IL-1β) and tumor necrosis factor-α (TNF-α), promote the destruction of pancreatic endocrine islets via islet-infiltrating immune cells [5]. It has been demonstrated that many functional abnormalities associated with diabetes can partially contribute to failure in appropriate inflammatory responses. Some researchers have suggested the concurrent occurrence of allergic disorders in T1DM [6]. In addition, it has been proposed that mast cells and eosinophil accumulation are decreased in the pleural cavity due to allergic reactions in diabetes mellitus patients [7]. Mast cells (MCs) have central effector and regulatory roles in inflammatory diseases (autoimmunity, allergic diseases, and parasitic infections) [8]. They are located in many tissues in the body, such as the airways, skin, gastrointestinal tract, and lymphoid tissues, and have the ability to release proinflammatory and immunoregulatory mediators [6]. The autoimmune response against islet β cells is believed to result from a disorder of immunoregulation. Macrophages