WO2015034519A1 - Peptides cibles pour l'immunothérapie et le diagnostic - Google Patents

Peptides cibles pour l'immunothérapie et le diagnostic Download PDF

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WO2015034519A1
WO2015034519A1 PCT/US2013/058477 US2013058477W WO2015034519A1 WO 2015034519 A1 WO2015034519 A1 WO 2015034519A1 US 2013058477 W US2013058477 W US 2013058477W WO 2015034519 A1 WO2015034519 A1 WO 2015034519A1
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composition
seq
peptide
hla
cells
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PCT/US2013/058477
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Donald F. Hunt
Jeffrey Shabanowitz
Stacy A. MALAKER
Victor H. Engelhard
Angela Zarling
Kara L. CUMMINGS
Rebecca C. OBENG
Mark Cobbold
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University Of Virginia Patent Foundation
The University Of Birmingham
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Priority claimed from PCT/US2013/057856 external-priority patent/WO2014036562A2/fr
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Publication of WO2015034519A1 publication Critical patent/WO2015034519A1/fr

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    • A61K39/001102—Receptors, cell surface antigens or cell surface determinants
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    • A61K39/001102—Receptors, cell surface antigens or cell surface determinants
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    • A61K39/46—Cellular immunotherapy
    • A61K39/461—Cellular immunotherapy characterised by the cell type used
    • A61K39/4611—T-cells, e.g. tumor infiltrating lymphocytes [TIL], lymphokine-activated killer cells [LAK] or regulatory T cells [Treg]
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    • A61K2039/55516—Proteins; Peptides
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Definitions

  • the presently disclosed subject matter relates to the area of diagnostics and therapeutics.
  • it relates to immunotherapies and diagnostics in the context of proliferative diseases such as but not limited to cancer.
  • T cells The mammalian immune system has evolved a variety of mechanisms to protect the host from cancerous cells. An important component of this response is mediated by cells referred to as T cells. Cytotoxic T lymphocytes (CTL) are specialized T cells that primarily function by recognizing and killing cancerous cells or infected cells, but they can also function by secreting soluble molecules referred to as cytokines that can mediate a variety of effects on the immune system. T helper cells primarily function by recognizing antigen on specialized antigen presenting cells, and in turn secreting cytokines that activate B cells, T cells, and macrophages. A variety of evidence suggests that immunotherapy designed to stimulate a tumor- specific CTL response would be effective in controlling cancer.
  • CTL Cytotoxic T lymphocytes
  • Melanoma or skin cancer, is a disease that is diagnosed in approximately
  • MHC-peptide complex which is located on the surface of the cancerous cell.
  • MHC major histocompatibility-complex
  • class I and class II MHC-encoded molecules MHC molecules are referred to as human leukocyte antigens (HLA).
  • HLA human leukocyte antigens
  • HLA- A HLA-A
  • HLA-B HLA-C
  • the genes that can be encoded at each of these loci are extremely polymorphic, and thus, different individuals within the population express different class I MHC molecules on the surface of their cells.
  • HLA-A1, HLA-A2, HLA-A3, HLA-B7, HLA- B14, HLA-B27, and HLA-B44 are examples of different class I MHC molecules that can be expressed from these loci.
  • the peptides which associate with the MHC molecules can either be derived from proteins made within the cell, in which case they typically associate with class I MHC molecules (Rock & Goldberg, 1999); or they can be derived from proteins which are acquired from outside of the cell, in which case they typically associate with class II MHC molecules (Watts, 1997).
  • the peptides that evoke a cancer-specific CTL response most typically associate with class I MHC molecules.
  • the peptides themselves are typically nine amino acids in length, but can vary from a minimum length of eight amino acids to a maximum of fourteen amino acids in length.
  • Tumor antigens may also bind to class II MHC molecules on antigen presenting cells and provoke a T helper cell response.
  • the peptides that bind to class II MHC molecules are generally twelve to nineteen amino acids in length, but can be as short as ten amino acids and as long as thirty amino acids.
  • antigen processing The process by which intact proteins are degraded into peptides is referred to as antigen processing.
  • Two major pathways of antigen processing occur within cells (Rock & Goldberg, 1999).
  • One pathway which is largely restricted to professional antigen presenting cells such as dendritic cells, macrophages, and B cells, degrades proteins that are typically phagocytosed or endocytosed into the cell. Peptides derived from this pathway can be presented on either class I or to class II MHC molecules.
  • a second pathway of antigen processing is present in essentially all cells of the body. This second pathway primarily degrades proteins that are made within the cells, and the peptides derived from this pathway primarily bind to class I MHC molecules.
  • Antigen processing by this latter pathway involves polypeptide synthesis and proteolysis in the cytoplasm, followed by transport of peptides to the plasma membrane for presentation.
  • These peptides initially being transported into the endoplasmic reticulum of the cell, become associated with newly synthesized class I MHC molecules and the resulting complexes are then transported to the cell surface.
  • Peptides derived from membrane and secreted proteins have also been identified. In some cases these peptides correspond to the signal sequence of the proteins which is cleaved from the protein by the signal peptidase. In other cases, it is thought that some fraction of the membrane and secreted proteins are transported from the endoplasmic reticulum into the cytoplasm where processing subsequently occurs.
  • the peptides are recognized by antigen-specific receptors on CTL.
  • CTL antigen-specific receptors on CTL.
  • Several methods have been developed to identify the peptides recognized by CTL, each method of which relies on the ability of a CTL to recognize and kill only those cells expressing the appropriate class I MHC molecule with the peptide bound to it.
  • Mere expression of the class I MHC molecule is insufficient to trigger the CTL to kill the target cell if the antigenic peptide is not bound to the class I MHC molecule.
  • Such peptides can be derived from a non-self source, such as a pathogen (for example, following the infection of a cell by a bacterium or a virus) or from a self-derived protein within a cell, such as a cancerous cell.
  • a pathogen for example, following the infection of a cell by a bacterium or a virus
  • a self-derived protein within a cell such as a cancerous cell.
  • the tumor antigens from which the peptides are derived can broadly be categorized as differentiation antigens, cancer/testis antigens, mutated gene products, widely expressed proteins, viral antigens and most recently, phosphopeptides derived from dysregulated signal transduction pathways. (Zarling et ah, 2006).
  • Adoptive T cell therapy of melanoma is described in two recent publications: Dudley et ah, 2008 and Rosenberg & Dudley, 2009.
  • late stage metastatic melanoma patients are treated as if they were undergoing an organ transplant operation. Tumor is resected and cytotoxic T cells that have infiltrated the tumor are harvested and exposed to a particular class I peptide antigen (MART-1). Those that recognize this antigen are then allowed to expand until the total number of MART-1 specific cells reach 100 billion.
  • the patient receives whole body irradiation and chemotherapy to wipe out 98% of his/her immune system.
  • the MART specific T cells are then given back to the patient and circulate throughout the body looking for tumor.
  • tumors in 72% of the patients showed objective responses with this therapy at all sites of metastasis including lymph nodes, bone, lung, liver, and brain. Twenty-eight percent of the patients had complete remission of the disease.
  • Immunization with melanoma-derived, class I or class II MHC-encoded molecule associated peptides, or with a precursor polypeptide or protein that contains the peptide, or with a gene that encodes a polypeptide or protein containing the peptide, are forms of immunotherapy that can be employed in the treatment of melanoma. Identification of the immunogens is a necessary first step in the formulation of the appropriate immunotherapeutic agent or agents. Although a large number of tumor-associated peptide antigens recognized by tumor reactive CTL have been identified, there are few examples of antigens that are derived from proteins that are selectively expressed on a broad array of tumors, as well as associated with cellular proliferation and/or transformation.
  • Attractive candidates for this type of antigen are peptides derived from proteins that are differentially phosphorylated on serine (Ser), threonine (Thr), and tyrosine (Tyr). See Zarling et ⁇ , 2000. Due to the increased and dysregulated phosphorylation of cellular proteins in transformed cells as compared to normal cells, tumors are likely to present a unique subset of phosphorylated peptides on the cell surface that are available for recognition by cytotoxic T-lymphocytes (CTL). Presently, there is no way to predict which protein phosphorylation sites in a cell will be unique to tumors, survive the antigen processing pathway, and be presented to the immune system in the context of 8-14 residue phosphopeptides bound to class I MHC molecules.
  • CTL cytotoxic T-lymphocytes
  • ⁇ -catenin a protein involved in cell adhesion and a downstream mediator of Wnt signaling, has been implicated in tumor development and progression (Takemaru et al, 2008).
  • ⁇ -catenin translocates into the nucleus by an unknown mechanism where it associates with TCF/Lef proteins to activate transcription of genes such as cyclin Dl (Tetsu & McCormick, 1999), c-myc (He et al, 1998), and metalloproteases (Crawford et al, 1999; Takahashi et al, 2002), which promote tumorigenesis and metastasis.
  • genes such as cyclin Dl (Tetsu & McCormick, 1999), c-myc (He et al, 1998), and metalloproteases (Crawford et al, 1999; Takahashi et al, 2002), which promote tumorigenesis and metastasis.
  • ⁇ -catenin in melanoma cells diminishes with disease progression (Sanders et al, 1999; Kageshita et al, 2001; Maelandsmo et al, 2003; Krengel et al, 2004; Hoek et al, 2006; Pecina-Slaus et al, 2007).
  • nuclear ⁇ -catenin has been observed in melanoma samples and may be transcriptionally active in promoting invasive behavior of melanoma cells (Rimm et al, 1999; Bachmann et al, 2005; Chien et al, 2009; Arozarena et al, 2011).
  • Degradation of ⁇ -catenin is dependent on phosphorylation of the protein at S33, S37, and T41 by GSK-3P (Kimelman & Xu, 2006). Thus detection of this phosphorylated form of the protein in cells indicates that ⁇ -catenin has been marked for degradation. Phosphorylated ⁇ -catenin has been detected in metastatic melanomas and to a lesser extent, primary melanomas (Kielhorn et al., 2003) but the relative abundances of the different forms of phosphorylated ⁇ -catenin (S33/S37/T41, S37/T41, S33/S37, T41, S37, or S33 only) were not distinguished.
  • the presently disclosed subject matter provides an isolated and purified target peptide that consists of between 8 and 50 contiguous amino acid residues derived from a native human protein.
  • the target peptide is a peptide that comprises a sequence selected from SEQ ID NO: 1- 2167 and 2374.
  • the target peptide is a phosphopeptide that comprises a sequence selected from SEQ ID NO: 1-2163 in which at least one serine, threonine, or tyrosine residue in the selected sequence is phosphorylated with a hydro lyzable or non-hydro lyzable phosphate group.
  • the peptide is an comprises an O-GlcNAcylated peptide that comprises an amino acid sequence selected from SEQ ID NOs: 2163-2167 and 2374.
  • contiguous amino acids adjacent to the selected sequence in the phosphopeptide are selected from the adjacent residues in the native human protein.
  • the phosphopeptide is phosphorylated with a non-hydro lyzable phosphate group.
  • a composition is administered to the mammal that activates CD8 + T cells.
  • the composition comprises a phosphopeptide that consists of between 8 and 50 contiguous amino acid residues derived from a native human protein.
  • the target peptide is a peptide that comprises a sequence selected from SEQ ID NO: 1-2167 and 2374.
  • the target peptide is a phosphopeptide that comprises a sequence selected from SEQ ID NO: 1-2163 in which at least one serine, threonine, or tyrosine residue in the selected sequence is phosphorylated with a hydro lyzable or non-hydrolyzable phosphate group.
  • the peptide is an comprises an O-GlcNAcylated peptide that comprises an amino acid sequence selected from SEQ ID NOs: 2163-2167 and 2374.
  • contiguous amino acids adjacent to the selected sequence in the phosphopeptide are selected from the adjacent residues in the native human protein.
  • the phosphopeptide is phosphorylated with a non-hydrolyzable phosphate group.
  • a sample isolated from a patient is contacted with an antibody that specifically binds to a phosphopeptide.
  • the phosphopeptide consists of between 8 and 50 contiguous amino acid residues derived from a native human protein.
  • the target peptide is a peptide that comprises a sequence selected from SEQ ID NO: 1-2167 and 2374.
  • the target peptide is a phosphopeptide that comprises a sequence selected from SEQ ID NO: 1-2163 in which at least one serine, threonine, or tyrosine residue in the selected sequence is phosphorylated with a hydrolyzable or non-hydrolyzable phosphate group.
  • the peptide is an comprises an O-GlcNAcylated peptide that comprises an amino acid sequence selected from SEQ ID NOs: 2163-2167 and 2374.
  • contiguous amino acids adjacent to the selected sequence in the phosphopeptide are selected from the adjacent residues in the native human protein.
  • the antibody does not bind to a peptide consisting of the same amino acid sequence but devoid of phosphorylation.
  • antibody bound to the sample is measured or detected.
  • the presently disclosed subject matter also provides in some embodiments molecules that comprise an antigen-binding region of an antibody.
  • the molecule specifically binds to a phosphopeptide and does not bind to a peptide consisting of the same amino acid sequence but devoid of phosphorylation.
  • the phosphopeptide consists of between 8 and 50 contiguous amino acid residues derived from a native human protein.
  • the target peptide is a peptide that comprises a sequence selected from SEQ ID NO: 1-2167 and 2374.
  • the target peptide is a phosphopeptide that comprises a sequence selected from SEQ ID NO: 1-2163 in which at least one serine, threonine, or tyrosine residue in the selected sequence is phosphorylated with a hydro lyzable or non-hydro lyzable phosphate group.
  • the peptide is an comprises an O-GlcNAcylated peptide that comprises an amino acid sequence selected from SEQ ID NOs: 2163-2167 and 2374.
  • contiguous amino acids adjacent to the selected sequence in the phosphopeptide are selected from the adjacent residues in the native human protein.
  • kits for measuring a phosphoprotein that in some embodiments consists of between 8 and 50 contiguous amino acids.
  • the phosphoprotein comprises a sequence selected from SEQ ID NO: 1-2163 that includes a phosphorylated serine, threonine, or tyrosine residue.
  • the kit comprises a molecule comprising an antigen-binding region of an antibody, wherein the molecule specifically binds to the phosphoprotein and does not bind to a protein consisting of the same amino acid sequence but devoid of phosphorylation.
  • dendritic cells are contacted in vitro with an isolated phosphopeptide consisting of between 8 and 50 contiguous amino acids.
  • the target peptide is a peptide that comprises a sequence selected from SEQ ID NO: 1-2167 and 2374.
  • the target peptide is a phosphopeptide that comprises a sequence selected from SEQ ID NO: 1- 2163 in which at least one serine, threonine, or tyrosine residue in the selected sequence is phosphorylated with a hydrolyzable or non-hydrolyzable phosphate group.
  • the peptide is an comprises an O-GlcNAcylated peptide that comprises an amino acid sequence selected from SEQ ID NOs: 2163-2167 and 2374.
  • the dendritic cells thereby become phosphopeptide- loaded.
  • the phosphopeptide is phosphorylated with a non-hydrolyzable phosphate group.
  • the dendritic cells made by the presently disclosed methods provide in vitro compositions of dendritic cells, which in some embodiments are useful as immunotherapeutic agents.
  • the presently disclosed subject matter also provides in some embodiments synthetic phosphopeptides.
  • the synthetic phosphopeptides comprise from 10-50 amino acid residues.
  • the synthetic phosphopeptides comprise the amino acid sequence RVAsPTSGVK (SEQ ID NO: 65) or the amino acid sequence RVAsPTSGVKR (SEQ ID NO: 66), wherein in some embodiments the serine residue at position 4 is phosphorylated with a hydrolyzable or non-hydrolyzable phosphate group, and wherein in some embodiments adjacent amino acid residues to the sequence are adjacent sequences in the human insulin substrate-2 (IRS-2) protein.
  • the phosphopeptide is useful for loading dendritic cells so that they present phosphopeptide on HLA-A*0301 molecules.
  • the presently disclosed subject matter also provides in some embodiments isolated and purified phosphopeptides.
  • the isolated and purified phosphopeptides consist of between 8 and 50 contiguous amino acid residues derived from a native human protein.
  • the isolated and purified phosphopeptides comprise a sequence selected from SEQ ID NO: 1-2163, wherein at least one serine, threonine, or tyrosine residue in the selected sequence is phosphorylated with a hydrolyzable or non-hydrolyzable phosphate group, wherein in some embodiments the contiguous amino acids adjacent to the selected sequence in the phosphopeptide are the adjacent contiguous amino acid residues in the native human protein.
  • the phosphopeptides are substantially free of other peptides.
  • compositions comprising the target peptides that are in some embodiments substantially free of human cells.
  • the compositions comprise an admixture with one or more distinct peptides.
  • the composition comprises melanoma-specific peptides or leukemia-specific peptides.
  • the composition comprises an immune adjuvant.
  • the composition is an admixture of target peptides, wherein a least one target peptide that binds to each of an HLA-A*0101, HLA-A*0301, HLA-B*4402, HLA-B*2705, and HLA-B*0702 molecule is present in the admixture.
  • the composition comprises at least one target peptide that binds to HLA-A*0201.
  • compositions comprising a target peptide as disclosed herein in a complex with an HLA-A*0101, HLA-A*0301, HLA-B*4402, HLA-B*2705, HLA-B* 1402, or HLA- B*0702 molecule.
  • the complex is a tetramer.
  • compositions for treating a proliferative disease comprise a tetanus peptide and one or more synthetic target peptides.
  • each of synthetic target peptides is at least or about 8, 9, 10, 11, 12, 13, 14, or 15 amino acids long and comprises an amino acid sequence that is at least 90% identical to any one of SEQ ID NOs: 1-2167 and 2374.
  • the tetanus peptide comprises an amino acid sequence that is selected from the group consisting of an amino acid sequence that is at least 90% identical to SEQ ID NO: 2376 or SEQ ID NO: 2377 and an amino acid sequence that is 100% identical to SEQ ID NO: 2376 or SEQ ID NO: 2377.
  • the tetanus peptide is about or at least 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25 natural or non-natural amino acids in length.
  • the tetanus peptide comprises an amino acid sequence that is at least 90% identical to an 10-25 amino acid subsequence of a wild type tetanus toxoid protein.
  • the tetanus peptide binds to one or more MHC Class II molecules when administered to a subject. In some embodiments, the tetanus peptide is modified so as to prevent formation of tetanus peptide secondary structures.
  • the one or more synthetic target peptides are selected from the group consisting of (a) a first synthetic target peptide comprising a sequence selected from the group consisting of SEQ ID NO: 398, SEQ ID NO: 2000, SEQ ID NO: 2001, and SEQ ID NO: 2002; (b) a second synthetic target peptide comprising a sequence selected from the group consisting of SEQ ID NO: 418, SEQ ID NO: 2062, and SEQ ID NO: 2063; (c) a third synthetic target peptide comprising a sequence selected from the group consisting of SEQ ID NO: 427; SEQ ID NO: 2078, SEQ ID NO: 2079, SEQ ID NO: 2080, SEQ ID NO: 2081, SEQ ID NO: 2082, SEQ ID NO: 2083, and SEQ ID NO: 2084; (d) a fourth synthetic target peptide selected from the group consisting of SEQ ID NO: 396; and SEQ ID NO: 1996; and (
  • the composition has an ability to stimulate a T cell-mediated immune response to the one or more synthetic target peptides and the composition is capable of eliciting a memory T cell response to the one or more synthetic target peptides.
  • the first synthetic target peptide is SEQ ID NO: 398
  • the second synthetic target peptide is SEQ ID NO: 2080
  • the third synthetic target peptide is SEQ ID NO: 418.
  • At least one serine residue in any of the synthetic target peptides is replaced with a homoserine relative to any one of SEQ ID NOs: 1-2167 and 2374.
  • the composition comprises a non-hydrolyzable phosphate.
  • At least one of the synthetic target peptides binds a MHC class I molecule at least 500% more tightly than its native counterpart.
  • at least one of the synthetic target peptides is capable of eliciting more activated CD8 + T cells specific for MHC class I molecule complexed with the phosphopeptide of SEQ ID NO: 427 than a control composition comprising the same target peptides wherein SEQ ID NO: 427 is used rather than SEQ ID NO: 2080.
  • the composition is at least 100% more immunogenic than a control composition comprising the same target peptides wherein SEQ ID NO: 427 is used rather than SEQ ID NO: 2080.
  • the composition is capable of reducing tumor size in a NOD/SCID/I- 2Ryc ⁇ / ⁇ mouse comprising transgenic T cells specific for human beta-catenin phosphopeptides such as SEQ ID NO: 427, by at least 30%> compared to a control composition comprising the same peptides wherein SEQ ID NO: 427 is used rather than SEQ ID NO: 2080.
  • the composition is immunologically suitable for at least 60 to 88% of melanoma patients.
  • the composition comprises at least 5, 10, or 15 different synthetic target peptides.
  • At least one, more than one, or all of the synthetic target peptide are capable of binding to an MHC class I molecule selected from the group consisting of HLA-A*0201, HLA-A*0101, HLA-A*0301, HLA-B*4402, HLA-B*0702, HLA-B*-2705 and HLA-B* 1402.
  • at least one, more than one, or all of the synthetic target peptides are capable of binding to an MHC class I molecule selected from the group consisting of HLA-A*0101, HLA-A*0301, HLA-B*4402, HLA-B*0702, HLA-B*-2705 and HLA-B* 1402.
  • At least one, more than one, or all of the synthetic target peptides are capable of binding to an MHC class I molecule of the HLA-A*0201, HLA-A*0101 or HLA-B*0702 alleles.
  • the composition is capable of increasing the 5 -year survival rate of malignant melanoma patients treated with the composition by at least 20 percent relative to average 5 -year survival rates that could have been expected without treatment with the composition.
  • the composition is capable of increasing the survival rate of malignant melanoma patients treated with the composition by at least 20 percent relative to a survival rate that could have been expected without treatment with the composition.
  • the composition is capable of increasing the treatment response rate of malignant melanoma patients treated with the composition by at least 20 percent relative to a treatment rate that could have been expected without treatment with the composition.
  • the composition is capable of increasing the overall median survival of patients of malignant melanoma patients treated with the composition by at least two months relative to an overall median survival that could have been expected without treatment with the composition.
  • the composition further comprises at least one peptide derived from MelanA (MART -I), g lOO (Pmel 17), tyrosinase, TRP-1, TRP-2, MAGE-1, MAGE-3, BAGE, GAGE-1, GAGE-2, pl5(58), CEA, RAGE, NY-ESO (LAGE), SCP-1, Hom/Mel-40, PRAME, p53, H-Ras, HER-2/neu, BCR-ABL, E2A-PRL, H4-RET, IGH-IGK, MYL-RAR, Epstein Barr virus antigens, EBNA, human papillomavirus (HPV) antigens E6 and E7, TSP-180, MAGE-4, MAGE-5, MAGE-6, pl85erbB2, pl80erbB-3, c-met, nm- 23H1, PSA, TAG-72-4, CA 19-9, CA 72-4, CAM
  • the composition further comprises an agent selected from the group consisting of a CTLA-4 antagonist, vermurafenib, ipilimumab, dacarbazine, carmustine, tamoxifen, IL-2, temozolomide, imatinib, gefitinib, erlotinib, sunitinib, a tyrphostin, a PD-1 agonist, and telatinib.
  • the composition further comprises darcarbazine, carmustine, and tamoxifen.
  • the composition further comprises an adjuvant selected from the group consisting of montanide ISA-51 (Seppic, Inc.), QS-21 (Aquila Pharmaceuticals, Inc.), , GM-CSF, cyclophosphamide, bacillus Calmette-Guerin (BCG), corynbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenezene (DNCB), keyhole limpet hemocyanins (KLH), Freunds adjuvant (complete and incomplete), mineral gels, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, dinitrophenol, diphtheria toxin (DT).
  • an adjuvant selected from the group consisting of montanide ISA-51 (Seppic, Inc.), QS-21 (Aquila Pharmaceuticals, Inc.), , GM-CSF, cyclophosphamide, bac
  • the presently disclosed subject matter also provides in some embodiments methods for immunizing a mammal to diminish the risk of, the growth of, or the invasiveness of a proliferative disease such as cancer.
  • the presently disclosed methods comprise administering to the mammal a target peptide composition, whereby CD8 + T cells are activated be the phosphopeptide.
  • the phosphopeptide comprises at least 15 amino acid residues.
  • the presently disclosed methods further comprise administering TLR- ligand oligonucleotide-CpG.
  • at least two target peptides are administered that share a sequence of at least 6 amino acid residues.
  • the mammal is a transgenic non-human comprising a human HLA. In some embodiments, the mammal is a dog, cat, horse, or mouse. In some embodiments, the mammal has a melanoma. In some embodiments, the mammal has metastatic melanoma. In some embodiments, the mammal has an increased risk of developing a melanoma.
  • the presently disclosed subject matter also provides in some embodiments methods for contacting a sample isolated from a patient with an antibody that specifically binds to the target peptide and does not bind to a peptide consisting of the same amino acid sequence but devoid of phosphorylation/O-GlcNAC moieties and measuring or detecting antibody bound to the sample.
  • the sample is tissue, blood, serum, plasma, lymph, urine, saliva, mucus, stool, or skin.
  • the sample is a biopsy sample from tumor or normal tissue.
  • the sample is from a lymph node.
  • the presently disclosed subject matter also provides in some embodiments molecules comprising an antigen-binding region of an antibody, wherein the molecule specifically binds to the target peptide and does not bind to a peptide consisting of the same amino acid sequence but devoid of phosphorylation and/or O-GlcNAC moieties.
  • the antibody is a monoclonal antibody.
  • the molecule is a single chain variable region (ScFv).
  • kits for measuring a phosphoprotein comprising a sequence selected from SEQ ID NO: 1-2163 and including a phosphorylated serine, threonine, or tyrosine residue.
  • the presently disclosed kits comprise a molecule comprising an antigen-binding region of an antibody, wherein the molecule specifically binds to the target peptide and does not bind to a protein consisting of the same amino acid sequence but devoid of a phosphorylation/O-GlcNAC moiety.
  • the kit comprises an antibody that specifically binds to a portion of the molecule that is distinct from the antigen-binding region.
  • the kit further comprises a detectable label.
  • the kit further comprises a solid support on which binding complexes of the molecule and the target peptides can be captured.
  • the presently disclosed subject matter also provides in some embodiments methods comprising contacting dendritic cells in vitro with an isolated phosphopeptide comprising between 8 and 50 contiguous amino acids comprising a sequence selected from SEQ ID NO: 1-2163, said phosphopeptide including at least one serine, threonine, or tyrosine residue that is phosphorylated, whereby the dendritic cells become phosphopeptide-loaded.
  • the methods involve transfusing or injecting the phosphopeptide-loaded dendritic cells into a cancer patient, optionally a leukemia patient, wherein the sequence is selected from the group consisting of SEQ ID NO: 267, 269-270, 272-274, 276, 282-289, 291-298, 302-308, 310, 312-325, 327-328, 330-331, 333-334, 336-340, 342-352, 356, 358-361, 363, 366-368, 370-371, 374-375, 377-379, 382-383, 385-389, 391-392, 1529-1534, 1539-1544, 1549-1570, 1576-1578, 1594-1617, 1622-1627, 1634-1646, 1656-1680, 1684-1687, 1691-1735, 1739-1744, 1748-1754, 1758-1763, 1767-1784, 1788-1826, 1836-1842, 1846-1874, 1878-1885, 1892-1905, 1909-19
  • the methods involve transfusing the stimulated CD8 + T cells into a melanoma or leukemia patient.
  • the CD8 + T cells are autologous to the patient.
  • the CD8 + T cells are allogeneic to the patient.
  • the dendritic cells are contacted with a plurality of said isolated phosphopeptides.
  • the dendritic cells are contacted with a plurality of said isolated phosphopeptides which are linked by a spacer of 10-50 amino acid residues.
  • the presently disclosed subject matter also provides in vitro compositions comprising dendritic cells.
  • the in vitro population of dendritic cells comprises a composition for treating a proliferative disease as disclosed herein or a composition comprising at least one target peptide having an amino acid sequence at least 90% identical to any of SEQ ID NOs: 1-2167 and 2374.
  • the dendritic cells are loaded with a phosphopeptide consisting of between 8 and 14 contiguous amino acids comprising a sequence selected from SEQ ID NO: 1-2163, said phosphopeptide including at least one serine, threonine, or tyrosine residue that is phosphorylated.
  • the phosphopeptide comprises at least one amino acid residue that is not in its native human protein.
  • the at least one amino acid residue is an optimal anchor residue for its corresponding HLA molecule.
  • the phosphopeptide is phosphorylated with a non-hydrolyzable phosphate group, which in some embodiments is a -CF 2 -PO 3 H group.
  • the phosphopeptide is phosphorylated with a non-hydrolyzable phosphate group that in some embodiments is a -CH 2 -PO 3 H group.
  • the presently disclosed subject matter also provides in some embodiments synthetic phosphopeptides consisting of from 10-50 amino acid residues, comprising the sequence RVAsPTSGVK (SEQ ID NO: 65) or RVAsPTSGVKR (SEQ ID NO: 66), wherein the serine residue at position 4 is phosphorylated with a hydrolyzable or non-hydrolyzable phosphate group, and wherein adjacent amino acid residues to the sequence are adjacent sequences in human insulin substrate-2 (IRS-2) protein.
  • the composition comprises the synthetic phosphopeptide in a complex with A* 0301.
  • the presently disclosed subject matter also provides in some embodiments concatamers of at least two phosphopeptides that are linked by a spacer of 10-50 amino acid residues.
  • compositions comprising at least three synthetic peptides which are exactly, about, or at least 8, 9, 10, 11, 12, 13, 14, or 15 or more amino acids long.
  • the first peptide comprises a sequence selected from the group consisting of selected from a group consisting of SEQ ID NO: 398, SEQ ID NO: 2000, SEQ ID NO: 2001, and SEQ ID NO: 2002 (BCAR3).
  • the second peptide comprises a sequence selected from the group consisting of SEQ ID NO: 427, SEQ ID NO: 2078, SEQ ID NO: 2079, SEQ ID NO: 2080, SEQ ID NO: 2081, SEQ ID NO: 2082, SEQ ID NO: 2083, and SEQ ID NO: 2084 (beta-catenin).
  • the third peptide comprises a sequence selected from the group consisting of SEQ ID NO: 418, SEQ ID NO: 2062, and SEQ ID NO: 2063 (IRS-2) wherein said composition has the ability to stimulate an immune response to said first second or third peptides.
  • the first peptide is SEQ ID NO: 398.
  • the second peptide is SEQ ID NO: 2080.
  • the third peptide is SEQ ID NO: 418.
  • at least one serine residue in any of the peptides is replaced with a homo-serine.
  • the composition comprises a non-hydrolyzable phosphate.
  • at least one of the peptides binds MHC class I at least 500% more tightly than its native counterpart.
  • At least one of the peptides is capable of eliciting more activated CD8 + T cells specific for MHC class I molecule complexed with the phosphopeptide of SEQ ID NO: 427 than a control composition comprising the same peptides except SEQ ID NO: 427 rather than SEQ ID NO: 2080.
  • the compositions are at least 100% more immunogenic than a control composition comprising the same peptides except SEQ ID NO: 427 rather than SEQ ID NO: 2080.
  • the compositions are capable of reducing tumor size in a NOD/SCID/IL-2Ryc ⁇ ⁇ mouse by at least 30% compared to a control composition comprising the same peptides except SEQ ID NO: 427 rather than SEQ ID NO: 2080.
  • the compositions are immunologically suitable for at least 60% to 88% of melanoma patients.
  • the compositions comprise at least 5, 10, or 15 different peptides.
  • the compositions comprise a peptide capable of binding to an MHC class I molecule selected from the group consisting of HL A- A* 0201, HLA-A*0101, HLA-A*0301, HLA-B*4402, HLA-B*0702, HLA-B*-2705, and HLA-B* 1402.
  • the compositions comprise a peptide capable of binding to an MHC class I molecule selected from the group consisting of HLA-A*0101, HLA-A*0301, HLA-B*4402, HLA-B*0702, HLA-B*-2705, and HLA-B* 1402.
  • the compositions comprise a peptide capable of binding to an HLA- A*0101 or an HLA-B*0702 MHC class I molecule.
  • the compositions are capable of increasing the 5-year survival rate of malignant melanoma patients treated with the composition by at least 20 percent relative to average 5-year survival rates that could have been expected without treatment with the composition. In some embodiments, the compositions are capable of increasing the survival rate of malignant melanoma patients treated with the composition by at least 20 percent relative to a survival rate that could have been expected without treatment with the composition. In some embodiments, the compositions are capable of increasing the treatment response rate of malignant melanoma patients treated with the composition by at least 20 percent relative to a treatment rate that could have been expected without treatment with the composition. In some embodiments, the compositions are capable of increasing the overall median survival of patients of malignant melanoma patients treated with the composition by at least two months relative to an overall median survival that could have been expected without treatment with the composition.
  • the compositions comprise at least one peptide derived from a MelanA (MART -I) polypeptide, a gplOO (Pmel 17) polypeptide, a tyrosinase polypeptide, a TRP-1 polypeptide, a TRP-2 polypeptide, a MAGE-1 polypeptide, a MAGE-3 polypeptide, a BAGE polypeptide, a GAGE-1 polypeptide, a GAGE-2 polypeptide, a pl5(58) polypeptide, a CEA polypeptide, a RAGE polypeptide, an NY- ESO (LAGE) polypeptide, an SCP-1 polypeptide, a Hom/Mel-40 polypeptide, a PRAME polypeptide, a p53 polypeptide, an H-Ras polypeptide, a HER-2/neu polypeptide, a BCR-ABL polypeptide, an E2A-PRL polypeptide, an H4-RET polypeptide
  • the compositions comprise an agent selected from the group consisting of a CTLA-4 antagonist, vermurafenib, ipilimumab, dacarbazine, IL- 2, temozolomide, imatinib, gefitinib, erlotinib, sunitinib, tyrphostins and telatinib.
  • the compositions comprise dacarbazine, carmustine and tamoxifen.
  • compositions comprise an adjuvant selected from the group consisting of montanide ISA-51 (Seppic, Inc., Fairfield, New Jersey, United States of America), QS-21 (Aquila Biopharmaceuticals, Inc., Lexington, Massachusetts, United States of America), tetanus helper peptides, GM-CSF, cyclophosamide, bacillus Calmette-Guerin (BCG), corynbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenezene (DNCB), keyhole limpet hemocyanins (KLH), Freunds adjuvant (complete and incomplete), mineral gels, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, dinitrophenol, diphtheria toxin (DT).
  • montanide ISA-51 Seppic, Inc., Fairfield, New Jersey, United States of America
  • the presently disclosed subject matter also provides compositions for treating a proliferative disease.
  • the compositions comprise (i) a tetanus peptide; and (ii) at least or about 1 , 2, 3, 4, 5, or more synthetic target peptides, each of which is at least or about 8, 9, 10, 1 1 , 12, 13, 14, 15, or more amino acids long.
  • the tetanus peptide comprises an amino acid sequence at least 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identical to SEQ ID NO: 2376 or SEQ ID NO: 2377.
  • the tetanus peptide comprises an amino acid sequence that is at least 90% identical to SEQ ID NO: 2376 or SEQ ID NO: 2377. In some embodiments, the tetanus peptide comprises an amino acid sequence that is 100% identical to SEQ ID NO: 2376 or SEQ ID NO: 2377.
  • the at least or about 1 , 2, 3, 4, 5, or more synthetic target peptide(s) is/are selected from the group consisting of (A) a first target peptide comprising a sequence selected from the group consisting of SEQ ID NO: 398, SEQ ID NO: 2000, SEQ ID NO: 2001 , and SEQ ID NO: 2002; (B) a second target peptide comprising a sequence selected from the group consisting of SEQ ID NO: 418, SEQ ID NO: 2062, and SEQ ID NO: 2063; (C) a third target peptide comprising a sequence selected from the group consisting of SEQ ID NO: 427; SEQ ID NO: 2078, SEQ ID NO: 2079, SEQ ID NO: 2080, SEQ ID NO: 2081 , SEQ ID NO: 2082, SEQ ID NO: 2083, and SEQ ID NO: 2084; (D) a fourth target peptide selected from the group consisting of SEQ ID NO: 396; and SEQ ID NO
  • the first target peptide is SEQ ID NO: 398.
  • the second target peptide is SEQ ID NO: 2080.
  • the third target peptide is SEQ ID NO: 418.
  • at least one serine residue in any of the target peptides is replaced with a homoserine.
  • the composition for treating a proliferative disease comprises a non-hydrolyzable phosphate.
  • At least one of the target peptides binds a MHC class I molecule at least 500% more tightly than its native counterpart.
  • At least one of the target peptides is capable of eliciting more activated CD8 + T cells specific for MHC class I molecule complexed with the phosphopeptide of SEQ ID NO: 427 than a control composition comprising the same target peptide(s) but wherein SEQ ID NO: 427 is present rather than SEQ ID NO: 2080.
  • the composition is at least 100% more immunogenic than a control composition comprising the same target peptide(s) but wherein SEQ ID NO: 427 is present in the composition rather than SEQ ID NO: 2080.
  • the composition is capable of reducing tumor size in a NOD/SCID/IL-2RYC ⁇ ⁇ mouse comprising transgenic T cells specific for human ⁇ -catenin phosphopeptides such as SEQ ID NO: 427, by at least 30% compared to a control composition comprising the same peptides wherein SEQ ID NO: 427 is present in the composition rather than SEQ ID NO: 2080.
  • the composition is immunologically suitable for at least 60 to 88% of melanoma patients.
  • the composition for treating a proliferative disease comprises at least 5 different target peptides. In some embodiments, the composition for treating a proliferative disease comprises at least 10 different target peptides. In some embodiments, the composition for treating a proliferative disease comprises at least 15 different target peptides.
  • the composition for treating a proliferative disease comprises a target peptide capable of binding to an MHC class I molecule selected from the group consisting of HLA-A*0201 , HLA-A*0101 , HLA-A*0301 , HLA- B*4402, HLA-B*0702, HLA-B*-2705 and HLA-B* 1402.
  • the composition for treating a proliferative disease comprises a target peptide capable of binding to an MHC class I molecule selected from the group consisting of HLA- A*0101, HLA-A*0301, HLA-B*4402, HLA-B*0702, HLA-B*-2705 and HLA- B* 1402.
  • the composition for treating a proliferative disease comprises a target peptide capable of binding to an MHC class I molecule of the HLA-A*0201, HLA-A*0101 or HLA-B*0702 alleles.
  • the composition for treating a proliferative disease is capable of increasing the 5 -year survival rate of malignant melanoma patients treated with the composition by at least 20 percent relative to average 5 -year survival rates that could have been expected without treatment with the composition. In some embodiments, the composition for treating a proliferative disease the composition is capable of increasing the survival rate of malignant melanoma patients treated with the composition by at least 20 percent relative to a survival rate that could have been expected without treatment with the composition. In some embodiments, the composition for treating a proliferative disease is capable of increasing the treatment response rate of malignant melanoma patients treated with the composition by at least 20 percent relative to a treatment rate that could have been expected without treatment with the composition. In some embodiments, the composition for treating a proliferative disease is capable of increasing the overall median survival of patients of malignant melanoma patients treated with the composition by at least two months relative to an overall median survival that could have been expected without treatment with the composition.
  • the composition for treating a proliferative disease comprises at least one peptide derived from MelanA (MART-I), gplOO (Pmel 17), tyrosinase, TRP-1, TRP-2, MAGE-1, MAGE-3, BAGE, GAGE-1, GAGE-2, pl5(58), CEA, RAGE, NY-ESO (LAGE), SCP-1, Hom/Mel-40, PRAME, p53, H-Ras, HER- 2/neu, BCR-ABL, E2A-PRL, H4-RET, IGH-IGK, MYL-RAR, Epstein Barr virus antigens, EBNA, human papillomavirus (HPV) antigens E6 and E7, TSP-180, MAGE-4, MAGE-5, MAGE-6, pl85erbB2, pl80erbB-3, c-met, nm-23Hl, PSA, TAG-72-4, CA 19-9, CA 72-4,
  • the composition for treating a proliferative disease comprises an agent selected from the group consisting of a CTLA-4 antagonist, vermurafenib, ipilimumab, dacarbazine, IL-2, temozolomide, imatinib, gefitinib, erlotinib, sunitinib, tyrphostins, a PD-1 agonist and telatinib.
  • the composition for treating a proliferative disease further comprises darcarbazine, carmustine and tamoxifen.
  • the composition for treating a proliferative disease comprises an adjuvant selected from the group consisting of montanide ISA-51 (Seppic, Inc.), QS-21 (Aquila Pharmaceuticals, Inc.), , GM-CSF, cyclophosamide, bacillus Calmette-Guerin (BCG), corynbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenezene (DNCB), keyhole limpet hemocyanins (KLH), Freunds adjuvant (complete and incomplete), mineral gels, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, dinitrophenol, diphtheria toxin (DT).
  • an adjuvant selected from the group consisting of montanide ISA-51 (Seppic, Inc.), QS-21 (Aquila Pharmaceuticals, Inc.), , GM-CSF, cyclophos
  • the presently disclosed subject matter also provides in some embodiments in vitro populations of dendritic cells comprising at least one of the aforementioned target peptide compositions.
  • the presently disclosed subject matter also provides in some embodiments in vitro populations of CD8 + T cells capable of being activated upon being brought into contact with a population of dendritic cells, wherein the dendritic cells comprise at least one of the aforementioned target peptide compositions.
  • the presently disclosed in vitro populations of CD8 + T cells are capable of being activated upon being brought into contact with a population of dendritic cells that comprise a composition for treating a proliferative disease as disclosed herein or a composition comprising at least one target peptide having an amino acid sequence at least 90% identical to any of SEQ ID NOs: 1-2167 and 2374.
  • the presently disclosed subject matter also provides in some embodiments an antibody or antibody-like molecule that specifically binds to any of the target peptides disclosed herein.
  • the presently disclosed antibody or antibodylike molecule specifically binds to both a first complex of MHC class I molecule and a peptide represented by SEQ ID NO: 2080 and a second complex of MHC class I molecule and a peptide represented by SEQ ID NO: 427; wherein the antibody or antibody-like molecule does not bind the same complexes containing an unphosphorylated version of SEQ ID NO: 2080 or SEQ ID NO: 427.
  • the antibody or antibody-like molecule is a member of the immunoglobulin superfamily.
  • the antibody or antibody-like molecule comprises a binding member selected from the group consisting an Fab, Fab', F(ab') 2 , Fv, and a single-chain antibody.
  • the antibody or antibody-like molecule comprises a therapeutic agent selected from the group consisting of an alkylating agent, an antimetabolite, a mitotic inhibitor, a taxoid, a vinca alkaloid and an antibiotic.
  • the antibody or antibody- like molecule is a T cell receptor, optionally linked to a CD3 agonist.
  • the presently disclosed subject matter also provides in some embodiments an in vitro population of T cells transfected with mRNA encoding a T cell receptor that specifically binds to any of the target peptides disclosed herein.
  • the presently disclosed subject matter also provides in some embodiments antibodies or antibody-like molecules that specifically bind to both a first complex of MHC class I molecule and a peptide represented by SEQ ID NO: 2080 and a second complex of MHC class I molecule and a peptide represented by SEQ ID NO: 427.
  • the antibodies or antibody-like molecules do not bind the same complexes containing an unphosphorylated version of SEQ ID NO: 2080 or SEQ ID NO: 427.
  • the antibodies or antibody-like molecules are members of the immunoglobulin superfamily.
  • the antibodies or antibody-like molecules comprise a binding member selected from the group consisting of an Fab, Fab', F(ab') 2 , Fv, and a single-chain antibody.
  • the antibodies or antibody-like molecules comprise a therapeutic agent selected from the group consisting of an alkylating agent, an antimetabolite, a mitotic inhibitor, a taxoid, a vinca alkaloid and an antibiotic.
  • the antibodies or antibody- like molecules are T cell receptors.
  • the presently disclosed subject matter also provides in some embodiments in vitro populations of T cells comprising a recombinant nucleic acid encoding the presently disclosed T cell receptors such that recombinant TCRs are expressed on their surfaces.
  • the presently disclosed subject matter also provides in some embodiments methods for treating and/or preventing cancer, such as but not limited to melanoma or leukemia.
  • the presently disclosed methods comprise administering to a patient in need thereof a dose of the aforementioned target peptide compositions in combination with a pharmaceutically acceptable carrier.
  • the presently disclosed subject matter also provides in some embodiments methods for treating and/or preventing cancer.
  • the presently disclosed methods comprise administering to a patient in need thereof a dose of the aforementioned activated CD8 + T cells in combination with a pharmaceutically acceptable carrier.
  • the presently disclosed subject matter also provides in some embodiments methods for treating and/or preventing cancer comprising administering to a patient in need thereof a dose of the aforementioned population of the dendritic cells in combination with a pharmaceutically acceptable carrier.
  • the presently disclosed subject matter also provides in some embodiments methods for of treating and/or preventing cancer comprising administering to a patient in need thereof the population T cells transfected with m NA encoding a TCR that specifically binds to any of the target peptides disclosed herein in combination with a pharmaceutically acceptable carrier.
  • the TCR is optionally linked to a CD3 agonist.
  • the methods can in some embodiments comprise administering to a patient in need thereof a dose of a composition for treating a proliferative disease as presented herein, a dose of an in vitro population of CD8+ T cells as disclosed herein, and/or a population of dendritic cells as disclosed herein.
  • the presently disclosed subject matter also provides in some embodiments methods for making a cancer vaccine.
  • the presently disclosed methods comprise combining the target peptide compositions with a chemotherapeutic agent, an adjuvant, a pharmaceutically acceptable carrier; and placing the composition, adjuvant and pharmaceutical carrier into a syringe into a syringe.
  • the presently disclosed methods comprise (a) combining the composition of any of claims 1-29 and a pharmaceutically acceptable carrier, optionally a carrier that is pharmaceutically acceptable for use in a human, with an adjuvant selected from the group consisting of montanide ISA-51 (Seppic, Inc.), QS-21 (Aquila Pharmaceuticals, Inc.), , GM-CSF, cyclophosamide, bacillus Calmette-Guerin (BCG), corynbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenezene (DNCB), keyhole limpet hemocyanins (KLH), Freunds adjuvant (complete and incomplete), mineral gels, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, dinitrophenol, diphtheria toxin (DT); and (b) placing the composition, adjuvant, and pharmaceutical carrier into a
  • the presently disclosed subject matter also provides in some embodiments, methods for screening target peptides for inclusion in an immunotherapy.
  • the presently disclosed methods comprise (a) contacting a target peptide with a population of human T cells; (b) determining whether the target peptide is capable of inducing a target peptide-specific memory T cell response in a portion of the population of human T cells; and (c) selecting the target peptide for inclusion in the immunotherapy composition if the target peptide elicits a memory T cell response in the portion.
  • the presently disclosed subject matter also provides methods for determining the prognosis of a cancer patient.
  • the presently disclosed methods comprise (a) contacting a target peptide with a population of human T cells obtained from the patient; (b) determining whether the target peptide is capable of inducing a target peptide-specific memory T cell response in a portion of the population ; and (c) determining that the cancer patient has a better prognosis if the portion mounts a memory T cell response to said target peptide than if the portion did not mount a memory T cell response to said target peptide.
  • the presently disclosed subject matter also provides methods for inducing a target peptide specific memory T cell response in a patient having a proliferative disorder.
  • the presently disclosed subject matter methods comprise (a) administering to a patient in need thereof a composition comprising at least one target peptide and an adjuvant; and (b) inducing the memory T cell response to the at least one target peptide wherein the memory T cell response is capable of treating the disorder.
  • the at least one target peptide comprises (i) a first peptide selected from the group consisting of SEQ ID NO: 398, SEQ ID NO: 2000, SEQ ID NO: 2001, and SEQ ID NO: 2002; and/or (ii) a second peptide comprising a sequence selected from the group consisting of SEQ ID NO: 418, SEQ ID NO: 2062, and SEQ ID NO: 2063; and/or (iii) a third peptide comprising a sequence selected from the group consisting of SEQ ID NO: 427; SEQ ID NO: 2078, SEQ ID NO: 2079, SEQ ID NO: 2080, SEQ ID NO: 2081, SEQ ID NO: 2082, SEQ ID NO: 2083, and SEQ ID NO: 2084; and/or (iv) a fourth peptide selected from the group consisting of SEQ ID NO: 396 and SEQ ID NO: 1996; and/or (v) a fifth peptide from the group consisting of SEQ ID NO:
  • the proliferative disorder is cancer.
  • the cancer is melanoma.
  • the adjuvant is selected from the group consisting of a TLR agonist, a Montanide ISA-51, and a tetanus helper peptide.
  • the composition comprises at least one peptide derived from MelanA (MART-I), gplOO (Pmel 17), tyrosinase, TRP-1, TRP-2, MAGE-1, MAGE-3, BAGE, GAGE-1, GAGE-2, pl5(58), CEA, RAGE, NY-ESO (LAGE), SCP-1, Hom/Mel-40, PRAME, p53, H-Ras, HER- 2/neu, BCR-ABL, E2A-PRL, H4-RET, IGH-IGK, MYL-RAR, Epstein Barr virus antigens, EBNA, human papillomavirus (HPV) antigens E6 and E7, TSP-180, MAGE-4, MAGE-5, MAGE-6, pl85erbB2, pl80erbB-3, c-met, nm-23Hl, PSA, TAG-72-4, CA 19-9, CA 72-4, CAM 17.
  • MART-I MelanA
  • the composition is immunologically suitable for at least 60 to 88% of melanoma patients. In some embodiments, the composition comprises at least 5, 10, or 15 different target peptides. In some embodiments, the composition comprises a peptide capable of binding to an MHC class I molecule selected from the group consisting of HLA-A*0201, HLA- A*0101, HLA-A*0301, HLA-B*4402, HLA-B*0702, HLA-B*-2705 and HLA- B* 1402.
  • the composition comprises a peptide capable of binding to an MHC class I molecule selected from the group consisting of HLA- A*0101, HLA-A*0301, HLA-B*4402, HLA-B*0702, HLA-B*-2705, HLA-B* 1402 and combinations thereof.
  • the composition comprises a peptide capable of binding to an MHC class I molecule of the HLA-A*0201, HLA-A*0101 or HLA-B*0702 alleles.
  • the composition comprises an agent selected from the group consisting of CTLA-4 antagonists, vermurafenib, ipilimumab, dacarbazine, IL-2, temozolomide, imatinib, gefitinib, erlotinib, sunitinib, tyrphostins, a PD-1 agonist and telatinib.
  • an agent selected from the group consisting of CTLA-4 antagonists, vermurafenib, ipilimumab, dacarbazine, IL-2, temozolomide, imatinib, gefitinib, erlotinib, sunitinib, tyrphostins, a PD-1 agonist and telatinib.
  • the methods increase the 5 -year survival rate of the patients treated with the composition by at least 20 percent relative to average 5 -year survival rates that could have been expected without treatment with the composition. In some embodiments of the presently disclosed methods, the methods are capable of increasing the overall median survival of patients treated with the composition by at least two months relative to an overall median survival that could have been expected without treatment with the composition.
  • the presently disclosed methods further comprise the step of administering to the patient darcarbazine, carmustine, and tamoxifen.
  • the presently disclosed methods comprise the step of administering to the patient an adjuvant selected from the group consisting of montanide ISA-51 (Seppic, Inc.), QS-21 (Aquila Pharmaceuticals, Inc.), a tetanus helper peptide, GM-CSF, cyclophosamide, bacillus Calmette-Guerin (BCG), corynbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenezene (DNCB), keyhole limpet hemocyanins (KLH), Freunds adjuvant (complete and incomplete), mineral gels, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, dinitrophenol, diphtheria toxin (DT).
  • an adjuvant selected from the group consisting of montanide ISA-51 (Seppic, Inc.), QS-21 (Aquila Pharmaceuticals, Inc.
  • the target peptides are administered individually. In some embodiments, the target peptides are administered simultaneously. In some embodiments, the at least one target peptide is selected from the group consisting of SEQ ID NOs: 2164, 2165, 2166, 2167, and 2374; or a combinations thereof.
  • the presently disclosed methods further comprise the additional step of determining that the T cell memory response is a T cell central memory response (TCM).
  • TCM T cell central memory response
  • kits comprising various target peptide compositions.
  • the kits also comprise an adjuvant and/or a cytokine.
  • the cytokine is selected from the group consisting of a transforming growth factor (TGF) such as but not limited to TGF-a and TGF- ⁇ ; insulin-like growth factor-I and/or insulin-like growth factor-II; erythropoietin (EPO); an osteoinductive factor; an interferon such as but not limited to interferon-a, - ⁇ , and - ⁇ ; a colony stimulating factor (CSF) such as but not limited to macrophage-CSF (M-CSF); granulocyte-macrophage-CSF (GM- CSF); and granulocyte-CSF (G-CSF).
  • TGF transforming growth factor
  • EPO erythropoietin
  • an osteoinductive factor an interferon such as but not limited to interferon-a, - ⁇ , and - ⁇
  • CSF colony
  • the cytokine is selected from the group consisting of nerve growth factors such as NGF- ⁇ ; platelet-growth factor; a transforming growth factor (TGF) such as but not limited to TGF-a and TGF- ⁇ ; insulin-like growth factor-I and insulin-like growth factor-II; erythropoietin (EPO); an osteoinductive factor; an interferon (IFN) such as but not limited to IFNa, ⁇ , and IFNy; a colony stimulating factor (CSF) such as macrophage-CSF (M- CSF); granulocyte-macrophage-CSF (GM-CSF); and granulocyte-CSF (G-CSF); an interleukin (II) such as but not limited to IL-1, IL-la, IL-2, IL-3, IL-4, IL-5, IL-6, IL- 7, IL-8, IL-9, IL-10, IL-11, IL-12; IL-13, IL-14,
  • the adjuvant selected from the group consisting of montanide ISA-51 (Seppic, Inc.), QS-21 (Aquila Pharmaceuticals, Inc.), a tetanus helper peptide, GM-CSF, cyclophosamide, bacillus Calmette-Guerin (BCG), corynbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenezene (DNCB), keyhole limpet hemocyanins (KLH), Freunds adjuvant (complete and incomplete), mineral gels, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, dinitrophenol, diphtheria toxin (DT).
  • montanide ISA-51 Seppic, Inc.
  • QS-21 Amla Pharmaceuticals, Inc.
  • a tetanus helper peptide GM-CSF
  • cyclophosamide
  • kits further comprise an agent selected from the group consisting of CTLA-4 antagonist, vermurafenib, ipilimumab, dacarbazine, IL-2, temozolomide, imatinib, gefitinib, erlotinib, sunitinib, tyrphostins a PD-1 agonist and telatinib.
  • an agent selected from the group consisting of CTLA-4 antagonist, vermurafenib, ipilimumab, dacarbazine, IL-2, temozolomide, imatinib, gefitinib, erlotinib, sunitinib, tyrphostins a PD-1 agonist and telatinib.
  • the presently disclosed kit comprises at least one target peptide composition comprising at least one target peptide and a cytokine and/or an adjuvant. In some embodiments, the kit comprises at least 2, 3, 4, or 5 target peptide compositions. In some embodiments, the kit comprises a composition as disclosed herein.
  • the presently disclosed kit further comprises at least one peptide derived from MelanA (MART -I), gplOO (Pmel 17), tyrosinase, TRP-1 , TRP-2, MAGE-1, MAGE-3, BAGE, GAGE-1, GAGE-2, pl5(58), CEA, RAGE, NY- ESO (LAGE), SCP-1, Hom/Mel-40, PRAME, p53, H-Ras, HER-2/neu, BCR-ABL, E2A-PRL, H4-RET, IGH-IGK, MYL-RAR, Epstein Barr virus antigens, EBNA, human papillomavirus (HPV) antigens E6 and E7, TSP-180, MAGE-4, MAGE-5, MAGE-6, pl85erbB2, pl80erbB-3, c-met, nm-23Hl, PSA, TAG-72-4, CA 19-9, CA 72-4, CAM 17.1,
  • the at least one target peptide is selected from the group consisting of SEQ ID NOs: 2164, 2165, 2166, 2167, 2374 and combinations thereof.
  • the at least one target peptide composition comprises target peptides is selected from the HLA groupings shown in Tables 14 and 15.
  • the presently disclosed kit comprises at least two target peptides wherein the at least two target peptides are in separate containers.
  • the presently disclosed kit further comprises instructions related to determining whether the at least one target peptide of the composition is inducing a T cell memory response that is a T cell central memory response (Tcm) in a patient.
  • Tcm T cell central memory response
  • Figures 1A-1E show that phosphoS33-P-catenin was broadly expressed in human melanoma.
  • Figure 1A is a tissue microarray composed of Stage III and IV metastatic melanoma samples that were evaluated for phosphoS33-P-catenin and total ⁇ -catenin expression by immunohistochemistry (IHC). Depicted are representative samples showing the range of expression of the protein based on a quantitative staining index (SI) and range in expression were determined as described in EXAMPLES 2-16 herein below. Scale bar: 5X - 250 ⁇ ; 40X - 100 ⁇ .
  • Figures IB and ID are bar graphs showing the distribution of phosphoS33-P-catenin and total ⁇ - catenin expression levels among metastatic melanoma and normal tissue samples, respectively.
  • Figure 1C shows representative samples of phosphoS33-P-catenin and ⁇ - catenin expression in normal tissues by IHC.
  • Figure IE is a representative tissue with strong staining for phosphoS33-P-catenin showing elevated phosphoS33-P-catenin expression in mitotic tumor cells (arrowheads) compared to non-mitotic cells (arrows) 40X; scale bar - 100 ⁇ .
  • Figures 2A-2G are a series of graphs and plots showing modification of the weakly immunogenic pS33-Pcat 3 o created a stronger immunogen in mice and humans.
  • Figure 2A is a plot showing human T cells that were cultured in microwells containing irradiated stimulators pulsed with pS33-Pcat 30 and evaluated for pS33- Pcat-specific responses in a 51 Cr-release assay after 3 and 7 weeks using targets pulsed with either the phosphorylated or unphosphorylated forms of the peptide at an effector to target ratio of 60: 1 (3 weeks) and 20:1 (7 weeks).
  • FIGs 2B and 2C AAD + mice were immunized with peptide-pulsed marrow-derived dendritic cells (BMDCs) and primary responses were evaluated by intracellular cytokine staining ex vivo 7 d later.
  • BMDCs peptide-pulsed marrow-derived dendritic cells
  • tecall responses were determined by priming AAD + mice with peptide-pulsed BMDCs, and boosting with peptide, CpG, and FGK45 28-30 days later. Pooled CD8 + T cells isolated from spleens and lymph nodes 5 days after the boost were evaluated for cytokine production.
  • the dot plots shown are representative of T cell responses from individual mice, gated on CD8 + cells.
  • pS33-Pcat 30 and a positive control peptide, IP30 were tested for their ability to compete with a standard peptide for HLA-A2 binding.
  • IC 50 values are as follows: pS33-Pcat 30 - 327 ng/ml; pS33- Pcat(V) 30 - 41 ng/ml; pS33/S37-Pcat 30 - 678 ng/ml; and IP30 - 27 ng/ml. Data are representative of three independent experiments showing triplicate wells per group. Error bars represent standard error of the mean (SEM).
  • human T cells were cultured in micro wells containing irradiated stimulators pulsed with either pS33-Pcat 30 or pS33-Pcat(V) 3 o and evaluated after 2 weeks of culture in a 51 Cr-release assay using targets pulsed with the phosphopeptides or unphosphorylated peptides at an effector to target ratio of 60: 1.
  • Each symbol represents a micro well culture. Data are representative of two independent experiments using two different donors.
  • Figures 3A-3C show that pS33-Pcat(V)-specific human and murine T cells were cross-reactive and antigenically distinct from the natural phosphopeptide.
  • human T cells were stimulated weekly with pS33-Pcat(V) 30 -pulsed stimulators as in Figure 2.
  • the proportion of CD8 T cells specific for either the modified or natural phosphopeptides was evaluated using tetramers composed of either pS33-Pcat 30 or pS33-Pcat(V) 3 o. Numbers on dot plots are % tetramer + of CD8 T cells.
  • the Right Panel shows a summary with each set of matching symbols representing one well. Data are representative of two independent experiments using two different donors.
  • Figure 3B shows the results of recognition of targets pulsed with graded doses of either pS33-Pcat(V) 3 o or pS33-Pcat 30 by CD8 T cells isolated from AAD + mice immunized with pS33-Pcat(V) 3 o.
  • the Left Panel shows recognition of targets pulsed with 1 ⁇ g/ml of each peptide. Each set of matching symbols represents T cells from a single mouse.
  • the Right Panel presents representative dose response curves for CD8 + T cells from one mouse.
  • FIGS 4A and 4B show that pS33-Pcat-specific T cells recognized endogenous levels of pS33-Pcat 30 on melanoma cells and control tumor growth.
  • the T cell cultures showed 70-85% reactivity on pS33-Pcat 30 -pulsed targets. Data are representative of two independent experiments.
  • the Upper Panel is a schematic of tumor control experiment.
  • the Lower Panel is a graph showing growth of subcutaneous SLM2 tumors in NOD/SCID IL- 2Ryc ⁇ ⁇ mice that received IL-2 only or pS33-Pcat-specific T cells + IL-2. Data are representative of two independent experiments with five (5) mice per group. Error bars indicate SEM. Statistical analysis was done by parametric modeling.
  • FIGS 5A-5C present the results of experiments showing that pS33-Pcat 30 was derived from GSK-3 mediated phosphorylation of ⁇ -catenin.
  • surface peptide-MHC complexes were denatured from untreated melanoma cells or those pretreated with 5 ⁇ of BIO or MeBIO (an inactive form of BIO) for 4 hours. The cells were then allowed to re-express peptide-MHC molecules in the presence of BIO, MeBIO, or 5 ⁇ lactacystin for 12 hours. T cell recognition of the cells was evaluated after 5 hours incubation with pS33-Pcat-specific T cells.
  • Figures 6A-6I show the results of experiments demonstrating that pS33-Pcat- specific T cell recognition correlated with total phosphoS33-P-catenin available for degradation and could be predicted by the subcellular localization of ⁇ -catenin in melanoma cells.
  • Figures 6A, 6B, 6H, and 61 show levels of phosphoS33-P-catenin and total ⁇ -catenin from melanoma cell lines that had been incubated with or without Lactacystin to block proteasome activity were determined by Western blot.
  • Figures 6A and 6H relate to data acquired with cells cultured in the absence of Lactacystin and using four times the amount of protein used for Figures 6B and 61.
  • Figures 6C and 6D present the results of experiments wherein integrated density values for phosphoS33-P-catenin and ⁇ -catenin were determined by scanning densitometry and normalized to those for GAPDH.
  • pS33-Pcat-specific T cell recognition data was from Figure 4A (T cell line 5). Data were analyzed by linear regression and is representative of two independent experiments.
  • Figure 6E depicts sections from formalin-fixed paraffin embedded cell pellets of melanoma cells that were evaluated for the subcellular localization of ⁇ -catenin by IHC as described in EXAMPLES 2-16. Scale bar - 100 ⁇ .
  • Figure 6F is a graph showing recognition of the melanoma cells in each category by pS33-Pcat-specific T cells from Figure 4A (T cell line 5) assessed in triplicate. Data were representative of two independent experiments. Error bars represent SEM.
  • Figure 6G is a bar graph showing metastatic melanoma samples from Figure 1 scored for subcellular localization as in Figure 6E.
  • Figures 7A-7D show expression of phosphoS33-P-catenin and presentation of pS33-Pcat 30 on other tumor types. Expression of phosphoS33-P-catenin and ⁇ -catenin in untreated or Lactacystin-treated melanoma (VMM 18 and DM331; Figure 7 A) and colorectal carcinoma (SW620) and breast carcinoma cell lines (Figure 7C) evaluated by Western blot. Data are representative of two independent experiments. With respect to Figures 7B and 7D, recognition of endogenously processed pS33-Pcat 30 on melanoma, colorectal, or breast cancer cell lines was evaluated after incubation with pS33-Pcat-specific T cell lines for 5 hours.
  • T cells used showed 85% (Figure 7B) and 92% (Figure 7D) reactivity on phosphopeptide-pulsed targets. Dot plots were gated on CD8. T cell recognition was assessed in triplicates and data is representative of two independent experiments. Error bars indicate SEM.
  • Figures 8A-8D present the results of experiments demonstrating that the level of phosphoS33-P-catenin and ⁇ -catenin expressed in Stage III and Stage IV metastatic melanomas did not correlate with survival.
  • the level of phosphoS33-P-catenin ( Figures 8A and 8B) and ⁇ -catenin ( Figures 8C and 8D) in metastatic melanoma tissues from Figure 1 were divided into low and high at the median of expression.
  • Kaplan-Meier survival curves from the date of surgery to the last follow-up were fitted by Cox proportional hazard model using the PHREG procedure in SAS 9.2 to examine survival against phosphoS33-P-catenin or ⁇ -catenin expression, adjusting for age and stage.
  • Figures 8B and 8D represent the number of subjects whose tumor samples showed high or low phosphoS33-P-catenin (Figure 8B) or ⁇ -catenin ( Figure 8D), that were at risk over the time period ranging from the date of surgery to the last follow-up.
  • Figures 9A and 9B are bar graphs of the recognition of naturally processed and presented phosphorylated peptides on cancer cells by the phosphopeptide-specific CTL.
  • Phosphopeptide-specific CTL were incubated with the following cancer cell lines or EBV-transformed B lymphoblastoid cell lines (BLCL): COV413.AAD.A4 ovarian carcinoma, DM331.AAD.A4 and SLM2.AAD.A1 melanomas, MCF7.AAD.A2 and MDAMB231.AAD breast carcinomas, and JY EBV-BLCL.
  • Supernatants were harvested and evaluated for the presence of murine IFNy (produced by murine CTL lines).
  • cancer cells were pulsed with the specific phosphopeptide to show that they are capable of presenting exogenously added peptide.
  • two phosphopeptide-specific CTL cell lines 6850 and 6960, that are specific for the phosphopeptide GLLGpSPVRA (SEQ ID NO: 396), recognized the phosphopeptide on all the cancer cell lines but not the control cell line.
  • the designation "pS” denotes a phosphoserine residue.
  • the ordinate indicates murine IFNy in pg/ml.
  • the abscissa indicates each cell line.
  • Figures 1 OA- 101 summarize analyses of identified phosphopeptides.
  • Figure 10A is a Venn diagram depicting the distribution of leukemia-associated phosphopeptide antigens. Distinct ALL- and AML-associated antigens were present, in contrast to CLL where all phosphoantigens were shared.
  • HLA-B7 alleles presented a greater number of phosphopeptides than HLA-A2 alleles (see Figure 10B) and malignant tissue expressed a greater repertoire of phosphopeptides than non- malignant tissue (see Figure IOC).
  • both HLA-A2- and HLA-B7-restricted antigens shared similar characteristics such as peptide length ( Figure 10D) and constrained phosphate position ( Figure 10E).
  • a logoplot of residue frequency within '9mer' HLA-B7 phosphopeptides ( Figure 10F) compared against previously identified 9mer non-phosphorylated B7-bound peptides ( Figure 10G) revealed common binding traits such as P2 Proline and P9 Leucine/Phenylalanine/Methionine. Letter height in Figures 1 OF- 101 is proportional to residue frequency at each position.
  • a logoplot of in silico predicted of B7-binding phosphopeptides (Figure 10H) revealed an even distribution of phosphoserine residues.
  • FIGS 11A-11G summarize generation of phosphopeptide-specific T cells.
  • HLA-A2 RQA(pS)IELPSMAV SEQ ID NO: 452
  • HLA-phosphopeptide tetramers were used to select RQA(pS)IELPSMAV (SEQ ID NO: 452)-specific T cells between re-stimulation rounds.
  • T cells were able to recognize RQA(pS)IELPSMAV (SEQ ID NO: 452)-loaded targets, but not those loaded with unphosphorylated RQA-V (SEQ ID NO: 2375) nor other phosphorylated A2 -restricted phosphopeptides (see Figure 1 IB).
  • the RQA(pS)IELPSMAV (SEQ ID NO: 452)-specific T cell lines were able to recognize tumor cell lines, both HLA-A2 + EBV-transformed lymphoblastoid cells, JY and FFLuc, but also the A2 + AML cell line THP-1 (see Figure 11C).
  • the ALL cell line, Jurkat was only recognized when transfected with A2.
  • Expanded RQA(pS)IELPSMAV (SEQ ID NO: 452) T cell lines are also able to kill JY and FFLuc tumor cells in addition to HLA-A2 transfected Jurkat (see Figure 11D). Ex vivo cytotoxicity was also demonstrated against HLA-A2 + primary AML and CLL cells, but not against HLA-A2- primary CLL cells (see Figure HE). Similarly, both anti-HLA-B7 pNCOAl and pMYL9-specific T cells grown from healthy donors were able to kill three different primary CLL cells ex vivo (see Figures 1 IF and 11G, resepctively).
  • Figures 12A-12E summarize phosphopeptide-specific immunity in healthy individuals.
  • Figure 12A summarizes HLA-A2 and HLA-B7 anti-phosphopeptide immunity in ten healthy donors assessed by ELISpot over 7 day cultures with individual phosphopeptides.
  • the data presented in columns 3-12 of Figure 12A show the results of ELISpot T cell recognition assays.
  • a blank box indicates that fewer than 10 spots per 200,000 CD8 T cells were detected; "1" indicates that 11-30 spots per 200,000 CD8 + T cells were detected; "2" indicates that 31-50 spots per 200,000 CD8 + T cells were detected; "3” indicates that 51-100 spots per 200,000 CD8 + T cells were detected; and "4" indicates that more than 100 spots per 200,000 CD8 + T cells were detected.
  • T cell-specific lines were readily generated resulting in high avidity phosphopeptide tetramer binding CD8 + T cells (Figure 12B).
  • Anti- phosphopeptide T cells did not recognize the non-phosphorylated counterpart peptides (Figure 12C) and resided mainly within the central memory (CM) CD8 + T cell subset, although some anti-phosphopeptide-specific T cells also resided within the effector memory (EM) and terminal effector (TE) subsets ( Figure 12D).
  • CM central memory
  • EM effector memory
  • TE terminal effector
  • FIGS 13A-13G summarize phosphopeptide-specific immunity in patients with CLL. Comparative ELISpot analysis of enriched CD8 + T cells from 14 patients with CLL and 10 healthy donors. T cells (200,000/well) were cultured with 20 ⁇ of phosphopeptide for 16 hours. Responses to individual phosphopeptides segregate CLL patients in two groups, Group 1 : absent anti phosphopeptide immunity and Group 2: present antiphosphopeptide immunity (see Figure 13 A). Overall (sum) anti- phosphopeptide responses between the groups (see Figure 13B) and statistical significant differences among phosphopeptides tested (see Figure 13C). ELISpot responses following mitogenic stimulation using anti-CD3 antibodies showed immunocompetence among all individuals tested (see Figure 13D). Progression-free survival (PFS; see Figure 13E), overall survival (OS; see Figure 13F) and time to first treatment (TTFT; see Figure 13G) analysis between CLL Group 1 and Group 2.
  • PFS progression-free survival
  • OS overall survival
  • TTFT time to first treatment
  • Figures 14A-14G summarize phosphopeptide-specific immunity in patients with AML.
  • Figure 14A shows comparative ELISpot analysis of PBMCs from 12 patients with AML (all with normal absolute lymphocyte counts) and 12 healthy donors.
  • PBMCs (lxl0 6 /well) were cultured with 20 ⁇ of phosphopeptide for 7 days.
  • Responses to individual phosphopeptides segregated AML patients in two groups: Group 1 - absent or small anti phosphopeptide immunity; Group 2 - present anti- phosphopeptide immunity (see Figure 14A).
  • Overall (sum) anti-phosphopeptide responses between the groups see Figure 14B
  • Figure 14C Overall (sum) anti-phosphopeptide responses between the groups (see Figure 14B) and statistical significant differences among phosphopeptides tested (see Figure 14C).
  • Anti-phosphopeptide immune responses following stem cell transplantation are also shown.
  • Figures 15A and 15B depict the results of experiments designed to determine phenotypes of phosphopeptide-specific CD8 + T cells.
  • Figure 15A is a representative flow cytometry T cell subset profile of freshly magnetically enriched CD8 + T cells from peripheral blood of healthy donors. N, naive; CM, central memory; EF, effector memory; TE, terminal effector.
  • Figure 15B is a ELISpot / CD8 + T cell subset mapping of anti-phosphopeptide responses following 7 day stimulations.
  • Figure 16 is a quantitative (rather than qualitative) reduction of anti- phosphopeptide immunity in patients with CLL.
  • Figure 16 presents a phosphopeptide comparison between enriched CD8 + T cells from a healthy donor (HD) and 5 patients with CLL who lacked antiphosphopeptide immunity stimulated in presence or absence of IL-2.
  • Figure 17 is a plot of immunocompetence of patients with AML showing anti- CD3 responses measured by ELISpot among healthy donors (HD) and patients with AML.
  • Tables 9-19 present tables of exemplary phosphopeptides.
  • Table 9 lists exemplary melanoma HLA A*0301 phosphopeptides, A*0101 phosphopeptides, B*4402 phosphopeptides, B*2705 phosphopeptides, and B* 1402 phosphopeptides.
  • Table 9 further includes exemplary phosphopeptides detected on transformed B-cell lines that are also detected on leukemia, including those presented on HLA A*0301, B*0702, A*0101, and B*2705.
  • Table 10 lists exemplary melanoma and/or leukemia HLA B*0702 phosphopeptides.
  • Table 11 lists exemplary melanoma phosphopeptides detected on HLA A*0201.
  • Table 12 lists exemplary leukemia or transformed B-cell line phosphopeptides detected on HLA A* 0201.
  • Table 13 lists exemplary phosphopeptides presented by class II molecules (DRB 1 *0404, 0101 or DRB4*0103) on melanoma and/or transformed B cells.
  • Table 14 lists exemplary HLA A*0201, A*0101, A*0301, B*0702, B*4402, and B*2705, and Class II MHC molecules (DRB1 *0404, 0101 or DRB4* 103) that can be used for immunotherapy of melanoma.
  • Table 15 lists exemplary HLA A*0202, A*0101, A*0301, B*0702 and Class II MHC molecules (DRB 1 *0404, 0101 or DRB4* 103) that can be used for immunotherapy of leukemia.
  • Table 16 lists exemplary melanoma HLA A* 0301 phosphopeptides, A*0101 phosphopeptides, B*4402 phosphopeptides, B*2705 phosphopeptides, and B* 1402 phosphopeptides, and exemplary sequence variants thereof.
  • Table 17 lists exemplary melanoma and/or leukemia HLA B*0702 phosphopeptides, and exemplary sequence variants thereof.
  • Table 18 lists exemplary melanoma HLA-A*0201 phosphopeptides, and exemplary sequence variants.
  • Table 19 lists exemplary O-GlcNAc class I peptides.
  • Tables 20-22 list characteristics of HLA-DR-associated phosphopeptides selectively expressed by melanoma cells.
  • Table 20 is a table derived from PCT International Patent Application Publication No. WO 2010/129537 that lists characteristics of HLA-DR-associated phosphopeptides selectively expressed by melanoma cells.
  • Tables 21 and 22 are derived from Depontieu et al. (2009) Proc Natl Acad Sci U S A 106: 12073-12078, including Depontieu et al. Supplemental Information, 10.1073 Proc Natl Acad Sci U S A 0903852106.
  • Table 21 lists characteristics of HLA-DR-associated phosphopeptides selectively expressed by EBV-transformed B Cells.
  • Table 22 lists characteristics of HLA-DR-associated phosphopeptides commonly expressed by melanoma and EBV-transformed B Cells.
  • Table 23 lists CLL cohort characteristics.
  • NA Not available
  • FC fludarabine/cyclophosphamide
  • FCR fludarabine/cyclophopshamide/rituximab
  • FCO fludarabine/cyclophopshamide/ ofatumumab
  • Chi chlorambucil
  • Chl/R chlorambucil/rituximab
  • Methylpred methylprednisolone.
  • Table 24 provides a listing of AML cohort characteristics.
  • MUD matched unrelated donor
  • ADE Ara-C, daunorubicin, etoposide
  • FLAG fludarabine
  • Ara-C idarubicin
  • DA daunorubicin, Ara-c
  • MID AC amsacrine
  • Ara-C etoposide, mitozantrone.
  • a peptide refers to one or more peptides.
  • the phrase “A, B, C, and/or D” includes A, B, C, and D individually, but also includes any and all combinations and subcombinations of A, B, C, and D.
  • phosphorylated amino acids are depicted in lowercase “s", “t”, or “y” for phosphoserine, phosphothreonine, or phosphotyrosine, respectively.
  • pS' refers to phosphoserine
  • pT refers to phosphothreonine
  • pY refers to phosphotyrosine.
  • the presently disclosed subject matter relates in some embodiments to post- translationally modified immunogenic therapeutic target peptides, e.g., phosphopeptides and/or O-GlcNAc peptides, for use in immunotherapy and diagnostic methods of using the target peptides, as well as methods of selecting the same to make compositions for immunotherapy, e.g., in vaccines and/or in compositions useful in adaptive cell transfer.
  • post- translationally modified immunogenic therapeutic target peptides e.g., phosphopeptides and/or O-GlcNAc peptides
  • the target peptides of the presently disclosed subject matter are post-translationally modified by being provided with a phosphate group, (i.e., "phosphopeptides") and/or an O-linked beta-N-acetylglucosamine (“O- GlcNAc”) moiety (i.e., "O-GlcNAc peptides").
  • phosphopeptides i.e., "phosphopeptides”
  • O- GlcNAc O-linked beta-N-acetylglucosamine
  • target peptides of the presently disclosed subject matter are in some embodiments not the entire proteins from which they are derived (i.e., are fragments and/or subsequences of larger polypeptides). They are in some embodiments from 8 to 50 contiguous amino acid residues of the native human protein. In some embodiments, they can contain exactly, about, or at least 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38,
  • the peptides of the presently disclosed subject matter can in some embodiments also have a length that falls in the ranges of 8-10, 9-12, 10-13, 11-14, 12-15, 15-20, 20-25, 25-30, 30-35, 35-
  • Target peptides can be modified and analogs can be synthesized that retain their ability to stimulate a particular immune response but which also gain one or more beneficial features, such as those described herein below.
  • a particular target peptide can, for example, have use for treating and vaccinating against multiple cancer types.
  • substitutions can be made in the target peptides at residues known to interact with the MHC molecule. Such substitutions can have the effect of increasing the binding affinity of the target peptides for the MHC molecule and can also increase the half-life of the target peptide-MHC complex, the consequence of which is that the substituted target peptide is a more potent stimulator of an immune response than is the original target peptide.
  • substitutions have no effect on the immunogenicity of the target peptide per se, but rather prolong its biological half-life and/or prevent it from undergoing spontaneous alterations which might otherwise negatively impact on the immunogenicity of the peptide.
  • the target peptides disclosed herein can have differing levels of immunogenicity, MHC binding, and ability to elicit CTL responses against cells displaying a native target peptide (e.g., on the surface of a tumor cell).
  • a phosphopeptide as disclosed herein is in some embodiments modified such that its immunogenicity and/or its binding is enhanced.
  • the modified target peptide binds to an MHC class I molecule about or at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 100%, 110%, 125%, 150%, 175%, 200%, 225%, 250%, 275%, 300%, 350%, 375%, 400%, 450%, 500%, 600%, 700%, 800%, 900%, 1000%, 10,000%, 100,000%, 1,000,000%, or more tightly than its native counterpart.
  • Target peptides of the presently disclosed subject matter can in some embodiments be mixed together to form a cocktail.
  • the target peptides can be in an admixture, or they can be linked together in a concatamer and/or in other arrangement as a single molecule.
  • Linkers between individual target peptides can be used; these can, for example, be formed in some embodiments by any 10 to 20 amino acid residues.
  • the linkers can be random sequences, or they can be optimized for degradation by dendritic cells.
  • a native amino acid residue in a native human protein can be altered to enhance its binding to an MHC class I molecule. These occur in “anchor" positions of the target peptides, often in positions 1, 2, 3, 9, or 10. Valine, alanine, lysine, leucine tyrosine, arginine, phenylalanine, proline, glutamic acid, threonine, serine, aspartic acid, tryptophan, and methionine can also be used as improved anchoring residues. Anchor residues for different HLA molecules are listed below in Table 1.
  • the immunogenicity of a target peptide is measured using transgenic mice expressing human MHC class I genes.
  • "ADD Tg mice” express an interspecies hybrid class I MHC gene, AAD, which contains the a-1 and a-2 domains of the human HLA-A2.1 gene and the a-3 transmembrane and cytoplasmic domains of the mouse H-2Dd gene, under the transcriptional control of the human HLA-A2.1 promoter.
  • AAD interspecies hybrid class I MHC gene
  • the chimeric HLA-A2.1/H2-Dd MHC Class I molecule mediates efficient positive selection of mouse T cells to provide a more complete T cell repertoire capable of recognizing peptides presented by HLA-A2.1 Class I molecules.
  • the peptide epitopes presented and recognized by mouse T cells in the context of the HLA-A2.1/H2-Dd class I molecule are the same as those presented in HLA- A2.1 + humans.
  • This transgenic strain enables the modeling of human T cell immune responses to HLA-A2 presented antigens, and identification of those antigens.
  • This transgenic strain is a preclinical model for design and testing of vaccines for infectious diseases or cancer therapy involving optimal stimulation of CD8 + cytolytic T cells.
  • the immunogenicity of a modified phosphopeptide is determined by the degree of Interferon gamma (IFNy) and/or tumor necrosis factor- alpha (TNF-a) production of T cells from ADD Tg mice immunized with the target peptide, e.g., by immunization with target peptide pulsed bone marrow derived dendritic cells.
  • IFNy Interferon gamma
  • TNF-a tumor necrosis factor- alpha
  • the modified target peptides are about or at least 10, 20, 30, 40, 50, 60, 70, 80, 90, 95, 100, 110, 125, 150, 175, 200, 225, 250, 275, 300, 350, 375, 400, 450, 500, 600, 700, 800, 1000, 1500, 2000, 2500, 3000, 4000, 5000% or more immunogenic, e.g., in terms of numbers of IFNy- and/or TNF-a-positive ⁇ i.e., "activated") T cells relative to numbers elicited by native target peptides in ADD Tg mice immunized with phosphopeptide-pulsed bone marrow derived dendritic cells (BMDCs).
  • BMDCs bone marrow derived dendritic cells
  • the target peptides are modified target peptides.
  • the modified target peptides are able to elicit CD8 + T cells that are cross-reactive with the modified and the native target peptide in general and when such modified and native target peptides are complexed with MHC class I molecules in particular.
  • the CD8 + T cells that are cross-reactive with the modified and the native target peptides are able to reduce tumor size by about or at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 97% or 99% in a NOD/SCID/IL-2RYC _/" knock out mouse relative to IL-2 treatment without such cross- reactive CD8 + T cells.
  • the phrase "capable of inducing a target peptide-specific memory T cell response in a patient” as used herein relates to eliciting a response from memory T cells (also referred to as "antigen-experienced T cell”), which are a subset of infection- and cancer-fighting T cells that have previously encountered and responded to their cognate antigen.
  • memory T cells also referred to as "antigen-experienced T cell”
  • Such T cells can recognize foreign invaders, such as bacteria or viruses, as well as cancer cells.
  • Memory T cells have become “experienced” by having encountered antigen during a prior infection, having encountered cancer, or via previous vaccination.
  • memory T cells can reproduce to mount a faster and stronger immune response than the first time the immune system responded to the invader (e.g., through the body's own consciously unperceived recognition of a target peptide being associated with diseased tissue). This behavior can be assayed in T lymphocyte proliferation assays, which can reveal exposure to specific antigens.
  • Memory T cells comprise two subtypes: central memory T cells (TC M cells) and effector memory T cells (T EM cells). Memory cells can be either CD4 + or CD8 . Memory T cells typically express the cell surface protein CD45RO. Central memory (TC M ) cells generally express L-selectin and CCR7, and they secrete IL-2 but not ⁇ or IL-4. Effector memory (T EM ) cells, however, generally do not express L- selectin or CCR7 but produce effector cytokines like IFNy and IL-4.
  • a memory T cell response generally results in the proliferation of memory T cells and/or the upregulation or increased secretion of factors such as CD45RO, L- selectin, CCR7, IL-2, IFNy, CD45RA, CD27, and/or IL-4.
  • the target peptides of the presently disclosed subject matter are capable of inducing a TC M cell response associated with L-selectin, CCR7, IL,-2 but not IFNy or IL-4 expression and/or secretion. See e.g., Hamann et ah, 1997.
  • a TC M cell response is associated with an at least or an about 1%, 5%, 10%, 15%, 20%>, 25%, 30%, 35%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 90%, 95%, 97%, 98%, 99%, 100%, 125%, 150%, 175%, 200%, 250%, 300%, 400%, 500%, 600%, 700%, 800%, 900%, 1000%, 1500%, 2000% or more increase in T cell CD45RO/RA, L- selectin, CCR7, or IL-2 expression and/secretion.
  • the target peptides of the presently disclosed subject matter are capable of inducing a CD8 + TC M cell response in a patient the first time that patient is provided the composition including the selected target peptides.
  • the target peptides of the presently disclosed subject matter can in some embodiments be referred to as "neo-antigens.”
  • target peptides might be considered "self for being derived from self-tissue, they generally are only found on the surface of cells with a dysregulated metabolism (e.g., aberrant phosphorylation), and they are likely never presented to immature T cells in the thymus. As such, these "self antigens act are neo-antigens because they are nevertheless capable of eliciting an immune response.
  • TCM cells activated by particular target peptide in a particular patient sample are TCM cells.
  • a patient sample is isolated exactly, about or at least 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1 , 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 , 22, 23, 24, 25, 26, 27, 28, 29, 30 or more days after an initial exposure to a particular target peptide and then assayed for target peptide-specific activated T cells and the proportion of T C M cells thereof.
  • compositions of the presently disclosed subject matter are able to elicit a CD8 + TCM cell response in at least or about 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 90%, 95%, 97%, 98%, or 99% of patients and/or healthy volunteers.
  • compositions of the presently disclosed subject matter are able to elicit a CD8 + TCM cell response in about or at least 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 90%, 95%, 97%), 98%o, 99%) of patients and/or healthy volunteers specific, and in some embodiments the CD8 + TCM cell response elicited is directed against all or at least or about 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10, or more target peptides that are present in the composition. In some embodiments, the aforementioned T cell activation tests are done by ELISpot assay.
  • O-GlcNAc peptides includes MHC class I- and MHC class II- specific O-GlcNAc peptides.
  • Exemplary MHC class I target peptides set forth in Table 19. Modification of proteins with O-linked ⁇ - ⁇ -acetylglucosamine (O-GlcNAc) was previously technically difficult to detect. However, it rivals phosphorylation in both abundance and distribution of the protein targets for this modification.
  • O-GlcNAcylation is a reversible modification of nuclear and cytoplasmic proteins and is characterized by the attachment of a single ⁇ - ⁇ -acetyl- glucosamine moiety to a hydroxyl group of a serine or a threonine residue. Modification by O -GlcNAcylation is often competitive with phosphorylation at the same sites or at proximal sites on proteins. Furthermore, crosstalk between O- GlcNAcylation and phosphorylation affects the posttranslational state of hundreds of proteins in response to nutrients and stress, and plays an important role in chronic diseases of metabolism such as but not limited to diabetes and neurodegeneration.
  • OGT O-GlcNAc transferase catalyzes the addition of the sugar moiety from the donor substrate uridine 5 '-diphosphate (UDP)-GlcNAc to proteins.
  • UDP uridine 5 '-diphosphate
  • OGT localizes to discrete structures, such as centrosomes (metaphase) and the spindle (anaphase), and then moves to the midbody during cytokinesis.
  • OGT along with O-GlcNAcase (OGA), the enzyme that removes the sugar, dynamically interact with Aurora Kinase B (AURKB) and protein phosphatase 1 (PP1) at the midbody.
  • AURKB Aurora Kinase B
  • PP1 protein phosphatase 1
  • these proteins form a complex regulating M-phase O-GlcNAcylation, which in turn influences the phosphorylation state, of vimentin.
  • AURKB Aurora Kinase B
  • PP1 protein phosphatas
  • Peptides modified with O-GlcNAc can be difficult to detect by standard mass spectrometric methods.
  • the modification is usually present at sub-stoichiometric amounts, modified and unmodified peptides co-elute during high-performance liquid chromatography (HPLC), and ionization of the modified peptide is suppressed in the presence of unmodified peptides. Consequently, sample enrichment is often required to successfully detect and characterize O-GlcNAcylated peptides. Enrichment can be achieved through chemoenzymatic approaches that biotinylate O-GlcNAc peptides and capture them by avidin chromatography.
  • a chemoenzymatic approach using a photocleavable biotin- alkyne reagent (PCbiotin-alkyne) tag can be used. See e.g., Figure SI A of Wang et al., 2010 ("Wang"), herein incorporated by reference.
  • Photocleavage not only allows efficient and quantitative recovery from the affinity column, but also tags the peptide with a charged moiety that facilitates O-GlcNAc site mapping by electron-transfer dissociation (ETD) mass spectrometry.
  • ETD electron-transfer dissociation
  • This tagging approach also makes it possible to use conventional collision-activated dissociation mass spectrometry (CAD MS) to screen samples for the presence of O-GlcNAc-modified peptides by monitoring for two-signature fragment ions characteristic of the tag (see Figure SIB of Wang).
  • CAD MS collision-activated dissociation mass spectrometry
  • O-GlcNAcylation rivals phosphorylation in both abundance and distribution of the modified proteins and alterations in O-GlcNAcylation disrupt both the chromosomal passenger complex - containing AURKB, inner centromere protein antigens 135/155 kDa (INCENP), PP1, Borealin, and Survivin - and the circuits regulating CDKl activity.
  • O-GlcNAc moieties are nearly as abundant as phosphates on proteins associated with the spindle and midbody. Many of the O-GlcNAcylation sites identified are identical or proximal to known phosphorylation sites. O-GlcNAcylation and phosphorylation work together to control complicated mitotic processes, such as spindle formation. For example, OGT overexpression altered the abundance of transcripts and proteins encoded by several mitotic genes, changed the localization of NuMAl, and disrupted the chromosomal passenger complex and the CDKl activation circuit.
  • O-GlcNAcylation and phosphorylation for several protein classes, most noticeably transcriptional regulators and cytoskeletal proteins.
  • Many of the O-GlcNAcylation and phosphorylation sites are located in the regulatory head domains of intermediate filament proteins. Phosphorylation of these sites causes filament disassociation during M phase.
  • vimentin is phosphorylated at multiple sites during M phase and there is an O-GlcNAcylation site that is also a mitotic phosphorylation site (Ser55; Slawson et al, 2005; Slawson et al, 2008; Wang et al, 2007; Molina et al, 2007).
  • OGT overexpression profoundly affects multiple mitotic signaling circuits. Although overexpression of OGT does not interfere with the formation of the midbody complex or localization of AURKB, AURKB activity is altered toward the cytoskeletal protein, vimentin. The reduction in the abundance of AURKB or INCENP dampens kinase activity to a point that retards mitotic progression especially during anaphase and telephase. Furthermore, OGT overexpression reduced phosphorylation of INCENP and borealin, but to what extent this alters the function of the midbody complex is unclear.
  • O-GlcNAcylation is directly coupled to nutrient uptake and metabolism, the sugar residue is an ideal metabolic sensor for regulating mitotic progression.
  • phosphorylation might act as a master switch initiating the mitotic process
  • O-GlcNAcylation could act as an adjuster of signals to make these processes more responsive to environmental cues.
  • How O-GlcNAcylation exerts control on specific mitotic proteins and how O-GlcNAcylation will integrate into well known signaling pathways represent another layer of cellular regulation.
  • phosphopeptides includes MHC class I- and MHC class II-specific phosphopeptides.
  • Exemplary MHC class I phosphopeptides are set forth in Tables 9- 22, for example.
  • the phosphopeptides contain the sequences of at least one of the MHC class I binding peptides listed in SEQ ID NO. 1-2163. Moreover, in some embodiments about, or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or more of the serine, homo-serine, threonine, or tyrosine residues within the recited sequences is phosphorylated.
  • the phosphorylation can be with a natural phosphorylation (-CH 2 -O-PO 3 H) or with an enzyme non-degradable, modified phosphorylation, such as but not limited to -CH 2 -CF 2 -PO 3 H or -CH 2 - CH 2 -PO 3 H.
  • Some phosphopeptides can contain more than one of the peptides listed in SEQ ID NO: 1-2163, for example, if they are overlapping, adjacent, or nearby within the native protein from which they are derived.
  • the chemical structure of a phosphopeptide mimetic appropriate for use in the presently disclosed subject matter can in some embodiments closely approximate the natural phosphorylated residue which is mimicked, and also be chemically stable (e.g., resistant to dephosphorylation by phosphatase enzymes). This can be achieved with a synthetic molecule in which the phosphorous atom is linked to the amino acid residue, not through oxygen, but through carbon. In some embodiments, a CF 2 group links the amino acid to the phosphorous atom. Mimetics of several amino acids which are phosphorylated in nature can be generated by this approach.
  • Mimetics of phosphoserine, phosphothreonine, and phosphotyrosme can be generated by placing a CF 2 linkage from the appropriate carbon to the phosphate moiety.
  • the mimetic molecule L-2-amino-4 (diethylphosphono)-4, 4-difluorobutanoic acid (F2Pab) can substitute for phosphoserine (Otaka et al., 1995).
  • L-2-amino-4-phosphono-4, 4- difluoro-3-methylbutanoic acid F2Pmb
  • L- 2-amino-4-phosphono (difluoromethyl) phenylalanine F2Pmp
  • the oxygen bridge of the natural amino acid can be replaced with a methylene group.
  • serine and threonine residues are substituted with homo-serine and homo-threonine residues, respectively.
  • ⁇ -catenin phosphorylated at S33 in human metastatic melanoma tissues and melanoma and breast cancer cell lines.
  • immunotherapeutic potential of the decapeptide YLD(pS)GIHSGA SEQ ID NO: 427
  • pS33-Pcatenrn 30 -39 or "pS33- Pcat 30 ", which corresponds to amino acids 30-39 of human ⁇ -catenin (CTNNB1) with a phosphoserine in the fourth position (i.e., amino acid 33 of human CTNNB1), and a modified form of the same phosphopeptide, pS33-Pcat(V)3o (see below).
  • pS33-Pcat 30 (SEQ ID NO: 427) is broadly and sufficiently presented by melanoma and breast cancer cells and is therefore a good target for cancer immunotherapy.
  • pS33-Pcat 30 as a phosphopeptide is a very weak immunogen in vivo. Secondary responses in mice elicited with pS33-Pcatenin 30 - 3 9 together with CpG and anti-Cd40 as adjuvants were almost undetectable. As such, it is not ideally suited for inclusion in a phosphopeptide composition vaccine.
  • pS33-Pcatenin 30 - 3 9 (SEQ ID NO: 427) was modified by replacing the Ala residue at the P10 position (amino acid 39 of human CTNNB1) with a Val residue. This modified peptides is referred to herein as pS33-Pcatenin 30 - 3 9(V), and it corresponds to SEQ ID NO: 2080.
  • the Ala to Val modification enhanced the HLA- A2 binding affinity by about 10 fold.
  • pS33-Pcat(V) 3 induced discernible primary and memory recall CD8 T cell responses. These T cells also specifically recognized the phosphorylated but not the unphosphorylated form of the modified peptide.
  • pS33-Pcat(V) 30 induced measurable in vitro human CD8 T cell responses after only 2 weeks, at which time no specific responses to pS33-Pcat 30 were detected. MHC-restricted peptides, even with conservative modifications, can thus elicit T cells incapable of recognizing the original epitope (Bertoletti et al., 1994; Klenerman et al. , 1994).
  • pS33-Pcat(V) 30 elicited activated CD8 T cells that demonstrated a high level of crossreactivity against the natural pS33-Pcat 30 phosphopeptide. Moreover, pS33-Pcat-specific T cells significantly delayed melanoma tumor outgrowth in NOD/SCID mouse model. Given that the pS33-Pcat 30 and pS33- Pcat(V) 3 o are antigenically distinct one might foresee a decrease in response to the pS33-Pcatenin 30 - 3 9 with increasing inoculation pS33-Pcat(V) 3 o antigen.
  • TNS3 Tensin 3
  • TNS4 Tensin-3
  • TNS3 also seems to be involved in mammary cell migration , and might be involved in cell migration and bone development.
  • the TNS3 phosphopeptide VMlGsPKKL (SEQ ID NO: 426) of the presently disclosed subject matter has been determined to have weak MHC binding affinity.
  • the breast cancer anti-estrogen resistance 3 (BCAR3) polypeptide activates the PI3K/Akt pathway and mediates migration and estrogen resistance in breast cancer cells, processes that are associated with malignancy.
  • BCAR3pT130 substitution of the P9 residue Leu with Val (i.e., SEQ ID NO: 398 vs. 2001, the latter of which is referred to herein as "modified BCAR3pT130") had no impact on HLA-A2 binding affinity.
  • the modified BCAR3pT130 is nevertheless, significantly immunogenic. This suggests that the modification altered the conformation of the phosphopeptide and that the immune response against the natural phosphopeptide is restricted by tolerance.
  • CD8 + T cells generated using the modified BCAR3pT130 produced IFNy, TNFa, and were cytotoxic based on CD 107a expression. Importantly, the T cells were equally reactive with the natural and modified phosphopeptides. This suggests that the natural BCAR3pT130 (i.e., SEQ ID NO: 398) phosphopeptide is an agonist and that the sequence modification creates a stronger agonist.
  • These T cells also recognized endogenously processed BCAR3pT130 on HLA-A2 human melanoma and breast cancer cells.
  • IRS-2 Insulin receptor substrate 2
  • IRS proteins are adapter proteins that link signaling from upstream activators to multiple downstream effectors to modulate normal growth, metabolism, survival, and differentiation. It is disclosed herein that phosphorylated IRS-2 is broadly displayed on multiple cancer types and the resulting phosphopeptide is endogenously processed and presented at levels that allow strong immune responses to be generated against it.
  • Phosphopeptide-specific CD8 + T cells can be generated from HLA-A2 transgenic mice upon immunization with the pIRS2 phosphopeptide, and these T cells are capable of recognizing and killing human melanoma and breast tumors in vitro and controlling tumor growth in a xenograft tumor model system.
  • Cell division cycle 25 is a dual-specificity phosphatase first isolated from the yeast Schizosaccharomyces pombe as a cell cycle defective mutant. Dual- specificity phosphatases are considered a subclass of protein tyrosine phosphatases. By removing inhibitory phosphate residues from target cyclin-dependent kinases (Cdks), CDC25 proteins control entry into and progression through various phases of the cell cycle, including mitosis and S-phase.
  • Cdks target cyclin-dependent kinases
  • the structure of the CDC25 proteins can be divided into two main regions: the N-terminal region, which is highly divergent and contains sites for its phosphorylation and ubiquitination that regulate the phosphatase activity; and the C-terminal region, which is highly homologous and contains the catalytic site.
  • the CDC25s, and in particular CDC25A and CDC25B, are proto-oncogenes in humans and have been shown to be overexpressed in a number of cancers.
  • the phosphopeptide compositions of the presently disclosed subject matter include the phosphopeptide GLLGpSPVRA (SEQ ID NO: 396).
  • the target peptides are combined into compositions that can be used in vaccine compositions for eliciting anti-tumor immune responses and/or in adoptive T cell therapy of cancer patients including, but not limited to melanoma patients.
  • Tables 9-16 list exemplary phosphopeptides that are presented on the surface of cancer cells. Exemplary variants and mimetics of these peptides and of additional class I MHC phosphopeptides are also provided, for example, in Tables 17 and 18.
  • HLA-A*0201 51%
  • HLA-A*0101 29%
  • HLA-A*0301 21%
  • HLA-B*4402 27%
  • HLA-B*0702 30%
  • HLA-B*2705 75%
  • target peptides which are immunologically suitable for each of the foregoing HLA alleles.
  • "Immunologically suitable” means that a target peptide will bind at least one allele of an MHC class I molecule in a given patient.
  • Compositions of the presently disclosed subject matter are in some embodiments immunologically suitable for a patient when at least one target peptide of the composition will bind at least one allele of an MHC class I molecule in a given patient.
  • Compositions of multiple target peptides presented by each of the most prevalent alleles used in a cocktail ensures coverage of the human population and to minimize the possibility that the tumor will be able to escape immune surveillance by down-regulating expression of any one class I target peptide.
  • compositions of the presently disclosed subject matter can in some embodiments comprise at least one target peptide specific for one or more of the following alleles: HLA-A*0201, HLA-A*0101, HLA-A*0301, HLA-B*4402, HLA- B*0702, HLA-B*-2705, and HLA-B* 1402.
  • the compositions of the presently disclosed subject matter can in some embodiments have at least one target peptide specific for one or more of the following alleles HLA-A*0201, HLA-A*0101, HLA- A*0301, HLA-B*4402, and HLA-B*0702.
  • compositions of the presently disclosed subject matter can in some embodiments have at least one target peptide specific for HLA-A*0201, HLA-A*0101, HLA-A*0301, HLA-B*4402, HLA-B*0702, HLA-B*-2705, HLA-B* 1402, or any combination thereof.
  • the compositions may have at least one phosphopeptide specific for about or at least 1, 2, 3, 4, 5, or all 6 of the aforementioned alleles.
  • compositions of the presently disclosed subject matter containing various combinations of target peptides are in some embodiments immunologically suitable for between or about 3-88%, 80-89%, 70-79%, 60-69%, 57-59%, 55-57%, 53-55% or 51-53% or 5-90%, 10-80%, 15-75%, 20-70%, 25-65%, 30-60%, 35-55% or 40-50% of the population of a particular cancer including, but not limited to melanoma and/or leukemia.
  • compositions of the presently disclosed subject matter are able to act as vaccine compositions for eliciting anti- tumor immune responses and/or in adoptive T cell therapy of melanoma patients wherein the compositions are immunologically suitable for about or at least 88, 87, 86, 85, 84, 83, 82, 81, 80, 79, 78, 77, 76, 75, 74, 73, 72, 71, 70, 69, 68, 67, 66, 65, 64, 63, 62, 61, 60, 59, 58, 57, 56, 55, 54, 53, 52, 51, 50, 49, 48, 47, 46, 45, 44, 43, 42, 41, 40, 39, 38, 37, 36, 35, 34, 33, 32, 31, 30, 29, 28, 27, 26, 25, 24, 23, 22, 20, 19, 18, 17, 16, 15, 14, 13, 12, 11, 10, 9, 8, 7, 6, 5, 4, or 3 percent of cancer such as, but not limited to melanoma patients.
  • target peptide compositions refers to at least one target peptide formulated, for example, as a vaccine; or as a preparation for pulsing cells in a manner such that the pulsed cells, e.g., dendritic cells, will display the at least one target peptide in the composition on their surface, e.g., to T cells in the context of adoptive T cell therapy.
  • compositions of the presently disclosed subject matter can in some embodiments include about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 50-55, 55-65, 65-80, 80-120, 90-150, 100-175, or 175-250 different target peptides.
  • compositions of the presently disclosed subject matter in some embodiments generally include MHC class I specific target peptide(s) but can also include one or more target peptides specific for MHC class II, such as but not limited to the peptides set forth in Tables 21-22, or other peptides associated with tumors ⁇ e.g., tumor associated antigen ("TAA”)) such as, but not limited to those disclosed in Table 2.
  • TAA tumor associated antigen
  • compositions comprising the target peptide are typically substantially free of other human proteins or peptides. They can be made synthetically or by purification from a biological source. They can be made recombinantly. Desirably they are in some embodiments at least 90%> pure, in some embodiments at least 92%> pure, in some embodiments at least 93%> pure, in some embodiments at least 94%> pure, in some embodiments at least 95% pure, in some embodiments at least 96% pure, in some embodiments at least 97% pure, in some embodiments at least 98% pure, and in some embodiments at least 99% pure.
  • compositions are typically devoid of cells, both human and recombinant producing cells.
  • the stimulated T cells can be used as an immunotherapy agent.
  • complexes can be formed in vitro or in vivo.
  • complexes are in some embodiments tetrameric with respect to an HLA-target peptide complex.
  • additional proteins or peptides can be added, for example, to make a cocktail having the ability to stimulate an immune response in a number of different HLA type hosts.
  • additional proteins and/or peptides can provide an interacting function within a single host, such as but not limited to an adjuvant function or a stabilizing function.
  • other tumor antigens can be used in admixture with the target peptides such that multiple different immune responses are induced in a single patient.
  • Target peptides to a mammalian recipient can be accomplished using long target peptides ⁇ e.g., longer than 15 residues), and/or using target peptide-loaded dendritic cells. See Melief, 2009.
  • an immediate goal of the administration of target peptides is to induce activation of CD8 + T cells in a subject.
  • Additional components that can be administered to the same subject, either at the same time and/or close in time include TLR-ligand oligonucleotide CpG and related target peptides that have overlapping sequences of at least six amino acid residues.
  • mammalian recipients should express the appropriate human HLA molecules to bind to the target peptides.
  • Transgenic mammals can be used as recipients, for example, if they express appropriate human HLA molecules. If a mammal's own immune system recognizes a similar target peptide then it can be used as model system directly without introducing a transgene.
  • Useful models and recipients can be at increased risk of developing metastatic cancer, such as metastatic melanoma. Other useful models and recipients can be predisposed, e.g., genetically and/or environmentally, to develop melanoma or other cancer.
  • T cells associated with these immune responses when expanded in vitro, are able to recognize and kill malignant tissue (both established cells lines and primary tumor samples).
  • Cold-target inhibition studies reveal that these target peptide-specific T cell lines kill primary tumor tissue in a target peptide-specific manner.
  • target peptides of the presently disclosed subject matter for inclusion in immunotherapy, e.g., in adaptive cell therapy or in the context of a vaccine, one can in some embodiments pick target peptides using one or more of the following criteria: 1) peptides associated with a particular cancer/tumor cell type; 2) a peptide derived from a gene product ⁇ e.g., a polypeptide) associated with cell proliferation, transformation, and/or malignancy; 3) a peptide that is specific for an HLA allele carried the group of patients to be treated; and/or 4) a peptide that is capable of inducing a target peptide-specific memory T cell response in the patients to be treated upon a first exposure to a composition including the selected target peptides.
  • the antigen target peptides can also be employed in a composition designed to vaccinate an individual.
  • the antigen target peptides can in some embodiments be injected alone and can in some embodiments be administered in combination with an adjuvant and/or a pharmaceutically acceptable carrier.
  • Vaccines are envisioned to prevent and/or treat certain diseases in general, and cancers in particular.
  • the target peptide-containing compositions of the presently disclosed subject matter can in some embodiments be used as a vaccine for cancer, and more specifically for melanoma, leukemia, ovarian, breast, colorectal, or lung squamous cancer, sarcoma, renal cell carcinoma, pancreatic carcinomas, squamous tumors of the head and neck, brain cancer, liver cancer, prostate cancer, ovarian cancer, and cervical cancer.
  • the compositions can include target peptides.
  • the vaccine compositions can in some embodiments include only the target peptides, or peptides disclosed herein, or they can include other cancer antigens that have been identified.
  • the vaccine compositions of the presently disclosed subject matter can be used prophylactically for the purposes of preventing, reducing the risk of, and/or delaying initiation of a cancer in an individual that does not currently have cancer. Alternatively, they can be used to treat an individual that already has cancer, so that recurrence or metastasis is delayed and/or prevented. Prevention relates to a process of prophylaxis in which the individual is immunized prior to the induction or onset of cancer. For example, in some embodiments individuals with a history of severe sunburn and at risk for developing melanoma can be immunized prior to the onset of the disease.
  • individuals that already have cancer can be immunized with the target peptide-containing compositions of the presently disclosed subject matter so as to stimulate an immune response that would be reactive against the cancer.
  • a clinically relevant immune response would be one in which the cancer partially or completely regresses and is eliminated from the patient, and it would also include those responses in which the progression of the cancer is blocked without being eliminated.
  • prevention need not be total, but may result in a reduced risk, delayed onset, or delayed progression or metastasis.
  • the vaccines of the presently disclosed subject matter can be used to treat malignant melanoma.
  • Malignant melanomas usually present at two extremes: at one end of the spectrum are patients with small skin lesions that may be curable by surgical resection and at the other are patients with widely metastatic disease, in whom the therapeutic options are limited and the prognosis is poor: e.g., with a median survival of only 6 to 9 months.
  • Prognosis also is related to the type of melanoma.
  • patents with Stage I disease have 5-year survival rate of greater than or about 90%.
  • Patients with Stage II disease have 5-year survival rate ranging from about 45 to about 77%
  • Patients with Stage III disease have 5-year survival rate ranging from about 27 to about 70%.
  • Patients with metastatic disease have a 5 -year survival rate of less than or about 20%>.
  • Stage IA Lesions less than or equal to 1 mm thick with no evidence of ulceration or metastases (TlaNOMO) are associated with a 5 -year survival rate of 95%.
  • Stage IB Lesions less than or equal to or about 1 mm thick with ulceration noted but without lymph node involvement (TlbNOMO) or lesions 1.01-2 mm thick without ulceration or lymph node involvement (T2aN0M0) are associated with a 5- year survival rate of approximately 91%.
  • Stage IIA Melanomas greater than 1 mm but less than or about 2.01 mm in thickness with no evidence of metastases but with evidence of ulceration (T2bN0M0) or lesions 2.01-4.0 mm without ulceration or lymph node involvement (T3aN0M0) are associated with an overall 5-year survival rate of 77-79%.
  • Stage IIB Melanomas 2.01-4 mm thick with ulceration but no lymph node involvement (T3bN0M0) or lesions greater than 4 mm without ulceration or lymph node involvement (T4aN0M0) are associated with a 5-year survival rate of 63-67%.
  • Stage IIC Lesions greater than 4 mm with ulceration but no lymph node involvement (T4bN0M0) are associated with a 5 -year survival rate of 45%.
  • Stage IIIA Patients with any depth lesion, no ulceration and 1 positive (micrometastatic) lymph node (Tl-4a, Nla, M0) have a 5-year survival rate of 70%. Tl-4a, N2a, M0 lesions (any depth lesion, no ulceration but 2-3 nodes positive for micrometastasis) are associated with a 5 -year survival rate of 63%.
  • Stage IIIB Patients with any depth lesion, positive ulceration, and 1 lymph node positive for micrometastasis (Tl-4b, Nla, M0) or 2-3 nodes positive for micrometastasis (Tl-4b, N2a, M0) have a 5-year survival rate of 50-53%. Patients with any depth lesion, no ulceration, and 1 lymph node positive for macrometastasis (Tl-4a, Nib, M0) or 2-3 nodes positive for macrometastasis (Tl-4a, N2b, M0) have a 5 -year survival rate of 46-59%.
  • Stage IIIC Patients with any depth lesion, positive ulceration, and 1 lymph node positive for macrometastasis (Tl-4b, Nib, M0) or 2-3 nodes positive for macrometastasis (Tl-4b, N2b, M0) or 4 or more metastatic lymph nodes, matted lymph nodes, or in transit met(s)/satellite(s) have a 5 -year survival rate of 24-29%.
  • Stage IV Melanoma metastatic to skin, subcutaneous tissue, or lymph nodes with normal LDH (Mia) is associated with a 5-year survival rate of 19%.
  • Mlb disease metalastatic disease to lungs with normal LDH
  • Mlc disease metalastatic disease to all other visceral organs and normal LDH or any distant disease with elevated LDH
  • the target peptide vaccines of the presently disclosed subject matter can in some embodiments be given to patients before, after, or during any of the aforementioned stages of melanoma. In some embodiments, they are given to patients with Stage IV melanoma.
  • the 5-year survival rate of patients treated with the vaccines of the presently disclosed subject matter is increased by a statistically significant amount: e.g., by about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, or 100 percent, or even greater than 100 percent,
  • the target peptide vaccine compositions of the presently disclosed subject matter increase survival rates in patients with metastatic melanoma by a statistically significant amount of time such as, but not limited to by about or at least 0.25, 0.5, 0.75, 1.0, 1.25, 1.5, 1.75, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 4.0, 4.25, 4.5, 4.75, 5.0, 5.25, 5.5, 5.75, 6.0, 6.25, 6.5, 6.75, 7.0, 7.25, 7.5, 7.75, 8.0, 8.25, 8.5, 8.75, 9.0, 9.25, 9.50, 9.75, 10.0, 10.25, 10.5, 10.75, 11.0, 11.25, 11.5, 11.75, or 12 months or more compared to what could have been expected without vaccine treatment at the time of filing of this specification.
  • the survival rate ⁇ e.g., the 1, 2, 3, 4, or 5-year survival rate) of patients treated with the vaccines of the presently disclosed subject matter is increased by a statistically significant amount such as, but not limited to about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97,
  • the target peptide vaccines of the presently disclosed subject matter are in some embodiments envisioned to illicit a T cell-associated immune response such as, but not limited to generating activated CD8 T cells specific for native target peptide/MHC class I expressing cells.
  • the CD8 + T cells specific for native target peptide/MHC class I expressing cells are specific for at least or about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more of the target peptides in the vaccine in a patient for about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74
  • the treatment response rates of patients treated with the target peptide vaccines of the presently disclosed subject matter are increased by a statistically significant amount such as, but not limited to about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51 , 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 07, 98, 99, 100, 150, 200, 250, 300
  • overall median survival of patients treated with the target peptide vaccines of the presently disclosed subject matter is increased by a statistically significant amount such as, but not limited to about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51 , 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 150, 200, 250, 300
  • the overall median survival of Stage IV melanoma patients treated the target peptide vaccines is envisioned to be about or at least 10.0, 10.25, 10.5, 10.75, 11.0, 11.25, 11.5, 11.75, 12, 12.25, 12.5, 12.75, 13, 13.25, 13.5, 13.75, 14, 14.25, 14.5, 14.75, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36 or more months.
  • tumor size of patients treated with the target peptide vaccines of the presently disclosed subject matter is decreased by a statistically statistically significant amount such as, but not limited to about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51 , 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 150, 200, 250,
  • compositions of the presently disclosed subject matter provide a clinical tumor regression that is by a statistically significant amount such as, but not limited to about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100 percent of patients treated with the composition.
  • compositions of the presently disclosed subject matter provide a CTL response specific for the cancer being treated, e.g., melanoma, by a statistically significant amount such as, but not limited to about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98,
  • compositions of the presently disclosed subject matter provide an increase in progression free survival in the cancer being treated, such as but not limited to melanoma, of about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 110, 120, 130, 140, 150
  • one or more of progression free survival, CTL response rates, clinical tumor regression rates, tumor size, survival rates are determined, assessed, calculated, and/or estimated weekly, monthly, bi-monthly, quarterly, semi-annually, annually, and/or bi-annually over a period of about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or more years or about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79
  • Adoptive cell transfer is the passive transfer of cells, in some embodiments immune-derived cells, into a recipient host with the goal of transferring the immunologic functionality and characteristics into the host. Clinically, this approach has been exploited to transfer either immune-promoting or tolerogenic cells (often lymphocytes) to patients to enhance immunity against cancer.
  • TIL autologous tumor infiltrating lymphocytes
  • ACT therapies achieve T cell stimulation ex vivo by activating and expanding autologous tumor-reactive T cell populations to large numbers of cells that are then transferred back to the patient. See Gattinoni et al., 2006.
  • the target peptides of the presently disclosed subject matter can in some embodiments take the form of antigenic peptides formulated in a composition added to autologous dendritic cells and used to stimulate a T helper cell or CTL response in vitro.
  • the in vitro generated T helper cells or CTL can then be infused into a patient with cancer (Yee et al., 2002), and specifically a patient with a form of cancer that expresses one or more of antigenic target peptides.
  • the target peptides can be added to dendritic cells (DCs) in vitro to produce loaded DCs, with the loaded DCs being subsequently transferred into an individual with cancer in order to stimulate an immune response.
  • the loaded DCs can be used to stimulate CD8 + T cells ex vivo with subsequent reintroduction of the stimulated T cells to the patient.
  • a particular target peptide might be identified on one particular cancer cell type, it might also be found on other cancer cell types.
  • the presently disclosed subject matter envisions treating cancer by providing a patient with cells pulsed with a composition of target peptides.
  • the use of DCs pulsed with target peptides peptide antigens enables manipulation of the immunogen in two ways: varying the number of cells injected and varying the density of antigen presented on each cell. Exemplary non-limiting methods for DC-based based treatments can be found, for example in Mackensen et al., 2000.
  • the target peptide compositions (or target peptide composition kits comprising the same) of the presently disclosed subject matter can in some embodiments also include at least one additional peptide derived from one or more tumor-associated antigens (TAAs).
  • TAAs include MelanA (MART -I), gplOO (Pmel 17), tyrosinase, TRP-1, TRP-2, MAGE-1, MAGE-3, BAGE, GAGE-1, GAGE-2, pl5(58), CEA, RAGE, NY-ESO (LAGE), SCP-1, Hom/Mel-40, PRAME, p53, H-Ras, HER-2/neu, BCR-ABL, E2A-PRL, H4-RET, IGH-IGK, MYL-RAR, Epstein Barr virus antigens, EBNA, human papillomavirus (HPV) antigens E6 and E7, TSP-180, MAGE-4, MAGE-5, MAGE-6, pl85er
  • Tumor-associated Antigen Peptides MAGE-A3 2 81-295 TSYVKVLHHMVKISG (SEQ ID NO: 2196)
  • Her2/neu 3 69-377 KIFGSLAFL (SEQ ID NO: 2200)
  • Her2/neuv5 4 -762 VLRENTSPK (SEQ ID NO: 2202)
  • tumor-specific peptides can be added to the target peptide compositions in a manner, number, and in an amount as if they were an additional target peptide added to the target peptide compositions as described herein.
  • the tumor-specific peptides added to the target peptide compositions of the presently disclosed subject matter comprise, consist essentially of, or consist of the amino acid sequences SDAEKSDICTDEY (SEQ ID NO: 2183), SSDYVIPIGTY (SEQ ID NO: 2184), EADPTGHSY (SEQ ID NO: 2185), EVDPIGHLY (SEQ ID NO: 2186), YMDGTMSQV (SEQ ID NO: 2187), IMDQVPFSV (SEQ ID NO: 2188), YLEPGPVTA (SEQ ID NO: 2189), GLYDGMEHL (SEQ ID NO: 2190), ALLAVGATK (SEQ ID NO: 2170), LIYRRRLMK (SEQ ID NO: 2179), SLFRAVITK (SEQ ID NO: 2205), ASGPGGGAPR (SEQ ID NO: 2192), or any combinations thereof.
  • SDAEKSDICTDEY SEQ ID NO: 2183
  • SSDYVIPIGTY SEQ ID NO: 2184
  • the target peptide compositions (or target peptide composition kits) of the presently disclosed subject matter are administered as a vaccine or in the form of pulsed cells as first, second, third, or fourth line treatment for the cancer.
  • the compositions of the presently disclosed subject matter are administered to a patient in combination with one or more therapeutic agents.
  • Exemplary, non-limiting therapeutic agents include anti- Programed Death- 1 (PD1) or PD1 -antagonists such as the anti-PDl antibody BMS- 936558 (Bristol-Myers Squibb Co., New York, New York, United States of America); anti-CTLA-4 or CTLA-4 antagonists; vermurafenib; ipilimumab; dacarbazine; IL-2; Temozolomide; receptor tyrosine kinase inhibitors, including but not limited to imatinib, gefitinib, erlotinib, sunitinib, tyrphostins, telatinib; sipileucel-T; a platinum- based agent; a taxane; an alkylating agent; an antimetabolite and/or a vinca alkaloid; and combinations thereof.
  • PD1 Programed Death- 1
  • BMS- 936558 Bristol-Myers Squibb Co.
  • the cancer is sensitive to and/or refractory, relapsed, and/or resistant to one or more chemotherapeutic agents such as, but not limited to a platinum-based agent, a taxane, an alkylating agent, an anthracycline (e.g., doxorubicin including but not limited to liposomal doxorubicin), an antimetabolite, and/or a vinca alkaloid.
  • chemotherapeutic agents such as, but not limited to a platinum-based agent, a taxane, an alkylating agent, an anthracycline (e.g., doxorubicin including but not limited to liposomal doxorubicin), an antimetabolite, and/or a vinca alkaloid.
  • chemotherapeutic agents such as, but not limited to a platinum-based agent, a taxane, an alkylating agent, an anthracycline (e.g., doxorubicin including but
  • the cancer is an ovarian cancer
  • the ovarian cancer is refractory, relapsed, or resistant to a platinum-based agent (e.g., carboplatin, cisplatin, oxaliplatin), a taxane (e.g., paclitaxel, docetaxel, larotaxel, cabazitaxel), and/or an anthracycline (e.g., doxorubicin including but not limited to liposomal doxorubicin).
  • a platinum-based agent e.g., carboplatin, cisplatin, oxaliplatin
  • a taxane e.g., paclitaxel, docetaxel, larotaxel, cabazitaxel
  • an anthracycline e.g., doxorubicin including but not limited to liposomal doxorubicin.
  • the cancer is colorectal cancer, and the cancer is refractory, relapsed, or resistant to an antimetabolite (e.g., an antifolate (e.g., pemetrexed, floxuridine, raltitrexed) a pyrimidine analogue (e.g., capecitabine, cytrarabine, gemcitabine, 5FU)), and/or a platinum-based agent (e.g., carboplatin, cisplatin, oxaliplatin).
  • an antimetabolite e.g., an antifolate (e.g., pemetrexed, floxuridine, raltitrexed)
  • a pyrimidine analogue e.g., capecitabine, cytrarabine, gemcitabine, 5FU
  • a platinum-based agent e.g., carboplatin, cisplatin, oxaliplatin
  • the cancer is lung cancer, and the cancer is refractory, relapsed, or resistant to a taxane (e.g., paclitaxel, docetaxel, larotaxel, cabazitaxel), a platinum-based agent (e.g., carboplatin, cisplatin, oxaliplatin), a vinca alkaloid (e.g., vinblastine, vincristine, vindesine, vinorelbine), a vascular endothelial growth factor (VEGF) pathway inhibitor, an epidermal growth factor (EGF) pathway inhibitor) and/or an antimetabolite (e.g., an antifolate including but not limited to pemetrexed, floxuridine, or raltitrexed), and a pyrimidine analogue (e.g., capecitabine, cytrarabine, gemcitabine, 5FU).
  • a taxane e.g., paclitaxel, docetaxel,
  • the cancer is breast cancer, and the cancer is refractory, relapsed, or resistant to a taxane (e.g., paclitaxel, docetaxel, larotaxel, cabazitaxel), a VEGF pathway inhibitor, an anthracycline (e.g., daunorubicin, doxorubicin including but not limited to liposomal doxorubicin, epirubicin, valrubicin, idarubicin), a platinum-based agent (e.g.
  • a taxane e.g., paclitaxel, docetaxel, larotaxel, cabazitaxel
  • a VEGF pathway inhibitor e.g., an anthracycline (e.g., daunorubicin, doxorubicin including but not limited to liposomal doxorubicin, epirubicin, valrubicin, idarubicin)
  • carboplatin e.g., carboplatin, cisplatin, oxaliplatin
  • an antimetabolite e.g., an antifolate including but not limited to pemetrexed, floxuridine, or raltitrexed
  • a pyrimidine analogue e.g., capecitabine, cytrarabine, gemcitabine, 5FU.
  • the cancer is gastric cancer, and the cancer is refractory, relapsed, or resistant to an antimetabolite (e.g., an antifolate including but not limited to pemetrexed, floxuridine, raltitrexed) and a pyrimidine analogue (e.g., capecitabine, cytrarabine, gemcitabine, 5FU) and/or a platinum-based agent (e.g., carboplatin, cisplatin, oxaliplatin).
  • an antimetabolite e.g., an antifolate including but not limited to pemetrexed, floxuridine, raltitrexed
  • a pyrimidine analogue e.g., capecitabine, cytrarabine, gemcitabine, 5FU
  • a platinum-based agent e.g., carboplatin, cisplatin, oxaliplatin.
  • DTIC Single-agent dacarbazine
  • melanoma Single-agent dacarbazine
  • the first regimen is the cisplatin, vinblastine, and DTIC (CVD) regimen.
  • the second commonly used regimen is the Dartmouth regimen, which is a combination of cisplatin, DTIC, carmustine, and tamoxifen.
  • DTIC was the first drug approved for the treatment of metastatic melanoma.
  • the overall response rate was 22%, with no impact on survival.
  • the response rate was 12% versus 13% (Middleton et al, 2000).
  • Carboplatin and paclitaxel have been tested in 2 small Phase II studies, and when used in combination with sorafenib, the response rate was 11-17%.
  • temozolomide is included in a first- line drug for melanoma.
  • the target peptide compositions (or target peptide composition kits) of the presently disclosed subject matter are associated with agents that inhibit T cell apoptosis or anergy thus potentiating a T cell response (referred to herein as a "T cell potentiator").
  • agents include B7RP1 agonists, B7-H3 antagonists, B7-H4 antagonists, HVEM antagonists, HVEM antagonists, GAL9 antagonists or alternatively CD27 agonists, OX40 agonists, CD 137 agonists, BTLA agonists, ICOS agonists CD28 agonists, or soluble versions of PDL1, PDL2, CD80, CD96, B7RP1, CD137L, OX40 or CD70. See Pardoll, 2012.
  • the T cell potentiator is a PDl antagonist.
  • Programmed death 1 (PDl) is a key immune checkpoint receptor expressed by activated T cells, and it mediates immunosuppression. PDl functions primarily in peripheral tissues, where T cells can encounter the immunosuppressive PDl ligands PD-Ll (B7-H1) and PD-L2 (B7-DC), which are expressed by tumor cells, stromal cells, or both.
  • the anti-PDl monoclonal antibody BMS-936558 also known as MDX- 1106 and ONO-4538; Bristol-Myers Squibb is used.
  • the T cell potentiator ⁇ e.g., PDl antagonist is administered as an intravenous infusion at least or about every 1, 1.5, 2, 2.5, 3, 3.5, or 4 weeks of each 4, 5, 6, 7, 8, 9, or 10-week treatment cycle of about for at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more cycles.
  • Exemplary, non-limiting doses of the PDl antagonists are in some embodiments exactly, about, or at least 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more mg/kg. See Brahmer et al. , 2012.
  • exemplary therapeutic agents listed herein above are envisioned to be administered at a concentration of in some embodiments about 1 to 100 mg/m 2 , in some embodiments about 10 to 80 mg/m 2 , and in some embodiments about 40 to 60 mg/m 2 .
  • Further exemplary dosages include, but are not limited to about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51 , 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91
  • cytokines such as lymphokines, monokines, growth factors, and traditional polypeptide hormones.
  • cytokines are growth hormones including but not limited to human growth hormone, N-methionyl human growth hormone, and bovine growth hormone; parathyroid hormone; thyroxine; insulin; proinsulin; relaxin; prorelaxin; glycoprotein hormones including but not limited to follicle stimulating hormone (FSH), thyroid stimulating hormone (TSH), and luteinizing hormone (LH); hepatic growth factor; prostaglandin, fibroblast growth factor; prolactin; placental lactogen, OB protein; TNF-a and TNF- ⁇ ; mullerian-inhibiting substance; mouse gonadotropin-associated peptide; inhibin; activin; VEGF; integrin; thrombopoietin (TPO); nerve growth hormones including but not limited to human growth hormone, N-methionyl human growth hormone, and bovine growth hormone; parathyroid hormone; thy
  • the target peptide compositions of the presently disclosed subject matter can in some embodiments be provided with administration of cytokines around the time of (including but not limited to about or at least 1, 2, 3, or 4 weeks or days before and/or after) the initial dose of a target peptide composition.
  • Exemplary non-limiting doses of the cytokine are in some embodiments about or at least 1-100, 10-80, 20-70, 30-60, 40-50, or 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 Mu/m 2 /day over about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, or 70 days.
  • the cytokine can in some embodiments be delivered at least or about once every 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, or 24 hours.
  • Cytokine treatment can be provided in at least or about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 cycles of at least or about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more weeks, wherein each cycle has at least or about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, or more cytokine doses.
  • Cytokine treatment can in some embodiments be on the same schedule as administration of the target peptide compositions or in some embodiments on a different schedule, which differing schedule can in some embodiments be an overlapping schedule.
  • the cytokine is IL-2 and is dosed in an amount about or at least 100,000 to 1,000,000; 200,000-900,000; 300,000-800,000; 450,000-750,000; 600,000-800,000; or 700,000-800,000 (in some embodiments. 720,000) units (IU)/kg administered, e.g., as a bolus, every 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 hours for 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or more days, in a cycle, for example.
  • IU unit
  • compositions of the presently disclosed subject matter are envisioned to be useful in the treatment of benign and/or malignant proliferative diseases.
  • Excessive proliferation of cells and turnover of cellular matrix contribute significantly to the pathogenesis of several diseases including but not limited to cancer, atherosclerosis, rheumatoid arthritis, psoriasis, idiopathic pulmonary fibrosis, scleroderma and cirrhosis of the liver, ductal hyperplasia, lobular hyperplasia, papillomas, and others.
  • the proliferative disease is cancer, including but not limited to breast cancer, colorectal cancer, squamous carcinoma of the lung, sarcoma, renal cell carcinoma, pancreatic carcinomas, squamous tumors of the head and neck, leukemia, brain cancer, liver cancer, prostate cancer, ovarian cancer, and cervical cancer.
  • the presently disclosed compositions and methods are used to treat melanoma, acute myelogenous leukemia (AML), acute lyphocytic leukemia (ALL), chronic lymphocytic lymphoma (CLL), chronic myelogenous leukemia (CML), breast cancer, renal cancer, pancreatic cancer, and/or ovarian cancer.
  • the target peptide compositions of the presently disclosed subject matter can be used to treat melanoma.
  • the melanoma can be in some embodiments Stage I, in some embodiments Stage II (including but not limited to Stages Ila and/or lib), Stage III, Stage IV, metastatic, malignant, or recurrent melanoma.
  • Stage II including but not limited to Stages Ila and/or lib
  • Stage III Stage IV
  • metastatic the melanoma is in some embodiments in the lung, bone, liver, or brain.
  • the cancer is a cancer described herein.
  • the cancer can be a cancer of the bladder (including but not limited to accelerated and metastatic bladder cancer), breast (including but not limited to estrogen receptor positive breast cancer, estrogen receptor negative breast cancer, HER-2 positive breast cancer, HER-2 negative breast cancer, triple negative breast cancer, and inflammatory breast cancer), colon (including but not limited to colorectal cancer), kidney (including but not limited to renal cell carcinoma), liver, lung (including but not limited to small cell lung cancer and non-small cell lung cancer such as but not limited to adenocarcinoma, squamous cell carcinoma, bronchoalveolar carcinoma and large cell carcinoma), genitourinary tract cancer, including but not limited to ovary (such as but not limited to fallopian, endometrial, and peritoneal cancers), cervix, prostate, and testes, lymphatic system, rectum, larynx, pancreas (including but not limited to exocrine pancreatic carcinoma), stomach (including but not
  • Exemplary non-limiting cancers also include melanoma, breast cancer (including but not limited to metastatic or locally advanced breast cancer), prostate cancer (including but not limited to hormone refractory prostate cancer), renal cell carcinoma, lung cancer (including but not limited to small cell lung cancer and non-small cell lung cancer (including adenocarcinoma, squamous cell carcinoma, bronchoalveolar carcinoma, and large cell carcinoma), pancreatic cancer, gastric cancer (including but not limited to gastroesophageal, upper gastric, and/or lower gastric cancer), colorectal cancer, squamous cell cancer of the head and neck, ovarian cancer (including but not limited to advanced ovarian cancer, platinum-based agent-resistant, and/or relapsed ovarian cancer), lymphoma (including but not limited to Burkitt's, Hodgkin's, or non- Hodgkin's lymphoma), leukemia (including but not limited to acute myeloid leukemia), and gastrointestinal cancer.
  • breast cancer including but
  • composition injections can be performed by intravenous (i.v.) injection, subcutaneous (s.c.) injection, intradermal (i.d.) injection, intraperitoneal (i.p.) injection, and/or intramuscular (i.m.) injection.
  • i.v. intravenous
  • s.c. subcutaneous
  • i.d. intradermal
  • i.p. intraperitoneal
  • i.m. intramuscular
  • Parenteral administration can be, for example, by bolus injection or by gradual perfusion over time.
  • administration can be by the oral route.
  • an injection is an intradermal (i.d.) injection.
  • the target peptide compositions are in some embodiments suitable for administration of the peptides by any acceptable route such as but not limited to oral (enteral), nasal, ophthal, and transdermal.
  • the administration is subcutaneous, and in some embodiments the subcutaneous administration is by an infusion pump.
  • compositions are generally added to the target peptide compositions or (target peptide compositions kits) that are compatible with the active ingredients and acceptable for pharmaceutical use.
  • examples of such carriers include but are not limited to water, saline solutions, dextrose, and/or glycerol. Combinations of carriers can also be used.
  • the vaccine compositions of the presently disclosed subject matter can further incorporate additional substances to stabilize pH and/or to function as adjuvants, wetting agents, and/or emulsifying agents, which can serve to improve the effectiveness of the vaccine.
  • the target peptide compositions may include one or more adjuvants such as for example: montanide ISA-51 (Seppic Inc., Fairfield, New Jersey, United States of America); QS-21 (Aquila Biopharmaceuticals, Inc., Framingham, Massachusetts, United States of America); Arlacel A; oeleic acid; tetanus helper peptides (such as but not limited to QYIKANSKFIGITEL (SEQ ID NO: 2376) and/or AQYIKANSKFIGITEL (SEQ ID NO: 2377); GM-CSF; cyclophosamide; bacillus Calmette-Guerin (BCG); Corynbacterium parvum; levamisole, azimezone; isoprinisone; dinitrochlorobenezene (DNCB); keyhole limpet hemocyanin (KLH); Freunds adjuvant (complete and incomplete); mineral gels; aluminum hydroxide (Alum); lysolecithin; plur
  • an adjuvant is a tetanus helper peptide (alternativedly referred to herein as a "tetanus peptide").
  • tetanus helper peptide and “tetanus peptide” refer to a peptide that comprises an amino acid sequence that is a subsequence of a wild type tetanus toxoid protein, or a derivative thereof.
  • the phrase "derivative thereof refers to a peptide that comprises an amino acid sequence that is in some embodiments at least 75%, in some embodiments at least 80%, in some embodiments at least 85%, in some embodiments at least 90%, in some embodiments at least 91%, in some embodiments at least 92%, in some embodiments at least 93%, in some embodiments at least 94%, in some embodiments at least 95%, in some embodiments at least 96%, in some embodiments at least 97%, in some embodiments at least 98%, or in some embodiments at least 99% identical to, or in some embodiments 100% identical to, a reference amino acid sequence.
  • the reference amino acid sequence is SEQ ID NO: 2376 or a subsequence thereof, and in some embodiments of a derivative of a tetanus peptide, the reference amino acid sequence is SEQ ID NO: 2377 or a subsequence thereof.
  • the tetanus peptide can be about or at least 10, 1 1, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, or more natural or non-natural amino acids in length.
  • the tetanus peptide is a fragment of a wild type and/or naturally occurring tetanus toxoid protein (i.e., comprises an amino acid sequence that is a subsequence of the amino acid sequence of a wild type and/or naturally occurring tetanus toxoid protein).
  • the tetanus toxoid peptide used herein is at least or about 70, 75, 80, 85, 90, 95, 98, 99%> identical to a 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25 amino acids segment of the wild type and/or naturally occurring tetanus toxoid protein.
  • the tetanus toxoid peptide used herein is at least or about 70, 75, 80, 85, 90, 95, 98, 99% identical to SEQ ID NOs: 2376 or 2377.
  • the tetanus peptide is binds to MHC Class II molecules.
  • the tetanus peptide is modified so as to prevent formation of tetanus peptide secondary structures.
  • Polyinosinic-Polycytidylic acid is a double-stranded RNA (dsRNA) that acts as a TLR3 agonist. To increase half-life, it has been stabilized with polylysine and carboxymethylcellulose as poly-ICLC. It has been used to induce interferon in cancer patients, with intravenous doses up to 300 ⁇ g/kg. Like poly-IC, poly-ICLC is a TLR3 agonist. TLR3 is expressed in the early endosome of myeloid DC; thus poly-ICLC preferentially activates myeloid dendritic cells, thus favoring a Thl cytotoxic T cell response. Poly-ICLC activates natural killer (NK) cells, induces cytolytic potential, and induces IFNy from myeloid DC.
  • NK natural killer
  • an adjuvant is provided at about or at least 10, 20, 30,
  • the adjuvant is provided in a dosage of at least or about 0.1 , 0.2, 0.3, 0.40, 0.50, 0.60, 0.70, 0.80, 0.90, 0.100, 1.10, 1.20, 1.30, 1.40, 1.50, 1.60, 1.70, 1.80, 1.90, 2.00, 2.10, 2.20, 2.30, 2.40, 2.50, 2.60, 2.70, 2.80, 2.90, 3.00, 3.10, 3.20, 3.30, 3.40, 3.50, 3.60, 3.70, 3.80, 3.90, 4.00, 4.10, 4.20, 4.30, 4.40, 4.50, 4.60, 4.70, 4.80, 4.90, 5.00, 5.10, 5.20, 5.30, 5.40, 5.50, 5.60, 5.70, 5.80, 5.90, 6.00, 6.10, 6.20, 6.30, 6.40, 6.50, 6.60, 6.70, 6.80, 6.90, 7.00, 7.10, 7.20, 7.30, 7.40, 7.50, 7.60, 7.70, 7.80,
  • the adjuvant is given at about or at least 10, 15, 20, 25, 50, 75, 100, 125, 150, 175, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, 400, 425, 450, 500, 525, 550, 575, 600, 625, 675, 700, 725, 750, 775, 800, 900, 1000, 1 100, 1200, 1300, 1400, 1500, 1600, 1700, 1800, 1900, or 2000 endotoxin units ("EU") per dose.
  • EU endotoxin units
  • the target peptide compositions of the presently disclosed subject matter can in some embodiments be provided with an administration of cyclophosamide around the time (e.g., about or at least 1 , 2, 3, or 4 weeks or days before and/or after) of the initial dose of a target peptide composition.
  • exemplary non-limiting doses of cyclophosamide are about or at least 100, 200, 300, 400, 500, 600, 700, 800, 900, or 1000 Mg/m 2 /day over about or at least 1 , 2, 3, 4, 5, 6, 7, 8, 9, or 10 days.
  • compositions can comprise the target peptides in the free form and/or in the form of a pharmaceutically acceptable salt.
  • a pharmaceutically acceptable salt refers to a derivative of a disclosed target peptide wherein the target peptide is modified by making acid or base salts of the agent.
  • acid salts are prepared from the free base (typically wherein the neutral form of the drug has a neutral -NH 2 group) involving reaction with a suitable acid.
  • Suitable acids for preparing acid salts include both organic acids such as but not limited to acetic acid, propionic acid, gly colic acid, pyruvic acid, oxalic acid, malic acid, malonic acid, succinic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p- toluenesulfonic acid, salicylic acid, and the like, as well as inorganic acids such as but not limited to hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid phosphoric acid, and the like.
  • organic acids such as but not limited to acetic acid, propionic acid, gly colic acid, pyruvic acid, oxalic acid, malic acid, malonic acid, succinic acid, maleic acid, fumaric acid, tartaric acid, citric acid, be
  • compositions can comprise target peptides as salts of acetic acid (acetates), ammonium, or hydrochloric acid (chlorides).
  • a composition can include one or more sugars, sugar alcohols, amino acids such but not limited to glycine, arginine, glutamic acid, and/or others as framework formers.
  • the sugars can be mono-, di-, or trisaccharides. These sugars can be used alone and/or in combination with sugar alcohols. Exemplary sugars include glucose, mannose, galactose, fructose, or sorbose as monosaccharides; sucrose, lactose, maltose, and trehalose as disaccharides; and raffmose as a trisaccharide.
  • a sugar alcohol can be, for example, mannitose.
  • the composition comprises sucrose, lactose, maltose, trehalose, mannitol, and/or sorbitol. In some embodiments, the composition comprises mannitol.
  • compositions can include physiological well-tolerated excipients (see Handbook of Pharmaceutical Excipients, 5 th ed., edited by Raymond Rowe, Paul Sheskey and Sian Owen, Pharmaceutical Press (2006)) such as antioxidants like ascorbic acid or glutathione; preserving agents such as phenol, m- cresol, methyl- or propylparabene, chlorobutanol, thiomersal/thimerosal, and/or benzalkoniumchloride; stabilizers, framework formers such as sucrose, lactose, maltose, trehalose, mannitose, mannitol, and/or sorbitol; mannitol and/or lactose and solubilizers such as polyethylene glycols (PEG; e.g.
  • physiological well-tolerated excipients see Handbook of Pharmaceutical Excipients, 5 th ed., edited by Raymond Rowe, Paul Sheskey and Sian Owen, Pharmaceutical Press (2006)
  • antioxidants
  • cyclodextrins e.g., hydroxypropyl- -cyclodextrin, sulfobutylethyl- -cyclodextrin, or ⁇ -cyclodextrin
  • dextranes e.g., poloxamer 407 or poloxamer 188
  • poloxamers e.g., poloxamer 407 or poloxamer 188
  • TWEEN® 20 or TWEEN® 80 e.g., one or more well-tolerated excipients can be included, optionally selected from the group consisting of antioxidants, framework formers, and stabilizers.
  • the pH for intravenous and/or intramuscular administration is selected from pH 2 to pH 12.
  • the pH for subcutaneous administration is selected from pH 2.7 to pH 9.0 as the rate of in vivo dilution is reduced resulting in more potential for irradiation at the injection site (Strickley, 2004).
  • a suitable dosage of a target peptide composition vaccine immunogen cam depend upon the age, sex, health, and/or weight of the recipient, the kind of concurrent treatment, if any, the frequency of treatment, and the nature of the effect desired. However, it is understood that dosages can be tailored to the individual subject, as determined by the researcher or clinician.
  • the total dose required for any given treatment will in some embodiments be determined with respect to a standard reference dose based on the experience of the researcher or clinician, such dose being administered either in a single treatment or in a series of doses, the success of which will depend on the production of a desired immunological result (such as but not limited to successful production of a T helper cell and/or CTL-mediated response to the target peptide immunogen composition, which response gives rise to the prevention and/or treatment desired).
  • a desired immunological result such as but not limited to successful production of a T helper cell and/or CTL-mediated response to the target peptide immunogen composition, which response gives rise to the prevention and/or treatment desired.
  • the overall administration schedule is considered in determining the success of a course of treatment and not whether a single dose, given in isolation, would or would not produce the desired immunologically therapeutic result or effect.
  • a therapeutically effective amount i.e., in some embodiments that amount that produces a desired T helper cell and/or CTL-mediated response
  • the efficacy of administering additional doses and/or of increasing or decreasing the interval can be continually re-evaluated in view of the recipient's immunocompetence (including but not limited to the level of T helper cell and/or CTL activity with respect to tumor- associated or tumor- specific antigens).
  • the concentration of the T helper or CTL stimulatory target peptides of the presently disclosed subject matter in pharmaceutical formulations can be subject to wide variation, including anywhere from less than 0.01% by weight to as much as 50% or more. Factors such as volume and viscosity of the resulting composition can in some embodiments also be considered.
  • the solvents or diluents used for such compositions can include water, phosphate buffered saline (PBS), and/or saline, or any other possible carriers or excipients.
  • the immunogens of the present presently disclosed subject matter can in some embodiments also be contained in artificially created structures such as liposomes, which structures in some embodiments can contain additional molecules such as but not limited to proteins or polysaccharides, inserted in the outer membranes of said structures and having the effect of targeting the liposomes to particular areas of the body and/or to particular cells within a given organ or tissue.
  • additional molecules such as but not limited to proteins or polysaccharides, inserted in the outer membranes of said structures and having the effect of targeting the liposomes to particular areas of the body and/or to particular cells within a given organ or tissue.
  • targeting molecules can in some embodiments comprise an immunoglobulin.
  • Antibodies can work particularly well for targeting of liposomes and/or other scaffolds to tumor cells.
  • Single i.d., i.m., s.c, i.p., and/or i.v. doses of in some embodiments about 1 to 50 ⁇ g, in some embodiments about 1 to 100 ⁇ g, in some embodiments about 1 to 500 ⁇ g, in some embodiments about 1 to 1000 ⁇ g, in some embodiments about 1 to 50 mg, in some embodiments about 1 to 100 mg, in some embodiments about 1 to 500 mg, or in some embodiments about 1 to 1000 mg of target peptide composition can be given and can depend from the respective compositions of target peptides with respect to total amount for all target peptides in the composition or alternatively for each individual target peptide in the composition.
  • a single dose of a target peptide vaccine composition of the presently disclosed subject matter can in some embodiments have a target peptide amount (e.g., total amount for all target peptides in the composition or alternatively for each individual target peptide in the composition) of about or at least 1 , 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, 400, 425, 450, 475, 500, 525, 550, 575, 600, 625, 650, 675, 700, 725, 750, 775, 800, 825, 850, 875, 900, or 950 ⁇ g.
  • a target peptide amount e.g., total amount for all target peptides in the composition or alternatively for each individual target peptide in the composition
  • a target peptide amount e.g., total
  • a single dose of a target peptide composition of the presently disclosed subject matter can have a total target peptide amount (e.g., total amount for all target peptides in the composition or alternatively for each individual target peptide in the composition) of about or at least 1 , 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, 400, 425, 450, 475, 500, 525, 550, 575, 600, 625, 650, 675, 700, 725, 750, 775, 800, 825, 850, 875, 900, or 950 mg.
  • the target peptides of a composition of the presently disclosed subject matter are present in equal amounts of about 100 micrograms per dose in combination with an adjuvant peptide present in an amount of about 200 micrograms per dose
  • the amount of each target peptide in the composition is in some embodiments equal or substantially equal.
  • a ratio of the target peptides present in the least amount relative to the target peptide present in the greatest amount is about or at least 1 : 1.25, 1 : 1.5, 1 : 1.75, 1 :2.0, 1 :2.25, 1 :2.5, 1 :2.75, 1 :3, 1 :4, 1 :5, 1 :6, 1 :7, 1 :8, 1 :9, 1 :10, 1 :20, 1 :30; 1 :40, 1 :50, 1 : 100, 1 :200, 1 :500, 1 : 1000, 1 :5000; 1 : 10,000; or 1 : 100,000.
  • a ratio of the target peptides present in the least amount relative to the target peptide present in the greatest amount is about or at least 1 or 2 to 25; 1 or 2 to 20; 1 or 2 to 15; 1 or 2 to 10; 1 to 3; 1 to 4; 1 to 5; 1 to 6; 1 to 7; 1 to 10; 2 to 3; 2 to 4; 2 to 5; 2 to 6; 2 to 7; 2 to 10; 3 to 4; 3 to 5; 3 to 6; 3 to 7; 3 to 10; 5 to 10; 10 to 15; 15 to 20; 20 to 25; 1 to 40; 1 to 30; 1 to 20; 1 to 15; 10 to 40; 10 to 30; 10 to 20; 10 to 15; 20 to 40; 20 to 30; or 20 to 25; 1 to 100; 25 to 100; 50 to 100; 75 to 100; 25 to 75, 25 to 50, or 50 to 75; 25 to 40; 25 to 50; 30 to 50; 30 to 40; or 30 to 75.
  • Single dosages can be given to a patient about or at least 1, 2, 3, 4, or 5 times per day.
  • Single dosages can be given to a patient about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 18, 19, 20, 21, 22, 23 , 24, 36, 48, 60, or 72 hours subsequent to a previous dose.
  • Single dosages can be given to a patient about or at least 1, 2, 3, 4, 5, 6, or 7 times per week, or every other, third, fourth, or fifth day.
  • Single doses can also be given every week, every other week, or only during 1, 2, or 3 weeks per month.
  • a course of treatment can in some embodiments last about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11. or 12 months.
  • the single dosages of the compositions of the presently disclosed subject matter can be provided to a patient in at least two phases: e.g., during an initial phase and then during a subsequent phase.
  • An initial phase can be about or at least 1, 2, 3, 4, 5, or 6 weeks in length.
  • the subsequent phase can last at least or about 1, 2, 3, 4, 5, 6, 7, or 8 times as long as the initial phase.
  • the initial phase can be separated from the subsequent phase by about or at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 weeks or months.
  • the target peptide composition dosage during the subsequent phase can be at least 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 300, 400, 500, 600, 700, 800, 900, or 1000 times greater than during the initial phase.
  • the target peptide composition dosage during the subsequent phase can be at least 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 30, 40, 50, 60, 70, 80, 90, 100, 200, 300, 400, 500, 600, 700, 800, 900, or 1000 times less than during the initial phase.
  • the initial phase is about three weeks and the second phase is about 9 weeks.
  • the target peptide compositions can be administered to the patient on or about days 1 , 8, 15, 36, 57, and 78.
  • a kit comprising (a) a container that contains at least one target peptide composition as described herein, in solution or in lyophilized form; (b) optionally, a second container containing a diluent or reconstituting solution for the lyophilized formulation; and (c) optionally, instructions for (i) use of the solution or (ii) reconstitution and/or use of the lyophilized formulation.
  • the kit may further comprise one or more of (iii) a buffer, (iv) a diluent, (v) a filter, (vi) a needle, or (v) a syringe.
  • the container is selected from the group consisting of: a bottle, a vial, a syringe, a test tube, or a multi- use container.
  • the target peptide composition is lyophilized.
  • kits can contain exactly, about, or at least 1 , 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1 ,
  • composition in the kit can be administered at the same time or at different times.
  • kits can comprise a lyophilized formulation of the presently disclosed compositions and/or vaccines in a suitable container and instructions for its reconstitution and/or use.
  • suitable containers include, for example, bottles, vials (e.g., dual chamber vials), syringes (such as dual chamber syringes), and test tubes.
  • the container can be formed from a variety of materials such as glass or plastic.
  • the kit and/or the container contain(s) instructions on or associated therewith that indicate(s) directions for reconstitution and/or use of a lyophilized formulation.
  • the label can indicate that the lyophilized formulation is to be reconstituted to target peptide concentrations as described herein.
  • the label can further indicate that the formulation is useful or intended for subcutaneous administration. Lyophilized and liquid formulations are typically stored at -20°C to -80°C.
  • the container holding the target peptide composition(s) can be a multi-use vial, which in some embodiments allows for repeat administrations (e.g. , from 2-6 or more administrations) of the reconstituted formulation.
  • the kit can further comprise a second container comprising a suitable diluent (e.g., sodium bicarbonate solution).
  • the final peptide concentration in the reconstituted formulation is at least or about 0.15, 0.20, 0.25, 0.5, 0.75, 1.0, 1.25, 1.5, 1.75, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.50, 3.75, 4.0, 4.25, 4.5, 4.75, 5.0, 6.0, 7.0, 8.0, 9.0, or 10 mg/mL/target peptide.
  • the final peptide concentration in the reconstituted formulation is at least or about 0.15, 0.20, 0.25, 0.5, 0.75, 1.0, 1.25, 1.5, 1.75, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.50, 3.75, 4.0, 4.25, 4.5, 4.75, 5.0, 6.0, 7.0, 8.0, 9.0, or 10 ⁇ g/mL/target peptide.
  • the kit can further include other materials desirable from a commercial and/or user standpoint, including other buffers, diluents, filters, needles, syringes, and package inserts with or without instructions for use.
  • kits can have a single container that contains the formulation of the target peptide compositions with or without other components (e.g., other compounds or compositions of these other compounds) or can have a distinct container for each component.
  • kits can include a formulation of the presently disclosed target peptide compositions and/or vaccines packaged for use in combination with the co-administration of a second compound (such as adjuvants including but not limited to imiquimod), a chemotherapeutic agent, a natural product, a hormone or antagonist, an anti-angiogenesis agent or inhibitor, an apoptosis-inducing agent or a chelator) or a composition thereof.
  • a second compound such as adjuvants including but not limited to imiquimod
  • a chemotherapeutic agent such as adjuvants including but not limited to imiquimod
  • a chemotherapeutic agent such as a chemotherapeutic agent, a natural product, a hormone or antagonist, an anti-angiogenesis agent or inhibitor, an apoptosis-inducing agent or a chelator
  • a second compound such as adjuvants including but not limited to imiquimod
  • a chemotherapeutic agent such as a chemotherapeutic agent,
  • the liquid solution is a sterile aqueous solution.
  • One or more of the components of the kit can also be provided as solids, which in some embodiments can be converted into liquids by addition of suitable solvents, which in some embodiments can be provided in another distinct container.
  • the container of a therapeutic kit can be a vial, a test tube, a flask, a bottle, a syringe, or any other structure suitable for enclosing a solid or liquid.
  • the kit contains a second vial or other container that allows for separate dosing.
  • the kit can also contain another container for a pharmaceutically acceptable liquid.
  • a therapeutic kit contains an apparatus (e.g., one or more needles, syringes, eye droppers, pipette, etc.), which enables administration of the agents of the disclosure that are components of the kit.
  • the vaccine compositions of the presently disclosed subject matter are in some embodiments envisioned to have certain physiological effects including but not limited to the induction of a T cell mediated immune response.
  • such techniques can be employed to assay patient samples including but not limited to formalin-fixed, paraffin-embedded tissue samples for the presence or absence of and/or for a level of expression of one or more of CD la, S I 00, CD83, DC-LAMP, CD3, CD4, CD8, CD20, CD45, CD79a, PNAd, TNFa, LIGHT, CCL19, CCL21 , CXCL12, TLR4, TLR7, FoxP3, PD-1 , and Ki67 gene products.
  • flow cytometry is used to determine an expression level for one or more of CD3, CD4, CD8, CD13, CD14, CD16, CD19, CD45RA, CD45RO, CD56, CD62L, CD27, CD28, CCR7, FoxP3 (intracellular), and MHC-peptide tetramers for I MHC associated (phospho)-peptides.
  • a positive control is employed, which in some embodiments can comprise a tissue sample comprising normal human peripheral blood lymphocytes (PBL), PBL activated with CD3/CD28 beads (activated PBL), human lymph node tissue from non-melanoma patients (LN), and/or inflamed human tissue from a surgical specimen of Crohn's disease (Crohn's), although any other positive control cell and/or tissue can be employed.
  • PBL peripheral blood lymphocytes
  • activated with CD3/CD28 beads activated with CD3/CD28 beads
  • LN human lymph node tissue from non-melanoma patients
  • Crohn's Crohn's
  • vaccination site infiltrating lymphocytes and lymphocytes from the sentinel immunized node (SIN) and vaccine site can be evaluated by ELISpot.
  • ELISpot permits the direct counting of T cells reacting to antigen by production of IFNy.
  • Peripheral blood lymphocytes can be evaluated by ELISpot assay for the number of peptide -reactive T cells.
  • Vaccine site infiltrating lymphocytes and SIN lymphocytes can be compared to those in peripheral blood. It is envisioned that positive results of the ELISpot assay correlates with increased patient progression free survival. Progression free survival is defined as the time from start of treatment until death from any cause or date of last follow up.
  • Peripheral blood lymphocytes and lymphocytes from the SIN and vaccine site can be evaluated by flow cytometry after incubation with MHC-peptide tetramers for the number of peptide-reactive T cells.
  • PBMC Peripheral blood mononuclear cells
  • vaccine-site inflammatory cells and/or lymphocytes from the SIN isolated from subjects can be evaluated for CD4 + T cell reactivity to, e.g., tetanus helper peptide mixture, using a 3 H-thymidine uptake assay.
  • Thl IL-2, ⁇ , TNFa
  • Th2 IL-4, IL-5, IL-10
  • Thl7 IL-17, and IL23
  • T-reg TGF- ⁇
  • one or both of the following peptides are used as negative controls: a tetanus peptide and the PADRE peptide (AK(X)VAAWTLKAA; SEQ ID NO: 2378).
  • tumor tissue collected prior to treatment or at the time of progression can be evaluated by routine histology and immunohistochemistry.
  • in vitro evaluations of tumor tissue and tumor infiltrating lymphocytes can be performed.
  • Patient samples can be studied for T cell homing receptors induced by vaccination with the compositions of the presently disclosed subject matter. These include, but are not limited to, integrins (including but not limited to ⁇ 7, ⁇ , ⁇ 4 ⁇ 1), chemokine receptors (including but not limited to CXCR3), and selectin ligands (including but not limited to CLA and PSL) on lymphocytes, and their ligands in the vaccine sites and SIN. In some embodiments, these can be assayed by immunohistochemistry, flow cytometry, and/or any other appropriate technique(s).
  • integrins including but not limited to ⁇ 7, ⁇ , ⁇ 4 ⁇ 1
  • chemokine receptors including but not limited to CXCR3
  • selectin ligands including but not limited to CLA and PSL
  • Differences in gene expression and/or differences in protein expression profiles can be determined by high-throughput screening assays (e.g., nucleic acid chips, protein arrays, etc.) of samples isolated from vaccine sites and/or SIN.
  • high-throughput screening assays e.g., nucleic acid chips, protein arrays, etc.
  • Antibodies and antibody-like molecules (including but not limited to T cell receptors) specific for target peptides and/or target peptide/MHC complexes are in some embodiments useful for analyzing biological samples.
  • an analysis can comprise determining the pathological nature of tumor margins.
  • Antibodies and antibody- like molecules can also be used as therapeutics.
  • such molecules can be used as therapeutics that target cells, including but not limited to tumor cells, which display target peptides on their surfaces.
  • antibodies and antibody-like molecules bind to phosphorylated target peptides and/or target peptide-MHC complex specifically and do not substantially cross react with the corresponding non-phosphorylated native peptides.
  • antibody As used herein, the terms “antibody”, “antibody peptide(s)”, and “antibodylike molecule(s)” refer to an intact antibody, a binding fragment thereof (i.e., a fragment of an antibody that comprises a paratope), or a polypeptide that can specifically recognize an antigen or epitope and bind to the same in a fashion that mimics antibody binding. In some embodiments, antibodies, antibody peptides, and antibody-like molecules compete with intact antibodies for specific binding to an antigen or epitope.
  • antibody fragments can be produced by recombinant DNA techniques and/or by enzymatic and/or chemical cleavage of intact antibodies.
  • Antibody fragments thus include but are not limited to Fab fragments, Fab' fragments, F(ab') 2 fragments, Fv, and single-chain antibodies including but not limited to single- chain fragment variable (scFv) antibodies.
  • An antibody is said to be "monospecific” if each of its paratopes is identical and/or binds to the same epitope.
  • "bispecific” or “bifunctional” antibodies comprise paratopes that bind to different antigens and/or epitopes.
  • an antibody substantially inhibits adhesion of a receptor to a counterreceptor when an excess of antibody reduces the quantity of receptor bound to counterreceptor by at least about 20%, 40%, 60%>, 80%>, 85%o, 90%o, 95%), or more as measured by, for example, an in vitro competitive binding assay.
  • MHC Major Histocompability Complex
  • HLA Human Leukocyte Antigens
  • HLA Human Leukocyte Antigens
  • MHC light chain and MHC heavy chain refer to particular portions of a MHC molecule.
  • class I molecules are heterodimers comprised of two noncovalently bound polypeptide chains, a larger "heavy” chain (a) and a smaller “light” chain ( ⁇ 2 -microglobulin or ⁇ 2 ⁇ ).
  • the polymorphic, polygenic heavy chain (45 kDa), encoded within the MHC on chromosome human 6 is subdivided into three extracellular domains (designated 1, 2, and 3), one intracellular domain, and one transmembrane domain. The two outermost extracellular domains, 1 and 2, together form the groove that binds to antigenic peptides and/or other epitopes.
  • Domain 3 of the molecule contains the recognition site for the CD8 protein on the CTL. This interaction serves to stabilize the contact between the T cell and an antigen-presenting cell (APC).
  • APC antigen-presenting cell
  • the invariant light chain (12 kDa), encoded on human chromosome 15, consists of a single, extracellular polypeptide.
  • MHC light chain The terms "MHC light chain”, “P2-microglobulin”, and “ ⁇ 2 ⁇ " are used interchangeably herein.
  • epitope includes any protein determinant capable of specific binding to an antibody, antibody peptide, and/or antibody-like molecule (including but not limited to a T cell receptor) as defined herein.
  • Epitopic determinants typically consist of chemically active surface groups of molecules such as amino acids or sugar side chains and generally have specific three dimensional structural characteristics as well as specific charge characteristics.
  • An antibody or antibody- like molecule is said to "specifically” bind an antigen when the dissociation constant (Ka) is in some embodiments less than about 1 ⁇ , in some embodiments less that about 100 nM, and in some embodiments less than about 10 nM.
  • Interactions between antibodies and antibody-like molecules and an epitope can also be characterized by an affinity constant (Ka). In some embodiments, a Ka of less than about 10 7 /M is considered "high affinity”.
  • antibody is used in the broadest sense, and covers monoclonal antibodies (including full length monoclonal antibodies), polyclonal antibodies, multispecific antibodies (e.g., bispecific and/or trispecific antibodies), and antibody fragments (including but not limited to Fab, F(ab') 2 and Fv fragments) as well as antibody- like molecules provided that they exhibit the desired biological activity (e.g., antigen binding).
  • Antibodies (Abs) and immunoglobulins (Igs) are glycoproteins that in some embodiments have the same structural characteristics.
  • antibody like molecules and other members of the immunoglobulin superfamily including, but not limited to T cell receptors, MHC molecules, and other polypeptides that contain one or more antigen-binding regions and/or variable regions including, but not limited to complementary determining regions (CD s) that specifically bind the target peptides disclosed herein.
  • CD s complementary determining regions
  • antibodies and antibody-like molecules bind to the target peptides disclosed herein but do not substantially and/or specifically crossreact with the same peptide in a modified form. See e.g., U.S. Patent Application Publication No. 2009/0226474, which is incorporated by reference.
  • the presently disclosed subject matter includes in some embodiments antibodies that recognize target peptides associated with a tumorigenic or disease state, wherein the peptides are displayed in the context of HLA molecules.
  • These antibodies can mimic the specificity of a T cell receptor (TCR) but can have higher binding affinities such that the molecules can be employed as therapeutic, diagnostic, and/or research reagents.
  • TCR T cell receptor
  • Methods of producing a T cell receptor mimic of the present presently disclosed subject matter comprise identifying a target peptide of interest, generating an isolating CD8 + T cells comprising T cell receptors (TCRs) that are specific for the target peptide, and cloning the genomic sequences present in the isolated CD8 + T cells that encode the TCRs that are specific for the target peptide.
  • TCRs T cell receptors
  • an immunogen comprising at least one target peptide/MHC complex is formed.
  • An effective amount of the immunogen is in some embodiments administered to a host to elicit an immune response in the host, and serum collected from the host can assayed to determine if antibodies that recognize a three-dimensional presentation of the target peptide in the binding groove of the MHC molecule have been produced.
  • the desired antibodies can in some embodiments differentiate the target peptide/MHC complex from the MHC molecule alone, the target peptide alone, and/or a complex of MHC and an irrelevant peptide (in some embodiments, a peptide having the same amino acid composition as a target peptide but wherein the amino acids are in a different order that in the target peptide).
  • the desired antibodies can be isolated.
  • antibody also encompasses soluble T cell receptor (TCR) cytoplasmic domains that are stable at low concentrations and which can recognize MHC-peptide complexes.
  • TCR soluble T cell receptor
  • Such soluble TCRs can in some embodiments be conjugated to immunostimulatory peptides and/or proteins, and/or moieties such as but not limited to CD3 agonists (e.g., anti-CD3 antibodies).
  • CD3 agonists e.g., anti-CD3 antibodies.
  • the CD3 antigen is present on mature human T cells, thymocytes, and a subset of natural killer cells. It is associated with the TCR and is involved in signal transduction of the TCR.
  • Antibodies specific for the human CD3 antigen are well known.
  • One such antibody is the murine monoclonal antibody OKT3 which was the first monoclonal antibody approved by the FDA.
  • OKT3 is reported to be a potent T cell mitogen (Van Wauve, 1980; U.S. Patent No. 4,361,539) and a potent T cell killer (Wong, 1990).
  • Other antibodies specific for the CD3 antigen have also been reported (see PCT International Patent Application Publication No. WO 2004/106380; U.S. Patent Application Publication No. 2004/0202657; U.S. Patent No. 6, 750, 325; U.S. Patent No.
  • Immune mobilizing mTCR Against Cancer are bifunctional proteins that combine affinity monoclonal T cell receptor (mTCR) targeting with a therapeutic mechanism of action (i.e., an anti-CD3 scFv).
  • Native antibodies and immunoglobulins are generally heterotetrameric glycoproteins of about 150,000 daltons (Da) composed of two identical light (L) chains and two identical heavy (H) chains. Each light chain is linked to a heavy chain by a covalent disulfide bond. Disulfide bonds also link the heavy chains of intact antibodies, although the number of disulfide bonds between the heavy chains of different immunoglobulin isotypes can vary. Each heavy and light chain also has regularly spaced intrachain disulfide bridges. Each heavy chain has at one end a variable domain (V H ) followed by a number of constant domains. Each light chain has a variable domain at one end (V L ) and a constant domain at its other end.
  • V H variable domain
  • V L variable domain at one end
  • the constant domain of the light chain is aligned with the first constant domain of the heavy chain, and the light chain variable domain is aligned with the variable domain of the heavy chain.
  • Particular amino acid residues are believed to form an interface between the light and heavy chain variable domains (Clothia et al., 1985; Novotny & Haber, 1985).
  • an “isolated” antibody is one which has been identified and/or separated and/or recovered from a component of the environment in which it was produced or otherwise present. Contaminant components of its production environment are materials that in some embodiments interfere with diagnostic and/or therapeutic uses for the antibody, and in some embodiments can include enzymes, hormones, and other proteinaceous or nonproteinaceous solutes.
  • an antibody can be purified as measurable by one or more of the following methods: 1) to greater than 50%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% by weight of antibody as determined by the Lowry method; 2) to a degree sufficient to obtain at least 10 or 15 residues of N-terminal or internal amino acid sequence by use of a spinning cup sequenator; or 3) to homogeneity by SDS-PAGE under reducing or non- reducing conditions using Coomassie blue or, in some embodiments, silver stain.
  • Isolated antibodies include an antibody in situ within recombinant cells since at least one component of the antibody's natural environment will not be present. Ordinarily, however, isolated antibodies will be prepared by a method that comprises at least one purification step.
  • antibody mutant and “antibody variant” refer to antibodies that relative to a reference antibody comprise one or more amino acid sequence differences, wherein one or more of the amino acid residues have been modified such as but not limited to substitution and/or deletion. Such mutants and/or variants comprise in some embodiments less than 100%, 99%, 98%, 97%, 96%, 95%, 90%, 85%o, 80%), or 75%) sequence identity and/or similarity to the amino acid sequence of either the heavy or light chain variable domain amino acid sequence of the reference antibody.
  • variable in the context of variable domain of antibodies, refers to the fact that certain portions of the variable domains differ extensively in sequence among antibodies and are used in the binding and specificity of each particular antibody for its particular antigen.
  • sequence variability is generally not evenly distributed throughout the variable domains of antibodies.
  • sequence variability is concentrated in three segments called complementarity determining regions (CDRs; also known as hypervariable regions) both in the light chain and heavy chain variable domains.
  • CDRs complementarity determining regions
  • variable domains of native heavy and light chains each comprise four FR regions, largely adopting a beta-sheet configuration, connected by three CDRs, which form loops connecting, and in some cases forming part of, the beta-sheet structure.
  • the CDRs in each chain are held together in close proximity by the FR regions and, with the CDRs from the other chain, contribute to the formation of the antigen binding site of antibodies (see Kabat et al., 1991)
  • the constant domains are generally not involved directly in binding between antibody and antigen, but exhibit various effector functions such as but not limited to participation of the antibody in antibody-dependent cellular toxicity.
  • antibody fragment refers to a portion of a full-length antibody, generally the antigen binding or variable region.
  • antibody fragments include Fab, Fab', F(ab') 2 , and Fv fragments.
  • Papain digestion of antibodies produces two identical antigen binding fragments, called the Fab fragment, each with a single antigen binding site, and a residual "Fc" fragment, so-called for its ability to crystallize readily.
  • Pepsin treatment yields an F(ab') 2 fragment that has two antigen binding fragments which are capable of cross-linking antigen, and a residual other fragment (which is termed pFc').
  • the phrase "functional fragment” with respect to antibodies refers in some embodiments to a fragment that contains at least one antigen-binding domain (referred to as a "paratope”), and thus includes, but is not limited to Fv, F(ab) and F(ab') 2 fragments.
  • an “Fv” fragment is the minimum antibody fragment which contains a complete antigen recognition and binding site.
  • This region consists of a heterodimer of one heavy and one light chain variable domain in a tight, non-covalent or covalent association (VH-VL dimer). It is in this configuration that the three CDRs of each variable domain interact to define an antigen binding site (paratope) on the surface of the VH-VL dimer.
  • VH-VL dimer tight, non-covalent or covalent association
  • the Fab or F(ab) fragment also contains the constant domain of the light chain and the first constant domain (CHI) of the heavy chain.
  • Fab' fragments differ from Fab fragments by the addition of a few residues at the carboxyl terminus of the heavy chain CHI domain including one or more cysteines from the antibody hinge region.
  • Fab'-SH is the designation herein for Fab' in which the cysteine residue(s) of the constant domains have a free thiol group.
  • F(ab') fragments are produced by cleavage of the disulfide bond at the hinge cysteines of the F(ab') 2 pepsin digestion product. Additional chemical couplings of antibody fragments are known to those of ordinary skill in the art.
  • the light chains of antibodies (immunoglobulin) from any vertebrate species can be assigned to one of two clearly distinct types, called kappa ( ⁇ ) and lambda ( ⁇ ), based on the amino sequences of the corresponding constant domain.
  • immunoglobulins can be assigned to different classes. There are at least five (5) major classes of immunoglobulins: IgA, IgD, IgE, IgG and IgM, and several of these may be further divided into subclasses or isotypes (e.g., IgGi, IgG 2 , IgG 3 , IgG 4 , IgAi, IgA 2 , etc.).
  • the heavy chains constant domains that correspond to the different classes of immunoglobulins are called alpha (a), delta ( ⁇ ), epsilon ( ⁇ ), gamma ( ⁇ ), and mu ( ⁇ ), respectively.
  • the subunit structures and three-dimensional configurations of different classes of immunoglobulins are well known.
  • monoclonal antibody refers to an antibody obtained from a population of substantially homogeneous antibodies, i.e., the individual antibodies comprising the population are identical except for possible naturally occurring mutations that can be present in minor amounts. Monoclonal antibodies are highly specific, being directed against a single antigenic site. Furthermore, in contrast to conventional (polyclonal) antibody preparations, which typically include different antibodies directed against different determinants (epitopes), each monoclonal antibody is directed against a single determinant on the antigen. In additional to their specificity, monoclonal antibodies can be advantageous in that they are typically synthesized from hybridomas and thus can be isolated in a form that is uncontaminated by other immunoglobulins. .
  • monoclonal antibodies indicates the character of the antibody as being obtained from a substantially homogeneous population of antibodies, and is not to be construed as requiring production of the antibody by any particular method.
  • monoclonal antibodies to be used in accordance with the presently disclosed subject matter can be made by the hybridoma method first described by Kohler & Milstein, 1975, or can be made by recombinant methods ⁇ see e.g., U.S. Patent No. 4,816,567; Harlow & Lane, 1988).
  • the monoclonal antibodies for use with the presently disclosed subject matter can be isolated from phage antibody libraries using the techniques described in Clackson et al. , 1991 and/or Marks et al, 1991.
  • Utilization of the monoclonal antibodies of the presently disclosed subject matter can in some embodiments comprise administering one or more monoclonal antibodies to a subject, such as but not limited to a human subject.
  • a subject such as but not limited to a human subject.
  • administration of such antibodies to a human patient can elicit an immune response, wherein the immune response is directed towards the administered antibodies themselves.
  • Such reactions can limit the duration and effectiveness of such a therapy.
  • the monoclonal antibodies of the presently disclosed subject matter can in some embodiments be "humanized", that is, the antibodies are engineered such that antigenic portions thereof are removed and like portions of a human antibody are substituted therefor, while the antibodies' affinity for specific peptide/MHC complexes is retained.
  • This engineering can involve a few amino acids, or can include the entire framework regions of the antibody, leaving only the complementarity determining regions of the parent antibody intact.
  • Several methods of humanizing antibodies are known in the art and are disclosed in U.S. Patent Nos. 6,180,370; 6,054,927; 5,869,619; 5,861,155; 5,712,120; and 4,816,567, the entire disclosure of each of which is hereby expressly incorporated herein by reference in its entirety.
  • Humanized forms of antibodies are thus chimeric immunoglobulins, immunoglobulin chains, or fragments thereof (such as Fv, Fab, Fab', F(ab') 2 or other antigen-binding subsequences of antibodies) that are principally comprised of the sequence of a human immunoglobulin, but that contain at least some subsequences derived from a non-human immunoglobulin. Humanization can be performed following the method of Winter and co-workers by substituting rodent CDRs or CDR sequences for the corresponding sequences of a human antibody (Jones et al, 1986; Riechmann et al, 1988; Verhoeyen et al, 1988; see also U.S. Patent No.
  • F v framework residues of a human immunoglobulin are replaced with corresponding non-human residues from an antibody of interest.
  • Humanized antibodies can also comprise residues which are found neither in the recipient antibody nor in the imported CDR or framework sequences.
  • the humanized antibody comprises substantially all of at least one, and typically two, variable domains, in which all or substantially all of the CDR regions correspond to those of a non-human immunoglobulin and all or substantially all of the framework regions are those of a human immunoglobulin consensus sequence.
  • the humanized antibody optimally can also comprise at least a portion of an immunoglobulin constant region (Fc), typically that of a human immunoglobulin (Jones et al, 1986; Riechmann et al. , 1988; and Presta, 1992).
  • Exemplary publications relating to the generation and/or use of humanized antibodies include Sandborn et al, 2001; Mihara et al, 2001; Yenari et al, 2001; Morales et al, 2000; Richards et al, 1999; Yenari et al, 1998; and Shinkura et al, 1998; each of which is expressly incorporated by reference herein in its entirety.
  • a treatment protocol that can be utilized in such a method includes a single dose, generally administered intravenously, of 10-20 mg of humanized mAb per kg ⁇ see e.g., Sandborn et al, 2001).
  • alternative dosing patterns can be appropriate, such as the use of three infusions, administered once every two weeks, of 800-1600 mg or even higher amounts of humanized mAb ⁇ see e.g., Richards et al, 1999).
  • the presently disclosed subject matter is not limited to the treatment protocols described herein, and further that other treatment protocols that are known to one of ordinary skill in the art can be employed in the methods of the presently disclosed subject matter.
  • the presently disclosed subject matter further relates to fully human monoclonal antibodies against specific target peptide/MHC complexes.
  • Fully human antibodies essentially relate to antibody molecules in which the entire sequence of both the light chain and the heavy chain, including the CDRs, arise from human genes. Such antibodies are referred to herein as “human antibodies” or “fully human antibodies”.
  • Human monoclonal antibodies can be prepared by the trioma technique (see U.S. Patent No. 4,714,681; PCT International Patent Application Publication No. WO 1999/047929); the human B-cell hybridoma technique (see Kozbor et al, 1983), and/or the EBV hybridoma technique (see Cole et al, 1985).
  • human monoclonal antibodies can be utilized in the practice of the presently disclosed subject matter and can be produced by using human hybridomas (see Cote et al, 1983) or by transforming human B-cells with Epstein Barr Virus in vitro (see Cole et al, 1985).
  • human antibodies can also be produced using additional techniques, such as but not limited to phage display libraries (Hoogenboom et al, 1991; Marks et al, 1991).
  • human antibodies can be made by introducing human immunoglobulin loci into transgenic animals, e.g., mice in which the endogenous immunoglobulin genes have been partially or completely inactivated. Upon challenge, human antibody production is observed, which closely resembles that seen in humans in all respects, including gene rearrangement, assembly, and antibody repertoire. This approach is described, for example, in U.S. Patent Nos.
  • Human antibodies can additionally be produced using transgenic non-human animals that have been modified to produce fully human antibodies in addition to or rather than the non-human animal's endogenous antibodies in response to challenge by an antigen. See PCT International Patent Application Publication No. WO 1994/02602.
  • endogenous genes encoding the heavy and light immunoglobulin chains present in the non-human animal have been deleted or otherwise inactivated, and nucleic acids encoding human heavy and light chain immunoglobulins have been inserted into the host's genome.
  • the human genes are incorporated, for example, using yeast artificial chromosomes containing the requisite human DNA segments. An animal that provides all the desired modifications is then obtained as progeny by crossbreeding intermediate transgenic animals containing fewer than the full complement of the modifications.
  • XENOMOUSETM produces B cells that secrete fully human immunoglobulins.
  • the antibodies can be obtained directly from the animal after immunization with an immunogen of interest, as, for example, a preparation of polyclonal antibodies, or alternatively from immortalized B cells derived from an immunized animal, such as hybridomas producing monoclonal antibodies. Additionally, the genes encoding the immunoglobulins with human variable regions can be recovered and expressed to obtain the antibodies directly and/or can be further modified to obtain analogs of antibodies such as, for example, single chain Fv molecules.
  • Non-human animal such as but not limited to a mouse that lacks expression of an endogenous immunoglobulin heavy chain
  • a non-human animal can be obtained by a method that comprises deleting the J segment genes from at least one endogenous heavy chain locus in an embryonic stem cell, thereby preventing rearrangement of the locus and formation of an RNA encoding a rearranged immunoglobulin heavy chain locus.
  • the deletion can be effected by a targeting vector that contains a selectable marker, Thereafter, a transgenic animal (e.g., a mouse) having somatic and germ cells containing the gene encoding the selectable marker can be produced from the embryonic stem cell.
  • a transgenic animal e.g., a mouse
  • the transgenic animal would be expected to be unable to rearrange its endogenous immunoglobulin heavy chain locus, and thus would be expected to be unable to produce endogenous immunoglobulins.
  • a method for producing an antibody of interest is also disclosed in U.S. Patent No. 5,916,771 , incorporated herein by reference. It includes introducing a first expression vector that contains a nucleotide sequence encoding a heavy chain into one mammalian host cell in culture, introducing a second expression vector containing a nucleotide sequence encoding a light chain into another mammalian host cell, and fusing the two cells to form a hybrid cell.
  • the hybrid cell can express thus an antibody made up of a heavy chain and a light chain encoded by the first and second expression vectors.
  • Target peptides disclosed herein are in some embodiments expressed on a variety of cancer cell types.
  • antibodies and antibody-like molecules can be used in treating, diagnosing, vaccinating, preventing, retarding, and attenuating a cancer such as but not limited to melanoma, ovarian cancer, breast cancer, colorectal cancer, squamous carcinoma of the lung, sarcoma, renal cell carcinoma, pancreatic carcinomas, squamous tumors of the head and neck, leukemia, brain cancer, liver cancer, prostate cancer, ovarian cancer, and cervical cancer.
  • a cancer such as but not limited to melanoma, ovarian cancer, breast cancer, colorectal cancer, squamous carcinoma of the lung, sarcoma, renal cell carcinoma, pancreatic carcinomas, squamous tumors of the head and neck, leukemia, brain cancer, liver cancer, prostate cancer, ovarian cancer, and cervical cancer.
  • Antibodies generated with specificity for a target peptide as disclosed herein can be used to detect the corresponding target peptides in a biological sample.
  • the biological sample is in some embodiments isolated from an individual who is suspected of having cancer, and thus detection could serve to diagnose the cancer.
  • the biological sample could be isolated from an individual known to have cancer, and detection of a target peptide therein can serve as an indicator of disease prognosis, cancer characterization, treatment efficacy, disease progression, or any combination thereof.
  • Immunoassays that can be employed for these purposes are known in the art and include, but are not limited to, immunohistochemistry, flow cytometry, radioimmunoassay, western blotting, and ELISA.
  • Biological samples suitable for such testing include, but are not limited to, cells, tissue biopsy specimens, whole blood, plasma, serum, sputum, cerebrospinal fluid, pleural fluid, and urine.
  • Antigens recognized by T cells are not recognized as intact proteins, but rather as small peptides that associate with class I or class II MHC proteins on the surface of cells.
  • antigens that are recognized in association with class II MHC molecules on antigen presenting cells are acquired from outside the cell, internalized, and processed into small peptides that associate with the class II MHC molecules.
  • Antigens that give rise to proteins that are recognized in association with class I MHC molecules are generally proteins that are produced within the cells, and these antigens are processed and associate with class I MHC molecules. It is now understood that the peptides that associate with given class I or class II MHC molecules are characterized as having a common binding motif, and the binding motifs for a large number of different class I and II MHC molecules have been determined. Synthetic peptides can also be synthesized that correspond to the amino acid sequence of a given antigen and that contain a binding motif for a given class I or
  • APCs can then be added to appropriate APCs, and the APCs can be used to stimulate a T helper cell or CTL response either in vitro or in vivo.
  • the binding motifs, methods for synthesizing the peptides, and methods for stimulating a T helper cell or CTL response are all known and readily available to one of ordinary skill in the art.
  • Kits can be prepared to assist in diagnosis, monitoring, and/or prognosis of diseases.
  • the kits facilitate the detection and/or measurement of cancer-specific phosphopeptides and/or phosphoproteins.
  • Such kits can contain, in a single or divided container, a molecule comprising an antigen-binding region.
  • such molecules are antibodies or antibody- like molecules.
  • Additional components that can be included in the kit include one or more of solid supports, detection reagents, secondary antibodies, instructions for use, vessels for running assays, gels, control samples, and the like.
  • an antibody or antibody-like molecules can optionally be directly or indirectly labeled.
  • the antibody or antibody-like molecules specific for phosphopeptides and/or phosphopeptide/MHC complexes can be conjugated to therapeutic agents.
  • therapeutic agents include, but are not limited to the following:
  • Alkylating agents are drugs that directly interact with genomic DNA to prevent cells from proliferating. This category of chemotherapeutic drugs represents agents that affect all phases of the cell cycle ⁇ i.e., they are not cell cycle phase-specific). Alkylating agents include, but are not limited to nitrogen mustards, ethylenimenes, methylmelamines, alkyl sulfonates, nitrosoureas, and triazines.
  • alkylating agents include but are not limited to busulfan, chlorambucil, cisplatin, cyclophosphamide (Cytoxan), dacarbazine, ifosfamide, mechlorethamine (mustargen), and melphalan.
  • Antimetabolites disrupt DNA and RNA synthesis. Unlike alkylating agents, they specifically influence the cell cycle during S phase. Antimetabolites can be differentiated into various categories, such as folic acid analogs, pyrimidine analogs, purine analogs, and related inhibitory compounds. Antimetabolites include but are not limited to 5-fluorouracil (5-FU), cytarabine (Ara- C), fludarabine, gemcitabine, and methotrexate.
  • Natural products generally refer to compounds originally isolated from a natural source and identified as having a desirable pharmacological activity. Such compounds, including analogs and derivatives thereof, can be isolated from a natural source, chemically synthesized, and/or recombinantly produced by any technique known to those of skill in the art. Natural products include such categories as mitotic inhibitors, antitumor antibiotics, enzymes, and biological response modifiers.
  • Mitotic inhibitors include plant alkaloids and other natural agents that can in some embodiments inhibit protein synthesis required for cell division and in some embodiments inhibit mitosis. They typically operate during a specific phase of the cell cycle. Mitotic inhibitors include, for example, docetaxel, etoposide (VP 16), teniposide, paclitaxel, taxol, vinblastine, vincristine, and vinorelbine, among others.
  • Mitotic inhibitors include, for example, docetaxel, etoposide (VP 16), teniposide, paclitaxel, taxol, vinblastine, vincristine, and vinorelbine, among others.
  • Taxoids are a class of related compounds isolated from the bark of the ash tree, Taxus brevifolia. Taxoids include but are not limited to compounds such as docetaxel and paclitaxel. Paclitaxel binds to tubulin (at a site distinct from that used by the vinca alkaloids) and promotes the assembly of microtubules.
  • Vinca alkaloids are a type of plant alkaloid identified to have pharmaceutical activity.
  • Exemplary vinca alkaloids include vinblastine (VLB) and vincristine.
  • Antibiotics Certain antibiotics have both antimicrobial and/or cytotoxic activity. These drugs also interfere with DNA by chemically inhibiting enzymes and mitosis or altering cellular membranes. These agents are typically not cell cycle phase-specific. Examples of cytotoxic antibiotics include but are not limited to bleomycin, dactinomycin, daunorubicin, doxorubicin (Adriamycin), plicamycin (mithramycin), and idarubicin.
  • Miscellaneous cytotoxic agents that do not fall into the previous categories include but are not limited to platinum coordination complexes, anthracenediones, substituted ureas, methyl hydrazine derivatives, amsacrine, L- asparaginase, and tretinoin.
  • Platinum coordination complexes include such compounds as carboplatin and cisp latin (cis-DDP).
  • An exemplary anthracenedione is mitoxantrone.
  • An exemplary substituted urea is hydroxyurea.
  • An exemplary methyl hydrazine derivative is procarbazine (N-methylhydrazine, MIH).
  • any known cytotoxic, cytostatic, and/or cytocidal agent can be attached to a targeting peptide of the presently disclosed subject matter and administered to a targeted organ, tissue, and/or cell type.
  • Chemotherapeutic (cytotoxic) agents including, but are not limited to, 5- fluorouracil, bleomycin, busulfan, camptothecin, carboplatin, chlorambucil, cisplatin (CDDP), cyclophosphamide, dactinomycin, daunorubicin, doxorubicin, estrogen receptor binding agents, etoposide (VP 16), farnesyl-protein transferase inhibitors, gemcitabine, ifosfamide, mechlorethamine, melphalan, mitomycin, navelbine, nitrosurea, plicomycin, procarbazine, raloxifene, tamoxifen, taxol, temazolomide (an aqueous form of DTIC), transplatinum, vinblastine, methotrexate, vincristine, and any analogs and/or derivatives or variants of the foregoing.
  • CDDP chlorambucil
  • chemotherapeutic agents fall into the categories of alkylating agents, antimetabolites, antitumor antibiotics, corticosteroid hormones, mitotic inhibitors, and nitrosoureas, hormone agents, miscellaneous agents, and any analog, derivative, or variant thereof.
  • PhosphoS33-P-catenin is broadly expressed in human metastatic melanoma tissues and cell lines and in breast cancer cell lines.
  • phosphoS33-P-catenin i.e., human ⁇ -catenin phosphorylated at Serine-33
  • pS33-Pcat 30 SEQ ID NO: 427 was found to be presented by melanoma and breast cancer cells and not cultured melanocytes.
  • the level of pS33-Pcat 30 epitope displayed on melanoma cells did not correlate with the steady state expression level of the phosphoprotein, but rather correlated with the total amount of phosphoprotein available for degradation. This, in turn, was influenced by the subcellular localization of ⁇ -catenin.
  • pS33-Pcat 30 (SEQ ID NO: 427) is only very weakly immunogenic. Surprisingly, however, replacement of the alanine with a valine at the C-terminus created an antigenically distinct phosphopeptide (SEQ ID NO: 2080) with an enhanced HLA*A0201 binding affinity and immunogenicity. Even more surprising, T cells generated from mice immunized with the modified phosphopeptide recognized endogenously processed pS33-Pcat 30 presented on melanoma and breast cancer cells and also controlled outgrowth of a melanoma xenograft.
  • pS33-Pcat 30 is disclosed herein to be a good immunotherapeutic target for melanoma and breast cancers and that effective pS33- Peat-specific T cells can be induced using the modified phosphopeptide pS33- Pcat(V) 30 (SEQ ID NO: 2080).
  • PhosphoS33-P-catenin was found to be homogenously expressed in the cytoplasm of the vast majority of metastatic melanoma samples. This is consistent with the fact that phosphorylation of ⁇ -catenin by GSK-3P occurs in the cytoplasm (Seidensticker & Behrens, 2000).
  • a previous study using an antibody directed against ⁇ -catenin phosphorylated at S33, S37, and/or T41 reported that phospho-P-catenin expression was exclusively nuclear in both primary and metastatic melanomas (Kielhorn et al., 2003). Elevated nuclear expression of ⁇ -catenin in a small number of samples was observed.
  • mitotic tumor cells with condensed chromosomes expressed elevated levels of phosphoS33-P-catenin.
  • ⁇ -catenin levels increase in the cytoplasm and nucleus up to the G2/M phase of the cell cycle, after which they rapidly decline, and degradation of ⁇ -catenin is apparently essential for cells to move beyond the G2/M phase (Olmeda et al., 2003).
  • pS33-Pcat 30 the levels of phosphoS33-P-catenin and total ⁇ -catenin detected in normal human spleen, liver, and kidney tissues were much lower than those of metastatic melanoma tissues.
  • Phospho33-P-catenin was also detected in cultured melanocytes in the steady state and the level of expression increased when proteasome degradation was inhibited, which raises the possibility that pS33-Pcat 30 could be presented by primary melanocytes.
  • pS33-Pcat 30 was not in the repertoire of phosphopeptides presented by cultured melanocytes. Melanocytes rarely proliferate in vivo (Jimbow et al, 1975) and when propagated in vitro, they divide at a much slower rate than melanoma cells. As such, the total amount of ⁇ -catenin that is phosphorylated and degraded in melanocytes is likely to be lower than in melanoma cells.
  • Phosphorylation of serine-37 in human ⁇ -catenin is a prerequisite for ⁇ 8 ⁇ -3 ⁇ - mediated phosphorylation of serine-33 (Fiol et al, 1988; Fiol et al, 1990) and phosphorylation of both sites is required for ubiquitination of ⁇ -catenin by ⁇ - transducin repeat-containing protein ( ⁇ -TrCP) to target it for proteasome degradation (Liu et al, 2002; Sadot et al, 2002).
  • ⁇ -TrCP ⁇ - transducin repeat-containing protein
  • the doubly phosphorylated peptide, pS33/S37 ⁇ cat 30 binds moderately well to HLA-A*0201, suggesting that that the lack of pS33/S37- ⁇ cat 3 o presentation on melanoma cells (Zarling et al, 2006) is likely due to the removal of the phosphate at S37 during antigen processing and presentation.
  • Peptides with a phosphate group at P4, such as pS33 ⁇ cat 30 , or P5 have been shown to be protected from phosphatases when they are bound to the MHC molecule (Petersen et al, 2009).
  • pS33-Pcat 3 o binds with moderate affinity to HLA-A*0201, it induced specific human T cells only after several weeks of in vitro culture and was very poorly immunogenic in vivo in HLA-A*0201 transgenic mice.
  • the lack of response to pS33- Pcat 3 o is because its HLA-A* 0201 -binding affinity is not high enough to allow sufficient antigen presentation in vivo. It has been shown that peptides with similar or even lower HLA-A*0201 binding affinities can induce immune responses in vivo (Sette et al, 1994; Bullock et al, 2000).
  • the enhanced immunogenicity of the modified pS33-Pcat(V) 3 o epitope might be due to the fact that it is antigenically distinct from pS33-Pcat 3 o and that it binds HLA-A*0201 with higher affinity. Regardless of the exact mechanisms, the more immunogenic modified phosphopeptide induced T cells that strongly cross-reacted with the natural phosphopeptide in an equivalent manner.
  • pS33-Pcat(V) 30 can be used advantageously in place of the natural phosphopeptide in vaccines or to generate antigen-specific T cells for adoptive immunotherapy.
  • Tumor antigens that are broadly expressed are appealing as immunotherapeutic targets, as the majority of antigens identified to date are expressed largely or exclusively in melanomas (Lucas & Coulie, 2008). Although a colorectal cancer cell line with a truncating mutation in APC that diminishes degradation of ⁇ - catenin was not recognized, breast cancer cells, which rarely have mutations in ⁇ - catenin or components of the destruction complex, were also effectively recognized by the pS33-Pcat-specific T cells.
  • pS33-Pcat 30 -targeted therapy might be of reduced applicability to cancers that have mutations in APC or frequent mutations in ⁇ -catenin and/or components of the destruction complex such as gastrointestinal (Morin et al, 1997) and endometriod ovarian (Oliva et al, 2006) cancers
  • pS33-Pcat 30 might be an effective target for renal (Kim et al., 2000), lung (Ohgaki et al., 2004), thyroid (Miyake et al., 2001), pituitary adenomas (Sun et al., 2005), and some types of pancreatic cancer (Gerdes et al., 1999), as these tumors rarely show mutations in ⁇ - catenin or proteins of the destruction complex.
  • pS33-Pcat 30 is a good target for cancer immunotherapy and is a broad tumor antigen.
  • phosphorylated antigens including many displayed on the surface of primary hematological malignant tissues. Many were HLA-B7-restricted and tumor-specific, and an additional several HLA-A2 -restricted tumor-specific antigens not found on healthy tissue were studied. Many of these antigens are derived from important oncoproteins linked to leukemogenesis, such as RUNX1, MLL, Myc, and Bcl-l lA. The present disclosure demonstrates that some HLA alleles present a dramatically larger number of phosphorylated antigens than others that are differentially displayed between normal and malignant tissue. The present disclosure establishes for the first time the surface expression of phosphorylated antigens on the surface of primary tumor tissue which are also analyzed on defined counterpart healthy tissue.
  • T cells when expanded in vitro, are able to recognize and kill malignant tissue: both established cells lines and primary tumor samples.
  • Cold-target inhibition studies reveal that these phosphopeptide-specific T cell lines kill primary tumor tissue in a phosphopeptide-specific manner.
  • these phosphopeptide-specific T cells bound HLA-phosphopeptide tetramers. This indicated that phosphopeptide-specific T cells express high affinity TCRs that have escaped thymic deletion, which embodies the greatest barrier for current immunotherapeutic strategies.
  • patients with leukemia can be divided into two groups: those with no detectable or barely detectable anti-phosphopeptide responses and those with intact immune responses very similar to healthy individuals (see also Figure IOC).
  • SCT stem cell transplantation
  • peptides identified and tested thus far in peptide-based vaccine approaches have generally fallen into one of three categories: 1) mutated on individual tumors, and thus not displayed on a broad cross-section of tumors from different patients; 2) derived from unmutated tissue-specific proteins, and thus compromised by mechanisms of self-tolerance; and 3) expressed in subsets of cancer cells and normal testes.
  • Antigens linked to transformation or oncogenic processes are of primary interest for immunotherapeutic development based on the hypothesis that tumor escape through mutation of these proteins could be more difficult without compromising tumor growth or metastatic potential
  • the target peptides of the presently disclosed subject matter are in some embodiments unique in that the identified target peptides are modified by intracellular modification. This modification is of particular relevance because it is associated with a variety of cellular control processes, some of which are dysregulated in cancer cells.
  • the source proteins for class I MHC-associated phosphopeptides are often known phosphoproteins, supporting the idea that the phosphopeptides are processed from folded proteins participating in signaling pathways.
  • the target peptides of the presently disclosed subject matter are unexpectedly superior than known tumor-associated antigen-derived peptides for use in immunotherapy because: 1) they only displayed on the surface of cells in which intracellular phosphorylation is dysregulated (i.e., cancer cells) and not normal thymus cells, and thus they are not compromised by self-tolerance (as opposed to TAAs generally, which are associated with overexpression or otherwise expressed on non-mutated cells); and/or 2) they identify a cell displaying them on their surface as having dysregulated phosphorylation.
  • post-translationally modified phosphopeptides that are differentially displayed on cancer cells and derived from source proteins objectively linked to cellular transformation and metastasis allow for more extensive anti-tumor responses to be elicited following vaccination.
  • Target peptides are, therefore, better immunogens in peptide-based vaccines, as target peptides are derived from proteins involved with cellular growth control, survival, and/or metastasis, and alterations in these proteins as a mechanism of immune escape might interfere with the malignant phenotype of tumors.
  • the presently disclosed subject matter also includes in some embodiments methods of identifying target peptides for use in immunotherapy which are displayed on transformed cells but are not substantially expressed on normal tissue in general or in the thymus in particular.
  • target peptides bind the MHC class I molecule more tightly than their non-phosphorylated native counterparts.
  • target peptides might have additional binding strength by having amino acid substitutions at certain anchor positions.
  • modified target peptides will remain cross-reactive with TCRs specific for native target peptide MHC complexes.
  • the target peptides associated with proteins involved in intracellular signaling cascades or cycle regulation are of particular interest for use in immunotherapy.
  • the TCR might specifically react with the phosphate groups on the target peptide being displayed on an MHC class I molecule.
  • a method for screening target peptides for use in immunotherapy involves determining whether the candidate target peptides are capable of inducing a memory T cell response.
  • the contemplated screening methods can include providing target peptides (including but not limited to those disclosed herein or those to be identified in the future) to a healthy volunteer and determining the extent to which a target peptide- specific T cell response is observed. In some embodiments, the extent to which the T cell response is a memory T cell response is also determined.
  • the extent to which a TCM response is elicited is determined.
  • those target peptides that are capable of inducing a memory T cell response in healthy and/or diseased patients are selected for inclusion in the therapeutic compositions of the presently disclosed subject matter.
  • the presently disclosed subject matter also provides methods for inducing a target peptide-specific memory T cell (e.g. , TCM) response in a patient by providing the patient with a composition comprising the target peptides disclosed herein.
  • a target peptide-specific memory T cell e.g. , TCM
  • the compositions are provided in a dosing regimen as disclosed herein.
  • the presently disclosed subject matter also relates to methods for determining a cancer disease prognosis. These methods can involve providing a patient with target peptide compositions and determining the extent to which the patient is able to mount a target peptide-specific T cell response.
  • the target peptide composition comprises target peptides selected in substantially the same manner that one would select target peptides for inclusion in a therapeutic composition. If a patient is able to mount a significant target peptide specific T cell response, then the patient is likely to have a better prognosis than a patient with the similar disease and therapeutic regimen who is not able to mount a target peptide specific T cell response.
  • the methods involve determining whether the target peptide specific T cell response is a T C M response.
  • the presence of a target peptide-specific T cell response as a result of the contemplated diagnostic method correlates with an at least or about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 125, 150, 175, 200, 250, 300, 400, 500 or more percent increase in progression free survival over standard of care.
  • the present EXAMPLE encompasses inter alia a set of phosphorylated peptides presented by HLA A*0101, A*0301, B*4402, B*2705, B* 1402, B*0702 and A* 0201 on the surface of melanoma cells that have the potential to (a) stimulate an immune response to the cancer, (b) to function as immunotherapeutics in adoptive T cell therapy or as a vaccine, (c) to facilitate antibody recognition of the tumor boundaries in surgical pathology samples, and (d) act as biomarkers for early detection of the disease.
  • class I MHC peptides presented on the surface of melanoma cells in association with the HLA molecules A*0101, A*0301, B*4402, B*2705, B* 1402, B*0702 and A*0201.
  • Tables 9-16 provide examples of target peptides within the scope of the presently disclosed subject matter. Sequence identifiers are listed in the first column. The UniProt database Accession numbers listed provide the sequences of the full human proteins from which the peptides are derived. The UniProt sequences are incorporated by reference. Also included are the Start and Stop amino acid positions as set forth in the listed UniProt database Accession numbers.
  • the class I phosphopeptide antigens reported here allow adoptive T cell therapy to be extended to melanoma patients that do not express the HLA- A* 0201 allele and also make it possible to treat a variety of other cancers by the same approach.
  • HLA A*0201 and HLA *A0301 both present peptides from the IRS-2 protein that contain the same phosphorylation site, Serl lOO.
  • RVApSPTSGV SEQ ID NO: 4108 binds to HLA A*0201 and both RVApSPTSSGVK (SEQ ID NO: 65) and RVApSPTSGVKR (SEQ ID NO: 66) bind to HLA A*0301.
  • RVApSPTSGV SEQ ID NO: 4108
  • RVApSPTSSGVK SEQ ID NO: 65
  • RVApSPTSGVKR SEQ ID NO: 66
  • mice expressing a chimeric class I MHC molecule comprised of the l and a2 domains of human HLA- A* 0201 and the a3 domain of murine H-2D d have been previously described (Newberg et al, 1992).
  • NOD/SCID IL- 2Ry-chain deficient mice were from The Jackson Laboratory, Bar Harbor, Maine, United States of America. The mice were housed and cared for in accordance with guidelines of the University of Virginia Animal Use and Care (University of Virginia, Charlottesville, Virginia, United States of America).
  • DM331, SLM2, VMM 12, and VMM 18 melanoma lines have been previously described (Zarling et al, 2006). 1363 Mel was from Dr. Susan Topalian (Johns Hopkins University, Baltimore, Maryland, United States of America). MCF7, MDAMB231, MDAMB468, and T47D breast cancer cell lines were from Dr. Sarah Parsons (University of Virginia, Charlottesville, Virginia, United States of America), and the SW620 colorectal cancer cell line (CCL-227) was purchased from the American Type Culture Collection (ATCC®; Manassas, Virginia, United States of America).
  • PhosphoS33-P-catenin and ⁇ -catenin specific antibodies were from Santa Cruz Biotechnology, Inc. (Dallas, Texas, United States of America) and Epitomics (an Abeam Company, Burlingame, California, United States of America).
  • HRP- conjugated anti-GAPDH was from Cell Signaling Technology, Inc. (Danvers, Massachusetts, United States of America).
  • aCD40 (FGK45; Fischbein et ah, 2000) was provided by Dr. Stephen Schoenberger (La Jolla Institute of Allergy and Immunology, La Jolla, California, United States of America).
  • Anti-CD8a (53.67), anti-IFNy (XMG1.2), and anti-TNFa (TN3-19) were from eBiosciences, Inc. (San Diego, California, United States of America).
  • HLA-A* 0201 -associated phosphopeptides were isolated from 1.05 x 10 9 cultured melanocytes pooled from four different donors using BB7.2 antibody and immobilized metal ion affinity chromatography and then analyzed by mass spectrometry as previously described (Zarling et ah, 2006).
  • Formalin-fixed paraffin-embedded cell line pellets and tissue microarrays of metastatic melanoma and normal tissue samples (Biorepository and Tissue Research Facility at the University of Virginia, Charlottesville, Virginia, United States of America) were deparaffmized, rehydrated, counterstained with hematoxylin, and imaged on an Aperio Scanner (Aperio, Vista, California, United States of America). Samples were incubated with anti-phosphoS33-P-catenin overnight at 4°C after antigen retrieval and antibody was detected using the IMMPACTTM AEC reagent (Vector Laboratories, Inc., Burlingame, California, United States of America).
  • Antibodies were removed with ethanol and acidified potassium permanganate and then reprobed with anti-P-catenin.
  • the staining index (SI) was calculated as total positive pixel count/mm 2 using ImageScope software. Results were compared to manual scores assigned by a pathologist to verify accuracy. SI ranged from less than 0.1-3.0 x 10 9 . Samples with SI less than 0.4 x 10 9 were scored as negative, 0.4-1.2 x 10 9 were scored as low, 1.2-2 x 10 9 were scored as moderate, and 2-3 x 10 9 were scored as high.
  • Membranous ⁇ -catenin was scored as follows: low: 0-25% of cells; moderate: 25-50% of cells; and high: greater than 50%>. Samples showing at least 10%> of cells with nuclear ⁇ -catenin were scored as positive.
  • T cells isolated using a Human Pan T cell isolation kit were co-cultured with autologous phosphopeptide -pulsed DCs matured with GM-CSF, IL-4 (both from R&D Systems, Inc., Minneapolis, Minnesota, United States of America), IL- ⁇ ⁇ , IL-6, TNFa (all from PeproTech, Rocky Hill, New Jersey, United States of America), and prostaglandin E 2 (Sigma-Aldrich Co. LLC, St. Louis, Missouri, United States of America) for 7 days.
  • GM-CSF GM-CSF
  • IL-4 both from R&D Systems, Inc., Minneapolis, Minnesota, United States of America
  • IL- ⁇ ⁇ IL-6
  • TNFa all from PeproTech, Rocky Hill, New Jersey, United States of America
  • prostaglandin E 2 Sigma-Aldrich Co. LLC, St. Louis, Missouri, United States of America
  • Monomers of phosphopeptide-MHC ⁇ 2 M complexes were generated as previously described (Altman et ah, 1996). Equimolar amount of streptavidin- conjugated PE fluorochrome was added slowly to biotinylated monomers to generate tetramers.
  • Affinity purified HLA-A*0201 was incubated with iodinated peptide FLPSPDYFPSV (SEQ ID NO: 2379), graded doses of test peptides, and ⁇ 2 ⁇ as previously described (Zarling et ah, 2000). Peptide-MHC complexes were captured in W6/32-coated ELISA plates after 48 hours and the dose at which test peptides inhibited binding of the indicator peptide by 50%> (IC 50 ) was calculated.
  • Murine bone marrow-derived dendritic cells (BMDCs) activated with CD40L- expressing 3T3 fibroblasts were prepared as previously described (Bullock et ah, 2000), pulsed with 10 ⁇ g/ml of peptide, and injected i.v. into AAD Tg mice. Seven days later, IFNy and TNFa production was evaluated by intracellular cytokine staining (ICS) in splenic CD8a T cells after incubation with peptide-pulsed C1R- AAD BLCL stimulators. For recall responses, mice previously immunized with peptide-pulsed BMDCs were boosted 28-30 days later i.v.
  • ICS cytokine staining
  • CD8 T cells isolated from mice 3 weeks after immunization with pS33- Pcat(V)3o-pulsed BMDCs were stimulated weekly with irradiated pS33-Pcat 30 or pS33-Pcat(V) 3 o-pulsed AAD + splenocytes as previously described (Zarling et ah, 2000).
  • mice 7-8 week old male NOD/SCID/IL-2Ryc ⁇ ⁇ mice were inoculated subcutaneously with 1.4-2 x 10 6 AAD + SLM2 cells. 6-7 x 10 6 effector pS33-Pcat- specific T cells were adoptively transferred 3 days later and an additional 0.3-1 x 10 6 effector T cells after an additional 4 days. All mice received 1500U of IL-2 (R&D Systems, Inc., Minneapolis, Minnesota, United States of America) i.p. every other day for 10 days. Tumor size was measured every 2-3 days with a digital caliper. Tumor size was calculated as L x W.
  • Lysates were prepared from -80% confluent cells in buffer containing 2% Triton X 100 and protease and phosphatase inhibitors. Samples were separated on 8% SDS-PAGE (Thermo Fischer Scientific Inc., Waltham, Massachusetts, United States of America) and transferred to PVDF membranes (Millipore Immobilon-FL, 0.45 ⁇ ; Millipore Corporation, Billerica, Massachusetts, United States of America). Blots were probed with phosphoS33-P-catenin, ⁇ -catenin, and GAPDH antibodies overnight at 4°C and developed by enhanced chemiluminescence (Millipore). Films were scanned and integrated density values determined using AlphaEase software and normalized to values obtained for GAPDH.
  • GSK-3 activity was inhibited using 5 ⁇ g BIO ((2'Z, 3'E)-6-Bromoindirubin-3'-oxime) and proteasomal degradation was blocked with 10 ⁇ g lactacystin (Calbiochem) before cells were lysed.
  • Unbound pS33/S37-Pcat 30 and pS33/S37-Pcat 30 bound to the MHC complex were treated separately with 0.2 U ⁇ g of alkaline phosphatase in 100 mM ammonium bicarbonate (pH 9) for 60 minutes at 37° C.
  • pS33-Pcat 30 To assess the immunogenicity of pS33-Pcat 30 , purified human T cells were cultured with peptide-pulsed stimulators in microwells, and their cytotoxic activity was evaluated after 3-7 weeks. pS33 -Peat-reactive T cells were detected in 4 out of 10 wells after 3 weeks of in vitro culture (see Figure 2A). After seven weeks of culture, these T cells also specifically recognized target cells pulsed with pS33-Pcat 30 but not those pulsed with Pcat 30 .
  • the weak in vivo immunogenicity of pS33-Pcat 30 might be because it binds with low affinity to HL A- A* 0201. Indeed, direct measurements indicated that it had a relatively low affinity ⁇ see Figure 2F).
  • the optimal C-terminal anchor residues for HLA-A*0201 binding peptides are leucine or valine (Ruppert et al, 1993), while pS33-Pcat 3 o has an alanine at this position.
  • the HLA-A*0201 binding affinity of pS33-Pcat 30 containing a valine in place of the alanine (pS33-Pcat(V) 30 ) is 8-fold higher than that of pS33-Pcat 3 o ⁇ see Figure 2F).
  • MHC-restricted peptides can elicit T cells incapable of recognizing the original epitope (Bertoletti et al, 1994; Klenerman et al, 1994).
  • the fraction of human CD8 + T cells staining with a pS33-Pcat 30 tetramer was 25-100% of that staining with a pS33-Pcat(V) 3 o tetramer (1-3%; see Figure 3A).
  • pS33-Pcat(V)-specific murine T cells recognized stimulators pulsed with the natural phosphopeptide at the maximal dose of 1 ⁇ g/ml, demonstrating a high level of crossreactivity against the natural phosphopeptide. More importantly, equivalent T cell recognition was observed at doses of pS33-Pcat 30 that were only 2-5-fold lower than those for pS33-Pcat(V) 3 o (see Figure 3B). Thus, most of the human and murine T cells induced with pS33-Pcat(V) 3 o are highly cross- reactive with the natural phosphopeptide.
  • Pcat 30 were modest (see Figure 3B), they suggested that the two peptides were nonetheless antigenically distinct. Indeed, it was found that different long-term murine T cell lines varied significantly in the dose-response curves for the natural and modified phosphopeptides.
  • One line (Line 1) showed a 73-fold difference in the dose- response curve for pS33-Pcat 30 and pS33-Pcat(V) 3 o (see Figure 3C, solid lines).
  • Residue serine-33 (S33) of human ⁇ -catenin is phosphorylated by GSK-3P in an obligatory sequence after phosphorylation of serine-41 (S41) and serine-37 (S37), and phosphorylation of both S33 and S37 is required for ubiquitination and degradation of the protein (Kimelman & Xu, 2006). Since pS33-Pcat 30 is phosphorylated at S33 but not S37, the hypothesis that its production was mediated by another kinase was tested.
  • Membrane-associated cadherins compete with APC for binding to ⁇ -catenin (Hulsken et al., 1994) and might therefore also limit degradation of ⁇ -catenin. Consistent with this hypothesis, T cell recognition (see Figure 6F) and the level of phosphoS33 ⁇ -catenin after proteasome blockade (see Figure 6A) was lower in cells with moderate to high levels of membranous ⁇ -catenin (DM331 and VMM12; see Figure 6E) or with a significant amount of nuclear ⁇ -catenin (1363Mel) than in cells with low levels of both (SLM2 and VMM 18).
  • Ub-carboxyl terminal hydrolase 10 (USP10) KLLpSPSNEKL
  • Interleukin enhancer binding factor 3 (ILF3) KLFPDpTPLAL Interleukin enhancer binding factor 3 (ILF3) KLFPDpTPLAL
  • ⁇ -catenin has been shown to be functionally important in the development and progression of several cancers, whether pS33-Pcat 30 was presented by tumors other than melanoma was determined.
  • the colorectal carcinoma cell line SW620 expressed high levels of both phosphoS33-P-catenin and total ⁇ -catenin, but no change in these levels was observed after proteasome blockade (see Figure 7A). Additionally, the level of phosphoS33-P-catenin was substantially higher in VMM18 than SW620 after proteasome blockade, indicating that phosphorylation of ⁇ -catenin was diminished in SW620.
  • pS33-Pcat-specific T cells recognized SW620 cells that had been pulsed with exogenous pS33-Pcat 30 .
  • unpulsed SW620 cells were not recognized by the T cells (see Figure 7B), indicating that this colorectal carcinoma cell line presented negligible amounts of pS33-Pcat 30 .
  • the levels of phosphoS33-P- catenin and total ⁇ -catenin increased substantially in four breast cancer cell lines after proteasome inhibition (see Figure 7C), and these cells were all recognized by pS33- Pcat 30 -specific T cells (see Figure 7D).
  • pS33-Pcat 30 would be a good immunotherapeutic target for cancers such as breast and melanoma that rarely exhibit mutations in ⁇ -catenin and the destruction complex.
  • Tissue Microarrays Tissue Microarrays
  • Antibodies that recognize the phosphosites for pSl 100-IRS2i 0 97 i io5, pT130- BCAPv3i27-i 3 6, pS42-CDC25b 3 g-46, anti-pS73-JunC/D 7 o-79, and pS33-Pcatenin 30 _ 3 9 were developed. They have been used to evaluate expression of the phosphosites and their source proteins in human cancer cell lines and pathological specimens using Western blotting, immunofluorescence, and immunohistochemistry.
  • the IRS-2 source protein phosphorylated at serine- 1100 is present in multiple cancer cell lines, including breast, ovarian, colorectal, bladder, non-small cell lung cancer, and melanoma, but not normal tissues.
  • siRNA knockdown of IRS- 2 abrogated pSl 100-IRS2io97 i io5-specific T cell recognition and led to cancer cell apoptosis, demonstrating that this protein is critical for cancer cell survival and the source of the class I MHC-restricted phosphopeptide.
  • the phosphorylated forms of BCAR3, ⁇ catenin, and CDC25b are broadly expressed among cancer cell lines representing multiple histological types. Expression of these phosphoproteins in melanoma and breast cancer were assayed using tissue microarrays (TMAs). About 80% of the melanomas in TMAs (178 samples of Stage 3 and 4 metastatic melanoma, and about 9 primary melanoma) stained positively for pS33-P-catenin. The majority of the tissues showed cytoplasmic staining, while a small fraction showed additional membranous or nuclear pS33-P- catenin.
  • TMAs tissue microarrays
  • mTCR expression of mTCR on the surface of up to 90% of cells using an antibody specific for the mouse TCR chain was detected.
  • the expression of the mTCR is maintained out to 5 days post-electroporation.
  • Expression of these mTCR maintained phosphopeptide-specific functional recognition based on induction of the release of the effector cytokine IFNy and initiation of the perforin/granzyme pathway based on cell surface mobilization of CD 107a.
  • expression of these TCR in human cells enhanced their avidity for peptide pulsed target cells and cancer cells that expressed the phosphopeptides after endogenous processing.
  • transfected T cells Utilizing these mTCR transfected T cells, it was established that the expression of phosphorylated source proteins in cancer cells was directly related to the level of phosphoepitope display at the cell surface. It is expected that such transfected T cells are capable of controlling human melanoma tumors growing as mouse xenografts, for example.
  • a vaccine having 1.5 ml of emulsion is prepared and 1 ml of this emulsion is administered subcutaneous ly and intradermally.
  • 1 ml contains 100 ⁇ g each of the 3 phosphopeptides and 200 ⁇ g of tetanus peptide emulsified in Montanide ISA-51 adjuvant.
  • PBL are evaluated by ELISpot assay for the number of peptide-reactive T cells per 10 5 cells. PBL are evaluated before vaccination and at several time points during and after the vaccination regimen.
  • the ELISpot assay measures the number of cells releasing IFNy specifically in response to the vaccination peptides, as recorded by the number of chromogen-defmed spots counted directly in the assay wells after exposure of participant lymphocytes to antigen in the presence of solid-phase antibody to IFNy. The number of spots is compared to two negative controls, one of which is generated by stimulation with an irrelevant peptide.
  • Responder T cells stimulated with PMA, ionomycin, PHA, and/or anti-CD3 are used as a positive control.
  • Assays are performed primarily on lymphocytes sensitized once in vitro. PBL are sensitized with the peptide mixture on day 0, and are assayed using individual peptides at day 14. Patients with reactivity after in vitro sensitization are optionally retested using cryopreserved lymphocytes that have not been sensitized or cultured ex vivo. For measures of T cell response without in vitro sensitization, the ELISpot assay is performed the same way, except that CD8 + cells are isolated first by negative selection on an antibody bead column.
  • immune response is summarized as a measure of fold-change.
  • ELISpot assays performed on PBL sensitized to peptide mixture once in vitro the response to peptide is considered positive if the following criteria are met:
  • T exp p 0S t the actual number of spots counted for an experimental peptide
  • the threshold for the number of spots over background (30) represents 30 spots per 100,000 lymphocytes, of which approximately 20% are CD8 + cells. Thus, 30 spots per 100,000 lymphocytes represent approximately 30 spots per 20,000 CD8 + cells (0.15%).
  • CD8 + cell separation ⁇ i.e., negative selection is performed first.
  • the response to peptide is considered positive if the following criteria are met:
  • T exp p 0S t the actual number of spots counted for an experimental peptide
  • the threshold for the number of spots over background (10) represents 10 spots per 100,000 CD8 + lymphocytes. Thus, 10 spots per 100,000 CD8 + lymphocytes represents approximately 0.01%. Background responses might be lower in these assays than in assays done after one stimulation.
  • PBL are evaluated for tetramer binding for assessment of immune response of lymphocyte subpopulations to a phosphopeptide.
  • PBL are evaluated before vaccination and at several time points during and after the vaccination regimen. In some embodiments, approximately 200,000 events are acquired by a FACSCALIBURTM flow cytometer (BD Biosciences) and analyzed by Flowjo software (Tree Star. Inc., Ashland, Oregon, United States of America). An irrelevant tetramer is used as a negative control. Cultured peptide-specific CTL (as determined by Elispot assays) is used as a positive control.
  • PBL are evaluated by a proliferation assay to determine whether T cell phosphopeptide-specific populations are present. PBL are evaluated before vaccination and at several time points during and after the vaccination regimen. Proliferation is measured by the incorporation of [ 3 H] thymidine. The specificity of responding T cells is confirmed using various negative controls, such as but not limited to "no peptide" and/or an irrelevant peptide. Responder T cells stimulated with PMA, ionomycin, PHA, and/or anti-CD3 are optionally used as positive controls.
  • cytokine profiles of their CD4 T cells are analyzed and characterized as Thl- or Th2-type cells.
  • CD8 + T cells are optionally depleted from PBL and SIN samples using separation columns (Vancouver, British Columbia, Canada). Cytokine production is measured using the BIO-PLEXTM Multiplex Cytokine Assay (Bio-Rad Laboratories, Inc., Hercules, California, United States of America). Cytokines measured include IL-2, IL-4, IL-5, IL-10, TNF-a, and IFNy.
  • responding T cells The specificity of responding T cells is confirmed using various negative controls, which optionally include "no peptide” and an irrelevant peptide.
  • Responder T cells stimulated with PMA, ionomycin, PHA, and/or anti-CD3 are optionally used as positive controls.
  • the 51 Cr release assay determines the relative killing activity of radioactively labeled target cells as the amount of CPM detected in the supernatant of assay wells after exposure of participant lymphocytes to radioactively labeled targets. Upon killing of the radioactively labeled target cells by the participant lymphocytes, radioactivity is released into the supernatant. Following the incubation period, the residual cells are pelleted and the amount of radioactivity released is determined using a gamma counter. The amount of non-specific release of radioactivity by the target cells is determined as a negative control (CPM MIN ).
  • CPM MIN negative control
  • Targets lysed with 1 N HCL are used as a positive control (CPM M A X )- Assays are performed primarily on lymphocytes sensitized once in vitro. PBL are sensitized with the peptide mixture on day 0, and are assayed using appropriate antigen- expressing HLA-A2 + targets on days 5-7. A net difference of at least or about 10- 25%, optionally at least or about 15% Specific Lysis between the positive and negative targets is a threshold for considering an individual culture to be positive for specific cytotoxic activity.
  • Novel leukemia-associated phosphorylated tumor antigens from primary leukemia samples are identified and immunity against these in both healthy individuals and patients with leukemia is assessed. These data demonstrate how the human CD8 T cell immune response is able to engage with tumor-associated "neo- antigens" and reveal immunotherapeutic strategies for treating cancer.
  • CLL chronic lymphocytic leukemia
  • MCL mantle cell lymphoma sample
  • ALL acute lymphoblastic leukemia
  • AML acute myeloid leukemia
  • ARID IB 343 4 2 1 3 2 3 4
  • HIVEP2 348 1 HIVEP2 348 1
  • ZFP106 370 1 Gene SEQ ID ALL1 CLL2 CLL4 HCL1 JY AML1 BM B T Name No. Cell Cell
  • Tables 6 and 7 provides listings of HLA-A*0201 and HLA-B*0702 phosphopeptides associated with leukemia samples.
  • CLL Chronic Lymphocytic Leukemia
  • MCL Mantle Cell Lymphoma
  • AML Acute Myeloid Leukemia
  • ALL Acute Lymphoblastic Leukemia
  • HCL Hairy Cell Leukemia
  • B-LCL EBV Transformed B Lymphoblastoid Cell Line (JY).
  • JY EBV Transformed B Lymphoblastoid Cell Line
  • no number indicates Not Detected; 1 indicates ⁇ 1 copy/cell, 2 indicates 1-5 copies/cell, 3 indicates 6-25 copies per cell, and 4 indicates >25 copies per cell.
  • Lowercase s, t, and y in the sequences correspond to serine-, threonine-, or tyrosine-associated phosphorylated residues, respectively.
  • HLA-B7-restricted phosphopeptide antigens Due to the greater number of HLA-B7-restricted phosphopeptide antigens identified, the distribution of phosphopeptides between tumor types and healthy tissue was analyzed (see Figure 10A). For all tissue types a greater number of phosphopeptides were identified for HLA-B7 than HLA-A2 (see Figure 10B), with more phosphopeptides identified on the aggressive tumors (AML and ALL) than other indolent tumors (CLL) or normal counterpart tissue (see Figure IOC).
  • the 57 AML-associated phosphopeptides were derived from a number of interesting oncogenes, many of which have been directly implicated in leukemogenesis, such as BCL-11A, MYC, RUNX1, EP300, SKI, GFI1 and MLL (see Tables 6 and 7 herein above). Forty-six phosphopeptides were identified on the ALL tumor sample whereas a total of 28 phosphopeptide antigens were identified on the surface of two CLL tumor samples (see Figure 10A). Of 57 HLA-B7 AML-associated peptides, only two were on healthy human bone marrow samples, 36 of these were only observed on the AML sample and no other tumor samples (see Figure 10B).
  • HLA-A2- and HLA-B7-bound Phosphopeptides Of the 86 HLA-B7-restricted phosphopeptides, five (6%) were 8-mers, 41 (48%) 9-mers, 24 (28%) 10-mers, 11 (13%) 11 -mers, and five (6%) either 12- or 13- mers were similar in length to the identified HLA-A2 phosphopeptides (see Figure 10D). All phosphopeptides were monophosphorylated, except two dual phosphorylated peptides, with 79/88 (90%>) bearing phosphoserine and 9 phosphothreonine residues. No phosphotyrosine residues were observed. The phosphate group was notably constrained to position four in 62/86 (72%) of HLA-B7 phosphopeptides a similar proportion to the HLA-A2 phosphopeptides (see Figure 10E).
  • HLA-A2 and two HLA-B7 phosphopeptides were derived from LSP-1, a protein previously identified as a potential tumor marker.
  • RQA(pS)IELPSMAV SEQ ID NO: 452
  • Monocyte-derived dendritic cells were generated from healthy donors and used to prime autologous T cells and HLA-phosphopeptide tetramers were used to enrich phosphopeptide-specific T cells, between each stimulation steps, to produce a monospecific T cell line ⁇ see Figure 11 A).
  • RQA(pS)IELPSMAV SEQ ID NO: 452-specific T cells produced IFNy in response to RQA(pS)IELPSMAV (SEQ ID NO: 452) phosphopeptide but not to the unphosphorylated RQASIELPSMAV (SEQ ID NO: 452) nor to closely related phosphopeptides such as RQA(pS)IELPSM (SEQ ID NO: 248) and was also identified on all HLA-A2 + primary tumor cells ⁇ see Figure 11B). Recognition was, therefore, phosphate-dependent and phosphopeptide-specific.
  • phosphopeptides encoded by some leukemia oncogenes most notably MYC, BCL-11A, and EP300; perhaps as both MYC and BCL-11A phosphopeptides were also observed on normal T cells.
  • phosphopeptides from other leading leukemia oncogenes such as MLL, GFI, and MEF2D elicited some of the strongest immune responses.
  • phosphopeptides derived from a single phosphoprotein could elicit differential responses.
  • LSP-1 derived peptides RQA(pS)IELPSMAV (SEQ ID NO: 452) and QPR(pT)PSPLVL (SEQ ID NO: 304) were associated with some of the strongest responses whereas RQA(pS)IELPSM (SEQ ID NO: 451) and KLIDRTE(pS)L (SEQ ID NO: 440) were not immunogenic despite the tumor-specific expression of KLIDRTE(pS)L (SEQ ID NO: 440). These data suggested that both antigen-expression and phosphorylation site can determine immunogenicity.
  • T cell specificity was confirmed using HLA-phosphopeptide multimers (see Figure 12B) that suggested that these T cells expressed moderate or high affinity T cell receptors. Furthermore, no responses were observed for the unphosphorylated counterpart peptides (see Figure 12C), confirming these responses were phosphoantigen-specific.
  • CD8 + T cells were flow-sorted from peripheral blood into na ' ive (T N ), central memory (TC M ), effector memory (T EM ), and terminal effector memory cells (T EMR A) according to the expression of CD45RA and CD27.
  • T N na ' ive
  • TC M central memory
  • T EM effector memory
  • T EMR A terminal effector memory cells
  • the level of leukemia-specific phosphoantigen-directed CD8 + T cell immunity in patients with leukemia was determined. Immunocompetent patients with early- stage CLL or patients in complete remission with AML were selected.
  • CLL is a heterogeneous disease where, in many cases, the disease behaves in an indolent manner, whilst for others the disease is aggressive, whether the level of phospho-directed immunity predicted patient outcome was evaluated.
  • Progression-free survival (PFS), overall survival (OS), and time to first treatment (TTFT) were analyzed between Group 1 and Group 2 (see Figures 13E-13G).
  • PFS progression-free survival
  • OS overall survival
  • TTFT time to first treatment
  • a cohort of 12 patients in complete remission (CR) with AML were assessed using 7-day recall responses, as measured by ELISpot, and compared against a cohort of 12 healthy donors (see Figures 14A and 16).
  • SCT Stem Cell Transplantation
  • All cell lines were grown at 37°C with 5% C0 2 in growth medium consisting of RPMI 1640 supplemented with 10% FCS and two mM L-glutamine.
  • Blood or leukapheresis samples were taken from patients with high-burden leukemia in heparin. Tumor cells were recovered by layering the blood over density gradient (Ficoll) and collecting the tumor layer following centrifugation. The tumor was washed in tris-buffered saline (TBS). The purity of the tumor was assessed using flow cytometry and was >98% pure in all cases. For healthy T and B-cell populations, a normal spleen sample processed and tonsil sample was collected and lymphocytes released through mechanical disruption.
  • Mononuclear cells were isolated using a density gradient and 10 9 T cells isolated using anti-CD 19 or anti-CD3 microbeads (Miltenyi Biotec Inc., Auburn, California, United States of America) with purity >98% were obtained. Bone marrow sample was obtained from an elective orthopedic procedure and red cell-depleted using hypotonic lysis. This sample was not processed further.
  • Class I MHC molecules were immunoaffinity purified from the JY cell line or from primary tumor samples, and their associated peptides were extracted as previously described in Zarling et al, 2006. Approximately 1.2-14 x 10 9 cells were lysed in a solution containing 20 mM Tris-HCl (pH 8.0), 150 mM NaCl, 1% CHAPS, one mM PMSF, five ⁇ g/mL aprotinin, 10 ⁇ g/mL leupeptin, 10 ⁇ g/mL pepstatin A, 1 ⁇ g/ml calyculin A, and phosphatase inhibitor (cocktails I and II; Sigma-Aldrich).
  • the mixture was subjected to centrifugation and the resulting supernatant was passed over protein A sepharose pre-loaded with the HLA-A2-specific antibody BB7.2 or HLA- B7-specific antibody ME1. Peptides were eluted from the purified class I MHC molecules with 10% acetic acid.
  • the cytotoxic specificity was determined with a standard 4 hour Cr release assay as previously described in Cobbold et ah, 2005.
  • PBMCs and CD8 T cells were isolated fresh from healthy donors and patients.
  • lxlO 6 PBMCs were isolated from both AML patients and healthy donors and resuspended in AIM-V media (10% human AB serum) in a 96 well plate.
  • Peptide or phosphopeptides were added individually at 10 ⁇ g/ml and placed at 37°C in C0 2 incubator for 7 days. Cells were then harvested, washed 4 times, and re-challenged with phosphopeptides, peptides, or anti-CD3 (OKT3, 100 ng/ml, Mabtech, Inc., Mariemont, Ohio, United States of America) as per the manufacturer's instructions.
  • CD8 + T cells were magnetically enriched using anti-CD8 microbeads (Miltenyi Biotec) to a purity of >99% for both healthy donors and patients with CLL. 200,000 CD8 + T cells from both patients and healthy donors were used for ELISpot analysis as described above.
  • HLA-A2 restricted RQA-V (SEQ ID NO: 2375) phosphopeptide-specific cytotoxic CD8 + T cells were generated from healthy donors as described previously in Ho et al, 2006. Briefly, PBMCs were cultured in flat-bottom 6-well plates at 10 7 cells per well in RPMI 1640 plus 10% heat-inactivated human AB serum (10% media).
  • GM-CSF 800 IU/mL
  • IL-4 1000 units/mL; PeproTech
  • DC dendritic cells
  • a maturation cocktail was added containing 100 ng/ml TNFa, 100 ng/ml IL- ⁇ , 10,000 IU/ml IL-6, 8,000 IU/ml GM-CSF, and 10 ⁇ g/ml PGE 2 .
  • DCs were harvested and loaded with phosphopeptide (20 ⁇ g/ml) and T cells added at a ratio of five T cells per DC.
  • Recombinant IL-7 (10 ng/ml) and IL-15 (10 ng/ml) were added on day 5.
  • T cells were harvested and re-stimulated by adding 10 7 irradiated PBMCs and 10 6 irradiated autologous LCLs pulsed with peptide with IL-7 (5 ng/ml), IL-15 (5 ng/ml), and IL-2 (20 IU/ml), and re-stimulated every 7 days in the same manner thereafter.
  • T cells were enriched using either anti-CD8 microbeads (Miltenyi Biotec) or by labeling with HLA-phosphopeptide tetramers and using anti-PE microbeads (Miltenyi Biotec).
  • HLA-B7-restricted anti-phosphopeptide T cells were grown in the absence of dendritic cells by plating 5xl0 6 PBMCs in 48 well plates in 10% media with individual phosphopeptides at 10 ⁇ g/ml for 7-10 days without cytokines. Re- stimulations with irradiated peptide-pulsed autologous PBMCs and cytokines took place thereafter once or twice and cytotoxicity assays performed as previously described.
  • the peptides disclosed in the EXAMPLES were synthesized with Fmoc chemistry, isolated by HPLC to >90% purity, and validated with mass spectrometry (EZ-Biolabs, Carmel, Indiana, United States of America and Genscript, Piscataway, New Jersey, United States of America).
  • HLA tetramers were synthesized by the use of standard methods, and the components of the HLA-peptide tetramers that were used in the study are shown in Table 3.
  • ELISpotPRO wells pre-coated with IFNy monoclonal antibody mAb 1-DlK (MabTech, product code: 3420-2APW-2) were washed four times with sterile PBS and blocked for 30 minutes with 200 ⁇ 10% RPMI 1640 after which the blocking medium was removed.
  • lxl 0 6 PBMCs were added to each well and peptide was added directly at a concentration of 10 ⁇ / ⁇ 1. Plates were cultured at 37°C for 24 hours after which wells were emptied and washed five times with 200 ⁇ sterile PBS.
  • the alkaline phosphatase (ALP)-labeled one step detection reagent 7-B6-1-ALP was diluted 1 :200 in PBS with 0.05% FBS. 100 ⁇ was added and incubated at room temperature for two hours. Wells were then emptied and washed five times with 200 ⁇ sterile PBS. 100 ⁇ filtered BCIP/NBT substrate was added to each well and incubated for 15 minutes at room temperature. To stop the reaction, plates were washed under running water and then dried by exposure to air. Spots were counted using an ELI Spot reader.
  • ALP alkaline phosphatase
  • Table 8 summarizes the results of a Day 7 ELISpot experiment that demonstrated that healthy humans had an immunological recall response to certain the leukemia class I phosphopeptides. Importantly, this response came from central memory T cells and was comparable to the recall response that the same individuals had to viral peptides presented as a result of flu, EBV, etc.
  • the left column lists various synthetic samples of melanoma class I A*00201 phosphopeptides including those from IRS2, b-catenin, CDC25B, BCAR3, Tensin 3, and Synemin. They were tested on six healthy A2 positive donors and memory T cell response for several of the peptides were observed.
  • APR is APRRYsSSL (SEQ ID NO: 267); “IMD” is IMDRtPEKL (SEQ ID NO: 398); “RTF” is RTFsPTYGL (SEQ ID NO: 416); “YLD” is YLDsGIHSGV (SEQ ID NO: 2080); “VMI” is VMIGsPK V (SEQ ID NO: 2232); “GLL” is GLLGsPVRA (SEQ ID NO: 396); “RVA” is RVAsPTSGV (SEQ ID NO: 418); “RVAk” is RVAsPTSGVK (SEQ ID NO: 65); “NLV” and “TPR” are cytomegalovirus (CMV) peptides, “GLC” and “RPP” are Epstein-Barr Virus (EBV) peptides; and “FLU” and “ADENO” are influenza and adenoviral peptides, respectively. Phosphopeptide sequences; pSer, p
  • APR (APRRYsSSL; SEQ ID NO: 267) is a B*0702 binding peptide that does not bind to A*0201 and was used as the control for the other peptides.
  • Two healthy donors (HD) responded to APR because they are both A*0201 and B*0702 positive.
  • RVA RVAsPTSGV; SEQ ID NO: 418) comes from IRS2 and binds to A*0301 so it did not bind to A*0201 and was employed as a control. None of the HD recognized or responded to it.
  • references listed in the instant disclosure including but not limited to all patents, patent applications and publications thereof, scientific journal articles, and database entries (including but not limited to GENBANK® database entries and including all annotations available therein) are incorporated herein by reference in their entireties to the extent that they supplement, explain, provide a background for, and/or teach methodology, techniques, and/or compositions employed herein.
  • the discussion of the references is intended merely to summarize the assertions made by their authors. No admission is made that any reference (or a portion of any reference) is relevant prior art. Applicants reserve the right to challenge the accuracy and pertinence of any cited reference.
  • beta-catenin is a suppressor of invasion.
  • Homfray et al. (1998) Defects in mismatch repair occur after APC mutations in the pathogenesis of sporadic colorectal tumours. Human Mutation 11 : 114-120. Hoogenboom et al. (1991) Nucleic Acids Res 19:4133. Horowitz et al. (1990) Graft- versus-leukemia reactions after bone marrow transplantation. Blood 75:555-562.
  • HIV-1 Gag variants Nature 369:403-407.

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Abstract

L'invention concerne un ensemble de peptides cibles, qui sont présentés par les HLA A*0101, A*0201, A*0301, B*4402, B*2705, B* 1402 et B*0702 sur la surface de cellules malades. Il est envisagé, entre autres, de (a) stimuler une réponse immunitaire vis-à-vis de la maladie proliférative, par exemple le cancer, (b) agir comme produits immunothérapeutiques dans une thérapie adoptive de lymphocytes T ou comme vaccin, (c) faciliter une reconnaissance d'anticorps de limites de tumeur dans des échantillons de pathologie chirurgicale, (d) agir comme biomarqueurs pour une détection et/ou un diagnostic précoce de la maladie, et (e) agir comme cibles dans la génération de molécules du type anticorps qui reconnaissent le complexe peptide cible/CMH.
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WO2017027403A1 (fr) 2015-08-07 2017-02-16 University Of Virginia Patent Foundation Identification de glycopeptides associés à mhc de catégorie i comme cibles d'immunothérapie de cancer
CN106456764A (zh) * 2014-05-29 2017-02-22 免疫医疗有限公司 用于治疗hpv阴性癌症的pdl‑1和pd‑1拮抗剂
WO2017030956A1 (fr) * 2015-08-14 2017-02-23 Agenus Inc. Procédé d'induction d'une réponse des lymphocytes t à des phosphopeptides à l'aide d'acides nucléiques codant pour des mimétiques de phosphopeptides
EP3452085A4 (fr) * 2016-05-05 2020-04-01 University Of Virginia Patent Foundation Peptides cibles pour le traitement et le diagnostic du cancer
WO2020191415A1 (fr) * 2019-03-21 2020-09-24 University Of Virginia Patent Foundation Compositions et méthodes pour le traitement de maladies et de troubles associés à une régulation anormale des protéines
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Publication number Priority date Publication date Assignee Title
CN106456764A (zh) * 2014-05-29 2017-02-22 免疫医疗有限公司 用于治疗hpv阴性癌症的pdl‑1和pd‑1拮抗剂
WO2016183486A1 (fr) 2015-05-13 2016-11-17 Agenus Inc. Vaccins pour le traitement et la prévention du cancer
WO2017027403A1 (fr) 2015-08-07 2017-02-16 University Of Virginia Patent Foundation Identification de glycopeptides associés à mhc de catégorie i comme cibles d'immunothérapie de cancer
WO2017030956A1 (fr) * 2015-08-14 2017-02-23 Agenus Inc. Procédé d'induction d'une réponse des lymphocytes t à des phosphopeptides à l'aide d'acides nucléiques codant pour des mimétiques de phosphopeptides
CN112940076A (zh) * 2015-10-08 2021-06-11 肿瘤疗法科学股份有限公司 Foxm1衍生的肽和包含它们的疫苗
EP3452085A4 (fr) * 2016-05-05 2020-04-01 University Of Virginia Patent Foundation Peptides cibles pour le traitement et le diagnostic du cancer
US11040027B2 (en) 2017-01-17 2021-06-22 Heparegenix Gmbh Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death
WO2020191415A1 (fr) * 2019-03-21 2020-09-24 University Of Virginia Patent Foundation Compositions et méthodes pour le traitement de maladies et de troubles associés à une régulation anormale des protéines
US20220387567A1 (en) * 2019-03-21 2022-12-08 University Of Virginia Patent Foundation Compositions and methods for treating diseases and disorders associated with aberrant regulation of proteins

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