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    • 6. 发明授权
    • Derivatives of soluble T-4
    • 可溶性T-4的衍生物
    • US5110906A
    • 1992-05-05
    • US160348
    • 1988-02-24
    • Paul J. MaddonRichard AxelRaymond W. SweetJames Arthos
    • Paul J. MaddonRichard AxelRaymond W. SweetJames Arthos
    • C12N15/09A61K38/00A61P31/12C07K14/00C07K14/725C07K14/73C07K16/28C12N5/10C12P21/02C12Q1/70C12R1/91
    • C12Q1/703C07K14/70514C07K16/2812A61K38/00Y10S435/974Y10S530/821Y10S930/221
    • This invention provides a therapeutic agent capable of specifically forming a complex with human immunodeficiency virus envelope glycoprotein which comprises a polypeptide. In one embodiment of the invention, the amino acid sequence of the polypeptide comprises the amino acid sequence shown in FIG. 6 from about +1 to about +185 fused to the amino acid sequence from about +353 to about +371. In another embodiment of the invention, the amino acid sequence of the polypeptide comprises the amino acid sequence shown in FIG. 6 from about +1 to about +106 fused to the amino acid sequence from about +353 to about +371. In yet a further embodiment of the invention, the amino acid sequence of the polypeptide comprises the amino acid sequence shown in FIG. 6 from about +1 to about +185.This invention also provides a method for treating a subject infected with a human immunodeficiency virus. The method comprises administering to the subject an effective amount of a pharmaceutical composition comprising an effective amount of a therapeutic agent of the invention and a pharmaceutically acceptable carrier.
    • 本发明提供能够特异性形成与包含多肽的人免疫缺陷病毒包膜糖蛋白复合物的治疗剂。 在本发明的一个实施方案中,多肽的氨基酸序列包含图1所示的氨基酸序列。 约1 + 1至约+ 18 5的氨基酸序列与约+353至约+ 371融合。 在本发明的另一个实施方案中,多肽的氨基酸序列包含图1所示的氨基酸序列。 与约+353至约+ 371的氨基酸序列融合的约1 + 1至约+ 10 6。 在本发明的另一个实施方案中,多肽的氨基酸序列包含图1所示的氨基酸序列。 6从约+1到约+185。 本发明还提供了治疗感染人免疫缺陷病毒的受试者的方法。 该方法包括向受试者施用有效量的包含有效量的本发明治疗剂和药学上可接受的载体的药物组合物。
    • 7. 发明授权
    • Internal deletion mutants of soluble T4(CD4)
    • 可溶性T4(CD4)的内部缺失突变体
    • US5422274A
    • 1995-06-06
    • US830489
    • 1992-02-05
    • Paul J. MaddonRichard AxelRaymond W. SweetJames Arthos
    • Paul J. MaddonRichard AxelRaymond W. SweetJames Arthos
    • C12N15/09A61K38/00A61P31/12C07K14/00C07K14/725C07K14/73C07K16/28C12N5/10C12P21/02C12Q1/70C12R1/91C12N15/00A61K39/00C07K1/00
    • C12Q1/703C07K14/70514C07K16/2812A61K38/00Y10S435/974Y10S530/821Y10S930/221
    • This invention provides a therapeutic agent capable of specifically forming a complex with human immunodeficiency virus envelope glycoprotein which comprises a polypeptide. In one embodiment of the invention, the amino acid sequence of the polypeptide has the amino acid sequence shown in FIG. 6 from about +1 to about +185 fused to the amino acid sequence from about +353 to about +371. In another embodiment of the invention, the amino acid sequence of the polypeptide has the amino acid sequence shown in FIG. 6 from about +1 to about +106 fused to the amino acid sequence from about +353 to about +371. In yet a further embodiment of the invention, the amino acid sequence of the polypeptide has the amino acid sequence shown in FIG. 6 from about +1 to about +185.This invention also provides a method for treating a subject infected with a human immunodeficiency virus. The method treats the subject with an effective amount of a pharmaceutical composition having an effective amount of a therapeutic agent of the invention and a pharmaceutically acceptable carrier.
    • 本发明提供能够特异性形成与包含多肽的人免疫缺陷病毒包膜糖蛋白复合物的治疗剂。 在本发明的一个实施方案中,多肽的氨基酸序列具有图1所示的氨基酸序列。 约1 + 1至约+ 18 5的氨基酸序列与约+353至约+ 371融合。 在本发明的另一个实施方案中,多肽的氨基酸序列具有图1所示的氨基酸序列。 与约+353至约+ 371的氨基酸序列融合的约1 + 1至约+ 10 6。 在本发明的又一个实施方案中,多肽的氨基酸序列具有图1所示的氨基酸序列。 6从约+1到约+185。 本发明还提供了治疗感染人免疫缺陷病毒的受试者的方法。 该方法用有效量的具有有效量的本发明的治疗剂和药学上可接受的载体的药物组合物治疗受试者。
    • 8. 发明授权
    • Derivatives of soluble T-4
    • 可溶性T-4的衍生物
    • US06673896B1
    • 2004-01-06
    • US08328500
    • 1994-10-25
    • Paul J. MaddonRichard Axel
    • Paul J. MaddonRichard Axel
    • C07K100
    • C12Q1/703A61K38/00C07K14/70514C07K16/2812
    • This invention provides a therapeutic agent capable of specifically forming a complex with human immunodeficiency virus envelope glycoprotein which comprises a polypeptide. In one embodiment of the invention, the amino acid sequence of the polypeptide comprises the amino acid sequence shown in FIG. 6 from about +1 to about +185 fused to the amino acid sequence from about +353 to about +371. In another embodiment of the invention, the amino acid sequence of the polypeptide comprises the amino acid sequence shown in FIG. 6 from about +1 to about +106 fused to the amino acid sequence from about +353 to about +371. In yet a further embodiment of the invention, the amino acid sequence of the polypeptide comprises the amino acid sequence shown in FIG. 6 from about +1 to about +185. This invention also provides a method for treating a subject infected with a human immunodeficiency virus. The method comprises administering to the subject an effective amount of a pharmaceutical composition comprising an effective amount of a therapeutic agent of the invention and a pharmaceutically acceptable carrier.
    • 本发明提供能够特异性形成与包含多肽的人免疫缺陷病毒包膜糖蛋白复合物的治疗剂。 在本发明的一个实施方案中,多肽的氨基酸序列包含图1所示的氨基酸序列。 约1 + 1至约+ 18 5的氨基酸序列与约+353至约+ 371融合。 在本发明的另一个实施方案中,多肽的氨基酸序列包含图1所示的氨基酸序列。 与约+353至约+ 371的氨基酸序列融合的约1 + 1至约+ 10 6。 在本发明的另一个实施方案中,多肽的氨基酸序列包含图1所示的氨基酸序列。 6为约+1至约+ 185.本发明还提供了一种治疗感染人类免疫缺陷病毒的受试者的方法。 该方法包括向受试者施用有效量的包含有效量的本发明治疗剂和药学上可接受的载体的药物组合物。