Eosinophils are produced in the bone marrow from multipotent hematopoietic stem cells. Hematopoietic differentiation involves the commitment of multipotent progenitors to a given lineage, followed by the maturation of the committed cells. From these stem cells, the myeloid lineage allows the development of the myeloblast with shared properties of basophils and eosinophils, and then into a separate eosinophil lineage.1 Each of the steps that ultimately lead to mature eosinophils is under the fine regulation of soluble mediators and transcription factors.

Several transcription factors are involved in eosinophilic lineage. Forced expression of the transcription C/EBP members (CCAAT/enhancer-binding protein family) in progenitor cells induces myeloid and eosinophil differentiation.2 PU.1, an ETS transcription factor family member, is only expressed in hematopoietic cells. At an early time point of the differentiation, PU.1 is involved in the transition between lymphoid and myeloid lineage. PU.1 expression level determines the fate of the cell and is necessary for dictating monocyte/macrophage and dendritic cell commitment and differentiation, as well as for neutrophil differentiation. In addition, high levels of PU.1 lead to an increase in myeloid differentiation.3 In most cells, PU.1 antagonizes GATA-1 (a zinc finger family member), the latter of which has synergistic activity in regulating eosinophil lineage specification and eosinophil granule protein transcription.4 The interferon consensus sequence binding protein (ICSBP) is also a key transcription factor for eosinophils and is demonstrated by a loss of eosinophils in ICSBP-deficient mice.5 Of these transcription factors, GATA-1 is clearly the most important for eosinophil lineage specification, based on loss of the eosinophil lineage in mice harboring a targeted deletion of the high affinity GATA-binding site in the GATA-1 promoter,6 and based on eosinophil differentiation experiments in vitro.7

Cytokines are indispensable for hematopoietic cell development, differentiation and maturation. Located on chromosome 5q31, IL-3, IL-5, and granulocyte/macrophage-colony stimulating factor (GM-CSF) are cytokines that are particularly important in regulating eosinophil development.8 These "eosinophilopoietins" likely provide permissive proliferative and differentiation signals following the instructive signals specified by the transcription factors GATA-1, PU.1, and C/EBPs. IL-3 and GM-CSF also induce the differentiation of other myeloid cells such as the mast cell, but IL-3, GM-CSF and IL-5 synergize toward the differentiation of eosinophils. Of these three cytokines, IL-5 is the most specific to the eosinophil lineage and is responsible for selective terminal differentiation of eosinophils.9 IL-5 also stimulates the release of eosinophils from the bone marrow into the peripheral circulation.10 The critical role of IL-5 in regulating eosinophils in humans has been demonstrated in several clinical trials with humanized anti-IL-5 antibodies (mepolizumab and reslizumab), currently a non-FDA approved drug, which dramatically lowers eosinophil levels in the blood in part by preventing eosinophil maturation in the bone marrow with arrest at the myelocyte and metamyelocyte stages.11,12

The life cycle of the eosinophil may be divided into bone marrow, blood, and tissue phases. Although the eosinophil is a formed element of the peripheral circulation, it is primarily a tissue-dwelling cell. In humans the tissue eosinophil/blood ratio is about 100:1.14 Furthermore, eosinophils tend to reside in those tissues where the epithelial surfaces are exposed to the external environment (gut); mast cells primarily reside in these tissues as well. Thus, eosinophils are considered merely to "pass through" the circulation en route to the tissues.15

Once the eosinophil has entered the blood, it has a short half-life, ranging from 8 to 18 hours. After circulating in the blood, eosinophils migrate into the tissues, probably by diapedesis at endothelial intercellular junctions4 by a mechanism involving cytokines and adhesion molecules. Under normal conditions, once eosinophils enter the tissues, most do not recirculate. The tissue life span of eosinophils ranges from 2 to 5 days, depending partly on the tissue studied. However, cytokines increase eosinophil survival in vitro to 14 days or longer; thus, they likely also prolong eosinophil survival in vivo.15

Under baseline conditions, most eosinophils traffic into the gastrointestinal tract where they normally reside within the lamina propria of all segments except the esophagus, where there are normally zero eosinophils.16 The gastrointestinal eosinophil is the predominant population of eosinophils. Under baseline conditions, eosinophil levels in the gastrointestinal tract occur independently of lymphocytes and enteric flora, indicating unique regulation compared with other leukocytes.16 Indeed, the recruitment of gastrointestinal eosinophils is regulated by the constitutive expression of eotaxin-1 (CCL11), demonstrated by the marked decrease of this population of eosinophils in eotaxin-1-deficient mice.17 The importance of eotaxin-1 in regulating the baseline level of eosinophils is reinforced by the observation that mice with a targeted deletion of CCR3 (but not eotaxin-2 (CCL24)-deficient mice) also have a deficiency in gastrointestinal eosinophils.17 In addition to trafficking into the gastrointestinal tract, eosinophils home into the thymus, mammary gland, and uterus under homeostatic conditions, also under the regulation of eotaxin-1.18 Of note, trafficking into the uterus is regulated by estrogen, as eosinophil and eotaxin-1 levels cycle along with estrus.19

While IL-5 does not appear to be nearly as important as chemokines for eosinophil recruitment, locally produced IL-5 does have an important function in increasing the survival of eosinophils once they have reached the tissues.

Both IL-3 and GM-CSF are pluripotent cytokines with activities on other hematopoietic lineages, whereas IL-5 is selective for the eosinophil lineage and plays a crucial role in driving committed eosinophil progenitor-cell proliferation, terminal differentiation, and post-mitotic priming and activation.80

It has been appreciated for some time that IL-3, GM-CSF and IL-5 enhance eosinophil survival when cultured in vitro for weeks, and thus it might be that in vivo eosinophil persistence in the tissues may be prolonged in their presence. From the human IL-5 data and in animal models, the ability of eosinophils to survive and function in the tissue is becoming an important focus. The development and maturation of eosinophils can occur in situ in peripheral sites of inflammation containing preexisting increased tissue eosinophils. Eosinophil progenitors are released into the circulation to reach such tissue sites.81 Eosinophils can release GM-CSF in an autocrine fashion,82 a cytokine which is stored in association with eosinophil granules.83 Other eosinophil-derived and stored cytokines (e.g., IL-4,84 IL-1385) and chemokines (e.g., RANTES (CCL5))48 may further amplify the inflammatory milieu. Thus, the local self-production of such factors by eosinophils may be important in tissue eosinophil reactions beyond IL-5. Local fibroblasts and epithelial cells produce IL-5 and GM-CSF. Eosinophils may enhance their own survival by directly stimulating CD4+ T cells within tissue to produce IL-5. Nasal explants from atopic patients were shown to survive ex vivo using similar mechanisms to promote extramedullary eosinophil maturation and survival.83 These, as well as lung explants of Brown-Norway rats, exhibited rapid (6 hours) accumulation of MBP-positive cells after allergen challenge of the explants in vitro.86 The major signaling pathway of these events is associated with IL-5 receptor ligation leading to phosphorylation of JAK-2 and Lyn kinases, decreased BAX translocation, and ultimately decreased apoptosis.87 Additionally, GM-CSF appears to have a strong role in inhibiting eosinophil apoptosis at the tissue level. Autocrine GM-CSF stimulation of eosinophils bound to fibronectin, via 4 integrins, promoted eosinophil survival for two weeks.82 Eosinophils, when instilled into the trachea of IL-5 knockout mice, not only survive in the absence of IL-5, but in concert with CD4+ T cells, migrate back into lung, and reconstitute the asthma phenotype of wild-type antigen-challenged animals.88 Overall, while IL-5 is essential in the maturation and differentiation of eosinophils in the bone marrow,89 the recruitment to tissues and function within tissues may be IL-5-independent.

Eosinophil apoptosis can be induced in response to specific ligands of the so-called 'death receptors' of the tumor necrosis factor (TNF) family.90 Studies on the role of TNF-α in the induction of eosinophil apoptosis have yielded inconsistent results. Currently available data suggest that induction of apoptosis occurs only under conditions in which nuclear factor-κB is suppressed.91 If this is not the case, TNF-α may even be anti-apoptotic for eosinophils. For instance, TNF-α was shown to activate the p38 mitogen-activated protein (MAP) kinase pathway resulting in delayed eosinophil apoptosis.92 Moreover, the survival effect of TNF-α under in vitro conditions was suggested to be mediated via GM-CSF induction in eosinophils, via activation of both TNF receptors, TNF-RI and TNF-RII.93 Both TNF-α and IL-1 interact synergistically with IL-4 and IL-13 to augment VCAM-1 expression as well as intercellular adhesion molecule-1 (ICAM-1, CD54) expression.94 Recent data suggest that TNF-α prolongs human eosinophil survival by activating both TNF receptor subtypes and NF-κB, but that the mechanism does not involve production of GM-CSF. Interestingly, glucocorticoids completely reversed TNF-α but not IL-5-afforded eosinophil survival.95 This would imply that the mechanism of TNF-α-induced eosinophil survival differs from that of IL-5. Glucocorticoids have been reported to inhibit NF-κB activation.96 In contrast, IL-5 does not cause discernible activation of NF-κB.97 This supports the idea that TNF-α induced eosinophil survival is mediated via activation of NF-κB pathway.

In vitro interferon (IFN)-α, IFN-β and IFN-γ each suppresses colony formation by both multipotential colony-forming units: granulocyte, erythroid, macrophage, and megakaryocyte and day 7 and 14 colony-forming unit granulocyte-macrophage.98 This effect is not dependent on the presence of monocytes, T or B lymphocytes, hence, IFNs appear able to block colony formation by a direct inhibitory effect on colony-forming cells. IFN-α may also act indirectly to reduce eosinophilia through its ability to up-regulate synthesis of IFN-γ,99 a proinflammatory product of Th1 CD4+ lymphocytes that inhibits differentiation of eosinophils from IL-3- and IL-5-stimulated umbilical cord mononuclear cells as well as their tissue migration.100 Both IFN-α and IFN-γ have complex effects on eosinophils. Both IFNs enhanced eosinophil viability in vitro, with IFN-γ being more effective.101 However, in cultures of human umbilical cord mononuclear cells, eosinophil viability decreased markedly after a 1-week culture with IFN-α or with IFN-γ,102 and the number of apoptotic eosinophils increased as well.

Leptin is a survival cytokine for human eosinophils, a finding with potential pathologic relevance in allergic and parasitic diseases.78 Leptin activates both phosphatidylinositol-3-OH (PI3) kinase and MAP kinase signaling pathways, resulting in the inhibition of the mitochondrial death pathway.103

Eosinophils have been shown to express the membrane receptor CD40, the ligation of which results in enhanced eosinophil survival as a consequence of autocrine GM-CSF release. Tissue eosinophils resident in nasal polyp tissue have been shown to have a high constitutive expression of CD40.104 The ligand for CD40, CD40L, is expressed by CD4+ T cells that are also present in nasal polyp tissue, which suggests an intriguing potential for a further relationship between eosinophils and T cells. CD40 engagement also enhances eosinophil survival through induction of cellular inhibitor of apoptosis protein 2 (c-IAP2) expression and suggests a role for this mechanism in allergic inflammation.79 CD40 was not expressed on freshly-isolated blood eosinophils, but was seen following culture.

IL-33 potently induces eosinophil adhesion and CD11b expression and enhances eosinophil survival, albeit not as effectively as IL-5. The IL-33-ST2 pathway might be an important regulator of eosinophil biology in the pathogenesis of Th2-biased allergic diseases.105

GM-CSF, IL-3 and IL-5 are cytokines important for eosinophil survival.101 The signaling pathways involved in cytokine-afforded eosinophil survival are complex and partly unknown. The receptors for IL-3 (CD123), IL-5 (CD125) and GM-CSF (CD116) each have unique α-chains but chare a common β-chain (CD131).106 The β-chain is essential for signal transduction and explains the overlapping activities of these cytokines. Cytokine receptors depend on dimerization for their activation, and upon dimerization, multiple tyrosine residues in the β-chain become phosphorylated.106 In general, the signaling events include the phosphorylation of tyrosine kinases, adapter proteins such as Shc and Grb-2, Ras-MAP kinase pathways, and janus kinase (Jak)-signal transducer and the activator of transcription (STAT) pathways (Fig. 2).

The intracellular pathways important in the inhibition of eosinophil apoptosis and their subsequent enhanced survival by IL-3, GM-CSF and IL-5 include the Lyn, Jak2, Raf1 and MAP kinases.108 Indeed, intracellular levels of protein tyrosine phosphorylation appear to be vital in determining whether an eosinophil will exhibit prolonged survival or undergo apoptosis, and a role for both tyrosine phosphorylation and the tyrosine kinase Lyn was recently demonstrated in Fas receptor-mediated apoptosis in eosinophils.109 The picture is complicated further by the observation that levels of intracellular reactive oxygen species in human eosinophils also appear to be involved in regulating their apoptosis and that antioxidants blocked Fasmediated eosinophil death.77

MAP kinases are serine and threonine kinases, which can be activated by phosphorylation in kinase cascades. The members include extracellular-regulated kinase (ERK) 1, 2, 5 and 6, JNK/SAPK, and various isoforms of p38.110

p38 MAP kinase is constitutively activated in surviving eosinophils, and when eosinophils are dying, it is de-activated in those cells. Furthermore inhibition of p38 MAP kinase activity enhances spontaneous apoptosis.92 These results suggest that p38 MAP kinase is involved in the signaling that supports eosinophil survival. The factor(s) that initially lead to p38 activation in eosinophils currently remain unknown.92 This leads to the interesting hypothesis that compounds that inhibit p38 MAP kinase activity may reduce eosinophilia. In fact, this may be true as a p38 MAP kinase inhibitor, SB239063 has been shown to almost completely abolish lung eosinophilia in ovalbumin-sensitized and challenged mice.111 In contrast to p38 MAP kinase, inhibition of ERK 1/2 activity seems not to alter the rate of spontaneous apoptosis in eosinophils.92

Sodium salicylate has been reported to induce JNK and p38 MAP kinase activation in human eosinophils as well as to induce apoptosis, but the effects of sodium salicylate on apoptosis could not be reversed by inhibiting JNK and p38 with antisense oligodeoxynucleotides or with the specific p38 MAP kinase inhibitor SB203580,112 thus suggesting that JNK and p38 MAP kinase are not mediating sodium salicylate-induced eosinophil apoptosis.

Despite a great variety of available apoptotic stimuli, final changes in the dying cell are similar and many of the signaling events appear to converge into common mechanisms involving activation of cysteine-containing proteases that cleave their target proteins at specific aspartic acids (caspases) (Fig. 3). Caspases are part of a family that so far comprise 14 members.113 They are present in the cells as inactive zymogens that must be cleaved to generate free catalytic subunits able to associate and form active heterotetramers.

The presence of caspases 3, 6, 7, 8 and 9 in eosinophils has been described and these caspases are associated with spontaneous eosinophil apoptosis.115 The family of caspases can be divided into two functional subgroups, the initiator and the executioner caspases. Many apoptotic responses are initiated by activation of the initiator caspases-8 or -9. Initiator caspases necessitate special mechanisms of activation of zymogens. For instance, caspase-8 can be activated following recruitment and clustering at multicomponent apoptosis-signaling complexes, resulting from ligation of cell surface molecules of the TNF receptor family, presumably by auto-processing of the zymogens according to the induced-proximity model.116 Caspase-9 is activated by recruitment to Apaf-1 in the presence of ATP following release of cytochrome c from mitochondria.117

Activation of either of these caspases can result in activation of executioner caspases such as caspase-3, leading eventually to apoptosis. Caspase-3 has been shown to be an important effector caspase in eosinophils following mitochondrial activation involving the Bcl-2 family protein Bax.115

IL-5 prevents the caspase activation.115 In one study, a caspase-9 inhibitor blocked eosinophil apoptosis, confirming the view that mitochondria are involved in pro-apoptotic signaling in eosinophils.118 In addition, broad-range caspase inhibitors also blocked eosinophil apoptosis, suggesting that caspases are indeed critical elements of the death machinery in eosinophils.

There have been several reports suggesting the involvement of members of the Bcl-2 family in the regulation of apoptosis that usually regulate the pro-apoptotic activity of mitochondria. This has been somewhat surprising since granulocytes have been described as cells with limited numbers of mitochondria.119 Recently published work, however, suggests that eosinophils contain small numbers of mitochondria, which are involved in the induction of apoptosis.118

Pro-apoptotic Bax molecules have been found to be expressed at high levels in eosinophils.120 Moreover, eosinophil apoptosis was associated with translocation of cytosolic Bax into the outer membrane of mitochondria where it forms pores, allowing the release of pro-apoptotic factors such as cytochrome c.115 Clearly, high levels of Bax may contribute but may not be sufficient to shorten the life span of eosinophils. The more proximal mechanisms that are responsible for Bax translocation to mitochondria in the absence of sufficient stimulation with survival cytokines remain to be determined.

Besides the pro-apoptotic Bax, eosinophils also express anti-apoptotic members of the Bcl-2 family. For instance, Bcl-xL was shown to play an antiapoptotic role and was inducible by IL-5 in eosinophils.120 In contrast, Bcl-2 appears not to be expressed in eosinophils,120 although there are some contrasting reports in the literature.121

Fas (CD95, APO-1) is a cell surface receptor expressed on many cells including eosinophils, which mediates apoptosis when ligated by agonistic antibodies or its natural ligand FasL. It seems that IFN-γ and TNF-α, both alone and synergistically, increase Fas receptor expression whereas IL-3/IL-5/GM-CSF do not modulate constitutive Fas receptor expression.122 After treatment with Fas antibody, electron microscopy of eosinophils and gel electrophoresis of DNA extracted from eosinophils demonstrated changes consistent with apoptosis. These data demonstrate that Fas antigen can modify eosinophil survival by inducing apoptosis through a pathway that is, at least in part, independent of the survival-promoting effects of IL-5.123 Fas-mediated apoptosis in eosinophils can be only partially overcome by IL-5124 and it can be further enhanced by glucocorticoids.125 Cross-linking of Fas can induce eosinophil apoptosis in ex vivo conditions in nasal polyps126 and in vivo in mouse lung.127 Interestingly, blood and tissue eosinophils from some donors did not express functional Fas receptors, although Fas protein was normally expressed in these cells.126

The signaling events induced by Fas in human eosinophils remain largely unknown. Ligation of Fas by agonistic antibody has been shown to result in tyrosine phosphorylation of several intracellular proteins and tyrosine kinase inhibitors lavendustin A and genistein have been reported to block Fas-receptor-induced cell death.109 Lyn phosphorylation by Fas has been reported, and decreases in the expression of Lyn by antisense technique resulted in partial reversal of Fas-induced cell death.109 Similarly, nitric oxide and cyclic adenosine 3':5'-monophosphate (cAMP) and cGMP have been reported to reverse Fas-induced eosinophil death.128 Fas-ligation induces caspase-3 and -8 activation and loss of mitochondrial membrane potential (ΔΨm). Interestingly, incubation of eosinophils with bongkrekic acid, an inhibitor of mitochondrial permeability transition pore opening, failed to modify Fas mediated loss in ΔΨm and apoptosis, whereas caspase inhibitors Z-VAD fmk (broad spectrum), Z-IETD-fmk (caspase-8) and Z-DEVD-fmk (caspase-3) inhibited Fas-induced apoptosis indicating that caspase-3 and -8 might play a role, but loss of ΔΨm is not involved in the signaling by Fas in eosinophils.124

More recently, a selective mechanism for the induction of human eosinophil apoptosis by surface Siglec-8 (sialic acid-binding immunoglobulin-like lectin 8) cross-linking has been identified.112 Siglec-8 is expressed on eosinophils but also on basophils and mast cells. Such cross-linking in eosinophils leads to increased caspase 3 activity, which is an enzyme responsible for the degradation of cellular contents in the final stages of the apoptotic pathway leading to increased cell apoptosis. This is the case even in the presence of IL-5 and GM-CSF.

Mechanistic studies implicated both caspases and reactive oxygen species generation resulting in mitochondrial injury in this cell death. A paradigm has emerged that engagement of Siglec-8 activates the apoptotic pathway involving generation of reactive oxygen species leading to down-stream mitochondrial dysfunction and caspase cleavage before apoptotic death ensues.129

One of the initially confusing observations regarding Siglec-8-induced cell death was that unlike most other eosinophil death pathways that can be overridden by counterbalanced survival signals such as those provided by the cytokines IL-5 and GM-CSF, Siglec-8-induced death was enhanced by these cytokines in that cells would die even more readily with even less of a Siglec-8 engagement signal.112 These results were subsequently confirmed in eosinophils primed in vivo in humans following allergen bronchoprovocation, and primed cells no longer used caspases in the apoptosis process, instead relying exclusively on reactive oxygen species generation and mitochondrial injury.130 Overall, these data suggest that activated eosinophils might be particularly susceptible to pharmacologic approaches that engage Siglec-8.

Intravenous immunoglobulin (IVIG) preparations that are used commercially contain autoantibodies to Siglec-8 at a high enough titer so as to also induce eosinophil apoptosis in vitro, especially in cytokine-primed cells.131

Using IL-5 transgenic mice and Northern blotting, Siglec-E, -F and -G were all expressed at the mRNA level in mouse eosinophils, but patterns of expression were markedly increased in IL-5 transgenic mice only for Siglec-F and Siglec-G.132 Ultimately, it was not until antibodies were generated that this issue was completely resolved, and it is now clear that Siglec-G is expressed on B lymphocytes133 while Siglec-F is most prominently expressed by mouse eosinophils and is considered the closest functional paralog to Siglec-8.134

Systemic administration of two different types of Siglec-F antibodies led to profound depletion of circulating and tissue eosinophils. It appears that the reduction in eosinophil numbers in vivo was due to apoptosis based on ex vivo studies with blood samples from Siglec-F-treated mice, as well as studies in which eosinophils from IL-5 transgenic mice were exposed to Siglec-F antibody in vitro and characteristic changes indicative of apoptosis were seen.135 Administration of anti-Siglec-F antibody in a mouse model of eosinophilic gastroenteritis significantly reduced levels of eosinophilic inflammation in the intestinal mucosa and this was associated with reduced intestinal permeability changes, normalization of intestinal villous crypt height, and restoration of weight gain,136 Siglec-F antibody administration also significantly reduced levels of allergen-induced eosinophilic airway inflammation and features of airway remodeling in a model of chronic mouse model of asthma, especially subepithelial fibrosis, by reducing the number of eosinophils and increasing the number of apoptotic eosinophils in lung and bone marrow.137

TGF-β is a pleiotropic immunoregulatory cytokine that, for instance, antagonizes the effects of IL-5 on eosinophils.138 In addition to blocking the anti-apoptotic effects of IL-5, it also inhibits eosinophil degranulation and cytokine production. The mechanisms of this inhibitory effect of TGF-β are unknown. It has been demonstrated that TGF-β blocks tyrosine phosphorylation of Jak2 and Lyn tyrosine kinases.139 Furthermore, it inhibits the activation of ERK MAP kinase and Stat1 nuclear factor. However, the signaling molecules mediating these effects have not yet been identified. Tyrosine phosphatases have been studied, but do not seem to be involved. It is possible that TGF-β activates some of the newly described inhibitors of tyrosine kinases, which subsequently mediate its inhibitory effects.

CD30, a member of the TNFR family, was originally identified as Ki-1, an antigen expressed on Reed-Sternberg cells in Hodgkin and non-Hodgkin lymphomas, particularly diffuse, large cell lymphoma and immunoblastic lymphoma.140 TNFR family members, including two receptors for TNF, the nerve growth factor receptor, Fas, CD27, CD40, OX40, 4-1BB, TRAIL receptors 1, 2, 3 and 4, as well as several soluble receptors of mammalian and viral origin, participate in cellular activation, induction of survival and/or apoptosis.141

The roles of the nuclear receptor family in eosinophil functions have not yet been clarified. CD30 stimulation recently has been shown to cause eosinophil-specific apoptosis.142 It has been further reported that CD30 stimulation markedly induced Nur77 and NOR1, NR4A nuclear receptor family, during eosinophil-specific apoptosis.143 However, CD30 stimulation did not alter Nurr1 expression in this system. Fas-signaling has also been shown to induce eosinophil apoptosis, but this effect is not eosinophil-specific; nor were Nur77 or NOR1 induced before apoptosis under these circumstances. Gene expression of the NR4A nuclear receptor family and subsequent eosinophil apoptosis were down-regulated by a MAP kinase inhibitor, but not by a p38 inhibitor. ERK1/2 phosphorylation by MEK1/2 downstream of CD30 signaling and upstream of the nuclear receptor family may be involved in apoptosis, but there still is no information on events downstream of these nuclear receptors.

Glucocorticoids can cause a striking reduction in eosinophil numbers in vivo144 and in their inhaled form remain the mainstay of anti-inflammatory therapy in asthma.145 Although the precise mechanism of action of steroids remains to be determined, glucocorticoids are likely to exert their effects on eosinophils by accelerating their apoptosis and engulfment by lung macrophages,146 by inhibiting the production of survival-enhancing cytokines or both. It is now clear that glucocorticoids suppress the transcription of the IL-5 and other cytokine genes. This inhibition of transcription is the consequence of inhibition of the potent inflammatory transcription factor NF-κB (Fig. 4).147

Eosinophils are highly sensitive to apoptosis induction by corticosteroids that can only be overcome by high concentrations of IL-5.148 Previous work with eosinophils derived from both healthy and asymptomatic allergic individuals has demonstrated an involvement of caspase-3 and -8 in glucocorticoid-induced apoptosis.149 One recent study has demonstrated that in vitro corticosteroid treatment of eosinophils in nasal polyp tissue sections enhanced their apoptosis induction,150 suggesting that eosinophil apoptosis induction by glucocorticoids might be relevant to their anti-inflammatory effects in sinus disease. Interestingly, there is evidence that the bronchodilating β-adrenoreceptor agonists block the anti-apoptotic effects of corticosteroids on eosinophils,151 which might have important implications for the over-usage of β2-agonists in asthma therapy.

Lidocaine and its analogues have been reported to inhibit IL-5-mediated eosinophil survival. This inhibition cannot be overcome by increasing concentrations of IL-5 and is not due to the blocking of Na+ channels by lidocaine.152

IRp60/CD300a is an inhibitory receptor on eosinophil. Although CD33 and p75/AIRM could inhibit proliferation of myeloid cell precursors, IRp60/CD300a could not suppress this feature, which suggests distinct functions for various inhibitory receptors.153 CD300a/IRp60 can also inhibit eosinophil survival.154 In contrast to Siglec-8, which induces eosinophil apoptosis, IRp60/CD300a inhibits survival signals delivered to eosinophils via the IL-3/IL-5/GM-CSF receptor βc.154 Cross-linking experiments have revealed that upon IRp60/CD300a activation, JAK2, p38, and extracellular signal-regulated kinase 1/2 phosphorylation are inhibited, probably from the recruitment of SHP-1 and not SHP-2.

The different outcome of Siglec-8 activation (induction of apoptosis) as opposed to IRp60/CD300 activation (inhibition of survival signals) may be partially explained by the fact that Siglec-8 contains both ITIM and ITSM motifs. ITSM motifs may recruit either inhibitory phosphatases such as SHP-1 and/or SHP-2 or activatory molecules such as slam-associated protein (SAP) and/or 2-Ewing's sarcoma-FLI activated transcript 2 (EAT-2).155