JP2014534266A - 新規な増強型セレクチンアンタゴニスト - Google Patents
新規な増強型セレクチンアンタゴニスト Download PDFInfo
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- JP2014534266A JP2014534266A JP2014543634A JP2014543634A JP2014534266A JP 2014534266 A JP2014534266 A JP 2014534266A JP 2014543634 A JP2014543634 A JP 2014543634A JP 2014543634 A JP2014543634 A JP 2014543634A JP 2014534266 A JP2014534266 A JP 2014534266A
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- PDTFCHSETJBPTR-UHFFFAOYSA-N phenylmercuric nitrate Chemical compound [O-][N+](=O)O[Hg]C1=CC=CC=C1 PDTFCHSETJBPTR-UHFFFAOYSA-N 0.000 description 1
- 239000008055 phosphate buffer solution Substances 0.000 description 1
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- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 1
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- RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 description 1
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- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
配列番号1は、ヒトPSGL−1のアミノ酸配列である。
配列番号2は、ヒトPSGL−1内に見出されるP−セレクチンおよびL−セレクチンに対する主要な結合部位のアミノ酸配列である。
配列番号3は、本発明の例証となるTSGL融合タンパク質である、タンデム可溶性糖タンパク質リガンド融合タンパク質、TSGL[PSGL1−19:PSGL5−19]−Fcをコードするヌクレオチド配列である。
配列番号4は、本発明の例証となるTSGL融合タンパク質である、タンデム可溶性糖タンパク質リガンド融合タンパク質、TSGL[PSGL1−19:PSGL5−19]−Fcをコードするタンパク質配列である。
ヒトPSGL−1は、17個のアミノ酸N末端シグナルペプチド(アミノ酸1〜17)、24個のアミノ酸N末端プロペプチド(アミノ酸18〜41)、および371個のアミノ酸P−セレクチン糖タンパク質リガンド1鎖(アミノ酸42〜412)を含む412個のアミノ酸タンパク質(配列番号1)である。
配列番号1
配列番号2:QATEYEYLDY DFLPETEPP
特定の実施形態において、組成物はさらに、1つまたは複数の界面活性剤を含む。例示的な界面活性剤には、天然の乳化剤(例えば、アラビアゴム、寒天、アルギン酸、アルギン酸ナトリウム、トラガカント、コンドラックス(chondrux)、コレステロール、キサンタン、ペクチン、ゼラチン、卵黄、カゼイン、羊毛脂、コレステロール、ワックス、およびレシチン)、コロイド粘土(例えば、ベントナイト[ケイ酸アルミニウム]およびVeegum[ケイ酸アルミニウムマグネシウム])、長鎖アミノ酸誘導体、高分子量アルコール(例えば、ステアリルアルコール、セチルアルコール、オレイルアルコール、モノステアリン酸トリアセチン、ジステアリン酸エチレングリコール、モノステアリン酸グリセリル、およびモノステアリン酸プロピレングリコール、ポリビニルアルコール)、カルボマー(例えば、カルボキシポリメチレン、ポリアクリル酸、アクリル酸ポリマー、およびカルボキシビニルポリマー)、カラギーナン、セルロース誘導体(例えば、カルボキシメチルセルロースナトリウム、粉末セルロース、ヒドロキシメチルセルロース、ヒドロキシプロピルセルロース、ヒドロキシプロピルメチルセルロース、メチルセルロース)、ソルビタン脂肪酸エステル(例えば、ポリオキシエチレンソルビタンモノラウレート[Tween 20]、ポリオキシエチレンソルビタン[Tween 60]、ポリオキシエチレンソルビタンモノオレエート[Tween 80]、ソルビタンモノパルミテート[Span 40]、ソルビタンモノステアレート[Span 60]、ソルビタントリステアレート[Span 65]、グリセリルモノオレエート、ソルビタンモノオレエート[Span80]、ポリオキシエチレンエステル(例えば、ポリオキシエチレンモノステアレート[Myrj 45]、ポリオキシエチレン水素化ヒマシ油)、ポリエトキシル化ヒマシ油、ポリオキシメチレンステアレート、およびSolutol)、スクロース脂肪酸エステル、ポリエチレングリコール脂肪酸エステル(例えば、Cremophor)、ポリオキシエチレンエーテル(例えば、ポリオキシエチレンラウリルエーテル[Brij 30])、ポリ(ビニルピロリドン)、ジエチレングリコールモノラウレート、トリエタノールアミンオレエート、オレイン酸ナトリウム、オレイン酸カリウム、オレイン酸エチル、オレイン酸、ラウリン酸エチル、ラウリル硫酸ナトリウム、Pluronic F 68、Poloxamer 188、臭化セトリモニウム、塩化セチルピリジニウム、塩化ベンザルコニウム、ドキュセートナトリウムなど、および/またはそれらの組み合わせが挙げられるが、それらに限定されない。特定の実施形態において、界面活性剤はTween界面活性剤(例えば、Tween 60、Tween 80など)である。
本発明の組成物およびキットは、P−セレクチン、E−セレクチン、またはL−セレクチン媒介性細胞内接着によって特徴づけられる状態を処置することにおいて有用であり得る。そのような状態には、非限定的に、心筋梗塞、細菌またはウイルスの感染、転移性状態、関節炎、痛風、ブドウ膜炎、急性呼吸窮迫症候群、喘息、肺気腫、遅延型過敏反応、全身性エリテマトーデス、火傷などの熱的傷害または凍傷、自己免疫性甲状腺炎、実験的アレルギー性脳脊髄炎、多発性硬化症、外傷に続発する多臓器傷害症候群、糖尿病、レイノー症候群、好中球性皮膚症(スウィート症候群)、炎症性腸疾患、グレーブス病、糸球体腎炎、歯肉炎、歯周炎、溶血性尿毒症症候群、潰瘍性大腸炎、クローン病、壊死性腸炎、顆粒球輸血関連症候群、サイトカイン誘導性毒性などの炎症性障害が挙げられる。
配列番号3
配列番号4
Claims (15)
- 同じポリペプチド鎖に沿ってタンデム配置で組み合わされた少なくとも2個の硫酸化P−セレクチン糖タンパク質リガンド(PSGL)ドメインを含む可溶性タンデムセレクチン糖タンパク質リガンド(TSGL)分子であって、PSGLドメインのそれぞれが、少なくとも1個の硫酸化チロシン、およびシアリルルイスx(sLex)エピトープを有する少なくとも1個のO連結型グリカンを含む、TSGL分子。
- 非TSGLポリペプチドに融合した、請求項1に記載のTSGL分子。
- 非TSGLポリペプチドが免疫グロブリンFcである、非TSGLポリペプチドに融合した請求項1に記載のTSGL分子。
- 非TSGLポリペプチドが、MAP−1、SolCD39、クニッツドメインポリペプチド、フィブロネクチンIII型ドメイン、またはXTENポリペプチドからなる群から選択される、非TSGLポリペプチドに融合した請求項1に記載のTSGL分子。
- 配列番号4のアミノ酸配列、または配列番号4のアミノ酸配列と少なくとも70%の配列同一性を有するその機能性変異体を含む、請求項1に記載のTSGL分子。
- 配列番号4のアミノ酸配列を含む、請求項5に記載のTSGL分子。
- 同じポリペプチド鎖に沿ってタンデム配置で組み合わされた少なくとも2個のP−セレクチン糖タンパク質リガンド(PSGL)ドメインを含む可溶性タンデムセレクチン糖タンパク質リガンド(TSGL)分子をコードするDNA配列であって、PSGLドメインが、少なくとも1個の硫酸化チロシン、およびシアリルルイスx(sLex)エピトープを有する少なくとも1個のO連結型グリカンを含む、DNA配列。
- 非TSGLポリペプチドに融合したTSGL分子をコードする、請求項7に記載のDNA配列。
- 非TSGLポリペプチドが免疫グロブリンFcである、非TSGLポリペプチドに融合したTSGL分子をコードする請求項7に記載のDNA配列。
- 非TSGLポリペプチドが、MAP−1、SolCD39、クニッツドメインポリペプチド、フィブロネクチンIII型ドメイン、またはXTENポリペプチドからなる群から選択される、非TSGLポリペプチドに融合したTSGL分子をコードする請求項7に記載のDNA配列。
- TSGL分子が、配列番号4のアミノ酸配列、または配列番号4のアミノ酸配列と少なくとも約70%の配列同一性を有するその機能性変異体を含む、TSGL分子をコードする請求項7に記載のDNA配列。
- TSGL分子が、配列番号4のアミノ酸配列を含む、請求項11に記載のDNA配列。
- 可溶性タンデムセレクチン糖タンパク質リガンド(TSGL)分子でヒト対象において障害を処置する方法であって、障害が、移植片対宿主病、炎症性障害、血栓性障害、多発性骨髄腫、および血管閉塞性障害からなる群から選択される、方法。
- TSGL分子が、配列番号4のアミノ酸配列、または配列番号4のアミノ酸配列と少なくとも約70%の配列同一性を有するその機能性変異体を含む、請求項13に記載の方法。
- TSGL分子が、配列番号4のアミノ酸配列を含む、請求項14に記載の方法。
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US11603406B2 (en) | 2017-03-14 | 2023-03-14 | Five Prime Therapeutics, Inc. | Antibodies binding to VISTA at acidic pH |
WO2019133454A2 (en) * | 2017-12-29 | 2019-07-04 | Shaw Gray D | Methods to improve the therapeutic index of activated t cells |
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JP2003529610A (ja) * | 2000-03-31 | 2003-10-07 | ジェネティクス インスティテュート,エルエルシー | 血栓症を抑制するためのp−セレクチン糖タンパク質リガンド−1(psgl−1)およびそのフラグメント |
JP2005507868A (ja) * | 2001-08-03 | 2005-03-24 | ジェネティクス インスティテュート,エルエルシー | 虚血後の白血球内皮相互作用の調節 |
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CA2377135A1 (en) * | 1999-04-23 | 2000-11-02 | Ceptyr, Inc. | Dsp-10 dual-specificity map kinsase phosphatase |
US20040086519A1 (en) * | 2000-09-12 | 2004-05-06 | Genetics Institute, Llc | Inhibition of stenosis or restenosis by P-selectin ligand antagonists |
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JP2003529610A (ja) * | 2000-03-31 | 2003-10-07 | ジェネティクス インスティテュート,エルエルシー | 血栓症を抑制するためのp−セレクチン糖タンパク質リガンド−1(psgl−1)およびそのフラグメント |
JP2005507868A (ja) * | 2001-08-03 | 2005-03-24 | ジェネティクス インスティテュート,エルエルシー | 虚血後の白血球内皮相互作用の調節 |
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US20130136741A1 (en) | 2013-05-30 |
CA2857019A1 (en) | 2013-06-06 |
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