JPH11514985A - 腫瘍性および感染性疾患の熱ショック/ストレスタンパク質による治療または予防 - Google Patents
腫瘍性および感染性疾患の熱ショック/ストレスタンパク質による治療または予防Info
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- JPH11514985A JPH11514985A JP9512063A JP51206397A JPH11514985A JP H11514985 A JPH11514985 A JP H11514985A JP 9512063 A JP9512063 A JP 9512063A JP 51206397 A JP51206397 A JP 51206397A JP H11514985 A JPH11514985 A JP H11514985A
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Abstract
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Claims (1)
- 【特許請求の範囲】 1.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質70から なる複合体を10〜600μgの範囲の量で含有する組成物をヒト個体に投与す ることを含んでなる、ヒト個体において免疫応答を引き出す方法。 2.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質90から なる複合体を50〜5000μgの範囲の量で含有する組成物をヒト個体に投与 することを含んでなる、ヒト個体において免疫応答を引き出す方法。 3.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質gp96 からなる複合体を10〜600μgの範囲の量で含有する組成物をヒト個体に投 与することを含んでなる、ヒト個体において免疫応答を引き出す方法。 4.前記の個体が肝臓癌、大腸癌、または乳癌をもつ、請求項1、2または3に 記載の方法。 5.前記複合体の量が10〜100μgの範囲である、請求項1に記載の方法。 6.前記複合体の量が約100μgの範囲である、請求項2に記載の方法。 7.前記複合体の量が10〜100μgの範囲である、請求項3に記載の方法。 8.インターフェロン−α、インターフェロン−γ、インターロイキン−2、イ ンターロイキン−4、インターロイキン−6、および腫瘍壊死因子よりなる群か ら選択される有効量の生物学的応答変更因子を前記個体に投与することをさらに 含んでなる、請求項1、2または3に記載の方法。 9.前記の投与ステップを1週間の間隔をおいて繰り返す、請求項1、2または 3に記載の方法。 10.前記複合体を筋肉内、皮下、腹腔内または静脈内に投与する、請求項1、2 または3に記載の方法。 11.前記の投与ステップを5回繰り返し、1回目の投与を左腕に、2回目の投与 を右腕に、3回目の投与を左腹部に、4回目の投与を右腹部に、5回目の投与を 左大腿に、そして6回目の投与を右大腿に行い、1〜6回目の投与を皮下に行う 、請求項1、2または3に記載の方法。 12.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質70から なる複合体を10〜600μgの範囲の量で含有する組成物をヒト個体に投与す ることを含んでなる、癌をもつヒト個体の治療方法。 13.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質90から なる複合体を50〜5000μgの範囲の量で含有する組成物をヒト個体に投与 することを含んでなる、癌をもつヒト個体の治療方法。 14.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質gp96 からなる複合体を10〜600μgの範囲の量で含有する組成物をヒト個体に投 与することを含んでなる、癌をもつヒト個体の治療方法。 15.癌が肉腫または癌からなり、繊維肉腫、粘液肉腫、脂肪肉腫、軟骨肉腫、骨 原性肉腫、脊索腫、血管肉腫、内皮肉腫、リンパ管肉腫、リンパ管内皮肉腫、滑 膜腫、中皮腫、ユーイング腫、平滑筋肉腫、横紋筋肉腫、大腸癌、膵臓癌、乳癌 、卵巣癌、前立腺癌、扁平上皮細胞癌、基底細胞癌、腺癌、汗腺癌、脂腺癌、乳 頭状癌、乳頭状腺癌、嚢胞腺癌、髄様癌、気管支原性癌、腎細胞癌、肝臓癌、胆 管癌、絨毛癌、精上皮腫、胎生期癌、ビルムス腫、子宮頸癌、精巣癌、肺癌、小 細胞肺癌、膀胱癌、上皮癌、神経膠腫、神経膠星状細胞腫、髄芽細胞腫、頭蓋咽 頭腫、上衣細胞腫、松果体腫、血管芽細胞腫、聴神経腫、乏突起膠腫、髄膜腫、 黒色腫、神経芽細胞腫、網膜芽細胞腫、白血病、リンパ腫、多発性骨髄腫、ワル デンシュトレームマクログロブリン血症、およびH鎖病よりなる群から選択され る、請求項12、13または14に記載の方法。 16.前記複合体の量が10〜100μgの範囲である、請求項12に記載の方法。 17.前記複合体の量が約100μgの範囲である、請求項13に記載の方法。 18.前記複合体の量が10〜100μgの範囲である、請求項14に記載の方法。 19.前記複合体が前記個体に由来する癌組織から調製される、請求項12、13また は14に記載の方法。 20.前記複合体が前記個体の同種異系に由来する癌組織から調製される、請求項 12、13または14に記載の方法。 21.インターフェロン−α、インターフェロン−γ、インターロイキン−2、イ ンターロイキン−4、インターロイキン−6、および腫瘍壊死因子よりなる群か ら選択される有効量の生物学的応答変更因子を前記個体に投与することをさ らに含んでなる、請求項12、13または14に記載の方法。 22.前記の投与ステップを1週間の間隔をおいて繰り返す、請求項12、13または 14に記載の方法。 23.前記の投与ステップを5回繰り返し、1回目の投与を左腕に、2回目の投与 を右腕に、3回目の投与を左腹部に、4回目の投与を右腹部に、5回目の投与を 左大腿に、そして6回目の投与を右大腿に行い、1〜6回目の投与を皮下に行う 、請求項16、17または18に記載の方法。 24.癌をもつヒト個体の治療方法であって、 (a)前記個体に、本質的にペプチドに非共有結合で結合された熱ショックタ ンパク質gp96からなる複合体を約25μg含有する組成物を投与し、ただし 、前記複合体は前記個体の癌組織から単離されたものであり、そして (b)前記ステップ(a)の投与を1週間の間隔で5週間繰り返し、1回目の投与 を左腕に、2回目の投与を右腕に、3回目の投与を左腹に、4回目の投与を右腹 に、5回目の投与を左腿に、そして6回目の投与を右腿に行い、前記1〜6回目 の投与を皮下に行う、 ことを含んでなる上記の方法。 25.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質70から なる複合体を10〜600μgの範囲の量で含有する組成物をヒト個体に投与す ることを含んでなる、癌の予防を希望するヒト個体において癌を予防する方法。 26.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質90から なる複合体を50〜5000μgの範囲の量で含有する組成物をヒト個体に投与 することを含んでなる、癌の予防を希望するヒト個体において癌を予防する方法 。 27.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質gp96 からなる複合体を10〜600μgの範囲の量で含有する組成物をヒト個体に投 与することを含んでなる、癌の予防を希望するヒト個体において癌を予防する方 法。 28.前記複合体の量が10〜100μgの範囲である、請求項25に記載の方法。 29.前記複合体の量が約100μgの範囲である、請求項26に記載の方法。 30.前記複合体の量が10〜100μgの範囲である、請求項27に記載の方法。 31.前記の抗原分子がin vivoで熱ショックタンパク質と内因的に結合している ペプチドであり、前記複合体が癌組織から単離される、請求項12、13または14に 記載の方法。 32.癌組織が前記個体に由来するものである、請求項31に記載の方法。 33.熱ショックタンパク質と抗原分子の非共有結合複合体がin vitroで作製され る、請求項12、13または14に記載の方法。 34.前記の抗原分子が腫瘍特異的抗原である、請求項33に記載の方法。 35.前記の抗原分子がin vivoで熱ショックタンパク質と内因的に結合している ペプチドである、請求項25、26または27に記載の方法。 36.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質70から なる複合体を10〜600μgの範囲の量で含有する組成物をヒト個体に投与す ることを含んでなる、感染症の治療または予防を希望するヒト個体において感染 症を治療または予防する方法。 37.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質90から なる複合体を50〜5000μgの範囲の量で含有する組成物をヒト個体に投与 することを含んでなる、感染症の治療または予防を希望するヒト個体において感 染症を治療または予防する方法。 38.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質gp96 からなる複合体を10〜600μgの範囲の量で含有する組成物をヒト個体に投 与することを含んでなる、感染症の治療または予防を希望するヒト個体において 感染症を治療または予防する方法。 39.前記複合体の量が10〜100μgの範囲である、請求項36に記載の方法。 40.前記複合体の量が約100μgの範囲である、請求項37に記載の方法。 41.前記複合体の量が10〜100μgの範囲である、請求項38に記載の方法。 42.前記の抗原分子が、感染症を引き起こす感染因子に感染した細胞内で、熱シ ョックタンパク質と内因的に結合しているペプチドである、請求項36、37または 38に記載の方法。 43.前記の抗原分子が感染症を引き起こす感染因子の抗原である、請求項36、37 または38に記載の方法。 44.感染因子がウイルス、細菌、原生動物、真菌または寄生体である、請求項43 に記載の方法。 45.腫瘍に特異的なMHCクラスI制限されたCD8+細胞傷害性Tリンパ球の 個体による産生を測定することを含んでなる、腫瘍をもつ個体においてin vivo で腫瘍拒絶を測定する方法。 46.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質70から なる複合体を10〜600μgの範囲の量で含有する組成物を容器内に含んでな るキット。 47.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質90から なる複合体を50〜5000μgの範囲の量で含有する組成物を容器内に含んで なるキット。 48.本質的に抗原分子に非共有結合で結合された熱ショックタンパク質gp96 からなる複合体を10〜600μgの範囲の量で含有する組成物を容器内に含ん でなるキット。 49.複数の容器を含んでなり、各容器が本質的に抗原分子に非共有結合で結合さ れた熱ショックタンパク質70からなる複合体を10〜600μgの範囲の量で 含有する組成物を含んでなるキット。 50.前記複合体の量が10〜100μgの範囲である、請求項46に記載のキット 。 51.前記複合体の量が約100μgの範囲である、請求項47に記載のキット。 52.前記複合体の量が10〜100μgの範囲である、請求項48に記載のキット 。 53.hsp70−ペプチド複合体を精製する方法であって、 (a)サンプル中のhsp70がADPと結合できるような条件下で、細胞性 タンパク質を含有するサンプルと固相支持体に固定したADPとを接触させ、そ して (b)ステップ(a)においてADPと結合したhsp70を溶出する、 ことを含んでなる上記の方法。 54.前記の接触がADP−アガロースによるカラムクロマトグラフィーにより行 われる、請求項53に記載の方法。 55.前記の細胞が腫瘍細胞である、請求項53に記載の方法。 56.前記の細胞がウイルスに感染している、請求項53に記載の方法。 57.前記の細胞が細菌に感染している、請求項53に記載の方法。 58.前記の細胞が原生動物に感染している、請求項53に記載の方法。 59.前記の細胞が寄生体に感染している、請求項53に記載の方法。 60.細胞からhsp70−ペプチド複合体を精製する方法であって、 (a)低張性緩衝液を用いて細胞をホモジナイズして細胞溶解物を調製し、 (b)該細胞溶解物を遠心して上清を回収し、 (c)該上清をADP−アガロースカラムに通し、 (d)該ADP−アガロースカラムをADP含有緩衝液で洗い、そして (e)該hsp70−ペプチド複合体を集める、 ことを含んでなる上記の方法。 61.hsp70−ペプチド複合体を精製する方法であって、 (a)サンプル中のhsp70が非加水分解性のATP類似体と結合できるよ うな条件下で、細胞性タンパク質を含有するサンプルと固相支持体に固定した非 加水分解性のATP類似体とを接触させ、そして (b)ステップ(a)において非加水分解性のATP類似体と結合したhsp70 を溶出する、 ことを含んでなる上記の方法。
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US08/527,391 US5837251A (en) | 1995-09-13 | 1995-09-13 | Compositions and methods using complexes of heat shock proteins and antigenic molecules for the treatment and prevention of neoplastic diseases |
PCT/US1996/014557 WO1997010001A1 (en) | 1995-09-13 | 1996-09-11 | Treatment or prevention of neoplastic and infectious diseases with heat shock/stress proteins |
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- 1996-09-11 EP EP96931527A patent/EP0859631B9/en not_active Expired - Lifetime
- 1996-09-11 JP JP9512063A patent/JPH11514985A/ja active Pending
- 1996-09-11 CA CA2232048A patent/CA2232048C/en not_active Expired - Fee Related
- 1996-09-11 WO PCT/US1996/014557 patent/WO1997010001A1/en active Application Filing
- 1996-09-11 AT AT96931527T patent/ATE456378T1/de not_active IP Right Cessation
- 1996-09-11 AU AU70181/96A patent/AU703101B2/en not_active Ceased
- 1996-09-13 ZA ZA967757A patent/ZA967757B/xx unknown
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JP2014208690A (ja) * | 2008-03-03 | 2014-11-06 | ザ ユニバーシティー オブ マイアミThe University Of Miami | 同種癌細胞による免疫療法 |
JP2014520875A (ja) * | 2011-07-21 | 2014-08-25 | バイオテック ツールズ エスエー | DnaKの投与量 |
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WO1997010001A1 (en) | 1997-03-20 |
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CA2232048A1 (en) | 1997-03-20 |
ES2340558T3 (es) | 2010-06-04 |
DE69638121D1 (de) | 2010-03-18 |
AU7018196A (en) | 1997-04-01 |
US5837251A (en) | 1998-11-17 |
EP0859631A1 (en) | 1998-08-26 |
ZA967757B (en) | 1997-04-07 |
ATE456378T1 (de) | 2010-02-15 |
US7601359B1 (en) | 2009-10-13 |
US6143299A (en) | 2000-11-07 |
US6139841A (en) | 2000-10-31 |
US6136315A (en) | 2000-10-24 |
US6162436A (en) | 2000-12-19 |
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