首页> 外国专利> COMBINATION THERAPY FOR PANCREATIC CANCER USING AN ANTIGENIC PEPTIDE AND CHEMOTHERAPEUTIC AGENT NAMELY GEMCITABINE

COMBINATION THERAPY FOR PANCREATIC CANCER USING AN ANTIGENIC PEPTIDE AND CHEMOTHERAPEUTIC AGENT NAMELY GEMCITABINE

机译:抗原肽和化学治疗剂即吉西他滨联合治疗胰腺癌

摘要

Disclosed is a an anti-cancer agent for treating cancer in a subject comprising (i) in combination with (ii); (i) one or more peptides inducing CTL selected from the group consisting of; (a) one or more peptides having the amino acid sequence selected from the group consisting of RFVPDGNRI (SEQ ID NO: 1), VYSSEEAEL (SEQ ID NO: 2), GYRIYDVVL (SEQ ID NO: 3), SYMISYAGM (SEQ ID NO: 4), KWEFPRDRL (SEQ ID NO: 5), and DFLTLEHLI (SEQ ID NO: 6), (b) the peptide of (a), in which 1, 2, or several amino acids are substituted, deleted, or added, and wherein said peptide has cytotoxic T cell inducibility; (c) the peptide of (b), wherein the second amino acid from the N-terminus is phenylalanine, tyrosine, methionine, or tryptophan; (d) the peptide of (b) or (c) , wherein the C-terminal amino acid is phenylalanine, leucine, isoleucine, tryptophan, or methionine; (e) one or more peptides having the amino acid sequence selected from the group consisting of AMFFWLLLV (SEQ ID NO: 7), VIAMFFWLL (SEQ ID NO: 8), AVIAMFFWL (SEQ ID NO: 9), KLIEIGVQT (SEQ ID NO: 10), YMISYAGMV (SEQ ID NO: 11), IQSDVWSFGV (SEQ ID NO: 12) and VLAMFFWLL (SEQ ID NO: 13); (f) the peptide of (e), in which 1, 2, or several amino acids are substituted, deleted, or added, and wherein said peptide has cytotoxic T cell inducibility; (g) the peptide of (f), wherein the second amino acid from the N terminus is leucine or methionine; and (h) the peptide of (f) or (g), wherein the C-terminal amino acid is valine or leucine, (ii) one or more chemotherapeutic agents selected from the group consisting of gemcitabine, a pharmaceutically acceptable salt thereof, and a prodrug thereof.
机译:公开了一种用于治疗对象的癌症的抗癌剂,其包含(i)与(ii)的组合; (i)一种或多种诱导CTL的肽,所述肽选自: (a)一种或多种具有选自RFVPDGNRI(SEQ ID NO:1),VYSSEEAEL(SEQ ID NO:2),GYRIYDVVL(SEQ ID NO:3),SYMISYAGM(SEQ ID NO。 :4),KWEFPRDRL(SEQ ID NO:5)和DFLTLEHLI(SEQ ID NO:6),(b)(a)的肽,其中1、2或几个氨基酸被取代,缺失或添加,并且其中所述肽具有细胞毒性T细胞诱导性; (c)(b)的肽,其中来自N端的第二个氨基酸是苯丙氨酸,酪氨酸,蛋氨酸或色氨酸; (d)(b)或(c)的肽,其中C端氨基酸是苯丙氨酸,亮氨酸,异亮氨酸,色氨酸或蛋氨酸; (e)一种或多种具有选自由AMFFWLLLV(SEQ ID NO:7),VIAMFFWLL(SEQ ID NO:8),AVIAMFFWL(SEQ ID NO:9),KLIEIGVQT(SEQ ID NO。 :10),YMISYAGMV(SEQ ID NO:11),IQSDVWSFGV(SEQ ID NO:12)和VLAMFFWLL(SEQ ID NO:13); (f)(e)的肽,其中1、2或几个氨基酸被取代,缺失或添加,并且其中所述肽具有细胞毒性T细胞诱导能力; (g)(f)的肽,其中来自N末端的第二个氨基酸是亮氨酸或蛋氨酸; (h)(f)或(g)的肽,其中C端氨基酸是缬氨酸或亮氨酸,(ii)一种或多种选自吉西他滨,其药学上可接受的盐的化学治疗剂,和其前药。

著录项

  • 公开/公告号NZ583578A

    专利类型

  • 公开/公告日2012-07-27

    原文格式PDF

  • 申请/专利权人 ONCOTHERAPY SCIENCE INC.;

    申请/专利号NZ20080583578

  • 发明设计人 YAMAUE HIROKI;

    申请日2008-08-19

  • 分类号A61K38;A61K31/7068;A61P35;

  • 国家 NZ

  • 入库时间 2022-08-21 17:23:29

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