| Literature DB >> 28410483 |
Caitlyn T Molloy1, Jennifer S Andonian2, Harrison M Seltzer1, Megan C Procario3, Michael E Watson1, Jason B Weinberg4.
Abstract
CD8 T cells are key components of the immune response to viruses, but their roles in the pathogenesis of adenovirus respiratory infection have not been characterized. We used mouse adenovirus type 1 (MAV-1) to define CD8 T cell contributions to the pathogenesis of adenovirus respiratory infection. CD8 T cell deficiency in β2m-/- mice had no effect on peak viral replication in lungs, but clearance of virus was delayed in β2m-/- mice. Virus-induced weight loss and increases in bronchoalveolar lavage fluid total protein, IFN-γ, TNF-α, IL-10, CCL2, and CCL5 concentrations were less in β2m-/- mice than in controls. CD8 T cell depletion had similar effects on virus clearance, weight loss, and inflammation. Deficiency of IFN-γ or perforin had no effect on viral replication or inflammation, but perforin-deficient mice were partially protected from weight loss. CD8 T cells promote MAV-1-induced pulmonary inflammation via a mechanism that is independent of direct antiviral effects.Entities:
Keywords: Adenovirus; CD8 T cells; Interferon gamma; Perforin; Respiratory infection
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Year: 2017 PMID: 28410483 PMCID: PMC5493992 DOI: 10.1016/j.virol.2017.04.005
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616