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Mucosal HIV-1 transmission and prevention strategies in BLT humanized mice

机译:BLT人源化小鼠的粘膜HIV-1传播和预防策略

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摘要

Clinical trials testing microbicides and related biomedical interventions to block HIV transmissions have produced contradictory results and to date it is unclear why. Further elucidation of the molecular basis of mucosa! HIV transmission and extensive pharmacokinetic and pharmacodynamic analyses are essential to implementing effective prevention strategies. Animal models are of critical importance to this effort and bone marrow-liver-thymus (BIT) humanized mice have recently emerged as a powerful small animal research platform for in vivo efficacy evaluation of mucosal and parenteral HIV-1 prevention interventions. The availability of this validated system for the pre-clinical evaluation of HIV-1 prevention approaches will accelerate the implementation of the best candidate interventions into clinical trials.
机译:测试杀菌剂和相关生物医学干预措施以阻止HIV传播的临床试验产生了矛盾的结果,到目前为止,尚不清楚原因。进一步阐明粘膜的分子基础! HIV传播以及广泛的药代动力学和药效学分析对于实施有效的预防策略至关重要。动物模型对此工作至关重要,最近,骨髓肝-胸腺(BIT)人源化小鼠已成为一种强大的小型动物研究平台,可用于评估粘膜和肠胃外HIV-1预防干预措施的体内功效。该经过验证的系统可用于对HIV-1预防方法进行临床前评估,这将加速在临床试验中实施最佳候选干预措施。

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