Patent Application
20200390902
The present disclosure relates to means and methods for specific delivery of drugs to diseased cells. More particularly, the present invention relates to antibody-drug conjugates and methods of using the same:
Antibody-drug conjugates (ADCs) comprise an antibody that is specific for a disease antigen, a linker and one or more drug molecules. The goal is to utilize the antibody as a means of specific delivery of the drug to diseased cells. Theoretically this should decrease systemic exposure to the drug and allow for use of a lower dose to avoid the severe side effects of drug therapy. In cancer, the approach employs an antibody-drug conjugate to target a tumor associated antigen and elicit cancer-specific cytotoxicity. To date there have been three ADCs approved by the US FDA for cancer treatment and many more are now in the development stage. The efficacy of any ADC is dependent on three factors; the antibody, the attached drug, and the linker used to connect them. While each of these factors is of import, with the growth of interest in ADCs for cancer therapy, the use of specific drugs and linkers has become more routine. Thus, the specificity of the tumor-associated antigen and the antibody used to target it are now, perhaps, the primary obstacles towards the development of novel ADCs.
Human aspartyl (asparaginyl) β-hydroxylase (HAAH), also known as aspartate β-hydroxylase (ASPH) is an embryonic/developmental protein, which is downregulated in normal cells after birth but overexpressed on the surface of many malignant cells. It has been demonstrated to be sufficient to induce cancer cell proliferation, motility, and invasiveness. The enzyme hydroxylates important residues in the NOTCH protein altering signal transduction pathways that lead to increased growth and metastatic potential. Increased levels of HAAH have been detected by immunohistochemistry in a diverse array of solid and hematological cancers (n>20), including: liver, bile duct, brain, breast; colon, prostate, ovary, pancreas, and lung cancers as well as various leukemias. HAAH is not found in measurable quantities in normal tissue (n>500) including normal adjacent tissue within cancer biopsy specimens or in benign proliferative disorders.
There is a need in the art for developing an approach for depleting, inhibiting and/or killing the growth and spread of HAAH-expressing cells involved in cancers. Accordingly, there is a need for anti-HAAH antibody-drug conjugates that are constructed in such a manner so as to be capable of having a clinically useful cytotoxic, cytostatic, gar immunosuppressive effect on HAAH-expressing cells, particularly without exerting undesirable effects on non-HAAH-expressing cells. Such compounds would be useful therapeutic agents against cancers that express HAAH.
The present disclosure relates to antibody-drug conjugates.
The present invention further relates to methods of making antibody-drug conjugates.
One embodiment of the present invention encompasses methods of treating cancer comprising contacting a cancer tumor with an antibody-drug conjugate.
An embodiment of the present invention encompasses a fully human anti-HAAH antibody conjugated to an anti-cancer drug. In some embodiments of the invention the cancer drug is auristatin or an auristatin derivative. In some embodiments of the invention the auristatin derivative is monomethyl auristatin E (MMAE) or monomethyl auristatin F (MMAF). In some embodiments of the invention the cancer drug is a maytansinoid or a derivative thereof. In some embodiments of the invention the maytansinoid is mertansine/emtansine (DM1) or ravtansine/soravtansine (DM4), In some embodiments of the invention the cancer drug is a duocarmycin or a derivative thereof. In some embodiments of the invention the duocarmycin is duocarmycin SA (DUO). In some embodiments of the invention the antibody is separated from the cancer drug by at least one linker. In some embodiments of the invention the linker is selected from a non-cleavable linker, a cleavable linker, and a combination thereof. In some embodiments of the invention, the non-cleavable linker is selected from maleimidocaproyl (MC). In some embodiments of the invention, the cleavable linker is selected from valine citruline (vc) combined with para-amino benzyl alcohol (PABA). In some embodiments of the invention, the fully human anti-ASPH antibody has a light chain comprising three complementarity determining regions CDR1, CDR2, and CDR3, where the amino acid sequence of CDR1, CDR2, and CDR3 have the amino acid sequence set forth in SEQ ID NO: 3 SEQ ID NO: 4; and SEQ ID NO: 5, In some embodiments of the invention, the anti-ASPH antibody has a light chain amino acid sequence as set forth in SEQ H) NO: 2, and a heavy chain amino acid sequence set forth in SEQ ID NO: 1. In some embodiments of the invention, SNS622 is the fully human anti-HAAH antibody.
The present invention farther provides pharmaceutical compositions comprising antibody-drug conjugates of the invention and a pharmaceutically acceptable medium.
Also provided herein are treatment methods comprising the administration of compositions comprising the antibody-drug conjugates of the invention in a pharmaceutically acceptable medium to a patient in need of treatment.
Embodiments of the present invention encompass antibody-drug conjugates and derivatives and methods relating to the use of such conjugates to treat HAAH-expressing cancers. The antibody, or other targeting moiety in the antibody-drug conjugate, binds to HAAH. A drug conjugated to the antibody or targeting moiety exerts a cytotoxic or cytostatic effect on HAAH-expressing cells to treat or prevent recurrence of HAAH-expressing cancers.
One embodiment of the present invention encompasses a hilly human anti-HAAH antibody conjugated to anti-cancer drug maytansinoid (DM1).
An embodiment of the present invention encompasses a fully human anti-HAAH antibody conjugated to monomethyl auristatin E (MMAE).
An embodiment of the present invention encompasses a fully human anti-HAAH antibody conjugated to duocarmycin (DUO).
An embodiment of the present invention encompasses a method of manufacturing an ASPH-directed ADC in which using a thiol directed linker-drug conjugate to yield a DAR of 2-8.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, methods and materials used are now described. All publications mentioned herein are incorporated herein by reference in their entirety.
In the present disclosure, “HAAH” and “ASPH” are used interchangeably and stand for human aspartyl (asparaginyl) beta-hydroxylase, ASPH is expressed by the majority of malignant neoplasms, such as cancers from the liver, bile duct, brain, breast, colon prostate, ovary, pancreas, and lung, and various leukemias.
In the present disclosure, “PAN-622” and “SNS622” are used interchangeably and stand for a high-affinity, fully-humanized monoclonal antibody against human aspartyl (asparaginyl) beta-hydroxylase. The PAN-622 antibody was initially developed and characterized by Yeung Y. A., et al. (2007, “Isolation and Characterization of Human Antibodies Targeting Human Aspartyl (asparaginyl) beta-Hydroxylose,” Hum. Antibodies 16: 163). The amino acid sequences of the light chain, heavy chain, and light chain complementarity determining regions for the PAN-622 antibody are presented in Table I, below:
In the present disclosure, the preparation and testing of ADCs comprising SNS622 are disclosed. These ADCs were prepared by conjugating the high-affinity, fully humanized anti-HAAH antibody SNS622 to mertansine (DM1), monomethyl auristatin E (MMAE), or duocarmycine (DUO), using, as linkers maleimidocaproyl (MC), valine-citrulline (vc), para-amino benzyl alcohol (PAB), a 4-unit polyethylene glycol (PEG4), or a combination of at least two of these linkers
In the present disclosure, “MIA-PaCa-2 HAAH” cells and “MIA-PaCa-2 ASPH” cells are used interchangeably and refer to MIA-PaCa-2 cells that have been transformed to overexpress ASPH.
In the present disclosure “MIA-PaCa-2 EV” cells are MIA-PaCa-2 cells transduced with an empty lentiviral vector.
For simplicity and illustrative purposes, the principles of the present invention are described by referring to various exemplary embodiments thereof. Although the preferred embodiments of the invention are particularly disclosed herein, one of ordinary skill in the art will readily recognize that the same principles are equally applicable to, and can be implemented in other systems, and that any such variation would be within such modifications that do not part from the scope of the present invention. Before explaining the disclosed embodiments of the present invention in detail, it is to be understood that the invention is not limited in its application to the details of any particular arrangement shown, since the invention is capable of other embodiments. The terminology used herein is for the purpose of description and not of limitation. Further, although certain methods are described with reference to certain steps that are presented herein in certain order, in many instances, these steps may be performed in any order as would be appreciated by one skilled in the art, and the methods are not limited to the particular arrangement of steps disclosed herein.
The present disclosure provides antibody-drug conjugates and derivatives and methods relating to the use of such conjugates to treat HAAH-expressing cancers. The antibody, or other targeting moiety in the antibody-drug conjugate, binds to HAIR A drug conjugated to the antibody or targeting moiety exerts a cytotoxic or cytostatic effect on HAAH-expressing cells to treat or prevent recurrence of HAAH-expressing cancers.
A suitable cytotoxic or cytostatic agent useful in the preparation of an ADC can be any agent approved by a healthcare regulatory agency such as the Food and Drug Administration (TDA) in the U.S.A Medicines & healthcare Products Regulatory Agency (MHRA) in the United Kingdom, Therapeutic Goods Administration in Australia, Health Canada in Canada, or European Medicines Agency (EMA) in Europe.
Suitable cytotoxic agents can be, for example, an auristatin, a DNA minor groove binding agent, a DNA minor groove alkylating agent, an enediyne, a lexitropsin, a duocarmycin, taxane, a puromycin, a dolastatin, a maytansinoid, and a vinca alkaloid. In specific embodiments, the drug is cytotoxic agent is APP, MMAF, MMAE, AEB, AEVB, auristatin E, paclitaxel, docetaxel, CC-1065, SN-38, topotecan, morpholino-doxorubicin, rhizoxin, cyanomorpholino-doxambicin, dolastatin-10, echinomycin, combretatstatin, chalicheamicin, maytansine, DM1, or netropsin. Other suitable cytotoxic agents include anti-tubulin agents, such as an auristatin, a vinca alkaloid, a podophyllotoxin, a taxane, a baccatin derivative, a cryptophysin, a maytansinoid, a combretastatin, or a dolastatin. In specific embodiments, the antitubulin agent is AFP, MMAF, MMAE, AEB, AEVB, auristatin E, vincristine, vinblastine, vindesine, vinorelbine, VP-16, camptothecin, paclitaxel, docetaxel, epothilone epothilone B, nocodazole, colchicines, colcimid, estramustine, cemadotin, discodermolide, maytansine, DM-1, or eleutherobin.
Other agents include, for example, ganciclovir, etanercept, cyclosporine, tacrolimus, rapamycin, cyclophosphamide, azathioprine, mycophenolate mofetil, methotrexate, cortisol, aldosterone, dexamethasone, a cyclooxygenase inhibitor, a 5-lipoxygenase inhibitor, or a leukotriene receptor antagonist.
Linkers accommodate different conjugation chemistries on both, antibodies and cytotoxic agents. Linkers contribute to the stability of the ADC complex in systematic circulation and dictate the cytotoxic agent release mechanisms once internalized and trafficked into designated cellular locations. Linkers are commonly categorized as cleavable linkers or non-cleavable linkers, based on their release mechanisms. Examples of cleavable linkers are peptide linkers, β-glucuronide linkers, pH-sensitive linkers, and Glutathione-sensitivity linkers.
Linkers should possess two crucial characteristics. First, linkers should possess stability in plasma for an extended period of time. In this manner the ADCs can reach and localize to the cancer cell in the original formation. After internalization, the linkers play a role as a trigger for releasing the cytotoxic drugs when the ADCs face particular circumstances in the cancer cells and the released cytotoxic drugs then bind to their targets. With the particular microenvironment of tumor cells and the delivery mechanism selected, the active formation of the cytotoxic drug may be efficiently released from ADCs by fracturing the designed linkers inside the target cells. The stability and rupturing capacity of linkers affect the overall pharmacokinetics (PK) properties, toxicities and therapeutic indexes of ADCs.
Linkers are classified in different categories according to the mechanism of drug release and their stability in circulation. Cleavable linkers rely on the physiological environment, such as there being high glutathione concentrations, low pH, and special protease, which could assist the linkers in enabling chemical or biochemical reactions by way of hydrolyzation or proteolysis. Non-cleavable linkers depend on the degradation of the monoclonal antibody after internalization of the ADC within the lysosomes and endosomes to generate the metabolites containing the active cytotoxic drugs with or without a portion of the linkers.
Each release strategy must account for many factors: the various activities of cytotoxic drugs, the characteristics of monoclonal antibodies, the nature and intracellular processing of the target antigen, and the particular disease, Optimal linkers designed to conjugate the cytotoxic drugs to monoclonal antibodies must meet the particular requirements.
Many non-cleavable linkers have been explored in the development of ADCs. The greatest advantage of non-cleavable linkers is their increased plasma stability. Examples of non-cleavable linkers are N-succinimidyl-4-(N-maleimidomethyl) cyclohexane-1-carboxylate (SMCC) linkers, and maleimidocaproyl linkers.
Cleavable linkers are stable in the blood circulation for a long period of time, and are efficiently released in the tumor microenvironment. Chemically labile linkers include acid-cleavable linkers and reducible linkers. Hydrazone and disulfide linkers are examples of acid-cleavable linkers. Enzyme cleavable linkers take advantage of the abundance of hydrolytic enzymes with the specificity to recognize the sequences of peptides or patterns of carbohydrate in order to degrade peptides and carbohydrates.
Peptide-based linkers are designed to keep ADCs intact in systemic circulation, and allow easy release of the cytotoxic drugs upon cleavage by specific intracellular proteases, such as cathepsin B. Examples of peptide-based linkers are valine-citrulline (Val-Cit) dipeptide phenylalanine-lysine (Phe-Lys) dipeptide linker, and β-glucuronide linker.
We have developed a fully human antibody against HAAH, PAN-622, which displays exquisite specificity for cancer. Here we explore PAN-622 drug conjugates for ultimate use in treating both hematological and solid tumors. PAN-622 was conjugated to three different drugs: a maytansinoid (DM1), monomethyl auristatin E (MMAE), or duocarmycin (DUO). DM1 was conjugated via a non-cleavable thioether linker, while MMAE and DUO were conjugated using valine-citruline containing linkers that are cleavable by cathepsin B in the endosomal compartment. Conjugation of drugs to the PAN-622 antibody had little effect on the affinity of the antibody for HAAH. Binding affinities were determined by immunoassay on fixed cancer cells (H460, human lung cancer line) and were ˜0.1, 0.2 and 0.5 nM for PAN-622-DM1, PAN-622-MMAE and PAN-622-DUO, respectively. The affinity of PAN-622 for HAAH as expressed on live cells has previously been shown to be ˜1 nM. Efficacies of the three ADCs for killing of H460 cells were determined using an MTS assay. The PAN-622-DM1 had an EC50 of ˜15 nM. The EC50 for PAN-622-MMAE was ˜60 nM and that for PAN-622-DUO was ˜300 nM, Importantly, both unconjugated PAN-622 and a non-relevant antibody conjugated to MMAE did not display any killing of the H460 cell line. Efficacy was also measured on a representative hematological cancer line, MOLM-14 (acute myelogenous leukemia) where EC50s were in the 20-50 nM range for all three ADCs. This work serves as a proof-of-concept; laying the groundwork for further development of HAAH-targeted ADCs.
The hypotriploid human cell line MIA PaCa-2 was obtained from the American Type Culture Collection (ATTC, Manassas, Va., U.S.A.; catalog No, CRL-1420). This cell line was established in 1975 by Yunis A A, et al. from tumor tissue of the pancreas obtained from a 65-year-old Caucasian male (1977, “Human pancreatic carcinoma (MIA PaCa-2) in continuous culture: sensitivity to asparaginase,” Int. J. Cancer 19: 128).
In the present disclosure, DAGIC1194-DM1 is a control, non-specific monoclonal ADC, The DAGIC1194 antibody was obtained from Creative DIagnostis (Shirley, N.Y., U.S.A.) and labeled by Goodwin Biotechnology, Inc, (Plantation, Fla., U.S.A) using the same procedures as used to label SNS622 with DM1.
Anti-ASPH SNS622 antibody was conjugated to linkers and cancer drugs at Goodwin Biotechnology (Plantation, Fla., U.S.A). Three different cytotoxic drugs were used, mertansine (DM1), monomethyl auristatin F (MMAE), or duocarmycine (DUO).
The SNS622 monoclonal antibody was conjugated to DM1, connected by the non-cleavable linker maleimidocaproyl (MC) to prepare SNS622-MC-DM1, or connected by MC and a combination of the cleavable linkers valine citruline and para-amino benzyl alcohol (vc-PAB) to prepare SNS622-MC-vc-PAB-DM1.
Similarly, the SNS622 monoclonal antibody was conjugated to MMAE connected by MC to prepare SNS622-MC-MMAE or connected by MC and vc-PAB to prepare SNS622-MC-vc-PAB-MMAE.
The SNS622 monoclonal antibody was conjugated to duocarmycin (DUO) connected by a combined linker of MC, a four unit of polyethylene glycol (PEG14), vc-PAB, and N,N-Dimethylethanolamine (DMEA) to prepare SNS622-MC-PEG4-vc-PAB-DMEA-DUO. An exemplary ADC construct comprising a monoclonal antibody conjugated to DUO, connected by the linkers MC, PEG4, vc-PAB, and DMEA is depicted in
Manufacture of ADCs was achieved through thiol-directed chemistry. Briefly linker-drug conjugates were purchased from Levena Biopharma (San Diego, Calif., U.S.A.). Antibody disulfide bonds were reduced by incubation for 1 hour at 25° C. in the presence of Tris(2-carboxyethyl) phosphine (TCEP) at a 5-fold molar excess for DM1 and MMAE conjugations, and at a 1.1 molar excess for DUO conjugation. Subsequently, linker-drug conjugates were added to the reduced antibodies at the indicated challenge ratio and incubated for 1 hour at 25° C. Finally, a molar excess of cysteine was added to quench the unreacted linker-drug moiety. Following the conjugation reaction, all conjugates were purified overnight using a SLIDE-A-LYZER 30 kDa MWCO Dialysis Device (ThermoFisher Scientific) with a total of three (3) buffer exchanges (1×PBS, 7.4) of at least 100 diavolume per dialysis.
Final Drug Antibody Ratios (DARs) were determined using UV absorption spectroscopy and hydrophobic interaction chemistry (HIC). Chromatograms of the final products are shown in
DAR values derived from HIC were lower than those derived from UV-absorbance, Highly payload-substituted species were less well-resolved on the HIC chromatograms due to peak broadening. DAR values are reported in Table II below.
All of the anti-ASPH ADCs showed anti-cancer activity when tested using an MTS assay with the human large cell lung carcinoma cell line H460 cells or with the adult acute myeloid leukemia cell line MOLM-14.
Human H460 cells were obtained from the American Type Culture Collection (ATCC; Manassas, Va., U.S.A.). The H460 cells were seeded at a density of 5,000 cells/well in 96-well plates and cultured in HG-DMEM (ThermoFisher Scientific, Waltham. Mass., U.S.A.; Catalog No. 11965-092) supplemented with 20 mM HEPES, 4 mM L-glutamine, 1 mM sodium pyruvate, 1× non-essential amino acids, 50 μg/ml gentamicin, and 10% fetal bovine serum (FBS)). Human MOLM-14 cells were obtained from Dr. Ashkan Emadi at University of Maryland (Baltimore. Md., U.S.A.). The MOLM-14 cells were seeded at a density of 5000 cells/well in 96-well plates and cultured in RPMI 1640 with 20% heat-inactivated FBS. The H460 and MOLM-14 cells were treated with naked antibodies or ADCs for 24 hours, starting at the time of cell seeding. By the end of experiment, the cell viability for both cell lines was determined quantitatively using CELL TITER 96 AQUOUS ONE SOLUTION cell proliferation assay, a colorimetric method for determining the number of viable cells (MTS; Promega, Madison. Wis., U.S.A.; Catalog No. G3582).
As seen in
In this comparison study, neither IgG1 nor SNS622 alone induced growth suppression of H460. Similarly, SNS622 did not suppress the in vitro growth of MOLM-14 either. In contrast, SNS622-drug conjugates SNS622-MC-DM1, SNS622-MC-vc-PAB-MMAE and SNS622-MC-PEG4-vc-PAB-DMEA-DUO all inhibit in vitro cell growth of both H460 and MOLM-14, providing a possibility for treating both HAAH-expressing solid tumors and blood cancers with each of them in vivo. SNS622-MC-DM1 demonstrated the stronger effect in suppressing cell growth of both cancer cell lines (IC50: 15 nM) than SNS622-MC-vc-PAB-MMAE (IC50: 60 nM), although SNS622-MC-DM1 has a less final DAR value than SNS622-MC-vc-PAB-MMAE. SNS622-MC-vc-PAB-MMAE has a 1.8-fold DAR value of that of SNS622-MC-PEG4-vc-PAB-DMEA-DUO, but IC50 of the latter is 5-fold of the former in suppression cell growth of H460. This results indicate that MC vc-PAB-MMAE is more cytotoxic than MC-PEG4-vc-PAB-DMEA-DUO when conjugated to SNS622.
As seen in
This example shows that the cytotoxic activity of SNS622-DM1 is dependent on the number of conjugated DM1, but there appears to be no correlation with the pH of the ADC. To determine if the cytotoxic activity is dependent on the drug antibody ration (DAR) or of the pH of the ADC, SNS622-MC-DM1s were synthesized by Goodwin Biotechnology using drug antibody ratios (DARs) of 2.5:1; 5:1; and 10:1; at pH 7 or pH8. The bioactivities of these SNS622 ADCs were examined using H460 cells. The cells were treated for 48 hours with these SNS622-MC-DM1s, or with SNS622 as control. Cell viability was evaluated at the end of the experiment using an MTS assay.
The final DAR for after each conjugation reaction is shown in Table III, below. The effects on H460 cell viability were determined with MTS assay after a 48-hour treatment, and the results are shown in
SNS622-MC-vc-PAB-DM1 and SNS622-MC-MMAE were also synthesized under different initial DAR ratios of 2.5:1, 5:1 and 10:1 at fixed pH8. The final DAR for each after conjugation reactions is shown in Table IV, below. The 460 cells were treated for 72 hours with ADCs SNS622-MC-vc-PAB-DM1 at with OAR 2.5:1; 5:1; and 10:1, or SNS622-MC-MMAE at with DAR 2.5:1; 5:1; and 10:1. The cell viability and cell death were separately quantified with MTA and lactate dehydrogenase (LDH) release assays.
As seen in
HAAH is highly expressed on the surface of cancer cells, but not on normal adult human cells. The specificity of SNS622-MC-DM1 was examined using human lung carcinoma cell line H460 and LONZA NHLF, a normal human lung fibroblasts (NHLF) cell line. Both cell lines were cultured in HG-DMEM (ThermoFisher Scientific Catalog No. 11965-092) supplemented with 20 mM HEPES (4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid), 4 mM L-glutamine, 1 mM sodium pyruvate, 1× non-essential amino acids, 50 μg/ml gentamicin and 10% fetal bovine serum (FBS). H460 and NHLF cells were seeded into 96-well plates at 5,000 cells per well, following a 2-day FBS deprivation, and released by culture in complete culture medium containing 10% FBS. The cells were allowed to grow for 2 days after releasing, and then treated with or without 32 nM SNS622-MC-DM1. By 72 hours post treatment, cell death was determined by observing cell morphology using a phase contrast microscope at 150×. As seen in
The cell death was also quantified using lactate dehydrogenase (LDH) releasing assay. For the LDH assay, a mixture of a 35 μl aliquot of culture medium and 17.5 μl of substrate, enzyme, and dye solutions (Sigma, St. Louis, Mo., U.S.A.) was incubated at room temperature for 30 minutes, and absorbance was measured at 490 nm using a plate reader (ELx805; BioTek, Winooski, Vt., U.S.A.). As seen on
The in vitro specificity of SNS622-MC-DM1 was also examined using the human pancreas cell line MIA-PaCa-2 ASPH. This cell line has a high level expression of ASPH. MIA-PaCa-2 cells were seeded at a density of 2,000 cells/well and cultured in high-glucose (25 mM D-glucose) Dulbecco's Modified Eagle's Medium (DMEM) with 10% FBS at 37° C. in a humidified atmosphere containing 5% CO2. The cells were treated with 10 nM IgG1-MC-DM1, 20 nM IgG1-MC-DM1, 50 nM IgG1-MC-DM1, 10 nM SNS622-MC-DM1, 20 nM SNS622-MC-DM1, or 50 nM SNS622-MC-DM1 for 48 hours. IgG1-MC-DM1 is a control ADC obtained from Goodwin Biotechnology, having catalog No. DAGIC1194, The cytotoxicity of the ADCs was measured using an MTS assay kit (Promega, Catalog No, G3582). After treatment for 1 hour with the MTS solution, absorbance was measured using a microplate reader at a 490 nm wavelength, with a reference at 690 nm. As seen in
The efficacy and specificity of SNS622-MC-DM1 was first examined in the mouse model with inoculation of pancreas cancer cells. In this model. 5 to 6-week-old female Nod Scid Gamma (NSG) mice (The Jackson Laboratory, Bar Harbor, Me., U.S.A.) were subcutaneously inoculated with 5×105 MIA-PaCa-2 EV cells (MIA-PaCa-2 cells transduced with an empty lentivirus vector) in 100 μl buffer solution on one shoulder, and with 5×105 MIA-PaCa-2 ASPH cells (MIA-PaCa-2 cells expressing high levels of ASPH) in 100 μl buffer solution on the other shoulder Two weeks post-inoculation, SNS622-MC-DM1 or IgG1-MC-DM1 was injected at 5 mg/kg through a tail vein once a week for 4 weeks. A representation of the schedule used for the ADC treatments is show n in
The volume of the tumors inoculated with the MIA-PaCa-2 ASPH cells was measured starting at day 1 of treatment with ADC, and the results are shown in
The expression of ASPH in MIA-PaCa-2 ASPH (also referred to here as MIA-PaCa-2 HAAH) cells (MIA-PaCa2 cells transformed to express high levels of HAAH), and MIA-PaCa-2 EVs cells (MIA-PaCa-2 cells transduced with an empty lentiviral vector) was studied using western blot analyses (
The response to treatment with SNS622-MC-DM1 of tumors derived from MIA-PaCa-2 HAAH cells and from MIA-PaCa-2 EV cells were compared in the same mouse.
The tumors were measured, and a graph of their volumes is shown in
Pancreatic ductular adenocarcinoma (PDAC) is a highly lethal malignancy with limited treatment options. HAAH is a cell surface protein that is highly expressed in 97.1 of PDACs. The specificity of SNS622-MC-DM1 was next examined in the patient-derived xenograft (PDx) mouse model PDAC. The patient-derived xenograft (PDx) murine model was established by using surgically resected PDAC (from Rhode Island Hospital, Providence, R.I., U.S.A.). Five to six-week-old female Nod Scid Gamma (NSG) mice were employed. The surgically resected tumor tissue was diced into 5×5×5 mm3 pieces, and a piece of tumor tissue was subcutaneously transplanted under anesthesia with isoflurane into each mouse via a small incision in the lower back, A buprenorphine analgesic was injected to each mouse for 3 days after surgery. The SNS622 antibody or the SNS622-MC-DM1 ADC was administered at a dose of 2.5 mg/kg by intravenous tail-vein injection every two weeks starting at day 17 post-surgery. Body weight and tumor size were measured twice a week and tumor volume was calculated using the modified ellipsoid formula (0.5×length×width2). To determine the effect of SNS622-MC-DM1 on lung metastasis, all lung tissues were immersed in Bouin's fixative solution (Sigma-Aldrich, St. Louis, Mo., U.S.A.; catalog No, HT10132) and metastatic nodules on the surface of the lungs were counted. Animal experiments were conducted in accordance with the guidelines of the Institutional Animal Care and Use Committee (IACUC) at Rhode. Island Hospital. As seen on
The PDx model was established from an individual with PDAC that exhibited spontaneous lung metastasis. This phenotype was maintained in the PDx model of NSG mouse. Serial passage of this PDAC in NSG mice confirmed the durability and transmissibility of this metastatic phenotype from the F2 to the F9 generation. Therefore, to evaluate the effect of SNS622-MC-DM1 administration on metastatic spread to the lung, this PDx model of PDAC w as employed. In this context, dose and period of administration of PAN-622 or SNS622-MC-DM1 for treatment of NSG mice was reduced to 1.9 mg/kg and the development and growth of metastatic nodules in the lungs after the treatment was assessed After 6 weeks of administration, the number of macroscopic metastatic nodules on the lung surface was determined. As seen in
To describe the specificity of SNS622-DM1 further, a binding assay of naked antibodies and ADCs against H460 lysate was conducted.
H460 cells were harvested, the cell density was adjusted to 2×106 cells/ml with PBS, and the resuspended cells sonicated on ice twice in 30 second pulses. After centrifugation at 300×g for 5 minutes the supernatant was collected and the protein concentration measured using a NANODROP spectrophotometer (ThermoFisher Scientific). A 96-well plate was coated with H460 lysate and dried at room temperature overnight. Following a 1-hour blockage with 1% non-fat dry milk in phosphate buffered saline (PBS), the plates were incubated for 45 minutes at 37° C. with each either 0.5 μg/ml IgG1λ (non-specific monoclonal antibody), IgG1λ-MC-DM1 (non-specific ADC), or SNS622-MC-DM1, or with 5 μg/ml SNS622. Following five PBS rinses to remove un-bound antibody. 1:100 goat anti-human IgG (8)-HRP was added and the plates incubated for 30 minutes at 37° C. Following five PBS rinses TMB substrate was added and, after incubation of the plates for 15 minutes at room temperature. Stop solution was added to terminate the reactions. The plates were read at 450 nm using a 96-well plate reader (ELx808, BioTek).
Table V, showing the percent of loading amount bound is shown below. Table V shows that SNS622 and SNS622-MC-DM1 demonstrated a high binding specificity to the H460 lysate (92% and 107%, respectively). In contrast, binding of IgG1λ and IgG1λ-MC-DM1 to the H460 lysate was minimal (<0.002% for both).
The catalytic domain of HAAH (HAAH-cat) is exposed at the surface of HAAH-expressing cancer cells. The binding of SNS622-MC-DM1 at different drug-antibody ratio (DAR) and pH to HAAH-cat was measured using IgG1λ as control. The plates were coated with HAAH by treating with 4 λg/ml HAAH catalytic domain overnight. Following blocking with 1% Non-Fat Dry Milk in PBS for one hour, the plates were incubated for 45 minutes at 37° C. with 11.1 mg/ml IgG1λ; 9.6 mg/ml SNS622; 4.8 mg/ml SNS622-MC-DM1 at DAR 2.5, pH 7.0; 5.9 mg/ml SNS622-MC-DM1 at DAR 2.5, pH8.0; 6.1 mg/ml SNS622-DM1 at DAR 5.0, pH 7.0; 5.7 mg/ml SNS622-MC-DM1 at DAR 5.0, pH8.0; 4.1 mg/ml SNS622-DM1 at DAR 10.0, pH7.0; or 4.4 mg/ml SNS622-MC-DM1 at DAR 10.0, pH8.0. Following 5 PBS rinses the plates were incubated with 1:100 goat anti-human IgG (8)-HRP for 30 minutes at 37° C., Following five PBS rinses TMB substrate was added, and after a 15-minute incubation at room temperature, Stop solution was added to terminate the reactions. The plates were read at 450 nm using a 96-well plate reader (ELx808, BioTek). The binding results are shown below in Table VI
The results show that almost 98% of SNS622 binds to the HAAH catalytic domain (HAAH-cat), while less than 1% of the non-specific antibody IgG1λ binds to the catalytic domain (<0.01%), Binding by SNS622-MC-DM1 s at different DARs and pH still keep high affinity to the catalytic domain (75-114%).
In general, these results in binding assays demonstrate high specific binding of SNS622-DM1 to the HAAH-expressing cancer cell line H460 lysate and to HAAH-cat. In contrast, nonspecific IgG1λ and IgG1-MC-DM1 have minimal binding to H460 lysate and to HAAH-cat. These provide the underlying mechanism for the in vitro and in vivo specificity of SNS622-MC-DM1 against cancer but not normal cells.
While the invention has been described with reference to certain exemplary embodiments thereof, those skilled in the art may make various modifications to the described embodiments of the invention without departing from the scope of the invention. The terms and descriptions used herein are set forth by way of illustration only and not meant as limitations. In particular, although the present invention has been described by way of examples, a variety of compositions and processes would practice the inventive concepts described herein. Although the invention has been described and disclosed in various terms and certain embodiments, the scope of the invention is not intended to be, nor should it be deemed to be, limited thereby and such other modifications or embodiments as may be suggested by the teachings herein are particularly reserved, especially as they fall within the breadth and scope of the claims here appended. Those skilled in the art will recognize that these and other variations are possible within the scope of the invention as defined in the following claims and their equivalents.
| Number | Date | Country | |
|---|---|---|---|
| 62548732 | Aug 2017 | US |
