Interleukin-15 Is Critical in the Pathogenesis of Influenza A Virus-Induced Acute Lung Injury

Author:

Nakamura Risa1,Maeda Naoyoshi12,Shibata Kensuke1,Yamada Hisakata1,Kase Tetsuo3,Yoshikai Yasunobu1

Affiliation:

1. Division of Host Defense, Research Center for Prevention of Infectious Diseases, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan

2. Division of Bioinformatics, Digital Medicine Initiative, Kyushu University, Fukuoka, Japan

3. Osaka Prefectural Institute of Public Health, Osaka, Japan

Abstract

ABSTRACT Highly pathogenic influenza A viruses cause acute severe pneumonia to which the occurrence of “cytokine storm” has been proposed to contribute. Here we show that interleukin-15 (IL-15) knockout (KO) mice exhibited reduced mortality after infection with influenza virus A/FM/1/47 (H1N1, a mouse-adapted strain) albeit the viral titers of these mice showed no difference from those of control mice. There were significantly fewer antigen-specific CD44 + CD8 + T cells in the lungs of infected IL-15 KO mice, and adoptive transfer of the CD8 + T cells caused reduced survival of IL-15 KO mice following influenza virus infection. Mice deficient in β 2 -microglobulin by gene targeting and those depleted of CD8 + T cells by in vivo administration of anti-CD8 monoclonal antibody displayed a reduced mortality rate after infection. These results indicate that IL-15-dependent CD8 + T cells are at least partly responsible for the pathogenesis of acute pneumonia caused by influenza A virus.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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