Interferon response to respiratory syncytial virus by bronchial epithelium from children with asthma is inversely correlated with pulmonary function

• Published in: Journal of allergy and clinical immunology Vol. 142; no. 2; pp. 451 - 459
• Main Authors: Altman, Matthew C., Reeves, Stephen R., Parker, Andrew R., Whalen, Elizabeth, Misura, Kira M., Barrow, Kaitlyn A., James, Richard G., Hallstrand, Teal S., Ziegler, Steven F., Debley, Jason S.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.08.2018; Elsevier Limited
• Subjects: Airway management; Apoptosis; Asthma; Children; Epithelial cells; Epithelium; Family medical history; Gene expression; Infections; Interferon; Lungs; Nitric oxide; Physiology; Respiratory function; Respiratory syncytial virus; Respiratory tract; Ribonucleic acid; RNA; sequence analysis; Studies; type I interferon; Viral infections; BEC; RNA; GO; epithelial cells; RIG-I; HRV; Asthma; type I interferon; BDR; LDH; MMP; RSV; FDR; ICS; sequence analysis; ISG; respiratory syncytial virus
• ISSN: 0091-6749; 1097-6825; 1097-6825
• DOI: 10.1016/j.jaci.2017.10.004

Respiratory viral infection in early childhood, including that from respiratory syncytial virus (RSV), has been previously associated with the development of asthma. We aimed to determine whether ex vivo RSV infection of bronchial epithelial cells (BECs) from children with asthma would induce specific gene expression patterns and whether such patterns were associated with lung function among BEC donors. Primary BECs from carefully characterized children with asthma (n = 18) and matched healthy children without asthma (n = 8) were differentiated at an air-liquid interface for 21 days. Air-liquid interface cultures were infected with RSV for 96 hours and RNA was subsequently isolated from BECs. In each case, we analyzed gene expression using RNA sequencing and assessed differences between conditions by linear modeling of the data. BEC donors completed spirometry to measure lung function. RSV infection of BECs from subjects with asthma, compared with uninfected BECs from subjects with asthma, led to a significant increase in expression of 6199 genes. There was significantly greater expression of 195 genes in BECs from children with asthma and airway obstruction (FEV1/forced vital capacity < 0.85 and FEV1 < 100% predicted) than in BECs from children with asthma without obstruction, or in BECs from healthy children. These specific genes were found to be highly enriched for viral response genes induced in parallel with types I and III interferons. BECs from children with asthma and with obstructive physiology exhibit greater expression of types I and III interferons and interferon-stimulated genes than do cells from children with normal lung function, and expression of interferon-associated genes correlates with the degree of airway obstruction. These findings suggest that an exaggerated interferon response to viral infection by airway epithelial cells may be a mechanism leading to lung function decline in a subset of children with asthma.