WO2013164355A1 - Compositions - Google Patents

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Publication number
WO2013164355A1
WO2013164355A1 PCT/EP2013/059025 EP2013059025W WO2013164355A1 WO 2013164355 A1 WO2013164355 A1 WO 2013164355A1 EP 2013059025 W EP2013059025 W EP 2013059025W WO 2013164355 A1 WO2013164355 A1 WO 2013164355A1
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WIPO (PCT)
Prior art keywords
amino acid
mimotope
group
acid residue
composition according
Prior art date
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PCT/EP2013/059025
Other languages
French (fr)
Inventor
Markus Mandler
Petra Gruber
Frank Mattner
Walter Schmidt
Original Assignee
Affiris Ag
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
Application filed by Affiris Ag filed Critical Affiris Ag
Priority to US14/398,204 priority Critical patent/US20150093431A1/en
Priority to CN201380033810.0A priority patent/CN104427996A/en
Priority to CA2872138A priority patent/CA2872138A1/en
Priority to AU2013255860A priority patent/AU2013255860A1/en
Priority to JP2015509424A priority patent/JP2015520739A/en
Priority to EP13723699.8A priority patent/EP2844281A1/en
Publication of WO2013164355A1 publication Critical patent/WO2013164355A1/en
Priority to US14/797,904 priority patent/US20150306194A1/en
Priority to HK15109009.3A priority patent/HK1208354A1/en

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/0005—Vertebrate antigens
    • A61K39/0007—Nervous system antigens; Prions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/0003—Invertebrate antigens
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/02—Bacterial antigens
    • A61K39/05—Actinobacteria, e.g. Actinomyces, Streptomyces, Nocardia, Bifidobacterium, Gardnerella, Corynebacterium; Propionibacterium
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/385—Haptens or antigens, bound to carriers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/39—Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
    • C07K14/34—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Corynebacterium (G)
    • 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
    • C07K14/43504—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from invertebrates
    • 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
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55505—Inorganic adjuvants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55511—Organic adjuvants
    • A61K2039/55555—Liposomes; Vesicles, e.g. nanoparticles; Spheres, e.g. nanospheres; Polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55511—Organic adjuvants
    • A61K2039/55566—Emulsions, e.g. Freund's adjuvant, MF59
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55511—Organic adjuvants
    • A61K2039/55572—Lipopolysaccharides; Lipid A; Monophosphoryl lipid A
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55511—Organic adjuvants
    • A61K2039/55577—Saponins; Quil A; QS21; ISCOMS
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/58—Medicinal preparations containing antigens or antibodies raising an immune response against a target which is not the antigen used for immunisation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/60—Medicinal preparations containing antigens or antibodies characteristics by the carrier linked to the antigen
    • A61K2039/6031—Proteins
    • A61K2039/6037—Bacterial toxins, e.g. diphteria toxoid [DT], tetanus toxoid [TT]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/60—Medicinal preparations containing antigens or antibodies characteristics by the carrier linked to the antigen
    • A61K2039/6031—Proteins
    • A61K2039/6081—Albumin; Keyhole limpet haemocyanin [KLH]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/55—Fusion polypeptide containing a fusion with a toxin, e.g. diphteria toxin

Definitions

  • the present invention relates to a medicament to be used to prevent and/or treat synucleinopathies.
  • Synucleinopathies are a diverse group of neurodegenerative disorders that share a common pathologic characteristic: in neu ⁇ ropathology examinations characteristic lesions can be detected containing abnormal aggregates of alpha-synuclein (alpha-syn, a- syn) protein in selected populations of neurons and glia cells.
  • Alpha-syn (initially identified as PARK1 and PARK4 ) is a 140 amino acid protein widely expressed in the neocortex, hippocam ⁇ pus, dentate gyrus, olfactory bulb, striatum, thalamus and cere ⁇ bellum. Alpha-Syn is also highly expressed in hematopoietic cells including B-, T-, and NK cells as well as monocytes and platelets. The exact role in these cells is not known but it has been implicated in the differentiation of megakaryocytes (plate ⁇ let precursors) .
  • the most common synucleinopathies include but are not lim ⁇ ited to Lewy body disorders (LBDs) like Parkinson's disease
  • neurodegenerative diseases can be clas ⁇ sified as synucleinopathies based on the occurrence of typical, a-syn containing lesions: progressive supranuclear palsy (PSP) , frontotemporal dementia (FTD) , Pick's disease (PiD) and cortico- basal degeneration (CBD) .
  • PSP progressive supranuclear palsy
  • FDD frontotemporal dementia
  • CBD cortico- basal degeneration
  • symptomatic medications such as L-dopa, anticholinergic drugs as well as inhibitors of monoamine oxi ⁇ dase.
  • all treatment opportunities currently present on ⁇ ly lead to symptomatic alleviation but do not induce a long lasting, disease modifying effect in patients.
  • Lewy body disorders are progressive neurodegenerative disorders characterized by tremor, rigidity, bradykinesia and by loss of dopaminergic neurons in the brain. In the case of DLB and PDD signs also include cognitive impairment. Up to 2% of the population above 60 years of age in western countries develop the typical signs of PD/LBD. Currently only symptomatic treat ⁇ ment is available. Unfortunately, these therapies only provide temporary relief from early symptoms and do not halt disease progression. The pathogenesis of PD/LBD is still incompletely understood, but it appears that genetic susceptibility and envi ⁇ ronmental factors are involved in the development of the dis ⁇ ease. Despite all genetic advances, PD/LBD is primarily a spo ⁇ radic disorder with no known cause (also called idiopathic
  • LBs Lewy bodies
  • tg transgenic mice
  • Drosophila melanogaster its key role in the pathogenesis of PD/LBD is underscored as these animal models mimic several characteristics of PD.
  • MSA Multiple System Atrophy
  • MSA is a sporadic neurodegenerative disorder that is characterised by symptoms of L-DOPA-resistant Parkinsonism, cerebellar ataxia, and dysautonomia . Patients suffer from multi ⁇ system neuronal loss affecting various brain areas including striatum, substantia nigra, cerebellum, pons, as well as the in ⁇ ferior olives and the spinal cord.
  • MSA is characterized by al ⁇ pha- syn-positive glial cytoplasmic (GCI) and rare neuronal in ⁇ clusions throughout the central nervous system.
  • GCI glial cytoplasmic
  • GCIs for the pathogene ⁇ sis of MSA are associated with striatonigral degeneration, olivoponto ⁇ cerebellar atrophy, and involvement of autonomic nuclei in me ⁇ dulla and spinal cord.
  • the importance of GCIs for the pathogene ⁇ sis of MSA is generally acknowledged and underscored by recent analysis of transgenic mouse models analysing the effect of al ⁇ pha-syn overexpression in oligodendroglia . In tg mice overex- pressing human alpha-syn both GCI-like aggregates and biochemical markers of MSA were observed.
  • alpha-syn has been identified in LBs .
  • modified alpha-syn have been identified including phosphory- lated, nitrated, and mono-, di-, or tri-ubiquitinated alpha-syn.
  • C-terminally truncated forms of the protein like alpha-syn 1-119, alpha-syn 1-122 and alpha-syn 1-123, have been detected in brain tissue from both transgenic mice and PD cases. It is currently believed that up to 15% of the alpha-syn detect ⁇ ed in LBs and lewy neurites is truncated. Previous in vitro studies using truncated alpha-syn could demonstrate that alpha- syn lacking the C-terminal 20-30 amino acids was showing an in ⁇ creased tendency to aggregate and to form filaments found in Lewy-neurites and LBs.
  • truncated versions could thus act in a similar way as truncated and modified forms of amyloid beta ( ⁇ ) ⁇ Alzheimer's disease (AD).
  • ⁇ amyloid beta
  • AD Alzheimer's disease
  • truncated and modified forms of ⁇ are thought to act as seed molecules for plaque dep ⁇ osition and show a higher aggregation propensity as well as high neurotoxicity and synaptotoxicity in vivo and in vitro.
  • alpha-syn as well as truncated and/or modi ⁇ fied forms of alpha-syn, which are showing potential seeding effects, are then believed to accumulate leading to oligomer- formation. Based on recent studies it is believed that such oli- gomer-formation for example in the synaptic terminals and axons plays an important role for PD/LBD development and could thus be enhanced by the presence of truncated forms of alpha-syn.
  • WO 2004/041067 means and methods for preventing or treating diseases associated with alpha-synuclein aggregation are disclosed which comprise the use of alpha- synuclein fragments.
  • diseases associated with alpha-synuclein aggregation comprise the use of alpha- synuclein fragments.
  • peptides are de ⁇ scribed which can be used to induce immune response to protein deposits.
  • US 2005/198694 relates to alpha-synuclein fragments comprising at least 100 amino acids and having a C-terminal de ⁇ letion of 1 to 23 amino acids.
  • Liang et al . (J. Neurochem. 99(2006): 470-482) studied the regulation of alpha-synuclein in rats. They observed that in alcohol preferring rats the expression rate of alpha-synuclein is increased compared to alcohol-non preferring rats.
  • immunogenic alpha-synuclein fragments which are able to induce an immune response against a specific epitope within residues 70-140 of alpha-synuclein.
  • WO 2006/045037 relates to C-terminal truncated alpha- synuclein molecules which can be used to screen for agents which have a pharmacological activity useful for treating a Lewy Body Disease .
  • antibodies produced by immunized animals also detected abnormal aggregated forms of al ⁇ pha-syn associated with the neuronal membrane and promoted the degradation of these aggregates, probably via lysosomal path ⁇ ways. Similar effects were observed using passive immunotherapy with an exogenously applied alpha-syn-specific antibody. These results suggest that vaccination is effective in reducing neu ⁇ ronal accumulation of alpha-syn aggregates and that further development of this approach might elicit beneficial effects in the treatment of LBD and synucleinopathies.
  • the present invention relates to a composition
  • a composition comprising at least one mimotope of an epitope of alpha-synuclein for use in a method for preventing and/or treating synucleinopathies, wherein said at least one mimotope is coupled or fused, preferably cou ⁇ pled, to a pharmaceutically acceptable carrier protein selected from the group consisting of a non-toxic diphtheria toxin mu ⁇ tant, keyhole limpet hemocyanin (KLH) , diphtheria toxin (DT) , tetanus toxid (TT) and Haemophilus influenzae protein D (protein D) .
  • KLH keyhole limpet hemocyanin
  • DT diphtheria toxin
  • TT tetanus toxid
  • protein D Haemophilus influenzae protein D
  • the immunogenicity of the mimotopes can surprisingly be in ⁇ creased if the mimotopes are fused or coupled to a carrier pro ⁇ tein selected from the group consisting of a non-toxic diphthe ⁇ ria toxin mutant, keyhole limpet hemocyanin (KLH) , diphtheria toxin (DT) , tetanus toxid (TT) and Haemophilus influenzae pro ⁇ tein D (protein D) , whereby non-toxic diphtheria toxin mutants, such as CRM197, are particularly preferred.
  • a carrier pro ⁇ tein selected from the group consisting of a non-toxic diphthe ⁇ ria toxin mutant, keyhole limpet hemocyanin (KLH) , diphtheria toxin (DT) , tetanus toxid (TT) and Haemophilus influenzae pro ⁇ tein D (protein D) , whereby non-toxic
  • epitope refers to an immunogenic region of an antigen which is recognized by a particular antibody molecule.
  • An antigen may possess one or more epitopes, each capable of binding an antibody that recognizes the particular epitope .
  • the term "mimotope" re ⁇ fers to a molecule which has a conformation that has a topology equivalent to the epitope of which it is a mimic.
  • the mimotope binds to the same antigen-binding region of an antibody which binds immunospecifically to a desired antigen.
  • the mimotope will elicit an immunological response in a host that is reactive to the antigen to which it is a mimic.
  • the mimotope may also act as a competitor for the epitope of which it is a mimic in in vitro inhibition assays (e.g. ELISA inhibition assays) which involve the epitope and an antibody binding to said epitope.
  • in vitro inhibition assays e.g. ELISA inhibition assays
  • a mimotope of the present invention may not necessarily prevent or compete with the binding of the epitope of which it is a mimic in an in vitro inhibition assay although it is capable to induce a specific immune response when administered to a mammal.
  • the compounds of the present invention comprising such mimotopes (also those listed above) have the advantage to avoid the for ⁇ mation of autoreactive T-cells, since the peptides of the com ⁇ pounds have an amino acid sequence which varies from those of naturally occurring alpha synuclein protein.
  • the mimotopes of the present invention can be synthetically produced by chemical synthesis methods which are well known in the art, either as an isolated peptide or as a part of another peptide or polypeptide.
  • the peptide mimotope can be produced in a microorganism which produces the peptide mimo ⁇ tope which is then isolated and if desired, further purified.
  • the peptide mimotope can be produced in microorganisms such as bacteria, yeast or fungi, in eukaryote cells such as a mammalian or an insect cell, or in a recombinant virus vector such as ade ⁇ novirus, poxvirus, herpesvirus, Simliki forest virus, baculovi- rus, bacteriophage, Sindbis virus or sendai virus.
  • Suitable bac ⁇ teria for producing the peptide mimotope include E.coli,
  • Suitable yeast types for expressing the peptide mimotope include Saccharomyces cere- visiae, Schizosaccharomyces pombe, Candida, Pichia pastoris or any other yeast capable of expressing peptides.
  • Corresponding methods are well known in the art. Also methods for isolating and purifying recombinantly produced peptides are well known in the art and include e.g. as gel filtration, affinity chromatog ⁇ raphy, ion exchange chromatography etc...
  • a fusion polypeptide may be made wherein the peptide mimotope is transla- tionally fused (covalently linked) to a heterologous polypeptide which enables isolation by affinity chromatography.
  • Typical heterologous polypeptides are His-Tag (e.g. His 6 ; 6 histidine resi ⁇ dues), GST-Tag (Glutathione-S-transferase) etc...
  • His-Tag e.g. His 6 ; 6 histidine resi ⁇ dues
  • GST-Tag Glutathione-S-transferase
  • the fusion polypep ⁇ tide may comprise a cleavage site at the junction between the peptide mimotope and the heterologous polypeptide.
  • the cleavage site consists of an amino acid sequence that is cleaved with an enzyme specific for the amino acid sequence at the site (e.g. proteases) .
  • the mimotopes of the present invention may also be modified at or nearby their N- and/or C-termini so that at said positions a cysteine residue is bound thereto.
  • the mimotopes according to the present invention preferably are antigenic polypeptides which in their amino acid sequence vary from the amino acid sequence of alpha synuclein.
  • the inventive mimotopes may not only comprise amino ac ⁇ id substitutions of one or more naturally occurring amino acid residues but also of one or more non-natural amino acids (i.e. not from the 20 "classical” amino acids) or they may be com ⁇ pletely assembled of such non-natural amino acids.
  • Suitable an ⁇ tibody-inducing antigens may be provided from commercially available peptide libraries.
  • these peptides are at least 7 amino acids, and preferred lengths may be up to 16, preferably up to 14 or 20 amino acids (e.g.
  • the mimotopes of the present invention may also be part of a polypeptide and consequently comprising at their N- and/or C-terminus at least one further amino acid residue.
  • peptide libraries are suitable, for instance produced by means of combinatorial chemistry or obtained by means of high throughput screening techniques for the most vary ⁇ ing structures (Display: A Laboratory Manual by Carlos F. Barbas (Editor), et al . ; Willats WG Phage display: practicalities and prospects. Plant Mol. Biol. 2002 Dec; 50 ( 6) : 837-54 ) .
  • epitope refers to an immunogenic region of an antigen to which a particular antibody molecule can specifically bind thereto.
  • An antigen may possess one or more epitopes, each capable of binding an antibody that recognizes the particular epitope.
  • composition of the present invention may comprise at least one, at least 2, at least 3, at least 4, at least 5 or at least 10 mimotopes as defined herein.
  • the non-toxic diphtheria toxin mutant is selected from the group consisting of CRM 197, CRM 176, CRM 228, CRM 45, CRM 9, CRM 102, CRM 103 and CRM 107, whereby CRM 197 is particularly preferred.
  • the mimotopes of the present invention are particularly pre ⁇ ferred fused or conjugated to non-toxic diphtheria toxin mu ⁇ tants, such as CRM 197 (a nontoxic but antigenically identical variant of diphtheria toxin), CRM 176, CRM 228, CRM 45 (Uchida et al J. Biol. Chem. 218; 3838-3844, 1973), CRM 9, CRM 45, CRM 102, CRM 103 and CRM 107 and other mutations described by
  • Another aspect of the present invention relates to a compo ⁇ sition comprising at least one mimotope of an epitope of alpha- synuclein for use in preventing and/or treating synucleinopa- thies .
  • the at least one mimotope can be fused or conjugated to a pharmaceutically acceptable carrier, prefera ⁇ bly KLH (Keyhole Limpet Hemocyanin) , tetanus toxoid, albumin- binding protein, bovine serum albumin, a dendrimer (MAP; Biol. Chem. 358: 581), peptide linkers (or flanking regions) as well as the substances described in Singh et al . , Nat. Biotech. 17
  • a pharmaceutically acceptable carrier prefera ⁇ bly KLH (Keyhole Limpet Hemocyanin) , tetanus toxoid, albumin- binding protein, bovine serum albumin, a dendrimer (MAP; Biol. Chem. 358: 581), peptide linkers (or flanking regions) as well as the substances described in Singh et al . , Nat. Biotech. 17
  • conjugation chemistry e.g. via hetero- bifunctional compounds such as GMBS and of course also others as described in "Bioconj ugate Techniques", Greg T. Hermanson) in this context can be selected from reactions known to the skilled man in the art.
  • the at least one mimotope can also be fused or conjugated to a pharmaceutically acceptable carrier protein selected from the group consisting of a non-toxic diph ⁇ theria toxin mutant, keyhole limpet hemocyanin (KLH) , diphtheria toxin (DT) , tetanus toxid (TT) and Haemophilus influenzae pro ⁇ tein D (protein D) as defined above.
  • a pharmaceutically acceptable carrier protein selected from the group consisting of a non-toxic diph ⁇ theria toxin mutant, keyhole limpet hemocyanin (KLH) , diphtheria toxin (DT) , tetanus toxid (TT) and Haemophilus influenzae pro ⁇ tein D (protein D) as defined above.
  • composition of the present invention may be administered by any suitable mode of application, e.g. i.d., i.v., i.p., i.m., intranasally, orally, subcutaneously, transdermally, in- tradermally etc. and in any suitable delivery device (O'Hagan et al . , Nature Reviews, Drug Discovery 2 (9), (2003), 727-735).
  • At least one mimotope of the present invention is preferably formulated for intravenous, subcutaneous, intra ⁇ dermal or intramuscular administration (see e.g. "Handbook of Pharmaceutical Manufacturing Formulations", Sarfaraz Niazi, CRC Press Inc, 2004) .
  • composition according to the present invention comprises the mimotope according to the invention in an amount of from 0.1 ng to 10 mg, preferably 10 ng to 1 mg, in particular 100 ng to 100 yg, or, alternatively, e.g. 100 fmol to 10 ymol, prefera ⁇ bly 10 pmol to 1 ymol, in particular 100 pmol to 100 nmol.
  • the vaccine may also contain auxiliary substances, e.g. buffers, stabilizers etc.
  • the composition of the present invention may also comprise auxiliary substances, e.g. buffers, stabilizers etc.
  • auxiliary substances e.g. a pharmaceutically acceptable excipient, such as water, buffer and/or stabilisers, are contained in an amount of 0.1 to 99 % (weight) , more pre ⁇ ferred 5 to 80% (weight) , especially 10 to 70 % (weight) .
  • Possible administration regimes include a weekly, biweekly, four-weekly (monthly) or bimonthly treatment for about 1 to 12 months; however, also 2 to 5, especially 3 to 4, initial vaccine admin ⁇ istrations (in one or two months) , followed by boaster vaccina ⁇ tions 6 to 12 months thereafter or even years thereafter are preferred - besides other regimes already suggested for other vaccines .
  • the at least one mimotope is administered to an individual in an amount of 0.1 ng to 10 mg, preferably of 0.5 to 500 yg, more preferably 1 to 100 yg, per immunization.
  • these amounts refer to all mimotopes present in the compo ⁇ sition of the present invention.
  • these amounts refer to each single mimotopes present in the com ⁇ position. It is of course possible to provide a vaccine in which the various mimotopes are present in different or equal amounts.
  • the mimotopes of the present invention may alternative ⁇ ly be administered to an individual in an amount of 0.1 ng to 10 mg, preferably 10 ng to 1 mg, in particular 100 ng to
  • the amount of mimotopes that may be combined with the carri ⁇ er materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.
  • the dose of the composition may vary according to factors such as the disease state, age, sex and weight of the individual, and the ability of antibody to elicit a desired response in the in ⁇ dividual. Dosage regime may be adjusted to provide the optimum therapeutic response. For example, several divided doses may be administered daily or the dose may be proportionally reduced as indicated by the exigencies of the therapeutic situation.
  • the dose of the vaccine may also be varied to provide optimum pre ⁇ ventative dose response depending upon the circumstances.
  • the mimotopes and compositions of the present inven ⁇ tion may be administered to an individual at intervals of sever ⁇ al days, one or two weeks or even months or years depending al ⁇ ways on the level of antibodies induced by the administration of the composition of the present invention.
  • the com ⁇ position is applied between 2 and 10, preferably between 2 and 7, even more preferably up to 5 and most preferably up to 4 times.
  • This number of immunizations may lead to a basic immun ⁇ isation.
  • the time interval between the subsequent vaccinations is chosen to be between 2 weeks and 5 years, preferably between 1 month and up to 3 years, more preferably between 2 months and 1.5 years.
  • An exem ⁇ plified vaccination schedule may comprise 3 to 4 initial vac ⁇ cinations over a period of 6 to 8 weeks and up to 6 months.
  • the repeated administration of the mimotopes of the pre ⁇ sent invention may maximize the final effect of a therapeutic vaccination .
  • the at least one mimotope is formulated with at least one adju ⁇ vant .
  • Adjuvants are compounds or a mixture that enhance the im ⁇ mune response to an antigen (i.e. mimotope) .
  • Adjuvants may act primarily as a delivery system, primarily as an immune modulator or have strong features of both. Suitable adjuvants include those suitable for use in mammals, including humans.
  • the at least one adjuvant used in the composition as defined herein is capable to stimulate the innate immune sys ⁇ tem.
  • Innate immune responses are mediated by toll-like receptors (TLR's) at cell surfaces and by Nod-LRR proteins (NLR) intracel- lularly and are mediated by Dl and DO regions respectively.
  • TLR's toll-like receptors
  • NLR Nod-LRR proteins
  • the innate immune response includes cytokine production in response to TLR activation and activation of Caspase-1 and IL- ⁇ secretion in response to certain NLRs (including Ipaf) .
  • This response is independent of specific antigens, but can act as an adjuvant to an adaptive immune response that is antigen specific.
  • the an ⁇ tigen may be supplied externally in the form of a vaccine or in ⁇ fection, or may be indigenous, for example, as is the case for tumor-associated antigens.
  • TLRs A number of different TLRs have been characterized. These TLRs bind and become activated by different ligands, which in turn are located on different organisms or structures.
  • the de ⁇ velopment of immunopotentiator compounds that are capable of eliciting responses in specific TLRs is of interest in the art.
  • US 4,666,886 describes certain lipopeptide mole ⁇ cules that are TLR2 agonists.
  • WO 2009/118296, WO 2008/005555, WO 2009/111337 and WO 2009/067081 each describe classes of small molecule agonists of TLR7.
  • WO 2007/040840 and WO 2010/014913 de ⁇ scribe TLR7 and TLR8 agonists for treatment of diseases.
  • These various compounds include small molecule immunopotentiators (SMIPs) .
  • the at least one adjuvant capable to stimulate the innate immune system preferably comprises or consists of a Toll-like receptor (TLR) agonist, preferably a TLR1, TLR2, TLR3, TLR4, TLR5, TLR7, TLR8 or TLR9 agonist, particularly preferred a TLR4 agonist .
  • TLR Toll-like receptor
  • TLR 2 agonist is Pam3CysSerLys4 , peptidoglycan (Ppg) , PamCys
  • a TLR3 agonist is IPH 31XX
  • a TLR4 agonist is an Aminoalkyl glucosaminide phosphate, E6020, CRX-527, CRX-601, CRX-675, 5D24.D4, RC-527
  • a TLR7 agonist is Imiquimod, 3M-003, Aldara, 852A, R850, R848, CL097
  • a TLR8 agonist is 3M-002
  • a TLR9 agonist is Flagellin, Vaxlmmune, CpG ODN (AVE0675,
  • the TLR agonist is selected from the group consisting of mono- phosphoryl lipid A (MPL) , 3-de-O-acylated monophosphoryl lipid A (3D-MPL), poly I:C, GLA, flagellin, R848, imiquimod and CpG.
  • composition of the present invention may comprise MPL.
  • MPL may be synthetically produced MPL or MPL obtainable from natural sources.
  • MPL chemically modified MPL. Examples of such MPL' s are known in the art.
  • the at least one adjuvant comprises or consists of a saponin, preferably QS21, a water in oil emulsion and a liposome .
  • the at least one adjuvant is preferably selected from the group consisting of MF59, AS01, AS02, AS03, AS04, aluminium hydroxide and aluminium phosphate.
  • alum e.g., aluminum phosphate, aluminum sulfate or aluminum hydrox ⁇ ide
  • calcium phosphate calcium phosphate
  • liposomes oil-in-water emulsions such as MF59 (4.3% w/v squalene, 0.5% w/v polysorbate 80 (Tween 80), 0.5% w/v sorbitan trioleate (Span 85)
  • water-in-oil emulsions such as Montanide
  • PLG poly (D, L-lactide-co-glycolide) mi- croparticles or nanoparticles .
  • Suitable immune modulatory type adjuvants include, but are not limited to sapo ⁇ nins extracts from the bark of the Aquilla tree (QS21, Quil A), TLR4 agonists such as MPL (Monophosphoryl Lipid A), 3DMPL (3-0- deacylated MPL) or GLA-AQ, LT/CT mutants, cytokines such as the various interleukins (e.g., IL-2, IL-12) or GM-CSF, and the like .
  • TLR4 agonists such as MPL (Monophosphoryl Lipid A), 3DMPL (3-0- deacylated MPL) or GLA-AQ
  • LT/CT mutants cytokines such as the various interleukins (e.g., IL-2, IL-12) or GM-CSF, and the like .
  • immune modulatory type adjuvants with both delivery and immune modulatory features that can be used in humans include, but are not limited to ISCOMS (see, e.g., Sjolander et al . (1998) J. Leukocyte Biol. 64:713;
  • GLA-EM which is a combination of a Toll-like receptor agonists such as a TLR4 agonist and an oil-in-water emulsion.
  • exemplary adjuvants to enhance effectiveness of the mimotope compositions of the present invention include, but are not limited to: (1) oil-in-water emulsion formulations (with or without other specific immunostimulating agents such as muramyl peptides (see below) or bacterial cell wall components) , such as for example (a) SAF, containing 10% Squalane, 0.4% Tween 80, 5% pluronic-blocked polymer L121, and thr-MDP either microfluidized into a submicron emulsion or vortexed to generate a larger particle size emulsion, and (b) RIBITM adjuvant system (RAS) , (Ribi Immunochem, Hamilton, Mont.) containing 2% Squalene, 0.2% Tween 80, and one or more bacterial cell wall components such as mono- phosphorylipid A (MPL) , trehalose dimycolate (TDM) , and cell wall skeleton (CWS) , preferably MPL+CWS
  • ISCOMS immunodeficiency virus
  • IFA Incom ⁇ plete Freund's Adjuvant
  • cytokines such as interleu- kins (e.g. IL-1, IL-2, IL-4, IL-5, IL-6, IL-7, IL-12
  • interferons e.g. gamma interferon
  • M-CSF macro ⁇ phage colony stimulating factor
  • MPL monophosphoryl lipid A
  • 3dMPL 3-O-deacylated MPL
  • GB-2220221 e.g., EP-A-0689454
  • WO00/56358 e.g., WO00/56358
  • combinations of 3dMPL with, for example, QS21 and/or oil-in-water emulsions see e.g. EP-A- 0835318, EP-A-0735898, EP-A-0761231
  • (7) a polyoxyethylene ether or a polyoxyethylene ester see e.g.
  • a polyoxyethylene sorbitan ester surfactant in combination with an octoxynol WO01/21207) or a polyoxyethylene alkyl ether or ester surfactant in combination with at least one additional non-ionic surfactant such as an octoxynol (WO01/21152) ;
  • a saponin and an immunostimulatory oligonucleotide e.g. a CpG oligonucleo ⁇ tide
  • WOO 0 / 62800 an immunostimulant and a particle of metal salt
  • Muramyl peptides include N- acetyl-muramyl-L-threonyl-D-isoglutamine (thr-MDP) , N-25 acetyl- normnuramyl-L-alanyl-D-isoglutamine (nor-MDP) , N-acetylmuramyl- L-alanyl-D-isoglutaminyl-L-alanine-2- (1 ' -2 ' -dipalmitoyl-sn- glycero-3-hydroxyphosphoryloxy) -ethylamine MTP-PE) , etc.
  • compositions of the present invention comprise as adjuvant an oil-in-water emulsion with or without Toll-like receptor agonists, as well as liposomes and/or sapo- nin-containing adjuvants, with or without Toll-like receptor ag ⁇ onists.
  • the composition of the present invention may also com ⁇ prise aluminium hydroxide with or without Toll-like receptor ag ⁇ onists as adjuvant.
  • the epitope comprises or consists of the amino acid sequence KNEEGAP or DMPVDPDN.
  • Mimotopes of the aforementioned epitopes are known to the person skilled in the art (see e.g. WO 2009/103105, WO
  • composition according to the present invention comprises preferably at least one mimotope comprising or consisting of the amino acid sequence
  • Xl is any amino acid residue
  • X2 is an amino acid residue selected from the group consist ⁇ ing of lysine (K) , arginine (R) , alanine (A) and histidine (H) ,
  • X3 is an amino acid residue selected from the group consist ⁇ ing of asparagine (N) , glutamine (Q) , serine (S) , glycine (G) and alanine (A) , preferably asparagine (N) , serine (S) , glycine (G) and alanine (A) ,
  • X4 is an amino acid residue selected from the group consist ⁇ ing of glutamic acid (E) , aspartic acid (D) and alanine (A)
  • X5 is an amino acid residue selected from the group consist ⁇ ing of glutamic acid (E) and aspartic acid (D) ,
  • XQ is an amino acid residue selected from the group consist ⁇ ing of alanine (A) and tyrosine (Y) ,
  • X7 is any amino acid residue
  • n and m independently, are 0 or an integer of more than 0, wherein the amino acid sequence according to Formula I is not identical with, or does not comprise the 7-mer polypeptide fragment of alpha-synuclein having the amino acid sequence
  • At least one mimotope comprising the amino acid sequence ac ⁇ cording to Formula I has a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence KNEEGAP.
  • peptide having a binding capacity to an antibody which is specific for an epitope of alpha-synuclein means that said peptide can be bound to alpha-synuclein specific antibody which has been produced by the administration of alpha-synuclein or fragments thereof to a mammal. Said peptide having said bind ⁇ ing capacity is able to induce the formation of alpha-synuclein specific antibodies in a mammal. The latter antibodies bind con ⁇ sequently to the compound of the present invention as well as to alpha-synuclein .
  • X 2 is an amino acid residue selected from the group consisting of lysine (K) and arginine (R) and/or Xe is ala ⁇ nine (A) .
  • the mimotope comprises or consists of an amino acid sequence se- lected from the group consisting of (Xl ) nKNDEGAP (X 7 ) mr
  • composition according to the present invention comprises preferably at least one mimotope comprising or consisting of an amino acid sequence selected from the group consisting of
  • Xi is any amino acid residue
  • X7 is any amino acid residue
  • n and m independently, are 0 or an integer of more than 0, said at least one mimotope having a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence KNEEGAP
  • Xi ' is any amino acid residue
  • X 2' is an amino acid residue selected from the group con ⁇ sisting of aspartic acid (D) and glutamic acid (E)
  • X3' is any amino acid residue
  • X 4' is any amino acid residue
  • X5' is an amino acid residue selected from the group con ⁇ sisting of proline (P) and alanine (A) ,
  • ⁇ ' is an amino acid residue selected from the group con ⁇ sisting of aspartic acid (D) and glutamic acid (E) ,
  • Xv is any amino acid residue
  • n' and m' independently, are 0 or an integer of more than 0, wherein the amino acid sequence according to Formula II is not identical with, or does not comprise the 8-mer polypeptide fragment of alpha-synuclein having the amino acid sequence
  • the at least one mimotope comprising the amino acid sequence according to Formula II has a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence DMPVDPDN.
  • X3' is an amino acid residue selected from the group consisting of glutamine (Q) , serine (S) , threonine (T) , arginine (R) , as- paragine (N) , valine (V) , histidine (H) , methionine (M) , tyro ⁇ sine (Y) , alanine (A) and leucin (L) .
  • X 4 * is an amino acid residue selected from the group consisting of glutamine (Q) , tryptophane (W) , threonine (T) , arginine (R) , aspartic acid(D), isoleucin (I), valine (V), histidine (H) , proline (P) , tyrosine (Y) , alanine (A) , serine (S) and leucin (L) .
  • the mimotope of the present invention which is part of the composition of the present invention has preferably an amino ac ⁇ id sequence selected from the group consisting of (C) DQPVLPD, (C)DMPVLPD, (C)DSPVLPD, (C) DSPVWAE, (C) DTPVLAE, (C) DQPVLPDN, (C)DMPVLPDN, (C) DSPVLPDN, (C) DQPVTAEN, (C) DSPVWAEN, (C) DTPVLAEN, (C)HDRPVTPD, (C)DRPVTPD, (C) DVPVLPD, (C) DTPVYPD, (C) DTPVIPD, (C) HDRPVTPDN, (C) DRPVTPDN, (C) DNPVHPEN, (C) DVPVLPDN,
  • C)DTPVYPDN (C)DTPVIPDN, (C) DQPVLPDG, (C) DMPVLPDG, (C) DSPVLPDG, (C)DSPVWAEG, (C)DRPVAPEG, (C)DHPVHPDS, (C) DMPVSPDR, (C) DSPVPPDD, (C)DQPVYPDI, (C)DRPVYPDI, (C) DHPVTPDR, (C)EYPVYPES, (C)DTPVLPDS, (C)DMPVTPDT, (C)DAPVTPDT, (C) DSPVVPDN, (C) DLPVTPDR, (C) DSPVHPDT, (C)DAPVRPDS, (C)DMPVWPDG, (C) DAPVYPDG, (C) DRPVQPDR,
  • C YDRPVQPDR, (C) DMPVDPEN, (C) DMPVDADN, DQPVLPD (C) , DMPVLPD (C) , (C)EMPVDPDN and (C)DNPVHPE.
  • n' and/or m' are 1 and Xi ' and/or X 7 * are cysteine (C) .
  • the mimotope comprises 7 to 30, preferably 7 to 20, more prefer ⁇ ably 7 to 16, most preferably 8 or 9, amino acid residues.
  • the mimotope comprises or consists of an amino acid sequence se ⁇ lected from the group consisting of DQPVLPD, DSPVLPD, DVPVLPD, DSPVLPDG, YDRPVQPDR, DHPVHPDS, DAPVRPDS, KNDEGAP, KQEEGAP and KSEEGAP, in particular DQPVLPD and YDRPVQPDR.
  • the mimotopes may comprise at the C- and/or N-terminal end a cysteine residue.
  • composition of the present invention comprises the following combinations of mimotopes and carriers and/or adjuvants (see Table A) .
  • These preferred adjuvant compo ⁇ sitions can be combined with the mimotopes of the present inven ⁇ tion to obtain a composition of the present invention.
  • the composition of the present invention comprises or consists of a combination of mimotopes, carriers and adju ⁇ vants selected from the group consisting of A-Cl-Al, A-C1-A3, A- C1-A4/A5/A6, A-C1-A9, A-C1-A12, A-C1-A14, A-C1-A16, A-C1-A17, A- C1-A18, A-C1-A21, A-C1-A26, E-C1-A1, E-C1-A3, E-Cl -A4 /A5 /A6 , E- C1-A9, E-C1-A12, E-C1-A14, E-C1-A16, E-C1-A17, E-C1-A18, E-Cl- A21, E-C1-A26, A-C2-A1, A-C2-A3, A-C2
  • the synucleinopathy to be treated and/or prevented and/or ameliorated with the composition and/or compounds of the present invention is selected from the group consisting of Lewy Body Disorders (LBDs) , preferably Parkinson's Disease (PD) , Parkison's Disease with Dementia (PDD) and Dementia with Lewy Bodies (DLB) , as well as Multiple System Atrophy (MSA) or Neuro- degeneration with Brain Iron Accumulation type I (NBIA Type I), progressive supranuclear palsy (PSP) , frontotemporal dementia
  • LBDs Lewy Body Disorders
  • PD Parkinson's Disease
  • PPD Parkison's Disease with Dementia
  • DLB Dementia with Lewy Bodies
  • MSA Multiple System Atrophy
  • NBIA Type I Neuro- degeneration with Brain Iron Accumulation type I
  • PSP progressive supranuclear palsy
  • FTD Fluorescence Activated Dermatylcholine
  • PiD Pick's disease
  • the motor symptoms of Parkinson's disease are selected from the group consisting of resting tremor, Bradykinesia, rigidity, pos ⁇ tural instability, stooped posture, dystonia, fatigue, impaired fine motor dexterity and motor coordination, impaired gross mo ⁇ tor coordination, poverty of movement (decreased arm swing) , akathisia, speech problems, loss of facial expression, mi- crographia, difficulty swallowing, sexual dysfunction and drool ⁇ ing .
  • a further aspect of the present invention relates to a meth ⁇ od for preventing and/or treating synucleinopathies as defined herein by administering to a subject in need thereof an appro ⁇ priate amount of a composition as defined in the claims.
  • preventing covers measures not only to prevent the occurrence of disease, such as risk factor reduction, but also to arrest its progress and reduce its conse ⁇ quences once established.
  • treatment or grammatical equiva ⁇ lents encompasses the improvement and/or reversal of the symp ⁇ toms of disease (e.g., neurodegenerative disease).
  • disease e.g., neurodegenerative disease
  • treatment refers to both therapeutic treatment and prophylactic or preventative measures.
  • those who may benefit from treatment with compositions and methods of the present invention include those already with a disease and/or disorder (e.g., neurodegenerative disease, lack of or loss of cognitive function) as well as those in which a disease and/or disorder is to be prevented (e.g., using a prophylactic treat ⁇ ment of the present invention) .
  • a disease and/or disorder e.g., neurodegenerative disease, lack of or loss of cognitive function
  • a disease and/or disorder e.g., using a prophylactic treat ⁇ ment of the present invention
  • Composition comprising at least one mimotope of an epitope of alpha-synuclein for use in a method for preventing and/or treating synucleinopathies , wherein said at least one mimotope is coupled or fused to a pharmaceutically acceptable carrier protein selected from the group consisting of a nontoxic diphtheria toxin mutant, keyhole limpet hemocyanin (KLH) , diphtheria toxin (DT) , tetanus toxid (TT) and Haemophilus influ ⁇ enzae protein D (protein D) .
  • KLH keyhole limpet hemocyanin
  • DT diphtheria toxin
  • TT tetanus toxid
  • protein D Haemophilus influ ⁇ enzae protein D
  • composition according to embodiment 1, wherein the nontoxic diphtheria toxin mutant is selected from the group con ⁇ sisting of CRM 197, CRM 176, CRM 228, CRM 45, CRM 9, CRM 102, CRM 103 and CRM 107, in particular CRM 197.
  • composition according to embodiment 1 or 2 wherein the at least one mimotope is formulated for subcutaneous, intrader ⁇ mal, transdermal or intramuscular administration.
  • composition according to embodiment 4 wherein at least one adjuvant is capable to stimulate the innate immune system.
  • composition according to embodiment 5 wherein at least one adjuvant capable to stimulate the innate immune system com ⁇ prises or consists of a Toll-like receptor (TLR) agonist, pref ⁇ erably a TLR1, TLR2, TLR3, TLR4, TLR5, TLR7, TLR8 or TLR9 ago ⁇ nist, particularly preferred a TLR4 agonist.
  • TLR Toll-like receptor
  • composition according to embodiment 6, wherein the TLR agonist is selected from the group consisting of monophosphoryl lipid A (MPL) , 3-de-O-acylated monophosphoryl lipid A (3D-MPL) , poly I:C, GLA, flagellin, R848, imiquimod and CpG.
  • MPL monophosphoryl lipid A
  • 3D-MPL 3-de-O-acylated monophosphoryl lipid A
  • poly I:C poly I:C
  • GLA flagellin
  • R848 imiquimod and CpG.
  • composition according to embodiment 4, wherein the at least one adjuvant is selected from the group consisting of
  • Xl is any amino acid residue
  • X2 is an amino acid residue selected from the group consist ⁇ ing of lysine (K) , arginine (R) , alanine (A) and histidine (H) ,
  • X3 is an amino acid residue selected from the group consist ⁇ ing of asparagine (N) , glutamine (Q) , serine (S) , glycine (G) and alanine (A) , preferably asparagine (N) , serine (S) , glycine (G) and alanine (A) ,
  • X4 is an amino acid residue selected from the group consist ⁇ ing of glutamic acid (E) , aspartic acid (D) and alanine (A)
  • X5 is an amino acid residue selected from the group consist ⁇ ing of glutamic acid (E) and aspartic acid (D) ,
  • XQ is an amino acid residue selected from the group consist ⁇ ing of alanine (A) and tyrosine (Y) ,
  • X7 is any amino acid residue
  • n and m independently, are 0 or an integer of more than 0, wherein the amino acid sequence according to Formula I is not identical with, or does not comprise the 7-mer polypeptide fragment of alpha-synuclein having the amino acid sequence KNEEGAP, and wherein
  • the at least one mimotope comprising the amino acid sequence according to Formula I has a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence KNEEGAP .
  • composition according to embodiment 11 or 12, wherein the mimotope comprises an amino acid sequence selected from the group consisting of ( Xi ) n KNDEGAP (X 7 ' mr (Xi) nANEEGAP (X 7 ) m ,
  • composition according to any one of embodiments 1 to 13 comprising at least one mimotope comprising an amino acid se ⁇ quence selected from the group consisting of (Xi) n QASFAME (X 7 ) m , (Xi) nTASWKGE (X 7 ) m , (Xi) n QASSKLD (X 7 ) m , (X 1 ) n TPAWKGE (X 7 ) m ,
  • Xi is any amino acid residue
  • X 7 is any amino acid residue
  • n and m independently, are 0 or an integer of more than 0, said at least one mimotope having a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence KNEEGAP
  • composition according to any one of embodiments 1 to 14, wherein the at least one mimotope comprises the amino acid se ⁇ quence (Xl')n'X2'X3'PVX 4 'X 5 'X 6 ' (X7')m' (Formula II) , wherein
  • Xi ' is any amino acid residue
  • X 2 ' is an amino acid residue selected from the group con ⁇ sisting of aspartic acid (D) and glutamic acid (E) ,
  • X3' is any amino acid residue
  • X 4 ' is any amino acid residue
  • X5' is an amino acid residue selected from the group con ⁇ sisting of proline (P) and alanine (A) ,
  • ⁇ ' is an amino acid residue selected from the group con ⁇ sisting of aspartic acid (D) and glutamic acid (E) ,
  • Xv is any amino acid residue
  • n' and m' independently, are 0 or an integer of more than 0, wherein the amino acid sequence according to Formula II is not identical with, or does not comprise the 8-mer polypeptide fragment of alpha-synuclein having the amino acid sequence
  • the at least one mimotope comprising the amino acid sequence according to Formula II has a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence DMPVDPDN.
  • X3' is an amino acid residue selected from the group consisting of glu- tamine (Q) , serine (S) , threonine (T) , arginine (R) , asparagine (N) , valine (V) , histidine (H) , methionine (M) , tyrosine (Y) , alanine (A) and leucin (L) .
  • composition according to embodiment 15 or 16 wherein X 4 ' is an amino acid residue selected from the group consisting of glutamine (Q) , tryptophane (W) , threonine (T) , arginine (R) , aspartic acid(D), isoleucin (I), valine (V), histidine (H) , pro ⁇ line (P) , tyrosine (Y) , alanine (A) , serine (S) and leucin (L) .
  • Q glutamine
  • W tryptophane
  • T threonine
  • R arginine
  • aspartic acid(D) aspartic acid(D)
  • isoleucin (I) isoleucin
  • V histidine
  • P pro ⁇ line
  • Y tyrosine
  • A alanine
  • S serine
  • L leucin
  • the mimotope has an amino acid sequence selected from the group consisting of (C) DQPVLPD, (C) DMPVLPD, (C) DSPVLPD, (C)DSPVWAE, (C) DTPVLAE, (C) DQPVLPDN, (C) DMPVLPDN, (C) DSPVLPDN, (C) DQPVTAEN, (C) DSPVWAEN, (C) DTPVLAEN, (C) HDRPVTPD, (C) DRPVTPD, (C)DVPVLPD, (C)DTPVYPD, (C) DTPVIPD, (C) HDRPVTPDN, (C) DRPVTPDN, (C) DRPVTPDN, (C)DNPVHPEN, (C) DVPVLPDN, (C) DTPVYPDN, (C) DTPVIPDN, (C) DQPVLPDG, (C)DMPVLPDG, (C) DSPV
  • LBDs Lewy Body Disorders
  • PD Parkinson's Dis ⁇ ease
  • MSA Multiple System Atrophy
  • NBIA Type I Neurodegeneration with Brain Iron Accumulation type I
  • PEP progressive supranuclear palsy
  • FTD frontotemporal dementia
  • PiD Pick's disease
  • DAPVRPDS KNDEGAP, KQEEGAP and KSEEGAP, in particular DQPVLPD and YDRPVQPDR
  • composition according to any one of embodiments 1 to 22 comprising a combination of at least one mimotope and carrier and/or adjuvant as defined in Table A, preferably A-C1-A1, A-Cl- A14, A-C1-A18, A-C1-A26, E-C1-A1, E-C1-A14, E-C1-A18, E-C1-A26, A-C2-A1, A-C2-A14, A-C2 -Al 8 , A-C2 -A26 , E-C2-A1, E-C2-A14, E-C2- A18 and E-C2-A26.
  • Fig. 1 (A) shows higher injected peptide specific immunogen- icity promoted by alternative adjuvants containing TLR4, saponin or oil in water emulsion when adjuvants are combined with
  • DQPVLPD-CRM197 conjugate compared to adjuvants alone or alumini ⁇ um hydroxide combined with DQPVLPD-CRM197 conjugate.
  • Fig. 1 (B) shows higher injected peptide specific immunogen- icity promoted by alternative adjuvants containing TLR4 and also to a lesser degree saponin or oil in water emulsion when adjuvants are combined with YDRPVQPDR-CRMl 97 conjugate compared to adjuvants alone or aluminium hydroxide combined with YDRPVQPDR- CRM197 conjugate.
  • Fig. 1 (C) shows higher injected peptide specific immunogen- icity promoted by alternative adjuvants containing TLR4 but not oil in water emulsion or saponin when adjuvants are combined with KNDEGAP-CRM197 conjugate compared to adjuvants alone or al ⁇ uminium hydroxide combined with KNDEGAP-CRM197 conjugate
  • Fig. 2 (A) shows higher injected peptide specific Immunogen- icity promoted by alternative adjuvants containing oil in water emulsion and TLR4 or saponin when adjuvants are combined with DQPVLPD-KLH conjugate compared to adjuvants alone or aluminium hydroxide combined with DQPVLPD-KLH conjugate.
  • Figures 2 (B) and (D) show higher injected peptide specific Immunogenicity promoted by alternative adjuvants containing TLR4 or oil in water emulsion but not saponin when adjuvants are combined with YDRPVQPDR-KLH (B) and DHPVHPDS-KLH (D) conjugate compared to adjuvants alone or aluminium hydroxide combined with YDRPVQPDR-KLH and DHPVHPDS-KLH conjugate, respectively.
  • Fig. 2 (C) shows higher injected peptide specific Immunogen ⁇ icity promoted by alternative adjuvants containing TLR4 and to a lesser degree oil in water emulsion or saponin when adjuvants are combined with KNDEGAP-KLH conjugate compared to adjuvants alone or aluminium hydroxide combined with KNDEGAP-KLH conju ⁇ gate .
  • Fig. 3 (A) shows higher Monocyte/Macrophage activation based on MCP-1 cytokine levels promoted by alternative adjuvants con ⁇ taining saponin and to a lesser degree TLR4 or oil in water emulsion when adjuvants are combined with DQPVLPD-CRM197 conjugate compared to adjuvants alone or aluminium hydroxide combined with DQPVLPD-CRM197 conjugate.
  • Quil-A alone already seems to promote monocyte/macrophage stimu ⁇ lation although on a rather low level.
  • Fig. 3 (C) shows higher Monocyte/Macrophage activation based on MCP-1 cytokine levels promoted by alternative adjuvants con ⁇ taining saponin or oil in water emulsion or TLR4 when adjuvants are combined with KNDEGAP-CRM197 conjugate compared to adjuvants alone or aluminium hydroxide combined with KNDEGAP-CRM197 conjugate.
  • Quil-A alone already seems to promote monocyte/macrophage stimulation although on a rather low level.
  • Fig. 3 (D) shows higher Monocyte/Macrophage activation based on MCP-1 cytokine levels promoted by alternative adjuvants con ⁇ taining saponin, TLR4 or oil in water emulsion when adjuvants are combined with DHPVHPDS-CRMl 97 conjugate compared to adju ⁇ vants alone or aluminium hydroxide combined with DHPVHPDS-CRMl 97 conjugate.
  • Quil-A alone already seems to promote mono ⁇ cyte/macrophage stimulation although on a rather low level.
  • Fig. 4 (A) shows higher Monocyte/Macrophage activation based on MCP-1 cytokine levels promoted by alternative adjuvants con ⁇ taining TLR4, saponin or oil in water emulsion when adjuvants are combined with DQPVLPD-KLH conjugate compared to adjuvants alone or aluminium hydroxide combined with DQPVLPD-KLH conju ⁇ gate .
  • Figures 4 (B) and (D) show higher Monocyte/Macrophage acti ⁇ vation based on MCP-1 cytokine levels promoted by alternative adjuvants containing TLR4, oil in water emulsion or saponin when adjuvants are combined with YDRPVQPDR-KLH (B) and DHPVHPDS-KLH (D) conjugate compared to adjuvants alone or aluminium hydroxide combined with YDRPVQPDR-KLH and DHPVHPDS-KLH conjugate, respectively.
  • Quil-A alone already seems to promote mono ⁇ cyte/macrophage stimulation
  • Fig. 4 (C) shows higher Monocyte/Macrophage activation based on MCP-1 cytokine levels promoted by alternative adjuvants con ⁇ taining oil in water emulsion or saponin but not TLR4 when adjuvants are combined with KNDEGAP-KLH conjugate compared to adju- vants alone or aluminium hydroxide combined with KNDEGAP-KLH conjugate.
  • Quil-A alone already seems to promote mono ⁇ cyte/macrophage stimulation.
  • Figures 5 (A) and (B) show a comparison of different adju ⁇ vants combined with CRM197-conjugates (A) and KLH-conj ugates (B) in respect to their influence on the size of the monocyte frac ⁇ tion in peripheral blood.
  • Monocyte percentage in all samples is within physiological range, although QuilA shows a trend to de ⁇ crease the number of monocytes alone as well as in combination with all mimotope-conj ugates tested. Absolute variances reflect assay variability.
  • Figures 6 (A) and (D) show a synergistic effect of alterna ⁇ tive adjuvants combined with KNDEGAP-CRM197 (A) and DHPVHPDS-KLH (D) on in vivo ⁇ uptake in peripheral blood monocytes when com ⁇ pared to aluminium hydroxide combined with KNDEGAP-CRM197 and DHPVHPDS-KLH conjugate, respectively.
  • Fig. 6 (B) shows a synergistic effect of TLR4 or oil in wa ⁇ ter emulsion adjuvants but not of saponin combined with
  • Fig. 6 (C) shows a synergistic effect of TLR4 but not oil in water emulsion or saponin combined with KNDEGAP-KLH on in vivo ⁇ uptake in peripheral blood monocytes when compared to alumin ⁇ ium hydroxide combined with KNDEGAP-KLH conjugate.
  • Mimotope peptides were coupled to the carrier CRM-197 or KLH by using the heterobifunctional crosslinking agent GMBS. Brief ⁇ ly, CRM-197/KLH was mixed with an excess of GMBS at room temperature to allow for activation, followed by removal of excess GMBS by dialysis. Excess mimotope peptide was then added to the activated carrier. The mimotope CRM-197/KLH conjugate was used for vaccine formulation.
  • Vaccines were formulated with different adjuvants and ap ⁇ plied to animals. Identical amounts of conjugated mimotope pep ⁇ tide (s) were injected per mouse when the CRM-197/KLH vaccines were compared to other vaccines or when different adjuvants were compared .
  • mice Female BALB/c mice, 6 mice per group, were immunized with mimotope-CRM-197/KLH conjugates using different adjuvants. Con ⁇ trol groups were immunized with CRM-197/KLH plus respective ad ⁇ juvants and/or PBS and/or adjuvants alone.
  • Example 1 Effect of mimotope-CRM197 conjugates using different adjuvant systems : Immunogenicity (Fig. 1)
  • mice are im ⁇ munized repeatedly with identical amounts of AFFITOPE peptides (the mimotopes disclosed herein) , comprising preferably a C or N-terminal cysteine residue, coupled to CRM-197 (10yg peptide per immunisation) .
  • AFFITOPE peptides the mimotopes disclosed herein
  • CRM-197 10yg peptide per immunisation
  • Adjuvants used in this example are:
  • the in vitro ELISA assay to determine the antibody titer following immunisation is performed with plasma of single mice (see method description below) .
  • peripheral blood was drawn from mice using heparin as anticoagulant and plasma was prepared from these samples.
  • the diluted plasma was then used for ELISA analy ⁇ sis.
  • the wells of the ELISA plates (Nunc Max- isorb) were coated with peptide-BSA conjugates. Subsequently, diluted plasma was added and the detection of peptide specific antibodies was performed with biotinylated anti-mouse IgG
  • Example 2 Effect of mimotope-KLH conjugates using different adjuvant systems : Immunogenicity (Fig. 2)
  • mice are im ⁇ munized repeatedly with identical amounts of mimotope peptides coupled to KLH (e.g. 10yg peptide per immunisation) .
  • KLH e.g. 10yg peptide per immunisation
  • suitable control groups e.g.: PBS alone or adjuvant alone or KLH plus adjuvant
  • Adjuvants used in this example are (as in example 1) :
  • Aluminium hydroxide Aluminium hydroxide, Aluminium hydroxide and MPLA, Addavax and QuilA.
  • the in vitro ELISA assay to determine the antibody titer following immunisation is performed with plasma of single mice (see method description as in example 1) .
  • Example 3 Effect of mimotope-CRM197 conjugates using different adjuvant systems: effect on peripheral monocyte/macrophage (Fig. 3)
  • Cytokine determination To determine the concentration of cytokines in the circula ⁇ tion of vaccinated animals, blood was collected from animals 2 hours after injection of vaccines. Subsequently, plasma was pre ⁇ pared from blood samples and cytokine concentration in individu ⁇ al samples was defined using the FlowCytomix bead array system (eBioscience) and flow cytometric analysis .
  • Example 4 Effect of mimotope-KLH conjugates using different adjuvant systems: effect on peripheral monocyte/macrophage
  • Example 5 Effect of immunotherapy on monocytes and monocytic alpha synuclein uptake (Fig. 5)
  • monocytes are considered the pe ⁇ ripheral blood precursor cells of brain microglia (Rezaie, P. , et al 1999. Dev . Brain Res . 115.-71-81 ; Mildner et al Nat
  • Markers such as CDllb and Ly6C are immunologicals markers that are present on such periph ⁇ eral blood monocytes and persist when these cells are infiltrat ⁇ ing the brain (Mildner et al . , 2007, Lebson L, et al . J Neurosci. 2010 Jul 21; 30 (29) : 9651-8) .
  • TLR agonist containing adjuvants or components thereof are contributing to changing the number of monocytes in the peripheral blood.
  • Peripheral blood was drawn from mice with K2-EDTA as antico- agulant, 24-Hour after last injection of the vaccines and anti ⁇ bodies, respectively.
  • Red blood cell lysis was performed on in ⁇ dividual animal samples using BD Pharm LyseTM (BD Pharmingen) .
  • Remaining peripheral blood cells were incubated with Rat anti- Mouse CD16/CD32 (BD Fc BlockTM by BD Biosciences) and cells were further incubated with a combination of directly conjugated an ⁇ tibodies as described by Mildner et al .
  • Monocytes were identified by their Forward/Side scatter properties and gated as CD3-/CD45R/B220-/Ly-6G-/NK1.1- (Lineage- )/CDllb+ cells.
  • CDllb+ monocyte frequency was reported as a per ⁇ centage of the total cells (excluding debris) .
  • mice were injected with HiLyte FluorTM488 labeled alpha-synuclein and blood was withdrawn 2h after injection.
  • Samples for alpha synuclein uptake determination were acquired on a flow cytometer (BD FACSCanto II) and data analyzed with the FACSDiva software (BD Biosciences) .
  • Monocytes were identified by their Side/Forward scatter properties, excluding debris and gated as CD3-/CD45R/B220-/Ly- 6G-/NK1.1- (Lineage-) /CDllb+ cells.
  • Alpha synuclein uptake was assessed by reporting the percentage of HiLyte fluorTM 488 alpha synuclein positive cells among gated monocytes.

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Abstract

The present invention relates to a composition comprising at least one mimotope of an epitope of alpha-synuclein for use in a method for preventing and/or treating synucleinopathies, wherein said at least one mimotope is coupled or fused to a pharmaceutically acceptable carrier protein selected from the group consisting of a non-toxic diphtheria toxin mutant, keyhole limpet hemocyanin (KLH), diphtheria toxin (DT), tetanus toxid (TT) and Haemophilus influenzae protein D (protein D).

Description

COMPOSITIONS
The present invention relates to a medicament to be used to prevent and/or treat synucleinopathies.
Synucleinopathies are a diverse group of neurodegenerative disorders that share a common pathologic characteristic: in neu¬ ropathology examinations characteristic lesions can be detected containing abnormal aggregates of alpha-synuclein (alpha-syn, a- syn) protein in selected populations of neurons and glia cells.
Alpha-syn (initially identified as PARK1 and PARK4 ) is a 140 amino acid protein widely expressed in the neocortex, hippocam¬ pus, dentate gyrus, olfactory bulb, striatum, thalamus and cere¬ bellum. Alpha-Syn is also highly expressed in hematopoietic cells including B-, T-, and NK cells as well as monocytes and platelets. The exact role in these cells is not known but it has been implicated in the differentiation of megakaryocytes (plate¬ let precursors) .
The most common synucleinopathies include but are not lim¬ ited to Lewy body disorders (LBDs) like Parkinson's disease
(PD) , Parkinson's disease with dementia (PDD) and dementia with Lewy bodies (DLB) , as well as Multiple System Atrophy (MSA) or Neurodegeneration with Brain Iron Accumulation type I (NBIA Type I) . In addition further neurodegenerative diseases can be clas¬ sified as synucleinopathies based on the occurrence of typical, a-syn containing lesions: progressive supranuclear palsy (PSP) , frontotemporal dementia (FTD) , Pick's disease (PiD) and cortico- basal degeneration (CBD) . The current treatment options for these diseases include symptomatic medications such as L-dopa, anticholinergic drugs as well as inhibitors of monoamine oxi¬ dase. However, all treatment opportunities currently present on¬ ly lead to symptomatic alleviation but do not induce a long lasting, disease modifying effect in patients.
Lewy body disorders (LBD) are progressive neurodegenerative disorders characterized by tremor, rigidity, bradykinesia and by loss of dopaminergic neurons in the brain. In the case of DLB and PDD signs also include cognitive impairment. Up to 2% of the population above 60 years of age in western countries develop the typical signs of PD/LBD. Currently only symptomatic treat¬ ment is available. Unfortunately, these therapies only provide temporary relief from early symptoms and do not halt disease progression. The pathogenesis of PD/LBD is still incompletely understood, but it appears that genetic susceptibility and envi¬ ronmental factors are involved in the development of the dis¬ ease. Despite all genetic advances, PD/LBD is primarily a spo¬ radic disorder with no known cause (also called idiopathic
PD/LBD) .
Patients suffering from this disease develop characteristic ubiquitinated intracellular inclusions called Lewy bodies (LBs) in the cortical and subcortical areas of the brain. Especially regions with high content of dopaminergic neurons or neuronal projections show this typical pathologic feature. Recently, sev¬ eral studies could show that the synaptic protein alpha-syn plays a central role in LBD pathogenesis. In LBD, alpha-syn ac¬ cumulates in LBs throughout affected brain areas. Additionally, it could be demonstrated that single point mutations as well as duplications or multiplications in the alpha-syn gene are asso¬ ciated with rare familial forms of Parkinsonism. Importantly, based on results from overexpression studies in transgenic (tg) mice as well as in Drosophila melanogaster its key role in the pathogenesis of PD/LBD is underscored as these animal models mimic several characteristics of PD.
Another very important synucleinopathy is Multiple System Atrophy (MSA) . MSA is a sporadic neurodegenerative disorder that is characterised by symptoms of L-DOPA-resistant Parkinsonism, cerebellar ataxia, and dysautonomia . Patients suffer from multi¬ system neuronal loss affecting various brain areas including striatum, substantia nigra, cerebellum, pons, as well as the in¬ ferior olives and the spinal cord. MSA is characterized by al¬ pha- syn-positive glial cytoplasmic (GCI) and rare neuronal in¬ clusions throughout the central nervous system. These inclusions are associated with striatonigral degeneration, olivoponto¬ cerebellar atrophy, and involvement of autonomic nuclei in me¬ dulla and spinal cord. The importance of GCIs for the pathogene¬ sis of MSA is generally acknowledged and underscored by recent analysis of transgenic mouse models analysing the effect of al¬ pha-syn overexpression in oligodendroglia . In tg mice overex- pressing human alpha-syn both GCI-like aggregates and biochemical markers of MSA were observed.
Although the exact mechanisms by which accumulation of al¬ pha- syn leads to the typical features of neurodegeneration in synucleopathies are not fully understood, recent studies imply that abnormal formation and accumulation of alpha-syn is involved in the degenerative processes underlying synucleinopathy . Recently, different forms of alpha-syn have been identified in LBs . Beside the full length form of the protein, different forms of modified alpha-syn have been identified including phosphory- lated, nitrated, and mono-, di-, or tri-ubiquitinated alpha-syn. In addition, C-terminally truncated forms of the protein, like alpha-syn 1-119, alpha-syn 1-122 and alpha-syn 1-123, have been detected in brain tissue from both transgenic mice and PD cases. It is currently believed that up to 15% of the alpha-syn detect¬ ed in LBs and lewy neurites is truncated. Previous in vitro studies using truncated alpha-syn could demonstrate that alpha- syn lacking the C-terminal 20-30 amino acids was showing an in¬ creased tendency to aggregate and to form filaments found in Lewy-neurites and LBs. These truncated versions could thus act in a similar way as truncated and modified forms of amyloid beta (Αβ)ίη Alzheimer's disease (AD). These truncated and modified forms of Αβ are thought to act as seed molecules for plaque dep¬ osition and show a higher aggregation propensity as well as high neurotoxicity and synaptotoxicity in vivo and in vitro.
Thus full length alpha-syn as well as truncated and/or modi¬ fied forms of alpha-syn, which are showing potential seeding effects, are then believed to accumulate leading to oligomer- formation. Based on recent studies it is believed that such oli- gomer-formation for example in the synaptic terminals and axons plays an important role for PD/LBD development and could thus be enhanced by the presence of truncated forms of alpha-syn. Hence, reduction of alpha-syn deposition and oligomerisation should be beneficial in the treatment of synucleopathies, especially of idiopathic LBD/PD and MSA and could present the first strategy for treatment of these neurodegenerative diseases in addition to the mere alleviation of symptoms resulting from current treat¬ ment strategies like L-DOPA application.
In Iwatsubo T. (Neuropathology 27 (5) (2007) : 474-478) the correlation of alpha-synuclein depositions as well as its phos¬ phorylation with a pathogenesis of alpha-synucleopathies is ex¬ amined. The author of this publication found that serine 129 of alpha-synuclein deposited in synucleopathy lesions is extensively phosphorylated . US 2007/213253 relates to mutant human alpha- synuclein as well as peptides derived therefrom which may be used for inhibiting the aggregation of the wild-type human al- pha-synuclein . In the WO 2004/041067 means and methods for preventing or treating diseases associated with alpha-synuclein aggregation are disclosed which comprise the use of alpha- synuclein fragments. In the US 2003/166558 peptides are de¬ scribed which can be used to induce immune response to protein deposits. US 2005/198694 relates to alpha-synuclein fragments comprising at least 100 amino acids and having a C-terminal de¬ letion of 1 to 23 amino acids.
Liang et al . (J. Neurochem. 99(2006): 470-482) studied the regulation of alpha-synuclein in rats. They observed that in alcohol preferring rats the expression rate of alpha-synuclein is increased compared to alcohol-non preferring rats.
In Hamilton BA (Genomics 83(2004): 739-742) the distribution of alpha-synuclein 53Thr and 53Ala in primates is examined.
In US 2005/0037013 immunogenic alpha-synuclein fragments are disclosed which are able to induce an immune response against a specific epitope within residues 70-140 of alpha-synuclein.
WO 2006/045037 relates to C-terminal truncated alpha- synuclein molecules which can be used to screen for agents which have a pharmacological activity useful for treating a Lewy Body Disease .
Although experimental therapies utilizing neurotrophic fac¬ tors and grafting of dopaminergic cells have yielded promising results, alternative approaches designed to reduce the neuronal accumulation of alpha-syn are required. There is compelling evidence accumulating that alpha-syn aggregates might be targeted by immunotherapy. Indeed, recently a potential for the treatment of synucleopathies has been shown. Tg mice overexpressing human alpha-syn were vaccinated with human alpha-syn protein. In mice that produced high relative affinity antibodies upon vaccina¬ tion, there was decreased accumulation of aggregated alpha-syn in neuronal cell bodies and synapses which was associated with reduced neurodegeneration . Furthermore, antibodies produced by immunized animals also detected abnormal aggregated forms of al¬ pha-syn associated with the neuronal membrane and promoted the degradation of these aggregates, probably via lysosomal path¬ ways. Similar effects were observed using passive immunotherapy with an exogenously applied alpha-syn-specific antibody. These results suggest that vaccination is effective in reducing neu¬ ronal accumulation of alpha-syn aggregates and that further development of this approach might elicit beneficial effects in the treatment of LBD and synucleinopathies.
It is an object of the present invention to provide a medic¬ ament to prevent and treat synucleinopathies on the basis of a vaccine .
The present invention relates to a composition comprising at least one mimotope of an epitope of alpha-synuclein for use in a method for preventing and/or treating synucleinopathies, wherein said at least one mimotope is coupled or fused, preferably cou¬ pled, to a pharmaceutically acceptable carrier protein selected from the group consisting of a non-toxic diphtheria toxin mu¬ tant, keyhole limpet hemocyanin (KLH) , diphtheria toxin (DT) , tetanus toxid (TT) and Haemophilus influenzae protein D (protein D) .
The immunogenicity of the mimotopes can surprisingly be in¬ creased if the mimotopes are fused or coupled to a carrier pro¬ tein selected from the group consisting of a non-toxic diphthe¬ ria toxin mutant, keyhole limpet hemocyanin (KLH) , diphtheria toxin (DT) , tetanus toxid (TT) and Haemophilus influenzae pro¬ tein D (protein D) , whereby non-toxic diphtheria toxin mutants, such as CRM197, are particularly preferred.
As used herein, the term "epitope" refers to an immunogenic region of an antigen which is recognized by a particular antibody molecule. An antigen may possess one or more epitopes, each capable of binding an antibody that recognizes the particular epitope .
According to the present invention the term "mimotope" re¬ fers to a molecule which has a conformation that has a topology equivalent to the epitope of which it is a mimic. The mimotope binds to the same antigen-binding region of an antibody which binds immunospecifically to a desired antigen. The mimotope will elicit an immunological response in a host that is reactive to the antigen to which it is a mimic. The mimotope may also act as a competitor for the epitope of which it is a mimic in in vitro inhibition assays (e.g. ELISA inhibition assays) which involve the epitope and an antibody binding to said epitope. However, a mimotope of the present invention may not necessarily prevent or compete with the binding of the epitope of which it is a mimic in an in vitro inhibition assay although it is capable to induce a specific immune response when administered to a mammal. The compounds of the present invention comprising such mimotopes (also those listed above) have the advantage to avoid the for¬ mation of autoreactive T-cells, since the peptides of the com¬ pounds have an amino acid sequence which varies from those of naturally occurring alpha synuclein protein.
The mimotopes of the present invention can be synthetically produced by chemical synthesis methods which are well known in the art, either as an isolated peptide or as a part of another peptide or polypeptide. Alternatively, the peptide mimotope can be produced in a microorganism which produces the peptide mimo¬ tope which is then isolated and if desired, further purified. The peptide mimotope can be produced in microorganisms such as bacteria, yeast or fungi, in eukaryote cells such as a mammalian or an insect cell, or in a recombinant virus vector such as ade¬ novirus, poxvirus, herpesvirus, Simliki forest virus, baculovi- rus, bacteriophage, sindbis virus or sendai virus. Suitable bac¬ teria for producing the peptide mimotope include E.coli,
B.subtilis or any other bacterium that is capable of expressing peptides such as the peptide mimotope. Suitable yeast types for expressing the peptide mimotope include Saccharomyces cere- visiae, Schizosaccharomyces pombe, Candida, Pichia pastoris or any other yeast capable of expressing peptides. Corresponding methods are well known in the art. Also methods for isolating and purifying recombinantly produced peptides are well known in the art and include e.g. as gel filtration, affinity chromatog¬ raphy, ion exchange chromatography etc...
To facilitate isolation of the peptide mimotope, a fusion polypeptide may be made wherein the peptide mimotope is transla- tionally fused (covalently linked) to a heterologous polypeptide which enables isolation by affinity chromatography. Typical heterologous polypeptides are His-Tag (e.g. His6; 6 histidine resi¬ dues), GST-Tag (Glutathione-S-transferase) etc... The fusion polypeptide facilitates not only the purification of the mimo¬ topes but can also prevent the mimotope polypeptide from being degraded during purification. If it is desired to remove the heterologous polypeptide after purification the fusion polypep¬ tide may comprise a cleavage site at the junction between the peptide mimotope and the heterologous polypeptide. The cleavage site consists of an amino acid sequence that is cleaved with an enzyme specific for the amino acid sequence at the site (e.g. proteases) .
The mimotopes of the present invention may also be modified at or nearby their N- and/or C-termini so that at said positions a cysteine residue is bound thereto.
The mimotopes according to the present invention preferably are antigenic polypeptides which in their amino acid sequence vary from the amino acid sequence of alpha synuclein. In this respect, the inventive mimotopes may not only comprise amino ac¬ id substitutions of one or more naturally occurring amino acid residues but also of one or more non-natural amino acids (i.e. not from the 20 "classical" amino acids) or they may be com¬ pletely assembled of such non-natural amino acids. Suitable an¬ tibody-inducing antigens may be provided from commercially available peptide libraries. Preferably, these peptides are at least 7 amino acids, and preferred lengths may be up to 16, preferably up to 14 or 20 amino acids (e.g. 5 to 16 amino acid residues) . According to the invention, however, also longer peptides may very well be employed as antibody-inducing antigens. Furthermore the mimotopes of the present invention may also be part of a polypeptide and consequently comprising at their N- and/or C-terminus at least one further amino acid residue.
For preparing the mimotopes of the present invention (i.e. the antibody-inducing antigens disclosed herein) , of course also phage libraries, peptide libraries are suitable, for instance produced by means of combinatorial chemistry or obtained by means of high throughput screening techniques for the most vary¬ ing structures (Display: A Laboratory Manual by Carlos F. Barbas (Editor), et al . ; Willats WG Phage display: practicalities and prospects. Plant Mol. Biol. 2002 Dec; 50 ( 6) : 837-54 ) .
As used herein, the term "epitope" refers to an immunogenic region of an antigen to which a particular antibody molecule can specifically bind thereto. An antigen may possess one or more epitopes, each capable of binding an antibody that recognizes the particular epitope.
The composition of the present invention may comprise at least one, at least 2, at least 3, at least 4, at least 5 or at least 10 mimotopes as defined herein.
According to a preferred embodiment of the present invention the non-toxic diphtheria toxin mutant is selected from the group consisting of CRM 197, CRM 176, CRM 228, CRM 45, CRM 9, CRM 102, CRM 103 and CRM 107, whereby CRM 197 is particularly preferred.
The mimotopes of the present invention are particularly pre¬ ferred fused or conjugated to non-toxic diphtheria toxin mu¬ tants, such as CRM 197 (a nontoxic but antigenically identical variant of diphtheria toxin), CRM 176, CRM 228, CRM 45 (Uchida et al J. Biol. Chem. 218; 3838-3844, 1973), CRM 9, CRM 45, CRM 102, CRM 103 and CRM 107 and other mutations described by
Nicholls and Youle in Genetically Engineered Toxins, Ed:
Frankel, Marcel Dekker Inc, 1992) . Methods for fusing peptides like mimotopes to other peptides, polypeptides or proteins are well known in the art.
Another aspect of the present invention relates to a compo¬ sition comprising at least one mimotope of an epitope of alpha- synuclein for use in preventing and/or treating synucleinopa- thies .
In such a composition the at least one mimotope can be fused or conjugated to a pharmaceutically acceptable carrier, prefera¬ bly KLH (Keyhole Limpet Hemocyanin) , tetanus toxoid, albumin- binding protein, bovine serum albumin, a dendrimer (MAP; Biol. Chem. 358: 581), peptide linkers (or flanking regions) as well as the substances described in Singh et al . , Nat. Biotech. 17
(1999), 1075-1081 (in particular those in Table 1 of that docu¬ ment), and 0 ' Hagan et al . , Nature Reviews, Drug Discovery 2 (9)
(2003) , 727-735 (in particular the endogenous immuno- potentiating compounds and delivery systems described therein) , or mixtures thereof. The conjugation chemistry (e.g. via hetero- bifunctional compounds such as GMBS and of course also others as described in "Bioconj ugate Techniques", Greg T. Hermanson) in this context can be selected from reactions known to the skilled man in the art. Of course the at least one mimotope can also be fused or conjugated to a pharmaceutically acceptable carrier protein selected from the group consisting of a non-toxic diph¬ theria toxin mutant, keyhole limpet hemocyanin (KLH) , diphtheria toxin (DT) , tetanus toxid (TT) and Haemophilus influenzae pro¬ tein D (protein D) as defined above.
The composition of the present invention may be administered by any suitable mode of application, e.g. i.d., i.v., i.p., i.m., intranasally, orally, subcutaneously, transdermally, in- tradermally etc. and in any suitable delivery device (O'Hagan et al . , Nature Reviews, Drug Discovery 2 (9), (2003), 727-735).
Therefore, that at least one mimotope of the present invention is preferably formulated for intravenous, subcutaneous, intra¬ dermal or intramuscular administration (see e.g. "Handbook of Pharmaceutical Manufacturing Formulations", Sarfaraz Niazi, CRC Press Inc, 2004) .
The composition according to the present invention comprises the mimotope according to the invention in an amount of from 0.1 ng to 10 mg, preferably 10 ng to 1 mg, in particular 100 ng to 100 yg, or, alternatively, e.g. 100 fmol to 10 ymol, prefera¬ bly 10 pmol to 1 ymol, in particular 100 pmol to 100 nmol. Typi¬ cally, the vaccine may also contain auxiliary substances, e.g. buffers, stabilizers etc.
Typically, the composition of the present invention may also comprise auxiliary substances, e.g. buffers, stabilizers etc.. Preferably, such auxiliary substances, e.g. a pharmaceutically acceptable excipient, such as water, buffer and/or stabilisers, are contained in an amount of 0.1 to 99 % (weight) , more pre¬ ferred 5 to 80% (weight) , especially 10 to 70 % (weight) . Possible administration regimes include a weekly, biweekly, four-weekly (monthly) or bimonthly treatment for about 1 to 12 months; however, also 2 to 5, especially 3 to 4, initial vaccine admin¬ istrations (in one or two months) , followed by boaster vaccina¬ tions 6 to 12 months thereafter or even years thereafter are preferred - besides other regimes already suggested for other vaccines .
According to a preferred embodiment of the present invention the at least one mimotope is administered to an individual in an amount of 0.1 ng to 10 mg, preferably of 0.5 to 500 yg, more preferably 1 to 100 yg, per immunization. In a preferred embodi¬ ment these amounts refer to all mimotopes present in the compo¬ sition of the present invention. In another preferred embodiment these amounts refer to each single mimotopes present in the com¬ position. It is of course possible to provide a vaccine in which the various mimotopes are present in different or equal amounts. However, the mimotopes of the present invention may alternative¬ ly be administered to an individual in an amount of 0.1 ng to 10 mg, preferably 10 ng to 1 mg, in particular 100 ng to
300 yg/kg body weight. The amount of mimotopes that may be combined with the carri¬ er materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration. The dose of the composition may vary according to factors such as the disease state, age, sex and weight of the individual, and the ability of antibody to elicit a desired response in the in¬ dividual. Dosage regime may be adjusted to provide the optimum therapeutic response. For example, several divided doses may be administered daily or the dose may be proportionally reduced as indicated by the exigencies of the therapeutic situation. The dose of the vaccine may also be varied to provide optimum pre¬ ventative dose response depending upon the circumstances. For instance, the mimotopes and compositions of the present inven¬ tion may be administered to an individual at intervals of sever¬ al days, one or two weeks or even months or years depending al¬ ways on the level of antibodies induced by the administration of the composition of the present invention.
In a preferred embodiment of the present invention the com¬ position is applied between 2 and 10, preferably between 2 and 7, even more preferably up to 5 and most preferably up to 4 times. This number of immunizations may lead to a basic immun¬ isation. In a particularly preferred embodiment the time interval between the subsequent vaccinations is chosen to be between 2 weeks and 5 years, preferably between 1 month and up to 3 years, more preferably between 2 months and 1.5 years. An exem¬ plified vaccination schedule may comprise 3 to 4 initial vac¬ cinations over a period of 6 to 8 weeks and up to 6 months.
Thereafter the vaccination may be repeated every two to ten years. The repeated administration of the mimotopes of the pre¬ sent invention may maximize the final effect of a therapeutic vaccination .
According to a preferred embodiment of the present invention the at least one mimotope is formulated with at least one adju¬ vant .
"Adjuvants" are compounds or a mixture that enhance the im¬ mune response to an antigen (i.e. mimotope) . Adjuvants may act primarily as a delivery system, primarily as an immune modulator or have strong features of both. Suitable adjuvants include those suitable for use in mammals, including humans.
According to a particular preferred embodiment of the pre- sent invention the at least one adjuvant used in the composition as defined herein is capable to stimulate the innate immune sys¬ tem.
Innate immune responses are mediated by toll-like receptors (TLR's) at cell surfaces and by Nod-LRR proteins (NLR) intracel- lularly and are mediated by Dl and DO regions respectively. The innate immune response includes cytokine production in response to TLR activation and activation of Caspase-1 and IL-Ιβ secretion in response to certain NLRs (including Ipaf) . This response is independent of specific antigens, but can act as an adjuvant to an adaptive immune response that is antigen specific. The an¬ tigen may be supplied externally in the form of a vaccine or in¬ fection, or may be indigenous, for example, as is the case for tumor-associated antigens.
A number of different TLRs have been characterized. These TLRs bind and become activated by different ligands, which in turn are located on different organisms or structures. The de¬ velopment of immunopotentiator compounds that are capable of eliciting responses in specific TLRs is of interest in the art. For example, US 4,666,886 describes certain lipopeptide mole¬ cules that are TLR2 agonists. WO 2009/118296, WO 2008/005555, WO 2009/111337 and WO 2009/067081 each describe classes of small molecule agonists of TLR7. WO 2007/040840 and WO 2010/014913 de¬ scribe TLR7 and TLR8 agonists for treatment of diseases. These various compounds include small molecule immunopotentiators (SMIPs) .
The at least one adjuvant capable to stimulate the innate immune system preferably comprises or consists of a Toll-like receptor (TLR) agonist, preferably a TLR1, TLR2, TLR3, TLR4, TLR5, TLR7, TLR8 or TLR9 agonist, particularly preferred a TLR4 agonist .
Agonists of Toll-like receptors are well known in the art. For instance a TLR 2 agonist is Pam3CysSerLys4 , peptidoglycan (Ppg) , PamCys, a TLR3 agonist is IPH 31XX, a TLR4 agonist is an Aminoalkyl glucosaminide phosphate, E6020, CRX-527, CRX-601, CRX-675, 5D24.D4, RC-527, a TLR7 agonist is Imiquimod, 3M-003, Aldara, 852A, R850, R848, CL097, a TLR8 agonist is 3M-002, a TLR9 agonist is Flagellin, Vaxlmmune, CpG ODN (AVE0675,
HYB2093), CYT005-15 AllQbGlO, dSLIM.
According to a preferred embodiment of the present invention the TLR agonist is selected from the group consisting of mono- phosphoryl lipid A (MPL) , 3-de-O-acylated monophosphoryl lipid A (3D-MPL), poly I:C, GLA, flagellin, R848, imiquimod and CpG.
The composition of the present invention may comprise MPL. MPL may be synthetically produced MPL or MPL obtainable from natural sources. Of course it is also possible to add to the composition of the present invention chemically modified MPL. Examples of such MPL' s are known in the art.
According to a further preferred embodiment of the present invention the at least one adjuvant comprises or consists of a saponin, preferably QS21, a water in oil emulsion and a liposome .
The at least one adjuvant is preferably selected from the group consisting of MF59, AS01, AS02, AS03, AS04, aluminium hydroxide and aluminium phosphate.
Examples of known suitable delivery-system type adjuvants that can be used in humans include, but are not limited to, alum (e.g., aluminum phosphate, aluminum sulfate or aluminum hydrox¬ ide) , calcium phosphate, liposomes, oil-in-water emulsions such as MF59 (4.3% w/v squalene, 0.5% w/v polysorbate 80 (Tween 80), 0.5% w/v sorbitan trioleate (Span 85)), water-in-oil emulsions such as Montanide, and poly (D, L-lactide-co-glycolide) (PLG) mi- croparticles or nanoparticles .
Examples of known suitable immune modulatory type adjuvants that can be used in humans include, but are not limited to sapo¬ nins extracts from the bark of the Aquilla tree (QS21, Quil A), TLR4 agonists such as MPL (Monophosphoryl Lipid A), 3DMPL (3-0- deacylated MPL) or GLA-AQ, LT/CT mutants, cytokines such as the various interleukins (e.g., IL-2, IL-12) or GM-CSF, and the like .
Examples of known suitable immune modulatory type adjuvants with both delivery and immune modulatory features that can be used in humans include, but are not limited to ISCOMS (see, e.g., Sjolander et al . (1998) J. Leukocyte Biol. 64:713;
WO90/03184, W096/11711, WO 00/48630, W098/36772, WO00/41720, WO06/134423 and WO07/026, 190) or GLA-EM which is a combination of a Toll-like receptor agonists such as a TLR4 agonist and an oil-in-water emulsion.
Further exemplary adjuvants to enhance effectiveness of the mimotope compositions of the present invention include, but are not limited to: (1) oil-in-water emulsion formulations (with or without other specific immunostimulating agents such as muramyl peptides (see below) or bacterial cell wall components) , such as for example (a) SAF, containing 10% Squalane, 0.4% Tween 80, 5% pluronic-blocked polymer L121, and thr-MDP either microfluidized into a submicron emulsion or vortexed to generate a larger particle size emulsion, and (b) RIBI™ adjuvant system (RAS) , (Ribi Immunochem, Hamilton, Mont.) containing 2% Squalene, 0.2% Tween 80, and one or more bacterial cell wall components such as mono- phosphorylipid A (MPL) , trehalose dimycolate (TDM) , and cell wall skeleton (CWS) , preferably MPL+CWS (DETOX™); (2) saponin adjuvants, such as QS21, STIMULON™ (Cambridge Bioscience,
Worcester, Mass.), Abisco® (Isconova, Sweden), or Iscomatrix®
(Commonwealth Serum Laboratories, Australia) , may be used or particles generated therefrom such as ISCOMs (immunostimulating complexes) , which ISCOMS may be devoid of additional detergent e.g. WO00/07621; (3) Complete Freund's Adjuvant (CFA) and Incom¬ plete Freund's Adjuvant (IFA); (4) cytokines, such as interleu- kins (e.g. IL-1, IL-2, IL-4, IL-5, IL-6, IL-7, IL-12
(W099/44636) , etc.), interferons (e.g. gamma interferon), macro¬ phage colony stimulating factor (M-CSF) , tumor necrosis factor
(TNF) , etc.; (5) monophosphoryl lipid A (MPL) or 3-O-deacylated MPL (3dMPL) (see e.g., GB-2220221, EP-A-0689454 ) , optionally in the substantial absence of alum when used with pneumococcal sac¬ charides (see e.g. WO00/56358); (6) combinations of 3dMPL with, for example, QS21 and/or oil-in-water emulsions (see e.g. EP-A- 0835318, EP-A-0735898, EP-A-0761231 ) ; (7) a polyoxyethylene ether or a polyoxyethylene ester (see e.g. W099/52549); (8) a polyoxyethylene sorbitan ester surfactant in combination with an octoxynol (WO01/21207) or a polyoxyethylene alkyl ether or ester surfactant in combination with at least one additional non-ionic surfactant such as an octoxynol (WO01/21152) ; (9) a saponin and an immunostimulatory oligonucleotide (e.g. a CpG oligonucleo¬ tide) (WOO 0 / 62800 ) ; (10) an immunostimulant and a particle of metal salt (see e.g. WO00/23105); (11) a saponin and an oil-in- water emulsion e.g. W099/11241; (12) a saponin (e.g.
QS21) +3dMPL+IM2 (optionally+a sterol) e.g. W098/57659; (13) oth¬ er substances that act as immunostimulating agents to enhance the efficacy of the composition. Muramyl peptides include N- acetyl-muramyl-L-threonyl-D-isoglutamine (thr-MDP) , N-25 acetyl- normnuramyl-L-alanyl-D-isoglutamine (nor-MDP) , N-acetylmuramyl- L-alanyl-D-isoglutaminyl-L-alanine-2- (1 ' -2 ' -dipalmitoyl-sn- glycero-3-hydroxyphosphoryloxy) -ethylamine MTP-PE) , etc.
Particularly preferred compositions of the present invention comprise as adjuvant an oil-in-water emulsion with or without Toll-like receptor agonists, as well as liposomes and/or sapo- nin-containing adjuvants, with or without Toll-like receptor ag¬ onists. The composition of the present invention may also com¬ prise aluminium hydroxide with or without Toll-like receptor ag¬ onists as adjuvant.
According to a preferred embodiment of the present invention the epitope comprises or consists of the amino acid sequence KNEEGAP or DMPVDPDN.
Mimotopes of the aforementioned epitopes are known to the person skilled in the art (see e.g. WO 2009/103105, WO
2011/020133) .
The composition according to the present invention comprises preferably at least one mimotope comprising or consisting of the amino acid sequence
(Xl)n 2 3X 5GX6P (X7)m (Formula I), wherein
Xl is any amino acid residue,
X2 is an amino acid residue selected from the group consist¬ ing of lysine (K) , arginine (R) , alanine (A) and histidine (H) ,
X3 is an amino acid residue selected from the group consist¬ ing of asparagine (N) , glutamine (Q) , serine (S) , glycine (G) and alanine (A) , preferably asparagine (N) , serine (S) , glycine (G) and alanine (A) ,
X4 is an amino acid residue selected from the group consist¬ ing of glutamic acid (E) , aspartic acid (D) and alanine (A) , X5 is an amino acid residue selected from the group consist¬ ing of glutamic acid (E) and aspartic acid (D) ,
XQ is an amino acid residue selected from the group consist¬ ing of alanine (A) and tyrosine (Y) ,
X7 is any amino acid residue,
n and m, independently, are 0 or an integer of more than 0, wherein the amino acid sequence according to Formula I is not identical with, or does not comprise the 7-mer polypeptide fragment of alpha-synuclein having the amino acid sequence
KNEEGAP, and wherein
at least one mimotope comprising the amino acid sequence ac¬ cording to Formula I has a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence KNEEGAP.
The term "peptide having a binding capacity to an antibody which is specific for an epitope of alpha-synuclein" means that said peptide can be bound to alpha-synuclein specific antibody which has been produced by the administration of alpha-synuclein or fragments thereof to a mammal. Said peptide having said bind¬ ing capacity is able to induce the formation of alpha-synuclein specific antibodies in a mammal. The latter antibodies bind con¬ sequently to the compound of the present invention as well as to alpha-synuclein .
According to a particularly preferred embodiment of the pre¬ sent invention X2 is an amino acid residue selected from the group consisting of lysine (K) and arginine (R) and/or Xe is ala¬ nine (A) .
According to a preferred embodiment of the present invention the mimotope comprises or consists of an amino acid sequence se- lected from the group consisting of (Xl ) nKNDEGAP (X7 ) mr
(Xl) nANEEGAP (Xv) mr (Xl) nKAEEGAP (X7) mr (Xl) nKNAEGAP (X7) mr
(Xl) nRNEEGAP (Xv) mr (Xl) nHNEEGAP (X7) mr (Xl) nKNEDGAP (X7) mr
(Xl) nKQEEGAP (Xv) mr (Xl) nKSEEGAP (X7) mr (Xl) nKNDDGAP (X7) mr
(Xl) nRNDEGAP (Xv) mr (Xl) nRNEDGAP (X7) mr (Xl) nRQEEGAP (X7) mr
(Xl) nRSEEGAP (Xv) mr (Xl) nANDEGAP (X7) mr (Xl) nANEDGAP (X7) mr
(Xl) nHSEEGAP (Xv) mr (Xl) nASEEGAP (X7) mr (Xl) nHNEDGAP (X7) mr
(Xl) nHNDEGAP (Xv) mr (Xl) nRNAEGAP (X7) mr (Xl) nHNAEGAP (X7) mr
(Xl) nKSAEGAP (Xv) mr (Xl) nKSDEGAP (X7) mr (Xl) nKSEDGAP (X7) mr
(Xl) nRQDEGAP (Xv) mr (Xl) nRQEDGAP (X7) mr (Xl) nHSAEGAP (X7) mr
(Xl) nRSAEGAP (Xv) mr (Xl) nRSDEGAP (X7) mr (Xl) nRSEDGAP (X7) mr
(Xl) nHSDEGAP (Xv) mr (Xl) nHSEDGAP (X7) mr (Xl) nRQDDGAP (X7) m, preferably
(Xl) nKNDEGAP (X2) mr (Xl) nRNEEGAP (X2) mr (Xl) nRNDEGAP (X2) mr
(Xl) nKNAEGAP (X2) mr (Xl) nKSDEGAP (X2) mr (Xl) nRNAEGAP (X2) m or
(Xl) nRSEEGAP (X2) m ·
The composition according to the present invention comprises preferably at least one mimotope comprising or consisting of an amino acid sequence selected from the group consisting of
(Xi)nQASFAME (X7)m, (Xi ) nTASWKGE (X7 ) m, (Xx) nQASSKLD (X7) m,
(Xi ) nTPAWKGE (X7 ) m, (X!)nTPSWAGE (X7)m, (X1 ) nTPSWKGE (X7 ) m,
wherein
Xi is any amino acid residue,
X7 is any amino acid residue,
n and m, independently, are 0 or an integer of more than 0, said at least one mimotope having a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence KNEEGAP
for use in preventing and/or treating synucleinopathies .
According to a preferred embodiment of the present invention the at least one mimotope comprises the amino acid sequence
(Xl' ) n'X2'X3' P X 'X5'X6' (Xv )m' (Formula II), wherein
Xi' is any amino acid residue,
X2' is an amino acid residue selected from the group con¬ sisting of aspartic acid (D) and glutamic acid (E) , X3' is any amino acid residue,
X4' is any amino acid residue,
X5' is an amino acid residue selected from the group con¬ sisting of proline (P) and alanine (A) ,
Χβ' is an amino acid residue selected from the group con¬ sisting of aspartic acid (D) and glutamic acid (E) ,
Xv is any amino acid residue,
n' and m' , independently, are 0 or an integer of more than 0, wherein the amino acid sequence according to Formula II is not identical with, or does not comprise the 8-mer polypeptide fragment of alpha-synuclein having the amino acid sequence
DMPVDPDN, and wherein
the at least one mimotope comprising the amino acid sequence according to Formula II has a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence DMPVDPDN. According to a preferred embodiment of the present invention X3' is an amino acid residue selected from the group consisting of glutamine (Q) , serine (S) , threonine (T) , arginine (R) , as- paragine (N) , valine (V) , histidine (H) , methionine (M) , tyro¬ sine (Y) , alanine (A) and leucin (L) .
According to a particularly preferred embodiment of the pre¬ sent invention X4 * is an amino acid residue selected from the group consisting of glutamine (Q) , tryptophane (W) , threonine (T) , arginine (R) , aspartic acid(D), isoleucin (I), valine (V), histidine (H) , proline (P) , tyrosine (Y) , alanine (A) , serine (S) and leucin (L) .
The mimotope of the present invention which is part of the composition of the present invention has preferably an amino ac¬ id sequence selected from the group consisting of (C) DQPVLPD, (C)DMPVLPD, (C)DSPVLPD, (C) DSPVWAE, (C) DTPVLAE, (C) DQPVLPDN, (C)DMPVLPDN, (C) DSPVLPDN, (C) DQPVTAEN, (C) DSPVWAEN, (C) DTPVLAEN, (C)HDRPVTPD, (C)DRPVTPD, (C) DVPVLPD, (C) DTPVYPD, (C) DTPVIPD, (C) HDRPVTPDN, (C) DRPVTPDN, (C) DNPVHPEN, (C) DVPVLPDN,
(C)DTPVYPDN, (C)DTPVIPDN, (C) DQPVLPDG, (C) DMPVLPDG, (C) DSPVLPDG, (C)DSPVWAEG, (C)DRPVAPEG, (C)DHPVHPDS, (C) DMPVSPDR, (C) DSPVPPDD, (C)DQPVYPDI, (C)DRPVYPDI, (C) DHPVTPDR, (C)EYPVYPES, (C)DTPVLPDS, (C)DMPVTPDT, (C)DAPVTPDT, (C) DSPVVPDN, (C) DLPVTPDR, (C) DSPVHPDT, (C)DAPVRPDS, (C)DMPVWPDG, (C) DAPVYPDG, (C) DRPVQPDR,
(C) YDRPVQPDR, (C) DMPVDPEN, (C) DMPVDADN, DQPVLPD (C) , DMPVLPD (C) , (C)EMPVDPDN and (C)DNPVHPE.
According to a particularly preferred embodiment of the pre¬ sent invention n' and/or m' are 1 and Xi ' and/or X7 * are cysteine (C) .
According to a preferred embodiment of the present invention the mimotope comprises 7 to 30, preferably 7 to 20, more prefer¬ ably 7 to 16, most preferably 8 or 9, amino acid residues.
According to a preferred embodiment of the present invention the mimotope comprises or consists of an amino acid sequence se¬ lected from the group consisting of DQPVLPD, DSPVLPD, DVPVLPD, DSPVLPDG, YDRPVQPDR, DHPVHPDS, DAPVRPDS, KNDEGAP, KQEEGAP and KSEEGAP, in particular DQPVLPD and YDRPVQPDR. Of course, in order to facilitate coupling of these mimotopes to a carrier pro¬ tein as defined herein, the mimotopes may comprise at the C- and/or N-terminal end a cysteine residue.
According to a particularly preferred embodiment of the pre- sent invention the composition of the present invention comprises the following combinations of mimotopes and carriers and/or adjuvants (see Table A) .
Table A:
Mimotope sequences (SEQ) : A = DQPVLPD, B = DSPVLPD, C = DVPVLPD, D = DSPVLPDG, E = YDRPVQPDR, F = DHPVHPDS, G = DAPVRPDS, H = KNDEGAP, I = KQEEGAP, J = KSEEGAP (the mimotopes comprise either a C- or N-terminal cysteine residue for coupling them to the carrier molecule)
Carrier (CAR) : CI = CRM197, C2 = KLH
Adjuvant (ADJ) : Al = Alum, A2 = saponin based formulation, A3 = QS21 (pure) , A4 = squalene based formulation, A5 = Addavax (Sor- bitan trioleate (0.5% w/v) in squalene oil (5% v/v) - Tween 80 (0.5% w/v) in sodium citrate buffer (10 mM, pH 6.5)), A6 = MF59 (0.5% Polysorbate 80, 0.5% Sorbitan Triolate, 4.3% Squalene, wa¬ ter for injection, 10 mM Na-citrate buffer), A7 = AS03, A8 = AF03, A9 = monophosphoryl-lipid A (MPL) , A10 = MPLA (derivative of lipid A from Salmonella minnesota lipopolysaccharide) , All = synthetic MPL, All = synthetic MPL, A12 = A1+A3, A13 = A1+A5, A14 = A1+A9, A15 = A3+A9, A16 = A3+A4, A17 = A4+A9, A18 =
A3+A4+A9, A19 = A1+A3+A4, A20 = A1+A4+A9, A21 = A1+A3+A9, A22 = Ribi adjuvant system, A23 = QS21 (encapsulated) , A24 = CpG, A25 = A1+A23, A26 = A1+A24, A27 = A1+A2, A28 = A1+A9+A24, A29 = A1+A3+A24, A30 = A1+A23+A24, A31 = A4+A3, A32 = A4+A9, A33 = A4+A23, A34 = A4+A24, A35 = A4+A9+A24, A36 = A4+A3+A24, A37 = A4+A23+A24, A38 = A4+A3+A9, A39 = A4+A23+A9, A40 = A4+A3+A9+A24 , A41 = A4+A23+A9+A24, A42 = A9+A23, A43 = A1+A3+A9+A24 , A44 = A1+A9+A23+A24
No. SEQ CAR ADJ No. SEQ CAR ADJ No. SEQ CAR ADJ
1 A CI Al 294 D CI A30 587 G C2 A15
2 B CI Al 295 E CI A30 588 H C2 A15
3 C CI Al 296 F CI A30 589 I C2 A15
4 D CI Al 297 G CI A30 590 J C2 A15
5 E CI Al 298 H CI A30 591 A C2 A16 F CI Al 299 I CI A30 592 B C2 A16
G CI Al 300 J CI A30 593 C C2 A16
H CI Al 301 A CI A31 594 D C2 A16
I CI Al 302 B CI A31 595 E C2 A16
J CI Al 303 C CI A31 596 F C2 A16
A CI A2 304 D CI A31 597 G C2 A16
B CI A2 305 E CI A31 598 H C2 A16
C CI A2 306 F CI A31 599 I C2 A16
D CI A2 307 G CI A31 600 J C2 A16
E CI A2 308 H CI A31 601 A C2 A17
F CI A2 309 I CI A31 602 B C2 A17
G CI A2 310 J CI A31 603 C C2 A17
H CI A2 311 A CI A32 604 D C2 A17
I CI A2 312 B CI A32 605 E C2 A17
J CI A2 313 C CI A32 606 F C2 A17
A CI A3 314 D CI A32 607 G C2 A17
B CI A3 315 E CI A32 608 H C2 A17
C CI A3 316 F CI A32 609 I C2 A17
D CI A3 317 G CI A32 610 J C2 A17
E CI A3 318 H CI A32 611 A C2 A18
F CI A3 319 I CI A32 612 B C2 A18
G CI A3 320 J CI A32 613 C C2 A18
H CI A3 321 A CI A33 614 D C2 A18
I CI A3 322 B CI A33 615 E C2 A18
J CI A3 323 C CI A33 616 F C2 A18
A CI A4 324 D CI A33 617 G C2 A18
B CI A4 325 E CI A33 618 H C2 A18
C CI A4 326 F CI A33 619 I C2 A18
D CI A4 327 G CI A33 620 J C2 A18
E CI A4 328 H CI A33 621 A C2 A19
F CI A4 329 I CI A33 622 B C2 A19
G CI A4 330 J CI A33 623 C C2 A19
H CI A4 331 A CI A34 624 D C2 A19
I CI A4 332 B CI A34 625 E C2 A19
J CI A4 333 C CI A34 626 F C2 A19
A CI A5 334 D CI A34 627 G C2 A19
B CI A5 335 E CI A34 628 H C2 A19
C CI A5 336 F CI A34 629 I C2 A19 D CI A5 337 G CI A34 630 J C2 A19
E CI A5 338 H CI A34 631 A C2 A20
F CI A5 339 I CI A34 632 B C2 A20
G CI A5 340 J CI A34 633 C C2 A20
H CI A5 341 A CI A35 634 D C2 A20
I CI A5 342 B CI A35 635 E C2 A20
J CI A5 343 C CI A35 636 F C2 A20
A CI A6 344 D CI A35 637 G C2 A20
B CI A6 345 E CI A35 638 H C2 A20
C CI A6 346 F CI A35 639 I C2 A20
D CI A6 347 G CI A35 640 J C2 A20
E CI A6 348 H CI A35 641 A C2 A21
F CI A6 349 I CI A35 642 B C2 A21
G CI A6 350 J CI A35 643 C C2 A21
H CI A6 351 A CI A36 644 D C2 A21
I CI A6 352 B CI A36 645 E C2 A21
J CI A6 353 C CI A36 646 F C2 A21
A CI A7 354 D CI A36 647 G C2 A21
B CI A7 355 E CI A36 648 H C2 A21
C CI A7 356 F CI A36 649 I C2 A21
D CI A7 357 G CI A36 650 J C2 A21
E CI A7 358 H CI A36 651 A C2 A22
F CI A7 359 I CI A36 652 B C2 A22
G CI A7 360 J CI A36 653 C C2 A22
H CI A7 361 A CI A37 654 D C2 A22
I CI A7 362 B CI A37 655 E C2 A22
J CI A7 363 C CI A37 656 F C2 A22
A CI A8 364 D CI A37 657 G C2 A22
B CI A8 365 E CI A37 658 H C2 A22
C CI A8 366 F CI A37 659 I C2 A22
D CI A8 367 G CI A37 660 J C2 A22
E CI A8 368 H CI A37 661 A C2 A23
F CI A8 369 I CI A37 662 B C2 A23
G CI A8 370 J CI A37 663 C C2 A23
H CI A8 371 A CI A38 664 D C2 A23
I CI A8 372 B CI A38 665 E C2 A23
J CI A8 373 C CI A38 666 F C2 A23
A CI A9 374 D CI A38 667 G C2 A23 B CI A9 375 E CI A38 668 H C2 A23
C CI A9 376 F CI A38 669 I C2 A23
D CI A9 377 G CI A38 670 J C2 A23
E CI A9 378 H CI A38 671 A C2 A24
F CI A9 379 I CI A38 672 B C2 A24
G CI A9 380 J CI A38 673 C C2 A24
H CI A9 381 A CI A39 674 D C2 A24
I CI A9 382 B CI A39 675 E C2 A24
J CI A9 383 C CI A39 676 F C2 A24
A CI A10 384 D CI A39 677 G C2 A24
B CI A10 385 E CI A39 678 H C2 A24
C CI A10 386 F CI A39 679 I C2 A24
D CI A10 387 G CI A39 680 J C2 A24
E CI A10 388 H CI A39 681 A C2 A25
F CI A10 389 I CI A39 682 B C2 A25
G CI A10 390 J CI A39 683 C C2 A25
H CI A10 391 A CI A40 684 D C2 A25
I CI A10 392 B CI A40 685 E C2 A25
J CI A10 393 C CI A40 686 F C2 A25
A CI All 394 D CI A40 687 G C2 A25
B CI All 395 E CI A40 688 H C2 A25
C CI All 396 F CI A40 689 I C2 A25
D CI All 397 G CI A40 690 J C2 A25
E CI All 398 H CI A40 691 A C2 A26
F CI All 399 I CI A40 692 B C2 A26
G CI All 400 J CI A40 693 C C2 A26
H CI All 401 A CI A41 694 D C2 A26
I CI All 402 B CI A41 695 E C2 A26
J CI All 403 C CI A41 696 F C2 A26
A CI A12 404 D CI A41 697 G C2 A26
B CI A12 405 E CI A41 698 H C2 A26
C CI A12 406 F CI A41 699 I C2 A26
D CI A12 407 G CI A41 700 J C2 A26
E CI A12 408 H CI A41 701 A C2 A27
F CI A12 409 I CI A41 702 B C2 A27
G CI A12 410 J CI A41 703 C C2 A27
H CI A12 411 A CI A42 704 D C2 A27
I CI A12 412 B CI A42 705 E C2 A27 J CI A12 413 C CI A42 706 F C2 A27
A CI A13 414 D CI A42 707 G C2 A27
B CI A13 415 E CI A42 708 H C2 A27
C CI A13 416 F CI A42 709 I C2 A27
D CI A13 417 G CI A42 710 J C2 A27
E CI A13 418 H CI A42 711 A C2 A28
F CI A13 419 I CI A42 712 B C2 A28
G CI A13 420 J CI A42 713 C C2 A28
H CI A13 421 A CI A43 714 D C2 A28
I CI A13 422 B CI A43 715 E C2 A28
J CI A13 423 C CI A43 716 F C2 A28
A CI A14 424 D CI A43 717 G C2 A28
B CI A14 425 E CI A43 718 H C2 A28
C CI A14 426 F CI A43 719 I C2 A28
D CI A14 427 G CI A43 720 J C2 A28
E CI A14 428 H CI A43 721 A C2 A29
F CI A14 429 I CI A43 722 B C2 A29
G CI A14 430 J CI A43 723 C C2 A29
H CI A14 431 A CI A44 724 D C2 A29
I CI A14 432 B CI A44 725 E C2 A29
J CI A14 433 C CI A44 726 F C2 A29
A CI A15 434 D CI A44 727 G C2 A29
B CI A15 435 E CI A44 728 H C2 A29
C CI A15 436 F CI A44 729 I C2 A29
D CI A15 437 G CI A44 730 J C2 A29
E CI A15 438 H CI A44 731 A C2 A30
F CI A15 439 I CI A44 732 B C2 A30
G CI A15 440 J CI A44 733 C C2 A30
H CI A15 441 A C2 Al 734 D C2 A30
I CI A15 442 B C2 Al 735 E C2 A30
J CI A15 443 C C2 Al 736 F C2 A30
A CI A16 444 D C2 Al 737 G C2 A30
B CI A16 445 E C2 Al 738 H C2 A30
C CI A16 446 F C2 Al 739 I C2 A30
D CI A16 447 G C2 Al 740 J C2 A30
E CI A16 448 H C2 Al 741 A C2 A31
F CI A16 449 I C2 Al 742 B C2 A31
G CI A16 450 J C2 Al 743 C C2 A31 H CI A16 451 A C2 A2 744 D C2 A31
I CI A16 452 B C2 A2 745 E C2 A31
J CI A16 453 C C2 A2 746 F C2 A31
A CI A17 454 D C2 A2 747 G C2 A31
B CI A17 455 E C2 A2 748 H C2 A31
C CI A17 456 F C2 A2 749 I C2 A31
D CI A17 457 G C2 A2 750 J C2 A31
E CI A17 458 H C2 A2 751 A C2 A32
F CI A17 459 I C2 A2 752 B C2 A32
G CI A17 460 J C2 A2 753 C C2 A32
H CI A17 461 A C2 A3 754 D C2 A32
I CI A17 462 B C2 A3 755 E C2 A32
J CI A17 463 C C2 A3 756 F C2 A32
A CI A18 464 D C2 A3 757 G C2 A32
B CI A18 465 E C2 A3 758 H C2 A32
C CI A18 466 F C2 A3 759 I C2 A32
D CI A18 467 G C2 A3 760 J C2 A32
E CI A18 468 H C2 A3 761 A C2 A33
F CI A18 469 I C2 A3 762 B C2 A33
G CI A18 470 J C2 A3 763 C C2 A33
H CI A18 471 A C2 A4 764 D C2 A33
I CI A18 472 B C2 A4 765 E C2 A33
J CI A18 473 C C2 A4 766 F C2 A33
A CI A19 474 D C2 A4 767 G C2 A33
B CI A19 475 E C2 A4 768 H C2 A33
C CI A19 476 F C2 A4 769 I C2 A33
D CI A19 477 G C2 A4 770 J C2 A33
E CI A19 478 H C2 A4 771 A C2 A34
F CI A19 479 I C2 A4 772 B C2 A34
G CI A19 480 J C2 A4 773 C C2 A34
H CI A19 481 A C2 A5 774 D C2 A34
I CI A19 482 B C2 A5 775 E C2 A34
J CI A19 483 C C2 A5 776 F C2 A34
A CI A20 484 D C2 A5 777 G C2 A34
B CI A20 485 E C2 A5 778 H C2 A34
C CI A20 486 F C2 A5 779 I C2 A34
D CI A20 487 G C2 A5 780 J C2 A34
E CI A20 488 H C2 A5 781 A C2 A35 F CI A20 489 I C2 A5 782 B C2 A35
G CI A20 490 J C2 A5 783 C C2 A35
H CI A20 491 A C2 A6 784 D C2 A35
I CI A20 492 B C2 A6 785 E C2 A35
J CI A20 493 C C2 A6 786 F C2 A35
A CI A21 494 D C2 A6 787 G C2 A35
B CI A21 495 E C2 A6 788 H C2 A35
C CI A21 496 F C2 A6 789 I C2 A35
D CI A21 497 G C2 A6 790 J C2 A35
E CI A21 498 H C2 A6 791 A C2 A36
F CI A21 499 I C2 A6 792 B C2 A36
G CI A21 500 J C2 A6 793 C C2 A36
H CI A21 501 A C2 A7 794 D C2 A36
I CI A21 502 B C2 A7 795 E C2 A36
J CI A21 503 C C2 A7 796 F C2 A36
A CI A22 504 D C2 A7 797 G C2 A36
B CI A22 505 E C2 A7 798 H C2 A36
C CI A22 506 F C2 A7 799 I C2 A36
D CI A22 507 G C2 A7 800 J C2 A36
E CI A22 508 H C2 A7 801 A C2 A37
F CI A22 509 I C2 A7 802 B C2 A37
G CI A22 510 J C2 A7 803 C C2 A37
H CI A22 511 A C2 A8 804 D C2 A37
I CI A22 512 B C2 A8 805 E C2 A37
J CI A22 513 C C2 A8 806 F C2 A37
A CI A23 514 D C2 A8 807 G C2 A37
B CI A23 515 E C2 A8 808 H C2 A37
C CI A23 516 F C2 A8 809 I C2 A37
D CI A23 517 G C2 A8 810 J C2 A37
E CI A23 518 H C2 A8 811 A C2 A38
F CI A23 519 I C2 A8 812 B C2 A38
G CI A23 520 J C2 A8 813 C C2 A38
H CI A23 521 A C2 A9 814 D C2 A38
I CI A23 522 B C2 A9 815 E C2 A38
J CI A23 523 C C2 A9 816 F C2 A38
A CI A24 524 D C2 A9 817 G C2 A38
B CI A24 525 E C2 A9 818 H C2 A38
C CI A24 526 F C2 A9 819 I C2 A38 D CI A24 527 G C2 A9 820 J C2 A38
E CI A24 528 H C2 A9 821 A C2 A39
F CI A24 529 I C2 A9 822 B C2 A39
G CI A24 530 J C2 A9 823 C C2 A39
H CI A24 531 A C2 A10 824 D C2 A39
I CI A24 532 B C2 A10 825 E C2 A39
J CI A24 533 C C2 A10 826 F C2 A39
A CI A25 534 D C2 A10 827 G C2 A39
B CI A25 535 E C2 A10 828 H C2 A39
C CI A25 536 F C2 A10 829 I C2 A39
D CI A25 537 G C2 A10 830 J C2 A39
E CI A25 538 H C2 A10 831 A C2 A40
F CI A25 539 I C2 A10 832 B C2 A40
G CI A25 540 J C2 A10 833 C C2 A40
H CI A25 541 A C2 All 834 D C2 A40
I CI A25 542 B C2 All 835 E C2 A40
J CI A25 543 C C2 All 836 F C2 A40
A CI A26 544 D C2 All 837 G C2 A40
B CI A26 545 E C2 All 838 H C2 A40
C CI A26 546 F C2 All 839 I C2 A40
D CI A26 547 G C2 All 840 J C2 A40
E CI A26 548 H C2 All 841 A C2 A41
F CI A26 549 I C2 All 842 B C2 A41
G CI A26 550 J C2 All 843 C C2 A41
H CI A26 551 A C2 A12 844 D C2 A41
I CI A26 552 B C2 A12 845 E C2 A41
J CI A26 553 C C2 A12 846 F C2 A41
A CI A27 554 D C2 A12 847 G C2 A41
B CI A27 555 E C2 A12 848 H C2 A41
C CI A27 556 F C2 A12 849 I C2 A41
D CI A27 557 G C2 A12 850 J C2 A41
E CI A27 558 H C2 A12 851 A C2 A42
F CI A27 559 I C2 A12 852 B C2 A42
G CI A27 560 J C2 A12 853 C C2 A42
H CI A27 561 A C2 A13 854 D C2 A42
I CI A27 562 B C2 A13 855 E C2 A42
J CI A27 563 C C2 A13 856 F C2 A42
A CI A28 564 D C2 A13 857 G C2 A42 272 B CI A28 565 E C2 A13 858 H C2 A42
273 C CI A28 566 F C2 A13 859 I C2 A42
274 D CI A28 567 G C2 A13 860 J C2 A42
275 E CI A28 568 H C2 A13 861 A C2 A43
276 F CI A28 569 I C2 A13 862 B C2 A43
277 G CI A28 570 J C2 A13 863 C C2 A43
278 H CI A28 571 A C2 A14 864 D C2 A43
279 I CI A28 572 B C2 A14 865 E C2 A43
280 J CI A28 573 C C2 A14 866 F C2 A43
281 A CI A29 574 D C2 A14 867 G C2 A43
282 B CI A29 575 E C2 A14 868 H C2 A43
283 C CI A29 576 F C2 A14 869 I C2 A43
284 D CI A29 577 G C2 A14 870 J C2 A43
285 E CI A29 578 H C2 A14 871 A C2 A44
286 F CI A29 579 I C2 A14 872 B C2 A44
287 G CI A29 580 J C2 A14 873 C C2 A44
288 H CI A29 581 A C2 A15 874 D C2 A44
289 I CI A29 582 B C2 A15 875 E C2 A44
290 J CI A29 583 C C2 A15 876 F C2 A44
291 A CI A30 584 D C2 A15 877 G C2 A44
292 B CI A30 585 E C2 A15 878 H C2 A44
293 C CI A30 586 F C2 A15 879 I C2 A44
880 J C2 A44
Particularly preferred adjuvant compositions comprise Al, A4, A12 = A1+A3, A14 = A1+A9, A18 = A3+A4+A9, A21 = A1+A3+A9, A26 = A1+A24, A28 = A1+A9+A24, A29 = A1+A3+A24, A34 = A4+A24, A38 = A4+A3+A9 and A42 = A9+A23. These preferred adjuvant compo¬ sitions can be combined with the mimotopes of the present inven¬ tion to obtain a composition of the present invention.
The adjuvants mentioned in table A are well known in the art (see e.g. Reed SG, Trend Immunol 30(2008): 23-32).
According to a particularly preferred embodiment of the pre¬ sent invention the composition of the present invention comprises or consists of a combination of mimotopes, carriers and adju¬ vants selected from the group consisting of A-Cl-Al, A-C1-A3, A- C1-A4/A5/A6, A-C1-A9, A-C1-A12, A-C1-A14, A-C1-A16, A-C1-A17, A- C1-A18, A-C1-A21, A-C1-A26, E-C1-A1, E-C1-A3, E-Cl -A4 /A5 /A6 , E- C1-A9, E-C1-A12, E-C1-A14, E-C1-A16, E-C1-A17, E-C1-A18, E-Cl- A21, E-C1-A26, A-C2-A1, A-C2-A3, A-C2 -A4 /A5 /A6 , A-C2-A9, A-C2- A12, A-C2-A14, A-C2-A16, A-C2-A17, A-C2-A18, A-C2-A21, A-C2-A26, E-C2-A1, E-C2-A3, E-C2 -A4 /A5 /A6 , E-C2-A9, E-C2-A12, E-C2-A14, Ε- C2-A16, E-C2-A17, E-C2-A18, E-C2-A21 and E-C2-A26, preferably Α- Cl-Al, A-C1-A14, A-C1-A18 , A-C1-A26, E-C1-A1, E-C1-A14, E-C1-A18, E-C1-A26, A-C2-A1, A-C2-A14, A-C2 -Al 8 , A-C2 -A26 , E-C2-A1, E-C2- A14, E-C2-A18 and E-C2-A26 whereby the variables are defined as in Table A (see above) .
According to a particularly preferred embodiment of the pre¬ sent invention the synucleinopathy to be treated and/or prevented and/or ameliorated with the composition and/or compounds of the present invention is selected from the group consisting of Lewy Body Disorders (LBDs) , preferably Parkinson's Disease (PD) , Parkison's Disease with Dementia (PDD) and Dementia with Lewy Bodies (DLB) , as well as Multiple System Atrophy (MSA) or Neuro- degeneration with Brain Iron Accumulation type I (NBIA Type I), progressive supranuclear palsy (PSP) , frontotemporal dementia
(FTD) , Pick's disease (PiD) and cortico-basal degeneration
(CBD) .
According to a preferred embodiment of the present invention the motor symptoms of Parkinson's disease are selected from the group consisting of resting tremor, Bradykinesia, rigidity, pos¬ tural instability, stooped posture, dystonia, fatigue, impaired fine motor dexterity and motor coordination, impaired gross mo¬ tor coordination, poverty of movement (decreased arm swing) , akathisia, speech problems, loss of facial expression, mi- crographia, difficulty swallowing, sexual dysfunction and drool¬ ing .
A further aspect of the present invention relates to a meth¬ od for preventing and/or treating synucleinopathies as defined herein by administering to a subject in need thereof an appro¬ priate amount of a composition as defined in the claims.
The term "preventing", as used herein, covers measures not only to prevent the occurrence of disease, such as risk factor reduction, but also to arrest its progress and reduce its conse¬ quences once established.
As used herein, the term "treatment" or grammatical equiva¬ lents encompasses the improvement and/or reversal of the symp¬ toms of disease (e.g., neurodegenerative disease). A compound which causes an improvement in any parameter associated with disease when used in the screening methods of the instant inven¬ tion may thereby be identified as a therapeutic compound. The term "treatment" refers to both therapeutic treatment and prophylactic or preventative measures. For example, those who may benefit from treatment with compositions and methods of the present invention include those already with a disease and/or disorder (e.g., neurodegenerative disease, lack of or loss of cognitive function) as well as those in which a disease and/or disorder is to be prevented (e.g., using a prophylactic treat¬ ment of the present invention) .
The present invention is further defined in the following embodiments :
1. Composition comprising at least one mimotope of an epitope of alpha-synuclein for use in a method for preventing and/or treating synucleinopathies , wherein said at least one mimotope is coupled or fused to a pharmaceutically acceptable carrier protein selected from the group consisting of a nontoxic diphtheria toxin mutant, keyhole limpet hemocyanin (KLH) , diphtheria toxin (DT) , tetanus toxid (TT) and Haemophilus influ¬ enzae protein D (protein D) .
2. Composition according to embodiment 1, wherein the nontoxic diphtheria toxin mutant is selected from the group con¬ sisting of CRM 197, CRM 176, CRM 228, CRM 45, CRM 9, CRM 102, CRM 103 and CRM 107, in particular CRM 197.
3. Composition according to embodiment 1 or 2, wherein the at least one mimotope is formulated for subcutaneous, intrader¬ mal, transdermal or intramuscular administration.
4. Composition according to any one of embodiments 1 to 3, wherein the at least one mimotope is formulated with at least one adjuvant.
5. Composition according to embodiment 4, wherein at least one adjuvant is capable to stimulate the innate immune system.
6. Composition according to embodiment 5, wherein at least one adjuvant capable to stimulate the innate immune system com¬ prises or consists of a Toll-like receptor (TLR) agonist, pref¬ erably a TLR1, TLR2, TLR3, TLR4, TLR5, TLR7, TLR8 or TLR9 ago¬ nist, particularly preferred a TLR4 agonist.
7. Composition according to embodiment 6, wherein the TLR agonist is selected from the group consisting of monophosphoryl lipid A (MPL) , 3-de-O-acylated monophosphoryl lipid A (3D-MPL) , poly I:C, GLA, flagellin, R848, imiquimod and CpG.
8. Composition according to any one of embodiments 4 to 7, wherein the at least one adjuvant comprises or consists of a saponin, preferably QS21, a water in oil emulsion and a liposome .
9. Composition according to embodiment 4, wherein the at least one adjuvant is selected from the group consisting of
MF59, AS01, AS02, AS03, AS04, aluminium hydroxide and aluminium phosphate .
10. Composition according to any one of embodiments 1 to 9, wherein the epitope comprises the amino acid sequence KNEEGAP or DMPVDPDN.
11. Composition according to any one of embodiments 1 to 10, wherein the at least one mimotope comprises the amino acid se¬ quence
(Xl)n 2 3X 5GX6P (X7)m (Formula I), wherein
Xl is any amino acid residue,
X2 is an amino acid residue selected from the group consist¬ ing of lysine (K) , arginine (R) , alanine (A) and histidine (H) ,
X3 is an amino acid residue selected from the group consist¬ ing of asparagine (N) , glutamine (Q) , serine (S) , glycine (G) and alanine (A) , preferably asparagine (N) , serine (S) , glycine (G) and alanine (A) ,
X4 is an amino acid residue selected from the group consist¬ ing of glutamic acid (E) , aspartic acid (D) and alanine (A) , X5 is an amino acid residue selected from the group consist¬ ing of glutamic acid (E) and aspartic acid (D) ,
XQ is an amino acid residue selected from the group consist¬ ing of alanine (A) and tyrosine (Y) ,
X7 is any amino acid residue,
n and m, independently, are 0 or an integer of more than 0, wherein the amino acid sequence according to Formula I is not identical with, or does not comprise the 7-mer polypeptide fragment of alpha-synuclein having the amino acid sequence KNEEGAP, and wherein
the at least one mimotope comprising the amino acid sequence according to Formula I has a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence KNEEGAP .
12. Composition according to embodiment 11, wherein X2 is an amino acid residue selected from the group consisting of lysine (K) and arginine (R) and/or Xe is alanine (A) .
13. Composition according to embodiment 11 or 12, wherein the mimotope comprises an amino acid sequence selected from the group consisting of ( Xi ) nKNDEGAP (X7 ' mr (Xi) nANEEGAP (X7) m,
(Xl) nKAEEGAP (X7) mr (Xl nKNAEGAP (X7; mr (Xl ) nRNEEGAP (X7 mr
(Xl) nHNEEGAP (X7) mr (Xl nKNEDGAP (X7; mr (Xl ) nKQEEGAP (X7 mr
(Xl) nKSEEGAP (X7) mr (Xl nKNDDGAP (X7; mr (Xl ) nRNDEGAP (X7 mr
(Xl) nRNEDGAP (X7) mr (Xl nRQEEGAP (X7; mr (Xl ) nRSEEGAP (X7 mr
(Xl) nANDEGAP (X7; mr (Xl nANEDGAP (X7; mr (Xl ) nHSEEGAP (X7 mr
(Xl) nASEEGAP (X7; mr (Xl nHNEDGAP (X7; mr (Xl ) nHNDEGAP (X7 mr
(Xl) nRNAEGAP (X7; mr (Xl nHNAEGAP (X7; mr (Xl ) nKSAEGAP (X7 mr
(Xl) nKSDEGAP (X7; mr (Xl nKSEDGAP (X7; mr (Xl ) nRQDEGAP (X7 mr
(Xl) nRQEDGAP (X7; mr (Xl nHSAEGAP (X7; mr (Xl ) nRSAEGAP (X7 mr
(Xl) nRSDEGAP (X7; mr (Xl nRSEDGAP (X7; mr (Xl ) nHSDEGAP (X7 mr
(Xl) nHSEDGAP (X7; mr (Xl nRQDDGAP (X7; mr preferably (Xi) nKNDEGAP (X2
(Xl) nRNEEGAP (X2) mr (Xl nRNDEGAP (X2) mr (Xi ) nKNAEGAP (X2 mr
(Xl) nKSDEGAP (X2) mr (Xl nRNAEGAP (X2) m or (Xi ) nRSEEGAP (X2 ) m .
14. Composition according to any one of embodiments 1 to 13 comprising at least one mimotope comprising an amino acid se¬ quence selected from the group consisting of (Xi) nQASFAME (X7) m, (Xi) nTASWKGE (X7) m, (Xi) nQASSKLD (X7) m, (X1 ) nTPAWKGE (X7 ) m,
(Xi) nTPSWAGE (X7) m, (Xi) nTPSWKGE (X7) m,
wherein
Xi is any amino acid residue,
X7 is any amino acid residue,
n and m, independently, are 0 or an integer of more than 0, said at least one mimotope having a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence KNEEGAP
for use in preventing and/or treating synucleinopathies .
15. Composition according to any one of embodiments 1 to 14, wherein the at least one mimotope comprises the amino acid se¬ quence (Xl')n'X2'X3'PVX4'X5'X6' (X7')m' (Formula II) , wherein
Xi ' is any amino acid residue,
X2 ' is an amino acid residue selected from the group con¬ sisting of aspartic acid (D) and glutamic acid (E) ,
X3' is any amino acid residue,
X4 ' is any amino acid residue,
X5' is an amino acid residue selected from the group con¬ sisting of proline (P) and alanine (A) ,
Χβ ' is an amino acid residue selected from the group con¬ sisting of aspartic acid (D) and glutamic acid (E) ,
Xv is any amino acid residue,
n' and m' , independently, are 0 or an integer of more than 0, wherein the amino acid sequence according to Formula II is not identical with, or does not comprise the 8-mer polypeptide fragment of alpha-synuclein having the amino acid sequence
DMPVDPDN, and wherein
the at least one mimotope comprising the amino acid sequence according to Formula II has a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence DMPVDPDN.
16. Composition according to embodiment 15, wherein X3' is an amino acid residue selected from the group consisting of glu- tamine (Q) , serine (S) , threonine (T) , arginine (R) , asparagine (N) , valine (V) , histidine (H) , methionine (M) , tyrosine (Y) , alanine (A) and leucin (L) .
17. Composition according to embodiment 15 or 16, wherein X4 ' is an amino acid residue selected from the group consisting of glutamine (Q) , tryptophane (W) , threonine (T) , arginine (R) , aspartic acid(D), isoleucin (I), valine (V), histidine (H) , pro¬ line (P) , tyrosine (Y) , alanine (A) , serine (S) and leucin (L) .
18. Composition according to any one of embodiments 15 to 17, wherein the mimotope has an amino acid sequence selected from the group consisting of (C) DQPVLPD, (C) DMPVLPD, (C) DSPVLPD, (C)DSPVWAE, (C) DTPVLAE, (C) DQPVLPDN, (C) DMPVLPDN, (C) DSPVLPDN, (C) DQPVTAEN, (C) DSPVWAEN, (C) DTPVLAEN, (C) HDRPVTPD, (C) DRPVTPD, (C)DVPVLPD, (C)DTPVYPD, (C) DTPVIPD, (C) HDRPVTPDN, (C) DRPVTPDN, (C)DNPVHPEN, (C) DVPVLPDN, (C) DTPVYPDN, (C) DTPVIPDN, (C) DQPVLPDG, (C)DMPVLPDG, (C) DSPVLPDG, (C) DSPVWAEG, (C) DRPVAPEG, (C)DHPVHPDS, (C)DMPVSPDR, (C)DSPVPPDD, (C)DQPVYPDI, (C)DRPVYPDI, (C) DHPVTPDR, (C)EYPVYPES, (C)DTPVLPDS, (C) DMPVTPDT, (C) DAPVTPDT, (C) DSPVVPDN, (C)DLPVTPDR, (C)DSPVHPDT, (C)DAPVRPDS, (C) DMPVWPDG, (C) DAPVYPDG, (C)DRPVQPDR, (C) YDRPVQPDR, (C) DMPVDPEN, (C) DMPVDADN, DQPVLPD (C) , DMPVLPD(C), (C)EMPVDPDN and (C)DNPVHPE.
19. Composition according to any one of embodiments 11 to 17, characterised in that n' and/or m' are 1 and Xi ' and/or X7 * are cysteine (C) .
20. Composition according to any one of embodiments 11 to 19, wherein the mimotope comprises 7 to 30, preferably 7 to 20, more preferably 7 to 16, most preferably 8 or 9, amino acid res¬ idues .
21. Composition according to any one of embodiments 1 to 20, wherein the synucleinopathy is selected from the group consist¬ ing of Lewy Body Disorders (LBDs) , preferably Parkinson's Dis¬ ease (PD) , Parkison's Disease with Dementia (PDD) and Dementia with Lewy Bodies (DLB) , as well as Multiple System Atrophy (MSA) or Neurodegeneration with Brain Iron Accumulation type I (NBIA Type I), progressive supranuclear palsy (PSP) , frontotemporal dementia (FTD) , Pick's disease (PiD) and cortico-basal degenera¬ tion (CBD) .
22. Composition according to any one of embodiments 1 to 21, wherein the at least one mimotope is selected from the group of DQPVLPD, DSPVLPD, DVPVLPD, DSPVLPDG, YDRPVQPDR, DHPVHPDS,
DAPVRPDS, KNDEGAP, KQEEGAP and KSEEGAP, in particular DQPVLPD and YDRPVQPDR
23. Composition according to any one of embodiments 1 to 22 comprising a combination of at least one mimotope and carrier and/or adjuvant as defined in Table A, preferably A-C1-A1, A-Cl- A14, A-C1-A18, A-C1-A26, E-C1-A1, E-C1-A14, E-C1-A18, E-C1-A26, A-C2-A1, A-C2-A14, A-C2 -Al 8 , A-C2 -A26 , E-C2-A1, E-C2-A14, E-C2- A18 and E-C2-A26.
The present invention is further illustrated by the follow¬ ing figures and examples, however, without being restricted thereto .
Fig. 1 (A) shows higher injected peptide specific immunogen- icity promoted by alternative adjuvants containing TLR4, saponin or oil in water emulsion when adjuvants are combined with
DQPVLPD-CRM197 conjugate compared to adjuvants alone or alumini¬ um hydroxide combined with DQPVLPD-CRM197 conjugate.
Fig. 1 (B) shows higher injected peptide specific immunogen- icity promoted by alternative adjuvants containing TLR4 and also to a lesser degree saponin or oil in water emulsion when adjuvants are combined with YDRPVQPDR-CRMl 97 conjugate compared to adjuvants alone or aluminium hydroxide combined with YDRPVQPDR- CRM197 conjugate.
Fig. 1 (C) shows higher injected peptide specific immunogen- icity promoted by alternative adjuvants containing TLR4 but not oil in water emulsion or saponin when adjuvants are combined with KNDEGAP-CRM197 conjugate compared to adjuvants alone or al¬ uminium hydroxide combined with KNDEGAP-CRM197 conjugate
Fig. 2 (A) shows higher injected peptide specific Immunogen- icity promoted by alternative adjuvants containing oil in water emulsion and TLR4 or saponin when adjuvants are combined with DQPVLPD-KLH conjugate compared to adjuvants alone or aluminium hydroxide combined with DQPVLPD-KLH conjugate.
Figures 2 (B) and (D) show higher injected peptide specific Immunogenicity promoted by alternative adjuvants containing TLR4 or oil in water emulsion but not saponin when adjuvants are combined with YDRPVQPDR-KLH (B) and DHPVHPDS-KLH (D) conjugate compared to adjuvants alone or aluminium hydroxide combined with YDRPVQPDR-KLH and DHPVHPDS-KLH conjugate, respectively.
Fig. 2 (C) shows higher injected peptide specific Immunogen¬ icity promoted by alternative adjuvants containing TLR4 and to a lesser degree oil in water emulsion or saponin when adjuvants are combined with KNDEGAP-KLH conjugate compared to adjuvants alone or aluminium hydroxide combined with KNDEGAP-KLH conju¬ gate .
Fig. 3 (A) shows higher Monocyte/Macrophage activation based on MCP-1 cytokine levels promoted by alternative adjuvants con¬ taining saponin and to a lesser degree TLR4 or oil in water emulsion when adjuvants are combined with DQPVLPD-CRM197 conjugate compared to adjuvants alone or aluminium hydroxide combined with DQPVLPD-CRM197 conjugate. However it has to be noted that Quil-A alone already seems to promote monocyte/macrophage stimu¬ lation although on a rather low level. Fig. 3 (B) shows higher Monocyte/Macrophage activation based on MCP-1 cytokine levels promoted by alternative adjuvants con¬ taining saponin, oil in water emulsion or TLR4 when adjuvants are combined with YDRPVQPDR-CRMl 97 conjugate compared to adju¬ vants alone or aluminium hydroxide combined with YDRPVQPDR- CRM197 conjugate. However it has to be noted that Quil-A alone already seems to promote monocyte/macrophage stimulation alt¬ hough on a rather low level.
Fig. 3 (C) shows higher Monocyte/Macrophage activation based on MCP-1 cytokine levels promoted by alternative adjuvants con¬ taining saponin or oil in water emulsion or TLR4 when adjuvants are combined with KNDEGAP-CRM197 conjugate compared to adjuvants alone or aluminium hydroxide combined with KNDEGAP-CRM197 conjugate. Quil-A alone already seems to promote monocyte/macrophage stimulation although on a rather low level.
Fig. 3 (D) shows higher Monocyte/Macrophage activation based on MCP-1 cytokine levels promoted by alternative adjuvants con¬ taining saponin, TLR4 or oil in water emulsion when adjuvants are combined with DHPVHPDS-CRMl 97 conjugate compared to adju¬ vants alone or aluminium hydroxide combined with DHPVHPDS-CRMl 97 conjugate. Quil-A alone already seems to promote mono¬ cyte/macrophage stimulation although on a rather low level.
Fig. 4 (A) shows higher Monocyte/Macrophage activation based on MCP-1 cytokine levels promoted by alternative adjuvants con¬ taining TLR4, saponin or oil in water emulsion when adjuvants are combined with DQPVLPD-KLH conjugate compared to adjuvants alone or aluminium hydroxide combined with DQPVLPD-KLH conju¬ gate .
Figures 4 (B) and (D) show higher Monocyte/Macrophage acti¬ vation based on MCP-1 cytokine levels promoted by alternative adjuvants containing TLR4, oil in water emulsion or saponin when adjuvants are combined with YDRPVQPDR-KLH (B) and DHPVHPDS-KLH (D) conjugate compared to adjuvants alone or aluminium hydroxide combined with YDRPVQPDR-KLH and DHPVHPDS-KLH conjugate, respectively. Quil-A alone already seems to promote mono¬ cyte/macrophage stimulation
Fig. 4 (C) shows higher Monocyte/Macrophage activation based on MCP-1 cytokine levels promoted by alternative adjuvants con¬ taining oil in water emulsion or saponin but not TLR4 when adjuvants are combined with KNDEGAP-KLH conjugate compared to adju- vants alone or aluminium hydroxide combined with KNDEGAP-KLH conjugate. Quil-A alone already seems to promote mono¬ cyte/macrophage stimulation.
Figures 5 (A) and (B) show a comparison of different adju¬ vants combined with CRM197-conjugates (A) and KLH-conj ugates (B) in respect to their influence on the size of the monocyte frac¬ tion in peripheral blood. Monocyte percentage in all samples is within physiological range, although QuilA shows a trend to de¬ crease the number of monocytes alone as well as in combination with all mimotope-conj ugates tested. Absolute variances reflect assay variability.
Figures 6 (A) and (D) show a synergistic effect of alterna¬ tive adjuvants combined with KNDEGAP-CRM197 (A) and DHPVHPDS-KLH (D) on in vivo Αβ uptake in peripheral blood monocytes when com¬ pared to aluminium hydroxide combined with KNDEGAP-CRM197 and DHPVHPDS-KLH conjugate, respectively.
Fig. 6 (B) shows a synergistic effect of TLR4 or oil in wa¬ ter emulsion adjuvants but not of saponin combined with
DHPVHPDS-CRMl 97 on in vivo Αβ uptake in peripheral blood mono¬ cytes when compared to aluminium hydroxide combined with
DHPVHPDS-CRMl 97 conjugate.
Fig. 6 (C) shows a synergistic effect of TLR4 but not oil in water emulsion or saponin combined with KNDEGAP-KLH on in vivo Αβ uptake in peripheral blood monocytes when compared to alumin¬ ium hydroxide combined with KNDEGAP-KLH conjugate.
EXAMPLES :
Material and Methods:
In vivo characterisation of mimotope-vaccine candidates : Conjugate production:
Mimotope peptides were coupled to the carrier CRM-197 or KLH by using the heterobifunctional crosslinking agent GMBS. Brief¬ ly, CRM-197/KLH was mixed with an excess of GMBS at room temperature to allow for activation, followed by removal of excess GMBS by dialysis. Excess mimotope peptide was then added to the activated carrier. The mimotope CRM-197/KLH conjugate was used for vaccine formulation.
Vaccines were formulated with different adjuvants and ap¬ plied to animals. Identical amounts of conjugated mimotope pep¬ tide (s) were injected per mouse when the CRM-197/KLH vaccines were compared to other vaccines or when different adjuvants were compared .
Animal experiments :
Female BALB/c mice, 6 mice per group, were immunized with mimotope-CRM-197/KLH conjugates using different adjuvants. Con¬ trol groups were immunized with CRM-197/KLH plus respective ad¬ juvants and/or PBS and/or adjuvants alone.
Animals were vaccinated 3 times in regular intervals (2 week interval) and plasma samples were taken regularly as well (one day before vaccination) .
Example 1: Effect of mimotope-CRM197 conjugates using different adjuvant systems : Immunogenicity (Fig. 1)
In several parallel experiments, female BALB/c mice are im¬ munized repeatedly with identical amounts of AFFITOPE peptides (the mimotopes disclosed herein) , comprising preferably a C or N-terminal cysteine residue, coupled to CRM-197 (10yg peptide per immunisation) . Different formulations using the same AFFI¬ TOPE conjugate are compared to suitable control groups (e.g.: PBS alone or adjuvant alone or CRM197 plus adjuvant)
The following peptide-conj ugates or combinations of conju¬ gates are used:
• DQPVLPD coupled to CRM197
• YDRPVQPDR coupled to CRM197
• DHPVHPDS coupled to CRM197
• KNDEGAP coupled to CRM197
Adjuvants used in this example are:
Aluminium hydroxide, Aluminium hydroxide and the TLR agonist MPLA, squalene-based, oil in water emulsion (=Addavax) , Saponin containing adjuvants (=QuilA) .
The in vitro ELISA assay to determine the antibody titer following immunisation is performed with plasma of single mice (see method description below) .
Peptide ELISA:
In order to perform ELISAs for detecting the immune responses in vaccinated animals, peripheral blood was drawn from mice using heparin as anticoagulant and plasma was prepared from these samples. The diluted plasma was then used for ELISA analy¬ sis. For this purpose, the wells of the ELISA plates (Nunc Max- isorb) were coated with peptide-BSA conjugates. Subsequently, diluted plasma was added and the detection of peptide specific antibodies was performed with biotinylated anti-mouse IgG
(Southern Biotech) and subsequent colour reaction using Strep- tavidin-POD (Roche) and ABTS.
Example 2: Effect of mimotope-KLH conjugates using different adjuvant systems : Immunogenicity (Fig. 2)
In several parallel experiments, female BALB/c mice are im¬ munized repeatedly with identical amounts of mimotope peptides coupled to KLH (e.g. 10yg peptide per immunisation) . Different formulations using the same mimotope conjugate are compared to suitable control groups (e.g.: PBS alone or adjuvant alone or KLH plus adjuvant)
The following peptide-conj ugates or combinations of conju¬ gates are used:
• DQPVLPD coupled to KLH
• YDRPVQPDR coupled to KLH
• DHPVHPDS coupled to KLH
• KNDEGAP coupled to KLH
Adjuvants used in this example are (as in example 1) :
Aluminium hydroxide, Aluminium hydroxide and MPLA, Addavax and QuilA.
The in vitro ELISA assay to determine the antibody titer following immunisation is performed with plasma of single mice (see method description as in example 1) .
Example 3: Effect of mimotope-CRM197 conjugates using different adjuvant systems: effect on peripheral monocyte/macrophage (Fig. 3)
In order to analyse whether mimotope-CRMl 97 adjuvanted with the different adjuvants described before, is able to change the cytokine milieu and thus influence peripheral mono¬ cyte/macrophage activation, the levels of Cytokines/Chemokines known to activate monocytes/macrophages or indicating mono¬ cyte/macrophage activation (e.g. CCL2/MCP1 etc.) were deter¬ mined. Cytokine/Chemokine levels are determined in plasma from treated animals 2 hours after injection of the different vac¬ cines .
Cytokine determination: To determine the concentration of cytokines in the circula¬ tion of vaccinated animals, blood was collected from animals 2 hours after injection of vaccines. Subsequently, plasma was pre¬ pared from blood samples and cytokine concentration in individu¬ al samples was defined using the FlowCytomix bead array system (eBioscience) and flow cytometric analysis .
Example 4 : Effect of mimotope-KLH conjugates using different adjuvant systems: effect on peripheral monocyte/macrophage
(Fig. 4)
In order to analyse whether mimotope-CRMl 97 adjuvanted with the different adjuvants described before, is able to change the cytokine milieu and thus influence peripheral mono¬ cyte/macrophage activation, the levels of Cytokines/Chemokines known to activate monocytes/macrophages or indicating mono¬ cyte/macrophage activation (e.g. CCL2/MCP1 etc.) were deter¬ mined. Cytokine/Chemokine levels are determined in plasma from treated animals 2 hours after injection of the different vac¬ cines (for details see method in example 3) .
Example 5: Effect of immunotherapy on monocytes and monocytic alpha synuclein uptake (Fig. 5)
The ability of the novel vaccine formulations to alter pe¬ ripheral CDllb+ monocyte numbers as well as to change monocytic alpha Synuclein uptake in vivo is also assessed.
As described previously, monocytes are considered the pe¬ ripheral blood precursor cells of brain microglia (Rezaie, P. , et al 1999. Dev . Brain Res . 115.-71-81 ; Mildner et al Nat
Neurosci. 2007 Dec; 10 (12) : 1544-53) . Markers such as CDllb and Ly6C are immunologicals markers that are present on such periph¬ eral blood monocytes and persist when these cells are infiltrat¬ ing the brain (Mildner et al . , 2007, Lebson L, et al . J Neurosci. 2010 Jul 21; 30 (29) : 9651-8) .
To investigate whether TLR agonist containing adjuvants or components thereof are contributing to changing the number of monocytes in the peripheral blood, a comparative analysis of the conjugate-formulations mentioned before is performed.
This result is again demonstrating a synergistic effect of AFFITOPE-vaccine induced immune responses (antibodies) with a TLR agonists used in the adjuvant.
Flow cytometry analysis :
Peripheral blood was drawn from mice with K2-EDTA as antico- agulant, 24-Hour after last injection of the vaccines and anti¬ bodies, respectively. Red blood cell lysis was performed on in¬ dividual animal samples using BD Pharm Lyse™ (BD Pharmingen) . Remaining peripheral blood cells were incubated with Rat anti- Mouse CD16/CD32 (BD Fc Block™ by BD Biosciences) and cells were further incubated with a combination of directly conjugated an¬ tibodies as described by Mildner et al . , 2007 or similar anti¬ bodies: PE-conj ugated Hamster anti-Mouse CD3, Rat anti-Mouse CD45R/B220, Rat anti-Mouse Ly-6G, Mouse anti-Mouse NK1.1; APC- conjugated Rat anti-Mouse CDllb; PE-Cy7-conjugated Hamster anti- Mouse CDllc, FITC- Rat Anti-Mouse Ly-6C and a suitable Rat anti- Mouse CD62L . (BD Biosciences)
Samples were acquired on a flow cytometer (BD FACSCanto II) and data were analyzed with the FACSDiva software (BD Bioscienc¬ es) including the automated compensation protocol for the used fluorescence channels.
Monocytes were identified by their Forward/Side scatter properties and gated as CD3-/CD45R/B220-/Ly-6G-/NK1.1- (Lineage- )/CDllb+ cells. CDllb+ monocyte frequency was reported as a per¬ centage of the total cells (excluding debris) .
Alpha Synuclein uptake assay (Fig. 6) :
To examine the function of monocytes in the peripheral blood, the capacity of those monocytes to uptake recombinant hu¬ man alpha synuclein was examined. In order to measure the phago¬ cytic activity, fluorescent recombinant human alpha-synuclein ( 1- 140; HiLyte Fluor™488 labeled, Anaspec Inc.) was used.
For that analysis mice were injected with HiLyte Fluor™488 labeled alpha-synuclein and blood was withdrawn 2h after injection. Samples for alpha synuclein uptake determination were acquired on a flow cytometer (BD FACSCanto II) and data analyzed with the FACSDiva software (BD Biosciences) .
Monocytes were identified by their Side/Forward scatter properties, excluding debris and gated as CD3-/CD45R/B220-/Ly- 6G-/NK1.1- (Lineage-) /CDllb+ cells. Alpha synuclein uptake was assessed by reporting the percentage of HiLyte fluor™ 488 alpha synuclein positive cells among gated monocytes.

Claims

Claims :
1. Composition comprising at least one mimotope of an epitope of alpha-synuclein for use in a method for preventing and/or treating synucleinopathies , wherein said at least one mimotope is coupled or fused to a pharmaceutically acceptable carrier pro¬ tein selected from the group consisting of a non-toxic diphthe¬ ria toxin mutant, keyhole limpet hemocyanin (KLH) , diphtheria toxin (DT) , tetanus toxid (TT) and Haemophilus influenzae pro¬ tein D (protein D) .
2. Composition according to claim 1, wherein the non-toxic diphtheria toxin mutant is selected from the group consisting of CRM 197, CRM 176, CRM 228, CRM 45, CRM 9, CRM 102, CRM 103 and CRM 107, in particular CRM 197.
3. Composition according to claim 1 or 2, wherein the at least one mimotope is formulated with at least one adjuvant.
4. Composition according to claim 3, wherein at least one adjuvant is capable to stimulate the innate immune system.
5. Composition according to claim 4, wherein at least one adjuvant capable to stimulate the innate immune system comprises or consists of a Toll-like receptor (TLR) agonist, preferably a TLR1, TLR2, TLR3, TLR4, TLR5, TLR7, TLR8 or TLR9 agonist, par¬ ticularly preferred a TLR4 agonist.
6. Composition according to claim 5, wherein the TLR agonist is selected from the group consisting of monophosphoryl lipid A (MPL) , 3-de-O-acylated monophosphoryl lipid A (3D-MPL) , poly I:C, GLA, flagellin, R848, imiquimod and CpG.
7. Composition according to any one of claims 3 to 6, wherein the at least one adjuvant comprises or consists of a saponin, preferably QS21, a water in oil emulsion and a liposome.
8. Composition according to claim 3, wherein the at least one adjuvant is selected from the group consisting of MF59, AS01, AS02, AS03, AS04, aluminium hydroxide and aluminium phosphate.
9. Composition according to any one of claims 1 to 8, wherein the epitope comprises the amino acid sequence KNEEGAP or
DMPVDPDN.
10. Composition according to any one of claims 1 to 9, wherein the at least one mimotope comprises the amino acid sequence
(Xl)n 2 3X 5GX6P (X7)m (Formula I), wherein
Xl is any amino acid residue,
X2 is an amino acid residue selected from the group consist¬ ing of lysine (K) , arginine (R) , alanine (A) and histidine (H) ,
X3 is an amino acid residue selected from the group consist¬ ing of asparagine (N) , glutamine (Q) , serine (S) , glycine (G) and alanine (A) , preferably asparagine (N) , serine (S) , glycine (G) and alanine (A) ,
X4 is an amino acid residue selected from the group consist¬ ing of glutamic acid (E) , aspartic acid (D) and alanine (A) , X5 is an amino acid residue selected from the group consist¬ ing of glutamic acid (E) and aspartic acid (D) ,
XQ is an amino acid residue selected from the group consist¬ ing of alanine (A) and tyrosine (Y) ,
X7 is any amino acid residue,
n and m, independently, are 0 or an integer of more than 0, wherein the amino acid sequence according to Formula I is not identical with, or does not comprise the 7-mer polypeptide fragment of alpha-synuclein having the amino acid sequence
KNEEGAP, and wherein
the at least one mimotope comprising the amino acid sequence according to Formula I has a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence KNEEGAP.
11. Composition according to claim 10, wherein the mimotope comprises an amino acid sequence selected from the group consisting of (Xi ) nKNDEGAP (X7)m, (Xi) nANEEGAP (X7) mr (Xi)nKAEEGAP (X7)m,
(Xl nKNAEGAP (X7; mr (Xl nRNEEGAP (X7 mr (Xl nHNEEGAP (X7 mr
(Xl nKNEDGAP (X7; mr (Xl nKQEEGAP (X7 mr (Xl nKSEEGAP (X7 mr
(Xl nKNDDGAP (X7; mr (Xl nRNDEGAP (X7 mr (Xl nRNEDGAP (X7 mr
(Xl nRQEEGAP (X7; mr (Xl nRSEEGAP (X7 mr (Xl nANDEGAP (X7 mr
(Xl nANEDGAP (X7; mr (Xl nHSEEGAP (X7 mr (Xl nASEEGAP (X7 mr
(Xl nHNEDGAP (X7; mr (Xl nHNDEGAP (X7 mr (Xl nRNAEGAP (X7 mr
(Xl nHNAEGAP (X7; mr (Xl nKSAEGAP (X7 mr (Xl nKSDEGAP (X7 mr
(Xl nKSEDGAP (X7; mr (Xl nRQDEGAP (X7 mr (Xl nRQEDGAP (X7 mr
(Xl nHSAEGAP (X7; mr (Xl nRSAEGAP (X7 mr (Xl nRSDEGAP (X7 mr
(Xl nRSEDGAP (X7; mr (Xl nHSDEGAP (X7 mr (Xl nHSEDGAP (X7 mr
(Xl nRQDDGAP (X7; mr preferably (Xi) nKNDEGAP (X2)m, (X^ nRNEEGAP (X2)m,
(Xl nRNDEGAP (X2; mr (Xi nKNAEGAP (X2 mr (Xl nKSDEGAP (X2 mr
(Xl nRNAEGAP (X2; m or (X!)nRSEEGAP (X2)m
12. Composition according to any one of claims 1 to 11 compris¬ ing at least one mimotope comprising an amino acid sequence se¬ lected from the group consisting of (Xi) nQASFAME (X7) m,
(Xi ) nTASWKGE (X7 ) m, (Xi) nQASSKLD (X7) m, (X1 ) nTPAWKGE (X7 ) m,
(Xi)nTPSWAGE (X7)m, (X!)nTPSWKGE (X7)m,
wherein
Xi is any amino acid residue,
X7 is any amino acid residue,
n and m, independently, are 0 or an integer of more than 0, said at least one mimotope having a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence KNEEGAP
for use in preventing and/or treating synucleinopathies.
13. Composition according to any one of claims 1 to 12, wherein the at least one mimotope comprises the amino acid sequence
(Xl' ) n'X2'X3' P X 'X5'X6' ( v )m' (Formula II), wherein
Xi' is any amino acid residue,
X2' is an amino acid residue selected from the group con¬ sisting of aspartic acid (D) and glutamic acid (E) ,
X3' is any amino acid residue, Χ4 ' is any amino acid residue,
X5 ' is an amino acid residue selected from the group con¬ sisting of proline (P) and alanine (A) ,
Χβ ' is an amino acid residue selected from the group con¬ sisting of aspartic acid (D) and glutamic acid (E) ,
Xv is any amino acid residue,
n' and m' , independently, are 0 or an integer of more than 0, wherein the amino acid sequence according to Formula II is not identical with, or does not comprise the 8-mer polypeptide fragment of alpha-synuclein having the amino acid sequence
DMPVDPDN, and wherein
the at least one mimotope comprising the amino acid sequence according to Formula II has a binding capacity to an antibody which is specific for an epitope of alpha-synuclein comprising the amino acid sequence DMPVDPDN.
14. . Composition according to claim 3, wherein the mimotope has an amino acid sequence selected from the group consisting of
(C) DQPVLPD, (C)DMPVLPD, (C ) DS PVLPD, (C )DSPVWAE, (C) DTPVLAE,
(C) DQPVLPDN, (C) DMPVLPDN, (C) DSPVLPDN, (C) DQPVTAEN, (C) DSPVWAEN,
(C) DTPVLAEN, (C) HDRPVTPD, (C) DRPVTPD, (C)DVPVLPD, ( C) DTPVYPD,
(C) DTPVIPD, (C) HDRPVTPDN, (C) DRPVTPDN, (C) DNPVHPEN, (C) DVPVLPDN,
(C) DTPVYPDN, (C) DTPVIPDN, (C) DQPVLPDG, (C) DMPVLPDG, (C) DSPVLPDG,
(C) DSPVWAEG, (C) DRPVAPEG, (C) DHPVHPDS, (C) DMPVSPDR, (C) DSPVPPDD,
(C) DQPVYPDI, (C) DRPVYPDI, (C) DHPVTPDR, (C) EYPVYPES, (C) DTPVLPDS,
(C) DMPVTPDT, (C) DAPVTPDT, (C) DSPVVPDN, (C) DLPVTPDR, (C) DSPVHPDT,
(C) DAPVRPDS, (C) DMPVWPDG, (C) DAPVYPDG, (C) DRPVQPDR,
(C) YDRPVQPDR, (C) DMPVDPEN, (C :) DMPVDADN , DQPVLPD (C), DMPVLPD (C) ,
(C) EMPVDPDN and (C)DNPVHPE
15. Composition according to any one of claims 10 to 14, charac- terised in that n' and/or m' are 1 and Xi ' and/or X7 * are cysteine (C) .
16. Composition according to any one of claims 1 to 15, wherein the at least one mimotope is selected from the group of DQPVLPD, DSPVLPD, DVPVLPD, DSPVLPDG, YDRPVQPDR, DHPVHPDS, DAPVRPDS,
KNDEGAP, KQEEGAP and KSEEGAP, in particular DQPVLPD and Ġ YDRPVQPDR.
PCT/EP2013/059025 2012-05-01 2013-04-30 Compositions WO2013164355A1 (en)

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