WO2023046202A1 - 一种抗体及其药物偶联物和用途 - Google Patents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/68—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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Definitions
- the present invention relates to antibodies and antibody-drug conjugates, more specifically to antibodies targeting Claudin18.2 (CLDN18.2) and antibody-drug conjugates (ADCs), compositions containing the antibodies or ADC molecules, and Therapeutic applications.
- CLDN18.2 Claudin18.2
- ADCs antibody-drug conjugates
- Gastric cancer is the third leading cause of cancer death worldwide, and the overall 5-year survival rate of patients with metastatic gastric cancer and gastroesophageal junction cancer (EGJA) is even less than 20%.
- EGJA gastroesophageal junction cancer
- Claudin18.2 is a member of the claudin family of tight junction proteins, which mediates tight junctions between cells.
- Claudin18.2 is highly expressed in gastric cancer and pancreatic cancer. In normal tissues, it is only expressed in gastric mucosal cells and not in other normal tissues. Therefore, it can be used as an ideal target for ADC (antibody-drug conjugate) drug development.
- ADC antibody-drug conjugate
- Claudin18.2 belongs to 4 transmembrane proteins, including 2 extracellular loops and 1 intracellular loop. Its sequence is very similar to the same family protein Claudin18.1, with only 8 amino acid differences in the first extracellular loop. Claudin18.1 is specifically expressed in the lung, so it is difficult and challenging to develop ADC drugs that only recognize Claudin18.2 but not Claudin18.1.
- the present invention provides an antibody-drug conjugate (ADC) having the following formula (I) or a pharmaceutically acceptable salt or solvate thereof:
- D represents a cytotoxic or cytostatic drug, for example, a topoisomerase I inhibitor
- the Ab comprises three CDRs of the heavy chain variable region (VH) sequence of SEQ ID NO: 1 or 3 and three CDRs of the light chain variable region (VL) sequence of SEQ ID NO: 2, preferably , wherein the CDRs are defined according to Kabat or IMGT or a combination thereof.
- the invention provides a composition comprising an ADC of the invention, or a pharmaceutically acceptable salt or solvate thereof.
- the present invention provides the use of the ADC of the present invention or its pharmaceutically acceptable salt or solvate and the composition thereof in the treatment of Claudin18.2 positive tumors.
- the present invention provides anti-Claudin18.2 antibodies, pharmaceutical compositions and uses thereof.
- Figures 1A-1I show that the positive rates of Claudin18.2 or Claudin18.1 expression in different cell lines of Example I-1 were detected by FACS technology using fluorescently labeled antibodies.
- the control is an isotype control antibody.
- Figure 1A HEK293T-Claudin18.2 (human) stable cell line was detected by PE fluorescently labeled anti-human Claudin18.2 antibody
- Figure 1B HEK293T-Claudin18 was detected by APC fluorescently labeled anti-human Claudin18.1 antibody.
- Figure 1C Detection of L929-Claudin18.2 (human) stable cell line using APC fluorescently labeled anti-human Claudin18.2 antibody.
- Figure 1D Detection of CHO-Claudin18.2 (human) stable cell line using APC fluorescently labeled anti-human Claudin18.2 antibody.
- Figure 1E Detection of HEK293T-Claudin18.2 (cynomolgus monkey) stable cell line using PE fluorescently labeled anti-monkey Claudin18.2 antibody.
- Figure 1F Detection of HEK293T-Claudin18.2 (rat) stable cell line using APC fluorescently labeled anti-rat Claudin18.2 antibody.
- Figure 1G Detection of HEK293T-Claudin18.2 (mouse) stable cell line using APC fluorescently labeled anti-mouse Claudin18.2 antibody.
- Figure 1H Detection of NUGC4-Claudin18.2 (human) stable cell line using APC fluorescently labeled anti-human Claudin18.2 antibody.
- Figure 1I Detection of NUGC4 tumor cell line using APC fluorescently labeled anti-human Claudin18.2 antibody.
- Figures 2A-2B show the detection of the cellular affinity of anti-human Claudin18.2 humanized antibody and reference antibody IMAB362 to NUGC4-Claudin18.2 (human) ( Figure 2A) and NUGC4 ( Figure 2B) in a cellular ELISA assay.
- Figures 3A-3C show that, using flow cytometry, the detection of anti-human Claudin18.2 humanized antibody and reference antibody IMAB362 and HEK293T-Claudin18.2 (human) ( Figure 3A), NUGC4-Claudin18.2 (human) ( Figure 3A) 3B) and the cellular affinity of NUGC4 (Fig. 3C).
- Figures 4A-4C show that, using flow cytometry, the detection of anti-human Claudin18.2 humanized antibody and reference antibody IMAB362 and HEK293T-Claudin18.2 (cynomolgus monkey) ( Figure 4A), HEK293T-Claudin18.2 (rat ) (Fig. 4B) and HEK293T-Claudin18.2 (mouse) (Fig. 4C) cell affinity.
- Figure 5 shows the ADCC killing activity assay results of the anti-human Claudin18.2 humanized antibody on HEK293T-Claudin 18.2 (human) cells.
- Figure 6 shows the CDC killing activity assay results of the anti-human Claudin18.2 humanized antibody on HEK293T-Claudin 18.2 (human) cells.
- Figure 7 shows the in vivo pharmacokinetic detection of the anti-Claudin18.2 humanized antibody in rats.
- Figures 8A-8B show the binding of anti-Claudin18.2 humanized antibody ADC to L929-Claudin18.2 cells ( Figure 8A) and NUGC4 cells ( Figure 8B) before and after toxin conjugation.
- Figures 9A-9E show that, in vitro experiments, the anti-Claudin18.2 humanized antibody ADC drug has an effect on HEK293T-Claudin 18.2 cells ( Figures 9A and 9B), HEK293T-Claudin 18.1 cells ( Figures 9C and 9D) and NUGC4-Claudin 18.2 Killing effect of cells (Fig. 9E).
- Figure 10 shows the tumor suppressive efficacy of the anti-Claudin18.2 humanized antibody ADC drug in the NUGC-4CDX model.
- Figure 11 shows the effect of anti-Claudin18.2 humanized antibody ADC drug on the body weight of mice.
- the trade name includes the product formulation, the generic drug and the active pharmaceutical ingredient for the product of the trade name.
- the term “comprising” or “comprising” means including stated elements, integers or steps, but not excluding any other elements, integers or steps.
- the term “comprising” or “comprises” is used, unless otherwise specified, it also covers the situation consisting of the mentioned elements, integers or steps.
- an antibody variable region that "comprises” a particular sequence it is also intended to encompass an antibody variable region that consists of that particular sequence.
- CLDN18 is a transmembrane protein that crosses the membrane four times. Both the N-terminus and the C-terminus are located in the cytoplasm, with extracellular loop 1 and extracellular loop 2. Comprising approximately 53 amino acids, the second extracellular loop (ie, extracellular loop 2) consists of approximately 30 amino acids.
- CLDN18 includes two splice variants, CLDN18.1 and CLDN18.2, which differ by 8 amino acids in the extracellular loop 1; in normal tissues, the expression of CLDN1 is restricted to the lung; the expression of CLDN2 is restricted to the gastric mucosa.
- CLDN18.1 preferably relates to human CLDN18.1, eg human CLDN18.1 having the amino acid sequence under NCBI_057453.1.
- the term also covers Claudin 18.1 from other species such as cynomolgus monkey, mouse and rat, but in the context of this document the term refers to human CLDN 18.1 unless otherwise specified.
- CLDN18.2 preferably relates to human CLDN18.2, eg human CLDN18.2 having the amino acid sequence under NCBI_001002026.1.
- the term also covers Claudin18.2 from other species, e.g., cynomolgus Claudin18.2 (e.g. amino acid sequence under XP_015300615.1), mouse Claudin18.2 (e.g. amino acid sequence under NP_001181850.1), Daphnia Murine Claudin18.2 (eg, amino acid sequence under NP_001014118.1).
- the term refers to human CLDN18.2.
- CLDN18 also cover post-translationally modified variants and conformational variants, as well as mutants, especially naturally occurring variants, allelic variants, species homologues.
- CLDN18.2-positive cells refers to cells that are positive for CLDN18.2 cell surface expression, such as cancer cells, modified cancer cells or modified non-tumor cells.
- the CLDN18.2 expression level on the cell surface can be determined by any conventional method known in the art for determining the expression level of the cell surface antigen, for example, a FACS detection method or an immunofluorescent staining method; and optionally compared with a predetermined reference value, Cells positive for cell surface expression of CLDN18.2 were identified.
- the measured value of CLDN18.2 expression level on positive cells is at least 2 times higher than a predetermined reference value.
- the predetermined reference value can be determined by those skilled in the art in a conventional manner.
- the predetermined reference value may be the expression level value of CLDN18.2 measured on normal cells other than gastric mucosa in the same assay method.
- the predetermined reference value can use the FACS method as described in Example I-1 of the present application, by comparing the fluorescence staining intensity produced by the specific CLDN18.2 antibody relative to the isotype control antibody on the cells To determine, for example, a predetermined reference value may be set at least 10 times greater than the mean fluorescent staining intensity of the isotype control antibody.
- CLDN18.2-positive cells express sufficiently high levels of CLDN18.2 on the surface so that they can be bound by CLDN18.2-specific antibodies in detection methods such as immunofluorescence staining or FACS, and produces a detection signal higher than a predetermined reference value, and/or produces a signal significantly different from non-cancerous normal cells other than gastric mucosa (for example, at least 2 times higher, or preferably at least 10 times or 100 times higher, or higher ).
- antibody refers to a polypeptide comprising at least a light or heavy chain immunoglobulin variable region that specifically recognizes and binds an antigen.
- the term encompasses various antibody structures including, but not limited to, monoclonal, polyclonal, single- or multi-chain antibodies, monospecific or multispecific (e.g., bispecific), chimeric, or human Antibodies, full-length antibodies, and antibody fragments are available as long as they exhibit the desired antigen-binding activity.
- a “whole antibody” refers to an antibody comprising at least two heavy (H) chains and two light chains (L) Immunoglobulin molecules.
- Each heavy chain is composed of a heavy chain variable region (abbreviated herein as VH) and a heavy chain constant region.
- Each light chain is composed of a light chain variable region (abbreviated herein as VL) and a light chain constant region.
- the variable region is the domain of an antibody's heavy or light chain that is involved in binding the antibody to its antigen.
- the constant regions are not directly involved in the binding of the antibody to the antigen, but exhibit various effector functions.
- the light chain of an antibody can be assigned to one of two classes, called kappa ( ⁇ ) and lambda ( ⁇ ), based on the amino acid sequence of its constant region.
- the heavy chains of antibodies can be divided into five main different classes based on the amino acid sequence of their constant regions: IgA, IgD, IgE, IgG, and IgM, and several of these classes can be further divided into subclasses, e.g., IgG1, IgG2, IgG3 and IgG4, IgA1 and IgA2.
- antibody fragment and “antigen-binding fragment” of an antibody are used interchangeably to refer to a molecule other than an intact antibody that comprises the portion of an intact antibody that binds the antigen to which the intact antibody binds.
- antibody fragments typically comprise amino acid residues from "complementarity determining regions" or "CDRs,” as those of skill in the art appreciate.
- Antibody fragments can be prepared by recombinant DNA techniques, or by enzymatic or chemical cleavage of intact antibodies.
- antibody fragments include, but are not limited to, Fab, scFab, disulfide-linked scFab, Fab', F(ab')2, Fab'-SH, Fv, scFv, disulfide-linked scFv, diabody ( diabody), triabody, tetrabody, minibody.
- antibody fragments comprise a portion of cysteine residues for interchain disulfide bond formation between the light chain and the heavy chain, for example, of the Fab region and/or hinge region of an IgG1 antibody. Cysteine residues to provide amino acid residue sites available for sulfhydryl coupling chemistry.
- antibody fragments comprise cysteine residues introduced into the Fc region to provide amino acid residue sites available for sulfhydryl coupling chemistry.
- immunoglobulin refers to a protein having the structure of a naturally occurring antibody.
- IgG class immunoglobulins are heterotetrameric proteins of approximately 150,000 Daltons consisting of two light chains and two heavy chains that are disulfide bonded.
- VH heavy chain variable region
- CH1 heavy chain constant domain
- CL light chain constant domain
- an antibody is an IgG antibody means that the antibody is a heterotetrameric protein having an IgG-like immunoglobulin structure.
- IgG antibodies usually the VH-CH1 of the heavy chain is paired with the VL-CL of the light chain to form a Fab fragment that specifically binds the antigen.
- an IgG antibody essentially consists of two Fab molecules and two dimerized Fc regions linked by an immunoglobulin hinge region.
- IgG immunoglobulins can be divided into subclasses based on the sequence of the heavy chain constant region, eg, gamma 1 (IgGl), gamma 2 (IgG2), gamma 3 (IgG3), and gamma 4 (IgG4).
- the light chains of IgG immunoglobulins can also be assigned to one of two types, called kappa and lambda, based on the amino acid sequence of their constant domains.
- an antibody according to the invention is an IgG antibody, such as an IgGl, IgG2, IgG3 or IgG4 antibody.
- antibodies according to the invention are IgGK or IgG ⁇ antibodies, eg, IgG1K or IgG1 ⁇ antibodies.
- CDR region As used herein, the terms “complementarity determining region” or “CDR region” or “CDR” or “hypervariable region” are used interchangeably to refer to antibody variable domains that are highly variable in sequence and form structurally defined regions. (“hypervariable loops") and/or regions containing antigen contact residues ("antigen contact points").
- the CDRs are primarily responsible for binding to antigenic epitopes.
- the CDRs of antibody heavy and light chains are numbered sequentially starting from the N-terminus, and are generally referred to as CDR1, CDR2 and CDR3.
- the CDRs located within the variable domain of an antibody heavy chain are also referred to as HCDR1, HCDR2, and HCDR3, while the CDRs located within the variable domain of an antibody light chain are referred to as LCDR1, LCDR2, and LCDR3.
- various schemes known in the art can be used to determine its CDR sequence.
- annotations of CDRs in a given light chain variable region or heavy chain variable region including those based on Kabat, AbM, Chothia, Contact, IMGT definitions, can be obtained at http://www.abysis.org/abysis/ CDR sequences.
- CDRs can also be determined based on having the same Kabat numbering position as the reference CDR sequence.
- residue positions in antibody variable regions including heavy chain variable region residues and light chain variable region residues
- Kabat numbering system Kabat et al., Sequences of Proteins of Immunological Interest, 5th Ed. Public Health Service, National Institutes of Health, Bethesda, Md. (1991)).
- a “variable region” or “variable domain” is a domain of an antibody's heavy or light chain that participates in the binding of the antibody to its antigen.
- the heavy chain variable region (VH) and the light chain variable region (VL) can be further subdivided into hypervariable regions (HVR, also known as complementarity determining regions (CDR)), interspersed with more conserved regions (i.e., framework Region (FR)).
- HVR hypervariable regions
- FR framework Region
- Each VH and VL consists of three CDRs and four FRs, arranged in the following order from the amino terminus to the carboxyl terminus: FR1, CDR1, FR2, CDR2, FR3, CDR3, FR4.
- one or more residues in one or both of the two variable domains may be modified, for example, in one or more CDR regions and/or in one or Residue modifications, especially conservative residue substitutions, are made in various framework regions to obtain antibody variants that still substantially retain at least one biological property (eg, antigen-binding ability) of the antibody molecule prior to the alteration.
- antibody variable regions can be modified by CDR grafting. Since the CDR sequences are responsible for most antibody-antigen interactions, recombinant antibody variants can be constructed that mimic the properties of known antibodies. In this antibody variant, CDR sequences from a known antibody are grafted onto the framework regions of a different antibody with different properties.
- Properties of the mutated and/or modified antibodies or ADC conjugates comprising the same can be assessed in in vitro or in vivo assays, such as target antigen binding properties or other desired functional properties, such as ADC endocytosis, pharmacokinetics, and tumor-killing activity in vivo.
- chimeric antibody refers to an antibody in which the variable region sequences are derived from one species and the constant region sequences are derived from another species, for example, an antibody in which the variable region sequences are derived from a mouse antibody and the constant region sequences are derived from a human antibody .
- humanized antibody refers to an antibody in which CDR sequences derived from the germline of another mammalian species, such as a mouse, have been joined to human framework sequences. Additional framework region modifications may be made within the human framework sequences, and/or additional amino acid modifications may be made in the CDR sequences, eg, for affinity maturation of antibodies.
- antibodies of the invention are humanized antibodies, having framework region sequences "derived from" specific human germline sequences.
- amino acid sequence of the framework region of the antibody is at least 90%, more preferably at least 95%, and even more preferably At least 96%, 97%, 98%, or 99% identity, and the antibody retains antigen binding activity, e.g., with 25C7A5-HZ1 or -HZ2, or with 2D3A11-HZ1 or -HZ2 is equivalent (e.g., ⁇ 10% ) CLDN18 binding affinity.
- the term "isolated" antibody is one that has been separated from components of its natural environment.
- antibodies are purified to greater than 95% or 99% purity, which can be determined by, for example, electrophoresis (e.g., SDS-PAGE, isoelectric focusing (IEF), capillary electrophoresis) or chromatography (e.g., ion exchange or reversed-phase HPLC) to determine.
- electrophoresis e.g., SDS-PAGE, isoelectric focusing (IEF), capillary electrophoresis
- chromatography e.g., ion exchange or reversed-phase HPLC
- epitope refers to the region of an antigen to which an antibody binds. Epitopes can be formed from contiguous amino acids or non-contiguous amino acids juxtaposed by the tertiary folding of the protein.
- the antibody according to the present invention binds to the natural epitope of human Claudin18.2, more preferably, binds to the natural epitope of human Claudin18.2 expressed on the cell surface.
- cell-based assays are used to detect binding of antibodies of the invention to native epitopes of human Claudin 18.2.
- affinity refers to an intrinsic binding affinity that reflects the interaction between members of a binding pair. Affinity can be measured by common methods known in the art. One specific method for measuring affinity is the cellular ELISA assay described in the Examples herein, another specific method is the FACS assay described in the Examples herein. In one embodiment, if the antibody has a comparable (i.e., ⁇ 10%) or less EC50 value and/or a comparable ( That is, ⁇ 10%) or higher maximum binding signal value, then the antibody is considered to have high affinity for Claudin18.2.
- the term "specifically binds” means that an antibody binds selectively or preferentially to a target antigen relative to a non-target antigen.
- the antibody binds (in particular with high affinity) to human Claudin18. binding), but does not bind or substantially does not bind to human Claudin18.1 expressed on the cell surface, then the antibody should be considered as an antibody that "specifically binds to human Claudin18.2".
- the binding of the antibody to human Claudin18.2 or human Claudin18.1 expressed on the cell surface can be assayed in a cell ELISA or FACS to determine the binding specificity of the antibody to Claudin18.2.
- an antibody is referred to as an antibody when it does not have significant affinity for human Claudin18.1 in a cell-based assay and does not significantly bind to human Claudin18.1, in particular does not produce a detectable signal that is significantly different from background. Does not bind or substantially does not bind human Claudin 18.1 (herein, this is also referred to as "no non-specific binding" to human Claudin 18.1).
- a recombinant cell line (such as a recombinant HEK293T stable cell line) with a positive rate of Claudin18.1 expression greater than 95% or greater than 98% is used , determined by FACS assay, for example, as described in Example 1.
- FACS assay for example, as described in Example 1.
- isotype controls can be used to eliminate background staining due to non-specific binding of antibodies to cells.
- an antibody that specifically binds human Claudin 18.2 and has no non-specific binding to human Claudin 18.1 may have cross-reactivity with Claudin 18.2 proteins from other species, as understood by those skilled in the art.
- cross-reactive refers to the ability of an antibody to bind Claudin 18.2 from a different species.
- an antibody according to the invention specific for human Claudin 18.2 may also bind Claudin 18.2 from other species (eg, cynomolgus monkey, mouse and/or rat Claudin 18.2).
- cross-reactivity examples include those described in the Examples as well as standard assays known in the art, for example by using flow cytometry techniques or cellular ELISA techniques.
- Species cross-reactivity of antibodies is advantageous in some circumstances. For example, when the target antibody has species cross-reactivity to preclinical experimental animals, such as mice, rats, or primates, it will facilitate the preclinical safety of the target antibody and its ADC conjugate before human therapeutic or diagnostic application sexuality and efficacy evaluation.
- the term "isotype" refers to the class of an antibody determined by the antibody heavy chain constant region.
- antibodies according to the invention may be IgA (e.g. IgA1 or IgA2), IgG1, IgG2 (e.g. IgG2a or IgG2b), IgG3, IgG4, IgE, IgM and IgD antibodies and have heavy chain constants of said immunoglobulin type. district.
- the antibody of the present invention may be an IgG1 antibody having a human IgG1 constant region.
- the present invention contemplates not only antibodies employing native sequence constant regions, but also antibodies comprising variant sequence constant regions.
- Fc region is used herein to define the C-terminal region of an immunoglobulin heavy chain that contains at least a portion of the constant region.
- the term includes native sequence Fc-regions and variant Fc-regions.
- the term "native sequence Fc region” encompasses naturally occurring Fc region sequences of various immunoglobulins, such as those of various Ig subclasses and their allotypes (Gestur Vidarsson et al., IgG subclasses and allotypes: from structure to effector functions, 20 October 2014, doi: 10.3389/fimmu.2014.00520.).
- the human IgG heavy chain Fc region has an amino acid sequence extending from Cys226 or from Pro230 to the carboxy-terminus of the heavy chain.
- the C-terminal terminal lysine (Lys447) of the Fc region may or may not be present.
- the human IgG heavy chain Fc region bears at the N-terminus a hinge sequence or a partial hinge sequence of a native immunoglobulin, eg, the sequence from E216 to T225 or the sequence from D221 to T225 according to EU numbering.
- variant sequence Fc region refers to an Fc region polypeptide comprising a modification relative to a native sequence Fc region polypeptide.
- the modification may be addition, deletion or substitution of amino acid residues. Substitutions can include naturally occurring amino acids and non-naturally occurring amino acids.
- the purpose of the modification may be to alter the binding of the Fc region to its receptor and the effector functions elicited thereby.
- effector functions refers to those biological activities attributable to the Fc region of an immunoglobulin that vary with immunoglobulin isotype.
- immunoglobulin effector functions include: C1q binding and complement-dependent cytotoxicity (CDC), Fc receptor binding, antibody-dependent cell-mediated cytotoxicity (ADCC), antibody-dependent cellular phagocytosis (ADCP) , cytokine secretion, immune complex-mediated antigen uptake by antigen-presenting cells, downregulation of cell surface receptors (eg, B-cell receptors), and B-cell activation.
- CDC complement-dependent cytotoxicity
- ADCC antibody-dependent cell-mediated cytotoxicity
- ADCP antibody-dependent cellular phagocytosis
- cytokine secretion immune complex-mediated antigen uptake by antigen-presenting cells
- downregulation of cell surface receptors eg, B-cell receptors
- B-cell activation e.g, B-cell activation
- ADCC refers to antibody-dependent cell-mediated cytotoxicity.
- ADCC is mainly mediated by natural killer cells (NK cells) in humans.
- NK cells natural killer cells
- the antibody binds to the antigen displayed on the surface of the target cell, and the Fc ⁇ RIIIA on the surface of the NK cell recognizes the Fc region of the antibody, so that the NK cell is activated, releases perforin and granule-dissolving enzyme, and leads to lysis and apoptosis of the target cell.
- the ADCC activity of antibodies can be assessed using a fluorescein reporter system such as that described in Example I. In some cases, when the ADCC effector activity of the antibody is not desired, the ADCC activity of the antibody can be removed by modifying the Fc region of the antibody.
- CDC refers to complement dependent cytotoxicity.
- the Fc region of the antibody binds to the complement molecule C1q, which in turn forms a membrane attack complex, resulting in the clearance of target cells.
- IgM is the most efficient isotype for complement activation. Both IgGl and IgG3 are also very effective at directing CDC through the classical complement activation pathway.
- the CDC activity of the antibody can be detected by the guinea pig serum killing test such as that described in Example 1. In some cases, when the CDC effector activity of the antibody is not desired, the CDC activity of the antibody can be removed by modifying the Fc region of the antibody.
- receptor-mediated endocytosis refers to the internalization and delivery of ligand/receptor complexes into the cytosol or The process of translocation to the appropriate intracellular compartment.
- the endocytosis rate can be measured by the method described in Example 1 to characterize the receptor-mediated endocytosis activity of the antibody.
- the antibody of the present invention can trigger endocytosis mediated by the Claudin18.2 receptor after binding to Claudin18.2 expressed on the cell surface, and the antibody of the present invention having this endocytic property can be combined with a drug (such as After coupling small molecule toxic drug molecule) to form ADC, it can be effectively used as a tool for carrying anti-tumor drugs into cancer cells.
- a drug such as After coupling small molecule toxic drug molecule
- sequence identity refers to the degree to which sequences are identical on a nucleotide-by-nucleotide or amino-acid-by-amino acid basis over a comparison window.
- Percent sequence identity can be calculated by comparing two optimally aligned sequences over a comparison window and determining the presence of identical nucleic acid bases (e.g., A, T, C, G, I) in the two sequences ) or the same amino acid residue (for example, Ala, Pro, Ser, Thr, Gly, Val, Leu, Ile, Phe, Tyr, Trp, Lys, Arg, His, Asp, Glu, Asn, Gln, Cys and Met) Number of positions To obtain the number of matching positions, the number of matching positions was divided by the total number of positions in the comparison window (ie, window size) and the result multiplied by 100 to yield the percent sequence identity.
- Optimal alignment for purposes of determining percent sequence identity can be achieved in various ways known in the art, for example, using publicly available computer software such as BLAST, BLAST-2, ALIGN or Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for aligning sequences, including any algorithms needed to achieve maximal alignment over the full length of the sequences being compared or over a region of sequence of interest.
- the percent amino acid sequence identity is determined by optimally aligning a candidate antibody sequence with a given antibody sequence, in a preferred embodiment according to the Kabat numbering rules .
- the comparison window ie the target antibody region to be compared
- the sequence identity may be spread over the entire heavy chain variable region and/or the entire light chain variable region, or the percent sequence identity may be limited to the framework regions only, while corresponding to the CDR regions. The sequence remains 100% the same.
- the "reference antibody IMAB362” refers to the anti-Claudin18.2 antibody constructed using the amino acid sequences of the heavy chain and light chain variable regions of the 175D10 monoclonal antibody published in patent CN 101312989 B.
- said reference antibody IMAB362 will have the same antibody structure as the antibody to be compared outside of the variable region, for example in both heavy and light chain constant region structures , have the same heavy and light chain constant region sequences.
- halogen generally refers to fluorine, chlorine, bromine, iodine, for example, it may be fluorine, chlorine.
- alkyl refers to a linear or branched saturated hydrocarbon group composed of carbon atoms and hydrogen atoms. Specifically, the alkyl group has 1-10 carbon atoms, such as 1 to 8, 1 to 6, 1 to 5, 1 to 4, 1 to 3 or 1 to 2 carbon atoms.
- C 1 -C 6 alkyl refers to a straight or branched saturated hydrocarbon group having 1 to 6 carbon atoms, examples of which are methyl, ethyl, propyl (including n-propyl and isopropyl), butyl (including n-butyl, isobutyl, sec-butyl or tert-butyl), pentyl (including n-pentyl, isopentyl, neopentyl), hexyl (including n-hexyl, 2-methylpentyl, 3-methylpentyl, 3,3-dimethylbutyl, 2,2-dimethylbutyl, 1,1-dimethylbutyl, 1,2 -Dimethylbutyl, 1,3-dimethylbutyl, 2,3-dimethylbutyl, 2-ethylbutyl), etc.
- alkenyl refers to a linear or branched unsaturated hydrocarbon group consisting of carbon atoms and hydrogen atoms and containing at least one double bond.
- alkenyl groups have 2-8, eg 2 to 6, 2 to 5, 2 to 4 or 2 to 3 carbon atoms.
- C 2 -C 6 alkenyl refers to a straight or branched alkenyl group having 2 to 6 carbon atoms, such as ethenyl, propenyl, allyl, 1-but Alkenyl, 2-butenyl, 1,3-butadienyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 1,3-pentadienyl, 1,4-pentenyl Dienyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 1,4-hexadienyl and the like.
- alkynyl refers to a straight or branched unsaturated hydrocarbon group consisting of carbon atoms and hydrogen atoms and containing at least one triple bond.
- alkynyl groups have 2-8, eg 2 to 6, 2 to 5, 2 to 4 or 2 to 3 carbon atoms.
- C 2 -C 6 alkynyl refers to a straight or branched alkynyl group having 2 to 6 carbon atoms, such as ethynyl, propynyl, propargyl, 1- Butynyl, 2-butynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-methyl-1-pentynyl, 1-hexynyl, 2-hexynyl , 3-hexynyl, 5-methyl-2-hexynyl, etc.
- alkylene refers to a divalent group obtained by removing two hydrogen atoms from the same or two different carbon atoms of a linear or branched saturated alkane. Specifically, the alkylene group has 1-10 carbon atoms, such as 1 to 6, 1 to 5, 1 to 4, 1 to 3 or 1 to 2 carbon atoms.
- C 1 -C 6 alkylene refers to a straight or branched chain alkylene group having 1 to 6 carbon atoms, including, but not limited to, methylene, ethylene group, propylene group, butylene group, etc.
- alkenylene refers to a divalent group obtained by removing two hydrogen atoms from the same or two different carbon atoms of a linear or branched unsaturated olefin containing at least one double bond.
- alkenylene has 2-8, eg 2 to 6, 2 to 5, 2 to 4 or 2 to 3 carbon atoms.
- C 2 -C 6 alkenylene refers to a straight or branched chain alkenylene having 2 to 6 carbon atoms, such as ethenylene, propenylene, allene group, butenylene, pentenylene, and hexenylene.
- alkynylene refers to a divalent group obtained by removing two hydrogen atoms from the same or two different carbon atoms of a linear or branched unsaturated alkyne containing at least one triple bond .
- an alkynylene group has 2-8, such as 2 to 6, 2 to 5, 2 to 4 or 2 to 3 carbon atoms.
- C 2 -C 6 alkynylene refers to a straight or branched chain alkynylene having 2 to 6 carbon atoms, such as ethynylene, propynylene, alkynylene Propyl, butynylene, pentynylene and hexynylene.
- cycloalkyl refers to a monocyclic, fused polycyclic, bridged polycyclic or spiro non-aromatic monovalent hydrocarbon ring structure having the specified number of ring atoms, which may be saturated or unsaturated, for example comprising 1 or more double bonds.
- a cycloalkyl group may contain 3 or more, such as 3-18, 3-10, or 3-8 carbon atoms in the ring, such as C 3-10 cycloalkyl, C 3-8 cycloalkyl, C 3-6 cycloalkyl, C 5-6 cycloalkyl.
- Examples of cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl.
- heterocycle refers to a 5-20 membered (eg 5-14 membered, 5- 8-membered, 5-6-membered) aromatic or non-aromatic monocyclic, bicyclic, or polycyclic ring systems.
- One or more N, C or S atoms in the heterocycle may be oxidized.
- the heterocycle is a 5-10 membered ring system, monocyclic or fused bicyclic.
- Representative examples include, but are not limited to, pyrrolidine, azetidine, piperidine, morpholine, tetrahydrofuran, tetrahydropyran, benzofuran, benzothiophene, indole, benzopyrazole, pyrrole, thiophene (thiophene ), furan, thiazole, imidazole, pyrazole, pyrimidine, pyridine, pyrazine, pyridazine, isothiazole and isoxazole. It should be understood that this term includes heteroaryl as defined herein.
- aryl refers to a monocyclic or polycyclic aromatic hydrocarbon group having 6-20, eg 6-12 carbon atoms in the ring portion.
- aryl is (C 6 -C 10 )aryl.
- Non-limiting examples include phenyl, biphenyl, naphthyl or tetrahydronaphthyl, each of which may be optionally substituted with 1-4 substituents such as alkyl, trifluoromethyl, cycloalkyl , halogen, hydroxyl, alkoxy, acyl, alkyl-C(O)-O-, aryl-O-, heteroaryl-O-, amino, mercapto, alkyl-S-, aryl-S- , nitro, cyano, carboxyl, alkyl-OC(O)-, carbamoyl, alkyl-S(O)-, sulfonyl, sulfonylamino, heterocyclyl, etc
- heteroaryl refers to a 5-20 membered (eg 5-14, 5-8, 5-6) aromatic monocyclic ring containing 1-4 heteroatoms selected from N, O or S or polycyclic ring systems, which may be substituted or unsubstituted.
- heteroaryl is a 5-10 membered ring system, monocyclic or fused bicyclic.
- heteroaryl groups include 2- or 3-thienyl, 2- or 3-furyl, 2- or 3-pyrrolyl, 2-, 4- or 5-imidazolyl, 3-, 4- or 5-pyrazolyl, 2-, 4- or 5-thiazolyl, 3-, 4- or 5-isothiazolyl, 2-, 4- or 5-oxazolyl, 3-, 4- or 5-iso Oxazolyl, 3- or 5-1,2,4-triazolyl, 4- or 5-1,2,3-triazolyl, tetrazolyl, 2-, 3- or 4-pyridyl, 3 - or 4-pyridazinyl, 3-, 4- or 5-pyrazinyl, 2-pyrazinyl, 2-, 4- or 5-pyrimidinyl.
- heteroalkyl means a fully saturated or containing 1 to 3 degrees of unsaturation consisting of the indicated number of carbon atoms and one to ten, preferably one to three, heteroatoms selected from O, N, Si and S Stable straight or branched chain hydrocarbons in which the nitrogen and sulfur atoms are optionally oxidized and the nitrogen heteroatoms are optionally quaternized.
- the heteroatoms O, N, Si and S can be located at any internal position of the heteroalkyl group or at the position where the heteroalkyl group is attached to the rest of the molecule.
- Up to two heteroatoms may be consecutive, such as for example -CH2-NH-OCH3 and -CH2-O-Si(CH3)3.
- a C1 to C4 heteroalkyl or heteroalkylene has 1 to 4 carbon atoms and 1 or 2 heteroatoms
- a C1 to C3 heteroalkyl or heteroalkylene has 1 to 3 carbon atoms and 1 or 2 a heteroatom.
- heteroalkyl and heteroalkylene are saturated.
- substituted used herein to define each group means that the corresponding group may be substituted by groups such as but not limited to: alkyl, alkenyl, alkynyl, cycloalkyl , aryl, heteroaryl, heterocyclyl, halogen, cyano, nitro, azido, carboxyl, hydroxyl, mercapto, amino, mono or dialkylamino, mono or dicycloalkylamino, mono or di Arylamino, mono- or diheterocyclylamino, mono- or diheteroarylamino, alkyl- or cycloalkyl- or heterocyclyl- or heteroaryl- or aryl-oxy, alkyl- or cyclo Alkyl- or heterocyclyl- or heteroaryl- or aryl-thio, alkyl- or cycloalkyl- or heterocyclyl- or heteroaryl- or aryl-acyl, alkyl-
- substituents include, but are not limited to, one or more groups independently selected from the group consisting of halogen, OH, SH, CN, NH 2 , NHCH 3 , N(CH 3 ) 2 , NO 2 , N 3 , C( O)CH 3 , COOH, C(O)-amino, OCOCH 3 , methyl, ethyl, propyl, iso-propyl, butyl, isobutyl, sec-butyl, tert-butyl, cyclopropyl, Methoxy, ethoxy, propoxy, oxo, trifluoromethyl, difluoromethyl, sulfonylamino, methylsulfonylamino, SO, SO 2 , phenyl, piperidinyl, piperazinyl and pyrimidinyl.
- substituted or “substituted” means that one or more (eg, 1, 2, 3, or 4) hydrogens on the designated atom are replaced by the designated group, provided that the designated group does not exceed the Atoms are bonded at their normal valences at the present situation and form stable compounds, and combinations of substituents and variables are permissible only if such combinations form stable compounds.
- linker refers to a bifunctional moiety that links a drug to an antibody in a drug-antibody conjugate.
- Linkers of the invention may have multiple components (eg, in some embodiments, a linker responsible for conjugation to the antibody; a degradable peptide unit; and optionally a spacer).
- PEG unit refers to an organic moiety comprising repeating ethyleneoxy subunits (PEG or PEG subunits), which may be polydisperse, monodisperse, or discrete (i.e., having a discrete number of ethylene-oxyl subunit).
- Polydisperse PEGs are a heterogeneous mixture of sizes and molecular weights, while monodisperse PEGs are usually purified from heterogeneous mixtures and thus have a single chain length and molecular weight.
- Preferred PEG units comprise discrete PEGs, which are compounds synthesized in a stepwise fashion rather than via a polymerization process. Discrete PEGs provide a single molecule with a defined and specified chain length.
- pharmaceutically acceptable salt means a salt that can maintain the biological effects and properties of the ADC conjugate of the present invention, and the salt is not biologically or otherwise undesirable.
- the ADC conjugates of the present invention may exist in the form of their pharmaceutically acceptable salts, including acid addition salts and base addition salts.
- a pharmaceutically acceptable non-toxic acid addition salt refers to a salt formed between the ADC conjugate in the present invention and an organic or inorganic acid
- the organic or inorganic acid includes but is not limited to hydrochloric acid, sulfuric acid, hydrobromic acid , hydriodic acid, phosphoric acid, nitric acid, perchloric acid, acetic acid, oxalic acid, maleic acid, fumaric acid, tartaric acid, benzenesulfonic acid, methanesulfonic acid, salicylic acid, succinic acid, citric acid, lactic acid, propionic acid, Benzoic acid, p-toluenesulfonic acid, malic acid, etc.
- the pharmaceutically acceptable non-toxic base addition salt refers to the salt formed by the ADC conjugate in the present invention and an organic or inorganic base, including but not limited to alkali metal salts, such as lithium, sodium or potassium salts; alkaline earth metal salts , such as calcium or magnesium salts; salts of organic bases, such as ammonium salts formed with organic bases containing N groups.
- alkali metal salts such as lithium, sodium or potassium salts
- alkaline earth metal salts such as calcium or magnesium salts
- salts of organic bases such as ammonium salts formed with organic bases containing N groups.
- solvate means an association formed by one or more solvent molecules and the ADC conjugate of the present invention.
- Solvents that form solvates include, but are not limited to, water, methanol, ethanol, isopropanol, ethyl acetate, tetrahydrofuran, N,N-dimethylformamide, dimethylsulfoxide, and the like.
- DAR drug:antibody ratio
- DAR refers to the ratio of drug moiety (D) to Ab moiety conjugated to the Ab moiety described herein in an ADC conjugate.
- DAR can be determined by q in formula I, for example, DAR can be 1 to 20, such as 2-18, 4-16, 5-12, 6-10, 2-8, 3- 8, 2-6, 4-6, 6-10, eg 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15.
- DAR can also be calculated as the average DAR of the population of molecules in the product, i.e., the Ab moieties conjugated to the Ab moieties described herein, measured by detection methods (e.g., by conventional methods such as mass spectrometry, ELISA assays, electrophoresis and/or HPLC).
- detection methods e.g., by conventional methods such as mass spectrometry, ELISA assays, electrophoresis and/or HPLC.
- the overall ratio of the small molecule drug fraction (D) to the Ab fraction of , this DAR is referred to as the average DAR in the text.
- the conjugates of the invention have an average DAR value of 1 to 20, such as 2-18, 4-16, 5-12, 6-10, 2-8, 3-8, 2-6, 4 -6, 6-10, such as 1.0-8.0, 2.0-6.0, such as 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6 ,2.7,2.8,2.9,3,3.1,3.2,3.3,3.4,3.5,3.6,3.7,3.8,3.9,4,4.1,4.2,4.3,4.4,4.5,4.6,4.7,4.8,4.9,5.0,5.1 , 5.2, 5.3, 5.4, 5.5, 5.6, 5.7, 5.8, 5.9, 6.0, 6.1, 6.2, 6.3, 6.4, 6.5, 6.6, 6.7, 6.8, 6.9, 7.0, 7.1, 7.2, 7.3, 7.4, 7.5, 7.6 ,7.7,7.8.0,7.9,8,8.1,8.2,8.3,8.
- drug encompasses any substance effective in the prevention or treatment of tumors, such as cancer, including chemotherapeutic agents, cytokines, angiogenesis inhibitors, cytotoxic agents, other antibodies, small molecule drugs, or immunomodulators (such as immunosuppressants).
- cytotoxic agent is used in the present invention to refer to a substance that inhibits or prevents cell function and/or causes cell death or destruction.
- examples of cytotoxic agents include, but are not limited to, camptothecins, auristatin, chlortetracycline, maytansinoids, ricin, ricin A chain, combrestatin, duocarcinogen Doxorubicin, doxorubicin, daunomycin, taxazole, cisplatin, cc1065, ethidium bromide, mitomycin, etoposide, tenoposide, vincristine , vinblastine, colchicine, dihydroxyanthracendione, actinomycin, diphtheria toxin, Pseudomonas exotoxin (PE) A, PE40, abrin, abrin A chain, lotus root toxin A Chain, ⁇ -sarcin, gelonin, mitogellin, retstrictocin
- small molecule drug refers to low molecular weight organic compounds capable of modulating biological processes.
- Small molecules are defined as molecules having a molecular weight of less than 10 kD, usually less than 2 kD and preferably less than 1 kD.
- Small molecules include, but are not limited to, inorganic molecules, organic molecules, organic molecules containing inorganic components, molecules containing radioactive atoms, synthetic molecules, peptide mimetics, and antibody mimetics. As therapeutic agents, small molecules can be more cell permeable, less susceptible to degradation, and less prone to eliciting an immune response than larger molecules.
- composition refers to a composition that is present in a form that permits the biological activity of the active ingredients contained therein to be effective and that does not contain additional substances that are unacceptably toxic to the subject to which the composition is administered. ingredients.
- pharmaceutical excipient refers to a diluent, adjuvant (such as Freund's adjuvant (complete and incomplete)), excipient, carrier or stabilizer, etc., which are administered together with the active substance.
- adjuvant such as Freund's adjuvant (complete and incomplete)
- excipient carrier or stabilizer, etc.
- non-fixed combination means that the active ingredients (e.g., (i) an ADC molecule of the invention or an antibody of the invention, and (ii) another therapeutic agent) are combined in separate entities simultaneously, with no specific time limit or in the same or Sequential administration to the patient at different time intervals, wherein such administration provides prophylactically or therapeutically effective levels of the two or more active agents in the patient.
- ADC molecules of the invention or antibodies of the invention and other therapeutic agents used in a pharmaceutical combination are administered at levels no greater than when they are used alone.
- fixed combination means that two or more active agents are administered to a patient simultaneously as a single entity. Dosages and/or intervals of two or more active agents are preferably selected such that the combined use of the parts produces a greater effect in treating a disease or condition than can be achieved by any one component alone.
- the components may each be in the form of separate formulations, which may be the same or different.
- combination therapy refers to the administration of two or more therapeutic agents or treatment modalities, such as radiation therapy or surgery, to treat a disease described herein.
- administration includes co-administration of the therapeutic agents in a substantially simultaneous manner, eg, in a single capsule with fixed ratios of the active ingredients.
- administration includes co-administration for each active ingredient in multiple or in separate containers (eg tablets, capsules, powders and liquids). Powders and/or liquids can be reconstituted or diluted to the desired dosage before administration.
- administration also includes using each type of therapeutic agent in a sequential manner at about the same time or at different times. In either case, the treatment regimen will provide for the beneficial effect of the drug combination in treating the disorders or conditions described herein.
- mammals include, but are not limited to, domesticated animals (e.g., cows, sheep, cats, dogs, and horses), primates (e.g., humans and non-human primates such as monkeys), rabbits, and rodents (e.g., mice and rodents). mouse).
- domesticated animals e.g., cows, sheep, cats, dogs, and horses
- primates e.g., humans and non-human primates such as monkeys
- rabbits e.g., mice and rodents.
- rodents e.g., mice and rodents.
- cancers suitable for treatment by the antibodies of the invention include gastric, pancreatic, or gastroesophageal junction cancers, including metastatic forms of those cancers.
- gastric, pancreatic, or gastroesophageal junction cancers including metastatic forms of those cancers.
- gastroesophageal junction cancers including metastatic forms of those cancers.
- the term also covers all neoplastic cell growth and proliferation, whether malignant or benign, and all pre-cancerous and cancerous cells and tissues.
- anti-tumor effect refers to a biological effect that can be exhibited by various means, including but not limited to, for example, reduction in tumor volume, reduction in tumor cell number, reduction in tumor cell proliferation, or reduction in tumor cell survival.
- treating means slowing, interrupting, arresting, alleviating, stopping, reducing, or reversing the progression or severity of an existing symptom, disorder, condition, or disease.
- prevention includes the inhibition of the occurrence or development of a disease or disorder or a symptom of a particular disease or disorder.
- subjects with a family history of cancer are candidates for prophylactic regimens.
- prevention refers to the administration of a drug prior to the onset of signs or symptoms of cancer, especially in subjects at risk of cancer.
- the term "effective amount” refers to such an amount or dose of the antibody drug conjugate of the present invention or its composition or combination, which, after being administered to a patient in single or multiple doses, is effective in a patient in need of treatment or prophylaxis. produce the expected effect.
- the term "therapeutically effective amount” refers to an amount effective, at dosages required, and for periods of time required, to achieve the desired therapeutic result.
- a therapeutically effective amount is also one in which any toxic or detrimental effects of the antibody drug conjugate of the invention or a composition or combination thereof are outweighed by the therapeutically beneficial effects.
- a “therapeutically effective amount” preferably achieves at least about 30%, even more preferably at least about 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90% or even 100% inhibition.
- prophylactically effective amount refers to an amount effective, at dosages required, and for periods of time required, to achieve the desired prophylactic result. Typically, a prophylactically effective amount will be less than a therapeutically effective amount because the prophylactic dose is administered in the subject before or at an earlier stage of the disease.
- the term "CLDN18.2 positive" tumor means that at least a part of cancer cells in tumor organs or tissues are positive for CLDN18.2 cell surface expression.
- the proportion of CLDN18.2 positive cancer cells in cancer tissue or cancer cell group is at least 10% or 20%, preferably at least 30%, 40%, 50%, 60%, 70%, 75% % or 80%.
- at least 40% or at least 50%, preferably 60%, 70%, 80% or 90% of the cancer cells in the tumor tissue or organ are positive for surface expression of CLDN18.2.
- cancer subjects treated according to the methods of the invention have increased cell surface expression levels of CLDN18.2 in diseased tissues or organs compared to corresponding tissues and organs in healthy subjects, e.g., by at least 10%, especially at least 20%, at least 50%, at least 100%, at least 200% or more.
- the CLDN18.2 positive tumor is selected from the group consisting of gastric cancer, esophageal cancer, pancreatic cancer, lung cancer (e.g., non-small cell lung cancer (NSCLC)), ovarian cancer, colon cancer, liver cancer, head and neck cancer, and gallbladder cancer, and Metastasis, especially gastric cancer metastasis.
- NSCLC non-small cell lung cancer
- the cancer is adenocarcinoma, especially advanced adenocarcinoma.
- Particularly preferred cancer diseases are adenocarcinomas of the stomach, esophagus, pancreatic duct, bile duct, lung and ovary.
- cancers treated in accordance with the invention are HER negative.
- the CLDN18.2 positive tumor is a cancer of the digestive system or a metastasis thereof.
- the cancer is selected from gastric cancer, esophageal cancer (especially lower esophageal cancer), cancer of the esophago-gastric junction and gastroesophageal cancer.
- the cancer is eg CLAUDIN 18.2 positive and HER2 negative gastric cancer.
- the cancer is gastroesophageal cancer, such as metastatic, refractory or recurrent advanced gastroesophageal cancer, in yet another embodiment, the cancer is metastatic gastric cancer or gastroesophageal junction cancer (EGJA) .
- EGJA gastroesophageal junction cancer
- the present invention provides an antibody-drug conjugate (ADC) having the following formula (I) or a pharmaceutically acceptable salt or solvate thereof:
- D represents a cytotoxic or cytostatic drug, for example, a topoisomerase I inhibitor
- the present inventors have developed and provided a humanized anti-Claudin18.2 monoclonal antibody with excellent properties.
- the antibody of the present invention not only exhibits high binding affinity and high specificity to cells expressing human Claudin18.2 on the surface (especially cells with low surface expression abundance), but also has the ability to express human Claudin18.2 antigen-mediated Therefore, it is suitable as a molecular component to couple with cytotoxic drugs to form antibody-drug conjugates.
- the ADC conjugate formed by the antibody of the present invention exhibits a potent in vivo tumor killing effect, and at the same time has good drug tolerance.
- the invention provides an antibody-drug conjugate (ADC) comprising an antibody of the invention that specifically binds Claudin 18.2 as the Ab unit of the conjugate of Formula I of the invention.
- ADC antibody-drug conjugate
- the Ab in formula (I) of the present invention comprises three CDRs of the heavy chain variable region (VH) sequence of SEQ ID NO: 1 or 3 and the light chain variable region of SEQ ID NO: 2 ( VL) three CDRs of the sequence, and preferably, wherein said CDRs are defined according to Kabat or IMGT or a combination thereof.
- the Ab of formula (I) of the invention comprises 3 heavy chain complementarity determining regions (HCDRs) and 3 light chain complementarity determining regions (LCDRs), wherein:
- HCDR1 comprises or consists of the amino acid sequence of SEQ ID NO:6
- HCDR2 comprises or consists of the amino acid sequence of SEQ ID NO:7
- HCDR3 comprises or consists of the amino acid sequence of SEQ ID NO:8
- LCDR1 comprises or consists of the amino acid sequence of SEQ ID NO:9
- LCDR2 comprises or consists of the amino acid sequence of SEQ ID NO:10
- LCDR3 comprises or consists of the amino acid sequence of SEQ ID NO:11;
- HCDR1 comprises or consists of the amino acid sequence of SEQ ID NO: 12
- HCDR2 comprises or consists of the amino acid sequence of SEQ ID NO: 13
- HCDR3 comprises or consists of the amino acid sequence of SEQ ID NO: 14
- LCDR1 comprises or consists of the amino acid sequence of SEQ ID NO:15
- LCDR2 comprises the amino acid sequence of SEQ ID NO:16 or consists of it
- LCDR3 comprises the amino acid sequence of SEQ ID NO:17 or consists of it.
- the Ab in formula (I) of the present invention comprises the heavy chain and light chain variable region sequences or variants thereof of any one of the exemplary antibodies 25C7A5-HZ1 and -HZ2 of the present invention, for example, having the same An antibody having the same CDR sequence as one of the exemplary antibodies and having the same or different framework region sequence.
- the Ab in formula (I) of the present invention comprises a heavy chain variable region, wherein: said heavy chain variable region comprises:
- amino acid sequence shown in SEQ ID NO: 1 or an amino acid sequence having at least 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity thereto, or
- amino acid sequence shown in SEQ ID NO: 3 or an amino acid sequence having at least 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity thereto.
- the Ab in formula (I) of the present invention comprises a light chain variable region, wherein: said light chain variable region comprises:
- amino acid sequence shown in SEQ ID NO: 2 or an amino acid sequence having at least 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity thereto.
- the Ab in formula (I) of the present invention comprises a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region comprises amino acids described in SEQ ID NO: 1 or 3 sequence or an amino acid sequence having at least 95%, 96%, 97%, 98% or 99% sequence identity therewith, and wherein said light chain variable region comprises the amino acid sequence shown in SEQ ID NO: 2, or has Amino acid sequences having at least 95%, 96%, 97%, 98% or 99% sequence identity.
- said antibody sequences are humanized. More preferably, the heavy chain variable region of the antibody has a framework region sequence derived from the human germline, and preferably has an amino acid Q or E, preferably an amino acid at position H6 according to Kabat numbering in the heavy chain variable region Q.
- the Ab in formula (I) of the present invention comprises the heavy chain variable region of SEQ ID No: 1 and the light chain variable region of SEQ ID No: 2.
- the Ab in formula (I) of the present invention comprises the heavy chain variable region of SEQ ID No:3 and the light chain variable region of SEQ ID No:2.
- the Ab in formula (I) of the present invention preferably further comprises the heavy chain constant region and/or the light chain constant region of the antibody.
- the heavy chain constant region is a heavy chain constant region derived from human immunoglobulin.
- the light chain constant region is a light chain constant region derived from human immunoglobulin.
- the heavy chain constant region comprised in the Ab can be of any isotype or subtype, such as an IgG1, IgG2, IgG3 or IgG4 isotype heavy chain constant region, and preferably an IgG1, IgG2 or IgG4 heavy chain constant region, especially the human IgG1 heavy chain constant region.
- the light chain constant region comprised in the Ab can be a kappa light chain constant region or a lambda light chain constant region, especially a human kappa light chain constant region.
- the Ab of formula (I) of the invention comprises a human IgGl heavy chain constant region.
- the heavy chain constant region comprises the amino acid sequence of SEQ ID NO: 4, or comprises at least one, two or three, but no more than 20, 10 or 5 amino acid sequences relative to the amino acid sequence of SEQ ID NO: 4
- the Ab of formula (I) of the invention comprises a human kappa light chain constant region.
- the light chain constant region comprises the amino acid sequence of SEQ ID NO: 5, or at least one, two or three, but no more than 20, 10 or 5 relative to the amino acid sequence of SEQ ID NO: 5 Amino acid sequence with amino acid changes, or a sequence with at least 95-99% identity to the amino acid sequence of SEQ ID NO:5.
- the Ab of formula (I) of the invention is a full-length antibody comprising a heavy chain constant region and a light chain constant region. In some embodiments, the Ab of formula (I) of the invention has a tetrameric structure formed by two light chains and two heavy chains. In still other embodiments, the Ab in formula (I) of the present invention is an IgG antibody, especially an IgG1 antibody. In a further embodiment, the Ab in formula (I) of the invention is a humanized antibody.
- the Ab in formula (I) of the present invention comprises a heavy chain and a light chain, wherein: the heavy chain comprises the amino acid sequence shown in SEQ ID NO: 18 or 19, or at least 80% thereof , 85%, 90%, 95%, 96%, 97%, 98% or 99% sequence identity of amino acid sequences, or consist thereof.
- the Ab in formula (I) of the present invention comprises a heavy chain and a light chain, wherein: the light chain comprises the amino acid sequence shown in SEQ ID NO: 20, or at least 80%, 85% thereof Amino acid sequences having %, 90%, 95%, 96%, 97%, 98% or 99% sequence identity.
- the Ab in formula (I) of the invention comprises a heavy chain and a light chain selected from:
- Antibody variants of the invention preferably retain at least 60%, 70%, 80%, 90%, or 100% of the biological activity (eg, antigen binding ability) of the pre-altered antibody. More preferably, the alterations do not result in the antibody variant losing binding to the antigen, but optionally confer properties such as increased affinity for the antigen and different effector functions. It is understood that the antibody heavy chain variable region or light chain variable region, or each CDR region can be altered individually or in combination. In addition, changes can also be made to the Fc region of the antibody. Alterations to the Fc region can be made alone, or in combination with the aforementioned changes to the framework and/or CDR regions.
- the Fc region can be altered, eg, to alter one or more functions of the antibody, such as serum half-life, complement fixation, Fc receptor binding, and/or antigen-dependent cellular cytotoxicity.
- antibodies of the invention may be chemically modified (eg, attached to PEG) or their glycosylation pattern altered.
- antibodies according to the invention can be conjugated to toxin-linkers using some of the natural attachment sites thereon.
- natural attachment sites are the sulfhydryl group of cysteine and the amino group of lysine.
- DAR drug-to-antibody ratio
- toxins are coupled to antibodies of the invention by sulfhydryl chemistry following reduction of the interchain disulfide bonds of the antibody to form ADC conjugates of formula (I).
- the introduction of artificial linking sites in the antibody can also be considered to achieve more site-specific conjugation.
- the drug D unit of the antibody-drug conjugate is also referred to herein as the payload of the ADC drug.
- the drug D that can be used in the ADC of the present invention is not particularly limited, and can be any drug or its prodrug that is toxic or inhibitory to cells. Those skilled in the art can select a suitable drug molecule as the payload of the ADC according to the required ADC drug onset mechanism and cell killing effect.
- Drug D is a cytotoxic agent.
- cytotoxic agents suitable for use as payloads have been reported, including, but not limited to,
- Microtubule inhibitory/destroying agents such as, but not limited to, auristatins (eg, MMAE or MMAF), maytansine derivatives (eg, DM2, DM4), Tubulysins, cryptocolistin (Cryptomycins), anti-mitotic EG5 inhibitors (eg, spindle kinesin KSP inhibitors);
- auristatins eg, MMAE or MMAF
- maytansine derivatives eg, DM2, DM4
- Tubulysins eg, cryptocolistin (Cryptomycins)
- anti-mitotic EG5 inhibitors eg, spindle kinesin KSP inhibitors
- DNA damaging agents such as, but not limited to, pyrrolobenzodiazepines (Pyrrolobenzodiazepines) (for example, pyrrolo[2,1-c][1,4]benzodiazepines (PBD )), Duocarmycin, Indolinobenzodiazepine; Duocarmycins; Calicheamicins;
- Topoisomerase inhibitors for example, but not limited to, camptothecins (eg, exitecan and its derivative Dxd);
- the drug D in the formula (I) of the present invention may be any compound selected from the above.
- drug D is an anti-tumor growth inhibitor selected from maytansine derivatives, calicheamicin derivatives, and auristatin derivatives.
- Drug D is a tubulin inhibitor/stability destabilizer such as vinca alkaloids, vincristine, paclitaxel and docetaxel.
- drug D is a DNA synthesis inhibitor, eg, methotrexate, 5-fluorouracil, cytarabine, gemcitabine, mercaptopurine, pentostatin, fludarabine, cladribine.
- drug D is a DNA topoisomerase inhibitor, e.g., topoisomerase I inhibitors (e.g., camptothecins) and topoisomerase II inhibitors (e.g., actinomycin D , doxorubicin, mitoxantrone).
- topoisomerase I inhibitors e.g., camptothecins
- topoisomerase II inhibitors e.g., actinomycin D , doxorubicin, mitoxantrone
- the drug D of the ADC according to the invention is a topoisomerase I inhibitor.
- a typical example of a topoisomerase I inhibitor is a camptothecin class of drugs such as, but not limited to, camptothecin (CPT), hydroxycamptothecin, 9-aminocamptothecin, exatecan, topotecan, belotecan, irinotecan , SN-38, and FL118, and their derivatives.
- CPT camptothecin
- CPT camptothecin
- hydroxycamptothecin hydroxycamptothecin
- 9-aminocamptothecin 9-aminocamptothecin
- exatecan topotecan
- belotecan belotecan
- irinotecan irinotecan
- SN-38 SN-38
- FL118 FL118
- the drug D of the ADC of the present invention is a camptothecin drug selected from the following:
- RA is selected from, for example, hydrogen, optionally substituted alkyl, wherein substituents include but are not limited to hydroxy, amino, wherein the amino moiety or hydroxy moiety may be substituted or unsubstituted, e.g., by alkyl, alkylacyl , or alkylsulfonyl substitution;
- substituents include but are not limited to hydroxy, amino, wherein the amino moiety or hydroxy moiety may be substituted or unsubstituted, e.g., by alkyl, alkylacyl , or alkylsulfonyl substitution;
- the drug D is selected from, for example, hydrogen, optionally substituted alkyl, wherein substituents include but are not limited to hydroxy, amino, wherein the amino moiety or hydroxy moiety may be substituted or unsubstituted, e.g., by alkyl, alkylacyl , or alkylsulfonyl substitution;
- the drug D is
- R B is selected from, for example, hydrogen, cycloalkyl, phenyl, optionally substituted alkyl, wherein the substituents include, but are not limited to, halogen, hydroxy, optionally substituted alkoxy, cycloalkyl, heterocyclic Alkyl, phenyl, amino, wherein the amino moiety may be optionally substituted; in one embodiment, the drug D is
- HCPT -10-hydroxy CPT
- R C is selected from, for example, optionally substituted alkyl and cycloalkyl;
- R' C is selected from, for example, H, alkanoyl or optionally substituted heterocycloalkyl acyl;
- the drug D It is 7-ethyl-10-hydroxy CPT (SN-38) or its prodrug irinotecan (irinotecan, CPT-11), or the drug D is topotecan
- the drug D is:
- F118 ((20S)-10,11-methylenedioxycamptothecin) was obtained by high-throughput screening compound library. Compared with other camptothecin derivatives, FL118 has been demonstrated to have much higher in vivo and in vitro anticancer activity in many different cancer types. In addition to inhibiting topoisomerase I, FL118 can also selectively inhibit gene promoter activity and endogenous expression of anti-apoptotic proteins such as survivin, XIAP, cIAP2 and Mcl-1.
- the conjugate formed by combining the compound with the antibody of the present invention and the linker not only effectively exerts this
- the compound has a tumor-killing effect, and overcomes the defects of the compound, and the formed conjugate has a small degree of aggregation and has good animal tolerance.
- the drug D of the ADC of the present invention is a FL118 derivative, especially a 7-substituted FL118.
- the drug D in formula (I) of the present invention is a camptothecin drug comprising the following formula D structure:
- R x , R y are each independently selected from H, halogen, -OH, C 1- C 6 alkyl, or R x and R y form together with the carbon atoms they are connected to have 1 or 2 selected from N, S and 5-6 membered heterocycle of O;
- R a is selected from H, halogen, -OH, optionally substituted C 1 -C 8 alkyl or C 3 -C 8 alkynyl or C 3 -C 8 alkenyl, optionally substituted C 1 -C 8 alkoxy Base, optionally substituted C 3- C 8 cycloalkyl, optionally substituted phenyl, optionally substituted heterocycloalkyl, optionally substituted heteroaryl,
- R a is selected from:
- R 1 and R 2 are independently selected from
- C 1 -C 8 alkyl optionally substituted with substituents selected from the group consisting of hydroxy, amino, amino substituted by one or two C 1 -C 4 alkyl, one or two C 1 -C 4 Amino groups substituted by hydroxyalkyl, amino groups substituted by (C 1 -C 4 hydroxyalkyl) and (C 1 -C 4 alkyl);
- R and R combined with the nitrogen atom to which they are attached form a 5-, 6- or 7-membered heterocyclic ring having 0 to 3 substituents selected from halogen, C 1 -C 4 alkyl , OH, C 1 -C 4 alkoxy, NH 2 , NH(C 1 -C 4 alkyl) and N(C 1 -C 4 alkyl) 2 ,
- cycloalkyl, heterocycloalkyl, phenyl, and heteroaryl are each independently optionally substituted by 0-3 substituents selected from the group consisting of OH, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, NH 2 , NH(C 1 -C 4 alkyl) and N(C 1 -C 4 alkyl) 2 substitutions.
- Rx and Ry are each independently H. In other preferred embodiments, Rx is F and Ry is methyl. In yet other preferred embodiments, R x and R y together with the carbon atoms to which they are attached form a 5 membered heterocyclic ring containing 2 O's.
- the drug D in formula (I) of the present invention is a camptothecin drug comprising the following formula D a or formula D b structure:
- camptothecins of formula (D a ) are especially camptothecins of formula (D a ).
- R a is selected from:
- R 1 and R 2 are independently selected from
- C 1 -C 8 alkyl optionally substituted with substituents selected from the group consisting of hydroxy, amino, amino substituted by one or two C 1 -C 4 alkyl, one or two C 1 -C 4 Amino groups substituted by hydroxyalkyl, amino groups substituted by (C 1 -C 4 hydroxyalkyl) and (C 1 -C 4 alkyl);
- R and R combined with the nitrogen atom to which they are attached form a 5-, 6- or 7-membered heterocyclic ring having 0 to 3 substituents selected from halogen, C 1 -C 4 alkyl , OH, C 1 -C 4 alkoxy, NH 2 , NH(C 1 -C 4 alkyl) and N(C 1 -C 4 alkyl) 2 ,
- cycloalkyl, heterocycloalkyl, phenyl, and heteroaryl are each independently optionally substituted by 0-3 substituents selected from the group consisting of OH, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, NH 2 , NH(C 1 -C 4 alkyl) and N(C 1 -C 4 alkyl) 2 substitutions.
- Ra is hydrogen
- R a is C 3 -C 8 cycloalkyl (eg, cyclopropyl, cycloheptyl, cyclopentyl).
- Ra is phenyl. In other embodiments, R a is phenyl substituted with NH 2 or NH(C 1 -C 4 alkyl).
- R a is C 1 -C 6 alkyl, for example, methyl, ethyl, propyl, 2-methylpropyl, butyl, isobutyl, 2,2-dimethyl- Propyl, 2,2-Dimethyl-butyl, n-hexyl, n-pentyl, 3-ethyl-pentyl.
- R a is C 1 -C 4 alkyl optionally substituted by hydroxy or C 1 -C 4 alkoxy, wherein alkoxy is optionally further replaced by -NH 2 , -NH( C 1 -C 4 alkyl) and -N(C 1 -C 4 alkyl) 2 substituted.
- R a is C 2 -C 4 alkenyl or C 2 -C 4 alkynyl, optionally substituted with hydroxy or amino.
- Ra is C 1 -C 4 alkyl substituted with 1 or 2 5-6 membered heterocycloalkyls selected from N, S, and O, wherein the heterocycloalkyl moiety is optionally Further substituted by C 1 -C 4 alkyl, preferably, the heterocycloalkyl is piperazinyl or morpholinyl.
- R a is C 1 -C 4 alkyl substituted by -NR 1 R 2 , especially -methylene-NR 1 R 2 , wherein R 1 and R 2 are independently selected from each other:
- Phenyl Halogenated phenyl
- R a is C 1 -C 4 alkyl substituted by -NR 1 R 2 , especially -methylene-NR 1 R 2 , wherein R 1 and R 2 are combined with the nitrogen atom to which they are attached A 5-, 6- or 7-membered heterocycloalkyl ring is formed.
- R 1 and R 2 combine with the nitrogen atom to which they are attached to form a 6-membered ring.
- the 6-membered ring is morpholinyl or piperazinyl.
- R a is -C 1 -C 4 alkylene-OH, -C 1 -C 4 alkylene-OC 1 -C 4 alkylene-NH 2 , or -C 1 -C 4 alkylene-NH 2 .
- R a is -C 1 -C 4 alkylene-OH.
- Ra is hydroxymethyl.
- Ra is hydroxyethyl.
- Ra is hydroxypropyl.
- R a is -C 1 -C 4 alkylene-NH 2 .
- Ra is aminomethyl.
- Ra is aminoethyl.
- Ra is aminopropyl.
- the drug D is linked to the linker L through a free hydroxyl or amino group on it, so as to be coupled to the antibody. More preferably, the drug D of formula D or formula D a or D b is connected to the linker L through the hydroxyl or amino group on R a to be coupled to the antibody.
- R a has a structure selected from the following after being connected with a linker:
- R a after being connected with the linker has a structure selected from the following:
- R a after linking with the linker has a structure selected from the following:
- the wavy line on the left indicates the position connected with the linker L
- the asterisk on the right indicates the position connected with the camptothecin mother nucleus.
- the L-D units in formula (I) of the present invention comprise the following structures:
- the L-D unit in formula (I) comprises the following structure:
- the linker L suitable for the present invention may be any linker capable of coupling the antibody of the present invention with a drug.
- the linker should be added to ensure sufficient stability of the ADC of the invention in the circulation, while providing rapid and efficient release of the active form of the toxic drug at the target site (eg, tumor cells or the tumor environment).
- the linker in formula (I) of the present invention is a non-degradable linker.
- a non-degradable linker includes, but is not limited to, N-succinimidyl-4-(N-maleimidomethyl)cyclohexane-1-carboxylate (SMCC).
- SMCC N-succinimidyl-4-(N-maleimidomethyl)cyclohexane-1-carboxylate
- ADCs containing such linkers must be internalized by the cell, and the antibody portion of the ADC is degraded by intracellular lysosomal proteases, releasing the pharmaceutically active molecule.
- the linker in formula (I) of the present invention is a degradable linker.
- Drug release from ADCs comprising such linkers is triggered by the nature of the cleavage site in the linker.
- the cleavage site of such linkers can be designed according to the characteristics of the target therapeutic site (eg, tumor cell lysosome and/or tumor environment).
- a degradable linker can consist of a coupling moiety, a degradable moiety, and optionally a spacer moiety.
- the conjugation moiety is responsible for the attachment of the antibody to the linker-drug and can be selected according to the desired antibody conjugation chemistry.
- the degradable moieties will comprise peptides or peptide analogs that are recognized by enzymes under an enzyme-based release mechanism, for example, Val-Ala, Val-Cit, Phe-Lys, Gly-Phe-Leu- Gly, Ala-Leu-Ala-Leu, Gly-Gly-Phe-Gly, cyclobutyl-Ala, cyclobutyl-Cit and other oligopeptides or oligopeptide analogues.
- ADC properties can be improved by introducing modifications in the linker at peptide residue positions adjacent to the enzymatic cleavage site, for example, the stability of the ADC in blood circulation and/or the drug resistance of the ADC at the target site.
- a spacer can also be introduced between the degradable part of the linker and the drug D to facilitate the release of the drug active molecule from the rest of the conjugate (especially, traceless release), for example , a p-aminobenzyl carbamate (PABA) or aminomethyl (-NHCH 2 -) spacer that can be eliminated spontaneously in acidic medium.
- PABA p-aminobenzyl carbamate
- -NHCH 2 - aminomethyl
- Linkers applicable to the present invention include, but are not limited to, those disclosed in WO2022/170971 (this document is hereby incorporated by reference).
- the linker L in formula (I) of the present invention has the structure of formula (II):
- Z is the linker connected with Ab
- Y is a peptide of 2-5 amino acids, preferably a dipeptide, tripeptide or tetrapeptide,
- M is absent, or is a spacer for attachment of drug D.
- the sulfur group of antibody cysteine exists in the form of a disulfide bond. Opening of antibody disulfide bonds provides free sulfhydryl groups as conjugation sites.
- One way to form ADC by conjugating antibody sulfhydryl groups is to make Michael addition reaction between the free sulfhydryl groups on the antibody and heterocyclic (eg maleimide) linkers.
- Another way is to make a nucleophilic substitution reaction between a linker comprising a heteroaryl ring substituted with a leaving group and a free sulfhydryl group in an antibody molecule to obtain an antibody-drug conjugate. Both approaches are applicable to the ADC conjugates of the present invention.
- linkers according to the invention may in some aspects comprise heterocyclic (eg maleimides) or heteroaromatic (eg pyrimidines) Z linkers; and, in some cases, preferably comprise heterocyclic Aromatic (eg, pyrimidine) linkers to provide conjugates with greater stability in blood circulation.
- Z in formula (II) has the following structure:
- Z is a 5-10 membered heterocyclic group, preferably containing 1 or 2 heteroatoms selected from N, S and O;
- Z 4 is a bond or a PEG unit represented by the formula
- R 5 is selected from C 1-4 alkylene, -NH-, -NH-C 1-4 alkylene-heteroaryl-, wherein heteroaryl is 5-membered or 6-membered nitrogen-containing heteroaryl , preferably triazolyl;
- Z is 5-10 membered heteroaryl.
- Z is selected from pyrimidine, thiazole, benzene optionally substituted with one or more independently selected from hydrogen, halogen, nitro, C1-6 alkyl and halogenated C1-6 alkyl Prothiazole, oxazole, quinazoline and pyrrolo[2,3d]pyrimidine.
- Z is heteroaryl selected from the group consisting of,
- Z2 is linked to Z1 through a carbon atom adjacent to the heteroatom.
- Z is pyrimidinylidene, preferably more preferred.
- the wavy line on the left indicates the position connected to Z 1 ; the wavy line on the right indicates the position connected to Z 3 .
- Z is maleimide
- the wavy line on the left indicates the position connected to Z 1 ; the wavy line on the right indicates the position connected to Z 3 .
- n' is 1-6, preferably, Z 3 is more preferred
- the wavy line on the left side represents the position connected with Z2
- the wavy line on the right side represents the position connected with Z4
- Z2 is a pyrimidinyl group
- Z 2 is pyrimidinylene
- Z 2 is maleimide
- Z 4 is a bond and Z 3 is directly linked to Y in formula (II).
- Z is selected from:
- Z in formula (I) of the present invention has the following structure:
- Z in formula (I) of the present invention has the following structure:
- Z in formula (I) of the present invention has the following structure:
- S is a sulfur atom in Ab
- R b is
- Z has the structure:
- Z in formula (I) of the present invention has the following structure:
- Z in formula (I) of the present invention has the following structure:
- antibody-drug conjugates For the purpose of limiting or minimizing the off-target toxicity of ADCs while ensuring release of the toxin molecules at the target tumor site, in some aspects it is advantageous to design antibody-drug conjugates so that they are highly selective in targeting Simultaneously to tumor cells, it can be degraded by proteolytic enzymes in tumor cells or in the environment (in particular, enzymes with significantly higher activity in tumor cells and/or in the tumor environment relative to blood).
- proteolytic enzymes in tumor cells or in the environment (in particular, enzymes with significantly higher activity in tumor cells and/or in the tumor environment relative to blood).
- oligopeptides or oligopeptide analogs that can be recognized and cleaved by such proteolytic enzymes can be included in the linker of such ADC conjugates.
- the Y unit that is part of the linker of the invention is a peptide-containing degradable moiety, e.g., containing two or more (e.g., 2-12, e.g. 2,3,4,5, or 6) degradable peptide linkers of continuous or discontinuous amino acids.
- Each amino acid of the peptide-containing unit may independently of one another be selected from natural amino acids or unnatural amino acids, for example from: alanine, arginine, aspartic acid, asparagine, histidine, glycine, glutamic acid , glutamine, phenylalanine, lysine, substituted lysine, leucine, serine, tyrosine, threonine, isoleucine, proline, tryptophan, valine , cysteine, methionine, selenocysteine, ornithine, beta-alanine, citrulline, and their derivatives.
- natural amino acids or unnatural amino acids for example from: alanine, arginine, aspartic acid, asparagine, histidine, glycine, glutamic acid , glutamine, phenylalanine, lysine, substituted lysine, leucine, serine, tyrosine, threonine,
- each amino acid is independently selected from alanine, arginine, aspartic acid, asparagine, histidine, glycine, glutamic acid, glutamine, phenylalanine, lysine amino acid, leucine, serine, tyrosine, threonine, isoleucine, proline, tryptophan, valine, cysteine, methionine and their derivatives.
- each amino acid is independently selected from alanine, arginine, aspartic acid, asparagine, histidine, glycine, glutamic acid, glutamine, phenylalanine, lysine amino acid, leucine, serine, tyrosine, threonine, isoleucine, proline, tryptophan and valine, N-methylglycine, ⁇ -alanine, and their derivatives .
- the amide bond in the Y unit will be recognized and degraded by enzymes in tumor cell lysosomes, releasing the drug moiety D.
- the amide bond in the Y unit can be recognized and degraded by enzymes in the tumor environment, releasing the drug moiety D.
- Linkers with such Y-containing peptide units will facilitate the release of toxin molecules in tumor cells and the environment by designing antibody-drug conjugates that favor tumor distribution.
- Y is a unit comprising a unit selected from the group consisting of: Val-Cit, Phe-Lys, Val-Ala, Val-Lys-Gly, Ala-Ala-Ala, Val-Ala, Gly-Phe-Leu-Gly , Ala-Leu-Ala-Leu, Gly-Gly-Phe-Gly, Cyclobutyl-Ala, Cyclobutyl-Cit.
- Y is a unit comprising a unit selected from the group consisting of: Val, Cit, Phe, Lys, D-Val, Leu, Gly, Ala, Asn, Cit-Val, Val-Ala, Lys-Val, Val-Lys (Ac), Phe-Lys, Phe-Lys(Ac), D-Val-Leu-Lys, Gly-Gly-Arg, Ala-Ala-Asn.
- Y is a dipeptide, tripeptide, tetrapeptide or pentapeptide comprising substituted lysines.
- the substituted lysine is:
- R 3 and R 4 are independently selected from: H, C 1-6 alkyl, -CO-NH 2 , -CONH (C 1-6 alkyl), and -CONH (C 1-6 alkyl) 2 , wherein the alkyl group is optionally substituted by a group selected from the group consisting of halogen, C 1-6 alkoxy, C 1-6 haloalkyl, C 3-6 cycloalkyl, 6-10 membered aryl and 5-14 membered heteroaryl.
- Y is a peptide having the following amino acid sequence from N-terminus to C-terminus;
- Xaa 1 is absent, or is an amino acid selected from valine, glycine, alanine and glutamic acid;
- Xaa 2 is an amino acid selected from phenylalanine, leucine, alanine and valine, preferably valine;
- Xaa 3 is unsubstituted or substituted lysine
- Xaa4 is an amino acid selected from leucine, glycine and alanine;
- Xaa 5 is absent, or is an amino acid selected from glycine and alanine;
- N-terminal of the amino acid sequence is connected to the Z unit of the linker, and the C-terminal is connected to the M unit or directly connected to the drug D,
- Xaa 3 is lysine in which the ⁇ -amino group is mono- or di-substituted by C 1 -C 3 alkyl,
- Y is a peptide selected from the group consisting of: Phe-Lys-Gly, Leu-lys-Gly, Gly-Val-Lys-Gly, Val-Lys-Gly-Gly, Val-Lys-Gly, Val-Lys- Ala, Val-Lys-Leu, wherein the Lys residue is lysine which is unsubstituted or mono- or di-substituted by C 1 -C 3 alkyl.
- the ADC conjugates of the invention have a spacer (M) between the releasable peptide-containing unit (Y) and the drug (D).
- the spacer can be a functional group that facilitates attachment of the peptide-containing unit (Y) to drug D, or can provide an additional structural component to further facilitate the release of drug D from the rest of the conjugate (e.g., a self-degrading group such as p-amino benzyl (PAB) component).
- PAB p-amino benzyl
- the M spacer between the Y and Drug D units can be selected from:
- the wavy line on the left indicates the connection with Y
- the wavy line on the right indicates the connection with the D unit of the drug.
- M is a covalent bond
- Y in formula I and drug D are directly connected, such as through an amide bond.
- the Y-M unit in linker L comprises the following structure:
- the Y-M unit is connected with the following Z unit:
- L in formula (I) of the present invention is a linker comprising the following structure:
- R3 and R4 are each independently selected from methyl, ethyl, propyl. In some more preferred embodiments, both R3 and R4 are methyl; or both R3 and R4 are ethyl; or both R3 and R4 are propyl.
- the L-D unit of formula I of the present invention is linked to the antibody by forming a thioether bond with the sulfhydryl group of the free cysteine of the light chain and/or heavy chain of Ab.
- the present invention provides an ADC conjugate having the following structure, or a pharmaceutically acceptable salt or solvate thereof:
- q represents an average DAR value of 1-20, such as an average DAR value of approximately 2, 4, 6 and 8.
- ADCs according to the present invention have at least one or more of the following advantages:
- the ADC according to the present invention may also have at least one or more of the following advantages:
- DAR can be as high as 8.
- conjugation of the drug-linker to the antibody is accomplished by reaction with amino acid residues of the antibody.
- a heteroaryl linker L with a leaving group is used to couple a drug D to a cysteine residue of an antibody to prepare a conjugate of formula I of the present invention.
- interchain disulfide bonds of the antibody are broken and free sulfhydryl groups are exposed for attachment to heteroaryl linkers by controlling the conditions under which the antibody is treated with a reducing agent such as tris(2-hydroxyethyl)phosphine (TCEP). - drug conjugation.
- TCEP tris(2-hydroxyethyl)phosphine
- Conjugates prepared by this method can contain zero, one, two, three, four, five, six, seven or eight drugs per antibody molecule.
- the drug loading of the conjugate is represented by the average DAR, which is the average number of drug molecules per antibody.
- the average number of drug per antibody of the antibody-drug conjugate composition produced by the preparation can be characterized by conventional means, such as mass spectrometry, ELISA assay and HPLC.
- the quantitative distribution expressed as q of the antibody-drug conjugate can also be determined.
- the separation, purification and characterization of homogeneous antibody-drug conjugates in which q is a certain value and antibody-drug conjugates with other drug loadings can be achieved by means such as reversed-phase HPLC or electrophoresis.
- q represents the number of drug-linker (L-D) moieties coupled to an individual antibody (Ab), and is preferably 1 to 16, 1 to 12, 1 to 10, or An integer from 1 to 8.
- the individual ADC conjugates may also be referred to as ADC compounds.
- on the ADC compound according to the invention there may be 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or 16
- Each drug linker moiety is coupled to a single antibody.
- q represents the average DAR of the prepared conjugate composition.
- q can be in the range of 1 to about 16, 1 to about 12, 1 to about 10, or 1 to about 8, 2 to about 16, 2 to about 12, 2 to about 10, or 2 to about An integer or decimal in the range of 8.
- q represents an average DAR of about 6.
- q represents an average DAR of about 8.
- the present invention provides a composition, preferably a pharmaceutical composition or pharmaceutical formulation, comprising any ADC described herein, or a pharmaceutically acceptable salt or solvate thereof.
- the composition further comprises pharmaceutical excipients.
- a composition eg, a pharmaceutical composition, comprises an ADC of the invention, or a pharmaceutically acceptable salt or solvate thereof, in combination with one or more other therapeutic agents.
- compositions comprising an ADC of the present invention, or a pharmaceutically acceptable salt or solvate thereof.
- compositions may also contain suitable pharmaceutical excipients, such as pharmaceutical carriers, pharmaceutical excipients, including buffers, known in the art.
- pharmaceutically acceptable carrier includes any and all solvents, dispersion media, isotonic and absorption delaying agents, and the like that are physiologically compatible.
- compositions of the invention can be in a variety of forms. These forms include, for example, liquid, semi-solid and solid dosage forms, such as liquid solutions (eg, injectable solutions and infusible solutions), powders or suspensions, liposomes and suppositories.
- liquid solutions eg, injectable solutions and infusible solutions
- powders or suspensions e.g., liposomes and suppositories.
- liposomes e.g., liposomes and suppositories.
- a medicament comprising an ADC as described herein may be prepared by admixing an ADC of the invention, or a pharmaceutically acceptable salt or solvate thereof, of the desired degree of purity with one or more optional pharmaceutical excipients, preferably in the form of a lyophilized in the form of preparations or aqueous solutions.
- compositions or formulations of the invention may also contain more than one active ingredient as required for the particular indication being treated, preferably those with complementary activities that do not adversely affect each other.
- active ingredients including chemotherapeutic agents, angiogenesis inhibitors, cytokines, cytotoxic agents, other antibodies, small molecule drugs, or immunomodulators (eg, immune checkpoint inhibitors or agonists), among others.
- the active ingredients are suitably present in combination in amounts effective for the intended use.
- sustained release formulations can be prepared. Suitable examples of sustained release formulations include semipermeable matrices of solid hydrophobic polymers containing the antibody in the form of shaped articles such as films or microcapsules.
- the present invention also provides a pharmaceutical combination or pharmaceutical combination product comprising an ADC of the present invention, or a pharmaceutically acceptable salt or solvate thereof, and one or more other therapeutic agents (e.g., therapeutic agents, including chemotherapy agents, angiogenesis inhibitors, cytokines, cytotoxic agents, other antibodies, small molecule drugs or immunomodulators (such as immune checkpoint inhibitors or agonists, etc.).
- therapeutic agents including chemotherapy agents, angiogenesis inhibitors, cytokines, cytotoxic agents, other antibodies, small molecule drugs or immunomodulators (such as immune checkpoint inhibitors or agonists, etc.).
- Another object of the present invention is to provide a kit of parts comprising the pharmaceutical combination of the present invention, preferably said kit is in the form of pharmaceutical dosage units. Dosage units may thus be presented according to a dosing regimen or interval between drug administrations.
- kit of parts of the invention comprises in the same package:
- a first container containing a pharmaceutical composition comprising an ADC of the invention or a pharmaceutically acceptable salt or solvate thereof;
- One aspect of the present invention provides a method for preventing or treating tumors (such as cancer) in a subject, comprising administering to the subject an effective amount of the ADC of the present invention or a pharmaceutically acceptable salt or solvate thereof, a pharmaceutical composition, a drug Combo or kit.
- CLDN18.2 is selectively expressed on the surface of cancer tissue cells from a variety of origins and is therefore a suitable target for the development of cancer immunotherapies. It has been found that CLDN18.2 is highly selectively expressed in digestive system cancers such as pancreatic cancer, esophageal cancer, gastric cancer and so on. Therefore, in one aspect, the present invention provides the use of the antibody of the present invention in preventing and/or treating CLAUDIN 18.2 positive tumors in a subject, comprising administering the antibody drug conjugate of the present invention in a preventive and/or therapeutically effective amount.
- the antibody drug conjugates of the invention can be the sole active agent, or can be administered in combination with other therapeutic or therapeutic agents.
- Said other therapies and therapeutic agents include, for example, drugs that target antigens on the surface of tumor cells to destroy tumors by binding and/or blocking these molecules; drugs that activate the subject's immune system to spontaneously destroy tumors .
- the tumors treated in accordance with the present invention may be early, intermediate or advanced or metastatic cancers. In some embodiments, the tumors treated in accordance with the present invention are previously treated tumors that have escaped the immune system.
- administration of the antibody-drug conjugates of the invention may include 1) therapeutic measures that cure, slow down, alleviate the symptoms of the diagnosed pathological condition or disorder and/or stop the diagnosed pathology or 2) prophylactic or preventative measures, which prevent and/or slow down the development of a pathological condition or disorder.
- the individual will benefit from the therapeutic or prophylactic measures and exhibit a greater risk of disease, disorder, condition, and and/or reduction or improvement in the onset, recurrence or progression of symptoms.
- the subject is receiving or has received other treatments, such as chemotherapy and/or radiation therapy, or other immunotherapy, prior to being treated by the methods of the invention.
- the antibody-drug conjugate of the present invention can kill CLDN18.2 positive tumor cells, and/or inhibit the proliferation of CLDN18.2 positive tumor cells.
- the antibody drug conjugate of the present invention can be administered by any suitable method, including parenteral administration, intratumoral administration and intranasal administration.
- Parenteral infusions include intramuscular, intravenous, intraarterial, intraperitoneal or subcutaneous administration. Administration may be by any suitable route, for example by injection, eg intravenous or subcutaneous injection, depending in part on whether the administration is short-term or chronic.
- Various dosing schedules are contemplated herein, including, but not limited to, single administration or multiple administrations at multiple time points, bolus administration, and pulse infusion.
- the appropriate dose of the antibody drug conjugate of the present invention (when used alone or in combination with one or more other therapeutic agents) will depend on the type of disease to be treated, the antibody drug conjugate Specific type, severity and course of disease, purpose of treatment, previous therapy, patient's clinical history and response to the antibody drug conjugate, and the judgment of the attending physician.
- the antibody drug conjugates of the present invention may be suitably administered to a patient in one treatment or over a series of treatments.
- the present invention also provides the use of the antibody-drug conjugate of the present invention in the preparation of a medicament for the aforementioned treatment and prevention methods.
- the present invention also provides a humanized anti-Claudin18.2 monoclonal antibody with various excellent properties, its encoding nucleic acid, a vector and a host cell comprising the nucleic acid, as well as an immunoconjugate comprising the antibody, and a multispecific antibody , pharmaceutical compositions and uses.
- the antibody of the present invention not only exhibits high binding affinity and high specificity to cells expressing human Claudin18.2 on the surface (especially cells with low surface expression abundance), but also has activities such as ADCC and/or CDC, derived from the Claudin18.2 antigen
- ADCC and/or CDC activities such as ADCC and/or CDC, derived from the Claudin18.2 antigen
- Favorable properties such as mediated endocytic activity, stability and/or pharmacokinetic properties, are therefore suitable for cancer therapy alone or in combination with other anticancer drugs, and are also suitable as molecular components for the formation of new drugs targeting cancer tissues.
- Anticancer molecules for example, are conjugated to cytotoxic drugs to form antibody-drug conjugates.
- the present invention provides antibodies or antigen-binding fragments thereof, especially humanized antibodies or antigen-binding fragments thereof, that specifically bind to Claudin18.2, preferably human Claudin18.2 protein (such as the human Claudin18.2 sequence of NM_001002026).
- the anti-Claudin18.2 antibody or antigen-binding fragment thereof according to the present invention comprises:
- the CDRs are defined according to Kabat or IMGT or a combination thereof.
- the present invention provides an antibody or antigen-binding fragment thereof that binds to Claudin18.2, comprising three complementarity determining regions HCDR of the variable region of the heavy chain, and three complementarity determining regions of the variable region of the light chain Decision area LCDR, where:
- HCDR1 comprises the amino acid sequence of SEQ ID NO:12 or consists of it
- HCDR2 comprises the amino acid sequence of SEQ ID NO:13 or 25 or consists of it
- HCDR3 comprises the amino acid sequence of SEQ ID NO:14 or Consisting of it
- LCDR1 comprises or consists of the amino acid sequence of SEQ ID NO:15
- LCDR2 comprises or consists of the amino acid sequence of SEQ ID NO:16
- LCDR3 comprises or consists of the amino acid sequence of SEQ ID NO:17; or
- HCDR1 comprises or consists of the amino acid sequence of SEQ ID NO:6
- HCDR2 comprises or consists of the amino acid sequence of SEQ ID NO:7
- HCDR3 comprises or consists of the amino acid sequence of SEQ ID NO:8
- LCDR1 comprises or consists of the amino acid sequence of SEQ ID NO:9
- LCDR2 comprises or consists of the amino acid sequence of SEQ ID NO:10
- LCDR3 comprises or consists of the amino acid sequence of SEQ ID NO:11; or
- HCDR1 comprises the amino acid sequence of SEQ ID NO:26 or consists of it
- HCDR2 comprises the amino acid sequence of SEQ ID NO:27 or 37 or consists of it
- HCDR3 comprises the amino acid sequence of SEQ ID NO:28 or Consisting of which, LCDR1 comprises or consists of the amino acid sequence of SEQ ID NO:32, LCDR2 comprises or consists of the amino acid sequence of SEQ ID NO:33, and LCDR3 comprises or consists of the amino acid sequence of SEQ ID NO:34,
- HCDR1 comprises the amino acid sequence of SEQ ID NO:29 or consists of it
- HCDR2 comprises the amino acid sequence of SEQ ID NO:30 or consists of it
- HCDR3 comprises the amino acid sequence of SEQ ID NO:31 or consists of it Composition
- LCDR1 comprises or consists of the amino acid sequence of SEQ ID NO:35
- LCDR2 comprises the amino acid sequence of SEQ ID NO:36 or consists of it
- LCDR3 comprises the amino acid sequence of SEQ ID NO:34 or consists of it.
- the invention also contemplates antibodies comprising a variant of one of the combinations of CDR sequences of (i)-(iv) above.
- the variant comprises at least one and no more than 5, 4, 3, 2 or 1 amino acid changes (preferably amino acid substitutions, preferably conservative substitutions) in the 6 CDR regions, and preferably the heavy chain CDR3 remains unchanged Change.
- the invention provides an anti-Claudin18.2 antibody or antigen-binding fragment thereof comprising a heavy chain variable region and a light chain variable region selected from:
- the anti-Claudin18.2 antibody or antigen-binding fragment thereof of the present invention comprises the exemplary antibody 25C7A5 of the present invention and its humanized antibodies (HZ1 and HZ2) and 2D3A11 and its humanized antibody (HZ1 and HZ2) heavy and light chain variable region sequences or variants thereof, for example, antibodies having the same CDR sequences as one of the exemplary antibodies and having the same or different framework region sequences.
- the anti-Claudin18.2 antibody or antigen-binding fragment thereof comprises a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region comprises SEQ ID NO:21 Amino acid sequence or an amino acid sequence having at least 95%, 96%, 97%, 98% or 99% sequence identity thereto, and wherein the light chain variable region comprises the amino acid sequence shown in SEQ ID NO: 22, or with it Amino acid sequences having at least 95%, 96%, 97%, 98% or 99% sequence identity.
- the antibody or antigen-binding fragment comprises the heavy chain variable region of SEQ ID No: 21 and the light chain variable region of SEQ ID No: 22.
- the anti-Claudin18.2 antibody or antigen-binding fragment thereof comprises a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region comprises SEQ ID NO: 1 or 3 said amino acid sequence or an amino acid sequence having at least 95%, 96%, 97%, 98% or 99% sequence identity therewith, and wherein said light chain variable region comprises the amino acid sequence shown in SEQ ID NO: 2, Or an amino acid sequence having at least 95%, 96%, 97%, 98% or 99% sequence identity thereto.
- the antibody is a humanized antibody. More preferably, the heavy chain variable region of the antibody has a framework region sequence derived from the human germline, and preferably has an amino acid Q or E, preferably an amino acid at position H6 according to Kabat numbering, in the heavy chain variable region Q.
- the antibody or antigen-binding fragment comprises the heavy chain variable region of SEQ ID No: 1 and the light chain variable region of SEQ ID No: 2.
- the antibody or antigen-binding fragment comprises the heavy chain variable region of SEQ ID No:3 and the light chain variable region of SEQ ID No:2.
- the anti-Claudin18.2 antibody or antigen-binding fragment thereof comprises a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region comprises SEQ ID NO: 23 Amino acid sequence or an amino acid sequence having at least 95%, 96%, 97%, 98% or 99% sequence identity thereto, and wherein the light chain variable region comprises the amino acid sequence shown in SEQ ID NO: 24, or with it Amino acid sequences having at least 95%, 96%, 97%, 98% or 99% sequence identity.
- the antibody or antigen-binding fragment comprises the heavy chain variable region of SEQ ID No: 23 and the light chain variable region of SEQ ID No: 24.
- the anti-Claudin18.2 antibody or antigen-binding fragment thereof comprises a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region comprises SEQ ID NO: 38 or 40 said amino acid sequence or an amino acid sequence having at least 95%, 96%, 97%, 98% or 99% sequence identity therewith, and wherein said light chain variable region comprises the amino acid sequence shown in SEQ ID NO:39, Or an amino acid sequence having at least 95%, 96%, 97%, 98% or 99% sequence identity thereto.
- the antibody is a humanized antibody. More preferably, the heavy chain variable region of the antibody has a framework region sequence derived from the human germline, and preferably has an amino acid Q or E, preferably an amino acid at position H6 according to Kabat numbering, in the heavy chain variable region Q.
- the antibody or antigen-binding fragment comprises the heavy chain variable region of SEQ ID No: 38 and the light chain variable region of SEQ ID No: 39.
- the antibody or antigen-binding fragment comprises the heavy chain variable region of SEQ ID No:40 and the light chain variable region of SEQ ID No:39.
- an antibody of the invention may comprise a heavy chain constant region and/or a light chain constant region.
- the heavy chain constant region is a heavy chain constant region derived from human immunoglobulin.
- the light chain constant region is a light chain constant region derived from human immunoglobulin.
- the heavy chain constant regions comprised in the antibodies of the invention may be of any isotype or subtype, eg, IgG1, IgG2, IgG3 or IgG4 isotype heavy chain constant regions.
- the invention provides an anti-Claudin18.2 antibody comprising an IgG1, IgG2, IgG3 or IgG4 heavy chain constant region, preferably an IgG1 heavy chain constant region, especially a human IgG1 heavy chain constant region.
- the light chain constant region contained in the antibody of the present invention may be a kappa light chain constant region or a lambda light chain constant region.
- the invention provides an anti-Claudin 18.2 antibody comprising a kappa light chain constant region or a lambda light chain constant region, preferably an antibody of the invention comprising a human kappa light chain constant region.
- antibodies according to the invention are IgG1 antibodies, more particularly IgG1 kappa or IgG1 lambda isotypes. Still more preferably, the antibody according to the invention is a human IgG1 ⁇ antibody.
- an anti-Claudin18.2 antibody of the invention comprises a human IgG1 heavy chain constant region.
- the heavy chain constant region comprises the amino acid sequence of SEQ ID NO: 4, or comprises at least one, two or three, but no more than 20, 10 or 5 amino acid sequences relative to the amino acid sequence of SEQ ID NO: 4
- an anti-Claudin 18.2 antibody of the invention comprises a human kappa light chain constant region.
- the light chain constant region comprises the amino acid sequence of SEQ ID NO: 5, or at least one, two or three, but no more than 20, 10 or 5 relative to the amino acid sequence of SEQ ID NO: 5 Amino acid sequence with amino acid changes, or a sequence with at least 95-99% identity to the amino acid sequence of SEQ ID NO:5.
- an antibody of the invention comprises a heavy chain sequence and a light chain sequence selected from the group consisting of:
- the present invention also provides variants of the antibodies comprising any one of (a)-(d) above, wherein the variants have amino acid changes in the heavy chain sequence and/or the light chain sequence.
- the variant comprises at least one, two or three, but no more than 20, 10 or 5 amino acid changes in the heavy chain sequence or the light chain sequence or both, compared to the corresponding antibody or an amino acid sequence having at least 80%, 85%, 90%, 92%, 95%, 97%, 98%, 99% or more identity.
- amino acid changes do not occur in the CDR regions, more preferably not in the variable regions.
- the invention also provides variants of any of the antibodies described herein, especially the exemplary antibodies 25C7A5 and its humanized antibodies (HZ1 and HZ2) and 2D3A11 and its humanized antibodies (HZ1 and HZ2) of the invention. variant of either.
- Antibody variants of the invention preferably retain at least 60%, 70%, 80%, 90%, or 100% of the biological activity (eg, antigen binding ability) of the pre-altered antibody. More preferably, the alterations do not result in the antibody variant losing binding to the antigen, but optionally confer properties such as increased affinity for the antigen and different effector functions. It is understood that the antibody heavy chain variable region or light chain variable region, or each CDR region can be altered individually or in combination.
- changes can also be made to the Fc region of the antibody. Alterations to the Fc region can be made alone, or in combination with the aforementioned changes to the framework and/or CDR regions.
- the Fc region can be altered, eg, to alter one or more functions of the antibody, such as serum half-life, complement fixation, Fc receptor binding, and/or antigen-dependent cellular cytotoxicity.
- antibodies of the invention may be chemically modified (eg, attached to PEG) or their glycosylation pattern altered.
- antibodies of the invention are preferably monospecific antibodies. However, in some embodiments, antibodies of the invention may also be multispecific antibodies comprising a first binding specificity for Claudin18.2 and a binding specificity for another antigen, e.g., for another antigen expressed on the surface of tumor cells. A second and/or third binding specificity for an antigen.
- an anti-Claudin18.2 antibody or antigen-binding fragment thereof of the invention has one or more of the following properties:
- the antibodies of the invention have high binding affinity and high binding specificity for Claudin18.2.
- the binding affinity and binding specificity of the antibodies of the invention to Claudin18.2 and/or to Claudin18.1 are determined by FACS or cellular ELSA assays (such as the assays described in Example 1-7) .
- the binding affinity of an antibody of the invention for Claudin 18.1 is at least 10-fold, 100-fold, 103-fold, 10 -fold lower relative to the binding affinity of said antibody for Claudin 18.2 in a cell-based assay times, 10 5 times or 10 6 times.
- the antibody of the present invention does not bind or substantially does not bind to Claudin18.1 expressing cells.
- an antibody of the invention exhibits a positive response to human Claudin 18.2 in a cell-based assay, for example, in a cellular ELISA assay using a recombinant cell line that expresses greater than 95% or greater than 98% positive expression of human Claudin 18.2.
- High binding affinity with an EC50 value of less than 300 ng/ml, especially less than about 100 ng/ml, such as about 1 ng/ml-50 ng/ml and preferably less than about 20 ng/ml.
- the assay is performed according to the cell ELISA assay method described in Example I-7.
- a recombinant HEK-293T cell line stably expressing human Claudin 18.2 is used in the assay.
- an antibody of the invention has comparable or greater binding affinity for human Claudin 18.2 relative to the reference antibody IMAB362 in a cell-based assay.
- the antibodies of the present invention exhibit comparable cell binding affinity on cells expressing high positive rate of human Claudin 18.2 surface cells (for example, the positive rate is greater than 95%); in other In an embodiment, the antibody of the present invention exhibits stronger cell-binding affinity on cells with a low positive rate (for example, a positive rate of less than 50%, such as about 2-30%) expressing human Claudin 18.2 on the surface.
- mammalian cell lines expressing human Claudin18.2 recombinantly such as HEK29 or L929 or NUGC4 cells can be used; tumor cell lines endogenously expressing human Claudin18.2 can also be used, such as NUGC4 cells.
- the cell ELISA assay method is used as described in Example I-7; or the FACS assay method is used as described in Example I-8.
- the antibody of the present invention exhibits stronger cell-binding activity for cells with an average lower expression level of Claudin18.2 on the cell surface, such as NUGC4 cells endogenously expressing human Claudin18.2.
- an antibody of the invention exhibits no specific binding to Claudin 18.1 in a cell-based assay.
- This binding property of antibodies to Claudin18.1 expressing cells can be determined in a FACS assay, optionally relative to negative and/or positive controls.
- the percent positive cell staining of the antibody and/or the value of the fluorescent staining intensity of the cells is determined.
- the positive cell rate of the antibody of the present invention is less than 3% (more preferably less than 2%, more preferably less than 1%) , again preferably less than 0.7%) and preferably, the median and/or mean fluorescent signal intensity produced by an antibody of the invention is comparable to the median/mean signal intensity produced by an isotype control antibody (e.g., ⁇ 20%, or preferably ⁇ 10%).
- the assay is performed according to the FACS assay method described in Example I-10.
- a recombinant HEK-293T cell line stably expressing human Claudin 18.1 is used in the assay.
- an antibody of the invention has ADCC activity.
- ADCC activity of antibodies of the invention can be assayed as described in Examples 1-11.
- antibodies of the invention exhibit an EC50 value of less than about 100 ng/ml, such as 80-50 ng/ml, or more preferably less than about 50 ng/ml in said assay.
- antibodies of the invention have CDC activity.
- CDC activity of antibodies of the invention can be assayed as described in Example 1-12.
- an antibody of the invention exhibits a CDC activity of less than about 5 ⁇ g/ml, such as about 1-4 ⁇ g/ml, in said assay.
- the antibody of the present invention has endocytic activity after binding to the receptor Claudin18.2 on the cell membrane surface.
- the endocytic activity of the antibodies of the invention can be assayed as described in Example 1-13.
- the endocytosis rate of the antibody of the present invention for example, the endocytosis rate at 37° C. for 4 hours, is at least 10%, for example, 10-25%, preferably at least 20%. %.
- the anti-Claudin18.2 antibody or antigen-binding fragment thereof of the present invention also has one or more of the following properties: (vii) good stability; and (viii) favorable pharmacokinetic properties.
- the stability of the antibodies of the invention can be determined as described in Examples 1-14.
- the antibody in the accelerated stability assay, has a SEC-HPLC purity of not less than 95%, preferably not less than 97%; and/or a non-reduced CE-SDS purity of not less than 90% after standing at 37°C for 3-14 days, Preferably not less than 93%, and/or reduced CE-SDS purity not less than 90%, preferably not less than 95%.
- the SEC-HPLC purity of the antibody is not less than 95%, preferably not less than 97%.
- the pharmacokinetic properties of the antibodies of the invention can be determined as described in Examples 1-15.
- the present invention provides a nucleic acid encoding any of the above anti-Claudin 18.2 antibodies or fragments thereof. Also provided are vectors comprising the nucleic acid; and host cells comprising the nucleic acid or the vector.
- the invention provides one or more vectors, including cloning vectors and expression vectors, comprising a nucleic acid of the invention.
- the vector is an expression vector, such as a eukaryotic expression vector.
- Vectors that can be used in the present invention include, but are not limited to, viruses, plasmids, cosmids, lambda phage, or yeast artificial chromosomes (YACs).
- the invention provides a host cell comprising a vector of the invention.
- Suitable host cells for cloning or expression of antibody-encoding vectors include prokaryotic or eukaryotic cells.
- antibodies can be produced in bacteria, especially when glycosylation and Fc effector functions are not required. After expression in bacteria such as E. coli, antibodies can be isolated from the bacterial cell paste in a soluble fraction and can be further purified.
- the host cell is a eukaryotic cell.
- the host cell is selected from yeast cells, mammalian cells, or other cells suitable for the production of antibodies or antigen-binding fragments thereof.
- Examples of useful mammalian host cell lines include, monkey kidney CV1 line (COS-7) transformed with SV40; human embryonic kidney line (293HEK or 293 cells); Chinese hamster ovary (CHO) cells, including DHFR - CHO cells; and myeloma cell lines such as Y0, NS0 and Sp2/0.
- COS-7 monkey kidney CV1 line
- SV40 human embryonic kidney line
- 293HEK or 293 cells human embryonic kidney line
- CHO Chinese hamster ovary (CHO) cells, including DHFR - CHO cells
- myeloma cell lines such as Y0, NS0 and Sp2/0.
- the invention provides methods of making anti-Claudin 18.2 antibodies of the invention.
- the method of the invention comprises, under conditions suitable for antibody expression, culturing a host cell comprising a nucleic acid encoding an antibody of the invention, and optionally recovering the host cell (or host cell culture medium) from the host cell (or host cell culture medium). said antibody.
- isolated or artificially or recombinantly synthesized nucleic acids encoding antibodies can be inserted into one or more vectors for further cloning in host cells and/or express.
- nucleic acids are readily isolated and sequenced using conventional procedures, for example, from hybridoma cells by using oligonucleotide probes that are capable of binding specifically to genes encoding the antibody heavy and light chains.
- the invention provides immunoconjugates produced by conjugating an antibody of the invention to a heterologous molecule.
- an antibody of the invention (or an antigen-binding fragment thereof) is conjugated to a therapeutic or diagnostic or detectable agent in an immunoconjugate.
- antibodies of the invention may be conjugated to heterologous molecules in the form of full-length antibodies or antibody fragments.
- linkers can be used to covalently link different entities of the conjugate. Suitable linkers include chemical linkers or peptide linkers.
- the linker is a "cleavable linker" which facilitates release of the polypeptide after delivery to the target site. For example, acid labile, peptidase sensitive, photolabile, dimethyl or disulfide containing linkers may be used.
- suitable therapeutic agents for the conjugate include, but are not limited to, cytotoxins (e.g., cytostatic or cytocidal agents), drugs, or radioisotopes.
- cytotoxins e.g., cytostatic or cytocidal agents
- diagnostic or detectable agents such conjugates may be used as part of a clinical assay (e.g., to determine the efficacy of a particular therapy) for monitoring or predicting the onset, development, progression of a disease or condition and/or severity.
- Such diagnosis and detection can be accomplished by conjugating the antibody to a detectable agent including, but not limited to, various enzymes such as horseradish peroxidase; prosthetic groups such as streptavidin/biotin; and avidin/biotin; fluorescent substances; luminescent substances; radioactive substances; and positron-emitting metals and non-radioactive paramagnetic metal ions used in various positron emission tomography procedures.
- a detectable agent including, but not limited to, various enzymes such as horseradish peroxidase; prosthetic groups such as streptavidin/biotin; and avidin/biotin; fluorescent substances; luminescent substances; radioactive substances; and positron-emitting metals and non-radioactive paramagnetic metal ions used in various positron emission tomography procedures.
- compositions comprising anti-Claudin18.2 antibodies or immunoconjugates thereof and compositions comprising polynucleotides encoding anti-Claudin18.2 antibodies or immunoconjugates thereof.
- compositions may also optionally contain suitable pharmaceutical excipients, such as pharmaceutical carriers, pharmaceutical excipients, including buffers, known in the art.
- suitable pharmaceutical excipients such as pharmaceutical carriers, pharmaceutical excipients, including buffers, known in the art.
- the anti-Claudin18.2 antibody or immunoconjugate of the present invention having the desired purity can be prepared by combining with one or more optional pharmaceutical excipients (Remington's Pharmaceutical Sciences, 16th edition) , Osol, A. Ed. (1980)) mixing to prepare pharmaceutical formulations comprising the present invention.
- the antibodies of the invention can be the sole active agent, or can be combined with other therapeutic agents.
- Therapeutic agents that can be combined with the antibodies of the invention include, but are not limited to, therapeutic agents that have beneficial therapeutic effects on the disease and/or condition being treated.
- the active ingredients may be as required for the particular indication being treated, preferably those with complementary activities that do not adversely affect each other.
- other pharmaceutical ingredients may provide anticancer activity.
- the antibodies of the present invention are present in pharmaceutical compositions and pharmaceutical preparations in appropriate combinations with active ingredients in amounts effective for the intended use.
- the invention also provides a combination product comprising an antibody or antigen-binding fragment thereof, multispecific antibody or immunoconjugate of the invention, and one or more other therapeutic agents (e.g., chemotherapeutics, other Antibodies, cytotoxic agents, antitumor drugs, etc.).
- therapeutic agents e.g., chemotherapeutics, other Antibodies, cytotoxic agents, antitumor drugs, etc.
- the components constituting the combination product such as the antibody of the present invention and other therapeutic agents, can be formulated in different formulations, and preferably contained in different containers. According to factors such as the disease to be treated and individual conditions, those skilled in the art can determine the administration method and administration sequence of each component of the combination product. Combinations of the invention may be used in the methods of treatment of the invention.
- the invention provides a combination product wherein the other therapeutic agent is, for example, a therapeutic agent such as an antibody effective to stimulate an immune response thereby further enhancing, stimulating or up-regulating the subject's immune response.
- the combination product is used to prevent or treat Claudin18.2 positive tumors.
- the invention provides methods and uses of the Claudin18.2 antibody or antigen-binding fragment thereof of the invention, for example, in vivo and in vitro for:
- the methods and uses of the invention relate to the treatment of disease in an individual subject.
- the methods and uses of the invention involve detecting the presence of Claudin18.2 in a sample from, eg, a subject.
- the present invention also provides the use of the anti-Claudin18.2 antibody or antigen-binding fragment thereof of the present invention in the preparation of products (such as pharmaceutical compositions or pharmaceutical products or combination products or detection products) for the above-mentioned purposes.
- the present invention provides the use of the antibody of the present invention in preventing and/or treating CLAUDIN 18.2 positive tumors in a subject, comprising administering the antibody of the present invention in a preventive and/or therapeutically effective amount.
- administration of the antibodies of the invention may include 1) therapeutic measures that cure, slow down, alleviate the symptoms of, and/or halt the progression of, the diagnosed pathological condition or disorder ; or 2) preventive or preventative measures, which prevent and/or slow down the development of a pathological condition or disorder.
- the subject can be an individual already suffering from a disorder, an individual prone to developing a disorder, or an individual in whom a disorder is to be prevented. Said individual will benefit from said therapeutic measure or prophylactic measure and exhibit an increased incidence, recurrence or progression of the disease, disorder, condition, and/or symptom compared to an individual not receiving said treatment alleviate or improve.
- the invention relates to the treatment of a disease or condition; in other embodiments, the invention relates to the prevention of a disease or condition.
- antibodies of the invention for use in the methods of the invention comprise an Fc region that elicits immune effector function and induces immune effects upon binding to cells expressing CLDN18.2 on the surface (e.g., cancer cells), e.g., ADCC and and/or CDC activity.
- an antibody, or fusion, conjugate or composition thereof, of the invention mediates CDC-mediated cell lysis, or ADCC-mediated cell lysis, or both. lead to cancer cell killing.
- the antibodies of the invention can be administered by any suitable method, including parenteral, intratumoral, and intranasal.
- Parenteral infusions include intramuscular, intravenous, intraarterial, intraperitoneal or subcutaneous administration. Administration may be by any suitable route, for example by injection, eg intravenous or subcutaneous injection, depending in part on whether the administration is short-term or chronic.
- Various dosing schedules are contemplated herein, including, but not limited to, single administration or multiple administrations at multiple time points, bolus administration, and pulse infusion.
- the present invention also provides methods and kits for detecting Claudin18.2 in a sample, wherein the method comprises: (a) contacting the sample with an antibody of the present invention or an antigen-binding fragment thereof or an immunoconjugate; and (b) detecting Formation of a complex between the antibody or antigen-binding fragment thereof or immunoconjugate and Claudin18.2 protein.
- the sample is from a cancer patient, such as a patient with digestive system cancer, such as gastric cancer, pancreatic cancer, or esophageal cancer.
- the detection can be in vitro or in vivo.
- the term "detection" as used herein includes quantitative or qualitative detection, and exemplary detection methods may involve immunohistochemistry, immunocytochemistry, flow cytometry (e.g., FACS), magnetic beads complexed with antibody molecules, ELISA assays methods, PCR-techniques (eg, RT-PCR).
- the biological sample is blood, serum, or other liquid sample of biological origin.
- a biological sample comprises cells or tissues.
- the biological sample is from a hyperproliferative or cancerous lesion.
- the Claudin18.2 to be detected is human Claudin18.2.
- an anti-Claudin18.2 antibody is used to select a subject suitable for treatment with an anti-Claudin18.2 antibody.
- the antibodies of the invention can be used to diagnose cancer or tumors, for example to evaluate (e.g., monitor) the treatment or progression of a disease described herein (e.g., a hyperproliferative or cancerous disease) in a subject, its diagnosis and / or in installments.
- labeled anti-Claudin 18.2 antibodies include, but are not limited to, labels or moieties that are detected directly (such as fluorescent labels, chromophore labels, electron-dense labels, chemiluminescent labels, and radioactive labels), as well as moieties that are detected indirectly, such as enzymes or ligands, for example, Through enzymatic reactions or molecular interactions.
- Embodiment 1 anti-Claudin18.2 preparation and characterization
- the amino acid sequence of human Claudin18.2 refers to NP_001002026.1 in the protein database of NCBI.
- the amino acid sequence of human Claudin18.1 refers to NP_057453.1 in the protein database of NCBI.
- the amino acid sequence of cynomolgus monkey Claudin18.2 refers to XP_015300615.1 in the protein database of NCBI.
- the amino acid sequence of mouse Claudin18.2 refers to NP_001181850.1 in the protein database of NCBI.
- the amino acid sequence of rat Claudin18.2 refers to NP_001014118.1 in the protein database of NCBI.
- the above amino acid sequence was codon-optimized by GenScript and synthesized on the lentiviral vector pLVX or pCDNA3.4 vector.
- the virus was prepared by a lentiviral packaging system, and after obtaining the virus, it was infected with HEK293T, L929, and CHO cells, and screened with puromycin to obtain CHO-Claudin18.2 (human), HEK293T-Claudin18.1 (human), HEK293T-Claudin18.2 (human), L929-Claudin18.2 (human), HEK293T-Claudin18.2 (cynomolgus monkey), HEK293T-Claudin18.2 (rat), HEK293T-Claudin18.2 (mouse) stable cell lines.
- NUGC4 is a gastric cancer cell line endogenously expressing Claudin18.2, and NUGC4 was selected for subsequent experiments (purchased from Nanjing Kebai, CBP60493); at the same time, recombinant NUGC4-Claudin18.2 (human) overexpressing human Claudin18.2 was purchased for stable The cell line (Beijing Kangyuan Bochuang, KC-1471) was used for subsequent experiments.
- the positive rate of Claudin18.2 was determined by flow cytometry (FACS) detection.
- the experimental steps are as follows: digest the adherent cultured cells, collect the cells by centrifugation, wash three times with pre-cooled PBS; resuspend the cells with 1% BSA (in PBS), add 3 ⁇ 105 cells to each well of a 96-well conical bottom plate, The volume is 50 ⁇ l; Dilute the IMAB362 antibody (sequence from patent: CN 101312989B, the heavy chain variable region amino acid sequence SEQ ID NO:135 and the light chain variable region amino acid sequence SEQ ID NO:135 of the antibody 175D10) with 1% BSA (in PBS) NO:142 was obtained by Anhui General Biosynthesis, expressed and purified by 293E cells) to 40 ⁇ g/mL, and 50 ⁇ l/well was added to the cells to make the final antibody concentration 20 ⁇ g/mL, mixed well, and incubated at 4°C for 1 hour; centrifuge
- the positive rate of Claudin18.1 cells was determined with the immunized mouse serum by the same method.
- mice 24 wild-type mice aged 5-6 weeks from 3 strains of Balb/C, KM and CD01 were selected, and pCDNA3.4-Claudin18.2 plasmid, CHO-Claudin18.2 (human) cells, L929-Claudin18.2 (Human) cells are immunized, and after 3-4 times of immunization, the serum titer is detected by flow cytometry.
- HEK293T-Claudin18.1 human
- HEK293T-Claudin18.2 human cells adherently cultured were collected by digestion and centrifugation, then washed three times with pre-cooled PBS, resuspended cells in PBS (containing 1% BSA), and Spread 3 ⁇ 105 cells in wells into a 96-well conical bottom plate, add serially diluted serum and incubate at 4°C for 1 hour, wash with pre-cooled PBS three times, add 1 ⁇ l anti-mouse IgG fluorescent secondary antibody to each well, incubate at 4°C for 0.5 hour, pre- After washing with cold PBS for three times, the cells were resuspended and detected by flow cytometry.
- mice with high affinity to HEK293T-Claudin18.2 (human) and low affinity to HEK293T-Claudin18.1 (human) were selected as candidates for fusion, and the numbers of the candidate mice were: 61, 64, 79, 89, and 91, respectively.
- mice The spleen and lymph nodes of mice were taken to prepare cell suspension, mixed with SP2/0 mouse myeloma cells at a ratio of 1:1, resuspended with cell electrofusion buffer, and electrofusion reaction was performed using BTX-ECM2001 cell electrofusion instrument. After the electrofusion reaction, resuspend with complete fusion medium (RPMI1640+20%FBS+1 ⁇ HAT), divide into 96-well cell culture plates according to 20000-25000 cells per well, and culture at 37°C and 5% CO2.
- complete fusion medium RPMI1640+20%FBS+1 ⁇ HAT
- L929-Claudin18.2 human cell ELISA method to screen hybridoma mother clones with higher affinity to human Claudin18.2, and exclude those capable of binding to Claudin18.1 by flow cytometry (FACS) mother clones for subcloning. After two rounds of fusion screening, a total of 52 mother clones were selected for subcloning.
- the affinity of anti-human Claudin18.2 mouse monoclonal antibody was evaluated by cell ELISA.
- the experimental steps are as follows: the day before the experiment, spread HEK293T-Claudin18.2 (human) cells into a 96-well plate, 5 ⁇ 10 4 cells per well; remove the supernatant on the day of the experiment, wash each well with 300 ⁇ l PBS once, and add 100 ⁇ l Fix with 4% paraformaldehyde at room temperature for 20 minutes; remove paraformaldehyde, wash twice with 300 ⁇ l PBS per well, add 100 ⁇ l 2% BSA (in PBS) to each well, block for 2 hours at 37°C; remove blocking solution, and serially dilute Antibody (dilute antibody with 2% BSA (in PBS), start at 10 ⁇ g/mL, 3-fold serial dilution, a total of 11 concentration points), add 100 ⁇ l/well to the plate, incubate at 37°C for 2 hours; remove the supernatant ,
- the specificity of anti-human Claudin18.2 mouse monoclonal antibody was evaluated by flow cytometry (FACS).
- the experimental steps are as follows: digest adherent cultured HEK293T-Claudin18.1 (human) cells, collect the cells by centrifugation, and wash three times with pre-cooled PBS; resuspend the cells with 1% BSA (in PBS), and place the Add 3 ⁇ 105 cells with a volume of 50 ⁇ l; dilute the antibody to be tested to 100 ⁇ g/mL with 1% BSA (in PBS), add 50 ⁇ l/well to the cells to make the final antibody concentration 50 ⁇ g/mL, mix well, Incubate at 4°C for 1 hour; collect cells by centrifugation, wash three times with pre-cooled PBS, resuspend cells with 50 ⁇ l 1% BSA (in PBS), add 1 ⁇ l fluorescent secondary antibody (Biolegend, catalog number: 405308) to each well, mix well, and incubate at 4°
- the product was amplified by PCR (Gold Medal MIX, TSE101), and the fragments were recovered by the agarose gel recovery kit; the sample was sent to Beijing Tingke Biotechnology Co., Ltd. for sequencing, and the sequence of the mouse antibody was measured through IMGT website analysis .
- Candidate murine antibody sequences are shown in Table 2.
- Humanized antibody 25C7A5-HZ1 (heavy chain variable region sequence SEQ ID NO: 1 and light chain variable region sequence SEQ ID NO: 2)
- 25C7A5-HZ2 (heavy chain variable region sequence SEQ ID NO: 3 and Light chain variable region sequence SEQ ID NO: 2)
- the variable region amino acid sequence of the reference antibody IMAB362 (sequence from patent: CN 101312989B, heavy chain variable region amino acid sequence SEQ ID NO: 135 of antibody 175D10 and light chain Variable region amino acid sequence (SEQ ID NO: 142), after codon optimization, gene synthesis (Anhui General Biology) was carried out, and it was constructed on the PTT5 vector.
- the plasmid was synthesized, it was directly extracted by shaking the bacteria, transfected into HEK293E cells by PEImax (Polysciences, 24765-1), expressed for about 7 days, and the supernatant was collected by centrifugation. The supernatant was purified using MabSelectSure Protein A affinity medium (GE).
- the expressed reference antibody has the same human IgG1 heavy chain constant region (SEQ ID NO:4) and human Kappa light chain constant region (SEQ ID NO:5) as the humanized antibody. All the purified antibodies were ultrafiltered into PBS buffer, the concentration was measured, and stored at -20°C.
- the affinity of anti-human Claudin18.2 humanized monoclonal antibody was determined by cell ELISA.
- the cell ELISA experiment procedure is as described in Example 1-3, and the cells are selected from L929-Claudin18.2 (human), HEK293T-Claudin18.2 cells (human), NUGC4-Claudin18.2 stably expressing human Claudin18.2 through transfection (human) cells and NUGC4 cells endogenously expressing human Claudin18.2.
- N 2 means 2 independent repeated experiments
- the affinity of anti-human Claudin18.2 humanized antibody was detected by flow cytometry.
- the experimental steps are as follows: digest HEK293T-Claudin18.2 (human), NUGC4-Claudin18.2 (human), and NUGC4 cells adherently cultured, collect the cells by centrifugation, wash three times with pre-cooled PBS; reconstitute with 1% BSA (in PBS) Suspend cells, add cells in a 96-well conical bottom plate, add 3 ⁇ 105 cells per well, the volume is 50 ⁇ l; dilute the antibody to be tested with 1% BSA (in PBS), start at 100 ⁇ g/mL, and use a 3-fold serial dilution , 10 concentration points; add 50 ⁇ l/well of the antibody to be tested into the cells in a gradient dilution, mix well, and incubate at 4°C for 1 hour; collect the cells by centrifugation, wash three times with pre-cooled PBS, and wash with 50 ⁇ l
- the affinity of anti-human Claudin18.2 humanized monoclonal antibody to different species of Claudin18.2 was determined by flow cytometry (FACS).
- the experimental steps are as follows: digest and centrifuge to collect HEK293T-Claudin18.2 (cynomolgus monkey) cells, HEK293T-Claudin18.2 (mouse) cells and HEK293T-Claudin18.2 (rat) cells, wash three times with pre-cooled PBS, 1% BSA (in PBS) resuspend cells, spread 3 ⁇ 105 cells per well into a 96-well conical bottom plate, add serially diluted antibodies and incubate at 4°C for 1 h, wash with pre-cooled PBS three times, add 1 ⁇ l fluorescent secondary antibody to each well (APC: Biolegend-410712), incubated at 4°C for 0.5h; washed three times with pre-cooled PBS, resuspended cells, and detected by flow
- the specificity of anti-human Claudin18.2 humanized monoclonal antibody was determined by flow cytometry (FACS).
- the experimental steps are as follows: digest and centrifuge to collect HEK293T-Claudin18.1 (human) cells, wash three times with pre-cooled PBS, resuspend the cells in 1% BSA (in PBS), and spread 3 ⁇ 105 cells per well into a 96-well conical bottom plate Add the antibody to be detected at a final concentration of 50 ⁇ g/mL and incubate at 4°C for 1 h, wash with pre-cooled PBS three times, add 1 ⁇ l of fluorescent secondary antibody (APC: Biolegend-410712; or PE: BioLegend-410708) to each well, and incubate at 4°C for 0.5 h.
- APC Biolegend-410712
- PE BioLegend-410708
- anti-human Claudin18.1 positive control antibody positive control antibody-1 and positive control antibody-2 were included in the experiment.
- the positive control antibody was selected from Example 1-3 which had significant binding to HEK293T-Claudin18.1 (human) cells, and the antibody clone numbers were: 13A6D2 (positive control antibody-1) and 15C12A2 (positive control antibody-2).
- Antibody name Median APC fluorescence signal value Mean APC fluorescence signal value Positive rate (%) 2D3A11-HZ1 233 281 0.69 2D3A11-HZ2 329 382 1 Positive Control Antibody-1 726 979 16.2 Antibody name Median PE fluorescence signal value Average PE fluorescence signal value Positive rate (%) 25C7A5-HZ1 504 583 0.54 25C7A5-HZ2 471 559 0.55 Positive Control Antibody-2 1055 1231 6.78 Negative Control Antibody (NC) 385 448 0.32
- the ADCC activity of anti-human Claudin18.2 humanized monoclonal antibody was detected by fluorescein reporter system. use Bio-Glory One-Step Firefly Luciferase Assay Kit (Ruian, Suzhou, RA-GL04), according to the manufacturer's instructions.
- the experimental steps are as follows: collect HEK293T-Claudin18.2 (human) cells by digestion and centrifugation, resuspend the cells with DMEM+1% FBS and plate 50,000 cells per well; collect Jurkat-NFAT-CD16a cells by centrifugation, and resuspend them with 1640+1% FBS After suspending cells, plate 100,000 cells per well; add serially diluted antibodies to be detected and incubate at 37°C for 5 hours; add 50 ⁇ l Bio-Glory One-Step luciferase substrate to each well, and read with a microplate reader (MD, SpectraMax i3x).
- MD Bio-Glory One-Step luciferase substrate
- the CDC activity of anti-human Claudin18.2 humanized monoclonal antibody was detected by guinea pig serum killing assay.
- the experimental steps are as follows: HEK293T-Claudin18.2 (human) cells were collected by digestion and centrifugation, and 50,000 cells were plated in each well overnight; the supernatant was discarded, and 100 ⁇ l of DMEM+20% guinea pig serum (Beijing Boerxi, BM361Y) was added to each well for serial dilution The antibody to be detected was incubated at 37°C for 5 hours, and 20 ⁇ l of CCK8 reagent (Suzhou Rui’an, QDY-003-D) was added to each well, reacted for 1-4 hours, and read on a microplate reader at 450 nm.
- HEK293T-Claudin18.2 cells were collected by digestion and centrifugation, incubated with the antibody to be detected at a concentration of 10ug/mL at 4°C for 1 hour, washed 3 times with PBS, resuspended cells with DMEM+10% FBS, divided into 4 parts and placed in Incubate at 37°C for 0, 1, 2, and 4 hours, wash with PBS three times, add 1 ⁇ l fluorescent secondary antibody (Biolegend, 410712), incubate at 4°C for 0.5h, wash with PBS three times, and resuspend the cells on the machine.
- FACS flow cytometry
- Negative antibodies are isotype control antibodies.
- SEC-HPLC detection method is as follows:
- Instrument parameters sample chamber temperature: 8°C; column temperature: 30°C; flow rate: 0.5ml/min; injection volume: 20 ⁇ g; detection wavelength: 280nm; isocratic operation: 30min.
- the CE-SDS detection method is as follows: the sample is diluted to 4mg/ml with ultrapure water. Take 25 ⁇ l into a centrifuge tube, add 75 ⁇ l premix solution (SDS Sample buffer+iodoacetamide), mix well, and centrifuge at 10000g for 1 minute. 70°C for 5 minutes. After taking it out, let it cool at room temperature, centrifuge at 10,000 g for 1 minute, mix well and transfer to a sampling bottle.
- Detection wavelength setting 220nm; acquisition frequency: 4Hz.
- the experimental results show that the 25C7A5 humanized antibody of the present invention has good stability under accelerated and repeated freeze-thaw conditions, the SEC purity is above 95%, the CE-SDS non-reduced purity is above 90%, and the CE-SDS reduced purity is above 90%. above 95.
- the metabolism of the anti-human Claudin18.2 humanized antibody was examined in the following manner.
- the samples to be tested, humanized antibody and IMAB362 antibody were administered to male rats (Chengdu Dashuo) through tail vein injection, 3 rats in each group, and the dosage was 10mg/kg; after administration, the samples were collected for 30min, 1h, 2h, 6h, 24h, 48h, 96h, 168h serum samples.
- Blood drug concentration was detected by L929-Claudin18.2 cell ELISA (method as described in Example 3).
- the results show that the humanized antibody of 25C7A5 of the present invention has comparable in vivo half-life in rats to the reference antibody IMAB362.
- Embodiment 1 Preparation of antibody-drug conjugate (ADC)
- Step 1 (S)-7-ethyl-7-hydroxy-14-(3-chloropropyl)-10,13-dihydro-11H-[1,3]dioxole[4, Synthesis of 5-g]pyrano[3',4':6,7]indoxazino[1,2-b]quinoline-8,11(7H)-dione (A1B)
- the reaction solution was stirred at 0° C. for 5 minutes, then warmed to room temperature, and stirred for 3 hours.
- the reaction solution was diluted with water (50 mL), extracted with ethyl acetate (80 mL ⁇ 2), the organic phase was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated to obtain a crude product.
- the crude product was further purified with a C18 column (acetonitrile/0.05% formic acid in water: 5%-60%) to obtain the target compound A1B (yellow solid, 400 mg, yield: 67%).
- Step 2 (S)-7-ethyl-7-hydroxy-14-(3-hydroxypropyl)-10,13-dihydro-11H-[1,3]dioxole[4, Synthesis of 5-g]pyrano[3',4':6,7]indoxazino[1,2-b]quinoline-8,11(7H)-dione (A1)
- Example 1.1.2 (S)-2-amino-N-((3-(7-ethyl-7-hydroxyl-8,11-dioxo-7,8,11,13-tetrahydro-10H -[1,3]dioxole[4,5-g]pyrano[3',4':6,7]indoleazino[1,2-b]quinoline-14- base) propoxy) methyl) acetamide (B1) synthesis
- Step 2 B1B (240mg) was dissolved in DMF (5ml), piperidine (1ml) was added, the compound was stirred for 20 minutes, the solution was removed under reduced pressure to remove low boiling point components, and the residue was directly used in the next step of synthesis. A small amount of crude product was purified by reverse phase chromatography (acetonitrile/0.05% FA in water: 5% to 50%) to obtain the target compound B1.
- Example 1.1.3 N 6 ,N 6 -Dimethyl-N 2 -((6-(2-(methylsulfonyl)pyrimidin-5-yl)hex-5-ynoyl)-L-valine )-L-lysine (C1)
- HOBT 1-hydroxybenzotriazole
- EDCI 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
- the reaction solution was directly purified by C18 column reverse phase (acetonitrile and 0.05% aqueous formic acid system) to obtain the target compound N 6 ,N 6 -dimethyl-N 2 -((6-(2-(methylsulfonyl)pyrimidine- 5-yl)hex-5-ynoyl)-L-valine)-L-lysine (C1, white solid, 327 mg).
- Example 1.1.4 N 6 , N 6 -diethyl-N 2 -((6-(2-(methylsulfonyl)pyrimidin-5-yl)hex-5-ynoyl)-L-valine )-L-lysine (C2)
- Example 1.1.5 N 6 , N 6 -di-n-propyl- N 2 -((6-(2-(methylsulfonyl)pyrimidin-5-yl)hex-5-ynoyl)-L-valline acid)-L-lysine (C3)
- the reaction solution was directly purified by C18 column reverse phase (acetonitrile and 0.05% aqueous formic acid system) to obtain the target compound N 6 , N 6 -di-n-propyl-N 2 -((6-(2-( Methylsulfonyl)pyrimidin-5-yl)hex-5-ynoyl)-L-valine)-L-lysine (C3, 50 mg, yield 28%), as a pale yellow solid.
- Example 1.2.1 N-((11S,14S)-11-(4-(di-n-propylamino)butyl)-1-((S)-7-ethyl-7-hydroxyl-8,11 -Dioxo-7,8,11,13-tetrahydro-10H-[1,3]dioxole[4,5-g]pyrano[3',4':6,7 ]indoleazino[1,2-b]quinolin-14-yl)-15-methyl-7,10,13-trioxo-4-oxa-6,9,12-triazadeca Hexa-14-yl)-6-(2-(methylsulfonyl)pyrimidin-5-yl)hex-5-yneamide (DL-01)
- Example 1.2.2 N-((11S,14S)-11-(4-(diethylamino)butyl)-1-((S)-7-ethyl-7-hydroxyl-8,11- Dioxo-7,8,11,13-tetrahydro-10H-[1,3]dioxole[4,5-g]pyrano[3',4':6,7] Indolazino[1,2-b]quinolin-14-yl)-15-methyl-7,10,13-trioxo-4-oxa-6,9,12-triazahexadecano Alk-14-yl)-6-(2-(methylsulfonyl)pyrimidin-5-yl)hex-5-yneamide (DL-02)
- Example 1.2.3 N-((11S,14S)-11-(4-(dimethylamino)butyl)-1-((S)-7-ethyl-7-hydroxyl-8,11- Dioxo-7,8,11,13-tetrahydro-10H-[1,3]dioxolano[4,5-g]pyrano[3',4':6,7] Indolazino[1,2-b]quinolin-14-yl)-15-methyl-7,10,13-trioxo-4-oxa-6,9,12-triazahexadecano Alk-14-yl)-6-(2-(methylsulfonyl)pyrimidin-5-yl)hex-5-yneamide (DL-03)
- Ab is an antibody.
- Example 1.4 Determination of the DAR value of the sample after coupling by mass spectrometry
- Sample treatment Take 50 ⁇ g of samples respectively, add 2 ⁇ l of 1M DTT, add 50 ⁇ l of ultrapure water to dilute to a concentration of about 1.0 mg/ml, mix well, and restore at room temperature for 30 minutes.
- Mass spectrometry conditions Gas1:45; Gas2:45; CUR: 30; TEM: 450; ISVF: 5000; DP: 120; CE: 12; mass range: 600-4000
- mAb represents an unconjugated monoclonal antibody
- LC represents an antibody light chain
- HC represents an antibody heavy chain
- DAR1 represents a conjugate containing a light chain or a heavy chain coupled to a toxin molecule
- DAR2 represents a conjugate containing a light chain Or a conjugate of two toxin molecules coupled to a heavy chain
- DAR3 represents a conjugate comprising three toxin molecules coupled to a light chain or a heavy chain; wherein, the theoretical molecular weight of the monoclonal antibody is calculated based on the G0F glycoform.
- mAb, LC, HC, DAR1, DAR2, and DAR3 are as described above.
- the detection results showed that the antibody light chain on CLDN18.2-ADC (DAR8) was coupled with 0 to 1 toxin molecule (the proportions of LC and DAR1 were 0% and 100%, respectively), and the heavy chain was coupled with 0 to 3 toxin molecules (mAb , DAR1, DAR2, and DAR3 are respectively 0%, 0%, 0%, and 100%), so the drug-antibody coupling ratio (DAR value) of CLDN18.2-ADC (DAR8) is calculated to be 8.0.
- the drug-antibody coupling ratio (DAR value) of other coupled samples can be measured by mass spectrometry.
- Antibody pretreatment Add 0.1M EDTA mother solution according to 1% of the antibody volume, and then use 1M disodium hydrogen phosphate mother solution to adjust the pH of the sample to 7.7 ⁇ 0.2.
- TCEP mother liquor weigh a certain mass of TCEP-HCL, add 80% TCEP solvent, then use 0.5M sodium hydroxide to adjust the pH to 7.7 ⁇ 0.2, and finally use TCEP solvent to make the TCEP concentration 20mM.
- Ultrafiltration Use an ultrafiltration tube to replace the reaction solution into an ultrafiltration buffer (10mM Hcl-His, pH 5.5) (after concentration, add more than 4 times the volume of buffer each time, and change the solution more than 3 times), and then Rinse the ultrafiltration membrane with a small amount of buffer to recover the sample.
- an ultrafiltration buffer (10mM Hcl-His, pH 5.5) (after concentration, add more than 4 times the volume of buffer each time, and change the solution more than 3 times), and then Rinse the ultrafiltration membrane with a small amount of buffer to recover the sample.
- Sample 1-2 and Sample 3-4 are two batches of preparations prepared separately.
- Example 2.2 the cell-binding affinity of the antibody before and after conjugation to the toxin was tested.
- Collect L929-claudin 18.2 (human) or NUGC4 cells by trypsinization and centrifugation, wash three times with pre-cooled PBS, resuspend the cells, spread 5 ⁇ 104 cells per well in a 96-well plate overnight, fix the cells with 4% paraformaldehyde, Block with 2% BSA (in PBS) at 37°C for 2 hours, add serially diluted ADC drugs or antibodies, incubate at 37°C for 2 hours, add HRP-labeled anti-human secondary antibody (Jackson, 109-035-088), and incubate at 37°C After 1 hour, TMB substrate was added for color development, and after termination with 2M HCl, the absorbance value at 450nM was read with a microplate reader.
- HEK293T-claudin 18.2 human
- HEK293T-claudin 18.1 human
- NUGC4-Claudin18.2 cells by trypsinization, resuspend the cells with DEME+2% FBS, and plate 10,000 cells per well; use DEME+2 %FBS gradient dilution of the antibody ADC drug to be tested is added to the plate, and incubated at 37°C for 72 hours; after the incubation is completed, add CCK8 reagent, 20uL/well, react for 2-4 hours, read at 450nm on a microplate reader and import it into Graphpad Prism for curve fitting .
- ADCs formed by coupling 25C7A5-HZ1 and 25C7A5-HZ2 can effectively kill HEK293T-claudin18.2 cells and NUGC-4-Claudin18.2 cells; After conjugation, HEK293T-claudin18.1 cells are basically not killed, indicating that the conjugated ADC will not non-specifically recognize claudin18.1 and has good stability.
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Abstract
Description
抗体名称 | 中位APC荧光信号值 | 平均APC荧光信号值 | 阳性率(%) |
2D3A11-HZ1 | 233 | 281 | 0.69 |
2D3A11-HZ2 | 329 | 382 | 1 |
阳性对照抗体-1 | 726 | 979 | 16.2 |
抗体名称 | 中位PE荧光信号值 | 平均PE荧光信号值 | 阳性率(%) |
25C7A5-HZ1 | 504 | 583 | 0.54 |
25C7A5-HZ2 | 471 | 559 | 0.55 |
阳性对照抗体-2 | 1055 | 1231 | 6.78 |
阴性对照抗体(NC) | 385 | 448 | 0.32 |
时间(min) | 1 | 5 | 7 | 7.1 | 10 |
流动相A | 90 | 40 | 10 | 90 | 90 |
流动相B | 10 | 80 | 80 | 10 | 10 |
No.* | 样品名 | SEC(%) | DAR |
1 | 25C7A5-HZ1-B82 | 98.85 | 6.82 |
2 | 25C7A5-HZ2-B82 | 99.34 | 7.10 |
3 | IgG-B81 | 98.4 | 8.00 |
4 | 25C7A5-HZ1-B81 | 98.4 | 7.97 |
Claims (28)
- 具有下式(I)的抗体-药物偶联物(ADC)或其可药用盐或溶剂化物:Ab-[L-D] q (I)其中,Ab表示抗Claudin18.2抗体,L表示连接体,D表示细胞毒性或细胞抑制性药物,例如,拓扑异构酶I抑制剂,且q=1-20,例如,q=1-10、1-8、2-8、4-8、或6-8,其中,所述Ab包含SEQ ID NO:1或3的重链可变区(VH)序列的三个CDR和SEQ ID NO:2的轻链可变区(VL)序列的三个CDR,优选地,其中所述CDR根据Kabat或IMGT或其组合进行定义。
- 根据权利要求1的抗体-药物偶联物或其可药用盐或溶剂化物,其中,所述Ab包含3个重链互补决定区(HCDR)以及3个轻链互补决定区(LCDR),其中:(i)根据IMGT定义,HCDR1包含SEQ ID NO:6的氨基酸序列或由其组成,HCDR2包含SEQ ID NO:7的氨基酸序列或由其组成,HCDR3包含SEQ ID NO:8的氨基酸序列或由其组成,LCDR1包含SEQ ID NO:9的氨基酸序列或由其组成,LCDR2包含SEQ ID NO:10的氨基酸序列或由其组成,且LCDR3包含SEQ ID NO:11的氨基酸序列或由其组成;或者(ii)根据Kabat定义,HCDR1包含SEQ ID NO:12的氨基酸序列或由其组成,HCDR2包含SEQ ID NO:13的氨基酸序列或由其组成,HCDR3包含SEQ ID NO:14的氨基酸序列或由其组成,LCDR1包含SEQ ID NO:15的氨基酸序列或由其组成,LCDR2包含SEQ ID NO:16的氨基酸序列或由其组成,且LCDR3包含SEQ ID NO:17的氨基酸序列或由其组成。
- 根据权利要求1-2任一项的抗体-药物偶联物或其可药用盐或溶剂化物,其中,所述Ab包含:-SEQ ID NO:1或3的重链可变区序列,或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%序列同一性的氨基酸序列;或-SEQ ID NO:2的轻链可变区序列,或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%序列同一性的氨基酸序列,优选地,所述Ab为IgG1抗体。
- 根据权利要求1-3任一项的抗体-药物偶联物或其可药用盐或溶剂化物,其中,D表示喜树碱类药物,优选地,FL118或其衍生物,例如,包含以下结构的喜树碱类药物:其中,R a选自:氢;C 3-C 8环烷基;苯基;任选被选自以下的取代基取代的C 1-C 8烷基:卤素、羟基、任选地被NH 2、NH(C 1-C 4烷基)和N(C 1-C 4烷基) 2取代的C 1-C 4烷氧基、C 3-C 8环烷基、杂环烷基、苯基、NR 1R 2,其中R 1和R 2彼此独立地选自氢;任选地被选自以下的取代基取代的C 1-C 8烷基:羟基、氨基、被一个或两个C 1-C 4烷基取代的氨基、被一个或两个C 1-C 4羟烷基取代的氨基、被(C 1-C 4羟烷基)和(C 1-C 4烷基)取代的氨基;被1或2个C 3-C 10环烷基、C 3-C 10杂环烷基、苯基或杂芳基取代的C 1-C 4烷基;C 3-C 10环烷基;C 3-C 10杂环烷基C 2-C 6杂烷基;杂芳基;任选卤代的苯基;任选被羟基或氨基取代的C 1-C 8烷基-C(=O)-;或者,R 1和R 2与各自连接的氮原子组合形成具有0至3个取代基的5-、6-或7-元杂环,所述取代基选自卤素、C 1-C 4烷基、OH、C 1-C 4烷氧基、NH 2、NH(C 1-C 4烷基)和N(C 1-C 4烷基) 2,其中环烷基、杂环烷基、苯基、杂芳基在每次出现时各自独立地任选被0-3个选自以下的取代基取代:OH、C 1-C 4烷基、C 1-C 4烷氧基、NH 2、NH(C 1-C 4烷基)和N(C 1-C 4烷基) 2取代,优选地,R a为-C 1-C 4烷基-OH、-C 1-C 4烷基-O-C 1-C 4烷基-NH 2、或-C 1-C 4烷基-NH 2,其中,优选地,所述药物D单元通过其上存在的羟基或氨基基团,与连接体L单元连接。
- 根据权利要求1-5任一项的抗体-药物偶联物或其可药用盐或溶剂化物,其中,L为含肽连接体,并包含以下式(II)的结构:-Z-Y-M-,其中Z为与Ab连接的连接基,Y是2-5个氨基酸的肽,优选二肽、三肽或四肽,M不存在,或是用于与药物D连接的间隔基。
- 根据权利要求6的抗体-药物偶联物或其可药用盐或溶剂化物,其中,Y为从N端到C端具有下式氨基酸序列的肽;Xaa 1-Xaa 2-Xaa 3-Xaa 4-Xaa 5,其中Xaa 1不存在,或为选自缬氨酸、甘氨酸、丙氨酸和谷氨酸的氨基酸;Xaa 2为选自苯丙氨酸、亮氨酸、和缬氨酸的氨基酸,优选缬氨酸;Xaa 3为未取代的或取代的赖氨酸;Xaa 4为选自亮氨酸、甘氨酸和丙氨酸的氨基酸;Xaa 5不存在,或为选自甘氨酸和丙氨酸的氨基酸;其中,所述氨基酸序列的N端与Z连接,且C端与M连接(如果M存在的话)或直接与药物D连接,优选地,Xaa 3为ε-氨基被C 1-C 3烷基单取代或二取代的赖氨酸,再优选地,Y为选自以下的肽:Phe-Lys-Gly、Leu-lys-Gly、Gly-Val-Lys-Gly、Val-Lys-Gly-Gly、Val-Lys-Gly、Val-Lys-Ala、Val-Lys-Leu,其中Lys残基为未取代的或被C 1-C 3烷基单取代或二取代的赖氨酸。
- 根据权利要求6-8的抗体-药物偶联物或其可药用盐或溶剂化物,其中,Z具有以下结构:-Z 1-Z 2-Z 3-Z 4-,其中Z 1为Ab中的硫原子,Z 2为5-10元杂环基,优选地含1或2个选自N,S和O的杂原子;Z 3选自键、-C(=O)-、-C 1-C 10亚烷基-C(=O)-、-C 3-C 10亚炔基-C(=O)-、-C 3-C 10亚烯基-C(=O)-、-C 1-C 10亚杂烷基-C(=O)-、-C 3-C 8亚环烷基-C(=O)-、-O-C 1-C 8亚烷基-C(=O)-、-亚芳基-C(=O)-、-C 1-C 10亚烷基-亚芳基-C(=O)-、-亚芳基-C 1-C 10亚烷基-C(=O)-、-C 1-C 10亚烷基-C 3-C 8亚环烷基-C(=O)-、- C 3-C 8亚环烷基-C 1-C 10亚烷基-C(=O)-、-C 3-C 8亚杂环基-C(=O)-、-C 1-C 10亚烷基-C 3-C 8亚杂环基-C(=O)-、-C 3-C 8亚杂环基-C 1-C 10亚烷基-C(=O)-,Z 4是键或是下式表示的PEG单元,其中,R 5选自C 1-4亚烷基、-NH-、-NH-C 1-4亚烷基-杂芳基-,其中杂芳基为5元或6元的含氮杂芳基,优选三唑基;R 6为-C(=O)-、C 1-4亚烷基、C 1-4亚烷基-C(=O)-、-NH-C(=O)-(CH 2OCH 2)-C(=O)-、C 1-4亚烷基-NH-C(=O)-(CH 2OCH 2)-C(=O)-,其中m为2-12的整数,例如m=2,4,6,或8,优选地,Z具有以下结构:其中,R b是亚炔基-C(=O)-或亚烯基-C-(=O)-、优选地,R b是其中,左侧波浪线表示与抗体(Ab)连接的位置;右侧波浪线表示与Y连接的位置;更优选地,Z具有结构:
- 根据权利要求11的抗体-药物偶联物或其可药用盐或溶剂化物,其中,R 3和R 4均为甲基;或R 3和R 4均为乙基;或R 3和R 4均为丙基。
- 权利要求1的抗体-药物偶联物或其可药用盐或溶剂化物,其中,所述式I的L-D单元通过与Ab的轻链和/或重链的半胱氨酸的巯基形成硫醚键,从而与抗体连接。
- 药物组合物,其包含前述权利要求1-14任一项的抗体-药物偶联物或其可药用盐或溶剂化物以及任选地药用辅料。
- 结合CLAUDIN 18.2的抗体或其抗原结合片段,其包含(i)如SEQ ID NO:1或3所示的重链可变区的HCDR1、2和3序列,以及如SEQ ID NO:2所示的轻链可变区的LCDR1、2和3序列,或者(ii)如SEQ ID NO:21所示的重链可变区的HCDR1、2和3序列,以及如SEQ ID NO:22所示的轻链可变区的LCDR1、2和3序列,或者(iii)如SEQ ID NO:23所示的重链可变区的HCDR1、2和3序列,以及如SEQ ID NO:24所示的轻链可变区的LCDR1、2和3序列,或者(iv)如SEQ ID NO:38或40所示的重链可变区的HCDR1、2和3序列,以及如SEQ ID NO:39所示的轻链可变区的LCDR1、2和3序列,或者(v)如SEQ ID NO:44所示的重链可变区的HCDR1、2和3序列,以及如SEQ ID NO:45所示的轻链可变区的LCDR1、2和3序列,或者(vi)如SEQ ID NO:46所示的重链可变区的HCDR1、2和3序列,以及如SEQ ID NO:47所示的轻链可变区的LCDR1、2和3序列,或者(vii)如SEQ ID NO:48所示的重链可变区的HCDR1、2和3序列,以及如SEQ ID NO:49所示的轻链可变区的LCDR1、2和3序列,或者(viii)如SEQ ID NO:50所示的重链可变区的HCDR1、2和3序列,以及如SEQ ID NO:51所示的轻链可变区的LCDR1、2和3序列,或者(ix)如SEQ ID NO:52所示的重链可变区的HCDR1、2和3序列,以及如SEQ ID NO:53所示的轻链可变区的LCDR1、2和3序列,优选地,其中所述CDR根据Kabat或IMGT或其组合进行定义。
- 权利要求16的抗体或其抗原结合片段,其中所述抗体或其抗原结合片段包含重链可变区和轻链可变区,其中:(i)重链可变区包含如SEQ ID NO:1或3所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,以及轻链可变区包含如SEQ ID NO:2所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,或者(ii)重链可变区包含如SEQ ID NO:21所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,以及轻链可变区包含如SEQ ID NO:22所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,或者(iii)重链可变区包含如SEQ ID NO:23所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,以及轻链可变区包含如SEQ ID NO:24所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,或者(iv)重链可变区包含如SEQ ID NO:38或40所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,以及轻链可变区包含如SEQ ID NO:39所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,或者(v)重链可变区包含如SEQ ID NO:44所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,以及轻链可变区包含如SEQ ID NO:45所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,或者(vi)重链可变区包含如SEQ ID NO:46所示的氨基酸序列或与其具有至少80%、85%、90%、95%、 96%、97%、98%或99%同一性的氨基酸序列,以及轻链可变区包含如SEQ ID NO:47所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,或者(vii)重链可变区包含如SEQ ID NO:48所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,以及轻链可变区包含如SEQ ID NO:49所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,或者(viii)重链可变区包含如SEQ ID NO:50所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,以及轻链可变区包含如SEQ ID NO:51所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,或者(ix)重链可变区包含如SEQ ID NO:52所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列,以及轻链可变区包含如SEQ ID NO:53所示的氨基酸序列或与其具有至少80%、85%、90%、95%、96%、97%、98%或99%同一性的氨基酸序列;优选地,其中所述抗体或其抗原结合片段包含选自以下的重链可变区和轻链可变区:(i)包含SEQ ID NO:1所示的氨基酸序列的重链可变区,和包含SEQ ID NO:2所示的氨基酸序列的轻链可变区,或者(ii)包含SEQ ID NO:3所示的氨基酸序列的重链可变区,和包含SEQ ID NO:2所示的氨基酸序列的轻链可变区,或者(iii)包含SEQ ID NO:21所示的氨基酸序列的重链可变区,和包含SEQ ID NO:22所示的氨基酸序列的轻链可变区,或者,其中所述抗体或其抗原结合片段包含选自以下的重链可变区和轻链可变区:(iv)包含SEQ ID NO:38所示的氨基酸序列的重链可变区,和包含SEQ ID NO:40所示的氨基酸序列的轻链可变区,或者(v)包含SEQ ID NO:39所示的氨基酸序列的重链可变区,和包含SEQ ID NO:40所示的氨基酸序列的轻链可变区,或者(vi)包含SEQ ID NO:23所示的氨基酸序列的重链可变区,和包含SEQ ID NO:24所示的氨基酸序列的轻链可变区。
- 权利要求16-17任一项的抗体或其抗原结合片段,其中所述抗体是IgG1,IgG2,IgG3或IgG4抗体,优选具有人IgG1重链恒定区和人Kappa轻链恒定区;或者所述抗原结合片段是选自以下的抗体片段:Fab、Fab’、Fab’-SH、Fv、单链抗体、scFv、scFab、二硫键连接的scFv,二硫键连接的scFab或(Fab’) 2片段。
- 权利要求16-18任一项的抗体或其抗原结合片段,其中所述抗体是鼠源抗体、或嵌合抗体、或人源化抗体,优选地为人源化抗体。
- 一种分离的核酸,其编码权利要求16-19任一项的抗CLAUDIN 18.2抗体或其抗原结合片段。
- 一种载体,其包含权利要求20的核酸,优选地所述载体是表达载体。
- 一种宿主细胞,其包含权利要求20的核酸或权利要求21的载体,优选地,所述宿主细胞是哺乳动物细胞。
- 免疫缀合物,其包含与治疗剂或诊断剂缀合的前述权利要求16-19中任一项的抗体或其抗原结合片段。
- 前述权利要求16-19任一项的抗体或其抗原结合片段的用途,所述用途选自在体内或在体外用于:(1)靶向性结合表面表达CLAUDIN 18.2的肿瘤细胞;和/或(2)引发针对表面表达CLAUDIN 18.2的肿瘤细胞的ADCC活性和/或CDC活性,以及(3)抑制和/或杀伤表面表达CLAUDIN 18.2的肿瘤细胞,或用于制备在前述任一项中使用的药物。
- 药物组合物,其包含前述权利要求16-19任一项的抗体或其抗原结合片段或权利要求23的免疫缀合物,以及任选地药用辅料。
- 在受试者中预防或治疗CLAUDIN 18.2阳性肿瘤的方法,所述方法包括向所述受试者施用有效量的前述权利要求1-14任一项的抗体-药物偶联物或其可药用盐或溶剂化物、或权利要求16-19任一项的抗体或其抗原结合片段,优选地,所述肿瘤是消化系统肿瘤或其转移瘤,例如胃癌、胰腺癌、食管癌、结肠癌、胆囊癌,肝癌,尤其是胃癌,例如,HER2阴性胃癌。
- 权利要求26的方法,其中CLAUDIN 18.2阳性肿瘤为晚期或转移性胃癌、或胃食管交界处癌(EGJA)。
- 检测样品中CLAUDIN 18.2的方法,所述方法包括(a)将样品与前述权利要求16-19中任一项的抗体或其抗原结合片段接触;和(b)检测所述抗体或其抗原结合片段和CLAUDIN 18.2间的复合物的形成;任选地,抗体是被可检测地标记的。
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Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101312989A (zh) | 2005-11-24 | 2008-11-26 | 加尼梅德药物公司 | 用于治疗癌症的针对密蛋白-18的单克隆抗体 |
WO2019195665A1 (en) | 2018-04-06 | 2019-10-10 | Seattle Genetics, Inc. | Camptothecin peptide conjugates |
CN111110862A (zh) * | 2018-11-01 | 2020-05-08 | 上海健信生物医药科技有限公司 | 抗cldn18.2抗体的药物偶联体及其制备方法和用途 |
CN111433188A (zh) * | 2018-12-17 | 2020-07-17 | 荣昌生物制药(烟台)股份有限公司 | 一种用于抗体药物偶联物的连接子及其应用 |
WO2020147321A1 (en) * | 2019-01-17 | 2020-07-23 | Beijing Mabworks Biotech Co. Ltd. | Antibodies binding human claudin 18.2 and uses thereof |
CN111867630A (zh) * | 2018-06-17 | 2020-10-30 | 上海健信生物医药科技有限公司 | 靶向cldn18.2的抗体、双特异性抗体、adc和car及其应用 |
WO2020228806A1 (zh) * | 2019-05-16 | 2020-11-19 | 齐鲁制药有限公司 | 针对密蛋白18a2的抗体及其应用 |
CN112237634A (zh) * | 2019-07-19 | 2021-01-19 | 上海复旦张江生物医药股份有限公司 | 抗体药物偶联物、其中间体、制备方法及应用 |
WO2022170971A1 (zh) | 2021-02-09 | 2022-08-18 | 苏州宜联生物医药有限公司 | 生物活性物偶联物及其制备方法和用途 |
-
2022
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Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101312989A (zh) | 2005-11-24 | 2008-11-26 | 加尼梅德药物公司 | 用于治疗癌症的针对密蛋白-18的单克隆抗体 |
WO2019195665A1 (en) | 2018-04-06 | 2019-10-10 | Seattle Genetics, Inc. | Camptothecin peptide conjugates |
CN111867630A (zh) * | 2018-06-17 | 2020-10-30 | 上海健信生物医药科技有限公司 | 靶向cldn18.2的抗体、双特异性抗体、adc和car及其应用 |
CN111110862A (zh) * | 2018-11-01 | 2020-05-08 | 上海健信生物医药科技有限公司 | 抗cldn18.2抗体的药物偶联体及其制备方法和用途 |
CN111433188A (zh) * | 2018-12-17 | 2020-07-17 | 荣昌生物制药(烟台)股份有限公司 | 一种用于抗体药物偶联物的连接子及其应用 |
WO2020147321A1 (en) * | 2019-01-17 | 2020-07-23 | Beijing Mabworks Biotech Co. Ltd. | Antibodies binding human claudin 18.2 and uses thereof |
WO2020228806A1 (zh) * | 2019-05-16 | 2020-11-19 | 齐鲁制药有限公司 | 针对密蛋白18a2的抗体及其应用 |
CN112237634A (zh) * | 2019-07-19 | 2021-01-19 | 上海复旦张江生物医药股份有限公司 | 抗体药物偶联物、其中间体、制备方法及应用 |
WO2022170971A1 (zh) | 2021-02-09 | 2022-08-18 | 苏州宜联生物医药有限公司 | 生物活性物偶联物及其制备方法和用途 |
Non-Patent Citations (7)
Title |
---|
"NCBI", Database accession no. NP_001014118.1 |
GESTUR VIDARSSON ET AL., IGG SUBCLASSES AND ALLOTYPES: FROM STRUCTURE TO EFFECTOR FUNCTIONS, 20 October 2014 (2014-10-20) |
KABAT ET AL.: "Sequences of Proteins of Immunological Interest", 1991, NATIONAL INSTITUTES OF HEALTH |
no. 2356229-58-6 |
R. C. ROWEP. J. SESKEYS. C. OWEN: "Handbook of Pharmaceutical Excipients", 1980, PHARMACEUTICAL PRESS |
VESELA KOSTOVA ET AL., THE CHEMISTRY BEHIND ADCS, PHARMACEUTICALS, vol. 14, 2021, pages 442, Retrieved from the Internet <URL:https://doi.org/10.3390/ph14050442> |
XIANG LING ET AL.: "A Novel Small Molecule FLU 8 That Selectively Inhibits Survivin, Mcl-1, XIAP and cIAP2 in a p53-Independent Manner, Shows Superior Antitumor Activity", PLOS ONE, vol. 7, no. 9, pages e45571 |
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