The Biology of Eosinophils and Their Role in Asthma

1The three main processes responsible for the clinical features of asthma are well recognized: bronchoconstriction, mucus hypersecretion, and airway inflammation. However, the underlying pathophysiology responsible for these processes is complex and nuanced, involving multiple cell types and cytokines. Furthermore, the activity and clinical impact of each cellular and subcellular component varies considerably between individuals and can change over time, as well as in response to drug therapy and environmental/lifestyle influences.

2Among these myriad cellular interactions and this extremely heterogeneous patient group, it is possible to identify certain key cells that are commonly involved—of which, arguably, the eosinophil is the most important.

3Eosinophil precursors originate in the bone marrow and following differentiation traffic to the lungs (among other sites) via the bloodstream. While high concentrations of circulating eosinophils are often measured in asthmatic patients, of more clinical relevance is the lung tissue eosinophilia that is also frequently present.

4The phenotype of “severe eosinophilic asthma” refers to a subgroup of asthmatic patients with evidence of eosinophilia that often require high maintenance doses of oral corticosteroids to maintain reasonable disease control. The notoriously non-specific mechanisms of action of corticosteroid therapy give rise to numerous well-documented adverse effects, which have driven decades of research focused on the development of targeted anti-eosinophil drug therapies. In order to understand how to better assist this group of patients, who currently have an unmet clinical need, it is helpful to understand the eosinophil itself, and the role that it plays in asthma. Targeted anti-eosinophil therapies will be touched upon but will be covered in greater detail by other reviews in this Research Topic.

5Eosinophils are granulocytes, typically measuring 10–16 µm in diameter. They possess segmented (usually bi-lobed) nuclei and their nucleus: cytoplasm ratio is approximately 30%. Eosinophils stain with acidophilic dyes—a feature noted in 1879 by Paul Ehrlich, who first described eosinophils and appreciated their increased presence in patients with asthma and helminth infections, among other conditions. See Figure 1 for an overview of the eosinophil ultrastructure.

6The presence of large specific granules, also known as secondary granules, is a characteristic feature that distinguishes eosinophils from other granulocytes (neutrophils and basophils). Specific granules consist of a dense crystalline core and a matrix, surrounded by a membrane. They contain a large number of mediators capable of inducing inflammation and/or tissue damage, including basic proteins, cytokines, chemokines, growth factors, and enzymes. The predominant substances are the proteins: major basic protein (MBP) is located in the core, while the matrix contains eosinophil cationic protein (ECP), eosinophil peroxidase (EPO), and eosinophil-derived neurotoxin (EDN).

7Primary granules tend to be smaller than specific granules. They are the principal location of Charcot–Leyden crystal protein (galactin-10): hexagonal bipyramidal crystals, which exhibit lysophospholipase activity and have been identified in tissues subject to eosinophilic inflammation.

8Lipid bodies are particularly important when considering the role of eosinophils in asthma, due to their involvement in the production of eicosanoids, including cysteinal leukotrienes, prostaglandins, and thromboxane. Lipid bodies are a key site of arachidonic acid esterification and eicosanoid production due to their high concentrations of relevant enzymes such as cyclooxygenases, 5-lipoxygenase, and leukotriene C4-synthase.

9Golgi bodies, endoplasmic reticulum, and mitochondria are also present and fulfill the fundamental duties of protein and adenosine triphosphate production within the eosinophil.

10The histological appearance of eosinophils varies depending on the level of activation. For example, higher numbers of vesicles such as eosinophil sombrero vesicles may be seen when the cell is undergoing piecemeal degranulation (PMD), a process described in detail further on.

11The varied roles of the eosinophil are reflected in its wide repertoire of surface molecules and receptors, which integrate eosinophils with both the innate and adaptive immune systems.

12The heterodimeric receptor for IL-5 is thought to be the most important cytokine receptor expressed by eosinophils. The beta-subunit is identical to the beta-subunit of the receptors for granulocyte–macrophage colony-stimulating factor (GM-CSF) and IL-3 (both of which are also present on eosinophil cell membranes). The alpha-subunit, IL-5Rα, is specific to IL-5 and has been identified as a therapeutic target for severe eosinophilic asthma and other eosinophil-mediated conditions. The IL-5 receptor is also expressed by basophils.

13Eosinophils also express receptors for multiple other cytokines and growth factors, including for IL-4, IL-13, IL-33, thymic stromal lymphopoietin, and transforming growth factor-β (TGF-β).

14Chemokines are small cytokines, which stimulate the migration of specific subsets of leukocytes. Chemokines are divided into four groups, depending on the presence or absence of one or more interposing amino acid(s) between two cysteine residues (known as CXC-, CX3C-, and CC-chemokines), or the presence of only one cysteine residue (XC-chemokines).

15CC-chemokine receptor-3 (CCR3) is an important G protein-coupled receptor expressed on eosinophil cell membranes. CCR3 binds to all three subtypes of eotaxin (a variety of CC-chemokine that functions as a selective eosinophil chemoattractant). CCR3 also binds to several other chemokines including monocyte chemoattractant protein-3 (MCP-3) and MCP-4. The airways of patients with asthma have been shown to contain higher numbers of cells expressing mRNA for CCR3 and its ligands, compared to non-asthmatic control subjects. In mouse models of allergic airway inflammation, antigen-induced airway eosinophilia may be inhibited by the administration of either a monoclonal antibody against CCR3 or a low molecular weight CCR3-antagonist.

16CCR1 is another key chemokine receptor on eosinophils, which is activated by chemoattractant cytokine ligand-3 (CCL-3) and CCL-5 (also known as RANTES—regulated on activation, normal T cell expressed and secreted).

17Eosinophils possess cell surface receptors for lipid mediators such as leukotrienes, prostaglandins, and platelet-activating factor, all of which have been shown to have a role in asthma pathophysiology.

18Pattern recognition receptors react to microbial pathogen-associated molecular patterns (PAMPs) or host-derived damage-associated molecular patterns (DAMPs) and regulate the immune response to these indicators of infection and/or tissue damage.

19Toll-like receptors (TLRs) are a family of PRRs, which are expressed by eosinophils, as well as multiple other cell lines. In humans there are 10 types of TLRs. TLRs are transmembrane glycoproteins, some of which are located at the cell surface and some in endosomes. The cytoplasmic domain resembles that of the IL-1 receptor, and the intracellular signals generated are therefore similar.

20Eosinophils also express several other families of PRR, including retinoic acid-inducible gene-I-like receptors, nucleotide-binding oligomerisation domain-like (NOD-like) receptors, and the receptor for advanced glycation endproducts (RAGE).

21Fc receptors to IgA, IgD, IgE, IgG, and IgM are expressed on the surface of eosinophils, facilitating interaction with the adaptive immune system.

22The high-affinity FcεR1 receptor binds IgE and signals via intracellular tyrosine kinases. On mast cells and basophils, where FcεR1 is expressed as a tetramer (αβγ2), stimulation by IgE results in degranulation. However, on eosinophils, FcεR1 is usually expressed in very small quantities as a trimer (without a β chain) and has no role in eosinophil activation. In contrast, cross-linking of FcαRI and FcγRII, with IgA and IgG, respectively, has been shown to trigger eosinophil activation.

23Eosinophils have an additional role as antigen-presenting cells, facilitated by the presence of MHC-II molecules and co-stimulatory molecules such as CD80 and CD86. In allergic patients, evaluated after segmental antigen challenge, expression of HLA-DR (a subtype of MHC-II molecule) was found to be approximately four times greater in lung eosinophils compared to blood eosinophils.

24Adhesion receptors, as their name suggests, allow cells such as the eosinophil to adhere to the extracellular matrix (ECM) and to other cells. They also allow the eosinophil to sense its surroundings and respond accordingly. Adhesion receptors are divided into four main groups: integrins, cadherins, selectins, and immunoglobulin-like cell adhesion molecules (Ig-CAM). Integrins and selectins are the main forms of adhesion receptors expressed on eosinophil cell membranes.

25Eosinophils express seven types of integrins, which are transmembrane glycoproteins, consisting of an α and a β chain. Examples include very late antigen-4 (VLA-4, CD49d/CD29) and the complement receptor CR3 (CD11b/CD18), which is otherwise known as macrophage-1 antigen (Mac-1).

26Selectins are single-chain transmembrane glycoproteins with multiple domains. There are three families: E-, L-, and P-selectin; the latter two are expressed by human eosinophils, whereas E-selectin is present on activated endothelium.

27Siglec-8 is a sialic acid immunoglobulin-like lectin (a carbohydrate-binding protein) expressed by eosinophils, mast cells, and basophils. Its physiological role has not yet been identified, although it is thought to represent a potential therapeutic target for eosinophil-mediated disease, due to the observation that administration of an antibody targeted against Siglec-8 can induce selective eosinophil apoptosis and inhibit mast cell degranulation.

28Eosinophils develop from pluripotent CD34+ granulocyte progenitor cells.

29Differentiation and maturation occurs as follows:

30Allergen challenge of mild asthmatics results in increased expression of IL-5Rα on CD34+ cells in the bone marrow, associated with blood and sputum eosinophilia. Eosinophil differentiation usually occurs in the bone marrow. However, eosinophil precursors have been isolated from the peripheral blood of atopic subjects at significantly higher concentrations compared to non-atopic controls. Increased numbers of CD34+/IL-5Rα+ eosinophil precursors have also been identified in bronchial biopsies of atopic asthmatics, compared to non-asthmatic control subjects (both atopic and non-atopic). Eosinophil-lineage committed cells have also been identified in lung tissue in a mouse model of allergic airway inflammation. More recently, eosinophil progenitors isolated from the blood of patients with severe eosinophilic asthma have been shown to have an exaggerated clonogenic response to IL-5 in vitro, compared to eosinophil precursors from mild asthmatics, suggesting that in situ eosinophilopoiesis may have a clinically relevant role in severe eosinophilic asthma.

31The differentiation of eosinophils is regulated by the transcription factors GATA-binding protein 1 (GATA-1), PU.1, and the CCAAT-enhancing binding protein (c/EBP) family. GATA-1 and PU.1 synergistically promote transcription of MBP. GATA-1 is thought to have the most important role, as disruption of the GATA-1 gene in mice results in a strain completely devoid of eosinophils.

32The cytokines IL-3, IL-5, and GM-CSF also synergistically contribute to the development of mature eosinophils. IL-5 is the most eosinophil-specific and also promotes the release of eosinophils from the bone marrow to the bloodstream, acting synergistically with eotaxin. Eosinophils are present in relatively low numbers in peripheral blood, usually accounting for no more than 5% of the total white blood cell count. They have a relatively short blood half-life of approximately 18 h. Migration to specific body sites, including the lungs and intestines, is mediated by eosinophil chemoattractants such as eotaxins. Eotaxins are a variety of CC-chemokines. There are three known subtypes: eotaxin-1 (CCL-11), eotaxin-2 (CCL-24), and eotaxin-3 (CCL-26). These bind to CCR3 receptors on the cell membranes of eosinophils and induce chemotaxis. 5-oxo 6, 8, 11, 14-eicosatetraenoic acid (5-oxo-ETE) is another eosinophil chemoattractant.

33In vitro, the presence of prostaglandin-D2 (PGD2) has been shown to significantly enhance the chemoattractant effects of eotaxin-1 and 5-oxo-ETE on eosinophils and—unlike eotaxin-1 or 5-oxo-ETE—PGD2 retains its chemoattractant effect in the presence of blood or plasma. It is therefore proposed that PGD2 acts as the initial chemoattractant, triggering the migration of circulating eosinophils to specific tissues, where eotaxins and 5-oxo-ETE then predominate. PGD2 is released from activated mast cells and acts via CRTh2 (chemoattractant receptor-homologous molecule expressed on TH2 cells).

34In allergic inflammation and asthma, circulating eosinophils adhere to the vascular endothelium and roll along it, before extravasating to the lung tissue. Initial tethering to the endothelium occurs as a result of the eosinophil cell membrane adhesion receptor P-selectin binding to P-selectin glycoprotein ligand-1 on the endothelium. Binding of the integrin VLA-4 to vascular cell adhesion molecule-1 promotes eosinophil activation and extravasation. IL-13 results in increased eosinophil expression of P-selectin and increased P-selectin mediated adhesion to endothelial cells.

35The eosinophil’s ability to store several preformed cytotoxic mediators ready for rapid release upon appropriate stimulation facilitates a much quicker reaction to pro-inflammatory stimuli, compared to other cells, whose responses depend on upregulating the transcription of genes coding for such proteins.

36The bronchial epithelium produces the cytokines IL-25, IL-33, and thymic stromal lymphopoietin, collectively known as the alarmins, in response to irritants such as allergens, pollutants, and pathogens. These cytokines trigger an inflammatory cascade involving, among others, T helper-2 (TH2) cells and type-2 innate lymphoid cells (ILC2s), resulting in increased production of numerous cytokines including IL-4, IL-5, and IL-13, therefore prompting eosinophil activation.

37High mobility group box 1 protein, acting via receptors TLR-2, TLR-4, and RAGE, also promotes eosinophilia, although less is known regarding its mechanism of action.

38Specific granule contents may be released via three different degranulation processes. Conventional exocytosis entails the specific granules fusing with the eosinophil cell membrane, resulting in the release of the entire contents of the specific granule. Alternatively, the eosinophil may be lysed (cytolysis), releasing all the cell contents, including the intact specific granules. These extracellular granules can be found in tissues affected by eosinophil-mediated disease and may subsequently release their contents in response to pro-inflammatory stimuli. However, the most common mechanism of eosinophil granulation is termed piecemeal degranulation (PMD). In this process, vesicles (both round and tubular) are released from specific granules and travel to the cell membrane to discharge their contents to the extracellular domain. The tubular vesicles tend to curl into a hoop-like morphology, giving rise to the term “eosinophil sombrero vesicles”. Vesicles with particular contents may be selectively released in response to particular cytokines, allowing eosinophils to supply a specific combination of cytotoxic mediators on demand.

39The activation of TLRs on eosinophils has been shown to promote adhesion and the release of certain cytokines and superoxides. Activation of TLR-2 and TLR-9 triggers eosinophil degranulation. In vitro, eosinophils from atopic subjects have been shown to produce more IL-8 and EDN in response to stimulation of TLR-7 and TLR-9, compared to healthy controls.

40Eosinophil survival is promoted by IL-3, IL-5, GM-CSF, and eotaxin. Activation of TLR-7 (the most abundant TLR subtype expressed by eosinophils) also enhances eosinophil survival.

41Among the type-2 cytokines, IL-3, IL-5, and GM-CSF are particularly important for the initiation and perpetuation of eosinophilic airway inflammation. These three cytokines are closely linked, in that the genes for all three are all located on chromosome 5, and their receptors also share a common β-subunit (βc).

42Monoclonal antibodies against IL-5 have been developed in order to treat eosinophil-mediated diseases such as eosinophilic asthma. Although inhibition of IL-5 activity in this manner (using mepolizumab) results in significant depletion of circulating eosinophils, the effect on bronchial tissue eosinophilia is less marked, with a median reduction of 55%. The residual tissue eosinophilia may reflect ongoing effects mediated by IL-3 and GM-CSF.

43In a mouse model of allergic airways inflammation, allergen-induced lung tissue eosinophilia was abolished in mice bred to lack the common β-subunit, therefore incapable of responding to IL-3, IL-5, and GM-CSF. In the same study, lung tissue from βc-deficient mice was found to contain fewer myeloid dendritic cells, and the local TH2 cells showed a reduced ability to proliferate and produce type-2 cytokines. These findings suggest a multifactorial role for the common β-subunit in the regulation of allergic airway inflammation.

44In comparison to the roles that eosinophils play in diseases and infections, relatively little is known about their purpose in health. However, an increasing number of homeostatic mechanisms have been attributed to—or at least associated with—eosinophils in recent years. This has prompted a call for a fundamental change of the perception of eosinophils purely as cytotoxic effector cells.

45In health, eosinophils are found in the thymus, spleen, lymph nodes, and gastrointestinal (GI) tract. The number of eosinophils in the thymus declines with age. Eosinophils may have a role in T cell selection. In a mouse model of MHC I-restricted acute negative selection, eosinophil recruitment to the corticomedullary region of the thymus and association with apoptotic bodies has been demonstrated. Eosinophils also enhance the ability of macrophages to phagocytose apoptotic thymic cells.

46Eosinophils migrate to the GI tract during embryonic development, i.e., prior to the development of any viable gut flora. In health, they are present throughout the GI tract—with the notable exception of the esophagus. Eosinophils contribute to the immune defense against gut microorganisms, due to multiple antimicrobial properties. (The antimicrobial properties of eosinophils are discussed in detail further on, with specific relation to respiratory pathogens.) Other potential homeostatic roles for eosinophils within the gut are not currently well defined but may relate to their ability to interact with the enteric neuronal system and increase smooth muscle reactivity (via release of MBP).

47In murine white adipose tissue, a positive correlation was identified between eosinophil counts and the numbers of arginase-1-expressing macrophages. Macrophages expressing arginase-1 are thought to contribute to glucose homeostasis, although macrophage classification is contentious. In a more recent study involving more than 9,000 human participants, the peripheral blood eosinophil percentage was found to be inversely associated with the risk of type-2 diabetes mellitus and insulin resistance.

48Eosinophils have also been implicated in the regeneration of liver tissue and skeletal muscle. The increased presence of eosinophils in preovulatory ovarian follicles and in endometrium has prompted speculation that they may have a role in tissue remodeling related to ovulation and menstruation.

49Eosinophils also perform several important immunomodulatory functions, discussed in the following section.

50Asthma pathophysiology is complex, and the relative contributions of the various cytokine networks involved vary between patients. Core features include airway hyperresponsiveness (AHR), mucus hypersecretion, tissue damage, and airway remodeling. See Figure 2 for an overview of the eosinophil’s role in asthma pathophysiology.

51It has long been observed that eosinophil counts in peripheral blood and bronchoalveolar lavage (BAL) fluid are higher in asthmatics compared to healthy controls. Analysis of BAL fluid obtained from patients with atopic asthma reveals increased expression of TH2 cytokines, including IL-5, which are strongly associated with eosinophilic inflammation. In general, the degree of eosinophilia correlates with disease severity and exacerbation frequency. However, non-eosinophilic asthma phenotypes are also recognized. Peripheral blood eosinophilia may also occur in numerous other conditions (see Box 1).

52Respiratory

53Eosinophilic granulomatosis with polyangiitis (EGPA)

54Allergic bronchopulmonary aspergillosis

55Sarcoidosis

56Hematological and neoplastic

57Myeloproliferative hypereosinophilic syndrome

58Lymphocytic-variant hypereosinophilic syndrome

59Certain leukemias and lymphomas

60Systemic mastocytosis

61Solid tumors—adenocarcinomas, squamous cell carcinomas, large cell lung carcinomas, transitional cell carcinoma of the bladder

62Infective

63Parasitic infection, in particular helminths

64Human immunodeficiency virus

65Dermatological

66Eczema

67Scabies infestation

68Iatrogenic

69Certain drug hypersensitivity reactions

70Graft vs host disease

71Eosinophils may be prompted to release a number of different mediators with the capacity to cause AHR. Human MBP is known to result in AHR when administered to primates and rats. In the former study, administration of EPO also caused AHR, although ECP and EDN did not. Data from the latter study suggested the mechanism of action involved the stimulation of bradykinin production. MBP can also trigger mast cells and basophils to release histamine, a potent mediator of bronchial hyperreactivity.

72Eosinophils are a source of several cytokines including IL-13, which causes AHR, and also promotes mucus hypersecretion via enhanced differentiation of goblet cells. IL-13 is also produced by TH2 cells and ILC2s. Lipid mediators such as leukotrienes, which are produced in eosinophil lipid bodies (and mast cells), also cause AHR and mucus hypersecretion.

73Studies involving two different strains of eosinophil-deficient mice have attempted to clarify the role of eosinophils in an ovalbumin model of asthma but yielded seemingly contradictory results. In one study, performed by Lee et al., eosinophil-deficient mice were protected from AHR and mucus hypersecretion. However, another study, led by Humbles, found that eosinophil deficiency was not protective in this regard. Several theories have been put forward to explain the conflicting results, including evidence of residual lung eosinophils in the Humbles study and differences between the underlying mouse strains.

74In terms of practical application, the existence in humans of eosinophilic bronchitis, a condition characterized by marked airway eosinophilia in the absence of AHR, calls into question the concept that eosinophils—acting alone—have a clinically significant impact on AHR. In patients with mild asthma, administration of a monoclonal antibody to IL-5 has been shown to reduce blood and sputum eosinophilia but had no effect on AHR. This may reflect the cellular redundancy of AHR pathophysiology, which involves several cell types including TH2 cells, ILC2s, and mast cells. In addition, the current evidence relating to AHR does not specifically study the pathophysiology of asthma exacerbations, during which it is possible that eosinophil degranulation may contribute to worsening AHR.

75Postulation that eosinophils are major effectors of lung tissue damage in asthma is well founded, given their propensity to release highly charged basic proteins, which exert multiple cytotoxic effects. MBP is toxic to respiratory epithelial cells in vitro and has been identified in postmortem lung tissue specimens of patients who have died of asthma, in association with epithelial damage. ECP and EDN share 67% amino acid sequence homology and tend to be grouped together as eosinophil-associated RNases, although ECP’s RNase activity is much less potent. ECP binds to cell membranes and alters their permeability. EDN, as its name suggests, is neurotoxic. It was first identified following the observation that, in rabbits, the intracerebral administration of eosinophils resulted in the destruction of cerebellar Purkinje cells and neurological features named “the Gordon phenomenon”. EPO catalyzes the oxidation of halides and thiocyanate, resulting in cytotoxic reactive oxidant species.

76Cell damage triggers the activation of repair pathways which, if excessive, may contribute to structural changes referred to as airway remodeling. The underlying pathological processes include hyperplasia of fibroblasts, airway smooth muscle (ASM) and goblet cells, deposition of ECM proteins, and angiogenesis. Airway remodeling is associated with the severity of asthma. It has been hypothesized that airway remodeling is responsible for the accelerated decline in lung function and development of fixed airway obstruction observed in some asthmatic patients. However, bronchial biopsies of children with difficult asthma have been shown to display reticular basement membrane thickening to a similar degree compared with adult asthmatics. Furthermore, there is evidence that some pathological features of airway remodeling can become evident within 24 h of allergen exposure.

77Eosinophils release multiple growth factors and fibrogenic mediators that promote airway remodeling (see Table 1). For example, eosinophils are known to produce TGF-β in disease states involving the skin (atopy), nose (nasal polyposis), and blood (idiopathic hypereosinophilic syndrome). Eosinophils are the main source of TGF-β in bronchial biopsies taken from asthmatic patients and can also stimulate epithelial cells to produce a number of mediators, including TGF-β. TGF-β is implicated in tissue remodeling via fibroblast proliferation and increased production of collagen and glycosaminoglycans.

78Eosinophils isolated from asthmatics, when cocultured with ASM cells, promote enhanced ASM proliferation, which is inhibited by the addition of the leukotriene antagonist montelukast. It appears that eosinophils and ASM enjoy a reciprocal relationship, as ASM cells are also known to produce pro-eosinophil cytokines. Mouse studies lend further support to the assertion that eosinophils have an important role in airway remodeling, as eosinophil-deficient mice are protected against airway deposition of collagen and smooth muscle.

79Treatment with the anti-IL-5 monoclonal antibody mepolizumab has been shown to reduce bronchial tissue eosinophilia, in association with decreased TGF-β1 in BAL specimens, and reduced reticular basement membrane procollagen III, tenascin, and lumican.

80Airway eosinophilia is an early feature of asthma exacerbations. In a study of steroid-dependent asthmatic patients, whose prednisolone dose was gradually reduced to below their maintenance requirement, the sputum eosinophil count started to rise 4 weeks before the blood eosinophil count and 6 weeks prior to spirometric and symptomatic deterioration. In fact, the adoption of an asthma treatment strategy based on sputum eosinophilia rather than traditional markers of disease activity (such as symptoms and spirometry) was found to reduce the frequency of exacerbations, with no overall increase in the average daily corticosteroid dose.

81The primary action of anti-IL-5 therapies appears to be a reduction in exacerbation frequency. Administration of mepolizumab to selected patient groups reduced exacerbation rates by approximately 50%. A similar reduction in exacerbation rates was seen with reslizumab, another anti-IL-5 monoclonal antibody. Mepolizumab has also been found to have a moderate glucocorticoid-sparing effect in a phase III clinical trial.

82Benralizumab is a monoclonal antibody targeted against the alpha subunit of the IL-5 receptor (IL-5Rα). As well as blocking the interaction between IL-5 and its receptor, benralizumab causes eosinophil cell death via antibody-dependent cell-mediated cytotoxicity, resulting in striking (95%) airway eosinophil depletion. Phase III clinical trials have demonstrated reductions in exacerbation rates.

83In addition to the direct effects of eosinophils on asthma pathophysiology, they have an important role in immunomodulation. MBP, released from eosinophil-specific granules, stimulates inflammatory responses from neutrophils (increased production of superoxide and IL-8) and mast cells (increased histamine release). Nerve growth factor (also released from specific granules) has also been shown to prolong the survival of neutrophils and mast cells. EDN promotes the activation of dendritic cells, which in turn trigger the proliferation of T cells (both helper and cytotoxic) and B cells via antigen presentation. Eosinophils themselves can also present antigens to T cells.

84The cytokines released from eosinophil-specific granules have various immunomodulatory effects. For example, IL-4 and IL-13 simulate the proliferation of B cells and IgE production, and IL-6 enhances survival of plasma cells Eosinophil-specific granules are also capable of releasing several chemokines. Depending on the stimulation they receive, these include CCL-17 and CCL-22, which attract TH2 cells, and CXCL-9 and CXCL-10, which are TH1 chemokines. In addition, eosinophils express indoleamine 2,3-dioxygenase (IDO), an enzyme that catalyzes the production of kynurenine, suppressing TH1 activity and promoting a type-2 inflammatory milieu.

85See Figure 3 for an overview of the eosinophil’s immunomodulatory roles in asthma.

86Eosinophils have traditionally been regarded as end-stage effector cells, responding to infections directly, i.e., by releasing substances that are toxic to pathogens (in particular, helminths) and resulting in the unwanted secondary effect of human tissue damage. However, research performed over the last 30 years has revealed additional roles fulfilled by the eosinophil, involving links with both the innate and adaptive immune systems. These roles include antigen presentation and interaction with other parts of the immune system, such as the complement pathway.

87Pattern recognition receptors on the cell membranes of eosinophils allow them to detect the presence of PAMPs such as lipopolysaccharide (LPS) and beta-glucans, cell wall components of bacteria and fungi, respectively. The cysteine and serine proteases produced by mites and fungi activate eosinophils via protease-activated receptors. TLR-7, the most common TLR expressed by eosinophils, is activated by viral single-stranded RNA.

88The contents of eosinophil-specific granules are directly cytotoxic to pathogens. MBP causes disruption of cell membranes due to its highly basic nature. ECP has antiviral activity and can also agglutinate Gram-negative bacteria by binding to LPS and peptidoglycans. EDN is only mildly toxic to helminths, compared to MBP and ECP. However, EDN significantly reduces the infectivity of respiratory syncytial virus group B, indicating a role in the immune response to viruses. EPO facilitates the generation of toxic reactive oxygen species.

89In addition to releasing cytotoxic proteins, eosinophils have been shown to phagocytose bacteria (albeit less efficiently than neutrophils). More recently, the “catapult-like” extrusion of “traps” consisting of mitochondrial DNA and eosinophil granule contents, in response to Gram-negative bacteria, has been observed.

90Eosinophils express receptors for various complement proteins, including C3a and C5a, which are known to promote eosinophil recruitment, extravasation, and activation. Complement is thought to facilitate eosinophil adherence to, and damage of, nematode larvae, although the development of secondary immunity is unaffected in complement-deficient mice.

91As fungi are known to trigger the production of TH2-associated cytokines (i.e., type-2 cytokines) and eosinophilia, it has been hypothesized that subclinical fungal infection/colonization of the airways may play a role in the genesis of diseases characterized by eosinophilia. Such diseases include severe eosinophilic asthma, as well as related conditions (e.g., chronic rhinosinusitis). One study of patients undergoing sinus surgery found that 74% of those with TH2-associated conditions had evidence of airway surface mycosis, compared to just 16% of controls. However, potential confounding factors such as inhaled and/or systemic corticosteroid usage must be considered.

92The increased susceptibility to respiratory viral infections observed in patients with asthma has been linked to reduced production of type I and type III interferons. Eosinophils may contribute to this impairment by producing TGF-β, which has been shown to diminish the ability of bronchial epithelial cells to produce interferons in response to human rhinovirus in vitro.

93The lung is known to harbor communities of bacteria, known as the lung microbiome, during health, which are deranged in disease states including asthma. Data have recently been published suggesting a possible link between the level of eosinophilia and microbiome community structure in asthma. Further dedicated studies, examining subject groups matched for baseline characteristics, are required.

94Although eosinophils have been associated with asthma since their initial discovery, our understanding of their roles in health and disease has evolved significantly over time. The eosinophil’s status as a cytotoxic effector cell appears to be justified, due its capacity to release potent destructive basic proteins, capable of antimicrobial effects as well as host tissue damage. However, its ability to modulate the innate and adaptive immune systems may be just as important.

95An appreciation of the numerous receptors expressed by eosinophils offers some insight into the many different interactions this versatile cell is capable of. Not only is the eosinophil recruited to the lungs in the context of pro-inflammatory type-2 cytokines but it is also a promoter of the type-2 inflammatory milieu, taking on roles such as antigen presentation and cytokine-mediated modulation of local lymphocytes.

96There is strong evidence that eosinophils contribute to airway remodeling in asthma. Mechanisms also exist by which eosinophils could promote AHR and mucus hypersecretion.

97The development of new anti-eosinophilic drugs, capable of selective depletion of eosinophils, offers great potential to explore further questions relating to the role of eosinophils in asthma and the consequences of their eradication. Research into variation in eosinophil-related gene expression between individuals may provide further insights regarding the relative contributions of eosinophils in different asthma phenotypes and the potential application of personalized medicine to this field.

98CM performed the initial literature review and drafted the article. AM-G provided critical review and additional content.

99CM has attended an international conference with Boehringer Ingelheim. AMG has attended advisory boards for Glaxo SmithKline, Novartis, Astra Zeneca, Boehringer Ingelheim and Teva. He has received speaker fees from Novartis, Astra Zeneca, Vectura, Boehringer Ingelheim and Teva. He has participated in research for which his institution has been renumerated with Hoffman La Roche, Glaxo SmithKline and Boehringer Ingelheim. He has attended international conferences with Napp and Astra Zeneca and has consultancy agreements with Astra Zeneca and Vectura.