JP2002514047A - 樹状細胞を活性化する方法 - Google Patents
樹状細胞を活性化する方法Info
- Publication number
- JP2002514047A JP2002514047A JP50534998A JP50534998A JP2002514047A JP 2002514047 A JP2002514047 A JP 2002514047A JP 50534998 A JP50534998 A JP 50534998A JP 50534998 A JP50534998 A JP 50534998A JP 2002514047 A JP2002514047 A JP 2002514047A
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- Prior art keywords
- antigen
- dendritic cells
- binds
- cells
- amino acid
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- 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.)
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Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.(a) 樹状細胞を回収し; (b) (i)抗原の取り込みおよび加工を促進する条件下で培養中に該樹状細胞を 抗原に暴露させる、もしくは(ii)該抗原をコードする遺伝子で該樹状細胞をトラ ンスフェクトすることによって、該樹状細胞に該抗原を発現させ;そして (c)該抗原を発現する樹状細胞を、可溶性CD40のCD40Lへの結合を最低約90%阻 害することが観察されることによって決定されるように、CD40に結合し、CD40の CD40Lへの結合を阻害することができるCD40結合蛋白質に暴露することによって 、該抗原を発現する樹状細胞を活性化する 工程により産生される、抗原を発現する活性化された樹状細胞の集団。 2.造血幹細胞もしくは始原細胞を、GM-CSF,flt3-L,IL-4,TNF-α,IL-3,c- kitリガンド,GM-CSFとIL-3の融合体、およびこれらの組み合わせからなるグル ープから選択される分子と接触させることによって、樹状細胞が得られる、請求 項1に記載の集団。 3.CD40結合蛋白質が: (a) SEQ ID NO:2のアミノ酸1から261,35から261,34から225,113から261 ,113から225,120から261もしくは120から225を含むペプチド; (b) CD40に結合する(a)によるペプチドの断片;並びに (c) (a)もしくは(b)のペプチドをコードするDNAに、ストリンジェントな条件 下(6×SSC、63℃で一晩ハイブリダイズ;3×SSC、55℃で洗浄)でハイブリダイ ズするDNAにコードされ、CD40に結合するペプチド、 並びにオリゴマー形成ペプチドから成るグループから選択される、可溶性オリゴ マーCD40リガンドである、請求項1に記載の集団。 4.可溶性オリゴマーCD40リガンドが: (a) SEQ ID NO:2にあげられたアミノ酸配列を持ち、アミノ酸194のシステイ ンが別のアミノ酸に置換されているポリペプチド;および (b) ムテイン(a)の断片でCD40に結合するポリペプチド; ここにおいて、アミノ酸194のシステインのかわりに置換されるアミノ酸は、ト リプトファン、セリン、アスパラギン酸およびリジンからなるグループから選択 される からなるグループから選択される、請求項3に記載の集団。 5.(a) 個体から樹状細胞を回収し; (b) (i)抗原の取り込みおよび加工を促進する条件下で培養中に該樹状細胞を 抗原に暴露させる、もしくは(ii)該抗原をコードする遺伝子で該樹状細胞をトラ ンスフェクトすることによって、該樹状細胞に該抗原を発現させ; (c)該抗原を発現する樹状細胞を、可溶性CD40のCD40Lへの結合を最低約90%阻 害することが観察されることによって決定されるように、CD40に結合し、CD40の CD40Lへの結合を阻害することができるCD40結合蛋白質に暴露することによって 、該抗原を発現する樹状細胞を活性化し;そして (d) 該活性化され抗原を発現する樹状細胞を該個体に投与する 工程を含む、個体における抗原に対する特異的な免疫反応を刺激する方法。 6.造血幹細胞もしくは始原細胞を該個体から回収し、該造血幹細胞もしくは 始原細胞をflt-3リガンド,GM-CSF,IL-4,TNF-α,IL-3,c-kitリガンド,GM-C SFとIL-3の融合体、および、これらの組み合わせからなるグループから選択され る分子と接触させることによって、樹状細胞が得られる、請求項5に記載の方法 。 7.CD40結合蛋白質が: (a) SEQ ID NO:2のアミノ酸1から261,35から261,34から225,113から261 ,113から225,120から261もしくは120から225を含むペプチド; (b) CD40に結合する(a)によるペプチドの断片;並びに (c) (a)もしくは(b)のペプチドをコードするDNAに、ストリンジェントな条件 下(6×SSC、63℃で一晩ハイブリダイズ;3×SSC、55℃で洗浄)でハイブリダイ ズするDNAにコードされ、CD40に結合するペプチド、 並びにオリゴマー形成ペプチドから成るグループから選択される、可溶性オリゴ マーCD40リガンドである、請求項6に記載の方法。 8.可溶性オリゴマーCD40リガンドが: (a) SEQ ID NO:2にあげられたアミノ酸配列を持ち、アミノ酸194のシステイ ンが別のアミノ酸に置換されているポリペプチド;および (b) ポリペプチド(a)の断片でCD40に結合するポリペプチド; ここにおいて、アミノ酸194のシステインのかわりに置換されるアミノ酸は、ト リプトファン、セリン、アスパラギン酸およびリジンからなるグループから選択 される からなるグループから選択される、請求項7に記載の集団。 9.該個体の血中の始原細胞数を増大させるため、flt-3リガンドが樹状細胞回 収前に該個体に投与される、請求項5に記載の方法。 10.造血幹細胞もしくは始原細胞を該個体から回収し、該造血幹細胞もしくは 始原細胞をflt-3リガンド,GM-CSF,IL-4,TNF-α,IL-3,c-kitリガンド,GM-C SFとIL-3の融合体、およびこれらの組み合わせからなるグループから選択される 分子と接触させることによって、樹状細胞が得られる、請求項9に記載の方法。 11.抗原を発現し、活性化された樹状細胞が、インターロイキン1,2,3,4,5,6, 7,10,12および15;顆粒球-マクロファージコロニー刺激因子、顆粒球コロニー 刺激因子;インターロイキン-3および顆粒球-マクロファージコロニー刺激因子 を含む融合蛋白質;インターフェロン-γ;TNF;TGF-β;flt-3リガンド;可溶 性CD40リガンド;可溶性CD83;これらサイトカインの生物学的活性のある誘導体 ;並びにこれらの組み合わせからなるグループから選択される分子と、同時に、 逐次的に、または別々に投与される、請求項5に記載の方法。 12.CD40結合蛋白質が: (a) SEQ ID NO:2のアミノ酸1から261,35から261,34から225,113から261 ,113から225,120から261もしくは120から225を含むペプチド; (b) CD40に結合する(a)によるペプチドの断片; (c) (a)もしくは(b)のペプチドをコードするDNAに、ストリンジェントな条件 下(6×SSC、63℃で一晩ハイブリダイズ;3×SSC、55℃で洗浄)でハイブリダイ ズするDNAにコードされ、CD40に結合するペプチド; (d) (a)によるポリペプチドで、アミノ酸194のシステインが、トリプトファ ン、セリン、アスパラギン酸およびリジンからなるグループから選択される別の アミノ酸に置換されている当該ポリペプチド;並びに (e) ポリペプチド(d)の断片でCD40に結合する当該断片; 並びにオリゴマー形成ペプチドから成るグループから選択される、可溶性オリゴ マーCD40リガンドである、請求項9に記載の方法。 13.CD40結合蛋白質が: (a) SEQ ID NO:2のアミノ酸1から261,35から261,34から225,113から261 ,113から225,120から261もしくは120から225を含むペプチド; (b) CD40に結合する(a)によるペプチドの断片; (c) (a)もしくは(b)のペプチドをコードするDNAに、ストリンジェントな条件 下(6×SSC、63℃で一晩ハイブリダイズ;3×SSC、55℃で洗浄)でハイブリダイ ズするDNAにコードされ、CD40に結合するペプチド; (d) (a)によるポリペプチドで、アミノ酸194のシステインが、トリプトファ ン、セリン、アスパラギン酸およびリジンからなるグループから選択される別の アミノ酸に置換されている当該ポリペプチド;並びに (e) ポリペプチド(d)の断片でCD40に結合する当該断片; 並びにオリゴマー形成ペプチドから成るグループから選択される、可溶性オリゴ マーCD40リガンドである、請求項10に記載の方法。 14.CD40結合蛋白質が: (a) SEQ ID NO:2のアミノ酸1から261,35から261,34から225,113から261 ,113から225,120から261もしくは120から225を含むペプチド; (b) CD40に結合する(a)によるペプチドの断片; (c) (a)もしくは(b)のペプチドをコードするDNAに、ストリンジェントな条件 下(6×SSC、63℃で一晩ハイブリダイズ;3×SSC、55℃で洗浄)でハイブリダイ ズするDNAにコードされ、CD40に結合するペプチド; (d) (a)によるポリペプチドで、アミノ酸194のシステインが、トリプトファ ン、セリン、アスパラギン酸およびリジンからなるグループから選択される別の アミノ酸に置換されている当該ポリペプチド;並びに (e) ポリペプチド(d)の断片でCD40に結合する当該断片; 並びにオリゴマー形成ペプチドから成るグループから選択される、可溶性オリゴ マーCD40リガンドである、請求項11に記載の方法。 15.(a) 個体から樹状細胞を回収し; (b) (i)抗原の取り込みおよび加工を促進する条件下で培養中に該樹状細胞を 抗原に暴露させる、もしくは(ii)該抗原をコードする遺伝子で該樹状細胞をトラ ンスフェクトすることによって、該樹状細胞に該抗原を発現させ; (c) 該抗原を発現する樹状細胞を、可溶性CD40のCD40Lへの結合を最低約90% 阻害することが観察されることによって決定されるように、CD40に結合し、CD40 のCD40Lへの結合を阻害することができるCD40結合蛋白質に暴露することによっ て、該抗原を発現する樹状細胞を活性化し;そして (d) T細胞に対して該樹状細胞に該抗原を提示させる 工程を含む、個体から抗原特異的T細胞を調製する方法。 16.抗原特異的T細胞が、該個体から回収され、抗原提示樹状細胞にex vivoで 暴露され、そして該個体に再投与される、請求項15に記載の方法。 17.CD40結合蛋白質が: (a) SEQ ID NO:2のアミノ酸1から261,35から261,34から225,113から261 ,113から225,120から261もしくは120から225を含むペプチド; (b) CD40に結合する(a)によるペプチドの断片; (c) (a)もしくは(b)のペプチドをコードするDNAに、ストリンジェントな条件 下(6×SSC、63℃で一晩ハイブリダイズ;3×SSC、55℃で洗浄)でハイブリダイ ズするDNAにコードされ、CD40に結合するペプチド; (d) (a)によるポリペプチドで、アミノ酸194のシステインが、トリプトファ ン、セリン、アスパラギン酸およびリジンからなるグループから選択される別の アミノ酸に置換されている当該ポリペプチド;並びに (e) ポリペプチド(d)の断片でCD40に結合する当該断片; 並びにオリゴマー形成ペプチドから成るグループから選択される、可溶性オリゴ マーCD40リガンドである、請求項15に記載の方法。 18.CD40結合蛋白質が: (a) SEQ ID NO:2のアミノ酸1から261,35から261,34から225,113から261 ,113から225,120から261もしくは120から225を含むペプチド; (b) CD40に結合する(a)によるペプチドの断片; (c) (a)もしくは(b)のペプチドをコードするDNAに、ストリンジェントな条件 下(6×SSC、63℃で一晩ハイブリダイズ;3×SSC、55℃で洗浄)でハイブリダ イズするDNAにコードされ、CD40に結合するペプチド; (d) (a)によるポリペプチドで、アミノ酸194のシステインが、トリプトファ ン、セリン、アスパラギン酸およびリジンからなるグループから選択される別の アミノ酸に置換されている当該ポリペプチド;並びに (e) ポリペプチド(d)の断片でCD40に結合する当該断片; 並びにオリゴマー形成ペプチドから成るグループから選択される、可溶性オリゴ マーCD40リガンドである、請求項16に記載の方法。 19.(a) 個体から樹状細胞を回収し; (b) (i)抗原の取り込みおよび加工を促進する条件下で培養中に該樹状細胞を 抗原に暴露させる、もしくは(ii)該抗原をコードする遺伝子で該樹状細胞をトラ ンスフェクトすることによって、該樹状細胞に該抗原を発現させ; (c) 該抗原を発現する樹状細胞を、可溶性CD40のCD40Lへの結合を最低約90% 阻害することが観察されることによって決定されるように、CD40に結合し、CD40 のCD40Lへの結合を阻害することができるCD40結合蛋白質に暴露することによっ て、該抗原を発現する樹状細胞を活性化し;そして (d) T細胞に対して該樹状細胞に該抗原を提示させる 工程によって産生される抗原特異的T細胞の集団。 20.CD40結合蛋白質が: (a) SEQ ID NO:2のアミノ酸1から261,35から261,34から225,113から261 ,113から225,120から261もしくは120から225を含むペプチド; (b) CD40に結合する(a)によるペプチドの断片; (c) (a)もしくは(b)のペプチドをコードするDNAに、ストリンジェントな条件 下(6×SSC、63℃で一晩ハイブリダイズ;3×SSC、55℃で洗浄)でハイブリダイ ズするDNAにコードされ、CD40に結合するペプチド; (d) (a)によるポリペプチドで、アミノ酸194のシステインが、トリプトファ ン、セリン、アスパラギン酸およびリジンからなるグループから選択される別の アミノ酸に置換されている当該ポリペプチド;並びに (e) ポリペプチド(d)の断片でCD40に結合する当該断片; 並びにオリゴマー形成ペプチドから成るグループから選択される、可溶性オリゴ マーCD40リガンドである、請求項19に記載の集団。
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JP2008515439A (ja) * | 2004-10-07 | 2008-05-15 | アルゴス セラピューティクス,インコーポレイティド | 成熟樹状細胞組成物およびその培養方法 |
JP2013121352A (ja) * | 2004-10-07 | 2013-06-20 | Argos Therapeutics Inc | 成熟樹状細胞組成物およびその培養方法 |
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EP0961824A1 (en) | 1999-12-08 |
NO986173D0 (no) | 1998-12-29 |
NZ333607A (en) | 2000-08-25 |
JP2008119004A (ja) | 2008-05-29 |
AU705647B2 (en) | 1999-05-27 |
EP0961824A4 (en) | 2003-01-29 |
KR20000022445A (ko) | 2000-04-25 |
IL127912A0 (en) | 1999-11-30 |
AU3655497A (en) | 1998-02-02 |
CA2259140C (en) | 2008-09-30 |
WO1998001538A1 (en) | 1998-01-15 |
CA2259140A1 (en) | 1998-01-15 |
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