Peptide Vaccine

Abstract

The present disclosure relates to a polypeptide and a pharmaceutical composition comprising the polypeptide, which are used for the prevention or treatment of cancer, particularly gastric cancer, lung cancer, melanoma, and bladder cancer. The present disclosure also relates to a method for inducing a cytotoxic T cell response or treating cancer in a subject by administering a pharmaceutical composition comprising the peptide, and a companion diagnostic method for identifying subjects for treatment. The peptide contains a T cell epitope that is immunogenic in a high proportion of patients. [Selection diagram] None

Description

[Technical field]

[0001] The present disclosure relates to polypeptides and vaccines for use in the prevention or treatment of cancer, particularly cancers that express specific antigens expressed in gastric cancer, lung cancer, melanoma, and bladder cancer. [Background technology]

[0002] Cancer kills millions of people worldwide because it cannot be effectively prevented or treated with existing drugs. Current checkpoint inhibitor immunotherapies, which reactivate existing immune responses, can provide clinical benefit to some cancer patients. Current cancer vaccines, which induce new immune responses, are poorly immunogenic and do not benefit most patients.

[0003] A recent analysis of 63,220 unique tumors revealed that the large heterogeneity of tumor genomes between individuals necessitates the need to tailor cancer vaccines specifically for each patient (Hartmaier et al. Genome Medicine 2017 9:16). Using state-of-the-art techniques, it is currently not feasible to scale up HLA-specific cancer vaccines to large populations. Summary of the Invention

[0004] In antigen-presenting cells (APCs), protein antigens, including tumor-associated antigens (TAA), are processed into peptides. These peptides bind to HLA molecules and are presented to T cells on the cell surface as peptide-HLA complexes. Different individuals express different HLA molecules, which present different peptides. The inventors have demonstrated that an epitope that binds to a single HLA class I allele expressed in a subject is essential, but not sufficient, to induce a tumor-specific T cell response. Instead, tumor-specific T cell responses are optimally activated when the epitope is recognized and presented by HLA molecules encoded by at least three HLA class I genes of an individual (WO 2018 / 158456, WO 2018 / 158457, WO 2018 / 158455, EP 3370065 and EP 3369431).

[0005] Based on this finding, the present inventors have identified T cell epitopes from specific gastric and / or lung and / or melanoma and / or bladder cancer-associated polypeptide antigens (tumor specific antigens (TSA) and / or cancer testis antigens (CTA)) that can bind to at least three class I HLAs in a high percentage of individuals. These T cell epitopes or fragments of antigens containing said T cell epitopes induce specific immune responses against tumor cells expressing these antigens and are useful for treating or preventing cancer.

[0006] In a first aspect, the present disclosure provides a method for producing a pharmaceutical composition comprising: (a) a fragment of up to 50 consecutive amino acids of a gastric cancer-associated antigen selected from DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and SSX1, the fragment comprising an amino acid sequence selected from any one of SEQ ID NOs: 1 to 30; (b) a fragment of up to 50 consecutive amino acids of a lung cancer-associated antigen selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1, the fragment comprising an amino acid sequence selected from any one of SEQ ID NOs: 90 to 119; (c) a fragment of up to 50 consecutive amino acids of a melanoma-associated antigen selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1, comprising an amino acid sequence selected from any one of SEQ ID NOs: 178 to 207; and / or (d) a fragment of up to 50 consecutive amino acids of a bladder cancer-associated antigen selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12, comprising an amino acid sequence selected from any one of SEQ ID NOs: 268 to 297. The present invention provides a polypeptide comprising:

[0007] In some particular cases, the present disclosure provides: (a) a fragment of a gastric cancer-associated antigen selected from DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and SSX1, the fragment comprising an amino acid sequence selected from any one of SEQ ID NOs: 1 to 30; or (b) two or more fragments of one or more gastric cancer-associated antigens selected from DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and SSX1, each fragment comprising a different amino acid sequence selected from any one of SEQ ID NOs: 1 to 30, and optionally comprising or consisting of overlapping or end-to-end fragments in the polypeptide; or (c) a fragment of a lung cancer-associated antigen selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1, the fragment comprising an amino acid sequence selected from any one of SEQ ID NOs: 90 to 119; or (d) two or more fragments of one or more lung cancer-associated antigens selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1, each fragment comprising a different amino acid sequence selected from any one of SEQ ID NOs: 90 to 119, and optionally comprising or consisting of overlapping or end-to-end fragments in the polypeptide; or (e) a fragment of a melanoma-associated antigen selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1, the fragment comprising an amino acid sequence selected from any one of SEQ ID NOs: 178 to 207; and / or (f) two or more fragments of one or more melanoma associated antigens selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1, each fragment comprising a different amino acid sequence selected from any one of SEQ ID NOs: 178 to 207, and optionally comprising or consisting of overlapping or end-to-end arranged fragments in the polypeptide; or (g) a fragment of a bladder cancer-associated antigen selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12, the fragment comprising an amino acid sequence selected from any one of SEQ ID NOs: 268 to 297; or (h) Two or more fragments of one or more bladder cancer-associated antigens selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12, each of which comprises a different amino acid sequence selected from any one of SEQ ID NOs: 268 to 297, and optionally comprises or consists of fragments that are overlapping or arranged end-to-end in the polypeptide. A polypeptide is provided.

[0008] In some particular cases, the polypeptide comprises or consists of fragments of at least two different cancer associated antigens, the cancer associated antigens being: (a) DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and SSX1, each of which contains a different amino acid sequence selected from SEQ ID NOs: 1 to 30; and / or (b) BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1, each of which contains a different amino acid sequence selected from SEQ ID NOs: 90 to 119; and / or (c) PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1, each fragment comprising a different amino acid sequence selected from SEQ ID NOs: 178 to 207; and / or (d) PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12, each of which contains a different amino acid sequence selected from SEQ ID NOs: 268 to 297. is selected from.

[0009] In some cases, the polypeptide comprises or consists of one or more amino acid sequences selected from SEQ ID NOs: 31-60, 90-119, 178-207, and / or 268-297.

[0010] In some cases, the polypeptide comprises or consists of one or more amino acid sequences selected from SEQ ID NOs: 61-75, 120-149, 208-237, and / or 298-327.

[0011] In a further aspect, the disclosure provides a panel of two or more polypeptides as described above, wherein each peptide comprises or consists of a different amino acid selected from SEQ ID NOs: 1 to 30; and / or SEQ ID NOs: 31 to 60; and / or SEQ ID NOs: 61 to 75; or selected from SEQ ID NOs: 90 to 119; and / or SEQ ID NOs: 120 to 149; and / or SEQ ID NOs: 150 to 164; or selected from SEQ ID NOs: 178 to 207; and / or SEQ ID NOs: 208 to 237; and / or SEQ ID NOs: 238 to 252; or selected from SEQ ID NOs: 268 to 297; and / or SEQ ID NOs: 298 to 327; and / or SEQ ID NOs: 328 to 342.

[0012] In a further aspect, the present disclosure provides a pharmaceutical composition or kit having as an active ingredient one or more of the panels of polypeptides or peptides as described above, or having as an active ingredient a polypeptide comprising at least two amino acid sequences selected from SEQ ID NOs: 1-30; SEQ ID NOs: 31-60; and / or SEQ ID NOs: 61-75; and / or SEQ ID NOs: 90-119; SEQ ID NOs: 120-149; and / or SEQ ID NOs: 150-164; and / or SEQ ID NOs: 178-207; and / or SEQ ID NOs: 208-237; and / or SEQ ID NOs: 238-252; and / or SEQ ID NOs: 268-297; and / or SEQ ID NOs: 298-327; and / or SEQ ID NOs: 328-342.

[0013] In a further aspect, the disclosure provides a method of inducing an immune response (e.g., vaccinating, providing immunotherapy, or inducing a CD8+ T cell response in a subject) comprising administering to the subject a pharmaceutical composition, kit, or panel of polypeptides as described above. The method may be a method of treating cancer, such as gastric cancer, lung cancer, melanoma, and bladder cancer.

[0014] In a further aspect, the present disclosure provides a method for producing a method for treating a cancer cell comprising: - a pharmaceutical composition, a kit or a panel of polypeptides as described above for use in a method for inducing an immune response or for use in a method for treating cancer, optionally gastric cancer, lung cancer, melanoma and bladder cancer; and - the use of a peptide or panel of peptides as defined above in the manufacture of a medicament for inducing an immune response or for treating cancer, optionally gastric cancer, lung cancer, melanoma and bladder cancer.

[0015] In a further aspect, the disclosure provides a method for identifying a human subject likely to have a CD8+ T cell response to administration of the pharmaceutical composition described above, comprising: (i) determining that the active ingredient polypeptide(s) contains a sequence that is a T cell epitope capable of binding to at least three HLA class I of the subject; (ii) identifying the subject as likely to have a CD8+ T cell response to administration of the pharmaceutical composition; The present invention provides a method comprising:

[0016] In a further aspect, the present disclosure provides a method for identifying a subject likely to have a clinical response to the above-described therapeutic method, comprising: (i) the active ingredient polypeptide(s) of the pharmaceutical composition comprises two or more different amino acid sequences, each of which is a. a T cell epitope capable of binding to at least three HLA class I molecules of the subject; and b. a cancer-associated antigen expressed by cancer cells of the subject, and optionally a fragment of the cancer-associated antigen present in a sample obtained from the subject. and determining that; (ii) identifying the subject as likely to have a clinical response to the treatment method; The present invention provides a method comprising:

[0017] In a further aspect, the present disclosure provides a method for determining the likelihood that a particular human subject will have a clinical response to the above-described treatment method, wherein one or more of the following factors correspond to a higher likelihood of clinical response: (a) the presence in the active ingredient polypeptide(s) of a greater number and / or different amino acid sequences that are T cell epitopes each capable of binding to at least three HLA class I of the subject; (b) A greater number of target polypeptide antigens A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; comprising at least one amino acid sequence, Optionally, the target polypeptide antigen is expressed in the subject, and further optionally, the target polypeptide antigen is present in one or more samples obtained from the subject; (c) the subject is administered a target polypeptide antigen, optionally a threshold number of the target polypeptide antigen, and / or optionally A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; a greater likelihood of expressing a target polypeptide antigen determined to include at least one amino acid sequence; and / or (d) a greater number of target polypeptide antigens that the subject is predicted to express, optionally a greater number of target polypeptide antigens that the subject expresses with a threshold probability, and / or optionally A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; A greater number of target polypeptide antigens determined to contain at least one amino acid sequence.

[0018] In some cases, the cancer associated antigen is a gastric cancer antigen selected from DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, SSX1, BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2NY - a lung cancer antigen selected from SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, MAGE-A1, a melanoma antigen selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, MAGE-A1, and / or a bladder cancer antigen selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8 and HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE A12. In some cases, the method includes determining that the subject's cancer cells express one or more cancer-associated antigens. The cancer-associated antigen(s) may be present in one or more samples obtained from the subject.

[0019] In some cases, administration of the pharmaceutical composition or active ingredient polypeptide of the kit may then be selected as a method of treatment for the subject. The subject may be further treated by administering the pharmaceutical composition or active ingredient polypeptide.

[0020] In a further aspect, the disclosure provides the above methods of treatment, wherein the subject has been identified as having a high likelihood of having a clinical response to treatment by the above method, or a likelihood of having a clinical response above a minimum threshold.

[0021] In a further aspect, the disclosure provides a method for identifying a human subject who is likely to not have a clinical response to the above-described therapeutic method, comprising: (i) determining that the active ingredient peptide(s) of the pharmaceutical composition does not contain two or more distinct sequences that are T cell epitopes each capable of binding to at least three HLA class I of the subject; (ii) identifying the subject as likely to not have a clinical response to the treatment method; The present invention provides a method comprising:

[0022] The above methods may include determining the subject's HLA class I and / or class II genotype.

[0023] The present disclosure includes a method of treating a human subject likely to respond to a polypeptide(s) of the present disclosure or a pharmaceutical composition comprising said polypeptide(s), comprising: (a) determining that the polypeptide(s) or pharmaceutical composition comprising said polypeptide(s) comprises an amino acid sequence that is a T cell epitope capable of binding to at least three HLA class I molecules in the human subject; and (b) administering said polypeptide or pharmaceutical composition to said human subject. In certain embodiments, the method includes determining whether the human subject is likely to respond to one or more polypeptide antigens expressed by cancer cells of the human subject, including (a) gastric cancer antigens DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and / or MAGE-A2-related antigens, using population expression data for each antigen. SSX1, and / or lung cancer antigens BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, MAGE-A1, and / or melanoma cancer antigens PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, MAGE-A1, and / or bladder cancer antigen P and (b) determining the likelihood of having a CD8+ T cell response targeting an antigen selected from IWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, and HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12; and (b) determining the likelihood of having a CD8+ T cell response targeting an antigen comprising an amino acid sequence that is a fragment of an active ingredient peptide of the pharmaceutical composition and a T cell epitope capable of binding to at least three HLA class I molecules of the human subject.

[0024] The present disclosure includes a method of treating a human subject likely to respond to a polypeptide(s) of the present disclosure or a pharmaceutical composition comprising said polypeptide(s), comprising: (a) determining that a polypeptide(s) or a pharmaceutical composition comprising said polypeptide comprises two or more distinct amino acid sequences, each of which is a T cell epitope capable of binding to at least three HLA class I molecules in a human subject; and a fragment of a cancer associated antigen expressed by cancer cells in the human subject, and optionally that said cancer associated antigen is present in a sample obtained from the human subject; and (b) administering said polypeptide or pharmaceutical composition to said human subject.

[0025] The present disclosure includes methods of treating a human subject likely to respond to a polypeptide(s) of the present disclosure or a pharmaceutical composition comprising said polypeptide(s), comprising determining any one of the following: (a) a greater number and / or different amino acid sequences are present in the polypeptide(s) or pharmaceutical composition comprising said polypeptide(s), each of which is a T cell epitope capable of binding to at least three HLA class I of the human subject; (b) a greater number of target polypeptide antigens in the human subject or in a sample from the human subject, which are contained in an active ingredient polypeptide and which comprise at least one amino acid sequence that is a T cell epitope capable of binding to at least three HLA class I of the human subject; (c) a greater number of target polypeptide antigens in the human subject or in a sample from the human subject, which target polypeptide antigens include at least one amino acid sequence that is a T cell epitope capable of binding to at least three HLA class I of the human subject; optionally, a higher probability of expressing a threshold number of target polypeptide antigens, and / or optionally, a target polypeptide antigen determined to comprise at least one amino acid sequence that is contained in the active ingredient polypeptide and that is a T cell epitope capable of binding to at least three HLA class I in the human subject; and / or (d) a higher number of target polypeptide antigens that the human subject is predicted to express, optionally, a higher number of target polypeptide antigens that the human subject expresses with a threshold probability, and / or optionally, a target polypeptide antigen determined to comprise at least one amino acid sequence that is contained in the active ingredient polypeptide and that is a T cell epitope capable of binding to at least three HLA class I in the human subject; and (e) administering the polypeptide or pharmaceutical composition to the human subject. In certain embodiments, the method further comprises identifying a polypeptide antigen targeted by the polypeptide(s) or pharmaceutical composition comprising said polypeptide(s) as comprising an amino acid sequence contained in an active ingredient polypeptide and which is a T cell epitope capable of binding to at least three HLA class I in a human subject, and using population expression data for each identified antigen to determine the probability that the human subject expresses one or more of the identified antigens which together comprise at least two distinct amino acid sequences; and administering the polypeptide or pharmaceutical composition to the human subject.In certain embodiments, the at least two different amino acid sequences are comprised in the amino acid sequences of two different polypeptide antigens targeted by the active ingredient polypeptide(s).

[0026] The present disclosure will now be described in more detail, by way of example and not by way of limitation, with reference to the accompanying drawings. Many equivalent modifications and variations will be apparent to those skilled in the art given this disclosure. Accordingly, the exemplary embodiments of the present disclosure described are considered to be illustrative and not limiting. Various modifications can be made to the described embodiments without departing from the scope of the present disclosure. All documents cited herein, whether above or below, are expressly incorporated by reference in their entirety.

[0027] The present disclosure includes combinations of the described embodiments and preferred features unless expressly stated to be unacceptable or to be explicitly avoided. As used in this specification and the appended claims, the singular forms "a," "an," and "the" include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to "a peptide" includes two or more such peptides.

[0028] The section headings used herein are for convenience only and are not to be construed as limiting in any way. [Brief description of the drawings]

[0029] [Figure 1] ROC curve for HLA-restricted PEPI biomarker. [Diagram 2] ROC curve of ≧1 PEPI3+ test for determining diagnostic accuracy. AUC=0.73 classifies the fair diagnostic value of the PEPI biomarker. [Figure 3A]Distribution of HLA class I PEPI3+ compared to CD8+ T cell responses measured by state of the art assays among peptide pools used in CD8+ T cell response assays. A: HLA class I restricted PEPI3+. 90% overall concordance (OPA) between T cell responses and PEPI3+ peptides indicates that the peptides of the invention are useful for predicting the set of vaccine-induced T cell responses in individuals (p<0.001). True positive (TP), both peptide and T cell responses were detected (shaded); True negative (TN), neither peptide nor T cell responses were detected (shaded); False negative (FN), only T cell responses were detected; False positive (FP), only peptide was detected. [Figure 3B] Distribution of HLA class I PEPI3+ epitopes compared to CD8+ T cell responses measured by state of the art assays among peptide pools used in the CD8+ T cell response assay. B: Class I HLA restricted epitopes (PEPI1+). The OPA between predicted epitopes and CD8+ T cell responses was 25% (not statistically significant). True positive (TP), both peptide and T cell responses were detected (shaded); True negative (TN), neither peptide nor T cell responses were detected (shaded); False negative (FN), only T cell responses were detected; False positive (FP), only peptides were detected. [Figure 4] Correlation between CD4 peptides predicted by the PEPI test and T cell reactivity measured with peptide pools in patients treated with SLP vaccine. A: PEPI binding to ≥3 HLA class II alleles; B: epitopes binding to one HLA class II allele. Grey: true positive (TP) and true negative (TN) responses; White: false negative (FN) and false positive (FP) responses. TP: both peptide and T cell responses detected; TN: neither peptide nor T cell responses detected; FN: only T cell responses detected; FP: only peptide detected. [Diagram 5]Multiple HLA-binding peptides defining HPV-16 LPV vaccine-specific T cell response sets in 20 VIN-3 patients and 5 cervical cancer patients. PEPI counts were compared with clinical responses after treatment with LPV. Predicted CD8+ T cell responders according to PEPI for HLA class I (A) and predicted CD4+ T cell responders according to PEPI for HLA class II (B). Correlation between PEPI counts for HLA class I (C) and class II (D) and clinical response during a 3-month follow-up period in VIN-3 patients. Predicted T cell responders: PEPI counts ≥ 1. Grey columns, patients with HPV16 E6 and / or E7-specific T cell responses; dashed columns, patients without T cell responses. CR, complete clinical responders; PR, partial clinical responders; NR, clinical non-responders. [Figure 6] Multiple HLA class I binding peptides that define HPV vaccine-specific T cell response sets for two patients. A: Four HPV antigens in the HPV vaccine. Boxes represent the length of amino acid sequence from N-terminus to C-terminus. B: Process of identifying multiple HLA binding peptides for two patients: Patient HLA sequences are labeled as 4-digit HLA genotypes from patient ID. Lines indicate the positions of the first amino acids of 54 and 91 epitopes that can bind to HLA (PEPI1+) of patient 12-11 and patient 14-5, respectively. PEPI2 represents peptides selected from PEPI1+ that can bind to multiple HLA of the patient (PEPI2+). PEPI3 represents peptides that can bind to ≧3 HLA of the patient (PEPI3+). PEPI4 represents peptides that can bind to ≧4 HLA of the patient (PEPI4+). PEPI5 represents peptides that can bind to ≧5 HLA of the patient (PEPI5+). PEPI6 represents peptides that can bind to 6 HLA of the patient (PEPI6). C: DNA vaccine-specific PEPI3+ sets of two patients characterize the vaccine-specific T cell responses of the patients. [Figure 7] Probability of developing TSA targeted by the IMA901 vaccine. [Figure 8]HLA class I allele binding characteristics of TUMAP of IMA901 peptide vaccine against 2,915 common alleles. (A) And for class I genotype (6 alleles) of 51 HLA-A*02+ RCC patients. Percentages at the bottom indicate the proportion of HLAs that TUMAP can bind. Dark grey lines indicate the binding HLA alleles. (B) Probability indicates the proportion of patients that can present a given number of TUMAP with 3 or more HLAs. AP indicates the number of antigens that can generate at least one PEPI. In this case, both antigens and predicted PEPIs are 9-mers, so AP=TUMAP=PEPI. [Figure 9] Correlation between immune responses measured for any TUMAP and immune responses to antigens expressed on tumors (AGPs) [Figure 10A] Correlation studies between immune response rate (IRR) and PEPI score, between objective response rate (ORR) and multi-PEPI score, and between objective response rate (ORR) and multi-Ag PEPI score. A: Preliminary experiment to investigate the relationship between PEPI score and immune response rate of therapeutic vaccine (r2=0.7, p=0.001). Dark gray dashed lines indicate 95% confidence intervals, and gray dashed lines indicate trend lines. [Figure 10B] Correlation studies between immune response rate (IRR) and PEPI score, between objective response rate (ORR) and multi-PEPI score, and between objective response rate (ORR) and multi-Ag PEPI score. B: Plot of IRR-PEPI score. (r2=0.47, p=0.001). Dark grey dashed lines indicate 95% confidence intervals, and grey dashed lines indicate trend lines. [Figure 10C] Correlation studies between immune response rate (IRR) and PEPI score, between objective response rate (ORR) and multi-PEPI score, and between objective response rate (ORR) and multi-Ag PEPI score. C: Multi-PEPI score and clinical response rate of therapeutic vaccine (r2=0.75, p=0.001). Dark grey dashed lines indicate 95% confidence intervals, and grey dashed lines indicate trend lines. [Figure 10D]Correlation studies between immune response rate (IRR) and PEPI score, between objective response rate (ORR) and multi-PEPI score, and between objective response rate (ORR) and multi-Ag PEPI score. D: ORR plotted against multi-PEPI score (r2=0.12, p=0.124). Dark grey dashed lines indicate 95% confidence intervals, and grey dashed lines indicate trend lines. [Figure 10E] Correlation studies between immune response rate (IRR) and PEPI score, between objective response rate (ORR) and multi-PEPI score, and between objective response rate (ORR) and multi-Ag PEPI score. E: ORR plotted against multi-Ag PEPI score for vaccines containing multiple antigens (r2=0.64, p=0.009). Dark grey dashed lines indicate 95% confidence intervals, grey dashed lines indicate trend lines. [Figure 10F] Correlation studies between immune response rate (IRR) and PEPI score, between objective response rate (ORR) and multi-PEPI score, and between objective response rate (ORR) and multi-Ag PEPI score. F: ORR plotted against multi-PEPI score for vaccines containing multiple antigens (r2=0.87, p=0.0002). Dark grey dashed lines indicate 95% confidence intervals, grey dashed lines indicate trend lines. [Figure 10G] Correlation studies between immune response rate (IRR) and PEPI score, between objective response rate (ORR) and multi-PEPI score, and between objective response rate (ORR) and multi-Ag PEPI score. G: ORR plotted against multi-PEPI score in patients with target antigen-positive disease (r2=0.56, p=0.005). Dark grey dashed lines indicate 95% confidence intervals, grey dashed lines indicate trend lines. [Figure 11] OBERTO Clinical Trial Design (NCT03391232) [Figure 12]Antigen expression in the CRC cohort of the OBERTO trial (n=10). A: Frequency of expression of PolyPEPI1018 source antigens based on 2391 biopsies. B: The PolyPEPI1018 vaccine design identified three of the seven TSAs as being expressed in CRC tumors with a probability of over 95%. C: On average, four out of ten patients had a pre-existing immune response to each target antigen, meaning that the TSA was actually expressed in the patient's tumor. D: Seven out of ten had a pre-existing immune response to at least one, and on average, three different TSAs. [Figure 13] The immunogenicity of PolyPEPI1018 in CRC patients confirms that the target antigen and target peptide were appropriately selected. Top: Target peptide selection and peptide design for the PolyPEPI1018 vaccine composition. Two 15mers were selected from the CRC-specific CTA (TSA) to contain the 9mer PEPI3+ that predominates in a representative model population. Table: The PolyPEPI1018 vaccine was retrospectively tested during preclinical trials in a CRC cohort and proved immunogenic for at least one antigen in all tested individuals by generating PEPI3+. Clinical immune responses specific for at least one antigen were measured in 90% of patients, and there was also a multi-antigen immune response against at least two antigens in 90% of patients and at least three antigens in 80% of patients when tested with an IFNy fluorescent spot assay specifically measured for the peptides that comprise the vaccine. [Figure 14A] Clinical response to PolyPEPI1018 treatment. A: Swimmer plot of clinical response from the OBERTO trial (NCT03391232). [Figure 14B] Clinical response to PolyPEPI1018 treatment. B: Association between progression-free survival (PFS) and AGP counts. [Figure 14C] Clinical response to PolyPEPI1018 treatment. C: Correlation between tumor volume and AGP count. [Figure 15]Example of peptide hotspot analysis: PRAME antigen hotspots in 433 patients of the model population. The y-axis is the 433 patients of the model population and the x-axis is the amino acid sequence of the PRAME antigen (CTA). Each data point represents PEPIs presented by ≥3 HLA class I of one patient starting at the specified amino acid position. The two most frequent PEPIs (called best EPIs) of the PRAME antigen are highlighted in dark grey (peptide hotspots = PEPI hotspots). [Figure 16] Tumor specific antigen (CTA) expression curve calculated by analyzing CTA expression frequency data in human gastric cancer tissues (cell line data not included). [Figure 17] Antigen expression distribution of gastric cancer based on calculation of multi-antigen response from expression frequency of 14 different selected CTAs. A: Non-cumulative distribution to calculate the expected value of the number of expressed antigens (AG50). This value indicates that 7.18 vaccine antigens are likely to be expressed in gastric tumor cells. B: Cumulative distribution curve of the minimum number of expressed antigens (CTA expression curve). This indicates that there is a 95% probability that at least 5 vaccine antigens are expressed in gastric cancer cells (AG95). [Figure 18] PEPIs representing antigens: Distribution of gastric cancer vaccine-specific CTA antigens with ≧1 PEPI (referred to as "AP") in a model population of gastric cancer vaccines (n=433). A: Non-cumulative distribution of APs with an average number of APs of AP50=7.98, which means that on average, nearly 8 CTAs have PEPI in the model population. B: Cumulative distribution curve of the minimum number of APs in the model population (n=433). This indicates that in 95% of the model population (n=433), at least 3 vaccine antigens have PEPI (AP95=3). [Figure 19]PEPI represented the distribution of expressed antigens (gastric cancer vaccine-specific CTA antigens expressed in tumors, ≧1 PEPI is predicted, called "AGP") in the model population (n=433) calculated using the CTA expression rate in gastric cancer. A: Non-cumulative distribution of AGPs, where the expected value of the number of expressed CTAs represented by PEPI is AGP50=3.86. AGP50 is a measure of the efficacy of the disclosed gastric cancer vaccine in attacking gastric tumors in an unselected patient population. AGP50=3.86 means that in the model population, at least three CTAs from the vaccine are likely to be expressed in gastric tumor cells and present PEPI. B: The cumulative distribution curve of the minimum number of AGPs in the model population (n=433) shows that at least one of the vaccine CTAs will present PEPI in 95% of the population, and the remaining 5% of the population is likely to have no AGPs at all (AGP95=1). [Figure 20] Tumor specific antigen (CTA) expression curve calculated by analyzing CTA expression frequency data in human lung cancer tissues (cell line data not included). [Figure 21] Antigen expression distribution of lung cancer based on calculation of multi-antigen response from expression frequency of 13 different selected CTAs. A: Non-cumulative distribution to calculate the expected value of the number of expressed antigens (AG50). This value indicates that 4.76 vaccine antigens are likely to be expressed in lung tumor cells. B: Cumulative distribution curve of the minimum number of expressed antigens (CTA expression curve). This indicates that there is a 95% probability that at least 2 vaccine antigens are expressed in lung cancer cells (AG95). [Figure 22] PEPIs representing antigens: Distribution of lung cancer vaccine-specific CTA antigens with ≧1 PEPI (referred to as "AP") in a model population of lung cancer vaccines (n=433). A: Non-cumulative distribution of APs with an average number of APs of AP50=7.6, which means that on average, approximately 8 CTAs have PEPI in the model population. B: Cumulative distribution curve of the minimum number of APs in the model population (n=433). This shows that in 95% of the model population (n=433), at least 2 vaccine antigens have PEPI (AP95=2). [Diagram 23]PEPI represented the distribution of expressed antigens (lung cancer vaccine-specific CTA antigens expressed in tumors, ≧1 PEPI is predicted, called "AGP") in the model population (n=433) calculated using the CTA expression rate in lung cancer. A: Non-cumulative distribution of AGPs, where the expected value of the number of expressed CTAs represented by PEPI is AGP50=2.77. AGP50 is a measure of the efficacy of the disclosed lung cancer vaccine in attacking lung tumors in an unselected patient population. AGP50=2.77 means that in the model population, at least three CTAs from the vaccine are likely to be expressed in lung tumor cells and present PEPI. B: The cumulative distribution curve of the minimum number of AGPs in the model population (n=433) shows that at least one of the vaccine CTAs presents PEPI in 91% of the population, and the remaining 9% of the population is likely to have no AGPs at all (AGP95=0). [Figure 24] Tumor-specific antigen (CTA) expression curve calculated by analyzing CTA expression frequency data in human melanoma (cell line data not included). [Diagram 25] Melanoma antigen expression distribution based on calculation of the multi-antigen response from the expression frequency of 15 different selected CTAs. A: Non-cumulative distribution to calculate the expected value of the number of expressed antigens (AG50). This value indicates that 7.62 vaccine antigens are likely to be expressed in gastric tumor cells. B: Cumulative distribution curve of the minimum number of expressed antigens (CTA expression curve). This indicates that there is a 95% probability that at least 5 vaccine antigens are expressed in melanoma cells (AG95). [Figure 26] PEPIs representing antigens: Distribution of melanoma vaccine-specific CTA antigens with ≥ 1 PEPI (referred to as "AP") in a model population of melanoma vaccines (n = 433). A: Non-cumulative distribution of APs with a mean number of APs AP50 = 8.29, meaning that on average 8 CTAs have PEPI in the model population. B: Cumulative distribution curve of the minimum number of APs in the model population (n = 433). This indicates that in 95% of the model population (n = 433), at least 3 vaccine antigens have PEPI (AP95 = 2). [Figure 27]PEPI represented the distribution of expressed antigens (melanoma vaccine-specific CTA antigens expressed in tumors, ≧1 PEPI is expected, called "AGP") in the model population (n=433) calculated using the CTA expression rate of melanoma. A: Non-cumulative distribution of AGPs, where the expected value of the number of expressed CTAs represented by PEPI is AGP50=4.22. AGP50 is a measure of the efficacy of the disclosed melanoma vaccine in attacking gastric tumors in an unselected patient population. AGP50=4.22 means that in the model population, at least three CTAs from the vaccine are likely to be expressed in gastric tumor cells and present PEPI. B: The cumulative distribution curve of the minimum number of AGPs in the model population (n=433) shows that at least one of the vaccine CTAs will present PEPI in 95% of the population, and the remaining 5% of the population is likely to have no AGPs at all (AGP95=1). [Figure 28] Tumor specific antigen (CTA) expression curve calculated by analyzing CTA expression frequency data in human bladder cancer tissues (cell line data not included). [Figure 29] Antigen expression distribution of bladder cancer based on calculation of multi-antigen response from expression frequency of 17 different selected CTAs. A: Non-cumulative distribution to calculate the expected number of expressed antigens (AG50). This value indicates that 8.85 vaccine antigens are likely to be expressed in bladder tumor cells. B: Cumulative distribution curve of the minimum number of expressed antigens (CTA expression curve). This indicates that there is a 95% probability that at least 4 vaccine antigens are expressed in bladder cancer cells (AG95). [Diagram 30] PEPIs representing antigens: Distribution of bladder cancer vaccine-specific CTA antigens with ≧1 PEPI (referred to as "AP") in a model population of bladder cancer vaccines (n=433). A: Non-cumulative distribution of APs with an average number of APs of AP50=9.44, which means that on average, approximately 8 CTAs have PEPI in the model population. B: Cumulative distribution curve of the minimum number of APs in the model population (n=433). This shows that in 95% of the model population (n=433), at least 3 vaccine antigens have PEPI (AP95=3). [Diagram 31] PEPI represented the distribution of expressed antigens (bladder cancer vaccine-specific CTA antigens expressed in tumors, ≧1 PEPI is predicted, called "AGP") in the model population (n=433) calculated using the CTA expression rate in bladder cancer. A: Non-cumulative distribution of AGPs, where the expected value of the number of expressed CTAs represented by PEPI is AGP50=3.90. AGP50 is a measure of the efficacy of the disclosed bladder cancer vaccine in attacking bladder tumors in an unselected patient population. AGP50=3.90 means that in the model population, at least three CTAs from the vaccine are likely to be expressed in bladder tumor cells and present PEPI. B: The cumulative distribution curve of the minimum number of AGPs in the model population (n=433) shows that at least one of the vaccine CTAs will present PEPI in 95% of the population, and the remaining 5% of the population is likely to have no AGPs at all (AGP95=1). [Diagram 32] Probability of vaccine antigens being expressed in patient A's tumor cells. There is a greater than 95% probability that 5 of the 13 target antigens in the vaccine regimen will be expressed in the patient's tumor. As a result, the 13 peptide vaccines combined have a 95% chance of inducing an immune response against at least 5 ovarian cancer antigens (AGP95). Each peptide has an 84% chance of inducing an immune response in patient A. The AGP50 is mean(expected)=7.9 (a measure of the vaccine's effectiveness in attacking patient A's tumor). [Diagram 33] Treatment schedule for Patient A [Diagram 34] T cell responses of patient A. A. Left: Vaccine peptide-specific T cell response (20mer). Right: CD8+ cytotoxic T cell response (9mer). The predicted T cell responses are confirmed by bioassay. [Diagram 35] MRI findings of Patient A treated with personalized (PIT) vaccine. This patient with advanced, heavily pretreated ovarian cancer had an unexpected objective response after treatment with PIT vaccine. These MRI findings suggest that the patient's tumor volume was significantly reduced by combining PIT vaccine with chemotherapy. [Diagram 36]Probability of vaccine antigens being expressed in tumor cells of patient B, and treatment schedule for patient B. A: The probability that 4 of the 13 target antigens in the vaccine are expressed in the patient's tumor is over 95%. B: As a result, the 12 peptide vaccines combined have a 95% probability of inducing an immune response against at least 4 breast cancer antigens (AGP95). Each peptide has an 84% probability of inducing an immune response in patient B. AGP50=6.45; a measure of the effectiveness of the vaccine in attacking patient B's tumor. C: Treatment schedule for patient B. [Figure 37] T cell responses of patient A. A. Left: P vaccine peptide-specific T cell responses (20mer). Right: Kinetics of vaccine-specific CD8+ cytotoxic T cell responses (9mer). The predicted T cell responses are confirmed by bioassay. [Figure 38] Treatment schedule for patient C. [Figure 39] T cell responses of patient C. A: Vaccine peptide-specific T cell response (20mer). B: Vaccine peptide-specific CD8+ T cell response (9mer). C-D: Kinetics of vaccine-specific CD4+ T cell and CD8+ cytotoxic T cell responses (9mer), respectively. After 14 months, there is a long-lasting immune response specific for CD4 and CD8 T cells. [Diagram 40] Treatment schedule for Patient D. [Diagram 41] Immune responses of patient D to PIT treatment. A: CD4+ specific T cell response (20mer) and B: CD8+ T cell specific T cell response (9mer). 0.5-4 months refers to the time period from the last vaccination until the collection of PBMC samples. [Diagram 42] Schematic diagram showing exemplary positions of amino acids in overlapping HLA class I and HLA class II binding epitopes in a 30-mer peptide. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0030] Array Description SEQ ID NOs: 1 to 30 show the 9-mer T cell epitopes listed in Table 20a. SEQ ID NOs: 31 to 60 show the 15-mer T cell epitopes listed in Table 20a. SEQ ID NOs: 61 to 75 show the gastric cancer vaccine peptides listed in Table 21a. SEQ ID NOs: 76 to 89 represent gastric cancer-associated antigens. SEQ ID NOs: 90 to 119 show the 9-mer T cell epitopes listed in Table 20b. SEQ ID NOs: 120 to 149 show the 15-mer T cell epitopes listed in Table 20b. SEQ ID NOs: 150 to 164 show the lung cancer vaccine peptides listed in Table 21b. SEQ ID NOs: 165 to 177 represent lung cancer-associated antigens. SEQ ID NOs: 178 to 207 show the 9-mer T cell epitopes listed in Table 20c. SEQ ID NOs: 208 to 237 show 15-mer T cell epitopes described in Table 20c. SEQ ID NOs: 238-252 show the melanoma vaccine peptides listed in Table 21c. SEQ ID NOs: 253 to 267 represent melanoma-associated antigens. SEQ ID NOs: 268 to 297 show the 9-mer T cell epitopes listed in Table 20d. SEQ ID NOs: 298 to 327 show 15-mer T cell epitopes listed in Table 20d. SEQ ID NOs: 328 to 342 show bladder cancer vaccine peptides listed in Table 21d. SEQ ID NOs: 343 to 359 represent bladder cancer-associated antigens. SEQ ID NOs: 360 to 372 show the sequences of the personalized vaccine for patient A and are listed in Table 22. SEQ ID NOs: 373-384 show the sequences of the personalized vaccine for patient B and are listed in Table 24. SEQ ID NO: 385 shows the 30 amino acid CRC_P3 peptide, FIG. SEQ ID NOs:386 to 394 show the sequences of the 9-mer shown in FIG.

[0031] Detailed Description HLA genotype HLA is encoded by the most polymorphic genes in the human genome. Each human has three HLA class I molecules (HLA-A * , HLA-B * , HLA-C * ) and four HLA class II molecules (HLA-DP*, HLA-DQ*, HLA-DRB1*, HLA-DRB3 * / 4 * / 5 * Each person has maternal and paternal alleles for HLA. In reality, each human expresses various combinations of six HLA class I and eight HLA class II molecules that present different epitopes from the same protein antigen. The function of HLA molecules is to control T cell responses.

[0032] The nomenclature used to name the amino acid sequences of HLA molecules is as follows: HLA-A * Gene name, such as 02:25 * Allele: Protein number. In this example, "02" refers to the allele. In most cases, alleles are defined by serotype, meaning that proteins of a given allele do not react with each other in serological assays. Protein numbers ("25" in the above example) are assigned consecutively as proteins are discovered. Any protein with a different amino acid sequence that determines the binding specificity for a non-self antigenic peptide is assigned a new protein number (e.g., even a single amino acid change in the sequence is considered a different protein number). Further information about the nucleic acid sequence of a given locus may be added to the HLA designation, but such information is not required for the methods described herein.

[0033] An individual's HLA class I genotype or HLA class II genotype may refer to the actual amino acid sequence of each class I or class II HLA of the individual, or may refer to a designation that minimally names the allele and protein number of each HLA gene, as described above. In some embodiments, an individual's HLA genotype is obtained or determined by assaying a biological sample from the individual. The biological sample typically contains the subject's DNA. The biological sample may be, for example, a blood, serum, plasma, saliva, urine, breath, cell, or tissue sample. In some embodiments, the biological sample is a saliva sample. In some embodiments, the biological sample is a buccal swab sample. The HLA genotype may be obtained or determined using any suitable method. For example, the sequence may be determined via sequencing the HLA locus using methods and protocols known in the art. In some embodiments, the HLA genotype is determined using sequence-specific primer (SSP) technology. In some embodiments, the HLA genotype is determined using sequence-specific oligonucleotide (SSO) technology. In some embodiments, HLA genotype is determined using sequence-based typing (SBT) technology. In some embodiments, HLA genotype is determined using next-generation sequencing. Alternatively, the HLA set of an individual can be stored in a database and accessed using methods known in the art.

[0034] Some subjects may have two HLA alleles that code for the same HLA molecule (e.g., homozygous HLA-A *02:25 is two copies). The HLA molecules encoded by these alleles bind to all of the same T cell epitopes. For the purposes of this disclosure, "binding to at least two HLA molecules of a subject" as used herein includes binding to HLA molecules encoded by two identical HLA alleles in a single subject. That is, "binding to at least two HLA molecules of a subject" etc. can also be expressed as "binding to HLA molecules encoded by at least two HLA alleles of a subject".

[0035] HLA-epitope binding A given HLA of a subject presents only a limited number of different peptides generated by processing of protein antigens in APCs to T cells. As used herein, "display" or "presentation", when used in relation to HLA, refers to the binding between a peptide (epitope) and HLA. In this context, "displaying" or "presenting" a peptide is synonymous with "binding" to a peptide.

[0036] As used herein, the term "epitope" or "T cell epitope" refers to a sequence of consecutive amino acids contained in a protein antigen that has binding affinity (can bind) to one or more HLA. Epitopes are HLA and antigen specific (HLA-epitope pairs, predicted by known methods), but not subject specific. An epitope, T cell epitope, polypeptide, fragment of a polypeptide, or composition comprising a polypeptide or fragment thereof is "immunogenic" to a particular human subject if it is capable of inducing a T cell response (cytotoxic T cell response or helper T cell response) in the subject. In some cases, the helper T cell response is a Th1 type helper T cell response. In some cases, an epitope, T cell epitope, polypeptide, fragment of a polypeptide, or composition comprising a polypeptide or fragment thereof is "immunogenic" to a particular human subject if it is more likely to induce a T cell or immune response in the subject than a different T cell epitope (or in some cases, two different T cell epitopes, respectively) that can bind to only one HLA molecule of the subject.

[0037] The terms "T cell response" and "immune response" are used interchangeably herein and refer to the activation of T cells and / or the induction of one or more effector functions after recognition of one or more HLA-epitope binding pairs. In some cases, the "immune response" includes an antibody response, since HLA class II molecules stimulate helper responses that are responsible for the induction of both long-lasting CTL and antibody responses. Effector functions include cytotoxicity, cytokine production, and proliferation. According to the present disclosure, an epitope, T cell epitope, or fragment of a polypeptide is immunogenic to a particular subject if it can bind to at least two, or in some cases at least three, class I HLAs of the subject, or at least two, or in some cases at least three, or at least four class II HLAs of the subject.

[0038] The term "personal epitope" or "PEPI" as used herein distinguishes subject-specific epitopes from HLA-specific epitopes. "PEPI" is a polypeptide fragment consisting of a sequence of consecutive amino acids of a polypeptide that is a T cell epitope that can bind to one or more HLA class I molecules of a specific human subject. In other cases, "PEPI" is a polypeptide fragment consisting of a sequence of consecutive amino acids of a polypeptide that is a T cell epitope that can bind to one or more HLA class II molecules of a specific human subject. That is, "PEPI" is a T cell epitope that is recognized by a specific individual's HLA set, and as a result, it is specific to the subject in addition to HLA and antigen. In contrast to "epitopes" that are only specific to HLA and antigen, PEPI is specific to an individual because different individuals have different HLA molecules, which each bind to a different T cell epitope. This subject specificity of PEPI allows the creation of personalized cancer vaccines.

[0039] "PEPI1," as used herein, refers to a peptide or polypeptide fragment that is capable of binding to one HLA class I molecule (or, in certain circumstances, an HLA class II molecule) of an individual. "PEPI1+" refers to a peptide or polypeptide fragment that is capable of binding to one or more HLA class I (or II) molecules of an individual.

[0040] "PEPI2" refers to a peptide or polypeptide fragment capable of binding to two HLA class I (or II) molecules of an individual. "PEPI2+" refers to a peptide or polypeptide fragment capable of binding to two or more HLA class I (or II) molecules of an individual, i.e., a fragment identified according to the methods of the present disclosure.

[0041] "PEPI3" refers to a peptide or polypeptide fragment capable of binding to three HLA class I (or II) molecules of an individual. "PEPI3+" refers to a peptide or polypeptide fragment capable of binding to three or more HLA class I (or II) molecules of an individual.

[0042] "PEPI4" refers to a peptide or polypeptide fragment capable of binding to four HLA class I (or II) molecules of an individual. "PEPI4+" refers to a peptide or polypeptide fragment capable of binding to four or more HLA class I (or II) molecules of an individual.

[0043] "PEPI5" refers to a peptide or polypeptide fragment capable of binding to five HLA class I (or II) molecules of an individual. "PEPI5+" refers to a peptide or polypeptide fragment capable of binding to five or more HLA class I (or II) molecules of an individual.

[0044] "PEPI6" refers to a peptide or polypeptide fragment capable of binding to all six HLA class I (or all six HLA class II) molecules of an individual.

[0045] Generally speaking, epitopes presented by HLA class I molecules are about 9 amino acids long, and epitopes presented by HLA class II molecules are about 15 amino acids long. However, for purposes of this disclosure, epitopes may be longer or shorter than 9 (for HLA class I) or 15 (for HLA class II) amino acids long, so long as they are capable of binding to HLA. For example, epitopes capable of binding to class I HLA may be from 7 amino acids long, or from 8 amino acids long, or from 9 amino acids long, or from 10 amino acids long, or from 11 amino acids long. Epitopes capable of binding to class II HLA may be from 13 amino acids long, or from 14 amino acids long, or from 15 amino acids long, or from 15 amino acids long, or from 16 amino acids long, or from 17 amino acids long.

[0046] The epitopes that bind to known HLA can be determined using techniques known in the art. Any suitable method can be used, as long as the method can be used to determine multiple HLA-epitope binding pairs that are directly compared. For example, biochemical analysis can be used. It is also possible to use a list of epitopes that are known to bind to a given HLA. It is also possible to use predictive or modeling software to determine which epitopes can bind to a given HLA. An example is provided in Table 1. In some cases, a T cell epitope can bind to a given HLA if the IC50 or predicted IC50 is less than 5000nM, less than 2000nM, less than 1000nM, or less than 500nM.

[0047] [Table 1]

[0048] HLA molecules control T cell responses. Until recently, it was thought that triggering of an immune response to an individual epitope was determined by recognition of the epitope by the product of a single HLA allele, i.e., an HLA-restricted epitope. However, HLA-restricted epitopes induce T cell responses in only a small proportion of individuals. Peptides that activate T cell responses in one individual are inactive in another individual, despite matching HLA alleles. Thus, it was unclear how an individual's HLA molecules present antigen-derived epitopes that actively activate T cell responses.

[0049] The inventors have found that in order to trigger a T cell response, multiple HLA expressed by an individual must present the same peptide. Thus, a fragment (epitope) of a polypeptide antigen that is immunogenic for a particular individual (PEPI) is one that can bind to multiple class I (activating CD8+ T cells, e.g., cytotoxic T cells) or class II (activating CD4+ T cells, e.g., helper T cells or CD4+ killer cells) HLA expressed by that individual. This discovery is described in International Application Nos. PCT / EP2018 / 055231, PCT / EP2018 / 055232, PCT / EP2018 / 055230, European Patent Nos. 3370065 and 3369431.

[0050] Polypeptides The present disclosure relates to polypeptides that are derived from CTA and that are immunogenic to a high percentage of the human population.

[0051] As used herein, the term "polypeptide" refers to a peptide characterized as a full-length protein, a portion of a protein, or a chain of amino acids. As used herein, the term "peptide" refers to a short polypeptide that contains 2 or more, or 3 or more, or 4 or more, or 5 or more, or 6 or more, or 7 or more, or 8 or more, or 9 or more, or 10 or more, or 11 or more, or 12 or more, or 13 or more, or 14 or more, or 15 or more, and 10 or less, or 11 or less, or 12 or less, or 13 or less, or 14 or less, or 15 or less, or 20 or less, or 25 or less, or 30 or less, or 35 or less, or 40 or less, or 45 or less, or 50 or less, or 55 or less, or 60 or less amino acids. Polypeptides are typically about 9-50 amino acids in length, or 15-40 amino acids in length, or 20-30 amino acids in length.

[0052] The term "fragment" or "fragment of a polypeptide" as used herein typically refers to a chain of amino acids or an amino acid sequence that is shorter in length than a reference polypeptide and contains an identical amino acid sequence to the reference polypeptide over the common portion. Such a fragment according to the present disclosure may be included in the larger polypeptide of which it is a component, if appropriate. In some cases, the fragment may include the entire polypeptide, for example, when the entire polypeptide, such as a 9 amino acid peptide, is a single T cell epitope. In some cases, the fragment referred to herein may be 2 or more, or 3 or more, or 4 or more, or 5 or more, or 6 or more, or 7 or more, or 8 or more, or 9 or more, and 20 or less, or 25 or less, or 30 or less, or 35 or less, or 40 or less, or 45 or less, or 50 or less amino acids.

[0053] In some embodiments, the peptide of the present disclosure may comprise or consist of one or more fragments of one or more CTAs. CTAs are typically not expressed in healthy cells after embryonic development. In healthy adults, CTA expression is restricted to male germ cells that do not express HLA and cannot present antigens to T cells. Thus, CTAs are considered expressible neoantigens when expressed in cancer cells.

[0054] CTAs are suitable targets for cancer vaccines because their expression is (i) tumor cell specific, (ii) more frequent in metastases than in primary tumors, and (iii) conserved among metastases from the same patient (Gajewski ed. Targeted Therapeutics in Melanoma. Springer New York. 2012).

[0055] Peptides of the present disclosure include DPPA2 (SEQ ID NO: 76, Q7Z7J5.1), CAGE-1 (SEQ ID NO: 77, Q8TC20.1), TSP50 (SEQ ID NO: 78, Q9UI38.1), HIWI (SEQ ID NO: 79, Q96J94.1), SURVIVIN (SEQ ID NO: 80, O15392.1), 5T4 (SEQ ID NO: 81, Q13641.1), PRAME (SEQ ID NO: 82, P78395.1), KK-LC-1 (SEQ ID NO: 83, Q5H943.1), MAGE-A2 (SEQ ID NO: 84, P43356.1), MAGE-A3 (SEQ ID NO: 85, P43357.1), and the like. ), LAGE-1 (SEQ ID NO: 86, O75638.1), MAGE-A10 (SEQ ID NO: 87, P43363.1), MAGE-A1 (SEQ ID NO: 88, P43355.1), and SSX1 (SEQ ID NO: 89, Q16384.1); and / or one or more gastric cancer associated antigens selected from BRDT (SEQ ID NO: 165, Q58F21.1), PRAME (SEQ ID NO: 166, P78395.1), NALP4 (SEQ ID NO: 167, Q96MN2.1), MAGE-A12 (SEQ ID NO: 168, P43365.1), MAGE-A2 (SEQ ID NO: 169, P43356 one or more lung cancer associated antigens selected from: SURVIVIN (SEQ ID NO: 170, O15392.1), DPPA2 (SEQ ID NO: 171, Q7Z7J5.1), NY-SAR-35 (SEQ ID NO: 172, Q8N0W7.1), LDHC (SEQ ID NO: 173, P07864.1), MAGE-C2 (SEQ ID NO: 174, Q9UBF1.1), MAGE-A3 (SEQ ID NO: 175, P43357.1), KK-LC-1 (SEQ ID NO: 176, Q5H943.1), and MAGE-A1 (SEQ ID NO: 177, P43355.1); and / or PRAME (SEQ ID NO: No. 253, P78395.1), MAGE-A2 (SEQ ID NO: 254, P43356.1), MAGE-C1 (SEQ ID NO: 255, P43355.1), SURVIVIN (SEQ ID NO: 256, O15392.1), MAGE-A12 (SEQ ID NO: 257, P43365.1), Ny-ESO-1 (SEQ ID NO: 258, P78358.1), MAGE-C2 (SEQ ID NO: 259, Q9UBF1.1), MAGE-A6 (SEQ ID NO: 260, P43360.1), BORIS (SEQ ID NO: 261, Q8NI51.1), LAGE-1 (SEQ ID NO: 262, O75638.one or more melanoma-associated antigens selected from MAGE-A11 (SEQ ID NO: 263, P43364.1), SSX-1 (SEQ ID NO: 264, Q16384.1), MAGE-A3 (SEQ ID NO: 265, P43357.1), MAGE-A10 (SEQ ID NO: 266, P43363.1), and MAGE-A1 (SEQ ID NO: 267, P43355.1); and / or PIW IL2 (SEQ ID NO: 343, Q8TC59.1), CTAGE1 (SEQ ID NO: 344, Q96RT6.1), MAGE-A9 (SEQ ID NO: 345, P43362.1), EpCAM (SEQ ID NO: 346, P16422.1), OY-TES-1 (SEQ ID NO: 347, Q8NEB7.1), NY-ESO-1 (SEQ ID NO: 348, P78358.1), SURVIVIN (SEQ ID NO: 349, O15392.1), MAGE-C1 (SEQ ID NO: 350, O60732.1), MAGE-A2 (SEQ ID NO: 351, P43356.1), LAGE-1 (SEQ ID NO: 352, O75638.1), MAGE-A3 (SEQ ID NO: 353, P43357.1), MAGE-A8 (SEQ ID NO: 354, P43361.1), HAGE (SEQ ID NO: 355, Q9NXZ2.1), MAGE-A1 (SEQ ID NO: 356, P43355.1), MAGE-C2 (SEQ ID NO: 357, Q9UBF1.1), MAGE-A10 (SEQ ID NO: 358, P43363.1), and MAGE-A12 (SEQ ID NO: 359, P43365.1). .

[0056] In some cases, the amino acid sequence is flanked at the N-terminus and / or C-terminus by additional amino acids that are not part of the sequence of the target polypeptide antigen, i.e., are not the same as the sequence of consecutive amino acids found adjacent to the selected fragment in the target polypeptide antigen. In some cases, the sequence is flanked at the N-terminus and / or C-terminus or between the target polypeptide fragments by up to 41, or 35, or 30, or 25, or 20, or 15, or 10, or 9, or 8, or 7, or 6, or 5, or 4, or 3, or 2, or 1 additional amino acids. In other cases, each polypeptide consists of a fragment of the target polypeptide antigen, or of two or more such fragments arranged end-to-end in a single peptide (sequentially arranged in the peptide end-to-end) or overlapping (where two or more of the fragments contain overlapping sequences, e.g., where two PEPIs in the same polypeptide are within 50 amino acids of each other). Typically, each polypeptide may comprise at least one fragment of a target polypeptide antigen, the fragment comprising an amino acid sequence that is a T cell epitope capable of binding to at least three or at least four HLA class II alleles in some subjects, or a high percentage of subjects, or a maximum percentage of subjects.

[0057] When fragments of different polypeptides or fragments from different regions of the same polypeptide are joined together in an artificial peptide, neoepitopes may be generated around the junction or junction point (Figure 42). Such neoepitopes encompass at least one amino acid from each fragment on either side of the junction or junction and are sometimes referred to herein as junction amino acid sequences. Neoepitopes may induce unwanted T cell responses against healthy cells (autoimmunity). Polypeptides may be designed or screened to avoid, eliminate, or minimize neoepitopes that correspond to fragments of proteins expressed in normal healthy human cells and / or that can bind to at least two, or in some cases at least three, or at least four HLA class I molecules of a subject, or in some cases at least two, or at least three, or four, or five HLA class II molecules of a subject. In some cases, peptides are designed or polypeptides are screened to exclude polypeptides having junction neoepitopes that can bind to at least two HLA class I molecules expressed by individual subjects in a population of human subjects that exceed a threshold percentage of the population. In some cases, the threshold is 20%, or 15%, or 10%, or 5%, or 2%, or 1%, or 0.5% of the population. Alignment can be determined using known methods such as the BLAST algorithm. Software for performing BLAST analysis is publicly available through the National Center for Biotechnology Information (http: / / www.ncbi.nlm.nih.gov / ).

[0058] The presence of at least two polypeptide fragments (epitopes) in a vaccine or immunotherapy composition that can bind to at least three HLA class I of an individual (≧2 PEPI3+) predicts a clinical response. In other words, if two or more PEPI3+ can be identified in the active ingredient polypeptide(s) of a vaccine or immunotherapy composition, the individual is likely to be a clinical responder. The at least two multiple HLA-binding PEPIs of the composition polypeptide may both target a single antigen (e.g., a polypeptide vaccine that includes two multiple HLA-binding PEPIs derived from a single tumor-associated antigen targeted by the vaccine) or may target different antigens (e.g., a polypeptide vaccine that includes one multiple HLA-binding PEPI derived from a tumor-associated antigen and a second multiple HLA-binding PEPI derived from a different tumor-associated antigen).

[0059] Without being bound by theory, the inventors believe that one of the reasons for the increased likelihood of clinical benefit from a vaccine / immunotherapy that includes at least two multiple HLA-binding PEPIs is that disease cell populations, such as cancer or tumor cells, or cells infected with a virus or pathogen, such as HIV, are often heterogeneous both within and between affected subjects. A particular cancer patient may or may not express or overexpress, for example, a particular cancer-associated target polypeptide antigen of the vaccine, or the patient's cancer may include a heterogeneous cell population, some of which (over)express the antigen and some of which do not. Furthermore, the more multiple HLA-binding PEPIs are included or targeted by the vaccine / immunotherapy, the less likely resistance will develop, because the patient is less likely to develop resistance to the composition through mutation of the target PEPI(s).

[0060] Currently, most vaccine and immunotherapy compositions target only a single polypeptide antigen. However, according to the present disclosure, in some cases, it is beneficial to provide a pharmaceutical composition that targets two or more different polypeptide antigens. For example, most cancers or tumors are heterogeneous, which means that different cancer or tumor cells of a subject (over)express different antigens. Also, tumor cells of different cancer patients express different combinations of tumor-associated antigens. Anti-cancer immunogenic compositions that are most likely to be effective are those that target multiple antigens expressed by tumors, and therefore more cancer or tumor cells, in individual human subjects or populations.

[0061] The beneficial effect of combining multiple best EPIs in one treatment (administration of one or more pharmaceutical compositions containing multiple PEPIs together) can be illustrated by the personalized vaccine polypeptide described in Example 21 below. Exemplary CTA expression probabilities in ovarian cancer are as follows: BAGE: 30%; MAGE A9: 37%; MAGE A4: 34%; MAGE A10: 52%. If patient A is treated with a vaccine containing PEPIs only for BAGE and MAGE A9, the probability of having mAGP (multiple expressed antigens with PEPIs) is 11%. If patient A is treated with a vaccine containing PEPIs only for MAGE A4 and MAGE A10 CTAs, the probability of having multiAGP is 19%. However, if the vaccine contains all four of these CTAs (BAGE, MAGE A9, MAGE A4, and MAGE A10), the probability of having mAGP is 50%. That is, the effect is greater than the sum of the probability of both mAGPs from treatment with two PEPIs (probability of mAGPs for BAGE / MAGE + probability of mAGPs for MAGE A4 and MAGE A10). The PIT vaccine for patient A described in Example 21 contains an additional 9 PEPIs, so the probability of having mAGPs is greater than 99.95%.

[0062] Similarly, exemplary CTA expression probabilities in breast cancer are as follows: MAGE C2: 21%; MAGE A1: 37%; SPC1: 38%; MAGE A9: 44%. Treatment of patient B with a vaccine containing PEPI in MAGE C2: 21% and MAGE A1 only has a mAGP probability of 7%. Treatment of patient B with a vaccine containing PEPI in SPC1: 38%; MAGE A9 only has a mAGP probability of 11%. Treatment of patient B with a vaccine containing PEPI in MAGE C2: 21%; MAGE A1: 37%; SPC1: 38%; MAGE A9 only has a mAGP probability of 44% (44>7+11). The patient's PIT vaccine described in Example 21 contains an additional 8 PEPIs, so the probability of having mAGP is greater than 99.93%.

[0063] Thus, in some cases, a polypeptide or panel of polypeptides of the disclosure, or an active ingredient polypeptide of a pharmaceutical composition or kit of the disclosure, may comprise or consist of any combination of 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, or 25 or more fragments of 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, or 25 of a cancer associated antigen or CTA, such as the CTAs listed above. In some cases, each fragment is selected from SEQ ID NOs: 1 to 30, SEQ ID NOs: 31 to 60, SEQ ID NOs: 90 to 119, SEQ ID NOs: 120 to 149, SEQ ID NOs: 178 to 207, SEQ ID NOs: 208 to 237, SEQ ID NOs: 268 to 297, and / or SEQ ID NOs: 298 to 327; or SEQ ID NOs: 1 to 2, or to 3, or to 4, or to 5, or to 6, or to 7, or to 8, or to 9, or to 10, or to 11, or to 12, or to 13, or to 14, or to 15, or to 16, or to 17, or to 18, or to 19, or to 20, or to 21, or to 22, or or selected from SEQ ID NOs: 31 to 32, or to 33, or to 34, or to 35, or to 36, or to 37, or to 38, or to 39, or to 40, or to 41 to 42, or to 43, or to 44, or to 45, or to 46, or to 47, or to 48, or to 49, or to 50, or to 51, or to 52, or to 53, or to 54, or to 55, or to 56, or to 57, or to 58, or to 59;or SEQ ID NO: 90 to 91, or ~92, or ~93, or ~94, or ~95, or ~96, or ~97, or ~98, or ~99, or ~100, or ~101, or ~102, or ~103, or ~104, or ~105, or ~106, or ~107, or ~108, or ~109, or ~110, or ~111, or ~112, or is selected from SEQ ID NOs: 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146, 147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160, 161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 203, 204, 205, 206, 207, 208, 209, 2010, 209, 2011, 5, or ~136, or ~137, or ~138, or ~139, or ~140, or ~141, or ~142, or ~143, or ~144, or ~145, or ~146, or ~147, or ~148, or ~149; or SEQ ID NO: 178 to 179, or ~180, or ~181, or ~182, or ~183, or ~184, or ~185, or selected from -186, or -187, or -188, or -189, or -190, or -191, or -192, or -193, or -194, or -195, or -196, or -197, or -198, or -199, or -200, or -201, or -202, or -203, or -204, or -205, or -206;or SEQ ID NO: 208 to 209, or ~210, or ~211, or ~212, or ~213, or ~214, or ~215, or ~216, or ~217, or ~218, or ~219, or ~220, or ~221, or ~222, or ~223, or ~224, or ~225, or ~226, or ~227, or ~228, or ~229, or ~230, or ~231, or ~232, or ~233, or ~234, or ~235, or SEQ ID NO: 268 to 269, or to 270, or to 271, or to 272, or to 273, or to 274, or to 275, or to 276, or to 277, or to 278, or to 279, or to 280, or to 281, or to 282, or to 283, or to 284, or to 285, or to 286, or to 287, or to 288, or to 289, or to 290, or to 291, or to 292, or to 293, or to 294, or or selected from SEQ ID NOs: 298 to 299, or ~300, or ~301, or ~302, or ~303, or ~304, or ~305, or ~306, or ~307, or ~308, or ~309, or ~310, or ~311, or ~312, or ~313, or ~314, or ~315, or ~316, or ~317, or ~318, or ~319, or ~320, or ~321, or ~322, or or any particular combination of sequences selected from any of these groups of sequences but which are within 50 to 60 amino acids of each other in any one or more of the antigens of SEQ ID NOs: 76 to 89, 165 to 177, 253 to 267, and / or 343 to 359, such as SEQ ID NOs: 3 and 8; SEQ ID NOs: 9 and 10; SEQ ID NOs: 12 and 16; SEQ ID NOs: 13, 18, and 25; SEQ ID NOs: 21 and 24; SEQ ID NOs: 23 and 30; SEQ ID NOs: 93 and 94; SEQ ID NOs: 99, 100, and 102;Each fragment may comprise or consist of a different target epitope having an amino acid sequence other than any combination of SEQ ID NOs: 109 and 111; SEQ ID NOs: 96, 101, and 113; SEQ ID NOs: 188 and 190; and / or SEQ ID NOs: 201 and 203; SEQ ID NOs: 268 and 270; SEQ ID NOs: 271 and 281; SEQ ID NOs: 272 and 275; and / or SEQ ID NOs: 288 and 291. In some cases, each fragment may comprise or consist of a different amino acid sequence selected from SEQ ID NOs: 60 or 61-75; SEQ ID NOs: 150-164; SEQ ID NOs: 238-252; and / or SEQ ID NOs: 328-342.

[0064] In some cases, the disclosure provides panels of two or more of any of the above peptides or peptides, for example, a panel may include 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, or more such peptides.

[0065] Pharmaceutical compositions, methods of treatment, and modes of administration In some aspects, the disclosure relates to pharmaceutical compositions, kits, or panels of polypeptides as described above having one or more polypeptides as active ingredient(s). These may be for use in methods of inducing an immune response, treating, vaccinating, or providing immunotherapy to a subject, and the pharmaceutical compositions may be vaccine or immunotherapy compositions. Such treatments include administering to a subject a pharmaceutical composition that includes one or more polypeptides, or all of the active ingredient polypeptides of the treatment together. Multiple polypeptides or pharmaceutical compositions may be administered together or sequentially, for example, all of the pharmaceutical compositions or polypeptides may be administered to a subject within a period of one year, or six months, or three months, or 60 days, or 50 days, or 40 days, or 30 days.

[0066] The term "active ingredient" as used herein refers to a polypeptide intended to induce an immune response and may include a polypeptide product of a vaccine or immunotherapy composition produced in vivo after administration to a subject. In the case of DNA or RNA immunotherapy compositions, the polypeptide may be produced in vivo by cells of the subject to which the composition is administered. In the case of cell-based compositions, the polypeptide may be processed and / or presented by cells of a composition pulsed with the polypeptide or containing an expression construct encoding the polypeptide, e.g., autologous dendritic cells or antigen-presenting cells. A pharmaceutical composition may include a polynucleotide or cell encoding one or more active ingredient polypeptides.

[0067] The composition / kit may optionally further comprise at least one pharma- ceutically acceptable diluent, carrier, or preservative, and / or an additional polypeptide that does not contain any PEPI. The polypeptide may be artificially produced, i.e., not naturally occurring. The kit may comprise one or more separate containers, each containing one or more of the active ingredient peptides. The composition / kit may be a personalized medicine for preventing, diagnosing, mitigating, treating, or curing a disease in an individual, such as cancer.

[0068] The immunogenic or pharmaceutical compositions or kits described herein may contain, in addition to one or more immunogenic peptides, pharma- ceutically acceptable excipients, carriers, diluents, buffers, stabilizers, preservatives, adjuvants, or other materials well known to those skilled in the art. Such materials are preferably non-toxic and preferably do not interfere with the pharmaceutical activity of the active ingredient(s). The pharmaceutical carrier or diluent may be, for example, a water-containing solution. The exact nature of the carrier or other material may depend on the route of administration, for example, oral, intravenous, cutaneous or subcutaneous, intranasal, intramuscular, intradermal, and intraperitoneal routes.

[0069] The pharmaceutical compositions of the present disclosure may contain one or more "pharmaceutical acceptable carriers". These are typically large, slowly metabolized macromolecules such as proteins, sugars, polylactic acids, polyglycolic acids, polymeric amino acids, amino acid copolymers, sucrose (Paoletti et al., 2001, Vaccine, 19:2118), trehalose (WO 00 / 56365), lactose and lipid aggregates (such as oil droplets or liposomes). Such carriers are well known to those skilled in the art. The pharmaceutical compositions may also contain diluents such as water, saline, glycerol, etc. Additionally, auxiliary substances such as wetting or emulsifying agents, pH buffering substances, etc. may be present. Sterile pyrogen-free phosphate-buffered saline is an exemplary carrier (Gennaro, 2000, Remington: The Science and Practice of Pharmacy, 20th edition, ISBN: 0683306472).

[0070] The pharmaceutical composition of the present disclosure may be lyophilized or in aqueous form, i.e., solution or suspension. This type of liquid formulation is ideal for injection, since it does not need to be reconstituted with an aqueous medium and the composition can be administered directly from the packaged form. The pharmaceutical composition may be provided in a vial or in a pre-filled syringe. The syringe may be supplied with or without a needle. The syringe may contain a single dose, while the vial may contain a single dose or multiple doses.

[0071] The liquid formulation of the present disclosure is also suitable for reconstituting other medicaments from lyophilized form.When the pharmaceutical composition is used for such immediate reconstitution, the present disclosure provides a kit that may include two vials, or may include one pre-filled syringe and one vial, and the contents of the syringe are used to reconstitute the contents of the vial before injection.

[0072] The pharmaceutical compositions of the present disclosure may contain an antibacterial agent, especially when packaged in a multi-dose format. Antibacterial agents such as 2-phenoxyethanol or parabens (methylparaben, ethylparaben, propylparaben) may be used. Any preservatives are preferably present at low levels. Preservatives may be added externally and / or may be a component of the bulk antigens that are mixed to form the composition (e.g., present as a preservative in pertussis antigens).

[0073] Pharmaceutical compositions of the present disclosure may also include detergents, such as Tween (polysorbate), DMSO (dimethylsulfoxide), DMF (dimethylformamide), etc. Detergents are generally present at low levels, e.g., <0.01%, but may be used at higher levels, e.g., 0.01-50%.

[0074] Pharmaceutical compositions of the present disclosure may contain sodium salts (e.g., sodium chloride) and free phosphate ions in solution (e.g., through the use of phosphate buffers).

[0075] In certain embodiments, the pharmaceutical composition may be encapsulated in a suitable vehicle to deliver the peptide to antigen-presenting cells or to enhance stability. As will be appreciated by those skilled in the art, a variety of vehicles are suitable for delivering the pharmaceutical composition of the present disclosure. Non-limiting examples of suitable structured fluid delivery systems include nanoparticles, liposomes, microemulsions, micelles, dendrimers, and other phospholipid-containing systems. Methods for incorporating pharmaceutical compositions into delivery vehicles are known in the art.

[0076] The pharmaceutical composition may also include one or more adjuvants and / or cytokines to enhance the immunogenicity of the composition.

[0077] Suitable adjuvants include aluminum salts, such as aluminum hydroxide or aluminum phosphate, but may also be calcium, iron, or zinc salts, or insoluble suspensions of acylated tyrosine or acylated sugars, or saccharides derivatized with cations or anions, polyphosphazenes, biodegradable microspheres, monophosphoryl lipid A (MPL), lipid A derivatives (e.g., those with reduced toxicity), 3-O-deacylated MPL [3D-MPL], Kir A, saponin, QS21, Freund's incomplete adjuvant (Difco Laboratories, Detroit, Mich.), Merck Adjuvant 65 (Merck and Company, Inc., Rahway, NJ), AS-2 (Smith-Kline The adjuvant may be a medicament for use as an adjuvant in the present disclosure, such as a medicament for use as an adjuvant in the present invention ...

[0078] In some embodiments, the composition comprises an adjuvant selected from the group consisting of Montanide ISA-51 (Seppic, Inc., Fairfield, NJ, United States of America), QS-21 (Aquila Biopharmaceuticals, Inc., Lexington, Mass, United States of America), GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corynbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete and incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, and diphtheria toxin (DT).

[0079] By way of example, the cytokine may be selected from the group consisting of transforming growth factors (TGFs), such as, but not limited to, TGF-α and TGF-β; insulin-like growth factor-I and / or insulin-like growth factor-II; erythropoietin (EPO); osteoinductive factors; interferons, such as, but not limited to, interferon-α, -β, and -γ; colony-stimulating factors (CSFs), such as, but not limited to, macrophage-CSF (M-CSF), granulocyte-macrophage-CSF (GM-CSF), and granulocyte-CSF (G-CSF). In some embodiments, the cytokine is a nerve growth factor, such as NGF-β; platelet growth factor; transforming growth factor (TGF), such as, but not limited to, TGF-α and TGF-β; insulin-like growth factor-I and insulin-like growth factor-II; erythropoietin (EPO); osteoconductive factors; interferons (IFN), such as, but not limited to, IFN-α, IFN-β, and IFN-γ; macrophage-CSF (M-CSF), granulocyte-macrophage-CSF (GM-CSF), and granulocyte-C. The antibody is selected from the group consisting of colony stimulating factors (CSF) such as SF (G-CSF); interleukins (Il) such as, but not limited to, IL-1, IL-1α, 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, IL-15, IL-16, IL-17, IL-18; LIF; Kit-ligand or FLT-3; angiostatin; thrombospondin; endostatin; tumor necrosis factor (TNF); and LT.

[0080] It is expected that the adjuvant or cytokine can be added in an amount of about 0.01 mg to about 10 mg per administration, preferably in an amount of about 0.2 mg to about 5 mg per administration, or alternatively, the adjuvant or cytokine may be at a concentration of about 0.01 to 50%, preferably at a concentration of about 2 to 30%.

[0081] In certain aspects, pharmaceutical compositions of the present disclosure are prepared by physically mixing adjuvants and / or cytokines with peptides of the present disclosure under appropriate sterile conditions according to known techniques to produce the final product.

[0082] Examples of suitable compositions and methods of administration of the polypeptide fragments of the invention are provided in Esseku and Adeyeye (2011) and Van den Mooter G. (2006). The preparation of vaccine and immunotherapy compositions is generally described in Vaccine Design ("The subunit and adjuvant approach" eds Powell MF & Newman MJ (1995) Plenum Press New York). Encapsulation in liposomes, which is also envisaged, is described in U.S. Patent No. 4,235,877 to Fullerton.

[0083] In some embodiments, the compositions disclosed herein are prepared as nucleic acid vaccines. In some embodiments, the nucleic acid vaccine is a DNA vaccine. In some embodiments, the DNA or genetic vaccine comprises a plasmid that includes a promoter and appropriate transcriptional and translational control elements, and a nucleic acid sequence that encodes one or more polypeptides of the present disclosure. In some embodiments, the plasmid also includes sequences for enhancing, for example, expression levels, intracellular targeting, or proteasomal processing. In some embodiments, the DNA vaccine comprises a viral vector that includes a nucleic acid sequence that encodes one or more polypeptides of the present disclosure. In additional aspects, the compositions disclosed herein comprise one or more nucleic acids that encode peptides that are determined to be immunoreactive to a biological sample. For example, in some embodiments, the composition comprises one or more nucleotide sequences encoding 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, or more peptides that contain fragments that are T cell epitopes capable of binding to at least three HLA class I molecules and / or at least three HLA class II molecules of a patient. In some embodiments, the peptides are derived from antigens expressed in the cancer. In some embodiments, the DNA or genetic vaccine also encodes an immunomodulatory molecule to manipulate the resulting immune response, such as to enhance vaccine efficacy, stimulate the immune system, or reduce immunosuppression. Strategies to enhance the immunogenicity of DNA or gene vaccines include encoding heterologous versions of the antigen, fusing the antigen to molecules that activate T cells or trigger associative recognition, priming with a DNA vector followed by boosting with a viral vector, and utilizing immune-modulating molecules. In some embodiments, DNA vaccines are delivered by needle, gene gun, aerosol injector, with a patch, through a microneedle, by abrasion, among other forms.In some forms, the DNA vaccine is incorporated into liposomes or other forms of nanobodies. In some embodiments, the DNA vaccine comprises a delivery system selected from the group consisting of transfection agents; protamine; protamine liposomes; polysaccharide particles; cationic nanoemulsions; cationic polymers; cationic polymer liposomes; cationic nanoparticles; cationic lipid and cholesterol nanoparticles; cationic lipid, cholesterol, and PEG nanoparticles; dendrimer nanoparticles. In some embodiments, the DNA vaccine is administered by inhalation or ingestion. In some embodiments, the DNA vaccine is introduced into the blood, thymus, pancreas, skin, muscle, tumor, or other site.

[0084] In some embodiments, the compositions disclosed herein are prepared as RNA vaccines. In some embodiments, the RNA is non-replicating mRNA or self-amplifying RNA derived from a virus. In some embodiments, the non-replicating mRNA encodes a peptide disclosed herein and contains 5' and 3' untranslated regions (UTRs). In some embodiments, the self-amplifying RNA derived from a virus encodes not only a peptide disclosed herein, but also the viral replication machinery that allows intracellular RNA amplification and expression of large amounts of protein. In some embodiments, the RNA is directly introduced into an individual. In some embodiments, the RNA is chemically synthesized or transcribed in vitro. In some embodiments, the mRNA is generated from a linear DNA template using T7, T3, or Sp6 phage RNA polymerase, and the resulting product contains an open reading frame encoding a peptide disclosed herein, adjacent UTRs, a 5' cap, and a poly(A) tail. In some embodiments, various versions of the 5' cap are added during or after the transcription reaction using vaccinia virus capping enzyme or by incorporating a synthetic cap or anti-reverse cap analog. In some embodiments, an optimal length poly(A) tail is added to the mRNA, either directly from a coding DNA template or by using poly(A) polymerase. The RNA encodes one or more peptides, including fragments that are T cell epitopes capable of binding to at least three HLA class I molecules and / or at least three HLA class II molecules of the patient. In some embodiments, the fragments are derived from antigens expressed in the cancer. In some embodiments, the RNA includes signals to enhance stability and translation. In some embodiments, the RNA also includes non-natural nucleotides to extend half-life or modified nucleotides to alter the immunostimulatory profile. In some embodiments, the RNA is introduced by needle, gene gun, aerosol injector, with a patch, through a microneedle, by abrasion, among other forms.In some forms, the RNA vaccines are incorporated into liposomes or other forms of nanobodies that facilitate cellular uptake of the RNA and protect the RNA from degradation. In some embodiments, the RNA vaccines are combined with transfection agents; protamine; protamine liposomes; polysaccharide particles; cationic nanoemulsions; cationic polymers; cationic polymer liposomes; cationic nanoparticles; cationic lipid and cholesterol nanoparticles; cationic lipid, cholesterol, and PEG nanoparticles; dendrimer nanoparticles; and / or naked mRNA; naked mRNA by in vivo electroporation; mRNA complexed with protamine; mRNA associated with positively charged oil-in-water cationic nanoemulsions; mRNA associated with chemically modified dendrimers and complexed with polyethylene glycol (PEG) lipids. mRNA complexed with protamine in a PEG-lipid nanoparticle; mRNA associated with a cationic polymer such as polyethylenimine (PEI); mRNA associated with a cationic polymer such as PEI and a lipid component; mRNA associated with a polysaccharide (e.g., chitosan) particle or gel; mRNA in a cationic lipid nanoparticle (e.g., 1,2-dioleoyloxy-3-trimethylammoniumpropane (DOTAP) or dioleoylphosphatidylethanolamine (DOPE) lipid); mRNA complexed with a cationic lipid and cholesterol; or mRNA complexed with a cationic lipid, cholesterol, and a PEG-lipid. In some embodiments, the RNA vaccine is administered by inhalation or ingestion. In some embodiments, the RNA is introduced into the blood, thymus, pancreas, skin, muscle, tumor, or other site, and / or by intradermal, intramuscular, subcutaneous, intranasal, intranodal, intravenous, intrasplenic, intratumoral, or other delivery route.

[0085] The polynucleotide or oligonucleotide components may be naked nucleotide sequences or may be combined with cationic lipids, polymers, or targeting systems. They may be delivered by any available technique. For example, polynucleotides or oligonucleotides may be introduced by needle injection, preferably intradermally, subcutaneously, or intramuscularly. Alternatively, polynucleotides or oligonucleotides may be delivered directly across the skin using a delivery device such as particle-mediated gene delivery. Polynucleotides or oligonucleotides may be administered topically to the skin, or to mucosal surfaces, for example, by intranasal, oral, or rectal administration.

[0086] Uptake of polynucleotide or oligonucleotide constructs can be enhanced by several known transfection techniques, including those involving the use of transfection agents. Examples of these agents include cationic agents, such as calcium phosphate and DEAE-dextran, and lipofection agents, such as lipofectam and transfectam. The dosage of polynucleotide or oligonucleotide administered can be varied.

[0087] Typically, a "prophylactically effective amount" or a "therapeutically effective amount" (although in some cases prevention may be considered treatment) is administered, which is an amount sufficient to effect a clinical response or show clinical benefit to the individual, e.g., an amount effective to prevent or delay the onset of a disease or condition, ameliorate one or more symptoms, induce or prolong remission, or delay recurrence or relapse.

[0088] The dose can be determined depending on various parameters, especially the substance used; the age, weight, and condition of the individual to be treated; the route of administration; and the regimen required. The amount of antigen in each dose is selected as an amount that induces an immune response. The physician can determine the route of administration and the dosage required for any particular individual. The dose can be provided as a single dose or as multiple doses, taken at regular intervals, for example, two, three, or four doses every hour. Typically, peptides, polynucleotides, or oligonucleotides are administered in the range of 1 pg to 1 mg, more typically 1 pg to 10 μg for particle-mediated delivery, and 1 μg to 1 mg for other routes, more typically 1 to 100 μg, more typically 5 to 50 μg. Generally, each dose is expected to contain 0.01 to 3 mg of antigen. The optimal amount of a particular vaccine can be ascertained by studies involving observation of immune responses in subjects.

[0089] Examples of the above mentioned techniques and protocols can be found in Remington's Pharmaceutical Sciences, 20th Edition, 2000, pub. Lippincott, Williams & Wilkins.

[0090] In some cases according to the present disclosure, more than one peptide or composition of peptides is administered. Two or more pharmaceutical compositions may be administered together / simultaneously and / or at different times or sequentially. Thus, the present disclosure includes a set of pharmaceutical compositions and their uses. To overcome the challenges of tumor genetic heterogeneity and individual HLA heterogeneity, it is important to use a combination of different peptides, optionally targeting different antigens. Combinations of peptides of the present disclosure are used to expand the population that can experience clinical benefits from vaccination. Multiple pharmaceutical compositions of peptides of the present disclosure manufactured for use in one regimen can define a formulation.

[0091] Routes of administration include, but are not limited to, intranasal, oral, subcutaneous, intradermal, and intramuscular. Subcutaneous administration is particularly preferred. Subcutaneous administration may be performed, for example, by injection into the abdomen, the lateral and anterior parts of the upper arms or thighs, the scapular region of the back, or the upper ventral and dorsal gluteal regions.

[0092] The composition of the present disclosure may also be administered in one or more doses and by other administration routes.For example, such other routes include intradermal, intravenous, intravascular, intraarterial, intraperitoneal, intrathecal, intratracheal, intracardiac, intralobular, intramedullary, intrapulmonary, and intravaginal.Depending on the desired duration of treatment, the composition of the present disclosure may be administered once or several times, and intermittently, for example, monthly, for several months or years, with different dosages.

[0093] The solid dosage form for oral administration includes capsules, tablets, caplets, pills, powders, pellets, and granules.In such solid dosage forms, active ingredient is usually combined with one or more pharma-ceutically acceptable excipients, the examples of which are detailed above.Also, oral agents may be administered as aqueous suspensions, elixirs, or syrups.In these cases, active ingredient may be combined with various sweeteners or flavorings, colorings, and if necessary, emulsifiers and / or suspending agents, as well as diluents such as water, ethanol, glycerin, and combinations thereof.

[0094] One or more compositions of the present disclosure may be administered, or methods and uses for treatment may be practiced according to the present disclosure, alone or in combination with other pharmacological compositions or therapies, such as chemotherapy and / or immunotherapy and / or vaccines. The other therapeutic compositions or therapies may be, for example, one or more of those discussed herein, and may be administered simultaneously or sequentially (before or after) with the compositions or therapies of the present disclosure.

[0095] In some cases, the treatment may be administered in combination with checkpoint blockade therapy, costimulatory antibodies, chemotherapy and / or radiation therapy, targeted therapy, or monoclonal antibody therapy. Chemotherapy has been demonstrated to sensitize tumors to be killed by tumor-specific cytotoxic T cells induced by vaccination (Ramakrishnan et al. J Clin Invest. 2010;120(4):1111-1124). Examples of checkpoint inhibitors are CTLA-4 inhibitors, and ipilimumab, programmed cell death-1 / programmed cell death ligand-1 (PD-1 / PD-L1) signaling inhibitors, nivolumab, pembrolizumab, atezolizumab, and durvalumab. Exemplary chemotherapeutic agents include alkylating agents including nitrogen mustards, e.g., mechlorethamine (HN2), cyclophosphamide, ifosfamide, melphalan (L-sarcolysin), and chlorambucil; anthracyclines; epothilones; nitrosoureas, e.g., carmustine (BCNU), lomustine (CCNU), semustine (methyl-CCNU), and streptozotocin (streptozotocin); triazenes, e.g., decarbazine (DTIC; dimethyltriazenoimidazole-carboxamide; ethylenimine / methylmelamines, e.g., hexamethylmelamine, thiotepa; alkylsulfonates, e.g., busulfan; antimetabolites including folic acid analogs, e.g., methotrexate (amethopterin); alkylating agents , antimetabolites, pyrimidine analogues such as fluorouracil (5-fluorouracil; 5-FU), floxuridine (fluorodeoxyuridine; FUdR), and cytarabine (cytosine arabinoside); purine analogues and related inhibitors such as mercaptopurine (6-mercaptopurine; 6-MP), thioguanine (6-thioguanine; TG), and pentostatin (2'-deoxycoformycin); epipodophyllotoxins; enzymes such as L-asparaginase; biological response modifiers such as IFNα, IL-2, G-CSF, and GM-CSF; platinum coordination complexes such as cisplatin (cis-DDP), oxaliplatin, and carboplatin; anthracenediones such as mitoxantrone and the anthracyclines;Substituted ureas, such as hydroxyurea; methylhydrazine derivatives, including procarbazine (N-methylhydrazine, MIH) and procarbazine; adrenal cortical suppressants, such as mitotane (o,p'-DDD) and aminoglutethimide; taxol and analogs / derivatives; adrenal cortical steroid antagonists, such as prednisone and equivalents, dexamethasone, and aminoglutethimide; progestins, such as hydroxyprogesterone caproate, medroxyprogesterone acetate, and megestrol acetate; estrogens, such as diethylstilbestrol and ethinyl estradiol equivalents; antiestrogens, such as tamoxifen; androgens, antiandrogens, including testosterone propionate and fluoxymesterone equivalents. Hormones and agonists / antagonists, including, for example, flutamide, gonadotropin releasing hormone analogs, and leuprolide, and nonsteroidal antiandrogens, for example, flutamide; vinca alkaloids, for example, vinblastine (VLB) and vincristine, epipodophyllotoxins, for example, etoposide and teniposide, antibiotics, for example, dactinomycin (actinomycin D), daunorubicin (daunomycin; rubidomycin), doxorubicin, bleomycin, plicamycin (mithramycin), and mitomycin (mitomycin C), enzymes, for example, L-asparaginase, and natural products, including biological response modifiers, for example, interferon alphenome;

[0096] In some cases, the method of treatment is a method of vaccination or a method of providing immunotherapy. As used herein, "immunotherapy" refers to preventing or treating a disease or condition by inducing or enhancing an immune response in an individual. In certain embodiments, immunotherapy refers to a treatment comprising administering one or more drugs to an individual to induce a T cell response. In certain embodiments, immunotherapy refers to a treatment comprising administering or expressing a polypeptide containing one or more PEPIs to an individual to induce a T cell response to recognize and kill cells that display one or more PEPIs on their cell surface in association with class I HLA. In another specific embodiment, immunotherapy comprises administering one or more PEPIs to an individual to induce a cytotoxic T cell response against cells that display a tumor-associated antigen (TAA), tumor-specific antigen (TSA), or cancer-testis antigen (CTA) containing the one or more PEPIs on their cell surface. In another embodiment, immunotherapy refers to a treatment comprising administering or expressing a polypeptide containing one or more PEPIs presented by class II HLA to an individual to induce a CD4+ T helper cell or CD4+ killer cell response to provide costimulation to cytotoxic T cells that recognize and kill disease cells that display the one or more PEPIs on their cell surface in conjunction with class I HLA. In yet another specific embodiment, immunotherapy refers to a treatment comprising administering to an individual one or more drugs that reactivate existing T cells to kill target cells. Theoretically, the cytotoxic T cell response will eliminate the cells displaying the one or more PEPIs, thereby improving the clinical condition of the individual. In some instances, immunotherapy may be used to treat tumors. In other instances, immunotherapy can be used to treat diseases or disorders based on intracellular pathogens.

[0097] In some cases, the disclosure relates to the treatment of cancer or solid tumors. In some cases, it is the treatment of gastric cancer, lung cancer, melanoma, and / or bladder cancer. In other cases, it may be the treatment of any other cancer or solid tumor expressing the target tumor-associated antigen of the peptide described herein, or any cancer in which such target polypeptide antigen is expressed in a portion or a high percentage of subjects. It may be the treatment of any cell, tissue, or organ type of cancer or malignant or benign tumor. The cancer may be metastatic or non-metastatic. Exemplary cancers include carcinoma, sarcoma, lymphoma, leukemia, germ cell tumor, or blastoma. The cancer may or may not be a hormone-related or dependent cancer (e.g., estrogen- or androgen-related cancer). The cancer may or may not be associated with or caused by viral infection and / or viral TAA.

[0098] Polypeptides and Patient Selection Certain polypeptide antigens, especially short peptides derived from such antigens that are commonly used in vaccination and immunotherapy, induce immune responses in only a small percentage of human subjects. The polypeptides of the present disclosure are specifically selected to induce immune responses in a high percentage of the general population, but may not be effective in all individuals due to the heterogeneity of HLA genotypes. The heterogeneity of HLA genotype populations means that immune or clinical response rates to the vaccines described herein differ between different human subpopulations. In some cases, the vaccines described herein are for use in treating specific or targeted subpopulations, such as, for example, Asian populations, or Vietnamese, Chinese, and / or Japanese populations.

[0099] The present disclosure also provides methods for identifying human subjects likely to have a CD8+ or cytotoxic T cell response (prospective responders) to administration of a pharmaceutical composition comprising a peptide of the present disclosure, or for predicting the likelihood that a subject will have a cytotoxic T cell response.

[0100] As provided herein, in order to trigger a T cell response, it is generally necessary for a T cell epitope to be presented by multiple HLAs of an individual.The inventors have determined that the best predictor of cytotoxic T cell response to a given polypeptide is the presence of at least one T cell epitope presented by three or more HLA class I of an individual (≧1 PEPI3+).Therefore, if one or more T cell epitopes that can bind to at least three HLAs of a subject are present in the active ingredient peptide of a pharmaceutical composition, it is predicted that the subject will have a cytotoxic T cell response to administration of the pharmaceutical composition.This subject is a potential immune responder.

[0101] In some cases, the T cell epitope capable of binding to at least three HLA class I of the subject has an amino acid sequence of any one of SEQ ID NOs: 1-30. In other cases, the T cell epitope may have a different amino acid sequence within one or more peptides of the pharmaceutical composition.

[0102] The inventors further found that the presence of at least two epitopes capable of binding to at least three HLAs of an individual in a vaccine or immunotherapy composition predicts clinical response. That is, if an individual has a total of two or more PEPI3+ in the active ingredient polypeptide(s) of the vaccine or immunotherapy composition, and these PEPI3+ are derived from antigen sequences that are actually expressed in the individual (e.g., the individual's target tumor cells express the target tumor-associated antigen), the individual is likely to be a clinical responder (i.e., a clinically relevant immune responder).

[0103] Thus, some aspects of the present disclosure relate to methods of identifying subjects likely to have a clinical response or predicting the likelihood that a subject will have a clinical response to a treatment method according to the present disclosure. "Clinical response" or "clinical benefit" as used herein may be prevention or delay of onset of a disease or condition, amelioration of one or more symptoms, induction or prolongation of remission, or delay of recurrence or relapse or worsening, or any other improvement or stabilization in a subject's disease state. Where appropriate, "clinical response" may correlate with "disease control" or "objective response" as defined by RECIST (Response Evaluation Criteria in Solid Tumors) guidelines.

[0104] In some embodiments, the method comprises the step of detecting the gastric cancer antigens DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1 SSX1, and / or the lung cancer antigens BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, MAGE-A1, and / or the melanoma cancer antigens PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX and determining that one or more cancer associated antigens selected from bladder cancer antigens PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, and HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12 are expressed in the cancer. For example, expression of the cancer associated antigens can be detected in a sample obtained from the subject, e.g., a tumor biopsy, using methods known in the art.

[0105] The inventors have found that it is insufficient for a vaccine or immunotherapy composition to target an antigen expressed by a patient's cancer or tumor cells, nor for the target sequence of that antigen to be able to bind to the patient's HLA class I (HLA-restricted epitope). The composition is likely to be effective only in patients who express the target antigen and have three or more different HLA class I molecules that bind to the same sequence of T cell epitopes of the target antigen. Furthermore, as mentioned above, at least two epitopes that bind to at least three HLAs of the patient are generally required to induce a clinically relevant immune response.

[0106] Thus, the method further includes determining that the active ingredient peptide(s) of the pharmaceutical composition comprises two or more different amino acid sequences, each of which is: a) a fragment of a cancer-associated antigen expressed by cancer cells of the subject, determined as described above; and b) a T cell epitope capable of binding to at least three HLA class I molecules of the subject.

[0107] In some cases, the likelihood of a subject having a clinical response to a peptide vaccine or immunotherapy composition such as those described herein can be determined without knowing whether the target antigen is expressed in the subject's cancer or tumor cells and / or without determining the subject's HLA class I genotype. Known antigen expression frequency in the disease (e.g., MAGE-A3 in tumor types such as gastric cancer, lung cancer, melanoma, or bladder cancer) and / or known frequency of the subject's HLA class I and class II genotype in the target population (e.g., ethnic population, general population, disease population) may be used instead. Furthermore, as identified and described herein, by combining peptides targeting the most frequently presented PEPIs (best EPIs) across the entire population in multiple target antigens frequently expressed in the disease, it is possible to design a cancer vaccine regime that is effective for a high proportion of patients. However, using the companion diagnostic methods described herein to preselect patients most likely to have a clinical response increases the clinical response rate among treated patients.

[0108] The likelihood that a subject will respond to treatment is increased by (i) the presence of more multiple HLA-binding PEPIs in the active ingredient polypeptide, (ii) the presence of more PEPIs in the target polypeptide antigen, and (iii) the expression of the target polypeptide antigen in the subject or in the diseased cells of the subject. In some cases, the expression of the target polypeptide antigen in the subject may be known, such as when the target polypeptide antigen is present in a sample obtained from the subject. In other cases, the probability that a particular subject or diseased cells of a particular subject (over)express a particular or any combination of target polypeptide antigens can be determined using population frequency data, for example the probability of expression of the antigen in gastric cancer, lung cancer, melanoma, or bladder cancer. The population frequency data can be for a subject and / or a disease-matched population, or a treatment intended population. For example, the frequency or probability of expression of a particular cancer-associated antigen in a subject with a particular cancer, such as gastric cancer, can be determined by detecting the antigen in a tumor sample, for example a tumor sample of gastric cancer. In some cases, such frequencies can be determined from published figures and scientific publications. In some cases, the methods of the disclosure include determining the frequency of expression of the relevant target polypeptide antigen in a relevant population.

[0109] A variety of pharmacodynamic biomarkers have been disclosed for predicting vaccine activity / efficacy in individual human subjects and populations of human subjects. These biomarkers can be used to facilitate the development of more effective vaccines and reduce development costs, and to evaluate and compare different compositions. Exemplary biomarkers are:

[0110] ·AG95 or AG50 - Vaccine Potency: The number of antigens in a cancer vaccine that a particular tumor type expresses with a 95% or 50% probability. AG95 and AG50 are indicators of vaccine potency and are independent of the immunogenicity of the vaccine antigens. AG95 and AG50 are calculated from tumor antigen expression data. Such data can be obtained from experiments published in peer-reviewed scientific journals. Technically, AG95 and AG50 are derived from a binomial distribution of antigens in the vaccine, taking into account all possible variations and expression rates.

[0111] PEPI3+ count - immunogenicity of the vaccine in a subject: PEPI3+ from the vaccine is a personal epitope that binds to at least three HLAs of the subject and induces a T cell response. PEPI3+ can be determined using the PEPI3+ test in subjects whose 4-digit HLA genotype is fully known.

[0112] AP count - antigenicity of the vaccine in the subject: the number of vaccine antigens with PEPI3+. The vaccine contains sequences from the target polypeptide antigens expressed by disease cells. AP count is the number of antigens in the vaccine that contain PEPI3+, and AP count represents the number of antigens in the vaccine that can induce a T cell response in the subject. AP count characterizes the vaccine antigen-specific T cell response of the subject, since it depends only on the subject's HLA genotype and is independent of the subject's disease, age, and medication. The exact value is between 0 (no antigens present PEPI) and the maximum number of antigens (all antigens present PEPI).

[0113] AP50 - antigenicity of a vaccine in a population: the average number of vaccine antigens with PEPI in a population. AP50 depends on the HLA genotype of the subjects in the population and is therefore suitable for characterizing vaccine antigen-specific T cell responses in a given population.

[0114] AGP Count - Vaccine efficacy in a subject: number of vaccine antigens expressed in tumors with PEPI. AGP Count indicates the number of tumor antigens that the vaccine recognizes and against which it induces a T cell response (hits the target). AGP Count depends on the vaccine antigen expression rate in the subject's tumor and on the subject's HLA genotype. The exact value is between 0 (no antigens present PEPI) and the maximum number of antigens (all antigens present PEPI).

[0115] · AGP50 - efficacy of cancer vaccine in a population: the average number of vaccine antigens expressed in a given tumor with PEPI in the population (i.e., AGP). AGP50 indicates the average number of tumor antigens that can be recognized by the T cell response induced by the vaccine. AGP50 depends on the expression rate of the antigen in a given tumor type and the immunogenicity of the antigen in the target population. AGP50 can estimate the efficacy of a vaccine in different populations and can also be used to compare different vaccines in the same population. The computational calculation of AGP50 is similar to that used for AG50, except that the expression is weighted by the occurrence rate of PEPI3+ in the subjects in the expressed vaccine antigen. In a theoretical population where each subject has PEPI from each vaccine antigen, AGP50 will be equal to AG50. In another theoretical population where there are no subjects with PEPI from any vaccine antigen, AGP50 will be 0. In general, the following statement is valid: 0≦AGP50≦AG50.

[0116] · mAGP - A potential biomarker for selecting potential responders: the likelihood that a cancer vaccine will induce a T cell response against multiple antigens expressed in a given tumor. mAGP is calculated from the expression rate of vaccine antigens in the tumor and the presence of vaccine-derived PEPIs in the subject. Technically, based on the AGP distribution, mAGP is the sum of the probabilities of multiple AGPs (2 or more AGPs).

[0117] Such prediction results can be used to inform a physician's decision regarding the treatment of a subject. Thus, in some cases, the method of the present disclosure predicts that a subject will have or is likely to have a T cell response and / or clinical response to a treatment described herein, and the method further comprises selecting a treatment for each human subject. In some cases, a subject is selected for treatment if the likelihood of a response targeting a predetermined number of target polypeptide antigens, optionally expressed (predicted to be expressed), is above a predetermined threshold. In some cases, the number of target polypeptide antigens or epitopes is two. In some cases, the number of target polypeptide antigens or epitopes is three, or four, or five, or six, or seven, or eight, or nine, or ten. The method may further comprise administering the treatment to the human subject. Alternatively, the method may predict that a subject will not have an immune response and / or clinical response, and may further comprise selecting a different treatment for each subject.

[0118] Further embodiments of the present disclosure - (1A) - Gastric cancer 1. A pharmaceutical composition comprising one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 61 to 75.

[0119] 2. The pharmaceutical composition according to item 1, comprising 2 or more peptides, 3 or more peptides, 4 or more peptides, 5 or more peptides, 6 or more peptides, 7 or more peptides, 8 or more peptides, 9 or more peptides, 10 or more peptides, 11 or more peptides, or 12 or more peptides.

[0120] 3. The pharmaceutical composition according to item 1, further comprising at least one additional peptide comprising a fragment of an antigen selected from DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and SSX1.

[0121] 4. The pharmaceutical composition according to item 3, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 1 to 30.

[0122] 5. The pharmaceutical composition according to item 3, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 31 to 60.

[0123] 6. The pharmaceutical composition according to item 1, further comprising a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0124] 7. The pharmaceutical composition according to item 6, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0125] 8. A pharmaceutical composition comprising one or more nucleic acid molecules encoding one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 61-75.

[0126] 9. The pharmaceutical composition according to item 8, wherein the one or more nucleic acid molecules encode two or more peptides, three or more peptides, four or more peptides, five or more peptides, six or more peptides, seven or more peptides, eight or more peptides, nine or more peptides, ten or more peptides, eleven or more peptides, or twelve or more peptides.

[0127] 10. The pharmaceutical composition of item 8, wherein the one or more nucleic acid molecules encode at least one additional peptide comprising a fragment of an antigen selected from DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and SSX1.

[0128] 11. The pharmaceutical composition according to item 10, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 1 to 30.

[0129] 12. The pharmaceutical composition according to item 10, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 31 to 60.

[0130] 13. The pharmaceutical composition according to item 8, further comprising a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0131] 14. The pharmaceutical composition according to item 13, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0132] 15. A method for identifying and treating a human subject having cancer who is likely to have a clinical response to administration of the pharmaceutical composition according to item 1, comprising: (i) assaying a biological sample from the subject to determine the HLA genotype of the subject; (ii) determining that the pharmaceutical composition comprises two or more sequences that are T cell epitopes capable of binding to at least three HLA class I molecules of the subject; (iii) using the population expression data for each antigen to determine the probability that the subject's tumor expresses one or more antigens corresponding to the T cell epitopes identified in step (ii) to identify the likelihood that the subject will have a clinical response to administration of the pharmaceutical composition; (iv) administering to the identified subject the composition described in item 1; The method includes:

[0133] 16. The method of claim 15, wherein the subject has gastric cancer.

[0134] 17. The method of claim 15, wherein the pharmaceutical composition comprises two or more peptides, three or more peptides, four or more peptides, five or more peptides, six or more peptides, seven or more peptides, eight or more peptides, nine or more peptides, ten or more peptides, eleven or more peptides, or twelve or more peptides.

[0135] 18. The method of claim 15, wherein the pharmaceutical composition further comprises at least one additional peptide comprising a fragment of an antigen selected from DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and SSX1.

[0136] 19. The method according to item 18, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 1 to 30.

[0137] 20. The method according to item 18, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 31 to 60.

[0138] 21. The method of claim 15, wherein the pharmaceutical composition further comprises a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0139] 22. The method according to item 21, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0140] 23. The method of claim 15, further comprising administering to the identified subject a chemotherapeutic agent, a checkpoint inhibitor, a targeted therapy, radiation therapy, another immunotherapy, a neoadjuvant therapy, or a combination thereof.

[0141] 24. Prior to the administration step: (i) assaying a tumor sample from the subject to determine whether the three or more peptides of the pharmaceutical composition comprise two or more different amino acid sequences, each of which is a. a fragment of a cancer-associated antigen expressed by the cancer cells of the subject as determined in step (i); and b. a T cell epitope capable of binding to at least three HLA class I molecules of the subject determining that; (ii) identifying the subject as likely to have a clinical response to the treatment method; 16. The method of claim 15, further comprising:

[0142] 25. A method for identifying and treating a human subject with cancer who is likely to have an immune response to administration of the pharmaceutical composition according to item 1, comprising: (i) assaying a biological sample from the subject to determine the HLA genotype of the subject; (ii) determining that the pharmaceutical composition comprises one or more sequences that are T cell epitopes capable of binding to at least three HLA class I molecules of the subject; (iii) administering to the identified subject the composition described in item 1; The method includes:

[0143] 26. a. a first pharmaceutical composition comprising one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 61 to 75; b. a second, different pharmaceutical composition comprising one or more peptides, each peptide comprising a different one of the amino acid sequences set forth in SEQ ID NOs: 61-75; Kit including:

[0144] 27. A pharmaceutical composition comprising a nucleic acid molecule expressing two or more polypeptides, each polypeptide comprising a fragment of up to 50 consecutive amino acids of an antigen selected from DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and SSX1, and each fragment comprising a different amino acid sequence selected from any one of SEQ ID NOs: 1 to 30.

[0145] Further embodiments of the present disclosure - (1B) - Lung cancer 1. A pharmaceutical composition comprising one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 150 to 164.

[0146] 2. The pharmaceutical composition according to item 1, comprising 2 or more peptides, 3 or more peptides, 4 or more peptides, 5 or more peptides, 6 or more peptides, 7 or more peptides, 8 or more peptides, 9 or more peptides, 10 or more peptides, 11 or more peptides, or 12 or more peptides.

[0147] 3. The pharmaceutical composition according to item 1, further comprising at least one additional peptide comprising a fragment of an antigen selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1.

[0148] 4. The pharmaceutical composition according to item 3, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 90 to 119.

[0149] 5. The pharmaceutical composition according to item 3, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 120 to 149.

[0150] 6. The pharmaceutical composition according to item 1, further comprising a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0151] 7. The pharmaceutical composition according to item 6, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0152] 8. A pharmaceutical composition comprising one or more nucleic acid molecules encoding one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 150 to 164.

[0153] 9. The pharmaceutical composition according to item 8, wherein the one or more nucleic acid molecules encode two or more peptides, three or more peptides, four or more peptides, five or more peptides, six or more peptides, seven or more peptides, eight or more peptides, nine or more peptides, ten or more peptides, eleven or more peptides, or twelve or more peptides.

[0154] 10. The pharmaceutical composition of item 8, wherein the one or more nucleic acid molecules encode at least one additional peptide comprising a fragment of an antigen selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1.

[0155] 11. The pharmaceutical composition according to item 10, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 90 to 119.

[0156] 12. The pharmaceutical composition according to item 10, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 120 to 149.

[0157] 13. The pharmaceutical composition according to item 8, further comprising a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0158] 14. The pharmaceutical composition according to item 13, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0159] 15. A method for identifying and treating a human subject having cancer who is likely to have a clinical response to administration of the pharmaceutical composition according to item 1, comprising: (i) assaying a biological sample from the subject to determine the HLA genotype of the subject; (ii) determining that the pharmaceutical composition comprises two or more sequences that are T cell epitopes capable of binding to at least three HLA class I molecules of the subject; (iii) using the population expression data for each antigen to determine the probability that the subject's tumor expresses one or more antigens corresponding to the T cell epitopes identified in step (ii) to identify the likelihood that the subject will have a clinical response to administration of the pharmaceutical composition; (iv) administering to the identified subject the composition described in item 1; The method includes:

[0160] 16. The method of claim 15, wherein the subject has lung cancer.

[0161] 17. The method of claim 15, wherein the pharmaceutical composition comprises two or more peptides, three or more peptides, four or more peptides, five or more peptides, six or more peptides, seven or more peptides, eight or more peptides, nine or more peptides, ten or more peptides, eleven or more peptides, or twelve or more peptides.

[0162] 18. The method of claim 15, wherein the pharmaceutical composition further comprises at least one additional peptide comprising a fragment of an antigen selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1.

[0163] 19. The method according to item 18, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 90 to 119.

[0164] 20. The method according to item 18, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 120 to 149.

[0165] 21. The method of claim 15, wherein the pharmaceutical composition further comprises a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0166] 22. The method according to item 21, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0167] 23. The method of claim 15, further comprising administering to the identified subject a chemotherapeutic agent, a checkpoint inhibitor, a targeted therapy, radiation therapy, another immunotherapy, a neoadjuvant therapy, or a combination thereof.

[0168] 24. Prior to the administration step: (i) assaying a tumor sample from the subject to determine whether the three or more peptides of the pharmaceutical composition comprise two or more different amino acid sequences, each of which is a. a fragment of a cancer-associated antigen expressed by the cancer cells of the subject as determined in step (i); and b. a T cell epitope capable of binding to at least three HLA class I molecules of the subject determining that; (ii) identifying the subject as likely to have a clinical response to the treatment method; 16. The method of claim 15, further comprising:

[0169] 25. A method for identifying and treating a human subject with cancer who is likely to have an immune response to administration of the pharmaceutical composition according to item 1, comprising: (i) assaying a biological sample from the subject to determine the HLA genotype of the subject; (ii) determining that the pharmaceutical composition comprises one or more sequences that are T cell epitopes capable of binding to at least three HLA class I molecules of the subject; (iii) administering to the identified subject the composition described in item 1; The method includes: 26. a. a first pharmaceutical composition comprising one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 150 to 164; b. a second, different pharmaceutical composition comprising one or more peptides, each peptide comprising a different one of the amino acid sequences set forth in SEQ ID NOs: 150 to 164; Kit including:

[0170] 27. A pharmaceutical composition comprising a nucleic acid molecule expressing two or more polypeptides, each polypeptide comprising a fragment of up to 50 consecutive amino acids of an antigen selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1, and each fragment comprising a different amino acid sequence selected from any one of SEQ ID NOs: 90 to 119.

[0171] Further embodiments of the present disclosure - (1C) - Melanoma 1. A pharmaceutical composition comprising one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 238 to 252.

[0172] 2. The pharmaceutical composition according to item 1, comprising 2 or more peptides, 3 or more peptides, 4 or more peptides, 5 or more peptides, 6 or more peptides, 7 or more peptides, 8 or more peptides, 9 or more peptides, 10 or more peptides, 11 or more peptides, or 12 or more peptides.

[0173] 3. The pharmaceutical composition according to item 1, further comprising at least one additional peptide comprising a fragment of an antigen selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1.

[0174] 4. The pharmaceutical composition according to item 3, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 178 to 207.

[0175] 5. The pharmaceutical composition according to item 3, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 208 to 237.

[0176] 6. The pharmaceutical composition according to item 1, further comprising a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0177] 7. The pharmaceutical composition according to item 6, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0178] 8. A pharmaceutical composition comprising one or more nucleic acid molecules encoding one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 61-75.

[0179] 9. The pharmaceutical composition according to item 8, wherein the one or more nucleic acid molecules encode two or more peptides, three or more peptides, four or more peptides, five or more peptides, six or more peptides, seven or more peptides, eight or more peptides, nine or more peptides, ten or more peptides, eleven or more peptides, or twelve or more peptides.

[0180] 10. The pharmaceutical composition of item 8, wherein the one or more nucleic acid molecules encode at least one additional peptide comprising a fragment of an antigen selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1.

[0181] 11. The pharmaceutical composition according to item 10, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 178 to 207.

[0182] 12. The pharmaceutical composition according to item 10, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 208 to 237.

[0183] 13. The pharmaceutical composition according to item 8, further comprising a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0184] 14. The pharmaceutical composition according to item 13, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0185] 15. A method for identifying and treating a human subject having cancer who is likely to have a clinical response to administration of the pharmaceutical composition according to item 1, comprising: (i) assaying a biological sample from the subject to determine the HLA genotype of the subject; (ii) determining that the pharmaceutical composition comprises two or more sequences that are T cell epitopes capable of binding to at least three HLA class I molecules of the subject; (iii) using the population expression data for each antigen to determine the probability that the subject's tumor expresses one or more antigens corresponding to the T cell epitopes identified in step (ii) to identify the likelihood that the subject will have a clinical response to administration of the pharmaceutical composition; (iv) administering to the identified subject the composition described in item 1; The method includes:

[0186] 16. The method of claim 15, wherein the subject has melanoma.

[0187] 17. The method of claim 15, wherein the pharmaceutical composition comprises two or more peptides, three or more peptides, four or more peptides, five or more peptides, six or more peptides, seven or more peptides, eight or more peptides, nine or more peptides, ten or more peptides, eleven or more peptides, or twelve or more peptides.

[0188] 18. The method of claim 15, wherein the pharmaceutical composition further comprises at least one additional peptide comprising a fragment of an antigen selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1.

[0189] 19. The method according to item 18, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 178 to 207.

[0190] 20. The method according to item 18, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 208 to 237.

[0191] 21. The method of claim 15, wherein the pharmaceutical composition further comprises a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0192] 22. The method according to item 21, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0193] 23. The method of claim 15, further comprising administering to the identified subject a chemotherapeutic agent, a checkpoint inhibitor, a targeted therapy, radiation therapy, another immunotherapy, a neoadjuvant therapy, or a combination thereof.

[0194] 24. Prior to the administration step: (iii) assaying a tumor sample from the subject to determine whether the three or more peptides of the pharmaceutical composition comprise two or more different amino acid sequences, each of which is c. a fragment of a cancer-associated antigen expressed by the cancer cells of the subject determined in step (i); and d. T cell epitopes capable of binding to at least three HLA class I molecules of the subject. determining that; (iv) identifying the subject as likely to have a clinical response to the treatment method; 16. The method of claim 15, further comprising:

[0195] 25. A method for identifying and treating a human subject with cancer who is likely to have an immune response to administration of the pharmaceutical composition according to item 1, comprising: (i) assaying a biological sample from the subject to determine the HLA genotype of the subject; (ii) determining that the pharmaceutical composition comprises one or more sequences that are T cell epitopes capable of binding to at least three HLA class I molecules of the subject; (iii) administering to the identified subject the composition described in item 1; The method includes:

[0196] 26. a. a first pharmaceutical composition comprising one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 238 to 267; b. a second, different pharmaceutical composition comprising one or more peptides, each peptide comprising a different one of the amino acid sequences set forth in SEQ ID NOs: 238-267; Kit including:

[0197] 27. A pharmaceutical composition comprising a nucleic acid molecule expressing two or more polypeptides, each polypeptide comprising a fragment of up to 50 consecutive amino acids of an antigen selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1, and each fragment comprising a different amino acid sequence selected from any one of SEQ ID NOs: 178 to 207.

[0198] Further embodiments of the present disclosure - (1D) - Bladder cancer 1. A pharmaceutical composition comprising one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 328 to 342.

[0199] 2. The pharmaceutical composition according to item 1, comprising 2 or more peptides, 3 or more peptides, 4 or more peptides, 5 or more peptides, 6 or more peptides, 7 or more peptides, 8 or more peptides, 9 or more peptides, 10 or more peptides, 11 or more peptides, or 12 or more peptides.

[0200] 3. The pharmaceutical composition according to item 1, further comprising at least one additional peptide comprising a fragment of an antigen selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12.

[0201] 4. The pharmaceutical composition according to item 3, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 268 to 297.

[0202] 5. The pharmaceutical composition according to item 3, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 298 to 327.

[0203] 6. The pharmaceutical composition according to item 1, further comprising a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0204] 7. The pharmaceutical composition according to item 6, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0205] 8. A pharmaceutical composition comprising one or more nucleic acid molecules encoding one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 328-342.

[0206] 9. The pharmaceutical composition according to item 8, wherein the one or more nucleic acid molecules encode two or more peptides, three or more peptides, four or more peptides, five or more peptides, six or more peptides, seven or more peptides, eight or more peptides, nine or more peptides, ten or more peptides, eleven or more peptides, or twelve or more peptides.

[0207] 10. The pharmaceutical composition of item 8, wherein the one or more nucleic acid molecules encode at least one additional peptide comprising a fragment of an antigen selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12.

[0208] 11. The pharmaceutical composition according to item 10, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 268 to 297.

[0209] 12. The pharmaceutical composition according to item 10, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 298 to 327.

[0210] 13. The pharmaceutical composition according to item 8, further comprising a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0211] 14. The pharmaceutical composition according to item 13, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0212] 15. A method for identifying and treating a human subject having cancer who is likely to have a clinical response to administration of the pharmaceutical composition according to item 1, comprising: (i) assaying a biological sample from the subject to determine the HLA genotype of the subject; (ii) determining that the pharmaceutical composition comprises two or more sequences that are T cell epitopes capable of binding to at least three HLA class I molecules of the subject; (iii) using the population expression data for each antigen to determine the probability that the subject's tumor expresses one or more antigens corresponding to the T cell epitopes identified in step (ii) to identify the likelihood that the subject will have a clinical response to administration of the pharmaceutical composition; (iv) administering to the identified subject the composition described in item 1; The method includes:

[0213] 16. The method of claim 15, wherein the subject has bladder cancer.

[0214] 17. The method of claim 15, wherein the pharmaceutical composition comprises two or more peptides, three or more peptides, four or more peptides, five or more peptides, six or more peptides, seven or more peptides, eight or more peptides, nine or more peptides, ten or more peptides, eleven or more peptides, or twelve or more peptides.

[0215] 18. The method of claim 15, wherein the pharmaceutical composition further comprises at least one additional peptide comprising a fragment of an antigen selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12.

[0216] 19. The method according to item 18, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 268 to 297.

[0217] 20. The method according to item 18, wherein the antigen fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 298 to 327.

[0218] 21. The method of claim 15, wherein the pharmaceutical composition further comprises a pharma- ceutically acceptable adjuvant, diluent, carrier, preservative, or a combination thereof.

[0219] 22. The method according to item 21, wherein the adjuvant is selected from the group consisting of Montanide ISA-51, QS-21, GM-CSF, cyclofosamide, Bacillus Calmette-Guerin (BCG), Corymbacterium parvum, levamisole, azimezone, isoprinisone, dinitrochlorobenzene (DNCB), keyhole limpet hemocyanin (KLH), Freund's adjuvant (complete), Freund's adjuvant (incomplete), mineral gel, aluminum hydroxide (Alum), lysolecithin, pluronic polyols, polyanions, oil emulsions, dinitrophenol, diphtheria toxin (DT), and combinations thereof.

[0220] 23. The method of claim 15, further comprising administering to the identified subject a chemotherapeutic agent, a checkpoint inhibitor, a targeted therapy, radiation therapy, another immunotherapy, a neoadjuvant therapy, or a combination thereof.

[0221] 24. Prior to the administration step: (v) assaying a tumor sample from the subject to determine whether the three or more peptides of the pharmaceutical composition comprise two or more different amino acid sequences, each of which is e. a fragment of a cancer-associated antigen expressed by the cancer cells of the subject determined in step (i); and f. a T cell epitope capable of binding to at least three HLA class I molecules of the subject determining that; (vi) identifying the subject as likely to have a clinical response to the treatment method; 16. The method of claim 15, further comprising:

[0222] 25. A method for identifying and treating a human subject with cancer who is likely to have an immune response to administration of the pharmaceutical composition according to item 1, comprising: (i) assaying a biological sample from the subject to determine the HLA genotype of the subject; (ii) determining that the pharmaceutical composition comprises one or more sequences that are T cell epitopes capable of binding to at least three HLA class I molecules of the subject; (iii) administering to the identified subject the composition described in item 1; The method includes:

[0223] 26. a. a first pharmaceutical composition comprising one or more peptides, each peptide comprising a different amino acid sequence selected from any one of SEQ ID NOs: 328-342; b. a second, different pharmaceutical composition comprising one or more peptides, each peptide comprising a different one of the amino acid sequences set forth in SEQ ID NOs: 328-342; Kit including:

[0224] 27. A pharmaceutical composition comprising a nucleic acid molecule expressing two or more polypeptides, each polypeptide comprising a fragment of up to 50 consecutive amino acids of an antigen selected from up to 50 consecutive amino acids of an antigen selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12, each fragment comprising a different amino acid sequence selected from any one of SEQ ID NOs: 268-297.

[0225] Further embodiments of the present disclosure - (2B) - Lungs 1. A polypeptide comprising a fragment of up to 50 consecutive amino acids of a lung cancer associated antigen selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1, wherein the fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 90 to 119, and optionally the fragment is flanked at the N- and / or C-terminus by additional amino acids that are not part of the sequence of the lung cancer associated antigen.

[0226] 2. a. A fragment of a lung cancer-associated antigen selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1, the fragment comprising an amino acid sequence selected from any one of SEQ ID NOs: 90 to 119; or b. The polypeptide according to item 1, comprising two or more fragments of one or more lung cancer-associated antigens selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1, each of which comprises a different amino acid sequence selected from any one of SEQ ID NOs: 90 to 119, and optionally comprising or consisting of fragments that are overlapping or end-to-end in the polypeptide.

[0227] 3. The polypeptide according to item 1 or 2, wherein the polypeptide comprises or consists of fragments of at least two different cancer-associated antigens, the cancer-associated antigens being selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1, and each fragment comprises a different amino acid sequence selected from SEQ ID NOs: 90 to 119.

[0228] 4. The polypeptide according to any one of items 1 to 3, comprising or consisting of one or more amino acid sequences selected from SEQ ID NOs: 120 to 149.

[0229] 5. A polypeptide according to any one of items 1 to 4, comprising or consisting of an amino acid sequence set forth in any one of SEQ ID NOs: 150 to 164.

[0230] 6. A panel of two or more polypeptides according to any one of items 1 to 5, wherein each polypeptide comprises a different amino acid sequence selected from SEQ ID NOs: 90 to 119.

[0231] 7. A pharmaceutical composition or kit comprising one or more polypeptides according to any one of items 1 to 5, or a panel of polypeptides according to item 6, or a polypeptide comprising at least two amino acid sequences selected from SEQ ID NOs: 90 to 119, or one or more polynucleic acids or vectors encoding the one or more polypeptides.

[0232] 8. A vaccination method for providing immunotherapy or inducing a cytotoxic T cell response in a subject, comprising administering to the subject a pharmaceutical composition or a peptide, polynucleic acid or vector of the kit according to item 7.

[0233] 9. The method of item 8, which is a method for treating cancer, optionally lung cancer.

[0234] 10. A method for identifying a human subject likely to have a cytotoxic T cell response to administration of a peptide, polynucleic acid, or vector of the pharmaceutical composition or kit according to item 7, comprising: (i) determining that the active component polypeptide(s) of the pharmaceutical composition or kit comprises a sequence which is a T cell epitope capable of binding to at least three HLA class I molecules of the subject; (ii) identifying the subject as likely to have a cytotoxic T cell response to administration of the pharmaceutical composition, or the peptide, polynucleic acid, or vector of the kit; The method includes:

[0235] 11. (a) selected from BRDT, PRAME, NALP4, MAGE-A12, MAGE-A2, SURVIVIN, DPPA2, NY-SAR-35, LDHC, MAGE-C2, MAGE-A3, KK-LC-1, and MAGE-A1; and (b) i. a fragment of the active ingredient peptide of the pharmaceutical composition; and ii. is a T cell epitope capable of binding to at least three HLA class I molecules of the subject. Contains an amino acid sequence, 11. The method of claim 10, further comprising using the population expression data for each antigen to determine the likelihood that the subject has a CD8+ T cell response targeted to one or more polypeptide antigens expressed by the subject's cancer cells.

[0236] 12. A method for identifying a subject who is likely to have a clinical response to the treatment method according to item 9, comprising: (i) the active ingredient polypeptide(s) of the pharmaceutical composition comprises two or more different amino acid sequences, each of which is a. a T cell epitope capable of binding to at least three HLA class I molecules of the subject; and b. a cancer-associated antigen expressed by cancer cells of the subject, and optionally a fragment of the cancer-associated antigen present in a sample obtained from the subject. and determining that; (ii) identifying the subject as likely to have a clinical response to the treatment method; The method includes:

[0237] 13. A method for determining the likelihood that a particular human subject will have a clinical response to the treatment method according to item 9, wherein one or more of the following factors correspond to a higher likelihood of clinical response: (a) the presence in the active ingredient polypeptide(s) of a greater number and / or different amino acid sequences that are T cell epitopes each capable of binding to at least three HLA class I of the subject; (b) A greater number of target polypeptide antigens A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; comprising at least one amino acid sequence, Optionally, the target polypeptide antigen is expressed in the subject, and further optionally, the target polypeptide antigen is present in one or more samples obtained from the subject; (c) the subject is administered a target polypeptide antigen, optionally a threshold number of the target polypeptide antigen, and / or optionally A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; a greater likelihood of expressing a target polypeptide antigen determined to include at least one amino acid sequence; and / or (d) a greater number of target polypeptide antigens that the subject is predicted to express, optionally a greater number of target polypeptide antigens that the subject expresses with a threshold probability, and / or optionally A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; A greater number of target polypeptide antigens determined to contain at least one amino acid sequence.

[0238] 14. (i) the polypeptide antigen targeted by the active ingredient polypeptide(s) is A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; identifying the sequence as comprising an amino acid sequence; (ii) using the population expression data for each antigen identified in step (i), determining the probability that the subject expresses one or more of the antigens identified in step (i), which together comprise at least two different amino acid sequences of step (i); (iii) determining the likelihood that the subject will have a clinical response to administration of the pharmaceutical composition, kit, or panel of polypeptides, wherein a higher probability determined in step (ii) corresponds to a higher likelihood of a clinical response. Item 14. The method according to item 13, comprising:

[0239] 15. The method according to item 14, wherein the at least two different amino acid sequences are contained in the amino acid sequences of two different polypeptide antigens targeted by the active ingredient polypeptide(s).

[0240] 16. The method according to any one of items 12 to 15, further comprising selecting or recommending administration of the pharmaceutical composition, or the peptide, polynucleic acid, or vector of the kit, as a method of treatment for the subject, and optionally further treating the subject by administering the pharmaceutical composition, or the peptide, polynucleic acid, or vector of the kit.

[0241] 17. The method of treatment according to item 9, wherein the subject has been identified as having a high likelihood of having a clinical response to treatment with the method according to any one of items 12 to 15, or as having a likelihood of having a clinical response above a minimum threshold.

[0242] 18. The method according to any one of items 8, 9, 16, and 17, wherein the treatment is administered in combination with chemotherapy, targeted therapy, or a checkpoint inhibitor.

[0243] 19. A method for identifying a human subject who is likely to not have a clinical response to the treatment method according to item 9, comprising: (i) determining that the active ingredient peptide(s) of the pharmaceutical composition does not contain two or more distinct sequences that are T cell epitopes, each of which is capable of binding to at least three HLA class I molecules of the subject; (ii) identifying the subject as likely to not have a clinical response to the treatment method; The method includes:

[0244] Further embodiments of the present disclosure - (3B) - Melanoma 1. A polypeptide comprising a fragment of up to 50 consecutive amino acids of a melanoma associated antigen selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1, wherein the fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 178-207, and optionally the fragment is flanked at the N- and / or C-terminus by additional amino acids that are not part of the sequence of the melanoma associated antigen.

[0245] 2. c. A fragment of a melanoma-associated antigen selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1, the fragment comprising an amino acid sequence selected from any one of SEQ ID NOs: 178 to 207; or d. The polypeptide according to item 1, comprising two or more fragments of one or more melanoma-associated antigens selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1, each fragment comprising a different amino acid sequence selected from any one of SEQ ID NOs: 178 to 207, and optionally comprising or consisting of fragments that are overlapping or arranged end-to-end in the polypeptide.

[0246] 3. The polypeptide according to item 1 or 2, wherein the polypeptide comprises or consists of fragments of at least two different cancer-associated antigens, the cancer-associated antigens being selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1, and each fragment comprises a different amino acid sequence selected from SEQ ID NOs: 178 to 207.

[0247] 4. The polypeptide according to any one of items 1 to 3, comprising or consisting of one or more amino acid sequences selected from SEQ ID NOs: 208 to 237.

[0248] 5. A polypeptide according to any one of items 1 to 4, comprising or consisting of any one of the amino acids in SEQ ID NOs: 238 to 252.

[0249] 6. A panel of two or more polypeptides according to any one of items 1 to 5, wherein each polypeptide comprises a different amino acid sequence selected from SEQ ID NOs: 178 to 207.

[0250] 7. A pharmaceutical composition or kit comprising one or more polypeptides according to any one of items 1 to 5, or a panel of polypeptides according to item 6, or a polypeptide comprising at least two amino acid sequences selected from SEQ ID NOs: 178 to 207, or one or more polynucleic acids or vectors encoding said one or more polypeptides.

[0251] 8. A vaccination method for providing immunotherapy or inducing a cytotoxic T cell response in a subject, comprising administering to the subject a pharmaceutical composition or a peptide, polynucleic acid or vector of the kit according to item 7.

[0252] 9. The method according to item 8, which is a method for treating cancer, optionally melanoma.

[0253] 10. A method for identifying a human subject likely to have a cytotoxic T cell response to administration of a peptide, polynucleic acid, or vector of the pharmaceutical composition or kit according to item 7, comprising: (i) determining that the active component polypeptide(s) of the pharmaceutical composition or kit comprises a sequence which is a T cell epitope capable of binding to at least three HLA class I molecules of the subject; (iii) identifying the subject as likely to have a cytotoxic T cell response to administration of the pharmaceutical composition, or the peptide, polynucleic acid, or vector of the kit; The method includes:

[0254] 11. (a) selected from PRAME, MAGE-A2, MAGE-C1, SURVIVIN, MAGE-A12, Ny-ESO-1, MAGE-C2, MAGE-A6, BORIS, LAGE-1, MAGE-A11, SSX-1, MAGE-A3, MAGE-A10, and MAGE-A1; and (b) i. a fragment of the active ingredient peptide of the pharmaceutical composition; and ii. is a T cell epitope capable of binding to at least three HLA class I molecules of the subject. Contains an amino acid sequence, 11. The method of claim 10, further comprising using the population expression data for each antigen to determine the likelihood that the subject has a CD8+ T cell response targeted to one or more polypeptide antigens expressed by the subject's cancer cells.

[0255] 12. A method for identifying a subject who is likely to have a clinical response to the treatment method according to item 9, comprising: (i) the active ingredient polypeptide(s) of the pharmaceutical composition comprises two or more different amino acid sequences, each of which is c. a T cell epitope capable of binding to at least three HLA class I molecules of the subject; and d. A cancer-associated antigen expressed by cancer cells of the subject, and optionally a fragment of the cancer-associated antigen present in a sample obtained from the subject. and determining that; (ii) identifying the subject as likely to have a clinical response to the treatment method; The method includes:

[0256] 13. A method for determining the likelihood that a particular human subject will have a clinical response to the treatment method according to item 9, wherein one or more of the following factors correspond to a higher likelihood of clinical response: (a) the presence in the active ingredient polypeptide(s) of a greater number and / or different amino acid sequences that are T cell epitopes each capable of binding to at least three HLA class I of the subject; (b) A greater number of target polypeptide antigens A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; comprising at least one amino acid sequence, Optionally, the target polypeptide antigen is expressed in the subject, and further optionally, the target polypeptide antigen is present in one or more samples obtained from the subject; (c) the subject is administered a target polypeptide antigen, optionally a threshold number of the target polypeptide antigen, and / or optionally A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; a greater likelihood of expressing a target polypeptide antigen determined to include at least one amino acid sequence; and / or (d) a greater number of target polypeptide antigens that the subject is predicted to express, optionally a greater number of target polypeptide antigens that the subject expresses with a threshold probability, and / or optionally A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; A greater number of target polypeptide antigens determined to contain at least one amino acid sequence.

[0257] 14. (iv) the polypeptide antigen targeted by the active ingredient polypeptide(s) is A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; identifying the sequence as comprising an amino acid sequence; (v) using the population expression data for each antigen identified in step (i), determining the probability that the subject expresses one or more of the antigens identified in step (i), which together comprise at least two different amino acid sequences of step (i); (vi) determining the likelihood that the subject will have a clinical response to administration of the pharmaceutical composition, kit, or panel of polypeptides, wherein a higher probability determined in step (ii) corresponds to a higher likelihood of a clinical response. Item 14. The method according to item 13, comprising:

[0258] 15. The method according to item 14, wherein the at least two different amino acid sequences are contained in the amino acid sequences of two different polypeptide antigens targeted by the active ingredient polypeptide(s).

[0259] 16. The method according to any one of items 12 to 15, further comprising selecting or recommending administration of the pharmaceutical composition, or the peptide, polynucleic acid, or vector of the kit, as a method of treatment for the subject, and optionally further treating the subject by administering the pharmaceutical composition, or the peptide, polynucleic acid, or vector of the kit.

[0260] 17. The method of treatment according to item 9, wherein the subject has been identified as having a high likelihood of having a clinical response to treatment with the method according to any one of items 12 to 15, or as having a likelihood of having a clinical response above a minimum threshold.

[0261] 18. The method according to any one of items 8, 9, 16, and 17, wherein the treatment is administered in combination with chemotherapy, targeted therapy, or a checkpoint inhibitor.

[0262] 19. A method for identifying a human subject who is likely to not have a clinical response to the treatment method according to item 9, comprising:

[0263] (i) determining that the active ingredient peptide(s) of the pharmaceutical composition does not contain two or more distinct sequences that are T cell epitopes, each of which is capable of binding to at least three HLA class I molecules of the subject; (ii) identifying the subject as likely to not have a clinical response to the treatment method; The method includes:

[0264] Further embodiments of the present disclosure - (4B) - Bladder 1. A polypeptide comprising a fragment of up to 50 consecutive amino acids of a bladder cancer associated antigen selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12, wherein the fragment comprises an amino acid sequence selected from any one of SEQ ID NOs: 268-297, and optionally the fragment is flanked at the N- and / or C-terminus by additional amino acids that are not part of the sequence of the bladder cancer associated antigen.

[0265] 2. e. A fragment of a bladder cancer-associated antigen selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12, the fragment comprising an amino acid sequence selected from any one of SEQ ID NOs: 268 to 297; or f. The polypeptide according to item 1, comprising two or more fragments of one or more bladder cancer-associated antigens selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12, each of which comprises a different amino acid sequence selected from any one of SEQ ID NOs: 268 to 297, and optionally comprising or consisting of fragments that are overlapping or arranged end-to-end in the polypeptide.

[0266] 3. The polypeptide according to item 1 or 2, wherein the polypeptide comprises or consists of fragments of at least two different cancer-associated antigens, the cancer-associated antigens being selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12, and each fragment comprises a different amino acid sequence selected from SEQ ID NOs: 268 to 297.

[0267] 4. The polypeptide according to any one of items 1 to 3, comprising or consisting of one or more amino acid sequences selected from SEQ ID NOs: 298 to 327.

[0268] 5. A polypeptide according to any one of items 1 to 4, comprising or consisting of an amino acid sequence set forth in any one of SEQ ID NOs: 328 to 342.

[0269] 6. A panel of two or more polypeptides according to any one of items 1 to 5, wherein each polypeptide comprises a different amino acid sequence selected from SEQ ID NOs: 268 to 297.

[0270] 7. A pharmaceutical composition or kit comprising one or more polypeptides according to any one of items 1 to 5, or a panel of polypeptides according to item 6, or a polypeptide comprising at least two amino acid sequences selected from SEQ ID NOs: 268 to 297, or one or more polynucleic acids or vectors encoding said one or more polypeptides.

[0271] 8. A vaccination method for providing immunotherapy or inducing a cytotoxic T cell response in a subject, comprising administering to the subject a pharmaceutical composition or a peptide, polynucleic acid or vector of the kit according to item 7.

[0272] 9. The method of item 8, which is a method for treating cancer, optionally bladder cancer.

[0273] 10. A method for identifying a human subject likely to have a cytotoxic T cell response to administration of a peptide, polynucleic acid, or vector of the pharmaceutical composition or kit according to item 7, comprising: (i) determining that the active component polypeptide(s) of the pharmaceutical composition or kit comprises a sequence which is a T cell epitope capable of binding to at least three HLA class I molecules of the subject; (iv) identifying the subject as likely to have a cytotoxic T cell response to administration of the pharmaceutical composition, or the peptide, polynucleic acid, or vector of the kit; The method includes:

[0274] 11. (a) selected from PIWIL2, CTAGE1, MAGE-A9, EpCAM, OY-TES-1, NY-ESO-1, SURVIVIN, MAGE-C1, MAGE-A2, LAGE-1, MAGE-A3, MAGE-A8, HAGE, MAGE-A1, MAGE-C2, MAGE-A10, and MAGE-A12; and (b) i. a fragment of the active ingredient peptide of the pharmaceutical composition; and ii. is a T cell epitope capable of binding to at least three HLA class I molecules of the subject. Contains an amino acid sequence, 11. The method of claim 10, further comprising using the population expression data for each antigen to determine the likelihood that the subject has a CD8+ T cell response targeted to one or more polypeptide antigens expressed by the subject's cancer cells.

[0275] 12. A method for identifying a subject who is likely to have a clinical response to the treatment method according to item 9, comprising: (i) the active ingredient polypeptide(s) of the pharmaceutical composition comprises two or more different amino acid sequences, each of which is e. a T cell epitope capable of binding to at least three HLA class I molecules of the subject; and f. a cancer-associated antigen expressed by cancer cells of the subject, and optionally a fragment of the cancer-associated antigen present in a sample obtained from the subject. and determining that; (ii) identifying the subject as likely to have a clinical response to the treatment method; The method includes:

[0276] 13. A method for determining the likelihood that a particular human subject will have a clinical response to the treatment method according to item 9, wherein one or more of the following factors correspond to a higher likelihood of clinical response: (a) the presence in the active ingredient polypeptide(s) of a greater number and / or different amino acid sequences that are T cell epitopes each capable of binding to at least three HLA class I of the subject; (b) A greater number of target polypeptide antigens A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; comprising at least one amino acid sequence, Optionally, the target polypeptide antigen is expressed in the subject, and further optionally, the target polypeptide antigen is present in one or more samples obtained from the subject; (c) the subject is administered a target polypeptide antigen, optionally a threshold number of the target polypeptide antigen, and / or optionally A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; a greater likelihood of expressing a target polypeptide antigen determined to include at least one amino acid sequence; and / or (d) a greater number of target polypeptide antigens that the subject is predicted to express, optionally a greater number of target polypeptide antigens that the subject expresses with a threshold probability, and / or optionally A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; A greater number of target polypeptide antigens determined to contain at least one amino acid sequence.

[0277] 14. (vii) the polypeptide antigen targeted by the active ingredient polypeptide(s) is A. the active ingredient is contained in a polypeptide; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; identifying the sequence as comprising an amino acid sequence; (viii) using the population expression data for each antigen identified in step (i) to determine the probability that the subject expresses one or more of the antigens identified in step (i), which together comprise at least two different amino acid sequences of step (i); (ix) determining the likelihood that the subject will have a clinical response to administration of the pharmaceutical composition, kit, or panel of polypeptides, wherein a higher probability determined in step (ii) corresponds to a higher likelihood of a clinical response. Item 14. The method according to item 13, comprising:

[0278] 15. The method according to item 14, wherein the at least two different amino acid sequences are contained in the amino acid sequences of two different polypeptide antigens targeted by the active ingredient polypeptide(s).

[0279] 16. The method according to any one of items 12 to 15, further comprising selecting or recommending administration of the pharmaceutical composition, or the peptide, polynucleic acid, or vector of the kit, as a method of treatment for the subject, and optionally further treating the subject by administering the pharmaceutical composition, or the peptide, polynucleic acid, or vector of the kit.

[0280] 17. The method of treatment according to item 9, wherein the subject has been identified as having a high likelihood of having a clinical response to treatment with the method according to any one of items 12 to 15, or as having a likelihood of having a clinical response above a minimum threshold.

[0281] 18. The method according to any one of items 8, 9, 16, and 17, wherein the treatment is administered in combination with chemotherapy, targeted therapy, or a checkpoint inhibitor.

[0282] 19. A method for identifying a human subject who is likely to not have a clinical response to the treatment method according to item 9, comprising: (i) determining that the active ingredient peptide(s) of the pharmaceutical composition does not contain two or more distinct sequences that are T cell epitopes, each of which is capable of binding to at least three HLA class I molecules of the subject; (ii) identifying the subject as likely to not have a clinical response to the treatment method; The method includes: EXAMPLES

[0283] Example 1 – HLA-epitope binding prediction process and validation Binding prediction between specific HLA and epitopes (9-mer peptides) was based on the Immune Epitope Database tool for epitope prediction (www.iedb.org).

[0284] We validated the HLA I-epitope binding prediction process by comparison with HLA class I-epitope pairs determined by laboratory experiments. A dataset of HLA I-epitope pairs reported in peer-reviewed publications or public immunological databases was compiled.

[0285] The concordance rate with the experimental dataset was calculated (Table 2). The binding HLA I-epitope pairs in the dataset were correctly predicted 93% of the time. Coincidentally, the non-binding HLA I-epitope pairs were also correctly predicted 93% of the time.

[0286] [Table 2]

[0287] We also determined the accuracy of predicting multiple HLA-binding epitopes (Table 3). Based on the specificity and sensitivity of the analysis, using a probability of 93% for both true positive and true negative predictions, and a probability of 7% (=100%-93%) for false positive and false negative predictions, we can calculate the probability of multiple HLA-binding epitopes in humans. The probability of multiple HLA binding to one epitope shows the relationship between the number of HLA binding to the epitope and the expected minimum number of actual bindings. According to the PEPI definition, the expected minimum number of HLA binding to an epitope is 3 (bold).

[0288] [Table 3]

[0289] A validated HLA-epitope binding prediction process was used to determine all HLA-epitope binding pairs described in the Examples below.

[0290] Example 2 – Epitope presentation by multiple HLA predicts cytotoxic T lymphocyte (CTL) responses

[0291] This study examines whether presentation of one or more epitopes of a polypeptide antigen by one or more HLA class I molecules of an individual predicts a CTL response.

[0292] This study was performed by retrospective analysis of six clinical trials conducted on 71 cancer patients and 9 HIV-infected patients (Table 4). Patients in these trials were treated with HPV vaccine, three different NY-ESO-1 specific cancer vaccines, one HIV-1 vaccine, and a CTLA-4 specific monoclonal antibody (ipilimumab) that has been shown to reactivate CTLs against the NY-ESO-1 antigen in melanoma patients. In all these clinical trials, antigen-specific CD8+ CTL responses (immunogenicity) were measured in the study subjects after vaccination. In some cases, correlations between CTL responses and clinical responses were reported.

[0293] No patients were excluded from the retrospective study for any reason other than data availability. The 157-patient dataset (Table 4) was randomized with a standard random number generator to create two independent cohorts for training and validation studies. In some cases, the cohorts contained multiple datasets from the same patient, resulting in a training cohort of 76 datasets from 48 patients and a testing / validation cohort of 81 datasets from 51 patients.

[0294] [Table 4]

[0295] The reported CD8+ T cell responses of the training dataset were compared to the HLA class I restriction profile of the epitopes (9mers) of the vaccine antigens. The antigen sequences and HLA class I genotypes of each patient were obtained from publicly available protein sequence databases or peer-reviewed publications, and the HLA I-epitope binding prediction process was blinded to the clinical CD8+ T cell response data of patients whose CD8+ T cells were IFN-y producing CTLs specific for the vaccine peptides (9mers). The number of epitopes from each antigen predicted to bind to at least one (PEPI1+), or at least two (PEPI2+), or at least three (PEPI3+), or at least four (PEPI4+), or at least five (PEPI5+), or all six (PEPI6) HLA class I molecules of each patient was determined, and the number of bound HLAs was used as a classifier of the reported CTL response. The true positive rate (sensitivity) and true negative rate (specificity) were determined separately from the training data set for each classifier (number of HLAs combined).

[0296] A ROC analysis was performed for each classifier. The ROC curves plotted the true positive rate (sensitivity) as a function of the false positive rate (1-specificity) for various cutoff points (Figure 1). Each point on the ROC curve represents a sensitivity / specificity pair corresponding to a particular discrimination threshold (epitope (PEPI) count). The area under the ROC curve (AUC) is a measure of how well the classifier can distinguish between two diagnostic groups (CTL responders or non-responders).

[0297] This analysis unexpectedly revealed that the predictive value of epitope presentation by a subject's multiple class I HLA (PEPI2+, PEPI3+, PEPI4+, PEPI5+, PEPI6) was in each case a better predictor of CD8+ T cell or CTL response than simply epitope presentation by one or more HLA class I (PEPI1+, AUC=0.48, Table 5).

[0298] [Table 5]

[0299] The CTL response of an individual is best predicted by considering the epitopes of the antigen that can be presented by at least three HLA class I alleles of the individual (PEPI3+, AUC=0.65, Table 5). The threshold count of PEPI3+ (the number of antigen-specific epitopes presented by three or more HLAs of an individual) that best predicted positive CTL response was 1 (Table 6). That is, if an epitope from at least one antigen is presented by at least three HLA class I of a subject (≧1 PEPI3+), the antigen can trigger at least one CTL clone, and the subject is a likely CTL responder. Using a threshold of ≧1 PEPI3+ to predict likely CTL responders ("≧1 PEPI3+ test"), a true positive rate (diagnostic sensitivity) of 76% was obtained (Table 6).

[0300] [Table 6]

[0301] Example 3 – Retrospective validation of the ≥1 PEPI3+ threshold as a novel biomarker for the PEPI test

[0302] In a retrospective analysis, a test cohort of 81 data sets from 51 patients was used to validate the ≧1 PEPI3+ threshold for predicting antigen-specific CD8+ T cell or CTL responses. For each data set in the test cohort, it was determined whether the ≧1 PEPI3+ threshold was met (at least one epitope from the antigen is presented by at least three class I HLAs of the individual). This was compared to the experimentally determined CD8+ T cell responses (CTL responses) reported in clinical trials (Table 7).

[0303] This retrospective validation demonstrated that PEPI3+ peptides induced CD8+ T cell responses (CTL responses) in individuals with a probability of 84%, the same value as that determined by analytical validation of PEPI3+ predictions, epitopes that bind to at least three HLAs in individuals (Table 3). These data provide strong evidence that immune responses can be induced by PEPI in individuals.

[0304] [Table 7]

[0305] The diagnostic accuracy was determined by ROC analysis using the PEPI3+ count as the cutoff value (Figure 2). The AUC value was 0.73. In ROC analysis, an AUC of 0.7 to 0.8 is generally considered to be a fair diagnostic value.

[0306] In the test dataset, a PEPI3+ count of at least 1 (≧1 PEPI3+) best predicted CTL responses (Table 8), a result that confirmed the thresholds determined during training (Table 5).

[0307] [Table 8]

[0308] Example 4 - Clinical validation of the ≧1 PEPI3+ threshold as a novel biomarker for the PEPI test Vaccine design based on the PEPI3+ biomarker was first tested in a Phase I clinical trial in patients with metastatic colorectal cancer (mCRC) in the OBERTO Phase I / II clinical trial (NCT03391232). The study evaluated the safety, tolerability, and immunogenicity of single or multiple doses of PolyPEPI1018 as an add-on to maintenance therapy in subjects with mCRC. PolyPEPI1018 is a peptide vaccine that contains 12 unique epitopes derived from seven conserved TSAs that are frequently expressed in mCRC (WO2018158455A1). These epitopes were designed to bind at least three self-HLA alleles, which are more likely to induce a T cell response than epitopes presented by a single HLA (see Examples 2 and 3). Vaccine (dose: 0.2 mg / peptide) was administered to mCRC patients in the first-line setting immediately after transition to fluoropyrimidine and bevacizumab maintenance therapy. Vaccine-specific T cell responses were predicted by first identifying PEPI3+-s in silico (using the patient's complete HLA genotype and CRC-specific antigen expression rates) and then measuring by ELISpot after one vaccination cycle (phase I part of the trial).

[0309] 70 data sets from 10 patients (phase 1 cohort and OBERTO trial data sets) were used to prospectively validate the PEPI3+ biomarker as predictive of antigen-specific CTL responses. For each data set, predictive PEPI3+-s were determined in silico and compared with vaccine-specific immune responses measured by ELISPOT assay from patients' blood. The diagnostic properties thus determined (positive predictive value, negative predictive value, overall concordance rate) were then compared with the retrospective validation results described in Example 3.

[0310] The overall concordance rate was 64% and the positive predictive value was high at 79%, which means that patients predicted as PEPI3+ have a 79% probability of generating a CD8+ T cell specific immune response against the analyzed antigen. The clinical trial data correlated significantly with the retrospective trial results (p=0.01), providing evidence for the calculation of PEPI3+ using the PEPI test to predict antigen-specific T cell responses based on the complete HLA genotype of the patient (Table 9).

[0311] [Table 9]

[0312] Example 5 - ≧1 PEPI3+ test predicts CD8+ T cell reactivity Supporting data are available showing that ≧1 PEPI3+ correlates with clinical immunogenicity data, whereas state-of-the-art single HLA-specific epitope definition does not correlate with vaccine-specific immunogenicity.

[0313] Calculation of > 1 PEPI3+ was compared to state of the art methods for predicting a particular human subject's CTL response to peptide antigens.

[0314] The HLA genotypes of 28 cervical cancer and VIN-3 patients who received the HPV-16 synthetic long peptide vaccine (LPV) in two different clinical trials were determined from DNA samples. LPV consists of a long peptide that encompasses the oncoproteins E6 and E7 of the HPV-16 virus. The amino acid sequence of LPV was obtained from MJ Welters, et al. Induction of tumor-specific CD4+ and CD8+ T-cell immunity in cervical cancer patients by a human papillomavirus type 16 E6 and E7 long peptides vaccine. Clin Cancer Res 14, 178-187 (2008), GG Kenter, et al. Vaccination against HPV-16 oncoproteins for vulvar intraepithelial neoplasia. N Engl J Med 361, 1838-1847 (2009), MJ Welters, et al. Success or failure of vaccination for HPV16-positive vulvar lesions correlates with kinetics and phenotype of induced T-cell responses. Proc Natl Acad Sci USA 107, 11895-11899 (2010). These publications also reported on the T cell responses of each vaccinated patient to the pool of overlapping peptides in the vaccine. Twenty-five patients (20 with VIN-3 and 5 with cervical cancer) had available immune response data, and 25 had available clinical response data.

[0315] For each patient, epitopes (9mers) of LPV presented by at least three patient class I HLA (PEPI3+) were identified and their distribution in the peptide pool was determined. Peptides containing at least one PEPI3+ (≧1 PEPI3+) were predicted to induce CD8+ T cell responses. Peptides without PEPI3+ were predicted not to induce CD8+ T cell responses.

[0316] A ≥1 PEPI3+ threshold correctly predicted 529 of 555 negative CD8+ T cell responses (95% true negative (TN) rate) and 9 of 45 positive CD8+ T cell responses (20% true positive (TP) rate) measured after vaccination (Figure 3A). Overall, there was 90% concordance between the ≥1 PEPI3+ threshold and experimentally determined CD8+ T cell reactivity (p<0.001).

[0317] For each patient, the distribution of epitopes presented by at least one patient's class I HLA (≧1 PEPI1+, HLA-restricted epitope prediction, prior art method) in the peptide pool was also determined. 42 HLA class I binding epitopes predicted 45 CD8+ T cell responses (TP rate 93%). In contrast, only 105 of the 555 negative T cell responses were excluded by HLA binding epitopes (TN rate 19%) (Figure 3B). Overall, the concordance rate between single HLA class I allele binding epitopes and CD8+ T cell responses was 25%, which was not statistically significant.

[0318] Example 6 – Prediction of HLA class II restricted CD4+ helper T cell epitopes CD4+ T helper responses after HPV vaccination were examined in 28 cervical cancer and VIN-3 patients who received HPV-16 synthetic long peptide vaccine (LPV) in two different clinical trials (detailed in Example 5) (Figure 4). The TP rate of prediction of HLA class II restricted epitopes was 95%, because the state-of-the-art tool predicted positive responses (positive CD4+ T cell reactivity to peptide pools for a person's HLA class II alleles) in 112 of 117 cases. TN rate was 0%, because 0 of the 33 negative T cell responses could be excluded. Overall, the concordance rate between PEPI prediction of HLA restricted class II and CD4+ T cell reactivity was 75% (not significant).

[0319] HLA class II-binding PEPI3+-s predicted 86 of 117 positive CD4+ T-cell responses (TP rate 73%) and excluded 17 of 33 negative T-cell responses (TN rate 52%). Overall, the concordance between HLA class II PEPI3+-s and CD4+ T-cell responses was 69% (p=0.005) (Figure 4A).

[0320] Example 7 - A ≧1 PEPI3+ test predicts T cell responses to full-length LPV polypeptides Using the same study reported in Examples 5 and 6, the ≧1 PEPI3+ test was used to predict patient CD8+ and CD4+ T cell responses to the full-length E6 and E7 polypeptide antigens of the LPV vaccine. Results were compared to reported experimentally determined responses. The test correctly predicted CD8+ T cell reactivity (PEPI3+) in 11 of 15 VIN-3 patients (sensitivity 70%, PPV 85%) and 2 of 5 cervical cancer patients (sensitivity 40%, PPV 100%) who had a positive CD8+ T cell reactivity test (Figure 5A). CD4+ T cell reactivity (PEPI3+) was correctly predicted in 100% of both VIN-3 and cervical cancer patients (Figure 5B).

[0321] We also observed that class I and class II HLA-restricted PEPI3+ counts correlated with the reported clinical benefit for patients vaccinated with LPV. Patients with higher PEPI3+ counts had either complete or partial responses already after 3 months. We also found a correlation between the number of PEPI and clinical response for HLA class II PEPIs, but not for HLA class I PEPIs, in patients with VIN-3, confirming the results of a post-hoc analysis of the clinical trial (Figures 5C and 5D).

[0322] Example 8 – Case study, correlation between PEPI3+ and vaccine-specific immunogenicity

[0323] "Vaccine-1" is an HPV16-based DNA vaccine containing full-length E6 and E7 antigens with a linker between them. "Vaccine-2" is an HPV18-based DNA vaccine containing full-length E6 and E7 antigens with a linker between them (Figure 6A). In a phase 2 clinical trial, T cell responses were examined in 17 HPV-infected cervical cancer patients who were vaccinated with both "Vaccine-1" and "Vaccine-2" (vaccine-3 vaccination, Bagarazzi et al. Science Translational Medicine. 2012;4(155):155ra138.).

[0324] Figure 6B shows the location of each epitope (9-mer) within the full-length sequences of two HPV-16 and two HPV-18 antigens for two exemplary patients (patient 12-11 and patient 14-5) that is presented by at least one (PEPI1+), at least two (PEPI2+), at least three (PEPI3+), at least four (PEPI4+), at least five (PEPI5+), or all six (PEPI6) class I HLAs in these patients.

[0325] Patient 12-11 had an overall PEPI1+ count of 54 for the combined vaccine (54 epitopes presented by one or more class I HLAs). Patient 14-5 had a PEPI1+ count of 91. Thus, patient 14-5 has a higher PEPI1+ count than patient 12-11 for the four HPV antigens. PEPI1+ represents a different set of vaccine antigen-specific HLA-restricted epitopes for patients 12-11 and 14-5. Only 27 PEPI1+ epitopes were common between these two patients.

[0326] For the PEPI3+ count (number of epitopes presented by 3 or more patient class I HLAs), the results for patients 12-11 and 14-5 were reversed: patient 12-11 had a PEPI3+ count of 8, containing at least one PEPI3+ in each of the four HPV16 / 18 antigens, whereas patient 14-5 had a PEPI3+ count of 0 (Figure 6C).

[0327] The reported immune responses of these two patients were consistent with the PEPI3+ counts but not with the PEPI1+ counts. Patient 12-11 developed an immune response to each of the four antigens after vaccination as measured by ELISpot, whereas patient 14-5 did not develop an immune response to any of the vaccine's four antigens. A similar pattern was observed when comparing the PEPI1+ and PEPI3+ sets of all 17 patients in the trial. There was no correlation between the PEPI1+ counts and the experimentally determined T cell responses reported from the clinical trial. However, there was a correlation between the T cell immunity predicted by a ≥1 PEPI3+ test and the reported T cell immunity. A ≥1 PEPI3+ test predicted immune responders to the HPV DNA vaccine.

[0328] Furthermore, the diversity of the patients' PEPI3+ sets was similar to the diversity of T cell responses typically seen in cancer vaccine trials. Patients 12-3 and 12-6 did not have PEPI3+, as did patient 14-5, predicting that the HPV vaccine would not be able to trigger T cell immunity. All other patients had at least one PEPI3, predicting that the HPV vaccine may be able to trigger T cell immunity. Eleven patients had multiple PEPI3+, predicting that the HPV vaccine would likely trigger a polyclonal T cell response. Patients 15-2 and 15-3 were able to mount extensive T cell immunity against E6 of both HPVs, but had poor immunity against E7. The other patients, 15-1 and 12-11, had similar magnitude responses against E7 of HPV18 and HPV16, respectively.

[0329] Example 9 -Design of model populations to conduct in silico trials on large populations and identify candidate precision vaccine targets Complete 4-digit HLA class I genotype (2 × HLA-A * xx:xx;2×HLA-B * xx:xx;2×HLA-C * We compiled an in silico human clinical trial cohort of 433 subjects with genotype (HLA genotype: genotype xx:xx) and demographic information. The model population has mixed ethnicity subjects with a total of 152 different HLA alleles representing >85% of the currently known allele G groups.

[0330] We also established a "big population" database containing 7,189 subjects characterized by 4-digit HLA genotype and demographic information. The big population has 328 different HLA class I alleles. The HLA allele distribution of the model population was significantly correlated with the big population (Table 10) (Pearson p<.001). Thus, the model population of 433 patients represents a 16-fold larger population.

[0331] The model population is representative of 85% of the human race as represented by HLA diversity in addition to HLA frequency.

[0332] [Table 10]

[0333] Example 10 – In silico clinical trials based on identification of multiple HLA-binding epitopes in the multi-peptide vaccine IMA901 predict immune response rates in reported clinical trials Probability of targeting multiple antigens in tumors of RCC patients IMA901 is a therapeutic vaccine for renal cell carcinoma (RCC) that contains nine peptides derived from tumor-associated antigens (TUMAPs). TUMAPs have been proven to be antigens that occur naturally in human cancer tissues and are commonly overexpressed in a subset of patients with a given cancer entity (Table 11). The probability of TSA expression in subjects treated with the IMA901 vaccine was estimated using data available from the scientific literature (Figure 7). Bayes' rule was used, assuming that the expression probability follows a beta distribution.

[0334] We defined AG50 as the number of TSAs (AGs) in a cancer vaccine that a particular tumor type has a 50% chance of expressing. AG50 modeling of cancer vaccines assumes that each AG exerts an effect proportional to the expression rate of the AG in the tumor type (if each AG in the vaccine is immunogenic).

[0335] For the IMA901 vaccine targeting nine antigens (nine TUMAPs), the AG50 value was 4.7, which means that about half of the antigens were overexpressed in 50% of the patients' tumors. Furthermore, the probability of targeting two expressed antigens was 100%, and for three antigens it was 96%. These results suggest the high efficacy of the IMA901 vaccine based on the selection of target antigens.

[0336] [Table 11]

[0337] Probability of inducing immune responses against multiple antigens in RCC patients' tumors A total of 96 patients with advanced RCC were randomly assigned to HLA-A *The 02+ subjects were treated with IMA901 (Walter S et al,Multipeptide immune response to cancer vaccine IMA901 after single-dose cyclophosphamide associates with longer patient survival,Nature Medicine,(2012),18,1254-1261). Each of the nine peptides in IMA901 binds to HLA-A * Based on currently accepted criteria, all nine peptides are strong candidates for boosting T cell responses against renal cancer because their presence has been detected in renal cancer patients and each peptide is present in at least one HLA molecule (HLA-A, HLA-B, HLA-C, HLA-D, HLA-E, HLA-F, HLA-G, HLA-H ... * 02). Despite this limitation, the immune response rates measured for at least one peptide in the vaccine in Phase I and Phase II clinical trials were 74% and 64%, respectively.

[0338] Analysis of the HLA binding properties of each TUMAP in IMA901 by in silico prediction revealed that eight of the nine TUMAPs had many HLA-A * 02 allele, validating the identification process (Figure 8). However, we found that each TUMAP was able to bind to many other HLA-B alleles. * and HLA-C * We found that it was able to bind to the allele (Figure 8A).

[0339] Because complete 4-digit HLA genotypes were not available for subjects enrolled in the IMA901 clinical trial, 51 HLA-A genotypes were obtained from a separate clinical trial. *Genotype data from RCC subjects selected in 02 were used to characterize the IMA901 vaccine (see: Chowell D, Morris LGT, Grigg CM, Weber JK, Samstein RM, et al. Patient HLA class I genotype influences cancer response to checkpoint blockade immunotherapy. Science. 2018;359(6375):582-587.). As presented in Figure 8B, only a few TUMAPs are able to bind to multiple HLAs in the same subject. The most immunogenic peptide in this context was MET-001, which was able to generate PEPIs in 35% of RCC patients. However, consistent with Figure 8A, CCN-001 was unable to generate PEPIs in any patient; CCN-001 was unable to generate PEPIs in any patient; * Based on Figure 8A, MUC-001 could theoretically bind to other alleles (both HLA-B and HLA-C), but these alleles were not present in patients in our model population, so this peptide was not able to generate PEPI.

[0340] The immunogenicity of the IMA901 vaccine as determined in two clinical trials was compared with the PEPI response rate determined using the PEPI test in our RCC model population. 67% (CI95 53-78%) had an immune response to at least one peptide of the IMA901 vaccine. * Thirty-three percent (CI95 22-47%) of 02+ subjects did not have the three HLAs that bind to any TUMAP. Interestingly, IMA901 did not bind to HLA-A or HLA-B in Phase I and II clinical trials, respectively. *02 did not induce a T cell response in 25% and 36% of subjects selected. Furthermore, the PEPI test predicted that 30% (CI95 19-43%) of subjects would have one PEPI against one TUMAP and 37% (CI95 25-51%) would have two or more PEPI against at least two IMA901 peptides, which is consistent with the average immune responses of 40% and 27% against one or more TUMAPs in both clinical trials (Table 12). The difference between immunogenicity seen in the three cohorts can be explained by the difference in HLA genotype of the study subjects and the potential error in measuring T cell responses and determining PEPI by PEPI test (see Example 1). The results of phase I and II trials show variability in immune response rates of the same vaccine in different clinical trial cohorts. However, the match between PEPI response rate and immunogenicity of peptide vaccines depends on the HLA sequence of the host.

[0341] [Table 12]

[0342] Similar to AG50, we define AP50 as the average number of antigens with PEPIs in the vaccine, which indicates the extent to which the vaccine can induce an immune response against the antigens targeted by the composition (cancer vaccine-specific immune response). Thus, AP depends on the HLA heterogeneity of the analyzed population, and does not depend on the expression of antigens in the tumor. The IMA901 composition can induce an immune response against an average of 1.06 vaccine antigens (AP50=1.06), i.e., HLA-A * In the RCC model population selected in 02, an immune response against at least one vaccine antigen can be induced, a result far less than the designed immunogenicity challenge (HLA-matched patients treated with 9 peptides).

[0343] Comparison of immunogenicity and clinical responses of TUMAP to IMA901 peptide vaccine The immune response induced by vaccine against a single antigen may not be sufficient for clinical activity because a given antigen may not be expressed in patients.Therefore, the inventors have defined the immune response targeting the expressed antigen as AGP, taking into account both the immunogenicity and expression probability of vaccine antigen in tumors as presented above.AGP depends on the antigen (AG) expression rate in applicable tumors and the HLA genotype of the subject that can make PEPI (P) in the test population.

[0344] Therefore, the correlation between immune responses to various numbers of antigens (TUMAP) and immune responses to antigens with high probability of expression (AGP) was investigated. It was found that the immune response induced by one peptide (one TUMAP) corresponds to 0.98 AGP, i.e., the probability that the immune response induced by any peptide of the IMA901 vaccine targets the antigen expressed in the tumor is 98% (Figure 9). However, the immune response induced by two or three TUMAPs corresponds to only 1.44 and 2.21 AGP, respectively. The 0.35 AGP, corresponding to 0 TUMAPs, shows the cumulative error of PEPI test prediction (see Example 1).

[0345] To characterize the efficacy of cancer vaccines, we define AGP50, which is a parameter that indicates the number of antigens that vaccine-induced CTL can recognize in tumors with a 50% probability.Computer calculation is similar to AG50, but in addition to expression, it also considers the occurrence of PEPI presentation in specific vaccine antigens.The AGP50 of IMA901 vaccine for RCC model population is 1.10.

[0346] In a retrospective analysis, IMA901 clinical trial investigators found that significantly more subjects who responded to multiple TUMAPs of IMA901 experienced disease control (DC, stable disease, or partial response) compared to subjects who did not respond or responded to only one TUMAP (Table 13). Because the presence of PEPI accurately predicted responders to TUMAP, we investigated the relationship between disease control rate and AGPs in the subpopulation of TUMAP responders. Similar to the investigators, we used our RCC model population to analyze the proportion of patients likely to have an immune response to expressed antigens (i.e., ≧1 AGP) for subpopulations predicted to have an immune response to 0, 1, or 2 TUMAPs. Interestingly, the proportion of patients with 1 AGP is similar to the proportion of patients with disease control in the subpopulations: 33% of patients had disease control, whereas 47% (CI95 23-67%) had 1 AGP, and in the subgroup with immune responses to two TUMAPs, significantly more patients had disease control and AGP, 75% vs. 90% (CI95 70, 97%), respectively. These results suggest that only patients with an immune response to at least one expressed tumor antigen are likely to experience clinical benefit. Furthermore, the proportion of patients with 1 AGP in our RCC model population is similar to the disease control rates in phase I and II clinical trials conducted with the IMA901 vaccine (Table 12).

[0347] [Table 13]

[0348] Analysis of IMA901 vaccine efficacy in multiple populations As shown in Table 14, an AG50 value of 4.7 was observed for the IMA901 vaccine, suggesting high efficacy based on the selection of the target antigen. However, the efficacy of the vaccine was not high in the unselected general population and in the HLA-A *In both unselected RCC model populations and HLA-A 02 selected subjects, the AP50 for IMA901 was only 0.75 and 1.12, respectively. * Similar results were obtained for the population selected in 02. The results were consistent with HLA-A * Although the higher abundance of .02 demonstrated improved antigenicity of IMA901, it did not guarantee the immunogenicity of the vaccine. As a result, the AGP50 values, which indicate the efficacy of the vaccine, were low in each population.

[0349] [Table 14]

[0350] Example 11 – In silico drug discovery based on identification of multiple HLA-binding epitopes predicts reported T cell response rates in clinical trials The objective of this study was to determine whether a model population such as that described in Example 9 could be used to predict vaccine CTL reactivity rates, i.e., to be used in in silico efficacy trials, and whether correlations could be made between clinical outcomes in vaccine trials and PEPI.

[0351] Published clinical trial results were collected from studies with therapeutic vaccines, which included 1,790 subjects in 64 clinical trials treated with 42 therapeutic vaccines covering 61 different antigens (Table 15). The same vaccines used in these clinical trials were used in an in silico clinical trial with a model population of 433 subjects with human leukocyte antigen (HLA) genotype (described in Example 9). No subjects were excluded for reasons other than data availability. IRR was defined as the proportion of subjects in the study population who had a T cell response induced by the study vaccine. ORR was defined as the proportion of subjects in the study population who achieved an objective response (complete response and partial response) after vaccination. In the in silico clinical trial, the proportion of subjects with PEPI (personal epitope that binds to the subject's three HLA alleles), multiple PEPIs, and PEPIs in multiple antigens were computed to obtain PEPI score, multi-PEPI score, and multi-AgPEPI score, respectively. Immune response rates and objective response rates (IRR and ORR) from published clinical trials were compared with the PEPI score, multi-PEPI score, and multi-AgPEPI score. All reported and calculated scores are summarized in Table 16.

[0352] [Table 15]

[0353] [Table 16-1]

[0354] [Table 16-2]

[0355] We investigated the correlation between a PEPI3+ score of ≥1 and immune response rate in a previous study of 12 cancer antigen-derived peptide vaccines that induced T cell responses in a subset of 172 subjects from 19 clinical trials identified from peer-reviewed publications. We compared the experimental response rates reported from the clinical trials with a PEPI3+ score of ≥1 and found a linear correlation (R 2 = 0.70) was found (p = 0.001) (Figure 10A). The correlation between ≥ 1 PEPI3+ score and immune response rate was then confirmed by analyzing 59 clinical trials involving 1,343 subjects treated with 40 different vaccines. Each vaccine was analyzed by comparing the published IRR from the clinical trials with the PEPI score from the model population (Figure 10B). The correlation between the IRR and PEPI score was significant (r 2 = 0.465 and p = 0.001). This result demonstrated that the PEPI score determined by in silico clinical trials in MP accurately predicted the IRR observed in clinical trials.

[0356] To test whether polyclonal T cell responses increase the likelihood of tumor shrinkage, we compared ORR and multi-PEPI scores. In preliminary experiments, we analyzed the relationship between clinical response (either ORR or DCR) and multi-PEPI scores in 17 clinical trials conducted with peptide and DNA-based immunotherapy vaccines. The results of these experiments demonstrated a significant correlation between clinical response rates and multi-PEPI scores (r 2 = 0.75, p < 0.001). To confirm these findings, ORR data were collected and analyzed from 27 clinical trials with 21 different vaccines involving 600 subjects (Figure 10C). Multi-PEPI score was calculated as the proportion of subjects in the model population with more than one PEPI from the study vaccine. The results of this experiment demonstrated that ORR did not correlate with multi-PEPI score (Figure 10D).

[0357] Results from previous studies suggested that T cell responses against multiple antigens are associated with longer progression-free and overall survival. Therefore, we hypothesized that inducing T cell responses against multiple tumor antigens would increase the chances of tumor shrinkage. To test this hypothesis, we collected and analyzed ORR data from 10 clinical trials using nine different vaccines involving 263 subjects treated with multi-antigen targeted vaccines. Multi-Ag PEPI scores were calculated as the proportion of subjects with vaccine-specific PEPI in at least two antigens. The results of this experiment showed a strong correlation between ORR and multi-Ag PEPI scores (r 2 = 0.64, p = 0.01), and between ORR and multi-PEPI score (r 2 = 0.88, p = 0.001) (Figures 10E and F, respectively). These results suggest that T cell responses to multiple tumor antigens may recognize a larger population of tumor cells, thereby increasing the likelihood of tumor shrinkage.

[0358] In a second analysis, we investigated whether PEPI-specific T cell responses against antigens expressed in the target tumor would increase the likelihood of tumor shrinkage. A total of 15 clinical trials enrolled subjects with target antigen-positive disease, and 11 trials did not preselect subjects based on antigen expression. The proportion of subjects who achieved an objective response was significantly higher in CTs that included target antigen-positive subjects compared to CTs that did not perform target preselection (21.0% vs. 3.6%, respectively, p=0.03).

[0359] The correlation between ORR and the multi-PEPI score was statistically significant in subjects with confirmed expression of the target antigen (r 2 = 0.56, p = 0.005) (Figure 10G). These results highlight the importance of the presence of cognate PEPI in the tumor and that its presence increases the likelihood of tumor shrinkage.

[0360] This study demonstrated that the association between subjects' HLA genotypes and PEPI was the most important factor in predicting clinical response to vaccines, and also demonstrated that the PEPI score could predict clinical outcomes of therapeutic vaccines.

[0361] Example 12 – Study design and preliminary safety data of the OBERTO Phase I / II clinical trial The OBERTO trial is a Phase I / II study of PolyPEPI1018 vaccine and CDx for the treatment of metastatic colorectal cancer (NCT03391232). The study design is shown in Figure 11.

[0362] Registration Criteria Histologically confirmed metastatic adenocarcinoma of the colon or rectum -At least one measurable reference lesion according to RECIST 1.1 Demonstrated PR or stable disease during first-line treatment with one systemic chemotherapy regimen and one biologic therapy regimen Maintenance therapy with a fluoropyrimidine (5-fluorouracil or capecitabine) plus the same biologic agent (bevacizumab, cetuximab, or panitumumab) used during induction is planned to begin before the first day of treatment with the investigational drug -Have had your last CT scan less than 3 weeks prior to the first day of treatment Subject Dropouts and Discontinuations If during the first study period (12 weeks) a patient experiences disease progression and requires initiation of second-line treatment, the patient will be dropped out of the study. If, during the second part of the study (after the second dose), a patient experiences disease progression and requires initiation of second-line treatment, they will remain in the study, receive their third vaccination as scheduled, and complete follow-up. - In addition to the expected transient local erythema and edema at the vaccination site, a flu-like syndrome with mild fever and fatigue was also observed. These reactions are already known for peptide vaccination and are usually associated with the mechanism of action, since fever and flu-like syndrome may be the consequence and sign of the induction of an immune response (which is known as a typical vaccine reaction in childhood vaccinations). Only one serious adverse event (SAE) “probably related” to the vaccine was recorded (Table 17). There was one non-vaccine related dose-limiting toxicity (DLT) (syncope).

[0363] Safety results are summarized in Table 17.

[0364] [Table 17]

[0365] Example 13 – Expression frequency-based target antigen selection during vaccine design and its clinical validation for mCRC Common tumor antigens allow precise targeting of all tumor types, including those with low mutational burden. Population expression data collected so far from 2,391 CRC biopsies represent the variability of antigen expression in CRC patients worldwide (Figure 12A).

[0366] PolyPEPI1018 is a peptide vaccine that we designed to contain 12 unique epitopes derived from seven conserved testis-specific antigens (TSAs) that are highly expressed in mCRC. In our model, by selecting TSAs that are highly expressed in CRC, targets are accurately identified and tumor biopsies are unnecessary. We calculated that the probability that three of the seven TSAs are expressed in each tumor is greater than 95%. (Figure 12B)

[0367] A phase I study evaluated the safety, tolerability, and immunogenicity of PolyPEPI1018 as an add-on to maintenance therapy in subjects with metastatic colorectal cancer (mCRC) (NCT03391232) (see also Example 4).

[0368] Immunogenicity measurements demonstrated pre-existing immune responses and indirectly confirmed the expression of target antigens in patients. Immunogenicity was measured by enrichment fluorescent spot assay (ELISPOT) from PBMC samples isolated at various time points before vaccination and after the next single immunization with PolyPEPI1018 to confirm vaccine-induced T cell responses; PBMC samples were stimulated in vitro with vaccine-specific peptides (9mer and 30mer) to determine vaccine-induced T cell responses above baseline. At least two patients, an average of four, had pre-existing CD8 T cell responses against each target antigen (Figure 12C). Seven out of ten patients had pre-existing immune responses against at least one antigen (average of 3) (Figure 12D). These results provide evidence that the target selection was appropriate, because CD8+ T cell responses against CRC-specific target TSAs confirmed the expression of that target antigen in the analyzed patients before vaccination with PolyPEPI1018 vaccine. Targeting the actual (expressed) TSA is a prerequisite for an effective tumor vaccine.

[0369] Example 14 – Preclinical and clinical immunogenicity of PolyPEPI1018 vaccine demonstrates proper peptide selection The PolyPEPI1018 vaccine contains six 30mer peptides, each designed by conjugating two immunogenic 15mer fragments (each containing a 9mer PEPI, so that there are two PEPIs in each 30mer, intentionally) derived from seven TSAs (Figure 13). These antigens are frequently expressed in CRC tumors based on the analysis of 2,391 biopsies (Figure 12).

[0370] Preclinical immunogenicity results calculated for the model population (n=433) and CRC cohort (n=37) yielded predicted immunogenicity of 98% and 100% based on the predictions of the PEPI test, which was clinically proven in the OBERTO trial (n=10), where immune responses to at least one antigen were measured in 90% of patients. More interestingly, 90% of patients had vaccine peptide-specific immune responses to at least two antigens, and 80% had CD8+ T cell responses to three or more different vaccine antigens, providing evidence that appropriate target antigens were selected during the design of PolyPEPI1018. CD4+ T cell-specific and CD8+ T cell-specific clinical immunogenicity are detailed in Table 18.

[0371] [Table 18]

[0372] High immune response rates were seen for both effector and memory effector T cells, and immune responses were boosted or de novo induced by the vaccine in 9 of 10 patients for both CD4+ and CD8+ T cells. Also, the percentage of CRC-reactive polyfunctional CD8+ and CD4+ T cells was increased by 2.5- and 13-fold, respectively, in PBMCs of patients after vaccination.

[0373] Example 15 – Clinical response to PolyPEPI1018 treatment The OBERTO clinical trial (NCT03391232), further described in Examples 4, 12, 13 and 14, was analyzed for preliminary objective tumor response rates (RECIST 1.1) (Figure 14). Of the 11 vaccinated patients on maintenance therapy, 5 had stable disease (SD) at the time of preliminary analysis (12 weeks), 3 experienced unexpected tumor responses (partial responses, PR) observed during treatment (maintenance therapy + vaccination), and 3 had progressive disease (PD) according to RECIST 1.1 criteria. Stable disease was achieved as best response in 69% of patients on maintenance therapy (capecitabine and bevacizumab). Patient 020004 had a sustained treatment response after 12 weeks, and patient 010004 was suitable for definitive surgery since he had a treatment response that lasted for a long period of time. After the third vaccination, this patient had no evidence of disease and was therefore a complete responder, as shown in the swimmer plot in Figure 14.

[0374] After one vaccination, the ORR was 27% and the DCR was 63%; in patients who received at least two doses (of three), two of five had an ORR (40%) and the DCR was as high as 80% (SD+PR+CR in four of five) (Table 19).

[0375] [Table 19]

[0376] Based on data from five patients who received multiple doses of the PolyPEPI1018 vaccine in the OBERTO-101 clinical trial, preliminary data suggest that higher AGP counts (>2) are associated with longer PFS and increased rates of tumor size reduction (Figures 14B and C).

[0377] Example 16 – Design of a gastric cancer peptide vaccine for the large population Using the PEPI3+ test described above, peptides were designed for use in a gastric cancer vaccine that would be effective in a high proportion of patients, taking into account both tumor antigen and patient HLA heterogeneity.

[0378] Gastric cancer CTAs were identified and ranked based on the overall expression frequency of antigens found in gastric cancer tumor samples as reported in peer-reviewed publications.

[0379] Based on the ranked expression rates, the most frequently expressed CTAs were selected as target antigens for gastric cancer vaccines. The expression rates of selected gastric cancer-specific CTAs are shown in Figure 16.

[0380] To select immunogenic peptides from the target CTA, the PEPI3+ test and model population described in Example 8 were used to identify 9-mer epitopes (PEPI3+) that were most frequently presented by at least three HLAs of individuals in the model population. These epitopes are referred to herein as "best EPIs." An illustrative example of "PEPI3+ hotspot" analysis and identification of best EPIs is shown in FIG. 15 for the PRAME antigen.

[0381] The reported expression frequency for each CTA was multiplied by the frequency of PEPI3+ hotspots in the model population to identify T cell epitopes (9mers) that induce cytotoxic T cell responses to gastric cancer antigens in the highest percentage of individuals (Table 20a). 15mers were then selected that encompass each of the selected 9mers (Table 20a). The 15mers were selected to bind to most HLA class II alleles in most subjects. These 15mers can induce both CTL and T helper responses in the highest percentage of subjects.

[0382] [Table 20]

[0383] Then, 15 30-mer peptides were designed (Table 21a). Each 30-mer can consist of two optimized 15-mer fragments, each of which is derived from a CTA of different general frequency and arranged end-to-end, with each fragment containing one of the 9-mers (best EPIs) in Table 2-a.

[0384] [Table 21]

[0385] Characterization of PolyPEPI131 Tumor heterogeneity can be addressed by including peptide sequences targeting multiple CTAs in a vaccine or immunotherapy regime. The PolyPEPI1311 composition targets 14 different CTAs. Based on the antigen expression rates of these 14 CTAs, we modeled the expected average number of antigens expressed in cancer cells (AG50) and the minimum number of antigens that have a 95% chance of being expressed (AG95). As shown in the antigen expression curve in Figure 17, 95% of individuals expressed at least 5 of the 14 target antigens (AG95=5).

[0386] The above AG value characterizes the vaccine regardless of the target patient population.The AG value can be used to predict the possibility that a particular cancer (e.g., gastric cancer) will express the antigen that a particular vaccine or immunotherapy composition targets.AG value is based on known tumor heterogeneity, but does not take into account HLA heterogeneity.

[0387] The HLA heterogeneity of a particular population can be characterized from the perspective of immunotherapy or vaccine composition by the number of antigens that display PEPI3+. These are vaccine-specific CTA antigens that are predicted to be ≧1 PEPI3+, referred to herein as "AP". The average number of antigens with PEPI3+ (AP50) indicates how well the vaccine can induce an immune response against the antigens targeted by the composition (gastric cancer vaccine-specific immune response). The PolyPEPI1311 composition can induce an immune response against an average of 8 vaccine antigens (AP50=7.98), and 95% of the model population can induce an immune response against at least 3 vaccine antigens (AP95=3) (Figure 18).

[0388] Vaccines can be further characterized by AGP values, which refer to antigens with PEPI. This parameter is a combination of two previously mentioned parameters: (1) AG depends on the frequency of antigen expression in a particular tumor type, but does not depend on the HLA genotype of individuals in the population, and (2) AP depends on the HLA genotype of individuals in the population, without considering the frequency of antigen expression. AGP depends on both the frequency of expression of the vaccine antigen in the disease and the HLA genotype of individuals in the population.

[0389] The AG and AP data of gastric cancer in the model population were combined to obtain the AGP value of PolyPEPI1311, which represents the probability distribution of vaccine antigens that induce an immune response to antigens expressed in gastric tumors. For PolyPEPI1311, the AGP50 value in the model population is 3.86. AGP95=1 means that 95% of subjects in the model population induce an immune response to at least one expressed vaccine antigen (Figure 19).

[0390] Example 17 –Patient selection using companion diagnostics for gastric, lung, melanoma, and bladder cancer vaccines The likelihood that a particular patient will have an immune or clinical response to treatment with one or more cancer vaccine peptides, such as those described above, can be determined based on (i) the identification of PEPI3+ in the vaccine peptide (a 9-mer epitope that can bind to at least three HLAs of the patient), and / or (ii) the determination of the expression of the target antigen in the patient's cancer cells, for example, measured in a tumor biopsy. Ideally, both parameters are determined to select the optimal combination of vaccine peptides for use in treating the patient. However, in cases where determining the tumor antigens expressed, for example, by biopsy, is not possible, not recommended, or unreliable due to biopsy errors (i.e., a biopsy tissue sample taken from a small portion of the tumor or a metastatic tumor does not represent the full repertoire of CTAs expressed in the patient), only PEPI3+ analysis may be used.

[0391] Example 18 – Design of a lung cancer peptide vaccine for large populations Using the above PEPI3+ test, 9mer and 15mer peptides were designed for use in lung cancer vaccines using the same method as described above in Example 16 for gastric cancer (Tables 20b, 21b). The expression rates of selected gastric cancer-specific CTAs are shown in Figure 20.

[0392] [Table 22]

[0393] [Table 23]

[0394] Characterization of PolyPEPI821 PolyPEPI821 composition targets 13 different CTAs. Based on the antigen expression rates of these 13 CTAs, we model the expected average number of antigens expressed in cancer cells (AG50) and the minimum number of antigens that are 95% likely to be expressed (AG95). As shown in the antigen expression curve in Figure 21, 95% of individuals express at least 2 of the 10 target antigens (AG95=2).

[0395] The PolyPEPI821 composition was able to induce an immune response to an average of nearly eight vaccine antigens (AP50=7.60), with 95% of the model population able to induce an immune response to at least two vaccine antigens (AP95=2) (Figure 22).

[0396] For PolyPEPI821, the AGP50 value in the model population is 2.77. AGP91=1 means that 91% of subjects in the model population will induce an immune response against at least one expressed vaccine antigen (Figure 23).

[0397] Example 19 –Design of a melanoma peptide vaccine for the large population Using the PEPI3+ test described above, 9-mer and 15-mer peptides were designed for use in melanoma vaccines using the same method described above in Example 16 for gastric cancer (Tables 20c, 21c). The expression rates of selected gastric cancer-specific CTAs are shown in Figure 24.

[0398] [Table 24]

[0399] Then, 15 30-mer peptides were designed (Table 21c). Each 30-mer can consist of two optimized 15-mer fragments, each of which is derived from a CTA of different general frequency and arranged end-to-end, with each fragment containing one of the 9-mers (best EPIs) in Table 20c.

[0400] [Table 25]

[0401] Characterization of PolyPEPI621 PolyPEPI621 composition targets 15 different CTAs. Based on the antigen expression rates of these 15 CTAs, we model the expected average number of antigens expressed in cancer cells (AG50) and the minimum number of antigens that are 95% likely to be expressed (AG95). As shown in the antigen expression curve in Figure 25, 95% of individuals express at least 5 of the 15 target antigens (AG95=5).

[0402] The PolyPEPI621 composition was able to induce an immune response to an average of eight vaccine antigens (AP50=8.29), with 95% of the model population able to induce an immune response to at least three vaccine antigens (AP95=2) (Figure 26).

[0403] The AG and AP data of melanoma in the model population were combined to obtain the AGP value of PolyPEPI621, which represents the probability distribution of vaccine antigens that induce an immune response to antigens expressed in gastric tumors. For PolyPEPI621, the AGP50 value in the model population is 2.77. AGP95=1 means that 95% of subjects in the model population induce an immune response to at least one expressed vaccine antigen (Figure 27).

[0404] Example 20 – Design of a bladder cancer peptide vaccine for the large population Using the above PEPI3+ test, 9mer and 15mer peptides were designed for use in bladder cancer vaccines using the same method as described above in Example 16 for gastric cancer (Tables 120d, 21d). The expression rates of selected gastric cancer-specific CTAs are shown in Figure 28.

[0405] [Table 26]

[0406] Then, 15 30-mer peptides were designed (Table 21d). Each 30-mer can consist of two optimized 15-mer fragments, each of which is derived from a CTA of different general frequency and arranged end-to-end, with each fragment containing one of the 9-mers (best EPIs) in Table 20d.

[0407] [Table 27]

[0408] Characterization of PolyPEPI1411 PolyPEPI1411 composition targets 17 different CTAs. Based on the antigen expression rates of these 17 CTAs, we model the expected average number of antigens expressed in cancer cells (AG50) and the minimum number of antigens that are 95% likely to be expressed (AG95). As shown in the antigen expression curve in Figure 29, 95% of individuals express at least 4 of the 17 target antigens (AG95=4).

[0409] The PolyPEPI1411 composition was able to induce an immune response against an average of 9 vaccine antigens (AP50=9.44), with 95% of the model population able to induce an immune response against at least 3 vaccine antigens (AP95=3) (Figure 30).

[0410] The AG and AP data of bladder cancer in the model population were combined to obtain the AGP value of PolyPEPI1411, which represents the probability distribution of vaccine antigens that induce an immune response to antigens expressed in bladder tumors. For PolyPEPI1411, the AGP50 value in the model population is 3.90. AGP95=1 means that 95% of subjects in the model population induce an immune response to at least one expressed vaccine antigen (Figure 31).

[0411] Example 21 –Personalized immunotherapy (PIT) design and treatment for ovarian, breast, and colorectal cancer This example provides proof-of-concept data from four metastatic cancer patients treated with a personalized immunotherapeutic vaccine composition to support the principle on which the present disclosure is based in part, that binding of epitopes by multiple HLA of a subject induces a cytotoxic T cell response.

[0412] Composition for the treatment of ovarian cancer using POC01-PIT (Patient A) This example describes the treatment of an ovarian cancer patient with an individualized immunotherapy composition designed specifically for the patient based on the patient's HLA genotype, based on the disclosure provided herein.

[0413] The HLA class I and class II genotypes of a patient with metastatic ovarian adenocarcinoma (Patient A) were determined from a saliva sample.

[0414] To generate a personalized pharmaceutical composition for patient A, 13 peptides were selected, each of which fulfills two criteria: (i) is derived from an antigen expressed in ovarian cancer, as reported in peer-reviewed scientific publications, and (ii) contains a fragment that is a T cell epitope capable of binding to at least three HLA class I of patient A (Table 22). Additionally, each peptide is optimized to bind to the maximum number of HLA class II of the patient.

[0415] [Table 28]

[0416] The 11 PEPI3 peptides in this immunotherapy composition can induce a T cell response in patient A with a probability of 84% and two PEPI4 peptides (POC01-P2 and POC01-P5) with a probability of 98% according to the validation of the PEPI test shown in Table 3. The T cell response targets 13 antigens expressed in ovarian cancer. The expression of these cancer antigens in patient A was not tested. Instead, the probability of successful cancer cell killing was determined based on the probability of antigen expression in the patient's cancer cells and the positive predictive value (AGP count) of a PEPI3+ test of ≧1. The AGP count predicts the efficacy of the vaccine in a subject: the number of vaccine antigens expressed in the patient's tumor (ovarian adenocarcinoma) with PEPI. The AGP count indicates the number of tumor antigens that the vaccine recognizes and induces a T cell response (hits the target) against the patient's tumor. The AGP count depends on the expression rate of the vaccine antigen in the subject's tumor and the subject's HLA genotype. The exact value is between 0 (no expressed antigens presenting PEPIs) and the maximum number of antigens (all antigens expressed and presenting PEPIs).

[0417] The probability that patient A expresses one or more of the 13 antigens is shown in Figure 32. AGP95 (AGP with 95% probability) = 5, AGP50 (mean of discrete probability distribution - expected value -) = 7.9, mAGP (probability that AGP is at least 2) = 100%, AP = 13.

[0418] The pharmaceutical composition for Patient A may contain at least two of the 13 peptides (Table 22), because it has been determined that the presence of at least two polypeptide fragments (epitopes) capable of binding to at least three HLA of an individual in a vaccine or immunotherapy composition (≧2 PEPI3+) predicts clinical response. The peptides are synthesized, dissolved in a pharma- ceutical acceptable solvent, mixed with an adjuvant, and then injected. It is desirable for the patient to receive personalized immunotherapy with at least two peptide vaccines, but more is preferable to increase the probability of killing cancer cells and reduce the chance of recurrence.

[0419] For the treatment of patient A, the 13 peptides were formulated as 4x3 or 4 peptides (POC01 / 1, POC01 / 2, POC01 / 3, POC01 / 4). One treatment cycle is defined as the administration of all 13 peptides within a 30 day period. Patient History: Diagnosis: Metastatic ovarian adenocarcinoma Age:51 Family medical history: colon and ovarian cancer (mother), breast cancer (grandmother) Tumor pathology: 2011: Initially diagnosed with ovarian adenocarcinoma; Wertheim surgery and chemotherapy; lymph node removal 2015: Metastasis to pericardial adipose tissue, resection 2016: Liver metastasis 2017: Progression in retroperitoneal and mesenteric lymph nodes; primary peritoneal carcinomatosis with small amount of ascites. Pretreatment: 2012: Paclitaxel-carboplatin (6x) 2014: Caelyx-Carboplatin (1x) 2016-2017 (9 months): Lymparza (olaparib) 2 × 400 mg / day, orally 2017: Hycamtin inf. 5 x 2.5 mg (3 x 1 seria / month) PIT vaccination treatment was started on April 21, 2017. Figure 33. 2017-2018: Patient A received 8 cycles of vaccination as add-on therapy and was still alive 17 months (528 days) after the start of treatment. During this interval, after the third and fourth vaccine treatments, the patient experienced a partial response as the best response. The patient died in October 2018.

[0420] Interferon (IFN)-γ ELISPOT bioassays confirmed the predicted T cell responses of patient A to the 13 peptides. Positive T cell responses (defined as >5-fold above control or >3-fold above control and >50 spots) were detected for all 13 20-mer peptides and all 13 9-mer peptides with the sequence of PEPI for each peptide capable of binding to the highest HLA class I allele in patient A ( FIG. 34 ).

[0421] Patient Tumor MRI Findings (Baseline April 15, 2016) (BL: Baseline for Tumor Response Assessment in Figure 35) Disease was primarily confined to the liver and lymph nodes. The use of MRI is limited to the detection of pulmonary (intrapulmonary) metastases. May 2016 to January 2017: Olaparib treatment (FU1: Follow-up observation 1 in Figure 35) December 25, 2016 (before PIT vaccine treatment). The tumor volume was dramatically reduced, and confirmation of response was obtained at (FU2: follow-up observation 2 in FIG. 35). January to March 2017 - TOPO Protocol (Topoisomerase) April 6, 2017 (FU3 in Fig. 35) Regrowth of existing lesions and emergence of new lesions leading to disease progression were demonstrated. Peritoneal carcinomatosis with increasing ascites volume. Progressive liver tumors and lymph nodes. April 21, 2017 PIT started July 26, 2017 (after PIT of the second cycle): (FU4 in Fig. 35) Progression / suspected progression Rapid progression, significant pleural and ascites in lymph nodes, liver, retroperitoneum, and chest. Carboplatin, gemcitabine, and Avastin were initiated. September 20, 2017 (after 3 cycles of PIT): (FU5 in Figure 35) Partial response Complete remission in the pleural area / pleural effusion and ascites Remission in the liver, retroperitoneal region, and lymph nodes These findings suggest pseudoprogression. November 28, 2017 (after 4 cycles of PIT): (FU6 in Figure 35) Partial response Complete remission in the thoracic region. Remission in the liver, retroperitoneal region, and lymph nodes. April 13, 2018: Progress Complete response in thoracic and retroperitoneal regions. Progression in liver centers and lymph nodes. June 12, 2018: Stable disease Complete response in thoracic and retroperitoneal regions. Minimal regression in central liver and lymph nodes. July 2018: Progress October 2018: Patient A dies Partial MRI data for patient A are shown in Table 23 and FIG.

[0422] [Table 29]

[0423] Design, Safety, and Immunogenicity of a Personalized Immunotherapeutic Composition (PBRC01) for Treating Metastatic Breast Cancer (Patient B) PT9 The HLA class I and class II genotypes of metastatic breast cancer patient B were determined from a saliva sample. To create a personalized pharmaceutical composition for patient B, 12 peptides were selected, each of which meets two criteria: (i) is derived from an antigen expressed in breast cancer, as reported in peer-reviewed scientific publications, and (ii) contains a fragment that is a T cell epitope that can bind to at least three HLA class I of patient B (Table 24). Furthermore, each peptide is optimized to bind to the maximum number of HLA class II of the patient. The 12 peptides target 12 breast cancer antigens. The probability that patient B expresses one or more of the 12 antigens is shown in Figure 36.

[0424] [Table 30]

[0425] Expected benefits: AGP95=4; 95% probability that the PIT vaccine will induce a CTL response against the four TSAs expressed on BRC09 breast cancer cells. Additional efficacy parameters: AGP50=6.45, mAGP=100%, AP=12.

[0426] For the treatment of patient B, 12 peptides were formulated as 4x3 peptides (PBR01 / 1, PBR01 / 2, PBR01 / 3, PBR01 / 4). One treatment cycle is defined as the administration of all 12 different peptide vaccines within 30 days (Figure 36C). Patient History: 2013: Diagnosis: Breast cancer; CT scan and bone scan ruled out metastatic disease. 2014: Double mastectomy, followed by chemotherapy 2016: Widespread metastatic disease with lymph node metastases both above and below the diaphragm. Multiple liver and lung metastases. Treatment: 2013-2014: Adriamycin-cyclophosphamide and paclitaxel 2017: Letrozole, palbociclib, and gozorelin, and the PIT vaccine 2018: The patient's condition worsened and he died in January PIT vaccine treatment was started on April 7, 2017. Treatment schedule and The main characteristics of the disease are shown in Table 25.

[0427] [Table 31]

[0428] Eight to twelve vaccine peptides were predicted with 95% confidence to induce T cell responses in patient B. Peptide-specific T cell responses were measured in all available PBMC samples using an interferon (IFN)-γ ELISPOT bioassay (Figure 37). The results confirmed the prediction: nine peptides showed a positive reaction, proving that T cells could recognize tumor cells of patient B expressing FISP1, BORIS, MAGE-A11, HOM-TES-85, NY-BR-1, MAGE-A9, SCP1, MAGE-A1, and MAGE-C2 antigens. Some tumor-specific T cells were present after the first vaccination and boosted with additional treatments (e.g., MAGE-A1), others were induced after the boost (e.g., MAGE-A9). Such a broad range of tumor-specific T cell responses is remarkable in patients with advanced cancer.

[0429] Patient B's medical history and results March 7, 2017: Pre-PIT vaccine treatment Multimetastatic disease of the liver with true extrinsic compression of the origin of the common bile duct and massive dilatation of the entire intrahepatic bile duct. Adenopathy of the peritoneum, porta hepatis, and retroperitoneum. March 2017: Treatment started - letrozole, palbociclib, gosorelin, and PIT vaccine May 2017: Drug withdrawal May 26, 2017: After one cycle of PIT Metabolic activity of the tumor decreased by 83% (PET CT) Liver, lungs, lymph nodes, and other metastases. June 2017: Normalization of neutrophil counts, as confirmed by the patient, indicates discontinuation of palbociclib Tumor marker rebound delayed by 4 months March-May 2017: CEA and CA remained elevated consistent with the patient's anti-cancer treatment outcome (Ban, Future Oncol 2018) June-September 2017: CEA and CA decreased consistent with delayed response to immunotherapy Quality of life February to March 2017: Hospitalized for illness and jaundice April to October 2017: Very good November 2017: (Deterioration of condition (tumor escape?) January 2018: Patient B dies.

[0430] The immunogenicity results are summarized in FIG.

[0431] Patient Clinical Outcome Measurements: One month prior to initiation of PIT vaccination treatment, PET CT confirmed extensive DFG avid disease with lymph node metastases both above and below the diaphragm (Table 25). The patient had progressive multiple liver, multifocal bone, and lung metastases, as well as retroperitoneal adenopathy. The patient's intrahepatic enzymes were elevated consistent with damage caused by liver metastases, with elevated bilirubin and jaundice. The patient was administered letrozole, palbociclib, and gozorelin as anticancer treatment. Two months after initiation of PIT vaccination, the patient felt very well and her quality of life had normalized. Indeed, the patient's PET CT showed significant morphological regression in liver, lung, bone, and lymph node metastases. At the supradiaphragmatic stage, metabolic adenopathy was not identifiable.

[0432] The combination of pablocilib and the personalized vaccine was likely responsible for the remarkable early response observed after vaccination. Pablocilib has been shown to improve the activity of immunotherapy by increasing HLA presentation of CTA and decreasing Treg proliferation: (Goel et al. Nature. 2017: 471-475). The treatment results of patient B suggest that maximum efficacy can be achieved using the PIT vaccine as an add-on to state-of-the-art therapy.

[0433] Patient B's tumor biomarkers were tracked to separate the effect of state-of-the-art therapy from that of the PIT vaccine. Tumor markers remained unchanged for the first 2-3 months of treatment, then declined rapidly, suggesting a delayed effect typical of immunotherapy (Table 25). Furthermore, by the time the tumor biomarkers declined, the patient had already voluntarily discontinued treatment, confirmed by an increase in neutrophil count.

[0434] After the fifth PIT treatment, the patient experienced symptoms. Tumor markers and liver enzyme levels were elevated again. Thirty-three days after the last PIT vaccination, the patient's PET CT showed significant metabolic progression in liver, peritoneum, skeleton, and left adrenal sites, confirming the laboratory findings. Isolated recurrence in distant metastases could be due to potential immune resistance; possibly caused by downregulation of both HLA expression impairing tumor recognition by PIT-induced T cells. However, PET CT detected complete regression of metabolic activity in all axillary and mediastinal axillary supradiaphragmatic targets (Table 25). These localized tumor responses could explain the known delayed and sustained responses to immunotherapy, since it is unlikely that these tumor sites will not recur after cessation of anticancer drug treatment.

[0435] Personalized immunotherapy composition PT13 for the treatment of a patient with metastatic breast cancer (Patient C) To treat a patient with metastatic breast cancer (Patient C), a PIT vaccine with a similar design to that described for Patient A and Patient B was prepared. The PIT vaccine contained 12 PEPIs. The predicted efficacy of the PIT vaccine is AGP=4. The treatment schedule of the patient is shown in Figure 38. Tumor Pathology Primary tumor in 2011. HER2-, ER+, sentinel node negative 2017 Multiple bone metastases: ER+, cytokeratin 7+, cytokeratin 20-, CA125-, TTF1-, CDX2- treatment 2011 Wide local excision, negative sentinel nodes; radiation therapy 2017~ Anticancer therapy (Tx): letrozole (2.5mg / day), denosumab; Radiation (Rx): 1 bone PIT vaccine (3 cycles) as an add-on to standard treatment Bioassays confirmed positive T cell responses (defined as >5-fold above control or >3-fold above control and >50 spots) to 11 of 12 20-mer peptides from the PIT vaccine and 11 of 12 9-mer peptides with the sequence of PEPI for each peptide capable of binding to the patient's highest HLA class I allele (Figure 39). Long-lasting memory T cell responses were detected 14 months after the last vaccination (FIGS. 24C-D). Treatment outcomes The clinical results of the treatment of Patient C are shown in Table 26. Patient C has a partial response and evidence of healing of bone metastases.

[0436] [Table 32]

[0437] The immune response is shown in Figure 39. Expected immunogenicity, PEPI=12 (CI95%[8,12]). Immunogenicity detected: 11 (20mer) and 11 (9mer) antigen-specific T cell responses after three PIT vaccinations (Fig. 39A, B). PIT vaccine-specific immune responses could still be detected 4.5, 11, or 14 months after the last vaccination (Fig. 39C, D).

[0438] Personalized immunotherapy composition PT16 for the treatment of a patient with metastatic colorectal cancer (Patient D) Tumor Pathology 2017 (February) mCRC (MSS) with liver metastases, surgery on primary tumor (sigmoid colon) pT3 pN2b(8 / 16)M1. KRAS G12D, TP53-C135Y, KDR-Q472H, MET-T1010I mutations. SATB2 expression. EGFR wt, PIK3CA-I391M (non-driver). 2017 (June) Partial liver resection: KRAS-G12D(35G>A)NRAS wt, May 2018: Second resection: SATB2 expression, lung metastasis 3→21 treatment 2017 FOLFOX-4 (oxaliplatin, calcium folinate, 5-FU) → Allergic reaction during the second treatment DeGramont (5-FU + Calcium folinate) June 2018 → FOLFIRI + ramucirumab, twice weekly; chemoembolization 2018 (October): PIT vaccination (13 patient-specific peptides, administered four times) as an add-on to standard treatment.

[0439] The patient treatment schedule is shown in FIG.

[0440] Treatment outcomes The patient's general condition was good, and pulmonary progression was confirmed by CT scan 8 months later. Using 9-mer and 20-mer peptides for stimulation, both PIT-induced and pre-existing T cell responses were measured by enriched fluorescent spots from PBMCs (FIG. 41).

[0441] A summary of immune response rates and immunogenicity results demonstrates that the vaccine is appropriately designed for target antigen selection and induction of multiple peptide-targeted immune responses, both CD4+ and CD8+ specific.

[0442] [Table 33]

Claims

1. A polypeptide comprising a fragment of 30 or fewer consecutive amino acids of gastric cancer associated antigen DPPA2, said fragment comprising the amino acid sequence of SEQ ID NO:1 or SEQ ID NO:

4.

2. A nucleic acid or nucleic acid vector encoding a polypeptide, said polypeptide comprising a fragment of 30 or fewer consecutive amino acids of gastric cancer associated antigen DPPA2, wherein said fragment comprises the amino acid sequence of SEQ ID NO:1 or SEQ ID NO:

4.

3. 3. A polypeptide according to claim 1 or a nucleic acid according to claim 2, wherein the polypeptide or the polypeptide encoded by the nucleic acid comprises: (i) a fragment of 30 or fewer consecutive amino acids of DPPA2 comprising SEQ ID NO:1 or SEQ ID NO:4; and (ii) a fragment of 30 or less consecutive amino acids of a second gastric cancer-associated antigen selected from CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and SSX1, wherein the fragment (ii) comprises an amino acid sequence selected from SEQ ID NOs: 2, 3, and 5-30. A polypeptide or nucleic acid comprising or consisting of:

4. A polypeptide according to claim 1 or 3 or a nucleic acid according to claim 2 or 3, wherein the polypeptide or the polypeptide encoded by the nucleic acid comprises or consists of the amino acid sequence of SEQ ID NO: 31 or 34.

5. 4. A polypeptide or nucleic acid according to claim 3, wherein the polypeptide or the polypeptide encoded by the nucleic acid comprises or consists of an amino acid sequence selected from SEQ ID NOs: 61, 71, 163 and 164.

6. 10. A combination of two or more polypeptides, wherein one polypeptide of said combination is a polypeptide according to any one of claims 1 and 3-5, and a second polypeptide of said combination comprises a fragment of 30 or less consecutive amino acids of a further gastric cancer associated antigen selected from CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and SSX1, wherein said fragment comprises an amino acid sequence selected from SEQ ID NOs: 2, 3 and 5-30.

7. (a) 15 polypeptides having the amino acid sequences of SEQ ID NOs: 61 to 75; or (b) 15 polypeptides having the amino acid sequences of SEQ ID NOs: 150 to 164.

7. The combination according to claim 6, comprising or consisting of:

8. 8. One or more nucleic acids encoding the combination of polypeptides according to claim 6 or 7, or one or more nucleic acid vectors comprising said one or more nucleic acids.

9. A pharmaceutical composition or a pharmaceutical kit comprising a polypeptide according to any one of claims 1 and 3 to 5, or a combination of polypeptides according to claim 6 or 7, or one or more nucleic acids according to any one of claims 2 to 5 and 8.

10. Use of a polypeptide according to any one of claims 1 and 3 to 5, a combination of polypeptides according to claim 6 or 7, or one or more nucleic acids according to any one of claims 2 to 5 and 8, in the manufacture of a medicament for vaccination to provide immunotherapy or to induce a cytotoxic T cell response in a subject.

11. A vaccination composition for providing immunotherapy or inducing a cytotoxic T cell response in a subject, said vaccination composition comprising a polypeptide described in any one of claims 1 and 3 to 5, a combination of the polypeptides described in claim 6 or 7, or one or more nucleic acids described in any one of claims 2 to 5 and 8.

12. The use according to claim 10, wherein the medicament is for treating cancer or gastric cancer.

13. The composition described in claim 11 for treating cancer or gastric cancer.

14. 10. A method for identifying a human subject likely to have a cytotoxic T cell response to administration of the polypeptide or a polypeptide encoded by the nucleic acid of the pharmaceutical composition or pharmaceutical kit of claim 9, comprising: (i) determining that the polypeptide(s) of the pharmaceutical composition or kit, or the polypeptide(s) encoded by the nucleic acid, comprises a sequence that is a T cell epitope capable of binding to at least three HLA class I molecules of the subject; (ii) identifying the subject as likely to have a cytotoxic T cell response to administration of the polypeptide or the polypeptide encoded by the nucleic acid of the pharmaceutical composition or the pharmaceutical kit; The method includes:

15. (a) selected from DPPA2, CAGE-1, TSP50, HIWI, SURVIVIN, 5T4, PRAME, KK-LC-1, MAGE-A2, MAGE-A3, LAGE-1, MAGE-A10, MAGE-A1, and SSX1; and (b) i. contained in a peptide contained in said pharmaceutical composition; and ii. comprises an amino acid sequence that is a T cell epitope capable of binding to at least three HLA class I molecules of the subject; 15. The method of claim 14, further comprising using the population expression data for each antigen to determine the likelihood that the subject has a CD8+ T cell response targeted to one or more polypeptide antigens expressed by cancer cells of the subject.

16. 10. A method for identifying a subject likely to have a clinical response to administration of said polypeptide or a polypeptide encoded by said nucleic acid of the pharmaceutical composition or pharmaceutical kit of claim 9, comprising: (i) the polypeptide(s) of the pharmaceutical composition or kit, or the polypeptide(s) encoded by the nucleic acid, comprises two or more different amino acid sequences, each of which is a. a T cell epitope capable of binding to at least three HLA class I molecules of the subject; and b. A cancer-associated antigen expressed by cancer cells of the subject or a fragment of a cancer-associated antigen present in a sample obtained from the subject. determining that; (ii) identifying the subject as likely to have a clinical response to administration of the polypeptide or the polypeptide encoded by the nucleic acid of the pharmaceutical composition or pharmaceutical kit; The method includes:

17. 10. A method for determining the likelihood that a particular human subject will have a clinical response to administration of said polypeptide or a polypeptide encoded by said nucleic acid of the pharmaceutical composition or pharmaceutical kit of claim 9, wherein one or more of the following factors correspond to a higher likelihood of clinical response: (a) a greater number and / or different amino acid sequences are present in the polypeptide(s) of said pharmaceutical composition or pharmaceutical kit, or in the polypeptide(s) encoded by said nucleic acid, each of which is a T cell epitope capable of binding to at least three HLA class I of said subject; (b) the greater the number of target polypeptide antigens, or the greater the number of target polypeptide antigens expressed in the subject, or the greater the number of target polypeptide antigens present in one or more samples obtained from the subject, A. contained in a polypeptide of the pharmaceutical composition or kit, or a polypeptide encoded by the nucleic acid; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; comprising at least one amino acid sequence; (c) the subject is more likely to express the target polypeptide antigen; or A. contained in a polypeptide of the pharmaceutical composition or kit, or a polypeptide encoded by the nucleic acid; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; a greater likelihood of expressing the target polypeptide antigen determined to comprise at least one amino acid sequence; and / or (d) the subject is predicted to express a greater number of target polypeptide antigens; or A. contained in a polypeptide of the pharmaceutical composition or kit, or a polypeptide encoded by the nucleic acid; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; A greater number of target polypeptide antigens determined to contain at least one amino acid sequence.

18. (i) the polypeptide antigen targeted by the polypeptide(s) of the pharmaceutical composition or pharmaceutical kit is A. contained in a polypeptide of the pharmaceutical composition or kit, or a polypeptide encoded by the nucleic acid; and B. a T cell epitope capable of binding to at least three HLA class I of the subject; identifying the amino acid sequence as comprising the (ii) using the population expression data for each antigen identified in step (i), determining the probability that the subject expresses one or more of the antigens identified in step (i), which together comprise at least two different amino acid sequences of step (i); (iii) determining the likelihood that the subject will have a clinical response to administration of the polypeptide or the polypeptide encoded by the nucleic acid of the pharmaceutical composition or pharmaceutical kit, wherein a higher probability determined in step (ii) corresponds to a higher likelihood of a clinical response.

20. The method of claim 17, comprising:

19. 20. The method of claim 18, wherein the at least two different amino acid sequences are comprised in the amino acid sequences of two different polypeptide antigens targeted by the pharmaceutical composition or kit.

20. 13. The use according to claim 10 or 12, wherein the medicament is an individualized medicine for a particular human subject, the subject being identified as likely to have a clinical response according to the method of any one of claims 15 to 18.

21. The composition of claim 11 or 13, wherein the composition is a personalized medicine for a particular human subject, the subject being identified as likely to have a clinical response to the method of any one of claims 15 to 18.

22. 21. The use according to any one of claims 10, 12 and 20, wherein the medicament is administered in combination with chemotherapy or a checkpoint inhibitor.

23. The composition of any one of claims 11, 13 and 21 administered in combination with chemotherapy or a checkpoint inhibitor.

24. 10. A method for identifying a human subject likely to not have a clinical response to administration of said polypeptide or nucleic acid of the pharmaceutical composition or pharmaceutical kit of claim 9, comprising: (i) determining that the polypeptide(s) of the pharmaceutical composition or kit, or the polypeptide encoded by the nucleic acid, does not contain two or more distinct amino acid sequences that are T cell epitopes each capable of binding to at least three HLA class I molecules of the subject; (ii) identifying the subject as likely to not have a clinical response to administration of the pharmaceutical composition, or the polypeptide or nucleic acid of the pharmaceutical kit; The method includes:

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