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
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.