Role of interferon gamma in the pathogenesis of primary respiratory syncytial virus infection in BALB/c mice

Citation
Sm. Van Schaik et al., Role of interferon gamma in the pathogenesis of primary respiratory syncytial virus infection in BALB/c mice, J MED VIROL, 62(2), 2000, pp. 257-266
Citations number
25
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF MEDICAL VIROLOGY
ISSN journal
01466615 → ACNP
Volume
62
Issue
2
Year of publication
2000
Pages
257 - 266
Database
ISI
SICI code
0146-6615(200010)62:2<257:ROIGIT>2.0.ZU;2-M
Abstract
Immunologic mechanisms are thought to contribute to the pathogenesis of res piratory syncytial virus (RSV) bronchiolitis in humans. RSV-infected BALB/c mice exhibit tachypnea and signs of outflow obstruction, similar to sympto ms in humans. Interferon gamma (IFN gamma) has been found to be the predomi nant cytokine produced in humans and mice with RSV infection. We therefore undertook this study to evaluate the role of IFN gamma in the development o f respiratory illness in RSV-infected mice. BALB/c mice were infected with RSV, and lung function was assessed by plethysmography. Bronchoalveolar lav age (BAL) fluids were analyzed for the concentration of interferon gamma (I FN gamma) and the presence of inflammatory cells, and lung tissue sections were examined for histopathologic changes. The role of IFN gamma was furthe r addressed in studies of IFN gamma knock-out mice (IFN gamma(-/-)) and of mice depleted of IFN gamma by in vivo administration of a neutralizing anti body. After infection, mice developed respiratory symptoms that were strong ly associated with the number of inflammatory cells in BAL, as well as with the concentrations of IFN-gamma. Both IFN-gamma(-/-) mice and mice treated with anti-IFN gamma developed more extensive inflammation of the airways t han control mice. However mice lacking IFN gamma exhibited less severe sign s of airway obstruction. Together these data suggest a protective role of I FN gamma in RSV infection in terms of limiting viral replication and inflam matory responses but also a pathogenic role in causing airway obstruction. (C) 2000 Wiley-Liss, Inc.