首页> 外国专利> RECOMBINANT PSEUDO-ADENOVIRUS PARTICLE, WHICH PRODUCES MODIFIED NANO-ANTIBODIES, WHICH LEARN THE MYCOPLASMA Of M.hominis, PHARMACEUTICAL COMPOSITION HUMS TO ITS BASIS AND METHOD OF ITS USE FOR THE THERAPY OF MYCOPLASMOSES

RECOMBINANT PSEUDO-ADENOVIRUS PARTICLE, WHICH PRODUCES MODIFIED NANO-ANTIBODIES, WHICH LEARN THE MYCOPLASMA Of M.hominis, PHARMACEUTICAL COMPOSITION HUMS TO ITS BASIS AND METHOD OF ITS USE FOR THE THERAPY OF MYCOPLASMOSES

机译:重组拟人腺病毒颗粒,可产生修饰的纳米抗体,可学习人型支原体的间质,其药物组合物的基础和使用其可用于治疗间质的

摘要

1. Recombinant psevdoadenovirusnaya particle on the basis of human adenovirus serotype 5 genome, containing an expression cassette with the modified chimeric gene insert nanoantibody binding to mycoplasma M.hominis, the nucleotide sequence of which is pre-modified by attaching an effector Fc-fragment of immunoglobulin G.2. Recombinant particles according to claim psevdoadenovirusnaya. 1, characterized in that the pre-modified nanoantibody gene sequence is the nucleotide sequence of SEQ ID 1.3. Recombinant psevdoadenovirusnaya particle according to claim. 1, characterized in that it activates the complement system mlekopitayuschih.4 immune system. A pharmaceutical composition comprising recombinant particles according to claim psevdoadenovirusnye. 1 and a pharmaceutically acceptable carrier, wherein upon administration to a mammal it activates the complement system and suppresses mycoplasma M.hominis.5. Method mycoplasma therapy M.hominis, by administering to a mammal in need thereof a therapeutically effective amount of a pharmaceutical according to claim. 4.6 composition. The method of claim. 5, characterized in that the pharmaceutical composition is administered by intravenous injection.
机译:1.基于人腺病毒血清型5基因组的重组伪狂犬病毒颗粒,其包含具有修饰的嵌合基因插入纳米抗体的表达盒,所述嵌合基因插入物与人支原体结合,所述核苷酸序列通过连接效应子Fc片段而被预先修饰。免疫球蛋白G.2。根据权利要求1所述的重组颗粒。如图1所示,其特征在于,所述预先修饰的纳米抗体基因序列是SEQ ID 1.3的核苷酸序列。 7.根据权利要求1的重组伪狂犬病毒颗粒。 1,特征在于它激活补体系统mlekopitayuschih.4免疫系统。 11.一种药物组合物,其包含根据权利要求1至7中任一项的重组颗粒。 1和药学上可接受的载体,其中当施用于哺乳动物时,其激活补体系统并抑制支原体支原体。5。方法支原体疗法通过向有需要的哺乳动物施用治疗有效量的权利要求的药物来治疗人型支原体。 4.6组成。权利要求的方法。如图5所示,其特征在于药物组合物通过静脉内注射给药。

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