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Development of a Comprehensive Human Immunodeficiency Virus Type 1 Screening Algorithm for Discovery and Preclinical Testing of Topical Microbicides▿

机译:用于局部杀微生物剂发现和临床前测试的全面人类免疫缺陷病毒1型筛选算法的开发▿

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摘要

Topical microbicides are self-administered, prophylactic products for protection against sexually transmitted pathogens. A large number of compounds with known anti-human immunodeficiency virus type 1 (HIV-1) inhibitory activity have been proposed as candidate topical microbicides. To identify potential leads, an in vitro screening algorithm was developed to evaluate candidate microbicides in assays that assess inhibition of cell-associated and cell-free HIV-1 transmission, entry, and fusion. The algorithm advances compounds by evaluation in a series of defined assays that generate measurements of relative antiviral potency to determine advancement or failure. Initial testing consists of a dual determination of inhibitory activity in the CD4-dependent CCR5-tropic cell-associated transmission inhibition assay and in the CD4/CCR5-mediated HIV-1 entry assay. The activity is confirmed by repeat testing, and identified actives are advanced to secondary screens to determine their effect on transmission of CXCR4-tropic viruses in the presence or absence of CD4 and their ability to inhibit CXCR4- and CCR5-tropic envelope-mediated cell-to-cell fusion. In addition, confirmed active compounds are also evaluated in the presence of human seminal plasma, in assays incorporating a pH 4 to 7 transition, and for growth inhibition of relevant strains of lactobacilli. Leads may then be advanced for specialized testing, including determinations in human cervical explants and in peripheral blood mononuclear cells against primary HIV subtypes, combination testing with other inhibitors, and additional cytotoxicity assays. PRO 2000 and SPL7013 (the active component of VivaGel), two microbicide products currently being evaluated in human clinical trials, were tested in this in vitro algorithm and were shown to be highly active against CCR5- and CXCR4-tropic HIV-1 infection.
机译:局部杀菌剂是自我管理的预防性产品,可防止性传播的病原体。已经提出了许多具有已知的抗人免疫缺陷病毒1型(HIV-1)抑制活性的化合物作为候选的局部杀菌剂。为了识别潜在的潜在客户,开发了一种体外筛选算法,以评估评估细胞相关和无细胞HIV-1传播,进入和融合的抑制作用的候选杀微生物剂。该算法通过在一系列定义的测定中进行评估来推进化合物的生成,这些测定会生成相对抗病毒效力的测量值以确定前进或失败。初始测试包括在CD4依赖性CCR5嗜性细胞相关的传播抑制试验和CD4 / CCR5介导的HIV-1进入试验中双重确定抑制活性。可以通过重复测试确认其活性,然后将鉴定出的活性物质进行第二次筛选,以确定它们在存在或不存在CD4的情况下对CXCR4-tropic病毒传播的影响及其抑制CXCR4-和CCR5-tropic包膜介导的细胞介导的能力。细胞融合。另外,在人精浆存在下,在结合了pH 4至7的pH值的测定中,以及在乳酸菌相关菌株的生长抑制方面,也要评估已证实的活性化合物。然后可以将导线提前进行专门测试,包括在人宫颈外植体和外周血单核细胞中针对主要HIV亚型的测定,与其他抑制剂的组合测试以及其他细胞毒性测定。目前正在人类临床试验中评估的两种杀菌剂产品PRO 2000和SPL7013(VivaGel的活性成分)已在该体外算法中进行了测试,并显示出对CCR5-和CXCR4-tropic HIV-1感染具有高活性。

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