Published in Volume
123, Issue 5
(May 1, 2013)J Clin Invest.
Copyright © 2013, American Society for Clinical Investigation
Eosinophil pathogenicity mechanisms and therapeutics in neuromyelitis optica
Departments of Medicine and Physiology, UCSF, San Francisco, California, USA.
Address correspondence to: Alan S. Verkman, 1246 Health Sciences East Tower, University of California, San Francisco, California 94143-0521, USA. Phone: 415.476.8530; Fax: 415.665.3847; E-mail:
First published April 8, 2013
Submitted: October 26,
2012; Accepted: February 12,
Eosinophils are abundant in inflammatory demyelinating lesions in neuromyelitis optica (NMO). We used cell culture, ex vivo spinal cord slices, and in vivo mouse models of NMO to investigate the role of eosinophils in NMO pathogenesis and the therapeutic potential of eosinophil inhibitors. Eosinophils cultured from mouse bone marrow produced antibody-dependent cell-mediated cytotoxicity (ADCC) in cell cultures expressing aquaporin-4 in the presence of NMO autoantibody (NMO-IgG). In the presence of complement, eosinophils greatly increased cell killing by a complement-dependent cell-mediated cytotoxicity (CDCC) mechanism. NMO pathology was produced in NMO-IgG–treated spinal cord slice cultures by inclusion of eosinophils or their granule toxins. The second-generation antihistamines cetirizine and ketotifen, which have eosinophil-stabilizing actions, greatly reduced NMO-IgG/eosinophil–dependent cytotoxicity and NMO pathology. In live mice, demyelinating NMO lesions produced by continuous intracerebral injection of NMO-IgG and complement showed marked eosinophil infiltration. Lesion severity was increased in transgenic hypereosinophilic mice. Lesion severity was reduced in mice made hypoeosinophilic by anti–IL-5 antibody or by gene deletion, and in normal mice receiving cetirizine orally. Our results implicate the involvement of eosinophils in NMO pathogenesis by ADCC and CDCC mechanisms and suggest the therapeutic utility of approved eosinophil-stabilizing drugs.
Neuromyelitis optica (NMO) is an inflammatory demyelinating disease that primarily affects the spinal cord and optic nerves, leading to paralysis and visual impairment (1, 2). Serum autoantibodies against astrocyte water channel aquaporin-4 (AQP4), called NMO immunoglobulin G (NMO-IgG), are present in most NMO patients and are believed to be pathogenic (3–5). Human NMO lesions show marked cellular infiltration with eosinophils, neutrophils, and macrophages, loss of astrocyte AQP4 and glial fibrillary acidic protein, perivascular deposition of activated complement, and demyelination (6–9). Current NMO therapies include immunosuppression, plasma exchange and B cell depletion (10, 11).
Eosinophil infiltration is a prominent feature in NMO lesions but not in other demyelinating diseases including multiple sclerosis (2, 7). Eosinophils are also found in cerebrospinal fluid in NMO (9). They can damage cells by the release of toxins contained in intracellular granules, including eosinophilic granule major basic protein (MBPe), eosinophil cationic protein (ECP), eosinophil peroxidase, and eosinophil-derived neurotoxin (12). Eosinophil degranulation can be triggered by immunoglobulin binding to Fc receptors and by soluble effectors such as complement anaphylotoxins C3a and C5a, chemokines, and lipid mediators (13). Differentiation and maturation of eosinophils in bone marrow is under the control of transcription factor GATA-1, as well as IL-3, IL-5, and GM-CSF (12). Eosinophils are normally present in the gastrointestinal tract, as well as in the thymus, mammary gland, and uterus. Eosinophilia and exaggerated eosinophil responses occur in some infections, asthma, hypereosinophilic syndrome, eosinophilic gastrointestinal diseases, and certain tumors (14). Eosinophil-based therapies target eosinophil production or eosinophil-derived products, which broadly include glucocorticoids, myelosuppressive drugs, leukotriene antagonists and inhibitors, some second-generation antihistamines, cromoglycate, tyrosine kinase inhibitors, IFN-α, and anti–IL-5 antibodies (13, 14).
Here, we utilize mouse models of NMO, including ex vivo spinal cord slice cultures (15) and a new in vivo intracerebral infusion model, as well as cell cultures, to investigate the mechanisms of eosinophil-dependent NMO pathology. We report evidence of antibody-dependent cell-mediated cytotoxicity (ADCC) and complement-dependent cell-mediated cytotoxicity (CDCC), in which eosinophil toxins secreted upon degranulation injure target cells. We also show protection against eosinophil-dependent NMO pathology by small-molecule inhibitors of eosinophil degranulation, including 2 widely used second-generation antihistamines.
Eosinophils produce NMO-IgG–dependent cytotoxicity. We performed in vitro experiments with murine eosinophils cultured from bone marrow. Cultures were treated with SCF and FLT3 ligand (FLT3-L) for 4 days to promote eosinophil progenitor cell growth, followed by IL-5 for 10 days to simulate eosinophil proliferation, and then GM-CSF for 24 hours before experiments to induce Fc receptor surface expression (16, 17). We produced a nearly pure suspension of eosinophils after 14 to 16 days in culture, showing cytoplasmic MBPe expression (Figure 1A).
Eosinophils produce NMO-IgG–dependent ADCC and CDCC in cell cultures. (A) Culture and characterization of eosinophils from murine bone marrow. Culture method shown at the left and MBPe immunofluorescence shown in the micrograph. Scale bar: 20 μm. (B) ADCC. AQP4-expressing CHO cells were incubated for 3 hours with 20 μg/ml NMO-IgG plus 300,000 eosinophils. Live/dead (green/red) staining is shown with percentage and density of live cells given below the micrographs (SEM, n = 10). Controls included untreated cultures, NMO-IgG or eosinophils alone, AQmabADCC plus eosinophils, and NMO-IgG plus eosinophils in nontransfected (AQP4-null) cells. Scale bar: 100 μm. (C) CDCC. Cells were incubated for 60 minutes with submaximal (5 μg/ml) NMO-IgG, 1% hc, and 100,000 eosinophils, with controls indicated. Percentage of dead cells quantified as in B (SEM, n = 10). Scale bar: 100 μm. Experiments were replicated 3 times. Eos, eosinophils; MPPs, multipotent progenitors.
The ability of eosinophils to produce NMO-IgG–dependent ADCC was studied after 3 hours’ incubation of AQP4-expressing CHO cell cultures with NMO-IgG and eosinophils. The percentage and density of live cells were quantified by live/dead (green/red) cell staining (Figure 1B). Substantial cell death was produced when NMO-IgG and eosinophils were present. Little cell death was seen in untreated (control) cells, in cells incubated with NMO-IgG or eosinophils alone, or in AQP4-null cells incubated with NMO-IgG and eosinophils. Also, little cell death was seen when NMO-IgG was replaced by a mutated NMO-IgG lacking ADCC effector function (AQmabADCC). Eosinophils can thus produce ADCC in the presence of NMO-IgG.
The ability of eosinophils to produce CDCC was measured similarly, except that cells were incubated with submaximal NMO-IgG and human complement (hc) to produce minimal cell death in the absence of eosinophils (Figure 1C). The inclusion of eosinophils greatly increased cell killing. The various controls indicate that eosinophil-dependent CDCC requires NMO-IgG, complement, and AQP4.
Eosinophils exacerbate NMO lesions in spinal cord slice cultures. The ability of eosinophils to produce NMO pathology by ADCC and CDCC mechanisms was investigated using an ex vivo spinal cord slice culture model (15). Vibratome-cut spinal cord slices from 7-day-old mice were cultured for 7 days, then NMO-IgG and eosinophils were added for 1 day, after which slices were immunostained for markers of NMO pathology. Figure 2A shows immunofluorescence staining for AQP4, glial fibrillary acidic protein (GFAP), myelin basic protein (MBP), and ionized calcium-binding adaptor molecule 1 (Iba1, activated microglia), with lesion scores (0: no pathology; 4: severe pathology) summarized at the bottom. We observed a loss of AQP4 and GFAP and increased Iba1 in slices exposed to NMO-IgG and eosinophils and little loss of MBP immunofluorescence. We also saw little pathology in control slices or in slices incubated with NMO-IgG or eosinophils alone, or with AQmabADCC and eosinophils. We saw little pathology in slices from AQP4-null mice incubated with NMO-IgG and eosinophils. Eosinophils can thus produce NMO-like pathology in spinal cord slice cultures by an ADCC mechanism. We postulated that toxic factors elaborated by degranulating eosinophils may be responsible for the cytotoxicity. To induce eosinophil degranulation, we added platelet-activating factor (PAF) to slice cultures. Figure 2B shows a marked loss of GFAP and AQP4 in slice cultures incubated with eosinophils in the presence of PAF (in the absence of NMO-IgG), but not in those incubated with eosinophils or PAF alone.
Eosinophils produce NMO-IgG–dependent pathology by an ADCC mechanism in ex vivo spinal cord slice cultures. (A) Vibratome-cut spinal cord slices from mouse were cultured on a porous support for 7 days, followed by the addition of NMO-IgG and/or cells for 1 day, and then stained for AQP4, GFAP, MBP, and Iba1. Immunofluorescence of spinal cord slices (from Aqp4+/+ and Aqp4–/– mice) were incubated as indicated (20 μg/ml NMO-IgG or AQmabADCC, 107 eosinophils). Pathology scores are summarized at the bottom (SEM; 6–11 slices per condition; *P < 0.001 versus the control group; 1-way ANOVA). Scale bar: 500 μm. (B) Eosinophil degranulation by PAF produces NMO-like pathology (107 eosinophils, 10 μg/ml PAF) (SEM; 5 slices per condition; *P < 0.01). Scale bar: 500 μm. Experiments were replicated 3 times.
Similar studies done in parallel with those in Figure 2A indicated the involvement of eosinophils in CDCC, in which spinal cord slice cultures were exposed to submaximal NMO-IgG and complement (Figure 3A). Incubation with eosinophils greatly increased NMO pathology. Control studies showed that eosinophil-dependent pathology was dependent on NMO-IgG, complement, and AQP4 expression. Replacement of NMO-IgG by a mutated NMO-IgG lacking complement-dependent cytotoxicity (CDC) effector function (AQmabCDC) indicated that the eosinophil-dependent pathology was complement dependent (C1q-binding dependent), implicating a CDCC mechanism. C5a is a complement anaphylotoxin that promotes eosinophil chemotaxis and degranulation (18). Figure 3B shows a marked loss of GFAP and AQP4 in slice culture incubated with eosinophils in the presence of C5a (in the absence of NMO-IgG), but not in culture incubated with eosinophils or C5a alone. We also found that the effect of eosinophils could be mimicked by the addition of purified human ECP, an eosinophil granule toxin, together with submaximal NMO-IgG and complement (Figure 3C).
Eosinophils produce NMO-IgG–dependent pathology by a CDCC mechanism in ex vivo spinal cord slice cultures. (A) Spinal cord slice cultures prepared as in Figure 2 were incubated with submaximal NMO-IgG and hc as indicated (5 μg/ml NMO-IgG or AQmabCDC, 3 × 106 eosinophils, 5% hc). The experiments were conducted in parallel with those in Figure 2A using the same control slice group (SEM; 8–11 slices per condition; *P < 0.001 versus the control group; 1-way ANOVA). Scale bar: 500 μm. (B) Eosinophil degranulation by recombinant human C5a produces NMO-like pathology (107 eosinophils pretreated with 5 μg/ml cytochalasin B, 30 ng/ml C5a) (SEM; 5 slices per condition; *P < 0.01). Scale bar: 500 μm. (C) Eosinophil toxin ECP produces NMO-like pathology (5 μg/ml NMO-IgG, 5% hc, 300 ng/ml ECP) (SEM; 4 slices per condition; *P < 0.01). Scale bar: 500 μm. Experiments were replicated 3 times.
Eosinophil-dependent NMO pathology in an in vivo mouse model of NMO. Prior passive-transfer mouse models of NMO involving intracerebral brain injection of NMO-IgG and complement produced NMO-like pathology, but without eosinophil infiltration (19, 20). After testing multiple variations of existing models, including eotaxin and IL-5 infusion together with NMO-IgG and complement administration, we found that human-like NMO pathology could be produced by 3-day continuous intracerebral infusion of NMO-IgG and hc (Figure 4A). Immunofluorescence showed lesions with astrocyte destruction, loss of AQP4, GFAP, and excitatory amino acid transporter 1 (EAAT1) immunoreactivity, as well as leukocyte infiltration and demyelination (Figure 4B). We did not observe lesions in identically treated Aqp4–/– mice. Within the lesion core, there was near-complete loss of AQP4 and myelin, perivascular deposition of activated complement, and prominent inflammation with eosinophil and neutrophil infiltration (Figure 4C); in the lesion periphery there was reduced AQP4 and myelin without complement deposition, and prominent perivascular infiltration of eosinophils and neutrophils. Figure 4D summarizes the extent of AQP4 loss, showing little pathology in Aqp4–/– mice or wild-type mice infused with NMO-IgG alone, or with control IgG with complement. Similar lesions were produced in mice infused continuously for 3 days with purified IgG from human NMO sera together with complement. Interestingly, after 1-day infusion with NMO-IgG and complement, the lesions contained many neutrophils but few eosinophils (Figure 4E).
In vivo mouse model of NMO with prominent eosinophil infiltration in lesions. (A) Mice were administered NMO-IgG and hc by 3-day continuous intracerebral injection using an implanted minipump. (B) Immunofluorescence staining of brain sections after 3-day infusion with NMO-IgG (3.3 μg/day) and complement (16.7 μl/day) stained for astrocyte markers AQP4, GFAP, and EAAT1, myelin marker MBP, and leukocyte marker CD45, in Aqp4+/+ and Aqp4–/– mice. White dotted lines demarcate the area of staining loss. Scale bar: 2 mm. (C) Higher magnification showing AQP4 and EAAT1, MBP, activated complement marker C9neo, markers of eosinophils (Siglec F) and neutrophils (Ly6G), and H&E staining in the lesion core, periphery, and contralateral side. Scale bars: 100 μm. Arrowhead indicates eosinophils in high magnificent H&E staining. Scale bar: 20 μm. (D) Percentage of area of loss of AQP4 staining (SEM; 3–6 mice per group; *P < 0.05). Mice were infused for 3 days as in B with NMO-IgG alone, control IgG plus complement, or IgG (66 μg/day) purified from 3 different NMO sera. (E) Immunofluorescence of AQP4, C9neo, Siglec F, and Ly6G after 1 day of minipump infusion (representative of 3 mice). Scale bar: 100 μm.
Several types of studies were conducted to demonstrate eosinophil-dependent NMO pathology in vivo. In an initial set of studies, lesions were compared in control mice receiving NMO-IgG and complement for 3 days with mice that were pretreated with anti–IL-5 to deplete eosinophils (21). Figure 5A summarizes peripheral eosinophil and neutrophil counts, showing the efficacy of the anti–IL-5 antibody. Figure 5B shows reduced lesion size and eosinophil infiltration in the anti-IL-5 antibody–treated mice. In a second set of studies, in order to isolate the effects of eosinophils versus neutrophils, we compared NMO lesions produced by NMO-IgG and complement in mice made neutropenic with anti-Ly6G antibody (20), without versus with anti–IL-5 antibody treatment. Treatment with anti-Ly6G antibody significantly reduced lesion size, which was further reduced by anti–IL-5 treatment (Figure 5C). Interestingly, in the neutropenic mice, the number of eosinophils in the lesion increased, particularly around blood vessels. In a third set of experiments, we tested the consequences of peripheral hypereosinophilia. Following infusion for 3 days with submaximal NMO-IgG and complement, lesions in transgenic hypereosinophilic (IL-5 Tg) mice showed marked eosinophil infiltration, with larger lesions compared with those in the control (normo-eosinophilic) mice (Figure 5D). Finally, studies in ΔdblGata1 mice, which lack eosinophils due to Gata1 promoter mutation, showed reduced lesion size (Figure 5E).
Eosinophil-dependent NMO pathology in mice. (A) Mice were intraperitoneally administered anti–IL-5 or anti-Ly6G antibodies, alone or together, to deplete eosinophils and/or neutrophils, followed by a 3-day NMO-IgG/hc infusion (top). Peripheral neutrophil (Nϕ) and eosinophil counts in control and treated mice (bottom) (SEM; 5 mice per group; P < 0.001). (B) Mice were infused for 3 days with 3.3 μg/day NMO-IgG and 16.7 μl/day hc, and sacrificed on day 3. Immunofluorescence staining of AQP4 and MBP (scale bar: 2 mm); Siglec F and Ly6G (scale bar: 100 μm). (C) Lesion severity assessed by loss of AQP4, myelin, and numbers of eosinophils and neutrophils in lesions (SEM; 4–8 mice per group; *P < 0.05; **P < 0.01). (D) Control and hypereosinophilic IL-5 Tg mice were infused for 3 days with NMO-IgG (3.3 μg/day) and submaximal hc (3.4 μl/day). Immunofluorescence staining of AQP4 (scale bar: 2 mm), Siglec F, and Ly6G (scale bar: 100 μm). Summary of lesion scores (SEM; 4 mice per group; *P < 0.05). (E) Control and Tg hypoeosinophilic ΔdblGata1 mice were infused for 3 days with NMO-IgG (3.3 μg/day) and hc (16.7 μl/day). AQP4 immunofluorescence and loss of AQP4 immunofluorescence are shown (SEM; 5 mice per group; *P < 0.05). Scale bar: 2 mm.
Eosinophil inhibitors reduce NMO-IgG–dependent pathology. We tested the possibility that compounds known to inhibit eosinophil degranulation would reduce NMO pathology. Figure 6A (left) shows in vitro inhibition of eosinophil degranulation, as assayed by EPO release, by cetirizine, a second-generation antihistamine, and IBMX, a phosphodiesterase inhibitor. The IC50 for cetirizine inhibition was approximately 1 μM. Figure 6A (center) shows relatively lower potency of other eosinophil stabilizers including theophylline, ketotifen, cromolyn, and loratadine. Control studies showed that these compounds did not protect against CDC in AQP4-expressing cells produced by NMO-IgG and complement in the absence of eosinophils (Figure 6A, right). Figure 6B shows that cetirizine reduced eosinophil degranulation in AQP4-expressing cell cultures treated with NMO-IgG and eosinophils, with low EPO activity in control (eosinophil alone) measurements. We found protective effects of cetirizine, ketotifen, and IBMX for eosinophil-dependent NMO pathology in spinal cord slice cultures. Figure 6C shows significant protection in the eosinophil-dependent ADCC (top) and CDCC (bottom) models established in Figures 2 and 3.
Small-molecule eosinophil inhibitors reduce NMO-IgG–dependent cytotoxicity and NMO lesions. (A) Reduced EPO release following 30-minute incubation of eosinophils with 5 μM PAF and indicated inhibitors (representative of 3 sets of experiments). Inset shows dose response for cetirizine (at 5 μM PAF, n = 6) (left). Summary of EPO release data (SEM; n = 6) (center). Lack of compound effect on NMO-IgG–mediated CDC in AQP4-expressing CHO cells (SEM; n = 8) (right). (B) EPO release into media for AQP4-expressing CHO cells treated for 1 hour with 106 eosinophils without or with 20 μg/ml NMO-IgG. Where indicated, 5 μM cetirizine was present (SEM; n = 6; *P < 0.05). (C) Spinal cord slice cultures were exposed to NMO-IgG without complement (top, ADCC), or with complement (bottom, CDCC), and without or with eosinophils, as done in Figures 2 and 3. Where indicated, cetirizine (1 μM), ketotifen (50 μM), or IBMX (300 μM) were present during the 24-hour incubation. Scale bars: 500 μm. (D) Intracerebral infusion was done (as in Figure 5) without versus with cetirizine administration (10 mg/kg b.i.d., 1 day prior to and during 3-day infusion). Immunofluorescence staining is shown on the top and lesion scores are summarized on the bottom (SEM; n = 4–6; *P < 0.05). Scale bars: 2 mm; 50 μm. (E) Chemical structures of cetirizine and analogs (left). Summary of EPO release data (SEM; n = 6) (center). Summary of data from intracerebral infusion model (right) (each compound was given 10 mg/kg b.i.d.) (SEM; n = 3–7 for each group; *P < 0.05).
Cetirizine, which showed the greatest potency in vitro and ex vivo, was tested in mice in vivo. Mice were administered cetirizine (10 mg/kg b.i.d.) orally, as done previously in other disease models in mice (22), 1 day prior to and during the 3-day intracerebral infusion with NMO-IgG and complement. Figure 6D shows remarkably fewer eosinophils in lesions, with significantly reduced lesion severity.
Three first-generation antihistamine analogs of cetirizine, chlorphenamine, mepyramine, and hydroxyzine (Figure 6E, left) were also tested in this model. The analogs showed weak inhibition of eosinophil degranulation in vitro as assessed by EPO (Figure 6E, center), and no significant reduction of NMO lesion size in vivo (Figure 6E, right).
The bulk of evidence supports an NMO pathogenic mechanism that involves NMO-IgG binding to AQP4 on astrocytes, which causes primary complement- and cell-dependent cytotoxicity and results in an inflammatory response involving cytokine release, blood-brain barrier disruption, and infiltration of granulocytes and macrophages (2, 4, 5). The consequent oligodendrocytic injury produces demyelination and neuronal death, resulting in neurological deficit. The supramolecular assembly of AQP4 in orthogonal arrays of particles is crucial for NMO pathogenesis, as AQP4 aggregates enhance NMO-IgG binding (23) and present NMO-IgG clusters for efficient C1q binding and consequent CDC (24). Several alternative NMO pathogenic mechanisms have been proposed but largely refuted, including astrocytic endocytosis of AQP4 and excitatory amino acid transporter-2, NMO-IgG inhibition of AQP4 water permeability, and cell membrane AQP4 clustering due to differential internalization of AQP4 M1 and M23 isoforms (25, 26). Elucidation of NMO pathogenesis is of clinical importance for the development of targeted, mechanism-based therapies, as current therapies, such as immunosuppression and B-cell depletion, are nonselective and of limited efficacy and can be associated with long-term adverse events.
Drug targeting of infiltrating granulocytes is a potential approach for NMO therapy. Eosinophils and neutrophils are the predominant infiltrating leukocytes, particularly in relatively early NMO lesions, with macrophages generally seen later (6, 19). Lymphocytes and NK cells are rarely seen. We postulated that granulocyte toxins, which are released in response to various inflammatory stimuli, may participate in NMO pathogenesis. We reported recently that neutrophils and neutrophil elastase exacerbate NMO pathology in spinal cord slice cultures exposed to NMO-IgG and complement, and that the neutrophil elastase inhibitor Sivelestat largely prevented the neutrophil-dependent pathology (15). NMO pathology was greatly exacerbated in neutrophilic mice administered NMO-IgG and complement by intraparenchymal injection, and was reduced in neutropenic mice or in normal mice treated with neutrophil elastase inhibitors (20). A recent case report described rapid clinical deterioration in an NMO patient made neutrophilic by inadvertent administration of G-CSF (27). Here, we show that eosinophils exacerbate NMO pathology produced by NMO-IgG alone via an ADCC mechanism, or that produced by NMO-IgG and complement via a CDCC mechanism. The approved, nonprescription drugs Zyrtec (cetirizine) and Zaditor (ketotifen) reduced eosinophil-dependent NMO pathology. Our studies suggest the potential clinical utility of granulocyte-targeted therapy with a neutrophil elastase inhibitor together with an eosinophil inhibitor.
Figure 7 diagrams a proposed mechanism for eosinophil-dependent NMO pathology. ADCC is mediated by a variety of leukocyte cell types, including granulocytes, NK cells, and macrophages (28). ADCC is the principal mechanism in cancer therapy involving the targeting of tumor cells by monoclonal antibodies (29). ADCC involves binding of the antibody Fc region to receptors on effector cells, such as CD16 (FcγRIII) on NK cells, and CD64 (FcγRI), CD32 (FcγRII), and CD16 on neutrophils and eosinophils (30–32). CDC is thought to be the major pathogenic mechanism in NMO, based in part on the perivascular deposition of activated complement in human NMO lesions, and the generation of NMO-like pathology in mice administered NMO-IgG and complement. The complement C5 inhibitor eculizumab, which binds to complement protein C5 and inhibits its cleavage by the C5 convertase, is in an open-label clinical trial based on the assumed dominant role of complement in NMO. The relative importance of ADCC in NMO pathogenesis is not clear. We showed recently that NK cells, acting through a pure ADCC mechanism, produced astrocyte cytotoxicity and NMO-like pathology in mouse models, but without marked inflammation or myelin loss (33). CDCC, which involves inflammatory cell activation by activated complement proteins, has been demonstrated to cause NMO pathology when NMO-IgG and complement are present, together with NK cells, neutrophils or macrophages (15, 33), and, as shown here, eosinophils. We thus conclude, as summarized in Figure 7, that NMO-IgG produces NMO pathology by a combination of CDC, CDCC, and ADCC mechanisms whose exact contributions may vary over time and remain to be quantified.
Proposed mechanism of eosinophil-dependent NMO pathogenesis. Eosinophils produce complement-independent and -dependent astrocyte damage. ADCC (left) involves binding of NMO-IgG to AQP4 on astrocytes, which causes eosinophil binding (involving Fcγ receptors) and degranulation. The released granule toxins damage astrocytes. Astrocyte damage is amplified when complement is present by CDCC (right), which involves multiple mechanisms, including complement-dependent enhancement of eosinophil binding to AQP4-IgG and increased eosinophil accumulation and degranulation.
Eosinophil degranulation occurs in response to various stimuli including IgG and IgE, and proinflammatory mediators and cytokines such as PAF, fMLP, and complement (12). Proteins contained within eosinophil granules can exacerbate NMO pathology by multiple mechanisms: the granule toxins MBP, ECP, and eosinophil neurotoxins damage adjacent cells directly, and released cytokines and chemokines induce granulocyte and macrophage infiltration (13). Here, we found that even in the absence of NMO-IgG, the release of eosinophil granule contents caused by C5a or PAF can produce or exacerbate NMO lesions in spinal cord slice cultures.
Cetirizine (Zyrtec) and ketotifen (Zaditor) are clinically approved nonprescription drugs that are long-acting, second-generation histamine H1 receptor antagonists used in the treatment of atopic dermatitis, urticaria, and allergic rhinitis (34). Both drugs are reported to have multiple actions on eosinophils, including inhibition of eosinophil degranulation, adhesion to endothelial cells, migration in response to fMLP, C5a, and LTB4 chemotaxin, and overall survival (13). The lack of protection by the first-generation cetirizine analogs chlorphenamine, mepyramine, and hydroxyzine indicates that the effects of cetritizine are histamine H1 receptor independent. Low concentrations of cetirizine increase lipid order in the exterior leaflet of the eosinophil plasma membranes, decrease membrane heterogeneity, and block PAF-induced changes in membrane fluidity (35). Cetirizine was originally designed for minimal brain-blood barrier penetration to reduce the sedative side effect of first-generation antihistamines. Notably, the blood-brain barrier is leaky in NMO lesions, suggesting effective penetration of cetirizine in these lesions. Pharmacokinetic studies showed a mean peak serum cetirizine concentration of 900 ng/ml (36), similar to its IC50 found here for the inhibition of eosinophil EPO release.
Though our data indicate the likely mechanisms by which eosinophil accumulation in NMO lesions produces NMO pathology, it is difficult to quantify the precise contribution of eosinophils in human NMO because of the limitations of available animal models of NMO. While cell cultures are useful for studying the mechanisms of NMO-IgG and AQP4-dependent cytotoxicity, the ex vivo and in vivo models of NMO can recapitulate the major features of human NMO pathology. An important advance here was the development of a continuous intracerebral infusion model that closely recapitulated NMO pathology, including prominent eosinophil and neutrophil infiltration. Nonetheless, as discussed (5), it is difficult to quantitatively extrapolate results from passive transfer models of NMO in rodents to human NMO. Improved animal models of NMO optic neuritis and transverse myelitis are needed, perhaps involving active immunity against AQP4.
In conclusion, our results support the involvement of eosinophils in NMO pathogenesis by ADCC and CDCC mechanisms, which amplify NMO-IgG–dependent astrocyte cytotoxicity and consequent blood-brain barrier disruption and oligodendrocytic injury. Our data thus provide a functional correlate to the prominent eosinophil infiltration in human NMO lesions and suggest the utility of eosinophil-targeted therapeutics in NMO.
Materials – mice, cell lines, antibodies, and drugs. AQP4-null mice have been described and extensively characterized (37). Experiments were done using weight-matched 16- to 18-week-old wild-type and AQP4-null mice on a CD1 genetic background. Some experiments were conducted using hypereosinophilic IL-5 Tg (Tg(Cd3d-Il5)NJ.1638Nal) mice (38) on a BALB/c background (provided by Richard Locksley, UCSF, San Francisco, California, USA) and ΔdblGata1 mice (C.Cg-Gata1tm6Sho/J mice; The Jackson Laboratory) that lack eosinophils because of Gata1 promoter mutation. Mice were maintained in air-filtered cages and fed normal mouse chow in the UCSF Animal Care Facility. CHO-K1 cells (ATCC CCL-61) were cultured at 37°C in 5% CO2/95% air in Ham’s F12 medium (Sigma-Aldrich) containing 10% FBS (Life Technologies) and 1% penicillin-streptomycin. Stably transfected cells expressing human M23-AQP4 were generated as described (24). Recombinant monoclonal NMO antibody rAb-53 (denoted as NMO-IgG) was generated from a clonally expanded plasma blast population from the cerebrospinal fluid of an NMO patient, as described and previously characterized (23, 39). Point mutations (K326W/E333S) were introduced into the IgG1 Fc sequence of the rAb-53 heavy chain to produce antibody AQmabADCC, which selectively lacks ADCC effector function (preserving CDC), and AQmabCDC (K322A), which selectively lacks CDC effector function (preserving ADCC) (40). NMO-IgGserum was purified from NMO human sera using a Melon Gel IgG Purification Kit (Thermo Scientific) and concentrated using Amicon Ultra Centrifugal Filter Units (Millipore). Ketotifen, cetirizine, loratadine and other chemicals were purchased from Sigma-Aldrich. Anti–IL-5 monoclonal antibody (TRFK-5 clone; BioLegend) was administered intraperitoneally for eosinophil depletion in mice, and anti-Lg6G monoclonal antibody (1A8 clone; BioLegend) for neutrophil depletion (with rat IgG1 as the control antibody).
Eosinophil culture. Bone marrow cells were collected from the femurs and tibiae of wild-type mice (8–12 weeks of age) by flushing the opened bones with Ca2+, Mg2+-free HBSS (Life Technologies) containing 0.5% FBS. Red blood cells were lysed in 6 ml of 0.2% NaCl followed by the addition of 14 ml of 1.2% NaCl. After centrifugation, the cells were washed and filtered using a 70-μm cell strainer (BD Biosciences). Cells were cultured at 106 per milliliter in RPMI 1640 (Life Technologies) containing 20% FBS, 1% penicillin-streptomycin, 2 mM glutamine, 25 mM HEPES, 1× nonessential amino acids, 1 mM sodium pyruvate and 50 μM 2-mercaptoethanol (Life Technologies), which was supplemented from days 0 through 4 with 100 ng/ml SCF (PeproTech) and 100 ng/ml FLT3-L (PeproTech). On day 4, SCF and FLT3-L were replaced by 10 ng/ml recombinant mouse (rm) IL-5 (PeproTech). On day 8, the cells were transferred to new flasks and maintained in fresh medium supplemented with rmIL-5. Thereafter, on every other day, one-half of the medium was replaced with fresh medium containing rmIL-5, and cell concentration was adjusted to 106 per milliliter. Cultures were used for experiments on days 14–16 after incubation with 10 ng/ml rm GM-CSF (PeproTech) for 24 hours. Eosinophil purity was greater than 95% as judged by immunofluorescence using anti-MBPe antibody (provided by the Lee Laboratory, Mayo Clinic, Scottsdale, Arizona, USA).
CDCC and ADCC measurements. Cells were grown in 96-well plates on glass coverslips until confluence. Eosinophils were used as the effector cells. For assay of CDCC, CHO cells expressing M23-AQP4 were incubated for specified times with 5 μg/ml NMO-IgG or control IgG at 37°C together with 1% hc (Innovative Research), with or without eosinophils at an effector/target cell ratio of 10:1. Calcein-AM and ethidium homodimer (Life Technologies) were added to stain live cells green and dead cells red. For assay of ADCC, cells were incubated for 3 hours at 37°C with 20 μg/ml NMO-IgG (or control IgG) and eosinophils at an effector/target cell ratio of 30:1. For assay of CDC, cells were incubated for 60 minutes at 37°C with 10 μg/ml NMO-IgG and 2% hc. In some experiments, test compounds were added for 30 minutes, followed 60 minutes later by complement and NMO-IgG. Cytotoxicity was measured by the AlamarBlue Assay (Life Technologies).
Spinal cord slice culture model. On postnatal day 7 mouse pups were decapitated and the spinal cord was rapidly removed and placed in ice-cold HBSS. Transverse slices of cervical spinal cord of 300-μm thickness were cut using a vibratome (VT-1000S; Leica). Individual slices were placed on transparent, noncoated membrane inserts (Millicell-CM 0.4 μm pores, 30-mm diameter; Millipore) in 6-well (35-mm diameter) plates containing 1 ml culture medium, with a thin film of culture medium covering the slices. The culture medium, consisting of 50% MEM (Life Technologies), 25% HBSS, 25% horse serum (Life Technologies), 1% penicillin-streptomycin, 0.65% glucose, and 25 mM HEPES, was changed every 3 days. The slices were cultured in 5% CO2 at 37°C for 7 days. NMO-IgG and/or complement were added to both sides of the porous membrane, with 1 ml of medium added above the porous filter to fully immerse the slice. Eosinophils were added to the solution above the porous filter bathing the slice. In some experiments PAF (Sigma-Aldrich), ECP (Sigma-Aldrich), or recombinant human C5a, together with cytochalasin B (Sigma-Aldrich), were added directly to the slice medium for 24 hours. AQP4- and GFAP-stained spinal cord slices were scored for lesion severity using the following scale: 0, intact slice with intact GFAP and AQP4 staining; 1, intact slice with some astrocyte swelling (seen from GFAP stain) with weak AQP4 staining; 2, at least 1 lesion with complete loss of GFAP and AQP4 staining; 3, multiple lesions with loss of GFAP and AQP4 staining in greater than 30% of slice area; and 4, extensive loss of GFAP and AQP4 staining affecting greater than 80% of the slice area (15).
Intracerebral infusion model. Mice were implanted with an osmotic minipump (Alzet 1003D) with the needle positioned in the right lateral brain (from the bregma, anterior-posterior, –2 mm; medial-lateral, +1.5 mm; dorsal-ventral, 2.5 mm below the dura). NMO-IgG and hc were dissolved in PBS and delivered for 3 days at 3.3 μg per day and 16.7 μl per day, respectively. For the IL-5 Tg mice, submaximal human complement (3.4 μl per day) was delivered together with NMO-IgG at 3.3 μg per day. In some studies, purified IgG from human NMO sera was delivered for 3 days at 66 μg per day. Control mice were implanted identically with an osmotic minipump with control (non–AQP4-binding) IgG1.
Immunofluorescence and immunochemistry. Slices were fixed with 4% paraformaldehyde for 15 minutes at room temperature, rinsed with PBS, and incubated in blocking solution (PBS containing 1% BSA and 0.3% Triton X-100) for 1 hour. Slices were then incubated for 2 hours with antibodies against mouse GFAP (1:1000; Millipore), AQP4 (1:200; Millipore), ionized calcium-binding adaptor molecule 1 (Iba1; 1:1,000; Wako), C5b-9 (1:100; Santa Cruz Biotechnology), or MBP (1:100; Santa Cruz Biotechnology), rinsed in PBS, and then incubated with secondary antibodies for 1 hour at room temperature. Secondary antibodies included Alexa Fluor 488–labeled donkey anti-mouse IgG, Alexa Fluor 555–labeled donkey anti-goat IgG, Alexa Fluor 555–labeled donkey anti-rabbit IgG, and Alexa Fluor 555–labeled goat anti-rat IgG (5 μg/ml each; Invitrogen). After rinsing in PBS, the slices were mounted on glass slides and coverslipped with VectaShield (Vector Laboratories). For the in vivo mouse model, frozen sections of brain were cut at 10-μm thickness and immunostained with the following primary antibodies at room temperature for 2 hours: rabbit anti-AQP4 (1:200); mouse anti-GFAP (1:500); goat anti-MBP (1:200); rabbit anti-Iba1 (1:500); rat anti-CD45 (1:10; BD Biosciences); rat anti-neutrophil (Ly6G antibody; 1:100; eBioscience); rat anti-eosinophil (Siglec F antibody; 1:50; BD Biosciences); mouse anti-EAAT1/GLAST (1:100; Miltenyi Biotec); or rabbit anti–C5b-9 (1:50; Santa Cruz Biotechnology), followed by the appropriate species-specific Alexa Fluor–conjugated secondary antibody (5 μg/ml each) or biotinylated secondary antibody (1:500; Vector Laboratories). When biotinylated secondary antibody was used, immunostaining was visualized as brown using the Vectastain horseradish peroxidase kit (Vector Laboratories), followed by diaminobenzidine/H2O2 according to the manufacturer’s protocol. Immunofluorescence was visualized on a Leica fluorescence microscope or a Nikon laser-scanning confocal microscope. Areas were defined by hand and quantified using ImageJ software (NIH). Data are presented as the percentage of immunonegative area (normalized to the total area of the hemibrain section).
Eosinophil peroxidase release activity. Release of eosinophil peroxidase was measured in cell supernatants by the o-phenylenediamine (OPD) method (41). Substrate solution was prepared by adding 800 μl of 5 mM OPD HCl (Sigma-Aldrich) to 4 ml of 1 M Tris buffer (pH 8.0) and 1.25 μl 30% H2O2. Eosinophils were collected by centrifugation and resuspended in RPMI 1640, without phenol red, at 250,000 cells per milliliter and 100 μl was added per well. EPO release from eosinophils was measured following the addition of PAF, which causes eosinophil degranulation (41). Substrate solution (100 μl) was added after 30 minutes, and the reaction stopped by 100 μl of 4 M sulfuric acid prior to the measurement of absorbence at 492 nm. In some experiments, eosinophil degranulation inhibitors (cetirizine, ketorizine, loratadine, cromolyn sodium, theophylline, IBMX) were added (separately) 30 minutes before PAF. EPO release was also measured after ADCC in which 250,000 cells in 100 μl were added to 96-well plates containing cultured CHO-AQP4 cells or CHO-null cells. NMO-IgG or control IgG was added and cells were incubated at 37°C, 5% CO2 for 1 hour. Samples were centrifuged at 250 g for 15 minutes at 4°C. The supernatants (50 μl; triplicate) were dispensed into each well of a microplate, and 50 μl of substrate solution was added to each well.
Statistics. Where appropriate, differences were evaluated using a 2-tailed Student’s t test, a Mann-Whitney rank sum test, or a 1-way ANOVA rank test, as calculated using SigmaStat software, version 3.5 (Systat Software). Data are presented as the mean ± SEM. A P value of 0.05 or less was considered significant.
Study approval. All mouse procedures were approved by the University of California, San Francisco Committee on Animal Research and were conducted in accordance with the NIH guidelines for the care and use of animals.
This work was supported by a grant from the Guthy-Jackson Charitable Foundation, and by grants from the NIH (EY13574, EB00415, DK35124, HL73856, DK86125, and DK72517). We thank Jeffrey Bennett of the University of Colorado Denver for providing recombinant monoclonal NMO antibody and for helpful advice, and Puay-Wah Phuan for help with CDC measurements.
Conflict of interest: The authors have declared that no conflict of interest exists.
Citation for this article:J Clin Invest. 2013;123(5):2306–2316. doi:10.1172/JCI67554.
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