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    • 专利摘要:
    The present invention relates to diltiazem for its use as an activating agent for the expression of at least one gene encoding a type III interferon, in the prevention and / or treatment of infections with at least one pathogenic microorganism of epitheliums of the respiratory and / or intestinal tracts.
    公开号:FR3081325A1
    申请号:FR1854307
    申请日:2018-05-23
    公开日:2019-11-29
    发明作者:Manuel Rosa-Calatrava；Olivier Terrier；Claire Nicolas De Lamballerie；Guy Boivin；Mario Andres Pizzorno
    申请人:Universite Laval；Centre National de la Recherche Scientifique CNRS；Universite Claude Bernard Lyon 1 UCBL；Institut National de la Sante et de la Recherche Medicale INSERM；Ecole Normale Superieure de Lyon；
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    DILTIAZEM FOR USE IN THE TREATMENT OF MICROBIAL INFECTIONS
    FIELD OF THE INVENTION
    The present invention relates to a compound for use in the prevention and / or treatment of infections by pathogenic microorganisms.
    More particularly, the present invention relates to a compound for its use in the prevention and / or treatment of infections by pathogenic microorganisms of the epithelia of the respiratory and / or intestinal tracts.
    STATE OF THE ART
    Infections by pathogenic microorganisms of the epithelia of the respiratory and / or intestinal tracts
    Acute respiratory infections (ARI) are one of the leading causes of consultations, hospitalizations and deaths worldwide, including being the number one killer of young children with almost 2 million deaths a year. Each year, trying to treat these various respiratory infections, the cost to companies is estimated between 1.5 to 2 billion euros.
    Among the etiological agents responsible for ARI, viruses occupy a preponderant place. They are indeed found in the majority of cases of childhood pneumonia and are a predisposing factor for bacterial pneumonia in adults. Among the viruses most representative in frequency and morbidity, there are in particular influenza viruses type A and B, which also constitute a recurrent pandemic risk factor, as well as respiratory syncytial virus (hRSV), parainfluenza viruses ( hPIV) and the human metapneumovirus (hMPV). In addition, the emergence of new viruses from the Coronaviridae family, such as SARS and the recently described MERS-CoV virus, is most likely a serious emerging health problem.
    Other agents responsible for ARI are bacteria. Among the most representative pathogenic bacteria, there are notably S. pneumonia, P. aeruginosa, S. aureus and H. influenza. These pathogenic bacteria are etiological agents contributing to increased comorbidity and co-mortality in the case of respiratory co-infections, and they are responsible for the emergence and increasing spread of strains of bacteria resistant to antibiotics which fundamentally question the effectiveness of conventional antibiotic treatments in both humans and animals.
    With the exception of influenza viruses, there is currently no effective vaccine or antiviral molecule to prevent or treat infections with these various pathogenic respiratory viruses. In addition, in the case of influenza viruses, the delay and varying effectiveness of vaccination, as well as the growing emergence of viruses resistant to antivirals, are of great concern today.
    With regard to the antibiotic resistance of pathogenic bacteria responsible for superinfections, the European Center for Disease Control estimates the number of deaths per year in Europe resulting from antibiotic resistance at 25,000. An equivalent excess mortality is observed in the United States by the Atlanta CDC. The increase in resistance will be responsible for a dramatic increase in these numbers as was modeled in Lord J. O'Neil's report on the impact of antibiotic resistance by 2050.
    In February 2017, the WHO published a list of resistant bacteria representing a threat on a global scale: P. aeruginosa represents, among other things, a critical emergency because it is resistant to a large number of antibiotics; Meticillin-resistant S. pneumonia and S. aureus (MRSA) are responsible for various infections of the lungs and bones, as well as sepsis, especially in the most sensitive patients.
    Thus, the development of new prophylactic and therapeutic treatments constitutes a major public health objective. The success of new treatment strategies for infections by these pathogens rests in large part on a better characterization of their cell biology and of their molecular and functional interactions with their host.
    Intestinal infections are also a major cause of hospitalizations and in some cases death. In developed countries, the most common causes of acute gastroenteritis in immunocompetent adults are noroviruses and rotaviruses, as well as the following species and genera of bacteria: Campylobacter spp., Salmonella spp., Escherichia coli, Staphylococcus aureus, Bacillus cereus, and Clostridium difficile.
    Type III interferons
    Type III interferons, also known as lambda interferons (λ), constitute the first line of antimicrobial defense in the epithelium of the respiratory and intestinal tracts, contributing to the initial inhibition of the dissemination of pathogens, without however triggering inflammatory response (Andreakos et al., 2017). These type III interferons are actually produced very early in response to activation by pathogens of host cell sensors, such as Toll-like receptors or cytoplasmic effectors. These type III interferons activate the expression of many so-called “ISGs” genes (via activation of the JAK / STAT pathways), which confer inhibitory activity against respiratory pathogens, by inactivating for example the cellular entry of viruses (gene IFITM), or their replication (CAS, OASL, IFIT1, IFIT2, IFIT13, ISG15 gene).
    This early anti-pathogenic response, known as “interferon type III”, is notably predominant in the initial response of the respiratory epithelium to infection by influenza viruses (Galani et al., 2017).
    Type III interferons have already been evaluated in a clinical trial to treat hepatitis B and C infections, and have shown less significant side effects compared to treatment with type I interferons (Chan et al., 2016). The use of type III interferons as a non-inflammatory antiviral treatment against influenza virus infections has been recently proposed (Davidson et al., 2016).
    It would be advantageous to stimulate the endogenous production of one or more interferons of the type
    III to fight against infections of the respiratory and / or intestinal epithelia, in particular against viral infections of these epithelia.
    However, at present, no therapeutic compound with this stimulating activity is known. Thus, only the administration of exogenous type III interferon has been tested so far.
    Diltiazem, a calcium channel blocker
    Diltiazem is a member of the benzothiazepines family, referenced under CAS number 42399-41-7. This molecule can be in the form of two enantiomers Lcis and D-cis, or a racemic mixture.
    Diltiazem has been known for more than 30 years and has been approved in Europe and the United States by the regulatory authorities for the drug. It can be administered as diltiazem hydrochloride. Cardizem®, Cartia®, Taztia® and Dilacor® are its most common trade names.
    Many formulations are available, especially sustained release formulations. Diltiazem is available in various galenical forms, such as a cream for topical application, in the form of tablets or capsules for oral administration, in the form of a powder for preparation of solution for injection or in the form of pharmaceutical preparations for inhalation (WO 02 / 094238, US 4,605,552).
    Its known physiological action is the inhibition of calcium channels, and therefore the inhibition of intracellular calcium flows. Diltiazem notably slows the entry of transmembrane calcium into the myocardial muscle fiber and the smooth muscle fiber of the vessels. This allows the intracellular calcium concentration reaching the contractile proteins to be reduced.
    In humans, the administration of diltiazem is indicated for its vasodilating action, with the aim of reducing cardiac work. It is thus used in the management of cardiac and circulatory disorders such as angina pectoris, high blood pressure, myocardial ischemia and tachycardia.
    Other therapeutic uses of diltiazem have also been proposed in the literature, although no drugs have already been approved by regulatory authorities for these new therapeutic applications.
    International application WO 87/07508 describes the use of therapeutic compounds which inhibit the influx of calcium into the cell, such as diltiazem, for the treatment of viral infections linked to cytomegalovirus or to herpes.
    International application WO 2011/066657 describes the use of a calcium channel blocker, such as verapamil or diltiazem, for the treatment or prevention of viral and / or bacterial infections, or even autoimmune diseases. Viruses affected include those of oral herpes, genital herpes and shingles.
    International application WO 2011/126071 describes the use of compounds which inhibit the influx of calcium into the cell, such as diltiazem, for the treatment of viral infections, in particular those linked to influenza viruses. It is specifically explained that diltiazem inhibits the interaction between the virus and calcium channels, and thus blocks the entry of the virus into cells.
    International application WO 2016/146836 discloses pharmaceutical or veterinary compositions comprising diltiazem for their use in the prevention and / or treatment of infection by influenza viruses.
    Patent EP 1,117,408 describes the use of diltiazem, as a calcium channel blocking compound, for treating pathologies linked to the degeneration of the photoreceptors of the retina.
    However, not all of the beneficial actions of diltiazem have been explored yet, and the technical effects associated with diltiazem used as a drug are likely not all known to date.
    STATEMENT OF THE INVENTION
    The technical problem underlying the present invention relates to the identification of molecules making it possible to stimulate the expression of genes coding for proteins of the interferon III type, with the aim of preventing and / or treating infections by pathogenic microorganisms of the epithelia. respiratory and / or intestinal tracts.
    Indeed, in the event of infection by microorganisms of the respiratory and / or intestinal tracts, it is advantageous to stimulate the response of the organism against these pathogens, without however inducing an inflammatory response, and thus avoid over-stimulation of the system. immune.
    However, at present, no therapeutic compound exhibiting this activity is known.
    Therapeutic compounds having the capacity to stimulate the expression of genes coding for proteins such as interleukin 29, interleukin 28A and / or interleukin 28B are therefore actively sought.
    Surprisingly, the inventors have highlighted the fact that diltiazem, an inhibitor of calcium channels, also has a stimulating action on the expression of these genes coding for proteins of interferon III type.
    Thus, diltiazem can be used for various therapeutic applications, and in particular to prevent and / or treat infections by at least one pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts.
    Diltiazem, as an activator of the expression of genes coding for one or more type III interferon (s), is particularly suitable for the treatment of viral or bacterial infections, but also co-infections linked to both in the presence of a virus and of a bacterium, and in particular is suitable for the treatment of bacterial superinfections concomitant with a primary viral infection.
    The present invention relates to diltiazem for its use as an agent which activates the expression of at least one gene coding for a type III interferon.
    As those skilled in the art know, in view of the abundant scientific literature on the subject, the activation of the “interferon III pathway” makes it possible to treat numerous physiological disorders, and in particular those linked to infections. by pathogens.
    In particular, the present invention relates to diltiazem for its use as an agent activating the expression of at least one gene coding for a type III interferon, in the prevention and / or treatment of infections by at least one pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts.
    The present invention also relates to a pharmaceutical or veterinary composition comprising diltiazem as an agent activating the expression of at least one gene coding for a type III interferon, for its use in the prevention and / or treatment of infections. by pathogenic microorganisms in the epithelia of the respiratory and / or intestinal tracts.
    According to a particular aspect, the pharmaceutical or veterinary composition is characterized in that it is in a galenical form suitable for administration by inhalation.
    DESCRIPTION OF THE FIGURES
    Figure 1. Characterization by RNAseq of the induction by diltiazem of the expression of type III interferon genes.
    1A- Ratios of expression of genes coding for type III interferons IFN-λΙ, IFN-X2 and IFN-X3 (designated respectively by IFNL1, IFNL2 and IFNL3) between:
    - the reconstituted human respiratory epithelia treated 3 days with diltiazem (90 μΜ) and
    - untreated reconstituted human respiratory epithelia (basal level of 1).
    1B- Ratios of expression of genes coding for IFI44L, IFIT1, IFIT2, IFIT3, IFITM1, ISG15, MX1, MX2, OAS1, OAS2, OAS3, OASL, RSAD2 and STAT1 between:
    - the reconstituted human respiratory epithelia treated 3 days with diltiazem (90 μΜ) and
    - untreated reconstituted human respiratory epithelia (basal level of 1).
    Figure 2. Rt-qPCR confirmation of diltiazem induction of 8 genes associated with the Interferon type III response.
    IFIT1, IFIT2, IFIT3, IFI27, IFN-λΙ (IFNL1), IFN-X2 (IFNL2), IFI44L and IFITM1 expression ratios between:
    - the reconstituted human respiratory epithelia treated 3 days with diltiazem (90 μΜ) (right) and
    - untreated reconstituted human respiratory epithelia (left).
    * P <0.05, ** P <0.01, *** P <0.001 and **** P <0.0001 compared to untreated epithelia.
    Figure 3. Measurement by ELISA assay of the secretion of lambda 1 interferon (IL-29).
    The secretion levels (pg / mL) of lambda 1 interferon (IL-29) at the apical and basal poles of reconstituted human respiratory epithelia treated and not treated with diltiazem were measured after 72 hours of treatment with ELISA.
    * P <0.05, ** P <0.01, *** P <0.001 and **** P <0.0001 compared to untreated epithelia.
    Figure 4. Diltiazem treatment reduces replication of the respiratory syncytial virus (RSV) in infected reconstituted epithelia.
    4A- Schematic representation of the chronology of treatments for human respiratory epithelia: after infection with RSV, the reconstituted epithelia are treated at 5 h post-infection (5 hpi) and then the following three days (1, 2 and 3 days pi). Viral quantification is carried out at 6 days pi.
    4B- Quantification of the number of copies of the viral genome (by quantifying the copies of the F gene) relative to the total quantity of RNA, by RT-qPCR, at the apical pole of the epithelium, that is to say in the supernatant culture of the epithelium.
    4C- Quantification of the number of copies of the viral genome (by quantifying the copies of the F gene) relative to the total amount of RNA, by RT-qPCR, within the epithelia.
    DETAILED DESCRIPTION OF THE INVENTION
    The present invention relates to a new therapeutic use of a known drug, diltiazem, a molecule member of the family of benzothiazepines referenced under CAS number 42399-41-7, of formula (1):
    Formula 1)
    For the purposes of the present invention, the term "diltiazem" means diltiazem in all its forms, in particular in the form of salts and in particular in the form of diltiazem hydrochloride. This term includes the racemic mixture as well as each of the enantiomers when these are isolated. This term also includes the derivatives of diltiazem, that is to say the molecules derived from formula (1), having the same biological activity of stimulating the expression of type III interferon proteins.
    The present invention relates to diltiazem for its use as an agent which activates the expression of at least one gene coding for a type III interferon.
    Until now, diltiazem has been used for its calcium channel blocking action; through this inhibition of intracellular calcium transport, the administration of diltiazem generates numerous physiological effects on the organisms of humans and animals.
    The inventors have highlighted a new technical effect of diltiazem, namely the activation of the expression of one or more genes coding for type III interferons.
    According to a preferred aspect of the invention, the gene or genes whose expression is activated are endogenous genes, that is to say the genes native to the organism considered, which have not undergone any genetic modification.
    A person skilled in the art knows the implication of type III interferons in different physiological situations, and can conclude, in the light of scientific literature, of the therapeutic potential of such a compound activating the synthesis of these type III interferons. In particular, cells sensitive to the effects of interferons III, i.e. cells expressing their receptors, have been listed in the literature. Thus, human and animal pathologies that may benefit from the use of diltiazem will be readily determined by those skilled in the art.
    More specifically, the present invention relates to diltiazem for its use as an agent for activating the expression of the genes coding for interleukin 29, interleukin 28A and interleukin 28B.
    Thus, for the first time, a therapeutic compound making it possible to activate the “interferon III pathway”, that is to say an agent activating the expression of one or more genes coding for interferons of the type III, is identified. It is the first compound with this activity to be identified.
    Type III interferons
    Type III interferons, also known as lambda interferons (λ), are the first line of defense for a human or animal organism from infection by pathogenic microorganisms.
    This new family of interferons, first described in 2003, includes the following four proteins in humans:
    Interferon lambda-1 (IFN-λΙ) or interleukin 29 (IL-29),
    Interferon lambda-2 (IFN-X2) or interleukin 28A (IL-28A),
    Interferon lambda-3 (IFN-X3) or interleukin 28B (IL-28B), Interferon lambda-4 (IFN-X4).
    In mice, only two proteins belonging to this family of interferons III have so far been identified (IFN-A2 / IL-28A and IFN-A2 / IL-28B).
    These type III interferons mediate their effects via their common receptor IFN-XR1, also known under the name IL-28RA. A heteromeric complex forms between this receptor and the IL-10R2 receptor to bind monomers of IFN-λ (see Donnelly & Kotenko, 2010, for review).
    For the purposes of the present invention, the term "gene coding for a type III interferon" means one of the following genes, or their counterparts:
    The gene coding for IFN-λΙ,
    The gene coding for IFN-X2,
    The gene coding for IFN-X3, and
    The gene coding for IFN-X4, as described in the publications by Kotenko et al., 2003 and O’Brien et al., 2014.
    It is understood that the genes mentioned above are the human genes, but that if diltiazem is used in a different animal species, the genes coding for the interferons of the type
    III whose expression is activated by diltiazem will be at least one of the homologous genes for the species in question.
    Infections by pathogenic microorganisms of the epithelia of the respiratory and / or intestinal tracts
    The IFN-XR1 receptor is exclusively expressed by cells of the epithelial type, thus limiting the effects of type III interferons to the epithelia.
    In infections with external pathogens, the epithelia of the respiratory and intestinal tracts are the first affected organs, due to their contact, respectively, with the aspirated air, and the water and food ingested.
    Thus, the present invention relates very particularly to diltiazem for its use as an agent activating the expression of at least one gene coding for a type III interferon, in the prevention and / or treatment of infections by at least a pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts.
    The expression “infection with at least one pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts” must be understood as being an infection generated by the presence of at least one pathogenic microorganism, this microorganism having infected the individual or the animal, or likely to infect the individual or animal.
    It is indeed understood that the present invention relates both to the prevention and / or treatment of infections affecting humans (also designated as "individuals"), as infections affecting animals, especially farm animals.
    The term "prevention" refers to preventing, or at least reducing the likelihood of, infection in a human or animal organism by at least one pathogenic microorganism. Under the action of the type III interferons produced, the organism's tissues, and in particular the epithelia, become more resistant and are more likely not to be infected by said microorganism.
    According to a particular implementation of the invention, diltiazem is used as an agent activating the expression of at least one gene coding for a type III interferon, in the prevention of infections by at least one pathogenic microorganism epithelia of the respiratory and / or intestinal tracts
    The term "treatment" refers to combating infection with at least one pathogenic microorganism in a human or animal organism. Thanks to the administration of diltiazem, the rate of viral, bacterial, fungal or parasitic infection in the body will gradually decrease or even disappear completely. The term "treatment" also refers to reducing the symptoms associated with the infection (fever, fatigue, etc.) and / or preventing / reducing the risk of complications, particularly secondary infection.
    According to a particular implementation of the invention, diltiazem is used as an agent activating the expression of at least one gene coding for a type III interferon, in the treatment of infections by at least one pathogenic microorganism epithelia of the respiratory and / or intestinal tracts.
    According to a preferred aspect, the present invention relates to diltiazem for its use as an agent activating the expression of at least one gene coding for a type III interferon, in the prevention and / or treatment of infections by at least one pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts, characterized in that said at least one gene is chosen from the gene coding for interleukin 29, the gene coding for interleukin 28A and the gene coding for interleukin 28B.
    According to a particular implementation, diltiazem is used as an activating agent for the expression of the three genes coding for interleukin 29, for interleukin 28A and for interleukin 28B.
    Pathogenic microorganisms
    Within the meaning of the invention, the expression “pathogenic microorganisms” designates any microorganism capable of creating a disease in other organisms, such as in humans or animals. This expression notably includes viruses, bacteria, fungi, protozoa, worms, and other pathogenic unicellular microorganisms.
    Preferably, the “pathogenic microorganism” is a microorganism sensitive to the cellular response of the “interferon III” type, that is to say a microorganism whose cellular infection will be prevented or inhibited, totally or partially, by expression and secretion of interferon III proteins.
    According to one aspect of the invention, the pathogenic microorganism is a microorganism which specifically infects the epithelia of the respiratory tracts.
    According to another aspect of the invention, the pathogenic microorganism is a microorganism which specifically infects the epithelia of the intestinal tracts.
    According to yet another aspect of the invention, the pathogenic microorganism is a microorganism capable of infecting any type of epithelia, especially those of the respiratory and intestinal tracts.
    According to a first aspect of the invention, the infection is a viral infection, that is to say that the pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts is a virus.
    Proteins belonging to the family of type III interferons are essential actors in the anti-viral response of epithelia targeted by viruses. Thus, an agent for activating the expression of the genes coding for said type III interferon proteins makes it possible to stimulate and optimize the anti-viral response of the infected epithelia.
    According to this aspect, the invention relates to diltiazem for its use as an agent activating the expression of at least one gene coding for a type III interferon, in the prevention and / or treatment of infections by at least a virus infecting the epithelia of the respiratory and / or intestinal tracts.
    Within the meaning of the invention, the term "virus" includes any type of virus but more particularly viruses infecting vertebrate eukaryotic organisms. It can be a DNA or RNA virus. In the context of the present invention, it is more particularly a question here of viruses infecting organisms via the epithelia of the respiratory and / or intestinal tracts.
    According to a particular aspect of the invention, the infection is not an infection with an influenza virus.
    The therapeutic use of diltiazem to treat influenza virus infections has already been proposed in documents WO 2011/126071 and WO 2016/146836. However, diltiazem is used in the prior art for its action on the calcium channels, and not for its action activating the expression of genes coding for type III interferons.
    According to a particular aspect of the invention, the pathogenic microorganism is a group I virus having a double-stranded DNA genome. This group of viruses includes viruses of the Herpes order, those of the papillomavirus family, as well as polyomaviruses and poxviridae.
    According to a particular aspect of the invention, the pathogenic microorganism is a group II virus having a single-stranded DNA genome, comprising in particular the viruses of the parvoviridae family.
    According to one aspect of the invention, the pathogenic microorganism is a group III virus having a double-stranded RNA genome, comprising in particular viruses of the rheoviridae family, such as rotaviruses.
    According to one aspect of the invention, the pathogenic microorganism is a group IV virus having a positive-polarity single-stranded RNA genome. This group includes:
    viruses of the order Nidovirales, such as those of the coronaviridae family;
    viruses of the family Caliciviridae, including the Norwalk virus;
    viruses of the family Flaviviridae, including in particular the yellow fever virus, the West Nile virus, the hepatitis C virus and the dengue virus;
    viruses of the Picornaviridae family, including polioviruses, rhinoviruses, and hepatitis A virus;
    viruses of the Togaviridae family, including rubella virus, Ross River virus, Sindbis virus and Chikungunya virus.
    According to one aspect of the invention, the pathogenic microorganism is a group V virus having a negative polarity single-stranded RNA genome (ssRNA). This group includes in particular viruses of the order Mononegavirales, such as:
    viruses of the Bornaviridae family, including Bornaviridae, viruses of the Filoviridae family, including Ebola virus and Marburg virus, viruses of the Paramyxoviridae family, including measles virus, mumps mumps virus and Henipaviruses, viruses of the Rhabdoviridae family, including the rabies virus, viruses of the Arenaviridae family, including the Lassa fever virus, viruses of the Bunyaviridae family, including the Hantaviruses and the Congo-Crimea fever, viruses of the Orthomyxoviridae family.
    According to a particular aspect of the invention, the pathogenic microorganism is a virus chosen from the human respiratory syncytial virus (hRSV), parainfluenza viruses (hPIV), human metapneumovirus (hMPV), Nipah virus, novoviruses, Swine virus fever, adenoviruses, coronaviruses, Zika virus, yellow fever virus, rheoviruses, rotaviruses, Dengue virus, and West Nile virus.
    According to a particular implementation, the invention relates to diltiazem for its use as an agent activating the expression of at least one gene coding for an interferon of the type
    III, in the prevention and / or treatment of infections with the human respiratory syncytial virus (hRSV).
    More particularly, the invention relates to diltiazem for its use in the prevention and / or treatment of infections with the human respiratory syncytial virus (hRSV).
    According to a second aspect of the invention, the infection is a non-viral infection. In particular, the pathogenic microorganism can be chosen from a bacterium, a fungus and a parasite.
    According to a particular aspect of the invention, the pathogenic microorganism is a bacterium.
    Among the pathogenic bacteria, mention may be made in particular of the bacteria of the following species: Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Salmonella Typhimurium and Streptococcus pneumoniae
    Mention may also be made of bacteria specific to intestinal infections such as Campylobacter spp., Salmonella spp., Shigella spp., Yersinia enterocolitica, Vibrio cholerae, Escherichia coli, Staphylococcus aureus, Bacillus cereus, and Clostridium difficile.
    According to a particular aspect of the invention, the pathogenic microorganism is a bacterium selected from the following bacterial species: Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Salmonella Typhimurus Typhimurus influenzae, Campylobacter spp., Salmonella spp., Shigella spp., Yersinia enterocolitica, Vibrio cholerae, Escherichia coli, Staphylococcus aureus, Bacillus cereus, and Clostridium difficile.
    According to a particular aspect of the invention, the pathogenic microorganism is a fungus.
    Among the pathogenic fungi there may be mentioned in particular Aspergillus fumigatus, Candida albicans, Pneumocystis jiroveci, Fusarium solari.
    The expression "at least one pathogenic microorganism" means that one or more pathogenic microorganisms are present in the infected organism, thereby generating an immune response from the organism.
    In particular, the organism may have been infected with both a virus and a bacterium, which is referred to as co-infection of the organism.
    According to a particular aspect, the invention relates to diltiazem for its use as described above, characterized in that the infection is a co-infection with at least one virus and at least one bacterium.
    Advantageously, diltiazem is then used for the concomitant treatment of a viral infection and a bacterial infection, which makes it possible to limit the number of active compounds administered to an individual or an animal suffering from this co-infection.
    More particularly, this co-infection may be linked to the presence in the infected epithelia of a combination of pathogenic microorganisms chosen from the following:
    A human respiratory syncytial virus (hRSV) and at least one bacterium of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Salmonella typhimure.
    a parainfluenza virus (hPIV) and at least one bacterium of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Salmonella typhimurusus streptus pneumoniae Streptococcus (hMPV) and at least one bacterium of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Salmonella typhimurium and Streptococcus pneumoniae a bacterium of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Salmonella typhimurium, Streptococcus pneumoniae and Haemophilus influenzae us and at least one bacterium of a species chosen from Campylobacter spp. Salmonella spp, Escherichia coli, Staphylococcus aureus, Bacillus cereus, and Clostridium difficile, a coronavirus and at least one bacteria of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus staphylococcus Salmonella typhimurium, Streptococcus pneumoniae and Haemophilus influenzae, Swine fever virus and at least one bacterium of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus epidaphorusus Staphylococcus aureus staphylococcus aureus staphylococcus and Haemophilus influenzae, an adenovirus and at least one bacterium of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Salmonella typ himurium, Streptococcus pneumoniae and Haemophilus influenzae, the Zika virus and at least one bacterium of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermococcus Sterm influenzae, the yellow fever virus and at least one bacterium of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Salmonella typhimurus pneumoniae Streptococcus rheovirus and at least one bacterium of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Salmonella typhimurium, Streptococcus pneumon iae and Haemophilus influenzae, a rotavirus and at least one bacterium of a species chosen from Campylobacter spp. Salmonella spp., Escherichia coli, Staphylococcus aureus, Bacillus cereus, and Clostridium difficile, the Dengue virus and at least one bacterium of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa , Staphylococcus epidermidis, Salmonella typhimurium, Streptococcus pneumoniae and Haemophilus influenzae, the virus l / l / est Nile and at least one bacterium of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonus aeronus Staphylococcus epidermidis, Salmonella typhimurium, Streptococcus pneumoniae and Haemophilus influenzae, and
    An influenza virus and at least one bacteria of a species chosen from Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, Salmonella typhimurium and Streptococcus pneumonia.
    According to a particular implementation of the invention, diltiazem as an agent activating the expression of at least one gene coding for a type III interferon will be used for both:
    i) Treat a viral infection of the epithelia of the respiratory and / or intestinal tracts; and ii) To prevent co-infection with at least one other pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts, such as bacterial superinfection.
    According to another particular implementation of the invention, diltiazem as an agent activating the expression of at least one gene coding for a type III interferon will be used for both:
    i) Treat a bacterial infection of the epithelia of the respiratory and / or intestinal tracts; and ii) To prevent co-infection with at least one other pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts, such as viral superinfection.
    According to another particular implementation of the invention, diltiazem as an agent activating the expression of at least one gene coding for a type III interferon will be used for both:
    i) Treat a viral infection of the epithelia of the respiratory and / or intestinal tracts; and ii) Treat a co-infection with at least one other pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts, such as a bacterial superinfection.
    Therapeutic combinations
    The present invention also relates to diltiazem for its therapeutic use as presented above, characterized in that it is used in combination with at least one other active agent, that is to say with one or more active agents.
    Preferably, this other active agent is a therapeutic compound having a beneficial action on a human or animal organism, with the aim of preventing or treating a pathology.
    This other active agent will in particular be chosen from an anti-viral compound, an antibacterial compound, an anti-parasitic compound, an anti-fungal compound, and a preventive or therapeutic vaccine.
    Preferably, this other active agent is chosen from an antiviral compound and an anti-bacterial compound.
    For the purposes of the invention, the term “antiviral compound” means a compound having either a direct inhibitory action on at least one virus (for example, inhibiting its replication), or an action on a target cell of the virus (for example, in inducing a cellular state unfavorable to a viral infection, thus preventing viral infection).
    Antiviral agents are classified into different categories according to their mode of action. We can cite in particular:
    - nucleotide analogs, which interfere or stop the synthesis of DNA or RNA; as well as inhibitors of enzymes involved in the synthesis of DNA or RNA (helicase, replicase);
    - the compounds which inhibit the stages of maturation of the virus during its replication cycle;
    - compounds that interfere with binding to the cell membrane, or the entry of viruses into host cells (fusion or entry inhibitors);
    - agents which prevent the virus from expressing itself in the host cell after it has entered, by blocking its disassembly within the cell;
    - agents that restrict the spread of viruses to other cells.
    In particular, the antiviral agent (s) is (are) chosen from:
    i) viral agents having a direct inhibitory action on viruses, such as for example ribavirin and favipiravir;
    ii) active agents inducing cellular states generally unfavorable to a viral infection; and iii) compounds chosen from the following compounds:
    • analogs of substituted 2-deoxyuridine;
    • nucleoside analogs;
    • pyrophosphate analogues;
    • protease inhibitors;
    • inhibitors of the penetration of a virus into cells, such as for example arbidol;
    • monoclonal antibodies, for example palivizumab, directed against an epitope of the antigenic site A of the fusion protein of the respiratory syncytial virus (RSV); and • antisense oligonucleotides having a virus-inhibiting action.
    Within the meaning of the invention, the term “anti-bacterial compound” means a compound having an anti-bacterial activity, that is to say inhibiting the replication of bacteria (bacteriostatic compounds) or destroying them (bactericidal compounds) or else by inhibiting their biosynthesis and / or secretion of toxic products. These are in particular antibiotics.
    In particular, the anti-bacterial agent (s) is (are) chosen from:
    i) antibiotics, and in particular those of the macrolide family, and in particular roxythromycin;
    ii) bacteriophages, natural predators of bacteria.
    Such anti-viral and anti-bacterial agents are commercially available, and their conditions of use are described in reference works such as Le Dictionnaire Vidal.
    According to another aspect of the invention, the other active agent used in combination with diltiazem is an anti-fungal compound or an anti-parasitic compound, in particular chosen from systemic anti-fungal compounds (amphotericin B, azoles, echinocandins) and systemic anti-parasitic compounds (for example antimalarial, anti-antibiotic, toxoplasmosis, leishmaniasis, pneumocytosis, anthelmintic).
    According to a particular implementation of the invention, the at least one other active agent is a vaccine.
    For the purposes of the invention, the term “vaccine” means a compound or a combination of compounds which specifically stimulate the immune system of a human or animal organism. A vaccine will in particular include an antigen, that is to say a compound inducing a specific immune response in the organism, which will keep its memory.
    Such a vaccine could be of the preventive vaccine type, that is to say intended to stimulate a specific immune response before infection of an organism by a pathogenic microorganism.
    Without limitation, there may be mentioned as examples different types of vaccines, classified according to the nature of the antigens from which they are prepared. The antigens conventionally used are the following: inactivated infectious agents, attenuated living agents, infectious agent subunits, toxoids, viral vectors expressing antigens derived from pathogens, vectors carrying nucleic acids (DNA or RNA), and antibodies.
    Such a vaccine could also be of the therapeutic vaccine type, that is to say intended to stimulate a specific immune response concomitantly with the infection of an organism by a pathogenic microorganism.
    In all cases, it is understood that this vaccine may be administered before, during or after treatment with diltiazem.
    Finally, according to a particular aspect of the invention, all of the active agents mentioned above may be used in combination with each other, for example combinations of the type: diltiazem, anti-viral compound and anti-bacterial compound, diltiazem , anti-viral compound and anti-parasitic compound, dilitiazem, anti-bacterial compound and anti-fungal compound, diltiazem and preventive vaccine; or diltiazem and therapeutic vaccine, may be administered concomitantly or sequentially to an individual or an animal having an infection, by one or more pathogenic microorganisms, of the epithelia of the respiratory and / or intestinal tracts.
    Pharmaceutical or veterinary composition
    The present invention also relates to a pharmaceutical or veterinary composition comprising diltiazem as an agent which activates the expression of at least one gene coding for a type III interferon.
    The present invention also relates to a pharmaceutical or veterinary composition comprising diltiazem as an agent activating the expression of at least one gene coding for a type III interferon, for its use in the prevention and / or treatment of infections. by pathogenic microorganisms in the epithelia of the respiratory and / or intestinal tracts.
    More specifically, this composition according to the invention will comprise diltiazem as well as a suitable pharmaceutical vehicle, and optionally another active agent.
    The term “suitable pharmaceutical vehicle” designates pharmaceutically acceptable vehicles or excipients, ie vehicles or excipients whose administration to an individual or an animal is not accompanied by significant deleterious effects, and which are well known to those skilled in the art.
    This composition according to the invention can be adapted for any type of administration and in particular for oral, sublingual, nasal and / or buccal administration by inhalation, subcutaneous, intramuscular, intravenous, transdermal, ocular or rectal.
    Appropriate dosage forms may for example be tablets, capsules, powders, granules and solutions or suspensions.
    According to a particular aspect, the pharmaceutical or veterinary composition is characterized in that it is in a galenical form suitable for administration by inhalation, that is to say by the nasal and / or buccal routes.
    Inhalation refers to absorption through the respiratory tract. It is a method of absorbing therapeutic compounds in the form of gases, micro-droplets or suspended powder.
    There are two types of administration by inhalation:
    • administration by insufflation when the compositions are in the form of powders, and • administration by nebulization when the compositions are in the form of aerosols (suspensions) or in the form of solutions, for example aqueous solutions, under pressure. The use of a nebulizer or sprayer will then be recommended for administering the pharmaceutical or veterinary composition.
    The dosage form suitable for administration of diltiazem by inhalation is chosen from: a powder, an aqueous suspension of droplets or a solution under pressure.
    According to one aspect of the invention, the pharmaceutical or veterinary composition comprises an effective amount of diltiazem, for its use as an agent activating the expression of at least one gene coding for a type III interferon, in the prevention and / or the treatment of infections with at least one pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts.
    A person skilled in the art will be able, from his general knowledge, to easily identify the effective amount of diltiazem which will have to be administered in order to obtain an action on the expression of at least one gene coding for a type III interferon.
    The present invention also relates to a combination product comprising:
    diltiazem as an agent which activates the expression of at least one gene coding for a type III interferon, and at least one other active agent chosen from an anti-viral compound, an anti-bacterial compound, and an agent for preventing infections by pathogenic microorganisms, for simultaneous, separate or sequential use for preventing and / or treating infection by pathogenic microorganisms of the respiratory and / or intestinal epithelia.
    The present invention also relates to a method for preventing and / or treating an infection in an individual infected or liable to be infected with at least one pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts, comprising the administration of diltiazem to this individual, to activate the expression of at least one gene coding for a type III interferon.
    The present invention also relates to a method for preventing and / or treating an infection in an individual infected or liable to be infected with at least one pathogenic microorganism of the epithelia of the respiratory and / or intestinal tracts, comprising the administration of diltiazem to this individual, diltiazem being used as an agent activating the expression of at least one gene coding for a type III interferon.
    The present invention also relates to a method of preventing and / or treating an infection in an animal infected or liable to be infected with at least one microorganism pathogenic to the epithelia of the respiratory and / or intestinal tracts, comprising the administration of diltiazem to this animal, to activate the expression of at least one gene coding for a type III interferon.
    This administration of diltiazem will preferably be carried out by inhalation.
    EXAMPLES
    It is understood that the examples presented in this section are in no way limiting, and that they only illustrate the invention as described above.
    Example 1. Characterization by RNAseq of the induction by diltiazem of the expression of type III interferon genes.
    Reconstituted human respiratory epithelia (MucilAir® HAE, Epithelix) and maintained in culture at the air-liquid interface according to the instructions of the supplier Epithelix, were treated or not with diltiazem (90 μΜ) via their culture medium at their basal pole . The diltiazem treatment was repeated for 3 consecutive days (3 administrations in total).
    The treated and untreated epithelia were then lysed with 150 μL of RLT buffer (Qiagen). Total RNA was extracted using the RNeasy kit (Qiagen) according to the supplier's instructions.
    CDNA libraries were prepared from 200 ng total RNA using the Scriptseq ™ complete Gold kit-Low Input kit (SCL6EP, Epicenter) according to the supplier's instructions. Each bank was amplified, quantified and indexed with primers provided in the ScriptSeq ™ Index PCR Primers kit (RSBC10948, Epicenter) and sequenced. The sequencing was carried out on an Illumina HiSeq 2500 system with a minimum required of 40 million “reads” sequenced by samples.
    Data demultiplexing and conversion of BCL files from sequencing to FASTQ files were performed using the Illumina bcl2fastq tool, in version 1.8.4. The FastQC software (http://www.bioinformatics.babraham.ac.uk/projects/fastqc) made it possible to carry out the necessary quality checks on the raw data. The “trimming” was carried out with the Trimmomatic tool, with a minimum quality threshold equal to Q30. A pseudoalignment of trimmed reads on the human genome (Homo Sapiens: GRCh38.p11) by the Kallisto software was carried out, followed by a statistical analysis using the R 3.3.1 software and the EdgeR 3.14.0 package.
    The difference in gene expression between cells treated with diltiazem and control cells was calculated using a linear model with a correction of the p value by the Benjamini-Hochberg method.
    Only the genes with an expression differential greater than or equal to 2, and a corrected p value less than 0.05, were considered in the rest of the analysis.
    These genes were subjected to functional enrichment analyzes using the DAVID 6.8 tool as well as association and interaction studies using the STRING tool.
    Are represented in FIG. 1A the expression ratios of the type III interferon genes IFN-λ1, IFN-X2 and IFN-X3 observed between the cells treated with diltiazem and the untreated control cells.
    Are represented in FIG. 1B the expression ratios of the type III interferon response genes such as IFI44L, IFIT1, IFIT2, IFIT3, IFITM1, ISG15, MX1, MX2, OAS1, OAS2, OAS3, OASL, RSAD2 and STAT1 observed between cells treated with diltiazem and untreated control cells.
    It clearly appears that the treatment of reconstituted human respiratory epithelia, for 3 days, modifies the level of expression of the genes coding for the type interferons
    III IFN — λ1, IFN-X2 and IFN-X3, significantly increasing it (from 100 to more than 200 times). In addition, this treatment also stimulates the expression of type III interferon response genes.
    Example 2. Confirmation by Rt-qPCR of the induction by diltiazem of the expression of 8 genes associated with the response "Interferon type III".
    Reconstituted human respiratory epithelia (MucilAir® HAE, Epithelix) were maintained in culture at the air-liquid interface according to the instructions of the supplier Epithelix, and were treated or not with diltiazem (90 μΜ) via their culture medium at their basal pole. The diltiazem treatment was repeated for 3 consecutive days (3 administrations in total).
    The treated and untreated epithelia were then lysed with 150 μL of RLT buffer (Qiagen). Total RNA was extracted using the RNeasy kit (Qiagen) according to the supplier's instructions. After a reverse transcription step, a quantitative real-time PCR reaction was carried out using the StepOnePlus ™ Real-Time PCR System (Applied Biosystems) in a 96-well plate.
    Quantitative PCR primers (GAPDH: Hs02758991_g1, IFNL1: Hs00601677_g1, IFNL2: Hs00820125_g1, IFIT1: Hs01675197_m1, IFIT2: Hs00533665_m1, IFIT3: Hs00382744_m1, IFI27: Hs01086373_g1, IFI44L: Hs00915292_m1, IFITM1: Hs01652522_g1) and probes (TaqMan gene assays term ) were provided by Thermo Fisher Scientific.
    Each sample was analyzed in triplicate and the “cycle threshold” (Ct) were normalized compared to the GAPDH reference.
    The expression ratios of the IFIT1, IFIT2, IFIT3, IFI27, IFN-λΙ, IFN-X2 ,, IFI44L and IFITM1 genes between the cells treated with diltiazem and the untreated cells were determined by the 2ΔΔΟί method (Livak and Schmittgen, 2001).
    Figure 2 shows the results obtained: after treatment with diltiazem, the reconstituted epithelia show a marked increase in the expression of the genes IFIT1, IFIT2, IFIT3, IFI27, IFN-λΙ, IFN-72, IFI44L and IFITMI.
    Example 3. Measurement by ELISA assay of the secretion, stimulated by diltiazem, of type III interferon lambda 1 (IL-29).
    Reconstituted human respiratory epithelia (MucilAir® HAE, Epithelix) were maintained in culture at the air-liquid interface according to the instructions of the supplier Epithelix, and were treated or not with diltiazem (90 μΜ) via their culture medium at their basal pole. The diltiazem treatment was repeated for 3 consecutive days (3 administrations in total).
    The secretion levels (pg / mL) of interferon lambda 1 (IL-29) at the apical and basal poles of the epithelia treated and not treated with diltiazem, were measured after 72 hours of treatment with ELISA according to the supplier's instructions (# 3570 -1 H, Mabtech, Stockhom, Sweden).
    FIG. 3 presents the results obtained: the secretion of IFN-11 is very markedly increased at the apical pole following a treatment with diltiazem; a less marked increase is also observed at the basal pole.
    Example 4. Treatment with diltiazem significantly reduces replication of the respiratory syncytial virus.
    Reconstituted human respiratory epithelia (MucilAir® HAE, Epithelix) were maintained in culture at the air-liquid interface according to the instructions of the supplier Epithelix, and were infected with respiratory syncytial virus (Long strain, ATCC VR-26) at a multiplicity of infection (MOI) 1, then treated or not with diltiazem (90 pM) via their culture medium at their basal pole. Treatment with diltiazem was carried out at 5 hours post-infection and then repeated for 3 consecutive days (4 administrations in total).
    At 6 days post-infection, the samples at the apical pole of the infected and treated and / or untreated epithelia, as well as the epithelia as such, were lysed with 150 μL of RLT buffer (Qiagen). The process of the experiment is schematically shown in Figure 4A.
    Total RNA was extracted using the RNeasy kit (Qiagen), according to the supplier's instructions, for quantification of the copy number of viral genome (F gene) by RT qPCR at the apical pole, i.e. in the supernatant (Figure 4B) as well as in the epithelia (Figure 4C).
    FIGS. 4B and 4C show that, when the reconstituted epithelia have been treated post-infection with diltiazem (90 μ la), the quantity of viral genome is much less than 5 times in the culture supernatant (FIG. 4B) and in the epithelium (Figure 4C). Diltiazem therefore has an anti-viral effect against respiratory syncytial virus
    REFERENCES
    PATENTS
    WO 02/094238
    US 4,605,552
    WO 87/07508
    WO 2011/066657
    WO 2011/126071
    WO 2016/146836
    EP 1,117,408
    BIBLIOGRAPHICAL REFERENCES
    Andreakos E, Salagianni M, Galani IE, Koltsida O. Interferon-As: Front-Line Guardians of Immunity and Homeostasis in the Respiratory Tract. Front Immunol. 2017 Sep 29; 8: 1232.
    Galani IE, Triantafyllia V, Eleminiadou EE, Koltsida O, Stavropoulos A, Manioudaki M, Thanos D, Doyle SE, Kotenko SV, Thanopoulou K, Andreakos E. Interferon-λ Mediates Nonredundant Front-Line Antiviral Protection against Influenza Virus Infection without Compromising Host fitness. Immunity. 2017 May 16; 46 (5): 875-890.e6.
    Chan HLY, Ahn SH, Chang TT, Peng CY, Wong D, Coffin CS, Lim SG, Chen PJ, Janssen HLA, Marcellin P, Serfaty L, Zeuzem S, Cohen D, Critelli L, Xu D, Wind-Rotolo M, Cooney E; LIRA-B Study Team. Peginterferon lambda for the treatment of HBeAg-positive chronic hepatitis B: A randomized phase 2b study (LIRA-B). J Hepatol. 2016 May; 64 (5): 1011-1019.
    Davidson S, McCabe TM, Crotta S, Gad HH, Hessel EM, Beinke S, Hartmann R, Wack A. IFNA is a potent anti-influenza therapeutic without the inflammatory side effects of IFNa treatment. EM BO Mol Med. 2016 Sep 1; 8 (9): 1099-112.
    Donnelly RP, Kotenko SV. Interferon-lambda: a new addition to an old family. J Interferon Cytokine Res. 2010 Aug; 30 (8): 555-64.
    Kotenko SV, Gallagher G, Baurin VV, Lewis-Antes A, Shen M, Shah NK, Langer JA, Sheikh F, Dickensheets H, Donnelly RP. IFN-lambdas mediate antiviral protection through a distinct class II cytokine receptor complex. Nat Immunol. 2003 Jan; 4 (1): 69-77.
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    2014 Nov; 34 (11): 829-38. doi: 10.1089 / jir.2013.0136.
    权利要求:
    Claims (12)
    [1" id="c-fr-0001]
    1. Diltiazem for its use as an agent which activates the expression of at least one gene coding for a type III interferon.
    [2" id="c-fr-0002]
    2. Diltiazem for its use as an agent which activates the expression of at least one gene coding for a type III interferon, in the prevention and / or treatment of infections with at least one pathogenic microorganism of the epithelia of the tracts respiratory and / or intestinal.
    [3" id="c-fr-0003]
    3. Diltiazem for its use according to one of claims 1 or 2, characterized in that said at least one gene is chosen from the gene coding for interleukin 29, the gene coding for interleukin 28A and the gene coding for interleukin 28B.
    [4" id="c-fr-0004]
    4. Diltiazem for its use according to one of claims 2 or 3, characterized in that the infection is not an infection by an influenza virus.
    [5" id="c-fr-0005]
    5. Diltiazem for its use according to one of claims 2 to 4, characterized in that the pathogenic microorganism is a virus chosen from human respiratory syncytial virus (hRSV), parainfluenza viruses (hPIV), human metapneumovirus (hMPV) , Nipah virus, novoviruses, coronaviruses, Swine fever virus, adenoviruses, Zika virus, yellow fever virus, rheoviruses, rotaviruses, Dengue virus, and l / l / est virus Nile.
    [6" id="c-fr-0006]
    6. Diltiazem for its use according to one of claims 2 or 3, characterized in that the pathogenic microorganism is chosen from a bacterium, a fungus and a parasite.
    [7" id="c-fr-0007]
    7. Diltiazem for its use according to claim 6 characterized in that the pathogenic microorganism is a bacterium chosen from the following bacterial species: Enterococcus faecalis, Borrelia burgdorferi, Listeria monocytogenes, Mycobacterium tuberculosis, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidum epidermis epidermis , Streptococcus pneumoniae, Haemophilus influenzae, Campylobacterspp., Salmonella spp., Shigella spp., Yersinia enterocolitica, Vibrio cholerae, Escherichia coli, Staphylococcus aureus, Bacillus cereus, and Clostridium difficile.
    [8" id="c-fr-0008]
    8. Diltiazem for its use according to one of claims 2 to 7, characterized in that the infection is a co-infection with at least one virus and at least one bacterium.
    [9" id="c-fr-0009]
    9. Diltiazem for its use according to one of claims 1 to 8, characterized
    5 in that it is used in combination with at least one other active agent.
    [10" id="c-fr-0010]
    10. Diltiazem for its use according to claim 9, characterized in that this other active agent is chosen from an anti-viral compound, an antibacterial compound, an anti-parasitic compound, an anti-fungal compound, and a preventive or therapeutic vaccine .
    11. Pharmaceutical or veterinary composition comprising diltiazem as an agent which activates the expression of at least one gene coding for a type III interferon, for its use in the prevention and / or treatment of infections by microorganisms pathogens of epithelia of the respiratory and / or intestinal tracts.
    [11" id="c-fr-0011]
    15
    [0012]
    12. Pharmaceutical or veterinary composition for its use according to claim 11, characterized in that it is in a galenical form suitable for administration by inhalation.
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    同族专利:
    公开号 | 公开日
    WO2019224489A1|2019-11-28|
    EP3796916A1|2021-03-31|
    BR112020023675A2|2021-02-17|
    KR20210013136A|2021-02-03|
    CA3101006A1|2019-11-28|
    AU2019273741A1|2020-12-24|
    CN112789046A|2021-05-11|
    US20210154205A1|2021-05-27|
    IL278895D0|2021-01-31|
    JP2021525250A|2021-09-24|
    FR3081325B1|2020-10-09|
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    法律状态:
    2019-05-13| PLFP| Fee payment|Year of fee payment: 2 |
    2019-11-29| PLSC| Search report ready|Effective date: 20191129 |
    2020-05-29| PLFP| Fee payment|Year of fee payment: 3 |
    2021-04-27| PLFP| Fee payment|Year of fee payment: 4 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1854307A|FR3081325B1|2018-05-23|2018-05-23|DILTIAZEM FOR USE IN THE TREATMENT OF MICROBIAL INFECTIONS|
    FR1854307|2018-05-23|FR1854307A| FR3081325B1|2018-05-23|2018-05-23|DILTIAZEM FOR USE IN THE TREATMENT OF MICROBIAL INFECTIONS|
    AU2019273741A| AU2019273741A1|2018-05-23|2019-05-23|Diltiazem for use in the treatment of microbial infections|
    US17/057,141| US20210154205A1|2018-05-23|2019-05-23|Diltiazem for use in the treatment of microbial infections|
    PCT/FR2019/051186| WO2019224489A1|2018-05-23|2019-05-23|Diltiazem for use in the treatment of microbial infections|
    JP2020565368A| JP2021525250A|2018-05-23|2019-05-23|Diltiazem for use in the treatment of microbial infections|
    EP19737813.6A| EP3796916A1|2018-05-23|2019-05-23|Diltiazem for use in the treatment of microbial infections|
    CA3101006A| CA3101006A1|2018-05-23|2019-05-23|Diltiazem for use in the treatment of microbial infections|
    KR1020207036694A| KR20210013136A|2018-05-23|2019-05-23|Diltiazem for use in the treatment of microbial infections|
    CN201980047805.2A| CN112789046A|2018-05-23|2019-05-23|Diltiazem for treating microbial infections|
    BR112020023675-6A| BR112020023675A2|2018-05-23|2019-05-23|diltiazem for use in the treatment of microbial infections|
    IL278895A| IL278895D0|2018-05-23|2020-11-22|Diltiazem for use in the treatment of microbial infections|
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