期刊
JOURNAL OF INFECTION
卷 66, 期 2, 页码 163-169出版社
W B SAUNDERS CO LTD
DOI: 10.1016/j.jinf.2012.11.008
关键词
Interferon beta; Rhinovirus; A549 cells; Primary bronchial epithelial cells; Asthma; COPD
资金
- Dutch Top Institute Pharma [D1.101]
Objectives: Interferon-beta (IFN beta) induces strong antiviral effects and is therefore an attractive agent to prevent or reduce the incidence of virus-mediated exacerbations in asthmatic or chronic obstructive pulmonary disease (COPD) patients. We therefore investigated the effects of prophylactic IFN beta on respiratory epithelial cells infected with rhinovirus (RV). Methods: A549 cells and primary bronchial epithelial cells (PBECs) were exposed for 18 h to IFN beta. Then, IFN beta was either removed or maintained in the supernatant for the rest of the experiment and cells were infected with RV-1B at t = 0 or 72 h after the initial exposure to IFN beta. Results: Viral RNA levels were decreased in both cell types. Furthermore, both viral RNA and infectious virus levels in the supernatant of infected A549 cells were still significantly reduced at 72 h after removal of IFN beta. This pronounced antiviral pre-treatment effect was associated with increased expression of the antiviral genes IFN-stimulated protein of MR15000 (ISG15) and Myxovirus resistance 1 (Mx1) and the effect was maintained even when IFN beta levels in the supernatant of A549 cells were undetectable. Conclusions: These data show that IFN beta has not only a strong, but also a long-lasting protective effect against RV infection of respiratory epithelium. (C) 2012 The British Infection Association. Published by Elsevier Ltd. All rights reserved.
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