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公开(公告)号:US09597382B2
公开(公告)日:2017-03-21
申请号:US14772003
申请日:2014-03-11
Applicant: ONCOTHERAPY SCIENCE, INC.
Inventor: Takuya Tsunoda , Ryuji Osawa , Sachiko Yoshimura , Tomohisa Watanabe
CPC classification number: A61K39/0011 , A61K38/00 , A61K2039/5154 , C07K7/06 , C07K14/47 , C07K16/18 , G01N33/505 , G01N33/57484
Abstract: Peptide vaccines against cancer are described herein. In particular, isolated epitope peptides derived from the KNTC2 gene that elicit CTLs and thus are suitable for use in the context of cancer immunotherapy are provided. The inventive peptides encompass both KNTC2-derived peptides and modified versions thereof, provided such modified versions retain the requisite CTL inducibility of the original sequences.
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公开(公告)号:US20140255437A1
公开(公告)日:2014-09-11
申请号:US14353261
申请日:2012-10-25
Applicant: c/o ONCOTHERAPY SCIENCE, INC.
Inventor: Yusuke Nakamura , Takuya Tsunoda , Ryuji Osawa , Sachiko Yoshimura , Tomohisa Watanabe , Gaku Nakayama
CPC classification number: A61K39/0011 , A61K38/00 , A61K39/0005 , A61K2039/5154 , A61K2039/572 , C07K7/06 , C07K14/4748 , C07K16/18 , C07K16/40 , C07K2317/34 , C12N9/12 , C12N9/1205 , C12Y207/12002 , G01N33/505 , G01N33/574
Abstract: The present invention provides isolated epitope peptides derived from TOPK and immunogenic fragments thereof have an ability to induce cytotoxic T lymphocytes (CTLs) and thus are suitable for use in cancer immunotherapy, more particularly as cancer vaccines. The peptides of the present invention encompass both of peptides including a TOPK-derived amino acid sequence and modified versions thereof, in which one, two, or several amino acids are substituted, deleted, inserted and/or added, provided such modified versions have CTL inducibility. Further provided are polynucleotides encoding any of the aforementioned peptides as well as pharmaceutical compositions that include any of the aforementioned peptides or polynucleotides. The peptides, polynucleotides, and pharmaceutical compositions of this invention find particular utility in either or both of the treatment and prevention of a number of cancers.
Abstract translation: 本发明提供了源自TOPK的分离的表位肽,其免疫原性片段具有诱导细胞毒性T淋巴细胞(CTL)的能力,因此适用于癌症免疫治疗,更特别地,作为癌症疫苗。 本发明的肽包括包括TOPK衍生的氨基酸序列和其修饰形式的两种肽,其中一个,两个或几个氨基酸被取代,缺失,插入和/或添加,只要这些修饰版本具有CTL 诱导性。 还提供了编码任何前述肽的多核苷酸以及包括任何上述肽或多核苷酸的药物组合物。 本发明的肽,多核苷酸和药物组合物在治疗和预防多种癌症中的任一者或两者中都具有特别的用途。
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公开(公告)号:US08759481B2
公开(公告)日:2014-06-24
申请号:US13744354
申请日:2013-01-17
Applicant: Oncotherapy Science, Inc.
Inventor: Takuya Tsunoda , Ryuji Ohsawa
IPC: C07K16/00
CPC classification number: C07K4/12 , A61K31/7088 , A61K38/00 , A61K39/00 , A61K39/0011 , A61K2039/572 , C07K7/06 , C07K14/47 , G01N2500/00
Abstract: The present invention provides peptides having an amino acid sequence as set forth in SEQ ID NO: 19, 22, 30, 34, 344, 358, 41, 44, 46, 48, 78, 376, 379, 80, 100, 101, 110, 111, 387, 112, 394, 114, 116, 117, 121, 395, 133, 135, 137, 426, 143, 147, 148, 149, 150, 152, 153, 154, 156, 160, 161, 162, 163, 166, 174, 178, 186, 194, 196, 202, 210, 213, 214, 217, 223, 227, 228, 233, 254, 271, 272 or 288, as well as peptides having the above-mentioned amino acid sequences in which 1, 2, or several (e.g., up to 5) amino acids are substituted, deleted, or added, provided the peptides possess cytotoxic T cell inducibility. The present invention also provides drugs for treating or preventing a disease associated with over-expression of the CDH3, EPHA4, ECT2, HIG2, INHBB, KIF20A, KNTC2, TTK and/or URLC10, e.g. cancers containing as an active ingredient one or more of these peptides. The peptides of the present invention find further utility as vaccines.
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公开(公告)号:US20200093849A1
公开(公告)日:2020-03-26
申请号:US16708134
申请日:2019-12-09
Applicant: ONCOTHERAPY SCIENCE, INC.
Inventor: Takuya Tsunoda , Ryuji Osawa , Sachiko Yamashita , Tomohisa Watanabe , Tetsuro Hikichi
IPC: A61K31/7088 , A61K38/00 , A61K39/00 , A61K48/00 , C12N15/09 , C07K7/06 , C07K7/08 , C12Q1/02 , G01N33/15 , G01N33/50 , C07K16/18 , C12N5/10 , C07K14/705
Abstract: The present invention provides URLC10-derived epitope peptides having the ability to induce cytotoxic T cells. The present invention further provides polynucleotides encoding the peptides, antigen-presenting cells presenting the peptides, and cytotoxic T cells targeting the peptides, as well as methods of inducing the antigen-presenting cells or CTLs. The present invention also provides compositions and pharmaceutical compositions containing them as an active ingredient. Further, the present invention provides methods of treating and/or preventing cancer, and/or preventing postoperative recurrence thereof, using the peptides, polynucleotides, antigen-presenting cells, cytotoxic T cells or pharmaceutical compositions of the present invention. Methods of inducing an immune response against cancer are also provided.
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公开(公告)号:US09975935B2
公开(公告)日:2018-05-22
申请号:US15228785
申请日:2016-08-04
Applicant: OncoTherapy Science, Inc.
Inventor: Takuya Tsunoda , Ryuji Ohsawa , Sachiko Yoshimura , Tomohisa Watanabe , Yusuke Nakamura , Yoichi Furukawa
CPC classification number: C07K14/4748 , A61K39/00 , A61K39/0011 , A61K39/39 , A61K2039/53 , A61K2039/572 , C12N9/88 , C12Y402/99018 , Y02A50/396
Abstract: The present invention provides isolated peptides or the fragments derived from SEQ ID NO: 45, which bind to an HLA antigen and induce cytotoxic T lymphocytes (CTL). The peptides may include the above mentioned amino acid sequence with substitution deletion, or addition of one, two, or several amino acids sequences. The invention also provides pharmaceutical compositions including these peptides. The peptides of this invention can be used for diagnosing or treating cancer.
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公开(公告)号:US09896492B2
公开(公告)日:2018-02-20
申请号:US15197278
申请日:2016-06-29
Applicant: OncoTherapy Science, Inc.
Inventor: Yusuke Nakamura , Takuya Tsunoda , Ryuji Ohsawa , Sachiko Yoshimura , Tomohisa Watanabe
Abstract: Isolated peptides derived from SEQ ID NO: 50 and fragments thereof that bind to an HLA antigen and induce cytotoxic T lymphocytes (CTL) and thus are suitable for use in the context of cancer immunotherapy, more particularly cancer vaccines are described herein. The inventive peptides encompasses both the above mentioned amino acid sequences and modified versions thereof, in which one, two, or several amino acids sequences substituted, deleted, added or inserted, provided such modified versions retain the requisite cytotoxic T cell inducibility of the original sequence. Further provided are nucleic acids encoding any of the aforementioned peptides as well as pharmaceutical agents, substances and/or compositions that include or incorporate any of the aforementioned peptides or nucleic acids. The peptides, nucleic acids, pharmaceutical agents, substances and compositions of this invention find particular utility in the treatment of cancers and tumors, including, for example, AML, bladder cancer, breast cancer, cervical cancer, cholangiocellular carcinoma, CML, colorectal cancer, esophagus cancer, Diffused-type gastric cancer, liver cancer, NSCLC, lymphoma, osteosarcoma, ovarian cancer, pancreatic cancer, prostate cancer, renal carcinoma, SCLC, soft tissue tumor and testicular tumor.
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公开(公告)号:US09849166B2
公开(公告)日:2017-12-26
申请号:US15203103
申请日:2016-07-06
Applicant: OncoTherapy Science, Inc.
Inventor: Yusuke Nakamura , Takuya Tsunoda , Ryuji Osawa , Sachiko Yoshimura , Tomohisa Watanabe , Gaku Nakayama
IPC: A61K38/00 , A61K39/00 , C07K16/18 , C07K7/06 , G01N33/574 , C07K14/47 , G01N33/50 , C12N9/12 , C07K16/40
CPC classification number: A61K39/0011 , A61K38/00 , A61K39/0005 , A61K2039/5154 , A61K2039/572 , C07K7/06 , C07K14/4748 , C07K16/18 , C07K16/40 , C07K2317/34 , C12N9/12 , C12N9/1205 , C12Y207/12002 , G01N33/505 , G01N33/574
Abstract: The present invention provides isolated epitope peptides derived from TOPK and immunogenic fragments thereof have an ability to induce cytotoxic T lymphocytes (CTLs) and thus are suitable for use in cancer immunotherapy, more particularly as cancer vaccines. The peptides of the present invention encompass both of peptides including a TOPK-derived amino acid sequence and modified versions thereof, in which one, two, or several amino acids are substituted, deleted, inserted and/or added, provided such modified versions have CTL inducibility. Further provided are polynucleotides encoding any of the aforementioned peptides as well as pharmaceutical compositions that include any of the aforementioned peptides or polynucleotides. The peptides, polynucleotides, and pharmaceutical compositions of this invention find particular utility in either or both of the treatment and prevention of a number of cancers.
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公开(公告)号:US09585948B2
公开(公告)日:2017-03-07
申请号:US14810287
申请日:2015-07-27
Applicant: ONCOTHERAPY SCIENCE, INC.
Inventor: Yusuke Nakamura , Takuya Tsunoda , Ryuji Osawa , Sachiko Yoshimura , Tomohisa Watanabe , Gaku Nakayama
IPC: A61K38/00 , A61K39/00 , C07K14/705 , G01N33/574 , C07K7/06 , C12N5/0783
CPC classification number: C07K7/06 , A61K38/00 , A61K39/00 , A61K39/0011 , A61K2039/5154 , A61K2039/5158 , A61K2039/53 , C07K14/705 , C12N5/0638 , C12N2501/998 , C12N2502/1114 , C12N2502/1121 , G01N33/57407
Abstract: The present invention provides isolated peptides or the fragments derived from SEQ ID NO: 42, which bind to an HLA antigen and induce cytotoxic T lymphocytes (CTL). The peptides may include one of the above mentioned amino acid sequences with substitution, deletion, or addition of one, two, or several amino acids sequences. The present invention also provides pharmaceutical compositions including these peptides. The peptides of this invention can be used for treating cancer.
Abstract translation: 本发明提供分离的肽或衍生自SEQ ID NO:42的片段,其结合HLA抗原并诱导细胞毒性T淋巴细胞(CTL)。 肽可以包括一个上述氨基酸序列中的一个,两个或几个氨基酸序列的取代,缺失或添加。 本发明还提供包含这些肽的药物组合物。 本发明的肽可用于治疗癌症。
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公开(公告)号:US09415096B2
公开(公告)日:2016-08-16
申请号:US14729752
申请日:2015-06-03
Applicant: ONCOTHERAPY SCIENCE, INC.
Inventor: Yasuharu Nishimura , Kazunori Yokomine , Takuya Tsunoda , Yusuke Nakamura
IPC: A61K38/00 , A61K39/00 , C12N5/0783 , C07K7/08 , C07K7/06
CPC classification number: A61K39/0011 , A61K38/00 , A61K2039/57 , A61K2039/572 , A61K2039/585 , C07K7/06 , C07K7/08 , C12N5/0636 , C12N5/0638 , C12N2501/998 , C12N2502/11
Abstract: An objective of the present invention is to provide a means for enabling cancer immunotherapy that targets approximately 30% of various cancer patients that highly express forkhead box M1 (FOXM1) among the Japanese, by identifying FOXM1-derived peptides that can activate cancer cell-damaging human killer T cells by binding to HLA-A2. The present invention provides a peptide of (A) or (B) below: (A) a peptide including the amino acid sequence of any one of SEQ ID NOs: 1 to 3; (B) a peptide which includes the amino acid sequence of any one of SEQ ID NOs: 1 to 3, wherein one, two, or several amino acid(s) are substituted, deleted, inserted, and/or added, and wherein the peptide shows cytotoxic (killer) T cell-inducing activity.
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公开(公告)号:US09284349B2
公开(公告)日:2016-03-15
申请号:US14274373
申请日:2014-05-09
Applicant: OncoTherapy Science, Inc.
Inventor: Takuya Tsunoda , Ryuji Ohsawa
CPC classification number: C07K4/12 , A61K31/7088 , A61K38/00 , A61K39/00 , A61K39/0011 , A61K2039/572 , C07K7/06 , C07K14/47 , G01N2500/00
Abstract: The present invention provides peptides having an amino acid sequence as set forth in SEQ ID NO: 19, 22, 30, 34, 344, 358, 41, 44, 46, 48, 78, 376, 379, 80, 100, 101, 110, 111, 387, 112, 394, 114, 116, 117, 121, 395, 133, 135, 137, 426, 143, 147, 148, 149, 150, 152, 153, 154, 156, 160, 161, 162, 163, 166, 174, 178, 186, 194, 196, 202, 210, 213, 214, 217, 223, 227, 228, 233, 254, 271, 272 or 288, as well as peptides having the above-mentioned amino acid sequences in which 1, 2, or several (e.g., up to 5) amino acids are substituted, deleted, or added, provided the peptides possess cytotoxic T cell inducibility. The present invention also provides drugs for treating or preventing a disease associated with over-expression of the CDH3, EPHA4, ECT2, HIG2, INHBB, KIF20A, KNTC2, TTK and/or URLC10, e.g. cancers containing as an active ingredient one or more of these peptides. The peptides of the present invention find further utility as vaccines.
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