Human Metapneumovirus Infection in Chronic Obstructive Pulmonary Disease: Impact of Glucocorticosteroids and Interferon

被引:23
作者
Kan-o, Keiko [1 ,2 ,3 ,7 ]
Ramirez, Ruben [4 ]
MacDonald, Martin I. [1 ]
Rolph, Michael [5 ]
Rudd, Penny A. [5 ]
Spann, Kirsten M. [6 ]
Mahalingam, Suresh [5 ]
Bardin, Philip G. [1 ,2 ,3 ]
Thomas, Belinda J. [1 ,2 ,3 ]
机构
[1] Monash Univ, Monash Lung & Sleep, Monash Med Ctr, Melbourne, Vic, Australia
[2] Monash Univ, Hudson Inst Med Res, Ctr Innate Immun & Infect Dis, Melbourne, Vic, Australia
[3] Monash Univ, Sch Clin Sci, Dept Mol & Translat Sci, Melbourne, Vic, Australia
[4] Univ Canberra, Fac Sci Appl, Southport, Qld, Australia
[5] Griffith Univ, Inst Glyc, Southport, Qld, Australia
[6] Queensland Univ Technol, Sch Biomed Sci, Brisbane, Qld, Australia
[7] Kyushu Univ, Grad Sch Med Sci, Res Inst Dis Chest, Fukuoka, Japan
基金
英国医学研究理事会;
关键词
human metapneumovirus; human primary bronchial epithelial cells; glucocorticosteroids; interferon; apoptosis; innate immune response; AIRWAY EPITHELIAL-CELLS; INHALED CORTICOSTEROIDS; RESPIRATORY-TRACT; VIRAL-INFECTIONS; YOUNG-CHILDREN; VIRUS; ASTHMA; COPD; EXACERBATIONS; RHINOVIRUS;
D O I
10.1093/infdis/jix167
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Human metapneumovirus (hMPV) infection is implicated in exacerbations of asthma and chronic obstructive pulmonary disease (COPD). Research into the pathogenesis of infection is restricted to animal models, and information about hMPV replication and inflammatory and immune responses in human disease is limited. Methods. Human primary bronchial epithelial cells (PBECs) from healthy and asthmatic subjects and those with COPD were infected with hMPV, with or without glucocorticosteroid (GCS) exposure. Viral replication, inflammatory and immune responses, and apoptosis were analyzed. We also determined whether adjuvant interferon (IFN) can blunt hMPV infection in vitro and in a murine model. Results. hMPV infected human PBECs and viral replication was enhanced in cells from patients with COPD. The virus induced gene expression of IFN-stimulated gene 56 (ISG56) and IFN-beta, as well as IFN-gamma-inducible protein 10 (IP-10) and regulated on activation, normal T cell expressed and secreted (RANTES), and more so in cells from patients with COPD. GCS exposure enhanced hMPV replication despite increased IFN expression. Augmented virus replication associated with GCS was mediated by reduced apoptosis via induction of antiapoptotic genes. Adjuvant IFN treatment suppressed hMPV replication in PBECs and reduced hMPV viral titers and inflammation in vivo. Conclusions. hMPV infects human PBECs, eliciting innate and inflammatory responses. Replication is enhanced by GCS and adjuvant IFN is an effective treatment, restricting virus replication and proinflammatory consequences of hMPV infections.
引用
收藏
页码:1536 / 1545
页数:10
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