JP2008283975A5 - - Google Patents

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JP2008283975A5
JP2008283975A5 JP2008148570A JP2008148570A JP2008283975A5 JP 2008283975 A5 JP2008283975 A5 JP 2008283975A5 JP 2008148570 A JP2008148570 A JP 2008148570A JP 2008148570 A JP2008148570 A JP 2008148570A JP 2008283975 A5 JP2008283975 A5 JP 2008283975A5
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sina molecule
nucleotide
nucleotides
fragment
sina
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JP2008148570A
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JP2008283975A (ja
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Priority claimed from PCT/US2002/009187 external-priority patent/WO2002081494A1/en
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Claims (17)

  1. RNA干渉(RNAi)によりC型肝炎ウイルス(HCV)RNAの発現を阻害する化学的に修飾された二本鎖短干渉核酸(siNA)分子であって,
    a) 前記siNA分子の各鎖は,独立して,18−24ヌクレオチドの長さであり,siNAデュープレックスは17−23塩基対を含み;
    b) 前記siNA分子の一方の鎖は前記HCV RNAに対して,siNA分子がRNA干渉によりHCV RNAの発現を阻害するのに十分な相補性を有するヌクレオチド配列を含み;および
    c) センスおよび/またはアンチセンスsiNA鎖の10個またはそれ以上のピリミジンヌクレオチドは,2’−デオキシ,2’−O−メチルまたは2’−デオキシ−2’−フルオロヌクレオチドで化学的に修飾されており,かつ,1またはそれ以上のホスホロチオエートヌクレオチド間結合を有するか,および/または,3’末端,5’末端,または3’および5’末端の両方に末端キャップ分子を有しており,これは同じ鎖または異なる鎖に存在する,
    ことを特徴とするsiNA分子。
  2. 前記siNA分子は,ヌクレオチド位置の約5%,10%,20%,30%,40%または50%にリボヌクレオチドを含む,請求項1に記載のsiNA分子。
  3. siNA分子は2つの別々のオリゴヌクレオチドフラグメントから組み立てられ,一方のフラグメントはセンス領域を含み,第2のフラグメントはアンチセンス領域を含む,請求項1に記載のsiNA分子。
  4. センス領域中のプリンヌクレオチドは2’−デオキシプリンヌクレオチドであり,センス領域中のピリミジンヌクレオチドは2’−デオキシ−2’−フルオロピリミジンヌクレオチドである,請求項3に記載のsiNA分子。
  5. センス領域中のピリミジンヌクレオチドは2’−O−メチルピリミジンヌクレオチドであり,センス領域中のプリンヌクレオチドはプリンリボヌクレオチドであり,センスフラグメントは5’末端および3’末端に末端キャップ成分を含む,請求項3に記載のsiNA分子。
  6. センス領域を含むフラグメントは,フラグメントの5’末端,3’末端,または5’末端および3’末端の両方に末端キャップ成分を含む,請求項3に記載のsiNA分子。
  7. アンチセンス領域のピリミジンヌクレオチドは2’−デオキシ−2’−フルオロピリミジンヌクレオチドであり,アンチセンス領域のプリンヌクレオチドは2’−O−メチルプリンヌクレオチドである,請求項3に記載のsiNA分子。
  8. アンチセンス領域のプリンヌクレオチドは2’−デオキシプリンヌクレオチドであり,アンチセンス領域のピリミジンヌクレオチドは2’−デオキシ−2’−フルオロピリミジンヌクレオチドである,請求項3に記載のsiNA分子。
  9. アンチセンス領域は3’末端にホスホロチオエートヌクレオチド間結合を含む,請求項3に記載のsiNA分子。
  10. siNA分子の2つのフラグメントはそれぞれ21ヌクレオチドを含む,請求項3に記載のsiNA分子。
  11. siNA分子の各フラグメントの約19ヌクレオチドはsiNA分子の他方のフラグメントの相補的ヌクレオチドと塩基対形成し,各フラグメントの少なくとも2つの3’末端ヌクレオチドは他方のフラグメントのヌクレオチドと塩基対形成しない,請求項10に記載のsiNA分子。
  12. アンチセンス領域のヌクレオチドはHCV RNAのヌクレオチド配列と相補的である,請求項3に記載のsiNA分子。
  13. アンチセンス領域を含むフラグメントの5’末端は任意にリン酸基を含んでいてもよい,請求項3に記載のsiNA分子。
  14. HCV RNAはHCVマイナス鎖RNAを含む,請求項1に記載のsiNA分子。
  15. HCV RNAはHCVプラス鎖RNAを含む,請求項1に記載のsiNA分子。
  16. 請求項1−15のいずれかに記載のsiNA分子を薬学的に許容しうる担体または希釈剤中に含む組成物。
  17. HCV感染の治療に用いるための,請求項1−15のいずれかに記載のsiNA分子。
JP2008148570A 2002-02-20 2008-06-05 短干渉核酸(siNA)を用いるC型肝炎ウイルス(HCV)遺伝子発現のRNA干渉媒介性阻害 Pending JP2008283975A (ja)

Applications Claiming Priority (9)

Application Number Priority Date Filing Date Title
US35858002P 2002-02-20 2002-02-20
US36312402P 2002-03-11 2002-03-11
PCT/US2002/009187 WO2002081494A1 (en) 2001-03-26 2002-03-26 Oligonucleotide mediated inhibition of hepatitis b virus and hepatitis c virus replication
US38678202P 2002-06-06 2002-06-06
US40110402P 2002-08-05 2002-08-05
US40678402P 2002-08-29 2002-08-29
US40837802P 2002-09-05 2002-09-05
US40929302P 2002-09-09 2002-09-09
US44012903P 2003-01-15 2003-01-15

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JP2008283975A5 true JP2008283975A5 (ja) 2011-03-17

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JP2003569657A Withdrawn JP2005517427A (ja) 2002-02-20 2003-02-20 短干渉核酸(siNA)を用いるC型肝炎ウイルス(HCV)遺伝子発現のRNA干渉媒介性阻害
JP2008148570A Pending JP2008283975A (ja) 2002-02-20 2008-06-05 短干渉核酸(siNA)を用いるC型肝炎ウイルス(HCV)遺伝子発現のRNA干渉媒介性阻害
JP2012230406A Withdrawn JP2013078311A (ja) 2002-02-20 2012-10-18 短干渉核酸(siNA)を用いるC型肝炎ウイルス(HCV)遺伝子発現のRNA干渉媒介性阻害

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US (1) US7915400B2 (ja)
EP (1) EP1430157B1 (ja)
JP (3) JP2005517427A (ja)
AT (1) ATE519774T1 (ja)
AU (1) AU2003219817B2 (ja)
CA (1) CA2457528C (ja)
GB (1) GB2397062B (ja)
WO (1) WO2003070750A2 (ja)

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