JPWO2008123308A1 - バソヒビン含有治療剤 - Google Patents
バソヒビン含有治療剤 Download PDFInfo
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- JPWO2008123308A1 JPWO2008123308A1 JP2009509145A JP2009509145A JPWO2008123308A1 JP WO2008123308 A1 JPWO2008123308 A1 JP WO2008123308A1 JP 2009509145 A JP2009509145 A JP 2009509145A JP 2009509145 A JP2009509145 A JP 2009509145A JP WO2008123308 A1 JPWO2008123308 A1 JP WO2008123308A1
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- Prior art keywords
- vasohibin
- therapeutic agent
- peritoneal
- cells
- diabetic nephropathy
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- A61K38/1703—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
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- A—HUMAN NECESSITIES
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- C12N2710/10011—Adenoviridae
- C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
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- C12N2710/10343—Use of virus, viral particle or viral elements as a vector viral genome or elements thereof as genetic vector
Abstract
Description
Jones M, Ibels L, Schenkel B, Zagari M、Kidney International、2004、Vol.65、p.757-767 An S. De Vriese, et al.、Journal of the American Society of Nephrology、2001、Vol.12、p.993-1000 Allan Flyvbjerg, et al.、Diabetes、2002、Vol.51、p.3090-30941 John D. Williams, et al.、Journal of the American Society of Nephrology、2002、Vol.13、p.470-479 Maria Yanez-Mo, et al.、The NEW ENGLAND JOURNAL of MEDICINE、2005、Vol.348、p.403-413 Peter J. Margetts, et al.、Journal of the American Society of Nephrology、2005、Vol.16、p.425-436 Sophie Combet, et al.、Journal of the American Society of Nephrology、2000、Vol.11、p.717-728 Hiroaki Io, et al.、Kidney International、2004、Vol.65、p.1927-1936 Yoko Yoshio, et al.、Kidney International、2004、Vol.66、p.1677-1685
〔1〕 バソヒビンを含有してなる、糖尿病性腎症の治療剤、
〔2〕 バソヒビンをコードするポリヌクレオチドを含むベクターを含有してなる、糖尿病性腎症の治療剤、
〔3〕 ベクターがウイルスベクターである前記〔2〕記載の糖尿病性腎症の治療剤、
〔4〕 ウイルスベクターがアデノウイルスベクターである前記〔3〕記載の糖尿病性腎症の治療剤、
〔5〕 糖尿病性腎症の治療剤の製造のための、バソヒビンの使用、
〔6〕 糖尿病性腎症の治療剤の製造のための、バソヒビンをコードするポリヌクレオチドの使用、
〔7〕 糖尿病性腎症の治療に使用するためのバソヒビン、
〔8〕 糖尿病性腎症の治療に使用するためのバソヒビンをコードするポリヌクレオチド、
〔9〕 前記〔1〕〜〔4〕いずれか記載の治療剤を投与する工程を含む、糖尿病性腎症の治療方法、
〔10〕 バソヒビンを含有してなる、腹膜硬化症の治療剤、
〔11〕 バソヒビンをコードするポリヌクレオチドを含むベクターを含有してなる、腹膜硬化症の治療剤、
〔12〕 ベクターがウイルスベクターである前記〔11〕記載の腹膜硬化症の治療剤、
〔13〕 ウイルスベクターがアデノウイルスベクターである前記〔12〕記載の腹膜硬化症の治療剤、
〔14〕 腹膜硬化症の治療剤の製造のための、バソヒビンの使用、
〔15〕 腹膜硬化症の治療剤の製造のための、バソヒビンをコードするポリヌクレオチドの使用、
〔16〕 腹膜硬化症の治療に使用するためのバソヒビン、
〔17〕 腹膜硬化症の治療に使用するためのバソヒビンをコードするポリヌクレオチド、及び
〔18〕 前記〔10〕〜〔13〕いずれか記載の治療剤を投与する工程を含む、腹膜硬化症の治療方法。
に関する。
バソヒビンは、Molecular Cloning:A Laboratory Manual,Second Edition(1989)(Cold Spring Harbor Laboratory Press)、Current Protocols in Molecular Biology(1994)(Wiley−Interscience)等に記載された方法等を用い、例えば、以下の方法により、バソヒビンの遺伝子を宿主細胞中で発現させ、作製することができる。
バソヒビン蛋白質の発現ベクターは、原核生物中で自立複製可能であると同時に、プロモーター、リボソーム結合配列、バソヒビンをコードする遺伝子、転写終結配列より構成されていることが好ましい。プロモーターを制御する遺伝子が含まれていてもよい。
宿主として動物細胞を用いる場合、発現ベクターとして、例えば、pcDNA1/Amp、pcDNA1、pCDM8、pREP4(インビトロジェン社製)、pHM6(ロシュダイアグノスティクス社製)、pKK223−3、pGEX(アマシャムバイオサイエンス社製)、pAGE107(Cytotechnology,3,133(1990))、pAGE103(The Journal of Biochemistry,101,1307(1987))、pAMo、pAMoA(pAMoPRSA)(The Journal of Biological Chemistry,268,22782−22787(1993))、pAS3−3(特開平2−22705)等を用いることができる。
宿主として昆虫細胞を用いる場合、発現ベクターとしては、例えば、pVL1392、pVL1393、pBlueBacIII、pFASTBac1(インビトロジェン社製)等が、感染用ウイルスとしては、例えば、ヨトウガ科昆虫に感染するバキュロウイルス(Vaculovirus)Autographa california nuclear polyhedrosis virus(AcMNPV)Bac−N−Blue DNA等が挙げられる。昆虫細胞の形質転換の方法は、例えば、Baculovirus Expression Vector:A Laboratory Manual(1992)(W.H.Freeman and Company)、Molecular Cloning:A Laboratory Manual,Second Edition(1989)(Cold Spring Harbor Laboratory Press)、Current Protocols in Molecular Biology(1994)(Wiley−Interscience)、Biotechnology,6,47(1988)等に記載の方法が用いられる。
バソヒビンをコードするDNAを組み込んだ発現用プラスミドを保有する形質転換体が、大腸菌、動物細胞等の細胞の場合、各種宿主に適した通常の培養方法に従って培養し、該タンパク質を産生・蓄積させ、形質転換体又は培養液より該タンパク質を回収することにより、該タンパク質を作製することができる。形質転換体が、動物個体又は植物個体の場合、各種宿主に適した通常の生育方法に従って飼育又は栽培し、該タンパク質を産生・蓄積させ、該動物個体又は植物個体より該タンパク質を回収することにより、該タンパク質を作製することができる。
バソヒビンは、形質転換体を培養し、培養液からバソヒビンを単離・精製することにより作製することができる。バソヒビンの単離・精製方法は、当該分野において周知慣用の常法により行うことができ、例えば、酵素の単離・精製方法やSandlerらの糖転移酵素の精製方法(Methods in Enzymology,83,458)を用いることができる。
遺伝子治療用ベクターの作製方法、細胞における発現方法等は上記「バソヒビンの作製方法」に記載の発現ベクターと同様である。
[組換えアデノウイルスの作成]
プラスミドpFLAG13−1036(WO02/090546参照)を、制限酵素NotI及びXbaI処理することにより回収したヒトVasohibin−1をコードするcDNAをT4DNAポリメラーゼ(タカラバイオ社)処理することにより平滑末端化し精製した。精製したcDNAを、制限酵素SmiI消化したコスミドベクターpAxCAwtit(タカラバイオ社製)に、ライゲーション・キットver.2(タカラバイオ社製)を用いて挿入し、制限酵素SmiIによる処理後、Gigapack III XL Extract(Stratagene社製)によりパッケージングを行い、大腸菌DH5αに感染させ、アンピシリン(Sigma社製)を含む寒天プレートに撒くことによりコスミドベクターpAxCAwtit−Vh1を得た。得られたベクターを、アデノウイルスゲノムDNA−TPC(タカラバイオ社製)と共にTransIT−293試薬(タカラバイオ社製)によりHEK293細胞に導入し、細胞内における相同組換えにより組換えアデノウイルス(Ad−Vasohibin−1)を産生する形質転換細胞を得た。この遺伝子導入293細胞を12時間時間培養後、EDTA/PBS(−)を用いて回収し、得られた懸濁液を段階希釈してコラーゲンコート96穴プレート(Corning社製)に撒きなおし、10%牛胎児血清(FCS)を含むダルベッコ変法イーグル培地(DMEM、Sigma社製)にて18日間培養した。細胞の変性が見られたウェルより細胞と培養液を回収し、ドライアイスと37℃温浴による凍結融解を6回繰り返し、4℃で5000r/min、5分間遠心した上清を1次ウイルス液として−80℃保存した。次に、コラーゲンコート24穴プレート(Corning社製)に70〜100%コンフルエントまで培養した293細胞に、ウェルあたり10μLの前記1次ウイルス液と5%FCSを含むDMEM0.1mLを加えて感染させた。この操作を15分ごと4回行い、5%FCSを含むDMEM0.4mLを加えた後、培養液ごと細胞を回収し凍結融解を6回繰り返し4℃で5000r/min、5分間遠心した上清を2次ウイルス液として−80℃保存した。なお、陰性対照として用いたbeta−galactosidase発現アデノウイルスAxCAiLacZはタカラバイオ社より購入した。
コラーゲンコート25cm2フラスコ(Corning社製)に100%コンフルエントまで培養した293細胞に、得られた2次ウイルス液15μLと5%FCSを含むDMEM0.5mLを加える操作を15分ごと4回行った後、5%FCSを含むDMEM4.5mLを加え3日間培養した。その後、培養液ごと回収した細胞を密閉型ソニケーターで破砕し、4℃で3000r/min、10分間遠心し上清を回収したものをドライアイスで急凍して−80℃保存した(3次ウイルス液)。同様に、この3次ウイルス液50μLと5%FCSを含むDMEM2mLを、コラーゲンコート75cm2フラスコ(Corning社製)に100%コンフルエントまで培養した293細胞に感染させ、5%FCSを含むDMEM13mLをさらに加えて3日間培養し、3次ウイルス液と同様にウイルス液を調製した(4次ウイルス液)。得られたウイルスの力価はTCID50法により測定した。なお、4次ウイルス液は、1mL/バイアルに分注し、ドライアイスで急凍後、使用するまで−80℃に保管した。
コラーゲンコート225cm2フラスコ(Corning社製)6本に70〜100%コンフルエントまで培養した293細胞に、約1.0pfu/mLの4次ウイルス液をそれぞれ加えて感染させた。この操作を15分ごと4回行った後、フラスコ1本あたり5%FCSを含むDMEM30mLを加え4日間培養し、培養液ごと回収した細胞を4℃で3000r/min、10分間遠心し、上清30mLを除去した。その後、残りを密閉型ソニケーターで破砕してウイルスを遊離させ、4℃で3000r/min、10分間遠心し上清を回収した。4M 塩化セシウム/10mM HEPES 10mL、2.2M 塩化セシウム/10mM HEPES 5mLの順に重層したチューブにウイルス液20mLを加え、スウィングローターにて4℃で25000r/min、2時間遠心後、ウイルスのバンドをシリンジで回収した。さらに、前記回収に使用したシリンジチューブ内で、前記回収したウイルス液に等量の飽和塩化セシウムを加えた後、4M塩化セシウム/10mM HEPES 2mL、2.2M塩化セシウム/10mM HEPES 4mLをこの順に重層し、スウィングローターにて4℃で35000r/min、3時間遠心し、ウイルスのバンドをシリンジで回収した。回収したウイルス液を10%グリセロールを含むPBS(−)1Lで終夜透析を行い、得られた精製ウイルス液を分注後、−80℃で使用するまで凍結保存した。
得られた精製ウイルス液の最適投与量を決定するために、以下の検討を行った。
得られた精製ウイルス液が糖尿病性腎症の進展抑制作用を有するかを調べるために、以下の検討を行った。
次に、得られた精製ウイルス液を投与することにより、腹膜におけるバソヒビンの発現量が亢進するかを調べるために、以下の検討を行った。
得られた精製ウイルス液が腹膜硬化症の進展抑制作用を有するかを調べるために、以下の検討を行った。
配列表の配列番号2は、KIAA1036ポリペプチドである。
配列表の配列番号3は、AY834202ポリヌクレオチドである。
配列表の配列番号4は、AY834202ポリペプチドである。
Claims (18)
- バソヒビンを含有してなる、糖尿病性腎症の治療剤。
- バソヒビンをコードするポリヌクレオチドを含むベクターを含有してなる、糖尿病性腎症の治療剤。
- ベクターがウイルスベクターである請求項2記載の糖尿病性腎症の治療剤。
- ウイルスベクターがアデノウイルスベクターである請求項3記載の糖尿病性腎症の治療剤。
- 糖尿病性腎症の治療剤の製造のための、バソヒビンの使用。
- 糖尿病性腎症の治療剤の製造のための、バソヒビンをコードするポリヌクレオチドの使用。
- 糖尿病性腎症の治療に使用するためのバソヒビン。
- 糖尿病性腎症の治療に使用するためのバソヒビンをコードするポリヌクレオチド。
- 請求項1〜4いずれか記載の治療剤を投与する工程を含む、糖尿病性腎症の治療方法。
- バソヒビンを含有してなる、腹膜硬化症の治療剤。
- バソヒビンをコードするポリヌクレオチドを含むベクターを含有してなる、腹膜硬化症の治療剤。
- ベクターがウイルスベクターである請求項11記載の腹膜硬化症の治療剤。
- ウイルスベクターがアデノウイルスベクターである請求項12記載の腹膜硬化症の治療剤。
- 腹膜硬化症の治療剤の製造のための、バソヒビンの使用。
- 腹膜硬化症の治療剤の製造のための、バソヒビンをコードするポリヌクレオチドの使用。
- 腹膜硬化症の治療に使用するためのバソヒビン。
- 腹膜硬化症の治療に使用するためのバソヒビンをコードするポリヌクレオチド。
- 請求項10〜13いずれか記載の治療剤を投与する工程を含む、腹膜硬化症の治療方法。
Priority Applications (1)
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JP2009509145A JP5256192B2 (ja) | 2007-03-29 | 2008-03-26 | バソヒビン含有治療剤 |
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JP2007089123 | 2007-03-29 | ||
JP2007089123 | 2007-03-29 | ||
JP2007089122 | 2007-03-29 | ||
JP2007089122 | 2007-03-29 | ||
PCT/JP2008/055744 WO2008123308A1 (ja) | 2007-03-29 | 2008-03-26 | バソヒビン含有治療剤 |
JP2009509145A JP5256192B2 (ja) | 2007-03-29 | 2008-03-26 | バソヒビン含有治療剤 |
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JPWO2008123308A1 true JPWO2008123308A1 (ja) | 2010-07-15 |
JP5256192B2 JP5256192B2 (ja) | 2013-08-07 |
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US (2) | US20100113354A1 (ja) |
EP (1) | EP2140876A4 (ja) |
JP (1) | JP5256192B2 (ja) |
WO (1) | WO2008123308A1 (ja) |
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JPWO2010074082A1 (ja) * | 2008-12-24 | 2012-06-21 | 塩野義製薬株式会社 | バソヒビン修飾体 |
KR101780584B1 (ko) | 2016-03-10 | 2017-09-21 | 인하대학교 산학협력단 | 바소히빈-1을 유효성분으로 포함하는 발기부전 예방 또는 치료용 조성물 |
CN113957150A (zh) * | 2021-11-18 | 2022-01-21 | 天津市肿瘤医院(天津医科大学肿瘤医院) | Vash2作为肺鳞癌标志物的应用 |
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JPS58110600A (ja) | 1981-12-25 | 1983-07-01 | Kyowa Hakko Kogyo Co Ltd | ヒトβ型インタ−フエロン遺伝子を含む組みかえ体プラスミド |
JP2564268B2 (ja) | 1985-08-28 | 1996-12-18 | 協和醗酵工業株式会社 | 融合抗原ポリペプチド |
ZA872705B (en) | 1986-04-22 | 1987-10-05 | Immunex Corporation | Human g-csf protein expression |
JPS63233798A (ja) | 1986-10-09 | 1988-09-29 | Kyowa Hakko Kogyo Co Ltd | 5′−グアニル酸の製造法 |
JPH0222705A (ja) | 1988-07-12 | 1990-01-25 | Fujitsu Ltd | 工程管理システムにおける特急製作指示装置 |
JPH0322979A (ja) | 1989-06-19 | 1991-01-31 | Kyowa Hakko Kogyo Co Ltd | 新規プラスミノーゲン活性化因子 |
JP3131322B2 (ja) | 1991-12-17 | 2001-01-31 | 協和醗酵工業株式会社 | 新規α2→3シアリルトランスフェラーゼ |
US20050158719A1 (en) * | 2001-05-07 | 2005-07-21 | Yasufumi Sato | Polypeptide serving as angiogenic marker and dna thereof |
WO2003086178A2 (en) * | 2002-04-11 | 2003-10-23 | Children's Medical Center Corporation | Methods for inhibiting vascular hyperpermeability |
US8216833B2 (en) * | 2003-04-18 | 2012-07-10 | Izumu Saito | Cosmid vector |
US20050250694A1 (en) * | 2003-10-10 | 2005-11-10 | Ma Jian-Xing | Compounds useful in inhibiting vascular leakage, inflammation and fibrosis and methods of making and using same |
WO2006073052A1 (ja) | 2005-01-05 | 2006-07-13 | Shionogi & Co., Ltd. | 新規血管新生抑制因子 |
US20090270314A1 (en) * | 2005-09-29 | 2009-10-29 | Tohoku University | Polypeptide having anti-angiogenic activity |
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- 2008-03-26 US US12/593,597 patent/US20100113354A1/en not_active Abandoned
- 2008-03-26 EP EP08738932A patent/EP2140876A4/en not_active Withdrawn
- 2008-03-26 WO PCT/JP2008/055744 patent/WO2008123308A1/ja active Application Filing
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Also Published As
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EP2140876A1 (en) | 2010-01-06 |
JP5256192B2 (ja) | 2013-08-07 |
WO2008123308A1 (ja) | 2008-10-16 |
EP2140876A4 (en) | 2011-08-03 |
US20120004287A1 (en) | 2012-01-05 |
US20100113354A1 (en) | 2010-05-06 |
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