WO2007057436A2 - Interferon in influenza - Google Patents
Interferon in influenza Download PDFInfo
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- WO2007057436A2 WO2007057436A2 PCT/EP2006/068588 EP2006068588W WO2007057436A2 WO 2007057436 A2 WO2007057436 A2 WO 2007057436A2 EP 2006068588 W EP2006068588 W EP 2006068588W WO 2007057436 A2 WO2007057436 A2 WO 2007057436A2
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- influenza
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/21—Interferons [IFN]
- A61K38/215—IFN-beta
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- the present invention relates to the use of an interferon (IFN) for the manufacture of a medicament for treatment and/or prevention of influenza.
- IFN interferon
- Influenza is a common infectious disease in humans, which is caused by influenza virus. Influenza virus is transmitted very easily by aerosols from infected people. The incubation time is 24-72 hours. The characteristic symptoms are a rapid onset of fever, together with cough, sore throat, as well as muscle pain, arthralgy and malaise. Additional symptoms can also be observed, like pharyngitis, conjonctivitis, bronchitis, diarrhoea or vomiting, but they are less frequent. Usually, patients recover within 1 and 2 weeks. However, a feeling of weakness can last for several weeks. Complications caused by influenza virus can be a respiratory distress, pneumonia caused by the influenza virus or by bacteria (staphylococcus, streptococcus, pneumococcus, Haemophilus influenzae).
- Avian influenza is an infectious disease of birds caused by type A strains of the influenza virus. The disease, which was first identified in Italy more than 100 years ago, occurs worldwide and may infect humans.
- the main object of the present invention is the use of an interferon (IFN) alone or in combination with an antiviral agent for the manufacture of a medicament for treatment and/or prevention of Influenza.
- IFN interferon
- Influenza viruses belong to the family of orthomyxoviruses. Three different types can be distinguished : influenza A, influenza B and influenza C viruses. The last one seems not to be associated with severe illness. The most severe symptoms are associated with influenza A viruses. Many sub-types of influenza A viruses are known and they are classified according to the origin of the hemagglutinin and of the neuraminidase : 15 types of hemagglutinin and 9 neuraminidase have been described. Influenza A subtypes still circulating in the population are influenza A (H3N2) appeared in 1968, and influenza A (H1 N1 ) reappeared in 1977.
- influenza A H3N2
- influenza A H1 N1
- influenza viruses of avian origin could be detected in humans. It was an influenza A (H5N1 ) and an influenza A (H9N2) strain. The first one caused the death of 6 persons in Hong Kong. The virus was directly transmitted from chickens to humans. The second one was detected in 2 hospitalized children Hong Kong. Patients showed weak symptoms and could be discharged from the hospital without any further problems.
- H5N1 influenza A
- H9N2 influenza A
- influenza virus Fifteen subtypes of influenza virus are known to infect birds, thus providing an extensive reservoir of influenza viruses potentially circulating in bird populations. To date, all outbreaks of the highly pathogenic form have been caused by influenza A viruses of subtypes H5 and H7. Recent research has shown that viruses of low pathogenicity can, after circulation for sometimes short periods in a poultry population, mutate into highly pathogenic viruses.
- influenza A viruses of subtypes H5 and H7 Recent research has shown that viruses of low pathogenicity can, after circulation for sometimes short periods in a poultry population, mutate into highly pathogenic viruses.
- the H5N2 virus initially caused low mortality, but within six months became highly pathogenic, with a mortality approaching 90%.
- the H7N1 virus initially of low pathogenicity, mutated within 9 months to a highly pathogenic form.
- H5N1 is of particular concern for several reasons. H5N1 mutates rapidly and has a documented propensity to acquire genes from viruses infecting other animal species. Its ability to cause severe disease in humans has now been documented on two occasions. In addition, laboratory studies have demonstrated that isolates from this virus have a high pathogenicity and can cause severe disease in humans. Birds that survive infection excrete virus for at least 10 days, orally and in faeces, thus facilitating further spread at live poultry markets and by migratory birds.
- Antiviral drugs are clinically effective against influenza A virus strains in otherwise healthy adults and children, but have some limitations. Some of these drugs are also expensive and supplies are limited.
- the present invention provides for the use of an interferon (IFN) or an isoform, mutein, fused protein, functional derivative, active fraction or salt thereof, for the manufacture of a medicament for treatment and/or prevention of influenza.
- IFN interferon
- an isoform, mutein, fused protein, functional derivative, active fraction or salt thereof for the manufacture of a medicament for treatment and/or prevention of influenza.
- the present invention provides for the use of an interferon (IFN) or an isoform, mutein, fused protein, functional derivative, active fraction or salt thereof for treatment and/or prevention of influenza.
- IFN interferon
- the present invention provides for an interferon (IFN) or an isoform, mutein, fused protein, functional derivative, active fraction or salt thereof for use in the treatment and/or prevention of influenza.
- IFN interferon
- interferon (IFN) variants hereinbelow.
- an interferon or an interferon variant include monotherapy, i.e. the interferon or the interferon variant is used as the only antiviral compound administered to the patient (monotherapy).
- the interferon or the interferon variant is administered in addition to, or together with, an antiviral agent as further defined hereinbelow (combination therapy).
- an IFN IFN
- an isoform, mutein, fused protein, functional derivative, active fraction or salt thereof in combination with an antiviral agent for the manufacture of a medicament for treatment and/or prevention of influenza for simultaneous, sequential or separate use.
- influenza is avian influenza.
- the avian influenza may be caused by a type A strain or a type B strain of influenza virus.
- the avian influenza is caused by a type A strain of influenza virus.
- the avian influenza is caused by a influenza virus of subtype H5, H7, or H9. In further preferred embodiments the avian influenza is caused by a influenza virus of any of the subtypes H5N2, H7N1 , H7N7, H9N2, or H5N1. In a particularly preferred embodiment the subtype is H5N1.
- interferon interferon
- an isoform, mutein, fused protein, functional derivative, active fraction or salt thereof is the only antiviral compound administered to the patient (monotherapy)
- the interferon (IFN) or an isoform, mutein, fused protein, functional derivative, active fraction or salt thereof is administered in addition to, or together with, an antiviral agent as further defined hereinbelow (combination therapy).
- the antiviral agent may be selected from the group of neuraminidase inhibitors, such as Oseltamivir (Tamiflu®) and Zanamivir (Relenza®), adamantanes, such as Amantadine (Symmetrel®) and Rimantadine (Flumadine®), or Ribavirin (Rebetol®).
- neuraminidase inhibitors such as Oseltamivir (Tamiflu®) and Zanamivir (Relenza®
- adamantanes such as Amantadine (Symmetrel®) and Rimantadine (Flumadine®)
- Ribavirin Rebetol®
- the antiviral agent is Ribavirin.
- interferon interferon
- an isoform, mutein, fused protein, functional derivative, active fraction or salt thereof is the only antiviral compound administered to the patient (monotherapy)
- the interferon (IFN) or an isoform, mutein, fused protein, functional derivative, active fraction or salt thereof is administered in addition to, or together with, an antiviral agent as further defined hereinbelow (combination therapy).
- the IFN is recombinant human IFN-beta.
- the recombinant human IFN-beta has a CHO cell-derived glycosylation.
- the IFN is consensus interferon.
- the IFN is a long-acting interferon-beta, such as for example a fused protein comprising an immunoglobulin (Ig) fragment, preferably the Fc portion of an immunoglobulin.
- the long-acting interferon-beta may be selected from pegylated interferon-beta or interferon-beta Fc-fusion proteins.
- the IFN may be administered at a dosage of about 1 to 50 ⁇ g per person per day, or about 10 to 30 ⁇ g per person per day or about 10 to 20 ⁇ g per person per day.
- the IFN may, for example, be administered daily or every other day.
- the IFN may, for example, be administered twice or three times per week.
- the IFN may, for example, be administered subcutaneously.
- the IFN may, for example, be administered intramuscularly.
- the IFN may be delivered by a spray device.
- the IFN is delivered within less than 3, preferably less than 2 days after infection with an influenza virus.
- the IFN is dosed at least at 44mcg s.c. per administration.
- the IFN is administered at least 3x weekly.
- the antiviral agent is administered at a dosage of about 100 to 2000 mg per person per day, or about 400 to 1200 mg per person per day, or about 800 to 1000 mg per person per day, or about 1000 to 1200 mg per person per day.
- Interferons are cytokines, i.e. soluble proteins that transmit messages between cells and play an essential role in the immune system by helping to destroy microorganisms that cause infection and repairing any resulting damage. Interferons are naturally secreted by infected cells and were first identified in 1957. Their name is derived from the fact that they "interfere" with viral replication and production.
- Interferons exhibit both antiviral and antiproliferative activity.
- human interferons On the basis of biochemical and immunological properties, the naturally-occurring human interferons are grouped into three major classes: interferon-alpha (leukocyte), interferon-beta
- fibroblast fibroblast
- interferon-gamma interferon-gamma
- Alpha-interferon is currently approved in the United States and other countries for the treatment of hairy cell leukemia, venereal warts, Kaposi's Sarcoma (a cancer commonly afflicting patients suffering from Acquired Immune Deficiency Syndrome (AIDS)), and chronic non-A, non-B hepatitis.
- AIDS Acquired Immune Deficiency Syndrome
- interferons are glycoproteins produced by the body in response to a viral infection. They inhibit the multiplication of viruses in protected cells. Consisting of a lower molecular weight protein, IFNs are remarkably non-specific in their action, i.e. IFN induced by one virus is effective against a broad range of other viruses. They are however species-specific, i.e. IFN produced by one species will only stimulate antiviral activity in cells of the same or a closely related species. IFNs were the first group of cytokines to be exploited for their potential anti-tumor and antiviral activities. The three major IFNs are referred to as IFN- ⁇ , IFN- ⁇ and IFN- ⁇ .
- IFNs Such main kinds of IFNs were initially classified according to their cells of origin (leukocyte, fibroblast or T cell). However, it became clear that several types might be produced by one cell. Hence leukocyte IFN is now called IFN- ⁇ , fibroblast IFN is IFN- ⁇ and T cell IFN is IFN- ⁇ . There is also a fourth type of IFN, lymphoblastoid IFN, produced in the "Namalwa" cell line (derived from Burkitt's lymphoma), which seems to produce a mixture of both leukocyte and fibroblast IFN.
- lymphoblastoid IFN produced in the "Namalwa" cell line (derived from Burkitt's lymphoma), which seems to produce a mixture of both leukocyte and fibroblast IFN.
- the interferon unit or International unit for interferon has been reported as a measure of IFN activity defined as the amount necessary to protect 50% of the cells against viral damage.
- the assay that may be used to measure bioactivity is the cytopathic effect inhibition assay as described (Rubinstein, et al. 1981 ; Familletti, P. C, et al., 1981 ).
- this antiviral assay for interferon about 1 unit/ml of interferon is the quantity necessary to produce a cytopathic effect of 50%.
- the units are determined with respect to the international reference standard for Hu- IFN-beta provided by the National Institutes of Health (Pestka, S. 1986). Every class of IFN contains several distinct types. IFN- ⁇ and IFN- ⁇ are each the product of a single gene.
- the proteins classified as IFNs- ⁇ are the most diverse group, containing about
- IFN- ⁇ genes There is a cluster of IFN- ⁇ genes on chromosome 9, containing at least 23 members, of which 15 are active and transcribed. Mature IFNs- ⁇ are not glycosylated.
- IFNs- ⁇ and IFN- ⁇ are all the same length (165 or 166 amino acids) with similar biological activities. IFNs- ⁇ are 146 amino acids in length, and resemble the ⁇ and ⁇ classes less closely. Only IFNs- ⁇ can activate macrophages or induce the maturation of killer T cells. These new types of therapeutic agents can are sometimes called biologic response modifiers (BRMs), because they have an effect on the response of the organism to the tumor, affecting recognition via immunomodulation.
- BRMs biologic response modifiers
- Human fibroblast interferon has antiviral activity and can also stimulate natural killer cells against neoplastic cells. It is a polypeptide of about 20,000 Da induced by viruses and double-stranded RNAs. From the nucleotide sequence of the gene for fibroblast interferon, cloned by recombinant DNA technology, (Derynk et al. 1980) deduced the complete amino acid sequence of the protein. It is 166 amino acid long.
- treatment within the context of this invention refers to any beneficial effect on progression of disease, including attenuation, reduction, decrease or diminishing of the pathological development after onset of disease.
- interferon is intended to include any molecule defined as such in the literature.
- IFN- ⁇ , IFN- ⁇ and IFN- ⁇ are included in the above definition.
- IFN- ⁇ is the preferred IFN according to the present invention.
- IFN- ⁇ suitable in accordance with the present invention is commercially available e.g. as Rebif® (Serono), Avonex® (Biogen) or Betaferon® (Schering).
- the use of interferons of human origin is also preferred in accordance with the present invention.
- the term interferon, as used herein, is intended to encompass salts, functional derivatives, variants, analogs and active fragments thereof.
- interferon-beta IFN- ⁇
- IFN- ⁇ interferon-beta
- fibroblast interferon in particular of human origin, as obtained by isolation from biological fluids or as obtained by DNA recombinant techniques from prokaryotic or eukaryotic host cells, as well as its salts, functional derivatives, variants, analogs and active fragments.
- muteins refers to analogs of IFN in which one or more of the amino acid residues of a natural IFN are replaced by different amino acid residues, or are deleted, or one or more amino acid residues are added to the natural sequence of IFN, without changing considerably the activity of the resulting products as compared to the wild type IFN.
- muteins are prepared by known synthesis and/or by site-directed mutagenesis techniques, or any other known technique suitable therefore.
- Preferred muteins include e.g. the ones described by Shepard et al. (1981 ) or Mark et al. (1984).
- Any such mutein preferably has a sequence of amino acids sufficiently duplicative of that of IFN, such as to have substantially similar or even better activity to an IFN.
- the biological function of interferon is well known to the person skilled in the art, and biological standards are established and available e.g. from the National Institute for Biological Standards and Control (http://immunology.org/links/NIBSC).
- Preferred changes for muteins in accordance with the present invention are what are known as "conservative" substitutions.
- Conservative amino acid substitutions of polypeptides or proteins of the invention may include synonymous amino acids within a group, which have sufficiently similar physicochemical properties that substitution between members of the group will preserve the biological function of the molecule. It is clear that insertions and deletions of amino acids may also be made in the above-defined sequences without altering their function, particularly if the insertions or deletions only involve a few amino acids, e.g., under thirty, and preferably under ten, and do not remove or displace amino acids which are critical to a functional conformation, e.g., cysteine residues. Proteins and muteins produced by such deletions and/or insertions come within the purview of the present invention.
- the synonymous amino acid groups are those defined in Table I. More preferably, the synonymous amino acid groups are those defined in Table II; and most preferably the synonymous amino acid groups are those defined in Table III.
- GIy Ala, Thr, Pro, Ser, GIy lie Met, Tyr, Phe, VaI, Leu, lie
- GIy GIy lie lie, Met, Phe, VaI, Leu
- GIy GIy lie lie, Met, Leu
- Examples of production of amino acid substitutions in proteins which can be used for obtaining muteins of IFN, for use in the present invention include any known method steps, such as presented in US patents 4,959,314, 4,588,585 and 4,737,462, to Mark et al; 5,1 16,943 to Koths et al., 4,965,195 to Namen et al; 4,879,1 11 to Chong et al; and 5,017,691 to Lee et al; and lysine substituted proteins presented in US patent No. 4,904,584 (Shaw et al). Specific muteins of IFN-beta have been described, for example by Mark et al., 1984.
- fused protein refers to a polypeptide comprising an IFN, or a mutein thereof, fused to another protein, which e.g., has an extended residence time in body fluids.
- An IFN may thus be fused to another protein, polypeptide or the like, e.g., an immunoglobulin or a fragment thereof.
- “Functional derivatives” as used herein cover derivatives of IFN, and their muteins and fused proteins, which may be prepared from the functional groups which occur as side chains on the residues or the N- or C-terminal groups, by means known in the art, and are included in the invention as long as they remain pharmaceutically acceptable, i.e. they do not destroy the activity of the protein which is substantially similar to the activity IFN, and do not confer toxic properties on compositions containing it.
- These derivatives may, for example, include polyethylene glycol side-chains, which may mask antigenic sites and extend the residence of IFN in body fluids.
- Other derivatives include aliphatic esters of the carboxyl groups, amides of the carboxyl groups by reaction with ammonia or with primary or secondary amines, N-acyl derivatives of free amino groups of the amino acid residues formed with acyl moieties (e.g. alkanoyl or carbocyclic aroyl groups) or O-acyl derivatives of free hydroxyl groups (for example that of seryl or threonyl residues) formed with acyl moieties.
- acyl moieties e.g. alkanoyl or carbocyclic aroyl groups
- O-acyl derivatives of free hydroxyl groups for example that of seryl or threonyl residues
- active fractions of IFN covers any fragment or precursors of the polypeptide chain of the protein molecule alone or together with associated molecules or residues linked thereto, e.g., sugar or phosphate residues, or aggregates of the protein molecule or the sugar residues by themselves, provided said fraction has no significantly reduced activity as compared to the corresponding IFN.
- salts herein refers to both salts of carboxyl groups and to acid addition salts of amino groups of the proteins described above or analogs thereof.
- Salts of a carboxyl group may be formed by means known in the art and include inorganic salts, for example, sodium, calcium, ammonium, ferric or zinc salts, and the like, and salts with organic bases as those formed, for example, with amines, such as triethanolamine, arginine or lysine, piperidine, procaine and the like.
- Acid addition salts include, for example, salts with mineral acids, such as, for example, hydrochloric acid or sulfuric acid, and salts with organic acids, such as, for example, acetic acid or oxalic acid.
- any such salts must retain the biological activity of the proteins (IFN) relevant to the present invention, i.e., the ability to bind to the corresponding receptor and initiate receptor signaling.
- R 1 of formula (I) is H.
- R 2 is OH.
- A is N.
- R 3 and R 5 form a 6-membered heterocyclic ring.
- the heterocyclic ring is a pyrimidine or a pyrimidine-one.
- antiviral can be used incombination with an interferon to potentiate its beneficial effects.
- the use of Ribavirin (1- ⁇ -D-ribofuranosyl-1 H-1 ,2,4-Triazole-3-carboxamide), as antiviral is especially preferred.
- the use of recombinant human IFN- beta and the compounds of the invention is further particularly preferred.
- Consensus interferons are non-naturally occurring variants of IFN (US 6,013,253). According to a preferred embodiment of the invention, the compounds of the invention are used in combination with a consensus interferon.
- human interferon consensus shall mean a non- naturally-occurring polypeptide, which predominantly includes those amino acid residues that are common to a subset of IFN-alpha's representative of the majority of the naturally-occurring human leukocyte interferon subtype sequences and which includes, at one or more of those positions where there is no amino acid common to all subtypes, an amino acid which predominantly occurs at that position and in no event includes any amino acid residue which is not existent in that position in at least one naturally-occurring subtype.
- IFN-con encompasses but is not limited to the amino acid sequences designated IFN-con1 , IFN-con2 and IFN-con3 which are disclosed in U.S. 4,695,623, 4,897,471 and 5,541 ,293.
- DNA sequences encoding IFN-con may be produced as described in the above-mentioned patents, or by other standard methods.
- the fused protein comprises an Ig fusion.
- the fusion may be direct, or via a short linker peptide which can be as short as 1 to 3 amino acid residues in length or longer, for example, 13 amino acid residues in length.
- Said linker may be a tripeptide of the sequence E-F-M (Glu-Phe-Met), for example, or a 13-amino acid linker sequence comprising Glu-Phe-Gly-Ala-Gly-Leu-Val-Leu-Gly-Gly- Gln-Phe-Met introduced between the sequence of IFN and the immunoglobulin sequence.
- the resulting fusion protein may have improved properties, such as an extended residence time in body fluids (half-life), increased specific activity, increased expression level, or the purification of the fusion protein is facilitated.
- IFN is fused to the constant region of an Ig molecule.
- it is fused to heavy chain regions, like the CH2 and CH3 domains of human IgGI , for example.
- Other isoforms of Ig molecules are also suitable for the generation of fusion proteins according to the present invention, such as isoforms IgG 2 , IgG ⁇ or IgG 4 , or other Ig classes, like IgM or IgA, for example. Fusion proteins may be monomeric or multimeric, hetero- or homomultimeric.
- the functional derivative comprises at least one moiety attached to one or more functional groups, which occur as one or more side chains on the amino acid residues.
- the moiety is a polyethylene (PEG) moiety. PEGylation may be carried out by known methods, such as the ones described in WO99/55377, for example.
- the dosage administered, as single or multiple doses, to an individual will vary depending upon a variety of factors, including pharmacokinetic properties, the route of administration, patient conditions and characteristics (sex, age, body weight, health, size), extent of symptoms, concurrent treatments, frequency of treatment and the effect desired.
- Standard dosages of human IFN-beta range from 80 000 IU/kg and 200 000
- IFN may preferably be administered at a dosage of about 1 to 50 ⁇ g, more preferably of about
- the administration of active ingredients in accordance with the present invention may be by intravenous, intramuscular or subcutaneous route.
- the preferred route of administration for IFN is the subcutaneous route.
- IFN may also be administered daily or every other day, of less frequent. Preferably, IFN is administered one, twice or three times per week
- the preferred route of administration is subcutaneous administration, administered e.g. three times a week.
- a further preferred route of administration is the intramuscular administration, which may e.g. be applied once a week.
- Preferably 22 to 44 ⁇ g or 6 MIU to 12 MIU of IFN-beta is administered three times a week by subcutaneous injection.
- IFN-beta may be administered subcutaneously, at a dosage of 250 to 300 ⁇ g or 8 MIU to 9.6 MIU, every other day. 30 ⁇ g or 6 MIU IFN-beta may further be administered intramuscularly once a week.
- Ribavirin is administered in combination with IFN- beta and it is administered at a dosage of about 100 to 2000 mg per person per day, preferably of about 400 to 1200 mg per person per day, more preferably about 800 to 1000 mg per person per day, or about 1000 to 1200 mg per person per day.
- the usual dose is 800 mg per day
- the usual dose is 1000 mg per day
- the usual dose is 1200 mg per day.
- the actual dosage employed may be varied depending upon the requirements of the patient and the severity of the condition being treated. Determination of the proper dosage regimen for a particular situation is within the skill of the art.
- Ribavirin is administered orally Ribavirin may be administered by injection or, preferably, orally.
- the compound can be formulated with the appropriate diluents and carriers to form ointments, creams, foams, and solutions having from about 0.01 % to about 15% by weight, preferably from about 1 % to about 10% by weight of the compound.
- Ribavirin is in the form of a solution or suspension, dissolved or suspended in physiologically compatible solution from about 10 mg/ml to about 1500 mg/ml. Injection may be intravenous, intermuscular, intracerebral, subcutaneous, or intraperitoneal.
- Ribavirin may be in capsule, tablet, oral suspension, or syrup form.
- the tablet or capsules may contain from about 10 to 500 mg of Ribavirin. Preferably they may contain about 300 mg of Ribavirin.
- the capsules may be the usual gelatin capsules and may contain, in addition to the Ribavirin in the quantity indicated above, a small quantity, for example less than 5% by weight, magnesium stearate or other excipient. Tablets may contain the foregoing amount of the compound and a binder, which may be a gelatin solution, a starch paste in water, polyvinyl pyrilidone, polyvinyl alcohol in water, etc. with a typical sugar coating.
- the compounds of the invention and IFN may be formulated in a pharmaceutical composition.
- the term "pharmaceutically acceptable” is meant to encompass any carrier, which does not interfere with effectiveness of the biological activity of the active ingredient and that is not toxic to the host to which it is administered.
- the active protein(s) may be formulated in a unit dosage form for injection in vehicles such as saline, dextrose solution, serum albumin and Ringer's solution.
- the active ingredients of the pharmaceutical composition according to the invention can be administered to an individual in a variety of ways.
- the routes of administration include intradermal, transdermal (e.g. in slow release formulations), intramuscular, intraperitoneal, intravenous, subcutaneous, oral, epidural, topical, and intranasal routes. Any other therapeutically efficacious route of administration can be used, for example absorption through epithelial or endothelial tissues or by gene therapy wherein a DNA molecule encoding the active agent is administered to the patient (e.g. via a vector), which causes the active agent to be expressed and secreted in vivo.
- the protein(s) according to the invention can be administered together with other components of biologically active agents such as pharmaceutically acceptable surfactants, excipients, carriers, diluents and vehicles.
- the subcutaneous route is preferred in accordance with the present invention.
- a vector for inducing and/or enhancing the endogenous production of IFN in a cell normally silent for expression of IFN, or which expresses amounts of IFN which are not sufficient, are is used for treatment of influenza.
- the vector may comprise regulatory sequences functional in the cells desired to express IFN.
- Such regulatory sequences may be promoters or enhancers, for example.
- the regulatory sequence may then be introduced into the right locus of the genome by homologous recombination, thus operably linking the regulatory sequence with the gene, the expression of which is required to be induced or enhanced.
- the technology is usually referred to as "endogenous gene activation" (EGA), and it is described e.g. in WO 91/09955.
- the invention further relates to the use of a cell that has been genetically modified to produce IFN in the manufacture of a medicament for the treatment and/or prevention of influenza.
- IFN can be formulated as a solution, suspension, emulsion or lyophilised powder in association with a pharmaceutically acceptable parenteral vehicle (e.g. water, saline, dextrose solution) and additives that maintain isotonicity (e.g. mannitol) or chemical stability (e.g. preservatives and buffers).
- a pharmaceutically acceptable parenteral vehicle e.g. water, saline, dextrose solution
- additives that maintain isotonicity e.g. mannitol
- chemical stability e.g. preservatives and buffers.
- the compounds of the invention and IFN can be administered prophylactically or therapeutically to an individual prior to, simultaneously or sequentially with other therapeutic regimens or agents (e.g. multiple drug regimens), in a therapeutically effective amount.
- Active agents that are administered simultaneously with other therapeutic agents can be administered in the same or different compositions.
- IFN The efficacy of IFN is studied in an experimental influenza virus infection model in the mouse.
- intranasal inoculation of the virus causes severe haemorrhagic pneumonia which leads to the death of the animals within 7 to 10 days of infection.
- the experimental design envisages evaluation of the therapeutic efficacy of the study substance, as assessed on the basis of survival of the infected animals.
- IFN is administered to the animals at various doses, on a daily basis for 7 days, starting from a few hours after infection.
- an avian influenza strain is used, such as in particular an H5N1 strain.
- Interferon preferably recombinant IFN-beta
- IFN Interferon
- antiviral agents such as neuraminidase inhibitors, such as Oseltamivir (Tamiflu®) and Zanamivir (Relenza®), adamantanes, such as Amantadine (Symmetrel®) and Rimantadine (Flumadine®), or Ribavirin (Rebetol®)
- neuraminidase inhibitors such as Oseltamivir (Tamiflu®) and Zanamivir (Relenza®
- adamantanes such as Amantadine (Symmetrel®) and Rimantadine (Flumadine®), or Ribavirin (Rebetol®)
- mice Four-week-old female inbred Balb/c AnCrIBR mice are used. A suitable IFN preparation is administered to the animals via the intraperitoneal route at various times after infection with the influenza virus. The IFN concentrations are chosen so as to obtain a range of doses in the animals' blood similar to the effective range in vitro.
- mice are inoculated intranasally (i.n.) with a suspension containing the influenza virus A/PR at a multiplicity of infection of 2 HAU/mouse, after light anaesthesia with ether.
- influenza virus at this multiplicity of infection produces haemorrhagic pneumonia that leads to the death of 80% of the animals by one week after infection.
- both virological and immunological parameters are monitored in addition to studying survival curves.
- the viral load is determined.
- the lungs of infected and control mice are taken as samples, weighed and homogenised in RPMI containing antibiotics. After centrifuging, the supernatants are suitably diluted and the viral load is analysed by means of the CPE-50% test.
- confluent MDCK cells are infected with the supernatants serially diluted in RPMI added with antibiotics at 2% FCS and incubated for three days at 37° C. in a 5% CO2 atmosphere. For each dilution, the wells showing positive effects are counted and compared with those showing negative cytopathic effects according to the Reed and Muench formula.
- the CPE-50% titre is calculated in units/ml.
- cytokine polyclonal antibody As an immunological parameter, levels of inflammatory cytokines are evaluated using the ELISA method.
- a 96-well plate is used for the experiment. The plate is coated with monoclonal antibodies to the cytokines to be studied, incubated overnight at 4° C. Later, 200 ⁇ I/well of 1 % BSA in carbonate buffer were added for 30 min at 37° C. Washings are then done with 0.25% TBS+Tween 20 and the samples are added for 4 hours at 37° C. As a reference curve recombinant cytokines in scalar dilution are used. Washings are then performed and an anti- cytokine polyclonal antibody, different from the first one, is added and left overnight at +4° C.
- the following antibodies are analysed: 1 ) monoclonal rat anti-mouse TNF-alpha/recombinant mouse IL-6; 2) recombinant mouse TNF-alpha/recombinant mouse IL-6; 3) polyclonal rabbit anti-mouse TNF-alpha/polyclonal goat anti-mouse IL-6; 4) goat anti-rabbit IgG-alkaline phosphatase/anti-goat IgG alkaline phoshatase.
- an avian influenza strain is used, such as in particular an H5N1 strain.
- Interferon preferably recombinant IFN-beta
- IFN Interferon
- antiviral agents such as neuraminidase inhibitors, such as Oseltamivir (Tamiflu®) and Zanamivir (Relenza®), adamantanes, such as Amantadine (Symmetrel®) and Rimantadine (Flumadine®), or Ribavirin (Rebetol®)
- neuraminidase inhibitors such as Oseltamivir (Tamiflu®) and Zanamivir (Relenza®
- adamantanes such as Amantadine (Symmetrel®) and Rimantadine (Flumadine®), or Ribavirin (Rebetol®)
- Pestka S. (1986) "Interferon Standards and General Abbreviations, in Methods in Enzymology (S. Pestka, ed.), Academic Press, New York 1 19, 14-23. 5. Rubinstein, S..Familletti, P. C, and Pestka, S. Convenient Assay for Interferons.
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Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
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AU2006314497A AU2006314497A1 (en) | 2005-11-18 | 2006-11-16 | Interferon in influenza |
EP06807823A EP1951285A2 (en) | 2005-11-18 | 2006-11-16 | Interferon in influenza |
US12/091,985 US20080260690A1 (en) | 2005-11-18 | 2006-11-16 | Interferon in Influenza |
JP2008540616A JP2009515933A (en) | 2005-11-18 | 2006-11-16 | Interferon in influenza |
CA002626056A CA2626056A1 (en) | 2005-11-18 | 2006-11-16 | Interferon in influenza |
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EP05110965 | 2005-11-18 | ||
EP05110965.0 | 2005-11-18 | ||
US73848305P | 2005-11-21 | 2005-11-21 | |
US60/738,483 | 2005-11-21 |
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US (1) | US20080260690A1 (en) |
EP (1) | EP1951285A2 (en) |
JP (1) | JP2009515933A (en) |
AU (1) | AU2006314497A1 (en) |
CA (1) | CA2626056A1 (en) |
WO (1) | WO2007057436A2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7858660B2 (en) | 2007-03-13 | 2010-12-28 | Adamas Pharmaceuticals, Inc. | Compositions and kits for treating influenza |
US20110177028A1 (en) * | 2007-05-18 | 2011-07-21 | Davies Donna | Interferon-beta and/or lambda for use in treating rhinovirus infection in the elderly |
US9421243B2 (en) | 2010-03-12 | 2016-08-23 | Synairgen Research Limited | Therapy for influenza like illness |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
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MX340972B (en) | 2008-10-08 | 2016-08-02 | Intrexon Corp | Engineered cells expressing multiple immunomodulators and uses thereof. |
MX362513B (en) * | 2010-03-23 | 2019-01-22 | Intrexon Corp | Vectors conditionally expressing therapeutic proteins, host cells comprising the vectors, and uses thereof. |
US8936782B2 (en) * | 2011-11-22 | 2015-01-20 | Cedars-Sinai Medical Center | Interferon beta as antibacterial agents |
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JPH06298665A (en) * | 1993-04-14 | 1994-10-25 | Toray Ind Inc | Antiviral agent |
US6083724A (en) * | 1995-03-06 | 2000-07-04 | Commonwealth Scientific And Industrial Research Organization | Recombinant avian interferon-gamma (IFN-γ) |
US20030021765A1 (en) * | 1998-10-16 | 2003-01-30 | Blake Pepinsky | Polymer conjugates of interferon beta-1a and uses |
EP1314436A1 (en) * | 1999-01-25 | 2003-05-28 | Petr Yakovlevich Gaponyuk | Antiviral agent in the form of nose drops |
WO2004075903A1 (en) * | 2003-02-25 | 2004-09-10 | Applied Research Systems Ars Holding N.V. | Combined use of ribavirin and interferon beta in demyelinating diseases |
Family Cites Families (3)
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ITRM20020562A1 (en) * | 2002-11-06 | 2004-05-07 | Sigma Tau Ind Farmaceuti | USE OF THE RESVERATROL FOR THE PREPARATION OF A USEFUL DRUG FOR THE TREATMENT OF INFLUENCE VIRUS INFECTIONS. |
US20060035859A1 (en) * | 2003-05-16 | 2006-02-16 | Hemispherx Biopharma | Treating severe and acute viral infections |
US20080292586A1 (en) * | 2005-02-04 | 2008-11-27 | Karen Jervis | Method and Use of Interferon Compositions For the Treatment of Avian Influenza |
-
2006
- 2006-11-16 EP EP06807823A patent/EP1951285A2/en not_active Withdrawn
- 2006-11-16 JP JP2008540616A patent/JP2009515933A/en active Pending
- 2006-11-16 US US12/091,985 patent/US20080260690A1/en not_active Abandoned
- 2006-11-16 CA CA002626056A patent/CA2626056A1/en not_active Withdrawn
- 2006-11-16 AU AU2006314497A patent/AU2006314497A1/en not_active Abandoned
- 2006-11-16 WO PCT/EP2006/068588 patent/WO2007057436A2/en active Application Filing
Patent Citations (5)
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JPH06298665A (en) * | 1993-04-14 | 1994-10-25 | Toray Ind Inc | Antiviral agent |
US6083724A (en) * | 1995-03-06 | 2000-07-04 | Commonwealth Scientific And Industrial Research Organization | Recombinant avian interferon-gamma (IFN-γ) |
US20030021765A1 (en) * | 1998-10-16 | 2003-01-30 | Blake Pepinsky | Polymer conjugates of interferon beta-1a and uses |
EP1314436A1 (en) * | 1999-01-25 | 2003-05-28 | Petr Yakovlevich Gaponyuk | Antiviral agent in the form of nose drops |
WO2004075903A1 (en) * | 2003-02-25 | 2004-09-10 | Applied Research Systems Ars Holding N.V. | Combined use of ribavirin and interferon beta in demyelinating diseases |
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TSANG ET AL: "H5N1 influenza pandemic: contingency plans" LANCET THE, LANCET LIMITED. LONDON, GB, vol. 366, no. 9485, 13 August 2005 (2005-08-13), pages 533-534, XP005025434 ISSN: 0140-6736 * |
XIA C ET AL: "The interferon-alpha genes from three chicken lines and its effects on H9N2 influenza viruses" ANIMAL BIOTECHNOLOGY, vol. 15, no. 1, 2004, pages 77-88, XP009062641 ISSN: 1049-5398 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7858660B2 (en) | 2007-03-13 | 2010-12-28 | Adamas Pharmaceuticals, Inc. | Compositions and kits for treating influenza |
US7981930B2 (en) | 2007-03-13 | 2011-07-19 | Adamas Pharmaceuticals, Inc. | Compositions and kits for treating influenza |
US20110177028A1 (en) * | 2007-05-18 | 2011-07-21 | Davies Donna | Interferon-beta and/or lambda for use in treating rhinovirus infection in the elderly |
US9421243B2 (en) | 2010-03-12 | 2016-08-23 | Synairgen Research Limited | Therapy for influenza like illness |
Also Published As
Publication number | Publication date |
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WO2007057436A3 (en) | 2007-07-05 |
CA2626056A1 (en) | 2007-05-24 |
EP1951285A2 (en) | 2008-08-06 |
JP2009515933A (en) | 2009-04-16 |
AU2006314497A1 (en) | 2007-05-24 |
US20080260690A1 (en) | 2008-10-23 |
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