The effect of infection history is ignored in most animal models of infectious disease. The attachment protein of respiratory syncytial virus (RSV) induces T helper cell type 2–driven pulmonary eosinophilia in mice similar to that seen in the failed infant vaccinations in the 1960s. We show that previous influenza virus infection of mice: (a) protects against weight loss, illness, and lung eosinophilia; (b) attenuates recruitment of inflammatory cells; and (c) reduces cytokine secretion caused by RSV attachment protein without affecting RSV clearance. This protective effect can be transferred via influenza-immune splenocytes to naive mice and is long lived. Previous immunity to lung infection clearly plays an important and underestimated role in subsequent vaccination and infection. The data have important implications for the timing of vaccinations in certain patient groups, and may contribute to variability in disease susceptibility observed in humans.
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6 November 2000
Article|
November 06 2000
Influenza Virus Lung Infection Protects from Respiratory Syncytial Virus–Induced Immunopathology
Gerhard Walzl,
Gerhard Walzl
bDepartment of Respiratory Medicine, National Heart and Lung Institute at St Mary's Hospital, Edgbaston, Birmingham B15 2TS, United Kingdom
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Sabrina Tafuro,
Sabrina Tafuro
dMolecular Immunology Group, Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, United Kingdom
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Paul Moss,
Paul Moss
cCancer Research Campaign Institute for Cancer Studies, University of Birmingham, Edgbaston, Birmingham B15 2TS, United Kingdom
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Peter J.M. Openshaw,
Peter J.M. Openshaw
bDepartment of Respiratory Medicine, National Heart and Lung Institute at St Mary's Hospital, Edgbaston, Birmingham B15 2TS, United Kingdom
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Tracy Hussell
Tracy Hussell
aDepartment of Biochemistry, Centre for Molecular Microbiology and Infection, Imperial College of Science, Technology and Medicine, London SW7 2AZ, United Kingdom
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Gerhard Walzl
bDepartment of Respiratory Medicine, National Heart and Lung Institute at St Mary's Hospital, Edgbaston, Birmingham B15 2TS, United Kingdom
Sabrina Tafuro
dMolecular Immunology Group, Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DS, United Kingdom
Paul Moss
cCancer Research Campaign Institute for Cancer Studies, University of Birmingham, Edgbaston, Birmingham B15 2TS, United Kingdom
Peter J.M. Openshaw
bDepartment of Respiratory Medicine, National Heart and Lung Institute at St Mary's Hospital, Edgbaston, Birmingham B15 2TS, United Kingdom
Tracy Hussell
aDepartment of Biochemistry, Centre for Molecular Microbiology and Infection, Imperial College of Science, Technology and Medicine, London SW7 2AZ, United Kingdom
Abbreviations used in this paper: BAL, bronchoalveolar lavage; β-gal, β-galactosidase; HA, hemagglutinin; LCMV, lymphocyte choriomeningitis virus; M2, second matrix protein; NP, nucleoprotein; QR, Quantum red; RSV, respiratory syncytial virus.
Received:
April 17 2000
Revision Requested:
August 24 2000
Accepted:
September 06 2000
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2000 The Rockefeller University Press
2000
The Rockefeller University Press
J Exp Med (2000) 192 (9): 1317–1326.
Article history
Received:
April 17 2000
Revision Requested:
August 24 2000
Accepted:
September 06 2000
Citation
Gerhard Walzl, Sabrina Tafuro, Paul Moss, Peter J.M. Openshaw, Tracy Hussell; Influenza Virus Lung Infection Protects from Respiratory Syncytial Virus–Induced Immunopathology. J Exp Med 6 November 2000; 192 (9): 1317–1326. doi: https://doi.org/10.1084/jem.192.9.1317
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