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Synthetic partially phosphorothioated antisense oligodeoxynucleotides and pharmaceutical compositions containing them

机译:合成的部分硫代磷酸反义寡脱氧核苷酸和包含它们的药物组合物

摘要

PCT No. PCT/EP93/00911 Sec. 371 Date Dec. 1, 1994 Sec. 102(e) Date Dec. 1, 1994 PCT Filed Apr. 15, 1993 PCT Pub. No. WO93/21202 PCT Pub. Date Oct. 26, 1993The invention relates to synthetic phosphorothioated or partially phosphorothioated oligodeoxynucleotides capable of selectively modulating hemopoietic bone marrow cells development. More particularly, the invention relates to synthetic antisense oligodeoxynucleotides directed against a region spanning the AUG initiation condon in human ACHE or 2HS genes, having phosphorothioate bonds linking between the nucleotide bases; synthetic antisense oligodeoxynucleotides directed against a region spanning the AUG initiation condon in human ACHE gene, 2HS gene or BCHE gene or against a 5'-region in the human CHED (cdc2 homolog) gene, having phosphorothioate bonds linking between the four 3'-terminus nucleotide bases. The invention also relates to pharmaceutical compositions comprising as active ingredient at least one synthetic phosphorothioated or partially phosphorothioated antisense oligodeoxynucleotides according to the invention in physiologically acceptable carrier in diluent. The antisense oligodeoxynucleotides of the invention and the pharmaceutical compositions containing them are suitable for inhibiting abnormal hemopoietic cells proliferation, inhibiting abnormal platelet proliferation, increasing stem cell fraction in bone marrow cell cultures, enhancing macrophage production and increasing stem cells counts, reducing immune response of organs to be transplanted, suppressing immune response of a recipient of an allotransplanted organ, and arresting growth of malignant tumors.
机译:PCT号PCT / EP93 / 00911第二部分371日期1994年12月1日102(e)1994年12月1日,PCT申请,1993年4月15日提交,PCT公开。 WO93 / 21202 PCT公开号日期,1993年10月26日,本发明涉及能够选择性地调节造血骨髓细胞发育的合成的硫代磷酸酯化或部分硫代磷酸化的寡脱氧核苷酸。更具体地,本发明涉及针对人ACHE或2HS基因中跨越AUG起始密码子的区域的合成反义寡脱氧核苷酸,其在核苷酸碱基之间具有硫代磷酸酯键。合成的反义寡聚脱氧核苷酸,其针对人类ACHE基因,2HS基因或BCHE基因中AUG起始密码子的区域,或针对人类CHED(cdc2同源物)基因中的5'区域,在四个3'末端之间具有硫代磷酸酯键核苷酸碱基。本发明还涉及药物组合物,其在生理上可接受的载体中在稀释剂中包含至少一种根据本发明的合成的硫代磷酸化或部分硫代磷酸化的反义寡脱氧核苷酸作为活性成分。本发明的反义寡脱氧核苷酸和包含它们的药物组合物适用于抑制异常造血细胞增殖,抑制异常血小板增殖,增加骨髓细胞培养物中的干细胞分数,增强巨噬细胞产生和增加干细胞计数,降低器官的免疫应答。可以抑制异体移植器官受体的免疫反应,并阻止恶性肿瘤的生长。

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