AU725048B2 - Treatment of asthma and airway diseases - Google Patents

Description

WO 97/42958 PCT/AU97/00286 TREATMENT OF ASTHMA AND AIRWAY DISEASES This invention relates to a method of treating chronic and acute inflammation of the airways, including asthmatic conditions. The invention also relates to steroid or steroid analogues used in the treatment, and to pharmaceutical compositions comprising these compounds as the active agent. In a preferred embodiment, the active component inhibits inflammation and smooth muscle cell proliferation in the airway wall.

It may also have at least one other activity selected from anti-angiogenesis, anti-oxidation and the ability to disrupt microtubule formation.

Background of the Invention Two distinct classes of agents are currently used in the treatment of asthma. Symptomatic relief is provided by using bronchodilators which include the Paadrenoceptor agonists such as salbutamol and salmeterol.

Other agents with bronchodilatory properties include the muscarinic-receptor antagonist, ipratropium bromide, and phosphodiesterase inhibitors such as theophylline.

The second class of agents is prophylactic, and includes glucocorticoids such as beclomethasone dipropionate. Disodium cromoglycate and nedocromil sodium are also used, even though these are less effective than the glucocorticoids.

However, none of these agents completely reverses airway hyperresponsiveness or prevents catastrophic life-threatening and fatal episodes of asthma in all patients. The fact that these conditions prevail and sometimes are the cause of death highlights the fact that the benefits from these agents are suboptimal.

S WO 97/42958 PCT/AU97/00286 2 Asthma is now regarded as a disease of chronic airways inflammation characterised by eosinophilic bronchitis [Frigas et al., 1991]. In common with other chronic inflammatory diseases, the inflammation in asthma initiates tissue remodelling, which has been documented in the airways in post mortem studies [Dunnill et al., 1969] and by bronchial biopsy from living donors [Brewster et al., 1990; Bai Pare, 1995].

The remodelling involves: epithelial sloughing; marked infiltration of eosinophils into the mucosa; activation of mast cells and lymphocytes; enlargement of mucous glands; deposition of wound-type collagen immediately below the true basement membrane of the epithelium and throughout the mucosa; and an increase in the number of myofibroblasts. In addition, there is an increase in the volume and number of blood vessels in asthmatic airways, indicating that an angiogenesis accompanies the remodelling process [Kuwano et al., 1993]. The overall volume of the airway wall is increased [James et al., 1989] in association with an increase in the volume of airway smooth muscle [Kuwano et al., 1993] which results from both hypertrophic and hyperplastic responses [Ebina et al., 1993].

Airway hyperresponsiveness (AHR) is the excessive bronchoconstrictor response of asthmatic subjects to a diverse array of stimuli. The concept that the airway wall thickening is central to the development of AHR has gained acceptance during the last years. The thickening of the airways has been shown by mathematical modelling studies to amplify the consequences of smooth muscle shortening a given amount of smooth muscle shortening is calculated to cause a much greater increase in airways resistance in asthmatics compared with healthy subjects (eg W WO 97/42958 PCT/AU97/00286 3 shortening gives a 15-fold increase in healthy subjects, but a 290-fold increase in asthmatics) [James et al., 1989]. The airway wall area is increased by 50-250%, with larger increments being observed in the larger airways [James et al., 1989]. The muscle increases in volume by 2-3 fold, and the extent of the increase is related to the severity of asthma [Kuwano et al., 1993].

The nature of the change has not been extensively investigated, but it comprises both hyperplasia and hypertrophy [Ebina et al., 1993]. After prolonged allergen avoidance by allergic asthmatics, decreases in airways responsiveness to the levels observed in healthy subjects have been demonstrated, and are accompanied by a resolution of the symptoms [Platts-Mills et al., 1987]. Studies such as this are consistent with the notion that the structural changes in the asthmatic airway are also reversible.

These long-term changes in the asthmatic airway offer new targets for therapeutic intervention [Stewart et al., 1993]. Consequently there has been considerable interest in identifying the mechanisms for this airway wall remodelling response and the influence of existing anti-asthma drugs on these processes. A large number of factors have been established as mitogens for cultured airway smooth muscle from various species, including humans [see Stewart et al., 1995a for a review]. As expected, the stimuli belonging to the growth factor families, including basic fibroblast growth factor (bFGF), platelet-derived growth factor (PDGF.) and epidermal growth factor (EGF) are the most effective proliferative agents [Hirst et al., 1992; Stewart et al., 1995a]. Thrombin is also an effective growth factor [Tomlinson et al., 1994], whereas bronchoconstrictors such as endothelin-1 and the 4 thromboxane A, mimetic, U46619, are only weakly active, and some other constrictors such as histamine and neurokinins are completely inactive [Stewart et al., 1995a].

In human cultured airway smooth muscle, continuous exposure to 3 -adrenoceptor agonists reduces the proliferative responses to a wide range of mitogens, including thrombin, EGF and the thromboxane A, analogue, U46619 (Tomlinson et al., 1994; 1995]. Furthermore, dexamethasone and other anti-inflammatory steroids also have an anti-proliferative effect on cultured airway smooth muscle [Stewart et al., 1995b], but the magnitude of the inhibition depends on the mitogen that stimulates proliferation in the first instance. It is also important to note that long-term treatment with inhaled anti-inflammatory steroids produces only a modest *reduction in AHR [Sotomayor et al., 1984; Lungren et al., 1988], whereas P,-agonists are reported to have either no effect or to increase AHR [Wahedna et al., 20 1993]. Thus, the two most commonly used and most effective drug classes for the treatment of asthma have sub-optimal effects on AHR, and are therefore unlikely to be effective in regulating the structural changes associated with airway remodelling that contribute to 25 the progression and development of the condition.

a 4A It will be clearly understood that, although a number of prior art publications are referred to herein, this reference does not constitute an admission that any of these documents forms part of the common general knowledge in the art, in Australia or in any other country.

We have been investigating potential ways of arresting or modulating the remodelling process and have surprisingly identified a steroid and analogues thereof which are suitable for this purpose.

e

S

E:\Simeona\Keep\Speci\26276-96.doc 28/07/00 ,I WO 97/42958 PCT/AU97/00286 5 Summary of the Invention 2-methoxyoestradiol is a natural metabolite of 17p-oestradiol, the physiological oestrogen in humans.

It is produced in a two-step process, involving JS hydroxylation of oestrogen to produce a catecholoestrogen followed by methoxylation to produce the corresponding methoxyoestrogen by an inducible cytochrome p450 pathway [Spink et al., 1994]. Hitherto considered to be biologically inactive [Rosner et al., 1991], in cell culture studies it has been established that 2 -methoxyoestradiol inhibits proliferation of certain transformed cell lines [Lottering et al., 1992] and of.actively proliferating or non-quiescent endothelial cells and fibroblasts [Fotsis et al., 1994].

Fotsis et al also showed that administration of 2 -methoxyoestradiol inhibited the growth of tumours by suppressing tumour-induced angiogenesis, rather than by direct inhibition of tumour cell proliferation. It was proposed that the compound reduced basal membrane breakdown, thus preventing cell migration into the extracellular matrix and rendering it a potential antiangiogenic agent for the treatment of solid tumours or angiogenic diseases. Inhibition of tumour neovascularization was also demonstrated in Klauber et al, 1997.

The anti-proliferative effects of 2methoxyoestradiol on cultured smooth muscle cells from rabbit aorta [Nishigaki et al., 1995] also suggested the usefulness of this compound in the prevention of progression of atherosclerosis, a disease caused by cellular events that differ from those seen in asthma and AHR.

The mechanism of the anti-proliferative effects has not yet been established. Lottering et al. (1992) WO 97/42958 PCT/AU97/00286" 6 suggested that elevation of cyclic adenosine monophosphate (cAMP) explains the inhibitory effects of 2 -methoxyoestradiol on DNA synthesis, whereas inhibition of microtubule assembly during spindle formation in mitosis is considered to explain the inhibitory effects on cell division [Fotsis et al., 1994]. The other biological effects of 2-methoxyoestradiol are not extensively characterized. In pig endometrial cell cultures, 2-methoxyoestradiol inhibits the synthesis of PGF. [Zhang Davis, 1992]. Non-genomic actions of 2-methoxyoestradiol include microtubule disruption via binding at the colchicine site on tubulin [D'Amato et al., 1994; Aizu-Yokota et al., 1995] and relaxation of vascular smooth muscle [Goyache et al., 1995].

In International patent publication No.

W095/04535, estradiol derivatives which exert antimitotic effects by inhibiting tubulin polymerisation in vitro are disclosed. It is inferred from the in vitro studies that the compounds inhibit endothelial cell proliferation.

The present invention relates to effects of 2-methoxyoestradiol and inhibition of inflammatory cell activation. It particularly relates to treatment or prevention of airway diseases such as asthma.

None of the documents referred to above suggest or disclose the invention. For example, inhibition of smooth muscle cell proliferation and inflammatory cell activation in the airway cannot be predicted by the in vitro observations described in W095/04535 and the mechanism of these activities do not appear to be related to actions on microtubule assembly.

The anti-proliferative effect of 2-methoxyoestradiol on rabbit vascular smooth muscle [Nishigaki et al, supra] also cannot be extrapolated to airway WO 97/42958 PCT/AU97/00286 7 smooth muscle, since there are known differences in responsiveness of the cells from these two different sources.

Some agents which enhance endothelial cell proliferation, eg. heparin, actually inhibit proliferation of airway smooth muscle cells. Therefore, the anti-proliferative effects of 2-methoxyoestradiol in endothelial cells [Fotsis et al, W095/04535, supra] do not suggest that smooth muscle would respond in the same way.

We have found that 2-methoxyoestradiol inhibits the release of myeloperoxidase from polymorphonuclear leukocytes obtained from human peripheral blood, as well as the phagocytic activity of these cells. The reduction of phagocytic activity in these cells provides evidence of its anti-inflammatory properties. This is surprising, particularly because 2-methoxyoestradiol is known not to have significant affinity for glucocorticoid or for oestrogen receptors [Merriam et al, 1980].

These properties render 2-methoxyoestradiol and related compounds of benefit in the treatment of conditions which include but are not limited to asthma, chronic obstructive airway diseases and other airway diseases characterised by inflammation. Other conditions amenable to treatment by the methods of the invention include, for example, emphysema, pneumonia or airway diseases characterised by one or both of proliferative and inflammatory conditions eg. neutrophil infiltration, or pulmonary infectious diseases the symptoms or sequelae of which result from activation of resident and inflammatory cells.

Conditions such as allergic rhinitis may also be treated, since we have also found that 2-methoxy- 'I WO 97/42958 PCT/AU97/00286" 8 oestradiol inhibits degranulation of the mast cellrelated cell line, RBL2H3. This inhibitory effect of 2 -methoxyoestradiol was selective for antigen-stimulated release since the response to the protein kinase C stimulant, PMA, and to the calcium ionophore A23187, were unaffected. Thus, the effect on antigen release is not likely to result from a non-specific action on microtubule-dependent granule extrusion. Our results indicate that 2 -methoxyoestradiol and related steroids having these activities are useful for treating allergic conditions that include but are not limited to rhinitis and atopic skin conditions. Without wishing to be bound to any particular mechanism of action, these data suggest that specific, signal transduction mechanisms involving receptors are involved and contribute to the inhibition of inflammation in the airway.

We have further found that 2-methoxyoestradiol inhibits DNA synthesis and cell division in airway smooth muscle stimulated with a range of growth factors, including FCS and bFGF. In addition, serotoninstimulated increases in protein synthesis rates are inhibited by 2 -methoxyoestradiol, raising the possibility of anti-hypertrophic effects, in addition to inhibition of cell proliferation. Our observations, together with the anti-angiogenic activity of 2methoxyoestradiol, indicate that this and related compounds may have therapeutic value in the treatment of airway diseases characterised by inflammation as described above, in particular in the treatment of chronic asthma, with particular impact on the airway wall remodelling and hence on airway hyperresponsiveness. Analogues of 2 -methoxyoestradiol were also tested for their ability to inhibit

DNA

synthesis, and the results indicate that these also may WO 97/42958 PCT/AU97/00286 9have therapeutic value.

In a first aspect, the invention provides a method of treating a disease characterised by chronic or acute airway inflammation, comprising the step of administering a steroid or steroid analogue having the ability to modulate remodelling of the airway to a mammal in need of such treatment. Preferably the mammal is a human, cat, horse or bovine, and more preferably is human. The steroid 2-methoxyoestradiol is especially preferred for use in accordance with the method of the invention. Steroids or analogues thereof which do not have effective glucocorticoid activity at the dosage level used in accordance with this invention are particularly desired.

In a second aspect, the invention provides a method of treating a disease characterised by chronic or acute airway inflammation, comprising the step of administering a steroid or steroid analogue to a mammal in need of such treatment, wherein said steroid or analogue inhibits phagocytic activity of polymorphonuclear leucocytes. Preferably, the release of myeloperoxidase from the leucocytes is also inhibited. The activation of macrophages may also be inhibited.

In one embodiment, the method according to the invention further modulates remodelling of the airway by inhibiting smooth muscle cell proliferation and inflammation. The remodelling may further be modulated by inhibition of one or more activities selected from the group consisting of angiogenesis, formation of oxidants and microtubule function in the airway wall.

In a particularly preferred embodiment, the method of the invention is used in the treatment of a disease selected from the group consisting of asthma, 1. WO 97/42958 PCT/AU97/00286 10 airway hyperresponsivness brochoconstriction, emphysema, pneumonia, atopic disease such as allergic rhinitis and pulmonary infection.

In a third aspect, the invention provides a steroid or steroid analogue which modulates airway remodelling by inhibiting inflammation of the airway wall. Preferably, the compound also has the ability to inhibit proliferation of airway smooth muscle cells, particularly in response to a mitogenic stimulus.

In a fourth aspect, the invention relates to a steroid or steroid analogue which modulates airway remodelling by inhibiting phagocytic activity. In a preferred embodiment, the phagocytic activity of polymorphonuclear leucocytes is inhibited by 2-methoxyestradiol. In another embodiment, the release of myeloperoxidase from polymorphonuclear leucocytes is also suppressed. In a particularly preferred embodiment, the steroid or steroid analogue does not exhibit glucocorticoid activity.

In a fifth aspect, the invention provides a steroid or analogue as described above, further having anti-angiogenic activity and/or anti-oxidant activity.

In a particularly preferred embodiment, the steroid or steroid analogue of the invention also has the ability to disrupt microtubules in the airway wall.

In a sixth aspect, the invention provides a composition comprising a steroid or steroid analogue as described above, optionally together with one or more pharmaceutically acceptable carriers and excipients.

Examples of such carriers and excipients include but are not limited to dry micronised powders together with lactose, or recently developed hydrofluoroalkanes. The composition of the invention may be used in formulations for administration via any standard route used in WO 97/42958 PCT/AU97/00286 11 treatment of airway diseases or asthma, for example, topical, oral, nasal administration or by inhalation.

These formulations may be in any conventional form such as capsules, cachets, tablets, aerosols, powder granules, micronised particles or as a solution.

Optionally, the steroid or steroid analogue may be complexed with cyclodextrin, and may also be in the form of an ester formed with a pharmaceutically acceptable acid such as sulphate, acetate, benzoate or the like. A person skilled in the art will be able by reference to standard texts, such as Remington's Pharmaceutical Sciences 17 t h edition, to determine how the formulations are to be made and how these may be administered.

The dose of the steroid or steroid analogue to be administered will depend on the condition to be treated and the route of administration, and will be at the discretion of the attending physician or veterinarian. Such a person will readily be able to determine a suitable dose, mode and frequency of administration. The composition of the invention may be used to treat conditions of chronic or acute airway inflammation, including asthma, airway hyperresponsiveness (AHR) or bronchoconstriction.

In a particularly preferred embodiment of the invention, inflammation and proliferation of smooth muscle cells in the airway wall of an asthmatic patient is inhibited by administration of a composition comprising 2 -methoxyoestradiol.

Although the invention will be described with particular reference to 2-methoxyoestradiol, it will be understood that analogues of this compound which have the requisite biological activities may also be used in accordance with the invention. These include but are not limited to 2 -hydroxyestradiol, 2-methoxyoestradiol-3 I. WO 97/42958 PCT/AU97/00286 12 methyl ether and 4-methoxyoestradiol.

A variety of compounds have been identified as oestradiol derivatives having anti-proliferative and/or anti-angiogenic activity in other tissues. See, for example, W095/04535 the entire disclosure of which is incorporated herein by this reference.

Such compounds may be suitable candidates for use in accordance with the present invention and are within the meaning of steroids, steroid analogues or steroid-like compounds for the purpose of the present invention. Preferred compounds have a methoxy group at the 2-position of the steroid backbone.

In addition, it is contemplated that further compounds not hitherto known will have sufficient structural similarity to the 2-methoxy steroids or steroid-like compounds of this invention to have biological activities within the scope of this invention. For the purposes of this specification, the terms "steroid", "steroid analogue" or "steroid-like" are to be understood to encompass 2-methoxyoestradiol., 2-hydroxyoestradiol, 2-methoxyoestradiol-3, methyl ether, 4-methoxyoestradiol and other compounds based around a steroid nucleus that have the relevant biological activities to be used for the purposes of the present invention. Other compounds may have sufficient structural and/or electronic resemblance (charge distribution) to 2-methoxyoestradiol and have biological activities within the scope of this invention without strictly having a steroid nucleus, such compounds are to be considered steroid analogous for the purposes of the present invention, for example compounds of W095/04535.

Compounds with such activities may be readily identified by using assays capable of indicating activities of the type described elsewhere in this specification. As an 13 example, a compound may be tested for its effects on chronic respiratory obstructive disease be measuring airway smooth muscle cell proliferation; effects on allergic rhinitis and on infectious diseases may be tested by determining the inhibition of inflammatory cell activation, eg. mast cells for rhinitis and neutrophils for infectious disease.

A person skilled in the art will be aware of alternative tests and can readily screen compounds for use in accordance with the invention.

Throughout the description and claims of this specification, the word "comprise" and variations of the word, such as "comprising" and "comprises", means ."including but not limited to", and is not intended to 15 exclude other additives, components, integers or steps".

Detailed Description of the Invention The invention will now be described in detail by way of example only, with reference to the following figures in which:- Figure 1 shows the lack of effect of 2e methoxyoestradiol on horseradish peroxidase-mediated :oxidation of tetramethyl benzidine.

Figure 2 shows the effect of 2-methoxyoestradiol (0.3 -10 WM, 30 min pretreatment) on mitogen-induced 25 incorporation of [3H]-thymidine in cultured human airway smooth muscle cells. Mitogens tested were 0.3 U/ml Thrombin, 1%FCS, 300 pM bFGF (Figure 2a) and 10% FCS, 3nM EGF (Figure 2b). Additional experiments of identical design to those depicted in Figure 2a b were carried out and the combination of this latter data and that in Figs 2a b is presented in Fig 2c. The time-course of the effect of 2-methoxyoestradiol (3 pM) on throbin (0.3 U/ml) induced DNA synthesis were also investigated Data are presented as the means and standard errors of the means of 3 experiments in 3 different cultures, and are expressed as a percentage of the [3H] -thymidine incorporation in ig non-pretreated H:\Bkrot\Keep\speci\26276-96.doc 3/04/00 WO 97/42958 PCT/AU97/00286 14 cells.

Figure 3 shows the effect of 2-methoxyoestradiol (0.3 -10 pM, 30 min pretreatment) on mitogen-induced incorporation of [3H]-leucine. Data are presented as the means and standard errors of the means of 3 experiments in 3 different cultures, and are expressed as a percentage of the ['H]-leucine incorporation in non-pretreated cells.

Figure 4 shows the effect of 2-methoxyoestradiol (0.3 -10 pM, 30 min pretreatment) on cell number in the presence of FCS or bFGF (300 pM). Data are presented as the means and standard errors of the means of 3 experiments in 3 different cultures, and are expressed as a percentage of the increase in cell number in non-pretreated cells.

Figure 5 shows the effect of the steroid receptor antagonist, RU 486 (1 pM), on 2methoxyoestradiol (3 pM) inhibition of FCS (1%)-induced DNA synthesis. Data are presented as the means and standard errors of the means of 3 experiments in 3 different cultures, and are expressed as a percentage of the PH] -thymidine incorporation in non-pretreated cells. RU 486 was added 30 min before 2methoxyoestradiol, which was added 30 min before FCS.

Figure 6 shows the effect of 173-oestradiol and 2 -hydroxyoestradiol (0.3 -10 M, 30 min pretreatment) on FCS (l%)-induced incorporation of -thymidine. Data are presented as the means and standard errors of the means of 3 experiments in 3 different cultures, and are expressed as a percentage of the [H]-thymidine incorporation in non-pretreated cells. Data relating to 2 -methoxyoestradiol are reproduced from figure 1 for ease of comparison.

WO 97/42958 PCT/AU97/00286 15 Figure 7 shows the effects of 2-methoxyoestrone and 2 -methoxyoestriol (0.3 -10 RM, 30 min pretreatment) on thrombin (0.3 U/ml)-induced incorporation of thymidine. Data are presented as the means and standard errors of the means of 3 experiments in 3 different cultures, and are expressed as a percentage of the thymidine incorporation in non-pretreated cells. Data relating to 2 -methoxyoestradiol are reproduced from figure 2a for ease of comparison.

Figure 8 shows the effect of 2-methoxyoestradiol on superoxide anion release in guinea-pig peritoneal macrophages. This compound completely blocked superoxide anion response of the macrophages to zymosan and reduced those to fMLP.

Figure 9 shows the effect of 2-methoxyoestradiol on prostacylin release in guinea-pig peritoneal macrophages. The results demonstrate that the estradiol completely blocked the macrophage response to fMLP whilst the response to PMA was inhibited by Figure 10 is a plot showing the effects of various concentrations of ovalbumin (DNP-OA) on mast cell (RBL2H3) degranulation, and the inhibition by 2methoxyoestradiol.

Figure 11 shows that 2-methoxyoestradiol reduced ovalbumin (DNP-OA)-stimulated release of 3 H]-5HT from guinea-pig peritoneal macrophages, but did not affect release in response to PMA.

Abbreviations Abbreviations used herein are as follows: AHR airway hyperresponsiveness bFGF basic fibroblast growth factor DNP-OA dinitro-phenyol treated ovalbumin EGF epidermal growth factor WO 97/42958 PCT/AU97/00286 16 fMLP formyl methiony leucyl Phenylalanine PDGF platelet-derived growth factor PMA phorbol myristate acetate serotonin General Methods Cell culture Human bronchial airway smooth muscle was obtained from macroscopically normal lung resection specimens from lung transplant donors or recipients provided by the Alfred Hospital (Melbourne). Cultures were prepared as previously described in detail (Tomlinson et al., 1994). Briefly, the tissue was partially digested in Dulbecco's Modified Eagle's Medium (DMEM), [supplemented with 2 mM L-glutamine, 100 [ig/ml streptomycin, 100 U/ml penicillin-G, 2 |Ig/ml amphotericin B, and 0.25% w/v bovine serum albumin (BSA)] containing 3 mg/ml collagenase for 30 minutes at 37 0 C, and approximately 0.5 g smooth muscle was further digested by a 2 hour incubation in 0.5 mg/ml elastase, followed by an 18 hour incubation in collagenase (3 mg/ml) at 37 0 C. Cell suspensions were centrifuged min, 100 x g, 25 0 washed three times in supplemented DMEM, resuspended in 25 ml DMEM containing 10% (v/v) heat-inactivated foetal calf serum (FCS), seeded into cm 2 Falcon culture flasks and incubated (37 0 C, 5% CO,) for 7 to 10 days until monolayer confluence was reached.

Cells were then harvested weekly by 10 min exposure to trypsin, 1 mM EDTA and passaged at a 1:3 split ratio into 75 cm 2 Falcon culture flasks. Cells at passage numbers 3 to 15 were used for experiments.

Immunocytochemistry Cells were subcultured into 8-well glass tissue culture chamber slides (Labtek), and grown to 100% WO 97/42958 PCT/AU97/00286 17 confluency in DMEM (10% FCS). Slides were washed three times in PBS, before fixation for 20 seconds in ice-cold acetone and stored for up to four weeks at 4 0 C before staining. Following rehydration in PBS/BSA for twenty minutes, the cells were permeabilized by incubation in 0.5% Triton X-100 (in PBS) and incubated with primary antibody for at least 60 minutes at 22 0

C.

The primary antibody was removed by washing 3 times with 0.25% BSA in PBS, and then the cells were exposed to the secondary antibody for at least 60 minutes at 22 0

C

(horseradish peroxidase (HRP)- conjugated goat antimouse ;Ig F(ab')2 fragment or goat anti-rabbit IgG).

Controls were provided by substituting the primary antibody for PBS/BSA The staining of the fixed cells was analysed by light microscopy (Olympus BH2 attached to a VideoPro 32 image analysis system, Faulding Imaging, Clayton, Victoria). The characteristics of the antibodies used to identify the smooth muscle in culture were established on native airway wall specimens. The antibodies used were raised against a-actin, myosin, calponin (all specific to smooth muscle), cytokeratin (epithelial cells) and PECAM-1 (CD31, which is a marker of endothelial cells).

The expression of smooth muscle a-actin, myosin and calponin was observed in all cultures used in this study. These cultures did not express detectable PECAM- 1 staining, and less than 5% of the cells were positive for staining with the monoclonal antibody against cytokeratin. Paraffin-embedded sections of the airway adjacent to that used for generation of cultures stained positively for smooth muscle a-actin and myosin in bundles of airway smooth muscle and blood vessels only.

WO 97/42958 PCT/AU97/00286 18 The antibody against PECAM-1 stained vascular endothelium, whereas that against cytokeratin stained only the epithelium, confirming the specificity of these antibodies for the target antigens.

DNA and protein synthesis Cells were subcultured into 24-well plates at a 1:3 ratio and allowed to grow to monolayer confluency over a 72-96 hour period in an atmosphere of 5% CO, in air at 37 0 C. The serum-containing medium was replaced with serum-free DMEM for a 24 hour period to produce growth arrest. In some experiments, the cells were pretreated with 2-methoxyoestradiol 30 min before the addition of mitogen. The stimulant (mitogen) was added to the appropriate wells together with a supplement containing insulin, transferrin, and selenium (Monomed A, 1% Monomed A was added to provide progression factors which are essential for the mitogenic activity of growth factors such as thrombin, epidermal growth factor (EGF) and basic fibroblast growth factor (bFGF) (Stewart et al., 1995a). Mitogens and inhibitors were left in contact with cells from the time of addition until the end of the experiment, unless indicated otherwise. Cells were incubated for 24 hours (37°C, CO,) before being pulsed with ['H]-thymidine (1 Ci/ml for four hours) to measure incorporation of radiolabel into newly synthesized DNA, according to our previous study (Stewart et al., 1995). Incorporation of radioactivity was determined by filtration at the end of the pulse-labelling period. The medium containing the radioactivity was aspirated and the cells were lysed by addition of 2 00Il of 0.1 M NaOH. The DNA was immobilised by filtration in a binding harvester (Packard Filtermate 196) on glass fibre filters WO 97/42958 PCT/AU97/00286 19 (Packard, standard), which were then washed with 3 x 3ml volumes of distilled water and a single 1 ml volume of 100% ethanol. The dried filters were counted in a Packard Topcount liquid scintillation counter. Protein synthesis rates were determined in experiments of analogous design to those described above, but leucine replaced ['H]-thymidine in the pulsing incubation of 4 hours. Furthermore, in experiments to determine the effects of mitogens and 2methoxyoestradiol on the rate of protein synthesis, incubations with mitogen were carried out for a period of 48 hours. The longer duration of these experiments was required to allow sufficient time for cell division to occur.

Cell counting The progression of airway smooth muscle cells through the cell-cycle to mitosis was determined by measuring changes in cell number in experiments of analogous design to those used for DNA synthesis, except that the incubations with mitogen were continued for 48 hours. Cells were removed from each of the wells of 6well culture plates used in these experiments by exposure to 200pl of 0.5% trypsin in PBS containing 1 mM EDTA, for a period of 30 45 min to ensure that the cells were completely dissociated from each other and from the culture plate to enable an accurate count to be made. At the end of this period, a further 200

L

1 of PBS FCS) was added to prevent cell lysis by trypsin and cells were counted directly in a haemocytometer.

Statistical analyses Each treatment in an individual experiment was carried out in quadruplicate for DNA and protein WO 97/42958 PCT/AU97/00286 20 synthesis experiments. Each experiment was performed in at least three different cultures obtained from three different individuals. For cell counting, single incubations were carried out in three cultures. Results are presented as grouped data from multiple cultures and are expressed as mean A S.E. of n cultures. The degree of increment was calculated by dividing the response of treated wells by that of the control wells on the same 24-well plate. The grouped data was analysed by paired t-test after normalisation by log transformation. The Bonferroni adjustment for multiple comparisons was used when necessary. Differences were considered to be significant when p<0.05.

Materials All chemicals used were of analytical grade or higher. The compounds used and their sources were as follows: 2-methoxyoestradiol (1,3,5[10]-estratriene- 2,3,17-triol 2-methylether lot 83H4065); 17P-oestradiol 3 ,5[10]-estratriene-3, 17p-diol, cat no. E8876); 2methoxyoestriol (1,3,5[10]-estratriene-2,3,16a, 17tetrol, lot 26F 4038; 2-methoxyoestrone, (2,3-dihydroxy 1, 3 ,5[10]-estratriene-17-one, lot 110F4003); 2hydroxyestradiol, (1,3,5[10]-estratriene-2,3,17p-triol lot 75H0853); L-glutamine, essentially fatty acid free bovine serum albumin fraction V (BSA), thrombin (bovine plasma), Sigma, USA; amphotericin B (Fungizone), human recombinant basic FGF (bFGF), Promega, USA; collagenase type CLS 1, elastase, Worthington Biochemical, USA; Dulbecco phosphate buffer saline (RBS), Oxoid, England; trypsin, versene, penicillin-G, Streptomycin, Monomed A, CSL, Australia, foetal calf serum (FCS), Flow Laboratories, Australia; Dulbecco's Modified Eagle's WO 97/42958 PCT/AU97/00286 21 Medium (DMEM), Flow Laboratories, Scotland. thymidine (185 GBq/mmol, 5 Ci/mmol), Amersham, UK; Microscint 0 scintillant, Canberra-Packard, Australia.

The antibodies used for immunocytochemistry were antismooth muscle a-actin (mouse monoclonal) (Dako M851), monoclonal mouse anti-PECAM-1 (DAKO-CD31,JC/70A) (Dako M823), Dako Corporation, USA; anti-cytokeratin (mouse monoclonal CY90, Sigma, USA) anti-mouse Ig F(ab')2 fragment FITC-conjugate (host sheep), sheep anti-rabbit Ig HRP-conjugate (Silenus DDAF), Silenus, Australia, and anti-smooth muscle myosin (rabbit polyclonal), provided by Professor M Sparrow, Perth, WA.

Example 1 Effect of 2-methoxyoestradiol on Leucocyte Activity Leucocyte activation is a feature of the pathology of asthma. The binding of 2-methoxyoestradiol to the colchicine binding site on tubulin raised the possibility that this compound interferes with leukocyte functions such as phagocytosis and locomotion.

Functional effects of 2-methoxyoestradiol were examined on polymorphonuclear leukocytes (PMN) and adherent monocytes obtained from human peripheral blood.

Superoxide anion generation was determined by superoxide dismutase sensitive reduction of cytochrome C (Stewart Harris, 1992). The release of myeloperoxidase was determined by oxidation of tetramethyl-benzidine (Menegazzi et al 1992). Phagocytosis was determined by radioiodination of zymosan particles (Shelton Hosking, 1975).

Guinea-pig peritoneal macrophages were harvested and cultured according to our previous studies (Stewart Phillips, 1989). Cells were incubated with stimuli including the chemotactic tripeptide, formyl methiony WO 97/42958 PCT/AU97/00286 22 leucyl Phenylalanine(fMLP, 100 nM), Zymosan (400 Jg/ml) or phorbol myristate acetate (PMA, 100nM) for 30 min in the presence or absence of 2-methoxyoestradiol (10 gM) added 15 min before the stimuli. Superoxide anion was determined by superoxide dismutase-sensitive reduction of cytochrome c (Stewart Harris, 1992) and the stable metabolite of prostacyclin, 6-oxo-PGFl was measured by radioimmunoassay (Stewart Phillips, 1989). All individual incubations were carried out in duplicate and experiments were carried out in macrophages from guinea-pigs.

RBL2H3 cells were cultured in RPMI 1640 containing 10% FCS and were passaged into 24 well plates for experiments. The cells were sensitised by a 48 hour incubation with 50% conditioned medium from a lymphoid cell line secreting anti-DNP ovalbumin antibody. During the last 24 hours of this incubation 3 H]-5HT (1 gCi/ml) was added to each of the wells to label granular amine stores. At the end of the incubation period, the medium was aspirated, the cells were washed twice in RPMI 1640 and incubated in RPMI 1640 (0.25% BSA) in the absence or presence of 2-methoxyoestradiol for 15 mins prior to stimulation with DNP-treated ovalbumin, A23187 or PMA for 30 mins at which time the supernatants were harvested, subjected to centrifugation (1000 x g, 4 0 C, 5 min) and aliquots taken for determination of the amount of 3 H]-5HT released.

All experiments were carried out in quadruplicate.

The results showed that 2-methoxyoestradiol (3lM) reduced oxidation of tetramethyl-benzidine in leukocytes stimulated with either zymosan (400 (ig/ml) or fMLP, as shown in Table 1. Cell-free supernatants from fMLP stimulated leukocytes also contained IWO 97/42958 PCT/AU97/00286 23 myeloperoxidase activity as determined by tetramethylbenzidine oxidation, but this activity was reduced only by the highest concentraction of 2-methoxy- oestradiol In addition, experiments were carried out to examine whether there was a direct effect of 2methoxyoestradiol on oxidation of tetramethyl benzidine by purified horseradish peroxidase. 2-methoxyoestradiol had no effect in this assay. Results are summarised in Figure 1.

Table 1: Tetramethylbenzidine oxidation by Human polymorphonuclear leukocytes Control fMLP Zymosan 100nM 400pg/ml Basal -0.001± 0.057± 0.26± 0.002 0.021 0.009 2-methoxy- -0.004± 0.028± 0.013± estradiol 3jM 0.001 0.03 0.012 Data are expressed as change in absorbance value.

Assays were carried out using 2 x 106 PMN in buffer.

In PMN, superoxide anion generation in response to fMLP (100nM) or zymosan (400 jlg/ml) was not reduced by concentrations of 2-methoxyoestradiol up to 10M. In phagocytosis experiments, radioiodination of zymosan particles by PMN was reduced by 2-methoxyoestradiol with significant effects being observed at both 3 and 10 M, as shown in Table 2.

WO 97/42958 PCT/AU97/00286 24 Table 2. 12 5 I uptake by Human polymorphonuclear leukocytes.

No PHS PHS* Control Zymosan Control Zymosan Basal 1.80± 2.83± 2.13± 4.33± 0.09 0.09 0.24 0.51 2-methoxy- 1.97± 1.97± 1.87± 3.27± oestradiol 3~M 0.44 0.48 0.46 0.64 2-methoxy- 2.05± 1.80± 1.75± 1.65± oestradiol 10pM 0.44 0.49 0.45 0.15 *PHS=pooled human serum Data are expressed as percentage of 12sI incorporation into glass fibre-filterable material. Assays were carried out using 1 x 106 PMN.

In adherent monocytes the oxidation of tetramethyl benzidine in respone to phorbol myristate acetate (1lM) PMA or zymosan (400jg/ml) was unaffected by 10M 2-methoxyoestradiol. Furthermore, superoxide anion generation in response to PMA was also unaffected in this cell type. However, zymosan-stimulated superoxide anion generation appeared to be markedly inhibited by 2-methoxyoestradiol (10lM) in monocytes from at least some donors.

The superoxide anion response of guinea-pig macrophages to zymosan or fMLP was reduced by 2-methoxyoestradiol as shown in Figure 8. However, the response to PMA (100 nM) was unaffected. In addition, fMLP (100 nM)-induced increases in 6-oxo-PGF1 a generation were completely blocked by 2-methoxyoestradiol, whereas the response to PMA was reduced by only 50%, and zymosan WO 97/42958 PCT/AU97/00286 25 did not stimulate an increase in the levels of the prostacyclin metabolite as shown in Figure 9.

Ovalbumin (DNP-OA) elicited a concentrationdependent release of 3 H]-5HT which was reduced by 10 pM 2 -methoxyoestradiol as can be seen in Figure However, the basal release of 3 H]-5HT and that in response to either PMA (100 nM) or the calcium ionophone A23187 (10 RM) were unaffected by 2-methoxyoestradiol as shown in Figure 11.

The inhibitory effects of 2-methoxyoestradiol on PMN myeloperoxidase release and activity, together with the reduction in phagocytosis, indicate that the compound will have an anti-inflammatory effect in vivo.

The selective inhibition of zymosan-stimulated superoxide anion generation suggests a specific effect on this phagocytic stimulus. These observations and our experiments showing inhibitory effects on macrophage function provide clear evidence of anti-inflammatory properties of benefit in asthma and other chronic obstructive airways diseases, particularly those with demonstrable PMN involvement.

Example 2 Effect of 2-methoxyoestradiol on DNA Synthesis Incubation of human cultured airway smooth muscle cells with 0.3 10 LM of 2-methoxyoestradiol for min before mitogen addition, and throughout the remaining 28 hours of the experiment, caused a concentration-dependent reduction in thrombin (0.3 U/ml)-stimulated incorporation of [EH]-thymidine, as shown in Figure 2a. At the highest concentration of 2methoxyoestradiol used (10 RM), the response to thrombin was reduced to approximately 10% of the control level.

WO 97/42958 PCT/AU97/00286 26 This inhibitory effect of 2-methoxyoestradiol on DNA synthesis was not restricted to the presence of thrombin, as similar concentration-related inhibitory effects of 2-methoxyoestradiol were observed in cells in which DNA synthesis was stimulated with either foetal calf serum (FCS, 1% v/v) or basic fibroblast growth factor (bFGF, 300 pM) (Figure 2a and 2b). However, DNA synthesis in the presence of either EGF (3 nM) or FCS was inhibited to a significantly lesser extent than responses to thrombin, bFGF or lower concentrations of FCS (Figure 2c). The DNA synthesis in response to FCS (27.2 7.8 times more than the unstimulated level of ['H]-thymidine incorporation) was significantly greater (p<0.05, paired Student's t-test) than the response to 0.3 U/ml thrombin (8.4 3.1 fold), 3 nM EGF 0.7) or 1% FCS (12.7 but not significantly different from the response to 300 pM bFGF (22.5 5.3).

Time-course studies were also carried out to determine whether addition of 2-methoxyoestradiol, after exposure to mitogens, still inhibited DNA synthesis.

Thrombin (0.3 U/ml)-stimulated DNA synthesis was inhibited when 2-methoxyoestradiol (3 M) was added up to 4 hours after the thrombin, with maximum inhibition being observed at 2 hours after thrombin addition.

Addition of 2-methoxyoestradiol between 4 and 14 hours after the thrombin resulted in a small inhibition whereas addition at 18 hours or later had no effect on the DNA synthesis in the presence of this mitogen as shown in Figure 2d. Subsequently, additional time points were examined and these studies indicated that the highest level of activity was observed when 2methoxyoestradiol was added either simultaneously or 1 hour after thrombin, but significant inhibition WO 97/42958 PCT/AU97/00286 27 persisted up to 6 hours after thrombin addition (Figure 2d).

Example 3 Effect of 2-methoxyoestradiol on protein synthesis and cell numbers In order to determine whether inhibition of DNA synthesis also resulted in arrest of cell-cycle progression and inhibition of mitosis, measurements of both protein synthesis and cell numbers after 48 hours of incubation with mitogens were made. The threshold concentration for inhibition of incorporation of leucine in the presence of thrombin (0.3 U/ml), FCS (1% v/v) or bFGF (300 pM) was 1 pM, and was similar to the results for inhibition of[3H]-thymidine incorporation.

The maximum percentage reduction of the response of approximately 30% was less than the value observed with DNA synthesis, and occurred at 3 tM. At 10 pJM, there was no significant inhibitory effect in the presence of thrombin or bFGF, as shown in Figure 3. 2methoxyoestradiol alone caused a small stimulation of ['H]-leucine incorporation at 0.3 Higher concentrations (1 and 3 lM) had small inhibitory effects and at 10 pM there was no effect. These results are summarised in Table 3. In contrast, the increases in cell number in response to either FCS v/v) or bFGF (300 pM) were more sensitive to inhibition by 2methoxyoestradiol than either protein or DNA synthesis, with complete inhibition of the proliferation responses being observed at 3 tM as shown in Figures 4a and b.

WO 97/42958 PTA9/08 PCT/AU97/00286 28 Table 3. Effect of 2-methoxyoestradiol on protein synthesis rates in unstimulated smooth muscle cells.

2-methoxyoestradiol (pM) [3H]-leucine incorporation (%6 control) mean±LSEM 100 0.3 135±t3* 84:L4* 77t3* 10.0 113t9 *p<0.05 paired Student's t-test, compared to 100% (no pretreatment) Example 4 Serotonin-stimulated (-IHJ-leucine incorPorationj in Smooth Muscle Cells.

Serotonin (5HT) at concentrations from 0.1 n14 up to 10 pLM had no effect on incorporation of [3H]thymidine, but 10 riM 5HT increased incorporation of 3H]-leucine. Preincubation with 0.3 10 tIM of 2methoxyoestradiol decreased the 5HT (10 n4) -stimulated increase in protein synthesis in a concentrationdependent manner, as summarized in Table 4.

WO 97/42958 PCT/AU97/00286 29 Table 4. Effect of 2-methoxyoestradiol on protein synthesis rates in 5HT-stimulated smooth muscle cells.

2 -methoxyoestradiol ['H]-leucine incorporation control) mean±SEM 100 0.3 91±5 62±2* 56±2* 10.0 51±6* *p<0.05 paired Student's t-test, compared to 100% (no pretreatment) Example Morphological effects of 2-methoxyoestradiol Morphological changes including the manifestation of a rounded appearance of the normally spindle-shaped cells were observed at concentrations of 3 and 10 pM of 2-methoxyoestradiol. The shape changes were relatively rapid in onset, being observed within 6 hours, and were maintained for the duration of the incubation. These shape changes weresimilar to those elicited by incubation of cells with the microtubule disaggregating agent, colchicine (0.1 10 pM). The steroid receptor antagonist, RU 486 [Stewart et al., 1995b] reduced the shape changes in response to either colchicine or 2-methoxyoestradiol, but had no effect on WO 97/42958 PCT/AU97/00286 30 the inhibition of DNA synthesis by 2-methoxyoestradiol.

These results are illustrated in Figure Example 6 Effects of analogues of 2-methoxyoestradiol Several compounds related to 2-methoxyoestradiol were examined for inhibition of FCS v/v)-stimulated DNA synthesis, including the parent compound, 173oestradiol, and the immediate precursor, 2hydroxyoestradiol. The lower concentrations of each of these compounds enhanced FCS (l%)-stimulated DNA synthesis, as shown in Figure 6. At higher concentrations, the enhancement was reversed, and inhibition was observed at 10 pM of these compounds.

The inhibitory effect of 2-hydroxyoestradiol (10M) was equivalent to 2-methoxyoestradiol (10pM). A biphasic effect was observed with analogues including 2methoxyoestrone and 2-methoxyoestriol, which enhanced thrombin-stimulated DNA synthesis at concentrations up to 3 gM, but the level of enhancement declined at 10 gM and is shown in Figure 7. The effects of 17oestradiol and 2-hydroxyoestradiol on protein synthesis are shown in Table WO 97/42958 PCT/AU97/00286 31 Table 5. Effect of 2-methoxyoestradiol on protein synthesis rates in unstimulated smooth muscle cells.

Concentration [3H] -leucine incorporation control) 17p- 2oestradiol hydroxyoestradiol mean SEM mean SEM 100 100 0.3 103 6 107 3 89 4 94 87 6 56 8* 10.0 100 9 51 *p<0.05 paired Student's t-test, compared to 100% (no pretreatment) We have shown here that 2-methoxyoestradiol, a natural metabolite of 173-oestradiol which was previously thought to be inactive, has anti-inflammatory activities and inhibits the DNA synthesis and subsequent division of airway smooth muscle cells cultured from human bronchi.

The anti-inflammatory property renders the compound and its analogues useful in the treatment of inflammatory diseases, e.g. treatment of asthma and other chronic obstructive airway diseases, particularly those with demonstrable PMN involvement.

The inhibitory effect on DNA synthesis is not a result of cytotoxicity, since protein synthesis rates were not altered by incubation of cells with the highest concentrations of 2-methoxyoestradiol (10 jiM) and no cell detachment from the culture plates was observed at WO 97/42958 PCT/AU97/00286 32 this concentration. Without wishing to be bound by any proposed mechanism for the observed advantages, it is possible that the steroid inhibits the cells early in the G1 phase of the cell-cycle (2.0 hours post-mitogen), causing maximal inhibition of DNA synthesis. It remains to be established whether post-mitogen addition of 2methoxyoestradiol retains its anti-proliferative effect.

2-methoxyoestradiol inhibited responses to bFGF, thrombin and FCS with similar potencies, indicating that the effect was not specific to any one mitogen.

This observation suggests that 2-methoxyoestradiol acts at early intracellular signalling step(s) used by each of these mitogens. Nevertheless, the inhibitory effect on DNA synthesis was surmountable, with higher concentrations of FCS being significantly less inhibited by preincubation with 2-methoxyoestradiol.

This resistance could be explained by the greater response to the higher concentration of FCS, but a similar argument cannot be made for the resistance to inhibition when the mitogen is EGF, which elicited smaller responses than those elicited by thrombin, FCS 1% or bFGF. However, the proliferative effects of EGF and 10% FCS may be inhibited by 2-methoxyoestradiol. We do not yet have any evidence linking the inhibition of DNA synthesis to inhibition of cell proliferation.

However, the fact that the latter effect is observed at lower concentrations of 2-methoxyoestradiol suggests that actions other than inhibition of DNA synthesis by 2-methoxyoestradiol also contribute to its antiproliferative actions.

Several analogues of 2-methoxyoestradiol were examined to determine whether they shared this antiproliferative effect. Both the parent compound 17oestradiol and the immediate precursor, 2-hydroxy- WO 97/42958 PCT/AU97/00286 33 oestradiol, at lower concentrations increased DNA synthesis in response to FCS and inhibited DNA synthesis at 3 and 10 pM. It was not established whether these changes in DNA synthesis resulted in corresponding changes in cell proliferation. The enhancement of thrombin-stimulated DNA synthesis by 2methoxyoestrone and 2-methoxyoestriol showed a bellshaped concentration-response curve, with a lesser effect at the higher concentrations. Collectively, our observations suggest that 2-methoxyoestradiol is the most potent of the analogues examined, consistent with earlier observations on the proliferative responses of endothelial cells [Fotsis et al., 1994].

It may also be possible to administer the parent compound, 173-estradiol, together with agents which induce metabolism to the active compound. For example, inducers of p450 cytochrome and of catecholamine methyl transferase may be used. Inhibitors of aryl sulphatase may also be considered.

The anti-proliferative effect of 2methoxyoestradiol and its ability to reduce SHT-induced increases in protein synthesis indicate both antihyperplastic and anti-hypertrophic effects. There is compelling evidence for hyperplasia and hypertrophy in asthmatic airways [Ebina et al., 1993], which account for a large part of the phenomenon of AHR [James et al., 1989]. Reductions in AHR are associated with complete resolution of symptoms in some asthmatics [Platts-Mills et al., 1987). Moreover, of all the structural changes documented in the airway wall remodelling response in asthma, an increase in the airway smooth muscle is considered to be of greatest importance [Pare Bai, 1995]. Thus a compound such as 2-methoxyoestradiol, which prevents the growth response of airway smooth WO 97/42958 PCT/AU97/00286 34 muscle, would reduce AHR and therefore reduce the symptoms of asthma. In addition, the anti-angiogenic activity of 2-methoxyoestradiol [Fotsis et al., 1994] is likely to limit the remodelling response, since it has been established that there is an angiogenic component to the remodelling [Kuwano et al., 1993]. It seems likely that this angiogenesis is required to support the metabolic needs of the increased tissue mass.

Therefore, prevention of the angiogenesis may arrest the remodelling response independently of any direct inhibitory effects of 2-methoxyoestradiol on smooth muscle and other cell types.

A number of other properties of 2methoxyoestradiol are likely to be of therapeutic benefit in the treatment of asthma, including its established ability to disrupt microtubule formation [D'Amato et al., 1994], which may reduce the exocytotic release of inflammatory mediators from mast cells, macrophages and eosinophils.

Our data indicate that 2-methoxyoestradiol inhibits antigen-induced mast cell degranulation. This activity supports the use of 2-methoxyoestradiol in a wide range of allergic conditions, including allergic rhinitis and atopic skin conditions. Inhibition of guinea-pig peritoneal macrophage activation by fMLP suggests that the action of 2-methoxyoestradiol may extend beyond events associated with the cytoskeleton, since fMLP activates G-protein-linked receptors rather than phagocytosis.

In addition, the anti-oxidant activities of 2methoxyoestradiol may also be of benefit, since the three key inflammatory cell types involved in airway inflammation each have the capacity to generate large amounts of oxygen radicals, and together with nitric iWO 97/42958 PCT/AU97/00286 35 oxide may cause significant oxidant damage. These activities also support the use of 2-methoxyoestradiol in the treatment of chronic obstructive airways disease, in which an important role for oxy radicals is well established and there is evidence of airway wall remodelling [Kuwano et al., 1993]. Finally, several studies indicate that 2-methoxyoestradiol and related compounds decrease calcium influx into smooth muscle [Goyache et al., 1995] which would, if also demonstrated for airways smooth muscle, counteract bronchospasm in asthma.

Although the examples have been described in some detail for the purpose of clarity and understanding, they represent guidelines only. The person skilled in the art will recognise that various modifications and alterations to the embodiments described herein may be made without departing from the scope of the invention.

References cited herein are listed on the following pages.

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Claims (14)

1. A method of treating a disease characterised by chronic or acute airway inflammation, comprising the step of administering an effective amount of a steroid or steroid analogue which does not exhibit glucocorticoid activity, but which modulates airway remodelling by inhibiting inflammation of the airway wall and/or by inhibiting smooth muscle cell proliferation to a mammal in need of such treatment.

2. A method according to claim 1, wherein the steroid or steroid analogue inhibits phagocytosis by leucocytes.

3. A method according to claim 2, wherein the steroid or steroid analogue inhibits release of myeloperoxidase from the leucocytes.

4. A method according to any one of claims 1 to 3, wherein the steroid or the analogue inhibits activation of macrophages. 20

5. A method according to any one of claims 1 to 4, wherein the remodelling of the airway is further modulated by inhibition of the one or more activities selected from the group consisting of angiogenesis, formation of oxidants and microtubule function in the airway wall. S' 25

6. A method according to any one of claims 1 to wherein the steroid or steroid analogue is selected from the group consisting of 2-methoxyoestradiol, 2- hydroxoestradiol, 2-methoxyoestrone, 2-methoxyoestradiol- 3-methyl ether and 4-methooxyoestradiol.

7. A method according to claim 6, wherein the steroid is 2-methoxyoestradiol.

8. A method according to any one of claims 1 to 7, wherein the disease to be treated is selected from the group consisting of asthma, airway hyperresponsiveness, brochoconstriction, emphysema, pneumonia, atopic disease and pulmonary infection.

9. A method according to claim 8, wherein the atopic H:\Bkrot\Keep\speci\26276-96doc 21/06/00 43 disease is allergic rhinitis.

A composition for inhalation comprising a steroid or steroid analogue which does not exhibit glucocorticoid activity, but which modulates airway remodelling by inhibiting inflammation of the airway wall and/or by inhibiting smooth muscle cell proliferation, wherein said composition is adapted for administration by inhalation with a particle size less than ten microns.

11. A composition according to claim 10, wherein the steroid or steroid analogue is selected from the group consisting of 2-methoxyoestradiol, 2-hydroxoestradiol, 2- methoxyoestrone, 2-methoxyoestradiol- 3-methyl ether and 4- methoxyoestradiol.

12. A composition according to claim 11, wherein the steroid is 2-methoxyoestradiol.

13. Use of a steroid or steroid analogue which does not exhibit glucocorticoid activity, but which modulates airway remodelling by inhibiting inflammation of the airway wall and/or by inhibiting smooth muscle cell proliferation in the manufacturer of a medicament used for treating a disease characterised by chronic or acute airway inflammation.

14. A method according to claim 1, substantially as hereinbefore described with reference to any one of the 25 examples. *Dated this 31st day of July 2000 SAMRAD OPERATIONS PTY LTD By their Patent Attorneys GRIFFITH HACK Fellows Institute of Patent and Trade Mark Attorneys of Australia E:\Simeona\Keep\Spci\26276-96.doc 28/0700