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. Author manuscript; available in PMC: 2018 Dec 1.
Published in final edited form as: Trends Immunol. 2017 Aug 4;38(12):942–954. doi: 10.1016/j.it.2017.07.003

Figure 1. Contrasting features of eosinophilic mild asthma and mixed neutrophilic/eosinophilic severe asthma.

Figure 1

Eosinophilic allergic asthma is characteristic of 50% of mild asthma. Other features of mild allergic asthma include increased type 2 inflammation in the airways accompanied by elevated serum IgE levels, mast cell activation and attenuation of symptoms by low dose inhaled corticosteroids. In mild allergic asthma, eosinophils typically undergo apoptosis in the presence of corticosteroids. In contrast, neutrophils can be detected in the airways of severe asthmatics, often in conjunction with eosinophils. Neutrophils infiltrate the airways of asthmatics during asthma exacerbations, and have been detected in the airways of individuals who died from an asthma attack. Pathogens, smoking and different co-morbidities can trigger neutrophil recruitment to the airways. The cytokines CXCL8, IL-17, tumor necrosis factor (TNF)-α, interferon (IFN)-γ and the leukotriene LTB4 promote neutrophil infiltration of the airways with the neutrophils themselves occasionally being a source of CXCL8 providing a feed-forward loop. While mediators released from neutrophils like reactive oxygen species (ROS) and proteases help in host defense, some of these proteases such as elastase and MMP-9 negatively regulate the levels of TIMP-1 and SLPI creating a protease-antiprotease imbalance, which can promote bronchoconstriction. Increased secretion of TGF-p by neutrophils promotes airway remodeling, a characteristic feature of persistent asthma. Neutrophils are generally resistant to the anti-inflammatory or pro-apoptotic effects of corticosteroids. Resistance to corticosteroid-induced apoptosis is also observed in the case of eosinophils in severe disease. Although neutrophilic airway inflammation is well described in asthmatics, there is insufficient information regarding their phenotype or state of activation or even their inflammatory or suppressive function in different asthmatics, which should be taken into consideration before targeting these cells to alleviate asthma.

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