TLR9 Differentiates Rapidly from Slowly Progressing Forms of Idiopathic Pulmonary Fibrosis

Abstract

Idiopathic pulmonary fibrosis is a generally progressive disorder with highly heterogeneous disease progression. The most common of the idiopathic interstitial pneumonias, idiopathic pulmonary fibrosis is characterized by a steady worsening of lung function and gas exchange cause by diffuse alveolar damage and severe fibrosis. We examined clinical features of patients with idiopathic pulmonary fibrosis to classify them as exhibiting rapid or slowly progressive over the first year of follow-up. We identified differences between the two groups in order to investigate the mechanism of rapid progression. Previous work from our laboratory has demonstrated that Toll-like receptor 9, a pathogen recognition receptor, promotes myofibroblast differentiation in lung fibroblasts cultured from biopsies of patients with idiopathic pulmonary fibrosis. Therefore, we hypothesized that TLR9 functions as both a sensor of pathogenic molecules and a profibrotic signal in rapidly progressive idiopathic pulmonary fibrosis. TLR9 was present at higher concentrations in surgical lung biopsies from rapidly progressive patients than in tissue from normal controls. Fibroblasts from rapid progressors were more responsive to the TLR9 agonist, CpG, than were fibroblasts from control patients. We used a humanized SCID mouse and demonstrated that there was increased fibrosis in murine lungs receiving human lung fibroblasts from rapid progressors than in mice receiving normal fibroblasts. This fibrosis was exacerbated by intranasal CpG challenges. Furthermore, CpG induced the differentiation of blood monocytes into fibrocytes and the epithelial-to-mesenchymal transition of A549 lung epithelial cells. These data suggest that TLR9 may drive the pathogenesis of rapidly progressive idiopathic pulmonary fibrosis and is a potential indicator of this subset of the disease.

TLR2-Mediated Production of IL-27 and Chemokines by Respiratory Epithelial Cells Promotes Bleomycin-Induced Pulmonary Fibrosis in Mice

“…Therefore, TLRs has been proposed to regulate pulmonary fibrosis by sensing alveolar epithelial cell damage. Consistent with this suggestion, several studies have shown that TLRs expressed in lung tissues regulate pulmonary fibrosis (11)(12)(13)(14).…”

Cellular crosstalk mechanism of Toll-like receptors in gingival overgrowth (Review)

“…Moreover, it has been reported that deficiency of MyD88, the common adaptor for all TLRs except TLR-3, protects mice from inflammation and fibrosis (51). In contrast to TLR-2 and TLR-4, TLR-9 appears to promote lung fibrosis (52). Those results were confirmed by another study, in which TLR-4 deficient mice exhibited a significant reduction in fibroblast accumulation and renal fibrosis (53).…”

Lung Pericytes and Resident Fibroblasts

“…11,19,20,22,44 Although ample evidence has accrued to strongly suggest that idiopathic pulmonary fibrosis originates with epithelial dysfunction, the pathological fibroblast from IPF patients has undergone durable reprogramming in the form of epigenetic modifications, as exemplified by the capacity of adoptively transplanted human IPF pathological fibroblasts to recapitulate lung disease in immunodeficient mice. 98 It is imperative that future studies focus on the epigenetic changes that could be modified to reduce myofibroblast differentiation and overactivated cell survival pathways.…”