DK1578446T3 - Anti-cd33-antistoffer og fremgangsmåde til behandling af akut myeloid leukæmi ved anvendelse heraf - Google Patents
Anti-cd33-antistoffer og fremgangsmåde til behandling af akut myeloid leukæmi ved anvendelse heraf Download PDFInfo
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- DK1578446T3 DK1578446T3 DK03779105.0T DK03779105T DK1578446T3 DK 1578446 T3 DK1578446 T3 DK 1578446T3 DK 03779105 T DK03779105 T DK 03779105T DK 1578446 T3 DK1578446 T3 DK 1578446T3
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Claims (16)
- ANTI-CD33-ANTISTOFFER OG FREMGANGSMÅDE TIL BEHANDLING AF AKUT MYELOID LEUKÆMI VED ANVENDELSE HERAF1. CD33-specifikt antistof omfattende: (i) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFQGK ATLT ADKS STT A YMQLS SLTSEDS AV Y YC ARE VRLR YFDV WGQGTTVTV SS; og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: EIVLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSOKNYLAWYQQIPGQSPRLLIYW ASTRES GVPDRFTGSGSGTDFTLTISSVQPEDLAIYYCHQYLSSRTFGQGTKLEIKR; (ii) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFQGK ATLT ADKS STT A YMOLS SLTSEDS AV YYC ARE VRLR YFDV WGQGTTVIVS S; og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: NIMLIQSPGSLAVSPGERVTMSCKSSQSVFFSSSOKNYLAWYQQIPGQSPKWYW ASTRES OVPDRFTGSOSOTDFTT TTSS VOPEDT ,ΑΤΥΥΓΗΟΥΤ .S S R TFGOGTKT .F.TKR; (iii) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: OVOLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFKGKATLT ADKSSTT AYMQLS SLTSEDS AV YYC AREVRLRYFDVWGQGTTVTVSS; og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: EIVLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSQKNYLAWYQQIPGQSPRLLIYVV ASTRE S GVPDRFTGS GSGTDFTLTIS S VQPEDL AI YYCHQ YLS SRTFGQGTKLEIKR; (iv) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFQGKATLT ADKSSTT AYMQLSSLTSEDS AVYYCARE VRLR YFDVWGQGTTVTVSS; og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: NIMLTQSPGSLAVSPGERVIMSCKSSQSVFFSSSQKNYLAWYQQIPGQSPRLLIYWASTRES G VPDRFTGSGS GTDFTLTIS S VQPEDLAIYY CHQYLS S RTFGQGTKLEIKR; (v) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFKGKATLTADKSSTTAYMQLSSLTSEDSAVYYCAREVRLR YFDVWGQGTTVTVSS; Og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: NIMLTQSPGSLAVSPGERVIMSCKSSQSVFFSSSQKNYLAWYQQIPGQSPRLLIYW ASTRES G VPDRFTGSGS GTDFTLTIS S VQPEDLAIYYCHQYLS S RTFGQGTKLEIKR; (vi) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFQGK ATLT ADKS STTAYMQLS SLTSEDS AV YY C ARE VRLRYFDV WGQGTTVTV SS; og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: ErVLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSQKNYLAWYQQIPGQSPKLLIYW ASTRES GVPDRFTGSGSGTDFTLTISSVQPEDLAIYYCHQYLSSRTFGQGTKLEIKR; (vii) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFKGK ATLT ADKS STT A YMQLS SLTSEDS AV YY C ARE VRLRYFDV WGQGTTVTV SS; og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: EIVLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSQKNYLAWYQQIPGQSPKLLIYW ASTRES GVPDRFTGSGSGTDFTLTISSVQPEDLAIYYCHQYLSSRTFGQGTKLEIKR; (viii) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYI HWIKQTPGQGLEWVGVIYPGNDDISYNQKFQGKATLTADKSSTTAYMQLSSLTSEDSAVY YC ARE VRLR YFD VWGQGTT VT VS S; og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: EIMLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSQKNYLAWYQQIPGQSPRLLIYW ASTRES G VPDRFTGSGS GTDFTLTIS S VQPEDLAI YY CHQYLS S RTFGQGTKLEIKR; (ix) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFKGKATLT ADKS STT AYMQLSSLTSEDS AV YY C ARE VRLRYFDVWGQGTTVTVSS; og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: EIMLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSQKNYLAWYQQIPGQSPRLLIYW ASTRES G VPDRFTGSGS GTDFTLTIS S VQPEDLAI YY CHQYLS S RTFGQGTKLEIKR; (x) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFQGK ATLT ADKS STTAYMQLS SLTSEDS AV YYC ARE VRLRYFDV VVGQGTT VI VS S °g en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: EIMLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSQKNYLAWYQQIPGQSPKLLIYW ASTRES G VPDRFTGSGS GTDFTLTIS S VQPEDLAIYYCHQYLS S RTFGQGTKLEIKR; (xi) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFKGK ATLT ADKS STT A YMQLSSLTSEDS AV YY C ARE VRLRYFDVWGQGTTVTV SS; og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: EIMLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSQKNYLAWYQQIPGQSPKLLIYW ASTRES GVPDRFTGSGSGTDFTLTISSVQPEDLAIYYCHQYLSSRTFGQGTKLEIKR; (xii) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFQGK ATLT ADKS STT A YMQLS SLTSEDS AV YY C ARE VRLRYFDV WGQGTTVTV SS; °g en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: NIVLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSQKNYLAWYQQIPGQSPRLLIYW ASTRES GVPDRFTGSGSGTDFTLTISSVQPEDLAIYYCHQYLSSRTFGQGTKLEIKR; (xiii) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFKGKATLTADKSSTTAYMQLSSLTSEDSAVYYCAREVRLRYFDVWGQGTTVTVSS; og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: NIVLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSQKNYLAWYQQIPGQSPRLLIYW ASTRES GVPDRFTGSGSGTDFTLTISSVQPEDLAIYYCHQYLSSRTFGQGTKLEIKR; (xiv) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFQGKATLTADKS STT AYMQLSSLTSEDS A V Y Y C ARE VRLRYFDVWGQGTTVTV SS; °g en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: NIVLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSQKNYLAWYQQI PGQSPKLLIYWASTRESGVPDRFTGSGSGTDFTLTISSVQPEDLAIYYCHQYLSSRTFGQGT KLEIKR; eller (xv) en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFKGKATLT ADKS STTAYMQLS SLTSEDS AV YY C ARE VRLRYFDVWGQGTTVTV SS; og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: NIVLTQSPGSLAVSPGERVIMSCKSSQSVFFSSSQKNYLAWYQQ1PGQSPKLLIWASTRESG VPDRFTGS GS GTDFTLTIS S VQPEDLAIYYCHQYLS SRTFGQGTKLEIKR.
- 2. CD33-specifikt antistof ifølge krav 1, hvilket antistof omfatter en variabel tungkæderegion omfattende en aminosyresekvens repræsenteret ved: QVQLQQPGAEVVKPGASVKMSCKASGYTFTSYYIHWIKQTPGQGLEWVGVIYPGNDDIS YNQKFQGKATLT ADKS STTAYMQLS SLTSEDS AV YYC ARE VRLRYFDVWGQGTTVTVSS (SEQ ID NO: 9), og en variabel letkæderegion omfattende en aminosyresekvens repræsenteret ved: EIVLTQSPGSLAVSPGERVTMSCKSSQSVFFSSSQKNYLAWYQQ IPGQSPRLLIYWASTRESGVPDRFTGSGSGTDFTLTISSVQPEDLAIYYCHQYLSSRTFGQGT KLEIKR (SEQ ID NO: 10).
- 3. Immunkonjugat, der omfatter antistoffet ifølge krav 1 eller 2, er bundet til et lægemiddel eller en prodrug.
- 4. Immunkonjugat ifølge krav 3, hvor lægemidlet eller prodrug’en er udvalgt fra gruppen bestående af et maytansinoid, et taxoid, CC-1065, en CC-1065-analog, dolastatin, en dolastatinanalog, methotrexat, daunorubicin, doxorubicin, vineristin, vinblastin, melphalan, mitomycin C, chlorambucil, calicheamicin og derivater deraf.
- 5. Sammensætning omfattende antistoffet ifølge krav 1 eller 2 og et lægemiddel eller en prodmg.
- 6. Farmaceutisk sammensætning omfattende antistoffet ifølge krav 1 eller 2, eller immunkonjugat eller sammensætning ifølge krav 3 til 5 og et farmaceutisk acceptabelt middel.
- 7. Fremgangsmåde in vitro til hæmning af væksten af en celle, der udtrykker CD33, hvilken fremgangsmåde omfatter etablering af kontakt mellem cellen og antistoffet ifølge krav 1 eller 2, immunkonjugatet ifølge krav 3 eller 4, sammensætningen ifølge krav 5 eller en farmaceutisk sammensætning ifølge krav 6.
- 8. Antistof ifølge krav 1 eller 2, immunkonjugat ifølge krav 3 eller 4, sammensætning ifølge krav 5 eller farmaceutisk sammensætning ifølge krav 6 til anvendelse som et medikament.
- 9. Anvendelse af antistoffet ifølge krav 1 eller 2, immunkonjugatet ifølge krav 3 eller 4, sammensætningen ifølge krav 5 eller den farmaceutiske sammensætning ifølge krav 6 i fremstillingen af et medikament til behandling af cancer.
- 10. Antistof ifølge krav 1 eller 2, immunkonjugat ifølge krav 3 eller 4, sammensætning ifølge krav 5 eller farmaceutisk sammensætning ifølge krav 6, til anvendelse i behandling af cancer.
- 11. Anvendelse eller antistof, immunkonugat, sammensætning eller farmaceutisk sammensætning til anvendelse ifølge krav 9 eller 10, hvor canceren er udvalgt fra gruppen bestående af akut myeloid leukæmi (AML), kronisk myeloid leukæmi (CML) og pro-myelocytisk leukæmi (PML).
- 12. Isoleret polynukleotid, der koder for antistoffet ifølge krav 1 eller 2.
- 13. Isoleret polynukleotid, der koder for en let og en tung kæde af antistoffet ifølge krav 1 eller 2.
- 14. Rekombinant vektor omfattende polynukleotidet ifølge krav 12 eller 13.
- 15. Værtscelle transformeret med den rekombinante vektor ifølge krav 14.
- 16. Fremgangsmåde til frembringelse af et CD33-specifikt antistof, hvilken fremgangsmåde omfatter (a) dyrkning af en værtscelle ifølge krav 15 på betingelser, således at værtscellen udtrykker antistoffet, og (b) indsamling af det således udtrykte antistof.
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GB9223377D0 (en) * | 1992-11-04 | 1992-12-23 | Medarex Inc | Humanized antibodies to fc receptors for immunoglobulin on human mononuclear phagocytes |
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CN1795009B (zh) * | 2002-11-07 | 2014-07-09 | 伊谬诺金公司 | 抗-cd33抗体及其用途 |
EA200702239A1 (ru) * | 2005-04-15 | 2008-10-30 | Иммьюноджен, Инк. | Уничтожение гетерогенной или смешанной клеточной популяции в опухолях |
KR20110028450A (ko) * | 2008-06-16 | 2011-03-18 | 이뮤노젠 아이엔씨 | 새로운 상승 효과 |
CA2947602A1 (en) * | 2014-05-20 | 2015-11-26 | Immunogen, Inc. | Methods for characterizing and treating acute myeloid leukemia |
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