WO2005101968A2

WO2005101968A2 - Antisense oligonucleotides against cpla2, compositions and uses thereof

Info

Publication number: WO2005101968A2
Application number: PCT/IL2005/000399
Authority: WO
Inventors: Rachel Levy
Original assignee: Mor Research Applications Ltd.; Ben-Gurion University Of The Negev Research And Development Authority
Priority date: 2004-04-22
Filing date: 2005-04-17
Publication date: 2005-11-03
Also published as: AU2005235286A1; IL178764A0; IL178764A; WO2005101968A3; EP1758996B1; CA2563741A1; US8735368B2; EP1758996A2; US20120277292A1; AU2005235286B2; MXPA06012157A; IL161579A0; EP1758996A4; US20140303233A1; CN101072788A; US8242255B2; US20080287380A1; JP2007533318A

Abstract

Antisense oligonucleotides against cPLA2 are provided, which are capable of inhibiting cPLA2 expression as well as superoxide production, especially in phagocytes. These antisense oligonucleotides are powerful agents for the treatment of inflammatory conditions, in particular arthritis, as well as in neurodegenerative diseases. The antisense oligonucleotides or compositions comprising the same may be used in methods of treatment of such diseases.

Description

ANTISENSE OLIGONUCLEOTIDES AGAINST CPLA2, COMPOSITIONS AND USES THEREOF

Field of the Invention

The present invention relates to the field of use of antisense oligonucleotides in the treatment of medical conditions. More specifically, the present invention describes novel antisense oligonucleotides for inhibition of phospholipase A2 (PLA2) and treatment of conditions associated with the activation of this molecule.

Background of the Invention

All publications mentioned throughout this application are fully incorporated herein by reference, including all references cited therein.

Inflammation is the body's response- to injury, infection or to molecules perceived by the immune system as foreign. Absent, excessive or uncontrolled inflammation results in a vast array of diseases such as asthma, arthritis and autoimmune diseases, adult respiratory distress syndrome (ARDS), cardiovascular inflammation and gastrointestinal inflammation. Numerous studies have demonstrated the participation of primed neutrophils, monocytes and macrophages in such inflammatory diseases. More recently, the role of superoxides release by microglia cells in the pathogenesis of neurodegenerative diseases such as Alzheimer's disease (AD), Parkinson's disease (PD) and amyotrophic lateral sclerosis (ALS) as well as brain ischemic and traumatic injury has also been documented.

The production of superoxides by the phagocyte NADPH oxidase and pro- inflammatory lipid mediators by phospholipase A₂ are among the most important functions for host defense. However, during altered physiological states, superoxides and lipid mediators promote inflammatory reactions and participate in processes that lead to tissue injury and the pathophysiology of various inflammatory diseases. Nowadays, non-steroidal anti-inflammatory drugs (NSAIDs) are one of the most widely prescribed drugs for the treatment of inflammatory conditions. However, they present unwanted side effects, the most common being ulceration and bleeding in the gastrointestinal tract. Moreover, these drugs reduce only the production of prostaglandins and do not affect the production of leukotrienes which have a pivotal role in the recruitment of neutrophils to the site of inflammation. Thus, the search for new anti-inflammatory drugs with fewer side effects continues. Numerous trials have been conducted with agents that block the inflammatory cascade, like corticosteroids, antiendotoxin antibodies, TNF antagonists, IL-1 receptor antagonists and other agents, without significant success.

The present inventor has developed a cell line, stable clones of PLB-985 cells lacking the expression of cytosolic phospholipase A₂ (CPLA2), and demonstrated that cPLA₂, in addition to its known role in the production of pro-inflammatory lipid mediators, is essential* for activation of the phagocyte NADPH oxidase complex after its assembly. The association between these two enzymes provides the molecular basis for activation of the assembled NADPH oxidase by arachidonic acid (AA) released by cPLA₂ [Dana, R. et al. (1998) J. Biol. Chem. 273:441-5; Lowenthal, A. and Levy, R. (1999) J. Biol. Chem. 274: 21603- 10; Levy, R. et al. (2000) Blood. 95:660-5; Pessach, I. et al. (2001) J. Biol. Chem. 276:33495-503; Shmelzer, Z. et al. (2003) J. Cell Biol. 162:683-692; Tarsi-Tsuk, D. and Levy, R. (1990) J. Immunol.; 144:2665-2670; Dana, R. et al. (1994) Biochem J. 297:217-223; Hazan-Halevy, I. et al. (2000) J. Biol. Chem. 275:12416-12423]. Since cPLA.2 is required for oxidase activation, its inhibition should not only diminish the formation of inflammatory mediators, but should also regulate the uncontrolled accelerated release of oxygen radicals that participate in the pathogenesis of inflammatory diseases. Moreover, the inventor's studies have shown that during inflammation in υiυo or inflammatory conditions in vitro, the level and activity of both cPLA₂ and NADPH oxidase enzymes are elevated in neutrophils and monocytes [Levy, R. et al. (1994) Biochim. Biophys. Ada 1220:261-265; Shaked, G. et al. (1994) J. Trauma 37:22-29; Levy, R. et al. (2000) Blood 95:660-665; Levy, R. and Malech, H. (1991) J. Immunol. 147:3066-3071; Levy, R. et al. (1994) Biochim. Biophys. Ada 1220:253-260; Reizenberg, K. et al. (1997) Eur. J. Clin. Invest. 27:398- 404]. Surprisingly, a recent report described that addition of cPLA₂ inhibitor pyrrolidine to neutrophils did not inhibit NADPH oxidase activity [Rubin, B.B. et al. (2005) J. Biol. Chem. 280:7519-29], however this effect might have been due to the methodology applied, which did not allow sufficient accumulation of the drug in the neutrophils (data not shown). Although methods of treating inflammatory conditions by inhibiting CPLA2 have been described, they involved the use of substances like trifuoromethylketone (TFMK), causing dose-dependent attenuation of airway inflammation [US Patent Application No. 20020165119, USSN 062730], or indole compounds, which inhibited various forms of PLA₂ [US 6,797,708], but no inhibitor unique to cPLA.2 has been described for treatment of inflammation to date. Currently, potent cytosolic PLA2 inhibitors are not available for clinical use in human or animals. All inhibitors against cPLA₂ so far were engineered to compete with the substrate. Since all types of PLA2 cleave the fatty acid from the sn-2 position of phospholipids, they are also inhibited by the same inhibitors (although some times with lower efficiency). Although several compounds were described as specific inhibitors of cPLA.2, they were found to also inhibit other PLA2 enzymes and vice versa. Because of the lack of specific inhibitor for each PLA2 subtype, the antisense technology provides an effective approach to inhibit a specific type of PLA2. Indeed, the results presented herein suggest that a drug targeted directly to cPLA₂ will specifically inhibit cPLA₂ activity. Moreover it also results in the regulation of both CPLA2 and NADPH oxidase to produce pro-inflammatory mediators and superoxides.

Antisense oligonucleotides targeted against the cPLA₂ mRNA sequence have been reported in the past as capable of inhibiting CPLA2 transcript expression [US 6,008,344]. However, these oligonucleotides did not demonstrate inhibition of CPLA2 protein expression, an.d were introduced into ceils in the presence of lipofectin.

In addition, three other antisense oligonucleotides targeted to cPLA₂ have been described: PI (Table 1, SEQ. ID. No.8) [Roshak, A. (1994) J. Biol. Chem. 269(42): 25999-26005; Muthalif, M.M. et al. (1996) J. Biol. Chem. 271(47): 30149-30157; Marshall, L. (1997) J. Biol. Chem. 272(2): 759-765; Anderson, KM. et al. (1997) J. Biol. Chem. 272(48): 30504-30511]; P2 (Table 1, SEQ. ID. No.9) [Li, Q. and Cathcart, M.K. (1997) J. Biol. Chem. 272(4): 2404-2411; Zhao, X. et al. (2002) J. Biol. Chem. 277(28): 25385-25392]; and P3 (5'- GTGCTGGTAAGGATCTAT-3'; SEQ. ID. No.12) [Locati, M. (1996) J. Biol. Chem. 271(11): 6010-6016], mainly evaluating the effect of inhibiting cPLA₂ in smooth muscle cells and human monocytes function. PI was used together with lipofectin. Pi and P2, with phosphorothioate modifications in all bases, had a significant effect only when used at 5 μM, which the present inventor found to be toxic to the cells. P3 was used at 10 μM (or even higher concentration, 10 times higher than what was used by the present inventor). - -

Thus, it is an object of the present invention to provide novel antisense oligonucleotides against the cPLA₂ mRNA, and their use in the inhibition of cPLA.2 expression and superoxide production, in order to inhibit pro- inflammatory processes. Consequently, the antisense oligonucleotides claimed in the present invention are also sought as anti-inflammatory agents.

Other uses and objects of the invention will become clear as the description proceeds.

Summary of the Invention

In a first aspect, the present invention provides antisense oligonucleotides directed against the open reading frame (ORF) of the cytosolic phospholipase A₂ (cPLA.2) mRNA sequence, and functional analogs, derivatives or fragments thereof, wherein the complementarity of said antisense oligonucleotide is within the region between nucleotides 145 to 400 of said ORF, and wherein said antisense oligonucleotide is capable of inhibiting the expression of the cPLA₂ protein.

In one embodiment, the antisense oligonucleotide of the invention is from 15 up to 30 nucleotides long, preferably 17 to 21 nucleotides long.

Said antisense oligonucleotide directed against the 5' region of the open reading frame of the cPLA₂ mRNA sequence has the sequence as denoted by any one of SEQ. ID. No.l, SEQ. ID. No.2, SEQ. ID. No.3, SEQ. ID. No.4, SEQ. ID. No.5, and SEQ. ID. No.6, and as detailed in Table 1.

The antisense oligonucleotides of the invention can be chemically modified, so as to possess improved endonuclease resistance.

Thus, in another embodiment of the antisense oligonucleotide of the invention, a phosphorothioate modification may be present on the first three and/or the last three nucleotides of said oligonucleotides. In addition, another phosphorothioate modification may be found on the tenth nucleotide of said oligonucleotide, as for example in the oligonucleotides denoted by SEQ. ID. Nos. 4 and 5.

In a further embodiment of the antisense oligonucleotide of the invention, further modifications, like 2-O-methylation, may be found in the first three and/or the last three nucleotides of said oligonucleotide.

As a result of the properties presented in the present study, the antisense oligonucleotide may be used as an inhibitor of inflammation processes related to cPLA₂ expression.

Therefore, the antisense oligonucleotide of the invention is for use in the treatment and/or prevention of any one of rheumatoid arthritis, adult respiratory distress syndrome (ARDS), asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease, and neurodegenerative diseases, such as for example Alzheimer's disease (AD), Parkinson's disease (PD), amyotrophic lateral sclerosis (ALS), as well as brain ischemic and traumatic injury, i.e. in all diseases where oxidative stress has a significant role in its pathogenesis, and in which there is accelerated release of eicosanoids and superoxides by reactive microglia.

Thus, the antisense oligonucleotide of the invention may be used for inhibiting superoxide production and release. In particular, said inhibition is effectuated in neutrophils, monocytes and macrophages, preferably in neutrophils.

Optionally the antisense oligonucleotide of the invention may be labeled with one of fluorescent, radioactive, metal particle, and any suitable labeling means.

In a second aspect, the present invention relates to a pharmaceutical composition comprising as active agent at least one antisense oligonucleotide as defined in the invention, or functional analogs, derivatives or fragments thereof.

Thus, the antisense oligonucleotide of the invention is generally provided in the form of pharmaceutical compositions. Said compositions are for use by injection, topical administration, or oral uptake.

Alternatively, the pharmaceutical composition of the invention may comprise as active agent a combination of at least two antisense oligonucleotides as defined in the invention, or functional analogs, derivatives or fragments thereof. Preferably, said combination comprises the following oligonucleotides:

SEQ. ID. No.l together with SEQ. ID. No.3, or SEQ. ID. No.l together with SEQ. ID. No.2, or SEQ. ID. No.l together with SEQ. ID. No.6, or SEQ. ID. No.l together with SEQ. ID. No.2 and SEQ. ID. No.3, or SEQ. ID. No.4 together with SEQ. ID. No.6, or SEQ. ID. No.2 together with SEQ. ID. No.6, or SEQ. ID. No.2 together with SEQ. ID. No.3, or SEQ. ID. No.3 together with SEQ. ID. No.6.

The pharmaceutical composition of the invention is intended for medical use.

In one embodiment, the pharmaceutical composition of the invention is intended for the treatment of inflammation processes related to CPLA2 expression and/or free radical release by phagocyte NADPH oxidase.

In another embodiment, the pharmaceutical composition of the invention is intended for the treatment of inflammatory conditions, wherein said inflammatory conditions may be any one of rheumatoid arthritis, ARDS, asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial isehemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease, CNS-related diseases such as the neurodegenerative diseases AD, PD, ALS, as well as brain ischemic and traumatic injury, i.e. in all diseases where oxidative stress has a significant role in its pathogenesis, and in which there is accelerated release of eicosanoids and superoxides by reactive microglia.

In a further embodiment, the pharmaceutical composition of the invention is intended for the treatment of conditions related to Aβ plaque accumulation. Said conditions are generally CNS-related diseases, particularly the neurodegenerative diseases Alzheimer's, Parkinson's and ALS, or brain ischemic and traumatic head injury.

The pharmaceutical composition of the invention may optionally further comprise buffers, additives, stabilizers, diluents and/or excipients. In another aspect, the present invention provides the use of the antisense oligonucleotide as defined in the invention, for the preparation of a pharmaceutical composition for the treatment and/or prevention of inflammatory conditions, wherein said inflammatory conditions may be any one of rheumatoid arthritis, ARDS, asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease, neurodegenerative diseases such as AD, PD and ALS, as well as brain ischemic and traumatic injury, i.e. in all diseases where oxidative stress has a significant role in its pathogenesis, and in which there is accelerated release of eicosanoids and superoxides by reactive microglia.

In a further aspect, the present invention provides the use of an antisense oligonucleotide as defined in the invention for the treatment of conditions associated with CPLA2 activation.

In addition, the present invention presents the use of an antisense oligonucleotide as defined in the invention, for the treatment and/or prevention of conditions related to Aβ plaque accumulation. Generally said conditions are CNS-related diseases selected from the group consisting of Alzheimer's disease, Parkinson's disease, ALS, brain ischemic injury and traumatic head injury.

In an even further aspect, the present invention presents a method of treatment of conditions associated with cPLA.2 activation^ comprising administering a therapeutically effective amount of at least one antisense oligonucleotide as defined in the invention, or compositions comprising thereof, to a subject in need.

Therefore, in yet another aspect, the present invention provides a method of treatment of inflammatory conditions, wherein said inflammatory conditions are any one of rheumatoid arthritis, ARDS, asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease, neurodegenerative diseases such as AD, PD and

ALS, as well as brain ischemic and traumatic injury, i.e. in all diseases where oxidative stress has a significant role in its pathogenesis, and in which there is accelerated release of eicosanoids and superoxides by reactive microglia, comprising administering a therapeutically effective amount of at least one antisense oligonucleotide as defined in the invention, or compositions comprising thereof, to a subject in need.

In one more aspect, the present invention provides a method of treatment of conditions related to Aβ plaque accumulation, comprising administering a therapeutically effective amount of at least one antisense oligonucleotide as defined in the invention, or compositions comprising thereof, to a subject in need. Said conditions are generally neurodegenerative diseases, particularly Alzheimer's and Parkinson's disease.

Finally, the present invention provides an in vivo, ex vivo or in vitro method of inhibiting cPLA₂ expression and/or activity, comprising contacting cells, preferably phagocytes, i.e. neutrophils, monocytes, macrophages and/or microglia, with the antisense oligonucleotide described in the invention or with compositions comprising thereof, for a suitable amount of time. These antisense oligonucleotides inhibited the cPLA2 activity in fibroblasts, neuronal cells and endothelial cells, but with lower efficiency compared to phagocytes, probably due to lower permeability of the former cells to the antisense oligonucleotides (data not shown). Brief Description of the Figures

Figure 1: cDNA Sequence of CPLA2 (SEQ. ID. No. 7), with position of antisense oligonucleotides C2, C3, C4, C8, C9 and CIO highlighted.

C2 encompasses nucleotides 347-366; C3 encompasses nucleotides 155-174; C4 encompasses nucleotides 379-399; C8 encompasses nucleotides 330-346; C9 encompasses nucleotides 183-202; and CIO encompasses nucleotides 290-306.

Figure 2: Comparison between two anti-cPLA2 antibodies (Ab): Fig. 2A: Levy's Ab [Hazan et al. (1997) id ibid.] Fig. 2B: commercial antibodies. Dil.=dilution.

Figure 3A-3B: Effect of CPLA2 antisense PPS oligonucleotides on CPLA2 expression and superoxide production in human peripheral blood monocytes.

Fig. 3A: Western blot analysis showing inhibition of CPLA2 expression detected by anti-cPLA₂ antibodies after treatment with antisense PPS oligonucleotides C2, C3, C4, C9, and the combination of C2+C4 (2+4), in comparison to control and to the antisense PI [Roshak, A et al. (1994) id ibid.; Marshall, L. et al. (1997) id ibid.; Muthalif, M.M. et al. (1996) id ibid.; Anderson, K. M. et al. (1997) id ibid.] and P2 [Li, Q. and Cathcart, M.K. (1997) id ibid.]. The level of cPLA.2 in the different treatment was quantified by densitometry and is presented below the Western blot analysis. Lev.=levels; dens.= densitometry. Fig. 3B: Histogram showing inhibition of superoxide production (SO prod.) by cPLA₂ antisense PPS oUgonucleotides C2, C3, C4, C9, and the combination of C2+C4 (2+4), in comparison to control and to the antisense Pi [Muthalif, M.M. et al. (1996) id ibid.; Anderson, K. M. et al. (1997) id ibid.] and P2 [Li, Q. and Cathcart, M.K. (1997) id ibid.].

It is important to note the higher efficiency of the antisense PPS oligonucleotides of the invention (denoted as 2, 3, 4 and 9) versus the antisense oligonucleotides Pi and P2 described previously. Figure 4A-4B: Effect of cPLA₂ antisense PPS oligonucleotides on CPLA2 expression and superoxide production in peripheral blood human monocytes.

Fig. 4A: Western blot analysis showing inhibition of CPLA2 expression detected by anti-cPLA2 antibodies after treatment with antisense partially phosphorothioated (PPS) oUgonucleotides C2, C8, C9, CIO and the combinations C3+C10 and C8+C10, in comparison to control and to the oligonucleotides IS1 and IS2 [US 6,008,344]. The level of cPLA₂ in the different treatment was quantified by densitometry and is presented below the Western blot analysis. Lev.=levels; dens.= densitometry.

Fig. 4B: Histogram showing inhibition of superoxide production (SO prod.) by CPLA2 antisense PPS oligonucleotides C2, C8, C9, CIO and the combinations C3+C10 and C8+C10, in comparison to control (cont.) and to the oligonucleotides IS1 and IS2 [US 6,008,344].

It is important to note the higher efficiency of the antisense oligonucleotides of the invention (denoted as 2, 8, 9, and 10 in the Figure) versus the antisense oligonucleotides described in-US-6,008,344 (ISl and IS2).

Figure 5A-5C: Effect of CPLA2 antisense PPS oligonucleotides on

CPLA2 expression and superoxide production in peritoneal murine macrophages.

Fig. 5A: Western blot analysis showing inhibition of CPLA2 expression detected by anti-cPLA2 antibodies after treatment with antisense PPS oligonucleotides

C3 and C4 and the combination C3+C4.

Fig. 5B: Histogram showing inhibition of superoxide production by cPLA₂ antisense PPS oligonucleotides C3 and C4 and the combination C3+C4.

Fig. 5C: Histogram showing inhibition of superoxide production by CPLA2 antisense PPS oUgonucleotides C2, C3, C4, CIO and the combinations C2+C10,

C3+C10, C4+C10 and C3+C4.

Abbreviations: cont., control; SO gen., superoxide generation. Figure 6: Correlation between inhibition of cPLA₂ expression (exp.) and superoxide production (SO prod.) following treatment with cPLA₂ antisense PPS oligonucleotides. Cont.=control.

Figure 7A-7C: Effect of cPLA₂ antisense PPS oligonucleotides on cPLA₂ expression and superoxide production in peripheral blood human neutrophils.

Fig. 7A: Western blot analysis showing inhibition of cPLA₂ expression detected by anti-cPLA.2 antibodies after treatment with antisense PPS oligonucleotides

C2 or C4 and the combination C2+C4. The level of cPLA.2 in the different treatment was quantified by densitometry and is presented below the Western blot analysis.

Fig. 7B: Histogram showing inhibition of superoxide production by cPLA₂ antisense oUgonucleotides C2, C4 or CIO and the combinations C2+C4,

C2+C10, C4+C10, C2+C4+C10 following PMA treatment.

Fig. 7C: Histogram showing inhibition of superoxide production by CPLA2 antisense oligonucleotides C2, C4 or CIO and the combinations C2+C4,

C2+C10, C4+C10, C2+C4+C10 following OZ treatment.

Abbreviations: Lev., levels; dens., densitometry; cont., control; SO gen., superoxide generation.

Figure 8A-F: Inhibition of superoxide production stimulated by physiologic agonists following cPLA₂ antisense PPS oligonucleotides treatment in neutrophils and macrophages.

Fig. 8A: Histogram showing inhibition of superoxide production in PMA- stimulated neutrophils foUowing 6 hours of incubation with the cPLA₂ antisense PPS oligonucleotides C3 or C4.

Fig. 8B: Histogram showing inhibition of superoxide production in fMLP- stimulated neutrophils foUowing 4 hours of incubation with the cPLA₂ antisense PPS oligonucleotides C3 or C4. Fig. 8C: Histogram showing inhibition of superoxide production in OZ- stimulated neutrophils foUowing 4 hours of incubation with the cPLA₂ antisense PPS oligonucleotides C3 or C4.

Fig. 8D: Histogram showing inhibition of superoxide production in PMA- stimulated monocytes following 16 hours of incubation with the cPLA₂ antisense PPS oligonucleotides C3 or C4.

Fig. 8E: Histogram showing inhibition of superoxide production in fMLP- stimulated monocytes following 16 hours of incubation with the CPLA2 antisense PPS oligonucleotides C3 or C4.

Fig. 8F: Histogram showing inhibition of superoxide production in OZ- stimulated monocytes following 16 hours of incubation with the CPLA2 antisense PPS oligonucleotides C3 or C4.

Abbreviations: SO prod., superoxide production; Act., activity.

Figure 9A-9D: Inhibition of stimulated superoxide production in rat microglia by CPLA2 antisense PPS oligonucleotides.

Fig. 9A: Western blot analysis showing- inhibition of CPLA2 expression detected by anti-cPLA.2 antibodies after treatment with antisense PPS oUgonucleotides

C2 or C4.

Fig. 9B: Graph demonstrating the kinetics of the inhibition of superoxide production in PMA-activated rat microglia cells foUowing treatment with the

CPLA2 antisense oligonucleotides C2, C4, C8 or CIO, and the combinations

C2+C10 or C4+ClO.

Fig. 9C: Histogram showing the effect of CPLA2 antisense PPS oligonucleotides

(C2, C4, C8 and CIO, and the combinations C2+C10 and C4+C10) on superoxide production in rat microglia cells foUowing PMA stimulation.

Fig. 9D: Histogram showing the effect of CPLA2 antisense PPS oligonucleotides

(C2, C4, C8 and CIO, and the combinations C2+C10 and C2+C4) on superoxide production in rat microglia cells foUowing Amyloid β stimulation.

Abbreviations: rest., resting; act., activated; as, antisense; kin., kinetics; T., time, min., minutes. Figure 10A-10C: Animal model of collagen-induced arthritis (CIA) Fig. 10A: A picture of exacerbated CIA in experimental compared to control (cont.) mice.

Fig. 10B: Histological assessment of representative section of joint histopathology on whole paws of CIA mice compared to control (cont.) (X100). Fig. IOC: Infiltration of inflammatory ceUs (X400) in CIA mice.

Figure 11A-11B: Treatment with a combination of 3 CPLA2 antisense

PPS oligonucleotides ("Cocktail") caused remission of arthritis.

Fig. HA: Photograph of swoUen limb of CIA mouse (top, art.=arthritis) and limb CIA mouse post-treatment with the cocktail (bottom, as=antisense treatment). Both photographs were taken at same magnification and same distance from the animal.

Fig. 11B: Reduction in disease severity score (dis. sev. sc), in serum (ser.) IL-6 and in serum TNFα after i.v. treatment with the cocktaU (mean+SEM, from 5 mice in each group).

Figure 12A-12B: Number and composition of peritoneal cell population after induction of sterile peritonitis.

Fig. 12A: Changes in peritoneal cell count in sterile peritonitis mice

(mean+SEM, from 6 mice in each group).

Fig. 12B: Changes in the composition of the peritoneal ceU population in sterile peritonitis mice.

Abbreviations: ce. no., ceU number; T., time; h, hours; neu, neutrophfls; mac, macrophages; lymp, lymphocytes.

Figure 13A-13B: LTB₄ levels after induction of sterile peritonitis. Fig. 13 A: LTB4 levels in the serum (ser.). Fig. 13B: LTB₄ levels in the peritoneal cavity (per. cav.). Mean+SEM from 5 mice in each group. T., time; h, hours. Figure 14A-14C: The effect of antisense PPS oligonucleotide cocktail treatment on peritoneal cell population and activity after 24 hours of induction.

Fig. 14A: FACS analysis of cell population (ce. pop.) composition.

Neu=neutrophfls.

Fig. 14B: Graph demonstrating cell count (ce. co.).

Fig. 14C: Superoxide production (SO prod.) by stimulated peritoneal cells of control healthy mice (H), of sterile peritonitis mice (P) and of sterile peritonitis mice after 24 h of cocktail i.v. injection (P+AS).

Figure 15A-15B: cPLAa antisense PPS oligonucleotide cocktail treatment decreased neutrophils number and superoxide production in inflammation site 24 hours after peritonitis induction.

Fig. 15A: Graph demonstrating percentage of neutrophils (neu) with and without antisense treatment.

Fig. 15B: Graph presenting stimulated superoxide production (SO prod.) by

PMA of peritoneal cells isolated from sterile peritonitis mice without and with antisense treatment.

Figure 16: cPLA₂ antisense PPS oligonucleotide cocktail treatment decreased unstimulated superoxide production by resting peritoneal cells in inflammation site 24 hours after peritonitis induction.

Shown is an example of detection of superoxide production by resting peritoneal cells isolated from sterile peritonitis mice assessed with 1 μM Dihydrorhodamine-123, without and with antisense treatment. Co.=counts.

Figure 17A-17B: Effect of CPLA . antisense PPS oligonucleotide cocktail treatment on the peritoneal cell composition in mice with sterile peritonitis.

Fig. 17A: Peritoneal cell composition during sterile peritonitis. Fig. 17B: Peritoneal ceU composition post antisense treatment. Abbreviations: ce. no., cell number; T., time; h, hours; neu, neutrophils; mac, macrophages; lymp, lymphocytes.

Abbreviations: Neu, neutrophils; mac, macrophages; lymp, lymphocytes; (means from 5 mice in each group).

Figure 18A-18B: Effect of cPLA₂ antisense PPS oligonucleotide treatment on stimulated superoxide production (SO prod.) by peritoneal cells during sterile peritonitis.

Fig. 18A: Stimulated superoxide production by peritoneal cells in mice with sterile peritonitis.

Fig. 18B: Stimulated superoxide production by peritoneal cells in mice with sterile peritonitis and treated with antisense oUgonucleotides.

Mean+SEM from 5 mice in each group. T.=time; h=hours.

Figure 19A-19B: cPLA₂ antisense PPS oligonucleotide cocktail treatment decreased peritoneal LTB4 levels.

Fig. 19A: LTB₄ levels in the peritoneum of sterile peritonitis mice.

Fig. 19B: LTB₄ levels in the peritoneum of sterile peritonitis mice treated with the cocktaU.

Mean+SEM from 5 mice in each group. T.=time; h=hours.

Figure 20 A-20B: cPLA₂ antisense PPS oligonucleotide cocktail treatment decreased peritoneal neutrophils count.

Fig. 20A: Number of neutrophils (Neu No) in the peritoneum of sterile peritonitis mice.

Fig. 20B: Number of neutrophils (Neu No) in the peritoneum of sterile peritonitis mice treated with the cocktail.

Mean+SEM from 5 mice in each group. T.=time; h=hours.

Figure 21A-21B: Accumulation of antisense oligonucleotides in peritoneal Mood cells 24 1-aoτtars after injection. ^~.?ig. 2 LA: Peritoneal blood cells, untreated. Fig. 2 IB: Peritoneal blood cells treated with the antisense (as) oligonucleotides.

Upper panel: light microscope. Lower panel: confocal microscopy.

Detailed Description of the Invention

In the present study, the inventors engineered six different antisense oligonucleotides against cytosolic phospholipase A2 (cPLA₂) mRNA. As shown in the following Examples, each antisense by itself is significantly potent in inhibiting the expression of cPLA₂, whfle different combinations of the oligonucleotides totaUy inhibited cPLA₂ expression in the different phagocytic, as well as microglia cells from humans, mice and rats. Moreover, there is a striking correlation between the inhibition of cPLA₂ expression by the antisense oligonucleotides and the inhibition of superoxide production by NADPH oxidase, which has not been previously demonstrated.

Thus, the present invention provides antisense oligonucleotides directed against the open reading frame (ORF) of the cPLA₂ mRNA sequence (indicated in Fig. 1), and functional analogs, derivatives or fragments thereof, wherein the complementarity of said antisense oligonucleotide is within the region between nucleotides 145 to 400 of said ORF, and wherein said antisense oligonucleotide is capable of inhibiting the expression of the cPLA₂ protein.

As shown in the following Examples, the antisense oligonucleotides provided by the invention can also inhibit superoxide production by inhibiting NADPH oxidase activity.

As referred to herein, SEQ. ID. No.7 relates to the cDNA sequence corresponding to the cPLA₂ mRNA sequence [GenBank No. M68874].

Said region between nucleotides 145 to 400 of the cPLA₂ mRNA is particularly useful for targeting, sinc3 it is much more efficient to prevent than to halt protein synthesis, once the process has already begun (the latter being the strategy used in US 6,008,344, for most of its cPLA₂ antisense sequences). Therefore, the antisense oUgonucleotides were designed as to target the region of translation site (beginning of the ORF).

Nonetheless, it is important to mention that antisense targeting is stiU very empirical, and a lot of experimentation is needed to find the specific sequence and the optimum conditions for most effective targeting. As described herein for example, the present inventors originally designed fourteen antisense oligonucleotides targeting the region between nucleotides 145-400 of the cPLA₂ sequence, corresponding to the beginning of the ORF, but only six of those worked efficiently, and were then studied in more detail.

Said antisense oUgonucleotide directed against the 5' region of the open reading frame of the cPLA₂ mRNA sequence has the sequence as denoted by any one of SEQ. ID. No.l, SEQ. ID. No.2, SEQ. ID. No.3, SEQ. ID. No. , SEQ. ID. No.5, and SEQ. ID. No.6-. which sequences are detailed in Table 1.

As mentioned, the antisense oligonucleotides of the invention can be chemically modified, so as to possess improved endonuclease resistance. Any chemical modification which confers resistance towards endonucleases, such as, but not limited to phosphorothioation or 2-O-methylation, may be adopted.

Thus, a phosphorothioate modification may be present on the first three and/or the last three nucleotides of the oUgonucleotides of the invention. In addition, another phosphorothioate modification may be found on the tenth nucleotide of said oUgonucleotide, an inner pyrimidine, as for example in the oligonucleotides denoted by SEQ. ID. Nos. 4 and 5. Phosphorothioation of inner pyrimidines has been shown to increase stability and protect from endonuclease cleavage [PiroUo, K.F. et al. (2003) Pharmacology & Therapeutics 90:55-77]. The antisense oUgonucleotides of the invention are partially phosphorothioated, and are thus less toxic than antisense oligonucleotides that have phosphorothioate modifications in all nucleotides.

Nevertheless, further modifications, like 2-O-methylation, may be found in the first three and/or the last three nucleotides of said oligonucleotide [EP 260,032].

As shown in Examples 5 to 7, the antisense oligonucleotides of the invention may be used as inhibitors of inflammation processes related to CPLA2 expression and activity.

The antisense oUgonucleotide of the invention is thus suitable for use in the treatment and/or prevention of any one of rheumatoid arthritis, ARDS, asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease, neurodegenerative diseases such as AD, PD and ALS, as well as brain ischemic and traumatic injury, i.e. in all diseases where oxidative stress has a significant role in its pathogenesis, and in which there is accelerated release of eicosanoids and superoxides by reactive microglia.

Although a study in human monocytes demonstrated that inhibition of CPLA2 expression also inhibits NADPH oxidase activity [Li, Q. and Cathcart, M.K. (1997) id ibid.], another report had shown that resident peritoneal macrophages from cPLA₂-deficient mice can, under normal stimulation, release superoxide [Gijon, M. A. et al. (2000) J. Biol. Chem. 275: 20146]. In contrast, the present inventors have now demonstrated that the antisense oligonucleotides, which were efficient in inhibiting cPLA₂ expression in mice macrophages, were also efficient in inhibiting superoxide production in macrophages, as weU as in monocytes, neutrophils and microglia cells. This disparity may be explained by the fact that often "knockout" animal models have normal phenotypes due to, for example, over expression and compensation of isoenzymes, and thus do not accurately mirror the effects of the lack of the gene (i.e., the protein or enzyme) in study. Most importantly, the present results were obtained using low levels of oligonucleotides of lμM (final concentration). It is important that the present antisense oligonucleotides are effective at low, non-toxic concentrations, which makes them suitable for use in clinical purposes, i.e., as a therapeutic agent for the treatment of conditions where inhibition of cPLA.2 is desirable, as discussed herein.

In addition, the antisense oligonucleotides of the invention are suitable for use in the treatment and/or prevention of conditions in which microglia cells are activated, for example by LPS, and release reactive oxygen species (ROS) and/or pro-inflammatory mediators, for example. Said conditions are selected from the group consisting of inflammations, infections, and ischemic disease.

The antisense oligonucleotide of the invention may also be used for inhibiting superoxide production and release. UsuaUy, said inhibition is effectuated in neutrophils, monocytes and macrophages, preferably in neutrophils.

Activated neutrophils are the first ceUs arriving at the inflammation site, which then release high levels of eicosanoid and superoxides which accelerates the inflammatory process. Consequently, neutrophils are direct effectors of the pathogenesis of the various inflammatory diseases, and directly inhibiting their function is an efficient way to reduce inflammatory processes. Monocytes (and macrophages) are the second cell population to arrive at the site of inflammation, and thus their inhibition is also important to staU inflammation.

In addition, the antisense oligonucleotides of the invention may be used for inhibiting eicosanoid and ROS production released by microgUa that are induced by amyloid β (Aβ) plaque formation or by other agents such as LPS or cytokines. ROS formation has been shown to be responsible for the dysfunction or death of neuronal ceUs that contributes to the pathogenesis of various neurological diseases.

By "analogs and derivatives" is meant the "fragments", "variants", "analogs" or "derivatives" of said nucleic acid molecule. A "fragment" of a molecule, such as any of the oligonucleotide sequences of the present invention, is meant to refer to any nucleotide subset of the molecule. A "variant" of such molecule is meant to refer a naturally occurring molecule substantially similar to either the entire molecule or a fragment thereof. An "analog" of a molecule can be without limitation a paralogous or orthologous molecule, e.g. a homologous molecule from the same species or from different species, respectively, i.e., an antisense oligonucleotide complementary to the equivalent region of the gene in a different species, which therefore may have sUght changes in the sequence.

Further derivatives of the antisense oUgonucleotides of the invention are those labeled or conjugated to a reporter molecule, such that the antisense oligonucleotide of the invention may be -traced and/or detected in the organism. Any label or reporter molecule that allow its detection may be suitable, like e.g. bio tin, fluorescein, rhodamine, 4-(4'-Dimethylamino-phenylazo)benzoic acid ("Dabcyl"); 4-(4'-Dimethylamino-phenylazo)sulfonic acid (sulfonyl chloride) ("Dabsyl"); 5-((2-aminoethyl)-amino)-naphtalene-l-sulfonic acid ("EDANS"); Psoralene derivatives, haptens, cyanines, acridines, fluorescent rhodol derivatives, cholesterol derivatives, radioactive labels, as well as metal particles (e.g. gold).

In a second aspect, the present invention relates to a pharmaceutical composition comprising as active agent at least one antisense oUgonucleotide as defined in the invention, or functional analogs, derivatives or fragments thereof. Thus, the antisense oligonucleotide of the invention is generaUy provided in the form of pharmaceutical compositions. Said compositions are for use by injection, topical administration, or oral uptake.

Alternatively, the pharmaceutical composition of the invention may comprise as active agent a combination of at least two antisense oUgonucleotides as defined in the invention, or functional analogs, derivatives or fragments thereof. Preferably, said combination comprises the following oligonucleotides: SEQ. ID. No.l together with SEQ. ID. No.3, or SEQ. ID. No.l together with SEQ. ID. No.2, or SEQ. ID. No.l together with SEQ. ID. No.6, or SEQ. ID. No.l together with SEQ. ID. No.2 and SEQ. ID. No.3, or SEQ. ID. No.4 together with SEQ. ID. No.6, or SEQ. ID. No.2 together with SEQ. ID. No.6, or SEQ. ID. No.2 together with SEQ. ID. No.3, or SEQ. ID. No.3 together with SEQ. ID. No.6.

In the Examples described herein below, it is clear how both inhibition of CPLA2 and inhibition of superoxide production were much more efficient when the antisense oligonucleotides were used in combination of two or three together in the same reaction.

In one embodiment, the pharmaceutical composition of the invention is intended for the treatment of inflammation processes related to cPLA.2 expression and/or free radical release by phagocyte NADPH oxidase.

In another embodiment, the pharmaceutical composition of the invention is intended for the treatment of inflammatory conditions, wherein said inflammatory conditions may be any one of rheumatoid arthritis, ARDS, asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease, neurodegenerative diseases such as AD, PE and ALS, as well as brain ischemic and traumatic injury, i.e. in aU diseases where oxidative stress has a significant role in its pathogenesis, and in which there is accelerated release of eicosanoids and superoxides by reactive microglia.

In a further embodiment, the pharmaceutical composition of the invention is intended for the treatment of conditions related to Aβ plaque accumulation. Said conditions are generally neurodegenerative diseases, preferably Alzheimer's, Parkinson's, ALS, or brain ischemic and traumatic injury.

The pharmaceutical composition of the invention is also intended to be used in the treatment and/or prevention of conditions, for example exposure to LPS, in which microglia ceUs are activated and release ROS and/or pro-inflammatory mediators (eicosanoid). Said conditions are selected from the group consisting of inflammations, infections, and ischemic disease.

Preferred uses of the pharmaceutical compositions of the invention by injection are subcutaneous injection, intraperitoneal injection, intravenous and intramuscular injection.

The pharmaceutical composition of the invention generally further comprises a dfluent, and/or a buffering agent, i.e. an agent which adjusts the osmolarity thereof, and optionaUy, one or more carriers, stabflizers, excipients and/or additives as known in the art, e.g., for the purposes of adding flavors, colors, lubrication, or the Uke to the pharmaceutical composition.

A preferred buffering agent is Tris, consisting of 10 mM Tris, pH 7.5-8.0, which solution is also adjusted for osmolarity.

For in vivo use, the antisense oligonucleotides are suspended is sterile distiUed water or in sterile saline. Carriers may include starch and derivatives thereof, ceUulose and derivatives thereof, e.g., microcrystalline ceUulose, xantham gum, and the like. Lubricants may include hydrogenated castor oil and the like.

The preparation of pharmaceutical compositions is weU known in the art and has been described in many articles and textbooks, see e.g., Remington's Pharmaceutical Sciences, Gennaro A. R. ed., Mack PubUshing Co., Easton, PA, 1990, and especially pp. 1521-1712 therein.

Pharmaceutical compositions for topical administration may include transdermal patches, ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders. Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable.

Compositions for oral administration include powders or granules, suspensions or solutions in water or non-aqueous media, capsules, sachets or tablets. Thickeners, flavoring agents, diluents,. emulsifiers, dispersing aids or binders may be desirable.

Compositions and formulations for parenteral, intrathecal or intraventricular administration may include sterile aqueous solutions which may also contain buffers, diluents and other suitable additives such as, but not limited to, penetration enhancers, carrier compounds and other pharmaceutically acceptable carriers or excipients.

The pharmaceutical compositions of the present invention include, but are not limited to, solutions, emulsions, and liposome-containing formulations. These compositions may be generated from a variety of components that include, but are not limited to, preformed liquids, self-emulsifying solids and self- emulsifying semisoUds.

The pharmaceutical compositions of the present invention, which may conveniently be presented in unit dosage form, may be prepared according to conventional techniques weU known in the pharmaceutical industry. Such techniques include the step of bringing into association the active ingredients with the pharmaceutical carrier(s) or excipient(s). In general the formulations are prepared by uniformly and intimately bringing into association the active ingredients with liquid carriers or finely divided solid carriers or both, and then, if necessary, shaping the product. Such compositions may be formulated into any of many possible dosage forms such as, but not limited to, tablets, capsules, Uquid syrups, soft gels, suppositories, and enemas. The compositions of the present invention may also be formulated as suspensions in aqueous, non-aqueous or mixed media. Aqueous suspensions may further contain substances which increase the viscosity of the suspension including, for example, sodium carboxymethylcellulose, sorbitol and/or dextran. The suspension may also contain stabilizers.

In one embodiment of the present invention the pharmaceutical compositions may be formulated and used as foams. Pharmaceutical foams include formulations such as, but not Umited to, emulsions, microemulsions, creams, jellies and liposomes. While basically simflar in nature these formulations vary in the components and the consistency of the final product.

The pharmaceutical composition of the invention may further comprise other active agents, e.g. antibiotics, analgesics and the like.

In another aspect, the present invention provides the use of the antisense oligonucleotide as defined in the invention, for the preparation of a pharmaceutical composition for the treatment and/or prevention of inflammatory conditions, wherein said inflammatory conditions may be any one of rheumatoid arthritis, ARDS, asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease neurodegenerative diseases such as AD, PD, and ALS, as well as brain ischemic and traumatic injury, i.e. in aU diseases where oxidative stress has a significant role in its pathogenesis, and in which there is accelerated release of eicosanoids and superoxides by reactive microglia.

Furthermore, the present invention provides the use of an antisense oligonucleotide as defined in the invention for the treatment of conditions associated with cPLA₂ activation, as weU as for the treatment and/or prevention of conditions related to Aβ plaque accumulation. Generally said conditions are neurodegenerative diseases, selected from the group consisting of Alzheimer's disease, Parkinson's disease, ALS, and brain ischemic and traumatic injury.

Hence, the present invention presents a method of treatment of conditions associated with CPLA2 activation, comprising administering a therapeutically effective amount of at least one antisense oligonucleotide as defined in the invention, or compositions comprising thereof, to a subject in need.

Said therapeutic effective amount, or dosing, is dependent on severity and responsiveness of the disease state to be treated, with the course of treatment lasting from several days to several months, or until a cure is effected or a diminution of the disease state is achieved. Optimal dosing schedules can be calculated from measurements of drug accumulation in the body of the patient. Persons of ordinary skiU can easily determine optimum dosages, dosing methodologies and repetition rates. Optimum dosages may vary depending on the relative potency of individual oligonucleotides, and can generally be estimated based on EC50, found to be effective in in vitro as well as in in vivo animal models. In general, dosage is from 0.01 μg to 10 mg per kg of body weight, and may be given once or more daily, weekly, monthly or yearly, or even once every 2 to 20 years. Persons of ordinary skill in the art can easily estimate repetition rates for dosing based on measured residence times and concentrations of the antisense oUgonucleotide in bodily fluids or tissues. Following successful treatment, it may be desirable to have the patient undergo maintenance therapy to prevent the recurrence of the disease state, wherein the oligonucleotide is administered in maintenance doses, ranging from 0.01 μg to 10 mg per kg of body weight, once or more daily.

As demonstrated in the following Examples 5 to 7, optimal dosage used for treatment of the inflammatory conditions is 1-2 mg/kg/day given daily for between 5 up to 14 days (Example 5), or given in one or two doses of 1-2 mg/kg/day after inflammation (Examples 6 and 7).

The use of antisense oligonucleotides for inhibiting cPLA₂ expression is an innovative treatment for local inflammatory diseases, since it wiU inhibit specificaUy the elevated cPLA₂ at the site of inflammation and wiU not affect normal CPLA2 expression. This treatment is potentiaUy even more effective when affecting also the activity of activated or primed phagocytes involved in the pathogenesis of such diseases, since these cells secrete high levels of eicosanoids and superoxides' which accelerate the inflammation process.

Therefore, the present invention also provides a method of treatment of inflammatory conditions, wherein said inflammatory conditions are any one of rheumatoid arthritis, ARDS, asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease, neurodegenerative diseases such as AD, PD and ALS, as well as brain ischemic and traumatic injury, i.e. in all diseases where oxidative stress has a significant role in its pathogenesis, and in which there is accelerated release of eicosanoids and superoxides by reactive microglia, comprising administering a therapeutically effective amount of at least one antisense oUgonucleotide as defined in the invention, or compositions comprising thereof, to a subject in need. In addition, involvement of cPLA₂ in the regulation of superoxide production by NADPH oxidase in microgUa ceUs suggests that CPLA2 antisense oligonucleotides may be used in the treatment of neurodegenerative diseases, selected from the group consisting of Alzheimer's disease, Parkinson's disease, ALS, and brain ischemic and traumatic injury.

Likewise, the present invention also provides a method for the treatment and/or prevention of conditions in which microglia cells are activated, exposed to LPS for example, and release ROS and or pro-inflammatory mediators, and wherein aid conditions are selected from the group consisting of inflammations, infections, and ischemic disease. Said method comprises administering a therapeutically effective amount of at least one antisense oligonucleotide as defined in the invention, or compositions comprising thereof, to a subject in need.

As a final aspect, the present invention provides a method of treatment of neurodegenerative diseases* as weU as brain damage (caused by stroke or trauma, for example), comprising administering a therapeutically effective amount of at least one antisense oUgonucleotide as defined in the invention, or compositions comprising thereof, to a subject in need. Said conditions are generally neurodegenerative diseases, preferably Alzheimer's and Parkinson's disease, or brain ischemic and traumatic injury, in which there is accelerated release of eicosanoid and superoxides by reactive microglia.

Various methods of administration may be used for deUvering the antisense oligonucleotide of the invention to a subject in need. OUgonucleotides may be deUvered via intravenous (i.v.), intramuscular (i.m.) intraperitoneal (i.p.) injections, oraUy (in liquid form or prepared as dosage unit forms like capsules, pills, lozenges, etc.). In order to be effective therapeutically, oUgonucleotides should be prepared in a way that would enable their stabiUty in the system following injection, or yet more preferably, foUowing oral administration. Alternatively, the oligonucleotides of the invention may also be delivered via transdermal delivery using patches, ointment or cream.

In addition, pharmaceutical compositions comprising as active agent the antisense oligonucleotides described in the present invention may be administered in a number of ways depending upon whether local or systemic treatment is desired and upon the area to be treated. Administration may be topical (including ophthalmic and to mucous membranes including vaginal and rectal deUvery), pulmonary, e.g., by inhalation or insufflation of powders or aerosols, including by nebulizer; intratracheal, intranasal, epidermal and transdermal), oral or parenteral. Parenteral administration includes intravenous, intraarterial, subcutaneous, intraperitoneal or intramuscular injection or infusion; or intracranial, e.g., intrathecal or intraventricular, administration. Oligonucleotides with at least one 2'-O-methoxyethyl modification are believed to be particularly useful for oral administration.

As shown in the following Examples, -preUminary trials with three different models of inflammation in mice and rats (arthritis, ARDS and peritonitis), demonstrate the effectiveness of the specific cPLA₂ antisense oligonucleotides as anti-inflammatory treatment.

The present invention is defined by the claims, the contents of which are to be read as included within the disclosure of the specification.

Disclosed and described, it is to be understood that this invention is not limited to the particular examples, process steps, and materials disclosed herein as such process steps and materials may vary somewhat. It is also to be understood that the terminology used herein is used for the purpose of describing particular embodiments only and not intended to be limiting since the scope of the present invention wiU be Umited only by the appended claims and equivalents thereof. It must be noted that, as used in this specification and the appended claims, the singular forms "a", "an" and "the" include plural referents unless the content clearly dictates otherwise.

Throughout this specification and the claims which foUow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", wiU be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.

The following Examples are representative of techniques employed by the inventors in carrying out aspects of the present invention. It should be appreciated that while these techniques are exemplary of preferred embodiments for the practice of the invention, those of skiU in the art, in light of the present disclosure, wiU recognize that numerous modifications can be made without departing from the intended scope of the invention.

Examples

Experimental Procedures

General Methods of Molecular Biology

A number of methods of the molecular biology art are not detailed herein, as they are well known to the person of skill in the art. Such methods include PCR, expression of cDNAs, transfection of mammaUan ceUs, and the Uke. Textbooks describing such methods are, e.g., Sambrook et al. (1989) Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Laboratory, ISBN: 0879693096; F. M. Ausubel (1988) Current Protocols in Molecular Biology, ISBN: 047150338X, John Wiley & Sons, Inc. Furthermore, a number of immunological techniques are not in each instance described herein in detafl, like for example Western Blot, as they are well known to the person of skill in the art. See, e.g., Harlow and Lane (1988) Antibodies: a laboratory manual. Cold Spring Earbor Laboratory. Oligonucleotides Table 1: Oligonucleotides used in the following examples

Note: the underline shows phosphorothioated nucleotides.

Example 1 Synthesis of anti-cPLA₂ antisense oligonucleotides Fourteen different partially phosphorothioated [Stein et al. (1988) Nucleic Acids Res. 16:3209-3221] oligonucleotides against cPLA₂ were originally synthesized. Prior to use, the oligonucleotides were purified by HPLC and tested for purity by mass spectrometry (Sigma, UK). Prior to selection, the sequences were analyzed by screening for uniqueness using the Blast program and were also tested for lack of secondary structure and oUgo pairing using Mulfold [Jaeger, J.A. (1989) Methods Enzymol. 183: 281-306]. Preliminary experiments (not shown) demonstrated that from those fourteen, only six oligonucleotides were found to be efficient in inhibiting cPLA₂ expression, and their sequences are detailed in Table 1 above.

The fact that only six antisense oligonucleotides displayed significant activity suggested that these have increased specificity for the target sequence. The remaining eight oligonucleotides were used in the experiments as controls.

The oligonucleotides carried phosphorothioate modifications on the last 3 bases at both 5' and 3' ends (as indicated by underUne, Table 1), and were engineered using computer based approach using RNADraw VI.1 [Mazura Multimedia, Sweden] for the first 400 hundred base pairs (N-terminal) of cPLA₂ mRNA (Table 1).

The partially phosphorothioated oUgonucleotides (PPS) are less toxic and more specific than the phosphorothioated oligonucleotides, but similar in their stability and cellular uptake. Some PPS contain GGGG (CIO) and GGG (C8 and C9) which have been shown to increase cellular uptake (see Table 1). PPS C8, C9 also contain phosphorothioated on inner pyrimidines (t) which have been shown to increase stability and protect from endonuclease cleavage (Table 1, underlined). Five of the antisense oligonucleotides did not contain CpG, which have been shown to stimulate immune responses. In all of the experiments presented herein, naked PPS were added since in this form they can be used for in vivo treatment [PiroUo, K.F. et al. (2003) id ibid.], in contrast to the pubUshed studies in vitro, which used different delivery systems to increase the antisense uptake. Hence, aU the cUnical trials with antisense oligonucleotides are carried out with naked oligonucleotides. For example, an in vivo clinical trial did not require cationic Upids for oUgonucleotide deUvery against Bcl-2 in cancer patients, in contrast to the experiments performed in tissue culture [Jansen, B. et al. (2000) Lancet 356: 1728-1733]. This is usuaUy the case in in vivo assays, and to date it is not well understood why a vector does not appear to e necessary. One hypothesis is that the oUgonucleotides interact with circulating proteins, which both protect them against degradation, and serve as carriers in ways not yet understood [Dias, N. and Stein, CA. (2002) Eur. J. Pharmac and Biopharmac. 54: 263-269].

As shown in Figures 3-7, there is a clear correlation between inhibition of cPLA₂ expression by the PPS antisense oligonucleotides and stimulated production of superoxides. Each PPS oligonucleotide caused significant inhibition of CPLA2 protein expression in different phagocytic cell types, and their combinations caused significantly improved inhibition.

As shown in Figures 3 and 4, the PPS antisense oligonucleotides of the invention are far more efficient than those previously reported [US 6,008,334; Roshak et al. (1994) id ibid; Muthalif et al. (1996) id ibid; Marshall et al (1997) id ibid; Anderson et al. (1997) id ibid ; Li, Q. and Cathcart, M.K. (1997) id ibid.; Zhao, X. et al. (2002) id ibid.]. Moreover, in the previous reports, these antisense oligonucleotides were tested only for their capacity to inhibit mRNA synthesis [US 6,008,334].

The effect of the number (and kind) of modifications at the two ends of the oligonucleotides was also evaluated (data not shown). The rank order of the efficiency in inhibiting cPLA₂ expression and NADPH oxidase observed was as follows:

PPS with 3 modifications > PPS with 2 modifications > PPS with 1 modification > no modification.

The PPS antisense oligonucleotides were more efficient in inhibiting cPLA₂ protein expression in the phagocytic ceUs, as shown for monocytes, than endothelial or epithelial cells (data not shown). This phenomenon has advantages especially regarding treatment of inflammation directly affecting the phagocyte at the site of inflammation, without affecting the organ. Example 2

Effect of cPLA2 antisense oligonucleotides on cPLA₂ expression and superoxide production in peripheral blood human monocytes

The expression of cPLA₂ protein was analyzed by Western blot analysis using antibodies against cPLA.2 that were raised by the inventors and which are much more efficient than those available on the commercial market (Fig. 2).

The effect of the different PPS antisense oUgonucleotides and their combinations on cPLA₂ expression and on superoxide production was studied in peripheral blood human monocytes (Figs. 3 and 4) and in murine macrophages (Fig. 5). Naked (free of transfection solutions like lipofectin, etc.) PPS antisense oligonucleotides (final concentration of 1 μM) were added to the cell suspension in RPMI containing 10% FCS for 16 h at 37°C. The same cells were analyzed for superoxide production stimulated with 5 ng/ml PMA (by cytochrome c reduction) and for the expression of cPLA₂ in cell lysates (by Western blot analysis). As shown, each of the PPS antisenses caused between 50-75% inhibition of superoxide production, which is in correlation with their effect on inhibiting cPLA₂ expression. The level of CPLA2 was quantitated by densitometry in a reflectance mode (Hoefer, Hoefer Scientific Instruments, San Francisco, USA). The correlation between these two parameters is demonstrated in Figure 6.

As shown in Figures 3 and 4, respectively, Pi [Roshak et al. (1994) id ibid; MuthaUf et al. (1996) id ibid; Marshall et al (1997) id ibid; Anderson et al. (1997) id ibid] and P2 [Li, Q. and Cathcart, M.K. (1997) id ibid.], and IS1 and IS2 [US 6,008,334] did not have any effect either on cPLA.2 expression or on superoxide production. Most importantly, oUgonucleotides ISl and IS2, were reported, in US 6,008,334, to cause 100% and 92% inhibition of mRNA expression, respectively. However, their effect was analyzed only by inhibition of mRNA expression and not by inhibition of cPLA₂ protein expression. In their original publications, Pi, P2 ISl and IS2 were synthesized with phosphorothioate modifications in all bases. The present inventor found that, when fully phosphorothioated, these oligonucleotides were toxic to the cells, and caused the killing of about 60-70% of the cells after 16 hours of incubation (data not shown). These results are consistent with a previous report showing that oligonucleotides with phosphorothioate modifications in all bases are much more toxic [PiroUo, K.F. et al. (2003) id ibid.]. Thus, it is important to note that, for this study, PI, P2, ISl and IS2, differently from the original oligonucleotides, were synthesized with phosphorothioate modifications only in the first and last three bases, in order to more accurately compare their effect to the effect of the PPS antisense oligonucleotides synthesized by the present inventor.

The results shown in Figures 2 and 3 demonstrate that the antisense oligonucleotides synthesized (and claimed) by the inventor are superior to the oligonucleotides described in the literature. In particular, it may be highlighted that the former are: a. Less toxic; b. Much more potent in inhibiting cPLA₂ protein expression.

The antisense oligonucleotides are especially preferred, compared to Pi, P2, ISl and IS2 since they may be introduced into the cells and perform their activity without cell delivery systems like lipofectin.

Example 3

Effect of cPLA₂ antisense oligonucleotides on cPLA₂ expression and superoxide production in peripheral blood human neutrophils

The effect of the different PPS antisense oUgonucleotides, and their combinations, on cPLA₂ expression and on superoxide production was studied in peripheral blood human neutrophils. Naked antisense oligonucleotides were added (at 1 μM final concentration) to 2xl0⁵ neutrophils for 6 h at 37°C. Neutrophils (95% purity) were isolated by Ficoll/Hypaque centrifugation, dextran sedimentation and hypotonic lysis of erythrocytes [Levy, R. et al. (2000) Blood 95:660-665]. As shown in Fig. 7, there was a sUght though significant (P<0.05) inhibition of superoxide production even after 6 hours of incubation with the neutrophils. In another experiment, a similar effect was shown after 16 h of incubation (data not shown).

Inhibition of superoxide production by the various oligonucleotide antisenses was significantly improved when the cells were stimulated by physiological agonists such as fMLP, opsonized zymosan (OZ) (Figure 8), LTB4, angiotensin II or AGEs (advanced glycation end products) (data not shown) which bind specific receptors on cell membranes.

The effect of the PPS was significantly higher when neutrophils were purified from patients with inflammatory diseases (Uke rheumatic arthritis, asthma or sepsis, data not shown), than when the neutrophils were from healthy controls. This phenomena is consistent with the inventor's earUer study [Levy, R. et al. (2000) id ibid.] which reported that the level of cPLA₂ in neutrophils is higher during the diseases indicating increase rate of synthesis, and thus more prone to targeting.

It is important to note that the experiments portrayed in Figures 3 to 6 were performed with the non-physiological stimulant PMA, an extremely potent activator of NADPH oxidase that bypasses the receptors and acts on PKC. This enabled the analysis of the role of the antisenses directly on NADPH oxidase, since under these conditions the effect of the expression of the different receptors and their binding to stimulants is eliminated.

Example 4

Effect of cPLA₂ antisense oligonucleotides on cPLA₂ expression and superoxide production in rat microglia

The effect of the antisenses and their combinations was studied on microglia isolated from rat brain. The PPS antisense oligonucleotides were added (at 1 μM final concentration) to microgUa ceUs for 16 h (similar to the conditions used for monocytes). There was a significant inhibition of cPLA₂ protein expression. The ceUs were stimulated with 2 mg/ml PMA or with 10 μM of Amyloid β, and superoxide production was analyzed by the fluorescence probe Amplex Red. As shown in Figure 9, the antisenses caused significant inhibition of superoxide production, in correlation with cPLA₂ protein expression. Interestingly, antisense C8, which did not match the rat sequence by 1 base, did not cause inhibition of superoxide production, indicating the high specificity of the antisenses. Inhibition was much higher when the ceUs were stimulated with Amyloid β. Incubation of microglia for 48 h with the antisense oligonucleotides caused higher inhibition of cPLA₂ expression and of superoxide production (data not shown). The results are of particular importance since Amyloid β plays an important role in the pathogenesis of brain and neurodegenerative diseases, such as Alzheimer.

Incubation of all cell types with X150 antisense concentration was not toxic to the ceUs and did not affect* cell functions which are not regulated by cPLA₂ (data not shown).

Example 5

Animal model of inflammation: Collagen-induced Arthritis

Collagen-induced arthritis (CIA) is an experimental model of autoimmune arthritis that has many clinical and pathological similarities to rheumatoid arthritis (RA). CIA is induced by immunizing susceptible animals (e.g. DBA black mice) with type II collagen (CII) as described [Bendele, A.M. et al. (2000) Arthritis & Rheumatism, 43:2648-58]. All mice were maintained in a specific pathogen-free environment, and fed standard mouse chow and water. Chick CII (Sigma-Aldrich, 2 mg/ml) was dissolved overnight at 4°C in 10 mM acetic acid and combined with an equal volume of CFA (complete Freund's adjuvant). CFA was prepared by mixing 100 mg of heat-kiUed M. tuberculosis (H37Ra, Difco, Detroit, Michigan, USA) with 20 ml of incomplete Freund's adjuvant (Sigma-Aidric-i, St. Louis, Missouri, USA). Mice (aged 7 to L0 weeks) were injected intradermally at the base of the tail and boosted at day 7 or 21.

Control mice were treated with CFA without CII. The severity of arthritis was monitored by direct examination with a digital caUper according to the following scale: grade 0, no swelling; 1, slight swelUng and erythema; 2, pronounced inflammation; and 3, joint rigidity. Each Umb was graded, giving a maximum possible score of 12 per animal. Fluid from animal paws was aspirated to determine cytokines (mRNA and protein level) and white blood ceUs. After sacrifice, paws were collected, fixed, decalcified, and paraffin embedded. Sections were stained with hematoxylin and eosin and scored according to the following scale: 0, no inflammation; 1, slight thickening of the synovial cell layer and/or some inflammatory ceUs in the subhning; 2, thickening of the synovial lining, infiltration of sublining, and localized cartilage erosions; and 3, infiltration in the synovial space, pannus formation, cartilage destruction, and bone erosion.

Detection of anti-CII antibodies: ELISA for antibodies to CII was performed by HRP-conjugated secondary antibody specific for IgGl, IgG2a, IgG2b, IgG3, or IgM and IgA.

Cell isolation: Positive selection of splenocyte subsets of synovial cells were performed using specific biotin-conjugated antibodies against CD lib, CD3, CD4, and CD8, and biotin binder Dynabeads. After positive selection of CDllb⁺ and CD3⁺ synovial cells, synovial ceUs were incubated with biotin CD45 and negatively selected using an excess of avidin-magnetic beads. The remaining CD45-negative cells were used for RNA extraction. Synovial fluid leukocytes were obtained from synovial effusions and purified by FicoU-Hypaque density gradient centrifugation.

The model of CIA was successfuUy developed by the inventors, as demonstrated, e.g. by the swollen limb of an exacerbated CIA mouse compared to the Umb of a control mouse (Fig. 10A). Histological assessment of the CIA mouse Umb (7ig. 10B) was in correlation with the severity of arthritis, monitored by direct examination of the limb as presented in Fig. 10A. Infiltration of inflammatory cells (especially neutrophils) is shown in a joint section of a CIA mouse (Fig. IOC). CIA mice showed severe difficulties in walking (data not shown).

Based on preliminary experiments performed with various PPS concentrations and combinations, the optimal concentration of 2mg/Kg was defined, for a combination of 3 different PPS (2, 4 and 10), also referred to herein as cocktaU. This concentration is within the range used for human therapy and in animal models.

For treatment of the inflammatory condition, sterile stock of antisenses (100 μM) is dissolved in sterile saline at the desired concentrations, and injected to sick mice either i.v., intradermally at the base of the tail, or at the inflamed joints.

As shown in Figure 11, intravenous injection of 2 mg/kg of the "cocktail" every day for 14 days caused significant remission of the arthritis, as detected by a reduction in swelling of the limb (Fig. 11A), by disease severity score, by full recovery of the mice ability to move and to run freely (data not shown), and by reduction in serum IL-6 and TNFα levels (Fig. 11B).

Example 6

Animal model of inflammation: Peritonitis

Model mice peritonitis is being developed in CD1 mice by injection of Candia as previously described [Levy, R. et al. (1989) J. Biol. Regul. Homeost. R Agents 3:5-12], or by injection of different doses of gram positive bacteria peritonitis wiU be induced with lethal doses of Candida or bacteria (S. epidermitis) or gram negative (E.Coli) which cause animal killing and with moderate doses which cause a moderate disease. The 50% lethal doses were determined as 6X10⁸ CFU for S. epidermitis and 1.5X10⁷ for CFU E. coli. The markers for infection and/or inflammation are: the number and population of blood cells in the peritonitis area, the concentration of inflammatory cytokines in the blood, such as TNF , ILl and IL6, and histological analyses of peritoneal sections. Mice injected with a lethal dose of bacteria are treated with antisenses 2 h after injection of the bacteria followed by antisenses injection in different time intervals. In these experiments, the effect of antisenses on mice survival is evaluated. For mice injected with lower doses of bacteria, the effect of antisenses (injected as described) is evaluated on the pathology by the infection and/or inflammation markers.

Example 7

Animal model of inflammation: Sterile Peritonitis

A model of sterile peritonitis was developed in ICR mice by intraperitoneal injection of 3 ml sterile 4% thioglycoUate (TG) as described previously [Segal, B.H. et al. (2002) J Leukoc Biol 71:410]. Assessment of inflammation was determined by the number and population of blood ceUs in the peritonitis cavity, the concentration of LTB and the presence of inflammatory cytokines, TNFα and IL6, in cell free peritoneal fluid and in serum. 10 ml of sterile PBS were injected to the peritoneal cavity in order to collect the ceUs. The number of cells was determined by microscopy after trypan blue staining. The composition of the cell population was determined by FACS using antibodies against anti mouse neutrophils (MCA771F), anti mouse macrophages (F4/80) and anti mouse lymphocytes (CD3). The composition of the cell population was also determined under microscopy after Giemsa staining. Figures 12A-12B present the changes in white blood cell count (Fig. 12A) and cell population (Fig. 12B) during 4 days of sterile peritonitis. High levels of neutrophils were detected 24 h after TG injection, which were later replaced by monocyte- macrophages. There was a significant elevation in stimulated phagocyte superoxide production, with the highest rate at 24 h post peritonitis induction.

The levels of LTB4 in the serum and in the peritoneal cavity during 24 h of sterile peritonitis are demonstrated in Figures 13A-13B. 1 hour after the induction of peritonitis there was a significant elevation of LTB4 levels in the blood. LTB4 levels stayed high during 5h and than decreased to half after 8 hours. At 16 h after peritonitis induction, LTB4 could not be detected in the blood. A similar pattern was observed in the peritoneal cavity, but the decay was slower and only after 24 h, LTB4 ceased to be detected.

According to the present results and consistent with the literature, the first ceUs to accumulate in the peritonitis model were neutrophils. Thus, in the first set of experiments the effect of the antisense oligonucleotides was analyzed primarily on neutrophil accumulation and activity, after 24 h of induction of sterile peritonitis. Two doses of a specific combination of PPS antisense oligonucleotides against CPLA2 (the "cocktail") dissolved in sterile water (0.2 ml) were administered i.v. in the tail of the mice 1 h and 4 h after induction of peritonitis. As demonstrated in Figures 14A-14C (results of two mice) this treatment caused a significant reduction in the number of neutrophils present in the peritoneal cavity (represented as cell number and cell population distribution detected by FACS analysis) and a slight inhibition of stimulated superoxide production by * the peritoneal cells 24 h after induction of inflammation. The efficiency of the cocktail on reduction of peritoneal recruited neutrophils and on superoxide production in 34 mice compared to 34 untreated mice with sterile peritonitis is presented in Figures 15A-15B. Superoxide release from unstimualted cells is of great importance since it reflects the behavior of the peritoneal cells in the peritoneum cavity. Thus, the release of superoxide from resting cells was assessed with the fluorescent probe Dihydrorhodamine-123 (1 mM) which is a very sensitive method and can detect low levels of superoxide. As shown in the representative results in Figure 16, the cocktail treatment for 24 h after induction of peritonitis significantly decreased the release of superoxides by peritoneal ceUs.

The effect of the antisense oUgonucleotide treatment was^" studied on peritoneal ceU population during 4 days of sterile peritonitis. The number of recruited neutrophils was dramaticaUy reduced and that of macrophages was significantly lower in the peritoneum of treated mice during the 4 days of peritonitis (Fig. 17A-17B). Stimulated superoxide production by the peritoneal cells of the antisense-treated mice was significantly lower than in the untreated mice during the four days of peritonitis (Fig. 18A-18B).

The antisense cocktail treatment reduced the levels of LTB in the peritoneal cavity as measured during 24h after induction of peritonitis (Figures 19A-19B) in correlation with the reduction of neutrophils recruited to peritoneal cavity (Figs. 20A-20B).

Accumulation of antisense oligonucleotides in peritoneal blood cells 24 h after i.v. injection was detected using fluorescently labeled antisense oligonucleotides (labeled with FITC at the last nucleotide) (Figs. 21A-21B). Distribution of the fluorescent antisense oligonucleotides in the different organs by histological section was also analyzed (data not shown). In further experiments, different antisense overdoses were administered, in order to determine their toxicity. A cocktail X100 was not toxic to the mice (data not shown).

Example 8

Animal model of inflammation: Experimental acute lung injury induced by:

1 - LPS/zymosan administration.

Mice are anesthetized and mechanically ventilated. During the experiments, oxygen gas is supplied continuously to the ventilatory system. One minute prior to intravenous (i.v.) administration, two deep inhalations (3x tidal volume) are delivered to standardize volume history and measurements are made as baseline. Mice then receive 3 mg/kg of LPS from Escherichia coli Olll:B4 (Sigma Chemical Co., St.Louis, MO) i.v. Two hours later, 10 mg/kg of zymosan A from Saccharomyces cerevisiae (Sigma) are administered i.v. In saline-treated group, animals receive saline instead of LPS and zymosan in the same manner, and serve as controls. In all groups, measurements are made at 30 minute intervals for 4 hours. In some animals, the observation period extended up to 6 hours. To assess the development of lung injury physiologically, EL (a reciprocal of lung compliance) is measured. Tracheal pressure (Ptr), flow and volume (V) will be measured. EL and lung resistance (RL, data not shown) are calculated by adjusting the equation of motion: Ptr =ELV +RL (dY/dt)+K, where ET is a constant. Changes in ΕL reflect lung parenchymal alterations and stiffening of the lungs.

2 - HCl aspiration.

After baseline measurements, anesthetized and mechanicaUy ventilated mice receive 2 ml/kg of HCl (pH =1.5) i.t., followed by a bolus of air (30 ml/kg). In saline-treated group, animals receive saline instead of HCl in the same manner and serve as controls. In all groups measurements are made at 30 minute intervals for 2 hours. In some animals, the observation period is up to 5 hours. ΕL measurement is a physiologic parameter to assess acute lung injury. Assessment of pulmonary edema - At the end of experiment, the lung wet/dry mass ratios are calculated to assess pulmonary edema. After the trapped blood is drained from the excised lungs, measurements of the lung wet mass are made. The lungs are then heated at 90°C to constant mass in a gravity convection oven for 72 h and the residue weighed as the lung dry mass. Bronchoalveolar lavage fluid - At the end of experiment, bronchoalveolar lavage (BAL) is performed (using 5x 1 ml phosphate-buffered saline) in each group. In each animal, 90% (4.5 ml) of the total injected volume is consistently recovered. After BAL fluid is centrifuged at 450 g for 10 minutes, the total and differential ceU counts of the BAL fluid is determined from the cell fraction. The supernatant is stored at -70 °C until measurement of protein content. The concentration of protein is measured by Lowry's method using bovine serum albumin as a standard.

Thromboxane and leukotriene measurement - is determined by using enzyme immunoassay (ΕIA) kits.

Claims

1. An antisense oUgonucleotide directed against the open reading frame (ORF) of the cytosolic phospholipase A2 (CPLA2) mRNA sequence, and functional analogs, derivatives or fragments thereof, wherein the complementarity of said antisense oUgonucleotide is within the region between nucleotides 145 to 400 of said ORF, and wherein said antisense oligonucleotide is capable of inhibiting the expression of the CP A2 protein.

2. The antisense oUgonucleotide of claim 1, wherein said antisense oligonucleotide is also capable of inhibiting NADPH oxidase activity.

3. An antisense oligonucleotide directed against the 5' region of the open reading frame of the cytosoUc phosphoUpase A2 (CPLA2) mRNA sequence, and functional analogs, derivatives or fragments thereof, wherein said antisense oligonucleotide has the sequence as denoted by any one of SEQ. ID. No.l, SEQ. ID. No.2, SEQ. ID. No.3, SEQ. ID. No.4 SEQ. ID No.5, and SEQ. ID. No.6.

4. The antisense oUgonucleotide of any one of claims 1 to 3, wherein said antisense oligonucleotide is from 15 up to 30 nucleotides long, preferably 17 to 21 nucleotides long.

5. The antisense oUgonucleotide of any one of claims 1 to 4, wherein the first three and/or the last three nucleotides of said oligonucleotide have a phosphorothioate modification.

6. The antisense oUgonucleotide of any one of claims 1 to 5, wherein the tenth nucleotide of said oligonucleotide has a phosphorothioate modification.

7. The antisense oUgonucleotide of any one of claims 1 to 4, wherein the first three and/or the last three nucleotides of said oUgonucleotides are 2-0- metjiylated.

8. The antisense oligonucleotide of any one of claims 1 to 7, for inhibiting superoxide production and release.

9. The antisense oligonucleotide of claim 8, wherein said inhibition occurs in any one of neutrophils, monocytes, and macrophages, preferably neutrophils.

10. The antisense oligonucleotide of claim 9, for the treatment of conditions related to Aβ plaque accumulation.

11. The antisense oligonucleotide of any one of claims 8 to 10, for the treatment and/or prevention of a central nervous system (CNS)-related disease, wherein said disease is selected from the group consisting of Alzheimer's disease, or Parkinson's disease, amyotrophic lateral sclerosis (ALS), brain ischemic injury and traumatic head injury.

12. The antisense oligonucleotide of any one of claims 1 to 7, for use as an inhibitor of inflammation processes related to cPLA₂ expression.

13. The antisense oligonucleotide of claim 12, for use in the treatment and/or prevention of inflammatory conditions.

14. The antisense oligonucleotide of claim 13, wherein said conditions are any one of rheumatoid arthritis, adult respiratory distress syndrome (ARDS), asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease.

15. The antisense oUgonucleotides of any one of claims 1 to 7, for use in the treatment and/or prevention of conditions in which microglia ceUs are activated and release reactive oxygen species (ROS) and/or pro-inflammatory mediators.

16. The antisense oligonucleotide of claim 15, wherein said conditions are selected from the group consisting of inflammations, infections, and ischemic disease.

17. The antisense oUgonucleotide of any one of the preceding claims, optionally labeled with one of fluorescent, radioactive, metal particle, and any suitable labeling means.

18. A pharmaceutical composition comprising as active agent at least one antisense oligonucleotide as defined in any one of claims 1 to 9.

19. A pharmaceutical composition comprising as active agent a combination of at least two antisense oligonucleotides as defined in any one of claims 1 to 9.

20. The pharmaceutical composition of claim 19, wherein said combination comprises the following oligonucleotides: SEQ. ID. No.l together with SEQ. ID. No.3, or SEQ. ID. No.l together with SEQ. ID. No.2, or SEQ. ID. No.l together with SEQ. ID. No.6, or SEQ. ID. No.l together with SEQ. ID. No.2 and SEQ. ID. No.3, or SEQ. ID. No.4 together with SEQ. ID. No.6, or SEQ. ID. No.2 together with SEQ. ID. No.6, or SEQ. ID. No.2 together with SEQ. ID. No.3, or SEQ. ID. No.3 together with SEQ. ID. No.6.

21. The pharmaceutical composition of any one of claims 18 to 20, for medical use.

22. The pharmaceutical composition of claim 21, for the treatment of inflammation processes related to cPLA₂ expression and/or free radical release by phagocyte NAEPH oxidase.

23. The pharmaceutical composition of claim 21, for the treatment of inflammatory conditions.

24. The pharmaceutical composition of claim 23, wherein said conditions are one of rheumatoid arthritis, ARDS, asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease.

25. The pharmaceutical composition of claim 21, for the treatment and/or prevention of conditions in which microglia cells are activated and release reactive oxygen species (ROS) and/or pro-inflammatory mediators.

26. The pharmaceutical composition of claim 25, wherein said conditions are selected from the group consisting of inflammations, infections, and ischemic disease.

27. A pharmaceutical composition comprising as active agent at least one antisense oUgonucleotide as defined in any one of claims 1 to 11, for the treatment of conditions related to Aβ plaque accumulation.

28. The pharmaceutical composition of claim 27, for the treatment and/or prevention of a CNS-related disease, wherein said disease is selected from the group consisting of Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis (ALS), and brain ischemic and traumatic head injury.

29. The pharmaceutical composition of any one of the preceding claims, optionally further comprising buffers, additives, stabilizers, dfluents and/or excipients.

30. Use of an antisense oUgonucleotide as defined in any one of claims 1 to 7 and 12 to 14, for the preparation of a pharmaceutical composition for the treatment and/or prevention of inflammatory conditions, wherein said conditions may be any one of rheumatoid arthritis, ARDS, asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease.

31. Use of an antisense oUgonucleotide as defined in any one of claims 1 to 7, 15 and 16, for the preparation of a pharmaceutical composition for the treatment and/or prevention of conditions in which microgUa ceUs are activated and release reactive oxygen species (ROS) and/or pro-inflammatory mediators, and wherein said conditions are selected from the group consisting of inflammations, infections, and ischemic disease.

32. Use of an antisense oUgonucleotide as defined in any one of claims 1 to 7 and 12 to 14 for the treatment of conditions associated with cPLA₂ activation.

33. Use of an antisense oligonucleotide as defined in any one of claims 1 to 11, for the treatment and/or prevention of conditions related to Aβ plaque accumulation.

34. The use of claim 33, for the treatment and/or prevention of neurodegenerative diseases, particularly Alzheimer's and Parkinson's.

35. A method of treatment of conditions associated with cPLA₂ activation, comprising administering a therapeuticaUy effective amount of at least one antisense oUgonucleotide as defined in any one of claims 1 to 7 and 12 to 14, or compositions comprising thereof, to a subject in need.

36. A method of treatment of inflammatory conditions, comprising administering a therapeutically effective amount of at least one antisense oligonucleotide as defined in any one of claims 1 to 7 and 12 to 14, or compositions comprising thereof, to a subject in need.

37. The method of claim 36, wherein said inflammatory conditions may be any one of rheumatoid arthritis, ARDS, asthma, rhinitis, idiopathic pulmonary fibrosis, peritonitis, cardiovascular inflammation, myocardial ischemia, reperfusion injury, atherosclerosis, sepsis, trauma, diabetes type II, retinopathy, psoriasis, gastrointestinal inflammation, cirrhosis and inflammatory bowel disease.

38. A method for the treatment and/or prevention of conditions in which microglia cells are activated and release reactive oxygen species (ROS) and/or pro-inflammatory mediators comprising administering a therapeutically effective amount of at least one antisense oligonucleotide as defined in any one of claims 1 to 7, 15 and 16, or compositions comprising thereof, to a subject in need.

39. The method of claim 38, wherein said conditions are selected from the group consisting of inflammations, infections, and ischemic disease.

40. A method of treatment of conditions related to Aβ plaque accumulation, comprising administering a therapeutically effective amount of at least one antisense oUgonucleotide as defined in any one of claims 1 to 11, or compositions comprising thereof, to a subject in need.

41. A method of treatment of neurodegenerative diseases, preferably Alzheimer's and Parkinson's disease, comprising administering a therapeutically effective amount of at least one antisense oUgonucleotide as defined in any one of claims 1 to 11, or compositions comprising thereof, to a subject in need.

42. An in vivo or in vitro method of inhibiting cPLA₂ expression, comprising contacting cells with the antisense oligonucleotide of any one of claims 1 to 8 or with compositions comprising thereof, for a suitable amount of time.

43. An in vivo or in vitro method of inhibiting CPLA2 activity, comprising contacting cells with the antisense oligonucleotide of any one of claims 1 to 8 or with compositions comprising thereof, for a suitable amount of time.

44. The method of claims 42 and 43, wherein said cells are phagocytic cells.