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In vitro screening assay for identification of compounds that inhibit cytopathicity of viral infection

机译:体外筛选测定法鉴定可抑制病毒感染细胞病变的化合物

摘要

The present invention includes the method of treating a viral infection, specifically one occurring as a result of infection by a human immunodeficiency virus (HIV-1). The method of treatment depends upon the ligand binding of the Ah receptor. Transformation and translocation of the receptor and DNA binding are not required. The study of compounds that interact with the Ah receptor, either as agonists, or antagonists, has resulted in the identification of compounds with useful therapeutic properties through perturbation of viral pathogenic signal transduction pathways. Antagonists of the Ah receptor are more likely candidates for treatment because the toxicity of such compounds is low. Identification of molecules affecting cellular targets, such as the Ah receptor, that inhibit viral pathologic signaling would be of great therapeutic potential as the activity of these molecules is not directed against the virus itself, therefore genetic viral mutation to escape such therapy would be far less likely to occur. The use of secondary compounds for use in combinational, synergistic, therapy is also enclosed. These second compounds are also known to have some effect on the treatment of cellular pathologic changes, together with those compounds found to be effective upon the regulation of the Ah receptor the compounds can more beneficially control virally induced cellular cytopathic changes.
机译:本发明包括治疗病毒感染的方法,特别是一种由于人免疫缺陷病毒(HIV-1)的感染而发生的病毒感染。治疗方法取决于Ah受体的配体结合。不需要受体的转化和易位以及与DNA的结合。与作为激动剂或拮抗剂与Ah受体相互作用的化合物的研究已导致通过扰动病毒致病性信号转导途径来鉴定具有有用治疗性质的化合物。由于此类化合物的毒性较低,因此Ah受体拮抗药更可能用于治疗。识别抑制病毒病理信号的影响细胞靶标的分子(例如Ah受体)将具有巨大的治疗潜力,因为这些分子的活性并不针对病毒本身,因此逃避此类治疗的遗传病毒突变将少得多可能发生。还涵盖了辅助化合物用于组合,协同治疗的用途。还已知这些第二化合物对细胞病理变化的治疗具有某些作用,以及发现对调节Ah受体有效的那些化合物,这些化合物可以更有利地控制病毒诱导的细胞胞质变化。

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