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体外结核肉芽肿模型:潜力与挑战。

In Vitro Granuloma Models of Tuberculosis: Potential and Challenges.

机构信息

National Institute for Health Research Biomedical Research Centre, Faculty of Medicine, University of Southampton, United Kingdom.

Department of Clinical and Experimental Medicine, Faculty of Medicine and Health Sciences, Linköping University, Sweden.

出版信息

J Infect Dis. 2019 May 24;219(12):1858-1866. doi: 10.1093/infdis/jiz020.

Abstract

Despite intensive research efforts, several fundamental disease processes for tuberculosis (TB) remain poorly understood. A central enigma is that host immunity is necessary to control disease yet promotes transmission by causing lung immunopathology. Our inability to distinguish these processes makes it challenging to design rational novel interventions. Elucidating basic immune mechanisms likely requires both in vivo and in vitro analyses, since Mycobacterium tuberculosis is a highly specialized human pathogen. The classic immune response is the TB granuloma organized in three dimensions within extracellular matrix. Several groups are developing cell culture granuloma models. In January 2018, NIAID convened a workshop, entitled "3-D Human in vitro TB Granuloma Model" to advance the field. Here, we summarize the arguments for developing advanced TB cell culture models and critically review those currently available. We discuss how integrating complementary approaches, specifically organoids and mathematical modeling, can maximize progress, and conclude by discussing future challenges and opportunities.

摘要

尽管进行了深入的研究,但结核病 (TB) 的几个基本发病机制仍未得到很好的理解。一个核心谜团是,宿主免疫对于控制疾病是必要的,但它通过引起肺部免疫病理学促进了传播。我们无法区分这些过程,这使得设计合理的新干预措施具有挑战性。阐明基本的免疫机制可能既需要体内分析,也需要体外分析,因为结核分枝杆菌是一种高度特化的人类病原体。经典的免疫反应是在细胞外基质中三维组织的结核肉芽肿。有几个小组正在开发细胞培养肉芽肿模型。2018 年 1 月,NIAID 召开了一次题为“3-D 人类体外结核肉芽肿模型”的研讨会,以推动该领域的发展。在这里,我们总结了开发先进的结核细胞培养模型的论点,并对现有的模型进行了批判性评价。我们讨论了如何整合互补的方法,特别是类器官和数学建模,以最大限度地取得进展,并最后讨论了未来的挑战和机遇。

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