eCite Digital Repository
Rapid Interferon g–dependent Clearance of Influenza A Virus and Protection from Consolidating Pneumonitis in Nitric Oxide Synthase 2–deficient Mice
Citation
Karupiah, G and Chen, J-H and Mahalingam, S and Nathan, CF and MacMicking, JD, Rapid Interferon g-dependent Clearance of Influenza A Virus and Protection from Consolidating Pneumonitis in Nitric Oxide Synthase 2-deficient Mice, The Journal of Experimental Medicine, 188, (8) pp. 1541-1546. ISSN 0022-1007 (1998) [Refereed Article]
![]() | PDF (Published version) 257Kb |
Copyright Statement
Author copyright 1998 Copyright The Rockefeller University Press
DOI: doi:10.1084/jem.188.8.1541
Abstract
Viral infection often activates the interferon (IFN)-g–inducible gene, nitric oxide synthase 2
(NOS2). Expression of NOS2 can limit viral growth but may also suppress the immune system
and damage tissue. This study assessed each of these effects in genetically deficient NOS22/2
mice after infection with influenza A, a virus against which IFN-g has no known activity. At
inocula sufficient to cause consolidating pneumonitis and death in wild-type control mice,
NOS22/2 hosts survived with little histopathologic evidence of pneumonitis. Moreover, they
cleared influenza A virus from their lungs by an IFN-g–dependent mechanism that was not evident in wild-type mice. Even when the IFN-g–mediated antiviral activity was blocked in
NOS22/2 mice with anti–IFN-g mAb, such mice failed to succumb to disease. Further evidence that this protection was independent of viral load was provided by treating NOS21/1
mice with the NOS inhibitor, Nv-methyl-l-arginine (l-NMA). l-NMA prevented mortality
without affecting viral growth. Thus, host NOS2 seems to contribute more significantly to the
development of influenza pneumonitis in mice than the cytopathic effects of viral replication.
Although NOS2 mediates some antiviral effects of IFN-g, during influenza infection it can
suppress another IFN-g–dependent antiviral mechanism. This mechanism was observed only
in the complete absence of NOS2 activity and appeared sufficient to control influenza A virus
growth in the absence of changes in cytotoxic T lymphocyte activity.
Item Details
Item Type: | Refereed Article |
---|---|
Keywords: | Nitric oxide; antiviral immunity; influenza A virus |
Research Division: | Biomedical and Clinical Sciences |
Research Group: | Immunology |
Research Field: | Innate immunity |
Objective Division: | Health |
Objective Group: | Clinical health |
Objective Field: | Prevention of human diseases and conditions |
UTAS Author: | Karupiah, G (Associate Professor Guna Karupiah) |
ID Code: | 142845 |
Year Published: | 1998 |
Web of Science® Times Cited: | 150 |
Deposited By: | Medicine |
Deposited On: | 2021-02-12 |
Last Modified: | 2021-05-27 |
Downloads: | 10 View Download Statistics |
Repository Staff Only: item control page