JPH11511968A - 抗原提示細胞上にて抗原密度を増加させる方法 - Google Patents
抗原提示細胞上にて抗原密度を増加させる方法Info
- Publication number
- JPH11511968A JPH11511968A JP9509560A JP50956097A JPH11511968A JP H11511968 A JPH11511968 A JP H11511968A JP 9509560 A JP9509560 A JP 9509560A JP 50956097 A JP50956097 A JP 50956097A JP H11511968 A JPH11511968 A JP H11511968A
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Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.細胞に接触させたペプチドの提示を変更するために、細胞のペプチドへの 接触前に細胞中のMHCクラスI経路関連成分の活性を阻害することからなる方 法。 2.MHCクラスI経路関連成分がTAP蛋白質である、請求項1記載の方法 。 3.MHCクラスI経路関連成分がLMP蛋白質である、請求項1記載の方法 。 4.LMP蛋白質がLMP2およびLMP7からなる群から選択される、請求 項3記載の方法。 5.MHCクラスI経路関連成分が熱ショック蛋白質である、請求項1記載の 方法。 6.熱ショック蛋白質がgp96、HSP90およびHSP70からなる群か ら選択される、請求項5記載の方法。 7.MHCクラスI経路関連成分がプロテオゾームである、請求項1記載の方 法。 8.プロテオゾームが26Sプロテオゾームである、請求項7記載の方法。 9.プロテオゾームが20Sプロテオゾームである、請求項7記載の方法。 10.請求項1記載の方法により生成された細胞。 11.MHCクラスI経路関連蛋白質の発現を減じるアンチセンスオリゴヌク レオチドを含む細胞。 12.MHCクラスI経路関連蛋白質の発現を減じるアンチセンス遺伝子を含 む細胞。 13.阻害が、MHCクラスI経路関連蛋白質をコードするmRNAのすべて または一部に相補なアンチセンスオリゴヌクレオチドを細胞に導入することによ りMHCクラスI経路関連蛋白質の翻訳を阻害することからなる、請求項1記載 の方法。 14.阻害が、MHCクラスI経路関連蛋白質をコードするmRNAのすべて または一部に相補なRNAをコードするアンチセンス遺伝子を細胞に導入するこ とによりMHCクラスI経路関連蛋白質の翻訳を阻害することからなる、請求項 1記載の方法。 15.病原体に感染した哺乳類に細胞を投与することをさらに含む、請求項1 記載の方法。 16.請求項10記載の細胞および薬学上受容可能な賦形剤を含むワクチン。 17.TAPがTAP−1である、請求項2記載の方法。 18.TAPがTAP−2である、請求項2記載の方法。 19.細胞がTリンパ球である、請求項1記載の方法。 20.細胞がRMA細胞である、請求項1記載の方法。 21.細胞が粘着性または非粘着性スプレノサイトである、請求項1記載の方 法。 22.細胞が粘着性または非粘着性末梢血単核細胞である、請求項1記載の方 法。 23.細胞が樹状細胞である、請求項1記載の方法。 24.細胞がマクロファージである、請求項1記載の方法。 25.細胞が胸腺腫の細胞である、請求項1記載の方法。 26.アンチセンスオリゴヌクレオチドが25から30ヌクレオチドの長さで あって配列: 5’AGGGCCTCAGGTAGGACAGCGCCAT3’(配列番号1) を含む、請求項13記載の方法。 27.アンチセンスオリゴヌクレオチドが25から30ヌクレオチドの長さで あって配列: 5.GCAGCAGGATATTGGCATTGAAAGG3’(配列番号2) を含む、請求項13記載の方法。 28.ペプチドが病原体により天然に発現される蛋白質の一部からなる6から 15のアミノ酸のポリペプチドである、請求項1記載の方法。 29.細胞がBリンパ球である、請求項1球の方法。 30.ペプチドが腫瘍特異性抗原である、請求項1記載の方法。 31.阻害が、MHCクラスI経路関連蛋白質に結合して該蛋白質の機能を阻 害するあとりのRNAを細胞に導入することからなる、請求項1記載の方法。 32.MHCクラスI経路関連蛋白質がTAP蛋白質およびLMP蛋白質から なる群から選択される、請求項31記載の方法。 33.阻害が、MHCクラスI経路関連蛋白質をコードするmRNAを特異的 に分断するリボザイムを細胞に導入してそれによりMHCクラスI経路関連蛋白 質の翻訳を阻害することからなる、請求項1記載の方法。 34.リボザイムがハンマーヘッドリボザイムである、請求項33記載の方法 。 35.MHCクラスI経路関連成分がTAP蛋白質およびLMP蛋白質からな る群から選択される、請求項33記載の方法。 36.阻害が、細胞をプロテアゾーム阻害剤に接触させることからなる、請求 項1記載の方法。 37.プロテアゾーム阻害剤がLLnL,MG115,MG132,CEP6 90,CEP1508,CEP1513,CEP1612,およびラクタシスチ ンからなる群から選択される、請求項36記載の方法。 38.プロテアゾーム阻害剤がMG132である、請求項37記載の方法。 39.細胞中のMHCクラスI経路関連成分の活性を阻害し、 細胞を腫瘍特異的抗原に接触させてそれにより抗原提示細胞を生成し、 そして 抗原提示細胞を哺乳類に投与すること からなる、哺乳類の癌の処置または予防方法。 40.MHCクラスI経路関連成分がTAPである、請求項39記載の方法。 41.MHCクラスI経路関連成分がLAPである、請求項39記載の方法。 42.MHCクラスI経路関連成分がプロテアゾームである、請求項39記載 の方法。 43.請求項10記載の細胞をTリンパ球に接触させることからなる、Tリン パ球のインビトロ増殖を刺激する方法。 44.細胞中のMHCクラスI経路関連成分の活性を阻害し、 細胞を腫瘍特異的抗原に接触させてそれにより抗原提示細胞を生成し、 そして 抗原提示細胞をTリンパ球に接触させることにより細胞毒性Tリンパ球 を生成すること により生成された細胞毒性Tリンパ球。 45.MHCクラスI経路関連成分がTAPである、請求項44記載の方法。 46.MHCクラスI経路関連成分がLAPである、請求項44記載の方法。 47.MHCクラスI経路関連成分がプロテアゾームである、請求項44記載 の方法。 48.請求項44記載の細胞毒性Tリンパ球を哺乳類に投与することからなる 、病原体に感染した哺乳類を処置する方法。 49.請求項44記載の細胞毒性Tリンパ球を哺乳類に投与することからなる 、哺乳類の癌を処置する方法。 50.プロテアゾーム阻害剤がCEP1601である、請求項36記載の方法 。
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US51737395A | 1995-08-21 | 1995-08-21 | |
US08/517,373 | 1995-08-21 | ||
PCT/US1996/013457 WO1997007128A1 (en) | 1995-08-21 | 1996-08-20 | A method to increase the density of antigen on antigen presenting cells |
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JPH11511968A true JPH11511968A (ja) | 1999-10-19 |
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JP9509560A Ceased JPH11511968A (ja) | 1995-08-21 | 1996-08-20 | 抗原提示細胞上にて抗原密度を増加させる方法 |
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US (1) | US5831068A (ja) |
EP (1) | EP0863913A4 (ja) |
JP (1) | JPH11511968A (ja) |
AU (1) | AU7008896A (ja) |
CA (1) | CA2230195A1 (ja) |
WO (1) | WO1997007128A1 (ja) |
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US5853719A (en) | 1996-04-30 | 1998-12-29 | Duke University | Methods for treating cancers and pathogen infections using antigen-presenting cells loaded with RNA |
SE9604581D0 (sv) * | 1996-12-12 | 1996-12-12 | Karolinska Innovations Ab | An agent against cancer and virus infections |
US6977073B1 (en) | 1997-02-07 | 2005-12-20 | Cem Cezayirli | Method for stimulating an immune response |
US6228640B1 (en) | 1997-02-07 | 2001-05-08 | Cem Cezayirli | Programmable antigen presenting cell of CD34 lineage |
US6251665B1 (en) | 1997-02-07 | 2001-06-26 | Cem Cezayirli | Directed maturation of stem cells and production of programmable antigen presenting dentritic cells therefrom |
US6133308A (en) | 1997-08-15 | 2000-10-17 | Millennium Pharmaceuticals, Inc. | Synthesis of clasto-lactacystin beta-lactone and analogs thereof |
CA2301054A1 (en) * | 1997-08-15 | 1999-02-25 | Francois Soucy | Synthesis of clasto-lactacystin .beta.-lactone and analogs thereof |
AU2674299A (en) * | 1998-02-11 | 1999-08-30 | Maxygen, Inc. | Targeting of genetic vaccine vectors |
EP1518927A3 (en) * | 1998-02-11 | 2005-06-22 | Maxygen, Inc. | Optimization of immunomodulatory properties of genetic vaccines |
AU755156B2 (en) * | 1998-03-20 | 2002-12-05 | Genzyme Corporation | Methods for enhanced antigen presentation on antigen-presenting cells and compositions produced thereby |
US6436392B1 (en) * | 1998-05-20 | 2002-08-20 | University Of Iowa Research Foundation | Adeno-associated virus vectors |
GB9817693D0 (en) * | 1998-08-14 | 1998-10-07 | Bridgehead Technologies Limite | Virally-mediated targeting of drugs and genetic material |
CN1339970A (zh) * | 1999-02-10 | 2002-03-13 | 鹤尾隆 | 抗癌药物增强剂 |
US7122335B1 (en) * | 1999-06-08 | 2006-10-17 | University Of Iowa Research Foundation | Compounds and methods to enhance rAAV transduction |
AU782966B2 (en) * | 1999-06-08 | 2005-09-15 | University Of Iowa Research Foundation, The | Compounds and methods to enhance RAAV transduction |
AT408721B (de) * | 1999-10-01 | 2002-02-25 | Cistem Biotechnologies Gmbh | Pharmazeutische zusammensetzung enthaltend ein antigen |
US7241447B1 (en) * | 1999-10-07 | 2007-07-10 | University Of Iowa Research Foundation | Adeno-associated virus vectors and uses thereof |
US6649593B1 (en) * | 1999-10-13 | 2003-11-18 | Tularik Inc. | Modulators of SREBP processing |
CA2520028A1 (en) * | 2003-03-31 | 2004-10-21 | University Of Iowa Research Foundation | Compounds and methods to enhance raav transduction |
US20060167106A1 (en) * | 2004-11-19 | 2006-07-27 | Mei Zhang | Compounds acting at the centrosome |
WO2007120863A2 (en) | 2006-04-14 | 2007-10-25 | Epicentre Technologies | Kits and methods for generating 5' capped rna |
EP2019964A2 (en) * | 2006-04-28 | 2009-02-04 | University of Iowa Research Foundation | Methods and compounds to modulate parvovirus transduction of mammalian cells or to alter virus infection. method to identify a viral receptor or co-receptor |
CN101484461B (zh) | 2006-08-18 | 2014-09-17 | 阿哥斯医疗公司 | Cd83在联合治疗中的用途 |
EP2557089A2 (en) | 2011-07-15 | 2013-02-13 | Fundació Institut d'Investigació Biomèdica de Bellvitge (IDIBELL) | Compositions and methods for immunomodulation |
WO2017139381A1 (en) | 2016-02-08 | 2017-08-17 | University Of Iowa Research Foundation | Methods to produce chimeric adeno-associated virus/bocavirus parvovirus |
AU2017229347A1 (en) | 2016-03-07 | 2018-11-01 | University Of Iowa Research Foundation | AAV-mediated expression using a synthetic promoter and enhancer |
WO2018132747A1 (en) | 2017-01-13 | 2018-07-19 | University Of Iowa Research Foundation | Bocaparvovirus small noncoding rna and uses thereof |
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AU660422B2 (en) * | 1990-09-06 | 1995-06-29 | Immulogic Pharmaceutical Corporation | Pathogen-specific CTL therapy |
DE69430315T2 (de) * | 1993-08-06 | 2002-11-21 | Epimmune, Inc. | Methoden zur (ex vivo) therapie mittels peptid - bestueckten antigen - praesentierenden zellen zur aktivierung von ctl |
ATE197609T1 (de) * | 1993-09-03 | 2000-12-15 | Chiron Corp | Verfahren zur unterdrückung der immunantwort durch gentherapie |
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1996
- 1996-08-20 AU AU70088/96A patent/AU7008896A/en not_active Abandoned
- 1996-08-20 CA CA002230195A patent/CA2230195A1/en not_active Abandoned
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WO1997007128A1 (en) | 1997-02-27 |
CA2230195A1 (en) | 1997-02-27 |
AU7008896A (en) | 1997-03-12 |
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