IL268626B2 - Immunogenic composition for modulating the immune system and methods to treat bacterial infections in a subject - Google Patents

Immunogenic composition for modulating the immune system and methods to treat bacterial infections in a subject

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Publication number
IL268626B2
IL268626B2 IL268626A IL26862619A IL268626B2 IL 268626 B2 IL268626 B2 IL 268626B2 IL 268626 A IL268626 A IL 268626A IL 26862619 A IL26862619 A IL 26862619A IL 268626 B2 IL268626 B2 IL 268626B2
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IL
Israel
Prior art keywords
inactivated
lysate
equal parts
salmonella
beta
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Application number
IL268626A
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Hebrew (he)
Other versions
IL268626A (en
IL268626B1 (en
Inventor
Alexandre Eduardo Nowill
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Alexandre Eduardo Nowill
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Publication date
Priority claimed from US15/431,329 external-priority patent/US10213504B2/en
Application filed by Alexandre Eduardo Nowill filed Critical Alexandre Eduardo Nowill
Publication of IL268626A publication Critical patent/IL268626A/en
Publication of IL268626B1 publication Critical patent/IL268626B1/en
Publication of IL268626B2 publication Critical patent/IL268626B2/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/02Bacterial antigens
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/396Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having three-membered rings, e.g. aziridine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41841,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/429Thiazoles condensed with heterocyclic ring systems
    • A61K31/43Compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula, e.g. penicillins, penems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/542Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/545Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/0002Fungal antigens, e.g. Trichophyton, Aspergillus, Candida
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/0005Vertebrate antigens
    • A61K39/0007Nervous system antigens; Prions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/002Protozoa antigens
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/02Bacterial antigens
    • A61K39/04Mycobacterium, e.g. Mycobacterium tuberculosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/02Bacterial antigens
    • A61K39/05Actinobacteria, e.g. Actinomyces, Streptomyces, Nocardia, Bifidobacterium, Gardnerella, Corynebacterium; Propionibacterium
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/02Bacterial antigens
    • A61K39/085Staphylococcus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/02Bacterial antigens
    • A61K39/09Lactobacillales, e.g. aerococcus, enterococcus, lactobacillus, lactococcus, streptococcus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/02Bacterial antigens
    • A61K39/095Neisseria
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/02Bacterial antigens
    • A61K39/102Pasteurellales, e.g. Actinobacillus, Pasteurella; Haemophilus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/12Viral antigens
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/12Viral antigens
    • A61K39/125Picornaviridae, e.g. calicivirus
    • A61K39/13Poliovirus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/12Viral antigens
    • A61K39/155Paramyxoviridae, e.g. parainfluenza virus
    • A61K39/165Mumps or measles virus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/12Viral antigens
    • A61K39/245Herpetoviridae, e.g. herpes simplex virus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/12Viral antigens
    • A61K39/245Herpetoviridae, e.g. herpes simplex virus
    • A61K39/25Varicella-zoster virus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/12Viral antigens
    • A61K39/275Poxviridae, e.g. avipoxvirus
    • A61K39/285Vaccinia virus or variola virus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/12Viral antigens
    • A61K39/29Hepatitis virus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K39/39Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/04Immunostimulants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies
    • A61K2039/58Medicinal preparations containing antigens or antibodies raising an immune response against a target which is not the antigen used for immunisation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Epidemiology (AREA)
  • Mycology (AREA)
  • Microbiology (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Oncology (AREA)
  • Pulmonology (AREA)
  • Engineering & Computer Science (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Claims (7)

1./ 1 CLAIMS 1. A synergistic pharmaceutical product comprising one or more antibiotics and: (a) i. 0,0036 ng/mL Koch’s Turberculin (inactivated Mycobacterium bovis lysate); ii. 0,0036 µg/mL PPD; iii. 6.31 µg/mL Inactivated Staphylococcus lysate (Staphylococcus aureus and Staphylococcus epidermidis in equal parts); iv. 6.31 µg/ml Inactivated Steptococcus lysate (Streptococcus pyogenes, Streptococcus pneumoniae and Enterococcus faecalis in equal parts); v. 0.404 µg/mL Streptokinase derived from inactivated beta-hemolytic Streptococcus lysate purification; vi. 0.101 µg/mL Dornase derived from inactivated beta-hemolytic Streptococcus lysate purification; vii. 6.31 µg/mL Oidiomycin (antigenic extract of Candida albicans); viii. 6.31 µg/mL Trichophytin (antigenic extract of Tricophyton sp); ix. 6.31 µg/mL Inactivated enteropathogenic Escherichia coli lysate (EPEC); x. 6.31 µg/mL Inactivated Salmonella lysate (Salmonella bongori, Salmonella enterica and Salmonella subterranea in equal parts); xi. 20 µg/mL Attenuated yellow fever virus strain 17 D204; xii. 7.5 mg/mL Sodium Chloride; xiii. 0.48 mg/mL Sodium phosphate dibasic heptahydrate; xiv. 0.06 mg/mL Potassium phosphate monobasic; xv. 2.5 mg/mL Phenol; and xvi. water; or (b) i. 0.004 ng/mL Koch’s Turberculin (inactivated Mycobacterium bovis lysate); ii. 0.004 g/mL PPD; iii. 6.94 µg/mL Inactivated Staphylococcus lysate (Staphylococcus aureus and Staphylococcus epidermidis in equal parts); iv. 6.94 µg/ml Inactivated Steptococcus lysate (Streptococcus pyogenes, Streptococcus pneumoniae and Enterococcus faecalis in equal parts); 268626/ 1 v. 0.444 µg/mL Streptokinase derived from inactivated beta-hemolytic Streptococcus lysate purification; vi. 0.111 µg/mL Dornase derived from inactivated beta-hemolytic Streptococcus lysate purification; vii. 6.94 µg/mL Inactivated Candida lysate (Candida albicans and Candida glabrata in equal parts); viii. 6.94 µg/mL Inactivated dermatophytes lysate (Epidermophytonfloccosum, Microsporum cannis, Trichophyton mentagrophytes of the interdigitale variety in equal parts); ix. 6.94 µg/mL Inactivated enteropathogenic Escherichia coli lysate (EPEC); x. 6.94 µg/mL Inactivated Salmonella lysate (Salmonella bongori, Salmonella enterica and Salmonella subterranea in equal parts); xi. 7.5 mg/mL Sodium Chloride; xii. 0.48 mg/mL Sodium phosphate dibasic heptahydrate; xiii. 0.06 mg/mL Potassium phosphate monobasic; xiv. 2.5 mg/mL Phenol; and xv. water.
2. The synergistic pharmaceutical product of claim 1 wherein the antibiotics are selected from the following classes: Amino Acid Derivatives, Aminoglycosides, Aureolic Acids, Aziridines, Ansamycins, Benzenoids, Benzimidazoles, Carbapenems, Cephalosporin, Coumarin-glycosides, Diphenyl Ether Derivatives, Epipolythiodioxopiperazines, Fatty Acid Derivatives, Glucosamine, Glycopeptides, Imidazoles, Indol Derivatives, Lipopeptides Macrolactams, Macrolides, Nucleosides. Penicillins and Cephalosporins (beta-Lactams), Peptides, Peptidyl Nucleosides, Phenicoles, Polyenes, Polyethers, Pyridines and Pyrimidines, Quinolones and Fluoroquinolones, Statins, Steroids, Sulfonamides, Taxoides and Tetracyclines.
3. The synergistic pharmaceutical product of claim 2 wherein the antibiotics are selected from the following classes: ansamycins, Penicillins, Cephalosporins, Carbapenems and Lipopeptides.
4. A synergistic effective amount of one or more antibiotics and (a) 268626/ 1 i. 0,0036 ng/mL Koch’s Turberculin (inactivated Mycobacterium bovis lysate); ii. 0,0036 µg/mL PPD; iii. 6.31 µg/mL Inactivated Staphylococcus lysate (Staphylococcus aureus and Staphylococcus epidermidis in equal parts); iv. 6.31 µg/ml Inactivated Steptococcus lysate (Streptococcus pyogenes, Streptococcus pneumoniae and Enterococcus faecalis in equal parts); v. 0.404 µg/mL Streptokinase derived from inactivated beta-hemolytic Streptococcus lysate purification; vi. 0.101 µg/mL Dornase derived from inactivated beta-hemolytic Streptococcus lysate purification; vii. 6.31 µg/mL Oidiomycin (antigenic extract of Candida albicans); viii. 6.31 µg/mL Trichophytin (antigenic extract of Tricophyton sp); ix. 6.31 µg/mL Inactivated enteropathogenic Escherichia coli lysate (EPEC); x. 6.31 µg/mL Inactivated Salmonella lysate (Salmonella bongori, Salmonella enterica and Salmonella subterranea in equal parts); xi. 20 µg/mL Attenuated yellow fever virus strain 17 D204; xii. 7.5 mg/mL Sodium Chloride; xiii. 0.48 mg/mL Sodium phosphate dibasic heptahydrate; xiv. 0.06 mg/mL Potassium phosphate monobasic; xv. 2.5 mg/mL Phenol; and xvi. water; or (b) i. 0.004 ng/mL Koch’s Turberculin (inactivated Mycobacterium bovis lysate); ii. 0.004 g/mL PPD; iii. 6.94 µg/mL Inactivated Staphylococcus lysate (Staphylococcus aureus and Staphylococcus epidermidis in equal parts); iv. 6.94 µg/ml Inactivated Steptococcus lysate (Streptococcus pyogenes, Streptococcus pneumoniae and Enterococcus faecalis in equal parts); v. 0.444 µg/mL Streptokinase derived from inactivated beta-hemolytic Streptococcus lysate purification; vi. 0.111 µg/mL Dornase derived from inactivated beta-hemolytic Streptococcus lysate purification; 268626/ 1 vii. 6.94 µg/mL Inactivated Candida lysate (Candida albicans and Candida glabrata in equal parts); viii. 6.94 µg/mL Inactivated dermatophytes lysate (Epidermophytonfloccosum, Microsporum cannis, Trichophyton mentagrophytes of the interdigitale variety in equal parts); ix. 6.94 µg/mL Inactivated enteropathogenic Escherichia coli lysate (EPEC); x. 6.94 µg/mL Inactivated Salmonella lysate (Salmonella bongori, Salmonella enterica and Salmonella subterranea in equal parts); xi. 7.5 mg/mL Sodium Chloride; xii. 0.48 mg/mL Sodium phosphate dibasic heptahydrate; xiii. 0.06 mg/mL Potassium phosphate monobasic; xiv. 2.5 mg/mL Phenol; and xv. water, for use in a method to treat sepsis and multi resistant bacterial infection in a human or an animal.
5. A synergistic effective amount of a composition comprising (a) i. 0,0036 ng/mL Koch’s Turberculin (inactivated Mycobacterium bovis lysate); ii. 0,0036 µg/mL PPD; iii.
6.31 µg/mL Inactivated Staphylococcus lysate (Staphylococcus aureus and Staphylococcus epidermidis in equal parts); iv. 6.31 µg/ml Inactivated Steptococcus lysate (Streptococcus pyogenes, Streptococcus pneumoniae and Enterococcus faecalis in equal parts); v. 0.404 µg/mL Streptokinase derived from inactivated beta-hemolytic Streptococcus lysate purification; vi. 0.101 µg/mL Dornase derived from inactivated beta-hemolytic Streptococcus lysate purification; vii. 6.31 µg/mL Oidiomycin (antigenic extract of Candida albicans); viii. 6.31 µg/mL Trichophytin (antigenic extract of Tricophyton sp); ix. 6.31 µg/mL Inactivated enteropathogenic Escherichia coli lysate (EPEC); x. 6.31 µg/mL Inactivated Salmonella lysate (Salmonella bongori, Salmonella enterica and Salmonella subterranea in equal parts); xi. 20 µg/mL Attenuated yellow fever virus strain 17 D204; 268626/ 1 xii.
7.5 mg/mL Sodium Chloride; xiii. 0.48 mg/mL Sodium phosphate dibasic heptahydrate; xiv. 0.06 mg/mL Potassium phosphate monobasic; xv. 2.5 mg/mL Phenol; and xvi. water; or (b) i. 0.004 ng/mL Koch’s Turberculin (inactivated Mycobacterium bovis lysate); ii. 0.004 g/mL PPD; iii. 6.94 µg/mL Inactivated Staphylococcus lysate (Staphylococcus aureus and Staphylococcus epidermidis in equal parts); iv. 6.94 µg/ml Inactivated Steptococcus lysate (Streptococcus pyogenes, Streptococcus pneumoniae and Enterococcus faecalis in equal parts); v. 0.444 µg/mL Streptokinase derived from inactivated beta-hemolytic Streptococcus lysate purification; vi. 0.111 µg/mL Dornase derived from inactivated beta-hemolytic Streptococcus lysate purification; vii. 6.94 µg/mL Inactivated Candida lysate (Candida albicans and Candida glabrata in equal parts); viii. 6.94 µg/mL Inactivated dermatophytes lysate (Epidermophytonfloccosum, Microsporum cannis, Trichophyton mentagrophytes of the interdigitale variety in equal parts); ix. 6.94 µg/mL Inactivated enteropathogenic Escherichia coli lysate (EPEC); x. 6.94 µg/mL Inactivated Salmonella lysate (Salmonella bongori, Salmonella enterica and Salmonella subterranea in equal parts); xi. 7.5 mg/mL Sodium Chloride; xii. 0.48 mg/mL Sodium phosphate dibasic heptahydrate; xiii. 0.06 mg/mL Potassium phosphate monobasic; xiv. 2.5 mg/mL Phenol; and xv. water, for use in a method to modulate an immune system response in a human or an animal who has a bacterial infection. For the Applicant Paulina Ben-Ami Patent Attorneys
IL268626A 2017-02-13 2018-02-15 Immunogenic composition for modulating the immune system and methods to treat bacterial infections in a subject IL268626B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US15/431,329 US10213504B2 (en) 2011-03-18 2017-02-13 Immunogenic composition for modulating the immune system and methods to treat bacterial infections in a subject
PCT/BR2018/000004 WO2018145180A1 (en) 2017-02-13 2018-02-15 Immunogenic composition for modulating the immune system and methods to treat bacterial infections in a subject

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IL268626A IL268626A (en) 2019-10-31
IL268626B1 IL268626B1 (en) 2023-12-01
IL268626B2 true IL268626B2 (en) 2024-04-01

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EP (1) EP3579868A4 (en)
JP (1) JP2020507629A (en)
KR (1) KR20190139209A (en)
CN (1) CN110709099B (en)
AU (1) AU2018217441A1 (en)
BR (1) BR112019016670A2 (en)
IL (1) IL268626B2 (en)
MX (1) MX2019009689A (en)
RU (1) RU2019128674A (en)
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Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012122618A1 (en) * 2011-03-17 2012-09-20 Nowill Alexandre Eduardo Immunogenic composition for immune system modulation and use thereof, method for treating and preventing diseases, method for inducing cell regeneration and method for restoring immune response

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004096270A1 (en) * 2003-04-30 2004-11-11 Medi Service S.R.L. Immunomodulating composition comprising a particulate fraction of bacterial mechanical lysates
CA2555253A1 (en) * 2004-02-06 2005-08-25 Yale University Compositions of pamps and listeria monocytogenes and methods of use
US20100166788A1 (en) * 2006-08-16 2010-07-01 Novartis Vaccines And Diagnostics Immunogens from uropathogenic escherichia coli
EP1938835A1 (en) * 2006-12-29 2008-07-02 Pevion Biotech AG Non-specific immunostimulating agents
EP2303236A4 (en) * 2008-07-01 2012-09-26 Univ Emory Synergistic induction of humoral and cellular immunity by combinatorial activation of toll-like receptors
CA2767536A1 (en) * 2009-07-07 2011-01-13 Novartis Ag Conserved escherichia coli immunogens
EP2464658B1 (en) * 2009-07-16 2014-10-01 Novartis AG Detoxified escherichia coli immunogens
US8980279B2 (en) * 2010-07-26 2015-03-17 Qu Biologics Personalized site-specific immunomodulation

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012122618A1 (en) * 2011-03-17 2012-09-20 Nowill Alexandre Eduardo Immunogenic composition for immune system modulation and use thereof, method for treating and preventing diseases, method for inducing cell regeneration and method for restoring immune response

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RU2019128674A3 (en) 2021-06-18
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AU2018217441A1 (en) 2019-10-03
CN110709099A (en) 2020-01-17
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WO2018145180A1 (en) 2018-08-16
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