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    • 4. 发明授权
    • Method for the production of recombinant virus, DNA constructs, recombinant virus and vaccine compositions
    • 生产重组病毒,DNA构建体,重组病毒和疫苗组合物的方法
    • US09539317B2
    • 2017-01-10
    • US14304387
    • 2014-06-13
    • Myrna Cristina BonaldoRicardo Galler
    • Myrna Cristina BonaldoRicardo Galler
    • A61K39/12C07K14/005A61K39/00
    • A61K39/12A61K2039/525A61K2039/5256A61K2039/575C07K14/005C07K2319/02C07K2319/03C07K2319/40C12N7/00C12N2770/24122C12N2770/24134C12N2770/24143C12N2770/24171Y02A50/386Y02A50/388
    • The purpose of the present invention is the production of recombinant virus through the cloning and expression of sequences of coding nucleotides of the whole or part of heterolog proteins, through the following method: (a) modification of the heterolog nucleotides sequences in such way that when cloned and expressed in the vector virus, they present in the 5′ region nucleotides present in the 5′ edge of the gene NS1 of this vector virus or of other virus or equivalent functional sequences, and in its 3′ region, the correspondent genome region in the whole or part of the spheres of the stem and anchor of the protein E of this vector virus or equivalent functional sequences, and not comprising the structure and the replication of the mention vector virus; (b) insertion of the modified heterolog sequences in (a) in the intergene region at the structural protein E level and of nonstructural NS1 vector virus; (c) obtaining the non-pathogenic recombinant virus and owner of the immunologic properties, having the heterolog sequences integrated in the viral genome according to the insertion described in (b) and, like that, expressing the heterolog antigen in such way that it can induce an appropriate immune response. The present invention is also addressed to vaccine compositions to immune against the Flavivirus and/or other pathogens.
    • 本发明的目的是通过以下方法通过克隆和表达编码全部或部分异源蛋白质的核苷酸的序列来生产重组病毒:(a)修饰异源核苷酸序列,使得当 在载体病毒中克隆并表达,它们存在于存在于该载体病毒或其他病毒或等效功能序列的NS1基因的5'边缘的5'区核苷酸中,并且在其3'区域中,相应的基因组区域 在该载体病毒的蛋白质E的茎和锚的全部或部分球体或相当的功能序列中,不包括提及载体病毒的结构和复制; (b)在(a)中在修饰的异源序列插入结构蛋白E水平的基因间区域和非结构性NS1载体病毒; (c)根据(b)中描述的插入获得非致病性重组病毒和免疫学性质的所有者,其具有整合在病毒基因组中的杂种序列,并且像以下那样表达异源抗原,使得它可以 诱导适当的免疫应答。 本发明还涉及免疫黄病毒和/或其他病原体的疫苗组合物。