Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University, Grand Rapids, Michigan.
Department of Pharmacology and Toxicology, Michigan State University, East Lansing, Michigan.
Am J Physiol Lung Cell Mol Physiol. 2021 Jun 1;320(6):L1147-L1157. doi: 10.1152/ajplung.00440.2020. Epub 2021 Apr 14.
Viral infections affecting the lower respiratory tract place enormous burdens on hospitals. As neither vaccines nor antiviral agents exist for many viruses, understanding risk factors and outcomes in each patient using minimally invasive analysis, such as blood, can lead to improved health care delivery. A cohort of PAXgene RNA sequencing of infants admitted with moderate or severe acute bronchiolitis and respiratory syncytial virus were compared with case-control statistical analysis and cohort-based outlier mapping for precision transcriptomics. Patients with severe bronchiolitis had signatures connected to the immune system, interferon signaling, and cytokine signaling, with marked sex differences in , , , and for severity. Several patients had unique secondary infections, cytokine activation, immune responses, biological pathways, and immune cell activation, highlighting the need for defining patient-level transcriptomic signatures. Balancing relative contributions of cohort-based biomarker discoveries with patient's biological responses is needed to understand the totality of mechanisms of adverse outcomes in viral bronchiolitis.
病毒感染影响下呼吸道,给医院带来巨大负担。由于许多病毒既没有疫苗也没有抗病毒药物,因此通过微创分析(如血液)了解每位患者的风险因素和结果,可以改善医疗服务的提供。对因中度或重度急性细支气管炎和呼吸道合胞病毒住院的婴儿进行 PAXgene RNA 测序的队列与病例对照统计分析和基于队列的离群值映射进行了比较,以进行精确转录组学分析。严重细支气管炎患者的特征与免疫系统、干扰素信号和细胞因子信号有关,严重程度在 、 、 和 方面存在明显的性别差异。一些患者有独特的继发感染、细胞因子激活、免疫反应、生物途径和免疫细胞激活,这突出表明需要确定患者水平的转录组特征。需要平衡基于队列的生物标志物发现与患者生物学反应的相对贡献,以了解病毒性细支气管炎不良结局的全部机制。