US20190175748A1 - Combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a tlr peptide agonist for use in medicine - Google Patents

Combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a tlr peptide agonist for use in medicine Download PDF

Info

Publication number
US20190175748A1
US20190175748A1 US16/084,170 US201716084170A US2019175748A1 US 20190175748 A1 US20190175748 A1 US 20190175748A1 US 201716084170 A US201716084170 A US 201716084170A US 2019175748 A1 US2019175748 A1 US 2019175748A1
Authority
US
United States
Prior art keywords
peptide
complex
antigen
immune checkpoint
cell penetrating
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US16/084,170
Other languages
English (en)
Inventor
Madiha Derouazi
Elodie BELNOUE
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Amal Therapeutics SA
Original Assignee
Amal Therapeutics SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from PCT/EP2016/000472 external-priority patent/WO2016146261A1/en
Application filed by Amal Therapeutics SA filed Critical Amal Therapeutics SA
Assigned to AMAL THERAPEUTICS SA reassignment AMAL THERAPEUTICS SA ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: DEROUAZI, Madiha
Publication of US20190175748A1 publication Critical patent/US20190175748A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
    • A61K47/66—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid the modifying agent being a pre-targeting system involving a peptide or protein for targeting specific cells
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/18—Growth factors; Growth regulators
    • 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
    • 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
    • A61K39/0011—Cancer 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
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
    • 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
    • A61K39/46—Cellular immunotherapy
    • A61K39/464—Cellular immunotherapy characterised by the antigen targeted or presented
    • A61K39/4643—Vertebrate antigens
    • A61K39/4644—Cancer antigens
    • A61K39/464402—Receptors, cell surface antigens or cell surface determinants
    • A61K39/464416—Receptors for cytokines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/42—Proteins; Polypeptides; Degradation products thereof; Derivatives thereof, e.g. albumin, gelatin or zein
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
    • A61K47/64—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
    • A61K47/64—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
    • A61K47/642—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent the peptide or protein in the drug conjugate being a cytokine, e.g. IL2, chemokine, growth factors or interferons being the inactive part of the conjugate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
    • A61K47/64—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
    • A61K47/6425—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent the peptide or protein in the drug conjugate being a receptor, e.g. CD4, a cell surface antigen, i.e. not a peptide ligand targeting the antigen, or a cell surface determinant, i.e. a part of the surface of a cell
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • 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
    • C07K14/475—Growth factors; Growth regulators
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
    • C07K16/2818—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against CD28 or CD152
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2863—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for growth factors, growth regulators
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2878—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the NGF-receptor/TNF-receptor superfamily, e.g. CD27, CD30, CD40, CD95
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K19/00—Hybrid peptides, i.e. peptides covalently bound to nucleic acids, or non-covalently bound protein-protein complexes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2/00—Peptides of undefined number of amino acids; Derivatives thereof
    • 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
    • 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
    • C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/62—DNA sequences coding for fusion proteins
    • C12N15/625—DNA sequences coding for fusion proteins containing a sequence coding for a signal sequence
    • 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
    • A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
    • 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
    • A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
    • A61K2039/507—Comprising a combination of two or more separate antibodies
    • 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
    • A61K2039/545—Medicinal preparations containing antigens or antibodies characterised by the dose, timing or administration schedule
    • 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
    • A61K2039/55516—Proteins; Peptides
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/75—Agonist effect on antigen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/01—Fusion polypeptide containing a localisation/targetting motif
    • C07K2319/10—Fusion polypeptide containing a localisation/targetting motif containing a tag for extracellular membrane crossing, e.g. TAT or VP22
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/40—Fusion polypeptide containing a tag for immunodetection, or an epitope for immunisation

Definitions

  • the present invention relates to the field of vaccination, in particular to cancer vaccines.
  • the immune system can recognize and to some extent eliminate tumor cells, however, this anti-tumor response is often of low amplitude and inefficient. Boosting this weak anti-tumor response with therapeutic vaccination has been a long sought goal for cancer therapy. Modulating the immune system to enhance immune responses has thus become a promising therapeutic approach in oncology as it can be combined with standard of care treatments.
  • CTLs cytotoxic T lymphocytes
  • cancer vaccines showed very limited clinical efficacy so far. Indeed, at the end of 2011, amongst the 300 hundred ongoing cancer vaccine clinical trials, only 19 phase III trials were reported ( globaldata, 2012). Amongst them, there are NeuVax, a peptide vaccine for breast cancer, Stimuvax, a liposome based vaccine for Non-Small Cell Lung Carcinoma (NSCLC) and breast cancer, TG4010, a vaccinia-based vaccine for NSCLC and GSK1572932A, an adjuvanted liposome for NSCLC. These four cancer vaccines are based on different technologies and have in common that they are targeting one single antigen.
  • Therapeutic cancer vaccines can be divided into two principal categories: personalized (autologous) and standardized vaccines, and further classified depending on the technology platform.
  • Current personalized vaccines include tumor lysate vaccines as well as dendritic cells based vaccine (hereinafter cell based).
  • cell based dendritic cells based vaccine
  • antigen loading can occur either with a pulse using tumor lysates, or transfection with RNA extracted from the tumors.
  • the antigens are tumor specific or associated, but are not clearly defined.
  • Dendritic cells can also be loaded with defined antigens either with peptide pulse or using a protein such as the Prostatic Acid Phosphatase (PAP) used to engineer the Provenge® vaccine.
  • PAP Prostatic Acid Phosphatase
  • subunits vaccines protein or peptides
  • APCs cell-based therapy
  • T cells T cells
  • CARs CARs
  • lysates subunits vaccines
  • subunits vaccines protein or peptides
  • the antigens are fully defined allowing for better immune-monitoring and reducing the risk of unwanted effects of vaccine component.
  • a therapeutic cancer vaccine is administrated to cancer patients to strengthen the capability of their immune system to recognize and kill the tumor cells.
  • the main goal of a therapeutic cancer vaccine is to generate killer T cells (also called cytotoxic T lymphocytes) specific for the tumor cells.
  • the vaccine must contain an antigen or an antigenic epitope that is also present in the tumor and that needs to be delivered to Antigen Presenting Cells (APCs), in particular dendritic cells (DCs), to initiate cancer immunity.
  • APCs Antigen Presenting Cells
  • DCs dendritic cells
  • the DCs process these tumor antigens into small peptides that are presented on cell surface expressed MHC class I or MHC class II molecules to T cells. Peptides that are then recognized by T cells and thereby induce their stimulation are called epitopes.
  • MHC class I and MHC class II molecules allow activation of two classes of T cells, CD8 + cytotoxic T lymphocytes (CTLs) and CD4 + helper T (T h ) cells, respectively.
  • CTLs cytotoxic T lymphocytes
  • T h helper T cells
  • co-stimulatory signal which is antigen non-specific and is provided by the interaction between co-stimulatory molecules expressed on the surface of APCs and the T cell. Therefore two major requirements for an efficient therapeutic cancer vaccine are (i) the specificity of the tumor antigens and (ii) the ability to deliver them efficiently to DCs.
  • induction of a tumor specific immune response thus requires three main steps: (i) an antigen must be delivered to dendritic cells, which will process it into epitopes, (ii) dendritic cells should receive a suitable activation signal, and (iii) activated tumor antigen-loaded dendritic cells must generate T-cell mediated immune responses in the lymphoid organs.
  • multi-epitopic antigen delivery provides an advantage.
  • protein based vaccines allow multi-epitopic antigen delivery to antigen presenting cells (APCs) such as dendritic cells (DCs) without the limitation of restriction to a single MHC allele.
  • APCs antigen presenting cells
  • DCs dendritic cells
  • Another strength is long-lasting epitope presentation recently described in dendritic cells loaded with proteins (van Montfoort N, Camps M G, Khan S, Filippov D V, Weterings J J, Griffith J M, et al.
  • Antigen storage compartments in mature dendritic cells facilitate prolonged cytotoxic T lymphocyte cross-priming capacity.
  • proteins require uptake and processing by DCs to achieve MHC restricted presentation of their constituent epitopes. This reduces the risk of inducing peripheral tolerance as shown after vaccination with short peptides that do not have such stringent processing requirements (Toes R E, Offringa R, Blom R J, Melief C J, Kast W M. Peptide vaccination can lead to enhanced tumor growth through specific T-cell tolerance induction. Proceedings of the National Academy of Sciences of the United States of America 1996; 93(15):7855-60).
  • peptide-pulsed DCs as vaccines have several limitations. For example, peptide degradation, rapid MHC class I turnover, and the disassociation of peptide from MHC class I molecules during the preparation and injection of DC/peptides may result in short half-lives of MHC class I/peptide complexes on the DC surface, leading to weak T-cell responses.
  • CPPs Cell penetrating peptides
  • Cell-penetrating peptides classes, origin, and current landscape. Drug Discov Today 2012). Alternatively, they are also called protein transduction domain (PTDs) reflecting their origin as occurring in natural proteins.
  • PTDs protein transduction domain
  • Several potent CPPs have been identified from proteins, including the Tat protein of human immunodeficiency virus, the VP22 protein of herpes simplex virus, and fibroblast growth factor (Berry C C. Intracellular delivery of nanoparticles via the HIV-1 tat peptide. Nanomedicine. 2008; 3:357-365; Deshayes S, Morris M C, Divita G, Heitz F. Cell-penetrating peptides: Tools for intracellular delivery of therapeutics. Cell Mol Life Sci.
  • adjuvants may be used.
  • Adjuvants may accomplish this task by mimicking conserved microbial components that are naturally recognized by the immune system. They include, for example, lipopolysaccharide (LPS), components of bacterial cell walls, and nucleic acids such as double-stranded RNA (dsRNA), single-stranded DNA (ssDNA), and unmethylated CpG dinucleotide-containing DNA. Their presence can increase the innate immune response to the antigen. Furthermore, this adjuvant should promote an adaptive immune response with CTLs and type polarized T h 1 rather than a humoral immune response resulting in antibody production.
  • LPS lipopolysaccharide
  • dsRNA double-stranded RNA
  • ssDNA single-stranded DNA
  • unmethylated CpG dinucleotide-containing DNA unmethylated CpG dinucleotide-containing DNA.
  • this adjuvant should promote an adaptive immune response with CTLs and type polarized T
  • TLR Toll Like Receptor
  • TLR-3 poly I:C
  • TLR-4 monophosphoryl lipid A
  • MPL monophosphoryl lipid A
  • TLR-5 flagellin
  • TLR-7 imiquimod
  • TLR-9 CpG
  • TLR ligand-peptide conjugate vaccines toward clinical application. Adv Immunol. 2012; 114:177-201).
  • TLR ligands for conjugate vaccine are the TLR2 agonist Pam2Cys and Pam3Cys (Fujita, Y. and H. Taguchi, Overview and outlook of Toll - like receptor ligand - antigen conjugate vaccines . Ther Deliv, 2012. 3(6): p. 749-60).
  • Immune checkpoints are molecules in the immune system, in particular on certain immune cells, that need to be activated (stimulatory or costimulatory checkpoint molecules) or inactivated (inhibitory checkpoint molecules) to start an immune response. Many of the immune checkpoints are regulated by interactions between specific receptor and ligand pairs. Often cancers protect themselves from the immune system by using these checkpoints to avoid being attacked by the immune system.
  • CTLA-4 and PD-1 received a lot of attention.
  • CTLA-4, PD-1 and their ligands are members of the CD28-B7 family of co-signaling checkpoint molecules that play important roles throughout all stages of T-cell function and other cell functions.
  • the PD-1 receptor is expressed on the surface of activated T cells and other immune cells, such as B cells. Its ligands (PD-L1 and PD-L2) are expressed on the surface of antigen-presenting cells, such as dendritic cells or macrophages, and other immune cells. Binding of PD-L1 or PD-L2 to PD1 triggers a signal in the T cell, which essentially switches the T cell off or inhibits it. Under non-pathological conditions, this interaction prevents T cells from attacking other cells in the body.
  • cancer cells often take advantage of this system and express high levels of PD-L1 on their surface. Thereby, cancer cells are able to switch off T cells expressing PD-1 and, thus, to suppress the anticancer immune response.
  • Inhibitors of PD1 and/or its ligands can boost the immune response against cancer cells and are, thus, promising in treating cancers.
  • Examples of inhibitory/antagonistic monoclonal antibodies against PD1, which are currently approved, include Opdivo® (Nivolumab; Bristol Myers Squibb) and Keytruda® (Pembrolizumab; Merck).
  • inhibitors of the PD1 pathway which are currently in clinical phase II and/or III include Pidilizumab (mAb inhibiting PD1; CureTech/Medivation), Durvalumab (mAb inhibiting PD-L1; MedImmune/AstraZeneca) and Atezolimab (mAb inhibiting PD-L1; Roche).
  • Yervoy® (Ipilimumab; Bristol Myers Squibb), another approved immune checkpoint modulator, is an inhibitory/antagonistic monoclonal antibody against cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4).
  • CTLA4 is also expressed on the surface of activated T cells and its ligands are expressed on the surface of professional antigen-presenting cells.
  • CTLA-4 is thought to regulate T-cell proliferation early in an immune response, primarily in lymph nodes and affects the functioning of regulatory T cells.
  • Another inhibitor of CTLA-4 which is currently in clinical phase II, is, for example, Tremelimumab (MedImmune/AstraZeneca).
  • checkpoint modulators which each other only targets endogenous tumor-specific immunity, in particular since no tumor-specific antigens are provided.
  • Another strategy for the treatment of cancer is to combine a checkpoint modulator with a vaccine containing an antigen or an antigenic epitope as described above, which provides specificity against a certain tumor.
  • the combination of a checkpoint modulator and a vaccine containing an antigen or an antigenic epitope may enhance or prolong an anti-tumor response in a subject.
  • a vaccine containing an antigen or an antigenic epitope with a checkpoint modulator may enhance or prolong the effects of the checkpoint modulator, enable a subject to respond to a checkpoint modulator, or enable the reduction of the toxicity or the dose of a checkpoint modulator.
  • the checkpoint modulator may remove the “immune brake” before pressing the “treatment gas pedal” by vaccine administration.
  • T h cells are involved in the maintenance of long-lasting cellular immunity and tumor infiltration by T h cells is also an essential step for the recruitment and function of CD8 + CTLs.
  • Immunological memory is essential to protect against tumor relapse.
  • the object of the present invention to overcome the drawbacks of current cancer vaccines outlined above and to provide a combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a TLR agonist for cancer immunotherapy applications representing a more potent vaccine, in particular cancer vaccine, having improved anti-tumor activity.
  • the present invention thus relates to a combination therapy to initiate, enable, enhance or improve an anti-tumor immune response, in particular which enables, enhances or improves the subject's or tumor response to checkpoint modulators.
  • the term “comprise”, and variations such as “comprises” and “comprising”, will be understood to imply the inclusion of a stated member, integer or step but not the exclusion of any other non-stated member, integer or step.
  • the term “consist of” is a particular embodiment of the term “comprise”, wherein any other non-stated member, integer or step is excluded. In the context of the present invention, the term “comprise” encompasses the term “consist of”.
  • the term “comprising” thus encompasses “including” as well as “consisting” e.g., a composition “comprising” X may consist exclusively of X or may include something additional e.g., X+Y.
  • the present invention provides a combination of
  • the components of the combination for use according to the present invention i.e. the immune checkpoint modulator and the complex comprising cell penetrating peptide, the at least one antigen or antigenic epitope and the at least one TLR peptide agonist, and preferred embodiments thereof, are described in detail.
  • a preferred embodiment of the combination for use according to the present invention comprises a preferred embodiment of the immune checkpoint modulator;
  • a preferred embodiment of the combination for use according to the present invention comprises a preferred embodiment of the complex comprising cell penetrating peptide, the at least one antigen or antigenic epitope and the at least one TLR peptide agonist;
  • a more preferred embodiment of the combination for use according to the present invention comprises a preferred embodiment of the immune checkpoint modulator and a preferred embodiment of the complex comprising cell penetrating peptide, the at least one antigen or antigenic epitope and the at least one TLR peptide agonist.
  • an immune checkpoint modulator refers to a molecule or to a compound that modulates (e.g., totally or partially reduces, inhibits, interferes with, activates, stimulates, increases, reinforces or supports) the function of one or more checkpoint molecules.
  • an immune checkpoint modulator may be an “immune checkpoint inhibitor” (also referred to as “checkpoint inhibitor” or “inhibitor”) or an “immune checkpoint activator” (also referred to as “checkpoint activator” or “activator”).
  • an “immune checkpoint inhibitor” (also referred to as “checkpoint inhibitor” or “inhibitor”) totally or partially reduces, inhibits, interferes with, or negatively modulates the function of one or more checkpoint molecules.
  • An “immune checkpoint activator” (also referred to as “checkpoint activator” or “activator”) totally or partially activates, stimulates, increases, reinforces, supports or positively modulates the function of one or more checkpoint molecules.
  • Immune checkpoint modulators are typically able to modulate (i) self-tolerance and/or (ii) the amplitude and/or the duration of the immune response.
  • the immune checkpoint modulator used according to the present invention modulates the function of one or more human checkpoint molecules and is, thus, a “human checkpoint modulator”.
  • the immune checkpoint modulator is an activator or an inhibitor of one or more immune checkpoint point molecule(s) selected from CD27, CD28, CD40, CD122, CD137, OX40, GITR, ICOS, A2AR, B7-H3, B7-H4, BTLA, CD40, CTLA-4, IDO, KIR, LAG3, PD-1, TIM-3, VISTA, CEACAM1, GARP, PS, CSF1R, CD94/NKG2A, TDO, GITR, TNFR and/or FasR/DcR3; or an activator or an inhibitor of one or more ligands thereof.
  • Checkpoint molecules are molecules, such as proteins, are typically involved in immune pathways and, for example, regulate T-cell activation, T-cell proliferation and/or T-cell function. Accordingly, the function of checkpoint molecules, which is modulated (e.g., totally or partially reduced, inhibited, interfered with, activated, stimulated, increased, reinforced or supported) by checkpoint modulators, is typically the (regulation of) T-cell activation, T-cell proliferation and/or T cell function. Immune checkpoint molecules thus regulate and maintain self-tolerance and the duration and amplitude of physiological immune responses.
  • immune checkpoint molecules belong to the B7:CD28 family or to the tumor necrosis factor receptor (TNFR) super family and, by the binding of specific ligands, activate signaling molecules that are recruited to the cytoplasmic domain (cf. Susumu Suzuki et al., 2016: Current status of immunotherapy. Japanese Journal of Clinical Oncology, 2016: doi: 10.1093/jjco/hyv201 [Epub ahead of print]; in particular Table 1).
  • B7-H3 Choval, A. I., et al., B 7- H 3 : a costimulatory molecule for T cell activation and IFN - gamma production . Nat Immunol, 2001. 2(3): p. 269-74
  • B7-H4 Sica, G. L., et al., B 7- H 4 , a molecule of the B 7 family, negatively regulates T cell immunity. Immunity, 2003.
  • CD28 is constitutively expressed on almost all human CD4+ T cells and on around half of all CD8 T cells. Binding with its two ligands are CD80 (B7-1) and CD86 (B7-2), expressed on dendritic cells, prompts T cell expansion.
  • the co-stimulatory checkpoint molecule CD28 competes with the inhibitory checkpoint molecule CTLA4 for the same ligands, CD80 and CD86 (cf. Buchbinder E. I. and Desai A., 2016: CTLA-4 and PD-1 Pathways—Similarities, Differences and Implications of Their Inhibition; American Journal of Clinical Oncology, 39(1): 98-106).
  • CTLA4 Cytotoxic T-Lymphocyte-Associated protein 4
  • CD152 Cytotoxic T-Lymphocyte-Associated protein 4
  • the ligands of CTLA-4 are CD80 (B7-1) and CD86 (B7-2), similarly to CD28.
  • binding of CTLA4 to B7 does not produce a stimulatory signal, but prevents the co-stimulatory signal normally provided by CD28.
  • CTLA4 binding to B7 is assumed to even produce an inhibitory signal counteracting the stimulatory signals of CD28:B7 and TCR:MHC binding.
  • CTLA-4 is considered the “leader” of the inhibitory immune checkpoints, as it stops potentially autoreactive T cells at the initial stage of na ⁇ ve T-cell activation, typically in lymph nodes (Buchbinder E. I. and Desai A., 2016: CTLA-4 and PD-1 Pathways: Similarities, Differences and Implications of Their Inhibition; American Journal of Clinical Oncology, 39(1): 98-106).
  • Preferred checkpoint inhibitors of CTLA4 include the monoclonal antibodies Yervoy® (Ipilimumab; Bristol Myers Squibb) and Tremelimumab (Pfizer/MedImmune).
  • CTLA-4 inhibitors include the anti-CTLA4 antibodies disclosed in WO 2001/014424, in WO 2004/035607, in US 2005/0201994, and in EP 1212422 B1. Additional preferred CTLA-4 antibodies are described in U.S. Pat. No. 5,811,097, in U.S. Pat. No. 5,855,887, in U.S. Pat. No. 6,051,227, in U.S. Pat. No. 6,984,720, in WO 01/14424 in WO 00/37504, in US 2002/0039581 and in US 2002/086014.
  • Other preferred anti-CTLA-4 antibodies that can be used in the context of the present invention include, for example, those disclosed in WO 98/42752; U.S. Pat.
  • PD1 Programmed Death 1 receptor
  • PD-L1 also known as B7-H1 and CD274
  • PD-L2 also known as B7-DC and CD273
  • the PD1 pathway regulates previously activated T cells at the later stages of an immune response, primarily in peripheral tissues.
  • An advantage of targeting PD1 is thus that it can restore immune function in the tumor microenvironment.
  • Preferred inhibitors of the PD1 pathway include Opdivo® (Nivolumab; Bristol Myers Squibb), Keytruda® (Pembrolizumab; Merck), Durvalumab (MedImmune/AstraZeneca), MEDI4736 (AstraZeneca; cf.
  • WO 2011/066389 A1 Atezolizumab (MPDL3280A, Roche/Genentech; cf. U.S. Pat. No. 8,217,149 B2), Pidilizumab (CT-011; CureTech), MEDIO0680 (AMP-514; AstraZeneca), Avelumab (Merck), MSB-0010718C (Merck), PDR001 (Novartis), BMS-936559 (Bristol Myers Squibb), REGN2810 (Regeneron Pharmaceuticals), MIH1 (Affymetrix), AMP-224 (Amplimmune, GSK), BGB-A317 (BeiGene) and Lambrolizumab (e.g.
  • hPD109A and its humanized derivatives h409AII, h409A16 and h409A17 in WO2008/156712; Hamid et al., 2013; N. Engl. J. Med. 369: 134-144).
  • Inducible T-cell costimulator (ICOS; also known as CD278) is expressed on activated T cells. Its ligand is ICOSL (B7-H2; CD275), expressed mainly on B cells and dendritic cells. The molecule seems to be important in T cell effector function.
  • B7-H3 (also known as CD276) was originally understood to be a co-stimulatory molecule but is now regarded as co-inhibitory.
  • a preferred checkpoint inhibitor of B7-H3 is the Fc-optimized monoclonal antibody Enoblituzumab (MGA271; MacroGenics; cf. US 2012/0294796 A1).
  • B7-H4 (also known as VTCN1), is expressed by tumor cells and tumor-associated macrophages and plays a role in tumor escape.
  • Preferred B7-H4 inhibitors are the antibodies described in Dangaj, D. et al., 2013; Cancer Research 73(15): 4820-9 and in Table 1 and the respective description of Jenessa B. Smith et al., 2014: B7-H4 as a potential target for immunotherapy for gynecologic cancers: A closer look. Gynecol Oncol 134(1): 181-189.
  • B7-H4 inhibitors include antibodies to human B7-H4 as disclosed, e.g., in WO 2013/025779 A1 and in WO 2013/067492 A1 or soluble recombinant forms of B7-H4, such as disclosed in US 2012/0177645 A1.
  • the TNF superfamily comprises in particular 19 protein-ligands binding to 29 cytokine receptors. They are involved in many physiological responses such as apoptosis, inflammation or cell survival (Croft, M., C. A. Benedict, and C. F. Ware, Clinical targeting of the TNF and TNFR superfamilies . Nat Rev Drug Discov, 2013. 12(2): p. 147-68). These commonly encountered effects make the TNF superfamily members highly attractive for drug development (more than 60 TNF family drugs in development in 2013 (Croft, M., C. A. Benedict, and C. F. Ware, Clinical targeting of the TNF and TNFR superfamilies . Nat Rev Drug Discov, 2013. 12(2): p.
  • TNFRSF4 (OX40/0X40L), TNFRSFS (CD40L/CD40), TNFRSF7 (CD27/CD70), TNFRSF8 (CD30/CD30L), TNFRSF9 (4-1BB/4-1BBL), TNFRSF10 (TRAILR/TRAIL)), TNFRSF12 (FN14/TWEAK), TNFRSF13 (BAFFRTACI/APRIL-BAFF) and TNFRSF18 (GITR/GITRL) (Avogadri, F., et al., Modulation of CTLA -4 and GITR/or cancer immunotherapy . Curr Top Microbiol Immunol, 2011. 344: p.
  • B- and T-lymphocyte attenuator (BTLA)/herpes virus entry mediator (HVEM) pathway should be considered as target for enhancing immune responses, just like the CTLA-4 blockade (Croft, M., C. A. Benedict, and C. F. Ware, Clinical targeting of the TNF and TNFRsuperfamilies . Nat Rev Drug Discov, 2013. 12(2): p. 147-68).
  • checkpoint modulators are preferred for the use in the treatment and/or prevention in cancer, which modulate one or more checkpoint molecules selected from TNFRSF4 (OX40/0X40L), TNFRSFS (CD40L/CD40), TNFRSF7 (CD27/CD70), , TNFRSF9 (4-1BB/4-1BBL), TNFRSF18 (GITR/GITRL), FasR/DcR3/Fas ligand, TNFRSF1 (TNF ⁇ /TNFR), BTLA/HVEM and CTLA4.
  • TNFRSF4 OX40/0X40L
  • TNFRSFS CD40L/CD40
  • TNFRSF7 CD27/CD70
  • TNFRSF9 4-1BB/4-1BBL
  • TNFRSF18 GTR/GITRL
  • FasR/DcR3/Fas ligand TNFRSF1 (TNF ⁇ /TNFR)
  • BTLA/HVEM BTLA/HVEM
  • OX40 (also known as CD134 or TNFRSF4) promotes the expansion of effector and memory T cells, but it is also able to suppress the differentiation and activity of T-regulatory cells and to regulate cytokine production.
  • the ligand of OX40 is OX40L (also known as TNFSF4 or CD252).
  • OX40 is transiently expressed after T-cell receptor engagement and is only upregulated on the most recently antigen-activated T cells within inflammatory lesions.
  • Preferred checkpoint modulators of OX40 include MEDI6469 (MedImmune/AstraZeneca), MEDI6383 (MedImmune/AstraZeneca), MEDI0562 (MedImmune/AstraZeneca), MOXR0916 (RG7888; Roche/Genentech) and GSK3174998 (GSK).
  • CD40 (also known as TNFRSF5) is expressed by a variety of immune system cells including antigen presenting cells. Its ligand is CD40L, also known as CD154 or TNFSF5, is transiently expressed on the surface of activated CD4+ T cells. CD40 signaling “licenses” dendritic cells to mature and thereby trigger T-cell activation and differentiation. However, CD40 can also be expressed by tumor cells. Thus, stimulation/activation of CD40 in cancer patients can be beneficial or deleterious.
  • CD40 checkpoint modulators include (i) agonistic anti-CD antibodies as described in Sufia Butt Hassan, Jesper Freddie Sorensen, Barbara Nicola Olsen and Anders Elm Pedersen, 2014: Anti-CD40-mediated cancer immunotherapy: an update of recent and ongoing clinical trials, Immunopharmacology and Immunotoxicology, 36:2, 96-104, such as Dacetuzumab (SGN-40), CP-870893, FGK 4.5/FGK 45 and FGK115, preferably Dacetuzumab, and (ii) antagonistic anti-CD antibodies as described in Sufia Butt Hassan, Jesper Freddie Sorensen, Barbara Nicola Olsen and Anders Elm Pedersen, 2014: Anti-CD40-mediated cancer immunotherapy: an update of recent and ongoing clinical trials, Immunopharmacology and Immunotoxicology, 36:2, 96-104, such as Lucatumumab (HCD122, CHIR-12.12). Further preferred
  • CD27 (also known as TNFRSF7) supports antigen-specific expansion of na ⁇ ve T cells and plays an important role in the generation of T cell memory. CD27 is also a memory marker of B cells.
  • CD70 also known as TNFSF7 or CD27L
  • TNFSF7 or CD27L The transient availability of its ligand, CD70 (also known as TNFSF7 or CD27L), on lymphocytes and dendritic cells regulates the activity of CD27.
  • CD27 co-stimulation is known to suppress Th17 effector cell function.
  • a preferred immune checkpoint modulator of CD27 is Varlilumab (Celldex).
  • Preferred immune checkpoint modulators of CD70 include ARGX-110 (arGEN-X) and SGN-CD70A (Seattle Genetics).
  • CD137 (also known as 4-1BB or TNFRSF9) is a member of the tumor necrosis factor (TNF) receptor family and is increasingly associated with costimulatory activity for activated T cells.
  • CD137 signaling via its ligand CD137L, also known as TNFSF9 or 4-1BBL results in T-cell proliferation and protects T cells, in particular, CD8+ T cells, from activation-induced cell death.
  • Preferred checkpoint modulators of CD137 include PF-05082566 (Pfizer) and Urelumab (BMS).
  • GITR Glucocorticoid-Induced TNFR family Related gene
  • TNFRSF18 Glucocorticoid-Induced TNFR family Related gene
  • GITRL TNFSF18
  • Antibodies to GITR have been shown to promote an anti-tumor response through loss of Treg lineage stability.
  • Preferred checkpoint modulators of GITR include BMS-986156 (Bristol Myers Squibb), TRX518 (GITR Inc) and MK-4166 (Merck).
  • BTLA B and T Lymphocyte Attenuator
  • CD272 B and T Lymphocyte Attenuator
  • BTLA also known as CD272
  • CD8+ T cells are in particular expressed by CD8+ T cells, wherein surface expression of BTLA is gradually downregulated during differentiation of human CD8+ T cells from the naive to effector cell phenotype.
  • tumor-specific human CD8+ T cells express high levels of BTLA.
  • BTLA expression is induced during activation of T cells, and BTLA remains expressed on Th1 cells but not Th2 cells.
  • BTLA interacts with a B7 homolog, B7H4.
  • BTLA displays T-Cell inhibition via interaction with tumor necrosis family receptors (TNF-R), not just the B7 family of cell surface receptors.
  • TNF-R tumor necrosis family receptors
  • BTLA is a ligand for tumor necrosis factor (receptor) superfamily, member 14 (TNFRSF14), also known as herpes virus entry mediator (HVEM; Herpesvirus Entry Mediator, also known as CD270).
  • HVEM herpes virus entry mediator
  • BTLA-HVEM complexes negatively regulate T-cell immune responses.
  • Preferred BTLA inhibitors are the antibodies described in Table 1 of Alison Crawford and E. John Wherry, 2009: Editorial: Therapeutic potential of targeting BTLA. Journal of Leukocyte Biology 86: 5-8, in particular the human antibodies thereof.
  • Other preferred antibodies in this context, which block human BTLA interaction with its ligand are disclosed in WO 2011/014438, such as “4C7” as described in WO 2011/014438.
  • Another checkpoint molecule family includes checkpoint molecules related to the two primary class of major histocompatibility complex (MHC) molecules (MHC class I and class II). Their function to trigger a response from the immune system through their respective pathways; killer Ig-like Receptor (KIR) for class I and lymphocyte activation gene-3 (LAG-3) for class II, seems opening novel immunotherapeutic strategies for cancer patients treatment (Hemon, P., et al., MHC class II engagement by its ligand LAG -3 ( CD 223) contributes to melanoma resistance to apoptosis . J Immunol, 2011. 186(9): p. 5173-83; Thielens, A., E. Vivier, and F. Romagne, NK cell MHC class/specific receptors ( KIR ): from biology to clinical intervention . Curr Opin Immunol, 2012. 24(2): p. 239-45).
  • MHC major histocompatibility complex
  • KIR Killer-cell Immunoglobulin-like Receptor
  • IPH 2102 Innate Pharma/BMS; cf. U.S. Pat. No. 8,119,775 B2 and Benson et al., 2012, Blood 120:4324-4333.
  • Lymphocyte Activation Gene-3 (LAG3, also known as CD223) signaling leads to suppression of an immune response by action to Tregs as well as direct effects on CD8+ T cells.
  • a preferred example of a LAG3 inhibitor is the anti-LAG3 monoclonal antibody BMS-986016 (Bristol-Myers Squibb).
  • Other preferred examples of a LAG3 inhibitor include LAG525 (Novartis), IMP321 (Immutep) and LAG3-Ig as disclosed in WO 2009/044273 A2 and in Brumble et al., 2009, Clin. Cancer Res.
  • T-cell Immunoglobulin domain and Mucin domain 3 (TIM-3, also known as HAVcr-2) is expressed on activated human CD4+ T cells and regulates Th1 and Th17 cytokines.
  • TIM-3 acts as a negative regulator of Th1/Tc1 function by triggering cell death upon interaction with its ligand, galectin-9 (GAL9).
  • GAL9 galectin-9
  • TIM-3 is a T helper type 1 specific cell surface molecule that is regulating the induction of peripheral tolerance.
  • TIM-3 inhibitors include antibodies targeting human TIM3 (e.g. as disclosed in WO 2013/006490 A2) or, in particular, the anti-human TIM3 blocking antibody F38-2E2 as disclosed by Jones et al., 2008, J Exp Med. 205 (12): 2763-79.
  • CEACAM1 Carcinoembryonic antigen-related cell adhesion molecule 1
  • a preferred checkpoint modulator of CEACAM1 is CM-24 (cCAM Biotherapeutics).
  • ARGX-115 is a preferred GARP checkpoint modulator.
  • phosphatidylserine also referred to as “PS”
  • PS phosphatidylserine
  • a preferred checkpoint modulator of phosphatidylserine (PS) is Bavituximab (Peregrine).
  • CSF1/CSF1R Another checkpoint pathway is CSF1/CSF1R (Zhu, Y., et al., CSF 1 /CSF 1 R Blockade Reprograms Tumor - Infiltrating Macrophages and Improves Response to T - cell Checkpoint Immunotherapy in Pancreatic Cancer Models . Cancer Research, 2014. 74(18): p. 5057-5069).
  • Preferred checkpoint modulators of CSF1R include FPA008 (FivePrime), IMC-CS4 (Eli-Lilly), PLX3397 (Plexxicon) and RO5509554 (Roche).
  • the CD94/NKG2A natural killer cell receptor is evaluated for its role in cervical carcinoma (Sheu, B. C., et al., Up - regulation of inhibitory natural killer receptors CD 94 /NKG 2 A with suppressed intracellular perform expression of tumor infiltrating CD 8 + T lymphocytes in human cervical carcinoma . Cancer Res, 2005. 65(7): p. 2921-9) and in leukemia (Tanaka, J., et al., Cytolytic activity against primary leukemic cells by inhibitory NK cell receptor ( CD 94 /NKG 2 A )-expressing T cells expanded from various sources of blood mononuclear cells. Leukemia, 2005. 19(3): p. 486-9).
  • a preferred checkpoint modulator of NKG2A is IPH2201 (Innate Pharma).
  • IDO the indoleamine 2,3-dioxygenase enzyme from the kynurenine pathway
  • Indoleamine 2,3-dioxygenase is a tryptophan catabolic enzyme with immune-inhibitory properties. IDO is known to suppress T and NK cells, generate and activate Tregs and myeloid-derived suppressor cells, and promote tumour angiogenesis.
  • IDO1 is overexpressed in many cancer and was shown to allow tumor cells escaping from the immune system (Liu, X., et al., Selective inhibition of IDOI effectively regulates mediators of antitumor immunity . Blood, 2010. 115(17): p. 3520-30; Ino, K., et al., Inverse correlation between tumoral indoleamine 2,3- dioxygenase expression and tumor - infiltrating lymphocytes in endometrial cancer: its association with disease progression and survival . Clin Cancer Res, 2008. 14(8): p. 2310-7) and to facilitate chronic tumor progression when induced by local inflammation (Muller, A.
  • IDO inhibitors include Exiguamine A, epacadostat (INCB024360; InCyte), Indoximod (NewLink Genetics), NLG919 (NewLink Genetics/Genentech), GDC-0919 (NewLink Genetics/Genentech), F001287 ( Flexusiii Biosciences/BMS) and small molecules such as 1-methyl-tryptophan, in particular 1-methyl-[D]-tryptophan and the IDO inhibitors listed in Table 1 of Sheridan C., 2015: IDO inhibitors move center stage in immune-oncology; Nature Biotechnology 33: 321-322.
  • TDO tryptophan-2,3-dioxygenase
  • Several studies already demonstrated the interest of TDO in cancer immunity and autoimmunity (Garber, K., Evading immunity: new enzyme implicated in cancer . J Natl Cancer Inst, 2012. 104(5): p. 349-52; Platten, M., W. Wick, and B. J. Van den Eynde, Tryptophan catabolism in cancer: beyond !DO and tryptophan depletion . Cancer Res, 2012. 72(21): p. 5435-40; Platten, M., et al., Cancer Immunotherapy by Targeting IDOI/TDO and Their Downstream Effectors . Front Immunol, 2014. 5: p. 673).
  • A2AR Another preferred immune checkpoint molecule to be modulated is A2AR.
  • the Adenosine A2A receptor (A2AR) is regarded as an important checkpoint in cancer therapy because the tumor microenvironment has typically relatively high concentrations of adenosine, which is activating A2AR.
  • A2AR antagonists Next generation checkpoint blockade for cancer immunotherapy. Computational and Structural Biotechnology journal 13: 265-272).
  • Preferred A2AR inhibitors include Istradefylline, PBS-509, ST1535, ST4206, Tozadenant, V81444, Preladenant, Vipadenant, SCH58261, SYN115, ZM241365 and FSPTP.
  • VISTA V-domain Ig suppressor of T cell activation
  • C10orf54 V-domain Ig suppressor of T cell activation
  • JNJ-61610588 ImmuNext
  • an anti-VISTA antibody which recently entered a phase 1 clinical trial.
  • CD122 is the Interleukin-2 receptor beta sub-unit. CD122 increases proliferation of CD8+ effector T cells.
  • checkpoint molecules include the “CTLA4-pathway” and the “PD1-pathway” with CTLA4 and its ligands CD80 and CD86 as well as PD1 with its ligands PD-L1 and PD-L2 (more details on CTLA4 and PD-1 pathways as well as further participants are described in Buchbinder E. I. and Desai A., 2016: CTLA-4 and PD-1 Pathways—Similarities, Differences and Implications of Their Inhibition; American Journal of Clinical Oncology, 39(1): 98-106).
  • checkpoint molecules include CD27, CD28, CD40, CD122, CD137, OX40, GITR, ICOS, A2AR, B7-H3, B7-H4, BTLA, CD40, CTLA-4, IDO, KIR, LAG3, PD-1, TIM-3, VISTA, CEACAM1, GARP, PS, CSF1R, CD94/NKG2A, TDO, GITR, TNFR and/or FasR/DcR3 as well as, in particular, their ligands.
  • Immune checkpoint molecules are responsible for co-stimulatory or inhibitory interactions of T-cell responses. Accordingly, checkpoint molecules can be divided into (i) (co-)stimulatory checkpoint molecules and (ii) inhibitory checkpoint molecules. Typically, (co-)stimulatory checkpoint molecules act positively in concert with T-cell receptor (TCR) signaling induced by antigen stimulation and inhibitory checkpoint molecules negatively regulate TCR signaling. Examples of (co-)stimulatory checkpoint molecules include CD27, CD28, CD40, CD122, CD137, OX40, GITR and ICOS.
  • inhibitory checkpoint molecules include CTLA4 as well as PD1 with its ligands PD-L1 and PD-L2; and A2AR, B7-H3, B7-H4, BTLA, IDO, KIR, LAG3, TIM-3, VISTA, CEACAM1, GARP, PS, CSF1R, CD94/NKG2A, TDO, TNFR and FasR/DcR3.
  • the immune checkpoint modulator is an activator of a (co-)stimulatory checkpoint molecule or an inhibitor of an inhibitory checkpoint molecule or a combination thereof.
  • the immune checkpoint modulator is more preferably (i) an activator of CD27, CD28, CD40, CD122, CD137, OX40, GITR and/or ICOS or (ii) an inhibitor of A2AR, B7-H3, B7-H4, BTLA, CD40, CTLA-4, IDO, KIR, LAG3, PD-1, PDL-1, PD-L2, TIM-3, VISTA, CEACAM1, GARP, PS, CSF1R, CD94/NKG2A, TDO, TNFR and/or FasR/DcR3.
  • CD27, CD28, CD40, CD122, CD137, OX40, GITR, ICOS, A2AR, B7-H3, B7-H4, CTLA-4, PD1, PDL-1, PD-L2, IDO, LAG-3, BTLA, TIM3, VISTA, KIR, CEACAM1, GARP, PS, CSF1R, CD94/NKG2A, TDO, TNFR and/or FasR/DcR3 modulators (inhibitors/activators) are known and some of them are already in clinical trials or even approved.
  • alternative immune checkpoint modulators may be developed in the (near) future.
  • known modulators of the preferred immune checkpoint molecules may be used as such or analogues thereof may be used, in particular chimerized, humanized or human forms of antibodies.
  • the immune checkpoint modulator is an inhibitor of an inhibitory checkpoint molecule (but preferably no inhibitor of a stimulatory checkpoint molecule). Accordingly, the immune checkpoint modulator is even more preferably an inhibitor of A2AR, B7-H3, B7-H4, BTLA, CTLA-4, IDO, KIR, LAG3, PD-1, PDL-1, PD-L2, TIM-3, VISTA, CEACAM1, GARP, PS, CSF1R, CD94/NKG2A, TDO, TNFR and/or DcR3 or of a ligand thereof.
  • the immune checkpoint modulator is an activator of a stimulatory or costimulatory checkpoint molecule (but preferably no activator of an inhibitory checkpoint molecule). Accordingly, the immune checkpoint modulator is more preferably an activator of CD27, CD28, CD40, CD122, CD137, OX40, GITR and/or ICOS or of a ligand thereof.
  • the immune checkpoint modulator is a modulator of the CD40 pathway, of the IDO pathway, of the CTLA-4 pathway and/or of the PD-1 pathway.
  • the immune checkpoint modulator is preferably a modulator of CD40, CTLA-4, PD-L1, PD-L2, PD-1 and/or IDO, more preferably the immune checkpoint modulator is an inhibitor of CTLA-4, PD-L1, PD-L2, PD-1 and/or IDO or an activator of CD40, even more preferably the immune checkpoint modulator is an inhibitor of CTLA-4, PD-L1, PD-1 and/or IDO and most preferably the immune checkpoint modulator is an inhibitor of CTLA-4 and/or PD-1.
  • the immune checkpoint modulator is a modulator of the CD40 pathway, of the IDO pathway, of the LAG3 pathway, of the CTLA-4 pathway and/or of the PD-1 pathway.
  • the immune checkpoint modulator is preferably a modulator of CD40, LAG3, CTLA-4, PD-L1, PD-L2, PD-1 and/or IDO, more preferably the immune checkpoint modulator is an inhibitor of CTLA-4, PD-L1, PD-L2, PD-1, LAG3, and/or IDO or an activator of CD40, even more preferably the immune checkpoint modulator is an inhibitor of CTLA-4, PD-L1, PD-1, LAG3 and/or IDO, even more preferably the immune checkpoint modulator is an inhibitor of LAG3, CTLA-4 and/or PD-1, and most preferably the immune checkpoint modulator is an inhibitor of CTLA-4 and/or PD-1.
  • the checkpoint modulator may be selected from known modulators of the CD40 pathway, the CTLA-4 pathway or the PD-1 pathway.
  • the checkpoint modulator may be selected from known modulators of the CD40 pathway, the LAG3 pathway, the CTLA-4 pathway or the PD-1 pathway.
  • Preferred inhibitors of the CTLA-4 pathway and of the PD-1 pathway include the monoclonal antibodies Yervoy® (Ipilimumab; Bristol Myers Squibb) and Tremelimumab (Pfizer/MedImmune) as well as Opdivo® (Nivolumab; Bristol Myers Squibb), Keytruda® (Pembrolizumab; Merck), Durvalumab (MedImmune/AstraZeneca), MEDI4736 (AstraZeneca; cf. WO 2011/066389 A1), MPDL3280A (Roche/Genentech; cf. U.S. Pat. No.
  • More preferred checkpoint inhibitors include the CTLA-4 inhibitors Yervoy® (Ipilimumab; Bristol Myers Squibb) and Tremelimumab (Pfizer/MedImmune) as well as the PD-1 inhibitors Opdivo® (Nivolumab; Bristol Myers Squibb), Keytruda® (Pembrolizumab; Merck), Pidilizumab (CT-011; CureTech), MEDIO0680 (AMP-514; AstraZeneca), AMP-224 and Lambrolizumab (e.g. disclosed as hPD109A and its humanized derivatives h409AII, h409A16 and h409A17 in WO2008/156712; Hamid O.
  • LAG3 inhibitor is the anti-LAG3 monoclonal antibody BMS-986016 (Bristol-Myers Squibb).
  • Other preferred examples of a LAG3 inhibitor include LAG525 (Novartis), IMP321 (Immutep) and LAG3-Ig as disclosed in WO 2009/044273 A2 and in Brumble et al., 2009, Clin. Cancer Res.
  • the immune checkpoint modulator is not a modulator of CD40.
  • the immune checkpoint modulator is not a CD40 ligand. It is also preferred that the immune checkpoint modulator is not an anti-CD40 antibody.
  • immune checkpoint modulator e.g., checkpoint inhibitor
  • at least 2, 3, 4, 5, 6, 7, 8, 9 or 10 distinct immune checkpoint modulators e.g., checkpoint inhibitors
  • 2, 3, 4 or 5 distinct immune checkpoint modulators e.g., checkpoint inhibitors
  • more preferably 2, 3 or 4 distinct immune checkpoint modulators e.g., checkpoint inhibitors
  • even more preferably 2 or 3 distinct immune checkpoint modulators e.g., checkpoint inhibitors
  • most preferably 2 distinct immune checkpoint modulators e.g., checkpoint inhibitors
  • “distinct” immune checkpoint modulators means in particular that they modulate (e.g., inhibit) different checkpoint molecule pathways.
  • an inhibitor of the PD-1 pathway is combined with an inhibitor of the CTLA-4 pathway.
  • an inhibitor of the CTLA-4 pathway is combined with an inhibitor of the CTLA-4 pathway.
  • a combination therapy with Nivolumab (anti-PD1) and Ipilimumab (anti-CTLA4) was approved by the FDA in 2015 for the treatment of patients with BRAF V600 wild-type, unresectable or metastatic melanoma.
  • immune checkpoint modulators of the PD-1 pathway and of the CTLA-4 pathway are (i) Nivolumab (anti-PD1) and Ipilimumab (anti-CTLA4) or (ii) Durvalumab (MEDI4736; anti-PD-L1) and Tremelimumab (anti-CTLA4).
  • Combinations thereof e.g. Nivolumab (anti-PD1) and Tremelimumab (anti-CTLA4) or Durvalumab (MEDI4736; anti-PD-L1) and Ipilimumab (anti-CTLA4) are also preferred.
  • a combination of checkpoint modulators modulating 4-1BB and inhibitors of CTLA-4 such as described in Curran et al., 2011, PLoS One 6(4): el 9499);
  • a combination of checkpoint modulators targeting PD1 and CD27 such as Novilumab/Varlilumab and Atezolizumab/Varlilumab
  • a combination of checkpoint modulators targeting OX40 and CTLA-4 such as MEDI6469/Tremelimumab
  • a combination of checkpoint modulators targeting OX40 and PD-1 such as MEDI6469/MEDI4736, MOXR0916/MPDL3280A, MEDI6383/MEDI4736 and GSK3174998/Pembrolizumab
  • a combination of checkpoint modulators targeting PD-1 and 4-1BB such as Novilumab/Urelumab, Pembroli
  • the combination of the immune checkpoint modulator and the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist for use according to the present invention comprises at least (i) an inhibitor of CTLA-4 and (ii) an inhibitor of PD-1, PD-L1 or PD-L2, preferably at least (i) an inhibitor of CTLA-4 and (ii) an inhibitor of PD-1.
  • Examples of such a preferred combination include a combination of Yervoy® (Ipilimumab; Bristol Myers Squibb) and Opdivo® (Nivolumab; Bristol Myers Squibb), a combination of Yervoy® (Ipilimumab; Bristol Myers Squibb) and Keytruda® (Pembrolizumab; Merck), a combination of Yervoy® (Ipilimumab; Bristol Myers Squibb) and Durvalumab (MedImmune/AstraZeneca), a combination of Yervoy® (Ipilimumab; Bristol Myers Squibb) and MEDI4736 (AstraZeneca; cf.
  • WO 2011/066389 A1 a combination of Yervoy® (Ipilimumab; Bristol Myers Squibb) and MPDL3280A (Roche/Genentech; cf. U.S. Pat. No. 8,217,149 B2), a combination of Yervoy® (Ipilimumab; Bristol Myers Squibb) and Pidilizumab (CT-011; CureTech), a combination of Yervoy® (Ipilimumab; Bristol Myers Squibb) and MEDIO0680 (AMP-514; AstraZeneca), a combination of Yervoy® (Ipilimumab; Bristol Myers Squibb) and MSB-0010718C (Merck), a combination of Yervoy® (Ipilimumab; Bristol Myers Squibb) and MIH1 (Affymetrix), a combination of Yervoy® (Ipilimumab; Bristol Myers Squib
  • WO 2011/066389 A1 a combination of Tremelimumab (Pfizer/MedImmune) and MPDL3280A (Roche/Genentech; cf. U.S. Pat. No. 8,217,149 B2), a combination of Tremelimumab (Pfizer/MedImmune) and Pidilizumab (CT-011; CureTech), a combination of Tremelimumab (Pfizer/MedImmune) and MEDIO0680 (AMP-514; AstraZeneca), a combination of Tremelimumab (Pfizer/MedImmune) and MSB-0010718C (Merck), a combination of Tremelimumab (Pfizer/MedImmune) and MIH1 (Affymetrix), a combination of Tremelimumab (Pfizer/MedImmune) and AMP-224 and a combination of Tremelimumab (Pfizer/MedImmune) and Lambrolizumab.
  • immune checkpoint modulator e.g., checkpoint inhibitor
  • at least 2, 3, 4, 5, 6, 7, 8, 9 or 10 immune checkpoint modulators (e.g., checkpoint inhibitors) of the same checkpoint pathway are used, preferably 2, 3, 4 or 5 immune checkpoint modulators (e.g., checkpoint inhibitors) of the same checkpoint pathway are used, more preferably 2, 3 or 4 immune checkpoint modulators (e.g., checkpoint inhibitors) of the same checkpoint pathway are used, even more preferably 2 or 3 immune checkpoint modulators (e.g., checkpoint inhibitors) of the same checkpoint pathway are used and most preferably 2 immune checkpoint modulators (e.g., checkpoint inhibitors) of the same checkpoint pathway are used.
  • Preferred checkpoint pathways to be modulated are the PD-1 pathway, the CTLA-4 pathway, the CD40 pathway or the IDO pathway, more preferably the PD-1 pathway, the CTLA-4 pathway or the CD40 pathway and even more preferably the PD-1 pathway or the CTLA-4 pathway.
  • a combination of MEDI4736 and MEDIO0680 may be used to modulate, in particular to inhibit, the PD-1 pathway.
  • immune checkpoint modulators may be any kind of molecule or agent, as long as it totally or partially reduces, inhibits, interferes with, activates, stimulates, increases, reinforces or supports the function of one or more checkpoint molecules as described above.
  • the immune checkpoint modulator binds to one or more checkpoint molecules, such as checkpoint proteins, or to its precursors, e.g. on DNA- or RNA-level, thereby modulating (e.g., totally or partially reducing, inhibiting, interfering with, activating, stimulating, increasing, reinforcing or supporting) the function of one or more checkpoint molecules as described above.
  • Preferred immune checkpoint modulators are oligonucleotides, siRNA, shRNA, ribozymes, anti-sense RNA molecules, immunotoxins, small molecule inhibitors and (e.g., checkpoint molecule blocking, antagonist or agonist of checkpoint molecule) antibodies or antigen binding fragments thereof.
  • the immune checkpoint modulator is an oligonucleotide.
  • an oligonucleotide is preferably used to decrease protein expression, in particular to decrease the expression of a checkpoint protein, such as the checkpoint receptors or ligands described above.
  • Oligonucleotides are short DNA or RNA molecules, typically comprising from 2 to 50 nucleotides, preferably from 3 to 40 nucleotides, more preferably from 4 to 30 nucleotides and even more preferably from 5 to 25 nucleotides, such as, for example 4, 5, 6, 7, 8, 9 or 10 nucleotides. Oligonucleotides are usually made in the laboratory by solid-phase chemical synthesis.
  • Oligonucleotides maybe single-stranded or double-stranded, however, in the context of the present invention the oligonucleotide is preferably single-stranded. More preferably, the checkpoint modulator oligonucleotide is an antisense-oligonucleotide.
  • Antisense-oligonucleotides are single strands of DNA or RNA that are complementary to a chosen sequence, in particular to a sequence chosen from the DNA or RNA sequence (or a fragment thereof) of a checkpoint protein.
  • Antisense RNA is typically used to prevent protein translation of messenger RNA strands, e.g. of mRNA for a checkpoint protein, by binding to the mRNA.
  • Antisense DNA is typically used to target a specific, complementary (coding or non-coding) RNA. If binding takes place, such a DNA/RNA hybrid can be degraded by the enzyme RNase H.
  • morpholino-antisense oligonucleotides can be used for gene knockdowns in vertebrates. For example, Kryczek et al., 2006 (Kryczek I, Zou L, Rodriguez P, Zhu G, Wei S, Mottram P, et al. B7-H4 expression identifies a novel suppressive macrophage population in human ovarian carcinoma. J Exp Med.
  • the immune checkpoint modulator is an siRNA.
  • Small interfering RNA (siRNA), sometimes known as short interfering RNA or silencing RNA, is a class of double-stranded RNA molecules, which is typically 20-25 base pairs in length.
  • RNAi RNA interference
  • siRNA interferes with the expression of specific genes, such as genes coding for checkpoint proteins, with complementary nucleotide sequences.
  • siRNA functions by causing mRNA to be broken down after transcription, resulting in no translation. Transfection of exogenous siRNA may be used for gene knockdown, however, the effect maybe only transient, especially in rapidly dividing cells. This may be overcome, for example, by RNA modification or by using an expression vector for the siRNA.
  • the siRNA sequence may also be modified to introduce a short loop between the two strands.
  • the resulting transcript is a short hairpin RNA (shRNA, also “small hairpin RNA”), which can be processed into a functional siRNA by Dicer in its usual fashion.
  • shRNA is an advantageous mediator of RNAi in that it has a relatively low rate of degradation and turnover.
  • the immune checkpoint modulator is preferably an shRNA.
  • shRNA typically requires the use of an expression vector, e.g. a plasmid or a viral or bacterial vector.
  • the immune checkpoint modulator is an immunotoxin.
  • Immunotoxins are chimeric proteins that contain a targeting moiety (such as an antibody), which is typically targeting an antigen on a certain cell, such as a cancer cell, linked to a toxin.
  • a targeting moiety such as an antibody
  • an immunotoxin comprising a targeting moiety, which targets a checkpoint molecule, is preferred.
  • the immunotoxin binds to a cell carrying the antigen, e.g. the checkpoint molecule, it is taken in through endocytosis, and the toxin can then kill the cell.
  • Immunotoxins preferably comprise a (modified) antibody or antibody fragment, linked to a (fragment of a) toxin.
  • the targeting portion of the immunotoxin typically comprises a Fab portion of an antibody that targets a specific cell type.
  • the toxin is usually cytotoxic, such as a protein derived from a bacterial or plant protein, from which the natural binding domain has been removed so that the targeting moiety of the immunotoxin directs the toxin to the antigen on the target cell.
  • immunotoxins can also comprise a targeting moiety other than an antibody or antibody fragment, such as a growth factor.
  • recombinant fusion proteins containing a toxin and a growth factor are also referred to as recombinant immunotoxins.
  • the immune checkpoint modulator is a small molecule drug (also referred to as “small molecule inhibitor”).
  • a small molecule drug is a low molecular weight (up to 900 daltons) organic compound that typically interacts with (the regulation of) a biological process.
  • a small molecule drug which is an immune checkpoint modulator is an organic compound having a molecular weight of no more than 900 daltons, which totally or partially reduces, inhibits, interferes with, or negatively modulates the function of one or more checkpoint molecules as described above.
  • the upper molecular weight limit of 900 daltons allows for the possibility to rapidly diffuse across cell membranes and for oral bioavailability.
  • the molecular weight of the small molecule drug which is an immune checkpoint modulator is no more than 500 daltons.
  • various A2AR antagonists known in the art are organic compounds having a molecular weight below 500 daltons.
  • the immune checkpoint modulator is an antibody or an antigen-binding fragment thereof, in particular antibodies, or antigen binding fragments thereof, that bind to immune checkpoint receptors or antibodies that bind to immune checkpoint receptor ligands.
  • antibodies, or antigen binding fragments thereof are agonists or antagonists of immune checkpoint receptors or of immune checkpoint receptor ligands.
  • antibody-type checkpoint modulators include immune checkpoint modulators, which are currently approved as described above, namely, Yervoy® (Ipilimumab; Bristol Myers Squibb), Opdivo® (Nivolumab; Bristol Myers Squibb) and Keytruda® (Pembrolizumab; Merck) and further anti-checkpoint receptor antibodies or anti-checkpoint ligand antibodies as described above.
  • the term “antibody” encompasses various forms of antibodies, preferably monoclonal antibodies, including but not being limited to whole antibodies, antibody fragments, human antibodies, chimeric antibodies, humanized antibodies and genetically engineered antibodies (variant or mutant antibodies) as long as the characteristic properties according to the invention are retained, which means that the antibody (or the antigen-binding fragment) modulates (e.g., totally or partially reduces, inhibits, interferes with, activates, stimulates, increases, reinforces or supports) the function of one or more checkpoint molecules as described above. In particular, the antibody (or the antigen-binding fragment) mediates this function by binding to a checkpoint molecule.
  • the antibody is preferably a “blocking” antibody (or the antigen-binding fragment), in particular an “antagonist” antibody (or the antigen-binding fragment), or an “agonist” antibody (or the antigen-binding fragment).
  • the term “antibody” includes both, glycosylated and non-glycosylated immunoglobulins of any isotype or subclass (preferably IgG) or to an antigen-binding region thereof that competes with the intact antibody for specific binding, unless otherwise specified.
  • antibodies include monoclonal antibodies, bispecific antibodies, minibodies, domain antibodies, synthetic antibodies, antibody mimetics, chimeric antibodies, humanized antibodies, human antibodies, antibody fusions, antibody conjugates, single chain antibodies, antibody derivatives, antibody analogues and fragments thereof, respectively.
  • antibody includes, in addition to antibodies comprising two full-length heavy chains and two full-length light chains, derivatives, variants, and fragments thereof. In some instances an “antibody” may include fewer chains.
  • human or humanized monoclonal antibodies and/or recombinant antibodies especially as recombinant human monoclonal antibodies.
  • Particularly preferred are human IgG-type antibodies.
  • human antibody is intended to include antibodies having variable and constant regions derived from human germ line immunoglobulin sequences.
  • Human antibodies are well-known in the state of the art (van Dijk, M. A., and van de Winkel, J. G., Curr. Opin. Chem. Biol. 5 (2001) 368-374).
  • Human antibodies can also be produced in transgenic animals (e.g., mice) that are capable, upon immunization, of producing a full repertoire or a selection of human antibodies in the absence of endogenous immunoglobulin production.
  • Human antibodies can also be produced in phage display libraries (Hoogenboom, H. R., and Winter, G., J. Mol. Biol. 227 (1992) 381-388; Marks, J.
  • human antibody as used herein also comprises such antibodies which are modified, e.g. in the variable region to generate the properties according to the invention.
  • recombinant antibody is intended to include all antibodies that are prepared, expressed, created or isolated by recombinant means, such as antibodies isolated from a host cell such as for example a CHO cell or from an animal (e.g. a mouse) that is transgenic for, e.g. human, immunoglobulin genes or antibodies expressed using a recombinant expression vector transfected into a host cell.
  • recombinant antibodies are antibodies that are prepared, expressed, created or isolated by recombinant means, such as (i) antibodies isolated from an animal (e.g., a mouse) that is transgenic for human immunoglobulin genes or a hybridoma prepared therefrom, (ii) antibodies isolated from a host cell transfected to express the antibody, e.g., from a transfectoma, (iii) antibodies isolated from a recombinant, combinatorial antibody library, and (iv) antibodies prepared, expressed, created or isolated by any other means that involve splicing of immunoglobulin gene sequences to other DNA sequences.
  • Such antibodies may have variable and constant regions derived from germline immunoglobulin sequences of two distinct species of animals.
  • Antibodies subjected to in vitro mutagenesis are also preferred, while the amino acid sequences of the V H and V L regions of such antibodies may be sequences that, while derived from and related to the germline V H and V L sequences of a particular species (e.g., human), may not naturally exist within that species' antibody germline repertoire in vivo.
  • Recombinant antibodies may have variable and constant regions in a rearranged form and/or, for example, certain mutations, which do not occur in nature.
  • antibody fragment As used herein, the terms “antigen binding fragment,” “fragment,” and “antibody fragment” are used interchangeably to refer to any fragment of an antibody of the invention that retains the specific binding activity of the antibody according to the invention.
  • antibody fragments include, but are not limited to, a single chain antibody, Fab, Fab′, F(ab′) 2 , Fv or scFv.
  • Fragments of the antibodies of the invention can be obtained from the antibodies by methods that include digestion with enzymes, such as pepsin or papain, and/or by cleavage of disulfide bonds by chemical reduction. Alternatively, fragments of antibodies can be obtained by cloning and expression of part of the sequences of the heavy and/or light chains.
  • “Fragments” include, but are not limited to, Fab, Fab′, F(ab′)2 and Fv fragments.
  • the invention also encompasses single-chain Fv fragments (scFv) derived from the heavy and light chains of an antibody of the invention.
  • scFv single-chain Fv fragments
  • the invention includes a scFv comprising the CDRs from an antibody of the invention.
  • heavy or light chain monomers and dimers single domain heavy chain antibodies, single domain light chain antibodies, as well as single chain antibodies, e.g., single chain Fv in which the heavy and light chain variable domains are joined by a peptide linker.
  • Antibody fragments of the invention may impart monovalent or multivalent interactions and be contained in a variety of structures as described above.
  • scFv molecules may be synthesized to create a trivalent “triabody” or a tetravalent “tetrabody.”
  • the scFv molecules may include a domain of the Fc region resulting in bivalent minibodies.
  • the sequences of the invention may be a component of multispecific molecules in which the sequences of the invention target the checkpoint molecule and other regions of the molecule bind to other targets.
  • Exemplary molecules include, but are not limited to, bispecific Fab2, trispecific Fab3, bispecific scFv, and diabodies (Holliger and Hudson, 2005 , Nature Biotechnology 9: 1126-1136).
  • antibody or “antibody of the invention” includes all categories of antibodies, namely, antigen binding fragment(s), antibody fragment(s), variant(s) and derivative(s) of antibodies. Further, the term “antibody” as used herein includes both antibodies and antigen binding fragments thereof.
  • the immune checkpoint modulators in the combination used according to the present invention are antibodies or antigen-binding fragments that can partially or totally block the PD-1 pathway (e.g., they can be partial or full antagonists of the PD-1 pathway), in particular PD-1, PD-L1 or PD-L2, more preferably, the antibody can partially or totally block PD-1 (e.g., they can be partial or full antagonists of PD-1).
  • Such antibodies or antigen-binding fragments include anti-PD-1 antibodies, human anti-PD-1 antibodies, mouse anti-PD-1 antibodies, mammalian anti-PD-1 antibodies, humanized anti-PD-1 antibodies, monoclonal anti-PD-1 antibodies, polyclonal anti-PD-1 antibodies, chimeric anti-PD-1 antibodies, anti-PD-L1 antibodies, anti-PD-L2 antibodies, anti-PD-1 adnectins, anti-PD-1 domain antibodies, single chain anti-PD-1 fragments, heavy chain anti-PD-1 fragments, and light chain anti-PD-1 fragments.
  • the anti-PD-1 antibody may be an antigen-binding fragment.
  • the anti-PD-1 antibody is able to bind to human PD-1 and to partially or totally block the activity of PD-1 (e.g., they can be partial or full antagonists of PD-1), thereby in particular unleashing the function of immune cells expressing PD-1.
  • the immune checkpoint modulators in the combination used according to the present invention are antibodies or antigen-binding fragments that can partially or totally block the CTLA-4 pathway (e.g., they can be partial or full antagonists of the CTLA-4 pathway).
  • Such antibodies or antigen-binding fragments include anti-CTLA4 antibodies, human anti-CTLA4 antibodies, mouse anti-CTLA4 antibodies, mammalian anti-CTLA4 antibodies, humanized anti-CTLA4 antibodies, monoclonal anti-CTLA4 antibodies, polyclonal anti-CTLA4 antibodies, chimeric anti-CTLA4 antibodies, MDX-010 (ipilimumab), tremelimumab, anti-CD28 antibodies, anti-CTLA4 adnectins, anti-CTLA4 domain antibodies, single chain anti-CTLA4 fragments, heavy chain anti-CTLA4 fragments, and light chain anti-CTLA4 fragments.
  • the anti-CTLA4 antibody may be an antigen-binding fragment.
  • the anti-CTLA4 antibody is able to bind to human CTLA4 and to partially or totally block the activity of CTLA4 (e.g., they can be partial or full antagonists of CTLA-4), thereby in particular unleashing the function of immune cells expressing CTLA4.
  • the combination for use according to the present invention comprises a complex comprising:
  • Such a complex comprised by the combination for use according to the present invention provides simultaneous (i) stimulation of multi-epitopic cytotoxic T cell-mediated immunity, (ii) induction of T h cells and (iii) promotion of immunological memory.
  • a complex comprised by the combination for use according to the present invention provides a potent vaccine, in particular having improved anti-tumor activity.
  • the complex comprised by the combination for use according to the present invention is a polypeptide or a protein, in particular a recombinant polypeptide or a recombinant protein, preferably a recombinant fusion protein or a recombinant fusion polypeptide.
  • recombinant as used herein (i.e. throughout the specification) means that it (here: the polypeptide or the protein) does not occur naturally.
  • the complex comprised by the combination for use according to the present invention which is a recombinant polypeptide or a recombinant protein, typically comprises components a) to c), wherein components a) to c) are of different origins, i.e. do not naturally occur in this combination.
  • peptide refers to peptide, oligopeptide, oligomer or protein including fusion protein, respectively, comprising at least two amino acids joined to each other, preferably by a normal peptide bond, or, alternatively, by a modified peptide bond, such as for example in the cases of isosteric peptides.
  • a peptide, polypeptide or protein can be composed of L-amino acids and/or D-amino acids.
  • a peptide, polypeptide or protein is either (entirely) composed of L-amino acids or (entirely) of D-amino acids, thereby forming “retro-inverso peptide sequences”.
  • the term “retro-inverso (peptide) sequences” refers to an isomer of a linear peptide sequence in which the direction of the sequence is reversed and the chirality of each amino acid residue is inverted (see e.g. Jameson et al., Nature, 368,744-746 (1994); Brady et al., Nature, 368,692-693 (1994)).
  • peptide also include “peptidomimetics” which are defined as peptide analogs containing non-peptidic structural elements, which peptides are capable of mimicking or antagonizing the biological action(s) of a natural parent peptide.
  • a peptidomimetic lacks classical peptide characteristics such as enzymatically scissile peptide bonds.
  • a peptide, polypeptide or protein can comprise amino acids other than the 20 amino acids defined by the genetic code in addition to these amino acids, or it can be composed of amino acids other than the 20 amino acids defined by the genetic code.
  • a peptide, polypeptide or protein in the context of the present invention can equally be composed of amino acids modified by natural processes, such as post-translational maturation processes or by chemical processes, which are well known to a person skilled in the art. Such modifications are fully detailed in the literature. These modifications can appear anywhere in the polypeptide: in the peptide skeleton, in the amino acid chain or even at the carboxy- or amino-terminal ends.
  • a peptide or polypeptide can be branched following an ubiquitination or be cyclic with or without branching. This type of modification can be the result of natural or synthetic post-translational processes that are well known to a person skilled in the art.
  • peptide in the context of the present invention in particular also include modified peptides, polypeptides and proteins.
  • peptide, polypeptide or protein modifications can include acetylation, acylation, ADP-ribosylation, amidation, covalent fixation of a nucleotide or of a nucleotide derivative, covalent fixation of a lipid or of a lipidic derivative, the covalent fixation of a phosphatidylinositol, covalent or non-covalent cross-linking, cyclization, disulfide bond formation, demethylation, glycosylation including pegylation, hydroxylation, iodization, methylation, myristoylation, oxidation, proteolytic processes, phosphorylation, prenylation, racemization, seneloylation, sulfatation, amino acid addition such as arginylation or ubiquitination.
  • the complex as described herein is a “classical” peptide, polypeptide or protein, whereby a “classical” peptide, polypeptide or protein is typically composed of amino acids selected from the 20 amino acids defined by the genetic code, linked to each other by a normal peptide bond.
  • the complex comprised by the combination for use according to the present invention is a polypeptide or a protein, it is preferred that it comprises at least 50, at least 60, at least 70, preferably at least 80, at least 90, more preferably at least 100, at least 110, even more preferably at least 120, at least 130, particularly preferably at least 140, or most preferably at least 150 amino acid residues.
  • the CPP allows for efficient delivery, i.e. transport and loading, in particular of at least one antigen or antigenic epitope, into the antigen presenting cells (APCs), in particular into the dendritic cells (DCs) and thus to the dendritic cells' antigen processing machinery.
  • APCs antigen presenting cells
  • DCs dendritic cells
  • CPPs cell penetrating peptides
  • Cell penetrating peptides is generally used to designate short peptides that are able to transport different types of cargo molecules across plasma membrane, and, thus, facilitate cellular uptake of various molecular cargoes (from nanosize particles to small chemical molecules and large fragments of DNA).
  • Cellular internalization of the cargo molecule linked to the cell penetrating peptide generally means transport of the cargo molecule across the plasma membrane and thus entry of the cargo molecule into the cell.
  • the cargo molecule can, then, be released in the cytoplasm, directed to an intracellular organelle, or further presented at the cell surface.
  • Cell penetrating ability, or internalization, of the cell penetrating peptide or of the complex (comprising said cell penetrating peptide) comprised by the combination for use according to the invention can be checked by standard methods known to one skilled in the art, including flow cytometry or fluorescence microscopy of live and fixed cells, immunocytochemistry of cells transduced with said peptide or complex, and Western blot.
  • Cell penetrating peptides typically have an amino acid composition that either contains a high relative abundance of positively charged amino acids such as lysine or arginine or have a sequence that contains an alternating pattern of polar/charged amino acids and non-polar, hydrophobic amino acids. These two types of structures are referred to as polycationic or amphipathic, respectively.
  • Cell-Penetrating peptides are of different sizes, amino acid sequences, and charges but all CPPs have a common characteristic that is the ability to translocate the plasma membrane and facilitate the delivery of various molecular cargoes to the cytoplasm or to an organelle of a cell.
  • CPP translocation distinguish three main entry mechanisms: direct penetration in the membrane, endocytosis-mediated entry, and translocation through the formation of a transitory structure.
  • CPP transduction is an area of ongoing research.
  • Cell-penetrating peptides have found numerous applications in medicine as drug delivery agents in the treatment of different diseases including cancer and virus inhibitors, as well as contrast agents for cell labeling and imaging.
  • cell penetrating peptides are peptides of 8 to 50 residues that have the ability to cross the cell membrane and enter into most cell types. Alternatively, they are also called protein transduction domain (PTDs) reflecting their origin as occurring in natural proteins. Frankel and Pabo simultaneously to Green and Lowenstein described the ability of the trans-activating transcriptional activator from the human immunodeficiency virus 1 (HIV-TAT) to penetrate into cells (Frankel, A. D. and C. O. Pabo, Cellular uptake of the tat protein from human immunodeficiency virus. Cell, 1988. 55(6): p. 1189-93).
  • HV-TAT human immunodeficiency virus 1
  • the first 16-mer peptide CPP called Penetratin having the amino acid sequence RQIKIYFQNRRMKWKK (SEQ ID NO: 1) was characterized from the third helix of the homeodomain of Antennapedia (Derossi, D., et al., The third helix of the Antennapedia homeodomain translocates through biological membranes. J Biol Chem, 1994. 269(14): p. 10444-50), followed in 1998 by the identification of the minimal domain of TAT, having the amino acid sequence YGRKKRRQRRR (SEQ ID NO: 2) required for protein transduction (Vives, E., P. Brodin, and B.
  • venoms e.g. melittin (Dempsey, C. E., The actions of melittin on membranes. Biochim Biophys Acta, 1990. 1031(2): p. 143-61), mastoporan (Konno, K., et al., Structure and biological activities of eumenine mastoparan-AF (EMP-AF), a new mast cell degranulating peptide in the venom of the solitary wasp ( Anterhynchium flavomarginatum micado ). Toxicon, 2000. 38(11): p.
  • maurocalcin Esteve, E., et al., Transduction of the scorpion toxin maurocalcine into cells. Evidence that the toxin crosses the plasma membrane. J Biol Chem, 2005. 280(13): p. 12833-9
  • crotamine Nascimento, F. D., et al., Crotamine mediates gene delivery into cells through the binding to heparan sulfate proteoglycans. J Biol Chem, 2007. 282(29): p. 21349-60
  • buforin Kobayashi, S., et al., Membrane translocation mechanism of the antimicrobial peptide buforin 2. Biochemistry, 2004.
  • CPPs were also designed including the poly-arginine (R8, R9, R10 and R12) (Futaki, S., et al., Arginine-rich peptides. An abundant source of membrane-permeable peptides having potential as carriers for intracellular protein delivery. J Biol Chem, 2001. 276(8): p. 5836-40) or transportani (Pooga, M., et al., Cell penetration by transportan. FASEB J, 1998. 12(1): p. 67-77). Any of the above described CPPs may be used as cell penetrating peptide, i.e.
  • component a), in the complex comprised by the combination for use according to the present invention may comprise the minimal domain of TAT, having the amino acid sequence YGRKKRRQRRR (SEQ ID NO: 2).
  • the component a), i.e. the CPP, in the complex comprised by the combination for use according to the present invention may comprise Penetratin having the amino acid sequence RQIKIYFQNRRMKWKK (SEQ ID NO: 1).
  • CPPs which can be used as cell penetrating peptide, i.e. as component a), in the complex comprised by the composition for use according to the present invention, are also disclosed in the review: Milletti, F., Cell-penetrating peptides: classes, origin, and current landscape. Drug Discov Today 17 (15-16): 850-60, 2012. In other words, the CPPs disclosed in Milletti, F., 2012, Cell-penetrating peptides: classes, origin, and current landscape. Drug Discov Today 17 (15-16): 850-60 can be used as cell penetrating peptide, i.e. as component a), in the complex comprised by the combination for use according to the present invention.
  • the cell penetrating peptide which is comprised by the complex
  • the cell penetrating peptide which is comprised by the complex
  • ZEBRA also known as Zta, Z, EB1, or BZLF1 generally means the basic-leucine zipper (bZIP) transcriptional activator of the Epstein-Barr virus (EBV).
  • bZIP basic-leucine zipper
  • EBV Epstein-Barr virus
  • the amino acid sequence of ZEBRA is disclosed under NCBI accession number YP_401673 and comprises 245 amino acids represented in SEQ ID NO: 3:
  • such a CPP can deliver multi-epitopic peptides to dendritic cells (DCs), and subsequently to promote CTL and Th cell activation and anti-tumor function.
  • DCs dendritic cells
  • Such a CPP can thus efficiently deliver the complex comprised by the combination for use according to the present invention to antigen presenting cells (APCs) and lead to multi-epitopic MHC class I and II restricted presentation.
  • APCs antigen presenting cells
  • MHC class I designates one of the two primary classes of the Major Histocompatibility Complex molecules.
  • the MHC class I (also noted “MHC I”) molecules are found on every nucleated cell of the body.
  • the function of MHC class I is to display an epitope to cytotoxic cells (CTLs).
  • CTLs cytotoxic cells
  • MHC class I molecules consist of two polypeptide chains, ⁇ - and ⁇ 2-microglobulin (b2m). Only the ⁇ chain is polymorphic and encoded by a HLA gene, while the b2m subunit is not polymorphic and encoded by the Beta-2 microglobulin gene.
  • MHC class II designates the other primary class of the Major Histocompatibility Complex molecules.
  • the MHC class II also noted “MHC II” molecules are found only on a few specialized cell types, including macrophages, dendritic cells and B cells, all of which are dedicated antigen-presenting cells (APCs).
  • APCs dedicated antigen-presenting cells
  • the sequence variant of a fragment of the minimal domain of ZEBRA as described above shares, in particular over the whole length, at least 70%, at least 75%, preferably at least 80%, more preferably at least 85%, even more preferably at least 90%, particularly preferably at least 95%, most preferably at least 99% amino acid sequence identity with the fragment of the minimal domain of ZEBRA as described above without abrogating the cell penetrating ability of the cell penetrating peptide.
  • a “fragment” of the minimal domain of ZEBRA as defined above is preferably to be understood as a truncated sequence thereof, i.e.
  • an amino acid sequence which is N-terminally, C-terminally and/or intrasequentially truncated compared to the amino acid sequence of the native sequence.
  • a “fragment” of the minimal domain of ZEBRA has preferably a length of 5 to 50 amino acids in total, preferably of 10 to 45 amino acids in total, more preferably of 15 to 45 amino acids in total.
  • sequence variant refers to any alteration in a reference sequence.
  • sequence variant includes nucleotide sequence variants and amino acid sequence variants.
  • a reference sequence is any of the sequences listed in the “Table of Sequences and SEQ ID Numbers” (Sequence listing), i.e. SEQ ID NO: 1 to SEQ ID NO: 47.
  • a sequence variant shares, in particular over the whole length of the sequence, at least 70%, at least 75%, preferably at least 80%, more preferably at least 85%, even more preferably at least 90%, particularly preferably at least 95%, most preferably at least 99% sequence identity with a reference sequence, whereby sequence identity is calculated as described below.
  • a sequence variant preserves the specific function of the reference sequence. Sequence identity is calculated as described below.
  • an amino acid sequence variant has an altered sequence in which one or more of the amino acids in the reference sequence is deleted or substituted, or one or more amino acids are inserted into the sequence of the reference amino acid sequence.
  • the amino acid sequence variant has an amino acid sequence which is at least 70%, at least 75%, preferably at least 80%, more preferably at least 85%, even more preferably at least 90%, particularly preferably at least 95%, most preferably at least 99% identical to the reference sequence.
  • variant sequences which are at least 90% identical have no more than 10 alterations, i.e. any combination of deletions, insertions or substitutions, per 100 amino acids of the reference sequence.
  • an amino acid sequence “sharing a sequence identity” of at least, for example, 95% to a query amino acid sequence of the present invention is intended to mean that the sequence of the subject amino acid sequence is identical to the query sequence except that the subject amino acid sequence may include up to five amino acid alterations per each 100 amino acids of the query amino acid sequence.
  • up to 5% (5 of 100) of the amino acid residues in the subject sequence may be inserted or substituted with another amino acid or deleted, preferably within the above definitions of variants or fragments.
  • nucleic acid sequences also applies similarly to nucleic acid sequences.
  • a “% identity” of a first sequence may be determined with respect to a second sequence.
  • these two sequences to be compared are aligned to give a maximum correlation between the sequences. This may include inserting “gaps” in either one or both sequences, to enhance the degree of alignment.
  • a % identity may then be determined over the whole length of each of the sequences being compared (so-called global alignment), that is particularly suitable for sequences of the same or similar length, or over shorter, defined lengths (so-called local alignment), that is more suitable for sequences of unequal length.
  • programs available in the Wisconsin Sequence Analysis Package, version 9.1 may be used to determine the % identity between two polynucleotides and the % identity and the % homology or identity between two polypeptide sequences.
  • BESTFIT uses the “local homology” algorithm of (Smith and Waterman (1981), J. Mol. Biol. 147, 195-197.) and finds the best single region of similarity between two sequences.
  • the fragments of the cell penetrating peptide or the variants thereof as described above further retain said peptide's ability to present a cargo molecule such as antigens or antigenic epitopes at the surface of a cell, such as an antigen-presenting cell, in the context of MHC class I and/or MHC class II molecules.
  • a cargo molecule such as antigens or antigenic epitopes at the surface of a cell, such as an antigen-presenting cell, in the context of MHC class I and/or MHC class II molecules.
  • a cell penetrating peptide or complex comprising said cell penetrating peptide to present a cargo molecule such as antigens or antigenic epitopes at the surface of a cell in the context of MHC class I and/or MHC class II molecules can be checked by standard methods known to one skilled in the art, including capacity to stimulate proliferation and/or function of MHC-restricted CD4 + or CD8 + T cells with specificity for these epitopes.
  • substitutions for one or more amino acids present in the referenced amino acid sequence should be made conservatively.
  • conservative substitutions include substitution of one aliphatic residue for another, such as lie, Val, Leu, or Ala for one another, or substitutions of one polar residue for another, such as between Lys and Arg; Glu and Asp; or Gin and Asn.
  • Other such conservative substitutions for example, substitutions of entire regions having similar hydrophobicity properties, are well known (Kyte and Doolittle, 1982 , J. Mol. Biol. 157(1):105-132).
  • Substitutions of one or more L-amino acids with one or more D-amino acids are to be considered as conservative substitutions in the context of the present invention.
  • Exemplary amino acid substitutions are presented in Table 1 below:
  • the preferred cell penetrating peptide which
  • such a preferred cell penetrating peptide has an amino acid sequence comprising a sequence according to the following general formula (I):
  • such a peptide, polypeptide or protein is either (entirely) composed of L-amino acids or (entirely) of D-amino acids, thereby forming “retro-inverso peptide sequences”.
  • the term “retro-inverso (peptide) sequences” refers to an isomer of a linear peptide sequence in which the direction of the sequence is reversed and the chirality of each amino acid residue is inverted (see e.g. Jameson et al., Nature, 368,744-746 (1994); Brady et al., Nature, 368,692-693 (1994)).
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 1 is K.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 2 is R.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 3 is Y.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 4 is K.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 5 is N.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 6 is R.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 7 is V.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 8 is A.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 9 is S.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 10 is R.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 11 is K.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 13 is R.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 14 is A.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 1s is K.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 16 is F.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein X 17 is K.
  • the cell penetrating peptide is as generically defined above by general formula (I), wherein the amino acid at position equivalent to position 12 relative to general formula (I) is a Ser (S).
  • a cell penetrating peptide which has an amino acid sequence comprising or consisting of an amino acid sequence according to SEQ ID NO: 6 (CPP3/Z13), SEQ ID NO: 7 (CPP4/Z14), SEQ ID NO: 8 (CPP5/Z15), or SEQ ID NO: 11 (CPP8/Z18), or sequence variants thereof without abrogating said peptide's cell penetrating ability, preferably sequence variants having 0, 1, 2, 3, 4, or 5 amino acids substituted, deleted and/or added without abrogating said peptide's cell penetrating ability.
  • a cell penetrating peptide is more preferred, which has an amino acid sequence comprising or consisting of an amino acid sequence according to SEQ ID NO: 6 (CPP3/Z13) or SEQ ID NO: 7 (CPP4/Z14) or sequence variants thereof without abrogating said peptide's cell penetrating ability, preferably sequence variants having 0, 1, 2, 3, 4, or 5 amino acids substituted, deleted and/or added without abrogating said peptide's cell penetrating ability.
  • a cell penetrating peptide which has an amino acid sequence comprising or consisting of an amino acid sequence according to SEQ ID NO: 6 (CPP3/Z13) or sequence variants thereof without abrogating said peptide's cell penetrating ability, preferably sequence variants having 0, 1, 2, 3, 4, or 5 amino acids substituted, deleted and/or added without abrogating said peptide's cell penetrating ability.
  • the cell penetrating peptide according to the invention has an amino acid sequence comprising or consisting of SEQ ID NO: 6 (CPP3/Z13).
  • the cell penetrating peptide according to the invention has an amino acid sequence comprising or consisting of SEQ ID NO: 7 (CPP4/Z14).
  • the cell penetrating peptide according to the invention has an amino acid sequence comprising or consisting of SEQ ID NO: 8 (CPP5/Z15).
  • the cell penetrating peptide according to the invention has an amino acid sequence comprising or consisting of SEQ ID NO: 11 (CPP8/Z18).
  • the primary amino acid sequence of the cell penetrating peptide may further be post-translationally modified, such as by glycosylation or phosphorylation, without departing from the invention.
  • the cell penetrating peptide optionally further comprises, in addition to its amino acid sequence as described above, any one of, or any combination of:
  • the cell penetrating peptide is linked to an antigen or antigenic epitope and facilitates the cellular internalization of said antigen or antigenic epitope.
  • the complex comprised by the combination for use according to the present invention may comprise one single cell penetrating peptide or more than one cell penetrating peptides.
  • the complex comprised by the combination for use according to the present invention comprises no more than five cell penetrating peptides, more preferably the complex comprised by the combination for use according to the present invention comprises no more than four cell penetrating peptides, even more preferably the complex comprised by the combination for use according to the present invention comprises no more than three cell penetrating peptides, particularly preferably the complex comprised by the combination for use according to the present invention comprises no more than two cell penetrating peptides and most preferably the complex comprised by the combination for use according to the present invention comprises one single cell penetrating peptide.
  • the complex comprised by the combination for use according to the present invention comprises as component b) at least one antigen or antigenic epitope.
  • an “antigen” is any structural substance which serves as a target for the receptors of an adaptive immune response, in particular as a target for antibodies, T cell receptors, and/or B cell receptors.
  • An “epitope”, also known as “antigenic determinant”, is the part (or fragment) of an antigen that is recognized by the immune system, in particular by antibodies, T cell receptors, and/or B cell receptors.
  • one antigen has at least one epitope, i.e. a single antigen has one or more epitopes.
  • epitope is mainly used to designate T cell epitopes, which are presented on the surface of an antigen-presenting cell, where they are bound to Major Histocompatibility Complex (MHC).
  • MHC Major Histocompatibility Complex
  • T cell epitopes presented by MHC class I molecules are typically, but not exclusively, peptides between 8 and 11 amino acids in length, whereas MHC class II molecules present longer peptides, generally, but not exclusively, between 12 and 25 amino acids in length.
  • the at least one antigen or antigenic epitope is selected from the group consisting of: (i) a peptide, a polypeptide, or a protein, (ii) a polysaccharide, (iii) a lipid, (iv) a lipoprotein or a lipopeptide, (v) a glycolipid, (vi) a nucleic acid, and (vii) a small molecule drug or a toxin.
  • the at least one antigen or antigenic epitope may be a peptide, a protein, a polysaccharide, a lipid, a combination thereof including lipoproteins and glycolipids, a nucleic acid (e.g. DNA, siRNA, shRNA, antisense oligonucleotides, decoy DNA, plasmid), or a small molecule drug (e.g. cyclosporine A, paclitaxel, doxorubicin, methotrexate, 5-aminolevulinic acid), or any combination thereof in particular if more than one antigen or antigenic epitope is comprised by the complex comprised by the combination for use according to the present invention.
  • a nucleic acid e.g. DNA, siRNA, shRNA, antisense oligonucleotides, decoy DNA, plasmid
  • a small molecule drug e.g. cyclosporine A, paclitaxel, doxorubicin, met
  • the at least one antigen or antigenic epitope can comprise for example at least one, i.e. one or more, peptides, polypeptides or proteins linked together and/or at least one, i.e. one or more, nucleic acids, e.g. where each one encodes one peptide or polypeptide.
  • the at least one antigen or antigenic epitope can be a combination of a protein, a lipid, and/or a polysaccharide including lipoproteins and glycolipids.
  • the complex comprised by the combination for use according to the present invention comprises more than one antigen or antigenic epitope
  • it can comprise more than one peptide, polypeptide, or protein, more than one polysaccharide, more than one lipid, more than one lipoprotein, more than one glycolipid, more than one nucleic acid, more than one small molecule drug or toxin, or a combination thereof.
  • the complex comprised by the combination for use according to the invention comprises at least one antigen or antigenic epitope comprising one or more epitope(s) from a cancer/tumor-associated antigen, a cancer/tumor-specific antigen, and/or an antigenic protein from a pathogen, including viral, bacterial, fungal, protozoal and multicellular parasitic antigenic protein.
  • the at least one antigen or antigenic epitope comprises or consists of (i) at least one pathogen epitope and/or (ii) at least one cancer/tumor epitope, in particular at least one tumor epitope.
  • the at least one antigen or antigenic epitope comprises or consists of at least one cancer/tumor epitope, in particular at least one tumor epitope.
  • the complex comprised by the combination for use according to the present invention comprises only such antigen(s) or antigenic epitope(s), which are cancer/tumor-associated antigen(s), cancer/tumor-specific antigen(s) and/or cancer/tumor epitope(s); in particular, which are tumor-associated antigen(s), tumor-specific antigen(s), and/or tumor epitope(s).
  • cancer epitope means an epitope from a cancer-associated antigen or from a cancer-specific antigen.
  • tumor epitope means an epitope from a tumor-associated antigen or from a tumor-specific antigen.
  • Such epitopes are typically specific (or associated) for a certain kind of cancer/tumor.
  • cancer/tumor epitopes include glioma epitopes.
  • cancer/tumor-associated (also cancer/tumor-related) antigens are antigens, which are expressed by both, cancer/tumor cells and normal cells. Accordingly, those antigens are normally present since birth (or even before).
  • Cancer/tumor-specific antigens are antigens, which are expressed specifically by cancer/tumor cells, but not by normal cells. Cancer/tumor-specific antigens include in particular neoantigens. In general neoantigens are antigens, which were not present before and are, thus, “new” to the immune system. Neoantigens are typically due to somatic mutations.
  • cancer/tumor-specific neoantigens were typically not present before the cancer/tumor developed and cancer/tumor-specific neoantigens are usually encoded by somatic gene mutations in the cancerous cells/tumor cells. Since neoantigens are new to the immune system, the risk of self-tolerance of those antigens is considerably lower as compared to cancer/tumor-associated antigens. However, every cancer's set of tumor-specific mutations appears to be unique.
  • cancer/tumor-specific antigens in particular neoantigens
  • neoantigens are identified in a subject diagnosed with a cancer by methods known to the skilled person, e.g., cancer genome sequencing.
  • the respective cancer/tumor-specific neoantigens and/or cancer/tumor-specific neoantigenic epitopes are used in the complex comprised by the combination for use according to the present invention.
  • a complex comprised by the combination for use according to the present invention comprises one or more cancer/tumor-associated epitopes and/or one or more cancer/tumor-associated antigens (but preferably no cancer/tumor-specific epitopes). It is also preferred that a complex comprised by the combination for use according to the present invention comprises one or more cancer/tumor-specific epitopes and/or one or more cancer/tumor-specific antigens (but preferably no cancer/tumor-associated epitopes).
  • a complex comprised by the combination for use according to the present invention may also preferably comprise both, (i) one or more cancer/tumor-associated epitopes and/or one or more cancer/tumor-associated antigens and (ii) one or more cancer/tumor-specific epitopes and/or one or more cancer/tumor-specific antigens.
  • Suitable cancer/tumor epitopes can be retrieved for example from cancer/tumor epitope databases, e.g. from van der Bruggen P, Stroobant V, Vigneron N, Van den Eynde B.
  • Peptide database T cell-defined tumor antigens. Cancer Immun 2013; URL: http://www.cancerimmunity.org/peptide/, wherein human tumor antigens recognized by CD4+ or CD8+ T cells are classified into four major groups on the basis of their expression pattern, or from the database “Tantigen” (TANTIGEN version 1.0, Dec.
  • cancer/tumor epitopes include e.g. TRP2-derived epitopes, glycoprotein 100 (gp100) melanoma antigen-derived epitopes, glycoprotein 70 (gp70) antigen-derived epitopes, survivin epitopes, IEa epitopes, IL13r ⁇ 2, Epha2 (ephrin type-A receptor 2), immunogenic fragments thereof, and fusions of such antigens and/or fragments.
  • cancer/tumor epitopes include epitopes of neoantigens, such as, for example, a neoantigen from MC-38 tumor cell line as described by Yadav et al. Nature. 2014 Nov. 27; 515(7528):572-6.
  • neoantigens are antigens, which are entirely absent from the normal human genome.
  • neoantigens are of relevance to tumor control, as the quality of the T cell pool that is available for these antigens is not affected by central T cell tolerance.
  • neoantigens may be based on individual tumor genomes. Potential neoantigens may be predicted by methods known to the skilled person, such as cancer genome sequencing or deep-sequencing technologies identifying mutations within the protein-coding part of the (cancer) genome.
  • cancer/tumor-associated, in particular tumor-related, or tissue-specific antigens useful in a complex comprised by the combination for use according to the present invention include, but are not limited to, the following antigens: Prostate: prostate-specific antigen (PSA), prostate-specific membrane antigen (PSMA), PAP, PSCA (PNAS 95(4) 1735-1740 1998), prostate mucin antigen (PMA) (Beckett and Wright, 1995, Int. J.
  • Cancer 62: 703-710) Prostase, Her-2neu, SPAS-1; Melanoma: TRP-2, tyrosinase, Melan A/Mart-1, gpIOO, BAGE, GAGE, GM2 ganglioside; Breast: Her2-neu, kinesin 2, TATA element modulatory factor 1, tumor protein D52, MAGE D, ING2, HIP-55, TGF-1 anti-apoptotic factor, HOM-Mel-40/SSX2, epithelial antigen (LEA 135), DF31MUC1 antigen (Apostolopoulos et al., 1996 Immunol. Cell. Biol. 74: 457-464; Pandey et al., 1995, Cancer Res.
  • Testis MAGE-1, HOM-Mel-40/SSX2, NY-ESO-1; Colorectal: EGFR, CEA; Lung: MAGE D, EGFR Ovarian Her-2neu; Baldder: transitional cell carcinoma (TCC) (Jones et al., 1997, Anticancer Res.
  • the cancer/tumor antigen or the cancer/tumor epitope is a recombinant cancer/tumor antigen or a recombinant cancer/tumor epitope.
  • a recombinant cancer/tumor antigen or a recombinant cancer/tumor epitope may be designed by introducing mutations that change (add, delete or substitute) particular amino acids in the overall amino acid sequence of the native cancer/tumor antigen or the native cancer/tumor epitope.
  • the introduction of mutations does not alter the cancer/tumor antigen or the cancer/tumor epitope so much that it cannot be universally applied across a mammalian subject, and preferably a human or dog subject, but changes it enough that the resulting amino acid sequence breaks tolerance or is considered a foreign antigen in order to generate an immune response.
  • Another manner may be creating a consensus recombinant cancer/tumor antigen or cancer/tumor epitope that has at least 85% and up to 99% amino acid sequence identity to its' corresponding native cancer/tumor antigen or native cancer/tumor epitope; preferably at least 90% and up to 98% sequence identity; more preferably at least 93% and up to 98% sequence identity; or even more preferably at least 95% and up to 98% sequence identity.
  • the recombinant cancer/tumor antigen or the recombinant cancer/tumor epitope has 95%, 96%, 97%, 98%, or 99% amino acid sequence identity to its' corresponding native cancer/tumor antigen or cancer/tumor epitope.
  • the native cancer/tumor antigen is the antigen normally associated with the particular cancer or cancer tumor.
  • the consensus sequence of the cancer/tumor antigen can be across mammalian species or within subtypes of a species or across viral strains or serotypes. Some cancer/tumor antigen do not vary greatly from the wild type amino acid sequence of the cancer/tumor antigen.
  • the aforementioned approaches can be combined so that the final recombinant cancer/tumor antigen or cancer/tumor epitope has a percent similarity to native cancer antigen amino acid sequence as discussed above.
  • the amino acid sequence of an epitope of a cancer/tumor antigen as described herein is not mutated and, thus, identical to the reference epitope sequence.
  • pathogen epitope means an epitope from an antigenic protein, an antigenic polysaccharide, an antigenic lipid, an antigenic lipoprotein or an antigenic glycolipid from a pathogen including viruses, bacteria, fungi, protozoa and multicellular parasites.
  • Antigenic proteins, polysaccharides, lipids, lipoproteins or glycolipids from pathogens include, herewith, proteins, polysaccharides, lipids, lipoproteins and glycolipids, respectively, from pathogens responsible of diseases which can be a target for vaccination including, for instance, Amoebiasis, Anthrax, Buruli Ulcer ( Mycobacterium ulcerans ), Caliciviruses associated diarrhoea, Campylobacter diarrhoea, Cervical Cancer (Human papillomavirus), Chlamydia trachomatis associated genital diseases, Cholera, Crimean-Congo haemorrhagic fever, Dengue Fever, Diptheria, Ebola haemorrhagic fever, Enterotoxigenic Escherichia coli (ETEC) diarrhoea, Gastric Cancer ( Helicobacter pylori ), Gonorrhea, Group A Streptococcus associated diseases, Group
  • the at least one antigen or antigenic epitope will be presented at the cell surface in an MHC class I and/or MHC class II context and/or in a CD1 context, whereby presentation at the cell surface in an MHC class I and/or MHC class II context is preferred.
  • the phrase “epitope presentation in the MHC class I context” refers in particular to a CD8 + epitope lying in the groove of a MHC class I molecule at the surface of a cell.
  • the phrase “epitope presentation in the MHC class II context” refers in particular to a CD4 + epitope lying in the groove of a MHC class II molecule at the surface of a cell.
  • the phrase “epitope presentation in the CD1 context” refers in particular to a lipidic epitope lying in the groove of a cluster of differentiation 1 molecule at the surface of a cell.
  • the complex comprised by the combination for use according to the invention comprises a cell penetrating peptide and at least one antigen or antigenic epitope, and allows the transport and presentation of said epitopes at the cell surface of antigen presenting cells in an MHC class I and MHC class II context, and is, thus, useful in vaccination and immunotherapy.
  • the complex comprised by the combination for use according to the present invention comprises at least one antigen or antigenic epitope, which is at least one CD4 + epitope and/or at least one CD8 + epitope.
  • CD4 epitope or “CD4-restricted epitope”, as used herein, designate an epitope recognized by a CD4 + T cell, said epitope in particular consisting of an antigen fragment lying in the groove of a MHC class II molecule.
  • a single CD4 + epitope comprised in the complex comprised by the combination for use according to the present invention preferably consists of about 12-25 amino acids. It can also consist of, for example, about 8-25 amino acids or about 6-100 amino acids.
  • CD8 + epitope or “CD8 + -restricted epitope”, as used herein, designate an epitope recognized by a CD8 + T cell, said epitope in particular consisting of an antigen fragment lying in the groove of a MHC class I molecule.
  • a single CD8 + epitope comprised in the complex comprised by the combination for use according to the present invention preferably consists of about 8-11 amino acids. It can also consist of, for example, about 8-15 amino acids or about 6-100 amino acids.
  • the at least one antigen can comprise or the at least one antigenic epitope can consist of a CD4 + epitope and/or a CD8 + epitope corresponding to antigenic determinant(s) of a cancer/tumor-associated antigen, a cancer/tumor-specific antigen, or an antigenic protein from a pathogen. More preferably, the at least one antigen can comprise or the at least one antigenic epitope can consist of a CD4 + epitope and/or a CD8 + epitope corresponding to antigenic determinant(s) of a cancer/tumor-associated antigen or a cancer/tumor-specific antigen.
  • the at least one antigen can comprise or the at least one antigenic epitope can consist of a CD4 + epitope and/or a CD8 + epitope corresponding to antigenic determinant(s) of a tumor-associated antigen or a tumor-specific antigen.
  • the complex comprised by the combination for use according to the present invention comprises at least two antigens or antigenic epitopes, wherein at least one antigen or antigenic epitope comprises or consists a CD4 + epitope and at least one antigen or antigenic epitope comprises or consists a CD8 + epitope.
  • a complex comprised by the combination for use according to the present invention comprising at least two antigens or antigenic epitopes, wherein at least one antigen or antigenic epitope comprises or consists of a CD4 + epitope and at least one antigen or antigenic epitope comprises or consists a CD8 + epitope, provides an integrated immune response allowing simultaneous priming of CTLs and T h cells and is thus preferable to immunity against only one CD8 + epitope or only one CD4 + epitope.
  • the complex comprised by the combination for use according to the present invention may preferably comprise an Ealpha-CD4 + epitope and a gp100-CD8 + epitope.
  • the complex comprised by the combination for use according to the present invention comprises at least two antigens or antigenic epitopes, wherein the at least two antigens or antigenic epitopes comprise or consist of at least two, e.g. 2, 3, 4, 5, 6, 7, 8, 9, or more, CD4 + epitopes and/or at least two, e.g. 2, 3, 4, 5, 6, 7, 8, 9, or more, CD8+ epitopes.
  • the at least two antigens or antigenic epitopes are preferably different antigens or antigenic epitopes, more preferably the at least two antigens or antigenic epitopes are different from each other but relating to the same kind of tumor.
  • a multi-antigenic vaccine will (i) avoid outgrowth of antigen-loss variants, (ii) target different tumor cells within a heterogeneous tumor mass and (iii) circumvent patient-to-patient tumor variability.
  • the complex comprised by the combination for use according to the present invention particularly preferably comprises at least four antigens or antigenic epitopes, in particular with at least two CD8 + epitopes and at least two CD4 + epitopes.
  • Such a complex comprised by the combination for use according to the present invention induces multi-epitopic CD8 CTLs and CD4 T h cells to function synergistically to counter tumor cells and promote efficient anti-tumor immunity.
  • T h cells are also involved in the maintenance of long-lasting cellular immunity that was monitored after vaccination.
  • Such a complex comprised by the combination for use according to the present invention induces polyclonal, multi-epitopic immune responses and poly-functional CD8 + and CD4 + T cells, and thus efficacious anti-tumor activity.
  • the complex comprised by the combination for use according to the present invention comprises at least two antigens or antigenic epitopes, more preferably the complex comprised by the combination for use according to the present invention comprises at least three antigens or antigenic epitopes, even more preferably the complex comprised by the combination for use according to the present invention comprises at least four antigens or antigenic epitopes, particularly preferably the complex comprised by the combination for use according to the present invention comprises at least five antigens or antigenic epitopes and most preferably the complex comprised by the combination for use according to the present invention comprises at least six antigens or antigenic epitopes.
  • the antigens or antigenic epitopes comprised by the complex may be the same or different, preferably the antigens or antigenic epitopes comprised by the complex are different from each other.
  • the complex comprises at least one CD4 + epitope and at least one CD8 + epitope.
  • the complex comprised by the combination for use according to the present invention comprises more than one CD4 + epitope, e.g. two or more CD4 + epitopes from the same antigen or from different antigens, and preferably no CD8 + epitope. It is also preferred that the complex comprised by the combination for use according to the present invention comprises more than one CD8 + epitope, e.g. two or more CD8 + epitopes from the same antigen or from different antigens, and preferably no CD4 + epitope. Most preferably, however, the complex comprised by the combination for use according to the present invention comprises (i) at least one CD4 + epitope, e.g.
  • CD4 + epitopes from the same antigen or from different antigens
  • CD8 + epitope e.g. two or more CD8 + epitopes from the same antigen or from different antigens.
  • the complex comprised by the combination for use according to the present invention may preferably comprise a gp100-CD8 + epitope, an Ealpha-CD4 + epitope, and a further CD4 + epitope and a further CD8 + epitope.
  • the complex comprised by the combination for use according to the present invention may comprise a polypeptide or protein comprising a gp 100-CD8 + epitope and an Ealpha-CD4 + epitope.
  • such a polypeptide or protein comprised by the complex comprised by the combination for use according to the present invention comprises or consists of an amino acid sequence according to SEQ ID NO: 14 or sequence variants thereof as defined above:
  • the complex comprised by the combination for use according to the present invention may preferably comprise a gp70-CD8 + epitope and/or a gp70-CD4 + epitope.
  • the complex comprised by the combination for use according to the present invention may comprise a polypeptide or protein comprising a gp70-CD8 + epitope and/or a gp70-CD4 + epitope.
  • such a polypeptide or protein comprised by the complex comprised by the combination for use according to the present invention comprises or consists of an amino acid sequence according to SEQ ID NO: 36 or sequence variants thereof as defined above:
  • the complex comprised by the combination for use according to the present invention may preferably comprise at least one survivin epitope, such as a survivin CD8 + epitope and/or a survivin CD4 + epitope. More preferably, the complex comprised by the combination for use according to the present invention may comprise a polypeptide or protein comprising a survivin CD8 + epitope and/or a survivin CD4 + epitope. More preferably, the complex comprised by the combination for use according to the present invention may comprise a polypeptide or protein comprising more than one survivin CD8 + epitope and/or more than one survivin CD4 + epitope, such as two different survivin CD8 + epitopes. For example, such a polypeptide or protein comprised by the complex comprised by the combination for use according to the present invention comprises or consists of an amino acid sequence according to SEQ ID NO: 37 or sequence variants thereof as defined above:
  • the complex comprised by the combination for use according to the present invention may preferably comprise an epitope from a neoantigen.
  • the complex comprised by the combination for use according to the present invention may comprise a polypeptide or protein comprising an epitope from a neoantigen, such as the neoantigen from MC-38 tumor cell line identified by Yadav et al. Nature. 2014 Nov. 27; 515(7528):572-6.
  • a polypeptide or protein comprised by the complex comprised by the combination for use according to the present invention comprises or consists of an amino acid sequence according to SEQ ID NO: 38 or sequence variants thereof as defined above:
  • the complex comprised by the combination for use according to the present invention may preferably comprise more than one, e.g. two or three, epitopes from neoantigens.
  • the complex comprised by the combination for use according to the present invention may comprise a polypeptide or protein comprising more than one, e.g. two or three, epitopes from neoantigens, such as the neoantigens from MC-38 tumor cell line identified by Yadav et al. Nature. 2014 Nov. 27; 515(7528):572-6.
  • such a polypeptide or protein comprised by the complex comprised by the combination for use according to the present invention comprises or consists of an amino acid sequence according to SEQ ID NO: 39 or sequence variants thereof as defined above:
  • SEQ ID NO: 39 LFRAAQLANDVVLQIMEHLELASMTNMELMSSIVVISASIIVFNLLELEG (Mad12-cargo comprising the epitope from a neo- antigen as described by Yadav et al. Nature. 2014 Nov. 27; 515(7528): 572-6).
  • the at least one antigen or antigenic epitope comprised by the complex comprised by the combination for use according to the present invention is a peptide, polypeptide, or a protein.
  • antigen or antigenic epitope of peptidic, polypeptidic, or proteic nature useful in the invention include cancer/tumor antigens or antigenic epitopes thereof, allergy antigens or antigenic epitopes thereof, auto-immune self-antigens or antigenic epitopes thereof, pathogenic antigens or antigenic epitopes thereof, and antigens or antigenic epitopes thereof from viruses, preferably from cytomegalovirus (CMV), orthopox variola virus, orthopox alastrim virus, parapox ovis virus, molluscum contagiosum virus, herpes simplex virus 1, herpes simplex virus 2, herpes B virus, varicella zoster virus, pseudorabies virus, human cytomegaly virus, human herpes virus 6, human
  • CMV
  • human immunodeficiency virus type 1 or human immunodeficiency virus type 2 influenza virus, Lassa virus, lymphocytic choriomeningitis virus, Tacaribe virus, Junin virus, Machupo virus, Borna disease virus, Bunyamwera virus, California encephalitis virus, Rift Valley fever virus, sand fly fever virus, Toscana virus, Crimean-Congo haemorrhagic fever virus, Hazara virus, Khasan virus, Hantaan virus, Seoul virus, Prospect Hill virus, Puumala virus, Dobrava Belgrade virus, Tula virus, sinari virus, Lake Victoria Marburg virus, Zaire Ebola virus, Sudan Ebola virus, Ivory Coast Ebola virus, influenza virus A, influenza virus B, influenza viruses C, parainfluenza virus, malaria parasite ( Plasmodium falciparum, Plasmodium vivax, Plasmodium ovale, Plasmodium malariae, Plasmodium knowlesi ), Marburg virus, meas
  • epitopes as well as variants of antigens as defined above exhibit a sequence homology or identity of about 10%, in particular at least 10%, about 20%, in particular at least 20%, about 30%, in particular at least 30%, about 40%, in particular at least 40%, about 50%, in particular at least 50%, about 60%, in particular at least 60%, about 70%, in particular at least 70%, about 80%, in particular at least 80%, about 90% in particular at least 90%, at least 95% or at least 98% with one of the antigens or antigen sequences as shown or described above.
  • epitopes and variants similarly applies as defined.
  • antigens or antigenic epitopes in the category of peptide, polypeptide or protein include a combination of multiple glioma epitopes such as those described in Novellino et al. (2005 , Cancer Immunol Immunother, 54(3):187-207), Vigneron et al. (2013 , Cancer Immun. 13:15).
  • a single complex comprised by the combination for use according to the present invention may also comprise only a subset, i.e. one or more of all of said glioma epitopes.
  • different complexes comprised by the combination for use according to the present invention comprise different subsets of all of said glioma epitopes, so that for example a vaccine according to the present invention comprising such different complexes comprises all of said glioma epitopes but distributed in the different complexes.
  • a complex comprised by the combination for use according to the invention may also comprise at least one antigen or antigenic epitope, wherein said antigen or antigenic epitope is a polysaccharide, a lipid, a lipoprotein, and/or a glycolipid, in particular a polysaccharidic, lipidic, lipoproteic, and/or glycolipidic epitope, which can be, for example, pathogen epitopes as defined herewith.
  • the complex comprised by the combination for use according to the invention may comprise at least one antigen or antigenic epitope, wherein said antigen or antigenic epitope is polysaccharidic, lipidic, lipoproteic, and/or glycolipidic, including viral, bacterial, fungal, protozoal and multicellular parasitic antigens or antigenic epitopes.
  • said epitopes will be presented at the cell surface in an MHC class I and/or MHC class II context.
  • said lipidic epitopes will be presented at the cell surface in a CD1 (cluster of differentiation 1) context.
  • the complex comprised by the combination for use according to the present invention may also comprise at least one antigen or antigenic epitope, wherein said antigen or antigenic epitope is a small molecule drug or toxin.
  • cargo molecules within the category of small molecule drugs or toxins useful in the invention include cyclosporine A, paclitaxel, doxorubicin, methotrexate, 5-aminolevulinic acid, diphtheria toxin, sunitinib and those molecules reviewed in De wit Amer (2010 , Neuro Oncol, 12(3):304-16).
  • the complex comprised by the combination for use according to the present invention comprises at least one antigen or antigenic epitope, preferably the complex comprised by the combination for use according to the present invention comprises more than one antigen or antigenic epitope, in particular 2, 3, 4, 5, 6, 7, 8, 9, 10 or more antigens or antigenic epitopes, more preferably the complex comprised by the combination for use according to the present invention comprises (at least) two or three antigens or antigenic epitopes, even more preferably the complex comprised by the combination for use according to the present invention comprises (at least) four or five antigens or antigenic epitopes.
  • antigen or antigenic epitope is comprised by the complex comprised by the combination for use according to the present invention it is understood that said antigen or antigenic epitope is in particular also covalently linked in the complex comprised by the combination for use according to the present invention, e.g. to another antigen or antigenic epitope and/or to a component a), i.e. a cell penetrating peptide, and/or to a component c), i.e. a TLR peptide agonist.
  • the various antigens or antigenic epitopes comprised by the complex may be the same or different.
  • the various antigens or antigenic epitopes comprised by the complex are different from each other, thus providing a multi-antigenic and/or multi-epitopic complex.
  • the more than one antigen or antigenic epitope in particular 2, 3, 4, 5, 6, 7, 8, 9, 10 or more antigens or antigenic epitopes, are positioned consecutively in the complex comprised by the combination for use according to the present invention.
  • all antigens and/or antigenic epitopes comprised by the complex are positioned in a stretch, which is neither interrupted by component a), i.e. a cell penetrating peptide, nor by component c), i.e. a TLR peptide agonist.
  • component a) and component c) are positioned in the complex for example before or after such a stretch of all antigens and/or antigenic epitopes.
  • the antigens and/or antigenic epitopes positioned consecutively in such a way may be linked to each other for example by a spacer or linker as described below, which is neither component a), i.e. a cell penetrating peptide, nor component c), i.e. a TLR peptide agonist.
  • the various antigens and/or antigenic epitopes may also be positioned in any other way in the complex comprised by the combination for use according to the present invention, for example with component a) and/or component c) positioned in between two or more antigens and/or antigenic epitopes, i.e. with one or more antigens and/or antigenic epitopes positioned between component a) and component c) (or vice versa) and, optionally, one or more antigens and/or antigenic epitopes positioned at the respective other end of component a) and/or component c).
  • a number of different antigens or antigenic epitopes relating to the same kind of disease, in particular to the same kind of tumor may be advantageously comprised by a single complex.
  • a number of different antigens or antigenic epitopes relating to the same kind of disease, in particular to the same kind of tumor may be distributed to subsets of different antigens or antigenic epitopes, in particular subsets complementing each other in the context of a certain kind of disease, e.g. tumor, which are comprised by different complexes, whereby such different complexes comprising different subsets may advantageously be administered simultaneously, e.g. in a single vaccine, to a subject in need thereof.
  • the complex according to the present invention comprises at least one tumor epitope, which is an epitope of an antigen selected from the group consisting of EpCAM, HER-2/neu, MUC-1, TOMM34, RNF 43, KOC1, VEGFR, ⁇ hCG, survivin, CEA, TGF ⁇ R2, p53, KRas, OGT, CASP5, COA-1, MAGE, SART, IL13Ralpha2, CMV, EGFRvIII, EphA2, gp100, hTert, TRP-2, YKL-40, brevican, neuroligin 4 and PTPRz1.
  • an antigen selected from the group consisting of EpCAM, HER-2/neu, MUC-1, TOMM34, RNF 43, KOC1, VEGFR, ⁇ hCG, survivin, CEA, TGF ⁇ R2, p53, KRas, OGT, CASP5, COA-1, MAGE, SART, IL13Ralpha2, CMV, EGFR
  • the complex according to the present invention comprises at least one tumor antigen selected from the group consisting of EpCAM, HER-2/neu, MUC-1, TOMM34, RNF 43, KOC1, VEGFR, ⁇ hCG, survivin, CEA, TGFR2, p53, KRas, OGT, CASP5, COA-1, MAGE, SART, IL13Ralpha2, CMV, EGFRvIII, EphA2, gp100, hTert, TRP-2, YKL-40, brevican, neuroligin 4 and PTPRz1 or a fragment thereof, or a sequence variant of a tumor antigen or a sequence variant of a fragment thereof.
  • tumor antigen selected from the group consisting of EpCAM, HER-2/neu, MUC-1, TOMM34, RNF 43, KOC1, VEGFR, ⁇ hCG, survivin, CEA, TGFR2, p53, KRas, OGT, CASP5, COA-1, MAGE, SART
  • the complex according to the present invention comprises at least one tumor epitope, which is an epitope of an antigen selected from the glioma antigens disclosed by Reardon, D. A., et al., An update on vaccine therapy and other immunotherapeutic approaches forglioblastoma . Expert Rev Vaccines, 2013. 12(6): p. 597-615.
  • a “fragment” of an antigen comprises at least 10 consecutive amino acids of the antigen, preferably at least 15 consecutive amino acids of the antigen, more preferably at least 20 consecutive amino acids of the antigen, even more preferably at least 25 consecutive amino acids of the antigen and most preferably at least 30 consecutive amino acids of the antigen.
  • a “sequence variant” is as defined above, namely a sequence variant has an (amino acid) sequence which is at least 70%, at least 75%, preferably at least 80%, more preferably at least 85%, even more preferably at least 90%, particularly preferably at least 95%, most preferably at least 99% identical to the reference sequence.
  • a “functional” sequence variant means in the context of an antigen/antigen fragment/epitope, that the function of the epitope(s), e.g. comprised by the antigen (fragment), is not impaired or abolished.
  • the amino acid sequence of the epitope(s), e.g. comprised by the cancer/tumor antigen (fragment) as described herein is not mutated and, thus, identical to the reference epitope sequence.
  • cancer/tumor epitopes of those antigens are known from the literature or can be identified by using cancer/tumor epitope databases, e.g. from van der Bruggen P, Stroobant V, Vigneron N, Van den Eynde B.
  • Peptide database T cell-defined tumor antigens. Cancer Immun 2013; URL: http://www.cancerimmunity.org/peptide/, wherein human tumor antigens recognized by CD4+ or CD8+ T cells are classified into four major groups on the basis of their expression pattern, or from the database “Tantigen” (TANTIGEN version 1.0, Dec. 1, 2009; developed by Bioinformatics Core at Cancer Vaccine Center, Dana-Farber Cancer Institute; URL: http://cvc.dfci.harvard.edu/tadb/).
  • the TLR peptide agonist allows an increased targeting of the vaccine towards dendritic cells along with self-adjuvancity.
  • Physical linkage of a TLR peptide agonist to the CPP and the at least one antigen or antigenic epitope in the complex comprised by the combination for use according to the present invention provides an enhanced immune response by simultaneous stimulation of antigen presenting cells, in particular dendritic cells, that internalize, metabolize and display antigen(s).
  • a “TLR peptide agonist” is an agonist of a Toll-like receptor (TLR), i.e. it binds to a TLR and activates the TLR, in particular to produce a biological response.
  • TLR peptide agonist is a peptide, a polypeptide or a protein as defined above.
  • the TLR peptide agonist comprises from 10 to 150 amino acids, more preferably from 15 to 130 amino acids, even more preferably from 20 to 120 amino acids, particularly preferably from 25 to 110 amino acids, and most preferably from 30 to 100 amino acids.
  • TLRs Toll like receptors
  • LRRs leucine-rich repeats
  • Toll like receptors include TLRs1-10. Compounds capable of activating TLR receptors and modifications and derivatives thereof are well documented in the art.
  • TLR1 may be activated by bacterial lipoproteins and acetylated forms thereof
  • TLR2 may in addition be activated by Gram positive bacterial glycolipids, LPS, LP A, LTA, fimbriae, outer membrane proteins, heat shock proteins from bacteria or from the host, and Mycobacterial lipoarabinomannans.
  • TLR3 may be activated by dsRNA, in particular of viral origin, or by the chemical compound poly(LC).
  • TLR4 may be activated by Gram negative LPS, LTA, Heat shock proteins from the host or from bacterial origin, viral coat or envelope proteins, taxol or derivatives thereof, hyaluronan containing oligosaccharides and fibronectins.
  • TLR5 may be activated with bacterial flagellae or flagellin.
  • TLR6 may be activated by mycobacterial lipoproteins and group B streptococcus heat labile soluble factor (GBS-F) or staphylococcus modulins.
  • TLR7 may be activated by imidazoquinolines.
  • TLR9 may be activated by unmethylated CpG DNA or chromatin—IgG complexes.
  • the TLR peptide agonist comprised by the complex comprised by the combination for use according to the present invention is an agonist of TLR1, 2, 4, 5, 6, and/or 10.
  • TLRs are expressed either on the cell surface (TLR1, 2, 4, 5, 6, and 10) or on membranes of intracellular organelles, such as endosomes (TLR3, 4, 7, 8, and 9).
  • the natural ligands for the endosomal receptors turned out to be nucleic acid-based molecules (except for TLR4).
  • the cell surface-expressed TLR1, 2, 4, 5, 6, and 10 recognize molecular patterns of extracellular microbes (Monie, T. P., Bryant, C. E., et al. 2009: Activating immunity: Lessons from the TLRs and NLRs. Trends Biochem. Sci. 34(11), 553-561).
  • TLRs are expressed on several cell types but virtually all TLRs are expressed on DCs allowing these specialized cells to sense all possible pathogens and danger signals.
  • the TLR peptide agonist comprised by the complex comprised by the combination for use according to the present invention is more preferably a peptide agonist of TLR2, TLR4 and/or TLR5.
  • the TLR peptide agonist is a TLR2 peptide agonist and/or a TLR4 peptide agonist.
  • the TLR peptide agonist is a TLR4 peptide agonist.
  • the TLR peptide agonist is one TLR peptide agonist, which is both, a TLR2 and a TLR4 agonist.
  • TLR2 can detect a wide variety of ligands derived from bacteria, viruses, parasites, and fungi.
  • the ligand specificity is often determined by the interaction of TLR2 with other TLRs, such as TLR1, 6, or 10, or non-TLR molecules, such as dectin-1, CD14, or CD36.
  • TLR1 TLR1, 6, or 10
  • non-TLR molecules such as dectin-1, CD14, or CD36.
  • TLR2 can identify triacyl lipoproteins or lipopeptides from (myco)bacterial origin, such as Pam3CSK4 and peptidoglycan (PGA; Gay, N. J., and Gangloff, M. (2007): Structure and function of Toll receptors and their ligands. Annu. Rev. Biochem.
  • TLR2 interacts with a broad and structurally diverse range of ligands, including molecules expressed by microbes and fungi.
  • Multiple TLR2 agonists have been identified, including natural and synthetic lipopeptides (e.g. Mycoplasma fermentas macrophage-activating lipopeptide (MALP-2)), peptidoglycans (PG such as those from S. aureus ), lipopolysaccharides from various bacterial strains (LPS), polysaccharides (e.g. zymosan), glycosylphosphatidyl-inositol-anchored structures from gram positive bacteria (e.g.
  • lipopeptides e.g. Mycoplasma fermentas macrophage-activating lipopeptide (MALP-2)
  • PG peptidoglycans
  • LPS lipopolysaccharides from various bacterial strains
  • polysaccharides e.g. zymosan
  • LTA lipoteichoic acid
  • lipo-arabinomannan from mycobacteria and lipomannas from M. tuberculosis .
  • Certain viral determinants may also trigger via TLR2 (Barbalat R, Lau L, Locksley R M, Barton G M. Toll-like receptor 2 on inflammatory monocytes induces type I interferon in response to viral but not bacterial ligands. Nat Immunol. 2009: 10(11):1200-7).
  • Bacterial lipopeptides are structural components of cell walls. They consist of an acylated s-glycerylcysteine moiety to which a peptide can be conjugated via the cysteine residue.
  • TLR2 agonists which are bacterial lipopeptides, include MALP-2 and it's synthetic analogue di-palmitoyl-S-glyceryl cysteine (Pam 2 Cys) or tri-palmitoyl-S-glyceryl cysteine (Pam 3 Cys).
  • TLR4 Monophosphoryl Lipid A from Salmonella minnesota R595 (MPLA), lipopolysaccharides (LPS), mannans ( Candida albicans ), glycoinositolphospholipids ( Trypanosoma ), viral envelope proteins (RSV and MMTV) and endogenous antigens including fibrinogen and heat-shock proteins.
  • MPLA Salmonella minnesota R595
  • LPS lipopolysaccharides
  • mannans Candida albicans
  • GMV glycoinositolphospholipids
  • RSV and MMTV viral envelope proteins
  • endogenous antigens including fibrinogen and heat-shock proteins.
  • Such agonists of TLR4 are for example described in Akira S, Uematsu S, Takeuchi O. Pathogen recognition and innate immunity. Cell. Feb. 24, 2006: 124(4):783-801 or in Kumar H, Kawai T, Akira S. Toll-like receptors and innate immunity. Biochem
  • LPS which is found in the outer membrane of gram negative bacteria, is the most widely studied of the TLR4 ligands. Suitable LPS-derived TLR4 agonist peptides are described for example in WO 2013/120073 (A1).
  • TLR5 is triggered by a region of the flagellin molecule expressed by nearly all motile bacteria.
  • flagellin, or peptides or proteins derived from flagellin and/or variants or fragments of flagellin are also suitable as TLR peptide agonists comprised by the complex.
  • TLR peptide agonists thus include the TLR2 lipopeptide agonists MALP-2, Pam 2 Cys and Pam 3 Cys or modifications thereof, different forms of the TLR4 agonist LPS, e.g. N. meningitidis wild-type L3-LPS and mutant penta-acylated LpxL1-LPS, and the TLR5 agonist flagellin.
  • the TLR peptide agonist comprised by the complex is neither a lipopeptide nor a lipoprotein, neither a glycopeptide nor a glycoprotein, more preferably, the TLR peptide agonist comprised by the complex is a classical peptide, polypeptide or protein as defined herein.
  • a preferred TLR2 peptide agonist is annexin II or an immunomodulatory fragment thereof, which is described in detail in WO 2012/048190 A1 and U.S. patent application Ser. No. 13/0331546, in particular a TLR2 peptide agonist comprising an amino acid sequence according to SEQ ID NO: 4 or SEQ ID NO: 7 of WO 2012/048190 A1 or fragments or variants thereof are preferred.
  • TLR2 peptide agonist comprising or consisting of an amino acid sequence according to SEQ ID NO: 15 or a sequence variant thereof as described above is particularly preferred as component c), i.e. as the at least one TLR peptide agonist, comprised by the complex.
  • SEQ ID NO: 15 STVHEILCKLSLEGDHSTPPSAYGSVKPYTNFDAE (TLR2 peptide agonist Anaxa)
  • a particularly preferred functional sequence variant of the TLR peptide agonist according to SEQ ID NO: 15 is the TLR peptide agonist according to SEQ ID NO: 47:
  • a TLR2 peptide agonist comprising or consisting of an amino acid sequence according to SEQ ID NO: 47 or a sequence variant thereof as described above is particularly preferred as component c), i.e. as the at least one TLR peptide agonist, comprised by the complex.
  • TLR peptides agonists are particularly preferred, which in particular correspond to motifs that bind to TLR4, in particular (i) peptides mimicking the natural LPS ligand (RS01: Gln-Glu-Ile-Asn-Ser-Ser-Tyr and RS09: Ala-Pro-Pro-His-Ala-Leu-Ser) and (ii) Fibronectin derived peptides.
  • the cellular glycoprotein Fibronectin (FN) has multiple isoforms generated from a single gene by alternative splicing of three exons. One of these isoforms is the extra domain A (EDA), which interacts with TLR4.
  • TLR peptide agonists comprise a fibronectin EDA domain or a fragment or variant thereof.
  • suitable fibronectin EDA domains or a fragments or variants thereof are disclosed in EP 1 913 954 B1, EP 2 476 440 A1, US 2009/0220532 A1, and WO 2011/101332 A1.
  • a TLR4 peptide agonist comprising or consisting of an amino acid sequence according to SEQ ID NO: 40 or a sequence variant thereof as described above is particularly preferred as component c), i.e. as the at least one TLR peptide agonist, comprised by the complex comprised by the combination for use according to the present invention.
  • high-mobility group box 1 protein HMGB1
  • peptide fragments thereof are assumed to be TLR4 agonists.
  • TLR4 agonists such as TLR4 agonists.
  • TLR4 agonist comprising or consisting of an amino acid sequence according to SEQ ID NO: 15 or 47 or a functional sequence variant thereof is particularly preferred as component c), i.e. as the at least one TLR peptide agonist, comprised by the complex.
  • the complex comprised by the combination for use according to the present invention comprises at least one TLR peptide agonist, preferably the complex comprised by the combination for use according to the present invention comprises more than one TLR peptide agonist, in particular 2, 3, 4, 5, 6, 7, 8, 9, 10 or more TLR peptide agonists, more preferably the complex comprised by the combination for use according to the present invention comprises (at least) two or three TLR peptide agonists, even more preferably the complex comprised by the combination for use according to the present invention comprises (at least) four or five TLR peptide agonists.
  • TLR peptide agonist is comprised by the complex it is understood that said TLR peptide agonist is in particular also covalently linked in the complex comprised by the combination for use according to the present invention, e.g. to another TLR peptide agonist and/or to a component a), i.e. a cell penetrating peptide, and/or to a component b), i.e. an antigen or antigenic epitope.
  • the complex comprised by the combination for use according to the present invention comprises one single TLR peptide agonist.
  • the complex comprised by the combination for use according to the present invention comprises one single TLR peptide agonist and no further component having TLR agonist properties except the one single TLR peptide agonist as described.
  • the various TLR peptide agonists comprised by the complex may be the same or different.
  • the various TLR peptide agonists comprised by the complex are different from each other.
  • the more than one antigen or antigenic epitope in particular 2, 3, 4, 5, 6, 7, 8, 9, 10 antigens or antigenic epitopes, or more TLR peptide agonists, in particular 2, 3, 4, 5, 6, 7, 8, 9, 10 TLR agonists, are positioned consecutively in the complex comprised by the combination for use according to the present invention.
  • all TLR peptide agonists comprised by the complex are positioned in a stretch, which is neither interrupted by component a), i.e. a cell penetrating peptide, nor by component b), i.e. at least one antigen or antigenic epitope.
  • component a) and component b) are positioned in the complex for example before or after such a stretch of all TLR peptide agonists.
  • the TLR peptide agonists positioned consecutively in such a way may be linked to each other for example by a spacer or linker as described below, which is neither component a), i.e. a cell penetrating peptide, nor component b), i.e. at least one antigen or antigenic epitope.
  • the various TLR peptide agonists may also be positioned in any other way in the complex comprised by the combination for use according to the present invention, for example with component a) and/or component b) positioned in between two or more TLR peptide agonists, i.e. with one or more TLR peptide agonist positioned between component a) and component b) (or vice versa) and, optionally, one or more TLR peptide agonists positioned at the respective other end of component a) and/or component b).
  • TLR peptide agonists activating the same or different TLR receptors may be advantageously comprised by a single complex.
  • a number of different TLR peptide agonists activating the same or different TLR receptors may be distributed to subsets of different TLR peptide agonists activating the same or different TLR receptors, which are comprised by different complexes, whereby such different complexes comprising different subsets may advantageously be administered simultaneously, e.g. in a single vaccine, to a subject in need thereof.
  • components a), b) and c) are covalently linked, i.e. the linkage between two out of the three components a), b), and c) of the complex is a covalent linkage.
  • two out of the three components a), b), and c) of the complex are covalently linked to each other (i.e. the “first” and the “second” component), and the third component out of the three components a), b), and c) is covalently linked either to the first component out of the three components a), b), and c) or to the second component out of the three components a), b), and c).
  • a linear molecule is formed.
  • each of the three components a), b), and c) is covalently linked to both of the other components out of the three components a), b), and c).
  • a “covalent linkage” refers to a chemical bond that involves the sharing of electron pairs between atoms.
  • a “covalent linkage” in particular involves a stable balance of attractive and repulsive forces between atoms when they share electrons. For many molecules, the sharing of electrons allows each atom to attain the equivalent of a full outer shell, corresponding to a stable electronic configuration.
  • Covalent bonding includes many kinds of interactions, including for example ⁇ -bonding, ⁇ -bonding, metal-to-metal bonding, agostic interactions, and three-center two-electron bonds. Accordingly, the complex comprised by the combination for use according to the present invention, may also be referred to as “compound”, in particular it may be referred to as “molecule”.
  • components a), b), and c) are covalently linked by chemical coupling in any suitable manner known in the art, such as cross-linking methods.
  • any suitable manner known in the art such as cross-linking methods.
  • chemical cross-linking methods are non-specific, i.e., they do not direct the point of coupling to any particular site on the components a), b), and c).
  • non-specific cross-linking agents may attack functional sites or sterically block active sites, rendering the fused components of the complex biologically inactive. It is referred to the knowledge of the skilled artisan to block potentially reactive groups by using appropriate protecting groups.
  • Coupling specificity can be increased by direct chemical coupling to a functional group found only once or a few times in components a), b), and/or c), which functional group is to be cross-linked to the another of the components a), b), and c).
  • the cystein thiol group may be used, if just one cystein residue is present in a certain component a), b), or c) of complex comprised by the combination for use according to the present invention.
  • a cross-linking reagent specific for primary amines will be selective for the amino terminus of the respective component.
  • cross-linking may also be carried out via the side chain of a glutamic acid residue placed at the N-terminus of the peptide such that a amide bond can be generated through its side-chain. Therefore, it may be advantageous to link a glutamic acid residue to the N-terminus of a certain component a), b), or c).
  • a cysteine residue is to be introduced into a certain component a), b), or c
  • introduction at or near its N- or C-terminus is preferred.
  • Conventional methods are available for such amino acid sequence alterations based on modifications of certain component a), b), or c) by either adding one or more additional amino acids, e.g.
  • cystein residue to the translocation sequence or by substituting at least one residue of the translocation sequence(s) being comprised in the respective component.
  • a cystein side chain is used for coupling purposes, a certain component a), b), or c) has preferably one cystein residue.
  • Any second cystein residue should preferably be avoided and can, optionally, be replaced when they occur in the respective component comprised by the complex.
  • a cysteine residue is replaced in the original sequence of a certain component a), b), or c)
  • Coupling of two out of the three components a), b), and c) can be accomplished via a coupling or conjugating agent including standard peptide synthesis coupling reagents such as HOBt, HBTU, DICI, TBTU.
  • a coupling or conjugating agent including standard peptide synthesis coupling reagents such as HOBt, HBTU, DICI, TBTU.
  • reagents for example, N-succinimidyl 3-(2-pyridyldithio)propionate (SPDP) or N,N′-(1,3-phenylene)bismaleimide; N,N′-ethylene-bis-(iodoacetamide) or other such reagent having 6 to 11 carbon methylene bridges; and 1,5-difluoro-2,4-dinitrobenzene.
  • SPDP N-succinimidyl 3-(2-pyridyldithio)propionate
  • N,N′-(1,3-phenylene)bismaleimide N,N′-ethylene-bis-(iodoacetamide) or other such reagent having 6 to 11 carbon methylene bridges
  • 1,5-difluoro-2,4-dinitrobenzene 1,5-difluoro-2,4-dinitrobenzene.
  • cross-linking agents useful for this purpose include: p,p′-difluoro-m,m′-dinitrodiphenylsulfone; dimethyl adipimidate; phenol-1,4-disulfonylchloride; hexamethylenediisocyanate or diisothiocyanate, or azophenyl-p-diisocyanate; glutaraldehyde and disdiazobenzidine.
  • Cross-linking agents may be homobifunctional, i.e., having two functional groups that undergo the same reaction.
  • a preferred homobifunctional cross-linking agent is bismaleimidohexane (BMH).
  • BMH contains two maleimide functional groups, which react specifically with sulfhydryl-containing compounds under mild conditions (pH 6.5-7.7).
  • the two maleimide groups are connected by a hydrocarbon chain. Therefore, BMH is useful for irreversible cross-linking of proteins (or polypeptides) that contain cysteine residues.
  • Cross-linking agents may also be heterobifunctional. Heterobifunctional cross-linking agents have two different functional groups, for example an amine-reactive group and a thiol-reactive group, that will cross-link two proteins having free amines and thiols, respectively.
  • heterobifunctional cross-linking agents are Succinimidyl-4-(N-maleimidomethyl)-cyclohexane-1-carboxylate (SMCC), m-maleimidobenzoyl-N-hydroxysuccinimide ester (MBS), and succinimide 4-(p-maleimidophenyl)butyrate (SMPB), an extended chain analog of MBS.
  • SMCC Succinimidyl-4-(N-maleimidomethyl)-cyclohexane-1-carboxylate
  • MBS m-maleimidobenzoyl-N-hydroxysuccinimide ester
  • SMPB succinimide 4-(p-maleimidophenyl)butyrate
  • cross-linking agents often have low solubility in water, a hydrophilic moiety, such as a sulfonate group, may be added to the cross-linking agent to improve its water solubility.
  • Sulfo-MBS and sulfo-SMCC are examples of cross-linking agents modified for water solubility.
  • Many cross-linking agents yield a conjugate that is essentially non-cleavable under cellular conditions. Therefore, some cross-linking agents contain a covalent bond, such as a disulfide, that is cleavable under cellular conditions.
  • cleavable cross-linkers For example, Traut's reagent, dithiobis (succinimidylpropionate) (DSP), and N-succinimidyl 3-(2-pyridyldithio)propionate (SPDP) are well-known cleavable cross-linkers.
  • DSP dithiobis
  • SPDP N-succinimidyl 3-(2-pyridyldithio)propionate
  • cleavable cross-linking agent permits the cell penetrating peptide, the at least one antigen or antigenic epitope and the at least one TLR peptide agonist comprised by the complex to separate from each other after delivery into the target cell.
  • direct disulfide linkage may also be useful.
  • Chemical cross-linking may also include the use of spacer arms.
  • Spacer arms provide intramolecular flexibility or adjust intramolecular distances between conjugated moieties and thereby may help preserve biological activity.
  • a spacer arm may be in the form of a protein (or polypeptide) moiety that includes spacer amino acids, e.g. proline.
  • a spacer arm may be part of the cross-linking agent, such as in “long-chain SPDP” (Pierce Chem. Co., Rockford, Ill., cat. No. 21651 H). Numerous cross-linking agents, including the ones discussed above, are commercially available. Detailed instructions for their use are readily available from the commercial suppliers.
  • Cross-linking agents for peptide or protein crosslinking include for example (i) amine-to-amine crosslinkers, e.g. homobifunctional amine-specific protein crosslinking reagents based on NHS-ester and imidoester reactive groups for selective conjugation of primary amines; available in short, long, cleavable, irreversible, membrane permeable, and cell surface varieties; (ii) sulfhydryl-to-carbohydrate crosslinkers, e.g. crosslinking reagents based on maleimide and hydrazide reactive groups for conjugation and formation of covalent crosslinks; (iii) sulfhydryl-to-sulfhydryl crosslinkers, e.g.
  • homobifunctional sulfhydryl-specific crosslinking reagents based on maleimide or pyridyldithiol reactive groups for selective covalent conjugation of protein and peptide thiols (reduced cysteines) to form stable thioether bonds;
  • photoreactive crosslinkers e.g. aryl azide, diazirine, and other photo-reactive (light-activated) chemical heterobifunctional crosslinking reagents to conjugate proteins, nucleic acids and other molecular structures involved in receptor-ligand interaction complexes via two-step activation;
  • amine-to-sulfhydryl crosslinkers e.g.
  • heterobifunctional protein crosslinking reagents for conjugation between primary amine (lysine) and sulfhydryl (cysteine) groups of proteins and other molecules; available with different lengths and types of spacer arms; and (vi) amine-to-amine crosslinkers, e.g. carboxyl-to-amine crosslinkers, e.g. Carbodiimide crosslinking reagents, DCC and EDC (EDAC), for conjugating carboxyl groups (glutamate, aspartate, C-termini) to primary amines (lysine, N-termini) and also N-hydroxysuccinimide (NHS) for stable activation of carboxylates for amine-conjugation.
  • amine-to-amine crosslinkers e.g. carboxyl-to-amine crosslinkers, e.g. Carbodiimide crosslinking reagents, DCC and EDC (EDAC)
  • carboxyl groups glutamate, aspartate, C-termini
  • crosslinkers in general which can be used in the complex comprised by the combination for use according to the present invention, include N-( ⁇ -Maleimidoacetoxy)-succinimide ester, N-5-Azido-2-nitrobenzyloxy-succinimide, 1,4-Bis-Maleimidobutane, 1,4-Bis-Maleimmidyl-2,3-dihydroxy-butane, Bis-Maleimidohexane, Bis-Maleimidoethane, N-(3-Maleimidopropionic acid)hydrazide*TFA, N-( ⁇ -Maleimidopropyloxy)succinimide ester, 1,8-Bis-Maleimidodiethylene-glycol, 1,11-Bis-Maleimidotriethyleneglycol, Bis (sulfosuccinimidyl)suberate, Bis (sulfosuccinimidyl)glutarate-d
  • linkage between two out of the three components a), b), and c) of the complex comprised by the combination for use according to the present invention may be directly or indirectly, i.e. two components directly adjoin or they may be linked by an additional component of the complex, e.g. a spacer or a linker.
  • a direct linkage may be realized preferably by an amide bridge, if the components to be linked have reactive amino or carboxy groups. More specifically, if the components to be linked are peptides, polypeptides or proteins, a peptide bond is preferred. Such a peptide bond may be formed using a chemical synthesis involving both components (an N-terminal end of one component and the C-terminal end of the other component) to be linked, or may be formed directly via a protein synthesis of the entire peptide sequence of both components, wherein both (protein or peptide) components are preferably synthesized in one step. Such protein synthesis methods include e.g., without being limited thereto, liquid phase peptide synthesis methods or solid peptide synthesis methods, e.g.
  • solid peptide synthesis methods according to Merrifield, t-Boc solid-phase peptide synthesis, Fmoc solid-phase peptide synthesis, BOP (Benzotriazole-1-yl-oxy-tris-(dimethylamino)-phosphonium hexafluorophosphate) based solid-phase peptide synthesis, etc.
  • BOP Benzotriazole-1-yl-oxy-tris-(dimethylamino)-phosphonium hexafluorophosphate
  • ester or ether linkages are preferred.
  • a linkage may occur via the side chains, e.g. by a disulfide bridge.
  • Further components of other chemical nature e.g. the at least one antigen or antigenic epitope if it is not of peptidic nature, may be likewise attached to the components of peptidic nature, e.g. the cell penetrating peptide, the at least one TLR peptide agonist, and the at least one antigen or antigenic epitope if it is of peptidic nature.
  • the linkage via a side chain will preferably be based on side chain amino, thiol or hydroxyl groups, e.g.
  • a linkage of a peptidic main chain with a peptidic side chain of another component may also be via an isopeptide bond.
  • An isopeptide bond is an amide bond that is not present on the main chain of a protein. The bond forms between the carboxyl terminus of one peptide or protein and the amino group of a lysine residue on another (target) peptide or protein.
  • the complex comprised by the combination for use according to the present invention may optionally comprise a spacer or linker, which are non-immunologic moieties, which are preferably cleavable, and which link component a) and b) and/or component a) and c), and/or component b) and c), and/or link consecutive antigens or antigenic epitopes, and/or link consecutive TLR peptide agonists, and/or link consecutive cell penetrating peptides, and/or which can be placed at the C-terminal part of components b) and/or c).
  • a spacer or linker which are non-immunologic moieties, which are preferably cleavable, and which link component a) and b) and/or component a) and c), and/or component b) and c), and/or link consecutive antigens or antigenic epitopes, and/or link consecutive TLR peptide agonists, and/or link consecutive cell penetr
  • a linker or spacer may preferably provide further functionalities in addition to linking of the components, and preferably being cleavable, more preferably naturally cleavable inside the target cell, e.g. by enzymatic cleavage.
  • further functionalities do in particular not include any immunological functionalities.
  • Examples of further functionalities, in particular regarding linkers in fusion proteins, can be found in Chen X. et al., 2013: Fusion Protein Linkers: Property, Design and Functionality. Adv Drug Deliv Rev. 65(10): 1357-1369, wherein for example also in vivo cleavable linkers are disclosed.
  • linkers e.g. flexible linkers and rigid linkers, and linker designing tools and databases, which can be useful in the complex comprised by the combination for use according to the present invention or to design a linker to be used in the complex.
  • Said spacer may be peptidic or non-peptidic, preferably the spacer is peptidic.
  • a peptidic spacer consists of about 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acids, more preferably of about 1, 2, 3, 4, or 5 amino acids.
  • the amino acid sequence of the peptidic spacer may be identical to that of the N-terminal or C-terminal flanking region of any of the components a), b), or c).
  • a peptidic spacer can consist of non-natural amino acid sequences such as an amino acid sequence resulting from conservative amino acid substitutions of said natural flanking regions or sequences of known cleavage sites for proteases such as an enterokinase target site (amino acid sequence: DDDK, SEQ ID NO: 16), factor Xa target site (amino acid sequence: IEDGR, SEQ ID NO: 17), thrombin target site (amino acid sequence: LVPRGS, SEQ ID NO: 18), protease TEV target site (amino acid sequence: ENLYFQG, SEQ ID NO: 19), PreScission protease target site (amino acid sequence LEVLFQGP, SEQ ID NO: 20), polycationic amino acids, e.g.
  • the peptidic spacer does not contain any Cys (C) residues.
  • the linker sequence contains at least 20%, more preferably at least 40% and even more preferably at least 50% Gly or ⁇ -alanine residues, e.g. GlyGlyGlyGlyGly (SEQ ID NO: 22), GlyGlyGlyGly (SEQ ID NO: 23), GlyGlyGly, CysGlyGly or GlyGlyCys, etc.
  • Appropriate linker sequences can be easily selected and prepared by a person skilled in the art. They may be composed of D and/or L amino acids. Further examples of a peptidic spacer include the amino acid sequences EQLE (SEQ ID NO: 24) or TEWT (SEQ ID NO: 25) or any conservative substitutions thereof.
  • a non-peptidic spacer can include or may be an ester, a thioester, and a di-sulfide.
  • the complex comprised by the combination for use according to the invention may comprise a spacer or linker, in particular a peptidic spacer, placed between component a) and b) and/or between component a) and c), and/or between component b) and c).
  • This peptidic spacer can be chosen by one skilled in the art so that it may be cut by the cell machinery once the complex comprising the cell penetrating peptide and the cargo molecule has been internalized.
  • each of the antigens or antigenic epitopes and/or each of the TLR peptide agonists comprised in the complex can be either directly linked to each other or linked via spacers or linkers such as, e.g., a peptidic spacer consisting of a few amino acids.
  • the complex comprised by the combination for use according to the present invention comprises several antigens or antigenic epitopes or when the complex comprises several TLR peptide agonists
  • some antigens or antigenic epitopes and/or some TLR peptide agonists comprised by the complex are directly linked to each other and some other antigens or antigenic epitopes and/or some other TLR peptide agonists are linked via spacers or linkers such as a peptidic spacer consisting of a few amino acids.
  • two successive antigens or antigenic epitopes or two successive TLR peptide agonists comprised in the complex are linked to each other by spacers consisting of the natural flanking regions of said antigens or antigenic epitopes or of said TLR peptide agonists, respectively.
  • the spacer used to link a first antigen/antigenic epitope or a first TLR peptide agonist to a second antigen/antigenic epitope or to a second TLR peptide agonist may consists of up to about 8 amino acids corresponding to up to about 4 amino acids of the N-terminal or C-terminal flanking region of the first antigen/antigenic epitope or the first TLR peptide agonist, followed by up to about 4 amino acids of the N-terminal or C-terminal flanking region of the second antigen/antigenic epitope or the second TLR peptide agonist.
  • the spacer used to link a first antigen/antigenic epitope or a first TLR peptide agonist (“antigen/epitope/TLR peptide agonist 1”) to a second epitope (“antigen/epitope/TLR peptide agonist 2”) consists of about 8 amino acids corresponding to any possible combination ranging from: 0 flanking amino acid of antigen/epitope/TLR peptide agonist 1 and 8 flanking amino acids of antigen/epitope/TLR peptide agonist 2, to 8 flanking amino acids of antigen/epitope/TLR peptide agonist 1 and 0 flanking amino acid of antigen/epitope/TLR peptide agonist 2, i.e.
  • the total of 8 amino acids constituting a spacer linking two consecutive antigen/epitope/TLR peptide agonist is not an absolute value and the spacer could also be composed of a total of, for instance, 3 amino acids, 4 amino acids, 5 amino acids, 6 amino acids, 7 amino acids, 9 amino acids or 10 amino acids.
  • equivalent combinations as mentioned above are also an illustration of the complex in the situation where a spacer has less or more than 8 amino acids.
  • the spacer used to link a first antigen/antigenic epitope or a first TLR peptide agonist (“antigen/epitope/TLR peptide agonist 1”) to a second antigen/antigenic epitope or to a second TLR peptide agonist, respectively, (“antigen/epitope/TLR peptide agonist 2”) consists of e.g. 1, 2, 3, 4, or 5 amino acids.
  • said spacer's amino acid sequence can correspond to the 4 amino acids of the N-terminal or C-terminal flanking region of antigen/epitope/TLR peptide agonist 1 or antigen/epitope/TLR peptide agonist 2.
  • a spacer as described above may also be placed at the C-terminal part of the last antigen/epitope/TLR peptide agonist comprised in the complex.
  • the technics for linking two of the three components a), b), and c) are well documented in the literature and can depend on the nature of the at least one antigen or antigenic epitope.
  • linkages between two of the three components a), b), and c) can be achieved via cleavable disulphide linkages through total stepwise solid-phase synthesis or solution-phase or solid-phase fragment coupling, stable amide, thiazolidine, oxime and hydrazine linkage, disulphide linkage, stable thiomaleimide linkage, peptide bond (including peptide bonds between amino acids of a fusion protein), or electrostatic or hydrophobic interactions.
  • the at least one antigen or antigenic epitope comprised by the complex as well as any optional spacer or linker comprised by the complex are of peptidic nature. More preferably, all components of the complex comprised by the combination for use according to the present invention, e.g. the cell penetrating peptide, the at least one antigen or antigenic epitope, which is a peptide, polypeptide or protein, the at least one TLR peptide agonist and any optional peptidic linker or spacer are linked in the complex comprised by the combination for use according to the present invention by a peptide bond.
  • the complex comprised by the combination for use according to the present invention is thus a peptide, polypeptide or protein, such as a fusion protein, e.g. a recombinant fusion protein.
  • a complex comprising or consisting of an amino acid sequence according to SEQ ID NO: 26, SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 31, SEQ ID NO: 32, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, or SEQ ID NO: 45; or a complex comprising or consisting of an amino acid sequence sharing at least 50%, at least 60%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95% or at least 98% sequence identity with any of SEQ ID NO: 26, SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 30, SEQ ID NO: 31, SEQ ID NO: 32, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43, SEQ ID NO: 44, or SEQ ID NO: 45 is preferred.
  • a complex comprising or consisting of an amino acid sequence according to SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO:31, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43 or SEQ ID NO: 45 or a complex comprising or consisting of an amino acid sequence sharing at least 50%, at least 60%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95% or at least 98% sequence identity with any of SEQ ID NO: 27, SEQ ID NO: 28, SEQ ID NO: 29, SEQ ID NO: 31, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43 or SEQ ID NO: 45 is more preferred.
  • a complex comprising or consisting of an amino acid sequence according to SEQ ID NO: 28, SEQ ID NO: 31, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43 or SEQ ID NO: 45 or a complex comprising or consisting of an amino acid sequence sharing at least 50%, at least 60%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95% or at least 98% sequence identity with SEQ ID NO: 28, SEQ ID NO: 31, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43 or SEQ ID NO: 45 is even more preferred.
  • a complex comprising or consisting of an amino acid sequence according to SEQ ID NO: 28, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43 or SEQ ID NO: 45 or a complex comprising or consisting of an amino acid sequence sharing at least 50%, at least 60%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95% or at least 98% sequence identity with SEQ ID NO: 28, SEQ ID NO: 41, SEQ ID NO: 42, SEQ ID NO: 43 or SEQ ID NO: 45 is particularly preferred.
  • SEQ ID NO: 26 MHHHHHHNID RPKGLAFTDV DVDSIKIAWE SPQGQVSRYR VTYSSPEDGI RELFPAPDGEDDTAELQGLR PGSEYTVSVV ALHDDMESQP LIGIQSTKRY KNRVASRKSR AKFKQLLQHY REVAAAKSSE NDRLRLLLKE SLKISQAVHA AHAEINEAGR EVVGVGALKV PRNQDWLGVP RFAKFASFEA QGALANIAVD KANLDVEQLE SIINFEKLTE WTGS SEQ ID NO: 27: MHHHHHHSTV HEILCKLSLE GDHSTPPSAY GSVKPYTNFD AEKRYKNRVA SRKSRAKFKQ LLQHYREVAA AKSSENDRLR LLLKESLKIS QAVHAAHAEI NEAGREVVGV GALKVPRNQD WLGVPRFAKF ASFEAQGALA NIAVDKANLD VEQLESIINF EKL
  • the components a), b), and c) may be arranged in the complex comprised by the combination for use according to the present invention in any way.
  • the more than one cell penetrating peptide may be positioned in a non-consecutive manner, i.e. at least one antigen or antigenic epitope (component b)) and/or at least one TLR peptide agonist (component c)) may interrupt a stretch of consecutively positioned cell penetrating peptides and/or the cell penetrating peptides may be positioned with component b) and/or with component c) in an alternating manner.
  • the more than one antigen or antigenic epitope may be positioned in a non-consecutive manner, i.e. at least one cell penetrating peptide (component a)) and/or at least one TLR peptide agonist (component c)) may interrupt a stretch of consecutively positioned antigens or antigenic epitopes and/or the antigens or antigenic epitopes may be positioned with component a) and/or with component c) in an alternating manner.
  • the more than one TLR peptide agonist may be positioned in a non-consecutive manner, i.e.
  • At least one cell penetrating peptide (component a)) and/or at least one antigen or antigenic epitope (component b)) may interrupt a stretch of consecutively positioned TLR peptide agonists and/or the TLR peptide agonists may be positioned with component a) and/or with component b) in an alternating manner.
  • the more than one cell penetrating peptide is positioned in the complex comprised by the combination for use according to the present invention in a consecutive manner and/or the more than one antigen or antigenic epitope is positioned in the complex comprised by the combination for use according to the present invention in a consecutive manner and/or the more than one TLR peptide agonist is positioned in the complex comprised by the combination for use according to the present invention in a consecutive manner.
  • all cell penetrating peptides, all antigens or antigenic epitopes or all TLR peptide agonists, which are comprised by the complex are positioned in a stretch, which is not interrupted by any of the other two components. Rather, the other two components are positioned in the complex for example before or after such a stretch of all single units of said certain component.
  • the single units of said certain component positioned consecutively in such a way may be linked to each other for example by a spacer or linker as described herein, which is not of the other two components.
  • each of the components a), b), and c) is positioned in a consecutive manner.
  • each component a), b), and c) typically comprises a single main chain and at least one side chain.
  • main chain also “backbone chain”
  • main chain refers to the main continuous chain of covalently bond atoms in a molecule.
  • main chain typically comprises alpha-carbon atoms and nitrogen atoms of the constituent amino acids linked by the peptide bond.
  • the backbone does not include the side chains.
  • side chain also “pendant chain”
  • side chains refers to a chemical group that is attached to a core part of the molecule called “main chain” or backbone.
  • the side chains typically represent the (main) parts of the constituent amino acids, which are attached to the alpha-carbon atoms of the backbone.
  • the components a), b), and c) may be covalently linked via a linker or spacer as described herein or they may be directly covalently linked.
  • a linker or spacer Independently of whether a spacer or linker is used for covalent linkage or not, there are in principle four options of how two of the three components are linked to each other in the complex comprised by the combination for use according to the present invention, namely:
  • all three components a), b), and c) are linked via main-chain/main-chain linkage, thus resulting in particular in a main chain of the complex, which comprises the main chain of one or more cell penetrating peptide(s), the main chain of one or more antigen(s) or antigenic epitope(s), and the main chain of one or more TLR peptide agonist(s).
  • the main chain of one or more cell penetrating peptide(s), the main chain of one or more antigen(s) or antigenic epitope(s), and the main chain of one or more TLR peptide agonist(s) constitute the main chain of the complex, optionally together with further components, for example linker(s), spacer(s), etc.
  • the following arrangements of the components a), b), and c) are preferred, in particular if the at least one antigen or antigenic epitope is a peptide, polypeptide or protein, whereby said preferred arrangements are shown below in N-terminus ⁇ C-terminus direction of the main chain of the complex and wherein all three components a), b), and c) are linked via main-chain/main-chain linkage and may be optionally linked by a linker, a spacer or another additional component:
  • the at least one antigen or antigenic epitope is positioned C-terminally of the cell penetrating peptide, whereby the cell penetrating peptide and the at least one antigen or antigenic epitope are optionally linked by a further component, e.g. a linker, a spacer, or by the at least one TLR peptide agonist. Accordingly, this corresponds to the arrangements ( ⁇ ), ( ⁇ ), and ( ⁇ ) from the arrangements shown above, i.e. from the above arrangements arrangements ( ⁇ ), ( ⁇ ), and ( ⁇ ) are more preferred.
  • the at least one antigen or antigenic epitope is positioned C-terminally of the cell penetrating peptide, whereby the cell penetrating peptide and the at least one antigen or antigenic epitope are optionally linked by a further component, e.g. a linker, a spacer, but not by the at least one TLR peptide agonist. Accordingly, this corresponds to the arrangements ( ⁇ ) and ( ⁇ ) from the arrangements shown above, i.e. from the above arrangements arrangements ( ⁇ ) and ( ⁇ ) are even more preferred.
  • the complex comprised by the combination for use according to the present invention is a recombinant polypeptide or a recombinant protein and the components a) to c) are positioned in N-terminus ⁇ C-terminus direction of the main chain of said complex in the order:
  • the at least one TLR agonist comprises or consists of at least one TLR2 agonist, for example:
  • TLR2 peptide agonist may also be arranged at other positions in the complex, for example:
  • the at least one TLR agonist comprises or consists of at least one TLR4 agonist, for example:
  • TLR4 peptide agonist may also be arranged at other positions in the complex, for example:
  • components a) and b) are linked via main-chain/main-chain linkage, resulting thus in the following arrangements of the components a) and b) in the complex, shown in N-terminus ⁇ C-terminus direction of the main chain of the complex, whereby the components a) and b) may be optionally linked by a further component, e.g. a linker, a spacer etc.:
  • component c) i.e. the at least one TLR peptide agonist
  • component c may then be arranged via main-chain/side-chain linkage, via side-chain/main-chain linkage or via side-chain/side chain linkage to either the cell penetrating peptide (a) or to the antigen/antigenic epitope (b) or, if present, to an additional component like a spacer or linker, which may be, for example, positioned between the cell penetrating peptide (a) and the antigen/antigenic epitope (b).
  • components b) and c) are linked via main-chain/main-chain linkage, resulting thus in the following arrangements of the components b) and c) in the complex, shown in N-terminus ⁇ C-terminus direction of the main chain of the complex, whereby the components b) and c) may be optionally linked by a further component, e.g. a linker, a spacer etc.:
  • component a i.e. the cell penetrating peptide
  • component a may then be arranged via main-chain/side-chain linkage, via side-chain/main-chain linkage or via side-chain/side chain linkage to either the antigen/antigenic epitope (b) or to the TLR peptide agonist (c) or, if present, to an additional component like a spacer or linker, which may be, for example, positioned between the antigen/antigenic epitope (b) and the TLR peptide agonist (c).
  • components a) and c) are linked via main-chain/main-chain linkage, resulting thus in the following arrangements of the components a) and b) in the complex, shown in N-terminus ⁇ C-terminus direction of the main chain of the complex, whereby the components a) and c) may be optionally linked by a further component, e.g. a linker, a spacer etc.:
  • component b i.e. the at least one antigen or antigenic epitope
  • component b may then be arranged via main-chain/side-chain linkage, via side-chain/main-chain linkage or via side-chain/side chain linkage to either the cell penetrating peptide (a) or to the TLR peptide agonist (c) or, if present, to an additional component like a spacer or linker, which may be, for example, positioned between the cell penetrating peptide (a) and the TLR peptide agonist (c).
  • Preferred combinations of a preferred immune checkpoint modulator and a preferred complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope
  • a preferred combination for use according to the present invention comprises a preferred immune checkpoint modulator as described herein.
  • a preferred combination for use according to the present invention comprises a preferred complex as described herein comprising a (preferred) cell penetrating peptide, at least one (preferred) antigen or antigenic epitope and at least one (preferred) TLR peptide agonist.
  • a more preferred combination for use according to the present invention comprises (i) a preferred immune checkpoint modulator as described herein and (ii) a preferred complex comprising as described herein comprising a (preferred) cell penetrating peptide, at least one (preferred) antigen or antigenic epitope and at least one (preferred) TLR peptide agonist.
  • a preferred immune checkpoint modulator as described herein
  • a preferred complex comprising as described herein comprising a (preferred) cell penetrating peptide, at least one (preferred) antigen or antigenic epitope and at least one (preferred) TLR peptide agonist.
  • the complex is a recombinant polypeptide or a recombinant protein wherein
  • the immune checkpoint modulator is a modulator of CD40, CTLA-4, PD-L1, PD-L2, PD-1 and/or IDO
  • the immune checkpoint modulator is an inhibitor of CTLA-4, PD-L1, PD-L2, PD-1 and/or IDO or an activator of CD40
  • the immune checkpoint modulator is an inhibitor of CTLA-4, PD-L1, PD-1 and/or IDO and even more preferably the immune checkpoint modulator is an inhibitor of CTLA-4 and/or PD-1.
  • the immune checkpoint modulator is a modulator of CD40, LAG3, CTLA-4, PD-L1, PD-L2, PD-1 and/or IDO
  • the immune checkpoint modulator is an inhibitor of LAG3, CTLA-4, PD-L1, PD-L2, PD-1 and/or IDO or an activator of CD40
  • the immune checkpoint modulator is an inhibitor of LAG3, CTLA-4, PD-L1, PD-1 and/or IDO and even more preferably the immune checkpoint modulator is an inhibitor of LAG3, CTLA-4 and/or PD-1.
  • immune checkpoint modulator e.g. checkpoint inhibitor
  • at least 2, 3, 4, 5, 6, 7, 8, 9 or 10 distinct immune checkpoint modulators, e.g. checkpoint inhibitors are used, preferably 2, 3, 4 or 5 distinct immune checkpoint modulators, e.g. checkpoint inhibitors, are used, more preferably 2, 3 or 4 distinct immune checkpoint modulators, e.g. checkpoint inhibitors, are used, even more preferably 2 or 3 distinct immune checkpoint modulators, e.g. checkpoint inhibitors, are used and most preferably 2 distinct immune checkpoint modulators, e.g. checkpoint inhibitors, are used.
  • an inhibitor of the CTLA-4 pathway in particular an inhibitor of CTLA-4 and (ii) an inhibitor of the PD-1 pathway, in particular an inhibitor of PD-1, PD-L1 or PD-L2 are used; preferably at least (i) an inhibitor of CTLA-4 and (ii) an inhibitor of PD-1 are used.
  • the combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein is for use in medicine.
  • Such a combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein is able to initiate or enhance the efficacy of checkpoint modulators.
  • a combination as described herein can simultaneously (i) stimulate multi-epitopic cytotoxic T cell-mediated immunity, (ii) induce T h cells and (iii) promote immunological memory, thereby generating potent, long lasting (anti-tumor) immunity. Immunological memory is essential to protect against relapse, in particular against tumor relapse.
  • the present invention thus provides to a combination as described herein which is able to initiate, enable, enhance or improve an immune response, in particular which enables, enhances or improves the subject's or tumor response to checkpoint modulators.
  • the combination for use according to the present invention can be useful in a variety of diseases.
  • the combination as described herein is for use (for the preparation of a medicament) for the prevention, treatment or stabilization of a disease or disorder, such as those which can be treated by immunotherapy, including cancers, infectious diseases, autoimmunity disorders, hematological diseases and transplant rejections.
  • a combination as described herein for use in the prevention, treatment or stabilization of a disease or disorder, such as those which can be treated by immunotherapy, including cancers, infectious diseases, autoimmunity disorders, hematological diseases and transplant rejections is preferred.
  • the combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein is used in the prevention and/or treatment of cancer.
  • disease as used in the context of the present invention is intended to be generally synonymous, and is used interchangeably with, the terms “disorder” and “condition” (as in medical condition), in that all reflect an abnormal condition of the human or animal body or of one of its parts that impairs normal functioning, is typically manifested by distinguishing signs and symptoms, and causes the human or animal to have a reduced duration or quality of life.
  • Preferred diseases to be treated and/or prevented by use of the combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein include cancer, hematological disorders, infectious diseases, autoimmunity disorders and transplant rejections. Thereby, treatment and/or prevention of cancer and infectious diseases is preferred and treatment and/or prevention of cancer is more preferred.
  • a malignant neoplasm of the brain or a malignant neoplasm of lymphoid, hematopoietic and related tissue are preferred and glioblastoma is more preferred.
  • the combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein may be used for (the preparation of a medicament for) the prophylaxis, treatment and/or amelioration of cancer or tumor diseases, including diseases caused by defective apoptosis, preferably selected from acusticus neurinoma, anal carcinoma, astrocytoma, basalioma, Behcet's syndrome, bladder cancer, blastomas, bone cancer, brain metastases, brain tumors, brain cancer (glioblastomas), breast cancer (mamma carcinoma), Burkitt's lymphoma, carcinoids, cervical cancer, colon carcinoma, colorectal cancer, corpus carcinoma, craniopharyngeomas, CUP syndrome, endometrial carcinoma, gall bladder cancer, genital tumors, including cancers of the genitourinary tract,
  • Burkitt's lymphoma EBV-induced B-cell lymphoma, cervix carcinoma), heptatitis B-induced tumors (hepatocell carcinomas), HTLV-1- and HTLV-2-induced lymphomas, vulval cancer, wart conditions or involvement, etc.
  • the terms “therapy” and “therapeutic” preferably mean to have at least some minimal physiological effect upon being administered to a living body.
  • a physiological effect upon administering a “therapeutic” anti-tumor compound may be the inhibition of tumor growth, or decrease in tumor size, or prevention reoccurrence of the tumor.
  • anti-tumor drug therefore preferably means any therapeutic agent having therapeutic effect against a tumor, neoplastic disease or cancer.
  • cancers to be treated with the combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein include brain cancer, prostate cancer, breast cancer, ovarian cancer, esophageal cancer, lung cancer, liver cancer, kidney cancer, melanoma, gut carcinoma, lung carcinoma, head and neck squamous cell carcinoma, chronic myeloid leukemia, colorectal carcinoma, gastric carcinoma, endometrial carcinoma, myeloid leukemia, lung squamous cell carcinoma, acute lymphoblastic leukemia, acute myelogenous leukemia, bladder tumor, promyelocytic leukemia, non-small cell lung carcinoma, and sarcoma.
  • the combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein are used to treat colorectal cancer.
  • the cancer may be a solid tumor, blood cancer, or lymphatic cancer.
  • the cancer may be benign or metastatic.
  • the cancer to be prevented and/or treated is a glioma, more preferably highly invasive glioblastoma multiforme (GBM).
  • Gliomas are the most frequent form of primary brain tumors in adults, with glioblastoma multiforme (GBM) having the poorest prognosis. This tumor is notorious for its highly invasive and aggressive behavior.
  • the combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein may be used in conjunction with existing modalities for glioma, more specifically highly invasive GBM.
  • T lymphocytes can actively seek out neoplastic cells in the brain, and have the potential to safely eliminate specific tumor cells without damaging the surrounding healthy tissues.
  • the combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein may be used for (the preparation of a medicament for) the prophylaxis, treatment and/or amelioration of infectious diseases, preferably viral, retroviral, bacterial or protozoological infectious diseases.
  • infectious diseases are typically selected from AIDS, anthrax, Japanese encephalitis, bacterial infectious diseases such as miscarriage (prostate inflammation), anthrax, appendicitis, borreliosis, botulism, Camphylobacter, Chlamydia trachomatis (inflammation of the urethra, conjunctivitis), cholera, diphtheria, donavanosis, epiglottitis, typhus fever, gas gangrene, gonorrhoea, rabbit fever, Heliobacter pylori , whooping cough, climatic bubo, osteomyelitis, Legionnaire's disease, chicken-pox, condyloma acuminata , cytomegalic virus (CMV), dengue fever, early summer meningoencephalitis (ESME), Ebola virus, colds, fifth disease, foot-and-mouth disease, herpes simplex type I, herpes simplex type II, herpes zoster,
  • human immunodeficiency virus type 1 or human immunodeficiency virus type 2 influenza virus, Lassa virus, lymphocytic choriomeningitis virus, Tacaribe virus, Junin virus, Machupo virus, Borna disease virus, Bunyamwera virus, California encephalitis virus, Rift Valley fever virus, sand fly fever virus, Toscana virus, Crimean-Congo haemorrhagic fever virus, Hazara virus, Khasan virus, Hantaan virus, Seoul virus, Prospect Hill virus, Puumala virus, Dobrava Belgrade virus, Tula virus, sinari virus, Lake Victoria Marburg virus, Zaire Ebola virus, Sudan Ebola virus, Ivory Coast Ebola virus, influenza virus A, influenza virus B, influenza viruses C, parainfluenza virus, measles virus, mumps virus, respiratory syncytial virus, human metapneumovirus, vesicular stomatitis Indiana virus, rabies virus, Mokola virus, Du
  • infectious diseases include diseases caused by viruses, bacteria, fungi, protozoa and multicellular parasites. They include, for instance, Amoebiasis, Anthrax, Buruli Ulcer ( Mycobacterium ulcerans ), Caliciviruses associated diarrhoea, Campylobacter diarrhoea, Cervical Cancer (Human papillomavirus), Chlamydia trachomatis associated genital diseases, Cholera, Crimean-Congo haemorrhagic fever, Dengue Fever, Diptheria, Ebola haemorrhagic fever, Enterotoxigenic Escherichia coli (ETEC) diarrhoea, Gastric Cancer ( Helicobacter pylori ), Gonorrhea, Group A Streptococcus associated diseases, Group B Streptococcus associated diseases, Haemophilus influenzae B pneumonia and invasive disease, Hepatitis A, Hepatitis B, Hepatitis
  • the combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein may be used for (the preparation of a medicament for) the prophylaxis, treatment and/or amelioration of autoimmune disorders, for example autoimmune diseases of the CNS, auto-inflammatory diseases, Celiac disease; Sjogren's syndrome, systemic lupus erythematosus etc.
  • autoimmune diseases arise from an abnormal immune response of the body against substances and tissues normally present in the body (autoimmunity). This may be restricted to certain organs (e.g.
  • Autoimmune diseases may be classified by corresponding type of hypersensitivity: type I (i.e. urticaria induced by autologous serum), type II, type III, or type IV.
  • type I i.e. urticaria induced by autologous serum
  • type II type III
  • type IV type IV
  • autoimmune diseases include Blau syndrome, Bullous pemphigoid, Cancer, Castleman's disease, Celiac disease, Chagas disease, Chronic inflammatory demyelinating polyneuropathy, Chronic recurrent multifocal osteomyelitis, chronic obstructive pulmonary disease, Churg-Strauss syndrome, Cicatricial pemphigoid, Cogan syndrome, Cold agglutinin disease, Complement component 2 deficiency, Contact dermatitis, Cranial arteritis, CREST syndrome, Crohn's disease, Cushing's Syndrome, Dercum's disease, Dermatitis herpetiformis, Dermatomyositis, Diabetes mellitus type 1, Diffuse cutaneous systemic sclerosis, Dressler's syndrome, lupus, Discoid lupus erythematosus, Eczema, Acute disseminated encephalomyelitis (ADEM), Addison's disease, Agammaglobulinemia, Amyotroph
  • the combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein may be used for (the preparation of a medicament for) the prophylaxis, treatment and/or amelioration of hematological disorders, which are typically disorders which primarily affect the blood. Thereby, hematological malignancies are preferred.
  • hematological diseases include myeloid disorders, including Hemoglobinopathies (congenital abnormality of the hemoglobin molecule or of the rate of hemoglobin synthesis), e.g. Sickle-cell disease, Thalassemia, Methemoglobinemia; Anemias (lack of red blood cells or hemoglobin), e.g.
  • Hemolytic anemias deficiency of red blood cells
  • Genetic disorders of RBC membrane such as Hereditary spherocytosis, Hereditary elliptocytosis, and Congenital dyserythropoietic anemia
  • Genetic disorders of RBC metabolism such as Glucose-6-phosphate dehydrogenase deficiency (G6PD), and Pyruvate kinase deficiency
  • Immune mediated hemolytic anemia direct Coombs test is positive
  • Autoimmune hemolytic anemia including Warm antibody autoimmune hemolytic anemia (such as Idiopathic, Systemic lupus erythematosus (SLE), and Evans' syndrome (antiplatelet antibodies and hemolytic antibodies)) and Cold antibody autoimmune hemolytic anemia (such as Idiopathic cold hemagglutinin syndrome, Infectious mononucle
  • Paroxysmal nocturnal hemoglobinuria rare acquired clonal disorder of red blood cell surface proteins
  • Direct physical damage to RBCs including Microangiopathic hemolytic anemia and Secondary to artificial heart valve(s)
  • Aplastic anemia such as Fanconi anemia, Diamond-Blackfan anemia (inherited pure red cell aplasia), and Acquired pure red cell aplasia; Decreased numbers of cells, e.g.
  • Myelodysplastic syndrome Myelofibrosis, Neutropenia (decrease in the number of neutrophils), Agranulocytosis, Glanzmann's thrombasthenia, and Thrombocytopenia (decrease in the number of platelets) including Idiopathic thrombocytopenic purpura (ITP), Thrombotic thrombocytopenic purpura (TTP), and Heparin-induced thrombocytopenia (HIT); Myeloproliferative disorders (Increased numbers of cells), e.g.
  • Polycythemia vera increase in the number of cells in general
  • Erythrocytosis increase in the number of red blood cells
  • Leukocytosis increase in the number of white blood cells
  • Thrombocytosis increase in the number of platelets
  • Myeloproliferative disorder Coagulopathies (disorders of bleeding and coagulation), e.g.
  • Thrombocytosis Recurrent thrombosis, Disseminated intravascular coagulation, Disorders of clotting proteins including Hemophilia such as Hemophilia A, Hemophilia B (also known as Christmas disease), and Hemophilia C, Von Willebrand disease, Disseminated intravascular coagulation, Protein S deficiency, and Antiphospholipid syndrome, and Disorders of platelets including Thrombocytopenia, Glanzmann's thrombasthenia, and Wiskott-Aldrich syndrome.
  • Hematological diseases also include hematological malignancies, e.g.
  • lymphomas including Hodgkin's disease and Non-Hodgkin's lymphoma such as Burkitt's lymphoma, Anaplastic large cell lymphoma, Splenic marginal zone lymphoma, Hepatosplenic T-cell lymphoma, and Angioimmunoblastic T-cell lymphoma (AILT), Myelomas such as Multiple myeloma, Waldenstrom macroglobulinemia, and Plasmacytoma, Leukemias such as Acute lymphocytic leukemia (ALL), Chronic lymphocytic leukemia (CLL), Acute myelogenous leukemia (AML), Chronic Idiopathic Myleofibrosis (MF), Chronic myelogenous leukemia (CML), T-cell prolymphocytic leukemia (T-PLL), B-cell prolymphocytic leukemia (B-PLL), Chronic neutrophilic leukemia (CNL), Hairy cell leukemia (HCL), T-cell large
  • examples of hematological diseases also include miscellaneous haematological diseases including Hemochromatosis, Asplenia, Hypersplenism such as Gauchers disease, Monoclonal gammopathy of undetermined significance, Hemophagocytic lymphohistiocytosis, and Tempi syndrome.
  • examples of hematological diseases also include hematological changes secondary to non-hematological disorders including Anemia of chronic disease, Infectious mononucleosis, AIDS, Malaria, and Leishmaniasis.
  • the combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein may be used for (the preparation of a medicament for) the prophylaxis, treatment and/or amelioration of transplant rejection, including e.g. graft-versus-host reaction.
  • Transplant rejection includes hyperacute rejection, acute rejection and chronic rejection of a transplant. Examples of transplant rejection include skin, kidney, heart, lung, pancreas, liver, blood cell, bone marrow, cornea, accidental severed limb, in particular fingers, hand, foot, face, nose, bone, cardiac valve, blood vessel or intestine transplant rejection reaction.
  • “combination of the immune checkpoint modulator as described herein and of the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein” means that the therapy with the immune checkpoint modulator as described herein is combined with the therapy with the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein.
  • the therapy with the immune checkpoint modulator as described herein is combined with the therapy with the complex comprising a cell penetrating peptide, at least one antigen or antigenic epitope and at least one TLR peptide agonist as described herein.
  • a combination in the context of the present invention does in particular not include the start of a therapy with one component (the checkpoint modulator or the complex) after the therapy with the other component (the other of checkpoint modulator or complex) is finished.
  • a “finished” therapy means in particular that the active component does not exert its effects anymore—i.e. a “therapy” may in particular be finished several minutes, hours or days after the last administration of the active component, depending on how long the active component exerts its effects.
  • one component may be administered once a week and the other component (the other of checkpoint modulator or complex) may be administered once a month.
  • the monthly administered component is to be administered at least once in the same week, in which also the weekly administered other component is administered.
  • the administration of the immune checkpoint modulator and/or of the complex comprised by the combination for use according to the present invention may require multiple successive administrations, e.g. multiple injections.
  • the administration may be repeated at least two times, for example once as primary immunization injections and, later, as booster injections.
  • the immune checkpoint modulator and/or the complex comprised by the combination for use according to the present invention may be administered repeatedly or continuously.
  • the immune checkpoint modulator and/or the complex comprised by the combination for use according to the present invention may be administered repeatedly or continuously for a period of at least 1, 2, 3, or 4 weeks; 2, 3, 4, 5, 6, 8, 10, or 12 months; or 2, 3, 4, or 5 years.
  • the immune checkpoint modulator comprised by the combination for use according to the present invention may be administered twice per day, once per day, every two days, every three days, once per week, every two weeks, every three weeks, once per month or every two months.
  • the complex comprised by the combination for use according to the present invention may be administered twice per day, once per day, every two days, every three days, once per week, every two weeks, every three weeks, once per month or every two months.
  • the complex comprised by the combination for use according to the present invention may be administered repeatedly, for example once per week or (once) every two weeks.
  • the immune checkpoint modulator and the complex are preferably administered at about the same time.
  • “At about the same time”, as used herein, means in particular simultaneous administration or that directly after administration of the immune checkpoint modulator the complex is administered or directly after administration of the complex the immune checkpoint modulator is administered.
  • “directly after” includes the time necessary to prepare the second administration—in particular the time necessary for exposing and disinfecting the location for the second administration as well as appropriate preparation of the “administration device” (e.g., syringe, pump, etc.).
  • Simultaneous administration also includes if the periods of administration of the checkpoint modulator and of the complex overlap or if, for example, one component (checkpoint modulator or complex) is administered over a longer period of time, such as 30 min, 1 h, 2 h or even more, e.g.
  • checkpoint modulator or complex by infusion, and the other component (checkpoint modulator or complex) is administered at some time during such a long period.
  • Administration of the immune checkpoint modulator and of the complex at about the same time is in particular preferred if different routes of administration and/or different administration sites are used.
  • the immune checkpoint modulator and the complex are administered consecutively.
  • the immune checkpoint modulator is preferably administered before the complex. It is also preferred that the immune checkpoint modulator is administered after the complex.
  • the time between administration of the first component (the checkpoint modulator or the complex) and administration of the second component (the other of the checkpoint modulator and the complex) is preferably no more than one week, more preferably no more than 3 days, even more preferably no more than 2 days and most preferably no more than 24 h. It is particularly preferred that the checkpoint modulator and the complex are administered at the same day with the time between administration of the first component (the checkpoint modulator of the complex) and administration of the second component (the other of the checkpoint modulator and the complex) being preferably no more than 6 hours, more preferably no more than 3 hours, even more preferably no more than 2 hours and most preferably no more than 1 h.
  • the immune checkpoint modulator comprised by the combination for use according to the present invention and the complex comprised by the combination for use according to the present invention are administered in a therapeutically effective amount.
  • a “therapeutically effective amount”, as used herein, is the amount which is sufficient for the alleviation of the symptoms of the disease or condition being treated and/or for prophylaxis of the symptoms of the disease or condition being prevented.
  • a “therapeutically effective amount” means an amount of the complex and/or of the checkpoint modulator that is sufficient to significantly induce a positive modification of a disease or disorder, i.e. an amount of the complex and/or of the checkpoint modulator, that elicits the biological or medicinal response in a tissue, system, animal or human that is being sought.
  • the term also includes the amount of the complex and/or of the immune checkpoint modulator sufficient to reduce the progression of the disease, notably to reduce or inhibit the tumor growth or infection and thereby elicit the response being sought, in particular such response could be an immune response directed against the antigens or antigenic epitopes comprised in by the complex (i.e. an “inhibition effective amount”).
  • an “inhibition effective amount” is preferably small enough to avoid serious side-effects, that is to say to permit a sensible relationship between advantage and risk. The determination of these limits typically lies within the scope of sensible medical judgment.
  • a “therapeutically effective amount” of the complex and/or of the checkpoint modulator will furthermore vary in connection with the particular condition to be treated and also with the age and physical condition of the patient to be treated, the body weight, general health, sex, diet, time of administration, rate of excretion, drug combination, the activity of the specific components (checkpoint modulator and complex), the severity of the condition, the duration of the treatment, the nature of the accompanying therapy, of the particular pharmaceutically acceptable carrier used, and similar factors, within the knowledge and experience of the accompanying doctor.
  • the dosage administered, as single or multiple doses, to an individual will thus vary depending upon a variety of factors, including pharmacokinetic properties, subject conditions and characteristics (sex, age, body weight, health, size), extent of symptoms, concurrent treatments, frequency of treatment and the effect desired.
  • the therapeutically effective dose of the complex comprised by the combination for use according to the present invention is from about 0.001 mg to 10 mg, preferably from about 0.01 mg to 5 mg, more preferably from about 0.1 mg to 2 mg per injection or from about 0.01 nmol to 1 mmol per injection, in particular from 1 nmol to 1 mmol per injection, preferably from 1 ⁇ mol to 1 mmol per injection.
  • the therapeutically effective dose of the complex comprised by the combination for use according to the present invention is (per kg body weight), in particular for cancer treatment, from about 0.01 mg/kg to 100 mg/kg, preferably from about 0.05 mg/kg to 50 mg/kg, more preferably from about 0.1 mg/kg to 25 mg/kg, even more preferably from about 0.5 mg/kg to 10 mg/kg and most preferably from about 1 mg/kg to 5 mg/kg.
  • the therapeutically effective dose of the immune checkpoint modulator comprised by the combination for use according to the present invention is (per kg body weight), in particular for cancer treatment, from about 0.01 mg/kg to 100 mg/kg, preferably from about 0.05 mg/kg to 50 mg/kg, more preferably from about 0.1 mg/kg to 25 mg/kg, even more preferably from about 0.5 mg/kg to 15 mg/kg and most preferably from about 1 mg/kg to 10 mg/kg.
  • the complex comprised by the combination for use according to the present invention and the immune checkpoint modulator comprised by the combination for use according to the present invention can be administered by various routes of administration, for example, systemically or locally.
  • Routes for systemic administration in general include, for example, transdermal, oral and parenteral routes, which include subcutaneous, intravenous, intramuscular, intraarterial, intradermal and intraperitoneal routes and/or intranasal administration routes.
  • Routes for local administration in general include, for example, topical administration routes, but also administration directly at the site of affliction, such as intratumoral administration.
  • the complex comprised by the combination for use according to the present invention and the immune checkpoint modulator comprised by the combination for use according to the present invention are administered by a parenteral route of administration. More preferably, the complex comprised by the combination for use according to the present invention and the immune checkpoint modulator comprised by the combination for use according to the present invention are administered via intravenous, intratumoral, intradermal, subcutaneous, intramuscular, intranasal, or intranodal route. Even more preferably, the complex comprised by the combination for use according to the present invention and the immune checkpoint modulator comprised by the combination for use according to the present invention are administered intravenously and/or subcutaneously. It is also more preferred that the complex comprised by the combination for use according to the present invention and the immune checkpoint modulator comprised by the combination for use according to the present invention are administered intradermally and/or subcutaneously
  • the complex comprised by the combination for use according to the present invention and the immune checkpoint modulator comprised by the combination for use according to the present invention are administered via the same route of administration, preferably via the same parenteral route of administration, more preferably intravenously or subcutaneously.
  • the complex comprised by the combination for use according to the present invention and the immune checkpoint modulator comprised by the combination for use according to the present invention are administered via distinct routes of administration, preferably via distinct parenteral routes of administration, more preferably the immune checkpoint modulator comprised by the combination for use according to the present invention is administered intravenously and the complex comprised by the combination for use according to the present invention is administered via intratumoral, intradermal, subcutaneous, intramuscular, intranasal, or intranodal route, preferably the complex comprised by the combination for use according to the present invention is administered subcutaneously. Even more preferably the immune checkpoint modulator comprised by the combination for use according to the present invention is administered intravenously and/or the complex comprised by the combination for use according to the present invention is administered subcutaneously or intradermally.
  • the complex comprised by the combination for use according to the present invention and the immune checkpoint modulator comprised by the combination for use according to the present invention may be provided in the same or in distinct compositions.
  • the complex comprised by the combination for use according to the present invention and the immune checkpoint modulator comprised by the combination for use according to the present invention are provided in distinct compositions.
  • different other components e.g. different vehicles
  • the complex and the immune checkpoint modulator can be administered via different routes of administration and the doses (in particular the relation of the doses) can be adjusted according to the actual need.
  • composition according to the present invention is described in more detail below (“composition according to the present invention”).
  • composition may be a pharmaceutical composition and/or a vaccine composition.
  • such a composition which comprises only the immune checkpoint modulator (and not the complex), only the complex (and not the checkpoint modulator) or both, is preferably a (pharmaceutical) composition which optionally comprises a pharmaceutically acceptable carrier and/or vehicle, or any excipient, buffer, stabilizer or other materials well known to those skilled in the art.
  • the (pharmaceutical) composition may in particular comprise a pharmaceutically acceptable carrier and/or vehicle.
  • a pharmaceutically acceptable carrier typically includes the liquid or non-liquid basis of the (pharmaceutical) composition. If the (pharmaceutical) composition is provided in liquid form, the carrier will typically be pyrogen-free water; isotonic saline or buffered (aqueous) solutions, e.g phosphate, citrate etc. buffered solutions.
  • water or preferably a buffer preferably an aqueous buffer
  • a sodium salt preferably at least 30 mM of a sodium salt
  • a calcium salt preferably at least 0.05 mM of a calcium salt
  • optionally a potassium salt preferably at least 1 mM of a potassium salt.
  • the sodium, calcium and, optionally, potassium salts may occur in the form of their halogenides, e.g. chlorides, iodides, or bromides, in the form of their hydroxides, carbonates, hydrogen carbonates, or sulfates, etc.
  • examples of sodium salts include e.g.
  • examples of the optional potassium salts include e.g. KCl, KI, KBr, K 2 CO 3 , KHCO 3 , K 2 SO 4
  • examples of calcium salts include e.g. CaCl 2 , CaI 2 , CaBr 2 , CaCO 3 , CaSO 4 , Ca(OH) 2 .
  • organic anions of the aforementioned cations may be contained in the buffer.
  • the buffer suitable for injection purposes as defined above may contain salts selected from sodium chloride (NaCl), calcium chloride (CaCl 2 )) and optionally potassium chloride (KCl), wherein further anions may be present additional to the chlorides.
  • CaCl 2 can also be replaced by another salt like KCl.
  • the salts in the injection buffer are present in a concentration of at least 30 mM sodium chloride (NaCl), at least 1 mM potassium chloride (KCl) and at least 0.05 mM calcium chloride (CaCl 2 ).
  • the injection buffer may be hypertonic, isotonic or hypotonic with reference to the specific reference medium, i.e.
  • the buffer may have a higher, identical or lower salt content with reference to the specific reference medium, wherein preferably such concentrations of the afore mentioned salts may be used, which do not lead to damage of cells due to osmosis or other concentration effects.
  • Reference media are e.g. liquids occurring in “in vivo” methods, such as blood, lymph, cytosolic liquids, or other body liquids, or e.g. liquids, which may be used as reference media in “in vitro” methods, such as common buffers or liquids.
  • Such common buffers or liquids are known to a skilled person. Saline (0.9% NaCl) and Ringer-Lactate solution are particularly preferred as a liquid basis.
  • the (pharmaceutical) composition which comprises the immune checkpoint modulator and/or the complex as described herein, further comprises arginine, such as L-arginine.
  • compatible solid or liquid fillers or diluents or encapsulating compounds may be used as well for the (pharmaceutical) composition, which are suitable for administration to a subject to be treated.
  • compatible means that these constituents of the (pharmaceutical) composition are capable of being mixed with the complex according to the present invention as defined above in such a manner that no interaction occurs which would substantially reduce the pharmaceutical effectiveness of the (pharmaceutical) composition under typical use conditions.
  • Pharmaceutically acceptable carriers, fillers and diluents must, of course, have sufficiently high purity and sufficiently low toxicity to make them suitable for administration to a subject to be treated.
  • Some examples of compounds which can be used as pharmaceutically acceptable carriers, fillers or constituents thereof are sugars, such as, for example, lactose, glucose and sucrose; starches, such as, for example, corn starch or potato starch; cellulose and its derivatives, such as, for example, sodium carboxymethylcellulose, ethylcellulose, cellulose acetate; powdered tragacanth; malt; gelatin; tallow; solid glidants, such as, for example, stearic acid, magnesium stearate; calcium sulfate; vegetable oils, such as, for example, groundnut oil, cottonseed oil, sesame oil, olive oil, corn oil and oil from theobroma; polyols, such as, for example, polypropylene glycol, glycerol, sorbitol, mannitol and polyethylene glycol; alginic acid.
  • sugars such as, for example, lactose, glucose and sucrose
  • starches such as, for example, corn star
  • the (pharmaceutical) composition may be administered orally, parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir.
  • parenteral as used herein includes subcutaneous, intravenous, intramuscular, intra-articular, intra-synovial, intrasternal, intrathecal, intrahepatic, intralesional, intracranial, transdermal, intradermal, intrapulmonal, intraperitoneal, intracardial, intraarterial, and sublingual injection or infusion techniques.
  • the (pharmaceutical) composition may be administered by parenteral injection, more preferably by subcutaneous, intravenous, intramuscular, intra-articular, intra-synovial, intrasternal, intrathecal, intrahepatic, intralesional, intracranial, transdermal, intradermal, intrapulmonal, intraperitoneal, intracardial, intraarterial, and sublingual injection or via infusion techniques.
  • Sterile injectable forms of the (pharmaceutical) compositions may be aqueous or oleaginous suspension. These suspensions may be formulated according to techniques known in the art using suitable dispersing or wetting agents and suspending agents.
  • the sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally-acceptable diluent or solvent, for example as a solution in 1,3-butanediol.
  • a non-toxic parenterally-acceptable diluent or solvent for example as a solution in 1,3-butanediol.
  • acceptable vehicles and solvents that may be employed are water, Ringer's solution and isotonic sodium chloride solution.
  • sterile, fixed oils are conventionally employed as a solvent or suspending medium.
  • any bland fixed oil may be employed including synthetic mono- or di-glycerides.
  • Fatty acids such as oleic acid and its glyceride derivatives are useful in the preparation of injectables, as are natural pharmaceutically-acceptable oils, such as olive oil or castor oil, especially in their polyoxyethylated versions.
  • oils such as olive oil or castor oil, especially in their polyoxyethylated versions.
  • These oil solutions or suspensions may also contain a long-chain alcohol diluent or dispersant, such as carboxymethyl cellulose or similar dispersing agents that are commonly used in the formulation of pharmaceutically acceptable dosage forms including emulsions and suspensions.
  • surfactants such as Tweens, Spans and other emulsifying agents or bioavailability enhancers which are commonly used in the manufacture of pharmaceutically acceptable solid, liquid, or other dosage forms may also be used for the purposes of formulation of the (pharmaceutical) composition.
  • the active ingredient will preferably be in the form of a parenterally acceptable aqueous solution which is pyrogen-free and has suitable pH, isotonicity and stability.
  • a parenterally acceptable aqueous solution which is pyrogen-free and has suitable pH, isotonicity and stability.
  • isotonic vehicles such as Sodium Chloride Injection, Ringer's Injection, Lactated Ringer's Injection.
  • Preservatives, stabilizers, buffers, antioxidants and/or other additives may be included, as required.
  • administration is preferably in a “therapeutically effective amount”, this being sufficient to show benefit to the individual.
  • the actual amount administered, and rate and time-course of administration, will depend on the nature and severity of what is being treated.
  • the (pharmaceutical) composition as described herein may also be administered orally in any orally acceptable dosage form including, but not limited to, capsules, tablets, aqueous suspensions or solutions.
  • carriers commonly used include lactose and corn starch.
  • Lubricating agents such as magnesium stearate, are also typically added.
  • useful diluents include lactose and dried cornstarch.
  • the active ingredient i.e. the inventive transporter cargo conjugate molecule as defined above, is combined with emulsifying and suspending agents. If desired, certain sweetening, flavoring or coloring agents may also be added.
  • the (pharmaceutical) composition may also be administered topically, especially when the target of treatment includes areas or organs readily accessible by topical application, e.g. including diseases of the skin or of any other accessible epithelial tissue. Suitable topical formulations are readily prepared for each of these areas or organs.
  • the (pharmaceutical) composition may be formulated in a suitable ointment, containing the inventive immunostimulatory composition, particularly its components as defined above, suspended or dissolved in one or more carriers.
  • Carriers for topical administration include, but are not limited to, mineral oil, liquid petrolatum, white petrolatum, propylene glycol, polyoxyethylene, polyoxypropylene compound, emulsifying wax and water.
  • the (pharmaceutical) composition can be formulated in a suitable lotion or cream.
  • suitable carriers include, but are not limited to, mineral oil, sorbitan monostearate, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol and water.
  • prescription of treatment e.g. decisions on dosage etc. when using the above (pharmaceutical) composition is typically within the responsibility of general practitioners and other medical doctors, and typically takes account of the disorder to be treated, the condition of the individual patient, the site of delivery, the method of administration and other factors known to practitioners. Examples of the techniques and protocols mentioned above can be found in REMINGTON'S PHARMACEUTICAL SCIENCES, 16th edition, Osol, A. (ed), 1980.
  • the (pharmaceutical) composition typically comprises a therapeutically effective amount of the components of the (pharmaceutical) composition, in particular of the complex and/or of the checkpoint modulator.
  • the (pharmaceutical) composition may be used for human and also for veterinary medical purposes, preferably for human medical purposes, as a (pharmaceutical) composition in general or as a vaccine.
  • compositions in particular vaccine compositions, or formulations according to the invention may be administered as a pharmaceutical formulation which can contain the complex as described herein and/or the checkpoint modulator as described herein in any form described herein.
  • pharmaceutical formulation and “pharmaceutical composition” as used in the context of the present invention refer in particular to preparations which are in such a form as to permit biological activity of the active ingredient(s) to be unequivocally effective and which contain no additional component which would be toxic to subjects to which the said formulation would be administered.
  • an “efficacy” of a treatment can be measured based on changes in the course of a disease in response to a use or a method according to the present invention.
  • the efficacy of a treatment of cancer can be measured by a reduction of tumor volume, and/or an increase of progression free survival time, and/or a decreased risk of relapse post-resection for primary cancer.
  • assessment of efficacy can be by the spectrum of clinical patterns of antitumor response for immunotherapeutic agents through novel immune-related response criteria (irRC), which are adapted from Response Evaluation Criteria in Solid Tumors (RECIST) and World Health Organization (WHO) criteria ( J. Natl. Cancer Inst.
  • the efficacy of prevention of infectious disease is ultimately assessed by epidemiological studies in human populations, which often correlates with titres of neutralizing antibodies in sera, and induction of multifunctional pathogen specific T cell responses.
  • Preclinical assessment can include resistance to infection after challenge with infectious pathogen.
  • Treatment of an infectious disease can be measured by inhibition of the pathogen's growth or elimination of the pathogen (and, thus, absence of detection of the pathogen), correlating with pathogen specific antibodies and/or T cell immune responses.
  • compositions in particular vaccine compositions, or formulations according to the invention may also be administered as a pharmaceutical formulation which can contain antigen presenting cells loaded with the complex as described herein in any form described herein.
  • the vaccine and/or the composition according to the present invention may also be formulated as (pharmaceutical) compositions and unit dosages thereof, in particular together with a conventionally employed adjuvant, immunomodulatory material, carrier, diluent or excipient as described above and below, and in such form may be employed as solids, such as tablets or filled capsules, or liquids such as solutions, suspensions, emulsions, elixirs, or capsules filled with the same, all for oral use, or in the form of sterile injectable solutions for parenteral (including subcutaneous and intradermal) use by injection or continuous infusion.
  • injectable compositions are typically based upon injectable sterile saline or phosphate-buffered saline or other injectable carriers known in the art.
  • Such (pharmaceutical) compositions and unit dosage forms thereof may comprise ingredients in conventional proportions, with or without additional active compounds or principles, and such unit dosage forms may contain any suitable effective amount of the active ingredient commensurate with the intended daily dosage range to be employed.
  • suitable adjuvants and/or immunomodulatory materials include MPL® (Corixa), aluminum-based minerals including aluminum compounds (generically called Alum), ASO1-4, MF59, CalciumPhosphate, Liposomes, Iscom, polyinosinic:polycytidylic acid (polyIC), including its stabilized form poly-ICLC (Hiltonol), CpG oligodeoxynucleotides, Granulocyte-macrophage colony-stimulating factor (GM-CSF), lipopolysaccharide (LPS), Montanide, polylactide co-glycolide (PLG), Flagellin, Soap Bark tree saponins (QS21), amino alkyl glucosamide compounds (e.g.
  • RC529 two component antibacterial peptides with synthetic oligodeoxynucleotides (e.g. IC31), Imiquimod, Resiquimod, Immunostimulatory sequences (ISS), monophosphoryl lipid A (MPLA), and Fibroblast-stimulating lipopeptide (FSL1).
  • compositions in particular pharmaceutical compositions and vaccines, according to the present invention may be liquid formulations including, but not limited to, aqueous or oily suspensions, solutions, emulsions, syrups, and elixirs.
  • the compositions may also be formulated as a dry product for reconstitution with water or other suitable vehicle before use.
  • Such liquid preparations may contain additives including, but not limited to, suspending agents, emulsifying agents, non-aqueous vehicles and preservatives.
  • Suspending agents include, but are not limited to, sorbitol syrup, methyl cellulose, glucose/sugar syrup, gelatin, hydroxyethyl cellulose, carboxymethyl cellulose, aluminum stearate gel, and hydrogenated edible fats.
  • Emulsifying agents include, but are not limited to, lecithin, sorbitan monooleate, and acacia.
  • Preservatives include, but are not limited to, methyl or propyl p-hydroxybenzoate and sorbic acid.
  • Dispersing or wetting agents include but are not limited to poly(ethylene glycol), glycerol, bovine serum albumin, Tween®, Span®.
  • compositions in particular pharmaceutical compositions and vaccines, according to the present invention may also be formulated as a depot preparation, which may be administered by implantation or by intramuscular injection.
  • compositions in particular pharmaceutical compositions and vaccines, according to the present invention may also be solid compositions, which may be in the form of tablets or lozenges formulated in a conventional manner.
  • tablets and capsules for oral administration may contain conventional excipients including, but not limited to, binding agents, fillers, lubricants, disintegrants and wetting agents.
  • Binding agents include, but are not limited to, syrup, accacia, gelatin, sorbitol, tragacanth, mucilage of starch and polyvinylpyrrolidone.
  • Fillers include, but are not limited to, lactose, sugar, microcrystalline cellulose, maizestarch, calcium phosphate, and sorbitol.
  • Lubricants include, but are not limited to, magnesium stearate, stearic acid, talc, polyethylene glycol, and silica.
  • Disintegrants include, but are not limited to, potato starch and sodium starch glycollate.
  • Wetting agents include, but are not limited to, sodium lauryl sulfate. Tablets may be coated according to methods well known in the art.
  • compositions in particular pharmaceutical compositions and vaccines, according to the present invention may also be administered in sustained release forms or from sustained release drug delivery systems.
  • compositions in particular pharmaceutical compositions and vaccines, according to the present invention may be adapted for delivery by repeated administration.
  • kits in particular a kit of parts, comprising
  • such a kit according to the present invention comprises (i) the immune checkpoint modulator as described above (in the context of the combination for use according to the present invention) and (ii) the complex as described above (in the context of the combination for use according to the present invention).
  • preferred embodiments of the immune checkpoint modulator as described above are also preferred in the kit according to the present invention.
  • preferred embodiments of the complex as described above are also preferred in the kit according to the present invention.
  • kits may be packaged in one or more containers.
  • the above components may be provided in a lyophilized or dry form or dissolved in a suitable buffer.
  • the kit may comprise a (pharmaceutical) composition comprising the immune checkpoint modulator as described above and a (pharmaceutical) composition comprising the complex as described above, e.g. with each composition in a separate container.
  • the kit may also comprise a (pharmaceutical) composition comprising both, the immune checkpoint modulator and the complex, as described above.
  • the kit may also comprise additional reagents including, for instance, preservatives, growth media, and/or buffers for storage and/or reconstitution of the above-referenced components, washing solutions, and the like.
  • kit-of-parts according to the present invention may optionally contain instructions of use.
  • the kit further comprises a package insert or label with directions to treat a disease as described herein, for example cancer, by using a combination of the immune checkpoint modulator and the complex.
  • kit may preferably be for use in medicine as described herein, in particular for use in the prevention and/or treatment of cancer as described herein.
  • the present invention also provides a vaccination kit for treating, preventing and/or stabilizing a disease, e.g. a cancer or an infectious disease, comprising the pharmaceutical composition comprising the immune checkpoint modulator as described herein and the pharmaceutical composition, in particular the vaccine, comprising the complex as described herein (wherein the pharmaceutical compositions may be the same or different) and instructions for use of said pharmaceutical composition or of said vaccine.
  • a disease e.g. a cancer or an infectious disease
  • a vaccine comprising the complex as described herein (wherein the pharmaceutical compositions may be the same or different) and instructions for use of said pharmaceutical composition or of said vaccine.
  • the present invention also provides a composition comprising
  • such a composition according to the present invention comprises (i) the immune checkpoint modulator as described above (in the context of the combination for use according to the present invention) and (ii) the complex as described above (in the context of the combination for use according to the present invention).
  • preferred embodiments of the immune checkpoint modulator as described above are also preferred in the composition according to the present invention.
  • preferred embodiments of the complex as described above are also preferred in the composition according to the present invention.
  • compositions comprising the immune checkpoint modulator as described above and the complex as described above and preferred embodiments of such a composition are described above (in the context of the combination for use according to the present invention). It is understood that the same description, in particular the same preferred embodiments as described above for the composition apply accordingly to the composition as described here.
  • composition preferably comprises a pharmaceutically acceptable carrier.
  • a pharmaceutically acceptable carrier are as described above.
  • composition comprises at least two different complexes.
  • a preferred composition comprises at least two different immune checkpoint modulators.
  • composition may preferably be for use in medicine as described herein, in particular for use in the prevention and/or treatment of cancer as described herein.
  • composition is a vaccine.
  • the term “vaccine” refers to a biological preparation that provides innate and/or adaptive immunity, typically to a particular disease, preferably cancer.
  • a vaccine supports in particular an innate and/or an adaptive immune response of the immune system of a subject to be treated.
  • the antigen or antigenic epitope of the complex as described herein typically leads to or supports an adaptive immune response in the patient to be treated, and the TLR peptide agonist of the complex as described herein may lead to or support an innate immune response.
  • the vaccine may also comprise a pharmaceutically acceptable carrier, adjuvant, and/or vehicle as defined below for the inventive pharmaceutical composition.
  • a pharmaceutically acceptable carrier is determined in principle by the manner in which the inventive vaccine is administered.
  • the inventive vaccine can be administered, for example, systemically or locally as described above. More preferably, vaccines may be administered by an intravenous, intradermal, subcutaneous, or intramuscular route.
  • the vaccine is therefore preferably formulated in liquid (or sometimes in solid) form.
  • the suitable amount of the vaccine to be administered can be determined by routine experiments with animal models. Such models include, without implying any limitation, rabbit, sheep, mouse, rat, dog and non-human primate models.
  • Preferred unit dose forms for injection include sterile solutions of water, physiological saline or mixtures thereof.
  • Suitable carriers for injection include hydrogels, devices for controlled or delayed release, polylactic acid and collagen matrices.
  • Suitable pharmaceutically acceptable carriers for topical application include those which are suitable for use in lotions, creams, gels and the like. If the inventive vaccine is to be administered orally, tablets, capsules and the like are the preferred unit dose form.
  • the pharmaceutically acceptable carriers for the preparation of unit dose forms which can be used for oral administration are well known in the prior art. The choice thereof will depend on secondary considerations such as taste, costs and storability, which are not critical for the purposes of the present invention, and can be made without difficulty by a person skilled in the art.
  • the vaccine can additionally contain one or more auxiliary substances in order to further increase its immunogenicity.
  • various mechanisms can come into consideration in this respect. For example, compounds that permit the maturation of dendritic cells (DCs), for example lipopolysaccharides or TNF-alpha, form a first class of suitable auxiliary substances.
  • DCs dendritic cells
  • TNF-alpha for example lipopolysaccharides or TNF-alpha
  • auxiliary substance any agent that influences the immune system in the manner of a “danger signal” (LPS, GP96, etc.) or cytokines, such as GM-CSF, which allow an immune response produced by the immune-stimulating adjuvant according to the invention to be enhanced and/or influenced in a targeted manner.
  • a “danger signal” LPS, GP96, etc.
  • cytokines such as GM-CSF
  • auxiliary substances are cytokines, such as monokines, lymphokines, interleukins or chemokines, that further promote the innate immune response, such as IL-1, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-12, IL-13, IL-14, IL-15, IL-16, IL-17, IL-18, IL-19, IL-20, IL-21, IL-22, IL-23, IL-24, IL-25, IL-26, IL-27, IL-28, IL-29, IL-30, IL-31, IL-32, IL-33, IFN-alpha, IFN-beta, IFN-gamma, GM-CSF, G-CSF, M-CSF, LT-beta or TNF-alpha, growth factors, such as hGH.
  • cytokines such as monokines, lymphokines, interleukins
  • emulsifiers such as, for example, Tween®
  • wetting agents such as, for example, sodium lauryl sulfate
  • colouring agents such as, for example, sodium lauryl sulfate
  • taste-imparting agents pharmaceutical carriers
  • tablet-forming agents such as, for example, stabilizers; antioxidants; preservatives.
  • the inventive vaccine can also additionally contain any further compound, which is known to be immune-stimulating due to its binding affinity (as ligands) to human Toll-like receptors TLR1, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TLR10, or due to its binding affinity (as ligands) to murine Toll-like receptors TLR1, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TLR10, TLR11, TLR12 or TLR13.
  • any further compound which is known to be immune-stimulating due to its binding affinity (as ligands) to human Toll-like receptors TLR1, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TLR10, TLR11, TLR12 or TLR13.
  • CpG nucleic acids in particular CpG-RNA or CpG-DNA.
  • a CpG-RNA or CpG-DNA can be a single-stranded CpG-DNA (ss CpG-DNA), a double-stranded CpG-DNA (dsDNA), a single-stranded CpG-RNA (ss CpG-RNA) or a double-stranded CpG-RNA (ds CpG-RNA).
  • the CpG nucleic acid is preferably in the form of CpG-RNA, more preferably in the form of single-stranded CpG-RNA (ss CpG-RNA).
  • the CpG nucleic acid preferably contains at least one or more (mitogenic) cytosine/guanine dinucleotide sequence(s) (CpG motif(s)).
  • CpG motif(s) cytosine/guanine dinucleotide sequence(s)
  • at least one CpG motif contained in these sequences in particular the C (cytosine) and the G (guanine) of the CpG motif, is unmethylated. All further cytosines or guanines optionally contained in these sequences can be either methylated or unmethylated.
  • the C (cytosine) and the G (guanine) of the CpG motif can also be present in methylated form.
  • the (pharmaceutical) composition, in particular the vaccine, as described above is for use in the prevention and/or treatment of diseases or disorders including for example cancers, hematological disorders, infectious diseases, autoimmunity disorders and transplant rejections, whereby cancer is preferred.
  • diseases or disorders including for example cancers, hematological disorders, infectious diseases, autoimmunity disorders and transplant rejections, whereby cancer is preferred.
  • the (pharmaceutical) composition in particular the vaccine, is used in a method for treating a subject, preferably a mammalian subject, and most preferably a human subject, who is suffering from a disease or disorder, in particular from a disorder that can be treated by immunotherapy such as cancers, infectious diseases, autoimmunity disorders and transplant rejections.
  • a subject preferably a mammalian subject, and most preferably a human subject, who is suffering from a disease or disorder, in particular from a disorder that can be treated by immunotherapy such as cancers, infectious diseases, autoimmunity disorders and transplant rejections.
  • the invention also provides a nucleic acid molecule comprising a polynucleotide encoding the immune checkpoint modulator according to the present invention as described above, wherein the immune checkpoint modulator is a (poly)peptide or a protein, and/or encloding the complex according to the present invention as described above, wherein the complex is a (poly)peptide or a protein, in particular a fusion (poly)peptide or a fusion protein.
  • the nucleic acid (molecule) encodes at least an exemplified complex as described herein or a functional sequence variant thereof.
  • the nucleic acid (molecule) most preferably comprises a polynucleotide encoding an amino acid sequence according to any of SEQ ID NOs: 26-32, or 41-45 or an amino acid sequence sharing at least 50%, at least 60%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95% or at least 98% sequence identity with any of SEQ ID NOs: 26-32, or 41-45.
  • nucleic acid molecules and/or polynucleotides include, e.g., a recombinant polynucleotide, a vector, an oligonucleotide, an RNA molecule such as an rRNA, an mRNA, an miRNA, an siRNA, or a tRNA, or a DNA molecule such as a cDNA.
  • vector refers to a nucleic acid molecule, preferably to a recombinant nucleic acid molecule, i.e. a nucleic acid molecule which does not occur in nature.
  • a vector in the context of the present invention is suitable for incorporating or harboring a desired nucleic acid sequence.
  • Such vectors may be storage vectors, expression vectors, cloning vectors, transfer vectors etc.
  • a storage vector is a vector which allows the convenient storage of a nucleic acid molecule.
  • the vector may comprise a sequence corresponding, e.g., to a desired complex according to the present invention as described above and/or a sequence corresponding, e.g., to a desired immune checkpoint modulator according to the present invention as described above.
  • An expression vector may be used for production of expression products such as RNA, e.g. mRNA, or peptides, polypeptides or proteins.
  • an expression vector may comprise sequences needed for transcription of a sequence stretch of the vector, such as a promoter sequence.
  • a cloning vector is typically a vector that contains a cloning site, which may be used to incorporate nucleic acid sequences into the vector.
  • a cloning vector may be, e.g., a plasmid vector or a bacteriophage vector.
  • a transfer vector may be a vector which is suitable for transferring nucleic acid molecules into cells or organisms, for example, viral vectors.
  • a vector in the context of the present invention may be, e.g., an RNA vector or a DNA vector.
  • a vector is a DNA molecule.
  • a vector in the sense of the present application comprises a cloning site, a selection marker, such as an antibiotic resistance factor, and a sequence suitable for multiplication of the vector, such as an origin of replication.
  • a vector in the context of the present application is a plasmid vector
  • the present invention provides a kit comprising
  • preferred immune checkpoint modulator are those as described herein and preferred complexes are those as described herein.
  • kits preferably also comprises a package insert or label, for example with directions to express the immune checkpoint modulator and the complex and/or to treat cancer by using a combination of the immune checkpoint modulator and the complex.
  • kit is preferably for use in medicine, for example for use in the prevention and/or treatment of cancer.
  • the nucleic acid molecule(s) in the kit are preferably selected from the group consisting of a vector as described above, such as an expression vector; an RNA molecule such as an rRNA, an mRNA, an miRNA, an siRNA, or a tRNA; or a DNA molecule, such as a cDNA.
  • the immune checkpoint modulator and the complex may be encoded by the same nucleic acid molecule or, preferably, by distinct nucleic acid molecules.
  • the present invention also provides a nucleic acid molecule comprising
  • nucleic acid molecule is preferably selected from the group consisting of a vector as described above, such as an expression vector; an RNA molecule such as an rRNA, an mRNA, an miRNA, an siRNA, or a tRNA; or a DNA molecule, such as a cDNA.
  • the nucleic acid molecule may be an expression vector or an RNA molecule, e.g. an mRNA molecule, encoding the complex and the immune checkpoint inhibitor in a biscistronic manner.
  • the present invention also provides a composition comprising
  • nucleic acid molecule(s) are preferably selected from the group consisting of a vector as described above, such as an expression vector; an RNA molecule such as an rRNA, an mRNA, an miRNA, an siRNA, or a tRNA; or a DNA molecule, such as a cDNA.
  • composition may also comprise further components, for example those described above for a (pharmaceutical) composition according to the present invention comprising the complex and/or the checkpoint inhibitor as described herein.
  • the present invention provides a method for treating a subject, preferably a mammalian subject, and most preferably a human subject, who is suffering from a disease or disorder, in particular from a disorder that can be treated by immunotherapy such as cancers, infectious diseases, autoimmunity disorders and transplant rejections, comprising administering to the subject
  • the present invention provides a method for treating cancer or initiating, enhancing or prolonging an anti-tumor-response in a subject in need thereof comprising administering to the subject
  • the present invention can be applied to any subject suffering from any disease or disorder, depending on the specificity in particular of the at least one antigen or antigenic epitope comprised by the complex comprised by the combination for use according to the present invention.
  • the therapeutic effect of the complex may be to elicit an immune response directed against said antigens or antigenic epitopes, in particular a response that is dependent on CD4 + helper T cells and/or CD8 + cytotoxic T cells and/or that is restricted by MHC class I molecules and/or MHC class II molecules and the therapeutic effect of the checkpoint modulator may be to enable or to enhance such an effect of the complex.
  • subjects according to the invention are subjects suffering from a cancer, for instance from a cancer of the brain, colon, head or neck, or from a cervical cancer. More preferably, subjects according to the invention are subjects suffering from a brain cancer including glioma.
  • subjects according to the invention have been subjected to a surgical removal of a tumor.
  • subjects according to the invention may preferably be subjects suffering from an infectious disease.
  • the present invention also provides a combination therapy for preventing and/or treating cancer, wherein the combination therapy comprises administration of
  • kits according to the present invention and the (pharmaceutical) composition, in particular the vaccine, according to the present invention may be used in the combination therapy according to the present invention.
  • Subjects to be treated with such a combination therapy are the same as described for the methods according to the present invention and diseases to be prevented and/or treated are the same as described herein, in the context of the combination for use according to the present invention.
  • FIG. 1 shows for Example 1 the tumor growth (A) and the survival rate (B) of 7 mice per group (mean ⁇ SEM).
  • C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank.
  • Mice of the groups “Z13Mad5Anaxa+Isotype” and “Z13Mad5Anaxa+anti-PD1” were vaccinated twice (d5 and d13) by subcutaneous injection of 2 nmol of Z13Mad5Anaxa in the right flank. 200 ⁇ g of anti-PD1 antibody were administered i.p.
  • FIG. 2 shows for Example 2 tumor growth of 8 mice per group (mean ⁇ SEM).
  • C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank.
  • Mice of the groups “Z13Mad5Anaxa+Isotype” and “Z13Mad5Anaxa+anti-PD1” were vaccinated twice (d5 and d13) by subcutaneous injection of 2 nmol of Z13Mad5Anaxa in the right flank.
  • 200 ⁇ g of anti-PD1 antibody were administered i.p. on each of days 5, 9 and 13 to mice of groups “anti-PD1” and “Z13Mad5Anaxa+anti-PD1”.
  • isotype 2A3 For control, 200 ⁇ g of isotype 2A3 were administered i.p. on each of days 5, 9 and 13 to mice of groups “isotype” and “Z13Mad5Anaxa+isotype”. Tumor size was measured with a caliper.
  • FIG. 3 shows for Example 2 the percentage of multimer-positive cells (in % of CD8 T cells) at the tumor site (Tumor-infiltrating cells, TILs) for the different experimental groups (A) and a correlation of multimer-positive cells (in % of CD8 T cells) at the tumor site (TILs) with tumor size (B). **, p ⁇ 0.01; ***, p ⁇ 0.001.
  • FIG. 4 shows for Example 2 the percentage of granulocytic MDSCs (in % of CD45+CD11b+ cells) for the different experimental groups in spleen (A) and TILs (B). *, p ⁇ 0.05; **, p ⁇ 0.01; ***, p ⁇ 0.001.
  • FIG. 5 shows for Example 2 the correlation of granulocytic MDSCs (in % of CD45+CD11b+ cells) with tumor size for the different experimental groups in spleen (A) and TILs (B).
  • FIG. 6 shows for Example 3 the tumor growth of mice treated with anti-PD1 and Z13Mad5Anaxa in distinct treatment protocols.
  • A Mice treated with anti-PD1 and Z13Mad5Anaxa according to the protocol of Example 1.
  • B Tumor growth of mice treated with anti-PD1 only after vaccination with Z13Mad5Anaxa was finished. ****, p ⁇ 0.0001.
  • FIG. 7 shows for Example 4 the percentage of SIINFEKL-specific CD8 T cells in blood (A) and the percentage of SIINFEKL-specific CD8 T cells in BILs (B).
  • FIG. 7C shows a summary of the percentage of SIINFEKL-specific CD8 T cells in blood and BILs.
  • C57BL/6 mice were implanted intracranially with 5 ⁇ 10 5 GI261-Quad tumor cells at day 0. After tumor implantation, mice of the groups “Z13Mad5Anaxa+Isotype” and “Z13Mad5Anaxa+anti-PD1” were vaccinated at days 7 and 21 by subcutaneous injection of 2 nmol of Z13Mad5Anaxa in the right flank.
  • 200 ⁇ g of anti-PD1 antibody were administered i.p. on each of days 7, 10, 14, 17 and 21 to mice of groups “anti-PD1” and “Z13Mad5Anaxa+anti-PD1”.
  • 200 ⁇ g of isotype mAB 2A3 were administered i.p. on each of days 7, 10, 14, 17 and 21 to mice of groups “isotype” and “Z13Mad5Anaxa+isotype”.
  • SIINFEKL-specific CD8 T cells were quantified in blood and in brain infiltrating leukocytes (BILs) at day 28 by multimer staining (5-8 mice per group). *, p ⁇ 0.05.
  • FIG. 8 shows for Example 4 the percentage of IFN- ⁇ producing cells (% of CD8 T cells) in BILs (A) and a summary of IFN- ⁇ and/or TNF ⁇ producing cells (% of CD8 T cells) in BILs (B) after stimulation with SIINFEKL peptide for 6 h. *, p ⁇ 0.05; **, p ⁇ 0.01.
  • FIG. 9 shows for Example 5 the survival rate of mice.
  • C57BL/6 mice were implanted intracranially with 5 ⁇ 10 5 GI261-Quad tumor cells at day 0.
  • mice of the groups “Z13Mad5Anaxa+Isotype” and “Z13Mad5Anaxa+anti-PD1” were vaccinated at days 7, 21 and 35 by subcutaneous injection of 2 nmol of Z13Mad5Anaxa in the right flank. 200 ⁇ g of anti-PD1 antibody were administered i.p. on each of days 7, 10, 14, 17 and 21 to mice of the group “Z13Mad5Anaxa+anti-PD1”.
  • isotype mAB 2A3 were administered i.p. on each of days 7, 10, 14, 17 and 21 to mice of groups “isotype” and “Z13Mad5Anaxa+isotype”.
  • the antibody was administered i.p. just after s.c. administration of Z13Mad5Anaxa.
  • Mice were weighed daily and euthanized when weight loss was more than 15%. *, p ⁇ 0.05; **, p ⁇ 0.01.
  • FIG. 10 shows for Example 6 the number of metastases.
  • C57B16 mice were implanted i.v. with 1 ⁇ 10 5 B16-OVA melanoma tumor cells at day 0.
  • mice of the group “Z13Mad5Anaxa+anti-PD1” (“Vaccine+anti-PD1”) were vaccinated at days 0 and 10 by subcutaneous injection of 0.5 nmol of Z13Mad5Anaxa in the right flank. 200 ⁇ g of anti-PD1 antibody were administered i.p. on each of days 0, 3 and 7 to mice of the groups “Z13Mad5Anaxa+anti-PD1” (“Vaccine+anti-PD1”) and “anti-PD1”.
  • isotype mAB 2A3 were administered i.p. on each of days 0, 3 and 7 to mice of the group “isotype”. Mice were euthanized at day 17 and lung recovered. Number of metastasis foci was counted for each lung. **, p ⁇ 0.01 (Unpaired T test).
  • FIG. 11 shows for Example 7 the tumor growth in the EG7 tumor model.
  • C57BL/6 mice (5-6 mice per group) were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank (day 0).
  • mice of the group “Z13Mad5Anaxa+aCTLA4 ip” were vaccinated at days 5 and 13 subcutaneously with 2 nmol of Z13Mad5Anaxa in the right flank.
  • 100 ⁇ g of anti-CTLA4 antibody were administered i.p. on each of days 5 and 13 to mice of groups “aCTLA4 ip” and “Z13Mad5Anaxa+aCTLA4 ip”.
  • group “Z13Mad5Anaxa+aCTLA4 ip” the antibody was administered i.p. just after s.c. administration of Z13Mad5Anaxa.
  • 100 ⁇ g of isotype mAB MPC-11 were administered i.p. on each of days 5 and 13 to mice of the group “control”. Tumor size was measured with a caliper.
  • A Summary of all experimental groups.
  • B Tumor growth in each mouse of the control group.
  • C Tumor growth in each mouse of the anti-CTLA4 alone group.
  • D Tumor growth in each mouse of the Z13Mad5Anaxa+aCTLA4 group. **, p ⁇ 0.01; ***, p ⁇ 0.001.
  • FIG. 12 shows for Example 8 the effect of the route of administration on tumor growth in the EG7 tumor model.
  • C57BL/6 mice (5-6 mice per group) were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank (day 0).
  • mice of the groups “Z13Mad5Anaxa+aCTLA4 ip” and “Z13Mad5Anaxa+aCTLA4 sc” were vaccinated at days 5 and 13 subcutaneously with 2 nmol of Z13Mad5Anaxa in the right flank. 100 ⁇ g of anti-CTLA4 antibody were administered i.p.
  • FIG. 13 shows for Example 9 the effect of a combination of a complex comprising a cell penetrating peptide, different antigens and a TLR peptide agonist and a CTLA4 inhibitor in the CT26 tumor model.
  • BALB/c mice (5 to 6 mice per group) were implanted s.c. with 2 ⁇ 10 5 CT26 tumor cells in the left flank (day 0).
  • mice of the group “Z13Mad8Anaxa+aCTLA4” were vaccinated at days 3 and 9 subcutaneously with 2 nmol of Z13Mad8Anaxa in the right flank and 100 ⁇ g of anti-CTLA4 antibody were administered i.p.
  • FIG. 14 shows for Example 10 the effect of a combination of a complex comprising a cell penetrating peptide, different antigens and a TLR peptide agonist, a PD1 inhibitor and a CTLA4 inhibitor.
  • BALB/c mice (5 to 6 mice per group) were implanted s.c. with 2 ⁇ 10 5 CT26 tumor cells in the left flank (day 0).
  • mice of the groups “Z13Mad8Anaxa+aCTLA4” and “Z13Mad8Anaxa+aCTLA4/aPD1” were vaccinated at days 3 and 9 by subcutaneous injection of 2 nmol of Z13Mad8Anaxa in the right flank.
  • anti-PD1 antibody 200 ⁇ g of anti-PD1 antibody were administered i.p. on each of days 3, 6 and 9 to mice of groups “aCTLA4/aPD1” and “Z13Mad8Anaxa+aCTLA4/aPD1”.
  • 100 ⁇ g of anti-CTLA4 antibody were administered i.p. on each of days 3, 6 and 9 to groups “aCTLA4/aPD1”, “Z13Mad8Anaxa+aCTLA4” and “Z13Mad8Anaxa+aCTLA4/aPD1”.
  • the antibodies were administered i.p. just after s.c.
  • FIG. 15 shows for Example 11 the effect of a combination of a complex comprising a cell penetrating peptide, different antigens and a TLR peptide agonist, a CD40 agonist.
  • C57BL/6 mice (4 mice per group) were vaccinated at days 0, 14, 28 and 42 by subcutaneous injection of 2 nmol of Z13Mad5Anaxa in the right flank.
  • 100 ⁇ g of anti-CD40 antibody were administered s.c. at days 0 and days 0 and 14 to mice of groups “Z13Mad5Anaxa+aCD40 at vac1” and “Z13Mad5Anaxa+aCD40 at vac1 and vac2” respectively.
  • A The percentage of multimer-positive cells (in % of CD8 T cells) for the different experimental groups.
  • B The percentage of KLRG1 positive cells among multimer-positive cells. All groups are significantly different compared to na ⁇ ve control group. *, p ⁇ 0.05.
  • FIG. 16 shows for Example 11 (A) the amount of IFN- ⁇ producing SIINFEKL-specific CD8 T cells (Elispot assay) and (B) the results of an intracellular staining of splenocytes for IFN- ⁇ , CD107 and TNF ⁇ for SIINFEKL-specific CD8 T cells.
  • FIG. 17 shows for Example 11 the FACS plots of the intracellular staining of splenocytes for IFN- ⁇ , CD107 and TNF ⁇ .
  • FIG. 18 shows for Example 12 the tumor growth of 7 mice per group (mean+SEM); *, p ⁇ 0.05 EDAZ13Mad5 versus control group (2-way Anova test).
  • C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank and vaccinated twice (d5 and d13) by subcutaneous injection of 10 nmol of EDAZ13Mad5, EDAMad5, Mad5 or Mad5 and MPLA (equimolar to EDA) s.c. in the right flank. Tumor size was measured with a caliper.
  • FIG. 19 shows for Example 12 individual tumor growth curves (7 individual mice per group).
  • C57B/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank and vaccinated twice (d5 and d13) by subcutaneous injection of 10 nmol of EDAZ13Mad5, EDAMad5, Mad5 or Mad5 and MPLA (equimolar to EDA) s.c. in the right flank. Tumor size was measured with a caliper.
  • FIG. 20 shows for Example 12 (A) the survival curve of 7 mice per group; *, p ⁇ 0.05 EDAZ13Mad5 versus control group (Log-rank test) and (B) the tumor-free progression curve of 7 mice per group; *, p ⁇ 0.05 EDAZ13Mad5 versus control group (Log-rank test).
  • FIG. 21 shows for Example 13 the effect of complexes having different CPPs on the immune response.
  • C57BL/6 mice were vaccinated five times (Wk0, Wk2, Wk4, Wk6 and Wk8) s.c. with either 2 nmol (A) or 0.5 nmol (B) of Z13Mad5Anaxa, Z14Mad5Anaxa or Z18Mad5Anaxa.
  • Mice were bled 7 days after the 2 nd , 3 rd , 4 th and 5 th vaccination and multimer staining was performed (one experiment with 4 mice per group).
  • * p ⁇ 0.05 between vaccinated versus na ⁇ ve mice at each time point except after Vac2 for Z18Mad5Anaxa-vaccinated mice.
  • FIG. 22 shows for Example 14 the effect of complexes having different CPPs on CD8 T cells in spleen (A), draining lymph nodes (B) and bone marrow (C).
  • C57B/6 mice were vaccinated five times (Wk0, Wk2, Wk4, Wk6 and Wk8) s.c. with 2 nmol of Z13Mad5Anaxa or Z14Mad5Anaxa.
  • mice were euthanized, organs recovered and multimer staining was performed.
  • FIG. 23 shows for Example 14 the effect of complexes having different CPPs on T cells in spleen (CD8 T cell response (A) and CD4 T cell response (B)).
  • C57BL6 mice were vaccinated five times (Wk0, Wk2, Wk4, Wk6 and Wk8) s.c. with 2 nmol of Z13Mad5Anaxa or Z14Mad5Anaxa.
  • Elispot assay was performed on spleen cells stimulated with SIINFEKL OVACD8 peptide.
  • Elispot assay was performed on spleen cells stimulated with OVACD4 peptide.
  • FIG. 24 shows for Example 14 the effect of complexes having different CPPs on CD8 T cell effector function.
  • C57BL/6 mice were vaccinated five times (Wk0, Wk2, Wk4, Wk6 and Wk8) s.c. with 2 nmol of Z13Mad5Anaxa or Z14Mad5Anaxa.
  • intracellular staining was performed on spleen cells stimulated with SIINFEKL OVACD8 peptide.
  • FIG. 25 shows for Example 15 the effect of complexes having different CPPs on tumor growth (A) and survival rates (B).
  • C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank and vaccinated twice (d5 and d13) by s.c. injection of 0.5 nmol of Z13Mad5Anaxa or Z14Mad5Anaxa in the right flank.
  • A Tumor growth of 7 mice per group (mean ⁇ SEM); *, p ⁇ 0.05; ****, p ⁇ 0.0001 (2-way Anova test at day 28).
  • FIG. 26 shows for Example 16 the effect of complexes having different CPPs on the immune response.
  • C57BL/6 mice were vaccinated three times (Wk0, Wk2 and Wk4) s.c. with 2 nmol (A) or 0.5 nmol (B) of EDAZ13Mad5, EDAZ14Mad5 or EDAZ18Mad5.
  • Mice were bled 7 days after the 3 rd vaccination and multimer staining was performed (one experiment with 4 mice per group). *, p ⁇ 0.05
  • FIG. 27 shows for Example 17 the effect of EDAZ14Mad5 on tumor growth (A) and survival rates (B).
  • C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank and vaccinated twice (d5 and d13) by s.c. injection of 2 nmoles of EDAZ14Mad5 in the right flank.
  • Left panel Tumor growth of 7 mice per group (mean ⁇ SEM); **, p ⁇ 0.01 (2-way Anova test at day 27).
  • Right panel Survival curve of 7 mice per group. Median survival is indicated on the graph (m.s.)
  • FIG. 28 shows for Example 18 the tumor growth of 7 mice per group (mean ⁇ SEM).
  • C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank and vaccinated twice (d5 and d13) by subcutaneous injection of 10 nmol of either AnaxZ13Mad5, Z13Mad5Anaxa or co-injection of Z13Mad5+Pam3CSK4 (equimolar to Anaxa) in the right flank.
  • Tumor size was measured with a caliper. *, p ⁇ 0.05; ***, p ⁇ 0.001, ****, p ⁇ 0.0001.
  • FIG. 29 shows for Example 18 the individual tumor growth curves (7 individual mice per group).
  • C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank and vaccinated twice (d5 and d13) by subcutaneous injection of 10 nmol of either AnaxZ13Mad5, Z13Mad5Anaxa or co-injection of Z13Mad5+Pam3CSK4 (equimolar to Anaxa) s.c. in the right flank. Tumor size was measured with a caliper.
  • FIG. 30 shows for Example 18 the survival curve of 7 mice per group.
  • C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank and vaccinated twice (d5 and d13) by subcutaneous injection of 10 nmol of either AnaxZ13Mad5, Z13Mad5Anaxa or co-injection of Z13Mad5+Pam3CSK4 (equimolar to Anaxa) in the right flank. Tumor size was measured with a caliper. *, p ⁇ 0.05, **, p ⁇ 0.01, ****, p ⁇ 0.0001 (Log-rank test).
  • FIG. 31 shows for Example 19 the tumor growth of 7 mice per group (mean ⁇ SEM).
  • C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank and vaccinated twice (d5 and d13) by subcutaneous injection of 2 nmoles of Hp91Z13Mad5, EDAZ13Mad5, Z13Mad5Anaxa, Z13Mad5EDA or Z13Mad5 and MPLA (equimolar to EDA) in the right flank.
  • FIG. 32 shows for Example 19 the individual tumor growth curves (7 individual mice per group).
  • C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank and vaccinated twice (d5 and d13) by subcutaneous injection of 2 nmoles of Hp91Z13Mad5, EDAZ13Mad5, Z13Mad5Anaxa, Z13Mad5EDA or Z13Mad5 and MPLA (equimolar to EDA) s.c. in the right flank.
  • FIG. 33 shows for Example 19 the survival curves of all 7 mice per group. Median survival is indicated on the graph (m.s.). *, p ⁇ 0.05; **, p ⁇ 0.01 (Log-rank test).
  • FIG. 34 shows for Example 20 the quantification of SIINFEKL-specific CD8 T cells in a Quad-GI261 glioblastoma model. Briefly, C57BL/6 mice were implanted i.c. with 5 ⁇ 10 5 GI261-Quad tumor cells and vaccinated twice (d7 and 21) by s.c. injection of 2 nmol of Z13Mad5Anaxa or 2 nmol of Z13Mad5 and 2 nmol of Anaxa. SIINFEKL-specific CD8 T cells were quantified in blood and in BILs at d28 by multimer staining (7-16 mice per group).
  • FIG. 35 shows for Example 20 the cytokine secretion.
  • C57BL/6 mice were implanted i.c. with 5 ⁇ 10 5 GI261-Quad tumor cells and vaccinated twice (d7 and 21) by s.c. injection of 2 nmol of Z13Mad5Anaxa or 2 nmol of Z13Mad5 and 2 nmol of Anaxa.
  • BILs were isolated and cultured during 6 h with matured BMDCs loaded or not with SIINFEKL peptide in presence of BrefeldinA before intracellular staining for cytokines.
  • FIG. 36 shows for Example 21 the quantification of SIINFEKL-specific CD8 T cells in na ⁇ ve mice. Briefly, C57BL/6 mice were vaccinated once (day 0) by s.c. injection of 2 nmol of Z13Mad5Anaxa (group “Z13Mad5Anaxa”) or 2 nmol of Z13Mad5 and 2 nmol of Anaxa (group “Z13Mad5+Anaxa”). SIINFEKL-specific CD8 T cells were quantified in blood at d7 by multimer staining (4-8 mice per group).
  • FIG. 37 shows for Example 22 the tumor growth (A) and the survival rate (B) of 7 mice per group (mean ⁇ SEM).
  • C57BL6 mice were implanted s.c. with 2 ⁇ 10 5 MC-38 tumor cells in the left flank.
  • Mice of the groups “Z13Mad12Anaxa” and “Z13Mad12Anaxa+anti-PD1” were vaccinated 3 times (d3, d10 and d17) by subcutaneous injection of 2 nmol of Z13Mad12Anaxa at the tail base. 200 ⁇ g of anti-PD1 antibody were administered i.p.
  • FIG. 38 shows for Example 22 individual tumor growth curves of 7 mice per group.
  • C57B/6 mice were implanted s.c. with 2 ⁇ 10 5 MC-38 tumor cells in the left flank.
  • Mice of the groups “Z13Mad12Anaxa” and “Z13Mad12Anaxa+anti-PD1” were vaccinated 3 times (d3, d10 and d17) by subcutaneous injection of 2 nmol of Z13Mad12Anaxa at the tail base.
  • 200 ⁇ g of anti-PD1 antibody were administered i.p. on each of days 6, 10, 13, 17, 20, 24, 27 and 31 to mice of groups “anti-PD1” and “Z13Mad12Anaxa+anti-PD1”. Tumor size was measured with a caliper.
  • FIG. 39 shows for Example 23 the tumor growth (A) and the survival rate (B) of 13 to 14 mice per group (mean ⁇ SEM).
  • C57BL6 mice were implanted s.c. with 2 ⁇ 10 5 MC-38 tumor cells on the back.
  • Mice of the groups “Z13Mad12Anaxa” and “Z13Mad12Anaxa+anti-PD1” were vaccinated 3 times (d3, d10 and d17) by subcutaneous injection of 2 nmol of Z13Mad12Anaxa at the tail base. 200 ⁇ g of anti-PD1 antibody were administered i.p.
  • FIG. 40 shows for Example 23 individual tumor growth curves of 13 to 14 mice per group.
  • C57BL/6 mice were implanted s.c. with 2 ⁇ 10 5 MC-38 tumor cells on the back.
  • Mice of the groups “Z13Mad12Anaxa” and “Z13Mad12Anaxa+anti-PD1” were vaccinated 3 times (d3, d10 and d17) by subcutaneous injection of 2 nmol of Z13Mad12Anaxa at the tail base.
  • 200 ⁇ g of anti-PD1 antibody were administered i.p. on each of days 6, 10, 13, 17, 20, 24 and 27 to mice of groups “anti-PD1” and “Z13Mad12Anaxa+anti-PD1”. Tumor size was measured with a caliper.
  • E.G7 is an OVA transfectant derived from the EL4 Thymoma cell line.
  • Z13Mad5Anaxa is a complex comprising a cell penetrating peptide, different antigens and a TLR peptide agonist as described herein.
  • Z13Mad5Anaxa is a fusion protein comprising the cell-penetrating peptide “Z13”, the antigenic cargo “MAD5” comprising OVA-CD4, gp100-CD8 + , Ealpha-CD4, and OVA-CD8 + epitopes, and the TLR peptide agonist “Anaxa”.
  • mice C57BL/6 mice (seven mice per group) were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank (day 0). After tumor implantation, mice of the groups “Z13Mad5Anaxa+Isotype” and “Z13Mad5Anaxa+anti-PD1” were vaccinated at days 5 and 13 subcutaneously with 2 nmol of Z13Mad5Anaxa in the right flank. 200 ⁇ g of anti-PD1 antibody RMP1-14 (BioXcell, West Riverside, N.H., USA) were administered i.p.
  • Example 1 In order to assess the effects of combination of a PD1 inhibitor and a complex comprising a cell penetrating peptide, different antigens and a TLR peptide agonist on homing of T cells to the tumor site and on MDSCs (myeloid-derived suppressor cells), the previous experiment (Example 1) was repeated with 8 mice per group and on day 22, mice were euthanized and FACS staining was performed to monitor the OVA-specific immune response and tumor microenvironment in the spleen and TILs (tumor-infiltrating lymphocytes).
  • FIG. 2 shows the tumor growth in the experimental groups (same experimental method as in Example 1).
  • treatment with the PD1 inhibitor alone or with Z13Mad5Anaxa alone resulted in significantly reduced tumor volume ( FIG. 2 ) as compared to the control group (“isotype”).
  • the combination of both, the PD1 inhibitor and Z13Mad5Anaxa resulted in the most pronounced improvement, namely in strongly decreased tumor volume and strongly increased survival rates. Accordingly, these data are in conformity with the results of Example 1 (cf. FIG. 1A ).
  • the data confirm that a combination of both, anti-PD1 therapy and Z13Mad5Anaxa vaccination, is more efficient than anti-PD1 therapy alone or Z13Mad5Anaxa vaccination alone and indicate a synergistic effect of anti-PD1 therapy and Z13Mad5Anaxa vaccination.
  • FIG. 3 shows the percentage of multimer-positive cells (in % of CD8 T cells) at the tumor site (TILs) for the different experimental groups ( FIG. 3A ) and a correlation of multimer-positive cells (in % of CD8 T cells) among TILs with tumor size ( FIG. 3B ).
  • FIG. 3A shows that antigen-specific T cells accumulate at the tumor site in vaccinated mice.
  • the lowest percentage of multimer-positive cells was found in control mice and in mice, which were treated with anti-PD1 only (“anti-PD1” group).
  • FIG. 4 shows the percentage of granulocytic MDSCs (in % of CD45+CD11b+ cells) for the different experimental groups in spleen ( FIG. 4A ) and TILs ( FIG. 4B ).
  • FIG. 5 shows a significant correlation between the percentage of granulocytic MDSCs (in % of CD45+CD11b+ cells) and tumor size for the different experimental groups in spleen ( FIG. 5A ) and TILs ( FIG. 5B ).
  • the present T cell data and MDSC data strongly support the synergistic effect of a combination of anti-PD1 therapy and Z13Mad5Anaxa vaccination observed for tumor growth and survival rate.
  • mice In a first experimental group “Z13Mad5Anaxa+anti-PD1” the PD1 inhibitor and Z13Mad5Anaxa were administered as described in Example 1. Briefly, C57BL/6 mice (six-seven mice per group) were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank (day 0). After tumor implantation, mice were vaccinated at days 5 and 13 subcutaneously with 2 nmol of Z13Mad5Anaxa in the right flank. 200 ⁇ g of anti-PD1 antibody RMP1-14 (BioXcell, West Riverside, N.H., USA) were administered i.p. on each of days 5, 9 and 13.
  • RMP1-14 BioXcell, West Riverside, N.H., USA
  • mice In a second experimental group “Z13Mad5Anaxa+anti-PD1” the PD1 inhibitor and Z13Mad5Anaxa were administered as follows: C57BL/6 mice (six-seven mice per group) were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank (day 0). After tumor implantation, mice were vaccinated at days 5 and 13 subcutaneously with 2 nmol of Z13Mad5Anaxa in the right flank—as in the first experimental group. However, in contrast to the first experimental group, in the second experimental group 200 ⁇ g of anti-PD1 antibody RMP1-14 (BioXcell, West Riverside, N.H., USA) were administered i.p.
  • RMP1-14 BioXcell, West Riverside, N.H., USA
  • the anti-PD1 treatment started only after the end of the Z13Mad5Anaxa treatment.
  • 200 ⁇ g of isotype mAB 2A3 were administered i.p. on each of days 17 and 20.
  • Results are shown in FIG. 6 with FIG. 6A showing the tumor growth in the first experimental group (protocol according to Example 1) and the respective control group and FIG. 6B showing the tumor growth in the second experimental group (anti-PD1 treatment only started after Z13Mad5Anaxa treatment was finished) and the respective control group.
  • the latter treatment protocol wherein anti-PD1 treatment only started after Z13Mad5Anaxa treatment was finished, resulted in a slight improvement (slightly decreased tumor growth, cf. FIG. 6B )
  • the “true combination” of anti-PD1 and Z13Mad5Anaxa resulted in a considerably stronger improvement, i.e. in a strongly pronounced decrease in tumor growth.
  • a murine glioblastoma model was used. T cell homing at the tumor site was thus analyzed in GI261-Quad tumor-bearing mice vaccinated twice (week 1 and week 3 after tumor implantation) with Z13Mad5Anaxa vaccine and treated or not with anti-PD1. At week 4, blood and the brain infiltrating leukocytes (BILs) were analyzed.
  • BILs brain infiltrating leukocytes
  • mice were implanted intracranially with 5 ⁇ 10 5 GI261-Quad tumor cells at day 0.
  • mice of the groups “Z13Mad5Anaxa+Isotype” and “Z13Mad5Anaxa+anti-PD1” were vaccinated at days 7 and 21 by subcutaneous injection of 2 nmol of Z13Mad5Anaxa in the right flank.
  • 200 ⁇ g of anti-PD1 antibody RMP1-14 BioXcell, West Riverside, N.H., USA
  • isotype mAB 2A3 were administered i.p. on each of days 7, 10, 14, 17 and 21 to mice of groups “isotype” and “Z13Mad5Anaxa+isotype”.
  • the antibody was administered i.p. just after s.c. administration of Z13Mad5Anaxa.
  • SIINFEKL-specific CD8 T cells were quantified in blood and in brain infiltrating leukocytes (BILs) at day 28 by multimer staining (5-8 mice per group).
  • FIG. 7 shows a summary of the percentage of SIINFEKL-specific CD8 T cells in blood and BILs.
  • FIG. 7C shows a summary of the percentage of SIINFEKL-specific CD8 T cells in blood and BILs.
  • low frequency of SIINFEKL-specific CD8 T cells was quantified in the blood.
  • a higher percentage of SIINFEKL-specific CD8 T cells was observed in the blood of Z13Mad5Anaxa-vaccinated mice treated or not with anti-PD1.
  • cytokine-producing cells were also assessed. To this end, intracellular cytokines were stained after restimulation with the SIINFEKL peptide for 6 hours in the presence of Brefeldin A (GolgiPlug, BD Bioscences) with mAb to IFN- ⁇ (XMG1.2), tumor necrosis factor (MP6-XT22) and corresponding isotype controls (BD Biosciences).
  • Brefeldin A GolgiPlug, BD Bioscences
  • mAb to IFN- ⁇ XMG1.2
  • MP6-XT22 tumor necrosis factor
  • corresponding isotype controls BD Biosciences
  • Results are shown in FIG. 8 with the percentage of IFN- ⁇ producing cells (% of CD8 T cells) shown in FIG. 8A and a summary of IFN- ⁇ and/or TNF ⁇ producing cells (% of CD8 T cells) shown in FIG. 8B .
  • Those data show that vaccination with Z13Mad5Anaxa alone and treatment with anti-PD1 alone result in an increased percentage of cytokine, in particular IFN- ⁇ , producing cells.
  • the strongest increase in percentage of cytokine, in particular IFN- ⁇ , producing cells was clearly observed in animals treated with a combination of Z13Mad5Anaxa and anti-PD1.
  • mice treated with a combination of anti-PD1 and Z13Mad5Anaxa were assessed in the glioblastoma model in an independent experiment.
  • mice were implanted intracranially with 5 ⁇ 10 5 GI261-Quad tumor cells at day 0.
  • mice of the groups “Z13Mad5Anaxa+Isotype” and “Z13Mad5Anaxa+anti-PD1” were vaccinated at days 7, 21 and 35 by subcutaneous injection of 2 nmol of Z13Mad5Anaxa in the right flank.
  • 200 ⁇ g of anti-PD1 antibody RMP1-14 BioXcell, West Riverside, N.H., USA
  • isotype mAB 2A3 were administered i.p. on each of days 7, 10, 14, 17 and 21 to mice of groups “isotype” and “Z13Mad5Anaxa+isotype”.
  • the antibody was administered i.p. just after s.c. administration of Z13Mad5Anaxa.
  • Mice were weighed daily and euthanized when weight loss was more than 15%.
  • Results are shown in FIG. 9 . These results show that Z13Mad5Anaxa therapeutic vaccination alone is more efficacious than the control group with a 10-days difference in the median survival. Again, the effects, i.e. the increase in the survival rate, are strongest for the combination of anti-PD1 and Z13Mad5Anaxa. In particular, combined anti-PD1/Z13Mad5Anaxa therapy is able to control glioblastoma growth.
  • mice C57BL/6 mice were implanted i.v. with 1 ⁇ 10 5 B16-OVA melanoma tumor cells at day 0.
  • mice of the group “Z13Mad5Anaxa+anti-PD1” (“Vaccine+anti-PD1”) were vaccinated at days 0 and 10 by subcutaneous injection of 0.5 nmol of Z13Mad5Anaxa in the right flank.
  • 200 ⁇ g of anti-PD1 antibody RMP1-14 BioXcell, West Riverside, N.H., USA
  • Results are shown in FIG. 10 .
  • the combined treatment with anti-PD1 and Z13Mad5Anaxa did not resulted in a significant decrease in the number of metastases. Accordingly, the combined treatment with anti-PD1 and Z13Mad5Anaxa was highly efficient in inhibiting the growth of melanoma metastasis in the lung.
  • an inhibitor of CTLA4 was used in the present experiment.
  • mice C57BL/6 mice (5-6 mice per group) were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank (day 0). After tumor implantation, mice of the group “Z13Mad5Anaxa+aCTLA4 ip” were vaccinated at days 5 and 13 subcutaneously with 2 nmol of Z13Mad5Anaxa in the right flank. 100 ⁇ g of anti-CTLA4 antibody 9D9 (BioXcell, West Riverside, N.H., USA) were administered i.p. on each of days 5 and 13 to mice of groups “aCTLA4 ip” and “Z13Mad5Anaxa+aCTLA4 ip”.
  • the EG7 tumor model was used.
  • mice C57BL/6 mice (5-6 mice per group) were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank (day 0).
  • mice of the groups “Z13Mad5Anaxa+aCTLA4 ip” and “Z13Mad5Anaxa+aCTLA4 sc” were vaccinated at days 5 and 13 subcutaneously with 2 nmol of Z13Mad5Anaxa in the right flank.
  • 100 ⁇ g of anti-CTLA4 antibody were administered i.p. on each of days 5 and 13 to mice of the group “Z13Mad5Anaxa+aCTLA4 ip” just after s.c.
  • Z13Mad5Anaxa administration of Z13Mad5Anaxa.
  • group “Z13Mad5Anaxa+aCTLA4 sc” on each of days 5 and 13 100 ⁇ g of anti-CTLA4 antibody were administered s.c. at the same site as Z13Mad5Anaxa 1 h after injection of Z13Mad5Anaxa.
  • 100 ⁇ g of isotype mAB MPC-11 were administered i.p. on each of days 5 and 13 to mice of the group “control”. Tumor size was measured with a caliper.
  • the most pronounced effect of the combination therapy of a complex comprising a cell penetrating peptide, different antigens and a TLR peptide agonist with a checkpoint modulator in decreasing tumor growth was achieved when the checkpoint modulator was administered intraperitoneally.
  • Subcutaneous administration of the checkpoint modulator also resulted in decreased tumor growth, however, the effect was less pronounced than after i.p. administration.
  • Z13Mad8Anaxa differs from Z13Mad5Anaxa (described in Example 1) in the antigenic cargoes.
  • Z13Mad8Anaxa is a fusion protein comprising the cell-penetrating peptide “Z13”, the antigenic cargo “MAD8” comprising CD8 and CD4 epitopes of glycoprotein 70, and the TLR peptide agonist “Anaxa”.
  • mice (seven mice per group) were implanted s.c. with 2 ⁇ 10 5 CT26 tumor cells in the left flank (day 0).
  • mice of the group “Z13Mad8Anaxa+aCTLA4” were vaccinated at days 3 and 9 subcutaneously with 2 nmol of Z13Mad8Anaxa in the right flank and 100 ⁇ g of anti-CTLA4 antibody 9D9 (BioXcell, West Riverside, N.H., USA) were administered i.p. on each of days 3, 6 and 9 (on days 3 and 9 just after s.c. administration of Z13Mad8Anaxa).
  • 100 ⁇ g of isotype mAB MPC-11 were administered i.p. on each of days 3, 6 and 9 to mice of the group “control”. Tumor size was measured with a caliper.
  • Results are shown in FIG. 13 . These data show that a combination of an inhibitor of CTLA4 with complex comprising a cell penetrating peptide, different antigens and a TLR peptide agonist is able to control tumor growth also in the CT26 colon cancer tumor model.
  • mice BALB/c mice (5 to 6 mice per group) were implanted s.c. with 2 ⁇ 10 5 CT26 tumor cells in the left flank (day 0). After tumor implantation, mice of the groups “Z13Mad8Anaxa+aCTLA4” and “Z13Mad8Anaxa+aCTLA4/aPD1” were vaccinated at days 3 and 9 by subcutaneous injection of 2 nmol of Z13Mad8Anaxa in the right flank. 200 ⁇ g of anti-PD1 antibody RMP1-14 (BioXcell, West Riverside, N.H., USA) were administered i.p.
  • Results are shown in FIG. 14 .
  • treatment with a combination of Z13Mad8Anaxa with a CTLA4 inhibitor resulted in a decrease in tumor growth.
  • treatment with a combination of checkpoint modulators anti-CTLA4 and anti-PD1
  • Z13Mad8Anaxa also resulted in a decrease in tumor growth.
  • the combination of all three, the two distinct checkpoint modulators and Z13Mad8Anaxa resulted in the most pronounced improvement, namely in strongly decreased tumor volume.
  • Example 11 Immunogenicity of Combination of a CD40 Agonist and a Complex Comprising a Cell Penetrating Peptide, Different Antigens and a TLR Peptide Agonist
  • an agonistic antibody targeting CD40 was used in the present experiment.
  • mice na ⁇ ve C57BL/6 mice (4 mice per group) were vaccinated at days 0, 14, 28 and 42 (weeks 0, 2, 4 and 6) subcutaneously with 2 nmol of Z13Mad5Anaxa in the right flank.
  • 100 ⁇ g of anti-CD40 antibody FGK45 BioXcell, West Riverside, N.H., USA
  • the anti-CD40 antibody was administered s.c.
  • cytokines were stained after restimulation with the SIINFEKL peptide for 6 hours in the presence of Brefeldin A (GolgiPlug, BD Bioscences) with mAb to IFN- ⁇ (XMG1.2), tumor necrosis factor (MP6-XT22), CD107a (1D4B) and corresponding isotype controls (BD Biosciences).
  • FIG. 15 shows the percentage of multimer-positive cells (in % of CD8 T cells) for the different experimental groups ( FIG. 15A ) and the percentage of KLRG1 positive cells among multimer-positive cells ( FIG. 158B ). All groups are significantly different compared to na ⁇ ve control group, confirming the immunogenicity of Z13Mad5Anaxa. However, the groups treated additionally with an anti-CD40 antibody showed even more multimer-positive cells and KLRG1 positive cells, which was most pronounced in the group receiving two treatments with anti-CD40. These results indicate a synergistic effect of a combination of a CD40 agonist and Z13Mad5Anaxa on immunogenicity.
  • Example 12 Efficacy of a Complex Having a Different TLR Agonist on Tumor Growth in a Benchmark EG.7-OVA Tumor Model
  • the complex is a fusion protein, comprising the cell-penetrating peptide “Z13”, a protein “MAD5”, which consists of different CD8 + and CD4 + epitopes from various antigens, and the TLR4 peptide agonist “EDA”. Accordingly, a fused protein with the EDA peptide at the N-terminal position and different control conjugated proteins without Z13 or EDA or both were designed.
  • mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank. After tumor implantation, mice were vaccinated at day 5 and 13 with 10 nmol of one of the following constructs (cf. Examples 1 and 2 for construct description): EDAZ13Mad5, EDAMad5, Mad5, or Mad5 and MPLA (equimolar to EDA) s.c. in the right flank. Tumor size was measured with a caliper.
  • FIG. 18 shows the tumor growth of 7 mice per group (mean+SEM); *, p ⁇ 0.05 EDAZ13Mad5 versus control group (2-way Anova test).
  • FIG. 19 shows individual tumor growth curves (7 individual mice per group).
  • FIG. 20 A shows the survival curve of 7 mice per group; *, p ⁇ 0.05 EDAZ13Mad5 versus control group (Log-rank test).
  • FIG. 20 B shows the tumor-free progression curve of 7 mice per group; *, p ⁇ 0.05 EDAZ13Mad5 versus control group (Log-rank test).
  • EDAZ13Mad5 was the only protein vaccine to significantly control the tumor growth compared to the control group with a significant better tumor free progression curve and survival curve.
  • construct protein EDAZ13Mad5 is a highly potent vaccine for controlling the tumor growth in a therapeutic setting.
  • fusion proteins which comprise CPPs other than Z13—namely Z14 (SEQ ID NO: 7) or Z18 (SEQ ID NO: 11).
  • Those fusion proteins also comprise the protein “MAD5”, which consists of different CD8 + and CD4 + epitopes from various antigens, and the TLR2 peptide agonist “Anaxa”. Accordingly, the following constructs were additionally designed:
  • mice were assigned to eight different groups (4 mice per group): three groups receiving 2 nmol of either Z13Mad5Anaxa, Z14Mad5Anaxa or Z18Mad5Anaxa and a respective control and three groups receiving 0.5 nmol of Z13Mad5Anaxa, Z14Mad5Anaxa or Z18Mad5Anaxa and a respective control.
  • the mice were vaccinated five times (Week0, Week2, Week4, Week6 and Week8) s.c. Mice were bled 7 days after the 2 nd , 3 rd , 4 th and 5 th vaccination and multimer staining was performed (one experiment with 4 mice per group).
  • C57BL/6 mice were assigned to three different groups (3-4 mice per group): na ⁇ ve, Z13Mad5Anaxa or Z14Mad5Anaxa.
  • mice of the Z13Mad5Anaxa group and of the Z14Mad5Anaxa group were vaccinated five times (Week0, Week2, Week4, Week6 and Week8) s.c. with 2 nmol of either Z13Mad5Anaxa or Z14Mad5Anaxa as described above.
  • mice vaccinated with Z13Mad5Anaxa or with Z14Mad5Anaxa showed a similar increase in multimer-positive cells, in particular in the spleen and bone marrow as well as a slight increase in draining lymph nodes.
  • mice vaccinated with Z13Mad5Anaxa showed a significant increase in IFN- ⁇ producing cells compared to na ⁇ ve mice.
  • Mice vaccinated with Z14Mad5Anaxa showed also an increase in IFN- ⁇ producing cells compared to na ⁇ ve mice, however, the increase was not significant, which may be due to the low number of mice (3 mice in Z14Mad5Anaxa group).
  • mice vaccinated with Z13Mad5Anaxa showed a highly significant increase in IFN- ⁇ producing cells compared to na ⁇ ve mice.
  • Mice vaccinated with Z14Mad5Anaxa showed also an increase in IFN- ⁇ producing cells compared to na ⁇ ve mice, however, the increase was not significant, which may be due to the low number of mice (3 mice in Z14Mad5Anaxa group).
  • mice intracellular staining was performed on spleen cells stimulated with SIINFEKL OVACD8 peptide (SEQ ID NO: 35) to identify CD107a + IFN- ⁇ + TNF- ⁇ + cells. Results are shown in FIG. 24 . Mice vaccinated with Z13Mad5Anaxa or with Z14Mad5Anaxa showed a similar increase in CD107a + IFN- ⁇ ′TNF- ⁇ + cells.
  • mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank and assigned to three different groups (na ⁇ ve, Z13Mad5Anaxa and Z14Mad5Anaxa). Mice were vaccinated twice at d5 and d13 after tumor implantation by s.c. injection of either 0.5 nmol of Z13Mad5Anaxa or Z14Mad5Anaxa in the right flank.
  • Results are shown in FIG. 25 .
  • Vaccination with Z13Mad5Anaxa or with Z14Mad5Anaxa resulted in significantly decreased tumor volumes compared to control mice ( FIG. 25 A) as well as to significantly increased survival rates compared to control mice ( FIG. 25 B).
  • Those results indicate that both complexes, Z13Mad5Anaxa and Z14Mad5Anaxa, are able to significantly decrease tumor growth and to significantly prolong survival.
  • fusion proteins which comprise CPPs other than Z13—namely Z14 (SEQ ID NO: 7) or Z18 (SEQ ID NO: 11).
  • Those fusion proteins also comprise the protein “MAD5”, which consists of different CD8 + and CD4 + epitopes from various antigens, and the TLR4 peptide agonist “EDA”. Accordingly, the following constructs were additionally designed:
  • mice were assigned to eight different groups (4 mice per group): three groups receiving 2 nmol of either EDAZ13Mad5, EDAZ14Mad5 or EDAZ18Mad5 and a respective control and three groups receiving 0.5 nmol of either EDAZ13Mad5, EDAZ14Mad5 or EDAZ18Mad5 and a respective control group.
  • the mice were vaccinated three times (Week0, Week2 and Week4) s.c. Mice were bled 7 days after the 2 nd and 3 rd vaccination and multimer staining was performed (one experiment with 4 mice per group).
  • mice On d0 C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank and assigned to two different groups (na ⁇ ve and EDAZ14Mad5). Mice were vaccinated twice at d5 and d13 after tumor implantation by s.c. injection of 0.5 nmol of EDAZ14Mad5 in the right flank.
  • Results are shown in FIG. 27 .
  • EDAZ13Mad5 cf. Example 12, FIGS. 18-20
  • vaccination with EDAZ14Mad5 resulted in significantly decreased tumor volumes compared to control mice ( FIG. 27 A) as well as to significantly increased survival rates compared to control mice ( FIG. 27 B).
  • Those results indicate that EDAZ14Mad5 is able to significantly decrease tumor growth and to significantly prolong survival—similarly to EDAZ13Mad5 (cf. Example 12, FIGS. 18-20 ).
  • Example 18 Superior Efficacy of Z13Mad5Anaxa Fusion Construct Compared to Z13Mad5 and a TLR Agonist Administered Separately
  • mice C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG7-OVA tumor cells in the left flank. After tumor implantation, the three groups of 7 mice each were vaccinated s.c. in the right flank at day 5 and 13 by subcutaneous injection of 10 nmol of either AnaxZ13Mad5 (group 1), Z13Mad5Anaxa (group 2) or Z13Mad5 and Pam3CSK4 (equimolar to Anaxa; group 3). Tumor size was measured with a caliper. Results are shown in FIG. 28-30 .
  • Z13Mad5Anaxa and AnaxaZ13Mad5 are better protein vaccines for controlling tumor growth compared to the control group, i.e. co-injection of Z13Mad5 and Pam3CSK4, with Z13Mad5Anaxa and AnaxaZ13Mad5 showing a significant better survival curve.
  • Z13Mad5Anaxa and AnaxaZ13Mad5 demonstrate significantly higher efficacy than Z13Mad5 administrated separately with Pam3CSK4. The results therefore suggest that the construct proteins Z13Mad5Anaxa and AnaxaZ13Mad5 are promising conjugate-vaccines for controlling the tumor growth in a therapeutic setting.
  • the goal of this study was to compare the efficacy of the different construct protein vaccines conjugated to different TLR agonist, namely EDAZ13Mad5 (SEQ ID NO: 26) and Z13Mad5Anaxa (SEQ ID NO: 28), on tumor growth control.
  • EDAZ13Mad5 SEQ ID NO: 26
  • Z13Mad5Anaxa SEQ ID NO: 28
  • C57BL/6 mice were implanted s.c. with 3 ⁇ 10 5 EG.7-OVA thymoma cells in the left flank as described previously.
  • Mice (7 individual mice per group) were vaccinated s.c. in the right flank at day 5 and 13 with 2 nmol of either EDAZ13Mad5, Z13Mad5Anaxa or co-injection of Z13Mad5+MPLA (equimolar to EDA).
  • Results are shown in FIGS. 31, 32 and 33 .
  • Z13Mad5Anaxa SEQ ID NO: 28
  • EDAZ13Mad5 SEQ ID NO: 26
  • Z13Mad5 SEQ ID NO: 46
  • Z13Mad5Anaxa is the best construct to significantly control tumor growth
  • EDAZ13Mad5 was slightly better than Z13Mad5+MPLA in this experimental setting.
  • Example 20 Superior Efficacy of Z13Mad5Anaxa Fusion Construct Compared to Z13Mad5 and Anaxa in a Glioblastoma Model
  • Z13Mad5Anaxa (SEQ ID NO: 28) was administered to one group of mice, whereas Z13Mad5 (SEQ ID NO: 46) and Anaxa (SEQ ID NO: 15) were administered (both together) to another group of mice.
  • T cell homing at the tumor site was analyzed in GI261-Quad tumor-bearing mice (7-16 mice per group) vaccinated twice, namely at day 7 and at day 21 after tumor implantation (day 0), with 2 nmol Z13Mad5Anaxa vaccine.
  • a group vaccinated with both, Z13Mad5 and Anaxa was used as control.
  • C57BL/6 mice were implanted i.c. (intracranially) with 5 ⁇ 10 5 GI261-Quad tumor cells and vaccinated twice (at d7 and d21 following implantation) by s.c.
  • FIG. 34 Results are shown in FIG. 34 .
  • a significantly higher percentage of SIINFEKL-specific CD8 T cells was observed in the blood of Z13Mad5Anaxa-vaccinated mice as compared to mice vaccinated with both, Z13Mad5 and Anaxa ( FIG. 34A ).
  • cytokine secretion was assessed.
  • C57BL/6 mice were implanted i.c. with 5 ⁇ 10 5 GI261-Quad tumor cells and vaccinated twice (d7 and 21) by s.c. injection of 2 nmol of Z13Mad5Anaxa or 2 nmol of Z13Mad5 and 2 nmol of Anaxa.
  • BILs were isolated and cultured during 6 h with matured BMDCs loaded or not with SIINFEKL peptide (SEQ ID NO: 35) in presence of BrefeldinA before intracellular staining for cytokines.
  • Results are shown in FIG. 35 .
  • a high level of cytokine secretion was observed for brain-infiltrating CD8 T cells from mice vaccinated with Z13Mad5Anaxa.
  • a significantly higher secretion of total IFN- ⁇ and of IFN- ⁇ and TNF- ⁇ together was observed for brain-infiltrating CD8 T cells from mice vaccinated with Z13Mad5Anaxa as compared to mice vaccinated with Z13Mad5 and Anaxa separately.
  • Z13Mad5Anaxa is efficacious for eliciting high brain infiltrating SIINFEKL-specific CD8 immune response.
  • Z13Mad5Anaxa is able to promote the secretion of cytokine by antigen-specific CD8 T cells in the brain.
  • Example 21 Superior Efficacy of Z13Mad5Anaxa Fusion Construct Compared to Z13Mad5 and Anaxa in Na ⁇ ve Mice
  • Z13Mad5Anaxa (SEQ ID NO: 28) was administered to one group of mice, whereas Z13Mad5 (SEQ ID NO: 46) and Anaxa (SEQ ID NO: 15) were administered (both together) to another group of mice.
  • results are shown in FIG. 36 .
  • a significantly higher percentage of SIINFEKL-specific CD8 T cells was observed in the blood of Z13Mad5Anaxa-vaccinated mice as compared to mice vaccinated with Z13Mad5 and Anaxa separately ( FIG. 36 ).
  • MC-38 is a colon carcinoma cell line.
  • Z13Mad12Anaxa is a complex comprising a cell penetrating peptide “Z13”, the antigenic cargo “MAD12” comprising three neoantigens as identified by Yadav et al. Nature. 2014 Nov. 27; 515(7528):572-6 from MC-38 tumor cell line, and the TLR peptide agonist “Anaxa”.
  • the amino acid sequence of Z13Mad12Anaxa is shown:
  • mice C57BL/6 mice (seven mice per group, female, 7 week old) were implanted s.c. with 2 ⁇ 10 5 MC-38 tumor cells in the left flank (day 0). After tumor implantation, mice of the groups “Z13Mad12Anaxa” and “Z13Mad12Anaxa+anti-PD1” were vaccinated at days 3, day 10 and 17 subcutaneously with 2 nmol of Z13Mad12Anaxa at the tail base. 200 ⁇ g of anti-PD1 antibody RMP1-14 (BioXcell, West Riverside, N.H., USA) were administered i.p.
  • FIGS. 37 and 38 treatment with the PD1 inhibitor alone or with Z13Mad12Anaxa alone resulted in significantly reduced tumor volume ( FIG. 37A ) and increased survival ( FIG. 37B ), as compared to the control group.
  • the combination of both, the PD1 inhibitor and Z13Mad12Anaxa resulted in the most pronounced improvement, namely in strongly decreased tumor volume and strongly increased survival rates.
  • Example 23 further animals were subdued to the experimental test of Example 22 in order to enlarge the group sizes of the different experimental groups of Example 22. Therefore, the experimental results “include” the results of the animals of Example 22 and those of additional animals.
  • MC-38 is a colon carcinoma cell line.
  • Z13Mad12Anaxa is a complex comprising a cell penetrating peptide “Z13”, the antigenic cargo “MAD12” comprising three neoantigens as identified by Yadav et al. Nature. 2014 Nov. 27; 515(7528):572-6 from MC-38 tumor cell line, and the TLR peptide agonist “Anaxa”.
  • the amino acid sequence of Z13Mad12Anaxa is shown:
  • mice C57BL/6 mice (thirteen to fourteen mice per group, female, 7 week old) were implanted s.c. with 2 ⁇ 10 5 MC-38 tumor cells in the left flank (day 0). After tumor implantation, mice of the groups “Z13Mad12Anaxa” and “Z13Mad12Anaxa+anti-PD1” were vaccinated at days 3, 10 and 17 subcutaneously with 2 nmol of Z13Mad12Anaxa at the tail base. 200 ⁇ g of anti-PD1 antibody RMP1-14 (BioXcell, West Riverside, N.H., USA) were administered i.p.
  • FIGS. 39 and 40 treatment with the PD1 inhibitor alone or with Z13Mad12Anaxa alone resulted in significantly reduced tumor volume ( FIG. 39A ) and increased survival ( FIG. 39B ), as compared to the control group.
  • the combination of both, the PD1 inhibitor and Z13Mad12Anaxa resulted in the most pronounced improvement, namely in strongly decreased tumor volume and strongly increased survival rates.
  • the “Z13Mad12Anaxa+aPD1” group only three mice developed tumors (whereas 10 mice remained tumor-free), whereas in the “aPD1” group and in the “Z13Mad12Anaxa” group eight and ten mice, respectively, developed tumors. In the control group all mice developed tumors.

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Immunology (AREA)
  • Genetics & Genomics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Zoology (AREA)
  • Biomedical Technology (AREA)
  • Biotechnology (AREA)
  • Wood Science & Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • Oncology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Cell Biology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Plant Pathology (AREA)
  • Endocrinology (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Toxicology (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Peptides Or Proteins (AREA)
US16/084,170 2016-03-16 2017-03-14 Combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a tlr peptide agonist for use in medicine Abandoned US20190175748A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
PCT/EP2016/000472 WO2016146261A1 (en) 2015-03-16 2016-03-16 Combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a tlr peptide agonist for use in medicine
EPPCT/EP2016/000472 2016-03-16
EPPCT/EP2016/070264 2016-08-26
EP2016070264 2016-08-26
PCT/EP2017/056034 WO2017157964A1 (en) 2016-03-16 2017-03-14 Combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a tlr peptide agonist for use in medicine

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2017/056034 A-371-Of-International WO2017157964A1 (en) 2016-03-16 2017-03-14 Combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a tlr peptide agonist for use in medicine

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US17/569,261 Continuation US20220118102A1 (en) 2016-03-16 2022-01-05 Combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a tlr peptide agonist for use in medicine

Publications (1)

Publication Number Publication Date
US20190175748A1 true US20190175748A1 (en) 2019-06-13

Family

ID=59851405

Family Applications (2)

Application Number Title Priority Date Filing Date
US16/084,170 Abandoned US20190175748A1 (en) 2016-03-16 2017-03-14 Combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a tlr peptide agonist for use in medicine
US17/569,261 Pending US20220118102A1 (en) 2016-03-16 2022-01-05 Combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a tlr peptide agonist for use in medicine

Family Applications After (1)

Application Number Title Priority Date Filing Date
US17/569,261 Pending US20220118102A1 (en) 2016-03-16 2022-01-05 Combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a tlr peptide agonist for use in medicine

Country Status (17)

Country Link
US (2) US20190175748A1 (hu)
EP (1) EP3429618B1 (hu)
JP (1) JP7189021B2 (hu)
AU (1) AU2017234192B2 (hu)
CA (1) CA3010779A1 (hu)
DK (1) DK3429618T5 (hu)
ES (1) ES2977541T3 (hu)
FI (1) FI3429618T3 (hu)
HR (1) HRP20240510T1 (hu)
HU (1) HUE066998T2 (hu)
LT (1) LT3429618T (hu)
PL (1) PL3429618T3 (hu)
PT (1) PT3429618T (hu)
RS (1) RS65430B1 (hu)
RU (2) RU2748378C2 (hu)
SI (1) SI3429618T1 (hu)
WO (1) WO2017157964A1 (hu)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180133327A1 (en) * 2015-03-16 2018-05-17 Amal Therapeutics Sa Cell Penetrating Peptides and Complexes Comprising the Same
CN113444687A (zh) * 2021-05-31 2021-09-28 浙江圣希澳医学科技有限公司 穿膜肽介导肿瘤抗原多肽致敏转染cd40l的dc疫苗及dc-ctl方法
US11338027B2 (en) 2016-09-21 2022-05-24 Amal Therapeutics Sa Fusion comprising a cell penetrating peptide, a multi epitope and a TLR peptide agonist for treatment of cancer
WO2023091747A1 (en) * 2021-11-22 2023-05-25 Axial Therapeutics, Inc. Modulator compounds, pharmaceutical compositions and uses thereof

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2016256911B2 (en) 2015-05-07 2022-03-31 Agenus Inc. Anti-OX40 antibodies and methods of use thereof
US11447557B2 (en) 2015-12-02 2022-09-20 Agenus Inc. Antibodies and methods of use thereof
CA3037380A1 (en) 2016-10-11 2018-04-19 Agenus Inc. Anti-lag-3 antibodies and methods of use thereof
MA46770A (fr) 2016-11-09 2019-09-18 Agenus Inc Anticorps anti-ox40, anticorps anti-gitr, et leurs procédés d'utilisation
EA201992755A1 (ru) 2017-05-19 2020-04-22 Уси Байолоджикс (Шанхай) Ко. Лтд. Новые моноклональные антитела к белку 4, ассоциированному с цитотоксическими т-лимфоцитами, (ctla-4)
GB201810058D0 (en) * 2018-06-19 2018-08-08 Cytovation As Combination therapy using a peptide
JP2023504907A (ja) * 2020-06-04 2023-02-07 ザ カトリック ユニバーシティ オブ コリア インダストリー－アカデミック コーオペレイション ファウンデーション フラジェリン由来のｔｌｒ５アゴニストを有効成分として含む抗がん剤組成物
EP4351639A1 (en) * 2021-05-19 2024-04-17 Queen's University At Kingston Combination therapy tumour cell vaccine
CN113945723B (zh) * 2021-10-28 2024-03-12 复旦大学附属中山医院 预测免疫检查点抑制剂治疗相关肺炎发生风险的系统、储存介质及其应用
WO2023155318A1 (zh) * 2022-02-21 2023-08-24 悦康药业集团股份有限公司 一种优化病毒膜融合抑制剂的方法及广谱抗冠状病毒脂肽和应用

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5851795A (en) 1991-06-27 1998-12-22 Bristol-Myers Squibb Company Soluble CTLA4 molecules and uses thereof
US6479055B1 (en) * 1993-06-07 2002-11-12 Trimeris, Inc. Methods for inhibition of membrane fusion-associated events, including respiratory syncytial virus transmission
US5811097A (en) 1995-07-25 1998-09-22 The Regents Of The University Of California Blockade of T lymphocyte down-regulation associated with CTLA-4 signaling
US5855887A (en) 1995-07-25 1999-01-05 The Regents Of The University Of California Blockade of lymphocyte down-regulation associated with CTLA-4 signaling
US6051227A (en) 1995-07-25 2000-04-18 The Regents Of The University Of California, Office Of Technology Transfer Blockade of T lymphocyte down-regulation associated with CTLA-4 signaling
AU6703198A (en) 1997-03-21 1998-10-20 Brigham And Women's Hospital Immunotherapeutic ctla-4 binding peptides
JP3793693B2 (ja) 1998-12-23 2006-07-05 ファイザー インコーポレーテッド Ｃｔｌａ−４に対するヒトモノクローナル抗体
US6682736B1 (en) 1998-12-23 2004-01-27 Abgenix, Inc. Human monoclonal antibodies to CTLA-4
US7109003B2 (en) 1998-12-23 2006-09-19 Abgenix, Inc. Methods for expressing and recovering human monoclonal antibodies to CTLA-4
US6984720B1 (en) 1999-08-24 2006-01-10 Medarex, Inc. Human CTLA-4 antibodies
US7605238B2 (en) 1999-08-24 2009-10-20 Medarex, Inc. Human CTLA-4 antibodies and their uses
JP2003520828A (ja) 2000-01-27 2003-07-08 ジェネティクス インスティテュート，エルエルシー Ｃｔｌａ４（ｃｄ１５２）に対する抗体、これを含む結合体、およびその使用
PL218660B1 (pl) 2002-10-17 2015-01-30 Genmab As Izolowane ludzkie przeciwciało monoklonalne wiążące ludzki CD20, związane z tym przeciwciałem transfektoma, komórka gospodarza, transgeniczne zwierzę lub roślina, kompozycja, immunokoniugat, cząsteczka bispecyficzna, wektor ekspresyjny, kompozycja farmaceutyczna, zastosowanie medyczne, zestaw oraz przeciwciało antyidiotypowe i jego zastosowanie
EP1768698A4 (en) 2004-06-17 2009-01-28 Medimmune Inc IMMUNOGENIC COMPOSITIONS COMPRISING HMGB1 POLYPEPTIDES
EP1791868B1 (en) 2004-07-01 2011-02-23 Novo Nordisk A/S Antibodies binding to receptors kir2dl1, -2, 3 but not kir2ds4 and their therapeutic use
ES2291071B1 (es) 2005-06-13 2009-03-16 Proyecto De Biomedicina Cima, S.L. Agentes y metodos basados en el uso del dominio eda de la fibronectina.
EP1987839A1 (en) 2007-04-30 2008-11-05 I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale Cytotoxic anti-LAG-3 monoclonal antibody and its use in the treatment or prevention of organ transplant rejection and autoimmune disease
NZ600758A (en) 2007-06-18 2013-09-27 Merck Sharp & Dohme Antibodies to human programmed death receptor pd-1
EP2044949A1 (en) 2007-10-05 2009-04-08 Immutep Use of recombinant lag-3 or the derivatives thereof for eliciting monocyte immune response
AR072999A1 (es) 2008-08-11 2010-10-06 Medarex Inc Anticuerpos humanos que se unen al gen 3 de activacion linfocitaria (lag-3) y los usos de estos
CN102245640B (zh) 2008-12-09 2014-12-31 霍夫曼-拉罗奇有限公司 抗-pd-l1抗体及它们用于增强t细胞功能的用途
CN102762593B (zh) 2009-07-31 2015-05-20 梅达雷克斯有限责任公司 抗btla的完全人抗体
CN102666581A (zh) 2009-08-31 2012-09-12 艾普利穆恩公司 用于抑制移植物排斥的方法和组合物
EP2476440B1 (en) * 2009-09-11 2017-08-02 Proyecto de Biomedicina Cima, S.L. Therapeutic compositions for the treatment of hpv-induced diseases
WO2011036211A1 (en) * 2009-09-23 2011-03-31 Institut National De La Sante Et De La Recherche Medicale (Inserm) Polypeptides and nucleic acids for treating erbb2-dependent cancers
MX359551B (es) 2009-11-24 2018-10-02 Medimmune Ltd Agentes de union diana contra b7-h1.
WO2011101332A1 (en) 2010-02-16 2011-08-25 Proyecto De Biomedicina Cima, S.L. Compositions based on the fibronectin extracellular domain a for the treatment of melanoma
US8802091B2 (en) 2010-03-04 2014-08-12 Macrogenics, Inc. Antibodies reactive with B7-H3 and uses thereof
US9555074B2 (en) 2010-10-08 2017-01-31 Regents Of The University Of Minnesota Annexin II compositions
US8841418B2 (en) 2011-07-01 2014-09-23 Cellerant Therapeutics, Inc. Antibodies that specifically bind to TIM3
JP6120848B2 (ja) 2011-08-15 2017-04-26 メディミューン，エルエルシー 抗ｂ７−ｈ４抗体およびその使用
WO2013067492A1 (en) 2011-11-03 2013-05-10 The Trustees Of The University Of Pennsylvania Isolated b7-h4 specific compositions and methods of use thereof
US9597393B2 (en) * 2012-02-09 2017-03-21 Av Therapeutics, Inc. Synthetic toll-like receptor-4 (TLR-4) agonist peptides
RU2670488C2 (ru) 2012-09-13 2018-10-23 Юниверсите Де Женев Новые проникающие в клетку пептиды
KR20160102314A (ko) * 2014-01-02 2016-08-29 메모리얼 슬로안-케터링 캔서 센터 면역 치료요법에 대한 암 반응의 결정인자

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180133327A1 (en) * 2015-03-16 2018-05-17 Amal Therapeutics Sa Cell Penetrating Peptides and Complexes Comprising the Same
US11338027B2 (en) 2016-09-21 2022-05-24 Amal Therapeutics Sa Fusion comprising a cell penetrating peptide, a multi epitope and a TLR peptide agonist for treatment of cancer
CN113444687A (zh) * 2021-05-31 2021-09-28 浙江圣希澳医学科技有限公司 穿膜肽介导肿瘤抗原多肽致敏转染cd40l的dc疫苗及dc-ctl方法
WO2023091747A1 (en) * 2021-11-22 2023-05-25 Axial Therapeutics, Inc. Modulator compounds, pharmaceutical compositions and uses thereof

Also Published As

Publication number Publication date
HRP20240510T1 (hr) 2024-07-05
HUE066998T2 (hu) 2024-09-28
LT3429618T (lt) 2024-05-10
AU2017234192B2 (en) 2024-04-04
SI3429618T1 (sl) 2024-06-28
WO2017157964A1 (en) 2017-09-21
RU2018135097A (ru) 2020-04-16
RU2748378C2 (ru) 2021-05-25
DK3429618T5 (da) 2024-09-16
DK3429618T3 (da) 2024-04-22
CA3010779A1 (en) 2017-09-21
ES2977541T3 (es) 2024-08-26
EP3429618B1 (en) 2024-02-21
US20220118102A1 (en) 2022-04-21
JP2019508444A (ja) 2019-03-28
RU2018135097A3 (hu) 2020-07-30
RS65430B1 (sr) 2024-05-31
PL3429618T3 (pl) 2024-07-01
PT3429618T (pt) 2024-04-02
FI3429618T3 (fi) 2024-03-15
EP3429618A1 (en) 2019-01-23
RU2769314C1 (ru) 2022-03-30
AU2017234192A1 (en) 2018-07-26
JP7189021B2 (ja) 2022-12-13

Similar Documents

Publication Publication Date Title
US20220118102A1 (en) Combination of an immune checkpoint modulator and a complex comprising a cell penetrating peptide, a cargo and a tlr peptide agonist for use in medicine
JP7190528B2 (ja) 神経膠芽腫を治療するための細胞透過性ペプチド、カーゴ、及びｔｌｒペプチドアゴニストを含む新規複合体
JP7346291B2 (ja) 癌を治療するための細胞透過性ペプチド、マルチエピトープ、及びｔｌｒペプチドアゴニストを含む融合体
RU2807135C2 (ru) Слитая конструкция, содержащая проникающий в клетку пептид, полиэпитоп и пептидный агонист tlr, предназначенная для лечения рака

Legal Events

Date Code Title Description
AS Assignment

Owner name: AMAL THERAPEUTICS SA, SWITZERLAND

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:DEROUAZI, MADIHA;REEL/FRAME:047259/0619

Effective date: 20181022

STPP Information on status: patent application and granting procedure in general

Free format text: APPLICATION DISPATCHED FROM PREEXAM, NOT YET DOCKETED

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION