room temperature. Antibodies were captured at starting at 10 ug/mL except for SI-105, SI-1X3, and SI-1X4 which started at 50 μg/mL for (reported in nM), all with 3× dilutions in PBST (1% BSA) for 1 hour at room temperature. Goat αhuman IgG-HRP antibody (Jackson ImmunoResearch, 109-035-098) was used for detection of the Fc portion of the antibodies at 1:2000 dilution in PBST (1% BSA) and developed in TMB (Thermo Scientific) for 5 minutes with 2M H2SO4 as a stop solution. 3 washes with PBST (1% BSA) were performed between each step. All data points were performed in triplicate and collected at 450 nm (
Kinetics determined using ForteBio Octet Red96 instrument with anti-human Fc sensors (ForteBio, AHC #18-5060). Binding experiments performed at 30° C. with 1000 RPM mixing. EGFR protein is extracellular domain (Met 1-Ser 645) of human EGFR with a C-terminal polyhistidine tag. All samples diluted in 10X Kinetics Buffer (ForteBio #18-5032). 105.2, 1X6 and 1X4.2 were loaded onto 8 sensors at 10 μg/ml each for 300 seconds followed by a Baseline for 60 seconds in 10X Kinetics Buffer. Association with EGFR protein was performed for 300 seconds with each sensor in a single concentration of EGFR protein (300, 100, 33.33, 11.11, 3.705, 1.235, 0.4116 and 0 nM). Dissociation was then performed in 10X Kinetics Buffer for 900 seconds. A typical association and dissociation trace for 105.2 and 1X4.2 is shown in
Data analysis was performed using ForteBio Data Analysis Software v9.0. Software curve-fitting was performed and the four most optimal curve fits for each 105.2 (TABLE 2), 1X4.2 (TABLE 3) and 1X6 (TABLE 4) were used and averaged to determine KD, k(on) and k(dis). The average KD for SI-105.2 and SI-1X4.2 were 19.2 nM and 18.4 nM respectively. The average KD for SI-1C6 was 3.04 nM 105.2 and 1X4.2 contained five amino acid changes as compared to 105 and 1X4 as described in example 1. These changes accounted for improved binding to EGFR ECD when compared to data generated for 105 and 1X4 in
The bispecific antibodies SI-1X1, SI-1X2, SI-1X3, SI-1X4, SI-1X5, and SI-1X6, as well as an isotype control were tested for binding to the tumor cell lines, A431 (epidermoid carcinoma, ATCC CRL-1555) and BxPC3 (pancreatic adenocarcinoma, ATCC CRL-1687) by flow cytometry. Cells were grown in RPMI-1640 medium containing 10% fetal bovine serum and were harvested for analysis while in exponential growth phase. Aliquots of 5×106 cells were washed once in PBS, then resuspended in 250 μl of PBS+1% bovine serum albumin (BSA) and incubated at 4° C. for 15 minutes to block membranes from non-specific binding. 250 μl of antibody, diluted to 10 μg/ml in PBS/1% BSA, was added to each sample for a final antibody concentration of 5 μg/ml. Cells were incubated in primary antibody for 1 hour at 4° C. with mixing. Cells were then washed twice with 1 ml PBS/1% BSA and then resuspended in 500 μl of PE-conjugated mouse-anti-human IgG-Fc and incubated at 4° C. with mixing for 45 minutes. Samples were again washed twice with 1 ml PBS/1% BSA, resuspended in 300 ml PBS and analyzed using a FACScalibur flow cytometer. For each sample, 10000 events were collected in the FL-2 channel. Histograms were generated using FCS Express software and SI-1X histograms were overlaid with histograms from the isotype control staining. All six bispecific antibodies displayed histogram shifts with respect to control staining indicating cell binding. This data is displayed in
The bispecific antibody, SI-1X4.2, monospecific antibodies, SI-105.2 and SI-1C1, as well as an isotype control were tested for binding to the tumor cell lines, A431 (epidermoid carcinoma, ATCC CRL-1555) (
To assess the growth inhibitory potential of anti-Her3/EGFR bispecific antibodies, the effect on proliferation of A431 cells (ATCC CRL-1555, Manassas, Va.) which are an epidermoid carcinoma tumor line was tested. The effect on proliferation of BxPC3 (ATCC CRL-1687, Manassas, Va.), a pancreatic adenocarcinoma tumor line was also tested. For each line, cells were seeded into 96-well tissue culture plates at a density of 6000 cells/well in 100 μl RPMI-1640 medium containing 1% fetal bovine serum. After 4 hours, test antibodies were added at various concentrations, ranging from 0.0015 nM to 100 nM. Cells were cultured in the presence of test antibodies for 72 hours. To each well, 20 μl of MTS reagent (Promega, Madison, Wis.) was added and cells were incubated at 37° C. for 2 hours. MTS is readily taken up by actively proliferating cells, reduced into formazan (which readily absorbs light at 490 nm), and then secreted into the culture medium. Following incubation, OD490 values were measured using a BioTek (Winooski, Vt.) ELx800 absorbance reader. OD490 values for control cells (treated with medium only) were also obtained in this manner at the time of antibody addition in order to establish baseline metabolic activity. Proliferation may be calculated by subtracting the control baseline OD490 from the 72 hour OD490. Data from antibody titrations was expressed at % of control population according to the following formula: % of control proliferation=(test proliferation/control proliferation)*100.
The effects of various bispecific anti-Her3/anti-EGFR antibodies on A431 cell proliferation are shown in
These molecules were also tested for antiproliferative effects in the BxPC3 cell line (
To assess the growth inhibitory potential of anti-Her3/EGFR bispecific antibodies, the effect on proliferation of FaDu (nasopharyngeal squamous cell carcinoma line, ATCC HTB-43) and A431 (epidermoid carcinoma, ATCC CRL-1555) cells were tested. Cells were seeded into 96-well tissue culture plates at a density of 6000 cells/well in 100 μl RPMI-1640 medium containing 1% fetal bovine serum. After 4 hours, test antibodies were added at various concentrations, ranging from 0.0015 nM to 100 nM. Cells were cultured in the presence of test antibodies for 72 hours. To each well, 11 μl of alamar blue reagent (Thermo Scientific) was added and cells were incubated at 37° C. for 2 hours. Alamar blue is readily taken up by actively proliferating cells, reduced, and then secreted into the culture medium. The reduced form of alamar blue is strongly fluorescent. Following incubation, fluorescence was measured using a Molecular Devices (Sunnyvale, Calif.) FilterMax F5 multi-mode plate reader using an excitation wavelength of 535 nm and an emission wavelength of 595 nm. Fluorescence values for control cells (treated with medium only) were also obtained in this manner at the time of antibody addition in order to establish baseline metabolic activity. Proliferation may be calculated by subtracting the control baseline fluorescence from the 72-hour fluorescence values. Data from antibody titrations was expressed at % of control population according to the following formula: % of control proliferation=(test proliferation/control proliferation)*100.
The effects of SI-105.2 and SI-1X4.2 on Fadu and A431 cell proliferation are shown in
The ability of SI-1X antibodies to mediate cellular cytotoxicity against several tumor cell lines was tested. Whole blood was obtained from normal, healthy volunteers. Blood was diluted with an equal volume of phosphate buffered saline (PBS). 20 ml aliquots of diluted blood were carefully layered over 15 ml Ficol Pacque PLUS (GE Life Sciences cat #17-1440-02; Pittsburgh, Pa.). Tubes were centrifuged at 300 g for 40 minutes with no brake. Following centrifugation most of the plasma layer was carefully aspirated and the buffy coat (containing PBMC) was carefully removed with a pipet in the smallest possible volume. PBMCs were pooled in 50 ml tubes and PBS added to bring each tube up to 50 ml. Tubes were centrifuged at 1300 RPM for 10 minutes and the supernatant was carefully aspirated. Cells were resuspended in 40 ml PBS and centrifuged again. The process was repeated for a total of 2 washes. Following the final wash, cells were resuspended in 30 ml RPMI-1630+10% FBS and incubated overnight at 37° C., 5% CO2.
Target cells tested were the head and neck squamous cell carcinoma line, FaDu (ATCC HTB-43, Manassas, Va.) and the non-small cell lung adenocarcinoma cell line, NCI-H1975 (ATCC CRL-5908, Manassas, Va.). Target cells were labeled with calcein as follows. Cells were grown as monolayers and were detached by incubation with accutase. Cells were washed twice in RPMI with no serum. 1 ml of cells at 4×106 cells/ml was mixed with 1 ml RPMI (no serum)+20 μM calcein AM (Sigma cat #C1359; St. Louis, Mo.). Cells were incubated at 37° C. for 30 minutes, with gentle mixing every 10 minutes. Following labeling, cells were washed twice with 14 ml RPMI+10% FBS+2.5 mM probenecid (assay medium). Probenecid (Sigma cat #P8761; St. Louis, Mo.) is an anionic transporter inhibitor and is known to reduce spontaneous release of intracellular calcein. Cells were resuspended in 20 ml assay medium and allowed to recover for 2 hours at 37° C., 5% CO2. Cells were then washed once with assay medium and diluted to 200,000 cells/ml. Aliquots of 50 μl (10,000 cells) calcein-labeled cells were aliquoted to 96-well round-bottom plates. 50 μl of antibody (at 3X final concentration) was added to cells and allowed to bind for 40 minutes on ice. PBMCs from the previous day were centrifuged at 300 g for 5 minutes, resuspended in 20 ml fresh assay medium, counted, and diluted to 6×106 cells/ml. 50 μl PBMC (300,000) were added to each well and plates incubated at 37° C., 5% CO2 for 4 hours. Each antibody was titrated in triplicate via 10-fold serial dilutions, starting at 50 nM and going down to 0.00005 nM. Control wells were also set up containing labeled target cells in the absence of antibody and effector cells in order to measure maximal and spontaneous calcein release.
At the end of the 4-hour incubation, 50 μl of assay medium containing 8% IGEPAL CA-630 (Sigma cat #18896; St. Louis, Mo.) was added to control wells containing labeled target cells only (to measure the maximal calcein release). 50 μl of assay medium was added to all the other wells to bring the total volume to 200 μl per well. Plates were centrifuged at 2000 RPM for 10 minutes and 150 μl supernatant was carefully transferred to V-bottom 96-well plates. These plates were centrifuged at 2000 RPM for an additional 10 minutes and 100 ml supernatant was carefully transferred to black, clear-bottom 96-well plates. Calcein in the supernatant was quantitated by measuring the fluorescence of each sample using an excitation wavelength of 485 nM and an emission wavelength of 535 nM. The percentage of specific lysis was calculated as follows:
% specific lysis=[(test sample value−spontaneous release)/(maximal release−spontaneous release)]*100
The data is shown in
Protein Thermal Shift Study was performed for protein thermal stability analysis. Protein melt reactions were set up using Protein Thermal Shift Buffer™ and the Protein Thermal Shift Dye™ (Applied Biosystems). In brief, the 20 ul reaction mixture contains 5 ug protein, 5 ul Protein Thermal Shift Buffer™ and 2.5μ 8× diluted Protein Thermal Shift™ Dye. For the negative control, PBS was used instead. The reaction mixture was added into MicroAmp Optical Reaction Plate and sealed with MicroAmp Optical Adhesive Film. Each sample consisted of 4 repeats. The protein melt reactions were run on Applied Biosystem Real-Time PCR System from 25-90° C. in 1% increment and then analyzed by Protein Thermal Shift Software™.
Serum stability of the molecules SI-105.2, SI-1C6.2, SI-1X4.2, and SI-1X6.4 was determined by comparative binding to monomeric EGFR ECD by ELISA after incubation at 100 μg/mL in 95% human serum (Atlanta Biologics, S40110) at 37° C. for Days 0, 3, and 7 time points with an extra time point of 55° C. on Day 7 to provide a known condition where degradation occurs. ELISA plates were coated with monomeric EGFR ECD (SI-2R4) at 3 μg/mL in PBS at 4° C. overnight. Coated ELISA plates were blocked with 3% BSA PBST for 2 hours at 25° C. and then washed 3 times with PBST. SI-1C6.2 and SI-1X6.4 were diluted 1:10 with 1% BSA PBST and diluted 4x across the plate. SI-105.2 and SI-1X4.2 were diluted 1:2 with 1% BSA PBST and diluted 4× across the plate and incubated at 25° C. for 1 hour. 3 more washes with PBST were performed before antigen capture with 1 μg/mL Her3 ECD Rabbit IgG1 (SI-1R1) for 1 hour at 25° C. in 1% BSA PBST. 3 more washes with PBST were performed before goat anti-rabbit IgG-HRP (Bio-Rad 172-1019) secondary antibody was applied at 1:5000 dilution in 1% BSA PBST at 25° C. for 1 hour. 3 final washes with PBST before development with 100 μl Pierce 1-step Ultra TMB ELISA (Pierce, 34028) for 10 minutes with a final quench of 100 μl 2M H2SO4. Plates were read at 450 nm. ELISA data was plotted and curves created using GraphPad Prism 6.
Results of the ELISA are reported by EC50 on
To test their half-life in vivo, pharmacokinetic experiments were performed in SD rats. A single, intravenous tail vein injection of bispecific Abs (1C6 10 mg/kg, 1X6 10 mg/kg, 1X2 10 mg/kg, 1X4 32 mg/kg) were given to groups of 4 female rats randomized by body weight (190-212 g range). Blood (˜150 μL) was drawn from the orbital plexus at each time point, processed for serum, and stored at −80° C. until analysis. Study durations were 28 days.
Antibody concentrations were determined using three ELISA assays. In assay 1 (EGFR ECD coated ELISA), recombinant EGFR-rabbit Fc was coated to the plate, wells were washed with PBST (phosphate buffered saline with 0.05% Tween) and blocked with 1% BSA in PBST. Serum or serum diluted standards were then added, followed by PBST washing, addition of HRP labeled rabbit-anti-human IgG (BOSTER), and additional PBST washing. TMB was then added and the plates were incubated 2.5 minutes in the dark. Color reaction was stopped by adding 2M sulfuric acid. Plate was read at 450 nm wavelength. For assay 2 (Hera coated ELISA), serum was detected using a similar ELISA, but recombinant HER3-His was used as capture reagent. For assay 3 (Sandwich ELISA), recombinant HER3-His was coated, serum or serum diluted standard were added, followed by PBST washing, addition of EGFR-rabbit Fc in PBST, and additional PBST washing. HRP labeled goat-anti-rabbit IgG (BOSTER) was then added. PK parameters were determined with a non-compartmental model.
The example tested the activity of SI-1X2, SI-1X4.2 and SI-1X6 of concomitant blockade of EGFR, HER3 in preclinical models of Fadu (head and neck squamous cell carcinoma xenograft model) and compared their potency with cetuximab and cetuximab in combination with an anti-HER3 antibody.
All mouse studies were conducted through Institutional Animal care and used committee-approved animal protocols in accordance with institutional guidelines. Six-week-old female Balb/c Nude mice were purchased from Beijing Vital River Laboratories and housed in air-filtered laminar flow cabinets with a 12-hour light cycle and food and water ad libitum. The size of the animal groups was calculated to measure means difference between placebo and treatment groups of 25% with a power of 80% and a P value of 0.01. Host mice carrying xenografts were randomly and equally assigned to either control or treatment groups. Animal experiments were conducted in a controlled and non-blinded manner. For cell line-derived xenograft studies, mice were injected subcutaneously with 2×1C6 Fadu suspended 150 μl of culture medium per mouse.
Once tumors reached an average volume of 100-250 mm3, mice were randomized into 9 groups, with 6 mice per group. Vehicle Control, 1C6 (25 mg/kg), 1C4 (25 mg/kg), 1C6+1C1 (25 mg/kg+50 mg/kg), SI-1X2 (25 mg/kg), SI-1X6 (10 mg/kg), SI-1X6 (25 mg/kg), and SI-1X4.2 (10 mg/kg) SI-1X4 (25 mg/kg). All test articles were administered once weekly via intravenous injection. Tumors were measured by digital caliper over the entire treatment period every 3 days and the volume was determined using the following formula: ½×length×width2. The body weight of mice were recorded before the first dose and followed by every week during the treatment period and recovery period.
All the test groups of SI-1X2, SI-1X6 and SI-1X4.2 and SI-1X6 combination yielded significantly tumor growth inhibition compared to positive control of SI-1C6 excluding the low dose SI-1X4.2 10 mg/kg group (
The term “effective amount” refers to an amount of a drug effective to achieve a desired effect, e.g., to ameliorate disease in a subject. Where the disease is a caner, the effective amount of the drug may inhibit (for example, slow to some extent, inhibit or stop) one or more of the following example characteristics including, without limitation, cancer cell growth, cancer cell proliferation, cancer cell motility, cancer cell infiltration into peripheral organs, tumor metastasis, and tumor growth. Wherein the disease is a caner, the effective amount of the drug may alternatively do one or more of the following when administered to a subject: slow or stop tumor growth, reduce tumor size (for example, volume or mass), relieve to some extent one or more of the symptoms associated with the cancer, extend progression free survival, result in an objective response (including, for example, a partial response or a complete response), and increase overall survival time. To the extent the drug may prevent growth and/or kill existing cancer cells, it is cytostatic and/or cytotoxic.
With respect to the formulation of suitable compositions for administration to a subject such as a human patient in need of treatment, the antibodies disclosed herein may be mixed or combined with pharmaceutically acceptable carriers known in the art dependent upon the chosen route of administration. There are no particular limitations to the modes of application of the antibodies disclosed herein, and the choice of suitable administration routes and suitable compositions are known in the art without undue experimentation.
Although many forms of administration are possible, an example administration form would be a solution for injection, in particular for intravenous or intra-arterial injection. Usually, a suitable pharmaceutical composition for injection may include pharmaceutically suitable carriers or excipients such as, without limitation, a buffer, a surfactant, or a stabilizer agent. Example buffers may include, without limitation, acetate, phosphate or citrate buffer. Example surfactants may include, without limitation, polysorbate. Example stabilizer may include, without limitation, human albumin.
Similarly, persons skilled in the art have the ability to determine the effective amount or concentration of the antibodies disclosed therein to effective treat a condition such as a cancer. Other parameters such as the proportions of the various components in the pharmaceutical composition, administration does and frequency may be obtained by person skilled in the art without undue experimentation. For example, a suitable solution for injection may contain, without limitation, from about 1 to about 20, from about 1 to about 10 mg antibodies per ml. The example dose may be, without limitation, from about 0.1 to about 20, from about 1 to about 5 mg/Kg body weight. The example administration frequency could be, without limitation, once per day or three times per week.
While the present disclosure has been described with reference to particular embodiments or examples, it may be understood that the embodiments are illustrative and that the disclosure scope is not so limited. Alternative embodiments of the present disclosure may become apparent to those having ordinary skill in the art to which the present disclosure pertains. Such alternate embodiments are considered to be encompassed within the scope of the present disclosure. Accordingly, the scope of the present disclosure is defined by the appended claims and is supported by the foregoing description.
This application is continuation-in-part of U.S. patent application Ser. No. 15/119,694, filed Aug. 17, 2016, which is a National Stage Entry of PCT/US15/66951, filed Dec. 19, 2015, which claims priority over U.S. Provisional Application No. 62/095,348, filed Dec. 22, 2014, titled “BISPECIFIC ANTIBODIES,” the disclosure of which are hereby incorporated by reference in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62095348 | Dec 2014 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15119694 | Aug 2016 | US |
| Child | 17143204 | US |
