This is consistent with the fact that anti-IL-5 had no effect on expression of major pro- and anti-inflammatory cytokines in thyroids of IFN-γ−/− mice. To our knowledge, this is the first report using a murine thyroiditis model to address the role of IL-5 and eosinophils in autoimmune inflammation. Eosinophilia is a classic feature of several human diseases such as parasitic infections, selleck kinase inhibitor inflammatory bowel disease, asthma, Churg–Strauss syndrome, eosinophilic esophagitis and eosinophilic gastroenteritis.9,34–38 Eosinophils have many functions, including antigen presentation and exacerbation of inflammatory responses through their ability to secrete various
cytokines and lipid mediators.9,35 Eosinophils are important inflammatory cells, for example in sites of allergic U0126 concentration inflammation, and they have been shown to affect both tissue injury and remodelling,9,37,39 and they have been implicated in promoting fibrosis in several diseases.10–14 IL-5 regulates the activation, differentiation, recruitment and survival of eosinophils,9 and neutralizing
IL-5 can block infiltration of eosinophils into synovial tissues34 and sites of allergic inflammation.40 Although the role of IL-5 in the differentiation, proliferation and migration of eosinophils has been well established,9 it remains unclear how important IL-5 and eosinophils are to the development and/or progression of clinical diseases including autoimmune diseases. In fact, several clinical trials using anti-IL-5 mAb in patients with asthma have failed to improve symptoms, although IL-5 seems to be responsible for the accumulation of eosinophils in blood and tissues.41–43 In this study, we took advantage of the differential migration of eosinophils versus neutrophils to thyroids of IFN-γ−/− and WT mice Phosphoprotein phosphatase during development of G-EAT to examine the potential role of eosinophil trafficking to sites of autoimmune inflammation in G-EAT induction and resolution. In this model, eosinophils contribute substantially to thyroid inflammation in IFN-γ−/− mice
with G-EAT, as they are one of the major cell types infiltrating IFN-γ−/− thyroids from day 10–21 after cell transfer.8 However, inhibition of the migration of most eosinophils to the thyroid by administration of anti-IL-5 had little effect on G-EAT severity scores. Although anti-IL-5 markedly reduced the contribution by eosinophils to thyroid inflammation, other cells such as neutrophils increased in number and the end result was a similar severity score (defined as the percentage of the thyroid replaced by infiltrating inflammatory cells) in thyroids of IFN-γ−/− mice given control IgG or anti-IL-5. Therefore, a similar degree of inflammation of the thyroid (severity score) can result from the activity of different inflammatory cells and cytokines or chemokines.
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