JP2012518609A - 癌の診断および治療のための方法および組成物 - Google Patents
癌の診断および治療のための方法および組成物 Download PDFInfo
- Publication number
- JP2012518609A JP2012518609A JP2011550483A JP2011550483A JP2012518609A JP 2012518609 A JP2012518609 A JP 2012518609A JP 2011550483 A JP2011550483 A JP 2011550483A JP 2011550483 A JP2011550483 A JP 2011550483A JP 2012518609 A JP2012518609 A JP 2012518609A
- Authority
- JP
- Japan
- Prior art keywords
- tumor antigen
- peptide
- acid sequence
- cancer
- nucleic acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 206010028980 Neoplasm Diseases 0.000 title claims abstract description 710
- 238000003745 diagnosis Methods 0.000 title claims abstract description 22
- 201000011510 cancer Diseases 0.000 title claims description 129
- 238000000034 method Methods 0.000 title claims description 108
- 238000011282 treatment Methods 0.000 title abstract description 28
- 239000000203 mixture Substances 0.000 title description 15
- 150000007523 nucleic acids Chemical class 0.000 claims abstract description 282
- 102000039446 nucleic acids Human genes 0.000 claims abstract description 235
- 108020004707 nucleic acids Proteins 0.000 claims abstract description 235
- 125000003275 alpha amino acid group Chemical group 0.000 claims abstract description 159
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 120
- 201000010099 disease Diseases 0.000 claims abstract description 112
- 230000001613 neoplastic effect Effects 0.000 claims abstract description 91
- 206010061535 Ovarian neoplasm Diseases 0.000 claims abstract description 85
- 208000020816 lung neoplasm Diseases 0.000 claims abstract description 36
- 239000000427 antigen Substances 0.000 claims description 475
- 102000036639 antigens Human genes 0.000 claims description 475
- 108091007433 antigens Proteins 0.000 claims description 475
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 368
- 210000004027 cell Anatomy 0.000 claims description 298
- 230000014509 gene expression Effects 0.000 claims description 112
- 239000012634 fragment Substances 0.000 claims description 100
- 108091054437 MHC class I family Proteins 0.000 claims description 93
- 102000043129 MHC class I family Human genes 0.000 claims description 85
- 206010033128 Ovarian cancer Diseases 0.000 claims description 66
- 210000001744 T-lymphocyte Anatomy 0.000 claims description 62
- 210000000056 organ Anatomy 0.000 claims description 52
- 210000004881 tumor cell Anatomy 0.000 claims description 52
- 108020004459 Small interfering RNA Proteins 0.000 claims description 49
- 206010061289 metastatic neoplasm Diseases 0.000 claims description 49
- 108091028043 Nucleic acid sequence Proteins 0.000 claims description 44
- 239000000126 substance Substances 0.000 claims description 42
- 230000003211 malignant effect Effects 0.000 claims description 39
- 230000001394 metastastic effect Effects 0.000 claims description 38
- 239000012472 biological sample Substances 0.000 claims description 36
- 238000001514 detection method Methods 0.000 claims description 31
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims description 29
- 239000008194 pharmaceutical composition Substances 0.000 claims description 28
- 208000005443 Circulating Neoplastic Cells Diseases 0.000 claims description 26
- 108091034117 Oligonucleotide Proteins 0.000 claims description 26
- 201000005202 lung cancer Diseases 0.000 claims description 26
- 208000009956 adenocarcinoma Diseases 0.000 claims description 24
- 230000001225 therapeutic effect Effects 0.000 claims description 23
- 238000012545 processing Methods 0.000 claims description 22
- 206010050017 Lung cancer metastatic Diseases 0.000 claims description 21
- 108091008874 T cell receptors Proteins 0.000 claims description 21
- 102000016266 T-Cell Antigen Receptors Human genes 0.000 claims description 21
- 206010041067 Small cell lung cancer Diseases 0.000 claims description 19
- 230000002611 ovarian Effects 0.000 claims description 19
- 208000000587 small cell lung carcinoma Diseases 0.000 claims description 19
- 208000005718 Stomach Neoplasms Diseases 0.000 claims description 18
- 230000000694 effects Effects 0.000 claims description 18
- 239000003446 ligand Substances 0.000 claims description 18
- 108020004414 DNA Proteins 0.000 claims description 17
- 239000012636 effector Substances 0.000 claims description 17
- 206010017758 gastric cancer Diseases 0.000 claims description 17
- 201000011549 stomach cancer Diseases 0.000 claims description 17
- 208000002154 non-small cell lung carcinoma Diseases 0.000 claims description 16
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims description 16
- 238000000338 in vitro Methods 0.000 claims description 14
- 206010009944 Colon cancer Diseases 0.000 claims description 13
- 230000002401 inhibitory effect Effects 0.000 claims description 13
- 206010006187 Breast cancer Diseases 0.000 claims description 11
- 208000026310 Breast neoplasm Diseases 0.000 claims description 11
- 206010061328 Ovarian epithelial cancer Diseases 0.000 claims description 11
- 239000003112 inhibitor Substances 0.000 claims description 11
- 238000011002 quantification Methods 0.000 claims description 11
- 229960005486 vaccine Drugs 0.000 claims description 11
- 208000036832 Adenocarcinoma of ovary Diseases 0.000 claims description 10
- 208000000453 Skin Neoplasms Diseases 0.000 claims description 10
- 208000029742 colonic neoplasm Diseases 0.000 claims description 10
- 230000001605 fetal effect Effects 0.000 claims description 10
- 208000013371 ovarian adenocarcinoma Diseases 0.000 claims description 10
- 201000006588 ovary adenocarcinoma Diseases 0.000 claims description 10
- 230000002381 testicular Effects 0.000 claims description 10
- 206010061902 Pancreatic neoplasm Diseases 0.000 claims description 9
- 241000700605 Viruses Species 0.000 claims description 9
- -1 iRNA Proteins 0.000 claims description 9
- 201000001441 melanoma Diseases 0.000 claims description 9
- 201000000849 skin cancer Diseases 0.000 claims description 9
- 206010008342 Cervix carcinoma Diseases 0.000 claims description 8
- 208000006105 Uterine Cervical Neoplasms Diseases 0.000 claims description 8
- 201000010881 cervical cancer Diseases 0.000 claims description 8
- 208000015486 malignant pancreatic neoplasm Diseases 0.000 claims description 8
- 201000002528 pancreatic cancer Diseases 0.000 claims description 8
- 208000008443 pancreatic carcinoma Diseases 0.000 claims description 8
- 206010005003 Bladder cancer Diseases 0.000 claims description 7
- 101710098119 Chaperonin GroEL 2 Proteins 0.000 claims description 7
- 208000008839 Kidney Neoplasms Diseases 0.000 claims description 7
- 206010025598 Malignant hydatidiform mole Diseases 0.000 claims description 7
- 206010038389 Renal cancer Diseases 0.000 claims description 7
- 206010039491 Sarcoma Diseases 0.000 claims description 7
- 208000024313 Testicular Neoplasms Diseases 0.000 claims description 7
- 206010057644 Testis cancer Diseases 0.000 claims description 7
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims description 7
- 208000002495 Uterine Neoplasms Diseases 0.000 claims description 7
- 208000035250 cutaneous malignant susceptibility to 1 melanoma Diseases 0.000 claims description 7
- 230000001939 inductive effect Effects 0.000 claims description 7
- 201000010982 kidney cancer Diseases 0.000 claims description 7
- 201000007270 liver cancer Diseases 0.000 claims description 7
- 208000014018 liver neoplasm Diseases 0.000 claims description 7
- 201000008824 placental choriocarcinoma Diseases 0.000 claims description 7
- 206010042863 synovial sarcoma Diseases 0.000 claims description 7
- 201000003120 testicular cancer Diseases 0.000 claims description 7
- 201000005112 urinary bladder cancer Diseases 0.000 claims description 7
- 208000010507 Adenocarcinoma of Lung Diseases 0.000 claims description 6
- 206010004146 Basal cell carcinoma Diseases 0.000 claims description 6
- 102000004190 Enzymes Human genes 0.000 claims description 6
- 108090000790 Enzymes Proteins 0.000 claims description 6
- 231100000433 cytotoxic Toxicity 0.000 claims description 6
- 230000001472 cytotoxic effect Effects 0.000 claims description 6
- 201000010536 head and neck cancer Diseases 0.000 claims description 6
- 208000014829 head and neck neoplasm Diseases 0.000 claims description 6
- 201000005249 lung adenocarcinoma Diseases 0.000 claims description 6
- 201000005243 lung squamous cell carcinoma Diseases 0.000 claims description 6
- 208000001608 teratocarcinoma Diseases 0.000 claims description 6
- 206010046766 uterine cancer Diseases 0.000 claims description 6
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims description 5
- 201000000274 Carcinosarcoma Diseases 0.000 claims description 5
- 108090000994 Catalytic RNA Proteins 0.000 claims description 5
- 102000053642 Catalytic RNA Human genes 0.000 claims description 5
- 108010021625 Immunoglobulin Fragments Proteins 0.000 claims description 5
- 102000008394 Immunoglobulin Fragments Human genes 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 208000006990 cholangiocarcinoma Diseases 0.000 claims description 5
- 208000004333 pleomorphic adenoma Diseases 0.000 claims description 5
- 230000000069 prophylactic effect Effects 0.000 claims description 5
- 108091092562 ribozyme Proteins 0.000 claims description 5
- 201000002314 small intestine cancer Diseases 0.000 claims description 5
- 206010044412 transitional cell carcinoma Diseases 0.000 claims description 5
- 206010004593 Bile duct cancer Diseases 0.000 claims description 4
- 208000019487 Clear cell papillary renal cell carcinoma Diseases 0.000 claims description 4
- 208000030808 Clear cell renal carcinoma Diseases 0.000 claims description 4
- 208000033133 Testicular seminomatous germ cell tumor Diseases 0.000 claims description 4
- 239000000074 antisense oligonucleotide Substances 0.000 claims description 4
- 238000012230 antisense oligonucleotides Methods 0.000 claims description 4
- 208000026900 bile duct neoplasm Diseases 0.000 claims description 4
- 206010073251 clear cell renal cell carcinoma Diseases 0.000 claims description 4
- 238000002405 diagnostic procedure Methods 0.000 claims description 4
- 206010073373 small intestine adenocarcinoma Diseases 0.000 claims description 4
- 210000000130 stem cell Anatomy 0.000 claims description 4
- 208000024662 testicular seminoma Diseases 0.000 claims description 4
- 208000004238 testicular teratoma Diseases 0.000 claims description 4
- 201000002312 ileal neoplasm Diseases 0.000 claims description 3
- 206010041823 squamous cell carcinoma Diseases 0.000 claims description 3
- 230000001737 promoting effect Effects 0.000 claims description 2
- JPOKAKNGULMYHZ-UILVTTEASA-N (2s)-6-amino-2-[[(2s)-2-[[(2s)-2-[[(2s)-2-[[(2s)-6-amino-2-[[(2s)-2-[[(2s)-6-amino-2-[[(2s)-6-amino-2-[[(2s)-2-amino-5-(diaminomethylideneamino)pentanoyl]amino]hexanoyl]amino]hexanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]hexanoyl]amino]-3-(4-hydroxyp Chemical compound C([C@@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CCCN=C(N)N)C1=CC=C(O)C=C1 JPOKAKNGULMYHZ-UILVTTEASA-N 0.000 claims 1
- 210000000270 basal cell Anatomy 0.000 claims 1
- 239000002435 venom Substances 0.000 claims 1
- 231100000611 venom Toxicity 0.000 claims 1
- 210000001048 venom Anatomy 0.000 claims 1
- 208000037841 lung tumor Diseases 0.000 abstract description 14
- 210000001519 tissue Anatomy 0.000 description 181
- 102000004196 processed proteins & peptides Human genes 0.000 description 64
- 108090000623 proteins and genes Proteins 0.000 description 62
- 102100038449 Claudin-6 Human genes 0.000 description 59
- 101000882898 Homo sapiens Claudin-6 Proteins 0.000 description 59
- 229920002477 rna polymer Polymers 0.000 description 47
- 235000001014 amino acid Nutrition 0.000 description 45
- 239000002773 nucleotide Substances 0.000 description 45
- 125000003729 nucleotide group Chemical group 0.000 description 45
- 210000001151 cytotoxic T lymphocyte Anatomy 0.000 description 44
- 229940024606 amino acid Drugs 0.000 description 42
- 102000004169 proteins and genes Human genes 0.000 description 42
- 150000001413 amino acids Chemical class 0.000 description 41
- 235000018102 proteins Nutrition 0.000 description 38
- 210000004443 dendritic cell Anatomy 0.000 description 25
- 108020004999 messenger RNA Proteins 0.000 description 24
- 238000004458 analytical method Methods 0.000 description 23
- 210000000170 cell membrane Anatomy 0.000 description 23
- 230000027455 binding Effects 0.000 description 22
- 210000000612 antigen-presenting cell Anatomy 0.000 description 21
- 239000000523 sample Substances 0.000 description 20
- 206010027476 Metastases Diseases 0.000 description 18
- 210000002919 epithelial cell Anatomy 0.000 description 18
- 238000003364 immunohistochemistry Methods 0.000 description 18
- 238000010186 staining Methods 0.000 description 18
- 208000006265 Renal cell carcinoma Diseases 0.000 description 17
- 230000028993 immune response Effects 0.000 description 17
- 102000053602 DNA Human genes 0.000 description 16
- 230000009401 metastasis Effects 0.000 description 16
- 210000004072 lung Anatomy 0.000 description 15
- 102000004127 Cytokines Human genes 0.000 description 14
- 108090000695 Cytokines Proteins 0.000 description 14
- JLCPHMBAVCMARE-UHFFFAOYSA-N [3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methyl [5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate Polymers Cc1cn(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c3nc(N)[nH]c4=O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3CO)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cc(C)c(=O)[nH]c3=O)n3cc(C)c(=O)[nH]c3=O)n3ccc(N)nc3=O)n3cc(C)c(=O)[nH]c3=O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)O2)c(=O)[nH]c1=O JLCPHMBAVCMARE-UHFFFAOYSA-N 0.000 description 14
- 238000004519 manufacturing process Methods 0.000 description 14
- 230000036755 cellular response Effects 0.000 description 13
- 230000003053 immunization Effects 0.000 description 13
- 238000009169 immunotherapy Methods 0.000 description 13
- 238000001727 in vivo Methods 0.000 description 13
- 210000004698 lymphocyte Anatomy 0.000 description 13
- 230000001105 regulatory effect Effects 0.000 description 13
- 238000006467 substitution reaction Methods 0.000 description 13
- 238000005259 measurement Methods 0.000 description 12
- 239000013612 plasmid Substances 0.000 description 12
- 230000004044 response Effects 0.000 description 12
- 238000002649 immunization Methods 0.000 description 11
- 239000002502 liposome Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- 102000008949 Histocompatibility Antigens Class I Human genes 0.000 description 10
- 239000002671 adjuvant Substances 0.000 description 10
- 230000000259 anti-tumor effect Effects 0.000 description 10
- 238000013459 approach Methods 0.000 description 10
- 210000002443 helper t lymphocyte Anatomy 0.000 description 10
- 210000004185 liver Anatomy 0.000 description 10
- 238000003753 real-time PCR Methods 0.000 description 10
- 241000894007 species Species 0.000 description 10
- 230000000692 anti-sense effect Effects 0.000 description 9
- 230000000890 antigenic effect Effects 0.000 description 9
- 230000000295 complement effect Effects 0.000 description 9
- 210000001672 ovary Anatomy 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 230000004936 stimulating effect Effects 0.000 description 9
- 238000012546 transfer Methods 0.000 description 9
- 238000002255 vaccination Methods 0.000 description 9
- 230000010056 antibody-dependent cellular cytotoxicity Effects 0.000 description 8
- 239000013604 expression vector Substances 0.000 description 8
- 210000000987 immune system Anatomy 0.000 description 8
- 210000002540 macrophage Anatomy 0.000 description 8
- 230000004048 modification Effects 0.000 description 8
- 238000012986 modification Methods 0.000 description 8
- 210000005059 placental tissue Anatomy 0.000 description 8
- 210000002536 stromal cell Anatomy 0.000 description 8
- 108091026890 Coding region Proteins 0.000 description 7
- 230000002159 abnormal effect Effects 0.000 description 7
- 210000003719 b-lymphocyte Anatomy 0.000 description 7
- 210000004369 blood Anatomy 0.000 description 7
- 239000008280 blood Substances 0.000 description 7
- 230000009089 cytolysis Effects 0.000 description 7
- 238000012217 deletion Methods 0.000 description 7
- 230000037430 deletion Effects 0.000 description 7
- 210000001165 lymph node Anatomy 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 230000035755 proliferation Effects 0.000 description 7
- 230000004043 responsiveness Effects 0.000 description 7
- 210000003491 skin Anatomy 0.000 description 7
- 238000013518 transcription Methods 0.000 description 7
- 210000003932 urinary bladder Anatomy 0.000 description 7
- 239000013598 vector Substances 0.000 description 7
- 201000009030 Carcinoma Diseases 0.000 description 6
- 108010033276 Peptide Fragments Proteins 0.000 description 6
- 102000007079 Peptide Fragments Human genes 0.000 description 6
- 230000005867 T cell response Effects 0.000 description 6
- IQFYYKKMVGJFEH-XLPZGREQSA-N Thymidine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](O)C1 IQFYYKKMVGJFEH-XLPZGREQSA-N 0.000 description 6
- 238000001574 biopsy Methods 0.000 description 6
- 210000004556 brain Anatomy 0.000 description 6
- 230000030833 cell death Effects 0.000 description 6
- 230000004540 complement-dependent cytotoxicity Effects 0.000 description 6
- 239000002299 complementary DNA Substances 0.000 description 6
- 210000004696 endometrium Anatomy 0.000 description 6
- 210000000981 epithelium Anatomy 0.000 description 6
- 238000009396 hybridization Methods 0.000 description 6
- 210000003405 ileum Anatomy 0.000 description 6
- 239000002955 immunomodulating agent Substances 0.000 description 6
- 238000011065 in-situ storage Methods 0.000 description 6
- 230000006698 induction Effects 0.000 description 6
- 238000003780 insertion Methods 0.000 description 6
- 230000037431 insertion Effects 0.000 description 6
- 210000003734 kidney Anatomy 0.000 description 6
- 230000001404 mediated effect Effects 0.000 description 6
- 210000001616 monocyte Anatomy 0.000 description 6
- 210000003101 oviduct Anatomy 0.000 description 6
- 108020003175 receptors Proteins 0.000 description 6
- 102000005962 receptors Human genes 0.000 description 6
- 210000000664 rectum Anatomy 0.000 description 6
- 239000013074 reference sample Substances 0.000 description 6
- 210000002784 stomach Anatomy 0.000 description 6
- 238000002560 therapeutic procedure Methods 0.000 description 6
- 230000035897 transcription Effects 0.000 description 6
- 239000013603 viral vector Substances 0.000 description 6
- 230000004913 activation Effects 0.000 description 5
- 238000007792 addition Methods 0.000 description 5
- 210000004100 adrenal gland Anatomy 0.000 description 5
- 230000006907 apoptotic process Effects 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 208000003373 basosquamous carcinoma Diseases 0.000 description 5
- 230000004663 cell proliferation Effects 0.000 description 5
- 238000003776 cleavage reaction Methods 0.000 description 5
- 239000003184 complementary RNA Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000003814 drug Substances 0.000 description 5
- 210000001198 duodenum Anatomy 0.000 description 5
- 210000004907 gland Anatomy 0.000 description 5
- 230000028996 humoral immune response Effects 0.000 description 5
- 210000002865 immune cell Anatomy 0.000 description 5
- 229940121354 immunomodulator Drugs 0.000 description 5
- 230000005764 inhibitory process Effects 0.000 description 5
- 230000003834 intracellular effect Effects 0.000 description 5
- 210000000496 pancreas Anatomy 0.000 description 5
- 230000002062 proliferating effect Effects 0.000 description 5
- 125000002652 ribonucleotide group Chemical group 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 230000007017 scission Effects 0.000 description 5
- 230000000638 stimulation Effects 0.000 description 5
- 230000008685 targeting Effects 0.000 description 5
- 238000013519 translation Methods 0.000 description 5
- 241001430294 unidentified retrovirus Species 0.000 description 5
- 108010047041 Complementarity Determining Regions Proteins 0.000 description 4
- 241000701022 Cytomegalovirus Species 0.000 description 4
- AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 description 4
- 108010087819 Fc receptors Proteins 0.000 description 4
- 102000009109 Fc receptors Human genes 0.000 description 4
- 108010017213 Granulocyte-Macrophage Colony-Stimulating Factor Proteins 0.000 description 4
- 102100039620 Granulocyte-macrophage colony-stimulating factor Human genes 0.000 description 4
- 108010054477 Immunoglobulin Fab Fragments Proteins 0.000 description 4
- 108091028664 Ribonucleotide Proteins 0.000 description 4
- 125000000539 amino acid group Chemical group 0.000 description 4
- 239000002246 antineoplastic agent Substances 0.000 description 4
- 210000000481 breast Anatomy 0.000 description 4
- 231100000504 carcinogenesis Toxicity 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 238000002512 chemotherapy Methods 0.000 description 4
- 208000009060 clear cell adenocarcinoma Diseases 0.000 description 4
- 230000024203 complement activation Effects 0.000 description 4
- 230000000139 costimulatory effect Effects 0.000 description 4
- 230000034994 death Effects 0.000 description 4
- 231100000517 death Toxicity 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 238000013461 design Methods 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 230000004069 differentiation Effects 0.000 description 4
- 238000010494 dissociation reaction Methods 0.000 description 4
- 230000005593 dissociations Effects 0.000 description 4
- 210000003238 esophagus Anatomy 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 230000006870 function Effects 0.000 description 4
- 210000000232 gallbladder Anatomy 0.000 description 4
- 230000002068 genetic effect Effects 0.000 description 4
- 230000001900 immune effect Effects 0.000 description 4
- 230000036039 immunity Effects 0.000 description 4
- 230000002163 immunogen Effects 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- 238000002372 labelling Methods 0.000 description 4
- 210000002429 large intestine Anatomy 0.000 description 4
- 208000037819 metastatic cancer Diseases 0.000 description 4
- 208000011575 metastatic malignant neoplasm Diseases 0.000 description 4
- 210000005259 peripheral blood Anatomy 0.000 description 4
- 239000011886 peripheral blood Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- 239000002336 ribonucleotide Substances 0.000 description 4
- 208000011581 secondary neoplasm Diseases 0.000 description 4
- 210000002027 skeletal muscle Anatomy 0.000 description 4
- 210000000952 spleen Anatomy 0.000 description 4
- 235000000346 sugar Nutrition 0.000 description 4
- 238000001356 surgical procedure Methods 0.000 description 4
- 230000004083 survival effect Effects 0.000 description 4
- 239000003053 toxin Substances 0.000 description 4
- 231100000765 toxin Toxicity 0.000 description 4
- 108700012359 toxins Proteins 0.000 description 4
- 241000701161 unidentified adenovirus Species 0.000 description 4
- 238000001262 western blot Methods 0.000 description 4
- 108091032973 (ribonucleotides)n+m Proteins 0.000 description 3
- 102000040650 (ribonucleotides)n+m Human genes 0.000 description 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 3
- 108020005544 Antisense RNA Proteins 0.000 description 3
- 108020004394 Complementary RNA Proteins 0.000 description 3
- 206010061818 Disease progression Diseases 0.000 description 3
- 206010014733 Endometrial cancer Diseases 0.000 description 3
- 206010014759 Endometrial neoplasm Diseases 0.000 description 3
- 241000282412 Homo Species 0.000 description 3
- 108060003951 Immunoglobulin Proteins 0.000 description 3
- 102000001706 Immunoglobulin Fab Fragments Human genes 0.000 description 3
- 102100037850 Interferon gamma Human genes 0.000 description 3
- 108010074328 Interferon-gamma Proteins 0.000 description 3
- 108010002350 Interleukin-2 Proteins 0.000 description 3
- 108010052285 Membrane Proteins Proteins 0.000 description 3
- 241000699670 Mus sp. Species 0.000 description 3
- 208000034176 Neoplasms, Germ Cell and Embryonal Diseases 0.000 description 3
- 206010029260 Neuroblastoma Diseases 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 206010060862 Prostate cancer Diseases 0.000 description 3
- 108020004511 Recombinant DNA Proteins 0.000 description 3
- 230000024932 T cell mediated immunity Effects 0.000 description 3
- 206010043276 Teratoma Diseases 0.000 description 3
- 230000030741 antigen processing and presentation Effects 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- IQFYYKKMVGJFEH-UHFFFAOYSA-N beta-L-thymidine Natural products O=C1NC(=O)C(C)=CN1C1OC(CO)C(O)C1 IQFYYKKMVGJFEH-UHFFFAOYSA-N 0.000 description 3
- 238000004422 calculation algorithm Methods 0.000 description 3
- 230000022534 cell killing Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000010367 cloning Methods 0.000 description 3
- 239000013068 control sample Substances 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 230000001461 cytolytic effect Effects 0.000 description 3
- 230000003013 cytotoxicity Effects 0.000 description 3
- 231100000135 cytotoxicity Toxicity 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 230000005750 disease progression Effects 0.000 description 3
- 230000012010 growth Effects 0.000 description 3
- 230000005847 immunogenicity Effects 0.000 description 3
- 102000018358 immunoglobulin Human genes 0.000 description 3
- 230000002584 immunomodulator Effects 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 230000009545 invasion Effects 0.000 description 3
- 201000005296 lung carcinoma Diseases 0.000 description 3
- 230000036210 malignancy Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000008883 metastatic behaviour Effects 0.000 description 3
- 201000010279 papillary renal cell carcinoma Diseases 0.000 description 3
- 210000004303 peritoneum Anatomy 0.000 description 3
- 210000002826 placenta Anatomy 0.000 description 3
- 230000003169 placental effect Effects 0.000 description 3
- 102000040430 polynucleotide Human genes 0.000 description 3
- 108091033319 polynucleotide Proteins 0.000 description 3
- 239000002157 polynucleotide Substances 0.000 description 3
- 229920001184 polypeptide Polymers 0.000 description 3
- 239000013641 positive control Substances 0.000 description 3
- 238000004393 prognosis Methods 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 238000012216 screening Methods 0.000 description 3
- 230000004614 tumor growth Effects 0.000 description 3
- 210000004291 uterus Anatomy 0.000 description 3
- 238000011179 visual inspection Methods 0.000 description 3
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 2
- IQFYYKKMVGJFEH-BIIVOSGPSA-N 2'-deoxythymidine Natural products O=C1NC(=O)C(C)=CN1[C@@H]1O[C@@H](CO)[C@@H](O)C1 IQFYYKKMVGJFEH-BIIVOSGPSA-N 0.000 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- 108010032595 Antibody Binding Sites Proteins 0.000 description 2
- 206010003445 Ascites Diseases 0.000 description 2
- 208000003174 Brain Neoplasms Diseases 0.000 description 2
- 241000283707 Capra Species 0.000 description 2
- 206010057248 Cell death Diseases 0.000 description 2
- 208000006332 Choriocarcinoma Diseases 0.000 description 2
- 208000001333 Colorectal Neoplasms Diseases 0.000 description 2
- 238000002965 ELISA Methods 0.000 description 2
- 102000018651 Epithelial Cell Adhesion Molecule Human genes 0.000 description 2
- 108010066687 Epithelial Cell Adhesion Molecule Proteins 0.000 description 2
- 208000000461 Esophageal Neoplasms Diseases 0.000 description 2
- 108010008177 Fd immunoglobulins Proteins 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 102100031573 Hematopoietic progenitor cell antigen CD34 Human genes 0.000 description 2
- 108010088652 Histocompatibility Antigens Class I Proteins 0.000 description 2
- 101000777663 Homo sapiens Hematopoietic progenitor cell antigen CD34 Proteins 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 108010065805 Interleukin-12 Proteins 0.000 description 2
- 102000013462 Interleukin-12 Human genes 0.000 description 2
- 208000005016 Intestinal Neoplasms Diseases 0.000 description 2
- FBOZXECLQNJBKD-ZDUSSCGKSA-N L-methotrexate Chemical compound C=1N=C2N=C(N)N=C(N)C2=NC=1CN(C)C1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 FBOZXECLQNJBKD-ZDUSSCGKSA-N 0.000 description 2
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 2
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 2
- 206010025323 Lymphomas Diseases 0.000 description 2
- 102000043131 MHC class II family Human genes 0.000 description 2
- 108700018351 Major Histocompatibility Complex Proteins 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 238000000636 Northern blotting Methods 0.000 description 2
- 101710163270 Nuclease Proteins 0.000 description 2
- 108020004711 Nucleic Acid Probes Proteins 0.000 description 2
- 206010030155 Oesophageal carcinoma Diseases 0.000 description 2
- 108010038807 Oligopeptides Proteins 0.000 description 2
- 102000015636 Oligopeptides Human genes 0.000 description 2
- 208000007571 Ovarian Epithelial Carcinoma Diseases 0.000 description 2
- 206010058823 Ovarian mass Diseases 0.000 description 2
- 102000004503 Perforin Human genes 0.000 description 2
- 108010056995 Perforin Proteins 0.000 description 2
- KHGNFPUMBJSZSM-UHFFFAOYSA-N Perforine Natural products COC1=C2CCC(O)C(CCC(C)(C)O)(OC)C2=NC2=C1C=CO2 KHGNFPUMBJSZSM-UHFFFAOYSA-N 0.000 description 2
- 206010036790 Productive cough Diseases 0.000 description 2
- 208000000236 Prostatic Neoplasms Diseases 0.000 description 2
- 108010029485 Protein Isoforms Proteins 0.000 description 2
- 102000001708 Protein Isoforms Human genes 0.000 description 2
- 201000010208 Seminoma Diseases 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 108091081024 Start codon Proteins 0.000 description 2
- 241000282887 Suidae Species 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 108091036066 Three prime untranslated region Proteins 0.000 description 2
- 208000024770 Thyroid neoplasm Diseases 0.000 description 2
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 2
- 108060008682 Tumor Necrosis Factor Proteins 0.000 description 2
- 102000000852 Tumor Necrosis Factor-alpha Human genes 0.000 description 2
- 241000700618 Vaccinia virus Species 0.000 description 2
- 210000001015 abdomen Anatomy 0.000 description 2
- 230000003187 abdominal effect Effects 0.000 description 2
- RJURFGZVJUQBHK-UHFFFAOYSA-N actinomycin D Natural products CC1OC(=O)C(C(C)C)N(C)C(=O)CN(C)C(=O)C2CCCN2C(=O)C(C(C)C)NC(=O)C1NC(=O)C1=C(N)C(=O)C(C)=C2OC(C(C)=CC=C3C(=O)NC4C(=O)NC(C(N5CCCC5C(=O)N(C)CC(=O)N(C)C(C(C)C)C(=O)OC4C)=O)C(C)C)=C3N=C21 RJURFGZVJUQBHK-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 description 2
- 238000010171 animal model Methods 0.000 description 2
- 230000005809 anti-tumor immunity Effects 0.000 description 2
- 230000006023 anti-tumor response Effects 0.000 description 2
- 238000011398 antitumor immunotherapy Methods 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 210000001124 body fluid Anatomy 0.000 description 2
- 239000010839 body fluid Substances 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- 210000001185 bone marrow Anatomy 0.000 description 2
- 210000003123 bronchiole Anatomy 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 238000009566 cancer vaccine Methods 0.000 description 2
- 229940022399 cancer vaccine Drugs 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- DQLATGHUWYMOKM-UHFFFAOYSA-L cisplatin Chemical compound N[Pt](N)(Cl)Cl DQLATGHUWYMOKM-UHFFFAOYSA-L 0.000 description 2
- 229960004316 cisplatin Drugs 0.000 description 2
- 210000001072 colon Anatomy 0.000 description 2
- 238000002591 computed tomography Methods 0.000 description 2
- 230000004940 costimulation Effects 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000005547 deoxyribonucleotide Substances 0.000 description 2
- 125000002637 deoxyribonucleotide group Chemical group 0.000 description 2
- 238000001212 derivatisation Methods 0.000 description 2
- 238000004520 electroporation Methods 0.000 description 2
- 230000002255 enzymatic effect Effects 0.000 description 2
- 201000004101 esophageal cancer Diseases 0.000 description 2
- 210000003527 eukaryotic cell Anatomy 0.000 description 2
- 239000013613 expression plasmid Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000002866 fluorescence resonance energy transfer Methods 0.000 description 2
- 230000000762 glandular Effects 0.000 description 2
- 210000003958 hematopoietic stem cell Anatomy 0.000 description 2
- 210000004408 hybridoma Anatomy 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 210000003297 immature b lymphocyte Anatomy 0.000 description 2
- 210000002861 immature t-cell Anatomy 0.000 description 2
- 230000002519 immonomodulatory effect Effects 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 238000001802 infusion Methods 0.000 description 2
- 229940117681 interleukin-12 Drugs 0.000 description 2
- 201000002313 intestinal cancer Diseases 0.000 description 2
- 210000000936 intestine Anatomy 0.000 description 2
- 230000003902 lesion Effects 0.000 description 2
- 231100000518 lethal Toxicity 0.000 description 2
- 230000001665 lethal effect Effects 0.000 description 2
- 210000000265 leukocyte Anatomy 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 239000006166 lysate Substances 0.000 description 2
- 230000005291 magnetic effect Effects 0.000 description 2
- 239000006249 magnetic particle Substances 0.000 description 2
- 210000004962 mammalian cell Anatomy 0.000 description 2
- 230000035800 maturation Effects 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 210000004379 membrane Anatomy 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 210000003716 mesoderm Anatomy 0.000 description 2
- 229960000485 methotrexate Drugs 0.000 description 2
- 239000002853 nucleic acid probe Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 229940124276 oligodeoxyribonucleotide Drugs 0.000 description 2
- 230000036961 partial effect Effects 0.000 description 2
- 230000037361 pathway Effects 0.000 description 2
- 229930192851 perforin Natural products 0.000 description 2
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 230000004962 physiological condition Effects 0.000 description 2
- 238000003752 polymerase chain reaction Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 210000001236 prokaryotic cell Anatomy 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 230000002285 radioactive effect Effects 0.000 description 2
- 238000001959 radiotherapy Methods 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 238000003757 reverse transcription PCR Methods 0.000 description 2
- 229930182490 saponin Natural products 0.000 description 2
- 150000007949 saponins Chemical class 0.000 description 2
- 235000017709 saponins Nutrition 0.000 description 2
- 230000009870 specific binding Effects 0.000 description 2
- 210000003802 sputum Anatomy 0.000 description 2
- 208000024794 sputum Diseases 0.000 description 2
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N squalane Chemical compound CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- 230000020382 suppression by virus of host antigen processing and presentation of peptide antigen via MHC class I Effects 0.000 description 2
- 229940124597 therapeutic agent Drugs 0.000 description 2
- 201000002510 thyroid cancer Diseases 0.000 description 2
- WYWHKKSPHMUBEB-UHFFFAOYSA-N tioguanine Chemical compound N1C(N)=NC(=S)C2=C1N=CN2 WYWHKKSPHMUBEB-UHFFFAOYSA-N 0.000 description 2
- 230000001875 tumorinhibitory effect Effects 0.000 description 2
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
- MZOFCQQQCNRIBI-VMXHOPILSA-N (3s)-4-[[(2s)-1-[[(2s)-1-[[(1s)-1-carboxy-2-hydroxyethyl]amino]-4-methyl-1-oxopentan-2-yl]amino]-5-(diaminomethylideneamino)-1-oxopentan-2-yl]amino]-3-[[2-[[(2s)-2,6-diaminohexanoyl]amino]acetyl]amino]-4-oxobutanoic acid Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@@H](N)CCCCN MZOFCQQQCNRIBI-VMXHOPILSA-N 0.000 description 1
- FDKXTQMXEQVLRF-ZHACJKMWSA-N (E)-dacarbazine Chemical compound CN(C)\N=N\c1[nH]cnc1C(N)=O FDKXTQMXEQVLRF-ZHACJKMWSA-N 0.000 description 1
- PNDPGZBMCMUPRI-HVTJNCQCSA-N 10043-66-0 Chemical compound [131I][131I] PNDPGZBMCMUPRI-HVTJNCQCSA-N 0.000 description 1
- PXFBZOLANLWPMH-UHFFFAOYSA-N 16-Epiaffinine Natural products C1C(C2=CC=CC=C2N2)=C2C(=O)CC2C(=CC)CN(C)C1C2CO PXFBZOLANLWPMH-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical group CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- WUIABRMSWOKTOF-OYALTWQYSA-N 3-[[2-[2-[2-[[(2s,3r)-2-[[(2s,3s,4r)-4-[[(2s,3r)-2-[[6-amino-2-[(1s)-3-amino-1-[[(2s)-2,3-diamino-3-oxopropyl]amino]-3-oxopropyl]-5-methylpyrimidine-4-carbonyl]amino]-3-[(2r,3s,4s,5s,6s)-3-[(2r,3s,4s,5r,6r)-4-carbamoyloxy-3,5-dihydroxy-6-(hydroxymethyl)ox Chemical compound OS([O-])(=O)=O.N([C@H](C(=O)N[C@H](C)[C@@H](O)[C@H](C)C(=O)N[C@@H]([C@H](O)C)C(=O)NCCC=1SC=C(N=1)C=1SC=C(N=1)C(=O)NCCC[S+](C)C)[C@@H](O[C@H]1[C@H]([C@@H](O)[C@H](O)[C@H](CO)O1)O[C@@H]1[C@H]([C@@H](OC(N)=O)[C@H](O)[C@@H](CO)O1)O)C=1NC=NC=1)C(=O)C1=NC([C@H](CC(N)=O)NC[C@H](N)C(N)=O)=NC(N)=C1C WUIABRMSWOKTOF-OYALTWQYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- FVFVNNKYKYZTJU-UHFFFAOYSA-N 6-chloro-1,3,5-triazine-2,4-diamine Chemical group NC1=NC(N)=NC(Cl)=N1 FVFVNNKYKYZTJU-UHFFFAOYSA-N 0.000 description 1
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical class CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 1
- 206010068873 Adenosquamous cell carcinoma Diseases 0.000 description 1
- 208000006468 Adrenal Cortex Neoplasms Diseases 0.000 description 1
- 241000589158 Agrobacterium Species 0.000 description 1
- 101710117290 Aldo-keto reductase family 1 member C4 Proteins 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- DCXYFEDJOCDNAF-UHFFFAOYSA-N Asparagine Natural products OC(=O)C(N)CC(N)=O DCXYFEDJOCDNAF-UHFFFAOYSA-N 0.000 description 1
- 241000711404 Avian avulavirus 1 Species 0.000 description 1
- 102000036365 BRCA1 Human genes 0.000 description 1
- 108700020463 BRCA1 Proteins 0.000 description 1
- 101150072950 BRCA1 gene Proteins 0.000 description 1
- 102000052609 BRCA2 Human genes 0.000 description 1
- 108700020462 BRCA2 Proteins 0.000 description 1
- 108020000946 Bacterial DNA Proteins 0.000 description 1
- DWRXFEITVBNRMK-UHFFFAOYSA-N Beta-D-1-Arabinofuranosylthymine Natural products O=C1NC(=O)C(C)=CN1C1C(O)C(O)C(CO)O1 DWRXFEITVBNRMK-UHFFFAOYSA-N 0.000 description 1
- 108010006654 Bleomycin Proteins 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 1
- 101150008921 Brca2 gene Proteins 0.000 description 1
- COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 description 1
- 239000002126 C01EB10 - Adenosine Substances 0.000 description 1
- 108010029697 CD40 Ligand Proteins 0.000 description 1
- 101150013553 CD40 gene Proteins 0.000 description 1
- 102100032937 CD40 ligand Human genes 0.000 description 1
- 102100032912 CD44 antigen Human genes 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 241000282472 Canis lupus familiaris Species 0.000 description 1
- 108090000565 Capsid Proteins Proteins 0.000 description 1
- 208000005623 Carcinogenesis Diseases 0.000 description 1
- DLGOEMSEDOSKAD-UHFFFAOYSA-N Carmustine Chemical compound ClCCNC(=O)N(N=O)CCCl DLGOEMSEDOSKAD-UHFFFAOYSA-N 0.000 description 1
- 102100023321 Ceruloplasmin Human genes 0.000 description 1
- 102000019034 Chemokines Human genes 0.000 description 1
- 108010012236 Chemokines Proteins 0.000 description 1
- JWBOIMRXGHLCPP-UHFFFAOYSA-N Chloditan Chemical compound C=1C=CC=C(Cl)C=1C(C(Cl)Cl)C1=CC=C(Cl)C=C1 JWBOIMRXGHLCPP-UHFFFAOYSA-N 0.000 description 1
- 108010049048 Cholera Toxin Proteins 0.000 description 1
- 102000009016 Cholera Toxin Human genes 0.000 description 1
- GUTLYIVDDKVIGB-OUBTZVSYSA-N Cobalt-60 Chemical compound [60Co] GUTLYIVDDKVIGB-OUBTZVSYSA-N 0.000 description 1
- 108020004705 Codon Proteins 0.000 description 1
- 102000016917 Complement C1 Human genes 0.000 description 1
- 108010028774 Complement C1 Proteins 0.000 description 1
- 102000000989 Complement System Proteins Human genes 0.000 description 1
- 108010069112 Complement System Proteins Proteins 0.000 description 1
- 241000699800 Cricetinae Species 0.000 description 1
- CMSMOCZEIVJLDB-UHFFFAOYSA-N Cyclophosphamide Chemical compound ClCCN(CCCl)P1(=O)NCCCO1 CMSMOCZEIVJLDB-UHFFFAOYSA-N 0.000 description 1
- PMATZTZNYRCHOR-CGLBZJNRSA-N Cyclosporin A Chemical compound CC[C@@H]1NC(=O)[C@H]([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C(C)C)NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O PMATZTZNYRCHOR-CGLBZJNRSA-N 0.000 description 1
- 108010036949 Cyclosporine Proteins 0.000 description 1
- HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 description 1
- 108010092160 Dactinomycin Proteins 0.000 description 1
- 241000702421 Dependoparvovirus Species 0.000 description 1
- 241000255581 Drosophila <fruit fly, genus> Species 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 102100025137 Early activation antigen CD69 Human genes 0.000 description 1
- 208000005431 Endometrioid Carcinoma Diseases 0.000 description 1
- 201000009273 Endometriosis Diseases 0.000 description 1
- 241000283086 Equidae Species 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 102000010834 Extracellular Matrix Proteins Human genes 0.000 description 1
- 108010037362 Extracellular Matrix Proteins Proteins 0.000 description 1
- 108050001049 Extracellular proteins Proteins 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 229920001917 Ficoll Polymers 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- GHASVSINZRGABV-UHFFFAOYSA-N Fluorouracil Chemical compound FC1=CNC(=O)NC1=O GHASVSINZRGABV-UHFFFAOYSA-N 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- 108700004714 Gelonium multiflorum GEL Proteins 0.000 description 1
- 108700028146 Genetic Enhancer Elements Proteins 0.000 description 1
- 108700039691 Genetic Promoter Regions Proteins 0.000 description 1
- 208000021309 Germ cell tumor Diseases 0.000 description 1
- 208000032612 Glial tumor Diseases 0.000 description 1
- 206010018338 Glioma Diseases 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- NYHBQMYGNKIUIF-UUOKFMHZSA-N Guanosine Chemical class C1=NC=2C(=O)NC(N)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O NYHBQMYGNKIUIF-UUOKFMHZSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 108010027412 Histocompatibility Antigens Class II Proteins 0.000 description 1
- 102000018713 Histocompatibility Antigens Class II Human genes 0.000 description 1
- 101000690301 Homo sapiens Aldo-keto reductase family 1 member C4 Proteins 0.000 description 1
- 101000868273 Homo sapiens CD44 antigen Proteins 0.000 description 1
- 101000934374 Homo sapiens Early activation antigen CD69 Proteins 0.000 description 1
- 101000935587 Homo sapiens Flavin reductase (NADPH) Proteins 0.000 description 1
- 101000930801 Homo sapiens HLA class II histocompatibility antigen, DQ alpha 2 chain Proteins 0.000 description 1
- 101000959820 Homo sapiens Interferon alpha-1/13 Proteins 0.000 description 1
- 101001116548 Homo sapiens Protein CBFA2T1 Proteins 0.000 description 1
- 101000914484 Homo sapiens T-lymphocyte activation antigen CD80 Proteins 0.000 description 1
- 101000611183 Homo sapiens Tumor necrosis factor Proteins 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 108010067060 Immunoglobulin Variable Region Proteins 0.000 description 1
- 108010047761 Interferon-alpha Proteins 0.000 description 1
- 102000006992 Interferon-alpha Human genes 0.000 description 1
- 108010002352 Interleukin-1 Proteins 0.000 description 1
- ZCYVEMRRCGMTRW-AHCXROLUSA-N Iodine-123 Chemical compound [123I] ZCYVEMRRCGMTRW-AHCXROLUSA-N 0.000 description 1
- OIRFJRBSRORBCM-UHFFFAOYSA-N Iopanoic acid Chemical compound CCC(C(O)=O)CC1=C(I)C=C(I)C(N)=C1I OIRFJRBSRORBCM-UHFFFAOYSA-N 0.000 description 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
- DCXYFEDJOCDNAF-REOHCLBHSA-N L-asparagine Chemical compound OC(=O)[C@@H](N)CC(N)=O DCXYFEDJOCDNAF-REOHCLBHSA-N 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 1
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 1
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 description 1
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 1
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 description 1
- 206010023774 Large cell lung cancer Diseases 0.000 description 1
- 108091026898 Leader sequence (mRNA) Proteins 0.000 description 1
- 108090001090 Lectins Proteins 0.000 description 1
- 102000004856 Lectins Human genes 0.000 description 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 1
- GQYIWUVLTXOXAJ-UHFFFAOYSA-N Lomustine Chemical compound ClCCN(N=O)C(=O)NC1CCCCC1 GQYIWUVLTXOXAJ-UHFFFAOYSA-N 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 108091054438 MHC class II family Proteins 0.000 description 1
- 208000030070 Malignant epithelial tumor of ovary Diseases 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 102000018697 Membrane Proteins Human genes 0.000 description 1
- BAQCROVBDNBEEB-UBYUBLNFSA-N Metrizamide Chemical compound CC(=O)N(C)C1=C(I)C(NC(C)=O)=C(I)C(C(=O)N[C@@H]2[C@H]([C@H](O)[C@@H](CO)OC2O)O)=C1I BAQCROVBDNBEEB-UBYUBLNFSA-N 0.000 description 1
- 108010063954 Mucins Proteins 0.000 description 1
- 102000015728 Mucins Human genes 0.000 description 1
- 241000699666 Mus <mouse, genus> Species 0.000 description 1
- 101000935589 Mus musculus Flavin reductase (NADPH) Proteins 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229930012538 Paclitaxel Natural products 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 108010067902 Peptide Library Proteins 0.000 description 1
- 108091093037 Peptide nucleic acid Proteins 0.000 description 1
- 108010043958 Peptoids Proteins 0.000 description 1
- 108010081690 Pertussis Toxin Proteins 0.000 description 1
- 206010057249 Phagocytosis Diseases 0.000 description 1
- 206010035226 Plasma cell myeloma Diseases 0.000 description 1
- 241000288906 Primates Species 0.000 description 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 1
- 101000762949 Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) Exotoxin A Proteins 0.000 description 1
- 108091030071 RNAI Proteins 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 208000015634 Rectal Neoplasms Diseases 0.000 description 1
- 241000702263 Reovirus sp. Species 0.000 description 1
- 241001068295 Replication defective viruses Species 0.000 description 1
- 108700008625 Reporter Genes Proteins 0.000 description 1
- 102000006382 Ribonucleases Human genes 0.000 description 1
- 108010083644 Ribonucleases Proteins 0.000 description 1
- PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 description 1
- 108010039491 Ricin Proteins 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- 241000710961 Semliki Forest virus Species 0.000 description 1
- 108091081021 Sense strand Proteins 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- 241000710960 Sindbis virus Species 0.000 description 1
- 208000021712 Soft tissue sarcoma Diseases 0.000 description 1
- 230000037453 T cell priming Effects 0.000 description 1
- 102100027222 T-lymphocyte activation antigen CD80 Human genes 0.000 description 1
- 210000000173 T-lymphoid precursor cell Anatomy 0.000 description 1
- 108700026226 TATA Box Proteins 0.000 description 1
- GKLVYJBZJHMRIY-OUBTZVSYSA-N Technetium-99 Chemical compound [99Tc] GKLVYJBZJHMRIY-OUBTZVSYSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 1
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 1
- 239000004473 Threonine Substances 0.000 description 1
- 108700009124 Transcription Initiation Site Proteins 0.000 description 1
- 206010066901 Treatment failure Diseases 0.000 description 1
- 102100040247 Tumor necrosis factor Human genes 0.000 description 1
- 102100040245 Tumor necrosis factor receptor superfamily member 5 Human genes 0.000 description 1
- 208000035896 Twin-reversed arterial perfusion sequence Diseases 0.000 description 1
- DRTQHJPVMGBUCF-XVFCMESISA-N Uridine Chemical class O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C=C1 DRTQHJPVMGBUCF-XVFCMESISA-N 0.000 description 1
- 208000008385 Urogenital Neoplasms Diseases 0.000 description 1
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 description 1
- 241000251539 Vertebrata <Metazoa> Species 0.000 description 1
- JXLYSJRDGCGARV-WWYNWVTFSA-N Vinblastine Natural products O=C(O[C@H]1[C@](O)(C(=O)OC)[C@@H]2N(C)c3c(cc(c(OC)c3)[C@]3(C(=O)OC)c4[nH]c5c(c4CCN4C[C@](O)(CC)C[C@H](C3)C4)cccc5)[C@@]32[C@H]2[C@@]1(CC)C=CCN2CC3)C JXLYSJRDGCGARV-WWYNWVTFSA-N 0.000 description 1
- 108020000999 Viral RNA Proteins 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- 210000000683 abdominal cavity Anatomy 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- RJURFGZVJUQBHK-IIXSONLDSA-N actinomycin D Chemical compound C[C@H]1OC(=O)[C@H](C(C)C)N(C)C(=O)CN(C)C(=O)[C@@H]2CCCN2C(=O)[C@@H](C(C)C)NC(=O)[C@H]1NC(=O)C1=C(N)C(=O)C(C)=C2OC(C(C)=CC=C3C(=O)N[C@@H]4C(=O)N[C@@H](C(N5CCC[C@H]5C(=O)N(C)CC(=O)N(C)[C@@H](C(C)C)C(=O)O[C@@H]4C)=O)C(C)C)=C3N=C21 RJURFGZVJUQBHK-IIXSONLDSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000003044 adaptive effect Effects 0.000 description 1
- 230000033289 adaptive immune response Effects 0.000 description 1
- 229960005305 adenosine Drugs 0.000 description 1
- 201000008395 adenosquamous carcinoma Diseases 0.000 description 1
- 201000005188 adrenal gland cancer Diseases 0.000 description 1
- 208000024447 adrenal gland neoplasm Diseases 0.000 description 1
- 229940009456 adriamycin Drugs 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000000556 agonist Substances 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- 125000005600 alkyl phosphonate group Chemical group 0.000 description 1
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- ROBVIMPUHSLWNV-UHFFFAOYSA-N aminoglutethimide Chemical compound C=1C=C(N)C=CC=1C1(CC)CCC(=O)NC1=O ROBVIMPUHSLWNV-UHFFFAOYSA-N 0.000 description 1
- 229960003437 aminoglutethimide Drugs 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- 230000033115 angiogenesis Effects 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 230000005875 antibody response Effects 0.000 description 1
- 229940034982 antineoplastic agent Drugs 0.000 description 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 235000009582 asparagine Nutrition 0.000 description 1
- 229960001230 asparagine Drugs 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- 230000002238 attenuated effect Effects 0.000 description 1
- 229960002170 azathioprine Drugs 0.000 description 1
- LMEKQMALGUDUQG-UHFFFAOYSA-N azathioprine Chemical compound CN1C=NC([N+]([O-])=O)=C1SC1=NC=NC2=C1NC=N2 LMEKQMALGUDUQG-UHFFFAOYSA-N 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 210000002469 basement membrane Anatomy 0.000 description 1
- 230000006399 behavior Effects 0.000 description 1
- MMIMIFULGMZVPO-UHFFFAOYSA-N benzyl 3-bromo-2,6-dinitro-5-phenylmethoxybenzoate Chemical compound [O-][N+](=O)C1=C(C(=O)OCC=2C=CC=CC=2)C([N+](=O)[O-])=C(Br)C=C1OCC1=CC=CC=C1 MMIMIFULGMZVPO-UHFFFAOYSA-N 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- HMFHBZSHGGEWLO-TXICZTDVSA-N beta-D-ribose Chemical group OC[C@H]1O[C@@H](O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-TXICZTDVSA-N 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229960002685 biotin Drugs 0.000 description 1
- 235000020958 biotin Nutrition 0.000 description 1
- 239000011616 biotin Substances 0.000 description 1
- 229960004395 bleomycin sulfate Drugs 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000004159 blood analysis Methods 0.000 description 1
- 210000000601 blood cell Anatomy 0.000 description 1
- 210000002798 bone marrow cell Anatomy 0.000 description 1
- 229940098773 bovine serum albumin Drugs 0.000 description 1
- 238000013276 bronchoscopy Methods 0.000 description 1
- 229960002092 busulfan Drugs 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229940095658 calcium ipodate Drugs 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 230000036952 cancer formation Effects 0.000 description 1
- 238000002619 cancer immunotherapy Methods 0.000 description 1
- 230000005773 cancer-related death Effects 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- OKTJSMMVPCPJKN-BJUDXGSMSA-N carbon-11 Chemical compound [11C] OKTJSMMVPCPJKN-BJUDXGSMSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 229960005243 carmustine Drugs 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 210000000845 cartilage Anatomy 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000021164 cell adhesion Effects 0.000 description 1
- 230000034196 cell chemotaxis Effects 0.000 description 1
- 230000032823 cell division Effects 0.000 description 1
- 230000010261 cell growth Effects 0.000 description 1
- 230000006037 cell lysis Effects 0.000 description 1
- 230000005859 cell recognition Effects 0.000 description 1
- 239000006285 cell suspension Substances 0.000 description 1
- 238000002659 cell therapy Methods 0.000 description 1
- 230000010307 cell transformation Effects 0.000 description 1
- 210000003850 cellular structure Anatomy 0.000 description 1
- 208000019065 cervical carcinoma Diseases 0.000 description 1
- HVZGHKKROPCBDE-HZIJXFFPSA-L chembl2068725 Chemical compound [Ca+2].CN(C)\C=N\C1=C(I)C=C(I)C(CCC([O-])=O)=C1I.CN(C)\C=N\C1=C(I)C=C(I)C(CCC([O-])=O)=C1I HVZGHKKROPCBDE-HZIJXFFPSA-L 0.000 description 1
- 125000003636 chemical group Chemical group 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 210000000038 chest Anatomy 0.000 description 1
- 210000004978 chinese hamster ovary cell Anatomy 0.000 description 1
- JCKYGMPEJWAADB-UHFFFAOYSA-N chlorambucil Chemical compound OC(=O)CCCC1=CC=C(N(CCCl)CCCl)C=C1 JCKYGMPEJWAADB-UHFFFAOYSA-N 0.000 description 1
- 229960004630 chlorambucil Drugs 0.000 description 1
- 210000000349 chromosome Anatomy 0.000 description 1
- 229960001265 ciclosporin Drugs 0.000 description 1
- 210000003040 circulating cell Anatomy 0.000 description 1
- 230000009137 competitive binding Effects 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 238000010668 complexation reaction Methods 0.000 description 1
- 238000004590 computer program Methods 0.000 description 1
- 210000002808 connective tissue Anatomy 0.000 description 1
- 210000004748 cultured cell Anatomy 0.000 description 1
- 229960004397 cyclophosphamide Drugs 0.000 description 1
- 229930182912 cyclosporin Natural products 0.000 description 1
- 229960003067 cystine Drugs 0.000 description 1
- 239000000824 cytostatic agent Substances 0.000 description 1
- 230000001085 cytostatic effect Effects 0.000 description 1
- 229940127089 cytotoxic agent Drugs 0.000 description 1
- 231100000599 cytotoxic agent Toxicity 0.000 description 1
- 239000002619 cytotoxin Substances 0.000 description 1
- 229960003901 dacarbazine Drugs 0.000 description 1
- 229960000640 dactinomycin Drugs 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 238000002059 diagnostic imaging Methods 0.000 description 1
- 210000000188 diaphragm Anatomy 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-N dithiophosphoric acid Chemical class OP(O)(S)=S NAGJZTKCGNOGPW-UHFFFAOYSA-N 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 230000003828 downregulation Effects 0.000 description 1
- 229960004679 doxorubicin Drugs 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 241001493065 dsRNA viruses Species 0.000 description 1
- 210000003981 ectoderm Anatomy 0.000 description 1
- 230000000235 effect on cancer Effects 0.000 description 1
- 230000002900 effect on cell Effects 0.000 description 1
- 210000001671 embryonic stem cell Anatomy 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000012202 endocytosis Effects 0.000 description 1
- 210000001900 endoderm Anatomy 0.000 description 1
- 201000003908 endometrial adenocarcinoma Diseases 0.000 description 1
- 208000028730 endometrioid adenocarcinoma Diseases 0.000 description 1
- 208000027858 endometrioid tumor Diseases 0.000 description 1
- 230000003511 endothelial effect Effects 0.000 description 1
- 239000002158 endotoxin Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 238000003114 enzyme-linked immunosorbent spot assay Methods 0.000 description 1
- 230000008995 epigenetic change Effects 0.000 description 1
- 230000008029 eradication Effects 0.000 description 1
- 238000009164 estrogen replacement therapy Methods 0.000 description 1
- VJJPUSNTGOMMGY-MRVIYFEKSA-N etoposide Chemical compound COC1=C(O)C(OC)=CC([C@@H]2C3=CC=4OCOC=4C=C3[C@@H](O[C@H]3[C@@H]([C@@H](O)[C@@H]4O[C@H](C)OC[C@H]4O3)O)[C@@H]3[C@@H]2C(OC3)=O)=C1 VJJPUSNTGOMMGY-MRVIYFEKSA-N 0.000 description 1
- 229960005420 etoposide Drugs 0.000 description 1
- 210000002744 extracellular matrix Anatomy 0.000 description 1
- 201000010972 female reproductive endometrioid cancer Diseases 0.000 description 1
- 238000000684 flow cytometry Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- YCKRFDGAMUMZLT-BJUDXGSMSA-N fluorine-18 atom Chemical compound [18F] YCKRFDGAMUMZLT-BJUDXGSMSA-N 0.000 description 1
- 229960002949 fluorouracil Drugs 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 230000037433 frameshift Effects 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 108020001507 fusion proteins Proteins 0.000 description 1
- 102000037865 fusion proteins Human genes 0.000 description 1
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 238000001502 gel electrophoresis Methods 0.000 description 1
- 230000009368 gene silencing by RNA Effects 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 210000003714 granulocyte Anatomy 0.000 description 1
- 230000005802 health problem Effects 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 208000013210 hematogenous Diseases 0.000 description 1
- 201000005787 hematologic cancer Diseases 0.000 description 1
- 208000024200 hematopoietic and lymphoid system neoplasm Diseases 0.000 description 1
- 210000003494 hepatocyte Anatomy 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- 102000054751 human RUNX1T1 Human genes 0.000 description 1
- 238000011577 humanized mouse model Methods 0.000 description 1
- 238000010191 image analysis Methods 0.000 description 1
- 230000005934 immune activation Effects 0.000 description 1
- 239000012642 immune effector Substances 0.000 description 1
- 230000036737 immune function Effects 0.000 description 1
- 238000010185 immunofluorescence analysis Methods 0.000 description 1
- 229940072221 immunoglobulins Drugs 0.000 description 1
- 229940055742 indium-111 Drugs 0.000 description 1
- APFVFJFRJDLVQX-AHCXROLUSA-N indium-111 Chemical compound [111In] APFVFJFRJDLVQX-AHCXROLUSA-N 0.000 description 1
- 239000000411 inducer Substances 0.000 description 1
- 230000002458 infectious effect Effects 0.000 description 1
- 208000021267 infertility disease Diseases 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 238000013152 interventional procedure Methods 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- XMBWDFGMSWQBCA-RNFDNDRNSA-M iodine-131(1-) Chemical compound [131I-] XMBWDFGMSWQBCA-RNFDNDRNSA-M 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229960002979 iopanoic acid Drugs 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 description 1
- 229960000310 isoleucine Drugs 0.000 description 1
- 230000009191 jumping Effects 0.000 description 1
- 210000002510 keratinocyte Anatomy 0.000 description 1
- 230000002147 killing effect Effects 0.000 description 1
- 208000003849 large cell carcinoma Diseases 0.000 description 1
- 239000002523 lectin Substances 0.000 description 1
- 208000032839 leukemia Diseases 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 229960002247 lomustine Drugs 0.000 description 1
- 201000009546 lung large cell carcinoma Diseases 0.000 description 1
- 210000002751 lymph Anatomy 0.000 description 1
- 210000003519 mature b lymphocyte Anatomy 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- MIKKOBKEXMRYFQ-WZTVWXICSA-N meglumine amidotrizoate Chemical compound C[NH2+]C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CC(=O)NC1=C(I)C(NC(C)=O)=C(I)C(C([O-])=O)=C1I MIKKOBKEXMRYFQ-WZTVWXICSA-N 0.000 description 1
- 210000002752 melanocyte Anatomy 0.000 description 1
- GLVAUDGFNGKCSF-UHFFFAOYSA-N mercaptopurine Chemical compound S=C1NC=NC2=C1NC=N2 GLVAUDGFNGKCSF-UHFFFAOYSA-N 0.000 description 1
- 229960001428 mercaptopurine Drugs 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 229960000554 metrizamide Drugs 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 229960000350 mitotane Drugs 0.000 description 1
- 108091005601 modified peptides Proteins 0.000 description 1
- 238000010369 molecular cloning Methods 0.000 description 1
- 229940035032 monophosphoryl lipid a Drugs 0.000 description 1
- 201000010879 mucinous adenocarcinoma Diseases 0.000 description 1
- 208000010492 mucinous cystadenocarcinoma Diseases 0.000 description 1
- 229940051875 mucins Drugs 0.000 description 1
- 230000035772 mutation Effects 0.000 description 1
- 201000000050 myeloid neoplasm Diseases 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 210000005170 neoplastic cell Anatomy 0.000 description 1
- 201000011330 nonpapillary renal cell carcinoma Diseases 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 230000005257 nucleotidylation Effects 0.000 description 1
- 238000011275 oncology therapy Methods 0.000 description 1
- 229940127234 oral contraceptive Drugs 0.000 description 1
- 239000003539 oral contraceptive agent Substances 0.000 description 1
- 210000003463 organelle Anatomy 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 210000004798 organs belonging to the digestive system Anatomy 0.000 description 1
- 229940127084 other anti-cancer agent Drugs 0.000 description 1
- 229960001592 paclitaxel Drugs 0.000 description 1
- 201000010198 papillary carcinoma Diseases 0.000 description 1
- 230000005298 paramagnetic effect Effects 0.000 description 1
- 239000013610 patient sample Substances 0.000 description 1
- 210000004197 pelvis Anatomy 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 108010091748 peptide A Proteins 0.000 description 1
- 238000010647 peptide synthesis reaction Methods 0.000 description 1
- 229940023041 peptide vaccine Drugs 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 210000003200 peritoneal cavity Anatomy 0.000 description 1
- 238000002823 phage display Methods 0.000 description 1
- 230000008782 phagocytosis Effects 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 150000004713 phosphodiesters Chemical class 0.000 description 1
- 150000008298 phosphoramidates Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 210000004694 pigment cell Anatomy 0.000 description 1
- 239000013600 plasmid vector Substances 0.000 description 1
- 108700028325 pokeweed antiviral Proteins 0.000 description 1
- 230000008488 polyadenylation Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 238000010837 poor prognosis Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 210000004986 primary T-cell Anatomy 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 208000030266 primary brain neoplasm Diseases 0.000 description 1
- 229960001586 procarbazine hydrochloride Drugs 0.000 description 1
- 208000037821 progressive disease Diseases 0.000 description 1
- 230000000770 proinflammatory effect Effects 0.000 description 1
- 229940021993 prophylactic vaccine Drugs 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- 201000001514 prostate carcinoma Diseases 0.000 description 1
- 230000002797 proteolythic effect Effects 0.000 description 1
- 230000002685 pulmonary effect Effects 0.000 description 1
- 238000007388 punch biopsy Methods 0.000 description 1
- 239000002213 purine nucleotide Substances 0.000 description 1
- 150000003212 purines Chemical class 0.000 description 1
- 239000002719 pyrimidine nucleotide Substances 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 230000007420 reactivation Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 206010038038 rectal cancer Diseases 0.000 description 1
- 201000001275 rectum cancer Diseases 0.000 description 1
- 230000022532 regulation of transcription, DNA-dependent Effects 0.000 description 1
- 208000015347 renal cell adenocarcinoma Diseases 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 238000002271 resection Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 201000009410 rhabdomyosarcoma Diseases 0.000 description 1
- 239000002342 ribonucleoside Substances 0.000 description 1
- 125000000548 ribosyl group Chemical group C1([C@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 230000003248 secreting effect Effects 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000012163 sequencing technique Methods 0.000 description 1
- 208000019694 serous adenocarcinoma Diseases 0.000 description 1
- 208000004548 serous cystadenocarcinoma Diseases 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- 239000004055 small Interfering RNA Substances 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 229940083542 sodium Drugs 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- ZEYOIOAKZLALAP-UHFFFAOYSA-M sodium amidotrizoate Chemical compound [Na+].CC(=O)NC1=C(I)C(NC(C)=O)=C(I)C(C([O-])=O)=C1I ZEYOIOAKZLALAP-UHFFFAOYSA-M 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 238000010532 solid phase synthesis reaction Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000013076 target substance Substances 0.000 description 1
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 description 1
- 229940056501 technetium 99m Drugs 0.000 description 1
- 229940021747 therapeutic vaccine Drugs 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
- 229940104230 thymidine Drugs 0.000 description 1
- 229960003087 tioguanine Drugs 0.000 description 1
- 239000003104 tissue culture media Substances 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 230000005026 transcription initiation Effects 0.000 description 1
- 230000002103 transcriptional effect Effects 0.000 description 1
- 238000010361 transduction Methods 0.000 description 1
- 230000026683 transduction Effects 0.000 description 1
- 238000001890 transfection Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 230000014621 translational initiation Effects 0.000 description 1
- 238000011269 treatment regimen Methods 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 238000009966 trimming Methods 0.000 description 1
- 230000001573 trophoblastic effect Effects 0.000 description 1
- 238000009810 tubal ligation Methods 0.000 description 1
- 210000005239 tubule Anatomy 0.000 description 1
- 210000003171 tumor-infiltrating lymphocyte Anatomy 0.000 description 1
- 230000004222 uncontrolled growth Effects 0.000 description 1
- 241001529453 unidentified herpesvirus Species 0.000 description 1
- 241001515965 unidentified phage Species 0.000 description 1
- 230000003827 upregulation Effects 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 208000037964 urogenital cancer Diseases 0.000 description 1
- 239000004474 valine Substances 0.000 description 1
- KDQAABAKXDWYSZ-PNYVAJAMSA-N vinblastine sulfate Chemical compound OS(O)(=O)=O.C([C@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 KDQAABAKXDWYSZ-PNYVAJAMSA-N 0.000 description 1
- 229960004982 vinblastine sulfate Drugs 0.000 description 1
- AQTQHPDCURKLKT-JKDPCDLQSA-N vincristine sulfate Chemical compound OS(O)(=O)=O.C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C=O)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 AQTQHPDCURKLKT-JKDPCDLQSA-N 0.000 description 1
- 229960002110 vincristine sulfate Drugs 0.000 description 1
- 229960004854 viral vaccine Drugs 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000005253 yeast cell Anatomy 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Images
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
- G01N33/57407—Specifically defined cancers
- G01N33/57449—Specifically defined cancers of ovaries
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7088—Compounds having three or more nucleosides or nucleotides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
- C12Q1/6883—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material
- C12Q1/6886—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for diseases caused by alterations of genetic material for cancer
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
- G01N33/57407—Specifically defined cancers
- G01N33/57423—Specifically defined cancers of lung
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
- G01N33/57484—Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/158—Expression markers
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/56—Staging of a disease; Further complications associated with the disease
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Immunology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Microbiology (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Biochemistry (AREA)
- Physics & Mathematics (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Pathology (AREA)
- Analytical Chemistry (AREA)
- Cell Biology (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- General Physics & Mathematics (AREA)
- Food Science & Technology (AREA)
- Hospice & Palliative Care (AREA)
- Biophysics (AREA)
- Plant Pathology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Mycology (AREA)
Abstract
Description
I.能動免疫療法(「癌ワクチン」)
免疫:
i)抗原またはペプチド(天然または修飾)
ii)抗原またはペプチドをコードする核酸
iii)抗原またはペプチドをコードする組換え細胞
iv)抗原またはペプチドをコードする組換えウイルス
v)抗原もしくはペプチド(天然もしくは修飾)でパルスした、または抗原もしくはペプチドをコードする核酸を導入した抗原提示細胞
vi)抗原を認識する抗体またはT細胞受容体の移入
vii)抗原(バルクまたはクローン化集団)に対してインビトロで感作された細胞の導入
viii)抗原を認識し、好ましくは腫瘍特異的MHCクラスI提示ペプチドに対して応答性であるT細胞受容体をコードする核酸を形質導入したエフェクター細胞(または幹細胞)の移入。
本明細書で使用される技術および方法は、本明細書で説明されるかまたはそれ自体が公知の方法でおよび、例えばSambrook et al.,Molecular Cloning:A Laboratory Manual,2nd Edition(1989)Cold Spring Harbor Laboratory Press,Cold Spring Harbor,N.Y.に記載されている技術および方法で実施される。キットおよび試薬の使用を含むすべての方法は、特に指示されない限り製造者の情報に従って実施される。
Claims (23)
- 腫瘍抗原の発現および/または活性の阻害剤を含有する医薬組成物であって、前記腫瘍抗原が、配列表の配列番号:1に従った核酸配列または前記核酸配列の変異体を含む核酸によってコードされるアミノ酸配列を含む、医薬組成物。
- (i)腫瘍抗原の発現の前記阻害剤が、前記配列表の配列番号:1に従った核酸配列もしくは前記核酸配列の変異体を含む核酸に選択的にハイブリダイズする阻害性核酸であり、前記阻害性核酸が、好ましくはアンチセンスオリゴヌクレオチド、リボザイム、iRNA、siRNAもしくはそれらをコードするDNAから成る群より選択されるか、または(ii)腫瘍抗原の活性の阻害剤が、前記腫瘍抗原に特異的に結合する抗体である、請求項1に記載の医薬組成物。
- 腫瘍抗原のリガンドまたは腫瘍抗原をコードする核酸のリガンドを含有する医薬組成物であって、前記腫瘍抗原が、配列表の配列番号:1に従った核酸配列または前記核酸配列の変異体を含む核酸によってコードされるアミノ酸配列を含み、前記腫瘍抗原のリガンドまたは腫瘍抗原をコードする核酸のリガンドが1またはそれ以上の治療効果部位に結合しており、前記治療効果部位が、好ましくは放射性標識、細胞毒または細胞毒性酵素である、医薬組成物。
- 前記腫瘍抗原の前記リガンドが前記腫瘍抗原に特異的に結合する抗体を含むか、または前記腫瘍抗原をコードする核酸の前記リガンドが前記核酸に選択的にハイブリダイズする核酸である、請求項3に記載の医薬組成物。
- (i)腫瘍抗原もしくは前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチド、または前記ペプチドの誘導体、
(ii)腫瘍抗原もしくは前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドをコードする核酸、または前記核酸の誘導体、
(iii)腫瘍抗原または前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドをコードする宿主細胞、
(iv)腫瘍抗原または前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドをコードするウイルス、
(v)腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドまたは前記ペプチドの誘導体を含む細胞、
(vi)腫瘍抗原または前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドに結合する抗体またはT細胞受容体、
(vii)腫瘍抗原または前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドを認識するようにインビトロで処理された免疫反応性細胞、および
(viii)腫瘍抗原または前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドを認識するT細胞受容体をコードする核酸を導入されたエフェクター細胞または幹細胞
からなる群より選択される1またはそれ以上の物質を含有する医薬組成物であって、前記腫瘍抗原が、配列表の配列番号:1に従った核酸配列または前記核酸配列の変異体を含む核酸によってコードされるアミノ酸配列を含み、前記腫瘍抗原ペプチドが、前記腫瘍抗原のフラグメントのアミノ酸配列に実質的に対応するアミノ酸配列を含む、医薬組成物。 - ペプチドが、MHCクラスIもしくはクラスII提示ペプチドであるか、またはMHCクラスIもしくはクラスII提示ペプチドをプロセッシングされて生じ得る、請求項5に記載の医薬組成物。
- 前記宿主細胞が、コードされる前記ペプチドまたはそのプロセッシング産物に結合するMHC分子を発現する、請求項5に記載の医薬組成物。
- 前記抗体が、モノクローナル、キメラ、ヒトもしくはヒト化抗体であるか、または抗体のフラグメントもしくは合成抗体である、請求項5に記載の医薬組成物。
- 治療用または予防用腫瘍ワクチンの形態である、請求項5乃至8のいずれか一項に記載の医薬組成物。
- 腫瘍性疾患を治療するまたは予防するうえでの使用のための、請求項5乃至9のいずれか一項に記載の医薬組成物。
- 請求項1乃至10のいずれか一項に記載の医薬組成物を患者に投与することを含む、腫瘍性疾患を有するまたは腫瘍性疾患を発症する危険性がある患者を治療する方法であって、前記投与が、好ましくは、配列表の配列番号:1に従った核酸配列または前記核酸配列の変異体を含む核酸によってコードされるアミノ酸配列を含む腫瘍抗原をMHCクラスIと共に提示する性質を有する腫瘍に対するCTL活性を誘導するまたは促進する、方法。
- 患者から単離された生物学的試料において、
(i)腫瘍抗原のアミノ酸配列を含むペプチドをコードする核酸、
(ii)腫瘍抗原もしくは前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチド、
(iii)腫瘍抗原もしくは前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドに結合する抗体、
(iv)腫瘍抗原もしくは前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドを認識するT細胞、および/または
(v)腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドを含む細胞
からなる群より選択される1またはそれ以上のパラメータを検出するおよび/またはその量を測定することを含む、腫瘍性疾患の診断、検出または観測のための方法であって、
前記腫瘍抗原が、配列表の配列番号:1に従った核酸配列または前記核酸配列の変異体を含む核酸によってコードされるアミノ酸配列を含み、前記腫瘍抗原ペプチドが、前記腫瘍抗原のフラグメントのアミノ酸配列に実質的に対応するアミノ酸配列を含む、方法。 - 患者から単離された播種性もしくは循環腫瘍細胞または転移性腫瘍細胞を含有するまたは含有することが疑われる生物学的試料において、(i)腫瘍抗原のアミノ酸配列を含むペプチドをコードする核酸、および/または(ii)腫瘍抗原もしくは前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチド、を検出するおよび/またはその量を測定することを含む、前記患者において循環腫瘍細胞を検出するための方法であって、
前記腫瘍抗原が、配列表の配列番号:1に従った核酸配列または前記核酸配列の変異体を含む核酸によってコードされるアミノ酸配列を含み、前記腫瘍抗原ペプチドが、前記腫瘍抗原のフラグメントのアミノ酸配列に実質的に対応するアミノ酸配列を含む、方法。 - 腫瘍を有する患者の組織または器官から単離された生物学的試料において、(i)腫瘍抗原のアミノ酸配列を含むペプチドをコードする核酸、および/または(ii)腫瘍抗原もしくは前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチド、を検出するおよび/またはその量を測定することを含む、前記患者において転移性卵巣癌細胞または転移性肺癌細胞を検出する方法であって、前記組織または器官が腫瘍を含まない場合、その細胞が前記核酸またはペプチドを実質的に発現せず、前記腫瘍抗原が、配列表の配列番号:1に従った核酸配列または前記核酸配列の変異体を含む核酸によってコードされるアミノ酸配列を含み、前記腫瘍抗原ペプチドが、前記腫瘍抗原のフラグメントのアミノ酸配列に実質的に対応するアミノ酸配列を含む、方法。
- 生物学的試料が組織または器官に由来し、前記組織または器官が腫瘍を含まない場合、その細胞が前記腫瘍抗原および/または前記腫瘍抗原をコードする核酸を実質的に発現しない、請求項12乃至14のいずれか一項に記載の方法。
- 前記検出および/または前記定量が、
(i)生物学的試料を、検出されるべきおよび/またはその量が測定されるべき核酸、ペプチド、抗体、T細胞または細胞に特異的に結合する物質と接触させること、ならびに
(ii)前記物質と、検出されるべきおよび/またはその量が測定されるべき核酸、ペプチド、抗体、T細胞または細胞との間の複合体の形成を検出するおよび/または複合体の量を測定すること
を含む、請求項12乃至15のいずれか一項に記載の方法。 - (i)核酸に特異的に結合する物質が、前記核酸に特異的にハイブリダイズするオリゴヌクレオチドを含む、(ii)ペプチドに特異的に結合する物質が、前記ペプチドに特異的に結合する抗体を含む、(iii)抗体に特異的に結合する物質が、前記抗体に特異的に結合するペプチドを含む、または(iv)T細胞に特異的に結合する物質が、MHC分子と前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドとの間の複合体を提示する細胞を含む、請求項16に記載の方法。
- 前記物質が、検出可能な標識をさらに含む、請求項16または17に記載の方法。
- (i)腫瘍抗原のアミノ酸配列を含むペプチドをコードする核酸、
(ii)腫瘍抗原もしくは前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチド、
(iii)腫瘍抗原もしくは前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドに結合する抗体、
(iv)腫瘍抗原もしくは前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドを認識するT細胞、および/または
(v)腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドを含む細胞
に特異的に結合する物質を含む診断試験キットであって、前記腫瘍抗原が、配列表の配列番号:1に従った核酸配列または前記核酸配列の変異体を含む核酸によってコードされるアミノ酸配列を含み、前記腫瘍抗原ペプチドが、前記腫瘍抗原のフラグメントのアミノ酸配列に実質的に対応するアミノ酸配列を含み、前記物質が、好ましくは検出可能な標識をさらに含む、診断試験キット。 - 腫瘍抗原または前記腫瘍抗原に由来する腫瘍抗原ペプチドのアミノ酸配列を含むペプチドに結合する物質であって、前記腫瘍抗原が、配列表の配列番号:1に従った核酸配列または前記核酸配列の変異体を含む核酸によってコードされるアミノ酸配列を含み、前記腫瘍抗原ペプチドが、前記腫瘍抗原のフラグメントのアミノ酸配列に実質的に対応するアミノ酸配列を含み、前記物質が、好ましくは抗体、より好ましくはモノクローナル、キメラ、ヒトもしくはヒト化抗体、抗体のフラグメントまたは合成抗体である、物質。
- 請求項20に記載の物質と治療効果部位または検出可能標識との間の複合体。
- 腫瘍抗原が、配列表の配列番号:2に従ったアミノ酸配列または前記アミノ酸配列の変異体を含む、請求項1乃至10のいずれか一項に記載の医薬組成物、請求項11乃至18のいずれか一項に記載の方法、請求項19に記載の診断試験キット、請求項20に記載の物質、または請求項21に記載の複合体。
- 腫瘍性疾患が、卵巣癌、特に卵巣腺癌および卵巣奇形癌、小細胞肺癌(SCLC)および非小細胞肺癌(NSCLC)を含む肺癌、特に肺扁平上皮癌および腺癌、胃癌、乳癌、肝癌、膵癌、皮膚癌、特に基底細胞癌および扁平上皮癌、悪性黒色腫、頭頸部癌、特に悪性多形腺腫、肉腫、特に滑膜肉腫および癌肉腫、胆管癌、膀胱の癌、特に移行上皮癌および乳頭状癌、腎癌、特に腎明細胞癌および乳頭状腎細胞癌を含む腎細胞癌、大腸癌、回腸の癌を含む小腸癌、特に小腸腺癌および回腸の腺癌、精巣胎生期癌、胎盤絨毛癌、子宮頸癌、精巣癌、特に精巣セミノーマ、精巣奇形腫および精巣胎生期癌、ならびに子宮癌、ならびにそれらの転移性形態、好ましくは卵巣癌、肺癌、転移性卵巣癌および転移性肺癌から成る群より選択される、請求項10もしくは22に記載の医薬組成物、または請求項11から12、14乃至18および22のいずれか一項に記載の方法。
Applications Claiming Priority (13)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15416709P | 2009-02-20 | 2009-02-20 | |
US61/154,167 | 2009-02-20 | ||
EP09002452.2 | 2009-02-20 | ||
EP09002452A EP2221375A1 (en) | 2009-02-20 | 2009-02-20 | Methods and compositions for diagnosis and treatment of cancer |
US23184309P | 2009-08-06 | 2009-08-06 | |
EP09010164 | 2009-08-06 | ||
EP09010164.3 | 2009-08-06 | ||
US61/231,843 | 2009-08-06 | ||
US26013509P | 2009-11-11 | 2009-11-11 | |
US61/260,135 | 2009-11-11 | ||
EP09014135.9 | 2009-11-11 | ||
EP09014135 | 2009-11-11 | ||
PCT/EP2010/001062 WO2010094499A1 (en) | 2009-02-20 | 2010-02-19 | Methods and compositions for diagnosis and treatment of cancer |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2012518609A true JP2012518609A (ja) | 2012-08-16 |
JP5808254B2 JP5808254B2 (ja) | 2015-11-10 |
Family
ID=42114454
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011550483A Active JP5808254B2 (ja) | 2009-02-20 | 2010-02-19 | 癌の診断および治療のための方法および組成物 |
Country Status (24)
Country | Link |
---|---|
US (4) | US9809815B2 (ja) |
EP (2) | EP2398902B1 (ja) |
JP (1) | JP5808254B2 (ja) |
KR (3) | KR102340685B1 (ja) |
CN (2) | CN102325885A (ja) |
AU (2) | AU2010215700B2 (ja) |
BR (1) | BRPI1008564B1 (ja) |
CA (1) | CA2750985C (ja) |
DK (1) | DK2398902T3 (ja) |
ES (1) | ES2963717T3 (ja) |
FI (1) | FI2398902T3 (ja) |
HR (1) | HRP20231525T1 (ja) |
HU (1) | HUE064745T2 (ja) |
IL (4) | IL214256A0 (ja) |
LT (1) | LT2398902T (ja) |
MX (3) | MX345316B (ja) |
NZ (1) | NZ594480A (ja) |
PL (1) | PL2398902T3 (ja) |
PT (1) | PT2398902T (ja) |
RS (1) | RS64937B1 (ja) |
SG (3) | SG173444A1 (ja) |
SI (1) | SI2398902T1 (ja) |
WO (1) | WO2010094499A1 (ja) |
ZA (1) | ZA201105471B (ja) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012518608A (ja) * | 2009-02-20 | 2012-08-16 | ガニメド ファーマシューティカルズ アーゲー | 癌の診断および治療のための方法および組成物 |
JP2013533247A (ja) * | 2010-07-06 | 2013-08-22 | ガニメド ファーマシューティカルズ アーゲー | インビボで標的指向抗体を用いるがん療法 |
US9321842B2 (en) | 2011-05-13 | 2016-04-26 | Ganymed Pharmaceuticals Ag | Antibodies for treatment of cancer |
US9487584B2 (en) | 2009-11-11 | 2016-11-08 | Ganymed Pharmaceuticals Ag | Antibodies specific for claudin 6 (CLDN6) |
JP2017518762A (ja) * | 2014-04-01 | 2017-07-13 | バイオエヌテック セル アンド ジーン セラピーズ ゲーエムベーハーBiontech Cell & Gene Therapies Gmbh | クローディン6特異的免疫受容体およびt細胞エピトープ |
US9809815B2 (en) | 2009-02-20 | 2017-11-07 | Ganymed Pharmaceuticals Ag | Methods and compositions for diagnosis and treatment of cancer |
JP2018138058A (ja) * | 2013-03-05 | 2018-09-06 | ボード・オブ・リージエンツ,ザ・ユニバーシテイ・オブ・テキサス・システム | 間葉及び上皮間葉形質転換循環腫瘍細胞のための特異的検出ツール |
US10604568B2 (en) | 2013-07-31 | 2020-03-31 | BioN Tech AG | Diagnosis and therapy of cancer involving cancer stem cells |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1762575A1 (en) * | 2005-09-12 | 2007-03-14 | Ganymed Pharmaceuticals AG | Identification of tumor-associated antigens for diagnosis and therapy |
EP1970384A1 (en) | 2007-03-14 | 2008-09-17 | Ganymed Pharmaceuticals AG | Monoclonal antibodies for treatment of cancer |
EP2166021A1 (en) * | 2008-09-16 | 2010-03-24 | Ganymed Pharmaceuticals AG | Monoclonal antibodies for treatment of cancer |
EP2547695B1 (en) | 2010-03-16 | 2018-05-09 | Biontech Protein Therapeutics GmbH | Tumor vaccination involving a humoral immune response against self-protein cldn18.2 |
EP2371864A1 (en) | 2010-03-23 | 2011-10-05 | Ganymed Pharmaceuticals AG | Monoclonal antibodies for treatment of cancer |
GB201312133D0 (en) * | 2013-07-05 | 2013-08-21 | Univ Birmingham | Immunotherapy |
CN105813650A (zh) | 2013-11-06 | 2016-07-27 | 施特姆森特克斯股份有限公司 | 新型抗-密蛋白抗体和使用方法 |
CN116999573A (zh) | 2017-09-29 | 2023-11-07 | 第一三共株式会社 | 抗体-药物偶联物及其制造方法、药物组合物及其在制备治疗肿瘤的药物中的应用 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11503014A (ja) * | 1995-03-27 | 1999-03-23 | アメリカ合衆国 | T細胞レセプター並びに治療および診断におけるその用途 |
JP2002536995A (ja) * | 1999-02-22 | 2002-11-05 | インサイト・ファーマスーティカルズ・インコーポレイテッド | 結腸の疾患に関連する遺伝子 |
JP2004537534A (ja) * | 2001-06-20 | 2004-12-16 | ジェネンテック・インコーポレーテッド | 腫瘍の診断及び治療のための組成物及び方法 |
JP2007529416A (ja) * | 2003-05-27 | 2007-10-25 | イゲネーオン・クレープス−イムンテラピー・フォルシュングス−ウント・エントヴィックルングス−アクチェンゲゼルシャフト | 直腸癌の免疫療法 |
JP2011501758A (ja) * | 2007-10-23 | 2011-01-13 | ガニメド ファーマシューティカルズ アーゲー | 診断及び治療のための腫瘍関連マーカーの同定 |
JP2011516580A (ja) * | 2008-04-11 | 2011-05-26 | バイオノボ・インコーポレーテッド | トウサイカチgleditsiasinensislamの抽出物を用いる抗癌方法 |
JP2012518608A (ja) * | 2009-02-20 | 2012-08-16 | ガニメド ファーマシューティカルズ アーゲー | 癌の診断および治療のための方法および組成物 |
Family Cites Families (67)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8601597D0 (en) | 1986-01-23 | 1986-02-26 | Wilson R H | Nucleotide sequences |
US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
WO1988007089A1 (en) | 1987-03-18 | 1988-09-22 | Medical Research Council | Altered antibodies |
GB8717430D0 (en) | 1987-07-23 | 1987-08-26 | Celltech Ltd | Recombinant dna product |
GB8809129D0 (en) | 1988-04-18 | 1988-05-18 | Celltech Ltd | Recombinant dna methods vectors and host cells |
US6255458B1 (en) | 1990-08-29 | 2001-07-03 | Genpharm International | High affinity human antibodies and human antibodies against digoxin |
GB9019812D0 (en) | 1990-09-11 | 1990-10-24 | Scotgen Ltd | Novel antibodies for treatment and prevention of infection in animals and man |
US6121022A (en) | 1995-04-14 | 2000-09-19 | Genentech, Inc. | Altered polypeptides with increased half-life |
US5677139A (en) | 1995-04-21 | 1997-10-14 | President And Fellows Of Harvard College | In vitro differentiation of CD34+ progenitor cells into T lymphocytes |
UA56132C2 (uk) | 1995-04-25 | 2003-05-15 | Смітклайн Бічем Байолоджікалс С.А. | Композиція вакцини (варіанти), спосіб стабілізації qs21 відносно гідролізу (варіанти), спосіб приготування композиції вакцини |
WO2002008284A2 (en) | 2000-07-20 | 2002-01-31 | Genentech, Inc. | Compositions and methods for the diagnosis and treatment of disorders involving angiogenesis |
US6277375B1 (en) | 1997-03-03 | 2001-08-21 | Board Of Regents, The University Of Texas System | Immunoglobulin-like domains with increased half-lives |
US5928631A (en) | 1997-06-09 | 1999-07-27 | The Procter & Gamble Company | Methods for controlling environmental odors on the body using compositions comprising uncomplexed cyclodextrins |
US20020127584A1 (en) | 1997-09-18 | 2002-09-12 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US5932445A (en) | 1997-11-07 | 1999-08-03 | Incyte Pharmaceuticals, Inc. | Signal peptide-containing proteins |
US6194551B1 (en) | 1998-04-02 | 2001-02-27 | Genentech, Inc. | Polypeptide variants |
NZ531664A (en) | 1998-09-01 | 2005-07-29 | Genentech Inc | Pro1317 polypeptides and sequences thereof with homology to the semaphorin B glycoprotein family |
JP2003524384A (ja) | 1998-11-03 | 2003-08-19 | アドヘレックス テクノロジーズ インコーポレイテッド | クラウディン媒介機能を調節するための化合物および方法 |
JP2002532083A (ja) | 1998-12-17 | 2002-10-02 | ヒューマン ジノーム サイエンシーズ, インコーポレイテッド | 47個のヒト分泌タンパク質 |
KR100358062B1 (ko) * | 1998-12-30 | 2003-01-24 | 주식회사 하이닉스반도체 | 플래쉬메모리셀및그의제조방법 |
CA2373915A1 (en) | 1999-06-02 | 2000-12-07 | Genentech, Inc. | Methods and compositions for inhibiting neoplastic cell growth |
AU2883700A (en) | 1999-06-23 | 2001-01-09 | Genentech Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
EP1514933A1 (en) * | 1999-07-08 | 2005-03-16 | Research Association for Biotechnology | Secretory protein or membrane protein |
WO2001053312A1 (en) | 1999-12-23 | 2001-07-26 | Hyseq, Inc. | Novel nucleic acids and polypeptides |
AU2001236470A1 (en) | 2000-01-14 | 2001-07-24 | Corixa Corporation | Ovarian tumor-associated sequences |
IL151928A0 (en) | 2000-03-30 | 2003-04-10 | Whitehead Biomedical Inst | Rna sequence-specific mediators of rna interference |
AU6531101A (en) | 2000-06-02 | 2001-12-17 | Genentech Inc | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
EP1309620A2 (en) | 2000-06-23 | 2003-05-14 | Genentech, Inc. | Compositions and methods for the diagnosis and treatment of disorders involving angiogenesis |
CA2416456A1 (en) | 2000-07-20 | 2002-01-31 | Genentech, Inc. | Secreted and transmembrane polypeptides and nucleic acids encoding the same |
US7351802B2 (en) | 2000-07-25 | 2008-04-01 | Genentech, Inc. | PRO19672 antibodies |
CA2634294A1 (en) | 2000-08-03 | 2002-02-14 | Therapeutic Human Polyclonals, Inc. | Production of humanized antibodies in transgenic animals |
ATE378403T1 (de) | 2000-11-30 | 2007-11-15 | Medarex Inc | Transchromosomale transgen-nagetiere zur herstellung von humänen antikörpern |
US20030133939A1 (en) | 2001-01-17 | 2003-07-17 | Genecraft, Inc. | Binding domain-immunoglobulin fusion proteins |
US7754208B2 (en) | 2001-01-17 | 2010-07-13 | Trubion Pharmaceuticals, Inc. | Binding domain-immunoglobulin fusion proteins |
US20040033493A1 (en) * | 2001-01-31 | 2004-02-19 | Tchernev Velizar T. | Proteins and nucleic acids encoding same |
CA2379661A1 (en) | 2002-03-28 | 2003-09-28 | Kursad Turksen | Paracellular drug delivery system |
KR20040101502A (ko) | 2002-04-16 | 2004-12-02 | 제넨테크, 인크. | 종양의 진단 및 치료 방법 및 이를 위한 조성물 |
US20070207142A1 (en) | 2002-05-08 | 2007-09-06 | Genentech, Inc. | Compositions and methods for the treatment of tumor of hematopoietic origin |
US20070224201A1 (en) | 2002-10-02 | 2007-09-27 | Genentech, Inc. | Compositions and methods for the diagnosis and treatment of tumor |
EP2330130B1 (en) | 2002-10-17 | 2014-08-27 | Genmab A/S | Human monoclonal antibodies against CD20 |
EP1578996A4 (en) | 2002-10-18 | 2007-12-19 | Genentech Inc | COMPOSITIONS AND METHODS FOR DIAGNOSING AND TREATING TUMORS |
EP1633309A4 (en) | 2003-05-30 | 2007-06-13 | Centocor Inc | METHOD FOR INHIBITING TUMOR GROWTH WITH ANTI-TISSUE FACTOR ANTIBODIES |
JP2007516693A (ja) | 2003-06-09 | 2007-06-28 | ザ・リージェンツ・オブ・ザ・ユニバーシティ・オブ・ミシガン | 癌の治療および診断のための組成物および方法 |
WO2006033664A1 (en) | 2004-03-08 | 2006-03-30 | Avalon Pharmaceuticals | Determining cancer-linked genes and therapeutic targets using molecular cytogenetic methods |
US7431927B2 (en) | 2005-03-24 | 2008-10-07 | Epitomics, Inc. | TNFα-neutralizing antibodies |
DE102005025041A1 (de) | 2005-05-30 | 2006-12-07 | Bell Flavors & Fragrances Duft Und Aroma Gmbh | Mittel zur Anwendung in Spülmaschinen sowie Vorrichtung für dessen dosierte Einbringung während der Spül- und Trocknungsphasen |
EP1790664A1 (en) | 2005-11-24 | 2007-05-30 | Ganymed Pharmaceuticals AG | Monoclonal antibodies against claudin-18 for treatment of cancer |
AU2007332473B2 (en) * | 2006-12-14 | 2012-09-27 | Forerunner Pharma Research Co., Ltd. | Anti-Claudin-3 monoclonal antibody, and treatment and diagnosis of cancer using the same |
WO2008114733A1 (ja) | 2007-03-16 | 2008-09-25 | Kyowa Hakko Kirin Co., Ltd. | 抗Claudin-4抗体 |
EP1997832A1 (en) | 2007-05-29 | 2008-12-03 | Ganymed Pharmaceuticals AG | Monoclonal antibodies against Claudin-18 for treatment of cancer |
WO2009025759A1 (en) * | 2007-08-17 | 2009-02-26 | Progenics Pharmaceuticals (Nevada), Inc. | Tight junction proteins associated with infection and entry of hepatitis c virus (hcv), methods and uses thereof |
WO2009028663A1 (ja) | 2007-08-30 | 2009-03-05 | Kyowa Hakko Kirin Co., Ltd. | 抗Claudin-3抗体 |
CN101918450A (zh) * | 2008-01-11 | 2010-12-15 | 国立大学法人东京大学 | 抗cldn6抗体 |
EP2352764B1 (en) | 2008-10-14 | 2018-03-28 | Ablynx N.V. | AMINO ACID SEQUENCES TARGETING HUMAN CD4 and CXCR4, CCR5, TLR4, ALPHAV INTEGRIN, BETA3-INTEGRIN,BETA1-INTEGRIN, HUMAN ALPHA2-INTEGRIN, CD81, SR-BI, CLAUDIN-1, CLAUDIN-6 AND/OR CLAUDIN-9, RESPECTIVELY, AND NEUTRALIZING VIRAL ENTRY |
DE102009026966A1 (de) | 2008-12-18 | 2010-07-01 | Robert Bosch Gmbh | Betrieb eines Bremskraftverstärkers als Pedalsimulator |
JP2010178650A (ja) | 2009-02-04 | 2010-08-19 | Univ Of Tokyo | 固形癌の再発予測のための試験方法および再発予防剤 |
LT2398902T (lt) | 2009-02-20 | 2023-12-27 | Astellas Pharma Inc. | Vėžio diagnostikos ir gydymo būdai bei kompozicijos |
DE102009010019B4 (de) | 2009-02-21 | 2012-05-31 | Jos. Schneider Optische Werke Gmbh | Verfahren zum berührungslosen Messen der Topographie |
LT2499161T (lt) | 2009-11-11 | 2017-11-27 | Ganymed Pharmaceuticals Gmbh | Specifiniai antikūnai, skirti klaudinui 6 (cldn6) |
EP2322555A1 (en) | 2009-11-11 | 2011-05-18 | Ganymed Pharmaceuticals AG | Antibodies specific for claudin 6 (CLDN6) |
WO2011105551A1 (ja) | 2010-02-26 | 2011-09-01 | 国立大学法人大阪大学 | 癌幹細胞の検出方法、及び癌の治療剤または再発予防剤 |
EP2404936A1 (en) | 2010-07-06 | 2012-01-11 | Ganymed Pharmaceuticals AG | Cancer therapy using CLDN6 target-directed antibodies in vivo |
LT3026064T (lt) | 2011-05-13 | 2019-01-25 | Ganymed Pharmaceuticals Gmbh | Antikūnai, skirti vėžio gydymui, ekspresuojantys klaudiną 6 |
US10018630B2 (en) | 2011-09-07 | 2018-07-10 | Chugai Seiyaku Kabushiki Kaisha | Cancer stem cell isolation |
EP2605017A1 (de) | 2011-12-16 | 2013-06-19 | Protagen AG | Markersequenzen für gynäkologisches Malignom und deren Verwendung |
AU2013292510A1 (en) | 2012-07-19 | 2015-02-05 | Amgen Inc. | Human BTNL3 proteins, nucleic acids, and antibodies and uses thereof |
WO2015014376A1 (en) | 2013-07-31 | 2015-02-05 | Biontech Ag | Diagnosis and therapy of cancer involving cancer stem cells |
-
2010
- 2010-02-19 LT LTEPPCT/EP2010/001062T patent/LT2398902T/lt unknown
- 2010-02-19 EP EP10705304.3A patent/EP2398902B1/en active Active
- 2010-02-19 CN CN201080008878XA patent/CN102325885A/zh active Pending
- 2010-02-19 HR HRP20231525TT patent/HRP20231525T1/hr unknown
- 2010-02-19 MX MX2014012968A patent/MX345316B/es unknown
- 2010-02-19 ES ES10705304T patent/ES2963717T3/es active Active
- 2010-02-19 SG SG2011052875A patent/SG173444A1/en unknown
- 2010-02-19 DK DK10705304.3T patent/DK2398902T3/da active
- 2010-02-19 CN CN201610818117.XA patent/CN107028969A/zh active Pending
- 2010-02-19 AU AU2010215700A patent/AU2010215700B2/en active Active
- 2010-02-19 SG SG10202005849RA patent/SG10202005849RA/en unknown
- 2010-02-19 US US13/201,702 patent/US9809815B2/en active Active
- 2010-02-19 KR KR1020207025131A patent/KR102340685B1/ko active IP Right Grant
- 2010-02-19 NZ NZ594480A patent/NZ594480A/xx unknown
- 2010-02-19 HU HUE10705304A patent/HUE064745T2/hu unknown
- 2010-02-19 KR KR1020187024634A patent/KR102152997B1/ko active IP Right Grant
- 2010-02-19 BR BRPI1008564-5A patent/BRPI1008564B1/pt active IP Right Grant
- 2010-02-19 FI FIEP10705304.3T patent/FI2398902T3/fi active
- 2010-02-19 JP JP2011550483A patent/JP5808254B2/ja active Active
- 2010-02-19 EP EP23200924.1A patent/EP4285911A3/en active Pending
- 2010-02-19 SG SG10201402493UA patent/SG10201402493UA/en unknown
- 2010-02-19 CA CA2750985A patent/CA2750985C/en active Active
- 2010-02-19 PT PT107053043T patent/PT2398902T/pt unknown
- 2010-02-19 PL PL10705304.3T patent/PL2398902T3/pl unknown
- 2010-02-19 MX MX2011008430A patent/MX2011008430A/es active IP Right Grant
- 2010-02-19 KR KR1020117021993A patent/KR20110128316A/ko active Application Filing
- 2010-02-19 WO PCT/EP2010/001062 patent/WO2010094499A1/en active Application Filing
- 2010-02-19 SI SI201032137T patent/SI2398902T1/sl unknown
- 2010-02-19 MX MX2017001051A patent/MX361432B/es unknown
- 2010-02-19 RS RS20231126A patent/RS64937B1/sr unknown
-
2011
- 2011-07-24 IL IL214256A patent/IL214256A0/en unknown
- 2011-07-25 ZA ZA2011/05471A patent/ZA201105471B/en unknown
-
2014
- 2014-12-30 IL IL236516A patent/IL236516B/en active IP Right Grant
-
2016
- 2016-02-19 AU AU2016201051A patent/AU2016201051B2/en active Active
-
2017
- 2017-10-05 US US15/726,063 patent/US20180119146A1/en not_active Abandoned
-
2018
- 2018-04-18 IL IL258794A patent/IL258794B/en active IP Right Grant
-
2019
- 2019-02-13 US US16/275,111 patent/US11473085B2/en active Active
- 2019-06-13 IL IL267342A patent/IL267342B/en unknown
-
2022
- 2022-08-24 US US17/821,997 patent/US20230193261A1/en active Pending
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11503014A (ja) * | 1995-03-27 | 1999-03-23 | アメリカ合衆国 | T細胞レセプター並びに治療および診断におけるその用途 |
JP2002536995A (ja) * | 1999-02-22 | 2002-11-05 | インサイト・ファーマスーティカルズ・インコーポレイテッド | 結腸の疾患に関連する遺伝子 |
JP2004537534A (ja) * | 2001-06-20 | 2004-12-16 | ジェネンテック・インコーポレーテッド | 腫瘍の診断及び治療のための組成物及び方法 |
JP2007529416A (ja) * | 2003-05-27 | 2007-10-25 | イゲネーオン・クレープス−イムンテラピー・フォルシュングス−ウント・エントヴィックルングス−アクチェンゲゼルシャフト | 直腸癌の免疫療法 |
JP2011501758A (ja) * | 2007-10-23 | 2011-01-13 | ガニメド ファーマシューティカルズ アーゲー | 診断及び治療のための腫瘍関連マーカーの同定 |
JP2011516580A (ja) * | 2008-04-11 | 2011-05-26 | バイオノボ・インコーポレーテッド | トウサイカチgleditsiasinensislamの抽出物を用いる抗癌方法 |
JP2012518608A (ja) * | 2009-02-20 | 2012-08-16 | ガニメド ファーマシューティカルズ アーゲー | 癌の診断および治療のための方法および組成物 |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9637548B2 (en) | 2009-02-20 | 2017-05-02 | Ganymed Pharmaceuticals Ag | Methods and compositions for diagnosis and treatment of cancer |
US11473085B2 (en) | 2009-02-20 | 2022-10-18 | Ganymed Pharmaceuticals Gmbh | Methods and compositions for diagnosis and treatment of cancer |
JP2012518608A (ja) * | 2009-02-20 | 2012-08-16 | ガニメド ファーマシューティカルズ アーゲー | 癌の診断および治療のための方法および組成物 |
US9809815B2 (en) | 2009-02-20 | 2017-11-07 | Ganymed Pharmaceuticals Ag | Methods and compositions for diagnosis and treatment of cancer |
US9932401B2 (en) | 2009-11-11 | 2018-04-03 | Ganymed Pharmaceuticals Ag | Antibodies specific for claudin 6 (CLDN6) |
US9487584B2 (en) | 2009-11-11 | 2016-11-08 | Ganymed Pharmaceuticals Ag | Antibodies specific for claudin 6 (CLDN6) |
US10745477B2 (en) | 2009-11-11 | 2020-08-18 | Ganymed Pharmaceuticals Gmbh | Antibodies specific for claudin 6 (CLDN6) |
US9718886B2 (en) | 2010-07-06 | 2017-08-01 | Ganymed Pharmaceuticals Ag | Cancer therapy using CLDN6 target-directed antibodies in vivo |
US9902778B2 (en) | 2010-07-06 | 2018-02-27 | Ganymed Pharmaceuticals Ag | Cancer therapy using CLDN6 target-directed antibodies in vivo |
US10844133B2 (en) | 2010-07-06 | 2020-11-24 | Ganymed Pharmaceuticals Gmbh | Cancer therapy using CLDN6 target-directed antibodies in vivo |
JP2013533247A (ja) * | 2010-07-06 | 2013-08-22 | ガニメド ファーマシューティカルズ アーゲー | インビボで標的指向抗体を用いるがん療法 |
US11859008B2 (en) | 2011-05-13 | 2024-01-02 | Ganymed Pharmaceuticals Gmbh | Antibodies for treatment of cancer expressing claudin 6 |
US9321842B2 (en) | 2011-05-13 | 2016-04-26 | Ganymed Pharmaceuticals Ag | Antibodies for treatment of cancer |
US10233253B2 (en) | 2011-05-13 | 2019-03-19 | Ganymed Pharmaceuticals Ag | Antibodies for treatment of cancer expressing claudin 6 |
US10919974B2 (en) | 2011-05-13 | 2021-02-16 | Ganymed Pharmaceuticals Gmbh | Antibodies for treatment of cancer expressing claudin 6 |
JP2018138058A (ja) * | 2013-03-05 | 2018-09-06 | ボード・オブ・リージエンツ,ザ・ユニバーシテイ・オブ・テキサス・システム | 間葉及び上皮間葉形質転換循環腫瘍細胞のための特異的検出ツール |
US10604568B2 (en) | 2013-07-31 | 2020-03-31 | BioN Tech AG | Diagnosis and therapy of cancer involving cancer stem cells |
US11795218B2 (en) | 2013-07-31 | 2023-10-24 | Biontech Ag | Diagnosis and therapy of cancer involving cancer stem cells |
JP2020096630A (ja) * | 2014-04-01 | 2020-06-25 | バイオエヌテック セル アンド ジーン セラピーズ ゲーエムベーハーBiontech Cell & Gene Therapies Gmbh | クローディン6特異的免疫受容体およびt細胞エピトープ |
JP2022046462A (ja) * | 2014-04-01 | 2022-03-23 | バイオエヌテック セル アンド ジーン セラピーズ ゲーエムベーハー | クローディン6特異的免疫受容体およびt細胞エピトープ |
JP2017518762A (ja) * | 2014-04-01 | 2017-07-13 | バイオエヌテック セル アンド ジーン セラピーズ ゲーエムベーハーBiontech Cell & Gene Therapies Gmbh | クローディン6特異的免疫受容体およびt細胞エピトープ |
JP7451858B2 (ja) | 2014-04-01 | 2024-03-19 | バイオエヌテック セル アンド ジーン セラピーズ ゲーエムベーハー | クローディン6特異的免疫受容体およびt細胞エピトープ |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5808254B2 (ja) | 癌の診断および治療のための方法および組成物 | |
JP5809067B2 (ja) | 癌の診断および治療のための方法および組成物 | |
JP6621473B2 (ja) | 癌の診断および処置のための方法および組成物 | |
EP2221375A1 (en) | Methods and compositions for diagnosis and treatment of cancer | |
JP2012525121A (ja) | 診断および治療のための腫瘍関連マーカーの同定 | |
AU2015255252B2 (en) | Methods and compositions for diagnosis and treatment of cancer |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20130116 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20140304 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20140602 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20140609 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140703 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20141007 |
|
RD01 | Notification of change of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7426 Effective date: 20141113 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20141203 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20150630 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20150713 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20150811 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20150908 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5808254 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313117 |
|
S533 | Written request for registration of change of name |
Free format text: JAPANESE INTERMEDIATE CODE: R313533 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |