Program in Translational Medicine, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON M5S 1A8, Canada.
Viruses. 2021 Sep 29;13(10):1960. doi: 10.3390/v13101960.
Respiratory Syncytial Virus (RSV) is the leading cause of acute lower respiratory infections in young children and infection has been linked to the development of persistent lung disease in the form of wheezing and asthma. Despite substantial research efforts, there are no RSV vaccines currently available and an effective monoclonal antibody targeting the RSV fusion protein (palivizumab) is of limited general use given the associated expense. Therefore, the development of novel approaches to prevent RSV infection is highly desirable to improve pediatric health globally. We have developed a method to generate alveolar-like macrophages (ALMs) from pluripotent stem cells. These ALMs have shown potential to promote airway innate immunity and tissue repair and so we hypothesized that ALMs could be used as a strategy to prevent RSV infection. Here, we demonstrate that ALMs are not productively infected by RSV and prevent the infection of epithelial cells. Prevention of epithelial infection was mediated by two different mechanisms: phagocytosis of RSV particles and release of an antiviral soluble factor different from type I interferon. Furthermore, intratracheal administration of ALMs protected mice from subsequent virus-induced weight loss and decreased lung viral titres and inflammation, indicating that ALMs can impair the pathogenesis of RSV infection. Our results support a prophylactic role for ALMs in the setting of RSV infection and warrant further studies on stem cell-derived ALMs as a novel cell-based therapy for pulmonary viral infections.
呼吸道合胞病毒(RSV)是导致婴幼儿急性下呼吸道感染的主要原因,感染与喘息和哮喘等持续性肺部疾病的发展有关。尽管进行了大量研究,但目前尚无 RSV 疫苗,而针对 RSV 融合蛋白的有效单克隆抗体(帕利珠单抗)由于费用高昂,其一般用途有限。因此,开发预防 RSV 感染的新方法对于改善全球儿科健康非常重要。我们已经开发出一种从多能干细胞中生成肺泡样巨噬细胞(ALM)的方法。这些 ALM 已显示出促进气道先天免疫和组织修复的潜力,因此我们假设 ALM 可被用作预防 RSV 感染的策略。在这里,我们证明 RSV 不能有效地感染 ALM,并且可以预防上皮细胞的感染。上皮细胞感染的预防是通过两种不同的机制介导的:RSV 颗粒的吞噬作用和释放不同于 I 型干扰素的抗病毒可溶性因子。此外,气管内给予 ALM 可保护小鼠免受随后的病毒诱导的体重减轻和肺部病毒滴度和炎症减少,表明 ALM 可损害 RSV 感染的发病机制。我们的结果支持 ALM 在 RSV 感染中的预防作用,并证明进一步研究干细胞衍生的 ALM 作为一种新型基于细胞的治疗肺部病毒感染的方法是合理的。