AU2001268863B2 - Modulation of FAS and FASL expression - Google Patents

Description

WO 02/18593 PCT/CA01/00845 1 MODULATION OF FAS AND FASL EXPRESSION FIELD OF THE INVENTION The present invention relates compositions useful for modulating Fas and Fas ligand expression on cells and for modulating efficacy of therapeutic agents.

BACKGROUND OF THE INVENTION The Fas (Apo-1, CD95) and Fas ligand (FasL, CD95L) system is one of the best-studied cell death systems. Fas is a type-I membrane protein abundantly expressed by cells in various tissues and particularly on activated T cells, heart cells, kidney cells and hepatocytes. FasL is a type-II transmembrane protein expressed particularly on activated T cells and natural killer cells (Nagata, S.

Ann. Rev. Genet. 33:29, 1999), and is expressed constitutively in immuneprivileged sites as, for example, the eye and testis (Griffith et al. Science 270:630, 1995).

Fas and FasL interactions (Fas/FasL) play an essential role in the regulation of immune cells and in the elimination of autoreactive cells (Sabelko- Downes et al. Curr. Opin. Immunol. 12:330, 2000). In addition, Fas/FasL mediates the killing of cancer cells and of virus-infected cells (Famularo et al.

Med. Hypoth. 53:50, 1999; Owen-Schaub et al. Int. J. Oncol. 17:5, 2000). In contrast, FasL, expressed on cancer cells, may attack cells of the immune system (O'Connell, J. Exp. Med. 184:1075, 1996) or facilitate local tumor invasion by killing surrounding tissue (Yoong et al. Am. J. Pathol. 154:693, 1999). FasL, expressed on activated T cells, may also participate in tissue damage in fulminant WO 02/18593 PCT/CA01/00845 2 hepatitis and in graft-versus-host disease (Kondo et al. Nature Med. 3:409, 1997; Braun et al. J. Exp. Med. 183:657, 1996).

Binding of FasL to Fas, or cross-linking of Fas with agonistic antibodies, induces apoptosis (Nagata, S. Ann. Rev. Genet. 33:29, 1999) that results in cell death. Apoptosis is an active cellular death process characterized by distinctive morphological changes that include condensation of nuclear chromatin, cell shrinkage, nuclear disintegration, plasma membrane blebbing, and the formation of membrane-bound apoptotic bodies (Wyllie et al. Int. Rev. Cytol. 68:251, 1980). A molecular hallmark of apoptosis is degradation of cellular nuclear DNA into oligonucleosomal-length fragments as the result of activation of endogenous endonucleases (Wyllie A. Nature 284:555, 1980). Caspases (cysteine-aspartylspecific proteases) have been implicated as key enzymes in the execution of the late stage of apoptosis. The binding of FasL to Fas activates a cascade of caspases via a FADD adaptor (Fas-associated protein with death domain), which leads to the cleavage of various cellular substrates and to DNA fragmentation (Nagata, S.

Ann. Rev. Genet. 33:29, 1999).

Synthetic oligonucleotides are polyanionic sequences that can be internalized by cells (Vlassov et al. Biochim. Biophys. Acta 1197:95, 1994) and bind selectively to nucleic acids (Wagner, R. Nature: 372:333, 1994), to specific cellular proteins (Bates et al. J. Biol. Chem. 274:26369, 1999) and to specific nuclear proteins (Scaggiante et al. Eur. J. Biochem. 252:207, 1998), and inhibit cell proliferation. Proliferation is the culmination of the progression of a cell through the cell cycle, resulting in the division of one cell into two cells.

Alterations in cell cycle progression occur in all cancers and may result from over-expression of genes, mutation of regulatory genes, or abrogation of DNA damage checkpoints (Hochhauser D. Anti-Cancer Chemotherapeutic Agents 8:903, 1997).

Synthetic phosphorothioate oligonucleotides containing unmethylated CpG dinucleotides flanked by two 5' purine and two 3' pyrimidine (CpG motifs) are reported to induce the synthesis of cytokines by macrophages and B cells, to increase the activity of NK cells and cytotoxic T lymphocytes, and to enhance Thelper 1 response (Ballas et al. J. Immunol. 157:1840, 1996; Klinman et al. Proc. Natl.

Acad. Sci. USA93:2879, 1996; Lipford et al. Eur. J. Immunol. 27:2340, 1997) A base synthetic CpG motif is reported to block Fas expression on activated B cells and to block apoptosis induced by anti-Fas monoclonal antibodies (Wang et al. Cell.

Immunol. 180:162, 1997). Irradiation is reported to upregulate the expression of Fas on cancer cells (Sheard et al. Int. J. Cancer 73:757, 1997; Nishioka et al. Int. J. Mol.

Med. 3:275, 1999).

The ability to modulate the Fas/FasL system has many clinical applications for use in diseases including, but not limited to, neoplastic autoimmune, degenerative cardiovascular diseases. However, most prior Fas/FasL modulating agents have proven to be less than adequate in clinical applications. Moreover, many of these agents are inefficient, toxic or have significant adverse effects.

Therefore, there is a continuing need for novel compositions and methods that modulate the expression of Fas and FasL on cells. There is also a need for novel compositions and methods that modulate the efficacy of Fas and FasL modulatory agents on disease. There is also a need for novel compositions and methods that modulate the expression of Fas and FasL on cells in order to treat diseases in animals or humans associated with altered expression of Fas or FasL on cells.

SUMMARY OF THE INVENTION The present invention fulfills these needs by providing a novel method, employing new compositions comprising a synthetic phosphodiester oligodeoxynucleotide (hereinafter, "sequence") selected from the group consisting of (GG)n, (GT)n, a(GT)nb, a(GA)nb and a (GC)nb, wherein n is an integer between 1 and 3, and a and b are independently either non or one or more As, Cs, Gs, or Ts, or combinations thereof, wherein the total number of bases in the composition is between 2 and 10, preferably 4 to 8, more preferably 5 to 7, and most preferably 6.

The present invention provides new uses for these compositions. This composition is combined with a pharmaceutically acceptable carrier, and is administered to an animal or a human in an amount effective to modulate Fas and FasL expression in the animal or the human. This composition is also combined with a pharmaceutically acceptable carrier, and is administered to an animal or a human having a disease in an amount effective to modulate Fas and FasL expression in order to treat the disease in the animal or the human. This composition is also administered to an animal or human to modulate the efficacy of Fas and FasL modulatory agents, comprising administration of the composition in an amount effective to modulate m:\specifications\090000\94000\94836desnew.doc 20/06 '07 16:56 FAX 613 8618 4199 FB RICE CO. 1011

O

O 4 efficacy of Fas and FasL modulatory agents to modulate Fas and FasL, or to treat an o animal or human having a disease. Another new use for this composition of the present Sinvention is to modulate, and preferentially potentiate, the efficacy of a therapeutic agent to treat a disease, comprising administration of the composition in a rC 5 pharmaceutically acceptable carrier, optionally in combination with a therapeutic agent, O in an amount effective to modulate efficacy of the therapeutic agent administered to an 00 animal or a human. The compositions of the present invention may be administered at C, any time before, during, or after administration of the therapeutic agent, in order to modulate the efficacy of the therapeutic agent. The compositions of the present o 10 invention may also be administered in vitro, for example to animal or human cells or Stissues.

In a preferred embodiment, the composition of the present invention comprises a sequence selected from the group consisting of (GT)n, a(GT)nb, a(GA),b and a wherein n is an integer between 1 and 3, and a and b are independently either none or one or more As, Cs, Gs, or Ts, or combinations thereof provided the total number of bases in the composition is 6. In another preferred embodiment, the composition of the present invention comprises this sequence of 6 bases in combination with a pharmaceutically acceptable carrier. In yet another preferred embodiment, the composition of the present invention comprises this sequence of 6 bases in combination with a therapeutic agent and a pharmaceutically acceptable carrier. These compositions may be used in any of the methods described in the preceding paragraphs and throughout the specification.

The unexpected and surprising ability of the sequences of the present invention to modulate the expression of Fas and FasL addresses a long felt unfulfilled need in the medical arts and provides an important benefit for animals, including humans- Accordingly, it is desirable that the present invention provide a new composition comprising a synthetic phosphodiester oligodeoxynucleotide (hereinafter, "sequence") selected from the group consisting of a(GT)nb, a(GA),b and a (GC)nb, wherein n is an integer between 1 and 3, and a and b are independently either none or one or more As, Cs, Gs, or Ts, or combinations thereof, wherein the total number of bases in the composition is 2 to The invention also provides a composition when used for modulating Fas or FasL expression in an animal or a human, the composition comprising a synthetic phosphodiester oligonucleotide sequence of 6 bases, selected from the group consisting of (GG)n, a(GT)nb, a(GA),b, and a(GC),b wherein n is an integer between 1 and 3, and a and b are independently either none or one or more As, Cs, Gs or Ts, or c;\nrportbl\meldocs\mjc\165627_1.doc COMS ID No: SBMI-07841754 Received by IP Australia: Time 15:58 Date 2007-06-20 20/06 '07 16:57 FAX 613 8618 4199 FB RICE CO. a 012 0 o 4a c( Scombinations thereof, wherein the composition is useful for modulating Fas or FasL Sexpression in the animal or the human when administered in an effective amount to the l animal.

In addition, the present invention also provides a composition when used for modulating the efficacy of a therapeutic agent in an animal or a human, the 00 composition comprising a synthetic phosphodiester oligonucleotide sequence of 6 00 bases, selected from the group consisting of (GT)n, a(GT)nb, a(GA)nb, and IS a(GC),b, wherein n is an integer between 1 and 3, and a and b are independently either o none or one or more As, Cs, Gs, or Ts, or combinations thereof, wherein the composition is useful for modulating efficacy of a therapeutic agent in the animal or the C human when administered in an effective amount to the animal.

The present invention also provides a composition comprising a synthetic phosphodiester oligonucleotide sequence of 6 bases, wherein the sequence is any one of SEQ ID NO: 1 to SEQ ID NO: 18, selected from the group consisting of(GG)., (GT)n, a(GT),b, a(GA),b, and a(GC),b wherein n is an integer between 1 and 3, and a and b are independently either none or one or more As, Cs, Gs or Ts, or combinations thereof, wherein the composition is useful for modulating Fas or FasL expression in an animal or a human when administered in an effective amount to the animal.

The present invention also provides a composition comprising a synthetic phosphodiester oligonucleotide sequence of 6 bases, wherein the sequence is any one of SEQ ID NO: 1 to SEQ ID NO: 18, selected from the group consisting of a(GT).b, and a(GC)nb, wherein n is an integer between I and 3, and a and b are independently either none or one or more As, Cs, Gs, or Ts, or combinations thereof, wherein the composition is useful for modulating efficacy of a therapeutic agent in an animal or a human when administered in an effective amount to the animal.

It is also desirable that the present invention provide a new composition comprising a synthetic phosphodiester oligodeoxynucleotide (hereinafter, "sequence") selected from the group consisting of a(GT)nb, a(GA)nb and a (GC).b, wherein n is an integer between 1 and 3, and a and b are independently either none or c;\nrportbl\meldocs\mje\1656 27 _1.doc COMS ID No: SBMI-07841754 Received by IP Australia: Time 15:58 Date 2007-06-20 1 one or more As, Cs, Gs, or Ts, combinations thereof, wherein the total number of bases in the composition is 4 to 8.

J It is also desirable that the present invention provide a new composition 00 Scomprising a synthetic phosphodiester oligodeoxynucleotide (hereinafter "sequence") selected from the group consisting of (GG)n, (GT)n, a(GT)nb, a(GA),b and a (GC),b, Cc wherein n is an integer between 1 and 3, and a and b are independently either none or 00 one or more As, Cs, Gs, or Ts, or combinations thereof, wherein the total number of 0 bases in the composition is 5 to 7.

(1 It is also desirable that the present invention provide a new composition comprising a synthetic phosphodiester oligodeoxynucleotide (hereinafter, "sequence") C selected from the group consisting of (GG)n, (GT)n, a(GT)nb, a(GA)nb and a (GC)nb, wherein n is an integer between 1 and 3, and a and b are independently either none or one or more As, Cs, Gs, or Ts, or combinations thereof, wherein the total number of bases in the composition is 6.

In yet another aspect, it is desirable that the present invention provides novel compositions comprising any of the sequences described herein, in combination with a pharmaceutically acceptable carrier.

It is also desirable that the present invention provides novel compositions comprising any of the sequences described herein, in combination with a therapeutic agent and a pharmaceutically acceptable carrier.

It is also desirable that the present invention provide for the use of any of the novel compositions described herein for the manufacture of a medicament.

It is also desirable that the present invention provide new uses for the compositions of the present invention.

It is also desirable that the present invention provide a method to modulate the Fas expression on cells.

It is also desirable that the present invention provide a method to modulate FasL expression on cells.

It is also desirable that the present invention provide a method to modulate the Fas expression on immune cells.

It is further desirable that the present invention provide a method to modulate FasL expression on immune cells.

It is also desirable that the present invention provide a method to modulate Fas expression on cancer cells.

It is also desirable that the present invention provide a method to modulate FasL expression on cancer cells.

m:\specifications\090000\94000\94836clmmjc.doc c It is also desirable that the present invention provide a method to treat a disease in an animal, including a human.

It is further desirable that the present invention provide a method to treat a 00 neoplastic disease.

It is also desirable that the present invention provide a method to treat an autoimmune disease.

00 It is desirable that the present invention provide a method to treat an 00 00inflammatory disease.

SIt is also desirable that the present invention provides a method to treat a proliferative disease It is desirable that the present invention provide a method to treat a lymphoproliferative disease.

It is also desirable that the present invention provides a method to treat a degenerative disease.

It is desirable that the present invention provide a method to treat a neurodegenerative disease.

It is also desirable that the present invention provides a method to treat a cardiovascular disease It is desirable that the present invention provide a method to treat a graft rejection.

It is also desirable that the present invention provides a method effective to treat an infection.

It is desirable that the present invention provide a method that modulates the effect of a therapeutic agent to treat disease.

It is desirable that the present invention provide a method that potentiates the effect of a therapeutic agent to treat disease.

It is also desirable that the present invention provides a method that potentiates the effect ofa Fas modulating agent.

It is desirable that the present invention provide a a method that potentiates the effect ofa FasL modulating agent.

It is also desirable that the present invention provides a method that potentiates the effect of an anti-neoplastic agent.

It is desirable that the present invention provide a method that potentiates the effect of an immunostimulatory agent.

It is also desirable that the present invention provides a method that potentiates the effect of an immunosuppressive agent.

m:\specifications\090000\94000\94836clmmjc.doc 0O 0 c It is desirable that the present invention provide a method that potentiates the y effect of an anti-inflammatory agent.

It is also desirable that the present invention provides a composition that is 00 0 simple to prepare.

It is desirable that the present invention provide a composition that is minimally Cc toxic to the recipient.

IND

00 00

ID

m:\specifications\090000\94000\94836clmmjc.doc WO 02/18593 PCT/CA01/00845 8 These and other objects, features and advantages of the present invention will become apparent after a review of the following detailed description of the disclosed embodiment and the appended claims.

DETAILED DESCRIPTION The present invention fulfills these needs by providing new compositions and new methods of using these compositions. The present compositions comprise a synthetic phosphodiester oligodeoxynucleotide (hereinafter, "sequence") selected from the group consisting of (GG)n, (GT)n, a(GT)nb, a(GA)nb, and a(GC)nb, wherein n is an integer between 1 and 3, and a and b are independently either none or one or more As, Cs, Gs, or Ts, or combinations thereof, wherein the total number of bases in the composition is between 2 and preferably 4 to 8, more preferably 5 to 7, and most preferably 6. The compositions of the present invention further comprise any of the sequences described herein in combination with a pharmaceutically acceptable carrier. The compositions of the present invention further comprise any of the sequences described herein in combination with a therapeutic agent and a pharmaceutically acceptable carrier.

The present invention provides new uses for these novel compositions.

This composition is combined with a pharmaceutically acceptable carrier, and is administered to an animal or a human an amount effective to modulate Fas and FasL expression in the animal or the human. This composition is also combined with a pharmaceutically acceptable carrier, and is administered to an animal or a human having a disease in an amount effective to modulate Fas and FasL expression in order to treat the disease in the animal or the human. This composition is also administered to an animal or human to modulate the efficacy of Fas and FasL modulatory agents, comprising administration of the composition in an amount effective to modulate efficacy of Fas and FasL modulatory agents to modulate Fas and FasL, or to treat an animal or a human having a disease.

Another new use for this composition of the present invention is to modulate, and preferentially potentiate, the efficacy of a therapeutic agent to treat a disease, comprising administration of the composition in a pharmaceutically acceptable carrier, optionally in a combination with a therapeutic agent, in an amount effective to modulate efficacy of the therapeutic agent administered to an animal or a human. The composition of the present invention may be administered at any time before, during, or after administration of the therapeutic agent, in order to modulate the efficacy of the therapeutic agent.

In a preferred embodiment the composition of the present invention comprises a sequence selected from the group consisting (GG)n, a(GT)nb, a(GA)nb and a (GC)nb, wherein n is an integer between 1 and 3, and a and b are independently either none or one or more As, Cs, Gs, or Ts, or combinations thereof provided the total number of bases in the composition is 6. In another preferred embodiment, the composition of the present invention comprises this sequence of 6 bases in combination with a pharmaceutically acceptable carrier. In yet another preferred embodiment, the composition of the present invention comprises this sequence of 6 bases in combination with a therapeutic agent and a pharmaceutically acceptable carrier. These compositions may be used in any of the methods described in this patent application.

As used herein the word "sequence" refers to a synthetic phosphodiester oligodeoxynucleotide comprised of adenine cytosine guanine and thymine with a total number of bases of 2 to 10, preferably 4 to 8, more preferably 5 to 7 and most preferably 6.

As used herein, the word "expression" refers to the cell surface concentration of Fas or of FasL.

As used herein, the words "response" refers to upregulation (increase) or downregulation (decrease) of Fas or of FasL expression.

As used herein, the word "modulates" refers to changes in the expression of Fas or of FasL. Such changes include upregulation and downregulation of Fas or of FasL expression. The word modulate is also employed to describe the ability of the novel sequences of the present invention to modulate the efficacy of therapeutic agents, including Gas and FasL modulating agents, to treat disease or to modulate Fas or FasL expression.

m:\speciflcations\090000\94000\94836desnew. doc WO 02/18593 PCT/CA01/00845 As used herein, the phrases "therapeutically effective", "effective amount" and "amount effective to" refer to an amount of a sequence effective to modulate the expression of Fas or of FasL.

As used herein, the word "disease" refers to a condition wherein bodily health is impaired.

As used herein, the phrase "therapeutic agent" is any agent approved by a regulatory agency of a country or a state government or listed in the U.S.

Pharmacopoeia or other generally recognized pharmacopoeia for use to treat a disease in an animal, including a human.

As used herein, the word "antineoplastic" refers to preventing the development, maturation, proliferation or spread of cancer cells As used herein, the word "potentiates" refers to a degree of synergism that is greater than additive.

As used herein, the word "synergism" refers to the coordinated action of two or more agents.

Administration of an effective amount of a sequence of the present invention to an animal, including a human, is a therapeutic treatment that prevents, treats or eliminates a disease including, but not limited to, neoplastic, autoimmune, proliferative, lymphoproliferative, degenerative, and cardiovascular disease; infection; inflammation; and, graft, tissue and cell rejection.

Compositions comprising one or more sequences and a pharmaceutically acceptable carrier are prepared by uniformly and intimately bringing into association the sequence and the pharmaceutically acceptable carrier.

Compositions comprising one or more sequences, a therapeutic agent and a pharmaceutically acceptable carrier are prepared by uniformly and intimately bringing into association the sequence, the therapeutic agent and the pharmaceutically acceptable carrier. Pharmaceutically acceptable carriers include liquid carriers, solid carriers or both. Liquid carriers are aqueous carriers, nonaqueous carriers or both and include, but are not limited to, solutions, suspensions and emulsions. Emulsions include, but are not limited to, oil emulsions, water in oil emulsions, water-in-oil-in-water emulsions, site-specific emulsions, longresidence emulsion, sticky-emulsions, microemulsions and nanoemulsions. Solid carriers are biological carriers, chemical carriers or both and include, but are not limited to, viral vector systems, plasmids, particles, microparticles, nanoparticles, microspheres, nanospheres, bacterial cell walls, minipumps, and biodegradable or nonbiodegradable natural or synthetic polymers that allow for sustained release of the sequences.

Preferred aqueous carriers include, but are not limited to, water, saline and pharmaceutically acceptable buffers. Preferred non-aqueous carriers include, but are not limited to, a mineral oil or a neutral oil including, but not limited to, a diglyceride, a triglyceride, a phospholipid, a lipid, an oil and mixtures thereof, wherein the oil contains an appropriate mix of polyunsaturated and saturated fatty acids. Optionally, stabilizing agents and excipients may be included regardless of the pharmaceutically acceptable carrier used to present the sequence to the cells.

The therapeutic effectiveness of a sequence may be increased by methods including, but not limited to, chemically modifying the base, sugar or phosphate backbone, chemically supplementing or biotechnologically amplifying the sequences using bacterial plasmids containing the appropriate sequences, complexing the sequences to biological or chemical carriers or coupling the sequences to tissue-type directed ligands or antibodies.

The composition of the present invention further comprises a composition comprising a sequence and a therapeutic agent, wherein, when the sequence and the therapeutic agent are combined with a pharmaceutically acceptable carrier and administered to an animal or human having a disease. The sequence modulates and preferentially potentiates the effect of the therapeutic agent on the disease.

Therapeutic agents include, but not limited to, anti-neoplastic, antiinflammatory, anti-autoimmune, anti-degenerative, Fas modulating and FasL modulating agents, or any combination thereof, and radiation therapy, or a combination of radiation therapy with therapeutic agents. These therapeutic agents include, but are not limited to, biologicals, drugs, chemotherapeutic drugs, immunostimulants, immunomodulators, immunotherapeutics, anti-virals, anti-infectives, antibiotics, cytokines, antigens, antibodies, nucleic acids, vaccines, aptabases, nucleic acids, antisense nucleic acids, telomerase inhibitors, caspase inducers, stable triple helix forming agents and genetic biology engineered and chemically synthesized agents, and agents that target cell death molecules for activation or inactivation.

Chemotherapeutic drugs include, but are no limited to, DNA damaging, DNAalkylating, DNA-cross-linking, anti-tumor antibiotic, topoisomerase inhibiting, purine m:\specification s\090000\94000\94836desn ew. doc inhibiting, pyrimidine inhibiting, microtubule stabilizing, microtubule-destabilizing, anti-metabolic, hormone antagonist, protein kinase inhibiting, HMG-CoA inhibiting, metaloproteinase inhibiting, CDK inhibiting, cycling inhibiting, angiogenesis inhibiting, differentiation enhancing and molecular biologically modified viral, bacterial and extotoxic agents.

Routes of administration include, but are not limited to, oral, topical, subcutaneous, transdermal, subdermal, intra-muscular, intra-peritoneal, intra-vesical, intra-articular, intra-prostatic, intra-arterial, intra-venous, intra-dermal, intra-cranial, intra-lesional, intra-tumoral, intra-ocular, intra-pulmonary, intra-spinal, placement within cavities of the body, nasal inhalation and impression into skin. It is to be understood that administration of the compositions of the present invention may occur in vivo, ex vivo or in vitro. For example, the compositions of the present invention may be administered to animal or human cells or tissues in vitro. Appropriate doses for in vitro administration are about 1 nM to 1 mM, preferably about 10 nM to 100 pM.

Depending on the route of administration, the volume per dose is preferably about 0.001 to 100 ml per dose, more preferable about 0.01 to 50 ml per dose and most preferably about 0.1 to 30 ml per dose. A sequence in a pharmaceutically acceptable carrier, or sequence plus therapeutic agent in a pharmaceutically acceptable carrier, can be administered in a single dose treatment, in multiple dose treatments or continuously infused on a schedule and over a period of time appropriate to the disease being treated, the condition of the recipient and the route of administration. Moreover, the therapeutic agent can be administered before, concurrently with, or after administration of the sequence.

Preferably, the amount of sequence administered per dose is from about 0.001 to 100 mg/kg, more preferably from about 0.01 to 10 mg/ml and most preferably from about 0.1 to 5 mg/kg. A sequence plus a chemotherapeutic agent is administered to an animal having a disease in an amount effective modulate and preferentially potentiate, the effect of the therapeutic agent. Preferably, the amount of therapeutic agent administered per dose is from about 0.001 to 1000 mg/m 2 or from about 0.01 to 1000 mg/kg, more preferably from about 0.01 to 500 mg/m 2 or about 0.01 to 500 mg/kg and most preferably from about 0.1 to 100 mg/m 2 or about 0.1 to 100 mg/kg. In one embodiment of a therapeutic agent, anti-Fas antibodies are employed and are administered in a dose of from about 0.003 to about 0.3 mg/kg, preferably 0.01 to about 0.1 mg/kg.

The particular sequence and the particular therapeutic agent administered, the amount per dose, the dose schedule and the route of administration should be decided m:\specifications\090000\94000\94836d esn ew. doc by the practitioner using methods known to those skilled in the art and will depend on the type of disease, the severity of the disease, the location of the disease and other clinical factors such as the size, weight and physical condition of the recipient. In addition, in vitro assays may optionally be employed to help identify optimal ranges for sequence and for sequence plus therapeutic agent administration.

The following examples will serve to further illustrate the present invention without, at the same time, however, constituting any limitation thereof On the contrary, it is to be clearly understood that resort may be had to various other embodiments, modifications, and equivalents thereof which, after reading the description herein, may suggest themselves to these skilled in the art without department from the spirit of the invention.

Example 1 Preparation of sequences Phosphodiester sequences were prepared by Sigma-Genosys (Woodlands, TX) using Abacus Segmented Synthesis Technology. Unless stated otherwise, the sequences were dispersed in autoclaved deionized water or in a pharmaceutically acceptable buffer such as, but not limited to, saline immediately prior to use.

Example 2 Cells All cell lines were obtained from the American Type Culture Collection (ATCC, Rockville, MD) and were cultured in the medium recommended by the ATCC. Table 1 shows the cell lines, their origins and their properties.

m:\specifications\090000\94000\94836desnew. doc Table 1 Cell lines CELL LINE ORIGIN PROPERTIES JURKAT Human T cell leukemia Suspension tumor model typical multi-drug resistance associated with protein UMUC-3 Human bladder cancer P-glycoprotein overexpression T-24 Human bladder cancer P53 mutated LNCaP Human prostate cancer Solid tumor model; metastatic TGFbeta 1 receptor-negative; androgendependent OVCAR-3 Human ovarian cancer Solid tumor model; metastatic p53 mutated; p21/waf-1/Cip-1 deleted SK-OV-3 Human ovarian cancer Solid tumor model; metastatic TGFbeta 1 receptor-negative; androgendependent MCF-7 Human breast cancer Solid tumor model; non-metastatic Caspase 3-negative; estrogen-depend Peripheral blood mononuclear cells (hereinafter, "PBMCs") were isolated from human blood by Ficoll-Hypaque (Amersham Pharmacia Biotech, Baie d"Urf6e, Quebec, Canada) density gradient centrifugation.

Cancer cells and PBMCs were seeded in 6 well flat-bottom microplates and were maintained at 37 0 C in a 5% CO 2 atmosphere. Unless stated otherwise, 2 X 105 cells/ml were incubated for 48 h with 0 ltg/ml (control) or 100 gg/ml (5.5 pM) (treated) of the sequences.

Example 3 Measurement ofFas and ofFasL at the cell surface Fas and FasL expression were measured by flow cytometry using anti-Fas FITC-conjugated monoclonal antibodies and anti-FasL PE-conjugated monoclonal antibodies in a FACScalibur Flow Cytometer (Becton Dickinson, San Jose, CA, USA) using the CELLQuest program (Becton Dickinson).

Results are expressed as percentage increase in the expression of Fas and FasL measured as treated cells compared to control cells.

m:\specifications\090000\94000\94836desnew.doc WO 02/18593 WO 0218593PCT/CA01I00845 Example 4 Modulation of Fas and FasL on Jurkat leukemia T cells Jurkat human leukemia T cells are an atypical multi-drug resistant human suspension tumor cell model. Jurkat T cells were incubated with the 6 base sequences shown in Table 2.

Table 2 Percentage increase of Fas and of FasL on Jurkat human leukemia T cells SEQUENCE INCREASE Fas FasL TGTGTG SEQ ED NO: I (6 bases) 52 93 GTGTGT SEQ ED NO:2 (6 bases) 52 43 TTTGTT SEQ ID NO:3 (6 bases) 258 497 GGTGGG SEQ ED NO:4 (6 bases) 61 22 GGGTGG SEQ ID NO:5 (6 bases) 150 145 TI'GITT SEQ ID NO:6 (6 bases) 126 140 AAGTAA SEQ ED NO:7 (6 bases) -4 -21 CCGTCC SEQ ID NO:8 (6 bases) 107 151 TGGTTG SEQ ID NO:9 (6 bases) 362 952 ATGTAT SEQ ID NO: 10 (6 bases) 246 393 CTGTCT SEQ EiD NO: 11 (6 bases) 203 413 TCGTTC SEQ ID NO: 12 (6 bases) 121 GGTTGG SEQ ID NO: 13 (6 bases) 99 86 GGAAGG SEQ ID NO: 14 bases) 67 88 GGCCGG SEQ lID NO: 15 (6 bases) 75 41 GGGGGG SEQ ID NO: 16 (6 bases) 118 49 GGGAGG SEQ ID NO: 17 (6 bases) 77 91 GGGCGG SEQ ID NO: 18 (6 bases) 208 356 WO 02/18593 WO 0218593PCT/CA01I00845 16 Example Modulation of Fas and of FasL on PBMCs PBMCs were incubated with the 6 base sequences shown in Table 3.

Table 3 Percentage increase of Fas and of FasL oilPBMCs SEQUENCE INCREASE Fas FasL TGTGTG SEQ ID NO:1 (6 bases) 126 260 GTGTGT SEQ ID NO:2 (6 bases) 94 99 TTTGTT SEQ ID NO:3 (6 bases) 1165 1528 GGTQOG SEQ lID NO:4 (6 bases) 57 59 GGGTGG SEQ ID NO: 5 (6 bases) 3 TTGTTT SEQ 11D NO:6 (6 bases) 338 441 AAGTAA SEQ ID NO:7 (6 bases) 13 -26 CCGTCC SEQ ID NO:28 (6 bases) 1046 1147 TG~iTTG SEQ ID NO:9 (6 bases) 1043 1322 ATGTAT SEQ IID NO: 10 (6 bases) 377 457 CTGTCT SEQ DD NO: I1I (6 bases) 310 476 TCGTTC SEQ ID NO: 12 (6 bases) 597 847 GUYTTUG SEQ ID NO: 13 (6 bases) -3 -32 GGAAGG SEQ IDNO: 14 bases) 112 162 GGCCGG SEQ ID NO: 15 (6 bases) 6 -29 GGGGGG SEQ ID NO: 16 (6 bases) 38 42 GGGAGG SEQ ID NO: 17 (6 bases) 266 356 GGGCGG SEQ ID NO:1IS (6 bases) 523 850 Example 6 Modulation of as and of FasL on T-24 bladder cancer cells T-24 bladder cancer cells are a p53 mutated human cell line T-24 cells X 10 cells/nil) were incubated with the 6 base sequences shown in Table 4.

WO 02/18593 WO 0218593PCT/CA01I00845 Table 4 Percentage increase of Fas and of FasL on T-24

SEQUENCE

bladder cancer cells

INCREASE

Fas FasL TGTGTG SEQ ID NO: t (6 bases) 84 213 GTGTGT SEQ ID NO:2 (6 bases) 93 77 TTTGTT SEQ ID NO:3 (6 bases) 279 549 GGTGGG SEQ ID) NO:4 (6 bases) 106 29 GGGTGG SEQ ED NO:5 (6 bases) 80 13 TT'GTTT SEQ ID NO:6 (6 bases) 116 152 AAGTAA SEQ ID NO:7 bases) 16 CCGTCC SEQ ID NO:8 (6 bases) 282 459 TGGTTG SEQ ID NO:9 (6 bases) 180 397 ATGTAT SEQ lID NO: 10 (6 bases) 90 150 CTGTCT SEQ lID NO: 11 (6 bases) 107 165 TCGTTC SEQ ID NO: 12 (6 bases) 105 74 GGTTGG SEQ ID NO: 13 (6 bases) 75 GGAAGG SEQ ID NO: 14 (6 bases) 46 14 GGCCGG SEQ DiD NO:15 (6 bases) 56 18 GGGGGG SEQ ID NO: 16 bases) 35 -14 GGGAGG SEQ ID NO: 17 (6 bases) 124 GGGCGG SEQID NO: 18 bases) 139 205 Example 7 Modulation of Fas and of FasL on UMIUC-3 bladder cancer cells UMUC-3 bladder cancer cells are a P-glycoprotein overexpressing human cell line. UMUC-3 cells (1.0 X 10 cells/mi) were incubated with the 6 base sequences shown in Table WO 02/18593 WO 0218593PCT/CA01/00845 18 Table Percentage increase of Fas and of FasL on UMUC-3 bladder cancer cells SEQUENCE INCREASE Fas FasL TGTGTG SEQ IIDNO:1 bases) 72 112 GTGTGT SEQ ID NO:2 (6 bases) 72 154 TTTGTT SEQ ID NO:3 (6 bases) 108 231 GGTGG:CT SEQ MD NO:4 (6 bases,) 62 113 GGGTGG SEQ ID NO:5 (6 bases) 67 143 TTGTTT SEQ ID NO:6 (6 bases) 57 132 AAGTAA SEQ ID NO:7 (6 bases) 6 -1 CCGTCC SEQ ID NO:8 (6 bases) 55 149 TGGTTG SEQ ID NOD9 (6 bases) 143 300 ATGTAT SEQ ID NO: 10 (6 bases) 42 CTGTCT SEQED NO:1I (6 bases) 45 156 TCGTTC SEQ ID NO: 12 (6 bases) 47 112 GGTTQG SEQ ID NO: 13 (6 bases) 47 98 GGAAGG SEQ ID NO: 14 -(6bases) 1 8 GGCCGG SEQJID NO: 15 (6 bases) 23 58 GGGGGG SEQ ID NO: 16 (6 bases) -5 GGGAGG SEQ ID NO: 17 (6 bases) 39 106 GGGCGG SEQ ID NO:1IS (6 bases) 72 250 Example 8 Modulation of Fas and of FasL on OVCAR-3 ovarian cancer cells OVCAR-3 ovarian cancer cells are a p53 mutated, p2 l/waf-l/Cip deleted, metastatic human solid tumor model. OVCAR-3 cells were incubated with the 6 base sequences shown in Table 6.

WO 02/18593 WO 0218593PCT/CA01/00845 Table 6 Percentage increase of Fas and of FasL on OVCAR-3 ovarian cancer cells SEQUENCE INCREASE Fas FasL TGTGTG SEQ ID NO:1I (6 bases) 64 GTGTGT SEQ ID NO:2 (6 bases) 77 69 TTTGTT SEQ ID NO:3 (6 bases) 193 341 GGTGGG SEQ ID NO:4 (6 bases) 41 14 GGGTGG SEQ ID NO:5 (6 bases) 43 9 TTGTTT SEQ ID NO:6 (6 bases) 65 98 AAGTAA SEQ ID NO:7 (6 bases) 16 -2 CCGTCC SEQ ID NO: S (6 bases) 83 TGGTTG SEQ ID NO:9 (6 bases) 221 270 ATGTAT SEQ ID NO: 10 (6 bases) 93 114 CTGTCT SEQ ID NO: I1I (6 bases) 52 93 TCGTTC SEQ ID NO: 12 (6 bases) 126 224 GGTTGG SEQ ID NO: 13 (6 bases) 22 GGAAGG SEQ ID NO: 14 bases) 15 1 GGCCGG SEQ lID NO: 15 (6 bases) 19 -2 GGGUGG SEQ ID NO: 16 bases) -1 7 GGGAGG SEQ ID NO: 17 (6 bases) 49 59 GGGCGG SEQ ID NO:1IS (6 bases) 65 142 Example 9 Modulation of Fas and of FasL on SK-0V3 ovarian cancer cells SK-OV-3 ovarian cancer cells are a p5 3 mutated, p21/waf-l/Cip deleted, ink4Bp 1 6 nk4 deleted metastatic human solid tumor model. SK-OV 3 cells X 10 5 cells/mI) were incubated with the 6 base sequences shown in Table 7.

WO 02/18593 WO 0218593PCT/CA01I00845 Table 7 Percentage increase of Fas and FasL on SK-OV-3 ovarian cancer cells SEQUENCE INCREASE Fas FasL TGTGTG SEQ ID NO:1I (6 bases) 49 37 GTGTGT SEQ ID NO:2 (6 bases) 60 24 TITGTT SEQ ID NO:3 (6 bases) 108 103 GGTGGG SEQ ID NO:1 (6 bases) -1 -17 GGGTGG SEQ lID NO:5 (6 bases) 3 -31 TTGTTT SEQ ID NO:6 (6 bases) 41 24 AAGTAA SEQ ID NO:7 (6 bases) -12 -22 CCGTCC SEQ ID NO: 8 (6 bases) 58 32 TGGTTG SEQ ID NO:9 (6 bases) 63 53 ATGTAT SEQ ID NO: 10 (6 bases) 34 33 CTGTCT SEQ ID NO:1I1 (6 bases) 15 26 TCGTTC SEQ lID NO:12 (6 bases) 9 -3 UOTTGG SEQ ID NO: 13 (6 bases) 16 -3 GGAAGG SEQ ID NO: 14 (6 bases) -15 -31 GGCCGG SEQ ID NO: 15 (6 bases) 0 -27 GGGGGG SEQ lID NO: 16 (6 bases) -14 -28 GGGAGG SEQ IDNO: 17 bases) -6 -16 GGGCGG SEQ ID NO: 18 (6 bases) 29 42 Example Modulation of Fas and of FasL on LNCaP prostate cancer cells LNCaP prostate cancer cells are a TGF-beta 1 receptor negative, androgen-independent, metastatic human solid tumor model. LNCaP cells were incubated with the 6 base sequences shown in Table 8.

WO 02/18593 WO 0218593PCT/CA01/00845 21 Table 8 Percentage increase of Fas and of FasL on LNCaP prostate cancer cells SEQUENCE INCREASE Fas FasL TGTGTG SEQ ID NO: 1 (6 bases) 29 GTGTGT SEQ ID NO:2 (6 bases) 34 7FITGTT SEQ ID NO:3 (6 bases) 199 344 GGTGGQ SEQ ID NO:4 (6 bases) 21 8 GGGTGG SEQ 11D NO:5 (6 bases) 15 -1 'ITGTTT SEQ ED NO:6 (6 bases) 40 73 AAGTAA SEQ ID NO:7 bases) 0 -16 CCGTCC SEQ ID NO: 8 (6 bases) 0 311 TGGTiTG SEQ ID NO:9 (6 bases) 184 241 ATGTAT SEQ -ED NO: 10 (6 bases) 44 68 CTGTCT SEQ IiDNO: 11 bases) 17 TCGTTC SEQ ID NO: 12 bases) ill 171 GGTTGG SEQ ID NO. 13 (6 bases) 23 -3 GGAAGG SEQ ID NO: 14 (6 bases) 26 -4 GGCCGG SEQ 11D NO:15 (6 bases) 12 -4 GGGGGG SEQ ID NO: 16 (6 bases) 6 13 GGGAGG SEQ IDNO: 17 (6 bases) 48 GGGCGG SEQ ID NO: 18 (6 bases) 55 126 Example 11 Modulation of Fas and of FasL on MCF-7 breast cancer cells MCF-7 human breast cancer cells are a caspase-3 negative, estrogendependent human solid tumor model. MCF-7 cells (1 X 10 5 cells/mi) were incubated with the 6 base sequences shown in Table 9.

WO 02/18593 WO 0218593PCT/CA01/00845 Table 9 Percentage increase of Fas and of FasL, on MCF-7 breast cancer cells SEQUENCE INCREASE Fas FasL TGTGTG SEQ ID NO:]I (6 bases) 122 121 GTGTGT SEQ ID NO:2 (6 bases) 155 135 TTTGTT SEQ ID NO:3 (6 bases) 361 528 GGTGGG SEQ lID NO:4 (6 bases) 106 110 GGGTGG SEQ ID NO:5 bases) 93 81 TTGTTT SEQ lID NO:6 (6 bases) 143 159 AAGTAA SEQ ED NO:7 (6 bases) 12 21 CCGTCC SEQ ID NO:8 (6 bases) 200 322 TGGTTG SEQ ID NO:9 (6 bases) 255 481 ATGTAT SEQ ID NO: 10 bases) 129 214 CTGTCT SEQ]ED NO: 11 (6 bases) 73 128 TCGTTC SEQ IID NO: 12 (6 bases) 56 98 GGTTGG SEQ IiDNO: 13 (6 bases) 99 83 GGAAGG SEQ ID NO: 14 (6 bases) 62 84 GGCCGG SEQ ID NO: 15 (6 bases) 63 78 GGGGGG SEQ ID NO: 16 bases) -7 18 GGGAGG SEQ IID NO: 17 (6 bases) 127 194 GGGCGG SEQ ID NO: 18 (6 bases) 165 322 Example 12 Inhibition of Fas expression on Jurkat human leukemia T cells by cycloheximide Jurkat human leukemia T cells were pre-incubated with 0.0 tg/ml CFIX) or with 0.1 jig/ml of cycloheximide CLIX) for 1 h. Ten ptghmi or 100 pLg/mi of 6 base SEQ ID NO:5 (GGGTGG) was added to both the C14X and CLIX cells and the incubation was continued for 24 hours and for 48 hours (Table WO 02/18593 WO 0218593PCT/CA01I00845 23 Table Percentage increase of Fas on Jurkat human leukemia T cells

INCREASE

SEQUENCE 24hl 48 h -CLIX ±CIIX -CliX +CIIX GGGTGG 63 5 91 51 SEQ ID NO:5 (6 bases) 10 jig/mI GGGTGG 62 22 150 115 SEQ ID) NO: 5 bases) 100 jig/mi As shown in Table 10, SEQ ID NO:5 upregulated Fas expression on Jurkat T cells. With 10 ig/m1 of SEQ ID NO cycloheximide decreased Fas expression 92% after 24 h and 44% after 48 h. With 100 4g/ml of SEQ ID cyclohexirnide decreased Fas expression 65% after 24 h and 23% after 48 h.

These data suggest that 6 base SEQ ID NO:5 stimulates de novo, synthesis of Fas.

Example 13 Synergistic effect of SEQ ID No.5 (GGGTGG) and agonistic anti-Fas antibodies on inhibition of UMUC-3 bladder cancer cell proliferation UMUC-3 bladder cancer cells were incubated for 48 hours with 0.00, 0.02 and 0.20 jig/mi of agonistic anti-Fas monoclonal antibodies (clone Gil-il: Coulter-Immunotech, Marseille, France) 0 or 10 jig/ml of SEQ ID NO:5. Cell proliferation was measured using dimethyithiazol-diphenyltetrazolium (MTT) reduction (Mosman et al. J. Immunol. Methods 65:55, 1983). MTT was measured at a wavelength of 570 nm using a multiplate spectrophotometer reader (ELX800, Bio-TEK Instruments Inc., Winooski, VT).

Table I11 Inhibition of UMUC-3 bladder cancer cell proliferation SEQUENCE INHIBITION Anti-Fas antibodies jig/mi 0.02 j[tg/ml 0.2 [tg/ml No sequence 0 7 17 GGGTGG 23 38 44 SEQ DD NO: 5-(6 bases) l0[tg/ml__ As shown in Table 11, 6 base SEQ ID NO:5 potentiated the inhibitory activity of 0.02 and 0.2 jig/mI of agonistic anti-Fas antibodies on UMUC-3 cell proliferation.

Example 14 Additive effect of SEQ ID NO.S (GGGTGG) and agonistic anti-Fas antibodies on inhibition of Jurkat leukemia T cell proliferation.

Jurkat T leukemia cells were incubated for 48 hours with 0.00, 0.002 and 0.20 ptg/mi of agonistic anti-Fas monoclonal antibodies (clone CH- 11) 0 and 10 jig/mI of SEQ ID NO: 5. Cell proliferation was measured as in Example 13.

Table 12 Inhibition of Jurkat leukemia T cell proliferation SEQUENCE INHIBITION Anti-Fas antibodies 0.0 jig/ml 0.02 jig/ml 0.2 jig/ml No sequence 0 16 33 GGGTGG 16 28 48 SEQ I1D NO: 5-(6 bases) jig/mI m:.\specifications\090000\94000\94836desflew. doc As shown in Table 12, the effects of base SEQ ID NO:5 and of 0.02 and 0.2 jIg/mi of agonistic anti-Fas antibodies on Jurkat T cell proliferation were additive.

Example Effect of 6 base sequences and agonistic anti-Fas antibodies on EL-4 murine T lymphomas.

m:\specifications\090000\94000\94836desnew. doc WO 02/18593 PCT/CA01/00845 EL-4 murine T lymphoma cells are implanted into C57/BL6 lpr/lpr (Fas negative mice). The mice are divided into 30 groups of 10 mice. On day 0, group 1 mice receive saline, group 2 mice receive 1, 10 or 100 mg/kg of SEQ. ID group 3 mice receive 1, 10 or 100 mg/kg of SEQ. ID NO:16, group 4 receive 1, or 100 mg/kg of SEQ. ID NO:17, group 5 mice receive 1, 10 or 100 mg/kg of SEQ. ID NO:18, group 6 mice receive anti-Fas antibodies, group 7 mice receive 1, or 100 mg/kg of SEQ. ID NO:5 anti-Fas antibodies, group 8 mice receive 1, or 100 mg/kg of SEQ. ID NO:16 anti-Fas antibodies, group 9 receive 1, or 100 mg/kg of SEQ. ID NO:17 anti-Fas antibodies, group 10 mice receive 1, 10 or 100 mg/kg of SEQ. ID NO:18 anti-Fas antibodies. In these different groups, anti-Fas antibodies are administered at any dose in the range of about 0.003 to about 0.3 mg/kg. Group 1 mice have the most tumor mass, groups 2, 3, 4, 5 and 6 mice have less tumor mass than group 1 mice, and group 7, 8, 9 and mice have the least tumor mass. The efficacy of the SEQ. ID NO:5, the SEQ. ID NO:16 and the SEQ. ID NO:17 is dose-dependent.

Example 16 Female (SJL/J x PL/J) Fl mice are injected subcutaneously in both femoral regions with an emulsion containing 0.5 mg of myelin basic protein (MBP) mixed with complete Freund's adjuvant. After 24 h, 400 ng of Bordetella pertussis toxin is administered intraperitoneally. On the day of onset (day 0), group 1 mice receive saline, group 2 mice receive 1, 10 or 100 mg/kg of SEQ. ID group 3 mice receive 1, 10 or 100 mg/kg of SEQ. ID NO:16, group 4 mice receive 1, 10 or 100 mg/kg of SEQ. ID NO:17, group 5 mice receive 1, 10 or 100 mg/kg of SEQ. ID NO: 18, group 6 mice receive anti-Fas antibodies, group 7 mice receive 1, 10 or 100 mg/kg of SEQ. ID NO:5 anti-Fas antibodies, group 8 mice receive 1, 10 or 100 mg/kg of SEQ. ID NO:16 anti-Fas antibodies, group 9 receive 1, 10 or 100 mg/kg of SEQ. ID NO:17 anti-Fas antibodies, group mice receive 1, 10 or 100 mg/kg of SEQ. ID NO:18 anti-Fas antibodies for 3 days by intracisternal administration (20 g/day). In these different groups, anti- Fas antibodies are administered at any dose in the range of about 0.003 to about 0.3 mg/kg. Group 6, 7, 8, 9 and 10 mice show less progression of EAE than group 1, 2, 3, 4 and 5 mice. Group 7, 8, 9 and 10 mice show the least progression of EAE. The efficacy of the SEQ.ID NO:5, the SEQ.ID NO:16 and the SEQ. ID NO:17 is dosedependent.

Any discussion of documents, acts, materials, devices, articles or the like which has been included in the present specification is solely for the purpose of providing a context for the present invention. It is not to be taken as an admission that any or all of these matters form part of the prior art base or were common general knowledge in the field relevant to the present invention as it existed before the priority date of each claim of this application.

Throughout this specification the word "comprise", or variations such as.

"comprises" or "comprising", will be understood to imply the inclusion of a stated element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps.

Finally, it will be appreciated by persons skilled in the art that numerous variations and/or modifications may be made to the invention as shown in the specific embodiments without departing from the spirit or scope of the invention as broadly described. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive.

Dated this twenty-fifth day of June 2003 Bioniche Life Sciences Inc.

Patent Attorneys for the Applicant: F B RICE CO m:\specifications\090000\94000\94836desnew. doc

Claims (13)

1. 3. The composition of Claim 1 or 2, wherein the sequence is any one of SEQ ID NO: 1 to SEQ ID NO: 18.
2. 4. A composition comprising a synthetic phosphodiester oligonucleotide sequence of 6 bases, wherein the sequence is any one of SEQ ID NO: 1 to SEQ ID NO: 18, selected from the group consisting of a(GT),b, a(GA),b, and a(GC),b wherein n is an integer between 1 and 3, and a and b are independently either none or one or more As, Cs, Gs or Ts, or combinations thereof, wherein the composition is useful for modulating Fas or FasL expression in an animal or a human when administered in an effective amount to the animal. A composition comprising a synthetic phosphodiester oligonucleotide sequence of 6 bases, wherein the sequence is any one of SEQ ID NO: 1 to SEQ ID NO: 18, selected from the group consisting of a(GT),b, a(GA),b, and wherein n is an integer between 1 and 3, and a and b are independently either none or one or more As, Cs, Gs, or Ts, or combinations thereof, wherein c:\nrportbhmeldocs\mjc\l1656 27 _1 .doc COMS ID No: SBMI-07841754 Received by IP Australia: Time 15:58 Date 2007-06-20 20/06 '07 16:58 FAX 613 8618 4199 FB RICE CO. 01014 O O 28 the composition is useful for modulating efficacy of a therapeutic agent in an o animal or a human when administered in an effective amount to the animal.
3. 6. The composition of any one of Claims 1 to 5, further comprising a pharmaceutically acceptable carrer. NO 00
4. 7. The composition of any one of Claims 1 to 6, farther comprising a therapeutic C agent.
5. 8. A composition comprising a synthetic phosphodiester oligonucleotide sequence c of 6 bases, wherein the sequence is any one of SEQ ID NO:1 to SEQ ID NO: 18.
6. 9. A method of modulating Fas or FasL expression in an animal or a human comprising administration of a composition of any one of Claims 1, 3, 7, or 8 and a pharmaceutically acceptable carrier to the animal or the human in an amount effective to modulate Fas or. FasL expression in the animal or the human. A method of modulating efficacy of a therapeutic agent in an animal or human comprising administration of an effective amount of the composition of any one of Claims 2, 3, 7, or 8 before, concurrently with, or after administration of the therapeutic agent, wherein the amount is effective to modulate efficacy of the therapeutic agent.
7. 11. The method of Claim 9 or 10, wherein the animal or human has a disease.
8. 12. The method of Claim 11, wherein the disease is cancer.
9. 13. The method of Claim 12, wherein the cancer is selected from the group consisting of ovarian, prostrate, breast, bladder, and leukaemia.
10. 14. The method of Claim 13, wherein the disease is autoimmune encephalomyelitis.
11. 15. The method of Claim 9 or 10, wherein the animal or human has inflammation, infection, graft rejection, tissue rejection or cell rejection. c:\nrportbl\meldocs\mjc\165627_ .doc COMS ID No: SBMI-07841754 Received by IP Australia: Time 15:58 Date 2007-06-20 20/06 '07 16:59 FAX 613 8618 4199 FB RICE CO. 0015 8 29 S16- Use of any one of the compositions of any of Claims 1-8 in the manufacture of a medicament. C
12. 17. Use of any one of the compositions of Claims 1, 3, 4, 7, or 8 for modulation of cn 5 Fas or FasL expression in cells of an animal or a human, comprising administration to animal or the human of any ore of the compositions of Claims 00 00 1, 3, 4, 7, or 8 in an amount effective to modulate Fas or FasL expression in the 0 cells of the animal or the human. C
13. 18. Use of any one of the compositions of Claims 2-8 for modulation of efficacy of 1 a therapeutic agent comprising administration to the animal or the human of any one of the compositions of Claims 2-8 in an amount effective to modulate efficacy of the therapeutic agent. Dated this twentieth day of June 2007 Bioniche Life Sciences Inc. Patent Attorneys for the Applicant: F B RICE CO c:\nrportbl\moldocs\mjc\1656271 .doc COMS ID No: SBMI-07841754 Received by IP Australia: Time 15:58 Date 2007-06-20