Mast cells have been regarded for a long time as effector cells in IgE mediated type I reactions and in host defence against parasites. However, they are resident in all environmental exposed tissues and express a wide variety of receptors, suggesting that these cells can also function as sentinels in innate immune responses. Indeed, studies have demonstrated an important role of mast cells during the induction of life-saving antibacterial responses. Furthermore, recent findings have shown that mast cells promote and modulate the development of adaptive immune responses, making them an important hinge of innate and acquired immunity. In addition, mast cells and several mast cell-produced mediators have been shown to be important during the development of allergic airway diseases. In the present review, we will summarize findings on the role of mast cells during the development of adaptive immune responses and highlight their function, especially during the development of allergic asthma.
Animals ; Anti-Infective Agents/pharmacology ; Asthma/*immunology/metabolism ; Cytokines/metabolism ; Histamine/metabolism ; Humans ; Hypersensitivity/*immunology/metabolism ; Immune System ; Immunoglobulin E/immunology ; Leukotrienes/metabolism ; Mast Cells/*cytology ; Mice ; Models, Biological ; Prostaglandins/metabolism ; Tumor Necrosis Factor-alpha/metabolism

Ambroxol is used in COPD and asthma to increase mucociliary clearance and regulate surfactant levels, perhaps through anti-oxidant and anti-inflammatory activities. To determine the role and effect of ambroxol in an experimental model of asthma, BALB/c mice were sensitized to ovalbumin (OVA) followed by 3 days of challenge. Airway hyperresponsiveness (AHR), lung cell composition and histology, and cytokine and protein carbonyl levels in bronchoalveolar lavage (BAL) fluid were determined. Ambroxol was administered either before the first OVA challenge or was begun after the last allergen challenge. Cytokine production levels from lung mononuclear cells (Lung MNCs) or alveolar macrophages (AM) were also determined. Administration of ambroxol prior to challenge suppressed AHR, airway eosinophilia, goblet cell metaplasia, and reduced inflammation in subepithelial regions. When given after challenge, AHR was suppressed but without effects on eosinophil numbers. Levels of IL-5 and IL-13 in BAL fluid were decreased when the drug was given prior to challenge; when given after challenge, increased levels of IL-10 and IL-12 were detected. Decreased levels of protein carbonyls were detected in BAL fluid following ambroxol treatment after challenge. In vitro, ambroxol increased levels of IL-10, IFN-γ, and IL-12 from Lung MNCs and AM, whereas IL-4, IL-5, and IL-13 production was not altered. Taken together, ambroxol was effective in preventing AHR and airway inflammation through upregulation of Th1 cytokines and protection from oxidative stress in the airways.
Ambroxol* ; Animals ; Asthma ; Bronchoalveolar Lavage ; Cytokines ; Eosinophilia ; Eosinophils ; Goblet Cells ; In Vitro Techniques ; Inflammation* ; Interleukin-10 ; Interleukin-12 ; Interleukin-13 ; Interleukin-4 ; Interleukin-5 ; Lung ; Macrophages, Alveolar ; Metaplasia ; Mice ; Models, Theoretical ; Mucociliary Clearance ; Neutrophils ; Ovalbumin ; Ovum ; Oxidative Stress ; Pulmonary Disease, Chronic Obstructive ; Up-Regulation