Patent Application
20230183377
The present disclosure provides activatable antigen binding proteins having immunoglobulin-like antigen binding activity, wherein the activatable antigen binding proteins comprise universal masking moieties that block binding between the antigen binding domain and its target antigen until the universal masking moieties are removed from blocking the antigen binding domain.
Antibodies have been successfully used as therapeutic reagents for various cancers. When administered to a subject, antibodies bind to both healthy and diseased tissues leading to deleterious side effects. To overcome the off-target effects, antibodies have been engineered to include masking moieties attached to a peptide linker. The masking moiety prevents antibody binding to the target antigen wherein the masking moiety either binds directly to the antigen binding domain or sterically hinders binding between the antigen binding domain and its target antigen. The peptide linkers are designed to be cleaved by proteases secreted by the diseased tissue which unmasks the antigen binding domain at the disease site and decreases off-target activity.
Described herein are activatable masked antigen binding proteins which offer many advantages over other masked antibody-like molecules (sometimes called “probodies”). The activatable masked antigen binding proteins described herein comprise an antigen binding protein attached to universal masking moieties by peptide linkers. The universal masking moieties dimerize with each other to form a dimerized masking complex that blocks binding between the antigen binding domain and its target antigen. The individual masking moieties and the dimerized masking complex do not bind specifically to the antigen binding domain. The masking moieties form stable dimers because their association with each other mimics homodimers or heterodimers found in naturally-occurring immunoglobulin or cell receptor molecules. The dimerization of the masking moieties does not involve covalent bonding and can be optimized by engineering interchain association through structure complementarity such as knob-in-hole. The masking moieties can potentially exhibit reduced immunogenicity because they are derived from the constant domains of immunoglobulin-like molecules (e.g., CH1, CH3 kappa, CH3 lambda) or T cell receptors (e.g., TCR alpha constant and TCR beta constant domains).
The masking moieties are attached to peptide linkers that can be cleaved by a protease, for example a protease localized at a disease tissue site. The masking moieties and peptide linkers operate together acting as a mask to sterically hinder binding between the antigen binding domain of the antibody and its target antigen. The peptide linkers having amino acid lengths and sequences that can be modified for improved flexibility and/or cleavage susceptibility. By modifying the peptide linker length and/or sequences, the steric hinderance of the masking moieties and cleavage susceptibility of the peptide linkers can be increased or decreased (e.g., tunable cleavability).
The length of the peptide linkers can be lengthened or shortened to obtain an optimal balance between linker flexibility to permit steric hinderance by the masking moieties and optimal cleavage susceptibility by the tumor-associated protease. For example, shorter peptide linkers may exhibit improved steric hinderance (improved masking) but may also exhibit reduced susceptibility to protease digestion. The peptide linkers can be designed to include amino acids (e.g., glycines) that confer linker flexibility. The cleavable site within the peptide linkers can be designed to confer modulated protease susceptibility. In one example, the peptide linkers can be designed to include 1-5 glycines on the C-terminal and/or N-terminal end of the peptide linker to increase or decrease protease susceptibility. In another example, certain amino acid sequences are readily cleavable with MMP9 protease but exhibit reduced levels of cleavage with MMP2 protease. Additionally, the junction sequence between the C-terminal end of the peptide linker and the N-terminal end of the heavy chain or light chain variable region can be mutated to include one or more amino acid substitutions, deletions and/or insertions to modulate protease susceptibility.
In the inactive state, the activatable masked antigen binding proteins exhibit reduced binding to healthy tissue that expresses low levels of tumor-associated protease. The activatable masked antigen binding proteins are converted from the inactive state to activated state upon cleavage of the peptide linkers at the diseased tissue site which expresses higher levels of the tumor-associated protease, thereby greatly reducing off-target activity and reducing toxicity. The activatable masked antigen binding proteins described herein have the potential to widen the therapeutic window.
The activatable masked antigen binding protein can be joined to a toxin by a chemical linker thereby forming an immunoconjugate. The toxin can be cytotoxic to cells and tissue. The immunoconjugate can be used to deliver the toxin to the target tumor.
Unless defined otherwise, technical and scientific terms used herein have meanings that are commonly understood by those of ordinary skill in the art unless defined otherwise. Generally, terminologies pertaining to techniques of cell and tissue culture, molecular biology, immunology, microbiology, genetics, transgenic cell production, protein chemistry and nucleic acid chemistry and hybridization described herein are well known and commonly used in the art. The methods and techniques provided herein are generally performed according to conventional procedures well known in the art and as described in various general and more specific references that are cited and discussed herein unless otherwise indicated. See, e.g., Sambrook et al. Molecular Cloning: A Laboratory Manual, 2d ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1989) and Ausubel et al., Current Protocols in Molecular Biology, Greene Publishing Associates (1992). A number of basic texts describe standard antibody production processes, including, Borrebaeck (ed) Antibody Engineering, 2nd Edition Freeman and Company, NY, 1995; McCafferty et al. Antibody Engineering, A Practical Approach IRL at Oxford Press, Oxford, England, 1996; and Paul (1995) Antibody Engineering Protocols Humana Press, Towata, N.J., 1995; Paul (ed.), Fundamental Immunology, Raven Press, N.Y, 1993; Coligan (1991) Current Protocols in Immunology Wiley/Greene, NY; Harlow and Lane (1989) Antibodies: A Laboratory Manual Cold Spring Harbor Press, NY; Stites et al. (eds.) Basic and Clinical Immunology (4th ed.) Lange Medical Publications, Los Altos, Calif., and references cited therein; Coding Monoclonal Antibodies: Principles and Practice (2nd ed.) Academic Press, New York, N.Y., 1986, and Kohler and Milstein Nature 256: 495-497, 1975. All of the references cited herein are incorporated herein by reference in their entireties. Enzymatic reactions and enrichment/purification techniques are also well known and are performed according to manufacturer’s specifications, as commonly accomplished in the art or as described herein. The terminology used in connection with, and the laboratory procedures and techniques of, analytical chemistry, synthetic organic chemistry, and medicinal and pharmaceutical chemistry described herein are well known and commonly used in the art. Standard techniques can be used for chemical syntheses, chemical analyses, pharmaceutical preparation, formulation, and delivery, and treatment of patients.
The headings provided herein are not limitations of the various aspects of the disclosure, which aspects can be understood by reference to the specification as a whole.
Unless otherwise required by context herein, singular terms shall include pluralities and plural terms shall include the singular. Singular forms “a”, “an” and “the”, and singular use of any word, include plural referents unless expressly and unequivocally limited on one referent.
It is understood the use of the alternative (e.g., “or”) herein is taken to mean either one or both or any combination thereof of the alternatives.
The term “and/or” used herein is to be taken mean specific disclosure of each of the specified features or components with or without the other. For example, the term “and/or” as used in a phrase such as “A and/or B” herein is intended to include “A and B,” “A or B,” “A” (alone), and “B” (alone). Likewise, the term “and/or” as used in a phrase such as “A, B, and/or C” is intended to encompass each of the following aspects: A, B, and C; A, B, or C; A or C; A or B; B or C; A and C; A and B; B and C; A (alone); B (alone); and C (alone).
As used herein, terms “comprising”, “including”, “having” and “containing”, and their grammatical variants, as used herein are intended to be non-limiting so that one item or multiple items in a list do not exclude other items that can be substituted or added to the listed items. It is understood that wherever aspects are described herein with the language “comprising,” otherwise analogous aspects described in terms of “consisting of” and/or “consisting essentially of” are also provided.
As used herein, the term “about” refers to a value or composition that is within an acceptable error range for the particular value or composition as determined by one of ordinary skill in the art, which will depend in part on how the value or composition is measured or determined, i.e., the limitations of the measurement system. For example, “about” or “approximately” can mean within one or more than one standard deviation per the practice in the art. Alternatively, “about” or “approximately” can mean a range of up to 10% (i.e., ±10%) or more depending on the limitations of the measurement system. For example, about 5 mg can include any number between 4.5 mg and 5.5 mg. Furthermore, particularly with respect to biological systems or processes, the terms can mean up to an order of magnitude or up to 5-fold of a value. When particular values or compositions are provided in the instant disclosure, unless otherwise stated, the meaning of “about” or “approximately” should be assumed to be within an acceptable error range for that particular value or composition.
The terms “peptide”, “polypeptide” and “protein” and other related terms used herein are used interchangeably and refer to a polymer of amino acids and are not limited to any particular length. Polypeptides may comprise natural and non-natural amino acids. Polypeptides include recombinant or chemically-synthesized forms. Polypeptides also include precursor molecules that have not yet been subjected to cleavage, for example cleavage by a secretory signal peptide or by non-enzymatic cleavage at certain amino acid residues. Polypeptides include mature molecules that have undergone cleavage. These terms encompass native and artificial proteins, protein fragments and polypeptide analogs (such as muteins, variants, chimeric proteins and fusion proteins) of a protein sequence as well as post-translationally, or otherwise covalently or non-covalently, modified proteins. Two or more polypeptides (e.g., 3 polypeptide chains) can associate with each other, via covalent and/or non-covalent association, to form a polypeptide complex. Association of the polypeptide chains can also include peptide folding. Thus, a polypeptide complex can be dimeric, trimeric, tetrameric, or higher order complexes depending on the number of polypeptide chains that form the complex.
The terms “nucleic acid”, “polynucleotide” and “oligonucleotide” and other related terms used herein are used interchangeably and refer to polymers of nucleotides and are not limited to any particular length. Nucleic acids include recombinant and chemically-synthesized forms. Nucleic acids include DNA molecules (cDNA or genomic DNA), RNA molecules (e.g., mRNA), analogs of the DNA or RNA generated using nucleotide analogs (e.g., peptide nucleic acids and non-naturally occurring nucleotide analogs), and hybrids thereof. Nucleic acid molecule can be single-stranded or double-stranded. In one embodiment, the nucleic acid molecules of the disclosure comprise a contiguous open reading frame encoding an antibody, or a fragment or scFv, derivative, mutein, or variant thereof. In one embodiment, nucleic acids comprise one type of polynucleotide or a mixture of two or more different types of polynucleotides. Nucleic acids encoding activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof, are described herein.
The term “recover” or “recovery” or “recovering”, and other related terms, refers to obtaining a protein (e.g., an antibody or an antigen binding portion thereof), from host cell culture medium or from host cell lysate or from the host cell membrane. In one embodiment, the protein is expressed by the host cell as a recombinant protein fused to a secretion signal peptide (leader peptide sequence) sequence which mediates secretion of the expressed protein from a host cell (e.g., from a mammalian host cell). The secreted protein can be recovered from the host cell medium. In one embodiment, the protein is expressed by the host cell as a recombinant protein that lacks a secretion signal peptide sequence which can be recovered from the host cell lysate. In one embodiment, the protein is expressed by the host cell as a membrane-bound protein which can be recovered using a detergent to release the expressed protein from the host cell membrane. In one embodiment, irrespective of the method used to recover the protein, the protein can be subjected to procedures that remove cellular debris from the recovered protein. For example, the recovered protein can be subj ected to chromatography, gel electrophoresis and/or dialysis. In one embodiment, the chromatography comprises any one or any combination or two or more procedures including affinity chromatography, hydroxyapatite chromatography, ion-exchange chromatography, reverse phase chromatography and/or chromatography on silica. In one embodiment, affinity chromatography comprises protein A or G (cell wall components from Staphylococcus aureus).
The term “isolated” refers to a protein (e.g., an antibody or an antigen binding portion thereof) or polynucleotide that is substantially free of other cellular material. A protein may be rendered substantially free of naturally associated components (or components associated with a cellular expression system or chemical synthesis methods used to produce the antibody) by isolation, using protein purification techniques well known in the art. The term isolated also refers in some embodiment to protein or polynucleotides that are substantially free of other molecules of the same species, for example other protein or polynucleotides having different amino acid or nucleotide sequences, respectively. The purity of homogeneity of the desired molecule can be assayed using techniques well known in the art, including low resolution methods such as gel electrophoresis and high resolution methods such as HPLC or mass spectrometry. In one embodiment, the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof, of the present disclosure are isolated.
The term “leader sequence” or “leader peptide” or “peptide signal sequence” or “signal peptide” or “secretion signal peptide” refers to a peptide sequence that is located at the N-terminus of a polypeptide. A leader sequence directs a polypeptide chain to a cellular secretory pathway and can direct integration and anchoring of the polypeptide into the lipid bilayer of the cellular membrane. Typically, a leader sequence is about 10-50 amino acids in length. A leader sequence can direct transport of a precursor polypeptide from the cytosol to the endoplasmic reticulum. In one embodiment, a leader sequence includes signal sequences comprising CD8α, CD28 or CD16 leader sequences. In one embodiment, the signal sequence comprises a mammalian sequence, including for example mouse or human Ig gamma secretion signal peptide. In one embodiment, a leader sequence comprises a mouse Ig gamma leader peptide sequence MEWSWVFLFFLSVTTGVHS.
An “antigen binding protein” and related terms used herein refers to a protein comprising a portion that binds to an antigen and, optionally, a scaffold or framework portion that allows the antigen binding portion to adopt a conformation that promotes binding of the antigen binding protein to the antigen. Examples of antigen binding proteins include antibodies, antibody fragments (e.g., an antigen binding portion of an antibody), antibody derivatives, and antibody analogs. The antigen binding protein can comprise, for example, an alternative protein scaffold or artificial scaffold with grafted CDRs or CDR derivatives. Such scaffolds include, but are not limited to, antibody-derived scaffolds comprising mutations introduced to, for example, stabilize the three-dimensional structure of the antigen binding protein as well as wholly synthetic scaffolds comprising, for example, a biocompatible polymer. See, for example, Korndorfer et al., 2003, Proteins: Structure, Function, and Bioinformatics, Volume 53, Issue 1: 121-129; Roque et al., 2004, Biotechnol. Prog. 20:639-654. In addition, peptide antibody mimetics (“PAMs”) can be used, as well as scaffolds based on antibody mimetics utilizing fibronection components as a scaffold. Antigen binding proteins comprising activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof, are described herein.
An antigen binding protein can have, for example, the structure of a naturally occurring immunoglobulin. In one embodiment, an “immunoglobulin” refers to a naturally-occurring tetrameric molecule composed of two identical pairs of polypeptide chains, each pair having one “light” (about 25 kDa) and one “heavy” chain (about 50-70 kDa). The amino-terminal portion of each chain includes a variable region of about 100 to 110 or more amino acids primarily responsible for antigen recognition. The carboxy-terminal portion of each chain defines a constant region primarily responsible for effector function. Human light chains are classified as kappa or lambda light chains. Heavy chains are classified as mu, delta, gamma, alpha, or epsilon, and define the antibody’s isotype as IgM, IgD, IgG, IgA, and IgE, respectively. Within light and heavy chains, the variable and constant regions are joined by a “J” region of about 12 or more amino acids, with the heavy chain also including a “D” region of about 10 more amino acids. See generally, Fundamental Immunology Ch. 7 (Paul, W., ed., 2nd ed. Raven Press, N.Y. (1989)) (incorporated by reference in its entirety for all purposes). The heavy and/or light chains may or may not include a leader sequence for secretion. The variable regions of each light/heavy chain pair form the antibody binding site such that an intact immunoglobulin has two antigen binding sites. In one embodiment, an antigen binding protein can be a synthetic molecule having a structure that differs from a tetrameric immunoglobulin molecule but still binds a target antigen or binds two or more target antigens. For example, a synthetic antigen binding protein can comprise antibody fragments, 1-6 or more polypeptide chains, asymmetrical assemblies of polypeptides, or other synthetic molecules. Antigen binding proteins having immunoglobulin-like properties that bind specifically to EGFR or CD38 are described herein.
The variable regions of immunoglobulin chains exhibit the same general structure of relatively conserved framework regions (FR) joined by three hypervariable regions, also called complementarity determining regions or CDRs. From N-terminus to C-terminus, both light and heavy chains comprise the domains FR1, CDR1, FR2, CDR2, FR3, CDR3 and FR4.
One or more CDRs may be incorporated into a molecule either covalently or noncovalently to make it an antigen binding protein. An antigen binding protein may incorporate the CDR(s) as part of a larger polypeptide chain, may covalently link the CDR(s) to another polypeptide chain, or may incorporate the CDR(s) noncovalently. The CDRs permit the antigen binding protein to specifically bind to a particular antigen of interest.
The assignment of amino acids to each domain is in accordance with the definitions of Kabat et al. in Sequences of Proteins of Immunological Interest, 5th Ed., US Dept. of Health and Human Services, PHS, NIH, NIH Publication no. 91-3242, 1991 (“Kabat numbering”). Other numbering systems for the amino acids in immunoglobulin chains include IMGT.RTM. (international ImMunoGeneTics information system; Lefranc et al, Dev. Comp. Immunol. 29:185-203; 2005) and AHo (Honegger and Pluckthun, J. Mol. Biol. 309(3):657-670; 2001); Chothia (Al-Lazikani et al., 1997 Journal of Molecular Biology 273:927-948; Contact (Maccallum et al., 1996 Journal of Molecular Biology 262:732-745, and Aho (Honegger and Pluckthun 2001 Journal of Molecular Biology 309:657-670.
An “antibody” and “antibodies” and related terms used herein refers to an intact immunoglobulin or to an antigen binding portion thereof that binds specifically to an antigen. Antigen binding portions may be produced by recombinant DNA techniques or by enzymatic or chemical cleavage of intact antibodies. Antigen binding portions include, inter alia, Fab, Fab′, F(ab′)2, Fv, domain antibodies (dAbs), and complementarity determining region (CDR) fragments, single-chain antibodies (scFv), chimeric antibodies, diabodies, triabodies, tetrabodies, and polypeptides that contain at least a portion of an immunoglobulin that is sufficient to confer specific antigen binding to the polypeptide.
Antibodies include recombinantly produced antibodies and antigen binding portions. Antibodies include non-human, chimeric, humanized and fully human antibodies. Antibodies include monospecific, multispecific (e.g., bispecific, trispecific and higher order specificities). Antibodies include tetrameric antibodies, light chain monomers, heavy chain monomers, light chain dimers, heavy chain dimers. Antibodies include F(ab′)2 fragments, Fab′ fragments and Fab fragments. Antibodies include single domain antibodies, monovalent antibodies, single chain antibodies, single chain variable fragment (scFv), camelized antibodies, affibodies, disulfide-linked Fvs (sdFv), anti-idiotypic antibodies (anti-Id), minibodies. Antibodies include monoclonal and polyclonal populations. Antibodies-like molecules comprising activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof, are described herein.
An “antigen binding domain,” “antigen binding region,” or “antigen binding site” and other related terms used herein refer to a portion of an antigen binding protein that contains amino acid residues (or other moieties) that interact with an antigen and contribute to the antigen binding protein’s specificity and affinity for the antigen. For an antibody that specifically binds to its antigen, this will include at least part of at least one of its CDR domains. Antigen binding domains from anti-EGFR or anti-CD38 antibodies are described herein.
The terms “specific binding”, “specifically binds” or “specifically binding” and other related terms, as used herein in the context of an antibody or antigen binding protein or antibody fragment, refer to non-covalent or covalent preferential binding to an antigen relative to other molecules or moieties (e.g., an antibody specifically binds to a particular antigen relative to other available antigens). In one embodiment, an antibody specifically binds to a target antigen if it binds to the antigen with a dissociation constant KD of 10-5 M or less, or 10-6 M or less, or 10-7 M or less, or 10-8 M or less, or 10-9 M or less, or 10-10 M or less, or 10-11 M or less. In one embodiment, activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that bind specifically to their target antigens (e.g., EGFR or CD38 antigen) are described herein.
In one embodiment, binding specificity can be measure by ELISA, radioimmune assay (RIA), electrochemiluminescence assays (ECL), immunoradiometric assay (IRMA), or enzyme immune assay (EIA).
In one embodiment, a dissociation constant (KD) can be measured using a BIACORE surface plasmon resonance (SPR) assay. Surface plasmon resonance refers to an optical phenomenon that allows for the analysis of real-time interactions by detection of alterations in protein concentrations within a biosensor matrix, for example using the BIACORE system (Biacore Life Sciences division of GE Healthcare, Piscataway, NJ).
An “epitope” and related terms as used herein refers to a portion of an antigen that is bound by an antigen binding protein (e.g., by an antibody or an antigen binding portion thereof). An epitope can comprise portions of two or more antigens that are bound by an antigen binding protein. An epitope can comprise non-contiguous portions of an antigen or of two or more antigens (e.g., amino acid residues that are not contiguous in an antigen’s primary sequence but that, in the context of the antigen’s tertiary and quaternary structure, are near enough to each other to be bound by an antigen binding protein). Generally, the variable regions, particularly the CDRs, of an antibody interact with the epitope. In one embodiment, activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that bind an epitope of EGFR or CD38 antigen are described herein.
An “antibody fragment”, “antibody portion”, “antigen-binding fragment of an antibody”, or “antigen-binding portion of an antibody” and other related terms used herein refer to a molecule other than an intact antibody that comprises a portion of an intact antibody that binds the antigen to which the intact antibody binds. Examples of antibody fragments include, but are not limited to, Fv, Fab, Fab′, Fab′—SH, F(ab′)2; Fd; and Fv fragments, as well as dAb; diabodies; linear antibodies; single-chain antibody molecules (e.g. scFv); polypeptides that contain at least a portion of an antibody that is sufficient to confer specific antigen binding to the polypeptide. Antigen binding portions of an antibody may be produced by recombinant DNA techniques or by enzymatic or chemical cleavage of intact antibodies. Antigen binding portions include, inter alia, Fab, Fab′, F(ab′)2, Fv, domain antibodies (dAbs), and complementarity determining region (CDR) fragments, chimeric antibodies, diabodies, triabodies, tetrabodies, and polypeptides that contain at least a portion of an immunoglobulin that is sufficient to confer antigen binding properties to the antibody fragment. In one embodiment, antigen-binding fragments include fragments of activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that bind specifically to their target antigens (e.g., EGFR or CD38 antigen) which are described herein.
The terms “Fab”, “Fab fragment” and other related terms refers to a monovalent fragment comprising a variable light chain region (VL), constant light chain region (CL), variable heavy chain region (VH), and first constant region (CH1). A Fab is capable of binding an antigen. An F(ab′)2 fragment is a bivalent fragment comprising two Fab fragments linked by a disulfide bridge at the hinge region. A F(Ab′)2 has antigen binding capability. An Fd fragment comprises VH and CH1 regions. An Fv fragment comprises VL and VH regions. An Fv can bind an antigen. A dAb fragment has a VH domain, a VL domain, or an antigen-binding fragment of a VH or VL domain (U.S. Pat. 6,846,634 and 6,696,245; U.S. published Application Nos. 2002/02512, 2004/0202995, 2004/0038291, 2004/0009507, 2003/0039958; and Ward et al., Nature 341:544-546, 1989). Fab fragments comprising antigen binding portions from anti-EGFR or anti-CD38 antibodies are described herein.
A single-chain antibody (scFv) is an antibody in which a VL and a VH region are joined via a linker (e.g., a synthetic sequence of amino acid residues) to form a continuous protein chain. Preferably the linker is long enough to allow the protein chain to fold back on itself and form a monovalent antigen binding site (see, e.g., Bird et al., 1988, Science 242:423-26 and Huston et al., 1988, Proc. Natl. Acad. Sci. USA 85:5879-83). Single chain antibodies comprising antigen binding portions from anti-EGFR or anti-CD38 antibodies are described herein.
Diabodies are bivalent antibodies comprising two polypeptide chains, wherein each polypeptide chain comprises VH and VL domains joined by a linker that is too short to allow for pairing between two domains on the same chain, thus allowing each domain to pair with a complementary domain on another polypeptide chain (see, e.g., Holliger et al., 1993, Proc. Natl. Acad. Sci. USA 90:6444-48, and Poljak et al., 1994, Structure 2:1121-23). If the two polypeptide chains of a diabody are identical, then a diabody resulting from their pairing will have two identical antigen binding sites. Polypeptide chains having different sequences can be used to make a diabody with two different antigen binding sites. Similarly, tribodies and tetrabodies are antibodies comprising three and four polypeptide chains, respectively, and forming three and four antigen binding sites, respectively, which can be the same or different. Diabody, tribody and tetrabody constructs can be prepared using antigen binding portions from any of the anti-EGFR or anti-CD38 antibodies described herein.
The term “human antibody” refers to antibodies that have one or more variable and constant regions derived from human immunoglobulin sequences. In one embodiment, all of the variable and constant domains are derived from human immunoglobulin sequences (e.g., a fully human antibody). These antibodies may be prepared in a variety of ways, examples of which are described below, including through recombinant methodologies or through immunization with an antigen of interest of a mouse that is genetically modified to express antibodies derived from human heavy and/or light chain-encoding genes. Fully human anti-EGFR or anti-CD38 antibodies and antigen binding proteins, or portions thereof are described herein.
A “humanized” antibody refers to an antibody having a sequence that differs from the sequence of an antibody derived from a non-human species by one or more amino acid substitutions, deletions, and/or additions, such that the humanized antibody is less likely to induce an immune response, and/or induces a less severe immune response, as compared to the non-human species antibody, when it is administered to a human subject. In one embodiment, certain amino acids in the framework and constant domains of the heavy and/or light chains of the non-human species antibody are mutated to produce the humanized antibody. In another embodiment, the constant domain(s) from a human antibody are fused to the variable domain(s) of a non-human species. In another embodiment, one or more amino acid residues in one or more CDR sequences of a non-human antibody are changed to reduce the likely immunogenicity of the non-human antibody when it is administered to a human subject, wherein the changed amino acid residues either are not critical for immunospecific binding of the antibody to its antigen, or the changes to the amino acid sequence that are made are conservative changes, such that the binding of the humanized antibody to the antigen is not significantly worse than the binding of the non-human antibody to the antigen. Examples of how to make humanized antibodies may be found in U.S. Pat. Nos. 6,054,297, 5,886,152 and 5,877,293.
The term “chimeric antibody” and related terms used herein refers to an antibody that contains one or more regions from a first antibody and one or more regions from one or more other antibodies. In one embodiment, one or more of the CDRs are derived from a human antibody. In another embodiment, all of the CDRs are derived from a human antibody. In another embodiment, the CDRs from more than one human antibody are mixed and matched in a chimeric antibody. For instance, a chimeric antibody may comprise a CDR1 from the light chain of a first human antibody, a CDR2 and a CDR3 from the light chain of a second human antibody, and the CDRs from the heavy chain from a third antibody. In another example, the CDRs originate from different species such as human and mouse, or human and rabbit, or human and goat. One skilled in the art will appreciate that other combinations are possible.
Further, the framework regions may be derived from one of the same antibodies, from one or more different antibodies, such as a human antibody, or from a humanized antibody. In one example of a chimeric antibody, a portion of the heavy and/or light chain is identical with, homologous to, or derived from an antibody from a particular species or belonging to a particular antibody class or subclass, while the remainder of the chain(s) is/are identical with, homologous to, or derived from an antibody (-ies) from another species or belonging to another antibody class or subclass. Also included are fragments of such antibodies that exhibit the desired biological activity (i.e., the ability to specifically bind a target antigen). Chimeric antibodies can be prepared from portions of any of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof are described herein.
As used herein, the term “variant” polypeptides and “variants” of polypeptides refers to a polypeptide comprising an amino acid sequence with one or more amino acid residues inserted into, deleted from and/or substituted into the amino acid sequence relative to a reference polypeptide sequence. Polypeptide variants include fusion proteins. In the same manner, a variant polynucleotide comprises a nucleotide sequence with one or more nucleotides inserted into, deleted from and/or substituted into the nucleotide sequence relative to another polynucleotide sequence. Polynucleotide variants include fusion polynucleotides.
As used herein, the term “derivative” of a polypeptide is a polypeptide (e.g., an antibody) that has been chemically modified, e.g., via conjugation to another chemical moiety such as, for example, polyethylene glycol, albumin (e.g., human serum albumin), phosphorylation, and glycosylation. Unless otherwise indicated, the term “antibody” includes, in addition to antibodies comprising two full-length heavy chains and two full-length light chains, derivatives, variants, fragments, and muteins thereof, examples of which are described below.
The term “Fc” or “Fc region” as used herein refers to the portion of an antibody heavy chain constant region beginning in or after the hinge region and ending at the C-terminus of the heavy chain. The Fc region comprises at least a portion of the CH and CH3 regions, and may or may not include a portion of the hinge region. Two polypeptide chains each carrying a half Fc region can dimerize to form an Fc region. An Fc region can bind Fc cell surface receptors and some proteins of the immune complement system. An Fc region exhibits effector function, including any one or any combination of two or more activities including complement-dependent cytotoxicity (CDC), antibody-dependent cell-mediated cytotoxicity (ADCC), antibody-dependent phagocytosis (ADP), opsonization and/or cell binding. An Fc region can bind an Fc receptor, including FcyRI (e.g., CD64), FcyRII (e.g., CD32) and/or FcyRIII (e.g., CD16a).
The term “labeled antibody” or related terms as used herein refers to antibodies and their antigen binding portions thereof that are unlabeled or joined to a detectable label or moiety for detection, wherein the detectable label or moiety is radioactive, colorimetric, antigenic, enzymatic, a detectable bead (such as a magnetic or electrodense (e.g., gold) bead), biotin, streptavidin or protein A. A variety of labels can be employed, including, but not limited to, radionuclides, fluorescers, enzymes, enzyme substrates, enzyme cofactors, enzyme inhibitors and ligands (e.g., biotin, haptens). Any of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that described herein can be unlabeled or can be joined to a detectable label or moiety.
The “percent identity” or “percent homology” and related terms used herein refers to a quantitative measurement of the similarity between two polypeptide or between two polynucleotide sequences. The percent identity between two polypeptide sequences is a function of the number of identical amino acids at aligned positions that are shared between the two polypeptide sequences, taking into account the number of gaps, and the length of each gap, which may need to be introduced to optimize alignment of the two polypeptide sequences. In a similar manner, the percent identity between two polynucleotide sequences is a function of the number of identical nucleotides at aligned positions that are shared between the two polynucleotide sequences, taking into account the number of gaps, and the length of each gap, which may need to be introduced to optimize alignment of the two polynucleotide sequences. A comparison of the sequences and determination of the percent identity between two polypeptide sequences, or between two polynucleotide sequences, may be accomplished using a mathematical algorithm. For example, the “percent identity” or “percent homology” of two polypeptide or two polynucleotide sequences may be determined by comparing the sequences using the GAP computer program (a part of the GCG Wisconsin Package, version 10.3 (Accelrys, San Diego, Calif.)) using its default parameters. Expressions such as “comprises a sequence with at least X% identity to Y” with respect to a test sequence mean that, when aligned to sequence Y as described above, the test sequence comprises residues identical to at least X% of the residues of Y.
In one embodiment, the amino acid sequence of a test antibody may be similar but not identical to any of the amino acid sequences of the polypeptides that make up the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that are described herein. The similarities between the test antibody and the polypeptides can be at least 95%, or at or at least 96% identical, or at least 97% identical, or at least 98% identical, or at least 99% identical, to any of the polypeptides that make up the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that are described herein. In one embodiment, similar polypeptides can contain amino acid substitutions within a heavy and/or light chain. In one embodiment, the amino acid substitutions comprise one or more conservative amino acid substitutions. A “conservative amino acid substitution” is one in which an amino acid residue is substituted by another amino acid residue having a side chain (R group) with similar chemical properties (e.g., charge or hydrophobicity). In general, a conservative amino acid substitution will not substantially change the functional properties of a protein. In cases where two or more amino acid sequences differ from each other by conservative substitutions, the percent sequence identity or degree of similarity may be adjusted upwards to correct for the conservative nature of the substitution. Means for making this adjustment are well-known to those of skill in the art. See, e.g., Pearson (1994) Methods Mol. Biol. 24: 307-331, herein incorporated by reference in its entirety. Examples of groups of amino acids that have side chains with similar chemical properties include (1) aliphatic side chains: glycine, alanine, valine, leucine and isoleucine; (2) aliphatic-hydroxyl side chains: serine and threonine; (3) amide-containing side chains: asparagine and glutamine; (4) aromatic side chains: phenylalanine, tyrosine, and tryptophan; (5) basic side chains: lysine, arginine, and histidine; (6) acidic side chains: aspartate and glutamate, and (7) sulfur-containing side chains are cysteine and methionine.
Antibodies can be obtained from sources such as serum or plasma that contain immunoglobulins having varied antigenic specificity. If such antibodies are subjected to affinity purification, they can be enriched for a particular antigenic specificity. Such enriched preparations of antibodies usually are made of less than about 10% antibody having specific binding activity for the particular antigen. Subjecting these preparations to several rounds of affinity purification can increase the proportion of antibody having specific binding activity for the antigen. Antibodies prepared in this manner are often referred to as “monospecific.” Monospecific antibody preparations can be made up of about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 75%, 80%, 85%, 90%, 95%, 97%, 99%, or 99.9% antibody having specific binding activity for the particular antigen. Antibodies can be produced using recombinant nucleic acid technology as described below.
A “vector” and related terms used herein refers to a nucleic acid molecule (e.g., DNA or RNA) which can be operably linked to foreign genetic material (e.g., nucleic acid transgene). Vectors can be used as a vehicle to introduce foreign genetic material into a cell (e.g., host cell). Vectors can include at least one restriction endonuclease recognition sequence for insertion of the transgene into the vector. Vectors can include at least one gene sequence that confers antibiotic resistance or a selectable characteristic to aid in selection of host cells that harbor a vector-transgene construct. Vectors can be single-stranded or double-stranded nucleic acid molecules. Vectors can be linear or circular nucleic acid molecules. A donor nucleic acid used for gene editing methods employing zinc finger nuclease, TALEN or CRISPR/Cas can be a type of a vector. One type of vector is a “plasmid,” which refers to a linear or circular double stranded extrachromosomal DNA molecule which can be linked to a transgene, and is capable of replicating in a host cell, and transcribing and/or translating the transgene. A viral vector typically contains viral RNA or DNA backbone sequences which can be linked to the transgene. The viral backbone sequences can be modified to disable infection but retain insertion of the viral backbone and the co-linked transgene into a host cell genome. Examples of viral vectors include retroviral, lentiviral, adenoviral, adeno-associated, baculoviral, papovaviral, vaccinia viral, herpes simplex viral and Epstein Barr viral vectors. Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e.g., bacterial vectors comprising a bacterial origin of replication and episomal mammalian vectors). Other vectors (e.g., non-episomal mammalian vectors) are integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome.
An “expression vector” is a type of vector that can contain one or more regulatory sequences, such as inducible and/or constitutive promoters and enhancers. Expression vectors can include ribosomal binding sites and/or polyadenylation sites. Expression vectors can include one or more origin of replication sequence. Regulatory sequences direct transcription, or transcription and translation, of a transgene linked to the expression vector which is transduced into a host cell. The regulatory sequence(s) can control the level, timing and/or location of expression of the transgene. The regulatory sequence can, for example, exert its effects directly on the transgene, or through the action of one or more other molecules (e.g., polypeptides that bind to the regulatory sequence and/or the nucleic acid). Regulatory sequences can be part of a vector. Further examples of regulatory sequences are described in, for example, Goeddel, 1990, Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. and Baron et al., 1995, Nucleic Acids Res. 23:3605-3606. An expression vector can comprise nucleic acids that encode at least a portion of any of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that are described herein.
A transgene is “operably linked” to a vector when there is linkage between the transgene and the vector to permit functioning or expression of the transgene sequences contained in the vector. In one embodiment, a transgene is “operably linked” to a regulatory sequence when the regulatory sequence affects the expression (e.g., the level, timing, or location of expression) of the transgene.
The terms “transfected” or “transformed” or “transduced” or other related terms used herein refer to a process by which exogenous nucleic acid (e.g., transgene) is transferred or introduced into a host cell. A “transfected” or “transformed” or “transduced” host cell is one which has been transfected, transformed or transduced with exogenous nucleic acid (transgene). The host cell includes the primary subject cell and its progeny. Exogenous nucleic acids encoding at least a portion of any of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that are described herein can be introduced into a host cell. Expression vectors comprising at least a portion of any of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that are described herein can be introduced into a host cell, and the host cell can express polypeptides comprising at least a portion of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that are described herein.
The terms “host cell” or “or a population of host cells” or related terms as used herein refer to a cell (or a population thereof) into which foreign (exogenous or transgene) nucleic acids have been introduced. The foreign nucleic acids can include an expression vector operably linked to a transgene, and the host cell can be used to express the nucleic acid and/or polypeptide encoded by the foreign nucleic acid (transgene). A host cell (or a population thereof) can be a cultured cell or can be extracted from a subject. The host cell (or a population thereof) includes the primary subject cell and its progeny without any regard for the number of passages. Progeny cells may or may not harbor identical genetic material compared to the parent cell. Host cells encompass progeny cells. In one embodiment, a host cell describes any cell (including its progeny) that has been modified, transfected, transduced, transformed, and/or manipulated in any way to express an antibody, as disclosed herein. In one example, the host cell (or population thereof) can be introduced with an expression vector operably linked to a nucleic acid encoding the desired antibody, or an antigen binding portion thereof, described herein. Host cells and populations thereof can harbor an expression vector that is stably integrated into the host’s genome, or can harbor an extrachromosomal expression vector. In one embodiment, host cells and populations thereof can harbor an extrachromosomal vector that is present after several cell divisions or is present transiently and is lost after several cell divisions.
Transgenic host cells can be prepared using non-viral methods, including well-known designer nucleases including zinc finger nucleases, TALENS or CRISPR/Cas. A transgene can be introduced into a host cell’s genome using genome editing technologies such as zinc finger nuclease. A zinc finger nuclease includes a pair of chimeric proteins each containing a non-specific endonuclease domain of a restriction endonuclease (e.g., FokI) fused to a DNA-binding domain from an engineered zinc finger motif. The DNA-binding domain can be engineered to bind a specific sequence in the host’s genome and the endonuclease domain makes a double-stranded cut. The donor DNA carries the transgene, for example any of the nucleic acids encoding a CAR or DAR construct described herein, and flanking sequences that are homologous to the regions on either side of the intended insertion site in the host cell’s genome. The host cell’s DNA repair machinery enables precise insertion of the transgene by homologous DNA repair. Transgenic mammalian host cells have been prepared using zinc finger nucleases (U.S. patent Nos. 9,597,357, 9,616,090, 9,816,074 and 8,945,868). A transgenic host cell can be prepared using TALEN (Transcription Activator-Like Effector Nucleases) which are similar to zinc finger nucleases in that they include a non-specific endonuclease domain fused to a DNA-binding domain which can deliver precise transgene insertion. Like zinc finger nucleases, TALEN also introduce a double-strand cut into the host’s DNA. Transgenic host cells can be prepared using CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats). CRISPR employs a Cas endonuclease coupled to a guide RNA for target specific donor DNA integration. The guide RNA includes a conserved multi-nucleotide containing protospacer adjacent motif (PAM) sequence upstream of the gRNA-binding region in the target DNA and hybridizes to the host cell target site where the Cas endonuclease cleaves the double-stranded target DNA. The guide RNA can be designed to hybridize to a specific target site. Similar to zinc finger nuclease and TALEN, the CRISPR/Cas system can be used to introduce site specific insertion of donor DNA having flanking sequences that have homology to the insertion site. Examples of CRISPR/Cas systems used to modify genomes are described for example in U.S. Pat. Nos. 8,697,359, 10,000,772, 9,790,490, and U. S. Pat. Application Publication No. US 2018/0346927. In one embodiment, transgenic host cells can be prepared using zinc finger nuclease, TALEN or CRISPR/Cas system, and the host target site can be a TRAC gene (T Cell Receptor Alpha Constant). The donor DNA can include for example any of the nucleic acids encoding a CAR or DAR construct described herein. Electroporation, nucleofection or lipofection can be used to co-deliver into the host cell the donor DNA with the zinc finger nuclease, TALEN or CRISPR/Cas system.
A host cell can be a prokaryote, for example, E. coli, or it can be a eukaryote, for example, a single-celled eukaryote (e.g., a yeast or other fungus), a plant cell (e.g., a tobacco or tomato plant cell), an mammalian cell (e.g., a human cell, a monkey cell, a hamster cell, a rat cell, a mouse cell, or an insect cell) or a hybridoma. In one embodiment, a host cell can be introduced with an expression vector operably linked to a nucleic acid encoding a desired antibody thereby generating a transfected/transformed host cell which is cultured under conditions suitable for expression of the antibody by the transfected/transformed host cell, and optionally recovering the antibody from the transfected/transformed host cells (e.g., recovery from host cell lysate) or recovery from the culture medium. In one embodiment, host cells comprise non-human cells including CHO, BHK, NS0, SP2/0, and YB2/0. In one embodiment, host cells comprise human cells including HEK293, HT-1080, Huh-7 and PER.C6. Examples of host cells include the COS-7 line of monkey kidney cells (ATCC CRL 1651) (see Gluzman et al., 1981, Cell 23: 175), L cells, C127 cells, 3T3 cells (ATCC CCL 163), Chinese hamster ovary (CHO) cells or their derivatives such as Veggie CHO and related cell lines which grow in serum- free media (see Rasmussen et al., 1998, Cytotechnology 28:31) or CHO strain DX-B 11, which is deficient in DHFR (see Urlaub et al., 1980, Proc. Natl. Acad. Sci. USA 77:4216-20), HeLa cells, BHK (ATCC CRL 10) cell lines, the CV⅟EBNA cell line derived from the African green monkey kidney cell line CV1 (ATCC CCL 70) (see McMahan et al., 1991, EMBO J. 10:2821), human embryonic kidney cells such as 293, 293 EBNA or MSR 293, human epidermal A431 cells, human Colo 205 cells, other transformed primate cell lines, normal diploid cells, cell strains derived from in vitro culture of primary tissue, primary explants, HL-60, U937, HaK or Jurkat cells. In one embodiment, host cells include lymphoid cells such as Y0, NS0 or Sp20. In one embodiment, a host cell is a mammalian host cell, but is not a human host cell. Typically, a host cell is a cultured cell that can be transformed or transfected with a polypeptide-encoding nucleic acid, which can then be expressed in the host cell. The phrase “transgenic host cell” or “recombinant host cell” can be used to denote a host cell that has been transformed or transfected with a nucleic acid to be expressed. A host cell also can be a cell that comprises the nucleic acid but does not express it at a desired level unless a regulatory sequence is introduced into the host cell such that it becomes operably linked with the nucleic acid. It is understood that the term host cell refers not only to the particular subject cell but also to the progeny or potential progeny of such a cell. Because certain modifications may occur in succeeding generations due to, e.g., mutation or environmental influence, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope of the term as used herein. A host cell, or a population of host cells, harboring a vector (e.g., an expression vector) operably linked to at least one nucleic acid encoding one or more activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof are described herein.
Polypeptides of the present disclosure (e.g., antibodies and antigen binding proteins) can be produced using any method known in the art. In one example, the polypeptides are produced by recombinant nucleic acid methods by inserting a nucleic acid sequence (e.g., DNA) encoding the polypeptide into a recombinant expression vector which is introduced into a host cell and expressed by the host cell under conditions promoting expression.
General techniques for recombinant nucleic acid manipulations are described for example in Sambrook et al., in Molecular Cloning: A Laboratory Manual, Vols. 1-3, Cold Spring Harbor Laboratory Press, 2 ed., 1989, or F. Ausubel et al., in Current Protocols in Molecular Biology (Green Publishing and Wiley-Interscience: New York, 1987) and periodic updates, herein incorporated by reference in their entireties. The nucleic acid (e.g., DNA) encoding the polypeptide is operably linked to an expression vector carrying one or more suitable transcriptional or translational regulatory elements derived from mammalian, viral, or insect genes. Such regulatory elements include a transcriptional promoter, an optional operator sequence to control transcription, a sequence encoding suitable mRNA ribosomal binding sites, and sequences that control the termination of transcription and translation. The expression vector can include an origin or replication that confers replication capabilities in the host cell. The expression vector can include a gene that confers selection to facilitate recognition of transgenic host cells (e.g., transformants).
The recombinant DNA can also encode any type of protein tag sequence that may be useful for purifying the protein. Examples of protein tags include but are not limited to a histidine tag, a FLAG tag, a myc tag, an HA tag, or a GST tag. Appropriate cloning and expression vectors for use with bacterial, fungal, yeast, and mammalian cellular hosts can be found in Cloning Vectors: A Laboratory Manual, (Elsevier, N.Y., 1985).
The expression vector construct can be introduced into the host cell using a method appropriate for the host cell. A variety of methods for introducing nucleic acids into host cells are known in the art, including, but not limited to, electroporation; transfection employing calcium chloride, rubidium chloride, calcium phosphate, DEAE-dextran, or other substances; viral transfection; non-viral transfection; microprojectile bombardment; lipofection; and infection (e.g., where the vector is an infectious agent). Suitable host cells include prokaryotes, yeast, mammalian cells, or bacterial cells.
Suitable bacteria include gram negative or gram positive organisms, for example, E. coli or Bacillus spp. Yeast, preferably from the Saccharomyces species, such as S. cerevisiae, may also be used for production of polypeptides. Various mammalian or insect cell culture systems can also be employed to express recombinant proteins. Baculovirus systems for production of heterologous proteins in insect cells are reviewed by Luckow and Summers, (Bio/Technology, 6:47, 1988). Examples of suitable mammalian host cell lines include endothelial cells, COS-7 monkey kidney cells, CV-1, L cells, C127, 3T3, Chinese hamster ovary (CHO), human embryonic kidney cells, HeLa, 293, 293T, and BHK cell lines. Purified polypeptides are prepared by culturing suitable host/vector systems to express the recombinant proteins. For many applications, the small size of many of the polypeptides disclosed herein would make expression in E. coli as the preferred method for expression. The protein is then purified from culture media or cell extracts. Any of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof, can be expressed by transgenic host cells.
Antibodies and antigen binding proteins disclosed herein can also be produced using cell-translation systems. For such purposes the nucleic acids encoding the polypeptide must be modified to allow in vitro transcription to produce mRNA and to allow cell-free translation of the mRNA in the particular cell-free system being utilized (eukaryotic such as a mammalian or yeast cell-free translation system or prokaryotic such as a bacterial cell-free translation system.
Nucleic acids encoding any of the various polypeptides disclosed herein may be synthesized chemically. Codon usage may be selected so as to improve expression in a cell. Such codon usage will depend on the cell type selected. Specialized codon usage patterns have been developed for E. coli and other bacteria, as well as mammalian cells, plant cells, yeast cells and insect cells. See for example: Mayfield et al., Proc. Natl. Acad. Sci. USA. 2003 100(2):438-42; Sinclair et al. Protein Expr. Purif. 2002 (1):96-105; Connell N D. Curr. Opin. Biotechnol. 2001 12(5):446-9; Makrides et al. Microbiol. Rev. 1996 60(3):512-38; and Sharp et al. Yeast. 1991 7(7):657-78.
Antibodies and antigen binding proteins described herein can also be produced by chemical synthesis (e.g., by the methods described in Solid Phase Peptide Synthesis, 2nd ed., 1984, The Pierce Chemical Co., Rockford, Ill.). Modifications to the protein can also be produced by chemical synthesis.
Antibodies and antigen binding proteins described herein can be purified by isolation/purification methods for proteins generally known in the field of protein chemistry. Non-limiting examples include extraction, recrystallization, salting out (e.g., with ammonium sulfate or sodium sulfate), centrifugation, dialysis, ultrafiltration, adsorption chromatography, ion exchange chromatography, hydrophobic chromatography, normal phase chromatography, reversed-phase chromatography, gel filtration, gel permeation chromatography, affinity chromatography, electrophoresis, countercurrent distribution or any combinations of these. After purification, polypeptides may be exchanged into different buffers and/or concentrated by any of a variety of methods known to the art, including, but not limited to, filtration and dialysis.
The purified antibodies and antigen binding proteins described herein are preferably at least 65% pure, at least 75 % pure, at least 85% pure, more preferably at least 95% pure, and most preferably at least 98% pure. Regardless of the exact numerical value of the purity, the polypeptide is sufficiently pure for use as a pharmaceutical product. Any of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that are described herein can be expressed by transgenic host cells and then purified to about 65-98% purity or high level of purity using any art-known method.
In certain embodiments, the antibodies and antigen binding proteins herein can further comprise post-translational modifications. Exemplary post-translational protein modifications include phosphorylation, acetylation, methylation, ADP-ribosylation, ubiquitination, glycosylation, carbonylation, sumoylation, biotinylation or addition of a polypeptide side chain or of a hydrophobic group. As a result, the modified polypeptides may contain non-amino acid elements, such as lipids, poly- or mono-saccharide, and phosphates. A preferred form of glycosylation is sialylation, which conjugates one or more sialic acid moieties to the polypeptide. Sialic acid moieties improve solubility and serum half-life while also reducing the possible immunogenicity of the protein. See Raju et al. Biochemistry. 2001 31; 40(30):8868-76.
In one embodiment, the antibodies and antigen binding proteins described herein can be modified to become soluble polypeptides which comprises linking the Antibodies and antigen binding proteins to non-proteinaceous polymers. In one embodiment, the non-proteinaceous polymer comprises polyethylene glycol (“PEG”), polypropylene glycol, or polyoxyalkylenes, in the manner as set forth in U.S. Pat. Nos. 4,640,835; 4,496,689; 4,301,144; 4,670,417; 4,791,192 or 4,179,337.
PEG is a water soluble polymer that is commercially available or can be prepared by ring-opening polymerization of ethylene glycol according to methods well known in the art (Sandler and Karo, Polymer Synthesis, Academic Press, New York, Vol. 3, pages 138-161). The term “PEG” is used broadly to encompass any polyethylene glycol molecule, without regard to size or to modification at an end of the PEG, and can be represented by the formula: X—O(CH2CH2O)n—CH2CH2OH (1), where n is 20 to 2300 and X is H or a terminal modification, e.g., a C1-4 alkyl. In one embodiment, the PEG terminates on one end with hydroxy or methoxy, i.e., X is H or CH3 (“methoxy PEG”). A PEG can contain further chemical groups which are necessary for binding reactions; which results from the chemical synthesis of the molecule; or which is a spacer for optimal distance of parts of the molecule. In addition, such a PEG can consist of one or more PEG side-chains which are linked together. PEGs with more than one PEG chain are called multiarmed or branched PEGs. Branched PEGs can be prepared, for example, by the addition of polyethylene oxide to various polyols, including glycerol, pentaerythriol, and sorbitol. For example, a four-armed branched PEG can be prepared from pentaerythriol and ethylene oxide. Branched PEG are described in, for example, EP-A 0 473 084 and U.S. Pat. No. 5,932,462. One form of PEGs includes two PEG side-chains (PEG2) linked via the primary amino groups of a lysine (Monfardini et al., Bioconjugate Chem. 6 (1995) 62-69).
The serum clearance rate of PEG-modified polypeptide may be modulated (e.g., increased or decreased) by about 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or even 90%, relative to the clearance rate of the unmodified antibodies and antigen binding proteins binding polypeptides. The PEG-modified antibodies and antigen binding proteins may have a half-life (t½) which is enhanced relative to the half-life of the unmodified polypeptide. The half-life of PEG-modified polypeptide may be enhanced by at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, 125%, 150%, 175%, 200%, 250%, 300%, 400% or 500%, or even by 1000% relative to the half-life of the unmodified antibodies and antigen binding proteins. In one embodiment, the protein half-life is determined in vitro, such as in a buffered saline solution or in serum. In other embodiments, the protein half-life is an in vivo half-life, such as the half-life of the protein in the serum or other bodily fluid of an animal.
The present disclosure provides therapeutic compositions comprising any of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that are described herein in an admixture with a pharmaceutically-acceptable excipient. An excipient encompasses carriers, stabilizers and excipients. Excipients of pharmaceutically acceptable excipients includes for example inert diluents or fillers (e.g., sucrose and sorbitol), lubricating agents, glidants, and anti-adhesives (e.g., magnesium stearate, zinc stearate, stearic acid, silicas, hydrogenated vegetable oils, or talc). Additional examples include buffering agents, stabilizing agents, preservatives, non-ionic detergents, anti-oxidants and isotonifiers.
Therapeutic compositions and methods for preparing them are well known in the art and are found, for example, in “Remington: The Science and Practice of Pharmacy” (20th ed., ed. A. R. Gennaro A R., 2000, Lippincott Williams & Wilkins, Philadelphia, Pa.). Therapeutic compositions can be formulated for parenteral administration may, and can for example, contain excipients, sterile water, saline, polyalkylene glycols such as polyethylene glycol, oils of vegetable origin, or hydrogenated napthalenes. Biocompatible, biodegradable lactide polymer, lactide/glycolide copolymer, or polyoxyethylene-polyoxypropylene copolymers may be used to control the release of the antibody (or antigen binding protein thereof) described herein. Nanoparticulate formulations (e.g., biodegradable nanoparticles, solid lipid nanoparticles, liposomes) may be used to control the biodistribution of the antibody (or antigen binding protein thereof). Other potentially useful parenteral delivery systems include ethylenevinyl acetate copolymer particles, osmotic pumps, implantable infusion systems, and liposomes. The concentration of the antibody (or antigen binding protein thereof) in the formulation varies depending upon a number of factors, including the dosage of the drug to be administered, and the route of administration.
Any of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof described herein may be optionally administered as a pharmaceutically acceptable salt, such as non-toxic acid addition salts or metal complexes that are commonly used in the pharmaceutical industry. Examples of acid addition salts include organic acids such as acetic, lactic, pamoic, maleic, citric, malic, ascorbic, succinic, benzoic, palmitic, suberic, salicylic, tartaric, methanesulfonic, toluenesulfonic, or trifluoroacetic acids or the like; polymeric acids such as tannic acid, carboxymethyl cellulose, or the like; and inorganic acid such as hydrochloric acid, hydrobromic acid, sulfuric acid phosphoric acid, or the like. Metal complexes include zinc, iron, and the like. In one example, the antibody (or antigen binding protein thereof) is formulated in the presence of sodium acetate to increase thermal stability.
Any of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof described herein may be formulated for oral use include tablets containing the active ingredient(s) in a mixture with non-toxic pharmaceutically acceptable excipients. Formulations for oral use may also be provided as chewable tablets, or as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium.
The term “subject” as used herein refers to human and non-human animals, including vertebrates, mammals and non-mammals. In one embodiment, the subject can be human, non-human primates, simian, ape, murine (e.g., mice and rats), bovine, porcine, equine, canine, feline, caprine, lupine, ranine or piscine.
The term “administering”, “administered” and grammatical variants refers to the physical introduction of an agent to a subject, using any of the various methods and delivery systems known to those skilled in the art. Exemplary routes of administration for the formulations disclosed herein include intravenous, intramuscular, subcutaneous, intraperitoneal, spinal or other parenteral routes of administration, for example by injection or infusion. The phrase “parenteral administration” as used herein means modes of administration other than enteral and topical administration, usually by injection, and includes, without limitation, intravenous, intramuscular, intraarterial, intrathecal, intralymphatic, intralesional, intracapsular, intraorbital, intracardiac, intradermal, intraperitoneal, transtracheal, subcutaneous, subcuticular, intraarticular, subcapsular, subarachnoid, intraspinal, epidural and intrasternal injection and infusion, as well as in vivo electroporation. In one embodiment, the formulation is administered via a non-parenteral route, e.g., orally. Other non-parenteral routes include a topical, epidermal or mucosal route of administration, for example, intranasally, vaginally, rectally, sublingually or topically. Administering can also be performed, for example, once, a plurality of times, and/or over one or more extended periods. Any of the activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof described herein can be administered to a subject using art-known methods and delivery routes.
The terms “effective amount”, “therapeutically effective amount” or “effective dose” or related terms may be used interchangeably and refer to an amount of an activatable masked IgG-type antibodies and dimeric antigen receptor (DAR) having activatable masking moieties or antigen-binding portions thereof that when administered to a subject, is sufficient to effect a measurable improvement or prevention of a disease or disorder associated with tumor or cancer antigen expression. Therapeutically effective amounts of antibodies provided herein, when used alone or in combination, will vary depending upon the relative activity of the antibodies and combinations (e.g. , in inhibiting cell growth) and depending upon the subject and disease condition being treated, the weight and age and sex of the subject, the severity of the disease condition in the subject, the manner of administration and the like, which can readily be determined by one of ordinary skill in the art.
In one embodiment, a therapeutically effective amount will depend on certain aspects of the subject to be treated and the disorder to be treated and may be ascertained by one skilled in the art using known techniques. In general, the polypeptide is administered at about 0.01 g/kg to about 50 mg/kg per day, preferably 0.01 mg/kg to about 30 mg/kg per day, most preferably 0.1 mg/kg to about 20 mg/kg per day. The polypeptide may be administered daily (e.g., once, twice, three times, or four times daily) or preferably less frequently (e.g., weekly, every two weeks, every three weeks, monthly, or quarterly). In addition, as is known in the art, adjustments for age as well as the body weight, general health, sex, diet, time of administration, drug interaction, and the severity of the disease may be necessary.
The present disclosure provides methods for treating a subject having a disease associated with expression of one or more tumor-associated antigens. The disease comprises cancer or tumor cells expressing the tumor-associated antigens, such as for example EGFR or CD38 antigen. In one embodiment, the cancer or tumor includes cancer of the prostate, breast, ovary, head and neck, bladder, skin, colorectal, anus, rectum, pancreas, lung (including non-small cell lung and small cell lung cancers), leiomyoma, brain, glioma, glioblastoma, esophagus, liver, kidney, stomach, colon, cervix, uterus, endometrium, vulva, larynx, vagina, bone, nasal cavity, paranasal sinus, nasopharynx, oral cavity, oropharynx, larynx, hypolarynx, salivary glands, ureter, urethra, penis and testis.
In one embodiment, the cancer comprises hematological cancers, including leukemias, lymphomas, myelomas and B cell lymphomas. Hematologic cancers include multiple myeloma (MM), non-Hodgkin’s lymphoma (NHL) including Burkitt’s lymphoma (BL), B chronic lymphocytic leukemia (B-CLL), systemic lupus erythematosus (SLE), B and T acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), diffuse large B cell lymphoma, chronic myelogenous leukemia (CML), hairy cell leukemia (HCL), follicular lymphoma, Waldenstrom’s Macroglobulinemia, mantle cell lymphoma, Hodgkin’s Lymphoma (HL), plasma cell myeloma, precursor B cell lymphoblastic leukemia/lymphoma, plasmacytoma, giant cell myeloma, plasma cell myeloma, heavy-chain myeloma, light chain or Bence-Jones myeloma, lymphomatoid granulomatosis, post-transplant lymphoproliferative disorder, an immunoregulatory disorder, rheumatoid arthritis, myasthenia gravis, idiopathic thrombocytopenia purpura, anti-phospholipid syndrome, Chagas’ disease, Grave’s disease, Wegener’s granulomatosis, poly-arteritis nodosa, Sjogren’s syndrome, pemphigus vulgaris, scleroderma, multiple sclerosis, anti-phospholipid syndrome, ANCA associated vasculitis, Goodpasture’s disease, Kawasaki disease, autoimmune hemolytic anemia, and rapidly progressive glomerulonephritis, heavy-chain disease, primary or immunocyte-associated amyloidosis, and monoclonal gammopathy of undetermined significance.
The term “in-tandem.” as used herein with respect to regions in a polypeptide chain or a protein complex, such as Fab regions, means that the regions are arranged head-to-tail without an intervening different region (e.g., Fc region) between the Fab regions. The in-tandem Fab regions may be separated by a linker. The exemplary structure illustrated in
The term “non-tandem” as used herein with respect to regions in a polypeptide chain or a protein complex, such as Fab regions, means that the regions are not in an “in-tandem” arrangement. The exemplary structure illustrated in
The present disclosure provides activatable masked antigen binding proteins comprising at least a first antigen binding domain which comprises a first heavy chain variable region and a first light chain variable region, wherein (i) the first heavy chain variable region is j oined to a first masking moiety via a first peptide linker, and (ii) the first light chain variable region is joined to a second masking moiety via a second peptide linker, and (iii) the first and second masking moieties associate with each other to form a first dimerized masking complex without covalent bonding, and (iv) the individual first and second masking moieties do not specifically bind the first antigen binding domain, and (v) the first dimerized masking complex does not specifically bind the first antigen binding domain. In one embodiment, the first and second masking moieties associate with each other to reduce the first antigen binding domain from binding to its target antigen. In one embodiment, the first peptide linker includes a first cleavable site. In one embodiment, the second peptide linker includes a second cleavable site.
In one embodiment, the activatable masked antigen binding proteins further comprises a second antigen binding domain which comprises a second heavy chain variable region and a second light chain variable region, wherein (i) the second heavy chain variable region is joined to a third masking moiety via a third peptide linker, and (ii) the second light chain variable region is joined to a fourth masking moiety via a fourth peptide linker, and (iii) the third and fourth masking moieties associate with each other to form a second dimerized masking complex without covalent bonding, and (iv) the individual third and fourth masking moieties do not specifically bind the second antigen binding domain, and (v) the second dimerized masking complex does not specifically bind the second antigen binding domain. In one embodiment, the third and fourth masking moieties associate with each other to reduce the second antigen binding domain from binding to its target antigen which may be the same or different target antigen compared to the target antigen bound by the first antigen binding domain. In one embodiment, the third peptide linker includes a third cleavable site. In one embodiment, the fourth peptide linker includes a fourth cleavable site.
In one embodiment, the first, second, third and/or fourth cleavable sites are cleavable with a cleaving condition which includes a protease, esterase, reductive condition, or oxidative condition. In one embodiment, the first, second, third and/or fourth cleavable sites are cleavable with the same or different cleaving condition. In one embodiment, the first, second third and/or fourth cleavable sites are cleavable with a protease that is present in a tumor microenvironment or are cleavable with a reductive or oxidative condition that is present in a tumor microenvironment. In one embodiment, the first, second, third and/or fourth cleavable sites are cleavable with the same or different proteases.
In one embodiment, the activatable masked antigen binding protein is joined to a toxin by a chemical linker thereby forming an immunoconjugate. In one embodiment, the toxin is joined to the chemical linker which in turn is j oined to a lysine residue of the activatable masked antigen binding protein by forming an amide bond with lysine side chain. In one embodiment, the lysine residue on the activatable masked antigen binding protein is selectively joined to the linker according to methods and chemical reactions described in U.S. Pat. No. 9,981,046. In one embodiment, the toxin is cytotoxic to cells and tissue. In one embodiment, the immunoconjugate can be used to deliver the toxin to a target cell or tissue (e.g., target tumor).
The present disclosure provides activatable masked antigen binding proteins comprising at least a first antigen binding domain which comprises a first heavy chain variable region and a first light chain variable region, wherein (i) the N-terminal end of the first heavy chain variable region is joined to a first masking moiety via a first peptide linker having a first cleavable site, and (ii) the N-terminal end of the first light chain variable region is joined to a second masking moiety via a second peptide linker having a second cleavable site, and (iii) the first and second masking moieties associate with each other to form a first dimerized masking complex without disulfide bonding, and (iv) the first and second masking moieties do not specifically bind the at least first antigen binding domain, and (v) the first dimerized masking complex does not specifically bind the at least first antigen binding domain, and (vi) the first cleavable site is cleavable with a first protease (e.g., the first protease comprises a tumor-associated protease), and (vii) the second cleavable site is cleavable with a second protease (e.g., the second protease comprises a tumor-associated protease), wherein the first and second cleavable sites are cleavable with the same or different proteases. In one embodiment, the first and second masking moieties associate with each other to reduce the capability of the first antigen binding domain from binding to its target antigen. In one embodiment, a first recombinant polypeptide comprises the first heavy chain variable region joined to the first peptide linker which is joined to the first masking moiety. In one embodiment, a second recombinant polypeptide comprises the first light chain variable region joined to the second peptide linker which is joined to the second masking moiety.
In one embodiment, the activatable masked antigen binding proteins further comprise a second antigen binding domain which comprises a second heavy chain variable region and a second light chain variable region, wherein (i) the N-terminal end of the second heavy chain variable region is joined to a third masking moiety via a third peptide linker having a third cleavable site, and (ii) the N-terminal end of the second light chain variable region is joined to a fourth masking moiety via a fourth peptide linker having a fourth cleavable site, and (iii) the third and fourth masking moieties associate with each other to form a second dimerized masking complex without disulfide bonding, and (iv) the third and fourth masking moieties do not specifically bind the second antigen binding domain, and (v) the second dimerized masking complex does not specifically bind the second antigen binding domain, and (vi) the third cleavable site is cleavable with a third protease (e.g., the third protease comprises a tumor-associated protease), and (vii) the fourth cleavable site is cleavable with a fourth protease (e.g., the fourth protease comprises a tumor-associated protease), wherein the third and fourth cleavable sites are cleavable with the same or different proteases. In one embodiment, the third and fourth masking moieties associates with each other to reduce the capability of the second antigen binding domain from binding to its target antigen. In one embodiment, a third recombinant polypeptide comprises the second heavy chain variable region joined to the third peptide linker which is joined to the third masking moiety. In one embodiment, a fourth recombinant polypeptide comprises the second light chain variable region joined to the fourth peptide linker which is joined to the fourth masking moiety.
In one embodiment, the activatable masked antigen binding protein comprises an IgG class antibody (e.g.,
In one embodiment, the activatable masked antigen binding protein is joined to a toxin by a chemical linker thereby forming an immunoconjugate. In one embodiment, the toxin is joined to the chemical linker which in turn is joined to a lysine residue of the activatable masked antigen binding protein by forming an amide bond with lysine side chain. In one embodiment, the lysine residue on the activatable masked antigen binding protein is selectively joined to the linker according to methods and chemical reactions described in U.S. Pat. No. 9,981,046. In one embodiment, the toxin is cytotoxic to cells and tissue. In one embodiment, the immunoconjugate can be used to deliver the toxin to a target cell or tissue (e.g., target tumor).
The present disclosure provides activatable masked antigen binding proteins comprising an IgG type antibody having (a) a first antigen binding domain which comprises a first heavy chain variable region and a first light chain variable region and (b) a second antigen binding domain which comprises a second heavy chain variable region and a second light chain variable region, wherein (i) the N-terminal end of the first heavy chain variable region is joined to a first masking moiety via a first peptide linker having a first cleavable site, (ii) the N-terminal end of the first light chain variable region is joined to a second masking moiety via a second peptide linker having a second cleavable site, (iii) the first and second masking moieties associate with each other without disulfide bonding, (iv) the first and second masking moieties do not specifically bind the first antigen binding domain, (v) the first cleavable site is cleavable with a first protease, and (vi) the second cleavable site is cleavable with a second protease, and wherein in the activatable masked antigen binding proteins further comprise an IgG type antibody having (vii) the N-terminal end of the second heavy chain variable region is joined to a third masking moiety via a third peptide linker having a third cleavable site, (viii) the N-terminal end of the second light chain variable region is joined to a fourth masking moiety via a fourth peptide linker having a fourth cleavable site, (ix) the third and fourth masking moieties associate with each other without disulfide bonding, (x) the third and fourth masking moieties do not specifically bind the second antigen binding domain, (xi) the third cleavable site is cleavable with a third protease, and (xii) the fourth cleavable site is cleavable with a fourth protease, wherein the first, second, third and fourth cleavable sites are cleavable with the same or different proteases.
In one embodiment, the activatable masked antigen binding protein comprises an IgG class antibody (e.g.,
In one embodiment, the C-terminal end of the first and third masking moiety is joined to the N-terminal end of the first and third peptide linkers, respectively. In one embodiment, the C-terminal end of the first and third peptide linkers are joined to the N-terminal end of the first and second heavy chain variable region, respectively.
In one embodiment, the C-terminal end of the second and fourth masking moiety is joined to the N-terminal end of the second and fourth peptide linkers, respectively. In one embodiment, the C-terminal end of the second and fourth peptide linkers are joined to the N-terminal end of the first and second light chain variable region, respectively.
In one embodiment, the activatable masked antigen binding proteins comprising an IgG type antibody can bind a target antigen (e.g., monospecific antibody) or can bind two different target antigens (e.g., bispecific antibody).
In one embodiment, the first and second masking moieties associates with each other to reduce the first antigen binding domain from binding to its target antigen. In one embodiment, the third and fourth masking moieties associates with each other to reduce the second antigen binding domain from binding to its target antigen.
In one embodiment, the first, second, third and/or fourth protease(s) is/are produced by the same tumor or by different tumors.
In one embodiment, the activatable masked antigen binding protein is joined to a toxin by a chemical linker.
The present disclosure provides activatable masked antigen binding proteins comprising an IgG type antibody and at least a first and second masking moiety. In one embodiment, the first and second masking moieties, and/or the third and fourth masking moieties, when associated (dimerized) with each other, interfere (obstruct) with the ability of the antigen binding protein to bind its target antigen. The first and second masking moieties, and/or the third and fourth masking moieties, when associated (dimerized) with each other, can block binding between the antigen binding protein and its target antigen by steric hinderance.
In one embodiment, the first and second masking moieties, and/or the third and fourth masking moieties, comprise polypeptides that associate (dimerize) with each other without forming a covalent bond (e.g., no disulfide or transglutamination bonding). The first and second masking moieties, and/or the third and fourth masking moieties, comprise polypeptides that can associate (dimerize) with each other by non-covalent interaction, including ionic interaction, hydrogen bonding, dipole-dipole interaction, hydrophilic interaction, hydrophobic interaction, affinity bonding, or bonds or associations involving van der Waals forces.
In one embodiment, the first and second masking moieties (paired first and second masking moieties), or the third and fourth masking moieties (paired third and fourth masking moieties), associate with each other as a homodimer or heterodimer.
In one embodiment, one of the masking moieties can be engineered to have a knob structure that forms an interchain steric complementarity structure to favor homo-dimerization or hetero-dimerization with another masking moiety which is engineered to have a hole structure.
The present disclosure provides activatable masked antigen binding proteins, wherein one or both of the masking moieties in a dimerized configuration includes one or more mutations that create a new interchain salt bridge. In one embodiment, a threonine residue in one masking moiety can be replaced with glutamic acid, and an asparagine at a corresponding position in another masking moiety is replaced with lysine, thereby creating an interchain salt bridge.
In one embodiment, the first, second, third and/or fourth masking moieties are derived from an immunoglobulin heavy chain constant region, for example from a mu, delta, gamma, alpha, or epsilon heavy chain. In one embodiment, the first, second, third and/or fourth masking moieties are derived from a gamma immunoglobulin constant region (e.g., CL, CH1, CH2 or CH3).
In one embodiment, die first or second, or third or fourth, masking moiety comprises a heavy chain constant region (CH1). In one embodiment, the second or first, or fourth or third, masking moiety comprises a kappa or lambda light chain constant region (CL kappa or CL lambda). In one embodiment, the first masking moiety comprises a heavy chain constant region (CH1) and the second masking moiety comprises a kappa or lambda light chain constant region (CL kappa or CL lambda). In one embodiment, the first masking moiety comprises a kappa or lambda light chain constant region (CL kappa or CL lambda) and the second masking moiety comprises a heavy chain constant region (CH1), In one embodiment, the third masking moiety comprises a heavy chain constant region (CH1) and the fourth masking moiety comprises a kappa or lambda light chain constant region (CL kappa or CL lambda). In one embodiment, the third masking moiety comprises a kappa or lambda light chain constant region (CL kappa or CL lambda) and the fourth masking moiety comprises a heavy chain constant region (CH1). In one embodiment, the first, second, third and/or fourth masking moiety comprises a CH1, CL (kappa) or CL (lambda) having the amino acid sequence of SEQ ID NO:21, 22 or 23. See also Tables 1 and 2 for a list of amino acid sequences of various masking moieties.
In one embodiment, the first or second, or third or fourth, masking moiety comprises an IgG1 or IgG4 gamma heavy chain constant region, for example CH3. In one embodiment, the first and second masking moieties comprise an IgG1 or IgG4 gamma heavy chain constant region CH3. In one embodiment, the third and fourth masking moieties comprise an IgG1 or IgG4 gamma heavy chain constant region CH3. In one embodiment, one of the masking moieties which comprises an IgG1 or IgG4 gamma heavy chain constant region CH3 is engineered to have a knob or hole structure that forms an interchain steric complementarity structure to favor dimerization (e.g., homo-dimerization) with another masking moiety which comprises an IgG1 or IgG4 gamma heavy chain constant region CH3 which is engineered to have hole or knob structure. In one embodiment, the first, second, third and/or fourth masking moiety comprises a CH3 (IgG1 or IgG4) having the amino acid sequence of SEQ ID NO:24, 25, 30 or 31. See also Tables 1 and 2 for a list of amino acid sequences of various masking moieties.
In one embodiment, at least one of the masking moieties is derived from an immunoglobulin heavy chain constant region and is joined to the heavy chain variable region of the activatable masked antibody. In one embodiment, at least one of the masking moieties is derived from an immunoglobulin heavy chain constant region and is joined to the light chain variable region of the activatable masked antibody.
In one embodiment, the first and second, or third and fourth, masking moieties are derived from T cell receptors alpha (α) and beta (β) constant regions In one embodiment, the first masking moiety comprises a T cell receptor alpha (α) constant regions and the second masking moiety comprises a T cell receptor beta (β) constant region. In one embodiment, the first masking moiety comprises a T cell receptor beta (β) constant regions and the second masking moiety comprises a T cell receptor alpha (α) constant region. In one embodiment, the third masking moiety comprises a T cell receptor alpha (α) constant regions and the fourth masking moiety comprises a T cell receptor beta (β) constant region. In one embodiment, the third masking moiety comprises a T cell receptor beta (β) constant regions and the fourth masking moiety comprises a T cell receptor alpha (α) constant region.
In one embodiment, at least one of the masking moieties is derived from a T cell receptor alpha (α) or beta (β) constant region and is joined to the heavy chain variable region of the activatable masked antibody. In one embodiment, at least one of the masking moieties is derived from a T cell receptor beta (β) or alpha (α) constant region and is joined to the light chain variable region of the activatable masked antibody. In one embodiment, the first, second, third and/or fourth masking moiety comprises a T cell receptor alpha (α) or beta (β) constant region having the amino acid sequence of SEQ ID NO:28 or 29. See Tables 1 and 2 for a list of amino acid sequences of various masking moieties.
In one embodiment, the first, second, third or fourth masking moiety comprises a variable heavy chain domain from a catalytic antibody (e.g., 38C2). In one embodiment, the first, second, third or fourth masking moiety comprises a variable light chain domain from a catalytic antibody (e.g., 38C2). In one embodiment, the first masking moiety comprises a variable heavy chain domain from 38C2 antibody and the second masking moiety comprise a variable light chain domain from 38C2 antibody. In one embodiment, the first masking moiety comprises a variable light chain domain from 38C2 antibody and the second masking moiety comprise a variable heavy chain domain from 38C2 antibody. In one embodiment, the third masking moiety comprises a variable heavy chain domain from 38C2 antibody and the fourth masking moiety comprise a variable light chain domain from 38C2 antibody. In one embodiment, the third masking moiety comprises a variable light chain domain from 38C2 antibody and the fourth masking moiety comprise a variable heavy chain domain from 38C2 antibody. In one embodiment, the first, second, third and/or fourth masking moiety comprises a variable heavy chain domain from a catalytic antibody (e.g., 38C2) having the amino acid sequence of SEQ ID NO:26 or 27. See Tables 1 and 2 for a list of amino acid sequences of various masking moieties.
In one embodiment, a masking moiety (e.g., first, second, third or fourth masking moiety) comprises two or more copies of a moiety arranged in-tandem along the same polypeptide chain. For example, a masking moiety comprises two antibody CH3 regions arranged in-tandem, or two antibody CH2 regions arranged in-tandem, or two antibody CH1 regions arranged in-tandem, or two antibody CL regions arranged in-tandem. Any of the CH3, CH2, CH1 or CL regions can include a knob or hole structure. For example, the masking moiety comprises two TCR alpha chain constant region arranged in-tandem, or two TCR beta chain constant region arranged in-tandem.
In one embodiment, a masking moiety (e.g., first, second, third or fourth masking moiety) comprises two or more different moieties arranged in-tandem along the same polypeptide chain. For example, the masking moiety comprises an antibody CH2 region and an antibody CH3 region arranged in-tandem.
The present disclosure provides activatable masked antigen binding proteins comprising an IgG type antibody and at least first and second peptide linkers have the same or different lengths (e.g., 5-10, 10-20, 20-30, 30-40 or 40-50 amino acids in length). In one embodiment, the first and/or second peptide linkers are glycine-rich (e.g., GS type linkers). In one embodiment, the first and the second peptide linkers have the same amino acid sequence or different amino acid sequences.
In one embodiment, the first peptide linker is cleavable with a first protease. In one embodiment, the first peptide linker has an amino acid sequence (first cleavable site) that is a substrate for cleavage by the first protease.
In one embodiment, the second peptide linker is cleavable with a second protease. In one embodiment, the second peptide linker has an amino acid sequence (second cleavable site) that is a substrate for cleavage by the second protease.
In one embodiment, the first peptide linker is cleavable with a first protease and the second peptide linker is cleavable with a second protease. In one embodiment, the first and second peptide linkers are cleavable with the same protease. In one embodiment, the first and second peptide linkers are cleavable with different proteases. In one embodiment, the first or the second peptide linker is not cleavable with a protease.
The present disclosure provides activatable masked antigen binding proteins comprising an IgG type antibody and further comprising third and fourth peptide linkers have the same or different lengths (e.g., 10-20, 20-30, 30-40 or 40-50 amino acids in length). In one embodiment, the third and/or fourth peptide linkers are glycine-rich (e.g., GS type linkers). In one embodiment, the third and the fourth peptide linkers have the same amino acid sequence or different amino acid sequences.
In one embodiment, the third peptide linker is cleavable with a third protease. In one embodiment, the third peptide linker has an amino acid sequence that is a substrate for cleavage by the third protease.
In one embodiment, the fourth peptide linker is cleavable with a fourth protease. In one embodiment, the fourth peptide linker has an amino acid sequence that is a substrate for cleavage by the fourth protease.
In one embodiment, the third peptide linker is cleavable with a third protease and the fourth peptide linker is cleavable with a fourth protease. In one embodiment, the third and fourth peptide linkers are cleavable with the same protease. In one embodiment, the third and fourth peptide linkers are cleavable with different proteases. In one embodiment, the third or the fourth peptide linker is not cleavable with a protease.
In one embodiment, the first, second, third and/or fourth proteases can be independently selected from: a matrix metalloprotease (MMP) including MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase); a disintegrin and metalloproteinase (ADAM) protease including ADAM10, ADAM12, ADAM17; a urokinase plasminogen activator (uPA) or uPAR; a serine protease; a cysteine protease; an aspartate protease; a threonine protease; a cathepsin (e.g., cysteine or aspartic cathepsins) including cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K or cathepsin L.
In one embodiment, the first, second, third and/or fourth peptide linker comprises the amino acid sequence that is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% identical the amino acid sequences of any one of SEQ ID NOS:32-40. See also the various peptide linker sequences listed in Tables 3-9.
The present disclosure provides activatable masked antigen binding proteins comprising an IgG type antibody having at least a first antigen binding domain which comprises a first heavy chain variable region and a first light chain variable region, wherein the first antigen binding domain binds a first target antigen (e.g., specifically binds a first target antigen). In one embodiment, the activatable masked antigen binding protein can further comprise a second antigen binding domain which comprises a second heavy chain variable region and a second light chain variable region, wherein the second antigen binding domain binds a second target antigen (e.g., specifically binds a second target antigen). In one embodiment, the first and second antigen binding domains bind the same target antigen. In another embodiment, the first and second antigen binding domains bind a different target antigen.
In one embodiment, the activatable masked antigen binding protein binds EGFR. antigen (SEQ ID NO:1) or CD38 antigen (SEQ ID NO:6).
In one embodiment, the antigen binding domain comprises a heavy chain variable region comprising an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity to a portion or full-length of SEQ ID NO:2 or 4 (e.g., anti-EGFR) or to a portion or full-length of SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18 or 20 (e.g., anti-CD38), or having 100% sequence identity to a portion or full-length of SEQ ID NO:2 or 4 (e.g., anti-EGFR) or a portion or full-length of SEQ ID NO: 7, 9, 11, 13, 14, 15, 16, 17, 18 or 20 (e.g., anti-CD38).
In one embodiment, the antigen binding domain comprises a light chain variable region comprising an amino acid sequence having at least 92%, or at least 93%), or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity to a portion or full-length of SEQ ID NO:3 or 5 (anti-EGFR) or a portion or full-length of SEQ ID NO:8, 10, 12 or 19 (e.g., anti-CD38), or having 100% sequence identity to a portion or full-length of SEQ ID NO:3 or 5 (e.g., anti-EGFR) or a portion or full-length of SEQ ID NO:8, 10, 12 or 19 (e.g., anti-CD38).
The present disclosure provides activatable masked antigen binding proteins that exhibit inactive and activated states which depend upon the ability of the masking moieties to obstruct binding between the antigen binding domain and its target antigen. In one embodiment, individual masking moieties are tethered to the N-terminus of the heavy chain and light chain variable regions by intact peptide linkers, and the masking moieties form a dimerized complex which obstructs the antigen binding domain resulting in an inactive state. Cleavage of one or both peptide linkers allows the dimerized complex to move away from the obstructing position to permit binding between the antigen binding domain and its target antigen. In one embodiment, cleavage of both peptide linkers liberates the dimerized complex to migrate away from the antigen binding protein.
In one embodiment, the activatable masked antigen binding proteins comprising an IgG type antibody is inhibited from binding to its target antigen (e.g., inactive) when the first and second peptide linkers and/or the third and fourth peptide linkers are in the un-cleaved state. In one embodiment, the activatable masked antigen binding proteins exhibit reduced binding capability to its target antigen (e.g., inactive) when the first and second peptide linkers and/or the third and fourth peptide linkers are in the un-cleaved state. In one embodiment, in an inactive state masked antigen binding protein, the first and second masking moieties and/or the third and fourth masking moieties may or may not be associated with each other.
In one embodiment, a masked antigen binding protein having intact first and second peptide linkers, and/or intact third and fourth peptide linkers, the binding capacity to the target antigen can be reduced by at least 25-50%, or at least 50-75%, or at least 75-95%, or at least 95-99% or more.
In one embodiment, a masked antigen binding protein having intact first and second peptide linkers, and/or intact third and fourth peptide linkers, the binding capacity to the target antigen can be reduced by about 2-20 fold, or about 20-100 fold, or about 100-200 fold, or about 200-500 fold, or about 500-1000 fold, or about 1,000-10,000 fold, or about 10,000-100,000 fold, or higher fold-levels of reduced binding capacity.
In one embodiment, a masked antigen binding protein having intact first and second peptide linkers, and/or intact third and fourth peptide linkers, the binding affinity (e.g., KD) of an inactive antigen binding protein is about 10-4 - 10-8 M. In one embodiment, the target antigen is a soluble antigen or a cell surface antigen.
The present disclosure provides activatable masked antigen binding proteins that are un-masked and capability of binding its target antigen (e.g., activated) when the first and second peptide linkers and/or the third and fourth peptide linkers are in the cleaved state. In one embodiment, the activatable masked antigen binding proteins exhibit increased binding capability to its target antigen (e.g., activated) when the first and second peptide linkers and/or the third and fourth peptide linkers are in the cleaved state. In one embodiment, in an activated state masked antigen binding protein, the first and second masking moieties and/or the third and fourth masking moieties may or may not be associated with each other.
In one embodiment, an un-masked antigen binding protein having cleaved first and/or second peptide linkers, and/or having cleaved third and/or fourth peptide linkers, the binding capacity to the target antigen can be increased by at least 25-50%, or at least 50-75%, or at least 75-95%, or at least 95-99% or more.
In one embodiment, an un-masked antigen binding protein having cleaved first and/or second peptide linkers, and/or having cleaved third and/or fourth peptide linkers, the binding capacity to the target antigen can be increased by about 2-20 fold, or about 20-100 fold, or about 100-200 fold, or about 200-500 fold, or about 500-1000 fold, or about 1,000-10,000 fold, or about 10,000-100,000 fold, or higher fold-levels of increased binding capacity.
In one embodiment, an un-masked antigen binding protein having cleaved first and/or second peptide linkers, and/or having cleaved third and/or fourth peptide linkers, the binding affinity (e.g., KD) of an activated antigen binding protein is about 10-5 - 10-12 M. In one embodiment, the target antigen is a soluble antigen or a cell surface antigen. In one embodiment, the binding affinity of the activated form of the antigen binding protein is higher compared to the inactive form.
In one embodiment, the difference in binding affinity between the inactive and activated antigen binding protein (e.g., KD of inactive vs. KD of activated) is about 10, 102, 103, 104 or 105 or higher differences in binding affinity.
The present disclosure provides activatable masked antigen binding proteins comprising an IgG type antibody, in an inactive or activated state, comprising an Fc region that exhibits effector function, including complement-dependent cytotoxicity (CDC), antibody-dependent cell-mediated cytotoxicity (ADCC) and/or antibody-dependent phagocytosis (ADP). In one embodiment, a mutation in the Fc region can increase or decrease any one or any combination of these functions. In one embodiment, the Fc region comprises a LALA-PG mutation (L234A, L235A, P329G) which reduces effector function.
In one embodiment, the Fc region mediates serum half-life of the activatable masked antigen binding proteins, and a mutation in the Fc region can increase or decrease the serum half-life of the activatable masked antigen binding proteins.
In one embodiment, the Fc region affects thermal stability of the activatable masked antigen binding proteins, and mutation in the Fc region can increase or decrease the thermal stability of the activatable masked antigen binding proteins.
The present disclosure provides activatable masked antigen binding proteins comprising an IgG type antibody and having one or more amino acid mutations in an Fc region where the mutation(s) lead to introducing knob-in-hole structures that promote dimerization of the first and second heavy chains, (Ridgeway 1996 Protein Engineering 9(7):617-621), or lead to introducing additional interchain disulfide bonding (Carter 2011 Journal of Immunological Methods 248:7-15), and/or lead to introducing new salt bridges.
In one embodiment, the Fc region includes mutations that create a protrusion (e.g., knob) on one heavy chain and a socket (e.g., hole) on the other heavy chain so that the protrusion and socket associate with each other. In one embodiment, the protrusion and socket promote association between the heavy chains, for example to promote dimerization. In one embodiment, one of the heavy chains is mutated by substituting a small amino acid with a larger one to create a protrusion. In one embodiment, the other heavy chain is mutated by substituting a larger amino acid with a smaller one to create a socket. In one embodiment, Fc region knob-in-hole mutations comprise a substitute mutation at any one Fc location or any combination of two or more Fc locations selected from a group consisting of T366, L368, T394, F405, Y407 and K409 (numbering is based on Kabat system). In one embodiment, Fc region knob-in-hole mutations comprise any one or any combination of two or more of the following mutations: T366Y, T366W, T366S, L368A, T394S, T394W, F405A, F405W, Y407A, Y407V, Y407T (numbering based on Kabat system).
The present disclosure provides nucleic acids encoding any of the activatable masked antigen binding proteins comprising an IgGtype antibody. For example, a nucleic acid encodes an activatable masked antigen binding protein comprising an IgG class antibody that binds a target antigen (e.g., monospecific). In another example, a nucleic acid encodes an activatable masked antigen binding protein comprising an IgG class antibody that binds two target antigens (e.g., bispecific).
In one embodiment, a first nucleic acid encodes a heavy chain comprising (i) a first or third masking moiety, (ii) a first or third peptide linker and (iii) a heavy chain variable region. In one embodiment, the first nucleic acid further encodes a heavy chain comprising (iv) a heavy chain constant region (CH1). In one embodiment, the first nucleic acid further encodes a heavy chain comprising (v) a hinge region. In one embodiment, the first nucleic acid further encodes a heavy chain comprising (vi) a heavy chain constant region (CH2 and/or CH3). In one embodiment, the first nucleic acid encodes a heavy chain constant region (CH2 and/or CH3) with a knob or hole. In one embodiment, the first linker comprises a first cleavable site. In one embodiment, the third linker comprises a third cleavable site. In one embodiment, the first nucleic acid comprises a recombinant nucleic acid molecule.
In one embodiment, the first nucleic acid encodes a heavy chain comprising a heavy chain variable region which comprises an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity to a portion or full-length of SEQ ID NO:2 or 4 (e.g., anti-EGFR) or to a portion or full-length of SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18 or 20 (e.g., anti-CD38), or having 100% sequence identity to a portion or full-length of SEQ ID NO:2 or 4 (e.g., anti-EGFR) or a portion or full-length of SEQ ID NO: 7, 9, 11, 13, 14, 15, 16, 17, 18 or 20 (e.g., anti-CD38).
In one embodiment, the first nucleic acid encodes a heavy chain comprising a first or third masking moiety comprising the amino acid sequence of any one of SEQ ID NO:21-31 (see Tables 1 and 2).
In one embodiment, the first nucleic acid encodes a heavy comprising a first or third peptide linker comprising the amino acid sequence of any one of SEQ ID NO:32-40 (see also Tables 3-9 and 12).
In one embodiment, a second nucleic acid encodes a light chain comprising (i) a second or fourth masking moiety, (ii) a second or fourth peptide linker and (iii) a light chain variable region. In one embodiment, the second nucleic acid further encodes a light chain constant region (CL). In one embodiment, the second linker comprises a second cleavable site. In one embodiment, the fourth linker comprises a fourth cleavable site. In one embodiment, the second nucleic acid comprises a recombinant nucleic acid molecule.
In one embodiment, the second nucleic acid encodes a light chain comprising a light chain variable region which comprises an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity to a portion or full-length of SEQ ID NO:3 or 5 (anti-EGFR) or a portion or full-length of SEQ ID NO:8, 10, 12 or 19 (e.g., anti-CD38), or having 100% sequence identity to a portion or full-length of SEQ ID NO:3 or 5 (e.g., anti-EGFR) or a portion or full-length of SEQ ID NO:8, 10, 12 or 19 (e.g., anti-CD38).
In one embodiment, the second nucleic acid encodes a light chain comprising a second or fourth masking moiety comprising the amino acid sequence of any one of SEQ ID NO:21-31 (see Tables 1 and 2).
In one embodiment, the second nucleic acid encodes a light chain comprising a second or fourth peptide linker comprising the amino acid sequence of any one of SEQ ID NO:32-40 (see also Tables 3-9 and 12).
The present disclosure provides individual vectors, including expression vectors, that are operably joined to nucleic acids encoding any of the activatable masked antigen binding proteins comprising an IgG type antibody. For example, the expression vector is operably joined to a nucleic acid encoding an activatable masked antigen binding protein comprising an IgG class antibody that binds a target antigen (e.g., monospecific). In another example, the expression vector is operably joined to a nucleic acid encoding an activatable masked antigen binding protein comprising an IgG class antibody that binds two target antigens (e.g., bispecific).
In one embodiment, the expression vector comprising one or more regulatory sequences (e.g., promoter and/or enhancer) that control transcription of the nucleic acids encoding any of the activatable masked antigen binding proteins comprising an IgG type antibody. In one embodiment, the expression vector comprises one or more regulatory sequences each operably joined to a nucleic acid encoding a heavy chain or light chain, and each regulatory sequence controls transcription of the nucleic acids encoding the heavy chain or light chain in a mono-cistronic manner. In one embodiment, the expression vector comprises a regulatory sequence operably joined to nucleic acids encoding a heavy chain and light chain, and the regulatory sequence controls transcription of the heavy chain and light chain in a poly-cistronic manner.
In one embodiment, the vector comprises multiple regulatory sequences that can be operably joined to individual nucleic acids each encoding a heavy chain or a light chain sequence.
In one embodiment, one expression vector is introduced into a host cell, wherein the expression vector within the host cell carries a promoter (and optionally an enhancer sequence), that is operably joined to a nucleic acid encoding a heavy chain and/or light chain sequence. Thus, the host cell can express the heavy chain and/or light chain that make up any of the activatable masked antigen binding proteins.
In one embodiment, multiple expression vectors are introduced into a host cell, wherein individual expression vectors within the host cell carry a promoter (and optionally an enhancer sequence), that is operably joined to a nucleic acid encoding a heavy chain or light chain sequence. Thus, the host cell can express the heavy chain and light chain that make up any of the activatable masked antigen binding proteins.
The vectors comprise promoters that are inducible or constitutive promoters. The vectors and host cells can be selected to generate transgenic host cells that transiently or stably express any of the heavy chains or light chains described herein.
The present disclosure provides host cells that harbor a single expression vector that is operably joined to one or more nucleic acids that encode the heavy chain and/or light chain that make up any of the activatable masked antigen binding proteins.
The present disclosure provides host cells that harbor two or more expression vectors each expression vector being operably joined to one or more nucleic acids that encode a heavy chain and/or light chain that make up any of the activatable masked antigen binding proteins.
The host cell can be a bacterial or mammalian cell. In one embodiment, the host cell comprises a Chinese hamster ovary (CHO) cell.
In one embodiment, at least one expression vector is introduced into the host cell via lipofection (e.g., using a lipid surfactant); electroporation; transfection employing calcium chloride, rubidium chloride, calcium phosphate, DEAE-dextran, or other substances; viral transfection; non-viral transfection; microprojectile bombardment; and infection (e.g., where the vector is an infectious agent).
In one embodiment, host cells harbor one expression vector which is operably joined to nucleic acids encoding the heavy chain and light chain. The host cells can express the heavy chain and light chain at a molar ratio for heavy chain:light chain of 1:1, 1:1.5, 1.5:1, 1:2, 2:1, 1:3, or 3:1. Other molar ratios are possible as well known in the art.
In one embodiment, host cells harbor expression two vectors, wherein the first expression vector is operably joined to nucleic acids encoding the heavy chain, and the second expression vector is operably joined to nucleic acid encoding the light chain. The host cells can express the heavy chain and light chain at a molar ratio for heavy chain:light chain of 1:1, 1:1.5, 1.5:1, 1:2, 2:1, 1:3, or 3:1. Other molar ratios are possible as well known in the art.
The present disclosure provide methods for preparing any of the activatable masked antigen binding proteins comprising an IgG type antibody described herein, the method comprising: culturing a population of host cells, wherein individual host cells in the population harbor at least one expression vector that is operably linked to any one or any combination of nucleic acids encoding any one or any combination of heavy chain and/or light chain described herein, wherein the culturing is conducted under conditions suitable for expressing the heavy chains and/or light chains by the population of host cells.
In one embodiment, the nucleic acids encoding the heavy chain and/or light chain further encodes a signal peptide for secretion of the expressed polypeptide chains. In one embodiment, the culturing is conducted under conditions suitable for secretion of the heavy chain and/or light chain by the population of host cells.
In one embodiment, the nucleic acids encoding any one or any combination of the heavy chain and/or light chain further encodes an affinity tag sequence for enriching the expressed polypeptides. Exemplary affinity tag sequences include histidine tag, FLAG tag, myc tag, HA tag, and GST tag.
In one embodiment, the methods for preparing any of the activatable masked antigen binding proteins comprising an IgG type antibody described herein further comprise isolating the expressed heavy chains and/or light chains.
In one embodiment, the culturing is conducted under conditions that are suitable for assembly or association of the heavy chain and light chain to form the activatable masked antigen binding proteins comprising an IgG type antibody.
In one embodiment, the method further comprises isolating or recovering the assembled activatable masked antigen binding proteins comprising an IgG type antibody. In one embodiment, the isolating is conducted using affinity chromatography. In one embodiment, the isolating is conducted using affinity chromatography with protein A or G from Staphylococcus aureus, glutathione S-transferase (GST), or immuno-affinity. In one embodiment, one or more additional isolating steps are conducted which includes cation exchange, anion exchange chromatography, hydrophobic interaction chromatography, mixed mode chromatography and/or hydroxyapatite chromatography.
In one embodiment, the assembled activatable masked antigen binding proteins comprising an IgG type antibody comprising heavy chains paired with light chains, wherein (1) the heavy chain comprises a first or third masking moiety, a first or third peptide linker, a heavy chain variable region, and optionally including heavy chain constant regions (CH1, CH2 and/or CH3), and (2) the light chain comprises a second or fourth masking moiety, a second or fourth peptide linker, a light chain variable region, and optionally including light chain constant regions (CL).
The activatable masked antigen binding proteins comprising an IgG type antibody can be prepared using transgenic host cell expression, phage display, yeast display and human antibody gene transgenic mice using methods that are well known in the art. In one embodiment, the yield of antigen binding proteins using transgenic host cell expression can be about 20-80%, or about 30-90%, or about 40-95%, or about 50-99% of the total activatable masked antigen binding proteins formed.
The present disclosure provide methods for cleaving at least one peptide linker of any of the activatable masked antigen binding proteins comprising an IgG type antibody described herein, the method comprising: (a) contacting at least one protease with an activatable masked antigen binding protein in an inactive form, wherein the first, second, third and fourth peptide linkers are in the un-cleaved state.
In one embodiment, the activatable masked antigen binding protein is contacted with an one or any combination of two or more proteases selected from: a matrix metalloprotease (MMP), MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase), a disintegrin and metalloproteinase (ADAM) protease, ADAM10, ADAM12, ADAM17, urokinase plasminogen activator (uPA), uPAR, serine proteases, cysteine proteases, aspartate proteases, threonine proteases, cathepsins (e.g., cysteine or aspartic cathepsins), cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K or cathepsin L.
In one embodiment, the activatable masked antigen binding protein is contacted essentially simultaneously (at the same time) with two or more proteases, or sequentially contacted with two or more proteases in any order.
In one embodiment, at least one of the peptide linkers of the activatable masked antigen binding protein used in step (a) comprises a cleavable site that is cleavable with one or more proteases, including a matrix metalloprotease (MMP), MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase), a disintegrin and metalloproteinase (ADAM) protease, ADAM10, ADAM12, ADAM17, urokinase plasminogen activator (uPA), uPAR, serine proteases, cysteine proteases, aspartate proteases, threonine proteases, cathepsins (e.g., cysteine or aspartic cathepsins), cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K or cathepsin L.
In one embodiment, the method further comprises: (b) cleaving at least one of the cleavable sites to convert the activatable masked antigen binding protein to an activated form. In one embodiment, the activated form can bind a target antigen.
In one embodiment, the method further comprises: (c) binding the activatable masked antigen binding protein (now in the activated state) to a target antigen.
In one embodiment, the steps of contacting, cleaving and binding are conducted in an in vitro or in vivo condition.
In one embodiment, the target antigen comprises a soluble antigen or a surface antigen expressed by a healthy or diseased cell.
In one embodiment, the diseased cell (e.g., tumor or cancer cell) that expresses the target antigen also expresses one or more proteases that cleaves the peptide linker. In one embodiment, the diseased cell expresses one or a combination of two or more proteases comprising a matrix metalloprotease (MMP), MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase), a disintegrin and metalloproteinase (ADAM) protease, ADAM10, ADAM12, ADAM17, urokinase plasminogen activator (uPA), serine proteases, cysteine proteases, aspartate proteases, threonine proteases, cathepsins, cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K and/or cathepsin L.
In one embodiment, method further comprises: (d) killing the diseased cell (e.g., tumor or cancer cell).
In one embodiment, at least one of the peptide linkers is cleavable with a protease that is present in a tumor microenvironment.
In one embodiment, the tumor microenvironment comprise a protease selected from a group consisting of a matrix metalloprotease (MMP), MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase), a disintegrin and metalloproteinase (ADAM) protease, ADAM10, ADAM12, ADAM17, urokinase plasminogen activator (uPA), serine proteases, cysteine proteases, aspartate proteases, threonine proteases, cathepsins (e.g., cysteine or aspartic cathepsins), cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K and cathepsin L.
The present disclosure provide methods treating a subject having a disease associated with expression or over-expression of a tumor-associated antigen, the method comprising: administering to the subject an effective amount of a therapeutic composition comprising one or any combination of two or more activatable masked antigen binding proteins comprising an IgG type antibody described herein. In one embodiment the activatable masked antigen binding proteins comprising an IgG type antibody (ies) are administered to the subject in an inactive form having the first, second, third and fourth peptide linkers in the un-cleaved state.
The present disclosure provides a method of treating a subject having a disease, disorder or condition associated with detrimental expression of a tumor antigen, wherein the disease is cancer, including, but not limited to hematologic cancer, breast cancer, ovarian cancer, prostate cancer, head and neck cancer, lung cancer, bladder cancer, melanoma, colorectal cancer, pancreatic cancer, lung cancer, liver cancer, renal cancer, esophageal cancer, leiomyoma, leiomyosarcoma, glioma, and glioblastoma, wherein the method for treating the subject comprises administering to the subject an effective amount of a therapeutic composition comprising one or any combination of two or more activatable masked antigen binding proteins comprising an IgG type antibody described herein.
In one embodiment, the cancer is a hematologic cancer selected from the group consisting of non-Hodgkin’s lymphoma (NHL), Burkitt’s lymphoma (BL), B chronic lymphocytic leukemia (B-CLL), B and T acute lymphocytic leukemia (ALL), T cell lymphoma (TCL), acute myeloid leukemia (AML), hairy cell leukemia (HCL), Hodgkin’s Lymphoma (HL), chronic myeloid leukemia (CML) and multiple myeloma (MM).
The present disclosure provides an in vitro cleavage-based method to detect protease activity and specificity for detecting, diagnosing, monitoring and/or staging a diseased tissue such as a cancer or tumor. A tumor or cancer mass can be extracted from a subject and contacted with one or any combination of two or more activatable masked antigen binding proteins comprising an IgG type antibody described herein, each having a known protease cleavage profile. The tumor or cancer mass from the subject produces one or more protease and is contacted with one or more activatable masked antigen binding proteins under conditions suitable for a protease(s) to cleave a peptide linker on the activatable masked antigen binding protein(s). The cleaved peptide linker product can be detected using any method. Thus, the type of protease produced by the tumor or cancer mass can be identified. In one embodiment, the peptide linker is cleavable with any one or any combination of two or more protease selected from a group consisting of a matrix metalloprotease (MMP), MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase), ADAM protease, urokinase plasminogen activator (uPA), serine proteases, cysteine proteases, aspartate proteases, threonine proteases, cathepsins (e.g., cysteine or aspartic cathepsins), cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K and cathepsin L.
The present disclosure provides a method for detecting the presence of a protease produced by a tumor from a subject, the method comprising: (a) contacting (i) a tumor obtained from the subject with (ii) at least one of the activatable masked antigen binding proteins comprising an IgG type antibody described herein, wherein the tumor sample produces a protease.
In one embodiment, the activatable masked antigen binding proteins each comprise at least a first antigen binding domain which comprises a first heavy chain variable region and a first light chain variable region, wherein (i) the first heavy chain variable region is joined to a first masking moiety via a first peptide linker, and (ii) the first light chain variable region is joined to a second masking moiety via a second peptide linker. In one embodiment, the activatable masked antigen binding proteins further comprise a second antigen binding domain which comprises a second heavy chain variable region and a second light chain variable region, wherein (i) the second heavy chain variable region is joined to a third masking moiety via a third peptide linker, and (ii) the second light chain variable region is j oined to a fourth masking moiety via a fourth peptide linker.
In one embodiment, the first peptide linker includes a first cleavable site and the second peptide linker includes a second cleavable site. In one embodiment, the third peptide linker includes a third cleavable site and the fourth peptide linker includes a fourth cleavable site. In one embodiment, the amino acid sequence of the first, second, third and/or fourth cleavable sites may or may not be a substrate for cleavage by the protease produced by the tumor sample. In one embodiment, the contacting in step (a) is performed under conditions suitable for the protease to cleave the first, second, third and/or fourth cleavable site to generate one or more cleavage products when the protease cleaves the first, second, third and/or fourth cleavable site.
In one embodiment, the method further comprises: (b) detecting the first, second, third and/or fourth cleavage product from the first, second, third and/or fourth peptide linker. In one embodiment, the method further comprises: (c) identifying the type of protease produced by the tumor from the subject by detecting the first, second, third and/or fourth cleavage product and correlating any of the cleavage products with the amino acid sequence of the first, second, third and/or fourth cleavable site.
In one embodiment, by identifying the type of protease produced by the tumor in the subject, the cancer in the subject can be diagnosed. In one embodiment, the first, second, third and/or fourth cleavage product can be detected by gel electrophoresis, Western blot analysis, immunology, immunohistochemistry, colorimetrically, spectrophotometrically, mass spectrometry, liquid chromatography, or by any combination thereof. In one embodiment, the tumor or cancer mass can be obtained from a prostate, breast, ovary, head and neck, bladder, skin, colorectal, anus, rectum, pancreas, lung (including non-small cell lung and small cell lung cancers), leiomyoma, brain, glioma, glioblastoma, esophagus, liver, kidney, stomach, colon, cervix, uterus, endometrium, vulva, larynx, vagina, bone, nasal cavity, paranasal sinus, nasopharynx, oral cavity, oropharynx, larynx, hypolarynx, salivary glands, ureter, urethra, penis, and testis. In one embodiment, the subject is a human, non-human primate, simian, ape, murine (e.g., mice and rats), bovine, porcine, equine, canine, feline, caprine, lupine, ranine or piscine. In one embodiment, the in vitro cleavage-based method can be used for detecting, diagnosing, monitoring and/or staging a cancer in the subject.
The present disclosure provides a kit comprising: at least one of the activatable masked antigen binding proteins comprising an IgG type antibody, and/or at least one nucleic acid encoding an activatable masked antigen binding proteins comprising an IgG type antibody. In one embodiment, the kit comprises one or more adjunct compounds selected from a group consisting of Tris, phosphate, carbonate, stabilizers, excipients, biocides and bovine serum albumin. In one embodiment, the kit comprises one or more adjunct compounds selected from a group consisting of Tris, phosphate, carbonate, stabilizers, excipients, biocides and bovine serum albumin. In one embodiment, the kit comprises one container which contains at least one activatable masked antigen binding proteins comprising an IgG type antibody (or nucleic acid encoding the protein thereof) and optionally one or more adjunct compound. In one embodiment, the kit comprises two or more containers, wherein one container contains at least one activatable masked antigen binding proteins comprising an IgG type antibody (or nucleic acid encoding the protein thereof) and a separate container contains one or more adjunct compounds.
The present disclosure provides activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) having a Fab fragment j oined to a transmembrane region and intracellular signaling regions, wherein the Fab fragment is joined to paired masking moieties. In one embodiment, the DAR construct includes an optional hinge region between the Fab fragment and the transmembrane region.
In one embodiment, the dimeric antigen receptors (DAR) comprise two polypeptide chains that dimerize to form a protein complex, wherein a first polypeptide chain comprises a heavy chain variable region and a second polypeptide chain comprises a light chain variable region, wherein the heavy chain variable region and the light chain variable region form an antigen binding domain. In one embodiment, the first polypeptide chain is linked to the second polypeptide chain by one or a plurality of disulfide bonds. The dimeric antigen receptors have antibody-like properties as they bind specifically to a target antigen.
In one embodiment, the dimeric antigen receptors (DAR) comprise two polypeptide chains that dimerize to form a protein complex, wherein a first polypeptide chain comprises a light chain variable region and a second polypeptide chain comprises a heavy chain variable region, wherein the light chain variable region and the heavy chain variable region form an antigen binding domain. In one embodiment, the first polypeptide chain is linked to the second polypeptide chain by one or a plurality of disulfide bonds. The dimeric antigen receptors have antibody-like properties as they bind specifically to a target antigen.
In one embodiment, the activatable masked antigen binding protein is joined to a toxin by a linker.
In one embodiment, the dimeric antigen receptors (DAR) lack a peptide linker and/or lack a masking moiety.
The present disclosure provides activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) having a first and a second polypeptide chain, wherein the (a) first polypeptide chain comprises regions: (i) an antibody heavy chain variable region (VH), (ii) an antibody heavy chain constant region (CH), (iii) an optional hinge region, (iv) a transmembrane region (TM), and (v) an intracellular signaling region, wherein the (b) second polypeptide chain comprises regions: (i) an antibody light chain variable region (VL) (e.g., kappa or lambda), and (ii) an antibody light chain constant region (CL), wherein the antibody heavy chain variable region (VH) and the antibody light chain variable region (VL) form an antigen binding domain that binds a target antigen.
In one embodiment, (i) the N-terminal end of the first polypeptide chain is joined to a first masking moiety via a first peptide linker having a first cleavable site, and (ii) the N-terminal end of the second polypeptide chain is joined to a second masking moiety via a second peptide linker having a second cleavable site, and (iii) the first and second masking moieties associate with each other without disulfide bonding, and (iv) the first and second masking moieties do not selectively bind the antigen binding domain, and (v) the first cleavable site is cleavable with a first protease, and (vi) the second cleavable site is cleavable with a second protease, wherein the first and second protease cleavable sites are cleavable with the same or different proteases. In one embodiment, the dimeric antigen receptors (DAR) lack a peptide linker and/or lack a masking moiety.
In one embodiment, the activatable masked antigen binding proteins comprising the dimeric antigen receptor (DAR) comprises a first and a second polypeptide chain, wherein the (a) first polypeptide chain comprises: (i) a first masking moiety, (ii) a first peptide linker, (iii) an antibody heavy chain variable region (VH), (iv) an antibody heavy chain constant region (CH), (v) an optional hinge region, (vi) a transmembrane region (TM), and (vii) an intracellular signaling region, wherein the (b) second polypeptide chain comprises: (i) a second masking moiety, (ii) a second peptide linker, (iii) an antibody light chain variable region (VL) (e.g., kappa or lambda), and (iv) an antibody light chain constant region (CL), wherein the antibody heavy chain variable region (VH) and the antibody light chain variable region (VL) form an antigen binding domain that binds a target antigen.
In one embodiment, the first and second masking moieties associates with each other to reduce the antigen binding domain from binding to its target antigen.
In one embodiment, the first and/or second cleavable sites are cleavable with the same or different proteases.
In one embodiment, the first and second proteases are produced by the same tumor or by different tumors.
In one embodiment, the hinge region is about 10 to about 100 amino acids in length. In one embodiment, the hinge region is independently selected from the group consisting of a PDGFR (platelet-derived growth factor receptor) hinge region or a fragment thereof, a CD8 hinge region or a fragment thereof, a CD8α hinge region or a fragment thereof, a hinge region of an antibody (IgG, IgA, IgM, IgE, or IgD) joining the constant domains CH1 and CH2 of an antibody. The hinge region can be derived from an antibody and may or may not comprise one or more constant regions of the antibody.
In one embodiment, the transmembrane domain can be derived from a membrane protein sequence region selected from the group consisting of CD8α, CD8β, 4-1BB/CD137, CD28, CD34, CD4, FcsRIγ, CD16, OX40/CD134, CD3ζ, CD3ε, CD3γ, CD3δ, TCRα, TCRβ, TCRζ, CD32, CD64, CD64, CD45, CD5, CD9, CD22, CD33, CD37, CD64, CD80, CD86, CD137, CD154, LFA-1 T cell co-receptor, CD2 T cell co-receptor/adhesion molecule, CD40, CD4OL/CD154, VEGFR2, FAS, and FGFR2B.
In one embodiment, the intracellular signaling region comprises any one or any combination of two or more intracellular signaling sequences selected from the group consisting of signaling regions from CD3-zeta chain, 4-1BB, CD28, CD27, OX40, CD30, CD40, PD-1, ICOS, lymph oocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, GITR (TNFRSF18), DR3 (TNFRSF25), TNFR2, CD226, and combinations thereof.
In one embodiment, the intracellular signaling region comprises 1, 2 or 3 different intracellular signaling sequences.
In one embodiment, the intracellular signaling region comprises any one or any combination of two or more signaling sequences selected from a group consisting of 4-1BB, CD28, CD3zeta (long) signaling sequence and/or CD3zeta (short) signaling sequence having an ITAM 3 motif.
In one embodiment, the activatable masked antigen binding protein is joined to a toxin by a linker.
The present disclosure provides activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) having a first and a second polypeptide chain, wherein the (a) first polypeptide chain comprises regions: (i) an antibody light chain variable region (VL) (e.g., kappa or lambda), (ii) an antibody light chain constant region (CL), (iii) an optional hinge region, (iv) a transmembrane region (TM), and (v) an intracellular signaling region, wherein the (b) second polypeptide chain comprises regions: (i) an antibody heavy chain variable region (VH), and (ii) an antibody heavy chain constant region (CH), wherein the antibody heavy chain variable region (VH) and the antibody light chain variable region (VL) form an antigen binding domain that binds a target antigen.
In one embodiment, (i) the N-terminal end of the first polypeptide chain is joined to a first masking moiety via a first peptide linker having a first cleavable site, and (ii) the N-terminal end of the second polypeptide chain is joined to a second masking moiety via a second peptide linker having a second cleavable site, and (iii) the first and second masking moieties associate with each other without disulfide bonding, and (iv) the first and second masking moieties do not selectively bind the antigen binding domain, and (v) the first cleavable site is cleavable with a first protease, and (vi) the second cleavable site is cleavable with a second protease, wherein the first and second protease cleavable sites are cleavable with the same or different proteases. In one embodiment, the dimeric antigen receptors (DAR) lack a peptide linker and/or lack a masking moiety.
In one embodiment, the activatable masked antigen binding proteins comprising the dimeric antigen receptor (DAR) comprises a first and a second polypeptide chain, wherein the (a) first polypeptide chain comprises: (i) a first masking moiety, (ii) a first peptide linker, (iii) an antibody light chain variable region (VL) (e.g., kappa or lambda), (iv) an antibody light chain constant region (CL), (v) an optional hinge region, (vi) a transmembrane region (TM), and (vii) an intracellular signaling region, wherein the (b) second polypeptide chain comprises: (i) a second masking moiety, (ii) a second peptide linker, (iii) an antibody heavy chain variable region (VH), and (iv) an antibody heavy chain constant region (CH), wherein the antibody heavy chain variable region (VH) and the antibody light chain variable region (VL) form an antigen binding domain that binds a target antigen.
In one embodiment, the first and second masking moieties associates with each other to reduce the antigen binding domain from binding to its target antigen.
In one embodiment, the first and/or second cleavable sites are cleavable with the same or different proteases.
In one embodiment, the first and second proteases are produced by the same tumor or by different tumors.
In one embodiment, the hinge region is about 10 to about 100 amino acids in length. In one embodiment, the hinge region is independently selected from the group consisting of a CD8 hinge region or a fragment thereof, a CD8α hinge region or a fragment thereof, a hinge region of an antibody (IgG, IgA, IgM, IgE, or IgD) joining the constant domains CH1 and CH2 of an antibody. The hinge region can be derived from an antibody and may or may not comprise one or more constant regions of the antibody.
In one embodiment, the transmembrane domain can be derived from a membrane protein sequence region selected from the group consisting of CD8α, CD8β, 4-1BB/CD137, CD28, CD34, CD4, FcsRIγ, CD16, OX40/CD134, CD3ζ, CD3ε, CD3γ, CD3δ, TCRα, TCRβ, TCRζ, CD32, CD64, CD64, CD45, CD5, CD9, CD22, CD33, CD37, CD64, CD80, CD86, CD137, CD154, LFA-1 T cell co-receptor, CD2 T cell co-receptor/adhesion molecule, CD40, CD4OL/CD154, VEGFR2, FAS, and FGFR2B.
In one embodiment, the intracellular signaling region comprises any one or any combination of two or more intracellular signaling sequences selected from the group consisting of signaling regions from CD3-zeta chain, 4-1BB, CD28, CD27, OX40, CD30, CD40, PD-1, ICOS, lymph oocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, GITR (TNFRSF 18), DR3 (TNFRSF25), TNFR2, CD226, and combinations thereof.
In one embodiment, the intracellular signaling region comprises 1, 2 or 3 different intracellular signaling sequences.
In one embodiment, the intracellular signaling region comprises any one or any combination of two or more signaling sequences selected from a group consisting of 4-1BB, CD28, CD3zeta (long) signaling sequence, and/or CD3zeta (short) signaling sequence having an ITAM 3 motif.
In one embodiment, the activatable masked antigen binding protein is joined to a toxin by a linker.
The present disclosure provides any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) described herein having at least a first and second masking moiety. In one embodiment, the first and second masking moieties when associated (dimerized) with each other, interfere (obstruct) with the ability of the antigen binding protein to bind its target antigen. The first and second masking moieties when associated (dimerized) with each other, can block binding between the antigen binding protein and its target antigen by steric hinderance.
In one embodiment, the first and second masking moieties comprise polypeptides that associate (dimerize) with each other without forming a covalent bond (e.g., no disulfide or transglutamination bonding). The first and second masking moieties comprise polypeptides that can associate (dimerize) with each other by non-covalent interaction, including ionic interaction, hydrogen bonding, dipole-dipole interaction, hydrophilic interaction, hydrophobic interaction, affinity bonding, or bonds or associations involving van der Waals forces.
In one embodiment, the first and second masking moieties associate with each other as a homodimer or heterodimer.
In one embodiment, one of the masking moieties can be engineered to have a knob structure that forms an interchain steric complementarity structure to favor homo-dimerization of, hetero-dimerization with another masking moiety which is engineered to have a hole structure.
The present disclosure provides activatable masked antigen binding proteins, wherein one or both of the masking moieties in a dimerized configuration includes one or more mutations that create a new interchain salt bridge. In one embodiment, a threonine residue in one masking moiety can be replaced with glutamic acid, and an asparagine at a corresponding position in another masking moiety is replaced with lysine, thereby creating an interchain salt bridge.
In one embodiment, the first and/or second masking moieties are derived from an immunoglobulin constant region (e.g., CL, CH1, CH2 or CH3).
In one embodiment, the first or second masking moiety comprises a heavy chain constant region (CH1). In one embodiment, the second or first masking moiety comprises a kappa or lambda light chain constant region (CL kappa or CL lambda). In one embodiment, the first masking moiety comprises a heavy chain constant region (CH1) and the second masking moiety comprises a kappa or lambda light chain constant region (CL kappa or CL lambda). In one embodiment, the first masking moiety comprises a kappa or lambda light chain constant region (CL kappa or CL lambda) and the second masking moiety comprises a heavy chain constant region (CH1). In one embodiment, the first and/or second masking moiety comprises a CH1, CL (lambda) or CL (kappa) having the amino acid sequence of SEQ ID NO:21, 22 or 23. See Tables 1 and 2 for a list of amino acid sequences of various masking moieties.
In one embodiment, the first or second masking moiety comprises an IgG1 or IgG4 gamma heavy chain constant region, for example CH3 In one embodiment, the first and second masking moieties comprise an IgG1 or IgG4 gamma heavy chain constant region CH3. In one embodiment, one of the masking moieties which comprises an IgGI or IgG4 gamma heavy chain constant region CH3 is engineered to have a knob or hole structure that forms an interchain steric complementarity structure to favor dimerization (e.g., homo-dimerization) with another masking moiety which comprises an IgG1 or IgG4 gamma heavy chain constant region CH3 which is engineered to have hole or knob structure. In one embodiment, the first and/or second masking moiety comprises a CH3 (IgG1 or (IgG4) having the amino acid sequence of SEQ ID NO:24, 25, 30 or 31. See Tables 1 and 2 for a list of amino acid sequences of various masking moieties.
In one embodiment, at least one of the masking moieties is derived from an immunoglobulin heavy chain constant region and is joined to the heavy chain variable region of the activatable masked antibody. In one embodiment, at least one of the masking moieties is derived from an immunoglobulin heavy chain constant region and is joined to the light chain variable region of the activatable masked antibody.
In one embodiment, die first and second masking moieties are derived from T cell receptors alpha (α) and beta (β) constant regions. In one embodiment, the first masking moiety comprises a T cell receptor alpha (α) constant regions and the second masking moiety comprises a T cell receptor beta (β) constant region. In one embodiment, the first masking moiety comprises a T cell receptor beta (β) constant regions and the second masking moiety comprises a T cell receptor alpha (α) constant region.
In one embodiment, at least one of the masking moieties is derived from a T cell receptor alpha (α) or beta (β) constant region and is joined to the heavy chain variable region of the activatable masked antibody. In one embodiment, at least one of the masking moieties is derived from a T cell receptor beta (β) or alpha (α) constant region and is joined to the light chain variable region of the activatable masked antibody. In one embodiment, the first and/or second masking moiety comprises a T cell receptor alpha (α) or beta (β) constant region having the amino acid sequence of SEQ ID NO:28 or 29. See Tables 1 and 2 for a list of amino acid sequences of various masking moieties.
In one embodiment, the first or second masking moiety comprises a variable heavy chain domain from a catalytic antibody (e.g., 38C2). In one embodiment, the first or second masking moiety comprises a variable light chain domain from a catalytic antibody (e.g., 38C2). In one embodiment, the first masking moiety comprises a variable heavy chain domain from 38C2 antibody and the second masking moiety comprise a variable light chain domain from 38C2 antibody. In one embodiment, the first and/or second masking moiety comprises a variable heavy chain domain from catalytic antibody 38C2 having the amino acid sequence of SEQ ID NO:26 or 27. See Tables 1 and 2 for a list of amino acid sequences of various masking moieties.
In one embodiment, a masking moiety (e.g., first or second masking moiety) comprises two or more copies of a moiety arranged in-tandem along the same polypeptide chain. For example, a masking moiety comprises two antibody CH3 regions arranged in-tandem, or two antibody CH2 regions arranged in-tandem, or two antibody CH1 regions arranged in-tandem, or two antibody CL regions arranged in-tandem. Any of the CH3, CH2, CH1 or CL regions can include a knob or hole structure. For example, the masking moiety comprises two TCR alpha chain constant region arranged in-tandem, or two TCR beta chain constant region arranged in-tandem.
In one embodiment, a masking moiety (e.g., first or second masking moiety) comprises two or more different moieties arranged in-tandem along the same polypeptide chain. For example, the masking moiety comprises an antibody CH2 region and an antibody CH3 region arranged in-tandem.
The present disclosure provides any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) described herein including at least first and second peptide linkers that have the same or different lengths (e.g., 10-20, 20-30, 30-40 or 40-50 amino acids in length). In one embodiment, the first and/or second peptide linkers are glycine-rich (e.g., GS type linkers). In one embodiment, the first and the second peptide linkers have the same amino acid sequence or different amino acid sequences.
In one embodiment, the first peptide linker is cleavable with a first protease. In one embodiment, the first peptide linker has an amino acid sequence (first cleavable site) that is a substrate for cleavage by the first protease.
In one embodiment, the second peptide linker is cleavable with a second protease. In one embodiment, the second peptide linker has an amino acid sequence (second cleavable site) that is a substrate for cleavage by the second protease.
In one embodiment, the first peptide linker is cleavable with a first protease and the second peptide linker is cleavable with a second protease. In one embodiment, the first and second peptide linkers are cleavable with the same protease. In one embodiment, the first and second peptide linkers are cleavable with different proteases. In one embodiment, the first or the second peptide linker is not cleavable with a protease.
In one embodiment, the first and second proteases can be independently selected from: a matrix metalloprotease (MMP) including MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase); a disintegrin and metalloproteinase (ADAM) protease including ADAM10, ADAM12, ADAM17; a urokinase plasminogen activator (uPA) or uPAR; a serine protease; a cysteine protease; an aspartate protease; a threonine protease; a cathepsin (e.g., cysteine or aspartic cathepsins) including cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K or cathepsin L.
In one embodiment, the first and/or second peptide linkers comprise the amino acid sequence that is at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% identical to the amino acid sequences of any one of SEQ ID NOS: 32-40. See also the various peptide linker sequences listed in Tables 3-9.
The present disclosure provides activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) having an antigen binding domain which comprises a first heavy chain variable region and a first light chain variable region, wherein the antigen binding domain binds a target antigen (e.g., specifically binds a target antigen).
In one embodiment, the activatable masked antigen binding protein binds EGFR antigen having the amino acid sequence of SEQ ID NO: 1 or bind CD38 antigen having the amino acid sequence of SEQ ID NO:6.
In one embodiment, the activatable masked antigen binding proteins binds an antigen from a human. In one embodiment, the activatable masked antigen binding proteins binds an antigen from a human and can bind (e.g., cross-react) with an antigen (e.g., homologous antigen) from any one or any combination of non-human animals such as dog, cat, mouse, rat, goat, rabbit, hamster and/or monkey (e.g., cynomolgus, rhesus or macaque).
The present disclosure provides activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) having a first and a second polypeptide chain.
In one embodiment, the first polypeptide chain comprises a first masking moiety comprising a CH1, CL (lambda or kappa) region having the amino acid sequence of SEQ ID NO:21, 22 or 23. In one embodiment, the first polypeptide chain comprises a first masking moiety comprising a CH3 (IgG1 or IgG4) region having the amino acid sequence of SEQ ID NO:24, 25, 30 or 31. In one embodiment, the first polypeptide chain comprises a first masking moiety comprising a T cell receptor alpha (α) or beta (β) constant region having the amino acid sequence of SEQ ID NO:28 or 29. In one embodiment, the first polypeptide chain comprises a first masking moiety comprising a variable heavy chain domain from catalytic antibody 38C2 having the amino acid sequence of SEQ ID NO:26 or 27.
In one embodiment, the second polypeptide chain comprises a second masking moiety comprising a CH1, CL (lambda or kappa) region having the amino acid sequence of SEQ ID NO:21, 22 or 23. In one embodiment, the second polypeptide chain comprises a second masking moiety comprising a CH3 (IgG1 or IgG4) region having the amino acid sequence of SEQ ID NO:24, 25, 30 or 31. In one embodiment, the second polypeptide chain comprises a second masking moiety comprising a T cell receptor alpha (α) or beta (β) constant region having the amino acid sequence of SEQ ID NO:28 or 29. In one embodiment, the second polypeptide chain comprises a second masking moiety comprising a variable heavy chain domain from catalytic antibody 38C2 having the amino acid sequence of SEQ ID NO:26 or 27.
In one embodiment, the first polypeptide chain comprises a first peptide linker comprising the amino acid sequence of one of SEQ ID NO:32-40 or comprising any one of the amino acid sequences listed in Tables 3-9.
In one embodiment, the second polypeptide chain comprises a second peptide linker comprising the amino acid sequence of one of SEQ ID NO:32-40 or comprising any one of the amino acid sequences listed in Tables 3-9.
In one embodiment, the first polypeptide chain comprises an antibody heavy chain variable region (VH) comprising an anti-EGFR heavy chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:2 or 4. In one embodiment, the first polypeptide chain comprises an antibody heavy chain variable region (VH) comprising an anti-CD38 heavy chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18 or 20.
In one embodiment, the first polypeptide chain comprises an antibody light chain variable region (VL) comprising an anti-EGFR light chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:3 or 5. In one embodiment, the first polypeptide chain comprises an antibody light chain variable region (VL) comprising an anti-CD38 light chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-lengthof SEQ ID NO:8, 10, 12 or 19.
In one embodiment, the second polypeptide chain comprises an antibody light chain variable region (VL) comprising an anti-EGFR light chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:3 or 5. In one embodiment, the second polypeptide chain comprises an antibody light chain variable region (VL) comprising an anti-CD38 light chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:8, 10, 12 or 19.
In one embodiment, the second polypeptide chain comprises an antibody heavy chain variable region (VH) comprising an anti-EGFR heavy chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:2 or 4. In one embodiment, the second polypeptide chain comprises an antibody heavy chain variable region (VH) comprising an anti-CD38 heavy chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18 or 20.
In one embodiment, the first polypeptide chain comprises an antibody heavy chain constant region (CH) comprising an anti-EGFR heavy chain constant region sequence (e.g., from SEQ ID NO:2 or 4). In one embodiment, the first polypeptide chain comprises an antibody heavy chain constant region (CH) comprising an anti-CD38 heavy chain constant region sequence (e.g., from SEQ ID NO: 7, 9, 11, 13, 14, 15, 16, 17, 18 or 20).
In one embodiment, the first polypeptide chain comprises an antibody light chain constant region (CL) comprising an anti-EGFR light chain constant region sequence (e.g., from SEQ ID NO:3 or 5). In one embodiment, the first polypeptide chain comprises an antibody light chain constant region (CL) comprising an anti-CD38 light chain constant region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19).
In one embodiment, the second polypeptide chain comprises an antibody light chain constant region (CL) comprising an anti-EGFR light chain constant region sequence (e.g., from SEQ ID NO:3 or 5). In one embodiment, the second polypeptide chain comprises an antibody light chain constant region (CL) comprising an anti-CD38 light chain constant region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19).
In one embodiment, the second polypeptide chain comprises an antibody heavy chain constant region (CH) comprising an anti-EGFR heavy chain constant region sequence (e.g., from SEQ ID NO:2 or 4). In one embodiment, the second polypeptide chain comprises an antibody heavy chain constant region (CH) comprising an anti-CD38 heavy chain constant region sequence (e.g., from SEQ ID NO: 7, 9, 11, 13, 14, 15, 16, 17, 18 or 20).
In one embodiment, the first polypeptide chain comprises a hinge region having the amino acid sequence of any one or any combination of two or more of: a CD28 hinge sequence (SEQ ID NO:44); a CD8 hinge sequence (SEQ ID NO:45); a long hinge comprising CD28 and CD8 hinge sequences (SEQ ID NO:46); and/or a PDGFR beta hinge sequence (SEQ ID NO:41).
In one embodiment, the first polypeptide chain comprises a transmembrane region having the amino acid sequence of a CD28 transmembrane sequence (SEQ ID NO:47) or a PDGFR beta transmembrane sequence (SEQ ID NO:42).
In one embodiment, the first polypeptide chain comprises 1 - 3 intracellular signaling sequences in any order and in any combination having the amino acid sequence(s) of: a 4-1BB signaling sequence (SEQ ID NO:48); a CD28 signaling sequence (SEQ ID NO:49); a CD3zeta signaling sequence (SEQ ID NO:50); and/or a CD3zeta short signaling sequence (SEQ ID NO:51).
The present disclosure provides activatable masked antigen binding proteins that exhibit inactive and activated states which depend upon the ability of the masking moieties to obstruct binding between the antigen binding domain and its target antigen. In one embodiment, individual masking moieties are tethered to the N-terminus of the heavy chain variable region (on the first polypeptide chain) and light chain variable region (on the second polypeptide chain) by intact peptide linkers, and the masking moieties form a dimerized complex which obstructs the antigen binding domain resulting in an inactive state. Cleavage of one or both peptide linkers allows the dimerized complex to move away from the obstructing position to permit binding between the antigen binding domain and its target antigen. In one embodiment, cleavage of both peptide linkers liberates the dimerized complex to migrate away from the antigen binding protein.
In one embodiment, the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) is inhibited from binding to its target antigen (e.g., inactive) when the first and second peptide linkers are in the un-cleaved state. In one embodiment, the activatable masked antigen binding proteins exhibit reduced binding capability to its target antigen (e.g., inactive) when the first and second peptide linkers are in the un-cleaved state. In one embodiment, in an inactive state masked antigen binding protein, the first and second masking moieties may or may not be associated with each other.
In one embodiment, a masked antigen binding protein having intact first and second peptide linkers, the binding capacity to the target antigen can be reduced by at least 25-50%, or at least 50-75%, or at least 75-95%, or at least 95-99% or more.
In one embodiment, a masked antigen binding protein having intact first and second peptide linkers, the binding capacity to the target antigen can be reduced by about 2-20 fold, or about 20-50 fold, or about 50-200 fold, or about 200-350 fold, or about 350-500 fold, or higher fold-levels of reduced binding capacity.
In one embodiment, a masked antigen binding protein having intact first and second peptide linkers, the binding affinity (e.g., KD) of an inactive antigen binding protein is about 10-4 - 10-8 M. In one embodiment, the target antigen is a soluble antigen or a cell surface antigen.
The present disclosure provides activatable masked antigen binding proteins that are un-masked and capable of binding its target antigen (e.g., activated) when the first and/or second peptide linkers are in the cleaved state. In one embodiment, the activatable masked antigen binding proteins exhibit increased binding capability to its target antigen (e.g., activated) when the first and/or second peptide linkers are in the cleaved state. For example, the activatable masked antigen binding proteins can bind its target antigen when only the first or second peptide linker is cleaved, or when the first and second linkers are cleaved. In one embodiment, in an activated state masked antigen binding protein, the first and second masking moieties may or may not be associated with each other.
In one embodiment, an un-masked antigen binding protein having cleaved first and/or second peptide linkers, the binding capacity to the target antigen can be increased by at least 25-50%, or at least 50-75%, or at least 75-95%, or at least 95-99% or more.
In one embodiment, an un-masked antigen binding protein having cleaved first and/or second peptide linkers, the binding capacity to the target antigen can be increased by about 2-20 fold, or about 20-50 fold, or about 50-200 fold, or about 200-350 fold, or about 350-500 fold, or higher fold-levels of increased binding capacity.
In one embodiment, an un-masked antigen binding protein having cleaved first and/or second peptide linkers, the binding affinity (e.g., KD) of an activated antigen binding protein is about 10-5- 10-12 M. In one embodiment, the target antigen is a soluble antigen or a cell surface antigen. In one embodiment, the binding affinity of the activated form of the antigen binding protein is higher compared to the inactive form.
In one embodiment, the difference in binding affinity between the inactive and activated antigen binding protein (e.g., KD of inactive vs. KD of activated) is about 10, 102, 103, 104 or 105 or higher differences in binding affinity.
The present disclosure provides a Version 1 (e.g., V1) dimeric antigen receptors (DAR) construct comprising a first polypeptide chain carrying heavy chain variable (VH) and heavy chain constant regions (CH), and a second polypeptide chain carrying light chain variable (VL) and light chain constant regions (CL), wherein (a) the first polypeptide chain comprising regions ordered from the amino terminus to the carboxyl terminus: (i) a first masking moiety, (ii) a first peptide linker, (iii) an antibody heavy chain variable region (VH), (iv) an antibody heavy chain constant region (CH), (v) a long hinge region comprising CD8 and CD28 hinge sequences (e.g., SEQ ID NO:46), (vi) a transmembrane region (TM) comprising CD28 transmembrane sequence (e.g., SEQ ID NO:47), and (vii) an intracellular signaling region comprising CD28 signaling sequence (e.g., SEQ ID NO:49) and CD3-zeta signaling sequence having ITAM motifs 1, 2 and 3 (e.g., SEQ ID NO:50); (b) a second polypeptide chain comprising regions ordered from the amino terminus to the carboxyl terminus: (i) a second masking moiety, (ii) a second peptide linker, (iii) an antibody light chain variable region (VL) (e.g., kappa or lambda), and (iv) an antibody light chain constant region (CL). In one embodiment, the V1 dimeric antigen receptors (DAR) lack a peptide linker and/or lack a masking moiety.
In one embodiment, the V1 DAR antibody heavy chain variable region (VH) comprises an anti-EGFR heavy chain variable region sequence (e.g., from SEQ ID NO:2 or 4) and the antibody heavy chain constant region (CH) comprises an anti-EGFR heavy chain constant region sequence (e.g., from SEQ ID NO:2 or 4). In one embodiment, the V1 DAR antibody heavy chain variable region (VH) comprises an anti-CD38 heavy chain variable region sequence (e.g., from SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18 or 20) and the antibody heavy chain constant region (CH) comprises an anti-CD38 heavy chain constant region sequence (e.g., from SEQ ID NO: 7, 9, 11, 13, 14, 15, 16, 17, 18 or 20).
In one embodiment, the V1 DAR antibody light chain variable region (VL) comprises an anti-EGFR light chain variable region sequence (e.g., from SEQ ID NO:3 or 5) and the antibody light chain constant region (CL) comprises an anti-EGFR light chain constant region sequence (e.g., from SEQ ID NO:3 or 5). In one embodiment, the V1 DAR antibody light chain variable region (VL) comprises an anti-CD38 light chain variable region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19) and the antibody light chain constant region (CL) comprises an anti-CD38 light chain constant region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19).
In one embodiment, the first polypeptide chain of the Version 1 (V1) DAR construct comprises a PDGFR beta hinge sequence (SEQ ID NO:41) and a PDGFR beta transmembrane sequence (SEQ ID NO:42).
The present disclosure provides a Version 2 (e.g., V2) dimeric antigen receptors (DAR) construct comprising a first polypeptide chain carrying heavy chain variable (VH) and heavy chain constant regions (CH), and a second polypeptide chain carrying light chain variable (VL) and light chain constant regions (CL), wherein (a) the first polypeptide chain comprising regions ordered from the amino terminus to the carboxyl terminus: (i) a first masking moiety, (ii) a first peptide linker, (iii) an antibody heavy chain variable region (VH), (iv) an antibody heavy chain constant region (CH), (v) a short hinge region comprising a CD28 hinge sequence (e.g., SEQ ID NO:44), (vi) a transmembrane region (TM) comprising CD28 transmembrane sequence (e.g., SEQ ID NO:47), and (vii) an intracellular signaling region comprising either (1) a 4-1BB signaling sequence (e.g., SEQ ID NO:48) and CD3-zeta having ITAM motifs 1, 2 and 3 (e.g., SEQ ID NO:50), or (2) CD28 (e.g., SEQ ID NO:49) signaling sequence and CD3-zeta having ITAM motifs 1, 2 and 3 (e.g., SEQ ID NO:50), or (3) 4-1BB (e.g., SEQ ID NO:48) signaling sequence and CD28 (e.g., SEQ ID NO:49) signaling sequence and CD3-zeta having ITAM motifs 1, 2 and 3 (e.g., SEQ ID NO:50); (b) a second polypeptide chain comprising regions ordered from the amino terminus to the carboxyl terminus: (i) a second masking moiety, (ii) a second peptide linker, (iii) an antibody light chain variable region (VL) (e.g., kappa or lambda), and (iv) an antibody light chain constant region (CL). In one embodiment, the V2 dimeric antigen receptors (DAR) lack a peptide linker and/or lack a masking moiety.
In one embodiment, the Version 2a (V2a) DAR construct comprises the intracellular signaling region having the 4-1BB signaling sequence (e.g., SEQ ID NO:48) and CD3-zeta having ITAM motifs 1, 2 and 3 (e.g., SEQ ID NO:50).
In one embodiment, the Version 2b (V2b) DAR construct comprises the intracellular signaling region having the CD28 (e.g., SEQ ID NO:49) signaling sequence and CD3-zeta having ITAM motifs 1, 2 and 3 (e.g., SEQ ID NO:50).
In one embodiment, the Version 2c (V2c) DAR construct comprises the intracellular signaling region having the 4-1BB (e.g., SEQ ID NO:48) signaling sequence and CD28 (e.g., SEQ ID NO:49) signaling sequence and CD3-zeta having ITAM motifs 1, 2 and 3 (e.g., SEQ ID NO:50).
In one embodiment, the DAR V2a and V2b are second generation DAR constructs, while the DAR V2c is a third generation DAR construct. In one embodiment, the antibody heavy chain variable region (VH) comprises an anti-EGFR heavy chain variable region sequence (e.g., from SEQ ID NO:2 or 4) and the antibody heavy chain constant region (CH) comprises an anti-EGFR heavy chain constant region sequence (e.g., from SEQ ID NO:2 or 4). In one embodiment, the antibody heavy chain variable region (VH) comprises an anti-CD38 heavy chain variable region sequence (e.g., from SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18 or 20) and the antibody heavy chain constant region (CH) comprises an anti-CD38 heavy chain constant region sequence (e.g., SEQ ID NO: 7, 9, 11, 13, 14, 15, 16, 17, 18 or 20).
In one embodiment, the V2 DAR antibody light chain variable region (VL) comprises an anti-EGFR light chain variable region sequence (e.g., from SEQ ID NO:3 or 5) and the antibody light chain constant region (CL) comprises an anti-EGFR light chain constant region sequence (e.g., from SEQ ID NO:3 or 5). In one embodiment, the V2 DAR antibody light chain variable region (VL) comprises an anti-CD38 light chain variable region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19) and the antibody light chain constant region (CL) comprises an anti-CD38 light chain constant region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19).
In one embodiment, the first polypeptide chain of the Version 2a, 2b or 2c DAR construct comprises a PDGFR beta hinge sequence (SEQ ID NO:41) and a PDGFR beta transmembrane sequence (SEQ ID NO:42).
The present disclosure provides a Version 3 (e.g., V3) dimeric antigen receptors (DAR) construct comprising a first polypeptide chain carrying heavy chain variable (VH) and heavy chain constant regions (CH), and a second polypeptide chain carrying light chain variable (VL) and light chain constant regions (CL), wherein (a) the first polypeptide chain comprising regions ordered from the amino terminus to the carboxyl terminus: (i) a first masking moiety, (ii) a first peptide linker, (iii) an antibody heavy chain variable region (VH), (iv) an antibody heavy chain constant region (CH), (v) a short hinge region comprising CD28 hinge sequences (e.g., SEQ ID NO:44), (vi) a transmembrane region (TM) comprising CD28 transmembrane sequence (e.g., SEQ ID NO:47), and (vii) an intracellular signaling region comprising 4-1BB signaling sequence (e.g., SEQ ID NO:48) and CD3-zeta signaling sequence having only ITAM motif3 (e.g., SEQ ID NO:51); (b) a second polypeptide chain comprising regions ordered from the amino terminus to the carboxyl terminus: (i) a second masking moiety, (ii) a second peptide linker, (iii) an antibody light chain variable region (VL) (e.g., kappa or lambda), and (iv) an antibody light chain constant region (CL). In one embodiment, the V3 dimeric antigen receptors (DAR) lack a peptide linker and/or lack a masking moiety.
In one embodiment, the antibody heavy chain variable region (VH) comprises an anti-EGFR heavy chain variable region sequence (e.g., from SEQ ID NO:2 or 4) and the antibody heavy chain constant region (CH) comprises an anti-EGFR heavy chain constant region sequence (e.g., from SEQ ID NO:2 or 4). In one embodiment, the antibody heavy chain variable region (VH) comprises an anti-CD38 heavy chain variable region sequence (e.g., from SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18 or 20) and the antibody heavy chain constant region (CH) comprises an anti-CD38 heavy chain constant region sequence (e.g., from SEQ ID NO: 7, 9, 11, 13, 14, 15, 16, 17, 18 or 20).
In one embodiment, the V3 DAR antibody light chain variable region (VL) comprises an anti-EGFR light chain variable region sequence (e.g., from SEQ ID NO:3 or 5) and the antibody light chain constant region (CL) comprises an anti-EGFR light chain constant region sequence (e.g., from SEQ ID NO:3 or 5). In one embodiment, the V3 DAR antibody light chain variable region (VL) comprises an anti-CD38 light chain variable region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19) and the antibody light chain constant region (CL) comprises an anti-CD38 light chain constant region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19).
In one embodiment, the first polypeptide chain of the Version 3 (V3) DAR construct comprises a PDGFR beta hinge sequence (SEQ ID NO:41) and a PDGFR beta transmembrane sequence (SEQ ID NO:42).
The present disclosure provides a Version 4 (e.g., V4) dimeric antigen receptors (DAR) construct comprising a first polypeptide chain carrying heavy chain variable (VH) and heavy chain constant regions (CH), and a second polypeptide chain carrying light chain variable (VL) and light chain constant regions (CL), wherein (a) the first polypeptide chain comprising regions ordered from the amino terminus to the carboxyl terminus: (i) a first masking moiety, (ii) a first peptide linker, (iii) an antibody heavy chain variable region (VH), (iv) an antibody heavy chain constant region (CH), (v) a transmembrane region (TM) comprising CD28 transmembrane sequence (e.g., SEQ ID NO:47), and (vi) an intracellular signaling region comprising 4-1BB signaling sequence (e.g., SEQ ID NO:48) and CD3-zeta signaling sequence having only ITAM motif 3 (e.g., SEQ ID NO:51); (b) a second polypeptide chain comprising regions ordered from the amino terminus to the carboxyl terminus: (i) a second masking moiety, (ii) a second peptide linker, (iii) an antibody light chain variable region (VL) (e.g., kappa or lambda), and (iv) an antibody light chain constant region (CL). The DAR V4 construct lacks a hinge sequence. In one embodiment, the V4 dimeric antigen receptors (DAR) lack a peptide linker and/or lack a masking moiety.
In one embodiment, the antibody heavy chain variable region (VH) comprises an anti-EGFR heavy chain variable region sequence (e.g., from SEQ ID NO:2 or 4) and the antibody heavy chain constant region (CH) comprises an anti-EGFR heavy chain constant region sequence (e.g., SEQ ID NO:2 or 4). In one embodiment, the antibody heavy chain variable region (VH) comprises an anti-CD38 heavy chain variable region sequence (e.g., from SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18 or 20) and the antibody heavy chain constant region (CH) comprises an anti-CD38 heavy chain constant region sequence (e.g., from SEQ ID NO: 7, 9, 11, 13, 14, 15, 16, 17, 18 or 20).
In one embodiment, the V4 DAR antibody light chain variable region (VL) comprises an anti-EGFR light chain variable region sequence (e.g., from SEQ ID NO:3 or 5) and the antibody light chain constant region (CL) comprises an anti-EGFR light chain constant region sequence (e.g., from SEQ ID NO:3 or 5). In one embodiment, the V4 DAR antibody light chain variable region (VL) comprises an anti-CD38 light chain variable region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19) and the antibody light chain constant region (CL) comprises an anti-CD38 light chain constant region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19).
In one embodiment, the first polypeptide chain of the Version 4 (V4) DAR construct comprises a PDGFR beta hinge sequence (SEQ ID NO:41) and a PDGFR beta transmembrane sequence (SEQ ID NO:42).
The present disclosure provides nucleic acids encoding a precursor polypeptide (e.g.,
In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising (i) heavy chain leader sequence, (ii) a first masking moiety, (iii) a first peptide linker, (iv) an antibody heavy chain variable region (VH), (v) an antibody heavy chain constant region (CH), (vi) an optional hinge region, (vii) a transmembrane region (TM), (viii) an intracellular signaling region, (ix) a self-cleaving sequence, (x) a light chain leader sequence, (xi) a second masking moiety, (xii) a second peptide linker, (xiii) an antibody light chain variable region (VL) (e.g., kappa or lambda), and (xiv) an antibody light chain constant region (CL). In one embodiment, the first peptide linker comprises a first cleavable site. In one embodiment, the second peptide linker comprises a second cleavable site. In one embodiment, the self-cleaving sequence comprises T2A (e.g., amino acid sequence EGRGSLLTCGDVEENPGP, P2A (e.g., amino acid sequence (GSG)ATNFSLLKQAGDVEENPG, PE2A (e.g., amino acid sequence (GSG)QCTNYALLKLAGDVESNPG, PF2A (e.g., amino acid sequence (GSG)VKQTLNFDLLKLAGDVESNPGP, wherein the amino acid sequence (GSG) is optional. In one embodiment, the nucleic acid encoding the precursor polypeptide chain comprises a recombinant nucleic acid molecule.
In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising (i) light chain leader sequence, (ii) a first masking moiety, (iii) a first peptide linker, (iv) an antibody light chain variable region (VL) (e.g., kappa or lambda), (v) an antibody light chain constant region (CL), (vi) an optional hinge region, (vii) a transmembrane region (TM), (viii) an intracellular signaling region, (ix) a self-cleaving sequence, (x) a heavy chain leader sequence, (xi) a second masking moiety, (xii) a second peptide linker, (xiii) an antibody heavy chain variable region (VH), and (xiv) an antibody heavy chain constant region (CH). In one embodiment, the first peptide linker comprises a first cleavable site. In one embodiment, the second peptide linker comprises a second cleavable site. In one embodiment, the second peptide linker comprises a second cleavable site. In one embodiment, the self-cleaving sequence comprises T2A (e.g., amino acid sequence EGRGSLLTCGDVEENPGP), P2A (e.g., amino acid sequence (GSG)ATNFSLLKQAGDVEENPG), PE2A (e.g., amino acid sequence (GSG)QCTNYALLKLAGDVESNPG), PF2A (e.g., amino acid sequence (GSG)VKQTLNFDLLKLAGDVESNPGP), wherein the amino acid sequence (GSG) is optional. In one embodiment, the nucleic acid encoding the precursor polypeptide chain comprises a recombinant nucleic acid molecule.
In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising a first and/or second masking moiety comprising a CH1, CL (lambda or kappa) region having the amino acid sequence of SEQ ID NO:21, 22 or 23. In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising a first and/or second masking moiety comprising a CH3 (IgG1 or IgG4) region having the amino acid sequence of SEQ ID NO:24, 25, 30 or 31. In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising a first and/or second masking moiety comprising a T cell receptor alpha (α) or beta (β) constant region having the amino acid sequence of SEQ ID NO:28 or 29. In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising a first and/or second masking moiety a variable heavy chain domain from catalytic antibody 38C2 having the amino acid sequence of SEQ ID NO:26 or 27.
In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising a first and/or second peptide linker comprising the amino acid sequence of one of SEQ ID NO:32-40 or comprising any one of the amino acid sequences listed in Tables 3-9.
In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising an antibody heavy chain variable region (VH) which comprises an anti-EGFR heavy chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%), or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:2 or 4. In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising an antibody heavy chain variable region (VH) which comprises an anti-CD38 heavy chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18 or 20.
In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising an antibody heavy chain constant region (CH) which comprises an anti-EGFR heavy chain constant region sequence (e.g., from SEQ ID NO:2 or 4). In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising an antibody heavy chain constant region (CH) which comprises an anti-CD38 heavy chain constant region sequence (e.g., from SEQ ID NO: 7, 9, 11, 13, 14, 15, 16, 17, 18 or 20).
In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising an antibody light chain variable region (VL) which comprises an anti-EGFR light chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:3 or 5. In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising an antibody light chain variable region (VL) which comprises an anti-CD38 light chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:8, 10, 12 or 19.
In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising an antibody light chain constant region (CL) which comprises an anti-EGFR light chain constant region sequence (e.g., from SEQ ID NO:3 or 5). In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising an antibody light chain constant region (CL) which comprises an anti-CD38 light chain constant region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19).
In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising a hinge region having the amino acid sequence of any one or any combination of two or more of: a CD28 hinge sequence (SEQ ID NO:44); a CD8 hinge sequence (SEQ ID NO:45); a long hinge comprising CD28 and CD8 hinge sequences (SEQ ID NO:46); and/or a PDGFR beta hinge sequence (SEQ ID NO:41).
In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising transmembrane region having the amino acid sequence of a CD28 transmembrane sequence (SEQ ID NO:47) or a PDGFR beta transmembrane sequence (SEQ ID NO:42).
In one embodiment, the nucleic acid encodes a precursor polypeptide chain comprising 1 - 3 intracellular signaling sequences in any order and in any combination having the amino acid sequence(s) of: a 4-1BB signaling sequence (SEQ ID NO:48); a CD28 signaling sequence (SEQ ID NO:49); a CD3zeta signaling sequence (SEQ ID NO:50); and/or a CD3zeta short signaling sequence (SEQ ID NO:51).
The present disclosure provides a first nucleic acid encoding a first polypeptide chain and a second nucleic acid encoding a second polypeptide chain (e.g.,
In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising (i) heavy chain leader sequence, (ii) a first masking moiety, (iii) a first peptide linker, (iv) an antibody heavy chain variable region (VH), (v) an antibody heavy chain constant region (CH), (vi) an optional hinge region, (vii) a transmembrane region (TM), and (viii) an intracellular signaling region (e.g.,
In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising (i) a light chain leader sequence, (ii) a second masking moiety, (iii) a second peptide linker, (iv) an antibody light chain variable region (VL) (e.g., kappa or lambda), and (x) an antibody light chain constant region (CL) (e.g.,
In one embodiment, the first peptide linker comprises a first cleavable site. In one embodiment, the second peptide linker comprises a second cleavable site. In one embodiment, the first and second nucleic acids which encode the first and second chains, respectively, comprise recombinant nucleic acid molecules.
In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising (i) light chain leader sequence, (ii) a first masking moiety, (iii) a first peptide linker, (iv) an antibody light chain variable region (VL) (e.g., kappa or lambda), (v) an antibody light chain constant region (CL), (vi) an optional hinge region, (vii) a transmembrane region (TM), and (viii) an intracellular signaling region (e.g.,
In one embodiment, the second nucleic acid encodes (i) a heavy chain leader sequence, (ii) a second masking moiety, (iii) a second peptide linker, (iv) an antibody heavy chain variable region (VH), and (x) an antibody heavy chain constant region (CH) (e.g.,
In one embodiment, the first peptide linker comprises a first cleavable site. In one embodiment, the second peptide linker comprises a second cleavable site. In one embodiment, the first and second nucleic acids which encode the first and second chains, respectively, comprise recombinant nucleic acid molecules.
In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising a first masking moiety comprising a CH1, CL (lambda or kappa) region having the amino acid sequence of SEQ ID NO:21, 22 or 23. In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising a first masking moiety comprising a CH3 (IgG1 or IgG4) region having the amino acid sequence of SEQ ID NO:24, 25, 30 or 31. In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising a first masking moiety comprising a T cell receptor alpha (a) or beta (β) constant region having the amino acid sequence of SEQ ID NO:28 or 29. In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising a first masking moiety comprising a variable heavy chain domain from catalytic antibody 38C2 having the amino acid sequence of SEQ ID NO:26 or 27.
In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising a second masking moiety comprising a CH1, CL (lambda or kappa) region having the amino acid sequence of SEQ ID NO:21, 22 or 23. In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising a second masking moiety comprising a CH3 (IgG1 or IgG4) region having the amino acid sequence of SEQ ID NO:24, 25, 30 or 31. In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising a second masking moiety comprising a T cell receptor alpha (α) or beta (β) constant region having the amino acid sequence of SEQ ID NO:28 or 29. In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising a second masking moiety comprising a variable heavy chain domain from catalytic antibody 38C2 having the amino acid sequence of SEQ ID NO:26 or 27.
In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising a first peptide linker comprising the amino acid sequence of one of SEQ ID NO:32-40 or comprising any one of the amino acid sequences listed in Tables 3-9.
In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising a second peptide linker comprising the amino acid sequence of one of SEQ ID NO:32-40 or comprising any one of the amino acid sequences listed in Tables 3-9.
In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising an antibody heavy chain variable region (VH) which comprises an anti-EGFR heavy chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:2 or 4. In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising an antibody heavy chain variable region (VH) which comprises an anti-CD38 heavy chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18 or 20.
In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising an antibody light chain variable region (VL) which comprises an anti-EGFR light chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:3 or 5. In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising an antibody light chain variable region (VL) which comprises an anti-CD38 light chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:8, 10, 12 or 19.
In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising an antibody light chain variable region (VL) which comprises an anti-EGFR light chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:3 or 5. In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising an antibody light chain variable region (VL) which comprises an anti-CD38 light chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:8, 10, 12 or 19.
In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising an antibody heavy chain variable region (VH) which comprises an anti-EGFR heavy chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:2 or 4. In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising an antibody heavy chain variable region (VH) which comprises an anti-CD38 heavy chain variable region sequence having an amino acid sequence having at least 92%, or at least 93%, or at least 94%, or at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% sequence identity, or having 100% sequence identity, to a portion or full-length of SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18 or 20.
In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising an antibody heavy chain constant region (CH) which comprises an anti-EGFR heavy chain constant region sequence (e.g., from SEQ ID NO:2 or 4). In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising an antibody heavy chain constant region (CH) which comprises an anti-CD38 heavy chain constant region sequence (e.g., from SEQ ID NO: 7, 9, 11, 13, 14, 15, 16, 17, 18 or 20).
In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising an antibody light chain constant region (CL) which comprises an anti-EGFR light chain constant region sequence (e.g., from SEQ ID NO:3 or 5). In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising an antibody light chain constant region (CL) which comprises an anti-CD38 light chain constant region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19).
In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising an antibody light chain constant region (CL) which comprises an anti-EGFR light chain constant region sequence (e.g., from SEQ ID NO:3 or 5). In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising an antibody light chain constant region (CL) which comprises an anti-CD38 light chain constant region sequence (e.g., from SEQ ID NO:8, 10, 12 or 19).
In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising an antibody heavy chain constant region (CH) which comprises an anti-EGFR heavy chain constant region sequence (e.g., from SEQ ID NO:2 or 4). In one embodiment, the second nucleic acid encodes the second polypeptide chain comprising an antibody heavy chain constant region (CH) which comprises an anti-CD38 heavy chain constant region sequence (e.g., from SEQ ID NO: 7, 9, 11, 13, 14, 15, 16, 17, 18 or 20).
In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising a hinge region having the amino acid sequence of any one or any combination of two or more of: a CD28 hinge sequence (SEQ ID NO:44); a CD8 hinge sequence (SEQ ID NO:45); a long hinge comprising CD28 and CD8 hinge sequences (SEQ ID NO:46); and/or a PDGFR beta hinge sequence (SEQ ID NO:41).
In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising a transmembrane region having the amino acid sequence of a CD28 transmembrane sequence (SEQ ID NO:47) or a PDGFR beta transmembrane sequence (SEQ ID NO:42).
In one embodiment, the first nucleic acid encodes the first polypeptide chain comprising 1-3 intracellular signaling sequences in any order and in any combination having the amino acid sequence(s) of: a 4-1BB signaling sequence (SEQ ID NO:48); a CD28 signaling sequence (SEQ ID NO:49); a CD3zeta signaling sequence (SEQ ID NO:50); and/or a CD3zeta short signaling sequence (SEQ ID NO:51).
The present disclosure provides vectors, including expression vectors, that are operably joined to nucleic acids encoding a precursor polypeptide of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, the expression vector comprises one or more regulatory sequences (e.g., promoter and/or enhancer) that control transcription of the nucleic acids encoding any of the precursor polypeptides of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR). In one embodiment, the expression vector comprises one or more regulatory sequences each operably joined to a nucleic acid encoding the precursor polypeptide.
In one embodiment, an expression vector is introduced into a host cell, wherein the expression vector within the host cell carries a promoter (and optionally an enhancer sequence), that is operably joined to a nucleic acid encoding a precursor polypeptide. Thus, the host cell can express (transcription and translation) the encoded precursor polypeptide that makes up any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) described herein.
In one embodiment, the precursor polypeptide can be processed by cleaving the precursor polypeptide at the self-cleaving sequence to release the first and second polypeptide chains and secreting the precursor, and/or anchoring the precursor in the cellular membrane of the host cell. In one embodiment, the precursor polypeptide can be cleaved at the self-cleaving sequence thereby generating first and second polypeptide chains each having a leader signal sequence at their N-terminal ends.
In one embodiment, after release of the first and second polypeptide chains, the first and second polypeptide chains can dimerize (assemble) via at least one disulfide bond between the antibody heavy chain constant region and the antibody light chain constant region.
The vectors comprise promoters that are inducible or constitutive promoters. The vectors and host cells can be selected to generate transgenic host cells that transiently or stably express any of the precursor polypeptides described herein.
The expression vector can include nucleic acid backbone sequences derived from a retrovirus, lentivirus or adenovirus. The expression vectors can include one or more regulatory sequences, such as inducible and/or constitutive promoters and enhancers. The expression vectors can include ribosomal binding sites and/or polyadenylation sites.
In one embodiment, the expression vector, which is operably linked to the nucleic acid encoding the dimeric antigen receptor (DAR) construct, can direct production of the dimeric antigen receptor (DAR) construct which can be displayed on the surface of the transgenic host cell or the dimeric antigen receptor can be secreted into the cell culture medium.
The present disclosure provides vectors that are operably joined to nucleic acids encoding a first polypeptide chain and/or encoding a second polypeptide chain, wherein the first and second polypeptide chains associate/dimerize with each other to form an the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, a first vector (e.g., a first expression vector) is operably joined to a first nucleic acid encoding a first polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, a second vector (e.g., a second expression vector) is operably joined to a second nucleic acid encoding a second polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, a first vector (e.g., a first expression vector) that is operably joined to a first nucleic acid encoding a first polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR), and the first vector is also operably joined to a second nucleic acid encoding a second polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, the expression vector comprises one or more regulatory sequences (e.g., promoter and/or enhancer) that control transcription of the nucleic acids encoding any of the precursor polypeptides of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR). In one embodiment, the expression vector comprises one or more regulatory sequences each operably joined to a nucleic acid encoding the precursor polypeptide.
In one embodiment, an expression vector is introduced into a host cell, wherein the expression vector within the host cell carries a promoter (and optionally an enhancer sequence), that is operably joined to a nucleic acid encoding a precursor polypeptide. Thus, the host cell can express (transcription and translation) the encoded precursor polypeptide that makes up any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) described herein.
In one embodiment, after expression of the first and second polypeptide chains, the first and second polypeptide chains can dimerize (assemble) via at least one disulfide bond between the antibody heavy chain constant region and the antibody light chain constant region (e.g.,
The vectors comprise promoters that are inducible or constitutive promoters. The vectors and host cells can be selected to generate transgenic host cells that transiently or stably express any of the precursor polypeptides described herein.
The expression vector can include nucleic acid backbone sequences derived from a retrovirus, lentivirus or adenovirus. The expression vectors can include one or more regulatory sequences, such as inducible and/or constitutive promoters and enhancers. The expression vectors can include ribosomal binding sites and/or polyadenylation sites.
In one embodiment, the expression vector, which is operably linked to the nucleic acid encoding the dimeric antigen receptor (DAR) construct, can direct production of the dimeric antigen receptor (DAR) construct which can be displayed on the surface of the transgenic host cell or the dimeric antigen receptor can be secreted into the cell culture medium.
The present disclosure provides a host cell, or a population of host cells, that harbor one or more expression vectors that are operably joined to any of the nucleic acids that encode the first and/or second polypeptide chains that can associate/dimerize with each other to become an activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, a first host cell, or a population of first host cells, harbors a first vector (e.g., a first expression vector) which is operably joined to a first nucleic acid encoding a first polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, a second host cell, or a population of second host cells, harbors a second vector (e.g., a second expression vector) which is operably joined to a second nucleic acid encoding a second polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, a first host cell, or a population of first host cells, harbors a first vector (e.g., a first expression vector) which is operably joined to a first nucleic acid encoding a first polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR), and the first host cell or the population of first host cells also harbors a second vector which is operably joined to a second nucleic acid encoding a second polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, a first host cell, or a population of first host cells, harbors a first vector (e.g., a first expression vector) which is operably joined to a first nucleic acid encoding a first polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR), and the first vector is also operably joined to a second nucleic acid encoding a second polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
The host cell can be a bacterial or mammalian cell. In one embodiment, the host cell comprises a Chinese hamster ovary (CHO) cell. The host cell or the population of host cells include T lymphocytes (e.g., T cells, regulatory T cells, gamma-delta T cells, and cytotoxic T cells), NK (natural killer) cells, macrophages, dendritic cells, mast cells, eosinophils, B lymphocytes, monocytes. In one embodiment, the NK cells comprise cord blood-derived NK cells, or placental derived NK cells.
In one embodiment, the first expression vector is introduced into the first host cell or the population of the first host cell, wherein the first expression vector is operably linked to a first nucleic acid encoding the first polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, the second expression vector is introduced into the second host cell or the population of the second host cell, wherein the second expression vector is operably linked to a second nucleic acid encoding the second polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, the first and the second expression vectors are introduced into the first host cell or the population of the first host cell, wherein the first expression vector is operably linked to a first nucleic acid encoding the first polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR), and wherein the second expression vector is operably linked to a second nucleic acid encoding the second polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, the first expression vector is introduced into the first host cell or the population of the first host cell, wherein the first expression vector is operably linked to a first nucleic acid encoding the first polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR), and wherein the first expression vector is also operably linked to a second nucleic acid encoding the second polypeptide chain of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, at least one expression vector is introduced into the host cell via lipofection (e.g., using a lipid surfactant); electroporation; transfection employing calcium chloride, rubidium chloride, calcium phosphate, DEAE-dextran, or other substances; viral transfection; non-viral transfection; microprojectile bombardment; and infection (e.g., where the vector is an infectious agent).
The present disclosure provide methods for preparing any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) described herein, including the second and third generation DAR constructs, and including the Versions V1, V2a, V2b, V2c, V3 and V4 DAR constructs, and including any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) that can bind EGFR or CD38. Methods for preparing the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) comprise: culturing a population of host cells, wherein individual host cells in the population harbor an expression vector that is operably linked to a first and/or a second nucleic acid encoding a first and/or second polypeptide chain described herein, wherein the culturing is conducted under conditions suitable for expressing the first and/or second polypeptide by the population of host cells.
In one embodiment, the nucleic acids encoding the first and/or second polypeptide chain further encodes a light chain and/or heavy chain leader sequence for secretion of the expressed first and/or second polypeptides by the host cell. In one embodiment, the culturing is conducted under conditions suitable for secretion of the first and/or second polypeptide by the population of host cells.
In one embodiment, the nucleic acids encoding the first and/or second polypeptide further encodes an affinity tag sequence for enriching the expressed polypeptides. Exemplary affinity tag sequences include histidine tag, FLAG tag, myc tag, HA tag, and GST tag.
In one embodiment, the methods for preparing any of the activatable masked antigen binding proteins comprising an IgG type antibody described herein further comprise isolating the expressed heavy chains and/or light chains.
In one embodiment, the culturing is conducted under conditions that are suitable for assembly or association of the heavy chain and light chain to form the activatable masked antigen binding proteins comprising an IgG type antibody.
In one embodiment, the method for preparing any of the activatable masked antigen binding proteins comprising a DAR type antibody described herein further comprises isolating the expressed precursor DAR polypeptides. In one embodiment, the method for preparing any of the activatable masked antigen binding proteins comprising a DAR type antibody described herein further comprises isolating the processed/cleaved/assembled polypeptides that form the dimeric antigen receptors (DAR).
In one embodiment, the culturing is conducted under conditions that are suitable for expression, secretion and cleavage of the precursor DAR polypeptide, and assembly of the two resulting polypeptide chains (first and second polypeptide chains) to form the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, the method for preparing any of the activatable masked antigen binding proteins comprising a DAR type antibody described herein further comprises isolating the expressed first and/or second polypeptides. In one embodiment, the method for preparing any of the activatable masked antigen binding proteins comprising a DAR type antibody described herein further comprises isolating the dimeric antigen receptors (DAR) which is formed by association/dimerization of the first and second Dar polypeptide chains.
In one embodiment, the culturing is conducted under conditions that are suitable for expression of the first and/or second polypeptide chains, and assembly of the first and second polypeptide chains to form the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR).
In one embodiment, the method further comprises isolating or recovering the assembled activatable masked antigen binding proteins comprising the dimeric antigen receptor (DAR). In one embodiment, the isolating is conducted using affinity chromatography. In one embodiment, the isolating is conducted using affinity chromatography with protein A or G from Staphylococcus aureus, glutathione S-transferase (GST), or immuno-affinity. In one embodiment, one or more additional isolating steps are conducted which includes cation exchange, anion exchange chromatography, hydrophobic interaction chromatography, mixed mode chromatography and/or hydroxyapatite chromatography.
In one embodiment, the assembled activatable masked antigen binding proteins comprising the dimeric antigen receptor (DAR) comprises a first and a second polypeptide chain, wherein the (a) first polypeptide chain comprises: (i) a first masking moiety, (ii) a first peptide linker, (iii) an antibody heavy chain variable region (VH), (iv) an antibody heavy chain constant region (CH), (v) an optional hinge region, (vi) a transmembrane region (TM), and (vii) an intracellular signaling region, wherein the (b) second polypeptide chain comprises: (i) a second masking moiety, (ii) a second peptide linker, (iii) an antibody light chain variable region (VL) (e.g., kappa or lambda), and (iv) an antibody light chain constant region (CL), wherein the antibody heavy chain variable region (VH) and the antibody light chain variable region (VL) form an antigen binding domain that binds a target antigen.
In one embodiment, the assembled activatable masked antigen binding proteins comprising the dimeric antigen receptor (DAR) comprises a first and a second polypeptide chain, wherein the (a) first polypeptide chain comprises: (i) a first masking moiety, (ii) a first peptide linker, (iii) an antibody light chain variable region (VL) (e.g., kappa or lambda), (iv) an antibody light chain constant region (CL), (v) an optional hinge region, (vi) a transmembrane region (TM), and (vii) an intracellular signaling region, wherein the (b) second polypeptide chain comprises: (i) a second masking moiety, (ii) a second peptide linker, (iii) an antibody heavy chain variable region (VH), and (iv) an antibody heavy chain constant region (CH), wherein the antibody heavy chain variable region (VH) and the antibody light chain variable region (VL) form an antigen binding domain that binds a target antigen.
The activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) can be prepared using transgenic host cell expression, phage display, yeast display and human antibody gene transgenic mice using methods that are well known in the art. In one embodiment, the yield of antigen binding proteins using transgenic host cell expression can be about 20-80%, or about 30-90%, or about 40-95%, or about 50-99% of the total activatable masked antigen binding proteins formed.
The present disclosure provide methods for cleaving at least one peptide linker of any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) described herein, the method comprising: (a) contacting at least one protease with an activatable masked antigen binding protein DAR in an inactive form, wherein the first and second peptide linkers are in the un-cleaved state.
In one embodiment, the activatable masked antigen binding protein is contacted with an one or any combination of two or more proteases selected from: a matrix metalloprotease (MMP), MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase), a disintegrin and metalloproteinase (ADAM) protease, ADAM10, ADAM12, ADAM17, urokinase plasminogen activator (uPA), serine proteases, cysteine proteases, aspartate proteases, threonine proteases, cathepsins (e.g., cysteine or aspartic cathepsins), cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K or cathepsin L.
In one embodiment, the activatable masked antigen binding protein is contacted essentially simultaneously (at the same time) with two or more proteases, or sequentially contacted with two or more proteases in any order.
In one embodiment, at least one of the peptide linkers of the activatable masked antigen binding protein used in step (a) comprises a cleavable site that is cleavable with one or more proteases, including a matrix metalloprotease (MMP), MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase), a disintegrin and metalloproteinase (ADAM) protease, ADAM10, ADAM12, ADAM17, urokinase plasminogen activator (uPA), serine proteases, cysteine proteases, aspartate proteases, threonine proteases, cathepsins (e.g., cysteine or aspartic cathepsins), cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K or cathepsin L.
In one embodiment, the method further comprises: (b) cleaving at least one of the peptide linkers to convert the un-cleaved activatable masked antigen binding protein to an activated form. In one embodiment, the activated form can bind a target antigen.
In one embodiment, the method further comprises: (c) binding the activatable masked antigen binding protein (now in the activated state) to a target antigen.
In one embodiment, the steps of contacting, cleaving and binding are conducted in an in vitro or in vivo condition.
In one embodiment, the target antigen comprises a soluble antigen or a surface antigen. In one embodiment, the target antigen is expressed by a healthy or diseased cell.
In one embodiment, the diseased cell (e.g., tumor or cancer cell) that expresses the target antigen also expresses one or more proteases that cleaves the peptide linker. In one embodiment, the diseased cell expresses one or a combination of two or more proteases comprising a matrix metalloprotease (MMP), MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase), a disintegrin and metalloproteinase (ADAM) protease, ADAM10, ADAM12, ADAM17, urokinase plasminogen activator (uPA), serine proteases, cysteine proteases, aspartate proteases, threonine proteases, cathepsins (e.g., cysteine or aspartic cathepsins), cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K and/or cathepsin L.
In one embodiment, method further comprises: (d) killing the diseased cell (e.g., tumor or cancer cell) by binding the activated masked antigen binding protein to the diseased cell.
In one embodiment, at least one of the peptide linkers is cleavable with a protease that is present in a tumor microenvironment.
In one embodiment, the tumor microenvironment comprise a protease selected from a group consisting of a matrix metalloprotease (MMP), MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase), a disintegrin and metalloproteinase (ADAM) protease, ADAM10, ADAM12, ADAM17, urokinase plasminogen activator (uPA), serine proteases, cysteine proteases, aspartate proteases, threonine proteases, cathepsins (e.g., cysteine or aspartic cathepsins), cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K and cathepsin L.
The present disclosure provide methods treating a subject having a disease associated with expression or over-expression of a tumor-associated antigen, the method comprising: administering to the subject an effective amount of a therapeutic composition comprising a population of host cells expressing any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) described herein. In one embodiment, the population of host cells express the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) in an inactive form having the first and second peptide linkers in the un-cleaved state (e.g., activatable). In one embodiment, the population of host cells can express any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR), including the second and third generation DAR constructs, and including the Versions V1,V2a, V2b, V2c, V3 and V4 DAR constructs, and including any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) that can bind EGFR or CD38. In one embodiment, the population of host cells that express any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) described herein are administered to the subject in an amount that is sufficient to effect a measurable improvement or prevention of a disease or disorder associated with tumor or cancer antigen expression.
In one embodiment, the host cell or population of host cells used to treat the subject are autologous and are derived from the subject receiving the treatment. In one embodiment, whole blood can be obtained from the subject and the desired cells (e.g., T lymphocytes, NK cells or macrophages) can be recovered from the whole blood.
In one embodiment, the host cell or population of host cells used to treat the subject are allogenic and are derived from a different subject. Allogenic cells can be obtained from whole blood from a different subject in the same manner employed for the autologous cells. In one embodiment, the allogenic cells are derived from placenta or chord tissue after pregnancy.
In one embodiment, the desired cells are obtained from the subject to receive treatment, or from a different subject, and are engineered to harbor one or more expression vectors that direct expression of any of the first or second polypeptides, or the precursor polypeptides, thereby generating transgenic host cells. The transgenic host cells can express the first or second polypeptides, or the precursor polypeptide. The host cells can express the first and second polypeptide chains which dimerize to form a dimeric antigen receptor that binds specifically to the tumor antigen in the subject. The host cells can express the precursor polypeptide chain which can be cleaved to form first and second polypeptide chains that dimerize to form a dimeric antigen receptor that binds specifically to the tumor antigen in the subject. The transgenic host cells (e.g., harboring the expression vector(s) or expressing the polypeptide chains) can be administered to the subject to treat the disease, disorder or condition associated with over- expression of a tumor antigen.
The present disclosure provides a method of treating a subject having a disease, disorder or condition associated with detrimental expression of a tumor antigen, wherein the disorder is cancer, including, but not limited to hematologic cancer, breast cancer, ovarian cancer, prostate cancer, head and neck cancer, lung cancer, bladder cancer, melanoma, colorectal cancer, pancreatic cancer, lung cancer, liver cancer, renal cancer, esophageal cancer, leiomyoma, leiomyosarcoma, glioma, and glioblastoma, wherein the method for treating the subject comprises administering to the subject an effective amount of a therapeutic composition comprising a population of host cells expressing any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) described herein.
In one embodiment, the cancer is a hematologic cancer selected from the group consisting of non-Hodgkin’s lymphoma (NHL), Burkitt’s lymphoma (BL), B chronic lymphocytic leukemia (B-CLL), B and T acute lymphocytic leukemia (ALL), T cell lymphoma (TCL), acute myeloid leukemia (AML), hairy cell leukemia (HCL), Hodgkin’s Lymphoma (HL), chronic myeloid leukemia (CML) and multiple myeloma (MM).
The present disclosure provides an in vitro cleavage-based method to detect protease activity and specificity for detecting, diagnosing, monitoring and/or staging a diseased tissue such as a cancer or tumor. A tumor or cancer mass can be extracted from a subject and contacted with one or any combination of two or more activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) described herein, each having at least one peptide linker with a known protease cleavage profile. The tumor or cancer mass from the subject produces one or more proteases. The method comprises: (a) contacting the diseased tissue with one or more activatable masked antigen binding proteins under conditions suitable for a protease(s) to cleave at least one peptide linker on the activatable masked antigen binding protein(s) to generate a cleaved peptide product. The method further comprises: (b) detecting the cleaved peptide product, for example using any method. Thus, the type of protease produced by the tumor or cancer mass can be identified. In one embodiment, the diseased tissue is contacted with one or more of an activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR), including the second and third generation DAR constructs, and including the Versions V1,V2a, V2b, V2c, V3 and V4 DAR constructs, and including any of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) that can bind EGFR or CD38.
In one embodiment, the peptide linker is cleavable with any one or any combination of two or more protease selected from a group consisting of a matrix metalloprotease (MMP), MMP1, MMP2, MMP3, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase), ADAM protease, urokinase plasminogen activator (uPA), serine proteases, cysteine proteases, aspartate proteases, threonine proteases, cathepsins (e.g., cysteine or aspartic cathepsins), cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K and cathepsin L.
The present disclosure provides a method for detecting the presence of a protease produced by a tumor from a subject, the method comprising: (a) contacting (i) a tumor obtained from the subject with (ii) at least one of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) described herein, wherein the tumor sample produces a protease.
In one embodiment, the first peptide linker includes a first cleavable site and the second peptide linker includes a second cleavable site. In one embodiment, the amino acid sequence of the first and/or second cleavable sites may or may not be a substrate for cleavage by the protease produced by the tumor sample. In one embodiment, the contacting in step (a) is performed under conditions suitable for the protease to cleave the first and/or second cleavable site to generate one or more cleavage products when the protease cleaves the first and/or second cleavable site.
In one embodiment, the method further comprises: (b) detecting the first and/or second cleavage product. In one embodiment, the method further comprises: (c) identifying the type of protease produced by the tumor from the subject by detecting the first and/or second cleavage product and correlating any of the cleavage products with the amino acid sequence of the first and/or second cleavable site.
In one embodiment, by identifying the type of protease produced by the tumor in the subject, the cancer in the subject can be diagnosed. In one embodiment, the first and/or second cleavage product can be detected by gel electrophoresis, Western blot analysis, immunology, immunohistochemistry, colorimetrically, spectrophotometrically, mass spectrometry, liquid chromatography, or by any combination thereof. In one embodiment, the tumor or cancer mass can be obtained from a prostate, breast, ovary, head and neck, bladder, skin, colorectal, anus, rectum, pancreas, lung (including non-small cell lung and small cell lung cancers), leiomyoma, brain, glioma, glioblastoma, esophagus, liver, kidney, stomach, colon, cervix, uterus, endometrium, vulva, larynx, vagina, bone, nasal cavity, paranasal sinus, nasopharynx, oral cavity, oropharynx, larynx, hypolarynx, salivary glands, ureter, urethra, penis, and testis. In one embodiment, the subject is a human, non-human primate, simian, ape, murine (e.g., mice and rats), bovine, porcine, equine, canine, feline, caprine, lupine, ranine or piscine. In one embodiment, the in vitro cleavage-based method can be used for detecting, diagnosing, monitoring and/or staging a cancer in the subject.
The present disclosure provides a kit comprising: at least one of the activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR), and/or at least one nucleic acid encoding a precursor polypeptide that can be cleaved and assembled to become an activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR). In one embodiment, the kit includes at least one of: a second or third generation DAR constructs, a Version V1,V2a, V2b, V2c, V3 or V4 DAR construct, and/or an activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) that can bind EGFR or CD38. In one embodiment, the kit comprises one or more adjunct compounds selected from a group consisting of Tris, phosphate, carbonate, stabilizers, excipients, biocides and bovine serum albumin. In one embodiment, the kit comprises one or more adjunct compounds selected from a group consisting of Tris, phosphate, carbonate, stabilizers, excipients, biocides and bovine serum albumin. In one embodiment, the kit comprises one container which contains at least one activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) (or nucleic acid encoding the protein thereof) and optionally one or more adjunct compound. In one embodiment, the kit comprises two or more containers, wherein one container contains at least one activatable masked antigen binding proteins comprising a dimeric antigen receptor (DAR) (or nucleic acid encoding the protein thereof) and a separate container contains one or more adjunct compounds.
The present disclosure provides any of the activatable masked antigen binding proteins described herein, including the IgG class antibodies, bispecific antibodies and dimeric antigen receptors (DARs), comprising paired hetero-dimeric masking moieties having amino acid sequences from Table 1. In one embodiment, the activatable masked antigen binding proteins comprising the IgG class antibodies or bispecific antibodies have first and second and/or third and fourth masking moieties having the amino acid sequence of any of the paired masking moieties listed in Table 1 below. In one embodiment, the activatable masked antigen binding proteins comprising the dimeric antigen receptor (DAR) comprise first and second masking moieties having the amino acid sequence of any of the paired masking moieties listed in Table 1.
L
VKGFYPSDIAVEWESNGQPENNYKTT
The present disclosure provides any of the activatable masked antigen binding proteins described herein, including the IgG class antibodies, bispecific antibodies and dimeric antigen receptors (DARs), comprising paired homo-dimeric masking moieties having amino acid sequences from Table 2. In one embodiment, the activatable masked antigen binding proteins comprising the IgG class antibodies or bispecific antibodies have first and second and/or third and fourth masking moieties having the amino acid sequence of any of the paired masking moieties listed in Table 2 below. In one embodiment, the activatable masked antigen binding proteins comprising the dimeric antigen receptor (DAR) comprise first and second masking moieties having the amino acid sequence of any of the paired masking moieties listed in Table 2.
The present disclosure provides any activatable masked antigen binding proteins described herein, including the IgG class antibodies, bispecific antibodies and dimeric antigen receptors (DARs), comprising at least first and/or second peptide linkers, and optionally further comprising third and/or fourth peptide linkers, carrying a cleavable site. In one embodiment, the cleavable site is cleavable with a cleaving condition which includes a protease, esterase, reductive condition, or oxidative condition. In one embodiment, the cleavable site is cleavable with a protease that is present in a tumor microenvironment or is cleavable with a reductive or oxidative condition that is present in a tumor microenvironment (Rakashanda et al., 2012 Biotechnology and Molecular Biology Review 7(4):90-101). In one embodiment, the cleaving condition comprises one protease or any combination of two or more proteases, including serine proteases, cysteine proteases, aspartate proteases, threonine proteases, glutamic acid proteases, metalloproteases, asparagine peptide lyases, serum proteases, matrix metalloproteinase (MMP), MMP1, MMP2, MMP3, MMP7, MMP8, MMP9, MMP11, MMP13, MMP14, MT1-MMP (membrane type 1 matrix metalloproteinase), urokinase plasminogen activator (uPA), enterokinase, prostate-specific antigen (PSA, hK3), interleukin-ḯβ converting enzyme, thrombin, FAP (FAP-a), dipeptidyl peptidase, meprins, granzymes (e.g., granzyme B), dipeptidyl peptidase IV (DPPIV/CD26), a disintegrin and metalloproteinase (e.g., ADAM proteases), ADAM10, ADAM12, ADAM17, hepsin, cathepsins (e.g., cysteine or aspartic cathepsins), cathepsin B, cathepsin C, cathepsin D, cathepsin E, cathepsin K, cathepsin L, kallikreins, hKl, hK10, hK15, plasmin, collagenase, Type IV collagenase, stromelysin, lysosomal enzyme, Factor Xa, chymotrypsin-like protease, trypsin-like protease, elastase- like protease, subtili sin-like protease, actinidain, bromelain, calpain, caspases, caspase-1, caspase-2, caspase-3, caspase-8, caspase-9, caspase-10, caspase-11, caspase-12, caspase-13, caspase-14, herpes simplex virus protease, HIV protease, CMV protease, Mirl- CP, papain, HIV-1 protease, HSV protease, CMV protease, chymosin, renin, pepsin, matriptase (e.g., matriptase 2, human ST14, or TMPRSS6), legumain, plasmepsin, nepenthesin, metalloexopeptidases, and/or metalloendopeptidases.
In one embodiment, the peptide linker comprises a cleavable site having an amino acid sequence that is at least 95%, or at least 96%, or at least 97%, or at least 98%, or at least 99% identical to a peptide that is cleavable with a matrix metalloprotease protease, for example the amino acid sequence of GGSGSGSGGSSGGGSGGGGS, TSGSGGSGGSV, TSGSGGSPLGMGGSGSV, TSGSGGSPLGVGGSGSV, TSGSGGSPAALGGSGSV, TSGSGGSPAGLGGSGSV, TSGSGGSPLGMVGV, TSGSGGSPLGVVGV, TSGSGGSPAALVGV, TSGSGGSPAGLVGV, TSGSGGSPLGMVLV, TSGSGGSPLGVVLV, TSGSGGSPAALVLV or TSGSGGSPAGLVLV.
In one embodiment, the cleavable site comprises the amino acid sequence LEATA which is recognized and cleaved by MMP9. In one embodiment, the cleavable site comprises the amino acid sequence PR(S/T)(L/I)(S/T) which is recognized and cleaved by MMP9. In one embodiment, the cleavable site comprises the amino acid sequence SGSGGSPLGMGGSGSVD, SGSGGSPAGLGGSCSVD, or SGSGGSPAGLVGVD. In one embodiment, the cleavable site comprises the amino acid sequence GGAANLVRGG which is recognized and cleaved by MMP11.
The present disclosure provides any activatable masked antigen binding proteins described herein, including the IgG class antibodies, bispecific antibodies and dimeric antigen receptors (DARs), comprising at least a first and/or second peptide linker, and optionally further comprising a third and/or fourth peptide linker, carrying a cleavable site having an amino acid sequence according to any of the peptide linkers listed in Table 3, 4, 5, 6, 7, 8 and/or 9.
The present disclosure provides any activatable masked antigen binding proteins described herein, including the dimeric antigen receptors (DARs), wherein the hinge region comprises any one or any combination of two or more regions comprising an upper, core or lower hinge sequences from an IgG1, IgG2, IgG3 or IgG4 immunoglobulin molecule. In one embodiment, the hinge region comprises an IgG1 upper hinge sequence EPKSCDKTHT. In one embodiment, the hinge region comprises an IgG1 core hinge sequence CPXC, wherein X is P, R or S. In one embodiment, the hinge region comprises a lower hinge/CH2 sequence PAPELLGGP. In one embodiment, the hinge is joined to an Fc region (CH2) having the amino acid sequence SVFLFPPKPKDT. In one embodiment, the hinge region includes the amino acid sequence of an upper, core and lower hinge and comprises EPKSCDKTHTCPPCPAP ELLGGP. In one embodiment, the hinge region comprises one, two, three or more cysteines that can form at least one, two, three or more interchain disulfide bonds.
The present disclosure provides any activatable masked antigen binding proteins described herein, including the IgG class antibodies, bispecific antibodies and dimeric antigen receptors (DARs), wherein the first, second, third and/or fourth peptide linker permits dimerization of the paired masking moieties (e.g., dimerization of first and second masking moieties, and/or dimerization of third and fourth masking moieties). In one embodiment, any of the peptide linkers have a length of 1-50 amino acids which optionally can include at least one amino acid analog. In one embodiment, at least one of the linkers is a flexible linker and comprises predominantly any combination of two or more amino acids glycine, serine, alanine and/or threonine. In one embodiment, at least one of the peptide linkers comprise at least one and up to four polymers of glycine-alanine, or alanine-serine, or other flexible linkers sequences. In one embodiment, at least one of the peptide linkers comprise an amino acid sequence selected from a group consisting of: (SG)n, (SGG)n, (SGGG)n, (SSG)n, (GS)n, (GGG)n, (GSGGS)n, (GSG)n, (GGGGS)n, (GGGS)n, (GGGGSGS)n, (GGSGGGSGG)n, (GGGGSGGS)n, and (GGS)n, where n is an integer of 1-6. In one embodiment, at least one of the peptide linkers comprise an amino acid sequence selected from a group consisting of: AKTTPKLEEGEFSEAR, AKTTPKLEEGEFSEARV, AKTTPKLGG, SAKTTPKLGG, AKTTPKLEEGEFSEARV, SAKTTP, SAKTTPKLGG, RADAAP, RADAAPTVS, RADAAAAGGPGS, RADAAAA(G4S)4 SAKTTP, SAKTTPKLGG, SAKTTPKLEEGEFSEARV, ADAAP, ADAAPTVSIFPP, TVAAP, TVAAPSVFIFPP, QPKAAP, QPKAAPSVTLFPP, AKTTPP, AKTTPPSVTPLAP, AKTTAP, AKTTAPSVYPLAP, ASTKGP, ASTKGPSVFPLAP, GENKVEYAPALMALS, GPAKELTPLKEAKVS and GHEAAAVMQVQYPAS.
The present disclosure provides any activatable masked antigen binding proteins described herein, including the IgG class antibodies, bispecific antibodies and dimeric antigen receptors (DARs), that bind an epitope or an antigen from a human. In one embodiment, the activatable masked antigen binding proteins binds an epitope or an antigen from a human and can bind (e.g., cross-react) with an epitope or antigen (e.g., homologous antigen) from any one or any combination of non-human animals such as dog, cat, mouse, rat, goat, rabbit, hamster and/or monkey (e.g., cynomolgus, rhesus or macaque). In one embodiment, the activatable masked antigen binding proteins bind an EFGR antigen comprising the amino acid sequence of SEQ ID NO:1.
The present disclosure provides any activatable masked antigen binding proteins described herein, including the IgG class antibodies, bispecific antibodies and dimeric antigen receptors (DARs), that bind an EGFR antigen, wherein the activatable masked antigen binding proteins comprises an antibody heavy chain having the amino acid sequence of SEQ ID NO:2 or 4, and comprising an antibody light chain having the amino acid sequence of SEQ ID NO:3 or 5, in any heavy/light chain combination. In one embodiment, the heavy chain variable region of SEQ ID NO:2 and 4 is underlined. In one embodiment, the light chain variable region of SEQ ID NO:3 and 5 is underlined.
QVQLKQSGPGLVQPSQSLSITCTVSGFSLTNYGVHWVRQSPGKGLEWLGV IWSGGNTDYNTPETSRLSINKDNSKSQVFFKMNSLQSNDTAIYYCARALT YYDYEFAYWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKD
DILLTQSPVILSVSPGERVSFSCRASQSIGTNIHWYQQRTNGSPRLLIKY ASESISGIPSRFGSGSGTDFTLSINSVESEDIADYYCQQNNNWPTTFGAG TKLELKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVD
QVQLKQSGPGLVQPSQSLSITCTVSGFSLTNYGVHWVRQSPGKGLEWLGV IWSGGNTDYNTPETSRLSINKDNSKSQVFFKMNSLQSNDTAIYYCARALT YYDYEFAYWGQGTLVTVSAASTKGPSVFPLAPSSKSTSGGTAALGCLVKD
DILLTQSPVILSVSPGERVSFSCRASQSIGTNIHWYQQRTNGSPRLLIKY ASESISGIPSRFSGSGSGTDFTLSINSVESEDIADYYCQQNNNWPTTFGA GTKLELKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKV
The present disclosure provides any activatable masked antigen binding proteins described herein, including the IgG class antibodies, bispecific antibodies and dimeric antigen receptors (DARs), that bind an epitope or an antigen from a human. In one embodiment, the activatable masked antigen binding proteins binds an epitope or an antigen from a human and can bind (e.g., cross-react) with an epitope or antigen (e.g., homologous antigen) from any one or any combination of non-human animals such as dog, cat, mouse, rat, goat, rabbit, hamster and/or monkey (e.g., cynomolgus, rhesus or macaque). In one embodiment, the activatable masked antigen binding proteins bind a CD38 antigen comprising the amino acid sequence of SEQ ID NO:6.
The present disclosure provides any activatable masked antigen binding proteins described herein, including the IgG class antibodies, bispecific antibodies and dimeric antigen receptors (DARs), that bind a CD38 antigen, wherein the activatable masked antigen binding proteins comprises an antibody heavy chain having the amino acid sequence of SEQ ID NO:7, 9, 11, 13, 14, 15, 16, 17, 18, or 20, and comprising an antibody light chain having the amino acid sequence of SEQ ID NO:8, 10, 12 or 19, in any heavy/light chain combination (see Table 10 below). In one embodiment, the heavy chain variable region of SEQ ID NO:7 is underlined. In one embodiment, the light chain variable region of SEQ ID NO:8 is underlined.
QVQLVESGGGLVKPGGSLRLSCAASGFTFSDDYMSWIRQAPGKGLEWVAS VSNGRPTTYYADSVRGRFTISRDNAKNSLYLQMNSLRAEDTAVYYCARED WGGEFTDWGQGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDY
QAGLTQPPSASGTSGQRVTISCSGSSSNIGINFVYWYQHLPGTAPKLLIY KNNQRPSGVPDRFSGSKSGNSASLAISGLRSEDEADYYCAAWDDSLSGYV FGSGTKVTVLGQPKAAPSVTLFPPSSEELQANKATLVCLISDFYPGAVTV
The following examples are meant to be illustrative and can be used to further understand embodiments of the present disclosure and should not be construed as limiting the scope of the present teachings in any way.
Various activatable masked IgG type antibodies that bind EGFR or CD3 8 antigens were prepared which comprises a first heavy chain variable region and a first light chain variable region, wherein (i) the N-terminal end of the first heavy chain variable region is joined to a first masking moiety via a first peptide linker having a first cleavable site, and (ii) the N-terminal end of the first light chain variable region is joined to a second masking moiety via a second peptide linker having a second cleavable site, and (iii) the first and second masking moieties associate with each other to form a first dimerized masking complex, and (iv) the first cleavable site is cleavable with a first protease, and (v) the second cleavable site is cleavable with a second protease, wherein the first and second cleavable sites are cleavable with the same or different proteases.
The various activatable masked IgG type antibodies also comprise a second heavy chain variable region and a second light chain variable region, wherein (i) the N-terminal end of the second heavy chain variable region is joined to a third masking moiety via a third peptide linker having a third cleavable site, and (ii) the N-terminal end of the second light chain variable region is joined to a fourth masking moiety via a fourth peptide linker having a fourth cleavable site, and (iii) the third and fourth masking moieties associate with each other to form a second dimerized masking complex, and (iv) the third cleavable site is cleavable with a third protease, and (v) the fourth cleavable site is cleavable with a fourth protease, wherein the third and fourth cleavable sites are cleavable with the same or different proteases.
The naming convention (designation) of the various activatable masking moieties is listed in Table 11 below.
The naming convention of the peptide linkers in the various activatable masked antibodies, and their amino acid sequences, is listed in Table 12 below. The peptide linker sequences are underlined in Table 12 below. The non-underlined sequences represent the C-terminal amino acid sequence of the adjoining masking moiety CH3 (e.g., see SEQ ID NOS:24 and 25).
For the “Deleted” peptide linker sequence, the C-terminal amino acids GK of the human Ig-gamma CH3 and the N-terminal amino acids GG of the MMP2/9 peptide linker are deleted (see Table 12 above).
CHO-S cells (or CHO-K1 cells) were incubated in a CO2 incubator to a cell density of 1- 2×106 cells/ml with viability no less than 90%. Separate expression vectors for heavy and light chain pairs were prepared using a commercial plasmid DNA extraction kit (e.g. Qiagen Maxi plasmid DNA extraction kit). The expression vectors used are similar to pEGFP (e.g., from CloneTech). The expression vector pCDNA (from Invitrogen) can also be used. A mouse Ig gamma leader peptide sequence (MEWSWVFLFFLSVTTGVHS) was used as the secretory peptide sequence for both heavy and light chain expression. DNA PEI complex for transfection was formed by mixing DNA and PEI (Polyethylenimine, from Polyscience catalog # 24765) at a ratio between 1:2-3 (weight/volume concentrations). CHO cells to DNA ratio was approximately 106 cells per microgram DNA. DNA and PEI complex was formed in OptiPRO media (Thermo Fisher) and added to the CHO cell cultures in shaker flasks and incubated at 37° C. with rotation overnight. On Day 2 the culture was expanded by doubling the culture media with CHO culturing media containing penicillin/streptomycin and placed in 30° C. incubator with rotation for 1 to 2 weeks depending on IgG titer and viability of the CHO cells. The activatable masked anti-EGFR antibodies were purified by batch type capturing of the molecules using commercial Protein A resins.
The expression levels of Protein A titer and IgG yield from 25 mL CHO transfections of various anti-EGFR activatable masked IgG type antibodies was determined for various activatable masked antibodies and control anti-EGFR antibody with no masking moieties, which are listed in Table 13:
Various activatable masked antibodies (anti-EGFR) having peptide linkers that are cleavable with either MMP2, MMP9 or uPA, were subjected to digestion with MMP2, MMP9 or uPA proteases, for various time ranges (1, 3, 6.5 or 23 hours) and the resulting digestion products were analyzed by gel electrophoresis on 4-20% gradient Tris-Glycine SDS-PAGE gels under non-reducing or reducing conditions (reducing agent is NUPAGE 10X Sample Reducing Agent from Invitrogen).
Digestion reactions contained 0.1 ug of proteases MMP2 (recombinant human MMP2 from RnD Systems, catalog # 902-MP-010) or MMP9 (recombinant human MMP9 from Origeen CAT#: TP302872, or RnD Systems CAT # 911-MP-010) per 10 or 20 ug of uncleaved activatable masked antibody were incubated in DPBS buffer at room temperature or at 37° C. for 1, 3, 6.5 or 23 hours. The final concentration of the uncleaved activatable masked antibody was 0.25 ug/uL or 0.5 ug/uL, with 0.4 ug of MMP9 protease or 0.75 ug of uPA protease. APMA activation was not conducted.
The anti-EGFR activatable masked antibodies digested with MMP2 are shown in
The anti-EGFR activatable masked antibodies digested with MMP9 are shown in
The amino acid sequences of the heavy and light chains of the various anti-EGFR IgG type activatable masked antibodies shown in
The masking moiety is a human Ig-gamma CH3 (bolded font) which includes a hole structure, joined to an MMP2/9 peptide linker (underlined italic font), joined to an anti-EGFR IgG antibody heavy chain:
GQPREPQVYTLPPSREEMTKNQVSLSCAVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFLVSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK
GGPLGVRGGQVQLKQSG
The masking moiety is a human Ig-gamma CH3 (bolded font) which includes a knob structure, joined to an MMP2/9 peptide linker (underlined italic font), joined to an anti-EGFR IgG antibody light chain:
GQPREPQVYTLPPSREEMTKNQVSLWCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK
GGPLGVRGGDILLTQSP
The predicted amino acid sequence of the heavy chain cleavage product of [HC-CH3 hole MMP2/9, LC-CH3 knob MMP2/9] after MMP2 or MMP9 cleavage (cleavage products confirmed by mass spectrometry as described in Example 6 below):
The predicted amino acid sequence of the light chain cleavage product of [HC-CH3 hole MMP2/9, LC-CH3 knob MMP2/9] after MMP2 or MMP9 cleavage (cleavage products confirmed by mass spectrometry as described in Example 6 below):
The masking moiety is a human Ig-gamma CH3 (bolded font) which includes a hole structure, joined to a uPA1 peptide linker (underlined italic font), joined to an anti-EGFR IgG antibody heavy chain:
GQPREPQVYTLPPSREEMTKNQVSLSCAVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFLVSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK
GGGGRRGGGGQVQLKQS
The masking moiety is a human Ig-gamma CH3 (bolded font) which includes a knob structure, joined to a uPA1 peptide linker (underlined italic font), joined to an anti-EGFR IgG antibody light chain:
GQPREPQVYTLPPSREEMTKNQVSLWCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDG SFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK
GGGGRRGGGGDILLTQS
The masking moiety is a human Ig-gamma CH1 (bolded font), joined to an MMP2/9 peptide linker (underlined italic font), joined to an anti-EGFR antibody IgG antibody heavy chain:
ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGL YSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKRVEPKSS
GGPLGVRGGQVQLKQSGPGLV
The masking moiety is a human Ig-gamma CL kappa (bolded font), joined to an MMP2/9 peptide linker (underlined italic font), joined to an anti-EGFR antibody IgG antibody light chain:
RTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSK DSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGES
GGPLGVRGGDILLTQSP
The predicted amino acid sequence of heavy chain cleavage product of [HC-CH1 MMP2/9, LC-CL kappa MMP2/9] after MMP2 or MMP9 cleavage:
The predicted amino acid sequence of light chain cleavage product of [HC-CH1 MMP2/9, LC-CL kappa MMP2/9] after MMP2 or MMP9 cleavage:
The masking moiety is a human Ig-gamma CH1 (bolded font), joined to an MMP2/9 peptide linker (underlined italic font), joined to an anti-EGFR antibody IgG antibody heavy chain:
The masking moiety is a human Ig-gamma CL lambda (bolded font), joined to an MMP2/9 peptide linker (underlined italic font), joined to an anti-EGFR antibody IgG antibody light chain:
GQPKAAPSVTLFPPSSEELQANKATLVCLISDFYPGAVTVAWKADSSPVKAGVETTTPSKQS NNKYAASSYLSLTPEQWKSHRSYSCQVTHEGSTVEKTVAPTESS
GGPLGVRGGDILLTQSPV
The predicted amino acid sequence of heavy chain cleavage product of [HC-CH1 MMP2/9, LC-CL lambda MMP2/9] after MMP2 or MMP9 cleavage:
The predicted amino acid sequence of light chain cleavage product of [HC-CH1 MMP2/9, LC-CL lambda MMP2/9] after MMP2 or MMP9 cleavage:
The masking moiety is a TCR alpha (bolded font), joined to an MMP2/9 peptide linker (underlined italic font), joined to an anti-CD38 IgG antibody heavy chain:
IQNPDPAVYQLRDSKSSDKSVCLFTDFDSQTNVSQSKDSDVYITDKTVLDMRSMDFKSNSAV AWSNKSDFACANAFNNSIIPEDTFFPSP
GGPLGVRGGPLGVRGGQVQLVESGGGLVKPGGSL
The masking moiety is a TCR beta (bolded font), joined to an MMP2/9 peptide linker (underlined italic font), joined to an anti-CD38 IgG antibody light chain:
KVFPPEVAVFEPSEAEISHTQKATLVCLATGFFPDHVELSWWVNGKEVHSGVSTDPQPLKEQ PALNDSRYSLSSRLRVSATFWQNPRNHFRCQVQFNGQIVSAEAWGRADS
GGPLGVRGGPEGV
Various activatable masked antibodies (anti-EGFR) having peptide linkers with modified MMP2/9 cleavage sequences were subjected to digestion with MMP2 or MMP9 proteases as described in Example 3 above except the digestion time was conducted at 0.5, 1, 2, 6 or 24 hours. The resulting digestion products were analyzed by gel electrophoresis on 4-20% gradient Tris-Glycine SDS-PAGE gels under reducing conditions (reducing agent is NUPAGE 10X Sample Reducing Agent from Invitrogen). The results are shown in
Various activatable masked antibodies (anti-EGFR) having peptide linkers with modified MMP2/9 cleavage sequences or uPA1cleavage sequences were subjected to digestion with MMP2, MMP9 or uPA proteases as described in Example 3 above except the digestion time was conducted at 1, 3, 5 or 20 hours. The resulting digestion products were analyzed by gel electrophoresis on 4-20% gradient Tris-Glycine SDS-PAGE gels under reducing conditions (reducing agent is NUPAGE 10X Sample Reducing Agent from Invitrogen). The results are shown in
The mass of protease-digested anti-EGFR activatable masked antibodies were determined by subjecting the antibodies to a de-glycosylation reaction and then analyzed by mass spectroscopy.
The activatable masked antibodies were either non-MMP9 digested or digested with MMP9 according to the procedure described in Example 3 above. These antibodies were not digested to yield Fab and Fc domains. Ten micrograms of the MMP9-digested activatable masked IgG type antibody was mixed with water in total volume of 8 uL, then 2 uL of 5X PNGase F Buffer (non-reducing format, New England BioLabs, Catalog # B0717S) was added to make a 10 uL total reaction volume, which was incubated for 5 minutes at 75° C. The mixture was allowed to cool to room temperature. The de-glycosylation reaction was conducted by adding 1 uL Rapid PNGase F (non-reducing format, New England BioLabs, Catalog # P0711) which was incubated for 10 minutes at 50° C.
Liquid chromatography mass spectrometry (LC-MS) was conducted by analyzing approximately 2 ug of the de-glycosylated sample on a VANQUISH HORIZON (from Thermo Fisher Scientific, Waltham, MA) with a HESI source connected to a Q EXACTIVE Plus BioPharma mass spectrometer (Thermo Fisher Scientific, Waltham, MA) in the positive ion mode. The intact antibodies were separated by UPLC Waters BEH C4 column (2.1 x 150 mm, 300 Angstrom pore size) at a flow rate of 0.35 mL/min with the column temperature maintained at 80° C. Mobile phase A was 0.1% (v/v) formic acid in water, and mobile phase B was 0.1% (v/v) formic acid in 100% acetonitrile. Beginning with 10% mobile phase B and hold at 10% B for 5 minutes, phase B linearly increased to 25% after 1 min and to 60% at 14 min, and then to 90% B at 15 minutes. MS data was acquired in HMR mode. Acquired MS data was analyzed using Thermo BioPharma Finder software.
The anti-EGFR IgG heavy chain contains arginine residues at position 88 (e.g., in the Fab region) and 299 (e.g, in the Fc region) which are potential post-translational glycosylation sites. The “N” residue is bolded and underlined in the heavy chain amino acid sequences in Example 3 above.
It is known that CHO cells expressing antibody heavy chains will cleave off the C-terminal lysine reside. Thus, expressed IgG-type antibodies (e.g., the activatable masked IgG type antibodies described herein) may contain a heterogeneous population of antibodies having the lysine residues removed from both heavy chains, or removed from one of the heavy chains, or both heavy chains retain the C-terminal lysine residue. The activatable masked IgG type antibodies described in the Examples herein were expressed in CHO cells. In the amino acid sequences of the activatable masked antibodies described in Example 3 above, the C-terminal lysine of the heavy chains is shown in bold underlined font.
The theoretical molecular weights for de-glycosylated forms of MMP-digested or intact activatable masked antibodies [HC-CH3 hole MMP2/9, LC-CH3 knob MMP2/9] and [HC-CH1 MMP2/9, LC-CL lambda MMP2/9] were calculated using the predicted amino acid sequences of the MMP9-cleaved masked antibodies listed in Example 3 above, and compared with the experimentally determined molecular weights.
In
The LC-MS data for un-digested [HC-CH3 hole MMP2/9, LC-CH3 knob MMP2/9] is shown in
The LC-MS data for MMP9 digested [HC-CH3 hole MMP2/9, LC-CH3 knob MMP2/9] is shown in
The LC-MS data for un-digested [HC-CH1 MMP2/9, LC-CL lambda MMP2/9] is shown in
The LC-MS data for MMP9 digested [HC-CH1 MMP2/9, LC-CL lambda MMP2/9] is shown in
Cell binding assays were conducting using flow cytometry to determine EC50 values of anti-EGFR activatable masked antibodies [HC-CH3 hole MMP2/9, LC-CH3 knob MMP2/9] that were uncut (solid circles) or cut (solid squares) with MMP9, compared to a control anti-EGFR antibody (solid triangles). Additionally, uncut and cut anti-EGFR activatable masked antibodies [HC-CH3 hole uPA1, LC-CH3 knob MMP2/9] were tested and compared to the control anti-EGFR antibody.
The activatable masked antibodies were digested with MMP9 according to the protocol described in Example 3 above. EGFR positive tumor cell lines MDA-MB-231 (low EGFR expression), A431 (high EGFR expression) and MDA-MB-468 (high EGFR expression) were used. Cells were washed and resuspended in FACS buffer. The cells were counted and diluted to 1 × 106 cells/mL in FACS buffer containing 0.01% sodium azide and 50 uL (~ 50,000 cells) were aliquoted into clear V-bottom 96-well plates and spun for 5 minutes at 1200 RPM. The supernatant was removed and 30 uL of serially-diluted antibody was added. The antibody was diluted to a starting concentration between 10 and 50 ug/mL and then serially diluted 3-fold using FACS buffer. Each antibody concentration was added to cells in duplicate or triplicate. After incubating one hour at 4° C., 110 uL of FACS buffer was added to each well and the plate was spun for 5 minutes at 1200 RPM. After removing the supernatant, an anti-human IgG-PE or -APC or -FITZ/Alexa488 secondary antibody was added at a 500-fold dilution in FACS buffer + 0.01% azide, and incubated for 25 minutes at 4° C. Cells were washed with 110 uL of FACS buffer and spun. The cells were resuspended in 30 uL of FACS buffer and analyzed by FACS for binding using the Intellicyt FACS. Data was analyzed using Flo-Jo and GraphPad Prism.
Cell binding assays were conducted with an activatable masked antibody having a first heavy chain variable region joined to a first peptide linker, and a first light chain variable region joined to a second peptide linker, wherein the first and second peptide linkers comprise different lengths and sequences and are cleavable with different proteases. For example, the cell binding ability of activatable masked antibody [HC-CH3 hole uPA1; LC-CH3 knob MMP2/9], either uncut or digested with MMP9 protease, was tested for MDA-MB-231, A431 and MDA-MB-468 cells. The EC50 values are listed in Table 20 below (see the uncut and cut antibodies designated with **).
The EC50 values obtained from these FACs assays and calculated EC50 ratios are listed in Table 20 below:
ELISA assays were conducted to compare binding characteristics of uncut and cut activatable masked anti-EGFR IgG type antibodies [HC-CH3 hole MMP2/9, LC-CH3 knob MMP2/9] and [HC-CH1 MMP2/9, LC-CL lambda MMP2/9] and compared to control anti-EGFR antibody.
The activatable masked antibodies were digested with MMP9 according to the protocol described in Example 3 above. Recombinant EGFR protein extracellular domain was adsorbed onto a microtiter plate followed by blocking with BLOCKER Casein in PBS (from Thermo Fisher Scientific, catalog #37528). The test or control antibody was added in a series of dilutions. An enzyme-labeled anti-Human IgG reagent that binds the test antibody was added. The chromogenic substrate 3,3′,5,5′-Tetramethylbenzidine (TMB) was added. A plate reader was used to detect color change. Wash steps are included between steps to remove excess unbound reagents.
The ELISA results are shown in
Label-free bio-layer interferometry was used to measure kinetic binding between a commercial human EGFR protein and either control anti-EGFR antibody or various anti-EGFR activatable masked antibodies. The carboxylic groups on an AR2G (amine reactive second generation) sensor were activated in aqueous solution of EDC (1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride) and NHS (N-hydroxysuccinimide). Commercial recombinant EGFR was immobilized onto the sensor in pH5.5 in acetate buffer at concentration of 5 ug/ml for 5 minutes. Time-dependent binding was detected between the EGFR protein and the control anti-EGFR antibody or activatable masked antibodies either uncut or digested with MMP9 or MMP2 protease. The control anti-EGFR antibody was not subjected to MMP9 digestion. All tested antibodies were in PBS buffer at equal molar concentration of 30 nM. Data analysis was performed according to manufacturer’s instructions. The data are shown in
Intrinsic tryptophan fluorescence shift measurements were used to determine thermal stability of the various IgG-type activatable masked antibodies. UNcle from Unchained Labs (Pleasanton, California) was used to measure Tm. In a typical run, 9 µL of antibody with a concentration range of 0.1 mg/mL to 100 mg/mL was loaded. The thermal ramping was performed from 30° C. to 90° C. at a scan rate of 1° C./min, and fluorescence at full 250-720 nm spectral range was captured using a CCD digital camera. The UNcle software automatically displays the fluorescence curve calculated by BCM, and the midpoint of a thermal transition temperature (Tm, or thermal transition temperature) was also displayed. The results are listed in Tables 30-33 below:
Transgenic HeLa that expressed membrane-anchored antigen binding proteins that mimicked CAR or DAR were prepared using FUGENE6 transfection reagent.
The membrane-anchored antigen binding protein DAR-mimic included (1) a first polypeptide comprising an antibody heavy chain variable region (VH), an antibody heavy chain constant region (CH), a hinge region, and a transmembrane region (TM), but lacked an intracellular signaling region, and (2) a second polypeptide comprising an antibody light chain variable region (VL) (e.g., kappa or lambda), and an antibody light chain constant region (CL). The DAR-mimic either lacked included or lacked activatable masking moieties. See the schematic of an activatable masked DAR construct in
The membrane-anchored antigen binding protein CAR-mimic that resembles an scFv molecule included an antibody heavy chain variable region (VH), a flexible linker, an antibody light chain variable region (VL), a hinge region, and a transmembrane region (TM), but lacked an intracellular signaling region. The CAR-mimics all lacked activatable masking moieties. CAR-mimics that bind EGFR, CD38 or BCMA antigen were prepared.
The first and second polypeptide chains of the DAR mimics were each operably joined to separate transient expression vectors that were co-introduced into HeLa cells. FUGENE HD Transfection Reagent (Promega, catalog No. E2311) was used to prepare transgenic HeLa cells that express either a CAR or DAR antigen binding protein, with or without activatable masking moieties. Transfection was conducted according the manufacturer’s instructions. Briefly, a transfection solution was prepared by mixing the FUGENE6 reagent in an EPPENDORF tube with serum free media (e.g., DMEM). The DMDM/FUGENE6 solution was added to another tube that contained the DNA encoding the CAR or DAR antigen binding proteins (e.g., expression plasmids or expression viral vectors). The quantity of the FUGENE6 and DNA used to make the DMEM/FUGENE6 and plasmid solution was according to the manufacture’s protocol. Typically, 2ug DNA with FUGENE6 reagent volume (in uL) varying between ratios of 1:2 and 1:3 for a 10 cm-well of cells (about 104 or 106 cells). A complex was allowed to form by incubating the DMEM media containing FUGENE6 and plasmid for 15 minutes at room temperature. The DMEM media containing the formed complex was added directly to the HeLa cells by dripping on top and swirling to mix. Cells were placed in an incubator overnight, and CAR or DAR expression was checked on day 2 or 3.
The hinge and transmembrane portions of the anti-EGFR and anti-CD38 DAR mimics (those having activatable masking moieties and those lacking activatable masking moieties) were derived from platelet-derived growth factor receptor (PDGFR).
In one embodiment, the anti-EGFR or anti-CD38 DAR or CAR (or DAR mimic or CAR mimic) having activatable masking moieties can include a hinge sequence derived from CD28 or CD8, or both CD28 and CD8.
In one embodiment, the anti-EGFR or anti-CD38 DAR or CAR (or DAR mimic or CAR mimic) having activatable masking moieties can include a transmembrane sequence derived from CD28.
In one embodiment, the anti-EGFR or anti-CD38 DAR or CAR having activatable masking moieties can include at least one intracellular signaling sequence.
Transgenic HeLa cells expressing various anti-EGFR DAR mimics having activatable masking moieties were subjected to digestion with MMP9. Approximately 2 × 104 transgenic HeLa cells were reacted with 0.4 ug MMP9 protease (recombinant human MMP9 from Origeen CAT#: TP302872, or RnD Systems CAT # 911-MP-010) in DPBS/2% fetal bovine serum at 25° C. for about 15 hours. APMA activation was not conducted.
The transgenic HeLa cells expressing an anti-EGFR DAR mimic having activatable masking moieties (as described in Example 11 above) were tested in a cell binding assay using flow cytometry to assess the level of antigen binding as a reflection of masking level and to assess the level of CAR or DAR mimic expression from transgenic HeLa cells. The anti-EGFR DAR mimic having activatable masking moieties are configured as shown in the schematic of
Compare the Q2 quadrant showing transgenic HeLa cells expressing anti-EGFR DAR mimic having activatable masking moieties [HC-CH1 MMP2/9, LC-CL kappa MMP2/9] in an uncut state (
The transgenic HeLa cells expressing an anti-CD38 DAR mimic having activatable masking moieties (as described in Example 11 above) were tested in a cell binding assay using flow cytometry to assess the level of antigen binding as a reflection of masking level and to assess the level of CAR or DAR mimic expression from transgenic HeLa cells. The anti-CD38 DAR mimic having activatable masking moieties are configured as shown in the schematic of
Compare the Q2 quadrant showing transgenic HeLa cells expressing anti-CD38 DAR mimic having activatable masking moieties [HC-CH3(IgG4) MMP2/9, LC-CH3(IgG4) MMP2/9] in an uncut state (
Compare the Q2 quadrant showing transgenic HeLa cells expressing anti-CD38 DAR mimic having activatable masking moieties [HC-CH3 hole MMP2/9, LC-CH3 knob MMP2/9] in an uncut state (
Compare the Q2 quadrant showing transgenic HeLa cells expressing anti-CD38 DAR mimic lacking activatable masking moieties (
Incucyte imaging system (from Sartorius) was used to assess the masking and binding capability of an anti-EGFR DAR mimic having activatable masking moieties [HC-CH MMP2/9, LC-CL kappa MMP2/9] in an uncut state, in the presence or absence of conditioned media from MM1R human multiple myeloma cells.
On day one, approximately 2 x 104 HeLa cells were transfected with expression vectors carrying sequences encoding either control anti-EGFR antibody lacking activatable masking moieties or encoding anti-EGFR DAR mimic with activatable masking moieties, and using the FUGENE6 reagent as described in Example 11 above. On day two, the media was replaced with MM1R conditioned media from freshly cultured tumor cell line MM1R and incubated at 37° C. for 24 hours. On day three, the HeLa cells were fixed with 4% paraformaldehyde for 15 minutes at room temperature, followed by two washes with DPBS. The cells were treated with 0.5% Triton X-100 for 10 minutes at room temperature, then washed twice with DPBS. A blocking step was conducted with 3% BSA/DPBS and double-stained with mouse anti-human LC kappa/goat anti-mouse Alexa 594 and EGFR Fc-labeled Alexa 488.
In
The second row shows images of negative control non-transgenic HeLa cells which do not express an anti-EGFR antibody.
The third row shows images of transgenic HeLa cells expressing anti-EGFR DAR mimic having masking moieties [HC-CH MMP2/9, LC-CL kappa MMP2/9] in an uncut state, in the absence of conditioned media from MM1R human multiple myeloma cells. The APC-staining intensity is similar between the control HeLa cells expressing the DAR mimic without masking moieties (top row) and HeLa cells expressing the DAR mimic with masking moieties (third row), which indicates that these transgenic HeLa cells express similar levels of anti-EGFR DAR mimics. The Alex 488-staining intensity of the positive control transgenic HeLa cells expressing the DAR mimic lacking a masking moieties is higher compared to the staining intensity of the transgenic HeLa cells expressing the DAR mimic having the masking moieties in the uncut state, which indicates that the intact masking moieties reduced binding between the DAR mimic and EGFR antigen.
The bottom row shows images of transgenic HeLa cells expressing anti-EGFR DAR mimic having masking moieties [HC-CH MMP2/9, LC-CL kappa MMP2/9] in an uncut state, in the presence of conditioned media from MM1R human multiple myeloma cells. The Alex 488-staining intensity is similar between the HeLa cells expressing the DAR mimic having masking moieties in the absence and the presence of MM1R-conditioned media, which indicates that the conditioned media did not contain adequate levels of MMP9 protease to cleave the activatable masking moieties and thus the masking moieties are intact which reduced binding between the DAR mimic and EGFR antigen.
ADCC assays were conducted to determine the EC50 values of various anti-EGFR IgG-type antibodies having activatable masking moieties. NK (natural killer) cells were purified from PBMCs using EASYSEP Human NK cell enrichment kit (StemCell Technologies, catalog #19055) and incubated in RPMI 10% FBS in the presence of 20-50 IU/ml IL2. EGFR-positive tumor cell line H292 cells (which were CFSE-labeled the day before) were seeded at 15,000 cells/well in a 96-well plate. Control anti-EGFR IgG-type antibody or various anti-EGFR IgG-type antibodies having masking moieties, in the uncut state, were serially diluted in PBS buffer and added at decreasing concentration from 100 nM to 1pM (0.000001 nM) to the H292 cells in the 96-well plate then incubated 20 minutes. NK cells were added to each well such that the E:T ratio (effector cell NK : target cell H292) was 1:1, and the plate was incubated in tissue culture chamber for approximately 14 hours. FACs was used to determine the percentage of apoptotic target cells using annexin-V staining reagent while gating on the CFSE-labeled target H292 cell population (see
The results of the ADCC assay indicate that the EC50 value of anti-EGFR IgG type antibody having activatable masking moieties [HC-CH1 MMP2/9, LC-CL lambda MMP2/9] in an uncut state is about 7-fold higher compared to the control anti-EGFR IgG antibody, and the EC50 value of anti-EGFR IgG type antibody having activatable masking moieties [HC-CH3 hole MMP2/9, LC-CH3 knob MMP2/9] or [HC-CH3 hole deleted, LC-CH3 knob deleted] in an uncut state is about 70-fold higher.
Phoenix-ECO (a human embryonic kidney cell line) were transfected using FuGENE to express anti-EFGR DAR (with intracellular signaling domain) with activatable masking moieties.
Nucleic acids encoding the anti-EGFR masked DAR precursor polypeptide chains were cloned into a MFG viral vector. Two million phoenix-ECO cells were seeded in T25 flask and cultured overnight at 37° C., 5% CO2. The next day, mixed together 8 ug DNA to 24 uL FuGENE (1:3 ratio) to phoenix-ECO cell and the cells were incubated at 37° C., 5% CO2. At 48 hour and 96 hour post-transfection, the viral supernatant was harvested by spinning at 1600 RPM for 8 minutes. The viral supernatant was used to transduce PG13 cells.
RetroNectin coated non-tissue treated 6 well plates were used for PG13 transduction. 2 mL viral supernatant collected from phoenix-ECO was added and spun at 2500 RPM at RT for 2 hours. The viral supernatant was aspirated, then added 0.6 million PG13 cells in 2 mL viral supernatant. Spun at 2500 RPM at RT for 1 hour. The cells were incubated overnight at 37° C., 5% CO2. The next day, the transduction was repeated. The transduction reaction was repeated 2-3 times until the DAR expression level was about 90% which required for transduction DAR into T cells. DAR expression levels were detected via flow cytometry using 1:200 APC anti-human kappa LC. The PG13 viral supernatant was harvested at 48 hours, 72 hours and 96 hours post-transduction, respectively. To transduce T cells, the PG13 viral supernatant was used freshly-prepared or was stored at -80° C. for a future T cell transduction reaction.
PBMC (either freshly-isolated from human blood or frozen) were treated with Human CD3/CD28 T Cell Activator: 3 uL of T cell Activator per million PBMC. At day 2 or 3 post-activation, the CD3 population and T cell activation marker CD25 were checked via flow cytometry. Generally, the CD3+ population was greater than 85%. Day 2 or 3 activated T cells were used for DAR transduction.
2 mL viral supernatant was collected from PG cells and added to RetroNectin coated 6 well plate, and spun at 2500 RPM at room temperature for 2 hours. The viral supernatant was aspirated, then added 1 million activated T cells in 2 mL viral supernatant. Spun at 2500 RPM for 1 hour. The transduced activated T cells were incubated for 3-4 hours, then the media was changed to T cell culture media + 300 IU/ml IL2. The transduced T cells were incubated overnight at 37° C., 5% CO2. The T cell transduction was repeated 1-4 times until optimal DAR expression was reached.
Anti-EGFR masked DARs include: a first and a second polypeptide chain, wherein the (a) first polypeptide chain comprises: (i) a first masking moiety having the amino acid sequence of SEQ ID NO:24; (ii) a first peptide linker cleavable with MMP9 or uPA, or carrying a non-cleavable linker, and having the amino acid sequence of SEQ ID NO:32, 52 or 34, respectively; (iii) an antibody heavy chain variable region (VH) having a portion of the amino acid sequence of SEQ ID NO:2; (iv) an antibody heavy chain constant region (CH) having a portion of the amino acid sequence of SEQ ID NO:2; (v) a CD28 hinge region having the amino acid sequence of SEQ ID NO:44; (vi) a CD28 transmembrane region (TM) having the amino acid sequence of SEQ ID NO:47; and (vii) an intracellular signaling region which includes 4-1BB and CD3zeta intracellular signaling domains and having the amino acid sequence of SEQ ID NOS:48 and 50, respectively; wherein the (b) second polypeptide chain comprises: (i) a second masking moiety having the amino acid sequence of SEQ ID NO:25; (ii) a second peptide linker cleavable with MMP9 or uPA, or carrying a non-cleavable linker, and having the amino acid sequence of SEQ ID NO:32, 52 or 34, respectively; (iii) an antibody light chain variable region (VL) having a portion of the amino acid sequence of SEQ ID NO:5; and (iv) an antibody light chain constant region (CL) having a portion of the amino acid sequence of SEQ ID NO:5. These anti-EGFR masked DARs contained a first and second intracellular signaling domain, but lacked a third intracellular domain (an embodiment of the DAR molecules shown in
Control anti-EGFR DAR: Transgenic T cells expressed a control anti-EGFR DAR precursor polypeptide chain that contained a first polypeptide chain, a self-cleaving sequence (e.g., T2A), and a second polypeptide chain, and comprising the amino acid sequence of SEQ ID NO:53 (See
Anti-EGFR DAR with MMP2/9 cleavable linkers: Transgenic T cells expressed an anti-EGFR DAR precursor polypeptide chain that contained a first polypeptide chain, a self-cleaving sequence (e.g., T2A), and a second polypeptide chain, and comprising the amino acid sequence of SEQ ID NO:56 (See
Anti-EGFR DAR with uPA cleavable linkers: Transgenic T cells expressed an anti-EGFR DAR precursor polypeptide chain that contained a first polypeptide chain, a self-cleaving sequence (e.g., T2A), and a second polypeptide chain, and comprising the amino acid sequence of SEQ ID NO:59 (See
Anti-EGFR DAR with non-cleavable linkers: Transgenic T cells expressed an anti-EGFR DAR precursor polypeptide chain that contained a first polypeptide chain, a self-cleaving sequence (e.g., T2A), and a second polypeptide chain, and comprising the amino acid sequence of SEQ ID NO:62 (See
The anti-EGFR masked DAR described in Example 17 above were cultured in T cell expansion SFM media with 300 IU/mL of I-2. The media was changed every 2-3 days. In-house EGFR-his conjugated with Alexa-488 were prepared. Approximately 50k DAR-T cells or masked DAR-T cells were washed once and resuspended in 50 uL binding buffer, 1:200 APC anti-human Kappa and 1:100 EGFR-Alexa-488 was added and incubated on ice for 30 minutes. The cells were rinsed once with PBS plus 2% FBS. The cells were assay via flow cytometry using IQueScreener. The results are shown in
Cytotoxicity assay was conducted with a Real Time Cytotoxicity Assay (RTCA) using xCELLigence instrument. The cell lined A549 was used a target cell line. A549 is a non-small cell lung carcinoma (NSCLC) tumor cell line that expresses a high level of EGFR. 10k/well of A549 cells were seeded in E-plates and incubated for 24 hours. The control anti-EGFR DAR T cells and anti-EGFR masked DAR T cells were added at 5:1 or 20:1 of effector-to-target ratio. The cell index value was monitored kinetically for up to 72 hours. This monitoring indicates cell viability. As negative controls included no effector (A549 cells alone) and activated T cells. Normalized Cell Index was at the time point when effector cells were added (see
The supernatants from the cytotoxicity assay described in Example 19 above were saved and used to conduct a cytokine release assay. An IFN-gamma HTFR assay kit was used. Samples and IFN standard were diluted 1: 3 with dilution buffer. 16 uL of sample or IFN-gamma standard was added into 96W low volume, white plates, and 4 uL of mixed donor and acceptor antibody was added. The plate was sealed and incubated at room temperature for at least 2 hours then the plate was read using the HTRF setting on TECAN. The amount of IFN-gamma was calculated based on the standard curve. The results are shown in
This application claims priority to U.S. Provisional Application No. 62/981,782, filed Feb. 26, 2020, the contents of which is incorporated by reference herein in its entirety. Throughout this application various publications, patents, and/or patent applications are referenced. The disclosures of the publications, patents and/or patent applications are hereby incorporated by reference in their entireties into this application in order to more fully describe the state of the art to which this disclosure pertains.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2021/019331 | 2/24/2021 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 62981782 | Feb 2020 | US |
