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The Hu-M? CIEA NOG Mouse?: A Novel Preclinical Platform for Testing the Efficacy of Therapeutics Against Cancer and Infectious Diseases

机译:hu-m? Ciea nog鼠标?:一种新型临床前平台,用于测试治疗患者对癌症和传染病的疗效

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As checkpoint blockade becomes a promising therapeutic avenue for cancer therapy, current preclinical models are not able to recapitulate the antitumor immune responses mediated by checkpoint blockade therapies. This is partly because of the inherent differences between the mouse and the human immune systems. The systematic production and generation of "humanized" mice is critical in order to address the high unmet need for a robust preclinical platform for testing immuno-therapies directed against cancer in the context of a human immune system. HuMurine's Hu-M? mice are constructed by injecting pre-qualified human CD34+ hematopoietic progenitor cells (HPCs) into newborn NOG mice resulting in stable multi-lineage human hematopoiesis at 10-15 weeks post engraftment.
机译:由于检查点封闭成为癌症治疗的有希望的治疗途径,目前的临床前模型不能重新承载由检查点封闭疗法介导的抗肿瘤免疫应答。这部分是因为小鼠与人类免疫系统之间的固有差异。系统的生产和生成“人源化”小鼠是至关重要的,以解决稳健的临床前平台的高未满足需要在人类免疫系统的背景下测试针对癌症的免疫疗法。湿湿的HU-M?通过将预先合格的人CD34 +造血祖细胞(HPC)注射到新生儿Nog小鼠中来构建小鼠,从而在植入后10-15周的稳定的多谱系人血液血液中。

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