MX343589B - Leucotoxina e/d como agente anti-inflamatorio novedoso y microbicida. - Google Patents
Leucotoxina e/d como agente anti-inflamatorio novedoso y microbicida.Info
- Publication number
- MX343589B MX343589B MX2013014630A MX2013014630A MX343589B MX 343589 B MX343589 B MX 343589B MX 2013014630 A MX2013014630 A MX 2013014630A MX 2013014630 A MX2013014630 A MX 2013014630A MX 343589 B MX343589 B MX 343589B
- Authority
- MX
- Mexico
- Prior art keywords
- leukotoxin
- microbicide
- inflammatory agent
- new anti
- subject
- Prior art date
Links
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/164—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/351—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom not condensed with another ring
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- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/439—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom the ring forming part of a bridged ring system, e.g. quinuclidine
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- A—HUMAN NECESSITIES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/46—8-Azabicyclo [3.2.1] octane; Derivatives thereof, e.g. atropine, cocaine
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A61K9/0034—Urogenital system, e.g. vagina, uterus, cervix, penis, scrotum, urethra, bladder; Personal lubricants
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2866—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for cytokines, lymphokines, interferons
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2896—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against molecules with a "CD"-designation, not provided for elsewhere
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
Abstract
La presente invención se refiere a métodos para prevenir o tratar la infección por el virus de inmunodeficiencia humana (VIH), afecciones inflamatorias y la enfermedad de injerto contra huésped (GVHD) en un sujeto. Las composiciones terapéuticas de la presente invención comprenden proteínas o polipéptidos de leucocidina E (LuKe) y/o D. La invención también referida a métodos para tratar infección por Staphylococcus aureus administrando una composición que comprende un antagonista de CCR5 o cualquier molécula que bloquea la interacción de LuKe/D con células CCR5' en una cantidad eficaz para tratar la infección por S. aureus en el sujeto.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161498606P | 2011-06-19 | 2011-06-19 | |
PCT/US2012/043182 WO2012177660A2 (en) | 2011-06-19 | 2012-06-19 | Leukotoxin e/d as a new anti-inflammatory agent and microbicide |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2013014630A MX2013014630A (es) | 2014-05-14 |
MX343589B true MX343589B (es) | 2016-11-11 |
Family
ID=47423178
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2013014630A MX343589B (es) | 2011-06-19 | 2012-06-19 | Leucotoxina e/d como agente anti-inflamatorio novedoso y microbicida. |
Country Status (14)
Country | Link |
---|---|
US (3) | US8846609B2 (es) |
EP (2) | EP2720754B1 (es) |
JP (1) | JP6093760B2 (es) |
KR (1) | KR20140071318A (es) |
CN (1) | CN103764228B (es) |
AU (1) | AU2012273125B2 (es) |
BR (1) | BR112013032911A2 (es) |
CA (1) | CA2839558A1 (es) |
CL (1) | CL2013003651A1 (es) |
ES (1) | ES2609817T3 (es) |
MX (1) | MX343589B (es) |
MY (1) | MY165115A (es) |
RU (1) | RU2609650C2 (es) |
WO (1) | WO2012177660A2 (es) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ764564A (en) * | 2011-06-19 | 2022-10-28 | Univ New York | Methods of treating and preventing staphylococcus aureus infections and associated conditions |
CN104428000A (zh) * | 2012-05-02 | 2015-03-18 | 纽约大学 | 治疗和预防金黄色葡萄球菌感染和相关病状的方法 |
US10301378B2 (en) | 2013-06-18 | 2019-05-28 | New York University | Cellular factors involved in the cytotoxicity of Staphylococcus aureus leukocidins: novel therapeutic targets |
CN104744451A (zh) * | 2013-12-30 | 2015-07-01 | 中国科学院上海药物研究所 | 一种1-(3-氨基丙基)取代环状胺类化合物、其制备方法、药物组合物及用途 |
BR112017021779A2 (pt) * | 2015-04-17 | 2018-07-10 | Arsanis Biosciences Gmbh | ?uma preparação combinada de anticorpos anti-staphylococcus aureus? |
EP3313412A4 (en) * | 2015-06-23 | 2019-01-16 | CytoDyn Inc. | CCL5 LIGAND BINDING INHIBITION TO CCR5 RECEPTOR AND CCR5 / CCL5 AXIS SIGNALING MODIFICATION IN INFLAMMATION, CANCER, AUTOIMMUNIT DISEASE OR OTHER CONDITIONS |
Family Cites Families (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1121135B1 (en) | 1998-09-14 | 2009-01-28 | Nabi Biopharmaceuticals | Compositions of beta-glucans and specific immunoglobulins |
US20070010509A1 (en) | 1999-12-08 | 2007-01-11 | Tatsuki Shiota | Cycloamine ccr5 receptor antagonists |
KR20030032916A (ko) * | 2000-02-09 | 2003-04-26 | 휴먼 게놈 사이언시즈, 인크. | Ccr5에 대한 항체 |
US6476062B2 (en) | 2000-03-30 | 2002-11-05 | Schering Corporation | Chemokine receptor antagonists |
AT410798B (de) | 2001-01-26 | 2003-07-25 | Cistem Biotechnologies Gmbh | Verfahren zur identifizierung, isolierung und herstellung von antigenen gegen ein spezifisches pathogen |
GB0107661D0 (en) | 2001-03-27 | 2001-05-16 | Chiron Spa | Staphylococcus aureus |
US20030171563A1 (en) | 2001-05-18 | 2003-09-11 | Mcnamara Peter J. | Regulators of bacterial virulence factor expression |
AU2003247772A1 (en) | 2002-06-27 | 2004-01-19 | Schering Aktiengesellschaft | Substituted quinoline ccr5 receptor antagonists |
EP1593680A4 (en) * | 2003-02-07 | 2008-05-07 | Takeda Pharmaceutical | PYRIDINE DERIVATIVES WITH CONDENSED RING, PROCESS FOR THEIR PREPARATION AND USE |
IL157398A0 (en) * | 2003-08-14 | 2004-02-19 | Hadasit Med Res Service | Pharmaceutical compositions comprising ccr5 antagonists |
US7622125B2 (en) * | 2004-05-05 | 2009-11-24 | Novartis Vaccines And Diagnostics, Inc. | Polycistronic HIV vector constructs |
EP2305294B1 (en) | 2004-09-22 | 2015-04-01 | GlaxoSmithKline Biologicals SA | Immunogenic composition for use in vaccination against staphylococcei |
ATE484500T1 (de) | 2005-01-06 | 2010-10-15 | Schering Corp | Synthese von ccr5 rezeptor antagonisten |
WO2011047011A2 (en) | 2009-10-13 | 2011-04-21 | University Of Medicine And Dentistry Of New Jersey | Treatment and diagnosis of inflammatory disorders |
WO2007062150A2 (en) | 2005-11-25 | 2007-05-31 | University Of Medicine And Dentistry Of New Jersey | Leukotoxin compositions and therapeutic methods |
US20110143992A1 (en) * | 2006-02-13 | 2011-06-16 | Dennis Taub | Methods and Compositions Related to GHS-R Antagonists |
CN101466376A (zh) * | 2006-06-12 | 2009-06-24 | 辉瑞产品公司 | 用于提高免疫重建并治疗hiv患者的机会感染的ccr5拮抗剂 |
CN102743747A (zh) | 2006-06-12 | 2012-10-24 | 葛兰素史密斯克蓝生物品公司 | α-毒素在治疗和预防葡萄球菌感染上的用途 |
JP2008013447A (ja) | 2006-07-03 | 2008-01-24 | Juntendo | 毒素検出方法 |
WO2008016006A1 (en) * | 2006-07-31 | 2008-02-07 | Ono Pharmaceutical Co., Ltd. | Compound having cyclic group bound thereto through spiro binding and use thereof |
EP2066674B1 (en) | 2006-09-18 | 2010-06-30 | F.Hoffmann-La Roche Ag | Octahydropyrrolo [3, 4-c] pyrrole derivatives and their use as antiviral agents |
EP2120928A2 (en) * | 2007-02-15 | 2009-11-25 | Pfizer Limited | Pharmaceutical compositions and methods for ccr5 antagonists |
DK2510947T3 (en) | 2009-04-14 | 2016-03-21 | Glaxosmithkline Biolog Sa | Compositions for Immunization against Staphylococcus aureus. |
US8409584B2 (en) | 2009-05-05 | 2013-04-02 | New York University | Immunotherapy targeting of the shared abnormal conformational state of amyloidogenic peptides/proteins |
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2012
- 2012-06-19 EP EP12802525.1A patent/EP2720754B1/en not_active Not-in-force
- 2012-06-19 EP EP16187708.9A patent/EP3135339A1/en not_active Withdrawn
- 2012-06-19 RU RU2014101489A patent/RU2609650C2/ru not_active IP Right Cessation
- 2012-06-19 CA CA 2839558 patent/CA2839558A1/en not_active Abandoned
- 2012-06-19 US US13/527,438 patent/US8846609B2/en active Active
- 2012-06-19 CN CN201280039369.2A patent/CN103764228B/zh not_active Expired - Fee Related
- 2012-06-19 BR BR112013032911A patent/BR112013032911A2/pt not_active IP Right Cessation
- 2012-06-19 MX MX2013014630A patent/MX343589B/es active IP Right Grant
- 2012-06-19 JP JP2014517101A patent/JP6093760B2/ja not_active Expired - Fee Related
- 2012-06-19 KR KR20147000899A patent/KR20140071318A/ko not_active Application Discontinuation
- 2012-06-19 AU AU2012273125A patent/AU2012273125B2/en not_active Ceased
- 2012-06-19 WO PCT/US2012/043182 patent/WO2012177660A2/en active Application Filing
- 2012-06-19 ES ES12802525.1T patent/ES2609817T3/es active Active
- 2012-06-19 MY MYPI2013004568A patent/MY165115A/en unknown
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2013
- 2013-12-19 CL CL2013003651A patent/CL2013003651A1/es unknown
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2014
- 2014-08-25 US US14/468,026 patent/US9480726B2/en not_active Expired - Fee Related
-
2016
- 2016-09-23 US US15/273,888 patent/US20170224768A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
KR20140071318A (ko) | 2014-06-11 |
RU2609650C2 (ru) | 2017-02-02 |
US20130039885A1 (en) | 2013-02-14 |
US20150056163A1 (en) | 2015-02-26 |
NZ619942A (en) | 2016-02-26 |
US20170224768A1 (en) | 2017-08-10 |
EP2720754A2 (en) | 2014-04-23 |
AU2012273125B2 (en) | 2017-05-25 |
EP2720754B1 (en) | 2016-10-19 |
CN103764228A (zh) | 2014-04-30 |
WO2012177660A2 (en) | 2012-12-27 |
AU2012273125A1 (en) | 2014-01-16 |
JP2014520150A (ja) | 2014-08-21 |
ES2609817T3 (es) | 2017-04-24 |
US8846609B2 (en) | 2014-09-30 |
EP3135339A1 (en) | 2017-03-01 |
US9480726B2 (en) | 2016-11-01 |
RU2014101489A (ru) | 2015-07-27 |
MY165115A (en) | 2018-02-28 |
CN103764228B (zh) | 2017-09-08 |
CL2013003651A1 (es) | 2014-09-26 |
WO2012177660A3 (en) | 2013-02-21 |
JP6093760B2 (ja) | 2017-03-08 |
CA2839558A1 (en) | 2012-12-27 |
BR112013032911A2 (pt) | 2017-01-24 |
MX2013014630A (es) | 2014-05-14 |
EP2720754A4 (en) | 2015-04-29 |
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