| First Author | Evans-Marin H | Year | 2018 |
| Journal | Arthritis Rheumatol | Volume | 70 |
| Issue | 12 | Pages | 1971-1983 |
| PubMed ID | 29975009 | Mgi Jnum | J:355128 |
| Mgi Id | MGI:7737857 | Doi | 10.1002/art.40657 |
| Citation | Evans-Marin H, et al. (2018) Microbiota-Dependent Involvement of Th17 Cells in Murine Models of Inflammatory Arthritis. Arthritis Rheumatol 70(12):1971-1983 |
| abstractText | OBJECTIVE: Intestinal microbiota are associated with the development of inflammatory arthritis. The aim of this study was to dissect intestinal mucosal immune responses in the preclinical phase of arthritis and determine whether the presence of Th17 cells, beyond involvement of the cytokine interleukin-17 (IL-17), is required for arthritis development, and whether the involvement of Th17 cells in arthritis depends on the composition of the host microbiota. METHODS: Mucosal T cell production of IL-17, interferon-gamma, tumor necrosis factor alpha (TNFalpha), IL-22, and granulocyte-macrophage colony-stimulating factor (GM-CSF) was analyzed by flow cytometry and Luminex assay before arthritis onset in mice immunized to develop collagen-induced arthritis (CIA). Pathogenic features of arthritis in mice with CIA and mice with antigen-induced arthritis were compared between Th17 cell-deficient (CD4-Cre(+) Rorc(flox/flox) ) and Th17 cell-sufficient (CD4-Cre(-) Rorc(flox/flox) ) mice. In addition, the impact of intestinal microbiota on the Th17 cell dependence of CIA was assessed. RESULTS: Lamina propria CD4 T cells were activated before the onset of arthritis in mice with CIA, with marked up-regulation of several cytokines, including IL-17A, TNFalpha, and GM-CSF. CD4-Cre(+) Rorc(flox/flox) mice showed a specific reduction in intestinal mucosal levels of Th17 cells and partially reduced levels of IL-17-producing CD8 T cells. However, total levels of IL-17A, mostly produced by gammadelta T cells and neutrophils, were unaffected. The severity of arthritis was significantly reduced in Th17 cell-deficient mice, suggesting that Th17 cells have additional, IL-17A-independent roles in inflammatory arthritis. Accordingly, antigen-stimulated T cells from Th17 cell-deficient mice produced less IL-17A, IL-17F, and GM-CSF. Importantly, the dependence of CIA on the involvement of Th17 cells was mitigated in the presence of an alternative microbiome. CONCLUSION: These data from murine models suggest that activation of mucosal immunity precedes the development of arthritis, and also that Th17 cells have a microbiota-dependent role in arthritis. Therefore, a microbiome-guided stratification of patients might improve the efficacy of Th17-targeted therapies. |
