Department of Applied Biochemistry, Technische Universität Berlin, Chair of Applied Biochemistry, 10623 Berlin, Germany.
Department of Internal Medicine/Infectious and Respiratory Diseases, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 10115 Berlin, Germany.
Viruses. 2021 Aug 11;13(8):1590. doi: 10.3390/v13081590.
Influenza A virus (IAV) continuously causes epidemics and claims numerous lives every year. The available treatment options are insufficient and the limited pertinence of animal models for human IAV infections is hampering the development of new therapeutics. Bioprinted tissue models support studying pathogenic mechanisms and pathogen-host interactions in a human micro tissue environment. Here, we describe a human lung model, which consisted of a bioprinted base of primary human lung fibroblasts together with monocytic THP-1 cells, on top of which alveolar epithelial A549 cells were printed. Cells were embedded in a hydrogel consisting of alginate, gelatin and collagen. These constructs were kept in long-term culture for 35 days and their viability, expression of specific cell markers and general rheological parameters were analyzed. When the models were challenged with a combination of the bacterial toxins LPS and ATP, a release of the proinflammatory cytokines IL-1β and IL-8 was observed, confirming that the model can generate an immune response. In virus inhibition assays with the bioprinted lung model, the replication of a seasonal IAV strain was restricted by treatment with an antiviral agent in a dose-dependent manner. The printed lung construct provides an alveolar model to investigate pulmonary pathogenic biology and to support development of new therapeutics not only for IAV, but also for other viruses.
甲型流感病毒(IAV)每年都会持续引发疫情并夺走许多人的生命。现有的治疗选择并不充分,而动物模型对人类 IAV 感染的有限相关性也阻碍了新疗法的开发。生物打印组织模型支持在人类微组织环境中研究致病机制和病原体-宿主相互作用。在这里,我们描述了一种人类肺模型,它由原代人肺成纤维细胞的生物打印基底和单核细胞 THP-1 细胞组成,肺泡上皮 A549 细胞打印在其顶部。细胞被嵌入由藻酸盐、明胶和胶原蛋白组成的水凝胶中。这些构建体在长期培养中保持 35 天,并分析其活力、特定细胞标志物的表达和一般流变学参数。当模型受到细菌毒素 LPS 和 ATP 的组合挑战时,观察到促炎细胞因子 IL-1β和 IL-8 的释放,这证实了该模型可以产生免疫反应。在生物打印肺模型的病毒抑制试验中,抗病毒药物的处理以剂量依赖的方式限制了季节性 IAV 株的复制。该打印的肺结构提供了一个肺泡模型,用于研究肺部致病生物学,并支持新疗法的开发,不仅针对 IAV,还针对其他病毒。