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Fcε-PE chimeric protein for targeted treatment of allergy responses a method for its production and pharmaceutical compositions containing the same

机译:用于靶向治疗变态反应的Fcε-PE嵌合蛋白,其生产方法和包含该蛋白的药物组合物

摘要

The present invention generally relates to a new approach for the therapy of allergic responses, based on targeted elimination of cells expressing the FcεRI receptor by a chimeric cytotoxin FC2′-3-PE40. A sequence encoding amino acids 301-437 of the Fc region of the mouse IgE molecule was genetically fused to PE40—a truncated form of PE lacking the cell binding domain. The chimeric protein, produced in E. coli, specifically and efficiently kills mouse mast cell lines expressing the FcεRI receptor, as well as primary mast cells derived from bone marrow. The present invention provides a chimeric protein for targeted elimination of FcεRI expressing cells especially useful for the therapy of allergic responses. The said chimeric protein is comprised of a cell targeting moiety for FcεRI expressing cells and a cell killing moiety. The preferred killing moiety is the bacterial toxin Pseudomonas exotoxin (PE). This Pseudomonas exotoxin is a product of Pseudomonas aeruginosa. The present invention also relates to a method for the preparation of said protein. This chimeric protein is prepared by genetically fusing the Fc region of the mouse IgE molecule to PE40, a truncated form of PE lacking the cell binding domain. The present invention also provides pharmaceutical compositions, for the treatment of allergic diseases and for the treatment of hyperplasias and malignancies, comprising as an active ingredient the above mentioned chimeric protein and a conventional adjuvant product.
机译:本发明总体上涉及一种用于治疗过敏反应的新方法,该方法基于通过嵌合细胞毒素FC 2′-3 -PE 40 定向表达FcεRI受体的细胞。子>。将编码小鼠IgE分子Fc区氨基酸301-437的序列与PE 40 融合,PE 40 是一种截短形式的PE,缺少细胞结合域。在中产生的嵌合蛋白。大肠杆菌可以特异性,有效地杀死表达FcεRI受体的小鼠肥大细胞系以及源自骨髓的原代肥大细胞。本发明提供了用于靶向消除表达FcεRI的细胞的嵌合蛋白,其特别用于治疗变态反应。所述嵌合蛋白由表达FcεRI的细胞的细胞靶向部分和细胞杀伤部分组成。优选的杀伤部分是细菌毒素假单胞菌外毒素(PE)。 假单胞菌毒素是铜绿假单胞菌的产物。本发明还涉及所述蛋白质的制备方法。该嵌合蛋白是通过将小鼠IgE分子的Fc区遗传融合到PE 40 (一种缺乏细胞结合域的PE的截短形式)中而制备的。本发明还提供了用于治疗变应性疾病以及用于治疗增生和恶性肿瘤的药物组合物,其包含上述嵌合蛋白和常规佐剂作为活性成分。

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