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 subjectInfo
- 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
- Authority
- IL
- Israel
- Prior art keywords
- inactivated
- lysate
- equal parts
- salmonella
- beta
- Prior art date
Links
- 208000035143 Bacterial infection Diseases 0.000 title claims 3
- 208000022362 bacterial infectious disease Diseases 0.000 title claims 3
- 238000000034 method Methods 0.000 title claims 3
- 239000000203 mixture Substances 0.000 title claims 2
- 210000000987 immune system Anatomy 0.000 title 1
- 230000002163 immunogen Effects 0.000 title 1
- 239000006166 lysate Substances 0.000 claims 48
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims 12
- 241000194017 Streptococcus Species 0.000 claims 12
- 238000000746 purification Methods 0.000 claims 12
- 241001377138 Atlantibacter subterranea Species 0.000 claims 6
- 241000222122 Candida albicans Species 0.000 claims 6
- 241000194032 Enterococcus faecalis Species 0.000 claims 6
- 241000588724 Escherichia coli Species 0.000 claims 6
- 241000186366 Mycobacterium bovis Species 0.000 claims 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 6
- 241000607142 Salmonella Species 0.000 claims 6
- 241000533331 Salmonella bongori Species 0.000 claims 6
- 241001138501 Salmonella enterica Species 0.000 claims 6
- 241000191940 Staphylococcus Species 0.000 claims 6
- 241000191967 Staphylococcus aureus Species 0.000 claims 6
- 241000191963 Staphylococcus epidermidis Species 0.000 claims 6
- 241000193998 Streptococcus pneumoniae Species 0.000 claims 6
- 241000193996 Streptococcus pyogenes Species 0.000 claims 6
- 108010023197 Streptokinase Proteins 0.000 claims 6
- 230000000890 antigenic effect Effects 0.000 claims 6
- 229940095731 candida albicans Drugs 0.000 claims 6
- PYLIXCKOHOHGKQ-UHFFFAOYSA-L disodium;hydrogen phosphate;heptahydrate Chemical compound O.O.O.O.O.O.O.[Na+].[Na+].OP([O-])([O-])=O PYLIXCKOHOHGKQ-UHFFFAOYSA-L 0.000 claims 6
- 229940032049 enterococcus faecalis Drugs 0.000 claims 6
- 230000000369 enteropathogenic effect Effects 0.000 claims 6
- 229910000402 monopotassium phosphate Inorganic materials 0.000 claims 6
- 235000019796 monopotassium phosphate Nutrition 0.000 claims 6
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 claims 6
- 239000011780 sodium chloride Substances 0.000 claims 6
- 229940031000 streptococcus pneumoniae Drugs 0.000 claims 6
- 229960005202 streptokinase Drugs 0.000 claims 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 6
- 230000002195 synergetic effect Effects 0.000 claims 5
- 239000003242 anti bacterial agent Substances 0.000 claims 4
- 229940088710 antibiotic agent Drugs 0.000 claims 4
- 241001480043 Arthrodermataceae Species 0.000 claims 3
- 241000222120 Candida <Saccharomycetales> Species 0.000 claims 3
- 229930186147 Cephalosporin Natural products 0.000 claims 3
- 241001480036 Epidermophyton floccosum Species 0.000 claims 3
- 241001480037 Microsporum Species 0.000 claims 3
- 241001045770 Trichophyton mentagrophytes Species 0.000 claims 3
- 241000710772 Yellow fever virus Species 0.000 claims 3
- 241000222126 [Candida] glabrata Species 0.000 claims 3
- 230000002238 attenuated effect Effects 0.000 claims 3
- 208000032343 candida glabrata infection Diseases 0.000 claims 3
- 229940124587 cephalosporin Drugs 0.000 claims 3
- 150000001780 cephalosporins Chemical class 0.000 claims 3
- 230000037304 dermatophytes Effects 0.000 claims 3
- 239000000825 pharmaceutical preparation Substances 0.000 claims 3
- 229940127557 pharmaceutical product Drugs 0.000 claims 3
- 229940051021 yellow-fever virus Drugs 0.000 claims 3
- 108010028921 Lipopeptides Proteins 0.000 claims 2
- 241001465754 Metazoa Species 0.000 claims 2
- 229930182555 Penicillin Natural products 0.000 claims 2
- 229940041011 carbapenems Drugs 0.000 claims 2
- 239000002777 nucleoside Substances 0.000 claims 2
- 150000002960 penicillins Chemical class 0.000 claims 2
- MSWZFWKMSRAUBD-IVMDWMLBSA-N 2-amino-2-deoxy-D-glucopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-IVMDWMLBSA-N 0.000 claims 1
- -1 Carbapenems Chemical class 0.000 claims 1
- 108010015899 Glycopeptides Proteins 0.000 claims 1
- 102000002068 Glycopeptides Human genes 0.000 claims 1
- 229940121710 HMGCoA reductase inhibitor Drugs 0.000 claims 1
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical class C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims 1
- 206010040047 Sepsis Diseases 0.000 claims 1
- 239000004098 Tetracycline Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 150000003862 amino acid derivatives Chemical class 0.000 claims 1
- 229940126575 aminoglycoside Drugs 0.000 claims 1
- 229940053200 antiepileptics fatty acid derivative Drugs 0.000 claims 1
- 150000001541 aziridines Chemical class 0.000 claims 1
- 150000001556 benzimidazoles Chemical class 0.000 claims 1
- MSWZFWKMSRAUBD-UHFFFAOYSA-N beta-D-galactosamine Natural products NC1C(O)OC(CO)C(O)C1O MSWZFWKMSRAUBD-UHFFFAOYSA-N 0.000 claims 1
- 229930182483 coumarin glycoside Natural products 0.000 claims 1
- 150000008140 coumarin glycosides Chemical class 0.000 claims 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims 1
- 229940124307 fluoroquinolone Drugs 0.000 claims 1
- 229960002442 glucosamine Drugs 0.000 claims 1
- 239000002471 hydroxymethylglutaryl coenzyme A reductase inhibitor Substances 0.000 claims 1
- 150000002460 imidazoles Chemical class 0.000 claims 1
- 230000000899 immune system response Effects 0.000 claims 1
- 239000003120 macrolide antibiotic agent Substances 0.000 claims 1
- 229940041033 macrolides Drugs 0.000 claims 1
- 125000003835 nucleoside group Chemical group 0.000 claims 1
- 150000004291 polyenes Chemical class 0.000 claims 1
- 229920000570 polyether Polymers 0.000 claims 1
- 108090000765 processed proteins & peptides Proteins 0.000 claims 1
- 102000004196 processed proteins & peptides Human genes 0.000 claims 1
- 150000003222 pyridines Chemical class 0.000 claims 1
- 150000003230 pyrimidines Chemical class 0.000 claims 1
- 150000007660 quinolones Chemical class 0.000 claims 1
- 150000003431 steroids Chemical class 0.000 claims 1
- 229940124530 sulfonamide Drugs 0.000 claims 1
- 150000003456 sulfonamides Chemical class 0.000 claims 1
- 235000019364 tetracycline Nutrition 0.000 claims 1
- 150000003522 tetracyclines Chemical class 0.000 claims 1
- 229940040944 tetracyclines Drugs 0.000 claims 1
- 150000003952 β-lactams Chemical class 0.000 claims 1
Classifications
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/396—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having three-membered rings, e.g. aziridine
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- A61K31/4164—1,3-Diazoles
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- A61K31/425—Thiazoles
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- A61K31/43—Compounds 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
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- A61K31/545—Compounds 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
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- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
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- Y02A50/30—Against 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)
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- 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)
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- Microbiology (AREA)
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- General Chemical & Material Sciences (AREA)
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
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- Tropical Medicine & Parasitology (AREA)
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- 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
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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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