Antigen Peptide Derived From the Sequence of Epidermal Growth Factor Receptor Having T790M Point Mutation

Abstract

The present application relates to an antigen peptide derived from the sequence of epidermal growth factor receptor having T790M point mutation and a pharmaceutical composition for the treatment of cancer comprising the peptide.

Claims

1-8. (canceled)

9. A method of treating cancer in a subject in need thereof, comprising administering peptide-specific cytotoxic T lymphocytes (CTLs) to the subject, wherein the CTLs are prepared by contacting a peptide consisting of the amino acid sequence of SEQ ID NO: 5,7 or 15 with peripheral blood mononuclear cells (PBMCs) to induce the CTLs; or administering antigen presenting cells that express a peptide consisting of the amino acid sequence of SEQ ID NO: 5,7 or 15 to the subject.

10. The method according to claim 9, comprising administering the CTLs to a subject in need thereof.

11. The method according to claim 9, comprising administering the antigen presenting cells to a patient in need thereof.

12. The method according to claim 11, wherein the antigen presenting cells are prepared by culturing cells in the presence of the peptide such that the peptide is bound to and presented on an human leukocyte antigen (HLA) molecule of the cells, or introducing a vector expressing the peptide into the cells such that the peptide is expressed in the cells.

13. The method according to claim 12, wherein the cells are dendritic cells.

14. The method according to claim 13, wherein the dendritic cells are prepared from peripheral blood mononuclear cells (PBMCs).

Description

BRIEF DESCRIPTION OF DRAWINGS

[0010] FIG. 1. Immunogenicity of T790M-5 and T790M-7 peptides in peripheral blood mononuclear cells (PBMCs) from normal donors. Immunogenicity of T790M-5 and T790M-7 peptides was examined with PBMCs from 6 different HLA-A2.sup.+ healthy donors. PBMCs were stimulated 5 times with T790M-5 or T790M-7 peptide (10 g/ml) every 3 or 4 days. The stimulated PBMCs (310.sup.4 cells/well) were examined for reactivity against T2 cells (110.sup.4 cells/well) pulsed with T790M-5 or T790M-7 or control HIV peptide (10 g/ml) by IFN- ELISPOT assay.

[0011] FIG. 2. Reactivity of T790M-5- or T790M-7-stimulated T cells against non-small cell lung cancer (NSCLC) cells having the EGFR T790M mutation. PBMCs from an HLA-A2.sup.+ healthy donor were stimulated 5 times with T790M-5 or T790M-7 peptide (10 g/ml) every 3 or 4 days. CD8.sup.+ T cells (210.sup.4 cells/well) that were isolated from the stimulated PBMCs by using anti-CD8 beads were examined for their reactivity against different NSCLC cell lines, NCI-H1975 (HLA-A2.sup. T790M.sup.+), NCI-H1975-A2 (HLA-A2.sup.+ T790M.sup.+), and HCC827 (HLA-A2.sup. T790M.sup.), by IFN- ELISPOT assay.

[0012] FIG. 3. Cytotoxicity of T790M-5- or T790M-7-stimulated T cells against NSCLC cell lines having the EGFR T790M mutation. PBMCs from an HLA-A2.sup.+ healthy donor were stimulated 5 times with T790M-5 or T790M-7 peptide (10 /ml) every 3 or 4 days. The stimulated PBMCs were examined for their cytotoxicity against NSCLC cell lines (NCI-H1975 (HLA-A2.sup. T790M.sup.+) and NCI-H1975-A2 (HLA-A2.sup.+ T790M.sup.+)) (210.sup.3 cells/well), at the indicated effector/target ratios. The cytotoxicity was calculated as follows: cytotoxicity(%)=[(test releasespontaneous release)/(maximal releasespontaneous release)]100.

[0013] FIG. 4. HLA class I-restricted reactivity of T790M-5- or T790M-7-stimulated T cells against NSCLC cell lines having the EGFR T790M mutation. PBMCs from an HLA-A2.sup.+ healthy donor were stimulated 5 times with T790M-5 or T790M-7 peptide (10 g/ml) every 3 or 4 days. The stimulated PBMCs were examined for their reactivity against NCI-H1975-A2 (HLA-A2.sup.+ T790M.sup.+) in the presence of anti-HLA class I (W6/32) or anti-HLA class II (L243) antibody by IFN- ELISPOT assay.

[0014] FIG. 5. Cross reactivity of T790M-5-stimulated T cells to a wild-type peptide. PBMCs from an HLA-A2.sup.+ healthy donor were stimulated 5 times with T790M-5 (10 g/ml) every 3 or 4 days. The stimulated PBMCs were examined for their reactivity to T790M-5 or a wild-type peptide by IFN- ELISPOT assay.

[0015] FIG. 6. HLA-A2-binding capability of EGFR-T790M-derived peptides. The binding of selected peptides to an HLA-A2 molecule was evaluated by HLA class I stabilization assay with TAP2-deficient T2 cells expressing HLA-A2.

[0016] FIG. 7. Immunogenicity of EGFR-T790M-derived candidate peptides in HLA-A2Tg mice. Immunogenicity of candidate peptides in HLA-A2Tg mice was examined by vaccination of dendritic cells. The result of T790M-B is shown.

[0017] FIG. 8. Immunogenicity of EGFR-T790M-derived candidate peptides in PBMCs from healthy donors. For evaluation of immunogenicity of candidate peptides, induction of peptide-specific CTLs from PBMCs of HLA-A2.sup.+ healthy donors was examined. The result of T790M-A is shown.

[0018] FIG. 9. Reactivity of T790M-A-specific CTL line against NSCLC cell lines having the EGFR T790M mutation (1). The established T790M-A-specific CTL line was examined for reactivity against NSCLC cell lines (NCI-H1975 (HLA-A2.sup. T790M.sup.+) and NCI-H1975-A2 (HLA-A2.sup.+ T790M.sup.+)) by IFN- ELISPOT assay.

[0019] FIG. 10. Reactivity of T790M-A-specific CTL line against NSCLC cell lines having the EGFR T790M mutation (2). The established T790M-A-specific CTL line was examined for reactivity against NSCLC cell lines (NCI-H1975 (HLA-A2.sup. T790M.sup.+) and NCI-H1975-A2 (HLA-A2.sup.+ T790M.sup.+)) by CD107a assay.

[0020] FIG. 11. Reactivity of T790M-A-specific CTL line against NSCLC cell lines having the EGFR T790M mutation (3). The established T790M-A-specific CTL line was examined for cytotoxicity against NSCLC cell lines (NCI-H1975 (HLA-A2.sup. T790M) and NCI-H1975-A2 (HLA-A2.sup.+ T790M.sup.+)).

DESCRIPTION OF EMBODIMENTS

[0021] The present application provides a peptide derived from the sequence of epidermal growth factor receptor (EGFR) having T790M point mutation (EGFR-T790M) comprising the amino acid sequence of SEQ ID NO: 5, 7, or 15 and having an ability to induce peptide-specific CTLs. The amino acid sequence of EGFR-T790M is shown in SEQ ID NO: 11. The peptide of the invention may be a peptide that can bind to an HLA molecule by itself, or may be a peptide that produces a peptide comprising the amino acid sequence of SEQ ID NO: 5, 7, or 15 and binding to an HLA molecule when fragmented in a cell. The peptide is preferably, but not limited to, 10-30 amino acids, 11-30 amino acids, or 9-30 amino acids, more preferably 10-15 amino acids, 11-15 amino acids, or 9-15 amino acids in length.

[0022] The ability of the peptide to induce peptide-specific CTLs may be examined, for example, by determining a cytokine such as interferon- (IFN-) produced from PBMCs stimulated with the peptide in response to antigen presenting cells pulsed with the same peptide, by a method such as ELISA or ELISPOT. Alternatively, the ability may be examined by determining cytotoxicity of the induced CTLs by a method such as a .sup.51Cr-release assay.

[0023] In a preferred embodiment, the peptide of the invention is a peptide consisting of the amino acid sequence of SEQ ID NO: 5, 7, or 15.

[0024] A constituent amino acid of the peptide of the invention may be a natural amino acid or an amino acid analogue. Examples of the amino acid analogue include N-acylated, O-acylated, esterified, acid amidated and alkylated amino acids. The peptide of the invention may comprise a modification at the constituent amino acid or a moiety such as a carboxylic group, so long as the modification does not significantly deteriorate the function of the peptide. The modification may be addition of formyl, acetyl or t-butoxycarbonyl group at the N-terminus- or free-amino group, or addition of methyl, ethyl, t-butyl or benzyl group at the C-terminus- or free carboxylic group.

[0025] The peptide of the invention may be synthesized by a conventionally used peptide synthesizing procedure. Examples of the conventionally used procedure are those described in the literatures including Peptide Synthesis, Interscience, New York, 1966; The Proteins, vol. 2, Academic Press Inc., New York, 1976; Pepuchido-Gosei, Maruzen Co. Ltd., 1975; Pepuchido-Gosei-no-Kiso-to-Jikkenn, Maruzen Co. Ltd., 1985; and Iyakuhin-no-Kaihatu, Zoku, vol. 14, Peputido-Gosei, Hirokawa Shoten, 1991, (those references are herein incorporated by reference).

[0026] The peptide of the invention, when administered to a patient, induces CTLs that recognize a complex of the cancer antigen peptide and an HLA molecule on cancer cells to kill the cells (i.e., cancer-reactive CTLs) inside the body of the patient, and thereby exerts an anti-cancer effect. Therefore, the peptide of the invention may be used as a pharmaceutical composition for the treatment of cancer, such as a cancer vaccine or a CTL inducer.

[0027] The pharmaceutical composition of the invention may be used to treat a cancer expressing EGFR-T790M. Preferably, the pharmaceutical composition of the invention is used to treat non-small cell lung cancer.

[0028] As used herein, the treatment of cancer includes both prophylactic and therapeutic treatments. The treatment of cancer includes, for example, tumor shrinkage or suppression of tumor growth, suppression of tumorous lesion appearance, prolonged survival, improvement or suppression of exacerbation of a subjective or objective symptom associated with tumor, suppression of metastasis, and prevention of recurrence.

[0029] The pharmaceutical composition of the invention may be administrated intradermally or subcutaneously. The pharmaceutical composition of the invention may comprise a pharmaceutically acceptable salt or carrier suitable for the administration. Examples of the salt may include an alkali metal hydrogencarbonate such as sodium chloride and sodium hydrogen carbonate. Preferably, for administration, the pharmaceutical composition is dissolved in a vehicle such as water to provide a solution isotonic to plasma. Examples of the carrier may include cellulose, amino acid polymers and albumin. The peptide of the invention may be conjugated with the carrier as appropriate.

[0030] The pharmaceutical composition of the invention may be formulated as a liposomal preparation, a particulate preparation in which the ingredient is bound to a bead having a diameter of several micro maters, or a preparation in which the ingredient is attached to a lipid. For effective establishment of immunity, the pharmaceutical composition of the invention may be administered along with incomplete Freund's adjuvant (ISA-51 (SEPPIC), for example) or a polysaccharide such as pullulan, which has conventionally been used for vaccination, or an immunopotentiating agent such as complete Freund's adjuvant, Bacillus Calmette-Gurin (BCG), Alum, GM-CSF, IL-2, and CpG.

[0031] The dosage of the pharmaceutical composition of the invention may be determined as appropriate based on a factor such as condition of the disease to be treated, or age or body weight of the patient to be treated. In general, the amount of the peptide in the pharmaceutical composition to be administered may be 0.0001 to 1000 mg, preferably 0.001 to 100 mg, more preferably 0.01 to 10 mg, still more preferably 0.1 to 5 mg or 0.5 to 3 mg per administration. Preferably, the pharmaceutical composition may be repeatedly administered once every several days, several weeks or several months.

[0032] The peptide of the invention may be used to induce cancer-reactive CTLs in vitro. Therefore, the present application provides a method for inducing cancer-reactive CTLs comprising the step of contacting the peptide of the invention with PBMCs collected from a patient. The CTLs may be induced, for example, by incubating PBMCs collected from a patient in vitro in the presence of the peptide of the invention. The method for inducing cancer-reactive CTLs is useful for adoptive immunotherapy, wherein CTLs induced from PBMCs of a patient are returned into the patient to kill cancer cells.

[0033] The peptide of the invention also may be used to prepare antigen presenting cells that induce cancer-reactive CTLs in a cancer patient. Therefore, the present application provides a method for preparing antigen presenting cells comprising the step of contacting the peptide of the invention with cells having antigen-presenting ability collected from a patient. The antigen presenting cells may be prepared by culturing cells having antigen-presenting ability collected from a patient in the presence of the peptide of the invention such that the peptide is bound to and presented on an HLA molecule. Alternatively, the antigen presenting cells may be prepared by introducing a vector being able to express the peptide into cells having antigen-presenting ability collected from a patient such that the peptide is expressed in the cells. Examples of the cells having antigen presenting ability include dendritic cells. Dendritic cells derived from a patient may be prepared from PBMCs collected from a patient by isolating cells adhered to the culture plate of the PBMC culture and then, incubating the isolated cells in the presence of IL-4 and GM-CSF for one week. The antigen presenting cells prepared by the method can induce CTLs that specifically recognize a complex between the peptide and an HLA molecule presented on the surface of cancer cells. When administered to a cancer patient, the antigen presenting cells can promote the induction of cancer-reactive CTLs inside the body of the patient. Accordingly, the antigen presenting cells prepared with the peptide of the invention may be used as a pharmaceutical composition for the treatment of cancer.

[0034] The present application provides a nucleic acid molecule encoding the peptide of the invention and a vector comprising the nucleic acid molecule. When introduced into antigen presenting cells, the vector comprising the nucleic acid molecule expresses the peptide of the invention, and then a complex between the expressed peptide and an HLA molecule is presented on the surface of the cells. The antigen presenting cells thus obtained can effectively increase CTLs that kills cancer cells expressing EGFR-T790M.

[0035] Examples of vectors in which the nucleic acid molecule of the invention is incorporated may include various plasmid vectors and viral vectors such as adenovirus, adeno-associated virus, retrovirus and vaccinia virus vectors (Liu M, Acres B, Balloul J M, Bizouarne N, Paul S, Slos P, Squiban P. Gene-based vaccines and immunotherapeutics. Proc Natl Acad Sci USA 101 Suppl, 14567-71, 2004, herein incorporated by reference). Methods for preparing the vectors have been well known in the art (Molecular Cloning: A laboratory manual, 2nd ed. New York, Cold Spring Harbor Laboratory, herein incorporated by reference).

[0036] The vector of the invention may be administered to a patient so that the peptide of the invention is expressed in antigen presenting cells inside the body of the patient. Alternatively, the vector may be introduced ex vivo into suitable cells, for example dendritic cells derived from a patient, so that the cells express the peptide of the invention, and then the cells thus obtained may be returned to the patient. Those methods are well known in the art (Hrouda D, Dalgleish A G. Gene therapy for prostate cancer. Gene Ther 3: 845-52, 1996, herein incorporated by reference).

[0037] When the vector is administered to a patient, the amount of the vector to be administered may vary depending on a factor such as condition of the disease to be treated or age or body weight of the patient to be treated. The vector may be administered 0.1 g to 100 mg, preferably 1 g to 50 mg as an amount of DNA. The vector may be administered, for example, intravenously, subcutaneously, or intradermally.

[0038] The present invention is further illustrated by the following examples, but is not restricted by these examples in any way.

EXAMPLE 1

1. Materials and Methods

(1) Peptides and Cell Lines

[0039] The peptides comprising the mutated residue at position 790 (T790M) of EGFR, a wild-type peptide, and control HLA-A2-restricted peptides, influenza M1.sub.58-66 (Flu-M1, GILGFVFTL) (SEQ ID NO: 9) and HIV-derived peptides (SLYNTVATL) (SEQ ID NO: 10), were provided by Thermo Fisher Scientific GmbH (Bremen, Germany) at the purities of higher than 90%. NSCLC cell lines, NCI-H1975, and HCC827 were obtained from American Type Culture Collection (ATCC; Manassas, Va., USA). NCI-H1975-A2 cells were established by stable transfection with the plasmid carrying HLA-A2 cDNA (pCMV-HLA-A2). These cell lines were maintained in RPMI 1640 medium (Invitrogen, Carlsbad, Calif.) supplemented with 10% heat inactivated fetal bovine serum (FBS), 100 g/ml streptomycin, and 100 IU/ml penicillin. Expression of HLA-A2 on their cell surface was examined by flow cytometry with anti-HLA-A2 mAb (BB7.2; BD Biosciences, San Jose, Calif.).

(2) Prediction of EGFR-T790M-Derived HLA-A2-Binding Peptides

[0040] Two servers, NetMHC 3.2 (http://www.cbs.dtu.dk/services/NetMHC) and BIMAS (http://www-bimas.cit.nih.gov/molbio/hla_bind), were employed to predict 9-mer or 10-mer HLA-A2 binding peptides from EGFR-T790M. For prediction of 11-mer HLA-A2 binding peptides, only NetMHC 3.2 was used. Peptides that showed better scores by either or both of these prediction servers were selected for further evaluation.

(3) HLA Class I Stabilization Assay

[0041] The actual binding of predicted peptides to an HLA-A2 molecule was evaluated by MHC class I stabilization assay with TAP2-deficient RMA-S cells stably transfected with the HLA-A2 gene (RMA-S/A2). Briefly, RMA-S/A2 cells were cultured for 18 hours at 26 C. in RPMI 1640 medium in the presence of each synthetic peptide (10 g/ml) and 2-microglobulin. After washing, the cells were cultured for 3 hours at 37 C., and then stained with anti-HLA-A2 mAb

[0042] (BB7.2), followed by analysis with flow cytometry. The binding capability of each peptide to an HLA-A2 molecule was evaluated by the increase in mean fluorescence intensity (MFI) of the HLA-A2 expression, as follows: MFI increase(%)=(MFI with a given peptideMFI without peptide)/(MFI without peptide)100. The HLA-A2-restricted influenza M1.sub.58-66 epitope (Flu-M1) was used as a positive control.

(4) Generation of Antigen-Specific T Cells

[0043] Peptide-specific T cell lines were generated according to the previously reported method with slight modifications. In brief, peripheral blood was obtained with written informed consent from HLA-A2.sup.+ healthy donors and lung cancer patients under the approval of the Institutional Review Board at Kurume University. HLA-A2 expression was confirmed by flow cytometry with anti-HLA-A2 mAb. PBMCs (110.sup.5 cells/well) purified by Ficoll-Paque density centrifugation were incubated with 10 g/ml of each peptide in 96 round well plates (Nunc, Roskilde, Denmark) in 200 l of the culture medium containing 45% RPMI 1640, 45% AIM-V medium (Gibco BRL, Gaithersburg, Md., USA), 10% FCS, 20 IU/ml IL-2, and 0.1 mM MEM nonessential amino-acid solution (Gibco BRL). At every 3 or 4 days, half of the culture medium was removed and replaced by new medium containing the same peptide (10 g/ml) and 20 IU/ml IL-2. After 14 days of culture, the cells were used for interferon (IFN)- ELSPOT or cytotoxicity assays.

(5) Immune Assays

[0044] For IFN- ELISPOT assay (MBL, Nagoya, Japan), the peptide-stimulated PBMC (310.sup.4 cells/well) were cultured for 18 hours at 37 C. with T2 cells (110.sup.4 cells/well) loaded without or with the control or specific peptide (10 g/ml) in 96-well ELISPOT plate (MultiScreen HTS, Millipore) coated with anti-human IFN- mAb. After washing, the spots were developed with biotin-conjugated anti-human IFN- mAb, streptavidin-ALP, and BCIP/NBT substrate, in accordance with the manufacturer's instructions. The spot numbers were then counted by an ELISPOT reader (CTL Technologies). The peptide-stimulated PBMCs were also tested for their reactivity against NCI-H1975 (HLA-A2.sup. T790M.sup.+), NCI-H1975-A2 (HLA-A2.sup.+ T790M.sup.+), and HCC827 (HLA-A2.sup. T790M.sup.) by IFN- ELISPOT assay. In some experiments, CD8.sup.+ T cells were isolated using a CD8 Negative Isolation Kit (Miltenyi Biotec) from the peptide-stimulated PBMCs. Anti-HLA class I (W6/32) or anti-HLA class II (L243) antibody was added at 10 g/ml. The anti-HLA class I (W6/32) and anti-HLA class II (L243) antibodies were obtained by purification of antibodies secreted from hybridoma cells purchased from ATCC.

[0045] Peptide-stimulated PBMCs were also tested for cytotoxicity against NCI-H1975 or NCI-H1975-A2 by a standard 6-h .sup.51Cr-release assay. Two thousand .sup.51Cr-labelled cells per well were cultured with effector cells in 96-round well plates at the indicated effector/target ratio (ratio of effector cells to target cells). The spontaneous and maximal release was determined by the target cells cultured in medium without or with 1% Triton X-100 (Wako Pure Chemical Industries, Osaka, Japan), respectively. The specific lysis was calculated as follows: specific lysis(%)=[(test releasespontaneous release)/(maximal releasespontaneous release)]100.

2. Results

(1) Prediction of EGFR-T790M-Derived HLA-A2-Binding Peptides

[0046] Peptides (9 to 11-mer) that would bind to an HLA-A2 molecule with higher probability were predicted by using NetMHC 3.2 and/or BIMAS servers. Eight peptides that showed better scores by either or both of these prediction servers were selected, and evaluated for the actual binding to the HLA-A2 molecule (Table 1).

TABLE-US-00001 TABLE1 HLA-A2-bindingcapabilityof predictedEGFR-T790M-derivedpeptides. HLAbinding Peptide Aminoacidsequence capability(%) T790M-1 VQLIMQLMPF(SEQIDNO:1) 0 T790M-2 QLIMQLMPFG(SEQIDNO:2) 0 T790M-3 LIMQLMPFGC(SEQIDNO:3) 0 T790M-4 IMQLMPFGCL(SEQIDNO:4) 0 T790M-5 MQLMPFGCLL(SEQIDNO:5) 266.7 T790M-6 LTSTVQLIMQL(SEQIDNO:6) 0 T790M-7 LIMQLMPFGCL(SEQIDNO:7) 31.2 T790M-8 IMQLMPFGCLL(SEQIDNO:8) 69.3 FluM1 GILGFVFTL(SEQIDNO:9) 229.1

(2) HLA-A2-Binding Capability of EGFR-T790M-Derived Peptides

[0047] The HLA-A2-binding capability of the selected peptides was confirmed by cell surface HLA class I stabilization assay with the TAP-deficient cell line RMA-S stably expressing HLA-A2. As illustrated in Table 1, three of the eight selected peptides showed substantial binding to HLA-A2. The binding affinity of T790M-5 to HLA-A2 was much stronger than those of T790M-7 and T790M-8.

(3) Immunogenicity of EGFR-T790M-Derived HLA-A2-Binding Peptides in CD8.sup.+ T Cells from Normal Donors

[0048] To know the immunogenicity of the EGFR-T790M-derived HLA-A2-binding peptides, PBMCs from 6 different HLA-A2.sup.+ healthy donors were repeatedly stimulated with the synthetic peptide, T790M-5, T790M-7, or T790M-8. As shown in FIG. 1, after repeated stimulation, T cell lines secreting IFN- in response to T790M-5 were established in 5 of 6 healthy donors. Also, after repeated stimulation, T cell lines secreting IFN- in response to T790M-7 were established in 3 of 6 healthy donors. However, none of the 6 healthy donors showed antigen-specific T cell response to T790M-8.

(4) Reactivity of Peptide-Stimulated T Cells Against NSCLC Cells Having the EGFR T790M Mutation.

[0049] CD8.sup.+ T cells purified from the PBMCs after repeated stimulation with T790M-5 or T790M-7 were examined for their reactivity against NSCLC cell lines (NCI-H1975 (HLA-A2.sup. T790M.sup.+), NCI-H1975-A2 (HLA-A2.sup.+ T790M.sup.+), and HCC827 (HLA-A2.sup. T790M.sup.)) by IFN- ELISPOT assay. As shown in FIG. 2, the T790M-5-stimulated CD8.sup.+ T cells as well as the T790M-7-stimulated CD8.sup.+ T cells showed a significant IFN- production in response to NCI-H1975-A2, but not to HLA-A2-negative parental NCI-H1975 cells. In addition, the T790M-5-stimulated CD8.sup.+ T cells and the T790M-7-stimulated CD8.sup.+ T cells showed no responses against an EGFR/T790M-negative cell line, HCC827. Moreover, the T790M-5-stimulated PBMCs and the T790M-7-stimulated PBMCs showed substantial cytotoxicity against NCI-H1975-A2, but not against HLA-A2-negative NCI-H1975 cells (FIG. 3). Further, PBMCs after repeated stimulation with T790M-5 or T790M-7 were examined for their reactivity against NCI-H1975-A2 (HLA-A2.sup.+ T790M.sup.+) in the presence of anti-HLA class I (W6/32) or anti-HLA class II (L243) antibody by IFN- ELISPOT assay. As shown in FIG. 4, the T790M-5-stimulated PBMCs and the T790M-7-stimulated PBMCs showed a significant IFN- production in response to NCI-H1975-A2 in the absence of the antibody or in the presence of the anti-HLA class II (L243) antibody. In contrast, the IFN- production reduced in the presence of the anti-HLA class I (W6/32) antibody. Those results suggests that the T790M-5 and T790M-7 epitopes are expressed on the cell surface of NSCLC cells having the EGFR T790M mutation in an MHC class I-restricted manner.

(5) Cross Reactivity of T790M-5-Stimulated T Cells to a Wild-Type Peptide.

[0050] PBMCs after repeated stimulation with T790M-5 were examined for their reactivity against a wild-type peptide (TQLMPFGCLL) (SEQ ID NO: 12) by IFN- ELISPOT assay. AS shown in FIG. 5, the T790M-5-stimulated PBMCs responded to a high concentration (1 g/ml), but not to a low concentration (10 ng/ml), of the wild-type peptide. In contrast, the T790M-5-stimulated PBMCs responded to T790M-5 even at a low concentration (10 ng/ml). Since the T790M-5-stimulated T cells showed a low reactivity to the wild-type peptide, the cells were considered to show a low reactivity to normal cells expressing the wild-type peptide. Those results indicate that T790M-5 is less likely to induce a response to normal cells expressing a wild-type peptide, that is, an autoimmune response, when administered to a living body as a vaccine antigen.

(6) Immunogenicity of T790M-5 and T790M-7 in Blood of HLA-A2.SUP.+ Lung Cancer Patients.

[0051] For evaluation of immunogenicity of T790M-5 and T790M-7 in blood of lung cancer patients, PBMCs of 17 HLA-A2.sup.+ lung cancer patients were repeatedly stimulated with T790M- or T790M-7 and examined for their ability to induce peptide-specific CTLs by IFN- ELISPOT assay. The peptide-specific CTLs were induced in 3 of 6 gefitinib-sensitive patients (50%) and in 2 of 11 gefitinib-resistant patients (18%) (Table 2). Those results suggest that T790M-specific T cells have disappeared in gefitinib-resistant patients and this destroys the immunosurveillance system and allows the appearance of cancer cells having T790M mutation. Therefore, the appearance of the EGFR tyrosine kinase inhibitor resistant-mutation (T790M) is expected to be prevented in lung cancer patients receiving gefitinib by the immunotherapy with T790M-5 or T790M-7 that could maintain the immunosurveillance system.

TABLE-US-00002 TABLE 2 Immunogenicity of T790M-5 and T790M-7 in blood of HLA-A2+ lung cancer patients. Case No. Age Sex T790M-5 T790M-7 Gefitinib-sensitive patients 1 59 M +* + 2 60 M ** 3 77 F + 4 65 F 5 64 F 6 67 F + Gefitinib-resistant patients 1 60 F 2 60 M 3 81 M 4 78 F 5 57 F 6 76 F 7 79 F 8 74 M 9 68 F + 10 59 M + 11 59 M *+, responsive to T790M-5 or T790M-7. **, not responsive to T790M-5 or T790M-7. M, male; F, female.

EXAMPLE 2

1. Materials and Methods

(1) Mice

[0052] HLA-A2 transgenic (Tg) mice (HHD, H-2D.sup.b/2m.sup./) were provided from Prof. Matsui of Saitama Medical University and maintained in the animal facility of National Cancer Center Hospital East.

(2) Peptides and Cell Lines

[0053] The peptides comprising the mutated residue at position 790 (T790M) of EGFR were obtained from SCRUM Inc (Tokyo, Japan) (purity>95%). The control HLA-A2-restricted peptides, HIV.sub.77-85-derived peptide (SLYNTVATL) (SEQ ID NO: 10) and CMV.sub.495-503 peptide (NLVPMVATV) (SEQ ID NO: 13), were obtained from American Peptide Co. (Sunnyvale, Calif., US). H-2K.sup.b-resticted OVA.sub.257-264 peptide (SIINFEKL) (SEQ ID NO: 14) was obtained from AnaSpec (Fremont, Calif., USA) (purity>95%). NSCLC cell lines, NCI-H1975 and NCI-H1975-A2 cells were provided from Prof. Yano of Kanazawa university and Prof. Sasada of Kurume university, respectively. An artificial antigen presenting cell (aAPC: K562/HLA-A2/CD80/CD83) was provided from Dr. Hirano of Dana-Farber Cancer Institute. RMA-S-HHD was provided from Prof. Matsui of Saitama Medical University. These cell lines were maintained in RPMI 1640 medium (Sigma Chemical Company, St. Louis, Mo., USA) supplemented with 10% heat inactivated fetal bovine serum (FBS), 100 g/ml streptomycin, and 100 IU/ml penicillin.

(3) Prediction of EGFR-T790M-Derived HLA-A2-Binding Peptides

[0054] BIMAS (http://www-bimas.cit.nih.gov/molbio/hla_bind) was employed to predict 9-mer or 10-mer HLA-A2 binding peptides from EGFR-T790M. Peptides that showed better scores by the prediction server and modified peptides thereof were selected for evaluation.

(4) HLA Class I Stabilization Assay

[0055] The binding of predicted peptides to an HLA-A2 molecule was evaluated by HLA class I stabilization assay with TAP2-deficient T2 cells (HLA-A2+) (RIKEN, Saitama, Japan). After overnight culture in RPMI 1640 medium at 26 C., T2 cells were cultured for 3 hours at 26 C. in the presence of each synthetic peptide. The cells were cultured for 2.5 hours at 37 C., and then stained with anti-HLA-A2 antibody (BB7.2) (MBL, Nagoya, Japan), followed by analysis with flow cytometry. The binding capability of each peptide to the HLA-A2 molecule was evaluated by comparing the mean fluorescence intensity (MFI) of HLA-A2 expression of the peptide with those of the positive and the negative controls. The HLA-A2-restricted HIV peptide and CMV peptide were used as positive controls, and H-2K.sup.b-resticted OVA peptide was used as a negative control.

(5) Preparation of Mouse Dendritic Cells

[0056] Bone-marrow cells were obtained by hemolysis of cells in whole bone marrow collected from an HLA-A2Tg mouse. The bone-marrow cells (410.sup.6 cells) were cultured for 1 week in RPMI medium in the presence of mouse GM-CSF and 2ME to provide mouse bone marrow-derived dendritic cells. The dendritic cells thus obtained were stained with anti I-A.sup.b, CD11c, CD14, CD40, and CD86 antibodies (BioLegend, San Diego, Calif., USA) to confirm the differentiation to dendritic cells by flow cytometry.

(6) Determination of Immunogenicity in Mouse

[0057] Mouse dendritic cells were loaded with each peptide (10 g/ml). For immunization, the dendritic cells (510.sup.5 cells) suspended in 200 l PBS were intraperitoneally-injected into an HLA-A2Tg mouse (8-10 weeks old) on Day 0 and Day 7. On Day 14, the spleen was collected from the mouse. CD8.sup.+ cells isolated from the spleen with microbeads (Miltenyi Biotec, Bergisch Gladbach, Germany) were examined for induction of peptide-specific CTLs by IFN- ELISPOT assay.

(7) Preparation of Human Dendritic Cells

[0058] Peripheral blood was obtained with written informed consent from HLA-A2.sup.+ healthy donors. HLA-A2 expression was confirmed by genetic typing in Mitsubishi Chemical Medicine Corporation. PBMCs were purified from the peripheral blood by Ficoll-Paque (General Electric Healthcare Bio-Sciences, Uppsala, Sweden) density centrifugation and CD14.sup.+ cells were isolated with microbeads. The CD14.sup.+ cells were cultured in RPIM medium in the presence of GM-CSF and IL-4 for 5 days, further cultured with INF- and PGE2 for differentiation into mature dendritic cells, and used on Day 7. The differentiation into mature dendritic cells was confirmed with anti HLA-DR antibody (Becton-Dickinson Co., Sunnyvale, Calif., USA), and anti CD11c, CD14, CD40, CD80, CD83, and CD86 antibodies (BD Biosciences, San Jose, Calif., USA).

(8) Generation of Antigen-Specific T Cells

[0059] CD8.sup.+ cells were isolated from PBMCs of HLA-A2.sup.+ healthy donors with microbeads. The CD8.sup.+ cells (210.sup.6 cells) were co-cultured with dendritic cells that were loaded with each peptide (10 g/ml) and irradiated with 100 Gy in 2 ml RPMI medium containing 10% AB serum (SIGMA). On Days 7 and 14, aAPCs that were loaded with each peptide (10 g/ml) and irradiated with 200 Gy were added to the culture. On Days 3, 10, and 17, IL-2 (10 IU/ml) and IL-15 (10 ng/ml) were added to the culture medium. On Day 21, the cultured cells were collected, and CD8.sup.+ cells were isolated with microbeads for further experiments.

(9) Immune Assays

[0060] The peptide-specific immune response was evaluated by IFN- ELISPOT assay. The mouse or human CD8.sup.+ cells as described in (6) or (8) above (110.sup.5 cells/well) were cultured with RMA-S-HHD or T2 cells (110.sup.5 cells/well) that were loaded with a peptide (10 g/ml) for 20 hours at 37 C. in 96-well ELISPOT plate coated with anti-human IFN- antibody. After washing, the spots were developed with biotin-conjugated anti IFN- mAb, streptavidin-HRP, and AEC substrate. The spot numbers were then counted by Eliphoto system (Minerva Tech, Tokyo, Japan). The induction of peptide specific CTLs against NCI-H1975 and NCI-H1975-A2 was also examined. The number of cells and concentration of the pulsed peptide were modified in some experiments.

(10) CD107a Assay and Establishment of Peptide-Specific CTL Line

[0061] The CD8.sup.+ cells as described in (8) above were cultured with target cells (peptide-loaded T2 or NCI-H1975-A2) at a effector/target ratio 2:1 in the presence of anti-CD107a antibody (BD Biosciences) for 3.5 hours at 37 C. and analyzed by a flow cytometer. CD8.sup.+CD107a.sup.+ cells were sorted by a cell sorter as peptide-specific CTLs to a 96-well plate (1-100 cells/well). The sorted peptide-specific CTLs were cultured with allo PBMCs irradiated with 100 Gy (810.sup.4 cells), which were used as feeder cells, for 14-21 days in AIM-V medium (Gibco, Carlsbad, Calif., USA) containing 10% AB serum, IL-2 (200 U/mL) and phytohemagglutinin-P (PHA) (5 g/mL) to establish a peptide-specific CTL line. The peptide specificity of the established CTL line was confirmed by IFN- ELISPOT assay.

(11) Cytotoxicity Assay

[0062] Cytotoxicity of peptide-specific CTLs was examined by an assay with Calcein labeling. Target cells (NCI-H1975 or NCI-H1975-A2) were labeled with Calcein AM (Dojindo, Kumamoto, Japan). The target cells (110.sup.4 cells) were co-cultured with effector cells at the following effector/target ratio for 4-6 hours in 96-well half plate (Corning, N.Y., USA). Cytotoxicity was determined with Terascan VPC system (Minerva Tech). The effector/target ratio was 3:1 or 10:1. The cytotoxicity was calculated as follows: cytotoxicity(%)=[(test releasespontaneous release)/(maximal releasespontaneous release)]100.

2. Results

(1) Prediction of EGFR-T790M-Derived HLA-A2-Binding Peptides

[0063] Peptides (9 to 10-mer) that would bind to an HLA-A2 molecule with higher probability were predicted by BIMAS server. Three peptides, T790M-A, T790M-B, and T790M-C, each of which showed a good score higher than that of the corresponding wild-type peptide lacking T790M mutation, were selected. Further, modified peptides were prepared by alteration of an anchor residue that was important for HLA binding such that the binding capability was increased. Five peptides, including two modified peptides comprising one amino acid alteration (T790M-D and T790M-E), were examined as candidates (Table 3).

TABLE-US-00003 TABLE3 Candidatepeptidespredicted asHLA-A2-bindingpeptides. BIMASscore Peptide Aminoacidsequence (wild-type) T790M-A IMQLMPFGC(SEQIDNO:15) 35.378 (0.68) T790M-B MQLMPFGCLL(SEQIDNO:5) 51.77 (30.453) T790M-C LIMQLMPFGC(SEQIDNO:3) 24.921 (6.735) T790M-D IMQLMPFGV(SEQIDNO:16) 495.288 T790M-E IMQLMPFGL(SEQIDNO:17) 152.124

(2) HLA-A2-Binding Capability of EGFR-T790M-Derived Peptides

[0064] The HLA-A2-binding capability of the selected peptides was confirmed by cell surface HLA class I stabilization assay with TAP-deficient cell line T2 expressing HLA-A2. As shown in FIG. 6, T790M-A, T790M-B, and T790M-C were confirmed to bind to HLA-A2. The modified peptides T790M-D and T790M-E showed a higher binding.

(3) Immunogenicity of EGFR-T790M-Derived Candidate Peptides in HLA-A2Tg Mice

[0065] Immunogenicity of the candidate peptides in HLA-A2Tg mice was examined by vaccination of dendritic cells. Dendritic cells were induced from bone marrow of an HLA-A2Tg mouse and loaded with each of the candidate peptides. The dendritic cells were intraperitoneally-injected into the HLA-A2Tg mouse twice for immunization. From the immunized mouse, the spleen was collected and examined by IFN- ELISPOT assay. As shown in FIG. 7, T790M-B-specific CTLs were induced in all of the five immunized mice. For other four peptides, no peptide-specific CTL was induced.

(4) Immunogenicity of EGFR-T790M-Derived Candidate Peptides in PBMCs from Healthy Donors

[0066] For evaluation of immunogenicity of the EGFR-T790M-derived candidate peptides, induction of peptide-specific CTLs from PBMCs of HLA-A2.sup.+ healthy donors was examined. CD8.sup.+ T cells were isolated and stimulated with peptide-loaded dendritic cells and aAPCs. T790M-A-specific CTLs were induced in all of 4 donors examined (FIG. 8). Similarly, T790M-B-specific CTLs were induced in 2 of 4 donors examined. For other three peptides, no peptide-specific CTL was induced. Then, from the T790M-A-specific CTLs thus induced, CD8.sup.+CD107a.sup.+ cells were sorted by CD107a assay to establish a T790M-A-specific CTL line.

(5) Reactivity of T790M-A-Specific CTL Line Against NSCLC Cell Lines Having the EGFR T790M Mutation.

[0067] The established T790M-A-specific CTL line was examined for reactivity against NSCLC cell lines (NCI-H1975 (HLA-A2.sup. T790M.sup.+) and NCI-H1975-A2 (HLA-A2.sup.+ T790M.sup.+)) by IFN- ELISPOT assay and CD107a assay. The CTL line showed a higher IFN- production against NCI-H1975-A2 than against HLA-A2-negative NCI-H1975 (FIG. 9). The CD107a assay also detected many CD107a-positive cells in the co-culture with NCI-H1975-A2 (FIG. 10). In addition, the T790M-A-specific CTL line showed cytotoxicity against NCI-H1975-A2, but not against HLA-A2-negative NCI-H1975 cells (FIG. 11). Those results suggest that CTLs recognize the 9-mer peptide, T790M-A, endogenously presented on NCI-H1975-A2 cells to kill the cells.

SEQUENCE FREE TEXT

[0068] SEQ ID NO: 1: Synthetic peptide [0069] SEQ ID NO: 2: Synthetic peptide [0070] SEQ ID NO: 3: Synthetic peptide [0071] SEQ ID NO: 4: Synthetic peptide [0072] SEQ ID NO: 5: Synthetic peptide [0073] SEQ ID NO: 6: Synthetic peptide [0074] SEQ ID NO: 7: Synthetic peptide [0075] SEQ ID NO: 8: Synthetic peptide [0076] SEQ ID NO: 9: Synthetic peptide [0077] SEQ ID NO: 10: Synthetic peptide [0078] SEQ ID NO: 11: Synthetic peptide [0079] SEQ ID NO: 12: Synthetic peptide [0080] SEQ ID NO: 13: Synthetic peptide [0081] SEQ ID NO: 14: Synthetic peptide [0082] SEQ ID NO: 15: Synthetic peptide [0083] SEQ ID NO: 16: Synthetic peptide [0084] SEQ ID NO: 17: Synthetic peptide