WO2019000045A1 - METHOD OF TREATMENT - Google Patents

METHOD OF TREATMENT Download PDF

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Publication number
WO2019000045A1
WO2019000045A1 PCT/AU2018/050667 AU2018050667W WO2019000045A1 WO 2019000045 A1 WO2019000045 A1 WO 2019000045A1 AU 2018050667 W AU2018050667 W AU 2018050667W WO 2019000045 A1 WO2019000045 A1 WO 2019000045A1
Authority
WO
WIPO (PCT)
Prior art keywords
seq
peptide
tlr7
amino acid
acid sequence
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/AU2018/050667
Other languages
English (en)
French (fr)
Inventor
Stavros SELEMIDIS
Doug A BROOKS
John O'leary
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Monash University
RMIT University
Melbourne Institute of Technology
Adelaide University
College of the Holy and Undivided Trinity of Queen Elizabeth near Dublin
Original Assignee
Royal Melbourne Institute of Technology Ltd
University of South Australia
Monash University
Melbourne Institute of Technology
College of the Holy and Undivided Trinity of Queen Elizabeth near Dublin
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from AU2017902545A external-priority patent/AU2017902545A0/en
Application filed by Royal Melbourne Institute of Technology Ltd, University of South Australia, Monash University, Melbourne Institute of Technology, College of the Holy and Undivided Trinity of Queen Elizabeth near Dublin filed Critical Royal Melbourne Institute of Technology Ltd
Priority to AU2018293925A priority Critical patent/AU2018293925B2/en
Priority to CN201880056934.3A priority patent/CN111417401A/zh
Priority to JP2019572724A priority patent/JP2020527546A/ja
Priority to US16/624,367 priority patent/US11319343B2/en
Priority to CN202411599223.4A priority patent/CN119548615A/zh
Priority to EP18823595.6A priority patent/EP3645030A4/en
Publication of WO2019000045A1 publication Critical patent/WO2019000045A1/en
Anticipated expiration legal-status Critical
Priority to US17/703,111 priority patent/US20220213143A1/en
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
    • C07K7/04—Linear peptides containing only normal peptide links
    • C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/177—Receptors; Cell surface antigens; Cell surface determinants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/70596—Molecules with a "CD"-designation not provided for elsewhere
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/01—Fusion polypeptide containing a localisation/targetting motif
    • C07K2319/10—Fusion polypeptide containing a localisation/targetting motif containing a tag for extracellular membrane crossing, e.g. TAT or VP22

Definitions

  • Autoimmune disorders include systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, Sjogren's syndrome, polymyositis, vasculitis, Wegener's granulomatosis, sarcoidosis, ankylosing spondylitis, Reiter's syndrome, psoriatic arthritis and Behcet's syndrome.
  • the autoimmune disorder is an immune complex associated disease.
  • X 3 is V or I or A or P
  • the carboxyl group may be modified by carbodiimide activation via O-acylisourea formation followed by subsequent derivitization, for example, to a corresponding amide.
  • Sulphydryl groups may be modified by methods such as carboxymethylation with iodoacetic acid or iodoacetamide; performic acid oxidation to cysteic acid; formation of a mixed disulfides with other thiol compounds; reaction with maleimide, maleic anhydride or other substituted maleimide; formation of mercurial derivatives using 4- chloromercuribenzoate, 4-chloromercuriphenylsulphonic acid, phenylmercury chloride, 2- chloromercuri-4-nitrophenol and other mercurials; carbamoylation with cyanate at alkaline pH.
  • Human IAV virus including seasonal H3N2 (A/New York/55/2004, A/Brisbane/9/2007), seasonal H1N1 (A/Brazil/11/1978, A/New Caledonia/20/1999, A/Solomon Islands/3/2006), A(HlNl)pdm09 strains (A/California/7/2009, A/Auckland/1/2009), rhinovirus (RV16 strain), respiratory synctitial virus (strain A2), human parainfluenza virus type-3 (C243), human metapneumovirus (strain CAN97-83), mumps virus (strain Enders) and Newcastle disease virus (strain V4) were provided by the Department of Immunology and Microbiology, University of Melbourne, The Peter Doherty Institute for Infection and Immunity.
  • Coupling reactions were carried out using Fmoc -protected amino acids with 013 (6- chlorobenzotriazol-l-yl)-N,N,N ,N -tetramethyluronium hexafluorophosphate (HCTU) as coupling agent and N,N-diisopropylethylamine (DIPEA) as activating agent. Reactions were monitored using the 2,4,6-trinitrobenzenesulfonic acid (TNBS) test to indicate the absence or presence of free amino groups. The alternating sequence of deprotection and coupling reactions was carried out manually for all 20 amino acid residues using the appropriate Fmoc- and side-chain protected amino acids.
  • HCTU 6- chlorobenzotriazol-l-yl)-N,N,N ,N -tetramethyluronium hexafluorophosphate
  • DIPEA N,N-diisopropylethylamine
  • TNBS 2,4,6-trinitro
  • cells were pretreated with superoxide dismutase (SOD; 300 U/mL), apocynin (300 M), gp91dstat (50 M) or bafilomycin A (100 nM), for 30 min prior to infection.
  • SOD superoxide dismutase
  • apocynin 300 M
  • gp91dstat 50 M
  • bafilomycin A 100 nM
  • the cells were washed with PBS (0.01 M) and fixed with 4% PFA for 15 min. After fixation, cells were then washed three times with PBS over 30 min. Cover slips were then mounted onto microscope slides with 10-20 L of DAPI for 3 min, then analyzed and photographed on an Nikon upright confocal fluorescence microscope (Nikon D-eclipse CI).
  • Bafilomycin A from Streptomyces, Cat # B 1793, Sigma was prepared as a stock solution of 100 M in aliquots of 10 L and stored at -20°C.
  • influenza A viruses which belong to the Group IV negative sense, ssRNA viruses of the Orthomyxoviridae family and are internalized by endocytosis were first considered. Exposure of mouse alveolar macrophages (AMs), mouse peritoneal RAW264.7 cells or bone marrow -derived macrophages (BMDMs) to influenza A virus strain HKx31 (H3N2) resulted in a dose and time-dependent increase in influenza nucleoprotein (NP) fluorescence, which was almost abolished by the dynamin inhibitor, Dynasore (100 M) indicating a clathrin-coated pit or caveolin-dependent mechanism of internalization.
  • AMs mouse alveolar macrophages
  • BMDMs bone marrow -derived macrophages
  • the drug is most likely on the luminal face of the endosome membrane and due to the TAT portion can penetrate the membrane and suppress NOX2 activity.
  • the drug might still be able to diffuse towards other sites or locations of NOX2, however, the immediate and primary site of action is proposed to be NOX2 activity at the endosome, given that the drug appears to be selectively delivered via the endocytic pathway.
  • FIG. 13 shows that C98i blocks TLR7 response to the TLR7 agonist, gardiquimod. No effect is shown on basal un-stimulated levels of IL- ⁇ ( Figure 13). There was also no effect on TLR9, a closely related family member which has a tryptophan at position 98, or on TLR4 agonist response or TLR2 agonist response. There is very little sequence homology between TLR7 and TLR4 and TLR7 and TLR2.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Immunology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Zoology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Cell Biology (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Toxicology (AREA)
  • Epidemiology (AREA)
  • Virology (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
PCT/AU2018/050667 2017-06-30 2018-06-29 METHOD OF TREATMENT Ceased WO2019000045A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
AU2018293925A AU2018293925B2 (en) 2017-06-30 2018-06-29 A method of treatment
CN201880056934.3A CN111417401A (zh) 2017-06-30 2018-06-29 一种治疗方法
JP2019572724A JP2020527546A (ja) 2017-06-30 2018-06-29 治療方法
US16/624,367 US11319343B2 (en) 2017-06-30 2018-06-29 Method of treatment
CN202411599223.4A CN119548615A (zh) 2017-06-30 2018-06-29 一种治疗方法
EP18823595.6A EP3645030A4 (en) 2017-06-30 2018-06-29 TREATMENT PROCEDURES
US17/703,111 US20220213143A1 (en) 2017-06-30 2022-03-24 Method of treatment

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AU2017902545A AU2017902545A0 (en) 2017-06-30 A method of treatment
AU2017902545 2017-06-30

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US16/624,367 A-371-Of-International US11319343B2 (en) 2017-06-30 2018-06-29 Method of treatment
US17/703,111 Continuation US20220213143A1 (en) 2017-06-30 2022-03-24 Method of treatment

Publications (1)

Publication Number Publication Date
WO2019000045A1 true WO2019000045A1 (en) 2019-01-03

Family

ID=64740713

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/AU2018/050667 Ceased WO2019000045A1 (en) 2017-06-30 2018-06-29 METHOD OF TREATMENT

Country Status (6)

Country Link
US (2) US11319343B2 (enExample)
EP (1) EP3645030A4 (enExample)
JP (1) JP2020527546A (enExample)
CN (2) CN111417401A (enExample)
AU (1) AU2018293925B2 (enExample)
WO (1) WO2019000045A1 (enExample)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022170396A1 (en) * 2021-02-12 2022-08-18 ViraLok Therapeutics Pty Ltd Agents and methods for therapy and prophylaxis

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3645030A4 (en) * 2017-06-30 2021-04-21 The Provost, Fellows, Foundation Scholars, and the other members of Board, of the College of the Holy & Undiv. Trinity of Queen Elizabeth near Dublin TREATMENT PROCEDURES
CN114532296B (zh) * 2021-12-14 2023-12-15 首都医科大学附属北京同仁医院 NOX2基因缺陷rd1小鼠模型及其制备方法和应用

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ525914A (en) * 1998-03-10 2004-03-26 Genentech Inc Novel polypeptides and nucleic acids encoding the same
US6943240B2 (en) * 2000-09-15 2005-09-13 Coley Pharmaceuticals Gmbh Nucleic acids for high throughput screening of CpG-based immuno-agonist/antagonist
WO2010017131A2 (en) * 2008-08-04 2010-02-11 Idera Pharmaceuticals, Inc. Modulation of toll-like receptor 7 expression by antisense oligonucleotides
BR112012032240A2 (pt) * 2010-06-16 2019-09-24 Dynavax Technologies Corporation método de tratamento utilizando inibidores tlr7 e/ou tlr9
US20140378531A1 (en) * 2012-02-01 2014-12-25 New York University Inhibition of pattern recognition receptors in pancreatic cancer treatment using tlr inhibitors
US9228184B2 (en) * 2012-09-29 2016-01-05 Dynavax Technologies Corporation Human toll-like receptor inhibitors and methods of use thereof
EP3560960A1 (en) * 2013-04-22 2019-10-30 The University of Tokyo Preventive or therapeutic agent for inflammatory disease
CN104211799B (zh) * 2013-05-29 2017-12-26 成都渊源生物科技有限公司 人源egf结构域蛋白及其应用
AU2014310935B2 (en) * 2013-08-21 2019-11-21 CureVac SE Combination vaccine
US10308938B2 (en) * 2014-06-20 2019-06-04 Yale University Compositions and methods to activate or inhibit toll-like receptor signaling
EP3645030A4 (en) * 2017-06-30 2021-04-21 The Provost, Fellows, Foundation Scholars, and the other members of Board, of the College of the Holy & Undiv. Trinity of Queen Elizabeth near Dublin TREATMENT PROCEDURES

Non-Patent Citations (12)

* Cited by examiner, † Cited by third party
Title
DATABASE GenBank [O] 24 July 2016 (2016-07-24), "toll-like receptor 7, partial [Sigmodon hispidus]", XP055569948, Database accession no. ACK58672.1 *
DATABASE Protein [O] 8 March 2013 (2013-03-08), "Toll-like receptor 7, partial [Mustela putorius furo]", XP055569948, Database accession no. AES08222 *
GILL, R. ET AL.: "Linking oxidative stress to inflammation: Toll-like receptors", FREE RADICAL BIOLOGY & MEDICINE, vol. 48, no. 9, May 2010 (2010-05-01), pages 1121 - 1132, XP055569978 *
HIPP, M.M. ET AL.: "The Processed Amino-Terminal Fragment of Human TLR7 Acts as a Chaperone To Direct Human TLR7 into Endosomes", JOURNAL OF IMMUNOLOGY, vol. 194, no. 11, June 2015 (2015-06-01), pages 5417 - 5425, XP055569954 *
HU , X. ET AL.: "Multimerization and interaction of Toll and Spätzle in Drosophila", THE PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, vol. 101, no. 25, June 2004 (2004-06-01), pages 9369 - 9374, XP055569975 *
KIM, T.Y. ET AL.: "Effects of human mesenchymal stem cells transduced with superoxide dismutase on imiquimod-induced psoriasis-like skin inflammation in mice", JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY & VENEREOLOGY, vol. 30, no. 6, July 2016 (2016-07-01), pages 94, XP055372108 *
LAMPHIER, M. ET AL.: "Novel Small Molecule Inhibitors of TLR7 and TLR9: Mechanism of Action and Efficacy In Vivo", MOLECULAR PHARMACOLOGY, vol. 85, no. 3, March 2014 (2014-03-01), pages 429 - 440, XP009510804 *
MA, D. ET AL.: "1 he neurotoxic ettect of astrocytes activated with toll-like receptor ligands", JOURNAL OF NEUROIMMUNOLOGY, vol. 254, no. 1-2, January 2013 (2013-01-01), pages 10 - 18, XP055569983 *
PRINZ, N. ET AL.: "Antiphospholipid antibodies induce translocation of TLR7 and TLR8 to the endosome in human monocytes and plasmacytoid dendritic cells", BLOOD, vol. 118, no. 8, August 2011 (2011-08-01), pages 2322 - 2332, XP055569964 *
See also references of EP3645030A4 *
TO, E. ET AL.: "NOX2 oxidase expressed in endosomes exacerbates influenza pathogenicity", EUROPEAN RESPIRATORY JOURNAL, vol. 48, no. 60, September 2016 (2016-09-01), XP009518178, DOI: 10.1183/13993003.congress-2016.PA2600 *
TO, E.E. ET AL.: "Endosomal NOX2 oxidase exacerbates virus pathogenicity and is a target for antiviral therapy", NATURE COMMUNICATIONS, vol. 8, no. 69, July 2017 (2017-07-01), pages 1 - 17, XP055569988 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022170396A1 (en) * 2021-02-12 2022-08-18 ViraLok Therapeutics Pty Ltd Agents and methods for therapy and prophylaxis

Also Published As

Publication number Publication date
US20200216494A1 (en) 2020-07-09
JP2020527546A (ja) 2020-09-10
AU2018293925B2 (en) 2024-06-13
US11319343B2 (en) 2022-05-03
CN111417401A (zh) 2020-07-14
US20220213143A1 (en) 2022-07-07
EP3645030A1 (en) 2020-05-06
EP3645030A4 (en) 2021-04-21
AU2018293925A1 (en) 2020-01-16
CN119548615A (zh) 2025-03-04

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