Compositions and methods for the therapy and diagnosis of colon cancer

Abstract

Compositions and methods for the therapy and diagnosis of cancer, particularly colon cancer, are disclosed. Illustrative compositions comprise one or more colon tumor polypeptides, immunogenic portions thereof, polynucleotides that encode such polypeptides, antigen presenting cell that expresses such polypeptides, and T cells that are specific for cells expressing such polypeptides. The disclosed compositions are useful, for example, in the diagnosis, prevention and/or treatment of diseases, particularly colon cancer.

Description

BACKGROUND OF THE INVENTION

[0002] 1. Field of the Invention

[0003] The present invention relates generally to therapy and diagnosis of cancer, such as colon cancer. The invention is more specifically related to polypeptides, comprising at least a portion of a colon tumor protein, and to polynucleotides encoding such polypeptides. Such polypeptides and polynucleotides are useful in pharmaceutical compositions, e.g., vaccines, and other compositions for the diagnosis and treatment of colon cancer.

[0004] 2. Description of Related Art

[0005] Cancer is a significant health problem throughout the world. Although advances have been made in detection and therapy of cancer, no vaccine or other universally successful method for prevention and/or treatment is currently available. Current therapies, which are generally based on a combination of chemotherapy or surgery and radiation, continue to prove inadequate in many patients.

[0006] Colon cancer is the second most frequently diagnosed malignancy in the United States as well as the second most common cause of cancer death. The five-year survival rate for patients with colorectal cancer detected in an early localized stage is 92%; unfortunately, only 37% of colorectal cancer is diagnosed at this stage. The survival rate drops to 64% if the cancer is allowed to spread to adjacent organs or lymph nodes, and to 7% in patients with distant metastases.

[0007] The prognosis of colon cancer is directly related to the degree of penetration of the tumor through the bowel wall and the presence or absence of nodal involvement, consequently, early detection and treatment are especially important. Currently, diagnosis is aided by the use of screening assays for fecal occult blood, sigmoidoscopy, colonoscopy and double contrast barium enemas. Treatment regimens are determined by the type and stage of the cancer, and include surgery, radiation therapy and/or chemotherapy. Recurrence following surgery (the most common form of therapy) is a major problem and is often the ultimate cause of death. In spite of considerable research into therapies for the disease, colon cancer remains difficult to diagnose and treat. In spite of considerable research into therapies for these and other cancers, colon cancer remains difficult to diagnose and treat effectively. Accordingly, there is a need in the art for improved methods for detecting and treating such cancers. The present invention fulfills these needs and further provides other related advantages.

[0008] In spite of considerable research into therapies for these and other cancers, colon cancer remains difficult to diagnose and treat effectively. Accordingly, there is a need in the art for improved methods for detecting and treating such cancers. The present invention fulfills these needs and further provides other related advantages.

SUMMARY OF THE INVENTION

[0009] In one aspect, the present invention provides polynucleotide compositions comprising a sequence selected from the group consisting of.

[0010] (a) sequences provided in SEQ ID NO:1-934;

[0011] (b) complements of the sequences provided in SEQ ID NO:1-934;

[0012] (c) sequences consisting of at least 20, 25, 30, 35, 40, 45, 50, 75 and 100 contiguous residues of a sequence provided in SEQ ID NO:1-934;

[0013] (d) sequences that hybridize to a sequence provided in SEQ ID NO:1-934, under moderate or highly stringent conditions;

[0014] (e) sequences having at least 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identity to a sequence of SEQ ID NO:1-934;

[0015] (f) degenerate variants of a sequence provided in SEQ ID NO:1-934.

[0016] In one preferred embodiment, the polynucleotide compositions of the invention are expressed in at least about 20%, more preferably in at least about 30%, and most preferably in at least about 50% of colon tumor samples tested, at a level that is at least about 2-fold, preferably at least about 5-fold, and most preferably at least about 10-fold higher than that for normal tissues.

[0017] The present invention, in another aspect, provides polypeptide compositions comprising an amino acid sequence that is encoded by a polynucleotide sequence described above.

[0018] In certain preferred embodiments, the polypeptides and/or polynucleotides of the present invention are immunogenic, i.e., they are capable of eliciting an immune response, particularly a humoral and/or cellular immune response, as further described herein.

[0019] The present invention further provides fragments, variants and/or derivatives of the disclosed polypeptide and/or polynucleotide sequences, wherein the fragments, variants and/or derivatives preferably have a level of immunogenic activity of at least about 50%, preferably at least about 70% and more preferably at least about 90% of the level of immunogenic activity of a polypeptide sequence encoded by a polynucleotide sequence set forth in SEQ ID NO:1-934.

[0020] The present invention further provides polynucleotides that encode a polypeptide described above, expression vectors comprising such polynucleotides and host cells transformed or transfected with such expression vectors.

[0021] Within other aspects, the present invention provides pharmaceutical compositions comprising a polypeptide or polynucleotide as described above and a physiologically acceptable carrier.

[0022] Within a related aspect of the present invention, the pharmaceutical compositions, e.g., vaccine compositions, are provided for prophylactic or therapeutic applications. Such compositions generally comprise an immunogenic polypeptide or polynucleotide of the invention and an immunostimulant, such as an adjuvant.

[0023] The present invention further provides pharmaceutical compositions that comprise: (a) an antibody or antigen-binding fragment thereof that specifically binds to a polypeptide of the present invention, or a fragment thereof; and (b) a physiologically acceptable carrier.

[0024] Within further aspects, the present invention provides pharmaceutical compositions comprising: (a) an antigen presenting cell that expresses a polypeptide as described above and (b) a pharmaceutically acceptable carrier or excipient. Illustrative antigen presenting cells include dendritic cells, macrophages, monocytes, fibroblasts and B cells.

[0025] Within related aspects, pharmaceutical compositions are provided that comprise: (a) an antigen presenting cell that expresses a polypeptide as described above and (b) an immunostimulant.

[0026] The present invention further provides, in other aspects, fusion proteins that comprise at least one polypeptide as described above, as well as polynucleotides encoding such fusion proteins, typically in the form of pharmaceutical compositions, e.g., vaccine compositions, comprising a physiologically acceptable carrier and/or an immunostimulant. The fusions proteins may comprise multiple immunogenic polypeptides or portions/variants thereof, as described herein, and may further comprise one or more polypeptide segments for facilitating the expression, purification and/or immunogenicity of the polypeptide(s).

[0027] Within further aspects, the present invention provides methods for stimulating an immune response in a patient, preferably a T cell response in a human patient, comprising administering a pharmaceutical composition described herein. The patient may be afflicted with colon cancer, in which case the methods provide treatment for the disease, or patient considered at risk for such a disease may be treated prophylactically.

[0028] Within further aspects, the present invention provides methods for inhibiting the development of a cancer in a patient, comprising administering to a patient a pharmaceutical composition as recited above. The patient may be afflicted with colon cancer, in which case the methods provide treatment for the disease, or patient considered at risk for such a disease may be treated prophylactically.

[0029] The present invention further provides, within other aspects, methods for removing tumor cells from a biological sample, comprising contacting a biological sample with T cells that specifically react with a polypeptide of the present invention, wherein the step of contacting is performed under conditions and for a time sufficient to permit the removal of cells expressing the protein from the sample.

[0030] Within related aspects, methods are provided for inhibiting the development of a cancer in a patient, comprising administering to a patient a biological sample treated as described above.

[0031] Methods are further provided, within other aspects, for stimulating and/or expanding T cells specific for a polypeptide of the present invention, comprising contacting T cells with one or more of: (i) a polypeptide as described above; (ii) a polynucleotide encoding such a polypeptide; and/or (iii) an antigen presenting cell that expresses such a polypeptide; under conditions and for a time sufficient to permit the stimulation and/or expansion of T cells. Isolated T cell populations comprising T cells prepared as described above are also provided.

[0032] Within further aspects, the present invention provides methods for inhibiting the development of a cancer in a patient, comprising administering to a patient an effective amount of a T cell population as described above.

[0033] The present invention further provides methods for inhibiting the development of a cancer in a patient, comprising the steps of: (a) incubating CD4+ and/or CD8+ T cells isolated from a patient with one or more of: (i) a polypeptide comprising at least an immunogenic portion of polypeptide disclosed herein; (ii) a polynucleotide encoding such a polypeptide; and (iii) an antigen-presenting cell that expressed such a polypeptide; and (b) administering to the patient an effective amount of the proliferated T cells, and thereby inhibiting the development of a cancer in the patient. Proliferated cells may, but need not, be cloned prior to administration to the patient.

[0034] Within further aspects, the present invention provides methods for determining the presence or absence of a cancer, preferably a colon cancer, in a patient comprising: (a) contacting a biological sample obtained from a patient with a binding agent that binds to a polypeptide as recited above; (b) detecting in the sample an amount of polypeptide that binds to the binding agent; and (c) comparing the amount of polypeptide with a predetermined cut-off value, and therefrom determining the presence or absence of a cancer in the patient. Within preferred embodiments, the binding agent is an antibody, more preferably a monoclonal antibody.

[0035] The present invention also provides, within other aspects, methods for monitoring the progression of a cancer in a patient. Such methods comprise the steps of: (a) contacting a biological sample obtained from a patient at a first point in time with a binding agent that binds to a polypeptide as recited above; (b) detecting in the sample an amount of polypeptide that binds to the binding agent; (c) repeating steps (a) and (b) using a biological sample obtained from the patient at a subsequent point in time; and (d) comparing the amount of polypeptide detected in step (c) with the amount detected in step (b) and therefrom monitoring the progression of the cancer in the patient.

[0036] The present invention further provides, within other aspects, methods for determining the presence or absence of a cancer in a patient, comprising the steps of: (a) contacting a biological sample, e.g., tumor sample, serum sample, etc., obtained from a patient with an oligonucleotide that hybridizes to a polynucleotide that encodes a polypeptide of the present invention; (b) detecting in the sample a level of a polynucleotide, preferably mRNA, that hybridizes to the oligonucleotide; and (c) comparing the level of polynucleotide that hybridizes to the oligonucleotide with a predetermined cut-off value, and therefrom determining the presence or absence of a cancer in the patient. Within certain embodiments, the amount of mRNA is detected via polymerase chain reaction using, for example, at least one oligonucleotide primer that hybridizes to a polynucleotide encoding a polypeptide as recited above, or a complement of such a polynucleotide. Within other embodiments, the amount of mRNA is detected using a hybridization technique, employing an oligonucleotide probe that hybridizes to a polynucleotide that encodes a polypeptide as recited above, or a complement of such a polynucleotide.

[0037] In related aspects, methods are provided for monitoring the progression of a cancer in a patient, comprising the steps of: (a) contacting a biological sample obtained from a patient with an oligonucleotide that hybridizes to a polynucleotide that encodes a polypeptide of the present invention; (b) detecting in the sample an amount of a polynucleotide that hybridizes to the oligonucleotide; (c) repeating steps (a) and (b) using a biological sample obtained from the patient at a subsequent point in time; and (d) comparing the amount of polynucleotide detected in step (c) with the amount detected in step (b) and therefrom monitoring the progression of the cancer in the patient.

[0038] Within further aspects, the present invention provides antibodies, such as monoclonal antibodies, that bind to a polypeptide as described above, as well as diagnostic kits comprising such antibodies. Diagnostic kits comprising one or more oligonucleotide probes or primers as described above are also provided.

[0039] These and other aspects of the present invention will become apparent upon reference to the following detailed description. All references disclosed herein are hereby incorporated by reference in their entirety as if each was incorporated individually.

BRIEF DESCRIPTION OF THE SEQUENCE IDENTIFIERS

[0040]

SEQ ID NO:1	is the determined cDNA sequence of clone	54262.1
SEQ ID NO:2	is the determined cDNA sequence of clone	54264.2
SEQ ID NO:3	is the determined cDNA sequence of clone	54266.1
SEQ ID NO:4	is the determined cDNA sequence of clone	54269.1
SEQ ID NO:5	is the determined cDNA sequence of clone	54270.2
SEQ ID NO:6	is the determined cDNA sequence of clone	54271.2
SEQ ID NO:7	is the determined cDNA sequence of clone	54272.2
SEQ ID NO:8	is the determined cDNA sequence of clone	54273.2
SEQ ID NO:9	is the determined cDNA sequence of clone	54274.2
SEQ ID NO:10	is the determined cDNA sequence of clone	54278.1
SEQ ID NO:11	is the determined cDNA sequence of clone	54280.2
SEQ ID NO:12	is the determined cDNA sequence of clone	54283.2
SEQ ID NO:13	is the determined cDNA sequence of clone	54284.2
SEQ ID NO:14	is the determined cDNA sequence of clone	54285.1
SEQ ID NO:15	is the determined cDNA sequence of clone	55658.1
SEQ ID NO:16	is the determined cDNA sequence of clone	55658.2
SEQ ID NO:17	is the determined cDNA sequence of clone	55659.3
SEQ ID NO:18	is the determined cDNA sequence of clone	55660.1
SEQ ID NO:19	is the determined cDNA sequence of clone	55661.1
SEQ ID NO:20	is the determined cDNA sequence of clone	55661.2
SEQ ID NO:21	is the determined cDNA sequence of clone	55664.1
SEQ ID NO:22	is the determined cDNA sequence of clone	55664.2
SEQ ID NO:23	is the determined cDNA sequence of clone	55666.1
SEQ ID NO:24	is the determined cDNA sequence of clone	55667.1
SEQ ID NO:25	is the determined cDNA sequence of clone	55668.3
SEQ ID NO:26	is the determined cDNA sequence of clone	55669.1
SEQ ID NO:27	is the determined cDNA sequence of clone	55671.1
SEQ ID NO:28	is the determined cDNA sequence of clone	55671.2
SEQ ID NO:29	is the determined cDNA sequence of clone	55672.2
SEQ ID NO:30	is the determined cDNA sequence of clone	55677.1
SEQ ID NO:31	is the determined cDNA sequence of clone	55677.2
SEQ ID NO:32	is the determined cDNA sequence of clone	55679.3
SEQ ID NO:33	is the determined cDNA sequence of clone	55682.1
SEQ ID NO:34	is the determined cDNA sequence of clone	55688.1
SEQ ID NO:35	is the determined cDNA sequence of clone	55688.2
SEQ ID NO:36	is the determined cDNA sequence of clone	55689.1
SEQ ID NO:37	is the determined cDNA sequence of clone	56568.1
SEQ ID NO:38	is the determined cDNA sequence of clone	56569.1
SEQ ID NO:39	is the determined cDNA sequence of clone	56574.2
SEQ ID NO:40	is the determined cDNA sequence of clone	56575.1
SEQ ID NO:41	is the determined cDNA sequence of clone	56576.1
SEQ ID NO:42	is the determined cDNA sequence of clone	56581.1
SEQ ID NO:43	is the determined cDNA sequence of clone	56584.2
SEQ ID NO:44	is the determined cDNA sequence of clone	56584.3
SEQ ID NO:45	is the determined cDNA sequence of clone	56588.1
SEQ ID NO:46	is the determined cDNA sequence of clone	56590.2
SEQ ID NO:47	is the determined cDNA sequence of clone	56591.1
SEQ ID NO:48	is the determined cDNA sequence of clone	56594.2
SEQ ID NO:49	is the determined cDNA sequence of clone	56594.3
SEQ ID NO:50	is the determined cDNA sequence of clone	56601.1
SEQ ID NO:51	is the determined cDNA sequence of clone	56603.2
SEQ ID NO:52	is the determined cDNA sequence of clone	56603.3
SEQ ID NO:53	is the determined cDNA sequence of clone	56604.2
SEQ ID NO:54	is the determined cDNA sequence of clone	56604.3
SEQ ID NO:55	is the determined cDNA sequence of clone	56606.2
SEQ ID NO:56	is the determined cDNA sequence of clone	56607.2
SEQ ID NO:57	is the determined cDNA sequence of clone	56609.2
SEQ ID NO:58	is the determined cDNA sequence of clone	56610.1
SEQ ID NO:59	is the determined cDNA sequence of clone	56612.1
SEQ ID NO:60	is the determined cDNA sequence of clone	56617.2
SEQ ID NO:61	is the determined cDNA sequence of clone	56618.3
SEQ ID NO:62	is the determined cDNA sequence of clone	56619.2
SEQ ID NO:63	is the determined cDNA sequence of clone	56620.1
SEQ ID NO:64	is the determined cDNA sequence of clone	56626.1
SEQ ID NO:65	is the determined cDNA sequence of clone	56629.1
SEQ ID NO:66	is the determined cDNA sequence of clone	62416325
SEQ ID NO:67	is the determined cDNA sequence of clone	62416326
SEQ ID NO:68	is the determined cDNA sequence of clone	62416327
SEQ ID NO:69	is the determined cDNA sequence of clone	62416329
SEQ ID NO:70	is the determined cDNA sequence of clone	62416330
SEQ ID NO:71	is the determined cDNA sequence of clone	62416331
SEQ ID NO:72	is the determined cDNA sequence of clone	62416332
SEQ ID NO:73	is the determined cDNA sequence of clone	62416333
SEQ ID NO:74	is the determined cDNA sequence of clone	62416334
SEQ ID NO:75	is the determined cDNA sequence of clone	62416337
SEQ ID NO:76	is the determined cDNA sequence of clone	62416344
SEQ ID NO:77	is the determined cDNA sequence of clone	62416345
SEQ ID NO:78	is the determined cDNA sequence of clone	62416347
SEQ ID NO:79	is the determined cDNA sequence of clone	62416348
SEQ ID NO:80	is the determined cDNA sequence of clone	62416350
SEQ ID NO:81	is the determined cDNA sequence of clone	62416351
SEQ ID NO:82	is the determined cDNA sequence of clone	62416355
SEQ ID NO:83	is the determined cDNA sequence of clone	62416356
SEQ ID NO:84	is the determined cDNA sequence of clone	62416357
SEQ ID NO:85	is the determined cDNA sequence of clone	62416358
SEQ ID NO:86	is the determined cDNA sequence of clone	62416360
SEQ ID NO:87	is the determined cDNA sequence of clone	62416361
SEQ ID NO:88	is the determined cDNA sequence of clone	62416362
SEQ ID NO:89	is the determined cDNA sequence of clone	62416363
SEQ ID NO:90	is the detennined cDNA sequence of clone	62416364
SEQ ID NO:91	is the determined cDNA sequence of clone	62416365
SEQ ID NO:92	is the determined cDNA sequence of clone	62416366
SEQ ID NO:93	is the determined cDNA sequence of clone	62416368
SEQ ID NO:94	is the determined cDNA sequence of clone	62416369
SEQ ID NO:95	is the determined cDNA sequence of clone	62416372
SEQ ID NO:96	is the determined cDNA sequence of clone	62416373
SEQ ID NO:97	is the determined cDNA sequence of clone	62416375
SEQ ID NO:98	is the determined cDNA sequence of clone	62416377
SEQ ID NO:99	is the determined cDNA sequence of clone	62416379
SEQ ID NO:100	is the determined cDNA sequence of clone	62416380
SEQ ID NO:101	is the determined cDNA sequence of clone	62416382
SEQ ID NO:102	is the determined cDNA sequence of clone	62416384
SEQ ID NO:103	is the determined cDNA sequence of clone	62416385
SEQ ID NO:104	is the determined cDNA sequence of clone	62416386
SEQ ID NO:105	is the determined cDNA sequence of clone	62416387
SEQ ID NO:106	is the determined cDNA sequence of clone	62416389
SEQ ID NO:107	is the determined cDNA sequence of clone	62416390
SEQ ID NO:108	is the determined cDNA sequence of clone	62416391
SEQ ID NO:109	is the determined cDNA sequence of clone	62416392
SEQ ID NO:110	is the determined cDNA sequence of clone	62416395
SEQ ID NO:111	is the determined cDNA sequence of clone	62416396
SEQ ID NO:112	is the determined cDNA sequence of clone	62416397
SEQ ID NO:113	is the determined cDNA sequence of clone	62416398
SEQ ID NO:114	is the detennined cDNA sequence of clone	62416399
SEQ ID NO:115	is the determined cDNA sequence of clone	62416400
SEQ ID NO:116	is the determined cDNA sequence of clone	62416402
SEQ ID NO:117	is the determined cDNA sequence of clone	62416403
SEQ ID NO:118	is the determined cDNA sequence of clone	62416404
SEQ ID NO:119	is the determined cDNA sequence of clone	62416405
SEQ ID NO:120	is the determined cDNA sequence of clone	62416406
SEQ ID NO:121	is the determined cDNA sequence of clone	62416407
SEQ ID NO:122	is the determined cDNA sequence of clone	62416410
SEQ ID NO:123	is the determined cDNA sequence of clone	62416414
SEQ ID NO:124	is the determined cDNA sequence of clone	62416415
SEQ ID NO:125	is the determined cDNA sequence of clone	62416416
SEQ ID NO:126	is the determined cDNA sequence of clone	62416417
SEQ ID NO:127	is the determined cDNA sequence of clone	62583567
SEQ ID NO:128	is the determined cDNA sequence of clone	62583568
SEQ ID NO:129	is the determined cDNA sequence of clone	62583569
SEQ ID NO:130	is the determined cDNA sequence of clone	62583571
SEQ ID NO:131	is the determined cDNA sequence of clone	62583573
SEQ ID NO:132	is the determined cDNA sequence of clone	62583576
SEQ ID NO:133	is the determined cDNA sequence of clone	62583578
SEQ ID NO:134	is the determined cDNA sequence of clone	62583579
SEQ ID NO:135	is the determined cDNA sequence of clone	62583586
SEQ ID NO:136	is the determined cDNA sequence of clone	62583587
SEQ ID NO:137	is the determined cDNA sequence of clone	62583588
SEQ ID NO:138	is the determined cDNA sequence of clone	62583589
SEQ ID NO:139	is the determined cDNA sequence of clone	62583592
SEQ ID NO:140	is the determined cDNA sequence of clone	62583594
SEQ ID NO:141	is the determined cDNA sequence of clone	62583595
SEQ ID NO:142	is the determined cDNA sequence of clone	62583597
SEQ ID NO:143	is the determined cDNA sequence of clone	62583598
SEQ ID NO:144	is the determined cDNA sequence of clone	62583601
SEQ ID NO:145	is the determined cDNA sequence of clone	62583602
SEQ ID NO:146	is the determined cDNA sequence of clone	62583604
SEQ ID NO:147	is the determined cDNA sequence of clone	62583605
SEQ ID NO:148	is the determined cDNA sequence of clone	62583606
SEQ ID NO:149	is the determined cDNA sequence of clone	62583609
SEQ ID NO:150	is the determined cDNA sequence of clone	62583610
SEQ ID NO:151	is the determined cDNA sequence of clone	62583611
SEQ ID NO:152	is the determined cDNA sequence of clone	62583612
SEQ ID NO:153	is the determined cDNA sequence of clone	62583613
SEQ ID NO:154	is the determined cDNA sequence of clone	62583614
SEQ ID NO:155	is the determined cDNA sequence of clone	62583618
SEQ ID NO:156	is the determined cDNA sequence of clone	62583620
SEQ ID NO:157	is the determined cDNA sequence of clone	62583622
SEQ ID NO:158	is the determined cDNA sequence of clone	62583623
SEQ ID NO:159	is the determined cDNA sequence of clone	62583624
SEQ ID NO:160	is the determined cDNA sequence of clone	62583625
SEQ ID NO:161	is the determined cDNA sequence of clone	62583627
SEQ ID NO:162	is the determined cDNA sequence of clone	62583628
SEQ ID NO:163	is the determined cDNA sequence of clone	62583630
SEQ ID NO:164	is the determined cDNA sequence of clone	62583631
SEQ ID NO:165	is the determined cDNA sequence of clone	62583632
SEQ ID NO:166	is the determined cDNA sequence of clone	62583633
SEQ ID NO:167	is the determined cDNA sequence of clone	62583635
SEQ ID NO:168	is the determined cDNA sequence of clone	62583637
SEQ ID NO:169	is the determined cDNA sequence of clone	62583638
SEQ ID NO:170	is the determined cDNA sequence of clone	62583644
SEQ ID NO:171	is the determined cDNA sequence of clone	62583646
SEQ ID NO:172	is the determined cDNA sequence of clone	62583647
SEQ ID NO:173	is the determined cDNA sequence of clone	62583648
SEQ ID NO:174	is the determined cDNA sequence of clone	62583649
SEQ ID NO:175	is the determined cDNA sequence of clone	62583651
SEQ ID NO:176	is the determined cDNA sequence of clone	62583652
SEQ ID NO:177	is the determined cDNA sequence of clone	62583653
SEQ ID NO:178	is the determined cDNA sequence of clone	62583654
SEQ ID NO:179	is the determined cDNA sequence of clone	62583655
SEQ ID NO:180	is the determined cDNA sequence of clone	62583657
SEQ ID NO:181	is the determined cDNA sequence of clone	62583658
SEQ ID NO:182	is the determined cDNA sequence of clone	62583659
SEQ ID NO:183	is the determined cDNA sequence of clone	62480459
SEQ ID NO:184	is the determined cDNA sequence of clone	62480460
SEQ ID NO:185	is the determined cDNA sequence of clone	62480461
SEQ ID NO:186	is the determined cDNA sequence of clone	62480462
SEQ ID NO:187	is the determined cDNA sequence of clone	62480463
SEQ ID NO:188	is the determined cDNA sequence of clone	62480465
SEQ ID NO:189	is the determined cDNA sequence of clone	62480466
SEQ ID NO:190	is the determined cDNA sequence of clone	62480469
SEQ ID NO:191	is the determined cDNA sequence of clone	62480470
SEQ ID NO:192	is the determined cDNA sequence of clone	62480471
SEQ ID NO:193	is the determined cDNA sequence of clone	62480474
SEQ ID NO:194	is the determined cDNA sequence of clone	62480475
SEQ ID NO:195	is the determined cDNA sequence of clone	62480476
SEQ ID NO:196	is the determined cDNA sequence of clone	62480478
SEQ ID NO:197	is the determined cDNA sequence of clone	62480479
SEQ ID NO:198	is the determined cDNA sequence of clone	62480481
SEQ ID NO:199	is the determined cDNA sequence of clone	62480482
SEQ ID NO:200	is the determined cDNA sequence of clone	62480484
SEQ ID NO:201	is the determined cDNA sequence of clone	62480485
SEQ ID NO:202	is the determined cDNA sequence of clone	62480486
SEQ ID NO:203	is the determined cDNA sequence of clone	62480487
SEQ ID NO:204	is the determined cDNA sequence of clone	62480490
SEQ ID NO:205	is the determined cDNA sequence of clone	62480494
SEQ ID NO:206	is the determined cDNA sequence of clone	62480499
SEQ ID NO:207	is the determined cDNA sequence of clone	62480502
SEQ ID NO:208	is the determined cDNA sequence of clone	62480507
SEQ ID NO:209	is the determined cDNA sequence of clone	62480509
SEQ ID NO:210	is the determined cDNA sequence of clone	62480511
SEQ ID NO:211	is the determined cDNA sequence of clone	62480512
SEQ ID NO:212	is the determined cDNA sequence of clone	62480513
SEQ ID NO:213	is the determined cDNA sequence of clone	62480515
SEQ ID NO:214	is the determined cDNA sequence of clone	62480516
SEQ ID NO:215	is the determined cDNA sequence of clone	62480518
SEQ ID NO:216	is the determined cDNA sequence of clone	62480520
SEQ ID NO:217	is the determined cDNA sequence of clone	62480522
SEQ ID NO:218	is the determined cDNA sequence of clone	62480523
SEQ ID NO:219	is the determined cDNA sequence of clone	62480524
SEQ ID NO:220	is the determined cDNA sequence of clone	62480525
SEQ ID NO:221	is the determined cDNA sequence of clone	62480531
SEQ ID NO:222	is the determined cDNA sequence of clone	62480532
SEQ ID NO:223	is the determined cDNA sequence of clone	62480533
SEQ ID NO:224	is the determined cDNA sequence of clone	62480534
SEQ ID NO:225	is the determined cDNA sequence of clone	62480538
SEQ ID NO:226	is the determined cDNA sequence of clone	62480540
SEQ ID NO:227	is the determined cDNA sequence of clone	62480541
SEQ ID NO:228	is the determined cDNA sequence of clone	62480544
SEQ ID NO:229	is the determined cDNA sequence of clone	62480545
SEQ ID NO:230	is the determined cDNA sequence of clone	62480546
SEQ ID NO:231	is the determined cDNA sequence of clone	62480550
SEQ ID NO:232	is the determined cDNA sequence of clone	62416605
SEQ ID NO:233	is the determined cDNA sequence of clone	62416606
SEQ ID NO:234	is the determined cDNA sequence of clone	62416607
SEQ ID NO:235	is the determined cDNA sequence of clone	62416608
SEQ ID NO:236	is the determined cDNA sequence of clone	62416609
SEQ ID NO:237	is the determined cDNA sequence of clone	62416611
SEQ ID NO:238	is the determined cDNA sequence of clone	62416612
SEQ ID NO:239	is the determined cDNA sequence of clone	62416617
SEQ ID NO:240	is the determined cDNA sequence of clone	62416619
SEQ ID NO:241	is the determined cDNA sequence of clone	62416620
SEQ ID NO:242	is the determined cDNA sequence of clone	62416621
SEQ ID NO:243	is the determined cDNA sequence of clone	62416623
SEQ ID NO:244	is the determined cDNA sequence of clone	62416625
SEQ ID NO:245	is the determined cDNA sequence of clone	62416626
SEQ ID NO:246	is the determined cDNA sequence of clone	62416627
SEQ ID NO:247	is the determined cDNA sequence of clone	62416628
SEQ ID NO:248	is the determined cDNA sequence of clone	62416629
SEQ ID NO:249	is the determined cDNA sequence of clone	62416630
SEQ ID NO:250	is the determined cDNA sequence of clone	62416633
SEQ ID NO:251	is the determined cDNA sequence of clone	62416635
SEQ ID NO:252	is the determined cDNA sequence of clone	62416636
SEQ ID NO:253	is the determined cDNA sequence of clone	62416638
SEQ ID NO:254	is the determined cDNA sequence of clone	62416641
SEQ ID NO:255	is the determined cDNA sequence of clone	62416643
SEQ ID NO:256	is the determined cDNA sequence of clone	62416645
SEQ ID NO:257	is the determined cDNA sequence of clone	62416646
SEQ ID NO:258	is the determined cDNA sequence of clone	62416647
SEQ ID NO:259	is the determined cDNA sequence of clone	62416648
SEQ ID NO:260	is the determined cDNA sequence of clone	62416649
SEQ ID NO:261	is the determined cDNA sequence of clone	62416651
SEQ ID NO:262	is the determined cDNA sequence of clone	62416652
SEQ ID NO:263	is the determined cDNA sequence of clone	62416653
SEQ ID NO:264	is the determined cDNA sequence of clone	62416654
SEQ ID NO:265	is the determined cDNA sequence of clone	62416655
SEQ ID NO:266	is the determined cDNA sequence of clone	62416658
SEQ ID NO:267	is the determined cDNA sequence of clone	62416660
SEQ ID NO:268	is the determined cDNA sequence of clone	62416661
SEQ ID NO:269	is the determined cDNA sequence of clone	62416662
SEQ ID NO:270	is the determined cDNA sequence of clone	62416666
SEQ ID NO:271	is the determined cDNA sequence of clone	62416667
SEQ ID NO:272	is the determined cDNA sequence of clone	62416669
SEQ ID NO:273	is the determined cDNA sequence of clone	62416670
SEQ ID NO:274	is the determined cDNA sequence of clone	62416672
SEQ ID NO:275	is the determined cDNA sequence of clone	62416673
SEQ ID NO:276	is the determined cDNA sequence of clone	62416674
SEQ ID NO:277	is the determined cDNA sequence of clone	62416675
SEQ ID NO:278	is the determined cDNA sequence of clone	62416676
SEQ ID NO:279	is the determined cDNA sequence of clone	62416678
SEQ ID NO:280	is the determined cDNA sequence of clone	62416679
SEQ ID NO:281	is the determined cDNA sequence of clone	62416680
SEQ ID NO:282	is the determined cDNA sequence of clone	62416681
SEQ ID NO:283	is the determined cDNA sequence of clone	62416684
SEQ ID NO:284	is the determined cDNA sequence of clone	62416685
SEQ ID NO:285	is the determined cDNA sequence of clone	62416686
SEQ ID NO:286	is the determined cDNA sequence of clone	62416687
SEQ ID NO:287	is the determined cDNA sequence of clone	62416689
SEQ ID NO:288	is the determined cDNA sequence of clone	62416690
SEQ ID NO:289	is the determined cDNA sequence of clone	62416691
SEQ ID NO:290	is the determined cDNA sequence of clone	62416692
SEQ ID NO:291	is the determined cDNA sequence of clone	62416695
SEQ ID NO:292	is the determined cDNA sequence of clone	62416977
SEQ ID NO:293	is the determined cDNA sequence of clone	62416978
SEQ ID NO:294	is the determined cDNA sequence of clone	62416979
SEQ ID NO:295	is the determined cDNA sequence of clone	62416981
SEQ ID NO:296	is the determined cDNA sequence of clone	62416982
SEQ ID NO:297	is the determined cDNA sequence of clone	62416983
SEQ ID NO:298	is the determined cDNA sequence of clone	62416984
SEQ ID NO:299	is the determined cDNA sequence of clone	62416985
SEQ ID NO:300	is the determined cDNA sequence of clone	62416986
SEQ ID NO:301	is the determined cDNA sequence of clone	62416988
SEQ ID NO:302	is the determined cDNA sequence of clone	62416989
SEQ ID NO:303	is the determined cDNA sequence of clone	62416990
SEQ ID NO:304	is the determined cDNA sequence of clone	62416991
SEQ ID NO:305	is the determined cDNA sequence of clone	62416994
SEQ ID NO:306	is the determined cDNA sequence of clone	62416995
SEQ ID NO:307	is the determined cDNA sequence of clone	62416996
SEQ ID NO:308	is the determined cDNA sequence of clone	62416997
SEQ ID NO:309	is the determined cDNA sequence of clone	62416998
SEQ ID NO:310	is the determined cDNA sequence of clone	62417002
SEQ ID NO:311	is the determined cDNA sequence of clone	62417004
SEQ ID NO:312	is the determined cDNA sequence of clone	62417005
SEQ ID NO:313	is the determined cDNA sequence of clone	62417008
SEQ ID NO:314	is the determined cDNA sequence of clone	62417010
SEQ ID NO:315	is the determined cDNA sequence of clone	62417011
SEQ ID NO:316	is the determined cDNA sequence of clone	62417013
SEQ ID NO:317	is the determined cDNA sequence of clone	62417014
SEQ ID NO:318	is the determined cDNA sequence of clone	62417015
SEQ ID NO:319	is the determined cDNA sequence of clone	62417016
SEQ ID NO:320	is the determined cDNA sequence of clone	62417017
SEQ ID NO:321	is the determined cDNA sequence of clone	62417018
SEQ ID NO:322	is the determined cDNA sequence of clone	62417019
SEQ ID NO:323	is the determined cDNA sequence of clone	62417021
SEQ ID NO:324	is the determined cDNA sequence of clone	62417023
SEQ ID NO:325	is the determined cDNA sequence of clone	62417024
SEQ ID NO:326	is the determined cDNA sequence of clone	62417025
SEQ ID NO:327	is the determined cDNA sequence of clone	62417026
SEQ ID NO:328	is the determined cDNA sequence of clone	62417027
SEQ ID NO:329	is the determined cDNA sequence of clone	62417028
SEQ ID NO:330	is the determined cDNA sequence of clone	62417030
SEQ ID NO:331	is the determined cDNA sequence of clone	62417031
SEQ ID NO:332	is the determined cDNA sequence of clone	62417032
SEQ ID NO:333	is the determined cDNA sequence of clone	62417033
SEQ ID NO:334	is the determined cDNA sequence of clone	62417034
SEQ ID NO:335	is the determined cDNA sequence of clone	62417037
SEQ ID NO:336	is the determined cDNA sequence of clone	62417038
SEQ ID NO:337	is the determined cDNA sequence of clone	62417039
SEQ ID NO:338	is the determined cDNA sequence of clone	62417040
SEQ ID NO:339	is the determined cDNA sequence of clone	62417041
SEQ ID NO:340	is the determined cDNA sequence of clone	62417042
SEQ ID NO:341	is the determined cDNA sequence of clone	62417043
SEQ ID NO:342	is the determined cDNA sequence of clone	62417046
SEQ ID NO:343	is the determined cDNA sequence of clone	62417047
SEQ ID NO:344	is the determined cDNA sequence of clone	62417050
SEQ ID NO:345	is the determined cDNA sequence of clone	62417051
SEQ ID NO:346	is the determined cDNA sequence of clone	62417052
SEQ ID NO:347	is the determined cDNA sequence of clone	62417053
SEQ ID NO:348	is the determined cDNA sequence of clone	62417054
SEQ ID NO:349	is the determined cDNA sequence of clone	62417058
SEQ ID NO:350	is the determined cDNA sequence of clone	62417060
SEQ ID NO:351	is the determined cDNA sequence of clone	62417061
SEQ ID NO:352	is the determined cDNA sequence of clone	62417063
SEQ ID NO:353	is the determined cDNA sequence of clone	62417064
SEQ ID NO:354	is the determined cDNA sequence of clone	62417065
SEQ ID NO:355	is the determined cDNA sequence of clone	62416418
SEQ ID NO:356	is the determined cDNA sequence of clone	62416420
SEQ ID NO:357	is the determined cDNA sequence of clone	62416422
SEQ ID NO:358	is the determined cDNA sequence of clone	62416423
SEQ ID NO:359	is the determined cDNA sequence of clone	62416424
SEQ ID NO:360	is the determined cDNA sequence of clone	62416425
SEQ ID NO:361	is the determined cDNA sequence of clone	62416426
SEQ ID NO:362	is the determined cDNA sequence of clone	62416429
SEQ ID NO:363	is the determined cDNA sequence of clone	62416430
SEQ ID NO:364	is the determined cDNA sequence of clone	62416432
SEQ ID NO:365	is the determined cDNA sequence of clone	62416433
SEQ ID NO:366	is the determined cDNA sequence of clone	62416434
SEQ ID NO:367	is the determined cDNA sequence of clone	62416435
SEQ ID NO:368	is the determined cDNA sequence of clone	62416436
SEQ ID NO:369	is the determined cDNA sequence of clone	62416437
SEQ ID NO:370	is the determined cDNA sequence of clone	62416438
SEQ ID NO:371	is the determined cDNA sequence of clone	62416439
SEQ ID NO:372	is the determined cDNA sequence of clone	62416440
SEQ ID NO:373	is the determined cDNA sequence of clone	62416442
SEQ ID NO:374	is the determined cDNA sequence of clone	62416445
SEQ ID NO:375	is the determined cDNA sequence of clone	62416446
SEQ ID NO:376	is the determined cDNA sequence of clone	62416447
SEQ ID NO:377	is the determined cDNA sequence of clone	62416450
SEQ ID NO:378	is the determined cDNA sequence of clone	62416451
SEQ ID NO:379	is the determined cDNA sequence of clone	62416452
SEQ ID NO:380	is the determined cDNA sequence of clone	62416453
SEQ ID NO:381	is the determined cDNA sequence of clone	62416455
SEQ ID NO:382	is the determined cDNA sequence of clone	62416456
SEQ ID NO:383	is the determined cDNA sequence of clone	62416457
SEQ ID NO:384	is the determined cDNA sequence of clone	62416459
SEQ ID NO:385	is the determined cDNA sequence of clone	62416461
SEQ ID NO:386	is the determined cDNA sequence of clone	62416462
SEQ ID NO:387	is the determined cDNA sequence of clone	62416463
SEQ ID NO:388	is the determined cDNA sequence of clone	62416464
SEQ ID NO:389	is the determined cDNA sequence of clone	62416465
SEQ ID NO:390	is the determined cDNA sequence of clone	62416466
SEQ ID NO:391	is the determined cDNA sequence of clone	62416468
SEQ ID NO:392	is the determined cDNA sequence of clone	62416469
SEQ ID NO:393	is the determined cDNA sequence of clone	62416470
SEQ ID NO:394	is the determined cDNA sequence of clone	62416471
SEQ ID NO:395	is the determined cDNA sequence of clone	62416472
SEQ ID NO:396	is the determined cDNA sequence of clone	62416473
SEQ ID NO:397	is the determined cDNA sequence of clone	62416474
SEQ ID NO:398	is the determined cDNA sequence of clone	62416476
SEQ ID NO:399	is the determined cDNA sequence of clone	62416478
SEQ ID NO:400	is the determined cDNA sequence of clone	62416479
SEQ ID NO:401	is the determined cDNA sequence of clone	62416480
SEQ ID NO:402	is the determined cDNA sequence of clone	62416481
SEQ ID NO:403	is the determined cDNA sequence of clone	62416482
SEQ ID NO:404	is the determined cDNA sequence of clone	62416485
SEQ ID NO:405	is the determined cDNA sequence of clone	62416488
SEQ ID NO:406	is the determined cDNA sequence of clone	62416489
SEQ ID NO:407	is the determined cDNA sequence of clone	62416490
SEQ ID NO:408	is the determined cDNA sequence of clone	62416491
SEQ ID NO:409	is the determined cDNA sequence of clone	62416492
SEQ ID NO:410	is the determined cDNA sequence of clone	62416494
SEQ ID NO:411	is the determined cDNA sequence of clone	62416495
SEQ ID NO:412	is the determined cDNA sequence of clone	62416496
SEQ ID NO:413	is the determined cDNA sequence of clone	62416497
SEQ ID NO:414	is the determined cDNA sequence of clone	62416498
SEQ ID NO:415	is the determined cDNA sequence of clone	62416499
SEQ ID NO:416	is the determined cDNA sequence of clone	62416500
SEQ ID NO:417	is the determined cDNA sequence of clone	62416501
SEQ ID NO:418	is the determined cDNA sequence of clone	62416502
SEQ ID NO:419	is the determined cDNA sequence of clone	62416503
SEQ ID NO:420	is the determined cDNA sequence of clone	62416504
SEQ ID NO:421	is the determined cDNA sequence of clone	62416506
SEQ ID NO:422	is the determined cDNA sequence of clone	62416509
SEQ ID NO:423	is the determined cDNA sequence of clone	62416510
SEQ ID NO:424	is the determined cDNA sequence of clone	62416883
SEQ ID NO:425	is the determined cDNA sequence of clone	62416885
SEQ ID NO:426	is the determined cDNA sequence of clone	62416886
SEQ ID NO:427	is the determined cDNA sequence of clone	62416887
SEQ ID NO:428	is the determined cDNA sequence of clone	62416888
SEQ ID NO:429	is the determined cDNA sequence of clone	62416889
SEQ ID NO:430	is the determined cDNA sequence of clone	62416890
SEQ ID NO:431	is the determined cDNA sequence of clone	62416891
SEQ ID NO:432	is the determined cDNA sequence of clone	62416892
SEQ ID NO:433	is the determined cDNA sequence of clone	62416894
SEQ ID NO:434	is the determined cDNA sequence of clone	62416896
SEQ ID NO:435	is the determined cDNA sequence of clone	62416898
SEQ ID NO:436	is the determined cDNA sequence of clone	62416900
SEQ ID NO:437	is the determined cDNA sequence of clone	62416901
SEQ ID NO:438	is the determined cDNA sequence of clone	62416902
SEQ ID NO:439	is the determined cDNA sequence of clone	62416905
SEQ ID NO:440	is the determined cDNA sequence of clone	62416906
SEQ ID NO:441	is the determined cDNA sequence of clone	62416908
SEQ ID NO:442	is the determined cDNA sequence of clone	62416910
SEQ ID NO:443	is the determined cDNA sequence of clone	62416911
SEQ ID NO:444	is the determined cDNA sequence of clone	62416913
SEQ ID NO:445	is the determined cDNA sequence of clone	62416916
SEQ ID NO:446	is the determined cDNA sequence of clone	62416918
SEQ ID NO:447	is the determined cDNA sequence of clone	62416920
SEQ ID NO:448	is the determined cDNA sequence of clone	62416921
SEQ ID NO:449	is the determined cDNA sequence of clone	62416923
SEQ ID NO:450	is the determined cDNA sequence of clone	62416924
SEQ ID NO:451	is the determined cDNA sequence of clone	62416925
SEQ ID NO:452	is the determined cDNA sequence of clone	62416926
SEQ ID NO:453	is the determined cDNA sequence of clone	62416929
SEQ ID NO:454	is the detennined cDNA sequence of clone	62416930
SEQ ID NO:455	is the determined cDNA sequence of clone	62416931
SEQ ID NO:456	is the determined cDNA sequence of clone	62416933
SEQ ID NO:457	is the determined cDNA sequence of clone	62416936
SEQ ID NO:458	is the determined cDNA sequence of clone	62416937
SEQ ID NO:459	is the determined cDNA sequence of clone	62416938
SEQ ID NO:460	is the determined cDNA sequence of clone	62416939
SEQ ID NO:461	is the determined cDNA sequence of clone	62416940
SEQ ID NO:462	is the determined cDNA sequence of clone	62416942
SEQ ID NO:463	is the determined cDNA sequence of clone	62416943
SEQ ID NO:464	is the determined cDNA sequence of clone	62416946
SEQ ID NO:465	is the determined cDNA sequence of clone	62416948
SEQ ID NO:466	is the determined cDNA sequence of clone	62416949
SEQ ID NO:467	is the determined cDNA sequence of clone	62416950
SEQ ID NO:468	is the determined cDNA sequence of clone	62416954
SEQ ID NO:469	is the determined cDNA sequence of clone	62416957
SEQ ID NO:470	is the determined cDNA sequence of clone	62416958
SEQ ID NO:471	is the determined cDNA sequence of clone	62416959
SEQ ID NO:472	is the determined cDNA sequence of clone	62416966
SEQ ID NO:473	is the determined cDNA sequence of clone	62416967
SEQ ID NO:474	is the determined cDNA sequence of clone	62416969
SEQ ID NO:475	is the determined cDNA sequence of clone	62416974
SEQ ID NO:476	is the determined cDNA sequence of clone	62416975
SEQ ID NO:477	is the determined cDNA sequence of clone	62480662
SEQ ID NO:478	is the determined cDNA sequence of clone	62480664
SEQ ID NO:479	is the determined cDNA sequence of clone	62480665
SEQ ID NO:480	is the determined cDNA sequence of clone	62480666
SEQ ID NO:481	is the determined cDNA sequence of clone	62480668
SEQ ID NO:482	is the determined cDNA sequence of clone	62480671
SEQ ID NO:483	is the determined cDNA sequence of clone	62480674
SEQ ID NO:484	is the determined cDNA sequence of clone	62480676
SEQ ID NO:485	is the determined cDNA sequence of clone	62480677
SEQ ID NO:486	is the detennined cDNA sequence of clone	62480678
SEQ ID NO:487	is the detennined cDNA sequence of clone	62480681
SEQ ID NO:488	is the determined cDNA sequence of clone	62480682
SEQ ID NO:489	is the determined cDNA sequence of clone	62480688
SEQ ID NO:490	is the determined cDNA sequence of clone	62480689
SEQ ID NO:491	is the determined cDNA sequence of clone	62480694
SEQ ID NO:492	is the determined cDNA sequence of clone	62480695
SEQ ID NO:493	is the determined cDNA sequence of clone	62480696
SEQ ID NO:494	is the determined cDNA sequence of clone	62480701
SEQ ID NO:495	is the determined cDNA sequence of clone	62480702
SEQ ID NO:496	is the determined cDNA sequence of clone	62480703
SEQ ID NO:497	is the determined cDNA sequence of clone	62480704
SEQ ID NO:498	is the determined cDNA sequence of clone	62480707
SEQ ID NO:499	is the determined cDNA sequence of clone	62480708
SEQ ID NO:500	is the determined cDNA sequence of clone	62480709
SEQ ID NO:501	is the determined cDNA sequence of clone	62480714
SEQ ID NO:502	is the determined cDNA sequence of clone	62480715
SEQ ID NO:503	is the determined cDNA sequence of clone	62480717
SEQ ID NO:504	is the determined cDNA sequence of clone	62480718
SEQ ID NO:505	is the determined cDNA sequence of clone	62480721
SEQ ID NO:506	is the determined cDNA sequence of clone	62480722
SEQ ID NO:507	is the determined cDNA sequence of clone	62480725
SEQ ID NO:508	is the determined cDNA sequence of clone	62480728
SEQ ID NO:509	is the determined cDNA sequence of clone	62480729
SEQ ID NO:510	is the determined cDNA sequence of clone	62480730
SEQ ID NO:511	is the determined cDNA sequence of clone	62480732
SEQ ID NO:512	is the determined cDNA sequence of clone	62480733
SEQ ID NO:513	is the determined cDNA sequence of clone	62480736
SEQ ID NO:514	is the determined cDNA sequence of clone	62480737
SEQ ID NO:515	is the determined cDNA sequence of clone	62480741
SEQ ID NO:516	is the determined cDNA sequence of clone	62480742
SEQ ID NO:517	is the determined cDNA sequence of clone	62480743
SEQ ID NO:518	is the determined cDNA sequence of clone	62480745
SEQ ID NO:519	is the determined cDNA sequence of clone	62480749
SEQ ID NO:520	is the determined cDNA sequence of clone	62480750
SEQ ID NO:521	is the determined cDNA sequence of clone	62480751
SEQ ID NO:522	is the determined cDNA sequence of clone	62480752
SEQ ID NO:523	is the determined cDNA sequence of clone	62465822
SEQ ID NO:524	is the determined cDNA sequence of clone	62465824
SEQ ID NO:525	is the determined cDNA sequence of clone	62465825
SEQ ID NO:526	is the determined cDNA sequence of clone	62465829
SEQ ID NO:527	is the determined cDNA sequence of clone	62465834
SEQ ID NO:528	is the determined cDNA sequence of clone	62465835
SEQ ID NO:529	is the determined cDNA sequence of clone	62465836
SEQ ID NO:530	is the determined cDNA sequence of clone	62465837
SEQ ID NO:531	is the determined cDNA sequence of clone	62465839
SEQ ID NO:532	is the determined cDNA sequence of clone	62465840
SEQ ID NO:533	is the determined cDNA sequence of clone	62465845
SEQ ID NO:534	is the determined cDNA sequence of clone	62465846
SEQ ID NO:535	is the determined cDNA sequence of clone	62465847
SEQ ID NO:536	is the determined cDNA sequence of clone	62465849
SEQ ID NO:537	is the determined cDNA sequence of clone	62465851
SEQ ID NO:538	is the determined cDNA sequence of clone	62465852
SEQ ID NO:539	is the determined cDNA sequence of clone	62465855
SEQ ID NO:540	is the determined cDNA sequence of clone	62465856
SEQ ID NO:541	is the determined cDNA sequence of clone	62465859
SEQ ID NO:542	is the determined cDNA sequence of clone	62465860
SEQ ID NO:543	is the determined cDNA sequence of clone	62465862
SEQ ID NO:544	is the determined cDNA sequence of clone	62465865
SEQ ID NO:545	is the determined cDNA sequence of clone	62465869
SEQ ID NO:546	is the determined cDNA sequence of clone	62465872
SEQ ID NO:547	is the determined cDNA sequence of clone	62465873
SEQ ID NO:548	is the determined cDNA sequence of clone	62465874
SEQ ID NO:549	is the determined cDNA sequence of clone	62465875
SEQ ID NO:550	is the determined cDNA sequence of clone	62465876
SEQ ID NO:551	is the determined cDNA sequence of clone	62465877
SEQ ID NO:552	is the determined cDNA sequence of clone	62465878
SEQ ID NO:553	is the determined cDNA sequence of clone	62465880
SEQ ID NO:554	is the determined cDNA sequence of clone	62465882
SEQ ID NO:555	is the determined cDNA sequence of clone	62465885
SEQ ID NO:556	is the determined cDNA sequence of clone	62465887
SEQ ID NO:557	is the determined cDNA sequence of clone	62465888
SEQ ID NO:558	is the determined cDNA sequence of clone	62465889
SEQ ID NO:559	is the determined cDNA sequence of clone	62465890
SEQ ID NO:560	is the determined cDNA sequence of clone	62465891
SEQ ID NO:561	is the determined cDNA sequence of clone	62465892
SEQ ID NO:562	is the determined cDNA sequence of clone	62465893
SEQ ID NO:563	is the determined cDNA sequence of clone	62465894
SEQ ID NO:564	is the determined cDNA sequence of clone	62465896
SEQ ID NO:565	is the determined cDNA sequence of clone	62465897
SEQ ID NO:566	is the determined cDNA sequence of clone	62465898
SEQ ID NO:567	is the determined cDNA sequence of clone	62465899
SEQ ID NO:568	is the determined cDNA sequence of clone	62465901
SEQ ID NO:569	is the determined cDNA sequence of clone	62465903
SEQ ID NO:570	is the determined cDNA sequence of clone	62465904
SEQ ID NO:571	is the determined cDNA sequence of clone	62465905
SEQ ID NO:572	is the determined cDNA sequence of clone	62465907
SEQ ID NO:573	is the determined cDNA sequence of clone	62465909
SEQ ID NO:574	is the determined cDNA sequence of clone	62465911
SEQ ID NO:575	is the determined cDNA sequence of clone	62465914
SEQ ID NO:576	is the determined cDNA sequence of clone	62417071
SEQ ID NO:577	is the determined cDNA sequence of clone	62417072
SEQ ID NO:578	is the determined cDNA sequence of clone	62417073
SEQ ID NO:579	is the determined cDNA sequence of clone	62417074
SEQ ID NO:580	is the determined cDNA sequence of clone	62417075
SEQ ID NO:581	is the determined cDNA sequence of clone	62417076
SEQ ID NO:582	is the determined cDNA sequence of clone	62417077
SEQ ID NO:583	is the determined cDNA sequence of clone	62417078
SEQ ID NO:584	is the determined cDNA sequence of clone	62417079
SEQ ID NO:585	is the determined cDNA sequence of clone	62417081
SEQ ID NO:586	is the determined cDNA sequence of clone	62417082
SEQ ID NO:587	is the determined cDNA sequence of clone	62417083
SEQ ID NO:588	is the determined cDNA sequence of clone	62417084
SEQ ID NO:589	is the determined cDNA sequence of clone	62417085
SEQ ID NO:590	is the determined cDNA sequence of clone	62417087
SEQ ID NO:591	is the detennined cDNA sequence of clone	62417092
SEQ ID NO:592	is the determined cDNA sequence of clone	62417095
SEQ ID NO:593	is the determined cDNA sequence of clone	62417099
SEQ ID NO:594	is the determined cDNA sequence of clone	62417102
SEQ ID NO:595	is the determined cDNA sequence of clone	62417104
SEQ ID NO:596	is the determined cDNA sequence of clone	62417105
SEQ ID NO:597	is the determined cDNA sequence of clone	62417108
SEQ ID NO:598	is the determined cDNA sequence of clone	62417109
SEQ ID NO:599	is the determined cDNA sequence of clone	62417110
SEQ ID NO:600	is the determined cDNA sequence of clone	62417111
SEQ ID NO:601	is the determined cDNA sequence of clone	62417112
SEQ ID NO:602	is the determined cDNA sequence of clone	62417114
SEQ ID NO:603	is the determined cDNA sequence of clone	62417115
SEQ ID NO:604	is the determined cDNA sequence of clone	62417116
SEQ ID NO:605	is the determined cDNA sequence of clone	62417117
SEQ ID NO:606	is the determined cDNA sequence of clone	62417118
SEQ ID NO:607	is the determined cDNA sequence of clone	62417119
SEQ ID NO:608	is the determined cDNA sequence of clone	62417123
SEQ ID NO:609	is the determined cDNA sequence of clone	62417124
SEQ ID NO:610	is the determined cDNA sequence of clone	62417126
SEQ ID NO:611	is the determined cDNA sequence of clone	62417127
SEQ ID NO:612	is the determined cDNA sequence of clone	62417128
SEQ ID NO:613	is the determined cDNA sequence of clone	62417132
SEQ ID NO:614	is the determined cDNA sequence of clone	62417134
SEQ ID NO:615	is the determined cDNA sequence of clone	62417135
SEQ ID NO:616	is the determined cDNA sequence of clone	62417138
SEQ ID NO:617	is the determined cDNA sequence of clone	62417141
SEQ ID NO:618	is the determined cDNA sequence of clone	62417147
SEQ ID NO:619	is the determined cDNA sequence of clone	62417148
SEQ ID NO:620	is the determined cDNA sequence of clone	62417149
SEQ ID NO:621	is the determined cDNA sequence of clone	62417150
SEQ ID NO:622	is the determined cDNA sequence of clone	62417151
SEQ ID NO:623	is the determined cDNA sequence of clone	62417152
SEQ ID NO:624	is the determined cDNA sequence of clone	62417153
SEQ ID NO:625	is the determined cDNA sequence of clone	62417154
SEQ ID NO:626	is the determined cDNA sequence of clone	62417156
SEQ ID NO:627	is the determined cDNA sequence of clone	62417157
SEQ ID NO:628	is the determined cDNA sequence of clone	62417158
SEQ ID NO:629	is the determined cDNA sequence of clone	62417160
SEQ ID NO:630	is the determined cDNA sequence of clone	62481711
SEQ ID NO:631	is the determined cDNA sequence of clone	62481712
SEQ ID NO:632	is the determined cDNA sequence of clone	62481713
SEQ ID NO:633	is the determined cDNA sequence of clone	62481714
SEQ ID NO:634	is the determined cDNA sequence of clone	62481718
SEQ ID NO:635	is the determined cDNA sequence of clone	62481719
SEQ ID NO:636	is the determined cDNA sequence of clone	62481721
SEQ ID NO:637	is the determined cDNA sequence of clone	62481722
SEQ ID NO:638	is the determined cDNA sequence of clone	62481724
SEQ ID NO:639	is the determined cDNA sequence of clone	62481725
SEQ ID NO:640	is the determined cDNA sequence of clone	62481727
SEQ ID NO:641	is the determined cDNA sequence of clone	62481728
SEQ ID NO:642	is the determined cDNA sequence of clone	62481729
SEQ ID NO:643	is the determined cDNA sequence of clone	62481730
SEQ ID NO:644	is the determined cDNA sequence of clone	62481731
SEQ ID NO:645	is the determined cDNA sequence of clone	62481734
SEQ ID NO:646	is the determined cDNA sequence of clone	62481735
SEQ ID NO:647	is the determined cDNA sequence of clone	62481737
SEQ ID NO:648	is the determined cDNA sequence of clone	62481739
SEQ ID NO:649	is the determined cDNA sequence of clone	62481740
SEQ ID NO:650	is the determined cDNA sequence of clone	62481741
SEQ ID NO:651	is the determined cDNA sequence of clone	62481743
SEQ ID NO:652	is the determined cDNA sequence of clone	62481746
SEQ ID NO:653	is the determined cDNA sequence of clone	62481747
SEQ ID NO:654	is the determined cDNA sequence of clone	62481752
SEQ ID NO:655	is the determined cDNA sequence of clone	62481753
SEQ ID NO:656	is the determined cDNA sequence of clone	62481756
SEQ ID NO:657	is the determined cDNA sequence of clone	62481757
SEQ ID NO:658	is the determined cDNA sequence of clone	62481758
SEQ ID NO:659	is the determined cDNA sequence of clone	62481759
SEQ ID NO:660	is the determined cDNA sequence of clone	62481762
SEQ ID NO:661	is the determined cDNA sequence of clone	62481763
SEQ ID NO:662	is the determined cDNA sequence of clone	62481764
SEQ ID NO:663	is the determined cDNA sequence of clone	62481765
SEQ ID NO:664	is the determined cDNA sequence of clone	62481766
SEQ ID NO:665	is the determined cDNA sequence of clone	62481768
SEQ ID NO:666	is the determined cDNA sequence of clone	62481769
SEQ ID NO:667	is the determined cDNA sequence of clone	62481771
SEQ ID NO:668	is the determined cDNA sequence of clone	62481772
SEQ ID NO:669	is the determined cDNA sequence of clone	62481775
SEQ ID NO:670	is the determined cDNA sequence of clone	62481776
SEQ ID NO:671	is the determined cDNA sequence of clone	62481777
SEQ ID NO:672	is the determined cDNA sequence of clone	62481778
SEQ ID NO:673	is the determined cDNA sequence of clone	62481780
SEQ ID NO:674	is the determined cDNA sequence of clone	62481782
SEQ ID NO:675	is the determined cDNA sequence of clone	62481785
SEQ ID NO:676	is the determined cDNA sequence of clone	62481789
SEQ ID NO:677	is the detennined cDNA sequence of clone	62481790
SEQ ID NO:678	is the determined cDNA sequence of clone	62481792
SEQ ID NO:679	is the determined cDNA sequence of clone	62481794
SEQ ID NO:680	is the determined cDNA sequence of clone	62481796
SEQ ID NO:681	is the determined cDNA sequence of clone	62481798
SEQ ID NO:682	is the determined cDNA sequence of clone	62481799
SEQ ID NO:683	is the determined cDNA sequence of clone	62481800
SEQ ID NO:684	is the determined cDNA sequence of clone	62481801
SEQ ID NO:685	is the determined cDNA sequence of clone	62480551
SEQ ID NO:686	is the determined cDNA sequence of clone	62480552
SEQ ID NO:687	is the determined cDNA sequence of clone	62480553
SEQ ID NO:688	is the determined cDNA sequence of clone	62480556
SEQ ID NO:689	is the determined cDNA sequence of clone	62480557
SEQ ID NO:690	is the determined cDNA sequence of clone	62480559
SEQ ID NO:691	is the determined cDNA sequence of clone	62480561
SEQ ID NO:692	is the determined cDNA sequence of clone	62480562
SEQ ID NO:693	is the determined cDNA sequence of clone	62480564
SEQ ID NO:694	is the determined cDNA sequence of clone	62480566
SEQ ID NO:695	is the determined cDNA sequence of clone	62480568
SEQ ID NO:696	is the determined cDNA sequence of clone	62480569
SEQ ID NO:697	is the determined cDNA sequence of clone	62480571
SEQ ID NO:698	is the determined cDNA sequence of clone	62480572
SEQ ID NO:699	is the determined cDNA sequence of clone	62480573
SEQ ID NO:700	is the determined cDNA sequence of clone	62480576
SEQ ID NO:701	is the determined cDNA sequence of clone	62480578
SEQ ID NO:702	is the determined cDNA sequence of clone	62480579
SEQ ID NO:703	is the determined cDNA sequence of clone	62480581
SEQ ID NO:704	is the determined cDNA sequence of clone	62480583
SEQ ID NO:705	is the determined cDNA sequence of clone	62480585
SEQ ID NO:706	is the determined cDNA sequence of clone	62480588
SEQ ID NO:707	is the determined cDNA sequence of clone	62480590
SEQ ID NO:708	is the determined cDNA sequence of clone	62480592
SEQ ID NO:709	is the determined cDNA sequence of clone	62480594
SEQ ID NO:710	is the determined cDNA sequence of clone	62480595
SEQ ID NO:711	is the determined cDNA sequence of clone	62480596
SEQ ID NO:712	is the determined cDNA sequence of clone	62480597
SEQ ID NO:713	is the determined cDNA sequence of clone	62480598
SEQ ID NO:714	is the determined cDNA sequence of clone	62480605
SEQ ID NO:715	is the determined cDNA sequence of clone	62480606
SEQ ID NO:716	is the determined cDNA sequence of clone	62480607
SEQ ID NO:717	is the determined cDNA sequence of clone	62480608
SEQ ID NO:718	is the determined cDNA sequence of clone	62480610
SEQ ID NO:719	is the determined cDNA sequence of clone	62480611
SEQ ID NO:720	is the determined cDNA sequence of clone	62480612
SEQ ID NO:721	is the determined cDNA sequence of clone	62480614
SEQ ID NO:722	is the determined cDNA sequence of clone	62480615
SEQ ID NO:723	is the determined cDNA sequence of clone	62480619
SEQ ID NO:724	is the determined cDNA sequence of clone	62480620
SEQ ID NO:725	is the determined cDNA sequence of clone	62480621
SEQ ID NO:726	is the determined cDNA sequence of clone	62480622
SEQ ID NO:727	is the determined cDNA sequence of clone	62480623
SEQ ID NO:728	is the determined cDNA sequence of clone	62480624
SEQ ID NO:729	is the determined cDNA sequence of clone	62480626
SEQ ID NO:730	is the determined cDNA sequence of clone	62480627
SEQ ID NO:731	is the determined cDNA sequence of clone	62480629
SEQ ID NO:732	is the determined cDNA sequence of clone	62480631
SEQ ID NO:733	is the determined cDNA sequence of clone	62480633
SEQ ID NO:734	is the determined cDNA sequence of clone	62480635
SEQ ID NO:735	is the determined cDNA sequence of clone	62480636
SEQ ID NO:736	is the determined cDNA sequence of clone	62480637
SEQ ID NO:737	is the determined cDNA sequence of clone	62480643
SEQ ID NO:738	is the determined cDNA sequence of clone	63805729
SEQ ID NO:739	is the determined cDNA sequence of clone	63805732
SEQ ID NO:740	is the determined cDNA sequence of clone	63805735
SEQ ID NO:741	is the determined cDNA sequence of clone	63805736
SEQ ID NO:742	is the determined cDNA sequence of clone	63805737
SEQ ID NO:743	is the determined cDNA sequence of clone	63805738
SEQ ID NO:744	is the determined cDNA sequence of clone	63805739
SEQ ID NO:745	is the determined cDNA sequence of clone	63805741
SEQ ID NO:746	is the determined cDNA sequence of clone	63805743
SEQ ID NO:747	is the determined cDNA sequence of clone	63805744
SEQ ID NO:748	is the determined cDNA sequence of clone	63805745
SEQ ID NO:749	is the determined cDNA sequence of clone	63805749
SEQ ID NO:750	is the determined cDNA sequence of clone	63805750
SEQ ID NO:751	is the determined cDNA sequence of clone	63805753
SEQ ID NO:752	is the determined cDNA sequence of clone	63805754
SEQ ID NO:753	is the determined cDNA sequence of clone	63805755
SEQ ID NO:754	is the determined cDNA sequence of clone	63805756
SEQ ID NO:755	is the determined cDNA sequence of clone	63805757
SEQ ID NO:756	is the determined cDNA sequence of clone	63805758
SEQ ID NO:757	is the determined cDNA sequence of clone	63805759
SEQ ID NO:758	is the detennined cDNA sequence of clone	63805760
SEQ ID NO:759	is the determined cDNA sequence of clone	63805762
SEQ ID NO:760	is the determined cDNA sequence of clone	63805763
SEQ ID NO:761	is the determined cDNA sequence of clone	63805764
SEQ ID NO:762	is the determined cDNA sequence of clone	63805765
SEQ ID NO:763	is the determined cDNA sequence of clone	63805767
SEQ ID NO:764	is the determined cDNA sequence of clone	63805769
SEQ ID NO:765	is the determined cDNA sequence of clone	63805775
SEQ ID NO:766	is the determined cDNA sequence of clone	63805777
SEQ ID NO:767	is the determined cDNA sequence of clone	63805781
SEQ ID NO:768	is the determined cDNA sequence of clone	63805782
SEQ ID NO:769	is the determined cDNA sequence of clone	63805783
SEQ ID NO:770	is the determined cDNA sequence of clone	63805785
SEQ ID NO:771	is the determined cDNA sequence of clone	63805788
SEQ ID NO:772	is the determined cDNA sequence of clone	63805789
SEQ ID NO:773	is the determined cDNA sequence of clone	63805790
SEQ ID NO:774	is the determined cDNA sequence of clone	63805791
SEQ ID NO:775	is the determined cDNA sequence of clone	63805792
SEQ ID NO:776	is the determined cDNA sequence of clone	63805793
SEQ ID NO:777	is the determined cDNA sequence of clone	63805797
SEQ ID NO:778	is the determined cDNA sequence of clone	63805798
SEQ ID NO:779	is the determined cDNA sequence of clone	63805799
SEQ ID NO:780	is the determined cDNA sequence of clone	63805801
SEQ ID NO:781	is the determined cDNA sequence of clone	63805802
SEQ ID NO:782	is the determined cDNA sequence of clone	63805803
SEQ ID NO:783	is the determined cDNA sequence of clone	63805804
SEQ ID NO:784	is the determined cDNA sequence of clone	63805805
SEQ ID NO:785	is the determined cDNA sequence of clone	63805806
SEQ ID NO:786	is the determined cDNA sequence of clone	63805807
SEQ ID NO:787	is the determined cDNA sequence of clone	63805808
SEQ ID NO:788	is the determined cDNA sequence of clone	63805809
SEQ ID NO:789	is the determined cDNA sequence of clone	63805810
SEQ ID NO:790	is the determined cDNA sequence of clone	63805811
SEQ ID NO:791	is the determined cDNA sequence of clone	63805814
SEQ ID NO:792	is the determined cDNA sequence of clone	63805815
SEQ ID NO:793	is the determined cDNA sequence of clone	63805816
SEQ ID NO:794	is the determined cDNA sequence of clone	63805819
SEQ ID NO:795	is the determined cDNA sequence of clone	63805821
SEQ ID NO:796	is the determined cDNA sequence of clone	74209.2
SEQ ID NO:797	is the determined cDNA sequence of clone	74210.1
SEQ ID NO:798	is the determined cDNA sequence of clone	74211.1
SEQ ID NO:799	is the determined cDNA sequence of clone	74212.1
SEQ ID NO:800	is the determined cDNA sequence of clone	74213.1
SEQ ID NO:801	is the determined cDNA sequence of clone	74214.1
SEQ ID NO:802	is the determined cDNA sequence of clone	74215.1
SEQ ID NO:803	is the determined cDNA sequence of clone	74216.1
SEQ ID NO:804	is the determined cDNA sequence of clone	74218.1
SEQ ID NO:805	is the determined cDNA sequence of clone	74220.1
SEQ ID NO:806	is the determined cDNA sequence of clone	74221.1
SEQ ID NO:807	is the determined cDNA sequence of clone	74226.2
SEQ ID NO:808	is the determined cDNA sequence of clone	74227.1
SEQ ID NO:809	is the determined cDNA sequence of clone	74228.2
SEQ ID NO:810	is the determined cDNA sequence of clone	74229.2
SEQ ID NO:811	is the determined cDNA sequence of clone	74231.1
SEQ ID NO:812	is the determined cDNA sequence of clone	74233.1
SEQ ID NO:813	is the determined cDNA sequence of clone	74234.2
SEQ ID NO:814	is the determined cDNA sequence of clone	74235.1
SEQ ID NO:815	is the determined cDNA sequence of clone	74238.2
SEQ ID NO:816	is the determined cDNA sequence of clone	74239.1
SEQ ID NO:817	is the determined cDNA sequence of clone	74240.1
SEQ ID NO:818	is the determined cDNA sequence of clone	74245.1
SEQ ID NO:819	is the determined cDNA sequence of clone	74249.1
SEQ ID NO:820	is the determined cDNA sequence of clone	74251.1
SEQ ID NO:821	is the determined cDNA sequence of clone	74252.1
SEQ ID NO:822	is the determined cDNA sequence of clone	74254.1
SEQ ID NO:823	is the detennined cDNA sequence of clone	74257.1
SEQ ID NO:824	is the determined cDNA sequence of clone	74258.1
SEQ ID NO:825	is the determined cDNA sequence of clone	74260.1
SEQ ID NO:826	is the determined cDNA sequence of clone	74262.2
SEQ ID NO:827	is the determined cDNA sequence of clone	74263.1
SEQ ID NO:828	is the determined cDNA sequence of clone	74265.1
SEQ ID NO:829	is the determined cDNA sequence of clone	74266.1
SEQ ID NO:830	is the determined cDNA sequence of clone	74267.1
SEQ ID NO:831	is the determined cDNA sequence of clone	74268.1
SEQ ID NO:832	is the determined cDNA sequence of clone	74269.2
SEQ ID NO:833	is the determined cDNA sequence of clone	74270.1
SEQ ID NO:834	is the determined cDNA sequence of clone	74271.1
SEQ ID NO:835	is the determined cDNA sequence of clone	74272.1
SEQ ID NO:836	is the determined cDNA sequence of clone	74273.2
SEQ ID NO:837	is the determined cDNA sequence of clone	74274.1
SEQ ID NO:838	is the determined cDNA sequence of clone	74275.1
SEQ ID NO:839	is the determined cDNA sequence of clone	74276.1
SEQ ID NO:840	is the determined cDNA sequence of clone	74280.1
SEQ ID NO:841	is the determined cDNA sequence of clone	74285.1
SEQ ID NO:842	is the determined cDNA sequence of clone	74286.1
SEQ ID NO:843	is the determined cDNA sequence of clone	74287.2
SEQ ID NO:844	is the determined cDNA sequence of clone	74289.1
SEQ ID NO:845	is the determined cDNA sequence of clone	74291.1
SEQ ID NO:846	is the determined cDNA sequence of clone	74293.2
SEQ ID NO:847	is the determined cDNA sequence of clone	74293.3
SEQ ID NO:848	is the determined cDNA sequence of clone	74295.2
SEQ ID NO:849	is the determined cDNA sequence of clone	74296.1
SEQ ID NO:850	is the determined cDNA sequence of clone	74296.2
SEQ ID NO:851	is the determined cDNA sequence of clone	74296.3
SEQ ID NO:852	is the determined cDNA sequence of clone	74298.1
SEQ ID NO:853	is the determined cDNA sequence of clone	74300.1
SEQ ID NO:854	is the determined cDNA sequence of clone	76267.1
SEQ ID NO:855	is the determined cDNA sequence of clone	76268.1
SEQ ID NO:856	is the determined cDNA sequence of clone	76270.3
SEQ ID NO:857	is the determined cDNA sequence of clone	76272.1
SEQ ID NO:858	is the determined cDNA sequence of clone	76275.1
SEQ ID NO:859	is the determined cDNA sequence of clone	76277.1
SEQ ID NO:860	is the determined cDNA sequence of clone	76279.1
SEQ ID NO:861	is the determined cDNA sequence of clone	76281.2
SEQ ID NO:862	is the determined cDNA sequence of clone	76282.2
SEQ ID NO:863	is the determined cDNA sequence of clone	76286.1
SEQ ID NO:864	is the determined cDNA sequence of clone	76293.1
SEQ ID NO:865	is the determined cDNA sequence of clone	76295.1
SEQ ID NO:866	is the determined cDNA sequence of clone	76297.1
SEQ ID NO:867	is the determined cDNA sequence of clone	76300.1
SEQ ID NO:868	is the determined cDNA sequence of clone	76304.1
SEQ ID NO:869	is the determined cDNA sequence of clone	76306.2
SEQ ID NO:870	is the determined cDNA sequence of clone	76307.2
SEQ ID NO:871	is the determined cDNA sequence of clone	76308.1
SEQ ID NO:872	is the determined cDNA sequence of clone	76309.3
SEQ ID NO:873	is the determined cDNA sequence of clone	76311.1
SEQ ID NO:874	is the determined cDNA sequence of clone	76317.2
SEQ ID NO:875	is the determined cDNA sequence of clone	76319.2
SEQ ID NO:876	is the determined cDNA sequence of clone	76320.1
SEQ ID NO:877	is the determined cDNA sequence of clone	76321.2
SEQ ID NO:878	is the determined cDNA sequence of clone	76327.2
SEQ ID NO:879	is the determined cDNA sequence of clone	76328.1
SEQ ID NO:880	is the determined cDNA sequence of clone	76333.1
SEQ ID NO:881	is the determined cDNA sequence of clone	76334.1
SEQ ID NO:882	is the determined cDNA sequence of clone	76335.1
SEQ ID NO:883	is the determined cDNA sequence of clone	76337.1
SEQ ID NO:884	is the determined cDNA sequence of clone	76337.2
SEQ ID NO:885	is the determined cDNA sequence of clone	76337.3
SEQ ID NO:886	is the determined cDNA sequence of clone	76342.1
SEQ ID NO:887	is the determined cDNA sequence of clone	76343.1
SEQ ID NO:888	is the determined cDNA sequence of clone	76347.1
SEQ ID NO:889	is the determined cDNA sequence of clone	76349.2
SEQ ID NO:890	is the determined cDNA sequence of clone	76351.1
SEQ ID NO:891	is the determined cDNA sequence of clone	73653.2
SEQ ID NO:892	is the determined cDNA sequence of clone	76354.1
SEQ ID NO:893	is the determined cDNA sequence of clone	76355.1
SEQ ID NO:894	is the determined cDNA sequence of clone	76357.1
SEQ ID NO:895	is the determined cDNA sequence of clone	76360.1
SEQ ID NO:896	is the determined cDNA sequence of clone	76843.2
SEQ ID NO:897	is the determined cDNA sequence of clone	76844.2
SEQ ID NO:898	is the determined cDNA sequence of clone	76845.2
SEQ ID NO:899	is the determined cDNA sequence of clone	76846.1
SEQ ID NO:900	is the determined cDNA sequence of clone	76847.1
SEQ ID NO:901	is the determined cDNA sequence of clone	76850.1
SEQ ID NO:902	is the determined cDNA sequence of clone	76851.1
SEQ ID NO:903	is the determined cDNA sequence of clone	76853.1
SEQ ID NO:904	is the determined cDNA sequence of clone	76854.1
SEQ ID NO:905	is the determined cDNA sequence of clone	76855.1
SEQ ID NO:906	is the determined cDNA sequence of clone	76856.1
SEQ ID NO:907	is the determined cDNA sequence of clone	76857.2
SEQ ID NO:908	is the determined cDNA sequence of clone	76858.1
SEQ ID NO:909	is the detennined cDNA sequence of clone	76859.1
SEQ ID NO:910	is the determined cDNA sequence of clone	76860.1
SEQ ID NO:911	is the determined cDNA sequence of clone	76861.1
SEQ ID NO:912	is the determined cDNA sequence of clone	76862.1
SEQ ID NO:913	is the determined cDNA sequence of clone	76863.2
SEQ ID NO:914	is the determined cDNA sequence of clone	76864.2
SEQ ID NO:915	is the determined cDNA sequence of clone	76865.1
SEQ ID NO:916	is the determined cDNA sequence of clone	76866.1
SEQ ID NO:917	is the determined cDNA sequence of clone	76869.1
SEQ ID NO:918	is the determined cDNA sequence of clone	76870.1
SEQ ID NO:919	is the determined cDNA sequence of clone	76871.1
SEQ ID NO:920	is the determined cDNA sequence of clone	76872.1
SEQ ID NO:921	is the determined cDNA sequence of clone	76873.1
SEQ ID NO:922	is the determined cDNA sequence of clone	76874.2
SEQ ID NO:923	is the determined cDNA sequence of clone	76875.1
SEQ ID NO:924	is the determined cDNA sequence of clone	76876.1
SEQ ID NO:925	is the determined cDNA sequence of clone	76878.1
SEQ ID NO:926	is the determined cDNA sequence of clone	76879.1
SEQ ID NO:927	is the determined cDNA sequence of clone	76880.1
SEQ ID NO:928	is the determined cDNA sequence of clone	76881.1
SEQ ID NO:929	is the determined cDNA sequence of clone	76882.1
SEQ ID NO:930	is the determined cDNA sequence of clone	76883.2
SEQ ID NO:931	is the determined cDNA sequence of clone	76884.2
SEQ ID NO:932	is the determined cDNA sequence of clone	76886.1
SEQ ID NO:933	is the determined cDNA sequence of clone	76887.1
SEQ ID NO:934	is the determined cDNA sequence of clone	76889.2

DETAILED DESCRIPTION OF THE INVENTION

[0041] The present invention is directed generally to compositions and their use in the therapy and diagnosis of cancer, particularly colon cancer. As described further below, illustrative compositions of the present invention include, but are not restricted to, polypeptides, particularly immunogenic polypeptides, polynucleotides encoding such polypeptides, antibodies and other binding agents, antigen presenting cells (APCs) and immune system cells (e.g., T cells).

[0042] The practice of the present invention will employ, unless indicated specifically to the contrary, conventional methods of virology, immunology, microbiology, molecular biology and recombinant DNA techniques within the skill of the art, many of which are described below for the purpose of illustration. Such techniques are explained fully in the literature. See, e.g., Sambrook, et al. Molecular Cloning: A Laboratory Manual (2nd Edition, 1989); Maniatis et al. Molecular Cloning: A Laboratory Manual (1982); DNA Cloning: A Practical Approach, vol. I & II (D. Glover, ed.); Oligonucleotide Synthesis (N. Gait, ed., 1984); Nucleic Acid Hybridization (B. Hames & S. Higgins, eds., 1985); Transcription and Translation (B. Hames & S. Higgins, eds., 1984); Animal Cell Culture (R. Freshney, ed., 1986); Perbal, A Practical Guide to Molecular Cloning (1984).

[0043] All publications, patents and patent applications cited herein, whether supra or infra, are hereby incorporated by reference in their entirety.

[0044] As used in this specification and the appended claims, the singular forms “a,” “an” and “the” include plural references unless the content clearly dictates otherwise.

[0045] Polypeptide Compositions

[0046] As used herein, the term “polypeptide” is used in its conventional meaning, i.e., as a sequence of amino acids. The polypeptides are not limited to a specific length of the product; thus, peptides, oligopeptides, and proteins are included within the definition of polypeptide, and such terms may be used interchangeably herein unless specifically indicated otherwise. This term also does not refer to or exclude post-expression modifications of the polypeptide, for example, glycosylations, acetylations, phosphorylations and the like, as well as other modifications known in the art, both naturally occurring and non-naturally occurring. A polypeptide may be an entire protein, or a subsequence thereof. Particular polypeptides of interest in the context of this invention are amino acid subsequences comprising epitopes, i.e., antigenic determinants substantially responsible for the immunogenic properties of a polypeptide and being capable of evoking an immune response.

[0047] Particularly illustrative polypeptides of the present invention comprise those encoded by a polynucleotide sequence set forth in any one of SEQ ID NO:1-934, or a sequence that hybridizes under moderately stringent conditions, or, alternatively, under highly stringent conditions, to a polynucleotide sequence set forth in any one of SEQ ID NO:1-934.

[0048] The polypeptides of the present invention are sometimes herein referred to as colon tumor proteins or colon tumor polypeptides, as an indication that their identification has been based at least in part upon their increased levels of expression in colon tumor samples. Thus, a “colon tumor polypeptide” or “colon tumor protein,” refers generally to a polypeptide sequence of the present invention, or a polynucleotide sequence encoding such a polypeptide, that is expressed in a substantial proportion of colon tumor samples, for example preferably greater than about 20%, more preferably greater than about 30%, and most preferably greater than about 50% or more of colon tumor samples tested, at a level that is at least two fold, and preferably at least five fold, greater than the level of expression in normal tissues, as determined using a representative assay provided herein. A colon tumor polypeptide sequence of the invention, based upon its increased level of expression in tumor cells, has particular utility both as a diagnostic marker as well as a therapeutic target, as further described below.

[0049] In certain preferred embodiments, the polypeptides of the invention are immunogenic, i.e., they react detectably within an immunoassay (such as an ELISA or T-cell stimulation assay) with antisera and/or T-cells from a patient with colon cancer. Screening for immunogenic activity can be performed using techniques well known to the skilled artisan. For example, such screens can be performed using methods such as those described in Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, 1988. In one illustrative example, a polypeptide may be immobilized on a solid support and contacted with patient sera to allow binding of antibodies within the sera to the immobilized polypeptide. Unbound sera may then be removed and bound antibodies detected using, for example, 125I-labeled Protein A.

[0050] As would be recognized by the skilled artisan, immunogenic portions of the polypeptides disclosed herein are also encompassed by the present invention. An “immunogenic portion,” as used herein, is a fragment of an immunogenic polypeptide of the invention that itself is immunologically reactive (i.e., specifically binds) with the B-cells and/or T-cell surface antigen receptors that recognize the polypeptide. Immunogenic portions may generally be identified using well known techniques, such as those summarized in Paul, Fundamental Immunology, 3rd ed., 243-247 (Raven Press, 1993) and references cited therein. Such techniques include screening polypeptides for the ability to react with antigen-specific antibodies, antisera and/or T-cell lines or clones. As used herein, antisera and antibodies are “antigen-specific” if they specifically bind to an antigen (i.e., they react with the protein in an ELISA or other immunoassay, and do not react detectably with unrelated proteins). Such antisera and antibodies may be prepared as described herein, and using well-known techniques.

[0051] In one preferred embodiment, an immunogenic portion of a polypeptide of the present invention is a portion that reacts with antisera and/or T-cells at a level that is not substantially less than the reactivity of the full-length polypeptide (e.g., in an ELISA and/or T-cell reactivity assay). Preferably, the level of immunogenic activity of the immunogenic portion is at least about 50%, preferably at least about 70% and most preferably greater than about 90% of the immunogenicity for the full-length polypeptide. In some instances, preferred immunogenic portions will be identified that have a level of immunogenic activity greater than that of the corresponding full-length polypeptide, e.g., having greater than about 100% or 150% or more immunogenic activity.

[0052] In certain other embodiments, illustrative immunogenic portions may include peptides in which an N-terminal leader sequence and/or transmembrane domain have been deleted. Other illustrative immunogenic portions will contain a small N- and/or C-terminal deletion (e.g., 1-30 amino acids, preferably 5-15 amino acids), relative to the mature protein.

[0053] In another embodiment, a polypeptide composition of the invention may also comprise one or more polypeptides that are immunologically reactive with T cells and/or antibodies generated against a polypeptide of the invention, particularly a polypeptide having an amino acid sequence disclosed herein, or to an immunogenic fragment or variant thereof.

[0054] In another embodiment of the invention, polypeptides are provided that comprise one or more polypeptides that are capable of eliciting T cells and/or antibodies that are immunologically reactive with one or more polypeptides described herein, or one or more polypeptides encoded by contiguous nucleic acid sequences contained in the polynucleotide sequences disclosed herein, or immunogenic fragments or variants thereof, or to one or more nucleic acid sequences which hybridize to one or more of these sequences under conditions of moderate to high stringency.

[0055] The present invention, in another aspect, provides polypeptide fragments comprising at least about 5, 10, 15, 20, 25, 50, or 100 contiguous amino acids, or more, including all intermediate lengths, of a polypeptide compositions set forth herein, such as those encoded by a polynucleotide sequence set forth in a sequence of SEQ ID NO:1-934.

[0056] In another aspect, the present invention provides variants of the polypeptide compositions described herein. Polypeptide variants generally encompassed by the present invention will typically exhibit at least about 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% or more identity (determined as described below), along its length, to a polypeptide sequences set forth herein.

[0057] In one preferred embodiment, the polypeptide fragments and variants provided by the present invention are immunologically reactive with an antibody and/or T-cell that reacts with a full-length polypeptide specifically set forth herein.

[0058] In another preferred embodiment, the polypeptide fragments and variants provided by the present invention exhibit a level of immunogenic activity of at least about 50%, preferably at least about 70%, and most preferably at least about 90% or more of that exhibited by a full-length polypeptide sequence specifically set forth herein.

[0059] A polypeptide “variant,” as the term is used herein, is a polypeptide that typically differs from a polypeptide specifically disclosed herein in one or more substitutions, deletions, additions and/or insertions. Such variants may be naturally occurring or may be synthetically generated, for example, by modifying one or more of the above polypeptide sequences of the invention and evaluating their immunogenic activity as described herein and/or using any of a number of techniques well known in the art.

[0060] For example, certain illustrative variants of the polypeptides of the invention include those in which one or more portions, such as an N-terminal leader sequence or transmembrane domain, have been removed. Other illustrative variants include variants in which a small portion (e.g., 1-30 amino acids, preferably 5-15 amino acids) has been removed from the N- and/or C-terminal of the mature protein.

[0061] In many instances, a variant will contain conservative substitutions. A “conservative substitution” is one in which an amino acid is substituted for another amino acid that has similar properties, such that one skilled in the art of peptide chemistry would expect the secondary structure and hydropathic nature of the polypeptide to be substantially unchanged. As described above, modifications may be made in the structure of the polynucleotides and polypeptides of the present invention and still obtain a functional molecule that encodes a variant or derivative polypeptide with desirable characteristics, e.g., with immunogenic characteristics. When it is desired to alter the amino acid sequence of a polypeptide to create an equivalent, or even an improved, immunogenic variant or portion of a polypeptide of the invention, one skilled in the art will typically change one or more of the codons of the encoding DNA sequence according to Table 1.

[0062] For example, certain amino acids may be substituted for other amino acids in a protein structure without appreciable loss of interactive binding capacity with structures such as, for example, antigen-binding regions of antibodies or binding sites on substrate molecules. Since it is the interactive capacity and nature of a protein that defines that protein's biological functional activity, certain amino acid sequence substitutions can be made in a protein sequence, and, of course, its underlying DNA coding sequence, and nevertheless obtain a protein with like properties. It is thus contemplated that various changes may be made in the peptide sequences of the disclosed compositions, or corresponding DNA sequences which encode said peptides without appreciable loss of their biological utility or activity.

TABLE 1
Amino Acids	Codons
Alanine	Ala	A	GCA	GCC	GCG	GCU
Cysteine	Cys	C	UGC	UGU
Aspartic acid	Asp	D	GAC	GAU
Glutamic acid	Glu	E	GAA	GAG
Phenylalanine	Phe	F	UUC	UUU
Glycine	Gly	G	GGA	GGC	GGG	GGU
Histidine	His	H	CAC	CAU
Isoleucine	Ile	I	AUA	AUC	AUU
Lysine	Lys	K	AAA	AAG
Leucine	Leu	L	UUA	UUG	CUA	CUC	CUG	CUU
Methionine	Met	M	AUG
Asparagine	Asn	N	AAC	AAU
Proline	Pro	P	CCA	CCC	CCG	CCU
Glutamine	Gln	Q	CAA	CAG
Arginine	Arg	R	AGA	AGG	CGA	CGC	CGG	CGU
Serine	Ser	S	AGC	AGU	UCA	UCC	UCG	UCU
Threonine	Thr	T	ACA	ACC	ACG	ACU
Valine	Val	V	GUA	GUC	GUG	GUU
Tryptophan	Trp	W	UGG
Tyrosine	Tyr	Y	UAC	UAU

[0063] In making such changes, the hydropathic index of amino acids may be considered. The importance of the hydropathic amino acid index in conferring interactive biologic function on a protein is generally understood in the art (Kyte and Doolittle, 1982, incorporated herein by reference). It is accepted that the relative hydropathic character of the amino acid contributes to the secondary structure of the resultant protein, which in turn defines the interaction of the protein with other molecules, for example, enzymes, substrates, receptors, DNA, antibodies, antigens, and the like. Each amino acid has been assigned a hydropathic index on the basis of its hydrophobicity and charge characteristics (Kyte and Doolittle, 1982). These values are: isoleucine (+4.5); valine (+4.2); leucine (+3.8); phenylalanine (+2.8); cysteine/cystine (+2.5); methionine (+1.9); alanine (+1.8); glycine (−0.4); threonine (−0.7); serine (−0.8); tryptophan (−0.9); tyrosine (−1.3); proline (−1.6); histidine (−3.2); glutamate (−3.5); glutamine (−3.5); aspartate (−3.5); asparagine (−3.5); lysine (−3.9); and arginine (−4.5).

[0064] It is known in the art that certain amino acids may be substituted by other amino acids having a similar hydropathic index or score and still result in a protein with similar biological activity, i.e. still obtain a biological functionally equivalent protein. In making such changes, the substitution of amino acids whose hydropathic indices are within ±2 is preferred, those within ±1 are particularly preferred, and those within ±0.5 are even more particularly preferred. It is also understood in the art that the substitution of like amino acids can be made effectively on the basis of hydrophilicity. U.S. Pat. No. 4,554,101 (specifically incorporated herein by reference in its entirety), states that the greatest local average hydrophilicity of a protein, as governed by the hydrophilicity of its adjacent amino acids, correlates with a biological property of the protein.

[0065] As detailed in U.S. Pat. No. 4,554,101, the following hydrophilicity values have been assigned to amino acid residues: arginine (+3.0); lysine (+3.0); aspartate (+3.0±1); glutamate (+3.0±1); serine (+0.3); asparagine (+0.2); glutamine (+0.2); glycine (0); threonine (−0.4); proline (−0.5±1); alanine (−0.5); histidine (−0.5); cysteine (−1.0); methionine (−1.3); valine (−1.5); leucine (−1.8); isoleucine (−1.8); tyrosine (−2.3); phenylalanine (−2.5); tryptophan (−3.4). It is understood that an amino acid can be substituted for another having a similar hydrophilicity value and still obtain a biologically equivalent, and in particular, an immunologically equivalent protein. In such changes, the substitution of amino acids whose hydrophilicity values are within ±2 is preferred, those within ±1 are particularly preferred, and those within ±0.5 are even more particularly preferred.

[0066] As outlined above, amino acid substitutions are generally therefore based on the relative similarity of the amino acid side-chain substituents, for example, their hydrophobicity, hydrophilicity, charge, size, and the like. Exemplary substitutions that take various of the foregoing characteristics into consideration are well known to those of skill in the art and include: arginine and lysine; glutamate and aspartate; serine and threonine; glutamine and asparagine; and valine, leucine and isoleucine.

[0067] In addition, any polynucleotide may be further modified to increase stability in vivo. Possible modifications include, but are not limited to, the addition of flanking sequences at the 5′ and/or 3′ ends; the use of phosphorothioate or 2′ O -methyl rather than phosphodiesterase linkages in the backbone; and/or the inclusion of nontraditional bases such as inosine, queosine and wybutosine, as well as acetyl- methyl-, thio- and other modified forms of adenine, cytidine, guanine, thymine and uridine.

[0068] Amino acid substitutions may further be made on the basis of similarity in polarity, charge, solubility, hydrophobicity, hydrophilicity and/or the amphipathic nature of the residues. For example, negatively charged amino acids include aspartic acid and glutamic acid; positively charged amino acids include lysine and arginine; and amino acids with uncharged polar head groups having similar hydrophilicity values include leucine, isoleucine and valine; glycine and alanine; asparagine and glutamine; and serine, threonine, phenylalanine and tyrosine. Other groups of amino acids that may represent conservative changes include: (1) ala, pro, gly, glu, asp, gln, asn, ser, thr; (2) cys, ser, tyr, thr; (3) val, ile, leu, met, ala, phe; (4) lys, arg, his; and (5) phe, tyr, trp, his. A variant may also, or alternatively, contain nonconservative changes. In a preferred embodiment, variant polypeptides differ from a native sequence by substitution, deletion or addition of five amino acids or fewer. Variants may also (or alternatively) be modified by, for example, the deletion or addition of amino acids that have minimal influence on the immunogenicity, secondary structure and hydropathic nature of the polypeptide.

[0069] As noted above, polypeptides may comprise a signal (or leader) sequence at the N-terminal end of the protein, which co-translationally or post-translationally directs transfer of the protein. The polypeptide may also be conjugated to a linker or other sequence for ease of synthesis, purification or identification of the polypeptide (e.g., poly-His), or to enhance binding of the polypeptide to a solid support. For example, a polypeptide may be conjugated to an immunoglobulin Fc region.

[0070] When comparing polypeptide sequences, two sequences are said to be “identical” if the sequence of amino acids in the two sequences is the same when aligned for maximum correspondence, as described below. Comparisons between two sequences are typically performed by comparing the sequences over a comparison window to identify and compare local regions of sequence similarity. A “comparison window” as used herein, refers to a segment of at least about 20 contiguous positions, usually 30 to about 75, 40 to about 50, in which a sequence may be compared to a reference sequence of the same number of contiguous positions after the two sequences are optimally aligned.

[0071] Optimal alignment of sequences for comparison may be conducted using the Megalign program in the Lasergene suite of bioinformatics software (DNASTAR, Inc., Madison, Wis.), using default parameters. This program embodies several alignment schemes described in the following references: Dayhoff, M. O. (1978) A model of evolutionary change in proteins—Matrices for detecting distant relationships. In Dayhoff, M. O. (ed.) Atlas of Protein Sequence and Structure, National Biomedical Research Foundation, Washington D.C. Vol. 5, Suppl. 3, pp. 345-358; Hein J. (1990) Unified Approach to Alignment and Phylogenes pp. 626-645 Methods in Enzymology vol. 183, Academic Press, Inc., San Diego, Calif.; Higgins, D. G. and Sharp, P. M. (1989) CABIOS 5:151-153; Myers, E. W. and Muller W. (1988) CABIOS 4:11-17; Robinson, E. D. (1971) Comb. Theor 11:105; Saitou, N. Nei, M. (1987) Mol. Biol. Evol. 4:406-425; Sneath, P. H. A. and Sokal, R. R. (1973) Numerical Taxonomy—the Principles and Practice of Numerical Taxonomy, Freeman Press, San Francisco, Calif.; Wilbur, W. J. and Lipman, D. J. (1983) Proc. Natl. Acad., Sci. USA 80:726-730.

[0072] Alternatively, optimal alignment of sequences for comparison may be conducted by the local identity algorithm of Smith and Waterman (1981) Add. APL. Math 2:482, by the identity alignment algorithm of Needleman and Wunsch (1970) J. Mol. Biol. 48:443, by the search for similarity methods of Pearson and Lipman (1988) Proc. Natl. Acad. Sci. USA 85: 2444, by computerized implementations of these algorithms (GAP, BESTFIT, BLAST, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group (GCG), 575 Science Dr., Madison, Wis.), or by inspection.

[0073] One preferred example of algorithms that are suitable for determining percent sequence identity and sequence similarity are the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al. (1977) Nucl. Acids Res. 25:3389-3402 and Altschul et al. (1990) J. Mol. Biol. 215:403-410, respectively. BLAST and BLAST 2.0 can be used, for example with the parameters described herein, to determine percent sequence identity for the polynucleotides and polypeptides of the invention. Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information. For amino acid sequences, a scoring matrix can be used to calculate the cumulative score. Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T and X determine the sensitivity and speed of the alignment.

[0074] In one preferred approach, the “percentage of sequence identity” is determined by comparing two optimally aligned sequences over a window of comparison of at least 20 positions, wherein the portion of the polypeptide sequence in the comparison window may comprise additions or deletions (i.e., gaps) of 20 percent or less, usually 5 to 15 percent, or 10 to 12 percent, as compared to the reference sequences (which does not comprise additions or deletions) for optimal alignment of the two sequences. The percentage is calculated by determining the number of positions at which the identical amino acid residue occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the reference sequence (i.e., the window size) and multiplying the results by 100 to yield the percentage of sequence identity.

[0075] Within other illustrative embodiments, a polypeptide may be a xenogeneic polypeptide that comprises an polypeptide having substantial sequence identity, as described above, to the human polypeptide (also termed autologous antigen) which served as a reference polypeptide, but which xenogeneic polypeptide is derived from a different, non-human species. One skilled in the art will recognize that “self” antigens are often poor stimulators of CD8+ and CD4+ T-lymphocyte responses, and therefore efficient immunotherapeutic strategies directed against tumor polypeptides require the development of methods to overcome immune tolerance to particular self tumor polypeptides. For example, humans immunized with prostase protein from a xenogeneic (non human) origin are capable of mounting an immune response against the counterpart human protein, e.g. the human prostase tumor protein present on human tumor cells. Accordingly, the present invention provides methods for purifying the xenogeneic form of the tumor proteins set forth herein, such as the polypeptides encoded by polynucleotide sequences set forth in SEQ ID NO:1-934.

[0076] Therefore, one aspect of the present invention provides xenogeneic variants of the polypeptide compositions described herein. Such xenogeneic variants generally encompassed by the present invention will typically exhibit at least about 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% or more identity along their lengths, to a polypeptide sequences set forth herein.

[0077] More particularly, the invention is directed to mouse, rat, monkey, porcine and other non-human polypeptides which can be used as xenogeneic forms of human polypeptides set forth herein, to induce immune responses directed against tumor polypeptides of the invention.

[0078] Within other illustrative embodiments, a polypeptide may be a fusion polypeptide that comprises multiple polypeptides as described herein, or that comprises at least one polypeptide as described herein and an unrelated sequence, such as a known tumor protein. A fusion partner may, for example, assist in providing T helper epitopes (an immunological fusion partner), preferably T helper epitopes recognized by humans, or may assist in expressing the protein (an expression enhancer) at higher yields than the native recombinant protein. Certain preferred fusion partners are both immunological and expression enhancing fusion partners. Other fusion partners may be selected so as to increase the solubility of the polypeptide or to enable the polypeptide to be targeted to desired intracellular compartments. Still further fusion partners include affinity tags, which facilitate purification of the polypeptide.

[0079] Fusion polypeptides may generally be prepared using standard techniques, including chemical conjugation. Preferably, a fusion polypeptide is expressed as a recombinant polypeptide, allowing the production of increased levels, relative to a non-fused polypeptide, in an expression system. Briefly, DNA sequences encoding the polypeptide components may be assembled separately, and ligated into an appropriate expression vector. The 3′ end of the DNA sequence encoding one polypeptide component is ligated, with or without a peptide linker, to the 5′ end of a DNA sequence encoding the second polypeptide component so that the reading frames of the sequences are in phase. This permits translation into a single fusion polypeptide that retains the biological activity of both component polypeptides.

[0080] A peptide linker sequence may be employed to separate the first and second polypeptide components by a distance sufficient to ensure that each polypeptide folds into its secondary and tertiary structures. Such a peptide linker sequence is incorporated into the fusion polypeptide using standard techniques well known in the art. Suitable peptide linker sequences may be chosen based on the following factors: (1) their ability to adopt a flexible extended conformation; (2) their inability to adopt a secondary structure that could interact with functional epitopes on the first and second polypeptides; and (3) the lack of hydrophobic or charged residues that might react with the polypeptide functional epitopes. Preferred peptide linker sequences contain Gly, Asn and Ser residues. Other near neutral amino acids, such as Thr and Ala may also be used in the linker sequence. Amino acid sequences which may be usefully employed as linkers include those disclosed in Maratea et al., Gene 40:39-46, 1985; Murphy et al., Proc. Natl. Acad. Sci. USA 83:8258-8262, 1986; U.S. Pat. Nos. 4,935,233 and 4,751,180. The linker sequence may generally be from 1 to about 50 amino acids in length. Linker sequences are not required when the first and second polypeptides have non-essential N-terminal amino acid regions that can be used to separate the functional domains and prevent steric interference.

[0081] The ligated DNA sequences are operably linked to suitable transcriptional or translational regulatory elements. The regulatory elements responsible for expression of DNA are located only 5′ to the DNA sequence encoding the first polypeptides. Similarly, stop codons required to end translation and transcription termination signals are only present 3′ to the DNA sequence encoding the second polypeptide.

[0082] The fusion polypeptide can comprise a polypeptide as described herein together with an unrelated immunogenic protein, such as an immunogenic protein capable of eliciting a recall response. Examples of such proteins include tetanus, tuberculosis and hepatitis proteins (see, for example, Stoute et al. New Engl. J. Med., 336:86-91, 1997).

[0083] In one preferred embodiment, the immunological fusion partner is derived from a Mycobacterium sp., such as a Mycobacterium tuberculosis-derived Ra12 fragment. Ra12 compositions and methods for their use in enhancing the expression and/or immunogenicity of heterologous polynucleotide/polypeptide sequences is described in U.S. patent application Ser. No. 60/158,585, the disclosure of which is incorporated herein by reference in its entirety. Briefly, Ra12 refers to a polynucleotide region that is a subsequence of a Mycobacterium tuberculosis MTB32A nucleic acid. MTB32A is a serine protease of 32 KD molecular weight encoded by a gene in virulent and avirulent strains of M. tuberculosis. The nucleotide sequence and amino acid sequence of MTB32A have been described (for example, U.S. patent application Ser. No. 60/158,585; see also, Skeiky et al., Infection and Immun. (1999) 67:3998-4007, incorporated herein by reference). C-terminal fragments of the MTB32A coding sequence express at high levels and remain as a soluble polypeptides throughout the purification process. Moreover, Ra12 may enhance the immunogenicity of heterologous immunogenic polypeptides with which it is fused. One preferred Ra12 fusion polypeptide comprises a 14 KD C-terminal fragment corresponding to amino acid residues 192 to 323 of MTB32A. Other preferred Ra12 polynucleotides generally comprise at least about 15 consecutive nucleotides, at least about 30 nucleotides, at least about 60 nucleotides, at least about 100 nucleotides, at least about 200 nucleotides, or at least about 300 nucleotides that encode a portion of a Ra12 polypeptide. Ra12 polynucleotides may comprise a native sequence (i.e., an endogenous sequence that encodes a Ra12 polypeptide or a portion thereof) or may comprise a variant of such a sequence. Ra12 polynucleotide variants may contain one or more substitutions, additions, deletions and/or insertions such that the biological activity of the encoded fusion polypeptide is not substantially diminished, relative to a fusion polypeptide comprising a native Ra12 polypeptide. Variants preferably exhibit at least about 70% identity, more preferably at least about 80% identity and most preferably at least about 90% identity to a polynucleotide sequence that encodes a native Ra12 polypeptide or a portion thereof.

[0084] Within other preferred embodiments, an immunological fusion partner is derived from protein D, a surface protein of the gram-negative bacterium Haemophilus influenza B (WO 91/18926). Preferably, a protein D derivative comprises approximately the first third of the protein (e.g., the first N-terminal 100-110 amino acids), and a protein D derivative may be lipidated. Within certain preferred embodiments, the first 109 residues of a Lipoprotein D fusion partner is included on the N-terminus to provide the polypeptide with additional exogenous T-cell epitopes and to increase the expression level in E. coli (thus functioning as an expression enhancer). The lipid tail ensures optimal presentation of the antigen to antigen presenting cells. Other fusion partners include the non-structural protein from influenzae virus, NS1 (hemaglutinin). Typically, the N-terminal 81 amino acids are used, although different fragments that include T-helper epitopes may be used.

[0085] In another embodiment, the immunological fusion partner is the protein known as LYTA, or a portion thereof (preferably a C-terminal portion). LYTA is derived from Streptococcus pneumoniae, which synthesizes an N-acetyl-L-alanine amidase known as amidase LYTA (encoded by the LytA gene; Gene 43:265-292, 1986). LYTA is an autolysin that specifically degrades certain bonds in the peptidoglycan backbone. The C-terminal domain of the LYTA protein is responsible for the affinity to the choline or to some choline analogues such as DEAE. This property has been exploited for the development of E. coli C-LYTA expressing plasmids useful for expression of fusion proteins. Purification of hybrid proteins containing the C-LYTA fragment at the amino terminus has been described (see Biotechnology 10:795-798, 1992). Within a preferred embodiment, a repeat portion of LYTA may be incorporated into a fusion polypeptide. A repeat portion is found in the C-terminal region starting at residue 178. A particularly preferred repeat portion incorporates residues 188-305.

[0086] Yet another illustrative embodiment involves fusion polypeptides, and the polynucleotides encoding them, wherein the fusion partner comprises a targeting signal capable of directing a polypeptide to the endosomal/lysosomal compartment, as described in U.S. Pat. No. 5,633,234. An immunogenic polypeptide of the invention, when fused with this targeting signal, will associate more efficiently with MHC class II molecules and thereby provide enhanced in vivo stimulation of CD4+ T-cells specific for the polypeptide.

[0087] Polypeptides of the invention are prepared using any of a variety of well known synthetic and/or recombinant techniques, the latter of which are further described below. Polypeptides, portions and other variants generally less than about 150 amino acids can be generated by synthetic means, using techniques well known to those of ordinary skill in the art. In one illustrative example, such polypeptides are synthesized using any of the commercially available solid-phase techniques, such as the Merrifield solid-phase synthesis method, where amino acids are sequentially added to a growing amino acid chain. See Merrifield, J. Am. Chem. Soc. 85:2149-2146, 1963. Equipment for automated synthesis of polypeptides is commercially available from suppliers such as Perkin Elmer/Applied BioSystems Division (Foster City, Calif.), and may be operated according to the manufacturer's instructions.

[0088] In general, polypeptide compositions (including fusion polypeptides) of the invention are isolated. An “isolated” polypeptide is one that is removed from its original environment. For example, a naturally-occurring protein or polypeptide is isolated if it is separated from some or all of the coexisting materials in the natural system. Preferably, such polypeptides are also purified, e.g., are at least about 90% pure, more preferably at least about 95% pure and most preferably at least about 99% pure.

[0089] Polynucleotide Compositions

[0090] The present invention, in other aspects, provides polynucleotide compositions. The terms “DNA” and “polynucleotide” are used essentially interchangeably herein to refer to a DNA molecule that has been isolated free of total genomic DNA of a particular species. “Isolated,” as used herein, means that a polynucleotide is substantially away from other coding sequences, and that the DNA molecule does not contain large portions of unrelated coding DNA, such as large chromosomal fragments or other functional genes or polypeptide coding regions. Of course, this refers to the DNA molecule as originally isolated, and does not exclude genes or coding regions later added to the segment by the hand of man.

[0091] As will be understood by those skilled in the art, the polynucleotide compositions of this invention can include genomic sequences, extra-genomic and plasmid-encoded sequences and smaller engineered gene segments that express, or may be adapted to express, proteins, polypeptides, peptides and the like. Such segments may be naturally isolated, or modified synthetically by the hand of man.

[0092] As will be also recognized by the skilled artisan, polynucleotides of the invention may be single-stranded (coding or antisense) or double-stranded, and may be DNA (genomic, cDNA or synthetic) or RNA molecules. RNA molecules may include HnRNA molecules, which contain introns and correspond to a DNA molecule in a one-to-one manner, and mRNA molecules, which do not contain introns. Additional coding or non-coding sequences may, but need not, be present within a polynucleotide of the present invention, and a polynucleotide may, but need not, be linked to other molecules and/or support materials.

[0093] Polynucleotides may comprise a native sequence (i.e., an endogenous sequence that encodes a polypeptide/protein of the invention or a portion thereof) or may comprise a sequence that encodes a variant or derivative, preferably and immunogenic variant or derivative, of such a sequence.

[0094] Therefore, according to another aspect of the present invention, polynucleotide compositions are provided that comprise some or all of a polynucleotide sequence set forth in any one of SEQ ID NO:1-934, complements of a polynucleotide sequence set forth in any one of SEQ ID NO:1-934, and degenerate variants of a polynucleotide sequence set forth in any one of SEQ ID NO:1-934. In certain preferred embodiments, the polynucleotide sequences set forth herein encode immunogenic polypeptides, as described above.

[0095] In other related embodiments, the present invention provides polynucleotide variants having substantial identity to the sequences disclosed herein in SEQ ID NO:1-934, for example those comprising at least 70% sequence identity, preferably at least 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% or higher, sequence identity compared to a polynucleotide sequence of this invention using the methods described herein, (e.g., BLAST analysis using standard parameters, as described below). One skilled in this art will recognize that these values can be appropriately adjusted to determine corresponding identity of proteins encoded by two nucleotide sequences by taking into account codon degeneracy, amino acid similarity, reading frame positioning and the like.

[0096] Typically, polynucleotide variants will contain one or more substitutions, additions, deletions and/or insertions, preferably such that the immunogenicity of the polypeptide encoded by the variant polynucleotide is not substantially diminished relative to a polypeptide encoded by a polynucleotide sequence specifically set forth herein). The term “variants” should also be understood to encompasses homologous genes of xenogenic origin.

[0097] In additional embodiments, the present invention provides polynucleotide fragments comprising or consisting of various lengths of contiguous stretches of sequence identical to or complementary to one or more of the sequences disclosed herein. For example, polynucleotides are provided by this invention that comprise or consist of at least about 10, 15, 20, 30, 40, 50, 75, 100, 150, 200, 300, 400, 500 or 1000 or more contiguous nucleotides of one or more of the sequences disclosed herein as well as all intermediate lengths there between. It will be readily understood that “intermediate lengths”, in this context, means any length between the quoted values, such as 16, 17, 18, 19, etc.; 21, 22, 23, etc.; 30, 31, 32, etc.; 50, 51, 52, 53, etc.; 100, 101, 102, 103, etc.; 150, 151, 152, 153, etc.; including all integers through 200-500; 500-1,000, and the like. A polynucleotide sequence as described here may be extended at one or both ends by additional nucleotides not found in the native sequence. This additional sequence may consist of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 nucleotides at either end of the disclosed sequence or at both ends of the disclosed sequence.

[0098] In another embodiment of the invention, polynucleotide compositions are provided that are capable of hybridizing under moderate to high stringency conditions to a polynucleotide sequence provided herein, or a fragment thereof, or a complementary sequence thereof. Hybridization techniques are well known in the art of molecular biology. For purposes of illustration, suitable moderately stringent conditions for testing the hybridization of a polynucleotide of this invention with other polynucleotides include prewashing in a solution of 5×SSC, 0.5% SDS, 1.0 mM EDTA (pH 8.0); hybridizing at 50° C.-60° C., 5×SSC, overnight; followed by washing twice at 65° C. for 20 minutes with each of 2×, 0.5× and 0.2×SSC containing 0.1% SDS. One skilled in the art will understand that the stringency of hybridization can be readily manipulated, such as by altering the salt content of the hybridization solution and/or the temperature at which the hybridization is performed. For example, in another embodiment, suitable highly stringent hybridization conditions include those described above, with the exception that the temperature of hybridization is increased, e.g., to 60-65° C. or 65-70° C.

[0099] In certain preferred embodiments, the polynucleotides described above, e.g., polynucleotide variants, fragments and hybridizing sequences, encode polypeptides that are immunologically cross-reactive with a polypeptide sequence specifically set forth herein. In other preferred embodiments, such polynucleotides encode polypeptides that have a level of immunogenic activity of at least about 50%, preferably at least about 70%, and more preferably at least about 90% of that for a polypeptide sequence specifically set forth herein.

[0100] The polynucleotides of the present invention, or fragments thereof, regardless of the length of the coding sequence itself, may be combined with other DNA sequences, such as promoters, polyadenylation signals, additional restriction enzyme sites, multiple cloning sites, other coding segments, and the like, such that their overall length may vary considerably. It is therefore contemplated that a nucleic acid fragment of almost any length may be employed, with the total length preferably being limited by the ease of preparation and use in the intended recombinant DNA protocol. For example, illustrative polynucleotide segments with total lengths of about 10,000, about 5000, about 3000, about 2,000, about 1,000, about 500, about 200, about 100, about 50 base pairs in length, and the like, (including all intermediate lengths) are contemplated to be useful in many implementations of this invention.

[0101] When comparing polynucleotide sequences, two sequences are said to be “identical” if the sequence of nucleotides in the two sequences is the same when aligned for maximum correspondence, as described below. Comparisons between two sequences are typically performed by comparing the sequences over a comparison window to identify and compare local regions of sequence similarity. A “comparison window” as used herein, refers to a segment of at least about 20 contiguous positions, usually 30 to about 75, 40 to about 50, in which a sequence may be compared to a reference sequence of the same number of contiguous positions after the two sequences are optimally aligned.

[0102] Optimal alignment of sequences for comparison may be conducted using the Megalign program in the Lasergene suite of bioinformatics software (DNASTAR, Inc., Madison, Wis.), using default parameters. This program embodies several alignment schemes described in the following references: Dayhoff, M. O. (1978) A model of evolutionary change in proteins—Matrices for detecting distant relationships. In Dayhoff, M. O. (ed.) Atlas of Protein Sequence and Structure, National Biomedical Research Foundation, Washington D.C. Vol. 5, Suppl. 3, pp. 345-358; Hein J. (1990) Unified Approach to Alignment and Phylogenes pp. 626-645 Methods in Enzymology vol. 183, Academic Press, Inc., San Diego, Calif.; Higgins, D. G. and Sharp, P. M. (1989) CABIOS 5:151-153; Myers, E. W. and Muller W. (1988) CABIOS 4:11-17; Robinson, E. D. (1971) Comb. Theor 11:105; Santou, N. Nes, M. (1987) Mol. Biol. Evol. 4:406-425; Sneath, P. H. A. and Sokal, R. R. (1973) Numerical Taxonomy—the Principles and Practice of Numerical Taxonomy, Freeman Press, San Francisco, Calif.; Wilbur, W. J. and Lipman, D. J. (1983) Proc. Natl. Acad., Sci. USA 80:726-730.

[0103] Alternatively, optimal alignment of sequences for comparison may be conducted by the local identity algorithm of Smith and Waterman (1981) Add. APL. Math 2:482, by the identity alignment algorithm of Needleman and Wunsch (1970) J. Mol. Biol. 48:443, by the search for similarity methods of Pearson and Lipman (1988) Proc. Natl. Acad. Sci. USA 85: 2444, by computerized implementations of these algorithms (GAP, BESTFIT, BLAST, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group (GCG), 575 Science Dr., Madison, Wis.), or by inspection.

[0104] One preferred example of algorithms that are suitable for determining percent sequence identity and sequence similarity are the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al. (1977) Nucl. Acids Res. 25:3389-3402 and Altschul et al. (1990) J. Mol. Biol. 215:403-410, respectively. BLAST and BLAST 2.0 can be used, for example with the parameters described herein, to determine percent sequence identity for the polynucleotides of the invention. Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information. In one illustrative example, cumulative scores can be calculated using, for nucleotide sequences, the parameters M (reward score for a pair of matching residues; always >0) and N (penalty score for mismatching residues; always <0). Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T and X determine the sensitivity and speed of the alignment. The BLASTN program (for nucleotide sequences) uses as defaults a wordlength (W) of 11, and expectation (E) of 10, and the BLOSUM62 scoring matrix (see Henikoff and Henikoff (1989) Proc. Natl. Acad. Sci. USA 89:10915) alignments, (B) of 50, expectation (E) of 10, M=5, N=−4 and a comparison of both strands.

[0105] Preferably, the “percentage of sequence identity” is determined by comparing two optimally aligned sequences over a window of comparison of at least 20 positions, wherein the portion of the polynucleotide sequence in the comparison window may comprise additions or deletions (i.e., gaps) of 20 percent or less, usually 5 to 15 percent, or 10 to 12 percent, as compared to the reference sequences (which does not comprise additions or deletions) for optimal alignment of the two sequences. The percentage is calculated by determining the number of positions at which the identical nucleic acid bases occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the reference sequence (i.e., the window size) and multiplying the results by 100 to yield the percentage of sequence identity.

[0106] It will be appreciated by those of ordinary skill in the art that, as a result of the degeneracy of the genetic code, there are many nucleotide sequences that encode a polypeptide as described herein. Some of these polynucleotides bear minimal homology to the nucleotide sequence of any native gene. Nonetheless, polynucleotides that vary due to differences in codon usage are specifically contemplated by the present invention. Further, alleles of the genes comprising the polynucleotide sequences provided herein are within the scope of the present invention. Alleles are endogenous genes that are altered as a result of one or more mutations, such as deletions, additions and/or substitutions of nucleotides. The resulting mRNA and protein may, but need not, have an altered structure or function. Alleles may be identified using standard techniques (such as hybridization, amplification and/or database sequence comparison).

[0107] Therefore, in another embodiment of the invention, a mutagenesis approach, such as site-specific mutagenesis, is employed for the preparation of immunogenic variants and/or derivatives of the polypeptides described herein. By this approach, specific modifications in a polypeptide sequence can be made through mutagenesis of the underlying polynucleotides that encode them. These techniques provides a straightforward approach to prepare and test sequence variants, for example, incorporating one or more of the foregoing considerations, by introducing one or more nucleotide sequence changes into the polynucleotide.

[0108] Site-specific mutagenesis allows the production of mutants through the use of specific oligonucleotide sequences which encode the DNA sequence of the desired mutation, as well as a sufficient number of adjacent nucleotides, to provide a primer sequence of sufficient size and sequence complexity to form a stable duplex on both sides of the deletion junction being traversed. Mutations may be employed in a selected polynucleotide sequence to improve, alter, decrease, modify, or otherwise change the properties of the polynucleotide itself, and/or alter the properties, activity, composition, stability, or primary sequence of the encoded polypeptide.

[0109] In certain embodiments of the present invention, the inventors contemplate the mutagenesis of the disclosed polynucleotide sequences to alter one or more properties of the encoded polypeptide, such as the immunogenicity of a polypeptide vaccine. The techniques of site-specific mutagenesis are well-known in the art, and are widely used to create variants of both polypeptides and polynucleotides. For example, site-specific mutagenesis is often used to alter a specific portion of a DNA molecule. In such embodiments, a primer comprising typically about 14 to about 25 nucleotides or so in length is employed, with about 5 to about 10 residues on both sides of the junction of the sequence being altered.

[0110] As will be appreciated by those of skill in the art, site-specific mutagenesis techniques have often employed a phage vector that exists in both a single stranded and double stranded form. Typical vectors useful in site-directed mutagenesis include vectors such as the M13 phage. These phage are readily commercially-available and their use is generally well-known to those skilled in the art. Double-stranded plasmids are also routinely employed in site directed mutagenesis that eliminates the step of transferring the gene of interest from a plasmid to a phage.

[0111] In general, site-directed mutagenesis in accordance herewith is performed by first obtaining a single-stranded vector or melting apart of two strands of a double-stranded vector that includes within its sequence a DNA sequence that encodes the desired peptide. An oligonucleotide primer bearing the desired mutated sequence is prepared, generally synthetically. This primer is then annealed with the single-stranded vector, and subjected to DNA polymerizing enzymes such as E. coli polymerase I Klenow fragment, in order to complete the synthesis of the mutation-bearing strand. Thus, a heteroduplex is formed wherein one strand encodes the original non-mutated sequence and the second strand bears the desired mutation. This heteroduplex vector is then used to transform appropriate cells, such as E. coli cells, and clones are selected which include recombinant vectors bearing the mutated sequence arrangement.

[0112] The preparation of sequence variants of the selected peptide-encoding DNA segments using site-directed mutagenesis provides a means of producing potentially useful species and is not meant to be limiting as there are other ways in which sequence variants of peptides and the DNA sequences encoding them may be obtained. For example, recombinant vectors encoding the desired peptide sequence may be treated with mutagenic agents, such as hydroxylamine, to obtain sequence variants. Specific details regarding these methods and protocols are found in the teachings of Maloy et al., 1994; Segal, 1976; Prokop and Bajpai, 1991; Kuby, 1994; and Maniatis et al., 1982, each incorporated herein by reference, for that purpose.

[0113] As used herein, the term “oligonucleotide directed mutagenesis procedure” refers to template-dependent processes and vector-mediated propagation which result in an increase in the concentration of a specific nucleic acid molecule relative to its initial concentration, or in an increase in the concentration of a detectable signal, such as amplification. As used herein, the term “oligonucleotide directed mutagenesis procedure” is intended to refer to a process that involves the template-dependent extension of a primer molecule. The term template dependent process refers to nucleic acid synthesis of an RNA or a DNA molecule wherein the sequence of the newly synthesized strand of nucleic acid is dictated by the well-known rules of complementary base pairing (see, for example, Watson, 1987). Typically, vector mediated methodologies involve the introduction of the nucleic acid fragment into a DNA or RNA vector, the clonal amplification of the vector, and the recovery of the amplified nucleic acid fragment. Examples of such methodologies are provided by U.S. Pat. No. 4,237,224, specifically incorporated herein by reference in its entirety.

[0114] In another approach for the production of polypeptide variants of the present invention, recursive sequence recombination, as described in U.S. Pat. No. 5,837,458, may be employed. In this approach, iterative cycles of recombination and screening or selection are performed to “evolve” individual polynucleotide variants of the invention having, for example, enhanced immunogenic activity.

[0115] In other embodiments of the present invention, the polynucleotide sequences provided herein can be advantageously used as probes or primers for nucleic acid hybridization. As such, it is contemplated that nucleic acid segments that comprise or consist of a sequence region of at least about a 15 nucleotide long contiguous sequence that has the same sequence as, or is complementary to, a 15 nucleotide long contiguous sequence disclosed herein will find particular utility. Longer contiguous identical or complementary sequences, e.g., those of about 20, 30, 40, 50, 100, 200, 500, 1000 (including all intermediate lengths) and even up to full length sequences will also be of use in certain embodiments.

[0116] The ability of such nucleic acid probes to specifically hybridize to a sequence of interest will enable them to be of use in detecting the presence of complementary sequences in a given sample. However, other uses are also envisioned, such as the use of the sequence information for the preparation of mutant species primers, or primers for use in preparing other genetic constructions.

[0117] Polynucleotide molecules having sequence regions consisting of contiguous nucleotide stretches of 10-14, 15-20, 30, 50, or even of 100-200 nucleotides or so (including intermediate lengths as well), identical or complementary to a polynucleotide sequence disclosed herein, are particularly contemplated as hybridization probes for use in, e.g., Southern and Northern blotting. This would allow a gene product, or fragment thereof, to be analyzed, both in diverse cell types and also in various bacterial cells. The total size of fragment, as well as the size of the complementary stretch(es), will ultimately depend on the intended use or application of the particular nucleic acid segment. Smaller fragments will generally find use in hybridization embodiments, wherein the length of the contiguous complementary region may be varied, such as between about 15 and about 100 nucleotides, but larger contiguous complementarity stretches may be used, according to the length complementary sequences one wishes to detect.

[0118] The use of a hybridization probe of about 15-25 nucleotides in length allows the formation of a duplex molecule that is both stable and selective. Molecules having contiguous complementary sequences over stretches greater than 15 bases in length are generally preferred, though, in order to increase stability and selectivity of the hybrid, and thereby improve the quality and degree of specific hybrid molecules obtained. One will generally prefer to design nucleic acid molecules having gene-complementary stretches of 15 to 25 contiguous nucleotides, or even longer where desired.

[0119] Hybridization probes may be selected from any portion of any of the sequences disclosed herein. All that is required is to review the sequences set forth herein, or to any continuous portion of the sequences, from about 15-25 nucleotides in length up to and including the full length sequence, that one wishes to utilize as a probe or primer. The choice of probe and primer sequences may be governed by various factors. For example, one may wish to employ primers from towards the termini of the total sequence.

[0120] Small polynucleotide segments or fragments may be readily prepared by, for example, directly synthesizing the fragment by chemical means, as is commonly practiced using an automated oligonucleotide synthesizer. Also, fragments may be obtained by application of nucleic acid reproduction technology, such as the PCR™ technology of U.S. Pat. No. 4,683,202 (incorporated herein by reference), by introducing selected sequences into recombinant vectors for recombinant production, and by other recombinant DNA techniques generally known to those of skill in the art of molecular biology.

[0121] The nucleotide sequences of the invention may be used for their ability to selectively form duplex molecules with complementary stretches of the entire gene or gene fragments of interest. Depending on the application envisioned, one will typically desire to employ varying conditions of hybridization to achieve varying degrees of selectivity of probe towards target sequence. For applications requiring high selectivity, one will typically desire to employ relatively stringent conditions to form the hybrids, e.g., one will select relatively low salt and/or high temperature conditions, such as provided by a salt concentration of from about 0.02 M to about 0.15 M salt at temperatures of from about 50° C. to about 70° C. Such selective conditions tolerate little, if any, mismatch between the probe and the template or target strand, and would be particularly suitable for isolating related sequences.

[0122] Of course, for some applications, for example, where one desires to prepare mutants employing a mutant primer strand hybridized to an underlying template, less stringent (reduced stringency) hybridization conditions will typically be needed in order to allow formation of the heteroduplex. In these circumstances, one may desire to employ salt conditions such as those of from about 0.15 M to about 0.9 M salt, at temperatures ranging from about 20° C. to about 55° C. Cross-hybridizing species can thereby be readily identified as positively hybridizing signals with respect to control hybridizations. In any case, it is generally appreciated that conditions can be rendered more stringent by the addition of increasing amounts of formamide, which serves to destabilize the hybrid duplex in the same manner as increased temperature. Thus, hybridization conditions can be readily manipulated, and thus will generally be a method of choice depending on the desired results.

[0123] According to another embodiment of the present invention, polynucleotide compositions comprising antisense oligonucleotides are provided. Antisense oligonucleotides have been demonstrated to be effective and targeted inhibitors of protein synthesis, and, consequently, provide a therapeutic approach by which a disease can be treated by inhibiting the synthesis of proteins that contribute to the disease. The efficacy of antisense oligonucleotides for inhibiting protein synthesis is well established. For example, the synthesis of polygalactauronase and the muscarine type 2 acetylcholine receptor are inhibited by antisense oligonucleotides directed to their respective mRNA sequences (U.S. Pat. Nos. 5,739,119 and 5,759,829). Further, examples of antisense inhibition have been demonstrated with the nuclear protein cyclin, the multiple drug resistance gene (MDG1), ICAM-1, E-selectin, STK-1, striatal GABAA receptor and human EGF (Jaskulski et al., Science. 1988 June 10;240(4858):1544-6; Vasanthakumar and Ahmed, Cancer Commun. 1989; 1 (4):225-32; Peris et al., Brain Res Mol Brain Res. 1998 June 15;57(2):310-20; U.S. Pat. Nos. 5,801,154; 5,789,573; 5,718,709 and 5,610,288). Antisense constructs have also been described that inhibit and can be used to treat a variety of abnormal cellular proliferations, e.g. cancer (U.S. Pat. Nos. 5,747,470; 5,591,317 and 5,783,683).

[0124] Therefore, in certain embodiments, the present invention provides oligonucleotide sequences that comprise all, or a portion of, any sequence that is capable of specifically binding to polynucleotide sequence described herein, or a complement thereof. In one embodiment, the antisense oligonucleotides comprise DNA or derivatives thereof. In another embodiment, the oligonucleotides comprise RNA or derivatives thereof. In a third embodiment, the oligonucleotides are modified DNAs comprising a phosphorothioated modified backbone. In a fourth embodiment, the oligonucleotide sequences comprise peptide nucleic acids or derivatives thereof. In each case, preferred compositions comprise a sequence region that is complementary, and more preferably substantially-complementary, and even more preferably, completely complementary to one or more portions of polynucleotides disclosed herein. Selection of antisense compositions specific for a given gene sequence is based upon analysis of the chosen target sequence and determination of secondary structure, Tm, binding energy, and relative stability. Antisense compositions may be selected based upon their relative inability to form dimers, hairpins, or other secondary structures that would reduce or prohibit specific binding to the target mRNA in a host cell. Highly preferred target regions of the mRNA, are those which are at or near the AUG translation initiation codon, and those sequences which are substantially complementary to 5′ regions of the mRNA. These secondary structure analyses and target site selection considerations can be performed, for example, using v.4 of the OLIGO primer analysis software and/or the BLASTN 2.0.5 algorithm software (Altschul et al., Nucleic Acids Res. 1997, 25(17):3389-402).

[0125] The use of an antisense delivery method employing a short peptide vector, termed MPG (27 residues), is also contemplated. The MPG peptide contains a hydrophobic domain derived from the fusion sequence of HIV gp41 and a hydrophilic domain from the nuclear localization sequence of SV40 T-antigen (Morris et al., Nucleic Acids Res. 1997 July 15;25(14):2730-6). It has been demonstrated that several molecules of the MPG peptide coat the antisense oligonucleotides and can be delivered into cultured mammalian cells in less than 1 hour with relatively high efficiency (90%). Further, the interaction with MPG strongly increases both the stability of the oligonucleotide to nuclease and the ability to cross the plasma membrane.

[0126] According to another embodiment of the invention, the polynucleotide compositions described herein are used in the design and preparation of ribozyme molecules for inhibiting expression of the tumor polypeptides and proteins of the present invention in tumor cells. Ribozymes are RNA-protein complexes that cleave nucleic acids in a site-specific fashion. Ribozymes have specific catalytic domains that possess endonuclease activity (Kim and Cech, Proc Natl Acad Sci U S A. 1987 December;84(24):8788-92; Forster and Symons, Cell. 1987 April 24;49(2):211-20). For example, a large number of ribozymes accelerate phosphoester transfer reactions with a high degree of specificity, often cleaving only one of several phosphoesters in an oligonucleotide substrate (Cech et al., Cell. 1981 December;27(3 Pt 2):487-96; Michel and Westhof, J Mol Biol. 1990 December 5;216(3):585-610; Reinhold-Hurek and Shub, Nature. 1992 May 14;357(6374):173-6). This specificity has been attributed to the requirement that the substrate bind via specific base-pairing interactions to the internal guide sequence (“IGS”) of the ribozyme prior to chemical reaction.

[0127] Six basic varieties of naturally-occurring enzymatic RNAs are known presently. Each can catalyze the hydrolysis of RNA phosphodiester bonds in trans (and thus can cleave other RNA molecules) under physiological conditions. In general, enzymatic nucleic acids act by first binding to a target RNA. Such binding occurs through the target binding portion of a enzymatic nucleic acid which is held in close proximity to an enzymatic portion of the molecule that acts to cleave the target RNA. Thus, the enzymatic nucleic acid first recognizes and then binds a target RNA through complementary base-pairing, and once bound to the correct site, acts enzymatically to cut the target RNA. Strategic cleavage of such a target RNA will destroy its ability to direct synthesis of an encoded protein. After an enzymatic nucleic acid has bound and cleaved its RNA target, it is released from that RNA to search for another target and can repeatedly bind and cleave new targets.

[0128] The enzymatic nature of a ribozyme is advantageous over many technologies, such as antisense technology (where a nucleic acid molecule simply binds to a nucleic acid target to block its translation) since the concentration of ribozyme necessary to affect a therapeutic treatment is lower than that of an antisense oligonucleotide. This advantage reflects the ability of the ribozyme to act enzymatically. Thus, a single ribozyme molecule is able to cleave many molecules of target RNA. In addition, the ribozyme is a highly specific inhibitor, with the specificity of inhibition depending not only on the base pairing mechanism of binding to the target RNA, but also on the mechanism of target RNA cleavage. Single mismatches, or base-substitutions, near the site of cleavage can completely eliminate catalytic activity of a ribozyme. Similar mismatches in antisense molecules do not prevent their action (Woolf et al., Proc Natl Acad Sci U S A. 1992 August 15;89(16):7305-9). Thus, the specificity of action of a ribozyme is greater than that of an antisense oligonucleotide binding the same RNA site.

[0129] The enzymatic nucleic acid molecule may be formed in a hammerhead, hairpin, a hepatitis δ virus, group I intron or RNaseP RNA (in association with an RNA guide sequence) or Neurospora VS RNA motif. Examples of hammerhead motifs are described by Rossi et al. Nucleic Acids Res. 1992 September 11;20(17):4559-65. Examples of hairpin motifs are described by Hampel et al. (Eur. Pat. Appl. Publ. No. EP 0360257), Hampel and Tritz, Biochemistry 1989 June 13;28(12):4929-33; Hampel et al., Nucleic Acids Res. 1990 January 25;18(2):299-304 and U.S. Pat. No. 5,631,359. An example of the hepatitis δ virus motif is described by Perrotta and Been, Biochemistry. 1992 December 1;31(47):11843-52; an example of the RNaseP motif is described by Guerrier-Takada et al., Cell. 1983 December;35(3 Pt 2):849-57; Neurospora VS RNA ribozyme motif is described by Collins (Saville and Collins, Cell. 1990 May 18;61(4):685-96; Saville and Collins, Proc Natl Acad Sci U S A. 1991 October 1;88(19):8826-30; Collins and Olive, Biochemistry. 1993 March 23;32(11):2795-9); and an example of the Group I intron is described in (U.S. Pat. No. 4,987,071). All that is important in an enzymatic nucleic acid molecule of this invention is that it has a specific substrate binding site which is complementary to one or more of the target gene RNA regions, and that it have nucleotide sequences within or surrounding that substrate binding site which impart an RNA cleaving activity to the molecule. Thus the ribozyme constructs need not be limited to specific motifs mentioned herein.

[0130] Ribozymes may be designed as described in Int. Pat. Appl. Publ. No. WO 93/23569 and Int. Pat. Appl. Publ. No. WO 94/02595, each specifically incorporated herein by reference) and synthesized to be tested in vitro and in vivo, as described. Such ribozymes can also be optimized for delivery. While specific examples are provided, those in the art will recognize that equivalent RNA targets in other species can be utilized when necessary.

[0131] Ribozyme activity can be optimized by altering the length of the ribozyme binding arms, or chemically synthesizing ribozymes with modifications that prevent their degradation by serum ribonucleases (see e.g., Int. Pat. Appl. Publ. No. WO 92/07065; Int. Pat. Appl. Publ. No. WO 93/15187; Int. Pat. Appl. Publ. No. WO 91/03162; Eur. Pat. Appl. Publ. No. 92110298.4; U.S. Pat. No. 5,334,711; and Int. Pat. Appl. Publ. No. WO 94/13688, which describe various chemical modifications that can be made to the sugar moieties of enzymatic RNA molecules), modifications which enhance their efficacy in cells, and removal of stem II bases to shorten RNA synthesis times and reduce chemical requirements.

[0132] Sullivan et al. (Int. Pat. Appl. Publ. No. WO 94/02595) describes the general methods for delivery of enzymatic RNA molecules. Ribozymes may be administered to cells by a variety of methods known to those familiar to the art, including, but not restricted to, encapsulation in liposomes, by iontophoresis, or by incorporation into other vehicles, such as hydrogels, cyclodextrins, biodegradable nanocapsules, and bioadhesive microspheres. For some indications, ribozymes may be directly delivered ex vivo to cells or tissues with or without the aforementioned vehicles. Alternatively, the RNA/vehicle combination may be locally delivered by direct inhalation, by direct injection or by use of a catheter, infusion pump or stent. Other routes of delivery include, but are not limited to, intravascular, intramuscular, subcutaneous or joint injection, aerosol inhalation, oral (tablet or pill form), topical, systemic, ocular, intraperitoneal and/or intrathecal delivery. More detailed descriptions of ribozyme delivery and administration are provided in Int. Pat. Appl. Publ. No. WO 94/02595 and Int. Pat. Appl. Publ. No. WO 93/23569, each specifically incorporated herein by reference.

[0133] Another means of accumulating high concentrations of a ribozyme(s) within cells is to incorporate the ribozyme-encoding sequences into a DNA expression vector. Transcription of the ribozyme sequences are driven from a promoter for eukaryotic RNA polymerase I (pol I), RNA polymerase II (pol II), or RNA polymerase III (pol III). Transcripts from pol II or pol III promoters will be expressed at high levels in all cells; the levels of a given pol II promoter in a given cell type will depend on the nature of the gene regulatory sequences (enhancers, silencers, etc.) present nearby. Prokaryotic RNA polymerase promoters may also be used, providing that the prokaryotic RNA polymerase enzyme is expressed in the appropriate cells Ribozymes expressed from such promoters have been shown to function in mammalian cells. Such transcription units can be incorporated into a variety of vectors for introduction into mammalian cells, including but not restricted to, plasmid DNA vectors, viral DNA vectors (such as adenovirus or adeno-associated vectors), or viral RNA vectors (such as retroviral, semliki forest virus, sindbis virus vectors).

[0134] In another embodiment of the invention, peptide nucleic acids (PNAs) compositions are provided. PNA is a DNA mimic in which the nucleobases are attached to a pseudopeptide backbone (Good and Nielsen, Antisense Nucleic Acid Drug Dev. 1997 7(4) 431-37). PNA is able to be utilized in a number methods that traditionally have used RNA or DNA. Often PNA sequences perform better in techniques than the corresponding RNA or DNA sequences and have utilities that are not inherent to RNA or DNA. A review of PNA including methods of making, characteristics of, and methods of using, is provided by Corey (Trends Biotechnol 1997 June;15(6):224-9). As such, in certain embodiments, one may prepare PNA sequences that are complementary to one or more portions of the ACE mRNA sequence, and such PNA compositions may be used to regulate, alter, decrease, or reduce the translation of ACE-specific mRNA, and thereby alter the level of ACE activity in a host cell to which such PNA compositions have been administered.

[0135] PNAs have 2-aminoethyl-glycine linkages replacing the normal phosphodiester backbone of DNA (Nielsen et al., Science 1991 December 6;254(5037):1497-500; Hanvey et al., Science. 1992 November 27;258(5087):1481-5; Hyrup and Nielsen, Bioorg Med Chem. 1996 January;4(l):5-23). This chemistry has three important consequences: firstly, in contrast to DNA or phosphorothioate oligonucleotides, PNAs are neutral molecules; secondly, PNAs are achiral, which avoids the need to develop a stereoselective synthesis; and thirdly, PNA synthesis uses standard Boc or Fmoc protocols for solid-phase peptide synthesis, although other methods, including a modified Merrifield method, have been used.

[0136] PNA monomers or ready-made oligomers are commercially available from PerSeptive Biosystems (Framingham, Mass.). PNA syntheses by either Boc or Fmoc protocols are straightforward using manual or automated protocols (Norton et al., Bioorg Med Chem. 1995 April;3(4):437-45). The manual protocol lends itself to the production of chemically modified PNAs or the simultaneous synthesis of families of closely related PNAs.

[0137] As with peptide synthesis, the success of a particular PNA synthesis will depend on the properties of the chosen sequence. For example, while in theory PNAs can incorporate any combination of nucleotide bases, the presence of adjacent purines can lead to deletions of one or more residues in the product. In expectation of this difficulty, it is suggested that, in producing PNAs with adjacent purines, one should repeat the coupling of residues likely to be added inefficiently. This should be followed by the purification of PNAs by reverse-phase high-pressure liquid chromatography, providing yields and purity of product similar to those observed during the synthesis of peptides.

[0138] Modifications of PNAs for a given application may be accomplished by coupling amino acids during solid-phase synthesis or by attaching compounds that contain a carboxylic acid group to the exposed N-terminal amine. Alternatively, PNAs can be modified after synthesis by coupling to an introduced lysine or cysteine. The ease with which PNAs can be modified facilitates optimization for better solubility or for specific functional requirements. Once synthesized, the identity of PNAs and their derivatives can be confirmed by mass spectrometry. Several studies have made and utilized modifications of PNAs (for example, Norton et al., Bioorg Med Chem. 1995 April;3(4):437-45; Petersen et al., J Pept Sci. 1995 May-June;1(3):175-83; Orum et al., Biotechniques. 1995 September;19(3):472-80; Footer et al., Biochemistry. 1996 August 20;35(33):10673-9; Griffith et al., Nucleic Acids Res. 1995 August 11;23(15):3003-8; Pardridge et al., Proc Natl Acad Sci U S A. 1995 June 6;92(12):5592-6; Boffa et al., Proc Natl Acad Sci U S A. 1995 March 14;92(6):1901-5; Gambacorti-Passerini et al., Blood. 1996 Augus 15;88(4):1411-7; Armitage et al., Proc Natl Acad Sci U S A. 1997 November 11;94(23):12320-5; Seeger et al., Biotechniques. 1997 September;23(3):512-7). U.S. Pat. No. 5,700,922 discusses PNA-DNA-PNA chimeric molecules and their uses in diagnostics, modulating protein in organisms, and treatment of conditions susceptible to therapeutics.

[0139] Methods of characterizing the antisense binding properties of PNAs are discussed in Rose (Anal Chem. 1993 December 15;65(24):3545-9) and Jensen et al. (Biochemistry. 1997 April 22;36(16):5072-7). Rose uses capillary gel electrophoresis to determine binding of PNAs to their complementary oligonucleotide, measuring the relative binding kinetics and stoichiometry. Similar types of measurements were made by Jensen et al. using BIAcore™ technology.

[0140] Other applications of PNAs that have been described and will be apparent to the skilled artisan include use in DNA strand invasion, antisense inhibition, mutational analysis, enhancers of transcription, nucleic acid purification, isolation of transcriptionally active genes, blocking of transcription factor binding, genome cleavage, biosensors, in situ hybridization, and the like.

[0141] Polynucleotide Identification, Characterization and Expression

[0142] Polynucleotides compositions of the present invention may be identified, prepared and/or manipulated using any of a variety of well established techniques (see generally, Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratories, Cold Spring Harbor, N.Y., 1989, and other like references). For example, a polynucleotide may be identified, as described in more detail below, by screening a microarray of cDNAs for tumor-associated expression (i.e., expression that is at least two fold greater in a tumor than in normal tissue, as determined using a representative assay provided herein). Such screens may be performed, for example, using the microarray technology of Affymetrix, Inc. (Santa Clara, Calif.) according to the manufacturer's instructions (and essentially as described by Schena et al., Proc. Natl. Acad. Sci. USA 93:10614-10619, 1996 and Heller et al., Proc. Natl. Acad. Sci. USA 94:2150-2155, 1997). Alternatively, polynucleotides may be amplified from cDNA prepared from cells expressing the proteins described herein, such as tumor cells.

[0143] Many template dependent processes are available to amplify a target sequences of interest present in a sample. One of the best known amplification methods is the polymerase chain reaction (PCR™) which is described in detail in U.S. Pat. Nos. 4,683,195, 4,683,202 and 4,800,159, each of which is incorporated herein by reference in its entirety. Briefly, in PCR™, two primer sequences are prepared which are complementary to regions on opposite complementary strands of the target sequence. An excess of deoxynucleoside triphosphates is added to a reaction mixture along with a DNA polymerase (e.g., Taq polymerase). If the target sequence is present in a sample, the primers will bind to the target and the polymerase will cause the primers to be extended along the target sequence by adding on nucleotides. By raising and lowering the temperature of the reaction mixture, the extended primers will dissociate from the target to form reaction products, excess primers will bind to the target and to the reaction product and the process is repeated. Preferably reverse transcription and PCR™ amplification procedure may be performed in order to quantify the amount of mRNA amplified. Polymerase chain reaction methodologies are well known in the art.

[0144] Any of a number of other template dependent processes, many of which are variations of the PCR™ amplification technique, are readily known and available in the art. Illustratively, some such methods include the ligase chain reaction (referred to as LCR), described, for example, in Eur. Pat. Appl. Publ. No. 320,308 and U.S. Pat. No. 4,883,750; Qbeta Replicase, described in PCT Intl. Pat. Appl. Publ. No. PCT/US87/00880; Strand Displacement Amplification (SDA) and Repair Chain Reaction (RCR). Still other amplification methods are described in Great Britain Pat. Appl. No. 2 202 328, and in PCT Intl. Pat. Appl. Publ. No. PCT/US89/01025. Other nucleic acid amplification procedures include transcription-based amplification systems (TAS) (PCT Intl. Pat. Appl. Publ. No. WO 88/10315), including nucleic acid sequence based amplification (NASBA) and 3SR. Eur. Pat. Appl. Publ. No. 329,822 describes a nucleic acid amplification process involving cyclically synthesizing single-stranded RNA (“ssRNA”), ssDNA, and double-stranded DNA (dsDNA). PCT Intl. Pat. Appl. Publ. No. WO 89/06700 describes a nucleic acid sequence amplification scheme based on the hybridization of a promoter/primer sequence to a target single-stranded DNA (“ssDNA”) followed by transcription of many RNA copies of the sequence. Other amplification methods such as “RACE” (Frohman, 1990), and “one-sided PCR” (Ohara, 1989) are also well-known to those of skill in the art.

[0145] An amplified portion of a polynucleotide of the present invention may be used to isolate a full length gene from a suitable library (e.g., a tumor cDNA library) using well known techniques. Within such techniques, a library (cDNA or genomic) is screened using one or more polynucleotide probes or primers suitable for amplification. Preferably, a library is size-selected to include larger molecules. Random primed libraries may also be preferred for identifying 5′ and upstream regions of genes. Genomic libraries are preferred for obtaining introns and extending 5′ sequences.

[0146] For hybridization techniques, a partial sequence may be labeled (e.g., by nick-translation or end-labeling with 32P) using well known techniques. A bacterial or bacteriophage library is then generally screened by hybridizing filters containing denatured bacterial colonies (or lawns containing phage plaques) with the labeled probe (see Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratories, Cold Spring Harbor, N.Y., 1989). Hybridizing colonies or plaques are selected and expanded, and the DNA is isolated for further analysis. cDNA clones may be analyzed to determine the amount of additional sequence by, for example, PCR using a primer from the partial sequence and a primer from the vector. Restriction maps and partial sequences may be generated to identify one or more overlapping clones. The complete sequence may then be determined using standard techniques, which may involve generating a series of deletion clones. The resulting overlapping sequences can then assembled into a single contiguous sequence. A full length cDNA molecule can be generated by ligating suitable fragments, using well known techniques.

[0147] Alternatively, amplification techniques, such as those described above, can be useful for obtaining a full length coding sequence from a partial cDNA sequence. One such amplification technique is inverse PCR (see Triglia et al., Nucl. Acids Res. 16:8186, 1988), which uses restriction enzymes to generate a fragment in the known region of the gene. The fragment is then circularized by intramolecular ligation and used as a template for PCR with divergent primers derived from the known region. Within an alternative approach, sequences adjacent to a partial sequence may be retrieved by amplification with a primer to a linker sequence and a primer specific to a known region. The amplified sequences are typically subjected to a second round of amplification with the same linker primer and a second primer specific to the known region. A variation on this procedure, which employs two primers that initiate extension in opposite directions from the known sequence, is described in WO 96/38591. Another such technique is known as “rapid amplification of cDNA ends” or RACE. This technique involves the use of an internal primer and an external primer, which hybridizes to a polyA region or vector sequence, to identify sequences that are 5′ and 3′ of a known sequence. Additional techniques include capture PCR (Lagerstrom et al., PCR Methods Applic. 1:111-19, 1991) and walking PCR (Parker et al., Nucl. Acids. Res. 19:3055-60, 1991). Other methods employing amplification may also be employed to obtain a full length cDNA sequence.

[0148] In certain instances, it is possible to obtain a full length cDNA sequence by analysis of sequences provided in an expressed sequence tag (EST) database, such as that available from GenBank. Searches for overlapping ESTs may generally be performed using well known programs (e.g., NCBI BLAST searches), and such ESTs may be used to generate a contiguous full length sequence. Full length DNA sequences may also be obtained by analysis of genomic fragments.

[0149] In other embodiments of the invention, polynucleotide sequences or fragments thereof which encode polypeptides of the invention, or fusion proteins or functional equivalents thereof, may be used in recombinant DNA molecules to direct expression of a polypeptide in appropriate host cells. Due to the inherent degeneracy of the genetic code, other DNA sequences that encode substantially the same or a functionally equivalent amino acid sequence may be produced and these sequences may be used to clone and express a given polypeptide.

[0150] As will be understood by those of skill in the art, it may be advantageous in some instances to produce polypeptide-encoding nucleotide sequences possessing non-naturally occurring codons. For example, codons preferred by a particular prokaryotic or eukaryotic host can be selected to increase the rate of protein expression or to produce a recombinant RNA transcript having desirable properties, such as a half-life which is longer than that of a transcript generated from the naturally occurring sequence.

[0151] Moreover, the polynucleotide sequences of the present invention can be engineered using methods generally known in the art in order to alter polypeptide encoding sequences for a variety of reasons, including but not limited to, alterations which modify the cloning, processing, and/or expression of the gene product. For example, DNA shuffling by random fragmentation and PCR reassembly of gene fragments and synthetic oligonucleotides may be used to engineer the nucleotide sequences. In addition, site-directed mutagenesis may be used to insert new restriction sites, alter glycosylation patterns, change codon preference, produce splice variants, or introduce mutations, and so forth.

[0152] In another embodiment of the invention, natural, modified, or recombinant nucleic acid sequences may be ligated to a heterologous sequence to encode a fusion protein. For example, to screen peptide libraries for inhibitors of polypeptide activity, it may be useful to encode a chimeric protein that can be recognized by a commercially available antibody. A fusion protein may also be engineered to contain a cleavage site located between the polypeptide-encoding sequence and the heterologous protein sequence, so that the polypeptide may be cleaved and purified away from the heterologous moiety.

[0153] Sequences encoding a desired polypeptide may be synthesized, in whole or in part, using chemical methods well known in the art (see Caruthers, M. H. et al. (1980) Nucl. Acids Res. Symp. Ser. 215-223, Horn, T. et al. (1980) Nucl. Acids Res. Symp. Ser. 225-232). Alternatively, the protein itself may be produced using chemical methods to synthesize the amino acid sequence of a polypeptide, or a portion thereof. For example, peptide synthesis can be performed using various solid-phase techniques (Roberge, J. Y. et al. (1995) Science 269:202-204) and automated synthesis may be achieved, for example, using the ABI 431A Peptide Synthesizer (Perkin Elmer, Palo Alto, Calif.).

[0154] A newly synthesized peptide may be substantially purified by preparative high performance liquid chromatography (e.g., Creighton, T. (1983) Proteins, Structures and Molecular Principles, WH Freeman and Co., New York, N.Y.) or other comparable techniques available in the art. The composition of the synthetic peptides may be confirmed by amino acid analysis or sequencing (e.g., the Edman degradation procedure). Additionally, the amino acid sequence of a polypeptide, or any part thereof, may be altered during direct synthesis and/or combined using chemical methods with sequences from other proteins, or any part thereof, to produce a variant polypeptide.

[0155] In order to express a desired polypeptide, the nucleotide sequences encoding the polypeptide, or functional equivalents, may be inserted into appropriate expression vector, i.e., a vector which contains the necessary elements for the transcription and translation of the inserted coding sequence. Methods which are well known to those skilled in the art may be used to construct expression vectors containing sequences encoding a polypeptide of interest and appropriate transcriptional and translational control elements. These methods include in vitro recombinant DNA techniques, synthetic techniques, and in vivo genetic recombination. Such techniques are described, for example, in Sambrook, J. et al. (1989) Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Press, Plainview, N.Y., and Ausubel, F. M. et al. (1989) Current Protocols in Molecular Biology, John Wiley & Sons, New York. N.Y.

[0156] A variety of expression vector/host systems may be utilized to contain and express polynucleotide sequences. These include, but are not limited to, microorganisms such as bacteria transformed with recombinant bacteriophage, plasmid, or cosmid DNA expression vectors; yeast transformed with yeast expression vectors; insect cell systems infected with virus expression vectors (e.g., baculovirus); plant cell systems transformed with virus expression vectors (e.g., cauliflower mosaic virus, CaMV; tobacco mosaic virus, TMV) or with bacterial expression vectors (e.g., Ti or pBR322 plasmids); or animal cell systems.

[0157] The “control elements” or “regulatory sequences” present in an expression vector are those non-translated regions of the vector-enhancers, promoters, 5′ and 3′ untranslated regions—which interact with host cellular proteins to carry out transcription and translation. Such elements may vary in their strength and specificity. Depending on the vector system and host utilized, any number of suitable transcription and translation elements, including constitutive and inducible promoters, may be used. For example, when cloning in bacterial systems, inducible promoters such as the hybrid lacZ promoter of the pBLUESCRIPT phagemid (Stratagene, La Jolla, Calif.) or pSPORT1 plasmid (Gibco BRL, Gaithersburg, Md.) and the like may be used. In mammalian cell systems, promoters from mammalian genes or from mammalian viruses are generally preferred. If it is necessary to generate a cell line that contains multiple copies of the sequence encoding a polypeptide, vectors based on SV40 or EBV may be advantageously used with an appropriate selectable marker.

[0158] In bacterial systems, any of a number of expression vectors may be selected depending upon the use intended for the expressed polypeptide. For example, when large quantities are needed, for example for the induction of antibodies, vectors which direct high level expression of fusion proteins that are readily purified may be used. Such vectors include, but are not limited to, the multifunctional E. coli cloning and expression vectors such as pBLUESCRIPT (Stratagene), in which the sequence encoding the polypeptide of interest may be ligated into the vector in frame with sequences for the amino-terminal Met and the subsequent 7 residues of .beta.-galactosidase so that a hybrid protein is produced; pIN vectors (Van Heeke, G. and S. M. Schuster (1989) J. Biol. Chem. 264:5503-5509); and the like. pGEX Vectors (Promega, Madison, Wis.) may also be used to express foreign polypeptides as fusion proteins with glutathione S-transferase (GST). In general, such fusion proteins are soluble and can easily be purified from lysed cells by adsorption to glutathione-agarose beads followed by elution in the presence of free glutathione. Proteins made in such systems may be designed to include heparin, thrombin, or factor XA protease cleavage sites so that the cloned polypeptide of interest can be released from the GST moiety at will.

[0159] In the yeast, Saccharomyces cerevisiae, a number of vectors containing constitutive or inducible promoters such as alpha factor, alcohol oxidase, and PGH may be used. For reviews, see Ausubel et al. (supra) and Grant et al. (1987) Methods Enzymol. 153:516-544.

[0160] In cases where plant expression vectors are used, the expression of sequences encoding polypeptides may be driven by any of a number of promoters. For example, viral promoters such as the 35S and 19S promoters of CaMV may be used alone or in combination with the omega leader sequence from TMV (Takamatsu, N. (1987) EMBO J. 6:307-311. Alternatively, plant promoters such as the small subunit of RUBISCO or heat shock promoters may be used (Coruzzi, G. et al. (1984) EMBO J. 3:1671-1680; Broglie, R. et al. (1984) Science 224:838-843; and Winter, J. et al. (1991) Results Probl. Cell Differ. 17:85-105). These constructs can be introduced into plant cells by direct DNA transformation or pathogen-mediated transfection. Such techniques are described in a number of generally available reviews (see, for example, Hobbs, S. or Murry, L. E. in McGraw Hill Yearbook of Science and Technology (1992) McGraw Hill, New York, N.Y.; pp. 191-196).

[0161] An insect system may also be used to express a polypeptide of interest. For example, in one such system, Autographa californica nuclear polyhedrosis virus (AcNPV) is used as a vector to express foreign genes in Spodoptera frugiperda cells or in Trichoplusia larvae. The sequences encoding the polypeptide may be cloned into a non-essential region of the virus, such as the polyhedrin gene, and placed under control of the polyhedrin promoter. Successful insertion of the polypeptide-encoding sequence will render the polyhedrin gene inactive and produce recombinant virus lacking coat protein. The recombinant viruses may then be used to infect, for example, S. frugiperda cells or Trichoplusia larvae in which the polypeptide of interest may be expressed (Engelhard, E. K. et al. (1994) Proc. Natl. Acad. Sci. 91 :3224-3227).

[0162] In mammalian host cells, a number of viral-based expression systems are generally available. For example, in cases where an adenovirus is used as an expression vector, sequences encoding a polypeptide of interest may be ligated into an adenovirus transcription/translation complex consisting of the late promoter and tripartite leader sequence. Insertion in a non-essential E1 or E3 region of the viral genome may be used to obtain a viable virus which is capable of expressing the polypeptide in infected host cells (Logan, J. and Shenk, T. (1984) Proc. Natl. Acad. Sci. 81:3655-3659). In addition, transcription enhancers, such as the Rous sarcoma virus (RSV) enhancer, may be used to increase expression in mammalian host cells.

[0163] Specific initiation signals may also be used to achieve more efficient translation of sequences encoding a polypeptide of interest. Such signals include the ATG initiation codon and adjacent sequences. In cases where sequences encoding the polypeptide, its initiation codon, and upstream sequences are inserted into the appropriate expression vector, no additional transcriptional or translational control signals may be needed. However, in cases where only coding sequence, or a portion thereof, is inserted, exogenous translational control signals including the ATG initiation codon should be provided. Furthermore, the initiation codon should be in the correct reading frame to ensure translation of the entire insert. Exogenous translational elements and initiation codons may be of various origins, both natural and synthetic. The efficiency of expression may be enhanced by the inclusion of enhancers which are appropriate for the particular cell system which is used, such as those described in the literature (Scharf, D. et al. (1994) Results Probl. Cell Differ. 20:125-162).

[0164] In addition, a host cell strain may be chosen for its ability to modulate the expression of the inserted sequences or to process the expressed protein in the desired fashion. Such modifications of the polypeptide include, but are not limited to, acetylation, carboxylation, glycosylation, phosphorylation, lipidation, and acylation. Post-translational processing which cleaves a “prepro” form of the protein may also be used to facilitate correct insertion, folding and/or function. Different host cells such as CHO, COS, HeLa, MDCK, HEK293, and WI38, which have specific cellular machinery and characteristic mechanisms for such post-translational activities, may be chosen to ensure the correct modification and processing of the foreign protein.

[0165] For long-term, high-yield production of recombinant proteins, stable expression is generally preferred. For example, cell lines which stably express a polynucleotide of interest may be transformed using expression vectors which may contain viral origins of replication and/or endogenous expression elements and a selectable marker gene on the same or on a separate vector. Following the introduction of the vector, cells may be allowed to grow for 1-2 days in an enriched media before they are switched to selective media. The purpose of the selectable marker is to confer resistance to selection, and its presence allows growth and recovery of cells which successfully express the introduced sequences. Resistant clones of stably transformed cells may be proliferated using tissue culture techniques appropriate to the cell type.

[0166] Any number of selection systems may be used to recover transformed cell lines. These include, but are not limited to, the herpes simplex virus thymidine kinase (Wigler, M. et al. (1977) Cell 11:223-32) and adenine phosphoribosyltransferase (Lowy, I. et al. (1990) Cell 22:817-23) genes which can be employed in tk.sup.- or aprt.sup.-cells, respectively. Also, antimetabolite, antibiotic or herbicide resistance can be used as the basis for selection; for example, dhfr which confers resistance to methotrexate (Wigler, M. et al. (1980) Proc. Natl. Acad. Sci. 77:3567-70); npt, which confers resistance to the aminoglycosides, neomycin and G-418 (Colbere-Garapin, F. et al (1981) J. Mol. Biol. 150:1-14); and als or pat, which confer resistance to chlorsulfuron and phosphinotricin acetyltransferase, respectively (Murry, supra). Additional selectable genes have been described, for example, trpB, which allows cells to utilize indole in place of tryptophan, or hisD, which allows cells to utilize histinol in place of histidine (Hartman, S. C. and R. C. Mulligan (1988) Proc. Natl. Acad. Sci. 85:8047-51). The use of visible markers has gained popularity with such markers as anthocyanins, beta-glucuronidase and its substrate GUS, and luciferase and its substrate luciferin, being widely used not only to identify transformants, but also to quantify the amount of transient or stable protein expression attributable to a specific vector system (Rhodes, C. A. et al. (1995) Methods Mol. Biol. 55:121-131).

[0167] Although the presence/absence of marker gene expression suggests that the gene of interest is also present, its presence and expression may need to be confirmed. For example, if the sequence encoding a polypeptide is inserted within a marker gene sequence, recombinant cells containing sequences can be identified by the absence of marker gene function. Alternatively, a marker gene can be placed in tandem with a polypeptide-encoding sequence under the control of a single promoter. Expression of the marker gene in response to induction or selection usually indicates expression of the tandem gene as well.

[0168] Alternatively, host cells that contain and express a desired polynucleotide sequence may be identified by a variety of procedures known to those of skill in the art. These procedures include, but are not limited to, DNA-DNA or DNA-RNA hybridizations and protein bioassay or immunoassay techniques which include, for example, membrane, solution, or chip based technologies for the detection and/or quantification of nucleic acid or protein.

[0169] A variety of protocols for detecting and measuring the expression of polynucleotide-encoded products, using either polyclonal or monoclonal antibodies specific for the product are known in the art. Examples include enzyme-linked immunosorbent assay (ELISA), radioimmunoassay (RIA), and fluorescence activated cell sorting (FACS). A two-site, monoclonal-based immunoassay utilizing monoclonal antibodies reactive to two non-interfering epitopes on a given polypeptide may be preferred for some applications, but a competitive binding assay may also be employed. These and other assays are described, among other places, in Hampton, R. et al. (1990; Serological Methods, a Laboratory Manual, APS Press, St Paul. Minn.) and Maddox, D. E. et al. (1983; J. Exp. Med. 158:1211-1216).

[0170] A wide variety of labels and conjugation techniques are known by those skilled in the art and may be used in various nucleic acid and amino acid assays. Means for producing labeled hybridization or PCR probes for detecting sequences related to polynucleotides include oligolabeling, nick translation, end-labeling or PCR amplification using a labeled nucleotide. Alternatively, the sequences, or any portions thereof may be cloned into a vector for the production of an mRNA probe. Such vectors are known in the art, are commercially available, and may be used to synthesize RNA probes in vitro by addition of an appropriate RNA polymerase such as T7, T3, or SP6 and labeled nucleotides. These procedures may be conducted using a variety of commercially available kits. Suitable reporter molecules or labels, which may be used include radionuclides, enzymes, fluorescent, chemiluminescent, or chromogenic agents as well as substrates, cofactors, inhibitors, magnetic particles, and the like.

[0171] Host cells transformed with a polynucleotide sequence of interest may be cultured under conditions suitable for the expression and recovery of the protein from cell culture. The protein produced by a recombinant cell may be secreted or contained intracellularly depending on the sequence and/or the vector used. As will be understood by those of skill in the art, expression vectors containing polynucleotides of the invention may be designed to contain signal sequences which direct secretion of the encoded polypeptide through a prokaryotic or eukaryotic cell membrane. Other recombinant constructions may be used to join sequences encoding a polypeptide of interest to nucleotide sequence encoding a polypeptide domain which will facilitate purification of soluble proteins. Such purification facilitating domains include, but are not limited to, metal chelating peptides such as histidine-tryptophan modules that allow purification on immobilized metals, protein A domains that allow purification on immobilized immunoglobulin, and the domain utilized in the FLAGS extension/affinity purification system (Immunex Corp., Seattle, Wash.). The inclusion of cleavable linker sequences such as those specific for Factor XA or enterokinase (Invitrogen. San Diego, Calif.) between the purification domain and the encoded polypeptide may be used to facilitate purification. One such expression vector provides for expression of a fusion protein containing a polypeptide of interest and a nucleic acid encoding 6 histidine residues preceding a thioredoxin or an enterokinase cleavage site. The histidine residues facilitate purification on IMIAC (immobilized metal ion affinity chromatography) as described in Porath, J. et al. (1992, Prot. Exp. Purif. 3:263-281) while the enterokinase cleavage site provides a means for purifying the desired polypeptide from the fusion protein. A discussion of vectors which contain fusion proteins is provided in Kroll, D. J. et al. (1993; DNA Cell Biol. 12:441-453).

[0172] In addition to recombinant production methods, polypeptides of the invention, and fragments thereof, may be produced by direct peptide synthesis using solid-phase techniques (Merrifield J. (1963) J. Am. Chem. Soc. 85:2149-2154). Protein synthesis may be performed using manual techniques or by automation. Automated synthesis may be achieved, for example, using Applied Biosystems 431A Peptide Synthesizer (Perkin Elmer). Alternatively, various fragments may be chemically synthesized separately and combined using chemical methods to produce the full length molecule.

[0173] Antibody Compositions Fragments Thereof and Other Binding Agents

[0174] According to another aspect, the present invention further provides binding agents, such as antibodies and antigen-binding fragments thereof, that exhibit immunological binding to a tumor polypeptide disclosed herein, or to a portion, variant or derivative thereof. An antibody, or antigen-binding fragment thereof, is said to “specifically bind,” “immunogically bind,” and/or is “immunologically reactive” to a polypeptide of the invention if it reacts at a detectable level (within, for example, an ELISA assay) with the polypeptide, and does not react detectably with unrelated polypeptides under similar conditions.

[0175] Immunological binding, as used in this context, generally refers to the non-covalent interactions of the type which occur between an immunoglobulin molecule and an antigen for which the immunoglobulin is specific. The strength, or affinity of immunological binding interactions can be expressed in terms of the dissociation constant (Kd) of the interaction, wherein a smaller Kd represents a greater affinity. Immunological binding properties of selected polypeptides can be quantified using methods well known in the art. One such method entails measuring the rates of antigen-binding site/antigen complex formation and dissociation, wherein those rates depend on the concentrations of the complex partners, the affinity of the interaction, and on geometric parameters that equally influence the rate in both directions. Thus, both the “on rate constant” (Kon) and the “off rate constant” (Koff) can be determined by calculation of the concentrations and the actual rates of association and dissociation. The ratio of Koff/Kon enables cancellation of all parameters not related to affinity, and is thus equal to the dissociation constant Kd. See, generally, Davies et al. (1990) Annual Rev. Biochem. 59:439-473.

[0176] An “antigen-binding site,” or “binding portion” of an antibody refers to the part of the immunoglobulin molecule that participates in antigen binding. The antigen binding site is formed by amino acid residues of the N-terminal variable (“V”) regions of the heavy (“H”) and light (“L”) chains. Three highly divergent stretches within the V regions of the heavy and light chains are referred to as “hypervariable regions” which are interposed between more conserved flanking stretches known as “framework regions,” or “FRs”. Thus the term “FR” refers to amino acid sequences which are naturally found between and adjacent to hypervariable regions in immunoglobulins. In an antibody molecule, the three hypervariable regions of a light chain and the three hypervariable regions of a heavy chain are disposed relative to each other in three dimensional space to form an antigen-binding surface. The antigen-binding surface is complementary to the three-dimensional surface of a bound antigen, and the three hypervariable regions of each of the heavy and light chains are referred to as “complementarity-determining regions,” or “CDRs.”

[0177] Binding agents may be further capable of differentiating between patients with and without a cancer, such as colon cancer, using the representative assays provided herein. For example, antibodies or other binding agents that bind to a tumor protein will preferably generate a signal indicating the presence of a cancer in at least about 20% of patients with the disease, more preferably at least about 30% of patients. Alternatively, or in addition, the antibody will generate a negative signal indicating the absence of the disease in at least about 90% of individuals without the cancer. To determine whether a binding agent satisfies this requirement, biological samples (e.g., blood, sera, sputum, urine and/or tumor biopsies) from patients with and without a cancer (as determined using standard clinical tests) may be assayed as described herein for the presence of polypeptides that bind to the binding agent. Preferably, a statistically significant number of samples with and without the disease will be assayed. Each binding agent should satisfy the above criteria; however, those of ordinary skill in the art will recognize that binding agents may be used in combination to improve sensitivity.

[0178] Any agent that satisfies the above requirements may be a binding agent. For example, a binding agent may be a ribosome, with or without a peptide component, an RNA molecule or a polypeptide. In a preferred embodiment, a binding agent is an antibody or an antigen-binding fragment thereof. Antibodies may be prepared by any of a variety of techniques known to those of ordinary skill in the art. See, e.g., Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, 1988. In general, antibodies can be produced by cell culture techniques, including the generation of monoclonal antibodies as described herein, or via transfection of antibody genes into suitable bacterial or mammalian cell hosts, in order to allow for the production of recombinant antibodies. In one technique, an immunogen comprising the polypeptide is initially injected into any of a wide variety of mammals (e.g., mice, rats, rabbits, sheep or goats). In this step, the polypeptides of this invention may serve as the immunogen without modification. Alternatively, particularly for relatively short polypeptides, a superior immune response may be elicited if the polypeptide is joined to a carrier protein, such as bovine serum albumin or keyhole limpet hemocyanin. The immunogen is injected into the animal host, preferably according to a predetermined schedule incorporating one or more booster immunizations, and the animals are bled periodically. Polyclonal antibodies specific for the polypeptide may then be purified from such antisera by, for example, affinity chromatography using the polypeptide coupled to a suitable solid support.

[0179] Monoclonal antibodies specific for an antigenic polypeptide of interest may be prepared, for example, using the technique of Kohler and Milstein, Eur. J. Immunol. 6:511-519, 1976, and improvements thereto. Briefly, these methods involve the preparation of immortal cell lines capable of producing antibodies having the desired specificity (i.e., reactivity with the polypeptide of interest). Such cell lines may be produced, for example, from spleen cells obtained from an animal immunized as described above. The spleen cells are then immortalized by, for example, fusion with a myeloma cell fusion partner, preferably one that is syngeneic with the immunized animal. A variety of fusion techniques may be employed. For example, the spleen cells and myeloma cells may be combined with a nonionic detergent for a few minutes and then plated at low density on a selective medium that supports the growth of hybrid cells, but not myeloma cells. A preferred selection technique uses HAT (hypoxanthine, aminopterin, thymidine) selection. After a sufficient time, usually about 1 to 2 weeks, colonies of hybrids are observed. Single colonies are selected and their culture supernatants tested for binding activity against the polypeptide. Hybridomas having high reactivity and specificity are preferred.

[0180] Monoclonal antibodies may be isolated from the supernatants of growing hybridoma colonies. In addition, various techniques may be employed to enhance the yield, such as injection of the hybridoma cell line into the peritoneal cavity of a suitable vertebrate host, such as a mouse. Monoclonal antibodies may then be harvested from the ascites fluid or the blood. Contaminants may be removed from the antibodies by conventional techniques, such as chromatography, gel filtration, precipitation, and extraction. The polypeptides of this invention may be used in the purification process in, for example, an affinity chromatography step.

[0181] A number of therapeutically useful molecules are known in the art which comprise antigen-binding sites that are capable of exhibiting immunological binding properties of an antibody molecule. The proteolytic enzyme papain preferentially cleaves IgG molecules to yield several fragments, two of which (the “F(ab)” fragments) each comprise a covalent heterodimer that includes an intact antigen-binding site. The enzyme pepsin is able to cleave IgG molecules to provide several fragments, including the “F(ab′)2” fragment which comprises both antigen-binding sites. An “Fv” fragment can be produced by preferential proteolytic cleavage of an IgM, and on rare occasions IgG or IgA immunoglobulin molecule. Fv fragments are, however, more commonly derived using recombinant techniques known in the art. The Fv fragment includes a non-covalent VH::VL heterodimer including an antigen-binding site which retains much of the antigen recognition and binding capabilities of the native antibody molecule. Inbar et al. (1972) Proc. Nat. Acad. Sci. USA 69:2659-2662; Hochman et al. (1976) Biochem 15:2706-2710; and Ehrlich et al. (1980) Biochem 19:4091-4096.

[0182] A single chain Fv (“sFv”) polypeptide is a covalently linked VH::VL heterodimer which is expressed from a gene fusion including VH- and VL-encoding genes linked by a peptide-encoding linker. Huston et al. (1988) Proc. Nat. Acad. Sci. USA 85(16):5879-5883. A number of methods have been described to discern chemical structures for converting the naturally aggregated—but chemically separated—light and heavy polypeptide chains from an antibody V region into an sFv molecule which will fold into a three dimensional structure substantially similar to the structure of an antigen-binding site. See, e.g., U.S. Pat. Nos. 5,091,513 and 5,132,405, to Huston et al.; and U.S. Pat. No. 4,946,778, to Ladner et al.

[0183] Each of the above-described molecules includes a heavy chain and a light chain CDR set, respectively interposed between a heavy chain and a light chain FR set which provide support to the CDRS and define the spatial relationship of the CDRs relative to each other. As used herein, the term “CDR set” refers to the three hypervariable regions of a heavy or light chain V region. Proceeding from the N-terminus of a heavy or light chain, these regions are denoted as “CDR1,” “CDR2,” and “CDR3” respectively. An antigen-binding site, therefore, includes six CDRs, comprising the CDR set from each of a heavy and a light chain V region. A polypeptide comprising a single CDR, (e.g., a CDR1, CDR2 or CDR3) is referred to herein as a “molecular recognition unit.” Crystallographic analysis of a number of antigen-antibody complexes has demonstrated that the amino acid residues of CDRs form extensive contact with bound antigen, wherein the most extensive antigen contact is with the heavy chain CDR3. Thus, the molecular recognition units are primarily responsible for the specificity of an antigen-binding site.

[0184] As used herein, the term “FR set” refers to the four flanking amino acid sequences which frame the CDRs of a CDR set of a heavy or light chain V region. Some FR residues may contact bound antigen; however, FRs are primarily responsible for folding the V region into the antigen-binding site, particularly the FR residues directly adjacent to the CDRS. Within FRs, certain amino residues and certain structural features are very highly conserved. In this regard, all V region sequences contain an internal disulfide loop of around 90 amino acid residues. When the V regions fold into a binding-site, the CDRs are displayed as projecting loop motifs which form an antigen-binding surface. It is generally recognized that there are conserved structural regions of FRs which influence the folded shape of the CDR loops into certain “canonical” structures—regardless of the precise CDR amino acid sequence. Further, certain FR residues are known to participate in non-covalent interdomain contacts which stabilize the interaction of the antibody heavy and light chains.

[0185] A number of “humanized” antibody molecules comprising an antigen-binding site derived from a non-human immunoglobulin have been described, including chimeric antibodies having rodent V regions and their associated CDRs fused to human constant domains (Winter et al. (1991) Nature 349:293-299; Lobuglio et al. (1989) Proc. Nat. Acad. Sci. USA 86:4220-4224; Shaw et al. (1987) J Immunol. 138:4534-4538; and Brown et al. (1987) Cancer Res. 47:3577-3583), rodent CDRs grafted into a human supporting FR prior to fusion with an appropriate human antibody constant domain (Riechmann et al. (1988) Nature 332:323-327; Verhoeyen et al. (1988) Science 239:1534-1536; and Jones et al. (1986) Nature 321:522-525), and rodent CDRs supported by recombinantly veneered rodent FRs (European Pat. Publication No. 519,596, published Dec. 23, 1992). These “humanized” molecules are designed to minimize unwanted immunological response toward rodent antihuman antibody molecules which limits the duration and effectiveness of therapeutic applications of those moieties in human recipients.

[0186] As used herein, the terms “veneered FRs” and “recombinantly veneered FRs” refer to the selective replacement of FR residues from, e.g., a rodent heavy or light chain V region, with human FR residues in order to provide a xenogeneic molecule comprising an antigen-binding site which retains substantially all of the native FR polypeptide folding structure. Veneering techniques are based on the understanding that the ligand binding characteristics of an antigen-binding site are determined primarily by the structure and relative disposition of the heavy and light chain CDR sets within the antigen-binding surface. Davies et al. (1990) Ann. Rev. Biochem. 59:439-473. Thus, antigen binding specificity can be preserved in a humanized antibody only wherein the CDR structures, their interaction with each other, and their interaction with the rest of the V region domains are carefully maintained. By using veneering techniques, exterior (e.g., solvent-accessible) FR residues which are readily encountered by the immune system are selectively replaced with human residues to provide a hybrid molecule that comprises either a weakly immunogenic, or substantially non-immunogenic veneered surface.

[0187] The process of veneering makes use of the available sequence data for human antibody variable domains compiled by Kabat et al., in Sequences of Proteins of Immunological Interest, 4th ed., (U.S. Dept. of Health and Human Services, U.S. Government Printing Office, 1987), updates to the Kabat database, and other accessible U.S. and foreign databases (both nucleic acid and protein). Solvent accessibilities of V region amino acids can be deduced from the known three-dimensional structure for human and murine antibody fragments. There are two general steps in veneering a murine antigen-binding site. Initially, the FRs of the variable domains of an antibody molecule of interest are compared with corresponding FR sequences of human variable domains obtained from the above-identified sources. The most homologous human V regions are then compared residue by residue to corresponding murine amino acids. The residues in the murine FR which differ from the human counterpart are replaced by the residues present in the human moiety using recombinant techniques well known in the art. Residue switching is only carried out with moieties which are at least partially exposed (solvent accessible), and care is exercised in the replacement of amino acid residues which may have a significant effect on the tertiary structure of V region domains, such as proline, glycine and charged amino acids.

[0188] In this manner, the resultant “veneered” murine antigen-binding sites are thus designed to retain the murine CDR residues, the residues substantially adjacent to the CDRs, the residues identified as buried or mostly buried (solvent inaccessible), the residues believed to participate in non-covalent (e.g., electrostatic and hydrophobic) contacts between heavy and light chain domains, and the residues from conserved structural regions of the FRs which are believed to influence the “canonical” tertiary structures of the CDR loops. These design criteria are then used to prepare recombinant nucleotide sequences which combine the CDRs of both the heavy and light chain of a murine antigen-binding site into human-appearing FRs that can be used to transfect mammalian cells for the expression of recombinant human antibodies which exhibit the antigen specificity of the murine antibody molecule.

[0189] In another embodiment of the invention, monoclonal antibodies of the present invention may be coupled to one or more therapeutic agents. Suitable agents in this regard include radionuclides, differentiation inducers, drugs, toxins, and derivatives thereof. Preferred radionuclides include 90Y, 123I, 125I, 131I, 186Re, 188Re, 211At, and 212Bi. Preferred drugs include methotrexate, and pyrimidine and purine analogs. Preferred differentiation inducers include phorbol esters and butyric acid. Preferred toxins include ricin, abrin, diptheria toxin, cholera toxin, gelonin, Pseudomonas exotoxin, Shigella toxin, and pokeweed antiviral protein.

[0190] A therapeutic agent may be coupled (e.g., covalently bonded) to a suitable monoclonal antibody either directly or indirectly (e.g., via a linker group). A direct reaction between an agent and an antibody is possible when each possesses a substituent capable of reacting with the other. For example, a nucleophilic group, such as an amino or sulfhydryl group, on one may be capable of reacting with a carbonyl-containing group, such as an anhydride or an acid halide, or with an alkyl group containing a good leaving group (e.g., a halide) on the other.

[0191] Alternatively, it may be desirable to couple a therapeutic agent and an antibody via a linker group. A linker group can function as a spacer to distance an antibody from an agent in order to avoid interference with binding capabilities. A linker group can also serve to increase the chemical reactivity of a substituent on an agent or an antibody, and thus increase the coupling efficiency. An increase in chemical reactivity may also facilitate the use of agents, or functional groups on agents, which otherwise would not be possible.

[0192] It will be evident to those skilled in the art that a variety of bifunctional or polyfunctional reagents, both homo- and hetero-functional (such as those described in the catalog of the Pierce Chemical Co., Rockford, Ill.), may be employed as the linker group. Coupling may be effected, for example, through amino groups, carboxyl groups, sulfhydryl groups or oxidized carbohydrate residues. There are numerous references describing such methodology, e.g., U.S. Pat. No. 4,671,958, to Rodwell et al.

[0193] Where a therapeutic agent is more potent when free from the antibody portion of the immunoconjugates of the present invention, it may be desirable to use a linker group which is cleavable during or upon internalization into a cell. A number of different cleavable linker groups have been described. The mechanisms for the intracellular release of an agent from these linker groups include cleavage by reduction of a disulfide bond (e.g., U.S. Pat. No. 4,489,710, to Spitler), by irradiation of a photolabile bond (e.g., U.S. Pat. No. 4,625,014, to Senter et al.), by hydrolysis of derivatized amino acid side chains (e.g., U.S. Pat. No. 4,638,045, to Kohn et al.), by serum complement-mediated hydrolysis (e.g., U.S. Pat. No. 4,671,958, to Rodwell et al.), and acid-catalyzed hydrolysis (e.g., U.S. Pat. No. 4,569,789, to Blattler et al.).

[0194] It may be desirable to couple more than one agent to an antibody. In one embodiment, multiple molecules of an agent are coupled to one antibody molecule. In another embodiment, more than one type of agent may be coupled to one antibody. Regardless of the particular embodiment, immunoconjugates with more than one agent may be prepared in a variety of ways. For example, more than one agent may be coupled directly to an antibody molecule, or linkers that provide multiple sites for attachment can be used. Alternatively, a carrier can be used.

[0195] A carrier may bear the agents in a variety of ways, including covalent bonding either directly or via a linker group. Suitable carriers include proteins such as albumins (e.g., U.S. Pat. No. 4,507,234, to Kato et al.), peptides and polysaccharides such as aminodextran (e.g., U.S. Pat. No. 4,699,784, to Shih et al.). A carrier may also bear an agent by noncovalent bonding or by encapsulation, such as within a liposome vesicle (e.g., U.S. Pat. Nos. 4,429,008 and 4,873,088). Carriers specific for radionuclide agents include radiohalogenated small molecules and chelating compounds. For example, U.S. Pat. No. 4,735,792 discloses representative radiohalogenated small molecules and their synthesis. A radionuclide chelate may be formed from chelating compounds that include those containing nitrogen and sulfur atoms as the donor atoms for binding the metal, or metal oxide, radionuclide. For example, U.S. Pat. No. 4,673,562, to Davison et al. discloses representative chelating compounds and their synthesis.

[0196] T Cell Compositions

[0197] The present invention, in another aspect, provides T cells specific for a tumor polypeptide disclosed herein, or for a variant or derivative thereof. Such cells may generally be prepared in vitro or ex vivo, using standard procedures. For example, T cells may be isolated from bone marrow, peripheral blood, or a fraction of bone marrow or peripheral blood of a patient, using a commercially available cell separation system, such as the Isolex™ System, available from Nexell Therapeutics, Inc. (Irvine, Calif.; see also U.S. Pat. Nos. 5,240,856; 5,215,926; WO 89/06280; WO 91/16116 and WO 92/07243). Alternatively, T cells may be derived from related or unrelated humans, non-human mammals, cell lines or cultures.

[0198] T cells may be stimulated with a polypeptide, polynucleotide encoding a polypeptide and/or an antigen presenting cell (APC) that expresses such a polypeptide. Such stimulation is performed under conditions and for a time sufficient to permit the generation of T cells that are specific for the polypeptide of interest. Preferably, a tumor polypeptide or polynucleotide of the invention is present within a delivery vehicle, such as a microsphere, to facilitate the generation of specific T cells.

[0199] T cells are considered to be specific for a polypeptide of the present invention if the T cells specifically proliferate, secrete cytokines or kill target cells coated with the polypeptide or expressing a gene encoding the polypeptide. T cell specificity may be evaluated using any of a variety of standard techniques. For example, within a chromium release assay or proliferation assay, a stimulation index of more than two fold increase in lysis and/or proliferation, compared to negative controls, indicates T cell specificity. Such assays may be performed, for example, as described in Chen et al., Cancer Res. 54:1065-1070, 1994. Alternatively, detection of the proliferation of T cells may be accomplished by a variety of known techniques. For example, T cell proliferation can be detected by measuring an increased rate of DNA synthesis (e.g., by pulse-labeling cultures of T cells with tritiated thymidine and measuring the amount of tritiated thymidine incorporated into DNA). Contact with a tumor polypeptide (100 ng/ml-100 μg/ml, preferably 200 ng/ml-25 μg/ml) for 3-7 days will typically result in at least a two fold increase in proliferation of the T cells. Contact as described above for 2-3 hours should result in activation of the T cells, as measured using standard cytokine assays in which a two fold increase in the level of cytokine release (e.g., TNF or IFN-γ) is indicative of T cell activation (see Coligan et al., Current Protocols in Immunology, vol. 1, Wiley Interscience (Greene 1998)). T cells that have been activated in response to a tumor polypeptide, polynucleotide or polypeptide-expressing APC may be CD4+ and/or CD8+. Tumor polypeptide-specific T cells may be expanded using standard techniques. Within preferred embodiments, the T cells are derived from a patient, a related donor or an unrelated donor, and are administered to the patient following stimulation and expansion.

[0200] For therapeutic purposes, CD4+ or CD8+ T cells that proliferate in response to a tumor polypeptide, polynucleotide or APC can be expanded in number either in vitro or in vivo. Proliferation of such T cells in vitro may be accomplished in a variety of ways. For example, the T cells can be re-exposed to a tumor polypeptide, or a short peptide corresponding to an immunogenic portion of such a polypeptide, with or without the addition of T cell growth factors, such as interleukin-2, and/or stimulator cells that synthesize a tumor polypeptide. Alternatively, one or more T cells that proliferate in the presence of the tumor polypeptide can be expanded in number by cloning. Methods for cloning cells are well known in the art, and include limiting dilution.

[0201] T Cell Receptor Compositions

[0202] The T cell receptor (TCR) consists of 2 different, highly variable polypeptide chains, termed the T-cell receptor α and β chains, that are linked by a disulfide bond (Janeway, Travers, Walport. Immunobiology, Fourth Ed., 148-159. Elsevier Science Ltd/Garland Publishing. 1999). The α/β heterodimer complexes with the invariant CD3 chains at the cell membrane. This complex recognizes specific antigenic peptides bound to MHC molecules. The enormous diversity of TCR specificities is generated much like immunoglobulin diversity, through somatic gene rearrangement. The β chain genes contain over 50 variable (V), 2 diversity (D), over 10 joining (J) segments, and 2 constant region segments (C). The α chain genes contain over 70 V segments, and over 60 J segments but no D segments, as well as one C segment. During T cell development in the thymus, the D to J gene rearrangement of the β chain occurs, followed by the V gene segment rearrangement to the DJ. This functional VDJβ exon is transcribed and spliced to join to a Cβ. For the α chain, a Vα gene segment rearranges to a Jα gene segment to create the functional exon that is then transcribed and spliced to the Cα. Diversity is further increased during the recombination process by the random addition of P and N-nucleotides between the V, D, and J segments of the β chain and between the V and J segments in the α chain (Janeway, Travers, Walport. Immunobiology. Fourth Ed., 98 and 150. Elsevier Science Ltd/Garland Publishing. 1999).

[0203] The present invention, in another aspect, provides TCRs specific for a polypeptide disclosed herein, or for a variant or derivative thereof. In accordance with the present invention, polynucleotide and amino acid sequences are provided for the V-J or V-D-J junctional regions or parts thereof for the alpha and beta chains of the T-cell receptor which recognize tumor polypeptides described herein. In general, this aspect of the invention relates to T-cell receptors which recognize or bind tumor polypeptides presented in the context of MHC. In a preferred embodiment the tumor antigens recognized by the T-cell receptors comprise a polypeptide of the present invention. For example, cDNA encoding a TCR specific for a colon tumor peptide can be isolated from T cells specific for a tumor polypeptide using standard molecular biological and recombinant DNA techniques.

[0204] This invention further includes the T-cell receptors or analogs thereof having substantially the same function or activity as the T-cell receptors of this invention which recognize or bind tumor polypeptides. Such receptors include, but are not limited to, a fragment of the receptor, or a substitution, addition or deletion mutant of a T-cell receptor provided herein. This invention also encompasses polypeptides or peptides that are substantially homologous to the T-cell receptors provided herein or that retain substantially the same activity. The term “analog” includes any protein or polypeptide having an amino acid residue sequence substantially identical to the T-cell receptors provided herein in which one or more residues, preferably no more than 5 residues, more preferably no more than 25 residues have been conservatively substituted with a functionally similar residue and which displays the functional aspects of the T-cell receptor as described herein.

[0205] The present invention further provides for suitable mammalian host cells, for example, non-specific T cells, that are transfected with a polynucleotide encoding TCRs specific for a polypeptide described herein, thereby rendering the host cell specific for the polypeptide. The α and β chains of the TCR may be contained on separate expression vectors or alternatively, on a single expression vector that also contains an internal ribosome entry site (IRES) for cap-independent translation of the gene downstream of the IRES. Said host cells expressing TCRs specific for the polypeptide may be used, for example, for adoptive immunotherapy of colon cancer as discussed further below.

[0206] In further aspects of the present invention, cloned TCRs specific for a polypeptide recited herein may be used in a kit for the diagnosis of colon cancer. For example, the nucleic acid sequence or portions thereof, of tumor-specific TCRs can be used as probes or primers for the detection of expression of the rearranged genes encoding the specific TCR in a biological sample. Therefore, the present invention further provides for an assay for detecting messenger RNA or DNA encoding the TCR specific for a polypeptide.

[0207] Pharmaceutical Compositions

[0208] In additional embodiments, the present invention concerns formulation of one or more of the polynucleotide, polypeptide, T-cell, TCR, and/or antibody compositions disclosed herein in pharmaceutically-acceptable carriers for administration to a cell or an animal, either alone, or in combination with one or more other modalities of therapy.

[0209] It will be understood that, if desired, a composition as disclosed herein may be administered in combination with other agents as well, such as, e.g., other proteins or polypeptides or various pharmaceutically-active agents. In fact, there is virtually no limit to other components that may also be included, given that the additional agents do not cause a significant adverse effect upon contact with the target cells or host tissues. The compositions may thus be delivered along with various other agents as required in the particular instance. Such compositions may be purified from host cells or other biological sources, or alternatively may be chemically synthesized as described herein. Likewise, such compositions may further comprise substituted or derivatized RNA or DNA compositions.

[0210] Therefore, in another aspect of the present invention, pharmaceutical compositions are provided comprising one or more of the polynucleotide, polypeptide, antibody, TCR, and/or T-cell compositions described herein in combination with a physiologically acceptable carrier. In certain preferred embodiments, the pharmaceutical compositions of the invention comprise immunogenic polynucleotide and/or polypeptide compositions of the invention for use in prophylactic and theraputic vaccine applications. Vaccine preparation is generally described in, for example, M. F. Powell and M. J. Newman, eds., “Vaccine Design (the subunit and adjuvant approach),” Plenum Press (NY, 1995). Generally, such compositions will comprise one or more polynucleotide and/or polypeptide compositions of the present invention in combination with one or more immunostimulants.

[0211] It will be apparent that any of the pharmaceutical compositions described herein can contain pharmaceutically acceptable salts of the polynucleotides and polypeptides of the invention. Such salts can be prepared, for example, from pharmaceutically acceptable non-toxic bases, including organic bases (e.g., salts of primary, secondary and tertiary amines and basic amino acids) and inorganic bases (e.g., sodium, potassium, lithium, ammonium, calcium and magnesium salts).

[0212] In another embodiment, illustrative immunogenic compositions, e.g., vaccine compositions, of the present invention comprise DNA encoding one or more of the polypeptides as described above, such that the polypeptide is generated in situ. As noted above, the polynucleotide may be administered within any of a variety of delivery systems known to those of ordinary skill in the art. Indeed, numerous gene delivery techniques are well known in the art, such as those described by Rolland, Crit. Rev. Therap. Drug Carrier Systems 15:143-198, 1998, and references cited therein. Appropriate polynucleotide expression systems will, of course, contain the necessary regulatory DNA regulatory sequences for expression in a patient (such as a suitable promoter and terminating signal). Alternatively, bacterial delivery systems may involve the administration of a bacterium (such as Bacillus-Calmette-Guerrin) that expresses an immunogenic portion of the polypeptide on its cell surface or secretes such an epitope.

[0213] Therefore, in certain embodiments, polynucleotides encoding immunogenic polypeptides described herein are introduced into suitable mammalian host cells for expression using any of a number of known viral-based systems. In one illustrative embodiment, retroviruses provide a convenient and effective platform for gene delivery systems. A selected nucleotide sequence encoding a polypeptide of the present invention can be inserted into a vector and packaged in retroviral particles using techniques known in the art. The recombinant virus can then be isolated and delivered to a subject. A number of illustrative retroviral systems have been described (e.g., U.S. Pat. No. 5,219,740; Miller and Rosman (1989) BioTechniques 7:980-990; Miller, A. D. (1990) Human Gene Therapy 1:5-14; Scarpa et al. (1991) Virology 180:849-852; Bums et al. (1993) Proc. Natl. Acad. Sci. USA 90:8033-8037; and Boris-Lawrie and Temin (1993) Cur. Opin. Genet. Develop. 3:102-109.

[0214] In addition, a number of illustrative adenovirus-based systems have also been described. Unlike retroviruses which integrate into the host genome, adenoviruses persist extrachromosomally thus minimizing the risks associated with insertional mutagenesis (Haj-Ahmad and Graham (1986) J. Virol. 57:267-274; Bett et al. (1993) J. Virol. 67:5911-5921; Mittereder et al. (1994) Human Gene Therapy 5:717-729; Seth et al. (1994) J. Virol. 68:933-940; Barr et al. (1994) Gene Therapy 1:51-58; Berkner, K. L. (1988) BioTechniques 6:616-629; and Rich et al. (1993) Human Gene Therapy 4:461-476).

[0215] Various adeno-associated virus (AAV) vector systems have also been developed for polynucleotide delivery. AAV vectors can be readily constructed using techniques well known in the art. See, e.g., U.S. Pat. Nos. 5,173,414 and 5,139,941; International Publication Nos. WO 92/01070 and WO 93/03769; Lebkowski et al. (1988) Molec. Cell. Biol. 8:3988-3996; Vincent et al. (1990) Vaccines 90 (Cold Spring Harbor Laboratory Press); Carter, B. J. (1992) Current Opinion in Biotechnology 3:533-539; Muzyczka, N. (1992) Current Topics in Microbiol. and Immunol. 158:97-129; Kotin, R. M. (1994) Human Gene Therapy 5:793-801; Shelling and Smith (1994) Gene Therapy 1:165-169; and Zhou et al. (1994) J. Exp. Med. 179:1867-1875.

[0216] Additional viral vectors useful for delivering the polynucleotides encoding polypeptides of the present invention by gene transfer include those derived from the pox family of viruses, such as vaccinia virus and avian poxvirus. By way of example, vaccinia virus recombinants expressing the novel molecules can be constructed as follows. The DNA encoding a polypeptide is first inserted into an appropriate vector so that it is adjacent to a vaccinia promoter and flanking vaccinia DNA sequences, such as the sequence encoding thymidine kinase (TK). This vector is then used to transfect cells which are simultaneously infected with vaccinia. Homologous recombination serves to insert the vaccinia promoter plus the gene encoding the polypeptide of interest into the viral genome. The resulting TK.sup.(−) recombinant can be selected by culturing the cells in the presence of 5-bromodeoxyuridine and picking viral plaques resistant thereto.

[0217] A vaccinia-based infection/transfection system can be conveniently used to provide for inducible, transient expression or coexpression of one or more polypeptides described herein in host cells of an organism. In this particular system, cells are first infected in vitro with a vaccinia virus recombinant that encodes the bacteriophage T7 RNA polymerase. This polymerase displays exquisite specificity in that it only transcribes templates bearing T7 promoters. Following infection, cells are transfected with the polynucleotide or polynucleotides of interest, driven by a T7 promoter. The polymerase expressed in the cytoplasm from the vaccinia virus recombinant transcribes the transfected DNA into RNA which is then translated into polypeptide by the host translational machinery. The method provides for high level, transient, cytoplasmic production of large quantities of RNA and its translation products. See, e.g., Elroy-Stein and Moss, Proc. Natl. Acad. Sci. USA (1990) 87:6743-6747; Fuerst et al. Proc. Natl. Acad. Sci. USA (1986) 83:8122-8126.

[0218] Alternatively, avipoxviruses, such as the fowlpox and canarypox viruses, can also be used to deliver the coding sequences of interest. Recombinant avipox viruses, expressing immunogens from mammalian pathogens, are known to confer protective immunity when administered to non-avian species. The use of an Avipox vector is particularly desirable in human and other mammalian species since members of the Avipox genus can only productively replicate in susceptible avian species and therefore are not infective in mammalian cells. Methods for producing recombinant Avipoxviruses are known in the art and employ genetic recombination, as described above with respect to the production of vaccinia viruses. See, e.g., WO 91/12882; WO 89/03429; and WO 92/03545.

[0219] Any of a number of alphavirus vectors can also be used for delivery of polynucleotide compositions of the present invention, such as those vectors described in U.S. Pat. Nos. 5,843,723; 6,015,686; 6,008,035 and 6,015,694. Certain vectors based on Venezuelan Equine Encephalitis (VEE) can also be used, illustrative examples of which can be found in U.S. Pat. Nos. 5,505,947 and 5,643,576.

[0220] Moreover, molecular conjugate vectors, such as the adenovirus chimeric vectors described in Michael et al. J. Biol. Chem. (1993) 268:6866-6869 and Wagner et al. Proc. Natl. Acad. Sci. USA (1992) 89:6099-6103, can also be used for gene delivery under the invention.

[0221] Additional illustrative information on these and other known viral-based delivery systems can be found, for example, in Fisher-Hoch et al., Proc. Natl. Acad. Sci. USA 86:317-321, 1989; Flexner et al., Ann. N.Y. Acad. Sci. 569:86-103, 1989; Flexner et al., Vaccine 8:17-21, 1990; U.S. Pat. Nos. 4,603,112, 4,769,330, and 5,017,487; WO 89/01973; U.S. Pat. No. 4,777,127; GB 2,200,651; EP 0,345,242; WO 91/02805; Berkner, Biotechniques 6:616-627, 1988; Rosenfeld et al., Science 252:431-434, 1991; Kolls et al., Proc. Natl. Acad. Sci. USA 91:215-219, 1994; Kass-Eisler et al., Proc. Natl. Acad. Sci. USA 90:11498-11502, 1993; Guzman et al., Circulation 88:2838-2848, 1993; and Guzman et al., Cir. Res. 73:1202-1207, 1993.

[0222] In certain embodiments, a polynucleotide may be integrated into the genome of a target cell. This integration may be in the specific location and orientation via homologous recombination (gene replacement) or it may be integrated in a random, non-specific location (gene augmentation). In yet further embodiments, the polynucleotide may be stably maintained in the cell as a separate, episomal segment of DNA. Such polynucleotide segments or “episomes” encode sequences sufficient to permit maintenance and replication independent of or in synchronization with the host cell cycle. The manner in which the expression construct is delivered to a cell and where in the cell the polynucleotide remains is dependent on the type of expression construct employed.

[0223] In another embodiment of the invention, a polynucleotide is administered/delivered as “naked” DNA, for example as described in Ulmer et al., Science 259:1745-1749, 1993 and reviewed by Cohen, Science 259:1691-1692, 1993. The uptake of naked DNA may be increased by coating the DNA onto biodegradable beads, which are efficiently transported into the cells.

[0224] In still another embodiment, a composition of the present invention can be delivered via a particle bombardment approach, many of which have been described. In one illustrative example, gas-driven particle acceleration can be achieved with devices such as those manufactured by Powderject Pharmaceuticals PLC (Oxford, UK) and Powderject Vaccines Inc. (Madison, Wis.), some examples of which are described in U.S. Pat. Nos. 5,846,796; 6,010,478; 5,865,796; 5,584,807; and EP Patent No. 0500 799. This approach offers a needle-free delivery approach wherein a dry powder formulation of microscopic particles, such as polynucleotide or polypeptide particles, are accelerated to high speed within a helium gas jet generated by a hand held device, propelling the particles into a target tissue of interest.

[0225] In a related embodiment, other devices and methods that may be useful for gas-driven needle-less injection of compositions of the present invention include those provided by Bioject, Inc. (Portland, Oreg.), some examples of which are described in U.S. Pat. Nos. 4,790,824; 5,064,413; 5,312,335; 5,383,851; 5,399,163; 5,520,639 and 5,993,412.

[0226] According to another embodiment, the pharmaceutical compositions described herein will comprise one or more immunostimulants in addition to the immunogenic polynucleotide, polypeptide, antibody, T-cell, TCR, and/or APC compositions of this invention. An immunostimulant refers to essentially any substance that enhances or potentiates an immune response (antibody and/or cell-mediated) to an exogenous antigen. One preferred type of immunostimulant comprises an adjuvant. Many adjuvants contain a substance designed to protect the antigen from rapid catabolism, such as aluminum hydroxide or mineral oil, and a stimulator of immune responses, such as lipid A, Bortadella pertussis or Mycobacterium tuberculosis derived proteins. Certain adjuvants are commercially available as, for example, Freund's Incomplete Adjuvant and Complete Adjuvant (Difco Laboratories, Detroit, Mich.); Merck Adjuvant 65 (Merck and Company, Inc., Rahway, N.J.); AS-2 (SmithKline Beecham, Philadelphia, Pa.); aluminum salts such as aluminum hydroxide gel (alum) or aluminum phosphate; salts of calcium, iron or zinc; an insoluble suspension of acylated tyrosine; acylated sugars; cationically or anionically derivatized polysaccharides; polyphosphazenes; biodegradable microspheres; monophosphoryl lipid A and quil A. Cytokines, such as GM-CSF, interleukin-2, -7, -12, and other like growth factors, may also be used as adjuvants.

[0227] Within certain embodiments of the invention, the adjuvant composition is preferably one that induces an immune response predominantly of the Th1 type. High levels of Th1-type cytokines (e.g., IFN-γ, TNFα, IL-2 and IL-12) tend to favor the induction of cell mediated immune responses to an administered antigen. In contrast, high levels of Th2-type cytokines (e.g., IL-4, IL-5, IL-6 and IL-10) tend to favor the induction of humoral immune responses. Following application of a vaccine as provided herein, a patient will support an immune response that includes Th1- and Th2-type responses. Within a preferred embodiment, in which a response is predominantly Th1-type, the level of Th1-type cytokines will increase to a greater extent than the level of Th2-type cytokines. The levels of these cytokines may be readily assessed using standard assays. For a review of the families of cytokines, see Mosmann and Coffman, Ann. Rev. Immunol. 7:145-173, 1989.

[0228] Certain preferred adjuvants for eliciting a predominantly Th1-type response include, for example, a combination of monophosphoryl lipid A, preferably 3-de-O-acylated monophosphoryl lipid A, together with an aluminum salt. MPL® adjuvants are available from Corixa Corporation (Seattle, Wash.; see, for example, U.S. Pat. Nos. 4,436,727; 4,877,611; 4,866,034 and 4,912,094). CpG-containing oligonucleotides (in which the CpG dinucleotide is unmethylated) also induce a predominantly Th1 response. Such oligonucleotides are well known and are described, for example, in WO 96/02555, WO 99/33488 and U.S. Pat. Nos. 6,008,200 and 5,856,462. Immunostimulatory DNA sequences are also described, for example, by Sato et al., Science 273:352, 1996. Another preferred adjuvant comprises a saponin, such as Quil A, or derivatives thereof, including QS21 and QS7 (Aquila Biopharmaceuticals Inc., Framingham, Mass.); Escin; Digitonin; or Gypsophila or Chenopodium quinoa saponins. Other preferred formulations include more than one saponin in the adjuvant combinations of the present invention, for example combinations of at least two of the following group comprising QS21, QS7, Quil A, β-escin, or digitonin.

[0229] Alternatively the saponin formulations may be combined with vaccine vehicles composed of chitosan or other polycationic polymers, polylactide and polylactide-co-glycolide particles, poly-N-acetyl glucosamine-based polymer matrix, particles composed of polysaccharides or chemically modified polysaccharides, liposomes and lipid-based particles, particles composed of glycerol monoesters, etc. The saponins may also be formulated in the presence of cholesterol to form particulate structures such as liposomes or ISCOMs. Furthermore, the saponins may be formulated together with a polyoxyethylene ether or ester, in either a non-particulate solution or suspension, or in a particulate structure such as a paucilamelar liposome or ISCOM. The saponins may also be formulated with excipients such as CarbopolR to increase viscosity, or may be formulated in a dry powder form with a powder excipient such as lactose.

[0230] In one preferred embodiment, the adjuvant system includes the combination of a monophosphoryl lipid A and a saponin derivative, such as the combination of QS21 and 3D-MPL® adjuvant, as described in WO 94/00153, or a less reactogenic composition where the QS21 is quenched with cholesterol, as described in WO 96/33739. Other preferred formulations comprise an oil-in-water emulsion and tocopherol. Another particularly preferred adjuvant formulation employing QS21, 3D-MPL® adjuvant and tocopherol in an oil-in-water emulsion is described in WO 95/17210.

[0231] Another enhanced adjuvant system involves the combination of a CpG-containing oligonucleotide and a saponin derivative particularly the combination of CpG and QS21 is disclosed in WO 00/09159. Preferably the formulation additionally comprises an oil in water emulsion and tocopherol.

[0232] Additional illustrative adjuvants for use in the pharmaceutical compositions of the invention include Montanide ISA 720 (Seppic, France), SAF (Chiron, Calif., United States), ISCOMS (CSL), MF-59 (Chiron), the SBAS series of adjuvants (e.g., SBAS-2 or SBAS-4, available from SmithKline Beecham, Rixensart, Belgium), Detox (Enhanzyn®) (Corixa, Hamilton, Mont.), RC-529 (Corixa, Hamilton, Mont.) and other aminoalkyl glucosaminide 4-phosphates (AGPs), such as those described in pending U.S. patent application Ser. Nos. 08/853,826 and 09/074,720, the disclosures of which are incorporated herein by reference in their entireties, and polyoxyethylene ether adjuvants such as those described in WO 99/52549A1.

[0233] Other preferred adjuvants include adjuvant molecules of the general formula

HO(CH2CH2O)n—A—R,  (I)

[0234] wherein, n is 1-50, A is a bond or —C(O)—, R is C1-50 alkyl or Phenyl C1-50 alkyl.

[0235] One embodiment of the present invention consists of a vaccine formulation comprising a polyoxyethylene ether of general formula (I), wherein n is between 1 and 50, preferably 4-24, most preferably 9; the R component is C1-50, preferably C4-C20 alkyl and most preferably C12 alkyl, and A is a bond. The concentration of the polyoxyethylene ethers should be in the range 0.1-20%, preferably from 0.1-10%, and most preferably in the range 0.1-1%. Preferred polyoxyethylene ethers are selected from the following group: polyoxyethylene-9-lauryl ether, polyoxyethylene-9-steoryl ether, polyoxyethylene-8-steoryl ether, polyoxyethylene-4-lauryl ether, polyoxyethylene-35-lauryl ether, and polyoxyethylene-23-lauryl ether. Polyoxyethylene ethers such as polyoxyethylene lauryl ether are described in the Merck index (12th edition: entry 7717). These adjuvant molecules are described in WO 99/52549.

[0236] The polyoxyethylene ether according to the general formula (I) above may, if desired, be combined with another adjuvant. For example, a preferred adjuvant combination is preferably with CpG as described in the pending UK patent application GB 9820956.2.

[0237] According to another embodiment of this invention, an immunogenic composition described herein is delivered to a host via antigen presenting cells (APCs), such as dendritic cells, macrophages, B cells, monocytes and other cells that may be engineered to be efficient APCs. Such cells may, but need not, be genetically modified to increase the capacity for presenting the antigen, to improve activation and/or maintenance of the T cell response, to have anti-tumor effects per se and/or to be immunologically compatible with the receiver (i.e., matched HLA haplotype). APCs may generally be isolated from any of a variety of biological fluids and organs, including tumor and peritumoral tissues, and may be autologous, allogeneic, syngeneic or xenogeneic cells.

[0238] Certain preferred embodiments of the present invention use dendritic cells or progenitors thereof as antigen-presenting cells. Dendritic cells are highly potent APCs (Banchereau and Steinman, Nature 392:245-251, 1998) and have been shown to be effective as a physiological adjuvant for eliciting prophylactic or therapeutic antitumor immunity (see Timmerman and Levy, Ann. Rev. Med. 50:507-529, 1999). In general, dendritic cells may be identified based on their typical shape (stellate in situ, with marked cytoplasmic processes (dendrites) visible in vitro), their ability to take up, process and present antigens with high efficiency and their ability to activate naive T cell responses. Dendritic cells may, of course, be engineered to express specific cell-surface receptors or ligands that are not commonly found on dendritic cells in vivo or ex vivo, and such modified dendritic cells are contemplated by the present invention. As an alternative to dendritic cells, secreted vesicles antigen-loaded dendritic cells (called exosomes) may be used within a vaccine (see Zitvogel et al., Nature Med. 4:594-600, 1998).

[0239] Dendritic cells and progenitors may be obtained from peripheral blood, bone marrow, tumor-infiltrating cells, peritumoral tissues-infiltrating cells, lymph nodes, spleen, skin, umbilical cord blood or any other suitable tissue or fluid. For example, dendritic cells may be differentiated ex vivo by adding a combination of cytokines such as GM-CSF, IL-4, IL-13 and/or TNFα to cultures of monocytes harvested from peripheral blood. Alternatively, CD34 positive cells harvested from peripheral blood, umbilical cord blood or bone marrow may be differentiated into dendritic cells by adding to the culture medium combinations of GM-CSF, IL-3, TNFα, CD40 ligand, LPS, flt3 ligand and/or other compound(s) that induce differentiation, maturation and proliferation of dendritic cells.

[0240] Dendritic cells are conveniently categorized as “immature” and “mature” cells, which allows a simple way to discriminate between two well characterized phenotypes. However, this nomenclature should not be construed to exclude all possible intermediate stages of differentiation. Immature dendritic cells are characterized as APC with a high capacity for antigen uptake and processing, which correlates with the high expression of Fcγ receptor and mannose receptor. The mature phenotype is typically characterized by a lower expression of these markers, but a high expression of cell surface molecules responsible for T cell activation such as class I and class II MHC, adhesion molecules (e.g., CD54 and CD11) and costimulatory molecules (e.g., CD40, CD80, CD86 and 4-1BB).

[0241] APCs may generally be transfected with a polynucleotide of the invention (or portion or other variant thereof) such that the encoded polypeptide, or an immunogenic portion thereof, is expressed on the cell surface. Such transfection may take place ex vivo, and a pharmaceutical composition comprising such transfected cells may then be used for therapeutic purposes, as described herein. Alternatively, a gene delivery vehicle that targets a dendritic or other antigen presenting cell may be administered to a patient, resulting in transfection that occurs in vivo. In vivo and ex vivo transfection of dendritic cells, for example, may generally be performed using any methods known in the art, such as those described in WO 97/24447, or the gene gun approach described by Mahvi et al., Immunology and cell Biology 75:456-460, 1997. Antigen loading of dendritic cells may be achieved by incubating dendritic cells or progenitor cells with the tumor polypeptide, DNA (naked or within a plasmid vector) or RNA; or with antigen-expressing recombinant bacterium or viruses (e.g., vaccinia, fowlpox, adenovirus or lentivirus vectors). Prior to loading, the polypeptide may be covalently conjugated to an immunological partner that provides T cell help (e.g., a carrier molecule). Alternatively, a dendritic cell may be pulsed with a non-conjugated immunological partner, separately or in the presence of the polypeptide.

[0242] While any suitable carrier known to those of ordinary skill in the art may be employed in the pharmaceutical compositions of this invention, the type of carrier will typically vary depending on the mode of administration. Compositions of the present invention may be formulated for any appropriate manner of administration, including for example, topical, oral, nasal, mucosal, intravenous, intracranial, intraperitoneal, subcutaneous and intramuscular administration.

[0243] Carriers for use within such pharmaceutical compositions are biocompatible, and may also be biodegradable. In certain embodiments, the formulation preferably provides a relatively constant level of active component release. In other embodiments, however, a more rapid rate of release immediately upon administration may be desired. The formulation of such compositions is well within the level of ordinary skill in the art using known techniques. Illustrative carriers useful in this regard include microparticles of poly(lactide-co-glycolide), polyacrylate, latex, starch, cellulose, dextran and the like. Other illustrative delayed-release carriers include supramolecular biovectors, which comprise a non-liquid hydrophilic core (e.g., a cross-linked polysaccharide or oligosaccharide) and, optionally, an external layer comprising an amphiphilic compound, such as a phospholipid (see e.g., U.S. Pat. No. 5,151,254 and PCT applications WO 94/20078, WO/94/23701 and WO 96/06638). The amount of active compound contained within a sustained release formulation depends upon the site of implantation, the rate and expected duration of release and the nature of the condition to be treated or prevented.

[0244] In another illustrative embodiment, biodegradable microspheres (e.g., polylactate polyglycolate) are employed as carriers for the compositions of this invention. Suitable biodegradable microspheres are disclosed, for example, in U.S. Pat. Nos. 4,897,268; 5,075,109; 5,928,647; 5,811,128; 5,820,883; 5,853,763; 5,814,344, 5,407,609 and 5,942,252. Modified hepatitis B core protein carrier systems, such as described in WO/99 40934, and references cited therein, will also be useful for many applications. Another illustrative carrier/delivery system employs a carrier comprising particulate-protein complexes, such as those described in U.S. Pat. No. 5,928,647, which are capable of inducing a class I-restricted cytotoxic T lymphocyte responses in a host.

[0245] In another illustrative embodiment, calcium phosphate core particles are employed as carriers, vaccine adjuvants, or as controlled release matrices for the compositions of this invention. Exemplary calcium phosphate particles are disclosed, for example, in published patent application No. WO/0046147.

[0246] The pharmaceutical compositions of the invention will often further comprise one or more buffers (e.g., neutral buffered saline or phosphate buffered saline), carbohydrates (e.g., glucose, mannose, sucrose or dextrans), mannitol, proteins, polypeptides or amino acids such as glycine, antioxidants, bacteriostats, chelating agents such as EDTA or glutathione, adjuvants (e.g., aluminum hydroxide), solutes that render the formulation isotonic, hypotonic or weakly hypertonic with the blood of a recipient, suspending agents, thickening agents and/or preservatives. Alternatively, compositions of the present invention may be formulated as a lyophilizate.

[0247] The pharmaceutical compositions described herein may be presented in unit-dose or multi-dose containers, such as sealed ampoules or vials. Such containers are typically sealed in such a way to preserve the sterility and stability of the formulation until use. In general, formulations may be stored as suspensions, solutions or emulsions in oily or aqueous vehicles. Alternatively, a pharmaceutical composition may be stored in a freeze-dried condition requiring only the addition of a sterile liquid carrier immediately prior to use.

[0248] The development of suitable dosing and treatment regimens for using the particular compositions described herein in a variety of treatment regimens, including e.g., oral, parenteral, intravenous, intranasal, and intramuscular administration and formulation, is well known in the art, some of which are briefly discussed below for general purposes of illustration.

[0249] In certain applications, the pharmaceutical compositions disclosed herein may be delivered via oral administration to an animal. As such, these compositions may be formulated with an inert diluent or with an assimilable edible carrier, or they may be enclosed in hard- or soft-shell gelatin capsule, or they may be compressed into tablets, or they may be incorporated directly with the food of the diet.

[0250] The active compounds may even be incorporated with excipients and used in the form of ingestible tablets, buccal tables, troches, capsules, elixirs, suspensions, syrups, wafers, and the like (see, for example, Mathiowitz et al., Nature 1997 March 27;386(6623):410-4; Hwang et al., Crit Rev Ther Drug Carrier Syst 1998;15(3):243-84; U.S. Pat. Nos. 5,641,515; 5,580,579 and 5,792,451). Tablets, troches, pills, capsules and the like may also contain any of a variety of additional components, for example, a binder, such as gum tragacanth, acacia, cornstarch, or gelatin; excipients, such as dicalcium phosphate; a disintegrating agent, such as corn starch, potato starch, alginic acid and the like; a lubricant, such as magnesium stearate; and a sweetening agent, such as sucrose, lactose or saccharin may be added or a flavoring agent, such as peppermint, oil of wintergreen, or cherry flavoring. When the dosage unit form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier. Various other materials may be present as coatings or to otherwise modify the physical form of the dosage unit. For instance, tablets, pills, or capsules may be coated with shellac, sugar, or both. Of course, any material used in preparing any dosage unit form should be pharmaceutically pure and substantially non-toxic in the amounts employed. In addition, the active compounds may be incorporated into sustained-release preparation and formulations.

[0251] Typically, these formulations will contain at least about 0.1% of the active compound or more, although the percentage of the active ingredient(s) may, of course, be varied and may conveniently be between about 1 or 2% and about 60% or 70% or more of the weight or volume of the total formulation. Naturally, the amount of active compound(s) in each therapeutically useful composition may be prepared is such a way that a suitable dosage will be obtained in any given unit dose of the compound. Factors such as solubility, bioavailability, biological half-life, route of administration, product shelf life, as well as other pharmacological considerations will be contemplated by one skilled in the art of preparing such pharmaceutical formulations, and as such, a variety of dosages and treatment regimens may be desirable.

[0252] For oral administration the compositions of the present invention may alternatively be incorporated with one or more excipients in the form of a mouthwash, dentifrice, buccal tablet, oral spray, or sublingual orally-administered formulation. Alternatively, the active ingredient may be incorporated into an oral solution such as one containing sodium borate, glycerin and potassium bicarbonate, or dispersed in a dentifrice, or added in a therapeutically-effective amount to a composition that may include water, binders, abrasives, flavoring agents, foaming agents, and humectants. Alternatively the compositions may be fashioned into a tablet or solution form that may be placed under the tongue or otherwise dissolved in the mouth.

[0253] In certain circumstances it will be desirable to deliver the pharmaceutical compositions disclosed herein parenterally, intravenously, intramuscularly, or even intraperitoneally. Such approaches are well known to the skilled artisan, some of which are further described, for example, in U.S. Pat. Nos. 5,543,158; 5,641,515 and 5,399,363. In certain embodiments, solutions of the active compounds as free base or pharmacologically acceptable salts may be prepared in water suitably mixed with a surfactant, such as hydroxypropylcellulose. Dispersions may also be prepared in glycerol, liquid polyethylene glycols, and mixtures thereof and in oils. Under ordinary conditions of storage and use, these preparations generally will contain a preservative to prevent the growth of microorganisms.

[0254] Illustrative pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions (for example, see U.S. Pat. No. 5,466,468). In all cases the form must be sterile and must be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms, such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (e.g., glycerol, propylene glycol, and liquid polyethylene glycol, and the like), suitable mixtures thereof, and/or vegetable oils. Proper fluidity may be maintained, for example, by the use of a coating, such as lecithin, by the maintenance of the required particle size in the case of dispersion and/or by the use of surfactants. The prevention of the action of microorganisms can be facilitated by various antibacterial and antifingal agents, for example, parabens, chlorobutanol, phenol, sorbic acid, thimerosal, and the like. In many cases, it will be preferable to include isotonic agents, for example, sugars or sodium chloride. Prolonged absorption of the injectable compositions can be brought about by the use in the compositions of agents delaying absorption, for example, aluminum monostearate and gelatin.

[0255] In one embodiment, for parenteral administration in an aqueous solution, the solution should be suitably buffered if necessary and the liquid diluent first rendered isotonic with sufficient saline or glucose. These particular aqueous solutions are especially suitable for intravenous, intramuscular, subcutaneous and intraperitoneal administration. In this connection, a sterile aqueous medium that can be employed will be known to those of skill in the art in light of the present disclosure. For example, one dosage may be dissolved in 1 ml of isotonic NaCl solution and either added to 1000 ml of hypodermoclysis fluid or injected at the proposed site of infusion, (see for example, “Remington's Pharmaceutical Sciences” 15th Edition, pages 1035-1038 and 1570-1580). Some variation in dosage will necessarily occur depending on the condition of the subject being treated. Moreover, for human administration, preparations will of course preferably meet sterility, pyrogenicity, and the general safety and purity standards as required by FDA Office of Biologics standards.

[0256] In another embodiment of the invention, the compositions disclosed herein may be formulated in a neutral or salt form. Illustrative pharmaceutically-acceptable salts include the acid addition salts (formed with the free amino groups of the protein) and which are formed with inorganic acids such as, for example, hydrochloric or phosphoric acids, or such organic acids as acetic, oxalic, tartaric, mandelic, and the like. Salts formed with the free carboxyl groups can also be derived from inorganic bases such as, for example, sodium, potassium, ammonium, calcium, or ferric hydroxides, and such organic bases as isopropylamine, trimethylamine, histidine, procaine and the like. Upon formulation, solutions will be administered in a manner compatible with the dosage formulation and in such amount as is therapeutically effective.

[0257] The carriers can further comprise any and all solvents, dispersion media, vehicles, coatings, diluents, antibacterial and antifingal agents, isotonic and absorption delaying agents, buffers, carrier solutions, suspensions, colloids, and the like. The use of such media and agents for pharmaceutical active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active ingredient, its use in the therapeutic compositions is contemplated. Supplementary active ingredients can also be incorporated into the compositions. The phrase “pharmaceutically-acceptable” refers to molecular entities and compositions that do not produce an allergic or similar untoward reaction when administered to a human.

[0258] In certain embodiments, the pharmaceutical compositions may be delivered by intranasal sprays, inhalation, and/or other aerosol delivery vehicles. Methods for delivering genes, nucleic acids, and peptide compositions directly to the lungs via nasal aerosol sprays has been described, e.g., in U.S. Pat. Nos. 5,756,353 and 5,804,212. Likewise, the delivery of drugs using intranasal microparticle resins (Takenaga et al., J Controlled Release 1998 March 2;52(1-2):81-7) and lysophosphatidyl-glycerol compounds (U.S. Pat. No. 5,725,871) are also well-known in the pharmaceutical arts. Likewise, illustrative transmucosal drug delivery in the form of a polytetrafluoroetheylene support matrix is described in U.S. Pat. No. 5,780,045.

[0259] In certain embodiments, liposomes, nanocapsules, microparticles, lipid particles, vesicles, and the like, are used for the introduction of the compositions of the present invention into suitable host cells/organisms. In particular, the compositions of the present invention may be formulated for delivery either encapsulated in a lipid particle, a liposome, a vesicle, a nanosphere, or a nanoparticle or the like. Alternatively, compositions of the present invention can be bound, either covalently or non-covalently, to the surface of such carrier vehicles.

[0260] The formation and use of liposome and liposome-like preparations as potential drug carriers is generally known to those of skill in the art (see for example, Lasic, Trends Biotechnol 1998 July;16(7):307-21; Takakura, Nippon Rinsho 1998 March;56(3):691-5; Chandran et al., Indian J Exp Biol. 1997 August;35(8):801-9; Margalit, Crit Rev Ther Drug Carrier Syst. 1995;12(2-3):233-61; U.S. Pat. Nos. 5,567,434; 5,552,157; 5,565,213; 5,738,868 and 5,795,587, each specifically incorporated herein by reference in its entirety).

[0261] Liposomes have been used successfully with a number of cell types that are normally difficult to transfect by other procedures, including T cell suspensions, primary hepatocyte cultures and PC 12 cells (Renneisen et al., J Biol Chem. 1990 September 25;265(27):16337-42; Muller et al., DNA Cell Biol. 1990 April;9(3):221-9). In addition, liposomes are free of the DNA length constraints that are typical of viral-based delivery systems. Liposomes have been used effectively to introduce genes, various drugs, radiotherapeutic agents, enzymes, viruses, transcription factors, allosteric effectors and the like, into a variety of cultured cell lines and animals. Furthermore, he use of liposomes does not appear to be associated with autoimmune responses or unacceptable toxicity after systemic delivery.

[0262] In certain embodiments, liposomes are formed from phospholipids that are dispersed in an aqueous medium and spontaneously form multilamellar concentric bilayer vesicles (also termed multilamellar vesicles (MLVs).

[0263] Alternatively, in other embodiments, the invention provides for pharmaceutically-acceptable nanocapsule formulations of the compositions of the present invention. Nanocapsules can generally entrap compounds in a stable and reproducible way (see, for example, Quintanar-Guerrero et al., Drug Dev Ind Pharm. 1998 December;24(12): 1113-28). To avoid side effects due to intracellular polymeric overloading, such ultrafine particles (sized around 0.1 μm) may be designed using polymers able to be degraded in vivo. Such particles can be made as described, for example, by Couvreur et al., Crit Rev Ther Drug Carrier Syst. 1988;5(1):1-20; zur Muhlen et al., Eur J Pharm Biopharm. 1998 March;45(2):149-55; Zambaux et al. J Controlled Release. 1998 January 2;50(1-3):31-40; and U.S. Pat. No. 5,145,684.

[0264] Cancer Therapeutic Methods

[0265] Immunologic approaches to cancer therapy are based on the recognition that cancer cells can often evade the body's defenses against aberrant or foreign cells and molecules, and that these defenses might be therapeutically stimulated to regain the lost ground, e.g. pgs. 623-648 in Klein, Immunology (Wiley-Interscience, New York, 1982). Numerous recent observations that various immune effectors can directly or indirectly inhibit growth of tumors has led to renewed interest in this approach to cancer therapy, e.g. Jager, et al., Oncology 2001;60(1):1-7; Renner, et al., Ann Hematol 2000 December;79(12):651-9.

[0266] Four-basic cell types whose function has been associated with antitumor cell immunity and the elimination of tumor cells from the body are: i) B-lymphocytes which secrete immunoglobulins into the blood plasma for identifying and labeling the nonself invader cells; ii) monocytes which secrete the complement proteins that are responsible for lysing and processing the immunoglobulin-coated target invader cells; iii) natural killer lymphocytes having two mechanisms for the destruction of tumor cells, antibody-dependent cellular cytotoxicity and natural killing; and iv) T-lymphocytes possessing antigen-specific receptors and having the capacity to recognize a tumor cell carrying complementary marker molecules (Schreiber, H., 1989, in Fundamental Immunology (ed). W. E. Paul, pp. 923-955).

[0267] Cancer immunotherapy generally focuses on inducing humoral immune responses, cellular immune responses, or both. Moreover, it is well established that induction of CD4+ T helper cells is necessary in order to secondarily induce either antibodies or cytotoxic CD8+ T cells. Polypeptide antigens that are selective or ideally specific for cancer cells, particularly colon cancer cells, offer a powerful approach for inducing immune responses against colon cancer, and are an important aspect of the present invention.

[0268] Therefore, in further aspects of the present invention, the pharmaceutical compositions described herein may be used to stimulate an immune response against cancer, particularly for the immunotherapy of colon cancer. Within such methods, the pharmaceutical compositions described herein are administered to a patient, typically a warm-blooded animal, preferably a human. A patient may or may not be afflicted with cancer. Pharmaceutical compositions and vaccines may be administered either prior to or following surgical removal of primary tumors and/or treatment such as administration of radiotherapy or conventional chemotherapeutic drugs. As discussed above, administration of the pharmaceutical compositions may be by any suitable method, including administration by intravenous, intraperitoneal, intramuscular, subcutaneous, intranasal, intradermal, anal, vaginal, topical and oral routes.

[0269] Within certain embodiments, immunotherapy may be active immunotherapy, in which treatment relies on the in vivo stimulation of the endogenous host immune system to react against tumors with the administration of immune response-modifying agents (such as polypeptides and polynucleotides as provided herein).

[0270] Within other embodiments, immunotherapy may be passive immunotherapy, in which treatment involves the delivery of agents with established tumor-immune reactivity (such as effector cells or antibodies) that can directly or indirectly mediate antitumor effects and does not necessarily depend on an intact host immune system. Examples of effector cells include T cells as discussed above, T lymphocytes (such as CD8+ cytotoxic T lymphocytes and CD4+ T-helper tumor-infiltrating lymphocytes), killer cells (such as Natural Killer cells and lymphokine-activated killer cells), B cells and antigen-presenting cells (such as dendritic cells and macrophages) expressing a polypeptide provided herein. T cell receptors and antibody receptors specific for the polypeptides recited herein may be cloned, expressed and transferred into other vectors or effector cells for adoptive immunotherapy. The polypeptides provided herein may also be used to generate antibodies or anti-idiotypic antibodies (as described above and in U.S. Pat. No. 4,918,164) for passive immunotherapy.

[0271] Monoclonal antibodies may be labeled with any of a variety of labels for desired selective usages in detection, diagnostic assays or therapeutic applications (as described in U.S. Pat. Nos. 6,090,365; 6,015,542; 5,843,398; 5,595,721; and 4,708,930, hereby incorporated by reference in their entirety as if each was incorporated individually). In each case, the binding of the labelled monoclonal antibody to the determinant site of the antigen will signal detection or delivery of a particular therapeutic agent to the antigenic determinant on the non-normal cell. A further object of this invention is to provide the specific monoclonal antibody suitably labelled for achieving such desired selective usages thereof.

[0272] Effector cells may generally be obtained in sufficient quantities for adoptive immunotherapy by growth in vitro, as described herein. Culture conditions for expanding single antigen-specific effector cells to several billion in number with retention of antigen recognition in vivo are well known in the art. Such in vitro culture conditions typically use intermittent stimulation with antigen, often in the presence of cytokines (such as IL-2) and non-dividing feeder cells. As noted above, immunoreactive polypeptides as provided herein may be used to rapidly expand antigen-specific T cell cultures in order to generate a sufficient number of cells for immunotherapy. In particular, antigen-presenting cells, such as dendritic, macrophage, monocyte, fibroblast and/or B cells, may be pulsed with immunoreactive polypeptides or transfected with one or more polynucleotides using standard techniques well known in the art. For example, antigen-presenting cells can be transfected with a polynucleotide having a promoter appropriate for increasing expression in a recombinant virus or other expression system. Cultured effector cells for use in therapy must be able to grow and distribute widely, and to survive long term in vivo. Studies have shown that cultured effector cells can be induced to grow in vivo and to survive long term in substantial numbers by repeated stimulation with antigen supplemented with IL-2 (see, for example, Cheever et al., Immunological Reviews 157:177, 1997).

[0273] Alternatively, a vector expressing a polypeptide recited herein may be introduced into antigen presenting cells taken from a patient and clonally propagated ex vivo for transplant back into the same patient. Transfected cells may be reintroduced into the patient using any means known in the art, preferably in sterile form by intravenous, intracavitary, intraperitoneal or intratumor administration.

[0274] Routes and frequency of administration of the therapeutic compositions described herein, as well as dosage, will vary from individual to individual, and may be readily established using standard techniques. In general, the pharmaceutical compositions and vaccines may be administered by injection (e.g., intracutaneous, intramuscular, intravenous or subcutaneous), intranasally (e.g., by aspiration) or orally. Preferably, between 1 and 10 doses may be administered over a 52 week period. Preferably, 6 doses are administered, at intervals of 1 month, and booster vaccinations may be given periodically thereafter. Alternate protocols may be appropriate for individual patients. A suitable dose is an amount of a compound that, when administered as described above, is capable of promoting an anti-tumor immune response, and is at least 10-50% above the basal (i.e., untreated) level. Such response can be monitored by measuring the anti-tumor antibodies in a patient or by vaccine-dependent generation of cytolytic effector cells capable of killing the patient's tumor cells in vitro. Such vaccines should also be capable of causing an immune response that leads to an improved clinical outcome (e.g., more frequent remissions, complete or partial or longer disease-free survival) in vaccinated patients as compared to non-vaccinated patients. In general, for pharmaceutical compositions and vaccines comprising one or more polypeptides, the amount of each polypeptide present in a dose ranges from about 25 μg to 5 mg per kg of host. Suitable dose sizes will vary with the size of the patient, but will typically range from about 0.1 mL to about 5 mL.

[0275] In general, an appropriate dosage and treatment regimen provides the active compound(s) in an amount sufficient to provide therapeutic and/or prophylactic benefit. Such a response can be monitored by establishing an improved clinical outcome (e.g. more frequent remissions, complete or partial, or longer disease-free survival) in treated patients as compared to non-treated patients. Increases in preexisting immune responses to a tumor protein generally correlate with an improved clinical outcome. Such immune responses may generally be evaluated using standard proliferation, cytotoxicity or cytokine assays, which may be performed using samples obtained from a patient before and after treatment.

[0276] Cancer Detection and Diagnostic Compositions, Methods and Kits

[0277] In general, a cancer may be detected in a patient based on the presence of one or more colon tumor proteins and/or polynucleotides encoding such proteins in a biological sample (for example, blood, sera, sputum urine and/or tumor biopsies) obtained from the patient. In other words, such proteins may be used as markers to indicate the presence or absence of a cancer such as colon cancer. In addition, such proteins may be useful for the detection of other cancers. The binding agents provided herein generally permit detection of the level of antigen that binds to the agent in the biological sample.

[0278] Polynucleotide primers and probes may be used to detect the level of mRNA encoding a tumor protein, which is also indicative of the presence or absence of a cancer. In general, a tumor sequence should be present at a level that is at least two-fold, preferably three-fold, and more preferably five-fold or higher in tumor tissue than in normal tissue of the same type from which the tumor arose. Expression levels of a particular tumor sequence in tissue types different from that in which the tumor arose are irrelevant in certain diagnostic embodiments since the presence of tumor cells can be confirmed by observation of predetermined differential expression levels, e.g., 2-fold, 5-fold, etc, in tumor tissue to expression levels in normal tissue of the same type.

[0279] Other differential expression patterns can be utilized advantageously for diagnostic purposes. For example, in one aspect of the invention, overexpression of a tumor sequence in tumor tissue and normal tissue of the same type, but not in other normal tissue types, e.g. PBMCs, can be exploited diagnostically. In this case, the presence of metastatic tumor cells, for example in a sample taken from the circulation or some other tissue site different from that in which the tumor arose, can be identified and/or confirmed by detecting expression of the tumor sequence in the sample, for example using RT-PCR analysis. In many instances, it will be desired to enrich for tumor cells in the sample of interest, e.g., PBMCs, using cell capture or other like techniques.

[0280] There are a variety of assay formats known to those of ordinary skill in the art for using a binding agent to detect polypeptide markers in a sample. See, e.g., Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, 1988. In general, the presence or absence of a cancer in a patient may be determined by (a) contacting a biological sample obtained from a patient with a binding agent; (b) detecting in the sample a level of polypeptide that binds to the binding agent; and (c) comparing the level of polypeptide with a predetermined cut-off value.

[0281] In a preferred embodiment, the assay involves the use of binding agent immobilized on a solid support to bind to and remove the polypeptide from the remainder of the sample. The bound polypeptide may then be detected using a detection reagent that contains a reporter group and specifically binds to the binding agent/polypeptide complex. Such detection reagents may comprise, for example, a binding agent that specifically binds to the polypeptide or an antibody or other agent that specifically binds to the binding agent, such as an anti-immunoglobulin, protein G, protein A or a lectin. Alternatively, a competitive assay may be utilized, in which a polypeptide is labeled with a reporter group and allowed to bind to the immobilized binding agent after incubation of the binding agent with the sample. The extent to which components of the sample inhibit the binding of the labeled polypeptide to the binding agent is indicative of the reactivity of the sample with the immobilized binding agent. Suitable polypeptides for use within such assays include full length colon tumor proteins and polypeptide portions thereof to which the binding agent binds, as described above.

[0282] The solid support may be any material known to those of ordinary skill in the art to which the tumor protein may be attached. For example, the solid support may be a test well in a microtiter plate or a nitrocellulose or other suitable membrane. Alternatively, the support may be a bead or disc, such as glass, fiberglass, latex or a plastic material such as polystyrene or polyvinylchloride. The support may also be a magnetic particle or a fiber optic sensor, such as those disclosed, for example, in U.S. Pat. No. 5,359,681. The binding agent may be immobilized on the solid support using a variety of techniques known to those of skill in the art, which are amply described in the patent and scientific literature. In the context of the present invention, the term “immobilization” refers to both noncovalent association, such as adsorption, and covalent attachment (which may be a direct linkage between the agent and functional groups on the support or may be a linkage by way of a cross-linking agent). Immobilization by adsorption to a well in a microtiter plate or to a membrane is preferred. In such cases, adsorption may be achieved by contacting the binding agent, in a suitable buffer, with the solid support for a suitable amount of time. The contact time varies with temperature, but is typically between about 1 hour and about 1 day. In general, contacting a well of a plastic microtiter plate (such as polystyrene or polyvinylchloride) with an amount of binding agent ranging from about 10 ng to about 10 μg, and preferably about 100 ng to about 1 μg, is sufficient to immobilize an adequate amount of binding agent.

[0283] Covalent attachment of binding agent to a solid support may generally be achieved by first reacting the support with a bifunctional reagent that will react with both the support and a functional group, such as a hydroxyl or amino group, on the binding agent. For example, the binding agent may be covalently attached to supports having an appropriate polymer coating using benzoquinone or by condensation of an aldehyde group on the support with an amine and an active hydrogen on the binding partner (see, e.g., Pierce Immunotechnology Catalog and Handbook, 1991, at A12-A13).

[0284] In certain embodiments, the assay is a two-antibody sandwich assay. This assay may be performed by first contacting an antibody that has been immobilized on a solid support, commonly the well of a microtiter plate, with the sample, such that polypeptides within the sample are allowed to bind to the immobilized antibody. Unbound sample is then removed from the immobilized polypeptide-antibody complexes and a detection reagent (preferably a second antibody capable of binding to a different site on the polypeptide) containing a reporter group is added. The amount of detection reagent that remains bound to the solid support is then determined using a method appropriate for the specific reporter group.

[0285] More specifically, once the antibody is immobilized on the support as described above, the remaining protein binding sites on the support are typically blocked. Any suitable blocking agent known to those of ordinary skill in the art, such as bovine serum albumin or Tween 20™ (Sigma Chemical Co., St. Louis, Mo.). The immobilized antibody is then incubated with the sample, and polypeptide is allowed to bind to the antibody. The sample may be diluted with a suitable diluent, such as phosphate-buffered saline (PBS) prior to incubation. In general, an appropriate contact time (i.e., incubation time) is a period of time that is sufficient to detect the presence of polypeptide within a sample obtained from an individual with colon cancer at least about 95% of that achieved at equilibrium between bound and unbound polypeptide. Those of ordinary skill in the art will recognize that the time necessary to achieve equilibrium may be readily determined by assaying the level of binding that occurs over a period of time. At room temperature, an incubation time of about 30 minutes is generally sufficient.

[0286] Unbound sample may then be removed by washing the solid support with an appropriate buffer, such as PBS containing 0.1% Tween 20™. The second antibody, which contains a reporter group, may then be added to the solid support. Preferred reporter groups include those groups recited above.

[0287] The detection reagent is then incubated with the immobilized antibody-polypeptide complex for an amount of time sufficient to detect the bound polypeptide. An appropriate amount of time may generally be determined by assaying the level of binding that occurs over a period of time. Unbound detection reagent is then removed and bound detection reagent is detected using the reporter group. The method employed for detecting the reporter group depends upon the nature of the reporter group. For radioactive groups, scintillation counting or autoradiographic methods are generally appropriate. Spectroscopic methods may be used to detect dyes, luminescent groups and fluorescent groups. Biotin may be detected using avidin, coupled to a different reporter group (commonly a radioactive or fluorescent group or an enzyme). Enzyme reporter groups may generally be detected by the addition of substrate (generally for a specific period of time), followed by spectroscopic or other analysis of the reaction products.

[0288] To determine the presence or absence of a cancer, such as colon cancer, the signal detected from the reporter group that remains bound to the solid support is generally compared to a signal that corresponds to a predetermined cut-off value. In one preferred embodiment, the cut-off value for the detection of a cancer is the average mean signal obtained when the immobilized antibody is incubated with samples from patients without the cancer. In general, a sample generating a signal that is three standard deviations above the predetermined cut-off value is considered positive for the cancer. In an alternate preferred embodiment, the cut-off value is determined using a Receiver Operator Curve, according to the method of Sackett et al., Clinical Epidemiology: A Basic Science for Clinical Medicine, Little Brown and Co., 1985, p. 106-7. Briefly, in this embodiment, the cut-off value may be determined from a plot of pairs of true positive rates (i.e., sensitivity) and false positive rates (100%-specificity) that correspond to each possible cut-off value for the diagnostic test result. The cut-off value on the plot that is the closest to the upper left-hand corner (i.e., the value that encloses the largest area) is the most accurate cut-off value, and a sample generating a signal that is higher than the cut-off value determined by this method may be considered positive. Alternatively, the cut-off value may be shifted to the left along the plot, to minimize the false positive rate, or to the right, to minimize the false negative rate. In general, a sample generating a signal that is higher than the cut-off value determined by this method is considered positive for a cancer.

[0289] In a related embodiment, the assay is performed in a flow-through or strip test format, wherein the binding agent is immobilized on a membrane, such as nitrocellulose. In the flow-through test, polypeptides within the sample bind to the immobilized binding agent as the sample passes through the membrane. A second, labeled binding agent then binds to the binding agent-polypeptide complex as a solution containing the second binding agent flows through the membrane. The detection of bound second binding agent may then be performed as described above. In the strip test format, one end of the membrane to which binding agent is bound is immersed in a solution containing the sample. The sample migrates along the membrane through a region containing second binding agent and to the area of immobilized binding agent. Concentration of second binding agent at the area of immobilized antibody indicates the presence of a cancer. Typically, the concentration of second binding agent at that site generates a pattern, such as a line, that can be read visually. The absence of such a pattern indicates a negative result. In general, the amount of binding agent immobilized on the membrane is selected to generate a visually discernible pattern when the biological sample contains a level of polypeptide that would be sufficient to generate a positive signal in the two-antibody sandwich assay, in the format discussed above. Preferred binding agents for use in such assays are antibodies and antigen-binding fragments thereof. Preferably, the amount of antibody immobilized on the membrane ranges from about 25 ng to about 1 μg, and more preferably from about 50 ng to about 500 ng. Such tests can typically be performed with a very small amount of biological sample.

[0290] Of course, numerous other assay protocols exist that are suitable for use with the tumor proteins or binding agents of the present invention. The above descriptions are intended to be exemplary only. For example, it will be apparent to those of ordinary skill in the art that the above protocols may be readily modified to use tumor polypeptides to detect antibodies that bind to such polypeptides in a biological sample. The detection of such tumor protein specific antibodies may correlate with the presence of a cancer.

[0291] A cancer may also, or alternatively, be detected based on the presence of T cells that specifically react with a tumor protein in a biological sample. Within certain methods, a biological sample comprising CD4+ and/or CD8+ T cells isolated from a patient is incubated with a tumor polypeptide, a polynucleotide encoding such a polypeptide and/or an APC that expresses at least an immunogenic portion of such a polypeptide, and the presence or absence of specific activation of the T cells is detected. Suitable biological samples include, but are not limited to, isolated T cells. For example, T cells may be isolated from a patient by routine techniques (such as by Ficoll/Hypaque density gradient centrifugation of peripheral blood lymphocytes). T cells may be incubated in vitro for 2-9 days (typically 4 days) at 37° C. with polypeptide (e.g., 5-25 μg/ml). It may be desirable to incubate another aliquot of a T cell sample in the absence of tumor polypeptide to serve as a control. For CD4+ T cells, activation is preferably detected by evaluating proliferation of the T cells. For CD8+ T cells, activation is preferably detected by evaluating cytolytic activity. A level of proliferation that is at least two fold greater and/or a level of cytolytic activity that is at least 20% greater than in disease-free patients indicates the presence of a cancer in the patient.

[0292] As noted above, a cancer may also, or alternatively, be detected based on the level of mRNA encoding a tumor protein in a biological sample. For example, at least two oligonucleotide primers may be employed in a polymerase chain reaction (PCR) based assay to amplify a portion of a tumor cDNA derived from a biological sample, wherein at least one of the oligonucleotide primers is specific for (i.e., hybridizes to) a polynucleotide encoding the tumor protein. The amplified cDNA is then separated and detected using techniques well known in the art, such as gel electrophoresis.

[0293] Similarly, oligonucleotide probes that specifically hybridize to a polynucleotide encoding a tumor protein may be used in a hybridization assay to detect the presence of polynucleotide encoding the tumor protein in a biological sample.

[0294] To permit hybridization under assay conditions, oligonucleotide primers and probes should comprise an oligonucleotide sequence that has at least about 60%, preferably at least about 75% and more preferably at least about 90%, identity to a portion of a polynucleotide encoding a tumor protein of the invention that is at least 10 nucleotides, and preferably at least 20 nucleotides, in length. Preferably, oligonucleotide primers and/or probes hybridize to a polynucleotide encoding a polypeptide described herein under moderately stringent conditions, as defined above. Oligonucleotide primers and/or probes which may be usefully employed in the diagnostic methods described herein preferably are at least 10-40 nucleotides in length. In a preferred embodiment, the oligonucleotide primers comprise at least 10 contiguous nucleotides, more preferably at least 15 contiguous nucleotides, of a DNA molecule having a sequence as disclosed herein. Techniques for both PCR based assays and hybridization assays are well known in the art (see, for example, Mullis et al., Cold Spring Harbor Symp. Quant. Biol., 51:263, 1987; Erlich ed., PCR Technology, Stockton Press, N.Y., 1989).

[0295] One preferred assay employs RT-PCR, in which PCR is applied in conjunction with reverse transcription. Typically, RNA is extracted from a biological sample, such as biopsy tissue, and is reverse transcribed to produce cDNA molecules. PCR amplification using at least one specific primer generates a cDNA molecule, which may be separated and visualized using, for example, gel electrophoresis. Amplification may be performed on biological samples taken from a test patient and from an individual who is not afflicted with a cancer. The amplification reaction may be performed on several dilutions of cDNA spanning two orders of magnitude. A two-fold or greater increase in expression in several dilutions of the test patient sample as compared to the same dilutions of the non-cancerous sample is typically considered positive.

[0296] In another aspect of the present invention, cell capture technologies may be used in conjunction, with, for example, real-time PCR to provide a more sensitive tool for detection of metastatic cells expressing colon tumor antigens. Detection of colon cancer cells in biological samples, e.g., bone marrow samples, peripheral blood, and small needle aspiration samples is desirable for diagnosis and prognosis in colon cancer patients.

[0297] Immunomagnetic beads coated with specific monoclonal antibodies to surface cell markers, or tetrameric antibody complexes, may be used to first enrich or positively select cancer cells in a sample. Various commercially available kits may be used, including Dynabeads® Epithelial Enrich (Dynal Biotech, Oslo, Norway), StemSep™ (StemCell Technologies, Inc., Vancouver, BC), and RosetteSep (StemCell Technologies). A skilled artisan will recognize that other methodologies and kits may also be used to enrich or positively select desired cell populations. Dynabeads® Epithelial Enrich contains magnetic beads coated with mAbs specific for two glycoprotein membrane antigens expressed on normal and neoplastic epithelial tissues. The coated beads may be added to a sample and the sample then applied to a magnet, thereby capturing the cells bound to the beads. The unwanted cells are washed away and the magnetically isolated cells eluted from the beads and used in further analyses.

[0298] RosetteSep can be used to enrich cells directly from a blood sample and consists of a cocktail of tetrameric antibodies that targets a variety of unwanted cells and crosslinks them to glycophorin A on red blood cells (RBC) present in the sample, forming rosettes. When centrifuged over Ficoll, targeted cells pellet along with the free RBC. The combination of antibodies in the depletion cocktail determines which cells will be removed and consequently which cells will be recovered. Antibodies that are available include, but are not limited to: CD2, CD3, CD4, CD5, CD8, CD10, CD11b, CD14, CD15, CD16, CD19, CD20, CD24, CD25, CD29, CD33, CD34, CD36, CD38, CD41, CD45, CD45RA, CD45RO, CD56, CD66B, CD66e, HLA-DR, IgE, and TCRαβ.

[0299] Additionally, it is contemplated in the present invention that mAbs specific for colon tumor antigens can be generated and used in a similar manner. For example, mAbs that bind to tumor-specific cell surface antigens may be conjugated to magnetic beads, or formulated in a tetrameric antibody complex, and used to enrich or positively select metastatic colon tumor cells from a sample. Once a sample is enriched or positively selected, cells may be lysed and RNA isolated. RNA may then be subjected to RT-PCR analysis using colon tumor-specific primers in a real-time PCR assay as described herein. One skilled in the art will recognize that enriched or selected populations of cells may be analyzed by other methods (e.g. in situ hybridization or flow cytometry).

[0300] In another embodiment, the compositions described herein may be used as markers for the progression of cancer. In this embodiment, assays as described above for the diagnosis of a cancer may be performed over time, and the change in the level of reactive polypeptide(s) or polynucleotide(s) evaluated. For example, the assays may be performed every 24-72 hours for a period of 6 months to 1 year, and thereafter performed as needed. In general, a cancer is progressing in those patients in whom the level of polypeptide or polynucleotide detected increases over time. In contrast, the cancer is not progressing when the level of reactive polypeptide or polynucleotide either remains constant or decreases with time.

[0301] Certain in vivo diagnostic assays may be performed directly on a tumor. One such assay involves contacting tumor cells with a binding agent. The bound binding agent may then be detected directly or indirectly via a reporter group. Such binding agents may also be used in histological applications. Alternatively, polynucleotide probes may be used within such applications.

[0302] As noted above, to improve sensitivity, multiple tumor protein markers may be assayed within a given sample. It will be apparent that binding agents specific for different proteins provided herein may be combined within a single assay. Further, multiple primers or probes may be used concurrently. The selection of tumor protein markers may be based on routine experiments to determine combinations that results in optimal sensitivity. In addition, or alternatively, assays for tumor proteins provided herein may be combined with assays for other known tumor antigens.

[0303] The present invention further provides kits for use within any of the above diagnostic methods. Such kits typically comprise two or more components necessary for performing a diagnostic assay. Components may be compounds, reagents, containers and/or equipment. For example, one container within a kit may contain a monoclonal antibody or fragment thereof that specifically binds to a tumor protein. Such antibodies or fragments may be provided attached to a support material, as described above. One or more additional containers may enclose elements, such as reagents or buffers, to be used in the assay. Such kits may also, or alternatively, contain a detection reagent as described above that contains a reporter group suitable for direct or indirect detection of antibody binding.

[0304] Alternatively, a kit may be designed to detect the level of mRNA encoding a tumor protein in a biological sample. Such kits generally comprise at least one oligonucleotide probe or primer, as described above, that hybridizes to a polynucleotide encoding a tumor protein. Such an oligonucleotide may be used, for example, within a PCR or hybridization assay. Additional components that may be present within such kits include a second oligonucleotide and/or a diagnostic reagent or container to facilitate the detection of a polynucleotide encoding a tumor protein.

[0305] The following Examples are offered by way of illustration and not by way of limitation.

EXAMPLES

Example 1

Identification of Colon Tumor Protein cDNAs

[0306] This Example illustrates the identification of cDNA molecules encoding colon tumor proteins.

[0307] A colon tumor cell line cDNA library was constructed using the Life Technologies SUPERSCRIPT PLASMID SYSTEM™ for cDNA synthesis and plasmid cloning. Briefly, mRNA was isolated from colon tumor cell line 391-12 total RNA (853A) and used as the template for cDNA synthesis. EcoR I/Not I adapters from Life Technologies and EcoR I/Not I-cut pZEro-2™ vector were substituted for components provided with the kit. The library was electroporated into Life Technologies ElectroMAX™ DH10B cells and amplified in liquid culture. 24 clones plated prior to liquid amplification were randomly selected for individual amplification. Turbo miniprep DNA was prepared from each clone and characterized by sequencing and database analysis. The sequences are disclosed herein as SEQ ID NO:1-14.

[0308] A colon tumor cell line subtracted library was generated by conventional, biotin-streptavidin subtraction. Briefly, 10 μg of plasmid DNA from the colon tumor cell line 391-12 library (754-1) was subtracted against 100 μg biotinylated driver [25% normal colon library, 25% normal liver and salivary gland library, and 50% pooled driver library (liver, pancreas, skin, bone marrow, resting PBMC, stomach, and whole brain)]. Two biotin-streptavidin subtractions were performed, one after an overnight hybridization and one after a 2-hour hybridization. cDNA remaining after the two subtractions was ligated into a Not I-cut pcDNA3.1(+) vector, electroporated into ElectroMAX™ DH10B cells, and grown on agar plates containing ampicillin. Clones were randomly selected for individual amplification. Turbo miniprep DNA was prepared from each clone and characterized by sequencing and database analysis. This subtraction generated a library representing genes that are over-expressed or exclusively expressed in colon tumor cell line CT391-12. These cDNA sequences are disclosed herein as SEQ ID NO:15-65.

[0309] The database analysis of the disclosed sequences revealed that the following sequences showed no significant similarity to sequences in public databases: SEQ ID No:6, 8, 15, 16, 38, 39, 53, 54 and 65. The remaining sequences showed some degree of similarity to GenBank nucleotide sequences, as shown in Table 2.

TABLE 2
SEQ ID NO: GenBank Nucleotide Database Search Results
17         Homo sapiens barrier-to-autointegration factor mRNA,
           complete cds
18         Homo sapiens ATP synthase, H+ transporting,
           mitochondrial 50 complex, subunit c (subunit 9), isoform 2
           (ATP5G2) mRNA
19, 20     Human histone (H2A.Z) mRNA, complete cds
21, 22     Human mRNA for elongation factor-1-beta
23         Homo sapiens mRNA for transcription factor BTF 3
24         Homo sapiens KRT8 mRNA for keratin 8
25         Homo sapiens ribosomal protein S2 (RPS2) mRNA
26         Homo sapiens ribosomal protein L11 mRNA, complete cds
27, 28     Human cyclin protein gene, complete cds
29         Human ferritin H chain mRNA, complete cds
30, 31     Human mRNA for lactate dehydrogenase B (LDH-B)
32         Homo sapiens ribosomal protein S6 (RPS6) mRNA
33         Human mRNA for elongation factor 1 alpha subunit
           (EF-1 alpha)
34, 35     Homo sapiens GTP binding protein mRNA, complete cds
36         Homo sapiens 12p12-31.7-37.2 BAC RP11-80N2 (Roswell
           Park Cancer Institute HumanBAC Library) complete
           sequence
37         Homo sapiens CDC28 protein kinase 1 (CKS1) mRNA
40         Human ribosomal protein L29 (humrpl29) mRNA,
           complete cds
41         Homo sapiens mRNA; cDNA DKFZp586O1224
42         RAN, member RAS oncogene family Homo sapiens RAN,
           member RAS oncogene family (RAN), mRNA
43, 44     Human DNA sequence from clone RP3-322L4 on
           chromosome 6, complete sequence
45         Human mitochondrial genome (cytochrome oxidase subunit
           II hits)
46         Homo sapiens eukoryotic translation elongation factor 1
           gamma (EEFIG) mRNA
47         Homo sapiens ribosomal protein L15 (RPL15) mRNA
48, 49     Human 28S ribosomal RNA gene, complete cds
50         Homo sapiens repressor of estrogen receptor activity (REA)
           mRNA, complete cds
51, 52     Homo sapiens guanine nucleotide binding protein
           (G protein), beta polypeptide 2-like 1 (GNB2L1), mRNA
55         Homo sapiens ribosomal protein S4, X-linked (RPS4X)
           mRNA
56         thymosin beta-10 [human, metastatic melanoma cell line,
           mRNA, 453nt]
57         Human thymosin beta-4 mRNA, complete cds
58         Homo sapiens U6 snRNA-associated Sm-like protein
           (LSM4), mRNA
59         Homo sapiens heterogenous nuclear ribonucleoprotein A1
           (HNRPA1) mRNA
60         Homo sapiens clone RP11-182J23 from 7p14-15, complete
           sequence
61         Human L23 mRNA for putative ribosomal protein
62         Homo sapiens hCPE-R mRNA for CPE-receptor, complete
           cds
63         Human somatic cytochrome c (HS7) processed pseudogene,
           complete cds
64         Homo sapiens HSPC198 mRNA, complete cds

[0310] Search results for additional sequences are shown in Table 3.

TABLE 3
SEQ
ID NO:		GenBank Nucleotide Database Search Results
1	54262	Human glyceraldehyde-3-phosphate dehydrogenase
		mRNA, complete cds
2	54264	Homo sapiens Chromosome 22q11.2 Cosmid Clone 2h
		In DGCR Region, complete sequence
3	54266	Human mitochondrial genome (cytochrome oxidase
		subunit II hits)
4	54269	Human mitochondrial genome
5	54270	Homo sapiens glycine cleavage system protein H
		(aminomethyl carrier) (GCSH) mRNA
7	54272	Homo sapiens cDNA FLJ11202 fis, clone
		PLACE1007746
9	54274	Homo sapiens chaperonin containing TCP1, subunit 2
		(beta) (CCT2) mRNA
10	54278	Homo sapiens lymphotoxin beta receptor (TNFR
		superfamily, member 3 (LTBR), mRNA
11	54280	Homo sapiens pyruvate dehydrogenase kinase
		isoenzyme 1 (PDK1) mRNA, complete cds
12	54283	Homo sapiens aspargine synthetase (ASNS) mRNA
13	54284	Homo sapiens mRNA for KIAA1393 protein, partial
		cds
14	54285	Homo sapiens mRNA for staufen protein, partial

Example 2

Additional cDNA Sequences from Colon Tumor Cell Subtracted Library

[0311] 1248 clones from the 391-12 colon tumor cell line subtracted library (754-1) were subjected to DNA sequence analysis by standard methodology. The cDNA sequences of 730 of those clones are disclosed herein as SEQ ID NO:66-795.

Example 3

Identification of Additional Colon Tumor Protein cDNAs from a Subtracted Serological Expression Library

[0312] A mammalian serological expression cloning system using COS-7 cells and subtracted libraries was developed to identify cDNAs overexpressed in colon tumors. Studies were performed essentially as follows: rabbit serum was generated against the membrane fraction of a colon tumor cell line and absorbed with normal human mammary epithelial cell (HMEC) lysate to remove non-specific reactivity. Colon tumor line 391-12 (CTL 391-12) cells and COS-7 cells were stained with the absorbed serum and analyzed by flow cytometry to determine if specific staining could be observed for the colon tumor line. Once specific staining was obtained, COS-7 cells were transfected with the colon tumor line subtraction 1 (CTLS1) library, generated as described in Example 1. COS-7 cells expressing antigen were isolated by selection over a magnetic column following primary staining with CTL 391-12 rabbit serum and secondary staining with magnetic bead-conjugated goat anti-rabbit IgG. Hirt DNA was isolated from the positive cells and transformed into E. coli. Plasmid DNA was purified and re-transfected into COS-7 cells for another round of selection. The selection process was repeated four times to isolate cDNAs that are specific for colon tumor cells. Individual cDNA clones were isolated from the third and fourth rounds of selection and analyzed by sequencing. Following is a detailed description of the protocol used to isolate cDNAs from this expression library.

[0313] Membrane and Antisera Generation

[0314] Membrane preparations were adapted from: Marshak, et al. “Strategies for Protein Purification and Characterization—A Lab Course Manual” Cold Spring Harbor Press 1996 pp 284-285. Briefly, 109 colon tumor 391-12 cells grown in X-vivo 15 media plus 1% rabbit sera were harvested and resuspended in 5 ml of 250 mM sucrose (Sigma, St. Louis), 10 mM HEPES pH=7.4 (Sigma), 1 mM EDTA (Sigma) and 1 COMPLETE Protease inhibitor tablet (Roche Biochemicals). The suspension was lysed by 15 strokes in a Dounce homogenizer and spun down at 800×g to remove organelles, and finally the membranes were harvested by ultracentrifugation at 100,000×g for 30 minutes. The pellet was resuspended in water and total protein (5-10 mg) was determined for this fraction. Two rabbits were immunized with this preparation in MPL adjuvant (1:1 [vol:vol] three times at monthly intervals) and immune serum was harvested post-second and third boost. Both sera were tested at a dilution of 1:500 against colon membranes and showed a strong positive signal. Freeze-thaw cell lysate was generated from 1.5×108 cells of a human mammary epithelial cell (HMEC) line. Ten ml of rabbit antisera was absorbed with this lysate (˜10 mg protein). The following experiments used absorbed antisera.

[0315] Flow Cytometry

[0316] COS-7 and colon tumor line 391-12 (CTL391-12) cells were harvested and incubated in staining buffer (5% FBS/0.1% sodium azide/1×PBS) with or without primary antibody for 30 minutes on ice. Approximately 500,000 cells were used per 50 μl staining. Cells were washed twice with staining buffer and resuspended in staining buffer containing 0.02 μg/μl fluorescein-conjugated goat anti-rabbit IgG F(ab′)2 antibody (Rockland). Cells were incubated another 30 minutes on ice, washed twice with staining buffer, and resuspended in 350 μl staining buffer with 2 μg/ml propidium iodide to stain dead cells. For each sample, data was collected from 10,000 live cells on a Becton-Dickenson FACSCalibur using CellQuest software. Flow cytometry revealed that colon tumor cells show specific staining with antiserum to colon tumor cell line membrane fraction.

[0317] Magnetic Selection

[0318] Transfection and Staining: COS-7 cells in 100 mm plates (Falcon 3003) were transfected with colon tumor cell line subtraction 1 (CTLS1) plasmid DNA using FuGENE™ 6 Transfection Reagent (RocheBiochemicals). After 40-48 hours, transfected cells were harvested by incubation with 1 ml Cell Dissociation Solution (Sigma) for 5-10 minutes at 37° C. Detached cells were washed once with staining buffer (5% FBS/0.1% sodium azide/1×PBS), pelleted at 300×g, and resuspended at a concentration of 107 cells/ml in staining buffer with 1:2000 rabbit anti-colon tumor line (391-12) membrane fraction absorbed with HMEC lysate (lot #3095L, 4-20-00). Cells were incubated 30 minutes on ice, washed twice with MACS buffer (0.5% bovine serum albumin/2 mM EDTA/1×PBS), and resuspended at a concentration of 107 cells per 80 μl MACS buffer. Added 20 μl goat anti-rabbit IgG microbeads (Miltenyi Biotech #486-02) was added per 107 cells and incubated for 30 minutes on ice.

[0319] MACS Separation: Stained cells were washed twice with MACS buffer and resuspended in 0.5 ml MACS buffer per MS+ positive selection column or 1 ml MACS buffer per LS selection column used (reagents from Miltenyi Biotec, Auburn, Calif.). A Filcons 130-33S filter was placed over each MS+ or LS column, and filters and columns were equilibrated with 500 μl (MS+) or 3 ml (LS) chilled MACS buffer. Resuspended cells were applied to each column through the filters, and the columns were washed with 3×500 μl (MS+) or 3×3 ml (LS) chilled MACS buffer. Positive cells were eluted from each column by a forceful flush of 2×1 ml (MS+) or 1×5 ml (LS) room temperature MACS buffer. Negative cells from the flow-through were pelleted and subjected to a second round of MACS separation.

[0320] Hirt DNA: Positive COS-7 cells were pooled and pelleted. Pellets were resuspended in 1-2 ml 0.6% SDS/10 mM EDTA and transferred to 1.5-ml microfuge tubes in 1 ml aliquots to lyse for 20 minutes at room temperature. 250 μl 5 M NaCl was added to each microfuge tube, samples were mixed well by inverting, and tubes were chilled in packed ice overnight. Precipitate was removed by centrifugation at >17,500×g for 10 minutes at 4° C. Supernatants were transferred to fresh tubes in aliquots of 500-600 μl and extracted twice with 25:24:1 phenol:chloroform:isoamyl alcohol. DNA in each tube was precipitated with 5 μg glycogen, 0.1×volume 3 M sodium acetate, and 0.7×volume 100% isopropanol, and centrifugation at >17,500×g for 30 minutes at 4° C. Precipitated DNA was washed once with 70% ethanol and resuspended in a total of 5 μl (1st and 2nd Hirt DNA) or 10 μl (3rd and 4th Hirt DNA) sterile water.

[0321] Transformation: 5 μl of resuspended Hirt DNA was electroporated into 100 μl ElectroMAX DH10B E. coli cells (Invitrogen™ Life Technologies). Bacteria transformed with 1st and 2nd Hirt DNA were grown overnight under antibiotic selection in 500 ml media, and plasmid DNA was isolated from 100 ml culture with a Plasmid Maxi Kit (QIAGEN). Bacteria transformed with 3rd and 4th Hirt DNA were plated out and grown overnight under antibiotic selection. Colonies were subsequently scraped off the plates and grown overnight under antibiotic selection in 500 ml media, and plasmid DNA was isolated from 100 ml culture with a Plasmid Maxi Kit (QIAGEN). Individual clones from the 3rd and 4th rounds of selection were sequenced (SEQ ID NO: 796-934) and searched against Genbank. Those sequences showing some degree of similarity with sequences in Genbank are listed in Table 4. Those showing no significant similarity to sequences in Genbank are listed in Table 5.

TABLE 4
COLON TUMOR PROTEIN cDNAS FROM A SUBTRACTED
SEROLOGICAL EXPRESSION LIBRARY SHOWING SOME
DEGREE OF SIMILARITY TO SEQUENCES IN GENBANK.
SEQ	Clone
ID NO	ID	5′	3′	GenbankID	Genbank Search Results
796	74209		.2	12006349	Homo sapiens 60S ribosomal protein L15 (EC45) mRNA,
					complete cds
798	74211	.1		12728616	Homo sapiens thymosin, beta 10 (TMSB10), mRNA
799	74212	.1		13278917	Homo sapiens, eukaryotic translation elongation factor 1
					gamma, clone MGC:4501, mRNA, complete cds
800	74213	.1		13273228	Homo sapiens mitochondrion, complete genome
801	74214	.1		12804026	Homo sapiens, ribosomal protein S7, clone MGC:10268,
					mRNA, complete cds
802	74215	.1		11136902	Human DNA sequence from clone RP11-183M13 on
					chromosome 1, complete sequence [Homo sapiens]
803	74216	.1		337384	Human 28S ribosomal RNA gene, complete cds
804	74218	.1		12653440	Homo sapiens, proliferating cell nuclear antigen, clone
					MGC:8367, mRNA, complete cds
805	74220	.1		332023	Mink cell focus-forming 247 MuLV env gene, 3′ end and
					LTR
806	74221	.1		12731525	Homo sapiens guanine nucleotide binding protein (G
					protein), betapolypeptide 2-like 1 (GNB2L1), mRNA
807	74226		.2	12804026	Homo sapiens, ribosomal protein S7, clone MGC:10268,
					mRNA, complete cds
808	74227	.1		114198983	Homo sapiens ribosomal protein L10 (RPL10), mRNA
809	74228		.2	134346409	Homo sapiens, ribosomal protein S3A, clone MGC:3883,
					mRNA, complete cds
810	74229		.2	8923000	Homo sapiens hypothetical protein FLJ11342 (FLJ11342),
					mRNA
811	74231	.1		337384	Human 28S ribosomal RNA gene, complete cds
812	74233	.1		11418676	Homo sapiens ribosomal protein S12 (RPS12), mRNA
813	74234		.2	13436409	Homo sapiens, ribosomal protein S3A, clone MGC:3883,
					mRNA, complete cds
814	74235	.1		337381	Human 28S ribosomal RNA gene
815	74238		.2	13111952	Homo sapiens, ribosomal protein S24, clone MGC:3989,
					mRNA, complete cds
816	74239	.1		12803036	Homo sapiens, glioma-amplified sequence-41, clone
					MGC:5009, mRNA, complete cds
817	74240	.1		12804728	Homo sapiens, Similar to ribosomal protein S2, clone
					MGC:3141, mRNA, complete cds
818	74245	.1		10834778	Homo sapiens PNAS-113 mRNA, complete cds
819	74249	.1		11558106	Homo sapiens mRNA for transmembrane protein (THW
					gene)
820	74251	.1		5031786	Homo sapiens imogen 38 (IMOGN38), mRNA
821	74252	.1		4504254	Homo sapiens H2A histone family, member Z (H2AFZ),
					mRNA
822	74254	.1		337384	Human 28S ribosomal RNA gene, complete cds
823	74257	.1		337384	Human 28S ribosomal RNA gene, complete cds
824	74258	.1		337384	Human 28S ribosomal RNA gene, complete cds
825	74260	.1		13375572	Homo sapiens GABA-A receptor-associated protein like 2
					(GABARAPL2) mRNA, complete cds
826	74262		.2	12655152	Homo sapiens, S100 calcium-binding protein A6
					(calcyclin), cloneMGC:2187, mRNA, compete cds
827	74263	.1		337384	Human 28S ribosomal RNA gene, complete cds
828	74265	.1		395086	H. sapiens mRNA for transcription factor BTF 3
829	74266	.1		13727523	Homo sapiens exonuclease NEF-sp mRNA, complete cds
830	74267	.1		2275186	Human BAC clone CTB-20D2 from 7q22, complete
					sequence [Homo sapiens]
831	74268	.1		337384	Human 28S ribosomal RNA gene, complete cds
832	74269		.2	12655034	Homo sapiens, ribosomal protein L4, clone MGC:2201,
					mRNA, complete cds
833	74270	.1		12731525	Homo sapiens guanine nucleotide binding protein (G
					protein), betapolypeptide 2-like 1 (GNB2L1), mRNA
834	74271	.1		337384	Human 28S ribosomal RNA gene, complete cds
835	74272	.1		12006349	Homo sapiens 60S ribosomal protein L15 (EC45) mRNA,
					complete cds
836	74273		.2	4506628	Homo sapiens ribosomal protein L29 (RPL29), mRNA
837	74274	.1		12803522	Homo sapiens, ribosomal protein L27, clone MGC:1642,
					mRNA, complete cds
838	74275	.1		9628654	Murine type C retrovirus, complete genome
839	74276	.1		12653440	Homo sapiens, proliferating cell nuclear antigen, clone
					MGC:8367, mRNA, complete cds
840	74280	.1		12653770	Homo sapiens, claudin 4, clone MGC:1778, mRNA,
					complete cds
841	74285	.1		11433251	Homo sapiens KIAA0101 gene product (KIAA0101),
					mRNA
842	74286	.1		3283923	Homo sapiens clone 24452 mRNA sequence
843	74287		.2	13111952	Homo sapiens, ribosomal protein S24, clone MGC:3989,
					mRNA, complete cds
844	74289	.1		12730302	Homo sapiens H2A histone family, member Z (H2AFZ),
					mRNA
845	74291	.1		9857564	Homo sapiens clone RP1-241P17, complete sequence
848	74295		.2	13273284	Homo sapiens mitochondrion, complete genome
852	74298	.1		5817036	Homo sapiens mRNA; cDNA DKFZp564D0164 (from
					clone DKFZp564D0164)
853	74300	.1		12742381	Homo sapiens hypothetical protein FLJ20550 (FLJ20550),
					mRNA
855	76268	.1		337384	Human 28S ribosomal RNA gene, complete cds
856	76270	.3		13436265	Homo sapiens, eukaryotic translation elongation factor 1
					beta 2, clone MGC:10551, mRNA, complete cds
858	76275	.1		11692629	Murine leukemia virus envelope protein (env) mRNA,
					complete cds
859	76277	.1		12730302	Homo sapiens H2A histone family, member Z (H2AFZ),
					mRNA
860	76279	.1		10281741	Homo sapiens clone TCBAP0781 mRNA sequence
862	76282		.2	12731525	Homo sapiens guanine nucleotide binding protein (G
					protein), betapolypeptide 2-like 1 (GNB2L1), mRNA
863	76286	.1		12653440	Homo sapiens, proliferating cell nuclear antigen, clone
					MGC:8367, mRNA, complete cds
864	76293	.1		12736773	Homo sapiens ferritin, heavy polypeptide 1 (FTH1),
					mRNA
865	76295	.1		11878115	Homo sapiens aspartyl beta-hydroxylase 2.8 kb transcript
					mRNA, complete cds; alternatively spliced
866	76297	.1		13177771	Homo sapiens, ribosomal protein, large, P0, clone
					MGC:4770, mRNA, complete cds
868	76304	.1		337384	Human 28S ribosomal RNA gene, complete cds
869	76306		.2	12804026	Homo sapiens, ribosomal protein S7, clone MGC:10268,
					mRNA, complete cds
870	76307		.2	395086	H. sapiens mRNA for transcription factor BTF 3
871	76308	.1		12742435	Homo sapiens HBV associated factor (XAP4), mRNA
872	76309	.3		12737278	Homo sapiens keratin 8 (KRT8), mRNA
873	76311	.1		12737278	Homo sapiens keratin 8 (KRT8), mRNA
874	76317		.2	12728616	Homo sapiens thymosin, beta 10 (TMSB10), mRNA
875	76319		.2	13529265	Homo sapiens, clone MGC:12520, mRNA, complete cds
876	76320	.1		12741419	Homo sapiens ribosomal protein S19 (RPS19), mRNA
877	76321		.2	8655645	Homo sapiens mRNA; cDNA DKFZp762B195 (from
					clone DKFZp762B195)
878	76327		.2	12653648	Homo sapiens, Similar to ribosomal protein L14, clone
					MGC: 1644, mRNA, complete cds
879	76328	.1		12730775	Homo sapiens MAD2 (mitotic arrest deficient, yeast,
					homolog)-like 1(MAD2L1), mRNA
880	76333	.1		337384	Human 28S ribosomal RNA gene, complete cds
882	76335	.1		12739361	Homo sapiens diaphorase (NADH/NADPH) (cytochrome
					b-5 reductase) (DIA4), mRNA
887	76343	.1		11640567	Homo sapiens MSTP030 mRNA, complete cds
888	76347	.1		12653770	Homo sapiens, claudin 4, clone MGC:1778, mRNA,
					complete cds
889	76349		.2	12736773	Homo sapiens ferritin, heavy polypeptide 1 (FTH1),
					mRNA
890	76351	.1		12653440	Homo sapiens, proliferating cell nuclear antigen, clone
					MGC:8367, mRNA, complete cds
891	76353		.2	12728616	Homo sapiens thymosin, beta 10 (TMSB10), mRNA
892	76354	.1		12729151	Homo sapiens hypothetical protein FLJ20432 (FLJ20432),
					mRNA
893	76355	.1		332023	Mink cell focus-forming 247 MuLV env gene, 3′ end and
					LTR
895	76360	.1		337381	Human 28S ribosomal RNA gene
896	76843		.2	12654114	Homo sapiens, annexin A3, clone MGC:5043, mRNA,
					complete cds
897	76844		.2	9954372	Homo sapiens zinc finger sarcoma gene short isoform
					(ZSG) mRNA, complete cds
898	76845		.2	12653770	Homo sapiens, claudin 4, clone MGC:1778, mRNA,
					complete cds
899	76846	.1		12731525	Homo sapiens guanine nucleotide binding protein (G
					protein), betapolypeptide 2-like 1 (GNB2L1), mRNA
900	76847	.1		12653770	Homo sapiens, claudin 4, clone MGC:1778, mRNA,
					complete cds
901	76850	.1		4505812	Homo sapiens dynein, cytoplasmic, light polypeptide
					(PIN), mRNA
902	76851	.1		11419204	Homo sapiens sorcin (SRI), mRNA
903	76853	.1		12653440	Homo sapiens, proliferating cell nuclear antigen, clone
					MGC:8367, mRNA, complete cds
904	76854	.1		178746	Human apurinic/apyrimidinic endonuclease (HPA1h)
					mRNA, complete cds
905	76855	.1		12003267	Homo sapiens C3orf1 mRNA, complete CDS
906	76856	.1		5453739	Homo sapiens myosin, light polypeptide, regulatory, non-
					sarcomeric (20 kD) (MLCB), mRNA
907	76857		.2	11907512	Homo sapiens mRNA for RECC, complete cds
908	76858	.1		12655072	Homo sapiens, similar to rat HREV107, clone MGC:1240,
					mRNA, complete cds
909	76859	.1		12736773	Homo sapiens ferritin, heavy polypeptide 1 (FTH1),
					mRNA
910	76860	.1		12728616	Homo sapiens thymosin, beta 10 (TMSB10), mRNA
911	76861	.1		6330699	Homo sapiens mRNA for KIAA1229 protein, partial cds
912	76862	.1		12736773	Homo sapiens ferritin, heavy polypeptide 1 (FTH1),
					mRNA
913	76863		.2	11418676	Homo sapiens ribosomal protein S12 (RPS12), mRNA
914	76864		.2	11419825	Homo sapiens ribosomal protein S4, X-linked (RPS4X),
					mRNA
916	76866	.1		12730302	Homo sapiens H2A histone family, member Z (H2AFZ),
					mRNA
917	76869	.1		12654176	Homo sapiens, clone MGC:5333, mRNA, complete cds
918	76870	.1		13543411	Homo sapiens, ribosomal protein, large, P0, clone
					MGC:3679, mRNA, complete cds
920	76872	.1		61651	Murine leukemia virus MGC13 LTR (LTR = long terminal
					repeat)
921	76873	.1		12006349	Homo sapiens 60S ribosomal protein L15(EC45) mRNA,
					complete cds
922	76874		.2	9628654	Murine type C retrovirus, complete genome
923	76875	.1		12730302	Homo sapiens H2A histone family, member Z (H2AFZ),
					mRNA
924	76876	.1		929656	H. sapiens mRNA for neutrophil gelatinase associate
					lipocalin
925	76878	.1		8894241	Human DNA sequence from clone RP5-875K15 on
					chromosome 11p12-14.1
926	76879	.1		13177771	Homo sapiens, ribosomal protein, large P0, clone
					MGC:4770, mRNA, complete cds
927	76880	.1		12736773	Homo sapiens ferritin, heavy polypeptide 1 (FTH1),
					mRNA
928	76881	.1		11425444	Homo sapiens small nuclear ribonuceloprotein D2
					polypeptide (16.5 kD) (SNRPD2), mRNA
929	76882	.1		7023162	Homo sapiens cDNA FLJ10861 fis, clone NT2RP4001571
930	76883		.2	13273284	Homo sapiens mitochondrion, complete genome
931	76884		.2	12734905	Homo sapiens argininosuccinate synthetase (ASS), mRNA
932	76886	.1		12653440	Homo sapiens, proliferating cell nuclear antigen, clone
					MGC:8367, mRNA, complete cds
933	76887	.1		522297	Mink cell focus forming virus long terminal repeat (LTR)
					RNA
846,	74293	.3	.2	12653440	Homo sapiens, proliferating cell nuclear antigen, clone
847					MGC:8367, mRNA, complete cds
849,	74296	.1 &	.2	2869145	Homo sapiens transcriptional coactivator ALY mRNA,
850,		.3		partial cds
851
883,	76337	.1 &	.2	11436804	Homo sapiens similar to dendritic cell protein (H. sapiens)
884,		.3			(LOC63319), mRNA
885

Table 5: Colon Tumor Protein cDNAs from a Subtracted Serological Expression

Library Showing no Significant Similarity to Sequence in Genbank

[0322]

	SEQ	Clone
	ID NO	ID	5′	3′
	797	74210	.1
	854	76267	.1
	857	76272	.1
	861	76281		.2
	867	76300	.1
	881	76334	.1
	886	76342	.1
	894	76357	.1
	915	76865	.1
	919	76871	.1
	934	76889		.2

Example 4

Analysis of cDNA Expression Using Microarry Technology

[0323] In additional studies, sequences disclosed herein are evaluated for overexpression in specific tumor tissues by microarray analysis. Using this approach, cDNA sequences are PCR amplified and their mRNA expression profiles in tumor and normal tissues are examined using cDNA microarray technology essentially as described (Shena, M. et al., 1995 Science 270:467-70). In brief, the clones are arrayed onto glass slides as multiple replicas, with each location corresponding to a unique cDNA clone (as many as 5500 clones can be arrayed on a single slide, or chip). Each chip is hybridized with a pair of cDNA probes that are fluorescence-labeled with Cy3 and Cy5, respectively. Typically, 1 μg of poly A+ is used to generate each cDNA probe. After hybridization, the chips are scanned and the fluorescence intensity recorded for both Cy3 and Cy5 channels. There are multiple built-in quality control steps. First, the probe quality is monitored using a panel of ubiquitously expressed genes. Secondly, the control plate also can include yeast DNA fragments of which complementary RNA may be spiked into the probe synthesis for measuring the quality of the probe and the sensitivity of the analysis. Currently, the technology offers a sensitivity of 1 in 100,000 copies of mRNA. Finally, the reproducibility of this technology can be ensured by including duplicated control cDNA elements at different locations.

Example 5

Analysis of cDNA Expression Using Real-time PCR

[0324] Real-time PCR (see Gibson et al., Genome Research 6:995-1001, 1996; Heid et al., Genome Research 6:986-994, 1996) is a technique that evaluates the level of PCR product accumulation during amplification. This technique permits quantitative evaluation of mRNA levels in multiple samples. Briefly, mRNA is extracted from tumor and normal tissue and cDNA is prepared using standard techniques. Real-time PCR is performed, for example, using a Perkin Elmer/Applied Biosystems (Foster City, Calif.) 7700 Prism instrument. Matching primers and fluorescent probes are designed for genes of interest using, for example, the primer express program provided by Perkin Elmer/Applied Biosystems (Foster City, Calif.). Optimal concentrations of primers and probes are initially determined by those of ordinary skill in the art, and control (e.g., β-actin) primers and probes are obtained commercially from, for example, Perkin Elmer/Applied Biosystems (Foster City, Calif.). To quantitate the amount of specific RNA in a sample, a standard curve is generated using a plasmid containing the gene of interest. Standard curves are generated using the Ct values determined in the real-time PCR, which are related to the initial cDNA concentration used in the assay. Standard dilutions ranging from 10-106 copies of the gene of interest are generally sufficient. In addition, a standard curve is generated for the control sequence. This permits standardization of initial RNA content of a tissue sample to the amount of control for comparison purposes.

[0325] An alternative real-time PCR procedure can be carried out as follows: The first-strand cDNA to be used in the quantitative real-time PCR is synthesized from 20 μg of total RNA that is first treated with DNase I (e.g., Amplification Grade, Gibco BRL Life Technology, Gaitherburg, Md.), using Superscript Reverse Transcriptase (RT) (e.g., Gibco BRL Life Technology, Gaitherburg, Md.). Real-time PCR is performed, for example, with a GeneAmp™ 5700 sequence detection system (PE Biosystems, Foster City, Calif.). The 5700 system uses SYBR™ green, a fluorescent dye that only intercalates into double stranded DNA, and a set of gene-specific forward and reverse primers. The increase in fluorescence is monitored during the whole amplification process. The optimal concentration of primers is determined using a checkerboard approach and a pool of cDNAs from colon tumors is used in this process. The PCR reaction is performed in 25 μl volumes that include 2.5 μl of SYBR green buffer, 2 μl of cDNA template and 2.5 μl each of the forward and reverse primers for the gene of interest. The cDNAs used for RT reactions are diluted approximately 1:10 for each gene of interest and 1:100 for the β-actin control. In order to quantitate the amount of specific cDNA (and hence initial mRNA) in the sample, a standard curve is generated for each run using the plasmid DNA containing the gene of interest. Standard curves are generated using the Ct values determined in the real-time PCR which are related to the initial cDNA concentration used in the assay. Standard dilution ranging from 20-2×106 copies of the gene of interest are used for this purpose. In addition, a standard curve is generated for β-actin ranging from 200 fg-2000 fg. This enables standardization of the initial RNA content of a tissue sample to the amount of β-actin for comparison purposes. The mean copy number for each group of tissues tested is normalized to a constant amount of β-actin, allowing the evaluation of the over-expression levels seen with each of the genes.

Example 6

Peptide Primimg of T-helper Lines

[0326] Generation of CD4+ T helper lines and identification of peptide epitopes derived from tumor-specific antigens that are capable of being recognized by CD4+ T cells in the context of HLA class II molecules, is carried out as follows:

[0327] Fifteen-mer peptides overlapping by 10 amino acids, derived from a tumor-specific antigen, are generated using standard procedures. Dendritic cells (DC) are derived from PBMC of a normal donor using GM-CSF and IL-4 by standard protocols. CD4+ T cells are generated from the same donor as the DC using MACS beads (Miltenyi Biotec, Auburn, Calif.) and negative selection. DC are pulsed overnight with pools of the 15-mer peptides, with each peptide at a final concentration of 0.25 μg/ml. Pulsed DC are washed and plated at 1×104 cells/well of 96-well V-bottom plates and purified CD4+ T cells are added at 1×105/well. Cultures are supplemented with 60 ng/ml IL-6 and 10 ng/ml IL-12 and incubated at 37° C. Cultures are restimulated as above on a weekly basis using DC generated and pulsed as above as antigen presenting cells, supplemented with 5 ng/ml IL-7 and 10 U/ml IL-2. Following 4 in vitro stimulation cycles, resulting CD4+ T cell lines (each line corresponding to one well) are tested for specific proliferation and cytokine production in response to the stimulating pools of peptide with an irrelevant pool of peptides used as a control.

Example 7

Generation of Tumor-specific CTL Lines Using In Vitro Whole-gene Priming

[0328] Using in vitro whole-gene priming with tumor antigen-vaccinia infected DC (see, for example, Yee et al, The Journal of Immunology, 157(9):4079-86, 1996), human CTL lines are derived that specifically recognize autologous fibroblasts transduced with a specific tumor antigen, as determined by interferon-γ ELISPOT analysis. Specifically, dendritic cells (DC) are differentiated from monocyte cultures derived from PBMC of normal human donors by growing for five days in RPMI medium containing 10% human serum, 50 ng/ml human GM-CSF and 30 ng/ml human IL-4. Following culture, DC are infected overnight with tumor antigen-recombinant vaccinia virus at a multiplicity of infection (M.O.I) of five, and matured overnight by the addition of 3 μg/ml CD40 ligand. Virus is then inactivated by UV irradiation. CD8+ T cells are isolated using a magnetic bead system, and priming cultures are initiated using standard culture techniques. Cultures are restimulated every 7-10 days using autologous primary fibroblasts retrovirally transduced with previously identified tumor antigens. Following four stimulation cycles, CD8+ T cell lines are identified that specifically produce interferon-γ when stimulated with tumor antigen-transduced autologous fibroblasts. Using a panel of HLA-mismatched B-LCL lines transduced with a vector expressing a tumor antigen, and measuring interferon-γ production by the CTL lines in an ELISPOT assay, the HLA restriction of the CTL lines is determined.

Example 8

Generation and Characterization of Anti-tumor Antigen Monoclonal Antibodies

[0329] Mouse monoclonal antibodies are raised against E. coli derived tumor antigen proteins as follows: Mice are immunized with Complete Freund's Adjuvant (CFA) containing 50 μg recombinant tumor protein, followed by a subsequent intraperitoneal boost with Incomplete Freund's Adjuvant (IFA) containing 10 μg recombinant protein. Three days prior to removal of the spleens, the mice are immunized intravenously with approximately 50 μg of soluble recombinant protein. The spleen of a mouse with a positive titer to the tumor antigen is removed, and a single-cell suspension made and used for fusion to SP2/O myeloma cells to generate B cell hybridomas. The supernatants from the hybrid clones are tested by ELISA for specificity to recombinant tumor protein, and epitope mapped using peptides that spanned the entire tumor protein sequence. The mAbs are also tested by flow cytometry for their ability to detect tumor protein on the surface of cells stably transfected with the cDNA encoding the tumor protein.

Example 9

Synthesis of Polypeptides

[0330] Polypeptides are synthesized on a Perkin Elmer/Applied Biosystems Division 430A peptide synthesizer using FMOC chemistry with HPTU (O-Benzotriazole-N,N,N′,N′-tetramethyluronium hexafluorophosphate) activation. A Gly-Cys-Gly sequence is attached to the amino terminus of the peptide to provide a method of conjugation, binding to an immobilized surface, or labeling of the peptide. Cleavage of the peptides from the solid support is carried out using the following cleavage mixture: trifluoroacetic acid:ethanedithiol:thioanisole:water:phenol (40:1:2:2:3). After cleaving for 2 hours, the peptides are precipitated in cold methyl-t-butyl-ether. The peptide pellets are then dissolved in water containing 0.1% trifluoroacetic acid (TFA) and lyophilized prior to purification by C18 reverse phase HPLC. A gradient of 0%-60% acetonitrile (containing 0.1% TFA) in water (containing 0.1% TFA) is used to elute the peptides. Following lyophilization of the pure fractions, the peptides are characterized using electrospray or other types of mass spectrometry and by amino acid analysis.

[0331] From the foregoing it will be appreciated that, although specific embodiments of the invention have been described herein for purposes of illustration, various modifications may be made without deviating from the spirit and scope of the invention. Accordingly, the invention is not limited except as by the appended claims.

Claims

1. An isolated polynucleotide comprising a sequence selected from the group consisting of: (a) sequences provided in SEQ ID NO:1-934; (b) complements of the sequences provided in SEQ ID NO:1-934; (c) sequences consisting of at least 20 contiguous residues of a sequence provided in SEQ ID NO:1-934; (d) sequences that hybridize to a sequence provided in SEQ ID NO:1-934, under highly stringent conditions; (e) sequences having at least 75% identity to a sequence of SEQ ID NO:1-934; (f) sequences having at least 90% identity to a sequence of SEQ ID NO:1-934; and (g) degenerate variants of a sequence provided in SEQ ID NO:1-934.

2. An isolated polypeptide comprising an amino acid sequence selected from the group consisting of: (a) sequences encoded by a polynucleotide of claim 1; and (b) sequences having at least 70% identity to a sequence encoded by a polynucleotide of claim 1; and (c) sequences having at least 90% identity to a sequence encoded by a polynucleotide of claim 1.

3. An expression vector comprising a polynucleotide of claim 1 operably linked to an expression control sequence.

4. A host cell transformed or transfected with an expression vector according to claim 3.

5. An isolated antibody, or antigen-binding fragment thereof, that specifically binds to a polypeptide of claim 2.

6. A method for detecting the presence of a cancer in a patient, comprising the steps of: (a) obtaining a biological sample from the patient; (b) contacting the biological sample with a binding agent that binds to a polypeptide of claim 2; (c) detecting in the sample an amount of polypeptide that binds to the binding agent; and (d) comparing the amount of polypeptide to a predetermined cut-off value and therefrom determining the presence of a cancer in the patient.

7. A fusion protein comprising at least one polypeptide according to claim 2.

8. An oligonucleotide that hybridizes to a sequence recited in SEQ ID NO:1-934 under highly stringent conditions.

9. A method for stimulating and/or expanding T cells specific for a tumor protein, comprising contacting T cells with at least one component selected from the group consisting of: (a) polypeptides according to claim 2; (b) polynucleotides according to claim 1; and (c) antigen-presenting cells that express a polynucleotide according to claim 1, under conditions and for a time sufficient to permit the stimulation and/or expansion of T cells.

10. An isolated T cell population, comprising T cells prepared according to the method of claim 9.

11. A composition comprising a first component selected from the group consisting of physiologically acceptable carriers and immunostimulants, and a second component selected from the group consisting of: (a) polypeptides according to claim 2; (b) polynucleotides according to claim 1;(c) antibodies according to claim 5; (d) fusion proteins according to claim 7; (e) T cell populations according to claim 10; and (f) antigen presenting cells that express a polypeptide according to claim 2.

12. A method for stimulating an immune response in a patient, comprising administering to the patient a composition of claim 11.

13. A method for the treatment of a colon cancer in a patient, comprising administering to the patient a composition of claim 11.

14. A method for determining the presence of a cancer in a patient, comprising the steps of: (a) obtaining a biological sample from the patient; (b) contacting the biological sample with an oligonucleotide according to claim 8; (c) detecting in the sample an amount of a polynucleotide that hybridizes to the oligonucleotide; and (d) compare the amount of polynucleotide that hybridizes to the oligonucleotide to a predetermined cut-off value, and therefrom determining the presence of the cancer in the patient.

15. A diagnostic kit comprising at least one oligonucleotide according to claim 8.

16. A diagnostic kit comprising at least one antibody according to claim 5 and a detection reagent, wherein the detection reagent comprises a reporter group.

17. A method for the treatment of colon cancer in a patient, comprising the steps of: (a) incubating CD4+ and/or CD8+ T cells isolated from a patient with at least one component selected from the group consisting of: (i) polypeptides according to claim 2; (ii) polynucleotides according to claim 1; and (iii) antigen presenting cells that express a polypeptide of claim 2, such that T cell proliferate; (b) administering to the patient an effective amount of the proliferated T cells, and thereby inhibiting the development of a cancer in the patient.