|
pubmed:abstractText |
Although ?herpesvirus infections are associated with enhanced lung fibrosis in both clinical and animal studies, there is limited understanding about fibrotic effects of ?herpesviruses on cell types present in the lung, particularly during latent infection. Wild-type mice were intranasally infected with a murine ?herpesvirus (?HV-68) or mock-infected with saline. Twenty-eight days postinfection (dpi), ?14 days following clearance of the lytic infection, alveolar macrophages (AMs), mesenchymal cells, and CD19-enriched cell populations from the lung and spleen express M(3) and/or glycoprotein B (gB) viral mRNA and harbor viral genome. AMs from infected mice express more transforming growth factor (TGF)-?(1), CCL2, CCL12, TNF-?, and IFN-? than AMs from mock-infected mice. Mesenchymal cells express more total TGF-?(1), CCL12, and TNF-? than mesenchymal cells from mock-infected mice. Lung and spleen CD19-enriched cells express more total TGF-?(1) 28 dpi compared with controls. The CD19-negative fraction of the spleen overexpresses TGF-?(1) and harbors viral genome, but this likely represents infection of monocytes. Purified T cells from the lung harbor almost no viral genome. Purified T cells overexpress IL-10 but not TGF-?(1). Intracellular cytokine staining demonstrated that lung T cells at 28 dpi produce IFN-? but not IL-4. Thus infection with a murine ?herpesvirus is sufficient to upregulate profibrotic and proinflammatory factors in a variety of lung resident and circulating cell types 28 dpi. Our results provide new information about possible contributions of these cells to fibrogenesis in the lungs of individuals harboring a ?herpesvirus infection and may help explain why ?HV-68 infection can augment or exacerbate fibrotic responses in mice.
|
