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Compositions for measuring resistance and methods, and compositions for screening antiviral agents and methods and anti-viral drug susceptibility

机译:用于测量抗性的组合物和方法,以及用于筛选抗病毒剂和方法以及抗病毒药物敏感性的组合物

摘要

(57) [Abstract] The present invention provides a method for determining the sensitivity of the HCMV antiviral agents or HCV: introducing into a host cell a resistance test vector comprising a marker gene and a segment derived from the patient (a) a step of culturing a host cell obtained step (b) in (a);; the steps of a step for determining the expression of the indicator gene in (c) target host cell, to give (d) in step (c) and a step of comparing the expression of the indicator gene measured when implemented steps (a) ~ (c) a in the absence of the antiviral agent, the expression of the indicator gene, steps (a) process - the process (c), the step (b) ~ process (c), or (c), the is to provide a method for causing the presence of HCV antiviral drug test concentration. The present invention provides a method for measuring the HCMV antiviral drug resistance or HCV in a patient: at the beginning (a), to measure the anti-viral drug susceptibility in the patient according to the above method, the segment from said patient The antiviral agent (c) steps (a) and it is measured in (b); at the time of (b) after the step of measuring the anti-viral drug susceptibility of the same patient; the step of obtaining from the patient at that time generally is reduction in time and a step of comparing the sensitivity and compared with sensitivity at the time of the first antiviral sensitivity at the time of the post, a way to indicate the development or progression of anti-viral drug resistance in the patient provide. The present invention also provides a method for evaluating the biological effects of HCMV antiviral drug candidate compounds or HCV. Resistance test vector comprising a patient-derived segment containing the HCMV gene or HCV, the indicator gene and host cells infected with said resistance test vector is provided.
机译:(57)[摘要]本发明提供了确定HCMV抗病毒剂或HCV敏感性的方法:将抗性测试载体引入宿主细胞,所述抗性测试载体包含标志物基因和源自患者的区段(a):培养在(a)中获得的步骤(b)的宿主细胞;步骤(a)〜(c)中确定指示基因在(c)靶宿主细胞中表达的步骤,得到(d)步骤(c)和比较所测量的指示基因表达的步骤(c)a。在不存在抗病毒剂的情况下,指示基因的表达,步骤(a)过程-过程(c),步骤(b)〜过程(c),或(c),是提供一种引起HCV抗病毒药物测试浓度存在的方法。本发明提供了一种用于测量患者的HCMV抗病毒药物抗性或HCV的方法:在开始时(a),根据上述方法测量患者的抗病毒药物敏感性,来自所述患者的片段。试剂(c)的步骤(a),并在(b)中测量; (b)在测量同一患者的抗病毒药物敏感性步骤之后;当时从患者那里获得的步骤通常是减少时间,以及比较敏感度并与之比较在发表时的第一抗病毒敏感度时与敏感度进行比较的步骤,这是一种指示病情发展或进展的方法。抗病毒药物的耐药性由患者提供。本发明还提供了评估HCMV抗病毒药物候选化合物或HCV的生物学作用的方法。提供了抗性测试载体,其包括含有HCMV基因或HCV的患者衍生片段,指示剂基因和被所述抗性测试载体感染的宿主细胞。

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