leptin has been researched along with Hypereosinophilic-Syndrome* in 1 studies
1 other study(ies) available for leptin and Hypereosinophilic-Syndrome
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Intravenous immunoglobulin preparations contain anti-Siglec-8 autoantibodies.
Human intravenous immunoglobulin (IVIg) preparations are used for the treatment of autoimmune and allergic diseases. Natural autoantibodies are believed to contribute to IVIg-mediated anti-inflammatory effects.. To address the question of whether IVIg preparations contain anti-sialic acid-binding Ig-like lectin-8 (anti-Siglec-8) autoantibodies.. The presence of possible anti-Siglec-8 autoantibodies in IVIg preparations was first examined by functional eosinophil death and apoptosis assays. Specificity of IVIg effects was shown by depleting anti-Siglec-8 autoantibodies from IVIg. Binding of purified anti-Siglec-8 autoantibodies to recombinant Siglec-8 was demonstrated by an immunodot assay.. IVIg exerts cytotoxic effects on purified human blood eosinophils. Both potency and efficacy of the IVIg-mediated eosinophil killing effect was enhanced by IL-5, granulocyte/macrophage colony-stimulating factor, IFN-gamma, TNF-alpha, and leptin. Similarly, inflammatory eosinophils obtained from patients suffering from the hypereosinophilic syndrome (HES) demonstrated increased Siglec-8 cytotoxic responses when compared with normal blood eosinophils. Pharmacologic blocking experiments indicated that the IVIg-mediated additional eosinophil death in the presence of cytokines is largely caspase-independent, but it depends on reactive oxygen species. Anti-Siglec-8 autoantibody-depleted IVIg failed to induce caspase-independent eosinophil death.. IVIg preparations contain natural anti-Siglec-8 autoantibodies.. Anti-Siglec-8 autoantibodies present in IVIg preparations may have therapeutic relevance in autoimmune and allergic diseases, respectively, such as Churg-Strauss syndrome. Topics: Adjuvants, Immunologic; Antigens, CD; Antigens, Differentiation, B-Lymphocyte; Apoptosis; Autoantibodies; Cell Death; Cells, Cultured; Eosinophils; Granulocyte-Macrophage Colony-Stimulating Factor; Humans; Hypereosinophilic Syndrome; Immunoglobulins, Intravenous; Interleukin-5; Lectins; Leptin | 2007 |