Abstract

BackgroundNeutrophils have been shown to play a role in host defence against highly virulent and mouse-adapted strains of influenza virus, however it is not clear if an effective neutrophil response is an important factor moderating disease severity during infection with other virus strains. In this study, we have examined the role of neutrophils during infection of mice with influenza virus strain HKx31, a virus strain of the H3N2 subtype and of moderate virulence for mice, to determine the role of neutrophils in the early phase of infection and in clearance of influenza virus from the respiratory tract during the later phase of infection.MethodsThe anti-Gr-1 monoclonal antibody (mAb) RB6-8C5 was used to (i) identify neutrophils in the upper (nasal tissues) and lower (lung) respiratory tract of uninfected and influenza virus-infected mice, and (ii) deplete neutrophils prior to and during influenza virus infection of mice.ResultsNeutrophils were rapidly recruited to the upper and lower airways following influenza virus infection. We demonstrated that use of mAb RB6-8C5 to deplete C57BL/6 (B6) mice of neutrophils is complicated by the ability of this mAb to bind directly to virus-specific CD8+ T cells. Thus, we investigated the role of neutrophils in both the early and later phases of infection using CD8+ T cell-deficient B6.TAP-/- mice. Infection of B6.TAP-/- mice with a low dose of influenza virus did not induce clinical disease in control animals, however RB6-8C5 treatment led to profound weight loss, severe clinical disease and enhanced virus replication throughout the respiratory tract.ConclusionNeutrophils play a critical role in limiting influenza virus replication during the early and later phases of infection. Furthermore, a virus strain of moderate virulence can induce severe clinical disease in the absence of an effective neutrophil response.

Highlights

  • Neutrophils have been shown to play a role in host defence against highly virulent and mouse-adapted strains of influenza virus, it is not clear if an effective neutrophil response is an important factor moderating disease severity during infection with other virus strains

  • Rapid and transient neutrophil response in the respiratory tract following influenza virus infection A number of studies have identified neutrophils by flow cytometry as Gr-1high inflammatory cells recruited to sites of infection [11,20]

  • Flow cytometric analysis of cells present in bronchoalveolar lavage (BAL) and nasal tissues (Fig. 1A) of mice infected with influenza virus strain HKx31 revealed a population of CD45+/Gr-1high cells, a phenotype consistent with that of neutrophils

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Summary

Introduction

Neutrophils have been shown to play a role in host defence against highly virulent and mouse-adapted strains of influenza virus, it is not clear if an effective neutrophil response is an important factor moderating disease severity during infection with other virus strains. Host defence against influenza virus infection depends on a complex interplay of innate (non-specific) and adaptive (specific) components. Crucial are pre-existing and rapidly induced innate defence mechanisms which play a critical role in the initial phase of a primary infection, providing a barrier to establishment of a virus and limiting its spread in host tissues in the days before a specific immune response devel-. The early inflammatory response aims to limit virus growth in the early phase of infection, prior to the recruitment and activation of virusspecific T lymphocytes (reviewed in [2])

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