Patent Application
20230321226
The file named “557 U.S. Corrected sequence listing” created on Jul. 12, 2019 with size of 3.16 KB, is hereby incorporated by reference into this specifciation.
The present invention relates to the field of liposomes, the lipid compounds thereof and the pharmaceutical uses thereof. In particular the present invention relates to new synthetic compounds and the formulation of new liposomes comprising at least one of these compounds for use in vaccination.
Developing new compounds that have advantageous properties for the preparation of liposomes represents a major stake in medical research. Liposomes form a very effective way for delivering a molecule of interest inside cells. Liposomes represent for example an alternative to viral vectors for the delivery of nucleic acids. They also are of major therapeutic interest in cancerology. In addition to being used as vectors for drugs, liposomes are indeed developed for a therapeutic vaccination aiming to induce an immune response against tumour cells.
So-called conventional liposomes are mainly comprised of phospholipids similar to those present in the membranes of bacteria or of eukaryotic cells. The medical use of these liposomes can however be limited by stability problems and targeting problems. In order to be able to be administered orally or through blood, liposomes must indeed be able to resist an acid environment and/or interactions with the proteins and lipoproteins of the blood. Moreover, liposomes must be recognised by the cells for which the molecules that they transport are intended. In particular liposomes used as vaccination vectors must be recognised and internalised by the antigen-presenting cells so that the latter can induce a specific immune response to the antigen delivered by the liposomes.
The problem of liposome stability can be resolved by the use of lipids called ether lipids or archaeolipids. These lipids, naturally present in the membranes of archaebacteria, are characterised by the presence of ether bonds linking the phytanyl aliphatic chains that they are comprised of to a glycerol. The lipids present in the membranes of archaebacteria are therefore generally diethers or tetraethers of phytanols. The structure of the ether lipids plays an important role in the resistance of archaebacteria to extreme conditions. Likewise, the liposomes comprising these lipids, also called archaeosomes, generally display an increased stability to oxidative stress, to high temperatures, to acidic or alkaline conditions, to the action of phospholipases, bile salts and serum proteins (Patel GB, Sprott GD. Archaeobacterial ether lipid liposomes (archeosomes) as novel vaccines and drug delivery systems. Crit Rev Biotechnol 1999; 19: 317-357). WO9308202 thus describes archaeosomes that display an increased stability, obtained using total polar lipids extracted from archaebacteria. CA2269502 describes lipids derived from tetraethers and liposomes that contain them. WO2006061396 describes synthetic tetraether lipids similar to those present in the membranes of archaebacteria and liposomes that integrate these tetraether lipids. In addition to their increased stability, archaeosomes also have the advantage of having an intrinsic adjuvant effect, independent of any molecule that they can transport. WO0126683 thus describes the in vitro and in vivo activation of mouse macrophages and of dendritic cells by empty archaeosomes comprised of total polar lipids extracted from archaebacteria.
The problem of addressing liposomes can be resolved by the use of compounds that contain a lipid bound to a polar group that can be recognised by receptors expressed on the surface of targeted cells. Thus, liposomes comprising such compounds having a sugar polar group can be recognised by the lectin receptors of antigen-presenting cells (Benvegnu et al., Glycolipid-based nanosystems for the delivery of drugs, genes and vaccine adjuvant applications, Carbohydr. Chem., 2014, 40: 341-377). In particular, Espuelas et al., describe the addition of one, two or four mannose group(s) via a PEG spacer to a synthetic dioleylglycerol (DOG) lipid having two non-phytanyl aliphaticchains linked to a glycerol via an ether bond (Espuelas et al., Influence of ligand valency on the targeting of immature human dendritic cells by mannosylated liposomes, Bioconjugate Chem. 2008, 19:2385-2393). Espuelas et al., show that liposomes containing these compounds can target and be bound by human immature dendritic cells but are not able on their own to induce the expression of surface markers CD83, CD86 and HLA-DR of these cells. The compounds described by Espuelas et al., therefore do not confer any intrinsic adjuvant effect to the liposomes that contain them. WO2007112567 describes hemisynthetic diethers or tetraethers lipids comprising only phytanyl chains obtained from extracts of total polar lipids of archaebacteria. After isolation, these lipids are attached to sugar groups and the compounds obtained are used in the preparation of archaeosomes.
Obtaining hemisynthetic compounds comprising a diether lipid extracted from archaebacteria requires setting up archaebacteria cultures, extraction and isolation methods that are difficult to implement on a large scale. It is therefore necessary to be able to obtain synthetic compounds comprising diether lipids bound to a sugar group that have the advantageous properties of archaebacteria lipids.
The present invention thus relates to synthetic compounds comprising a diether lipid linked to a sugar group and liposomes comprising these compounds. The compounds of the invention are characterised by the presence of a branched aliphatic chain and of an unsubstituted linear aliphatic chain and by the presence of a glycoside group grafted to the diether lipid via a PEG spacer. In an unprecedented manner, the synthetic compounds of the invention provide the liposomes that contain them an in vitro and in vivo intrinsic adjuvant effect.
The present invention thus relates to a compound of formula I:
wherein:
According to an embodiment, the present invention relates to a compound of formula I:
wherein:
According to an embodiment, the present invention relates to a compound of formula I:
wherein:
The present invention also relates to a compound of formula II: wherein:
According to an embodiment, the present invention relates to the compound of formula II: wherein:
The present invention also relates to a liposome comprising at least one compound according to the invention. According to an embodiment, the liposome of the invention comprises at least one compound of the invention in proportions between from about 1% to about 15% in mole percent with respect to the total number of moles of lipids, preferably from about 2% to about 10%, more preferably of about 5%.
The present invention also relates to a liposome of the invention further comprising at least one molecule of interest.
According to an embodiment, the molecule of interest contained in the liposome of the invention is able to induce an immune response.
According to an embodiment, the molecule of interest contained in the liposome of the invention is a nucleic acid.
According to an embodiment, the molecule of interest contained in the liposome of the invention is a cancer-associated antigen or a nucleic acid encoding a cancer-associated antigen.
According to an embodiment, the molecule of interest is a cancer-associated antigen selected from the group comprising: CAP-1, CD 4/m, cell surface proteins of the claudin family CLAUDIN-6, CLAUDIN-18.2 and CLAUDIN-12, c-myc, CT, GnT-V, HAGE, HAST-2, LAGE, NF1, NY-BR-1, proteinase 3, SAGE, SCGB3A2, SCP1, SCP2, SCP3, SSX, SURVrVin, TPI/m, TPTE, CDK4 (cyclin-dependent kinase 4), plS1″1′4′3, p53, AFP, β-catenin, caspase 8, mutated version of p21Ras, Bcr-abl chimera, MUM-I MUM-2, MUM-3, ELF2M, HSP70-2M, HST-2, KIAA0205, RAGE, myosin/m, 707-AP, CDC27/m, ETV6/AML, TEL/Amll, Dekcain, LDLR/FUT, Pml-RARαTEL/AMLI, NY-ESO-I, members of the MAGE family (Melanoma-associated antigen) MAGE-Al, MAGE-A2, MAGE-A3, MAGE-A4, MAGE-A5, MAGE-A6, MAGE-A7, MAGE-A8, MAGE-A9, MAGE-A10, MAGE-A11, MAGE-A12, MAGE-B, MAGE-C, BAGE, DAM-6, DAM-10, members of the GAGE family (G antigen) GAGE-1, GAGE-2, GAGE-3, GAGE-4, GAGE-5, GAGE-6, GAGE-7B, GAGE-8, NA-88A, CAG-3, RCC-associated antigen G250, oncoproteins E6 and E7 derived from HPV (human papilloma virus), Epstein Barr virus antigens EBNA2-6, LMP-I, LMP-2, gp77, gp100, MART-1/Melan-A, tyrosinase, TRP-I and TRP-2 (tyrosinase-related protein), TRP-2-INT2, PSA, PSM, MC1R, ART4, CAMEL, CEA, CypB, HER2/neu, hTERT, hTRT, iCE, Mucl, Muc2, PRAME RU1, RU2, SART-I, SART-2, SART-3, WT and WT1, or a nucleic acid encoding said cancer-associated antigen.
The present invention also relates to a compound according to the invention for use as a vaccine adjuvant. Furthermore, the present invention relates to a liposome comprising at least one compound according to the invention for use as a vaccine adjuvant.
The present invention also relates to a liposome comprising at least one compound of the invention and further comprising at least one molecule of interest capable of inducing an immune response, for use as a vaccine.
The present invention also relates to a pharmaceutical composition comprising the compound according to the invention and at least one pharmaceutically acceptable excipient. Furthermore, the present invention relates to the liposome according to the invention and at least one pharmaceutically acceptable excipient.
In the present invention, the following terms are defined in the following way:
The present invention relates to a compound comprising:
The present invention relates to a compound of formula I:
wherein:
According to an embodiment, the present invention relates to a compound of formula I:
wherein:
According to an embodiment, the present invention relates to a compound of formula I:
wherein:
According to an embodiment, the present invention relates to a compound of formula I:
wherein:
According to an embodiment, the present invention relates to a compound of formula I:
wherein:
According to an embodiment, the present invention relates to a compound of formula I:
wherein:
According to an embodiment, the present invention therefore relates to a tri-mannosylated compound of formula II: wherein:
According to a particular embodiment, this invention relates to a tri-mannosylated compound of formula II: wherein:
According to a particular embodiment, the present invention relates to a tri-mannosylated compound of formula II: wherein:
The present invention relates to a synthetic compound comprising a lipid that has structural characteristics specific to the lipids naturally present in the membranes of archaebacteria.
Lipids naturally present in the membranes of archaebacteria are characterised by the presence of ether bonds connecting their aliphatic chains to a glycerol molecule. They are also characterised by the presence of phytanyl aliphatic chains that are regularly branched. The lipid ethers present in the membranes of archaebacteria are thus generally diethers of phytanols (such as archaeol) or tetraethers of phytanols (such as caldarchaeol). The glycerolipids present in the membranes of bacteria and of eukaryotic cells, referred to as conventional lipids, have ester bonds connecting their fatty acids to a glycerol molecule. Moreover, the fatty acids of these conventional lipids are generally saturated or unsaturated aliphatic chains, that do not comprise any branches. The structure of the lipid ethers present in the membranes of archaebacteria plays an important role in the resistance of archaebacteria to extreme conditions such as high temperatures or an acid environment.
The present invention relates to a synthetic compound comprising two ether bonds, connecting a branched aliphatic chain and an unsubstituted linear aliphatic chain to a glycerol. The present invention relates to a compound comprising a diether lipid.
According to an embodiment, the diether lipid of the invention comprises two aliphatic chains, of which the linear structures, not including the branched carbons, are of the same length, connected to a glycerol via an ether bond, one of the aliphatic chains being a branched chain and the other aliphatic chain being an unsubstituted linear chain.
In an embodiment, the aliphatic chains of the diether lipid of the invention are saturated. In another embodiment, the aliphatic chains of the diether lipid of the invention are unsaturated. In another embodiment, the branched aliphatic chain is saturated and the unsubstituted linear aliphatic chain is unsaturated. In another embodiment, the branched aliphatic chain is unsaturated and the unsubstituted linear aliphatic chain is saturated.
In an embodiment, the linear structure of the same length of the branched chain and the unsubstituted linear chain of the diether lipid of the invention comprises between 12 and 20 carbons, preferably between 16 and 20 carbons, and more preferably 16 carbons.
In an embodiment the linear structure of the same length of the branched chain and the unsubstituted linear chain of the diether lipid of the invention comprises 12, 13, 14, 15, 16, 17, 18, 19 or 20 carbons.
The present invention relates to a compound comprising a diether lipid to which a hydrophilic group, or polar group is grafted.
In an embodiment, the hydrophilic group grafted to the diether lipid of the invention is a glycoside.
In an embodiment, the hydrophilic group grafted to the diether lipid of the invention is a sugar recognised by lectins, proteins able of binding sugar residues, and preferably by type C lectins.
In an embodiment, the hydrophilic group grafted to the diether lipid of the invention is a sugar recognised by lectins DC-SIGN (CD209), DEC205/CD205, langerin (CD207), CLEC9A, CLEC4D, CD40, and/or the mannose receptor (MR).
According to an embodiment, the hydrophilic group grafted to the diether lipid of the invention is a sugar chosen from the list comprising glycans terminated with a mannose, glycans terminated with a fucose, Lewis-A trisaccharide 3′-sulfate, Lewis-B trisaccharide (Leb), Lewis-X trisaccharide (Lex), tri-N-acetylglucosamine (tri-GlcNAc), PIMs (phosphatidylinositol mannosides), in particular PIM1 to PIM6 (phosphatidylinositol mono- to hexa-mannoside), Man9GlcNAc2 oligosaccharide, N-linked oligosaccharides rich in mannose, α-fucose-1-4GlcNAc oligosaccharide, lacto-N-fucopentaose III oligosaccharide containing the Lex trisaccharide, GlcNAc2 Man 3 oligosaccharide, Man 4 oligosaccharides, Manα1-3(Manα1-6)Manα1 oligosaccharide, lipoarabinomannans (LAMs), mannosylated lipoarabinomannans (ManLAMs) and the antennery sugars comprising from 2 to 5 sugar residues characterised in that the antennery sugar residues are attached by an oligo(propylene glycol)n spacer wherein n is ranging from 1 to 5 and preferably n = 2, the sugar residues being chosen independently from the list comprising mannose, glucose, fucose, and oligomannoses comprising from 2 to 10 mannose units.
According to an embodiment, the hydrophilic group grafted to the diether lipid of the invention is a sugar chosen from the list comprising glycans terminated with a mannose, glycans terminated with a fucose, Lewis-A trisaccharide 3′-sulfate, Lewis-B trisaccharide (Leb), Lewis-X trisaccharide (Lex), tri-N-acetylglucosamine (tri-GlcNAc), PIMs (phosphatidylinositol mannosides), in particular PIM1 to PIM6 (phosphatidylinositol mono- to hexa-mannoside), α-fucose-1-4GlcNAc oligosaccharide, lacto-N-fucopentaose III oligosaccharide containing the Lex trisaccharide, GlcNAc2 Man 3 oligosaccharide, lipoarabinomannans (LAMs), mannosylated lipoarabinomannans (ManLAMs) and the antennery sugars comprising from 2 to 5 sugar residues characterised in that the antennery sugar residues are attached by an oligo(propylene glycol)n spacer wherein n is ranging from 1 to 5 and preferably n = 2, the sugar residues being chosen independently from the list comprising mannose, glucose, fucose, and oligomannoses comprising from 2 to 10 mannose units.
According to an embodiment, the hydrophilic group grafted to the diether lipid of the invention is an antennery sugar comprising from 2 to 5 sugar residues characterised in that the antennery sugar residues are attached by an oligo(propylene glycol)n spacer wherein n is ranging from 1 to 5 and preferably n = 2, the sugar residues being chosen independently from the list comprising mannose, glucose, fucose, and oligomannoses comprising from 2 to 10 mannose units.
According to an embodiment, the hydrophilic group grafted to the diether lipid of the invention is an antennery sugar comprising 2, 3, 4 or 5 sugar residues attached by an oligo(propylene glycol)n spacer wherein n is ranging from 1 to 5 and preferably n = 2, the sugar residues being chosen independently from the list comprising mannose, glucose, fucose, and oligomannoses comprising from 2 to 10 mannose units.
According to an embodiment, the hydrophilic group grafted to the diether lipid of the invention is an antennery sugar comprising 3 sugar residues attached by an oligo(propylene glycol)n spacer wherein n is ranging from 1 to 5 and preferably n = 2, the sugar residues being chosen independently from the list comprising mannose, glucose, fucose, and oligomannoses comprising from 2 to 10 mannose units.
According to an embodiment, the hydrophilic group grafted to the diether lipid of the invention is an antennery sugar comprising 2, 3, 4 or 5 mannoses attached by an oligo(propylene glycol)n spacer wherein n is ranging from 1 to 5 and preferably n = 2.
According to an embodiment, the hydrophilic group grafted to the diether lipid of the invention is an antennery sugar comprising 2, 3, 4 or 5 glucoses attached by an oligo(propylene glycol)n spacer wherein n is ranging from 1 to 5 and preferably n = 2.
According to an embodiment, the hydrophilic group grafted to the diether lipid of the invention is an antennery sugar comprising 2, 3, 4 or 5 fucoses attached by an oligo(propylene glycol)n spacer wherein n is ranging from 1 to 5 and preferably n = 2.
According to an embodiment, the hydrophilic group grafted to the diether lipid of the invention is an antennery sugar comprising 2, 3, 4 or 5 oligomannoses comprising from 2 to 10 mannose units attached by an oligo(propylene glycol)n spacer wherein n is ranging from 1 to 5 and preferably n = 2.
The present invention relates to a compound comprising a diether lipid which is grafted to the hydrophilic group, or polar group, by the intermediary of a polyethylene glycol spacer (PEG).
In an embodiment, the PEG spacer has the following structure:
wherein c is between 1 and 130, preferably between 5 and 20.
According to an embodiment, c is equal to 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50.
According to an embodiment, c is an integer ranging from 2 to 30, preferably from 3 to 20, and more preferably from 4 to 10. According to a particular embodiment, c is equal to 5.
The synthesis of the compound of the invention can be carried out by different routes known to those skilled in the art.
In an embodiment (described in Laine et al., Folate-equipped pegylated archaeal lipid derivatives: synthesis and transfection properties, Chem. Eur. J. 2008, 14, 83330-8340), a diether lipid according to the invention can be obtained from a glycerol derivative, itself synthesised from a phytol and from a (R)-solketal. The reaction of this glycerol derivative with hexadecyl triflate in the presence of a proton sponge makes it possible to obtain the corresponding diether. The hydrogenolysis of the benzyloxy group leads to alcohol which can then be converted into carboxylic acid or into amine. The diethers lipid thus obtained, having a carboxylic acid function or an amine function, may be used for the synthesis of compounds according to the invention.
In an embodiment, the synthesis of the tri-mannosylated compound of formula II is carried out according to a four-step scheme starting from carboxylic acid tri-mannosylated ligand and 1-O-carboxyl-2-O-Phytanyl-3-O-hexadecane-sn-glycerol referred to hereinafter as diether lipid having a carboxylic acid function (or carboxylic acid diether):
The present invention also relates to a liposome comprising at least one compound of the invention.
According to an embodiment, the liposome of the invention comprises at least one compound of the invention in proportions rangingfrom about 1% to about 15% in mole percent with respect to the total number of moles of lipids, preferably from about 2% to about 10%, more preferably of about 5%.
In an embodiment, the liposome of the invention comprises at least one compound of the invention in proportions ranging from about 1% to about 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, or 15% in mole percent with respect to the total number of moles of lipids.
In an embodiment, the liposome of the invention comprises at least one compound of the invention in proportions ranging from about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, or 14%, to about 15% in mole percent with respect to the total number of moles of lipids.
In an embodiment, the liposome of the invention comprises about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14% or 15% of a compound of the invention in mole percent with respect to the total number of moles of lipids.
According to an embodiment, the liposome of the invention comprises at least one compound of the invention in proportions ranging from about 1% to about 15% by weight with respect to the total weight of the liposome, preferably from about 2% to about 10%, more preferably of about 5%.
In an embodiment, the liposome of the invention comprises about 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14% or 15% of a compound of the invention, by weight with respect to the total weight of the liposome.
In an embodiment, the liposome of the invention comprises at least one compound according to the invention alone or in a mixture with one or several synthetic, hemisynthetic or natural lipids.
According to an embodiment, the liposome of the invention comprises at least one compound according to the invention and the lipid KLN25 (O,O-dioleyl-N-[3N-(Nmethylimidazoliumbromide)propylene] phosphoramidate) of formula:
According to an embodiment, the liposome of the invention comprises at least one compound according to the invention and the lipid MM27 (O,O-dioleyl (-N-(histamine)phosphoramidate) of formula:
According to an embodiment, the liposome of the invention comprises at least one compound according to the invention, the lipid KLN25 and the lipid MM27.
According to an embodiment, the liposome of the invention comprises 5% of the compound according to the invention, 47.5% of lipid KLN25, and 47.5% of lipid MM27, in mole percent with respect to the total number of moles of lipids.
According to an embodiment, the liposome of the invention comprises at least one compound according to the invention and a cationic lipid. In an embodiment, the cationic lipid is a lipid that has one polar head consisting of an imidazolium group. In an embodiment, the liposome of the invention is a cationic liposome.
The preparation of the liposome of the invention can be carried out by different methods well-known to those skilled in the art. For example, the liposome of the invention can be prepared according to the method of hydrating a dry lipid film (Pichon C, Midoux P. (2013) Mannosylated and Histidylated LPR Technology for Vaccination with Tumor Antigen mRNA. Methods Mol Biol. 969:247-74).
According to an embodiment, the liposome of the invention comprises at least one molecule of interest. According to an embodiment, the liposome of the invention comprises at least one molecule of interest to be delivered in vitro or in vivo to a cell.
In an embodiment, the molecule of interest is comprised within the lipid bilayer of the liposome of the invention. In another embodiment, the molecule of interest is comprised within the hydrophilic compartment of the liposome of the invention.
In an embodiment, the molecule of interest is a nucleic acid, for example and without being limited to, the molecule of interest is a DNA, a RNA, a mRNA, a siRNA, or a microRNA. In another embodiment, the molecule of interest is a protein or a peptide. In another embodiment, the molecule of interest is a therapeutic agent. In another embodiment, the molecule of interest is a colouring agent or a marker.
In an embodiment, the molecule of interest is an immunogenic molecule. In an embodiment, the molecule of interest is able to induce an immune response.
In an embodiment, the molecule of interest is an antigen of bacterial origin, of fungal origin or of viral origin. In an embodiment, the molecule of interest is an antigen of bacterial origin chosen from the non-exhaustive list comprising the capsular polyoside (polyribosyl ribitol phosphate or PRP) of type b Hæmophilus influenzæ; polyoside serotypes 1, 2, 3, 4, 5, 6B, 7F, 8, 9N, 9V, 10A, 11A, 12F, 14, 15B, 17F, 18C, 19A, 19F, 20, 22F, 23F, 33F of Streptococcus pneumoniae; the polyoside of Neisseria meningitidis group A; the polyoside of Neisseria meningitidis group B; the capsular polyoside Vi of Salmonella typhi (Ty 2 strain).
In an embodiment, the molecule of interest is a cancer-associated antigen or a nucleic acid encoding a cancer-associated antigen.
In a preferred embodiment, the immunogenic molecule contained in the liposome of the invention is a tumour antigen or a nucleic acid encoding a tumour antigen. According to an embodiment, the tumour antigen can be chosen from the non-exhaustive list comprising: CDK4 (cyclin-dependent kinase 4), p1S1″1′4′3, p53, AFP, β-catenin, caspase 8, mutated version of p21Ras, Bcr-abl chimera, MUM-I MUM-2, MUM-3, ELF2M, HSP70-2M, HST-2, KIAA0205, RAGE, myosin/m, 707-AP, CDC27/m, ETV6/AML, TEL/Amll, Dekcain, LDLR/FUT, Pml-RARαTEL/AMLI, NY-ESO-I, members of the MAGE family (Melanoma-associated antigen) MAGE-Al, MAGE-A2, MAGE-A3, MAGE-A4, MAGE-A6, MAGE-10, MAGE-12, BAGE, DAM-6, DAM-10, members of the GAGE family (G antigen) GAGE-1, GAGE-2, GAGE-3, GAGE-4, GAGE-5, GAGE-6, GAGE-7B, GAGE-8, NA-88A, CAG-3, RCC-associated antigen G250, oncoproteins E6 and E7 derived from HPV (human papilloma virus), Epstein Barr virus antigens EBNA2-6, LMP-I, LMP-2, gp77, gp100, MART-1/Melan-A, tyrosinase, TRP-I and TRP-2 (tyrosinase-related protein), PSA, PSM, MC1R, ART4, CAMEL, CEA, CypB, HER2/neu, hTERT, hTRT, iCE, Muc1, Muc2, PRAME RU1, RU2, SART-I, SART-2, SART-3, and WT1. According to an embodiment, the tumour antigen can be chosen from the non-exhaustive list comprising: CAP-1, CD 4/m, cell surface proteins of the claudin family CLAUDIN-6, CLAUDIN-18.2 and CLAUDIN-12, c-myc, CT, GnT-V, HAGE, HAST-2, LAGE, NF1, NY-BR-1, proteinase 3, SAGE, SCGB3A2, SCP1, SCP2, SCP3, SSX, SURVrVin, TPI/m, TPTE, CDK4 cyclin-dependent kinase 4), p1S1″1′4′3, p53, AFP, β-catenin, caspase 8, mutated version of p21Ras, Bcr-abl chimera, MUM-I MUM-2, MUM-3, ELF2M, HSP70-2M, HST-2, KIAA0205, RAGE, myosin/m, 707-AP, CDC27/m, ETV6/AML, TEL/Amll, Dekcain, LDLR/FUT, Pml-RARαTEL/AMLI, NY-ESO-I, members of the MAGE family (Melanoma-associated antigen) MAGE-Al, MAGE-A2, MAGE-A3, MAGE-A4, MAGE-A5, MAGE-A6, MAGE-A7, MAGE-A8, MAGE-A9, MAGE-A10, MAGE-A11, MAGE-A12, MAGE-B, MAGE-C, BAGE, DAM-6, DAM-10, members of the GAGE family (G antigen) GAGE-1, GAGE-2, GAGE-3, GAGE-4, GAGE-5, GAGE-6, GAGE-7B, GAGE-8, NA-88A, CAG-3, RCC-associated antigen G250, oncoproteins E6 and E7 derived from HPV (human papilloma virus), Epstein Barr virus antigens EBNA2-6, LMP-I, LMP-2, gp77, gp100, MART-1/Melan-A, tyrosinase, TRP-I and TRP-2 (tyrosinase-related protein), TRP-2-INT2, PSA, PSM, MC1R, ART4, CAMEL, CEA, CypB, HER2/neu, hTERT, hTRT, iCE, Mucl, Muc2, PRAME RU1, RU2, SART-I, SART-2, SART-3, WT and WT1.
According to an embodiment, the tumour antigen is chosen from the list comprising oncoproteins E6 and E7 derived from HPV (human papilloma virus), MART-1/Melan-A. According to another embodiment, the tumour antigen is the oncoprotein E7 derived from HPV (human papilloma virus).
In an embodiment, the molecule of interest is a polypeptide. In an embodiment, the polypeptide is of bacterial origin, of fungal origin or of viral origin.
In an embodiment, the molecule of interest is a polypeptide of bacterial origin corresponding to a protein, or to a fragment of this protein, chosen from the non-exhaustive list comprising XcpQ and PopB of Pseudomonas aeruginosa; factor H binding protein (fHBP), Neisseria Heparin Binding Antigen (NHBA) of Neisseria meningitidis group B; Neisseria adhesin A (NadA) of Neisseria meningitidis group B, diphtheria toxoid of Corynebacterium diphtheriæ; tetanus toxoid of Clostridium tetani; pertussis toxoid (whooping cough toxoid), filamentous hemagglutinin, pertactin of Bordatella pertussis; recombinant cholera toxin B subunit (rCTB) of Vibrio choleræ.
In an embodiment, the molecule of interest is a polypeptide of viral origin corresponding to a protein, or a fragment of this protein, chosen from the non-exhaustive list comprising the proteins GAG (p24, p17, p9 and p7), Pol (p64, p51, p10 and p32) and Env (gp41 and gp120) of the human immunodeficiency virus (HIV); pre-membrane precursor protein (preM) and M (for membrane) protein of the Zika virus; EDIII domain of the E protein of the dengue virus; fusion glycoproteins (or RSV-F for respiratory syncytial virus F protein) of human respiratory syncytial virus; haemagglutinin of the influenza type A virus H5N1 subtype; nuclear protein NP of the influenza virus; surface antigen of the hepatitis B virus; S and pre-S2 proteins of the hepatitis B virus; L1 protein of type 6 human papillomavirus (HPV); L1 protein of type 11 human papillomavirus (HPV); L1 protein of type 16 human papillomavirus (HPV); L1 protein of type 18 human papillomavirus (HPV); L1 protein of type 31 human papillomavirus (HPV); L1 protein of type 33 human papillomavirus (HPV); L1 protein of type 45 human papillomavirus (HPV); L1 protein of type 52 human papillomavirus (HPV); L1 protein of type 58 human papillomavirus (HPV).
In an embodiment, the liposome of the invention forms a lipoplex comprising at least one compound of the invention. In other terms, in an embodiment, the liposome of the invention comprises at least one nucleic acid.
The preparation of the lipoplex of the invention can be carried out by different methods well known to those skilled in the art. For example, the lipoplex of the invention can be obtained by adding a solution of nucleic acid to a preparation of liposomes according to the invention.
According to an embodiment, the lipoplex of the invention is obtained by mixing a solution comprising a nucleic acid, preferably an mRNA, encoding a tumour antigen to a preparation of liposomes according to the invention.
According to an embodiment, the lipoplex of the invention is obtained by mixing a solution comprising a nucleic acid, preferably an mRNA, encoding a tumour antigen to a preparation of liposomes comprising 5% of the compound according to the invention, 47.5% of lipid KLN25, and 47.5% of lipid MM27, in mole percent with respect to the total number of moles of lipids.
In an embodiment, the liposome of the invention forms a lipopolyplex comprising at least one compound of the invention. In other terms, in an embodiment, the liposome of the invention comprises at least one nucleic acid complexed to a polycation.
The preparation of the lipopolyplex of the invention can be carried out by different methods well known to those skilled in the art. For example, the lipopolyplex of the invention can be obtained by mixing a complexed nucleic acid (cationic polymer) with a preparation of liposomes according to the invention.
According to an embodiment, the lipopolyplex of the invention is obtained by mixing:
According to an embodiment, the lipopolyplex of the invention is obtained by mixing:
According to an embodiment, the liposomes, lipoplexes or lipopolyplexes of the invention are dispersed in an aqueous solution. In a particular embodiment, the liposomes, lipoplexes or lipopolyplexes of the invention are dispersed in physiological serum or in PBS.
According to an embodiment, the invention also relates to an aqueous solution or a dispersion comprising the liposomes, lipoplexes or lipopolyplexes of the invention.
According to another embodiment, the present invention also relates to an emulsion comprising the liposomes, lipoplexes or lipopolyplexes of the invention.
In an embodiment, the emulsion comprising the liposomes, lipoplexes or lipopolyplexes of the invention is an oil-in-water emulsion, a water-in-oil emulsion or a water-in-oil-in-water emulsion.
According to an embodiment, the present invention also relates to a pharmaceutical composition comprising the liposomes, lipoplexes or lipopolyplexes of the invention and at least one pharmaceutically acceptable excipient. Examples of pharmaceutically acceptable excipients include, but are not limited to, water, saline water, dextrose, glycerol, and others, or combinations of these excipients. According to an embodiment, the pharmaceutical composition may also comprise humidifiers, emulsifiers, buffers, adjuvants, and others.
In an embodiment, the pharmaceutical composition further comprises at least one immune checkpoint inhibitor (ICI). Many tumours manage to express molecules that inhibit the immune response and thus to escape the control of the immune system. Immune checkpoint inhibitors are molecules that act against such inhibitor mechanisms developed by the tumour cells. Examples of immune checkpoint inhibitor include, without being limited to, CTLA-4 inhibitors (for example ipilumab), PD-1 inhibitors (for example pembrolizumab and nivolumab) and PD-L1 inhibitors (for example atezolizumab, avelumab and durvalumab).
According to an embodiment, the pharmaceutical composition of the invention can be administered to the subject by any suitable method of administration. Thus, according to an embodiment, the pharmaceutical composition of the invention can be formulated for oral administration, topical administration or an injection. According to an embodiment, the pharmaceutical composition of the invention can also be formulated for systemic, intravenous, intraperitoneal, intramuscular, intranodal, intracoronary, intra-arterially, subcutaneous, intradermal, transdermal, intratumoral, intraocular, pulmonary, by inhalation, direct injection into a tissue, or par electroporation or sonoporation administration. In a preferred embodiment, the pharmaceutical composition of the invention is formulated to be administered by injection, preferably by intradermal or intravenous injection, more preferably by intradermal injection.
In an embodiment, the pharmaceutical composition according to the invention is formulated for oral administration. Examples of forms suitable for oral administration include, but are not limited to, tablets (including extended-release tablet), capsules, powders, granules, pills (including sugar-coated pills), gelcaps (including flexible gelatin capsules), oral suspensions, drinkable solutions, and other similar forms.
In another embodiment, the pharmaceutical composition of the present invention is formulated to be injected. Examples of forms suitable for administration by injections include, but are not limited to, sterile aqueous solution, dispersions, emulsions, suspensions, solid forms suitable for the preparation of solutions or suspensions by adding a liquid before use such as, for example, powders.
In another embodiment, the pharmaceutical composition of the present invention is formulated for a topical application. Examples of forms suitable for administration by injections include, but are not limited to milks, creams, balms, oils, lotions, gels, salves, sprays or drops, such as eye drops.
According to an embodiment, the invention also relates to a vaccine adjuvant comprising the liposomes, lipoplexes or lipopolyplexes of the invention and at least one pharmaceutically acceptable excipient.
According to an embodiment, the invention also relates to a vaccine comprising the liposomes, lipoplexes or lipopolyplexes of the invention themselves comprising at least one immunogenic molecule, and at least one pharmaceutically acceptable excipient. In an embodiment, the vaccine of the invention can furthermore comprise at least one additional adjuvant. In another embodiment, the vaccine further comprises at least one immune checkpoint inhibitor.
In an embodiment, the vaccine of the invention can be formulated under different forms, including for example a solution, a dispersion or an emulsion.
In the embodiment according to which the vaccine of the invention is formulated under the form of an emulsion, the vaccine preferentially comprises one or several surfactant(s).
According to an embodiment and in order to improve the preservation thereof, the vaccine of the invention may be lyophilised. The vaccine of the invention can thus have a lyophilised form. In this embodiment, the vaccine comprises one or several agents assisting in lyophilisation. Agents assisting in lyophilisation are well known to those skilled in the art. These agents assisting in lyophilisation include in particular sugars such as lactose and mannitol.
In an embodiment, the vaccine of the invention can comprise one or several stabilising agents, for example in order to prolong the duration of the preservation of the vaccine or in order to improve the effectiveness of the lyophilisation. Examples of stabilising agents include, without being limited to, SPGA (Sucrose-Phosphate-Glutamate-Albumin), sugars such as sorbitol, mannitol, trehalose, starch, sucrose, dextran or glucose, proteins such as albumin or casein or the degradation products thereof, mixtures of amino acids such as lysine or glycine, and buffers such as alkali metal phosphates.
In an embodiment, the vaccine of the invention is administered to the subject by one of the conventional methods of vaccination including an injection, for example intradermal, intramuscular, intraperitoneal, or subcutaneous; a topical administration, for example a transdermal application or an application by intranasal spray; or an oral administration. The vaccine of the invention can be administered in a single dose or in several doses.
In the embodiment according to which the vaccine is injected, the formulation to be injected may have the form of a solution or sterile dispersion, or of a sterile lyophilised powder allowing for the extemporaneous preparation of a solution or sterile dispersion that can be injected. In order to prevent any contamination by microorganisms, one or several preservatives can be added to the vaccine such as for example antibacterial and antifungal agents such as parabens, chlorobutanol, phenol, sorbic acid, thiomersal and other similar agents. It may also be preferable to add to the vaccine one or several isotonic agents such as sugars or sodium chloride in order to reduce the pain caused by the injection. In order to prolong the absorption of an injected vaccine of the invention, one or several absorption-retarding agents can be added to the vaccine such as for example aluminium monostearate or gelatin.
It is understood that the total daily use of the liposome, lipoplex, lipopolyplex, pharmaceutical composition or vaccine of the invention will be adjusted by the attending physician in the framework of his medical opinion. The therapeutically effective dose specific to each patient will depend on a variety of factors including the disorder treated and the severity thereof; the activity of the compound used; the specific composition used; the age, weight, general health, gender and diet of the patient, the duration and the mode of administration; the duration of the treatment; the drugs used in combination or concomitantly with the compound used, and other similar factors known in the medical field.
According to an embodiment, the liposome, lipoplex, lipopolyplex, the pharmaceutical composition or the vaccine of the invention is administered once, twice, 3 times, 4 times, 5 times, 6 times, 7 times, 8 times, 9 times, or 10 times to the subject.
In an embodiment, the liposome, lipoplex, lipopolyplex, the pharmaceutical composition or the vaccine of the invention is administered to the subject at least once a day. Preferably, the liposome, lipoplex, lipopolyplex, the pharmaceutical composition or the vaccine of the invention is administered once a day. In another embodiment, the liposome, lipoplex, lipopolyplex, the pharmaceutical composition or the vaccine of the invention is administered to the subject at least once a week. For example, the liposome, lipoplex, lipopolyplex, the pharmaceutical composition or the vaccine of the invention can be administered once a week, twice, three times, four times or up to seven times per week.
In an embodiment, the liposome, lipoplex, lipopolyplex, the pharmaceutical composition or the vaccine of the invention is administered to the subject before the symptoms appear, i.e. the liposome, lipoplex, lipopolyplex, the pharmaceutical composition or the vaccine of the invention is administered prophylactically.
In an embodiment, the liposome, lipoplex, lipopolyplex, the pharmaceutical composition or the vaccine of the invention is administered to the subject after the symptoms have appeared, i.e. the liposome, lipoplex, lipopolyplex, the pharmaceutical composition or the vaccine of the invention is administered therapeutically.
In an embodiment, the liposome, lipoplex, lipopolyplex, the pharmaceutical composition or the vaccine of the invention is administered according to an optimal administration protocol. According to the invention, an optimal administration protocol comprises suitable dosage parameters and modes of administration that lead to the stimulation or to the triggering of an immune response in the subject.
The effective dosage parameters can be determined by conventional methods for a disease in particular. Examples of such methods include, but are not limited to survival rates, side effects, the progression or regression of the disease.
In particular, the effectiveness of the dose of liposomes, lipoplexes, lipopolyplexes, pharmaceutical composition or vaccine according to the invention for treating cancer can be determined by evaluating the response rate, which corresponds to the proportion of patients for whom the tumour regresses or does not grow under treatment.
The present invention also relates to a liposome, lipoplex or lipopolyplex according to the invention for its use for vectorisation, i.e. the transmembrane transfer of a molecule of interest. The present invention therefore also relates to the use of the liposome, lipoplex or lipopolyplex according to the invention for the vectorisation, i.e. the membrane transfer of a molecule of interest.
According to an embodiment the present invention relates to a liposome, lipoplex or lipopolyplex according to the invention for its use for the transfection of cells, preferably for the in vivo transfection of cells. According to another embodiment the present invention relates to the use of a liposome, lipoplex or lipopolyplex according to the invention for the in vitro or ex vivo transfection of cells.
The present invention therefore relates to a method of in vitro or ex vivo transfection of cells, comprising the use of a lipoplex or lipopolyplex according to the invention.
According to an embodiment, the present invention relates to a liposome, lipoplex or lipopolyplex according to the invention for its use for the delivery of prodrugs, sensitisers or visualising agent.
According to an embodiment, the present invention relates to a liposome, lipoplex or lipopolyplex according to the invention for its use for gene therapy, topical treatments (dermatology, ophthalmology) or bactericidal activities.
The invention further relates to a cosmetic composition comprising a liposome, lipoplex or lipopolyplex according to the invention. Another object of the invention is also the cosmetic use of a liposome, lipoplex or lipopolyplex according to the invention.
The invention also relates to a liposome, lipoplex or lipopolyplex according to the invention for its use for targeted vectorisation. The present invention therefore also relates to the use of the liposome, lipoplex or lipopolyplex according to the invention for targeted vectorisation. According to an embodiment, the compound of the invention contained in the liposome, lipoplex or lipopolyplex of the invention is recognised and bound by a particular type of cells.
In an embodiment, the compound of the invention contained in the liposome, lipoplex or lipopolyplex of the invention is recognised and bound by the cells expressing a lectin on their surface. In another embodiment, the compound of the invention contained in the liposome, lipoplex or lipopolyplex of the invention is recognised and bound by the cells expressing a type C lectin on their surface. In another embodiment, the compound of the invention contained in the liposome, lipoplex or lipopolyplex of the invention is recognised and bound by the cells expressing on their surface the lectins DC-SIGN (CD209), DEC205/CD205, langerin (CD207), CLEC9A, CLEC4D, CD40, and/or the mannose receptor (MR).
In an embodiment, the compound of the invention contained in the liposome, lipoplex or lipopolyplex of the invention is recognised and bound by antigen-presenting cells. In another embodiment, the compound of the invention contained in the liposome, lipoplex or lipopolyplex of the invention is recognised and bound by macrophages, dendritic cells and/or Langerhans cells. In a preferred embodiment, the compound of the invention contained in the liposome, lipoplex or lipopolyplex of the invention is recognised and bound by dendritic cells.
According to an embodiment the present invention relates to a liposome, lipoplex or lipopolyplex according to the invention for its use for the transfection of antigen-presenting cells, preferably for the transfection of macrophage, dendritic cells and/or Langerhans cells, more preferably for the transfection of dendritic cells.
The invention also relates to a compound of the invention, a liposome, lipoplex or lipopolyplex according to the invention for its use as an adjuvant.
In an embodiment, the compound of the invention, the liposome, lipoplex or lipopolyplex of the invention has an in vitro adjuvant effect. In an embodiment, the compound of the invention, the liposome, lipoplex or lipopolyplex of the invention has an in vivo adjuvant effect.
The invention also relates to a compound of the invention, a liposome, lipoplex or lipopolyplex according to the invention for its use as a vaccine adjuvant.
In an embodiment, the liposome, lipoplex or lipopolyplex of the invention administered to a subject induces an immune response in the subject. In an embodiment, the liposome, lipoplex or lipopolyplex of the invention administered to a subject induces an immune response in the subject that does not depend on the presence in the liposome, lipoplex or lipopolyplex of the invention of an immunogenic molecule of interest.
The invention also relates to a liposome, lipoplex or lipopolyplex according to the invention for its use for vaccination. The invention also relates to a liposome, lipoplex or lipopolyplex according to the invention comprising at least one molecule of interest capable of inducing an immune response for its use for vaccination. The invention also relates to a liposome, lipoplex or lipopolyplex according to the invention comprising at least one molecule of interest capable of inducing an immune response for its use as a vaccine.
In an embodiment, the liposome, lipoplex or lipopolyplex of the invention is used for a preventive vaccination. In another embodiment, the liposome, lipoplex or lipopolyplex of the invention is used for a therapeutic vaccination.
In an embodiment, the liposome, lipoplex or lipopolyplex of the invention is used as a cancer vaccine. In a preferred embodiment, the liposome, lipoplex or lipopolyplex of the invention is used for a therapeutic vaccination in the treatment of cancer.
In an embodiment, the term “cancer” or “tumour” includes all of the proliferative diseases. In an embodiment, proliferative diseases include neoplasms, dysplasia, premalignant or precancerous lesions, abnormal growths of cells, malignant tumours, and cancers or metastases. In an embodiment, the cancer is selected from the group comprising leukaemia, non-small cell lung cancer, small cell lung cancer, central nervous system cancer (CNS), melanoma, ovarian cancer, kidney cancer, prostate cancer, breast cancer, glioma, colon cancer, bladder cancer, sarcoma, pancreatic cancer, colorectal cancer, head and neck cancer, liver cancer, bone cancer, spinal cord cancer, stomach cancer, intestinal cancer, cancer of the oesophagus, thyroid cancer, hematologic cancer, and lymphoma.
In an embodiment, the cancer is a breast cancer, melanoma or hepatocellular carcinoma. In an embodiment, the breast cancer is a triple negative breast cancer, i.e. a cancer of the breast characterised by the absence of expression of the receptors to oestrogens, receptors to progesterone and HER2 (human epidermal growth factor receptor 2) by the cancer cells.
In an embodiment, the liposome, lipoplex or lipopolyplex of the invention used as a cancer vaccine comprises at least one tumour antigen or at least one nucleic acid encoding a tumour antigen. In an embodiment, the liposome, lipoplex or lipopolyplex of the invention used for a therapeutic cancer vaccination comprises at least one tumour antigen or at least one nucleic acid encoding a tumour antigen.
In an embodiment, the liposome, lipoplex or lipopolyplex of the invention used for a therapeutic cancer vaccination comprises at least one tumour antigen or at least one nucleic acid encoding a tumour antigen chosen from the non-exhaustive list comprising: CDK4 (cyclin-dependent kinase 4), p1S1″1′4′3, AFP, β-catenin, caspase 8, p53, mutated version of p21Ras, Bcr-abl chimera, MUM-I MUM-2, MUM-3, ELF2M, HSP70-2M, HST-2, KIAA0205, RAGE, myosin/m, 707-AP, CDC27/m, ETV6/AML, TEL/Amll, Dekcain, LDLR/FUT, Pml-RARαTEL/AMLI, NY-ESO-I, members of the MAGE family (Melanoma-associated antigen) MAGE-Al, MAGE-A2, MAGE-A3, MAGE-A4, MAGE-A6, MAGE-10, MAGE-12, BAGE, DAM-6, DAM-10, members of the GAGE family (G antigen) GAGE-1, GAGE-2, GAGE-3, GAGE-4, GAGE-5, GAGE-6, GAGE-7B, GAGE-8, NA-88A, CAG-3, RCC-associated antigen G250, oncoproteins E6 and E7 derived from HPV (human papilloma virus), Epstein Barr virus antigens EBNA2-6, LMP-I, LMP-2, gp77, gp100, MART-1/Melan-A, tyrosinase, TRP-I and TRP-2 (tyrosinase-related protein), PSA, PSM, MC1R, ART4, CAMEL, CEA, CypB, HER2/neu, hTERT, hTRT, iCE, Muc1, Muc2, PRAME, RU1, RU2, SART-1, SART-2, SART-3, and WT1. In an embodiment, the liposome, lipoplex or lipopolyplex of the invention used for therapeutic cancer vaccination comprises at least one tumour antigen or at least one nucleic acid encoding a tumour antigen chosen from the non-exhaustive list comprising: CAP-1, CD 4/m, cell surface proteins of the claudin family CLAUDIN-6, CLAUDIN-18.2 and CLAUDIN-12, c-myc, CT, GnT-V, HAGE, HAST-2, LAGE, NF1, NY-BR-1, proteinase 3, SAGE, SCGB3A2, SCP1, SCP2, SCP3, SSX, SURVrVin, TPI/m, TPTE, CDK4 (cyclin-dependent kinase 4), plS1″1′4′3, AFP, β-catenin, caspase 8, p53, mutated version of p21Ras, Bcr-abl chimera, MUM-I MUM-2, MUM-3, ELF2M, HSP70-2M, HST-2, KIAA0205, RAGE, myosin/m, 707-AP, CDC27/m, ETV6/AML, TEL/Amll, Dekcain, LDLR/FUT, Pml-RARαTEL/AMLI, NY-ESO-I, members of the MAGE family (Melanoma-associated antigen) MAGE-Al, MAGE-A2, MAGE-A3, MAGE-A4, MAGE-A5, MAGE-A6, MAGE-A7, MAGE-A8, MAGE-A9, MAGE-A1O, MAGE-A11, MAGE-A12, MAGE-B, MAGE-C, BAGE, DAM-6, DAM-10, members of the GAGE family (G antigen) GAGE-1, GAGE-2, GAGE-3, GAGE-4, GAGE-5, GAGE-6, GAGE-7B, GAGE-8, NA-88A, CAG-3, RCC-associated antigen G250, oncoproteins E6 and E7 derived from HPV (human papilloma virus), Epstein Barr virus antigens EBNA2-6, LMP-I, LMP-2, gp77, gp100, MART-1/Melan-A, tyrosinase, TRP-I and TRP-2 (tyrosinase-related protein), TRP-2-INT2, PSA, PSM, MC1R, ART4, CAMEL, CEA, CypB, HER2/neu, hTERT, hTRT, iCE, Muc1, Muc2, PRAME, RU1, RU2, SART-1, SART-2, SART-3, WT and WT1.
According to an embodiment, the liposome, lipoplex or lipopolyplex of the invention used for a therapeutic cancer vaccination comprises at least one tumour antigen or at least one nucleic acid encoding a tumour antigen chosen from the list comprising oncoproteins E6 and E7 derived from HPV (human papilloma virus), MART-1/Melan-A. According to another embodiment, the liposome, lipoplex or lipopolyplex of the invention used for a therapeutic cancer vaccination comprises at least oncoprotein E7 derived from HPV (human papilloma virus) or at least one nucleic acid encoding oncoprotein E7 or a peptide of oncoprotein E7.
In an embodiment, the subject is suceptible to or suspected of suffering from a disease, preferably an infectious disease or a cancer.
Examples of risks of developing cancer include, but are not limited to, a family history or genetic predisposition, age, consumption of alcohol, tobacco, exposure to toxic and/or carcinogenic substances, exposure to radiation, exposure to the sun, chronic inflammation, diet, and others.
Examples of risks of developing infectious diseases include, but are not limited to, exposure to bacteria, viruses, mushrooms, parasites, and others.
In an embodiment, the term “infectious diseases” includes all diseases caused by an infectious agent, such as a bacterium, a virus, a mushroom or other and diseases caused by a parasite.
In an embodiment, the infectious disease is selected from the flu, tuberculosis, pneumonias of bacterial origin, pneumonias of viral origin, Lyme disease, human immunodeficiency virus (HIV) infections, and acquired immunodeficiency syndrome (AIDS).
Examples of diseases caused by a virus include, but are not limited to human immunodeficiency virus (HIV) infections, acquired immunodeficiency syndrome (AIDS), adenovirus infections, alpha-virus infections, arbovirus infections, pneumonias of viral origin, Bell’s paralysis, Borna disease, infections with a virus of the Bunyaviridae family, infections with a virus of the Caliciviridae family, chicken pox, cold, condyloma accuminata, infections with a coronavirus, infections with coxsackievirus, infections with a cytomegalovirus, Chikungunya, dengue, infections wtih a DNA virus, infections with an RNA virus, contagious ecthyma, encephalitis, encephalitis caused by an arbovirus, encephalitis caused by herpes simplex virus, infections caused by the Epstein-Barr virus, infectious erythema, exanthema subitum (or roseola infantum), chronic fatigue syndrome, infections with a hantavirus, viral haemorrhagic fever, Ebola virus disease, Marburg virus disease, (viral hepatitis or infections with hepatitis A (HAV) virus, with hepatitis B (HBV) virus, with hepatitis C (HCV) virus or with hepatitis D (HDV) virus, herpes labialis, herpes simplex, herpes zoster (zona), infectious mononucleosis, flu, Lassa fever, measles, viral meningitis, molluscum contagiosum, smallpox, mumps, myelitis, infections with a papillomavirus, infections with a human papillomavirus (HPV), infections with a virus of the Paramyxoviridae family, sandfly fever, poliomyelitis, infections with a polyomavirus, postpoliomyelitis syndrome, rabies, respiratory infections due to respiratory syncytial virus (RSV), rubella, severe acute respiratory syndrome (SARS), subacute sclerosing panencephalitis, tick-borne diseases, warts, West Nile fever, viral diseases, infections caused by a virus of the genus Flavivirus, yellow fever, zika, zoonotic diseases, and others.
In an embodiment, the infectious disease is a disease caused by a virus and selected from acquired immunodeficiency syndrome (AIDS) or infection with human immunodeficiency virus (HIV), viral hepatitis or infections with hepatitis A (HAV) virus, with hepatitis B (HBV) virus, with hepatitis C (HCV) virus or with hepatitis D (HDV) virus, and infections with a human papillomavirus (HPV).
Examples of diseases caused by a bacterium or a mushroom include, but are not limited to abscess, actinomycosis, anaplasmosis, anthrax, reactive arthritis,aspergillosis, bacteraemia, bacterial infections and mycoses, infections with the Bartonella bacterium, botulism, brain abscess, brucellosis (or Malta fever), infections with a bacterium of the Burkholderia family, infections with a bacterium of the genus Campylobacter, candidiasis such as the candidiasis caused by Candida albicans, vulvovaginal candidiasis, cat-scratch disease (or benign inoculation lymphoreticulosis, or benign lymphogranuloma), cellulitis, infections of the central nervous system, canker, chlamydia infections, cholera, Clostridium infections, coccidioidomycoses such as coccidioidomycosis caused by Coccidioides immitis, corneal ulcer, cross-infections, blastomycosis, cryptococcosis, dermatomycoses, diphtheria, ehrlichiosis, pleural empyem, bacterial endocarditis, endophthalmitis, staphylococcal enterocolitis, erysipelas, infections caused by Escherichia coli, necrotizing fasciitis, Fournier gangrene, gas gangrene, furunculosis, infections with a bacterium of the genus Fusobacterium, gonorrhoea, infections wtih a gram-negative bacterium, infections with a gram-positive bacterium, granuloma inguinal, hidradenitis suppurativa, histoplasmosis, hordeolum (or stye), impetigo, infections with a bacterium of the genus Klebsiella, legionellosis (Legionnaires’ disease), leprosy, leptospirosis, Listeria infections, Ludwig’s angina, lung abscess, Lyme disease, lymphogranuloma venereum, eumycetoma, melioidosis, bacterial meningitis, Mycobacterium infections, infections by mycoplasma, mycoses, infections by Nocardia, onychomycosis, osteomyelitis, paronychia, pelvic inflammatory disease, plague, pneumonias of bacterial origin, pneumococcal infections, Pseudomona infections, psittacosi, puerperal infection, rat-bite fever, relapsing fever, respiratory tract infections, retropharyngeal abscess, rheumatic fever, rhinoscleroma, rickettsial infections, Rocky Mountain Spotted fever, Q fever, salmonella, scarlet fever, typhus, epidemic typhus, septicaemia, bacterial sexually transmitted infections, septic shock, bacterial skin diseases, infectious skin diseases, staphylococcal infections, streptococcal infections, syphilis, tetanus, tick-borne diseases, ringworm, trachoma, tuberculosis, tularaemia, typhoid fever, urinary tract infections, gastric ulcer linked to an infection by Helicobacter pylori, Whipple’s disease, whooping cough, infections caused by Vibrio, yaws, infections by Yersinia, zoonotic disease, mucormycosis or zygomycosis, and others.
Examples of diseases caused by a parasite include, but are not limited to malaria, sleeping sickness, leishmaniasi, toxoplasmosis, and others.
In another embodiment, the subject suffers from a disease, preferably an infectious disease or a cancer.
In an embodiment, the subject is an animal, preferably a mammal, more preferably a human. In an embodiment, the subject is a man. In another embodiment, the subject is a woman. In an embodiment, the subject is a child.
An object of the present invention is also a method for vectoring, i.e. transferring a molecule of interest through a membrane, comprising the use of a liposome, lipoplex or lipopolyplex according to the invention.
The present invention also relates to a method for inducing an immune response in a subject comprising the administration of the liposome, lipoplex or lipopolyplex according to the invention.
The present invention also relates to a method for vaccinating a subject comprising the administration of the liposome, lipoplex or lipopolyplex according to the invention, preferably a liposome, lipoplex or lipopolyplex comprising at least one molecule of interest capable of inducing an immune response.
According to an embodiment, the vaccination is preventive. According to another embodiment, the vaccination is therapeutic.
In an embodiment, the method for vaccinating a subject according to the invention is a method for vaccination against cancer, preferably a method of therapeutic vaccination against cancer.
Another object of the present invention relates to a method for preventing cancer in a subject comprising the administration of the liposome, lipoplex or lipopolyplex according to the invention, preferably a liposome, lipoplex or lipopolyplex comprising at least one tumour antigen or a nucleic acid encoding a tumour antigen.
The present invention invention also relates to a method for treating cancer in a subject comprising the administration of the liposome, lipoplex or lipopolyplex according to the invention, preferably a liposome, lipoplex or lipopolyplex comprising at least one tumour antigen or a nucleic acid encoding a tumour antigen.
This invention shall be understood better when reading the following examples that non-limitingly illustrate the invention.
Fourier-transform spectrometers BRUKER ARX 400 and BRUKER Avance 400 (400.13 MHz for the proton, 100.61 MHz for the carbon, ENSCR).
The chemical shifts are expressed in parts per million (ppm) with respect to the chemical shift of the deuterated solvent used as a reference. The multiplicity of signals is shown by using the following abbreviations: s, singlet; d, doublet; t, triplet; q, quadruplet; m, multiplet or massive that cannot be analysed. The coupling constants (J) are expressed in Hertz (Hz). The spectrometric data 13C is determined using fully decoupled spectra and heteronuclear 2D correlated spectra.
High resolution mass spectrometry MS/MS ZabSpec TOF Micromass (Centre Regional de Mesures Physiques de l′Ouest, Université de Rennes 1).
The ionisation mode used is positive electrospray (ESI+-MS). The ion acceleration voltage is 4 kV and the temperature of the source is equal to 60° C. (mode of introduction by infusion). The compounds are dissolved beforehand in methanol or in dimethylsulfoxide.
To a suspension of sodium hydride NaH (2.6 g, 90 mmol) in anhydrous DMF (100 mL), is added drop-by-drop the commercial pentaerythritol allyl ether (7.70 g; 300 mmol) purified beforehand by chromatography column on silica gel (eluent cyclohexane/ethyl acetate: 9/1, v/v). The medium is stirred 2 hours at 0° C. then benzyl bromide (7.7 g, 450 mmol) is added drop-by-drop at this temperature. The medium is left under stirring at ambient temperature for 17 hours then MeOH (6 mL) is added drop-by-drop at 0° C. The solvents are evaporated in the vacuum rotary evaporator then the vane pump. The yellowish residue is taken up in dichloromethane then is washed with water and by an aqueous solution saturated with NaCl. The organic phase is dried on MgSO4 and vacuum concentrated. The crude product is purified by chromatography on a column of silica gel (eluent: EP/AcOEt): 9/1, v/v) in order to provide the benzyl derivative (10.45 g) in the form of a colourless oil with a quantitative yield.
NMR 1H (CDCl3, 400 MHz) δ (ppm):
3.50 (6H, s, H3), 3.56 (2H, s, H2), 3.95 (6H, dt, J = 5.3, 1.5 Hz, H4), 4.65 (2H, s, H1), 5.12 (3H, dq, J = 10.4, 1.7 Hz, H6a), 5.24 (3H, dq, J = 17.2, 1.7 Hz, H6b), 5.87 (3H, m, H5), 7.24-7.35 (7H, m, Har).
The triallyl compound (10 g, 28.8 mmol) is dissolved in 50 mL of anhydrous dioxane. The 9-BBN (0.5 M in THF) (519 mL, 0.259 mol) is added to the reaction medium cooled beforehand to 0° C. and the mixture is stirred for 24 hours at ambient temperature. The sodium hydroxide 3 M (577 mL, 75 eq.) and the hydrogen peroxide 10 M (115 mL 1.15 mol) are added at 0° C. to the reaction medium and the mixture is stirred 12 hours at ambient temperature. The mixture is extracted 3 times with AcOEt then the organic phase is dried on MgSO4, filtered, concentrated under reduced pressure and purified by chromatography on silica gel (eluent AcOEt/EP/MeOH: 10/5/1) in order to give 9.57 g of triol in the form of a colourless oil with a yield of 83%.
NMR 1H (CDCl3, 400 MHz) δ (ppm):
1.75 (6H, p, J = 5.5, 5.3 Hz, H5), 3.28 (3H, s.large, OH), 3.42 (6H, s, H3), 3.44 (2H, s, H2), 3.56 (6H, t, J = 5.5 Hz, H4), 3.70 (6H, t, J = 5.3 Hz, H6), 4.62 (2H, s, H1), 7.24-7.35 (7H, m, Har).
The triol (7.8 g, 19.4 mmol) is dissolved in 100 mL of anhydrous DMF and is added drop-by-drop to the reaction medium containing potassium hydride (3.9 g, 97 mmol) in the DMF cooled beforehand to 0° C. The mixture is stirred 10 minutes at 0° C. before introducing drop-by-drop the allyl bromide (8.35 mL, 97 mmol). The stirring is prolonged 24 hours at ambient temperature and the excess potassium hydride is hydrolysed with 100 mL of distilled water. The reaction medium is extracted 3 times with diethyl ether then the organic phase is washed with a saturated aqueous solution of NaCl, dried on MgSO4, filtered, concentrated under reduced pressure and purified by chromatography on silica gel (eluent EP/AcOEt: 85/15) in order to give 8.63 g of the triallyl product in the form of a colourless oil with a yield of 78%.
NMR 1H (CDCl3, 400 MHz) δ (ppm):
1.81 (6H, q, J = 6.4 Hz, H5), 3.40 (6H, s, H3), 3.44-3.50 (14 H, m, H2, H4, H6), 3.95 (6H, ddd, J = 5.7, 1.5, H7), 4.48 (2H, s, H1), 5.15 (3H, ddd, J = 10.3, 3.3, 1.5 Hz, H9b), 5.26 (3H, ddd, J = 17.3, 3.5, 1.5 Hz, H9a), 5.90 (3H, ddt, J = 10.3, 6.8, 5.7 Hz, H8), 7.24-7.35 (7H, m, Har).
To a solution of the triallyl (7.9 g, 15 mmol) dissolved in 50 mL of anhydrous dioxane is added at 0° C. the 9-BBN (0.5 M in THF) (272 mL, 0.136 mol) and the mixture is stirred for 24 hours at ambient temperature. The sodium hydroxide 3 M (500 mL, 1.5 mol) and the aqueous hydrogen peroxide 35% (60 mL, 0.6 mol) are added at 0° C. to the reaction medium and the mixture is stirred 12 hours at ambient temperature. The mixture is extracted 3 times with AcOEt, dried on MgSO4, filtered, concentrated under reduced pressure and purified by chromatography on silica gel (eluent AcOEt/EP/MeOH: 10/5/1) in order to give 8.51 g of triol in the form of a colourless oil with a yield of 99%.
NMR 1H (CDCl3, 400 MHz) δ (ppm):
1.79 (12 H, p, J = 5.7 Hz, H8, H5), 2.62 (3H, s.large, OH), 3.42 (6H, s, H3), 3.49-3.43 (14 H, m, H2, H4, H6), 3.55 (6H, t, J = 5.7 Hz, H7), 3.73 (6H, t, J = 5.4 Hz, H9), 4.64 (2H, s, H1), 7.24-7.35 (7H, m, Har).
To a solution of trichloroacetimidate (10 g, 13.4 mmol) and of triol (1.03 g, 1.79 mmol) solubilised in 125 mL of anhydrous CH2Cl2 is added the solution at 5% in the CH2Cl2 of TMSOTf (640 µL, 0.179 mmol) and the mixture is stirred 12 hours at ambient temperature. After having added 2 g of sodium bicarbonate to the reaction, the reaction medium is filtered, the precipitate is rinsed several times with CH2Cl2 and the filtrate is vacuum concentrated. The residue is purified by chromatography on silica gel (eluent EP/AcOEt: 6/4) in order to give 3.44 g of tri-mannosylated product in the form of a light yellow powder with a yield of 82%.
NMR 1H (CDCl3, 400 MHz) δ (ppm):
1.77-1.84 (6H, m, J = 6.4 Hz, H5), 1.91-2.00 (6H, m, H8), 3.41-3.57 (26 H, m, H2, H3, H4, H6, H7), 3.57-3.68 (3H, m, H9b), 3.90-3.96 (3H, m, H9a), 4.40-4.50 (3H, m, H5′), 4.46-4.50 (5H, m, H1, H6b′), 5.08 (3H, d, J = 2.0 Hz, H1′), 5.70 (3H, dd, J = 3.2, 1.8 Hz, H2′), 5.91 (3H, dd, J = 10.1, 3.3 Hz, H3′), 6.11 (3H, t, J+10.1 Hz, H4′), 7.24-8.11 (65 H, m, Har).
To a solution of benzyl ether (3.44 g, 1.49 mmol) dissolved in 30 mL of a mixture CH2Cl2/MeOH (4/1) is added at ambient temperature the Pd/C (340 mg, 10% by weight). The reaction medium is stirred under a hydrogen atmosphere one night at ambient temperature. The medium is diluted with CH2Cl2, filtered on celite then vacuum concentrated. The compound is then purified by chromatography on silica gel (eluent Cyclohexane/AcOEt: 6/4) in order to give 2.61 g of alcohol in the form of a white powder with a yield of 79%.
NMR 1H (CDCl3, 400 MHz) δ (ppm):
1.81 (6H, p, J = 6.4 Hz, H5), 1.93 (6H, p, J = 6.4 Hz, H8), 3.04 (1H, t, J = 6.1 Hz, OH), 3.43 (6H, s, H3), 3.47 (6H, t, J = 6.3 Hz, H6), 3.50 (6H, t, J = 6.5 Hz, H4), 3.55 (6H, m, H7), 3.68 (5H, m, H9a, H2), 3.91 (3H, dt, J = 9.7, 6.4 Hz, H9b), 4.39-4.43 (3H, m, H5′), 4.47 (3H, dd, J = 12.0, 4.2 Hz, H6a′), 4.68 (3H, dd, J = 12.0, 2.4 Hz, H6b′), 5.07 (3H, d, J = 1.7 Hz, H1′), 5.69 (3H, dd, J = 3.3, 1.7 Hz, H2′), 5.91 (3H, dd, J = 10.1, 3.3 Hz, H3′), 6.11 (3H, t, J = 10.1 Hz, H4′), 7.23-7.41 (20H, m, Har meta), 7.41-7.58 (20H, m, Har para), 7.82-8.08 (20H, m, Har ortho).
NMR 13C (CDC13, 100 MHz) δ (ppm):
29.69 (C8), 29.95 (C5), 44.81 (C3a), 62.84 (C6′), 65.56 (C9), 66.05 (C2), 66.94 (C4′), 67.37 (C7), 68.11 (C4), 68.67 (C6), 68.78 (C5′), 70.14 (C3′), 70.53 (C2′), 71.46 (C3), 97.61 (C1′), 128.28 (CHar meta), 128.42 (CHar meta), 128.56 (CHar meta), 128.99 (Cqar), 129.09 (Cqar), 129.35 (Cqar), 129.72 (CHar ortho), 129.78 (CHar ortho), 129.83 (CHar ortho), 129.87 (Cqar), 133.03 (CHar para), 133.14 (CHar para), 133.41 (CHar para), 165.39 (COPh), 165.44 (COPh), 165.49 (COPh), 166.13 (COPh).
To a solution of alcohol (614 mg, 0.275 mmol) dissolved in 10 mL of AcOEt, are added 56 µL of an aqueous solution of KBr 0.5 M (0.028 mmol), the TEMPO (15 mg, 0.096 mmol), then at 0° C., 1.2 mL of NaOCl (0.84 mmol). After 3 hours at ambient temperature, the reaction is stopped and acidified with an aqueous solution of HCl at 5% (up to pH = 3), then 560 µL of NaO2Cl (1.68 mmol) are added. The reaction medium is stirred for one night at ambient temperature (yellow colouration) then it is extracted three times with the AcOEt. The organic phase is washed with a saturated solution of NaCl, dried on MgSO4, filtered then vacuum concentrated in order to give 614 mg of carboxylic acid in the form of a white powder with a yield of 99%.
NMR 1H (CDCl3, 400 MHz) δ (ppm):
1.83 (6H, p, J =, H5), 1.96 (6H, p, J = 6.2 Hz, H8), 3.51 (6H, t, J = 6.3 Hz, H6), 3.53 (6H, t, J = 6.1 Hz, H4), 3.56 (6H, m, H7), 3.64 (6H, s, H3), 3.66 (3H, td, J = 9.7, 6.4 Hz, H9b), 3.94 (3H, td, J = 9.7, 6.4 Hz, H9a), 4.47-4.41 (3H, m, H5′), 4.49 (3H. dd. J = 12.0. 4.2 Hz, H6b), 4.71 (3H, dd, J = 12.0, 2.4 Hz. H6a), 5.10 (3H, d, J = 1.7 Hz, H1′), 5.70 (3H, dd, J = 3.3, 1.7 Hz, H2′), 5.92 (3H, dd, J = 10.1, 3.3 Hz, H3′), 6.13 (3H, t, J = 10.0 Hz, H4′), 7.59-7.24 (36 H, m, Har), 8.11-7.82 (24 H, m, Har).
NMR 13C (CDCl3, 100 MHz) δ (ppm):
29.60 (C8), 29.77 (C5), 52.86 (C3a), 60.34 (C2) 62.79 (C6′), 65.46 (C9), 66.85 (C4′), 67.31 (C7), 67.87 (C6), 68.59 (C4), 68.73 (C5′), 69.07 (C3), 70.13 (C3′), 70.49 (C2′), 97.55 (C1′), 128.24 (CHar), 128.38 (CHar), 128.52 (CHar), 128.92 (Cqar), 129.00 (Cqar), 129.27 (Cqar), 129.68 (CHar), 129.73 (CHar), 129.78 (CHar), 133.02 (CHar), 133.12 (CHar), 133.37 (CHar), 133.39 (CHar), 165.39 (COPh), 165.42 (COPh), 165.50 (COPh), 166.15 (COPh), 173.45 (COOH).
To a mixture of the diether lipidcarboxylic acid (291 mg, 0.831 mmol) and TBTU (347 mg, 1.08 mmol) in anhydrous CH2Cl2 (15 mL), is added under an argon atmosphere the DIEA (188 µL, 1.08 mmol). The mixture is stirred at ambient temperature for 20 minutes under a nitrogen atmosphere. A solution of N3-PEG350-NH2 (291 mg, 0.831 mmol) in anhydrous CH2Cl2 (5 mL) is added under a nitrogen atmosphere. The reaction medium is stirred at ambient temperature for 12 hours under a nitrogen atmosphere. An aqueous solution of hydrochloric acid 1N is added and the organic phase (pH = 1) is washed with water. The organic phases are grouped together, dried (MgSO4), filtered and concentrated under reduced pressure. The residue is purified by chromatography on silica gel (eluent CH2Cl2/MeOH: 98/2) in order to isolate the azide coupling product (700 mg, 89%) in the form of a colourless oil.
NMR 1H (CDCl3, 400 MHz) δ (ppm):
0.83-0.87 (m, 18H, 6 CH3), 1.04-1.78 (m, 52H, 24 CH2, 4 CH), 3.37-3.40 (m, 2H, H-f), 3.41-3.50 (m, 4H, H-a, H-4), 3.53-3.57 (m, 4H, H-b, H-5), 3.58-3.69 (m, 23H, PEG, H-e, H-3α), 3.75-3.78 (m, 1H, H-3β), 3.88-3.90 (dd, J = 2.51, 5.92 Hz, 1H, H-2), 7.02-7.05 (m, 1H, NHCO).
NMR 13C (CDCl3, 100 MHz) δ (ppm):
14.10 (CH3), 19.58, 19.65, 19.72 (3 CH3), 22.60, 22.69 (2 CH3), 22.66, 24.36, 24.47, 24.78, 26.03 (5 CH2), 27.94, 29.84, 32.76, 32.78 (4 CH), 29.34, 29.46, 29.52, 29.63, 29.68, 31.89, 37.26, 37.36, 37.39, 37.45, 37.50, 39.32 (19 CH2), 38.67 (C-a), 50.63 (C-f), 69.72 (C-5), 69.83 (C-b), 70.3-70.7 (C-PEG, C-e), 71.47 (C-3), 71.68 (C-4), 80.48 (C-2), 170.57 (C-1).
To a solution of azide (212 mg, 0.224 mmol) in a THF/H2O mixture (25 mL, 1/1) is added the triphenylphosphine (88 mg, 0.337 mmol) by portion. The mixture is stirred at ambient temperature for 18 h. After concentration under reduced pressure, the residue is purified on silica gel chromatography (CH2Cl2/MeOH: 9/1) in order to isolate the amine (164 mg, 80%) in the form of a light yellow oil.
NMR 1H (CDCl3, 400 MHz) δ (ppm):
0.82-0.88 (m, 18H, 6 CH3), 0.99-1.69 (m, 52H, 24 CH2, 4 CH), 3.16-3.18 (m, 2H, H-f), 3.39-3.49 (m, 4H, H-a, H-4), 3.54-3.57 (m, 4H, H-b, H-5), 3.59-3.70 (m, 18H, PEG), 3.72-3.75 (m, 3H, H-c, H-3α), 3.76-3.77 (m, 1H, H-3β), 3.87-3.90 (m, 3H, H-2, H-e), 7.04-7.06 (m, 1H, NHCO).
NMR 13C (CDCl3, 100 MHz) δ (ppm):
14.10 (CH3), 19.58, 19.65, 19.72 (3 CH3), 22.61, 22.71 (2 CH3), 22.66, 24.34, 24.45, 24.76, 26.00 (5 CH2), 27.95, 29.77, 29.85, 32.79 (4 CH), 29.32, 29.45, 29.54, 20.61, 29.66, 31.88, 37.23, 37.34, 37.37, 37.43, 39.31 (19 CH2), 38.70 (C-a), 40.45 (C-f), 66.89 (C-e), 69.72-70.53 (C-PEG, C-5, C-b), 71.45 (C-3), 71.70 (C-4), 80.47 (C-2), 170.63 (C-1).
To a mixture of the carboxylic acid tri-mannosylated ligand (575 mg, 0.257 mmol) and of TBTU (124 mg, 0.386 mmol) in anhydrous CH2Cl2 (70 mL), is added under an argon atmosphere the DIEA (112 µL, 0.643 mmol). The mixture is stirred at ambient temperature for 20 minutes under a nitrogen atmosphere. A solution of the amide lipid (335 mg, 0.365 mmol) in anhydrous CH2Cl2 (50 mL) is added under a nitrogen atmosphere. The reaction medium is stirred at ambient temperature for 12 hours under a nitrogen atmosphere. An aqueous solution of hydrochloric acid 1N is added (pH = 1) and the organic phase is washed with water. The organic phases are grouped together, dried (MgSO4), filtered and concentrated under reduced pressure. The residue is purified by chromatography on silica gel (eluent Cyclohexane/AcOEt: 1:1 + 2% MeOH) in order to isolate the azide coupling product (500 mg, 62%) in the form of a translucent solid.
NMR 1H (CDCl3, 400 MHz) δ (ppm):
0.83-0.89 (m, 21H, CH3), 1-1.59 (m, 68H, alkyl chains), 1.79-1.86 (6H, q, H5), 1.93-1.99 (6H, q, H8), 3.40-3.68 (65H, m, H3, H4, H6, H7, H9b, Hia, Hj, Hl, HPEG), 3.75-3.78 (m, 1H, Ch)3.88-3.95(4H, m, H9a, Hib), 4.40-4.44 (3H, m, H5′), 4.48 (3H, dd, J = 4.1, 12.0 Hz, H6b′), 4.69 (3H, dd, J = 2.1, 12.1 Hz, H6a′), 5.09 (3H, d, J = 1.8 Hz, H1′), 5.69 (3H, dd, J = 1.6, 3.4 Hz, H2′), 5.91 (3H, dd, J = 3.2, 10.3 Hz, H3′), 6.11 (3H, t, J = 10.3 Hz, H4′), 7.24-8.11 (60H, m, Har).
NMR 13C (CDCl3, 100 MHz) δ (ppm):
14.12, 19.62, 19.68, 19.75, 22.63, 22.69 (CH3), 22.72-29.56 (CH2), 29.65 (C8), 29.70 (C5), 29.74, 29.84( C5), 29.91, 31.10, 31.43, 31.63, 31.92, 32.80, 53.03 (C3a), 60.40 (C2), 62.85 (C6′), 65.53 (C9), 66.91 (C4′), 67.36 (C7), 67.92 (C6), 68.61 (C4), 68.78 (C5′), 68.95 (C3), 70.15 (C3′), 70.55 (C2′), 80.53 (Ch), 97.64 (C1′), 128.30 (CHar), 128.44 (CHar), 128.57 (CHar), 129.00 (Cqar), 129.10 (Cqar), 129.35 (Cqar), 129.73 (CHar), 129.79 (CHar), 129.84 (CHar), 129.88 (CHar), 133.05 (CHar), 133.16 (CHar), 133.43 (COPh), 165.4 (COPh), 165.50 (COPh), 166.14 (COPh), 170.69 (CONH).
To a solution of the tri-mannosylated lipid in benzoylated form (435 mg, 0.139 mmol) in a CH2Cl2/MeOH mixture (100 mL, 1/1) is added a solution of MeONa in the methanol (5.3 M, 48.8 µL, 0.258 mmol) freshly prepared. The reaction medium is stirred for one night at ambient temperature. The mixture is neutralised thanks to the adding of Amberlite IR-120 H+ resin and the resin is filtered on cotton. After evaporation of the solvents under reduced pressure, a viscous light grey yellowish product is isolated (255 mg, 97%) corresponding to the target tri-mannosylated lipid. NMR 1H (MeOD+CDCl3, 70/30, 400 MHz) δ (ppm):
0.84-0.89 (m, 21H, CH3), 1.04-1.56 (m, 68H, alkyl chains), 1.79-1.84 (12H, m, H5, H8), 3.31-3.88 (88 H, m, H3, H4, H6, H7, H9, Hi, Hj, Hl, Ch, H3′, H4′, H5′, H6′, HPEG), 4.74 (3H, s, H1′), 7.55 (NH, s).
NMR 13C (MeOD+CDCl3, 70/30, 100 MHz) δ (ppm):
13.66, 19.26, 19.30, 19.33, 19.37, 19.40, 19.44, 22.22, 22.31, 22.50, 24.24, 24.31, 24.65, 25.92, 27.83, 29.21, 29.32, 29.39; 29.48, 29.50, 29.53, 29.64, 29.68, 29.72, 31.27, 31.78, 32.62, 32.64, 32.67, 36.59, 36.65, 36.72, 37.13, 37.23, 37.25, 37.30, 37.36, 37.39, 38.67, 38.95, 39.25, 52.25, 61.45, 64.22, 67.06, 67.52, 67.69, 68.41, 69.43, 69.48, 69.53, 69.61, 70.09, 70.11, 70.23, 70.33, 70.35, 70.37, 70.70, 71.11, 71.15, 71.33, 71.65, 72.56, 80.34, 80.29, 100.08 (C1′), 171.49 (CONH), 173.69 (CONH).
HRMSC194H1182N2O34: [M+Na]+: m/z theoretical = 1906.24662, measured = 1906.2448
The liposomes are prepared according to the method of hydrating a dry lipid film and dialysed against a buffer HEPES 10 mM, pH 7.4 (Pichon C, Midoux P. (2013) Mannosylated and Histidylated LPR Technology for Vaccination with Tumor Antigen mRNA. Methods Mol Biol. 969:247-74).
The compositions of liposomes used are:
The compositions of the fluorescent liposomes used are:
The mRNA was complexed with the partially histidinylated polylysine comprising one molecule of PEG 5 kDa (PEG-HpK) of which the synthesis is described in (Pichon C, Midoux P. (2013) Mannosylated and Histidylated LPR Technology for Vaccination with Tumor Antigen mRNA. Methods Mol Biol. 969:247-74).
The various LPR are prepared according to the method described in (Pichon C, Midoux P. (2013) Mannosylated and Histidylated LPR Technology for Vaccination with Tumor Antigen mRNA. Methods Mol Biol. 969:247-74).
In particular, for an in vitro transfection, the LPR are obtained in the following way. Briefly, 15 µg of PEG-HpK (in 10 µL of buffer 10 mM HEPES pH 7.4) are first added to the mRNA (5 µg in 25 µL of buffer 10 mM HEPES pH 7.4). The whole is vortexed for 4 sec then allowed to stand for 30 min at 20° C. The LPR are then formed by adding 10 µg of liposomes (5 µL to 5.4 mM in 10 mM HEPES buffer, pH 7.4) by stirring the solution via back-and-forth pipetting. The solution is allowed to stand for 15 minutes at 20° C. before use. For the in vitro transfection, the solution volume is adjusted to 1 ml with the medium without serum.
For an in vivo injection, the LPR are obtained by adding beforehand 50 µl (50 µg) of mRNA in a 1.5 ml Eppendorf tube containing 160 µl of sterile buffer HEPES 10 mM at pH 7.4 prepared in water without endonuclease. 100 µl (150 µg) of the solution of PEG-HpK are then added and mixed 4 seconds. After 30 min at 20° C., 50 µL of liposomes (100 µg in sterile buffer HEPES 10 mM at pH 7.4 prepared in water without endonuclease) are added to the polymer/mRNA complex and gently mixed by pipetting. The solution is allowed to stand for 15 min at 20° C. For the in vivo injection, the solution is adjusted to a final concentration in saccharose of 5% by adding 40 µl of a solution of saccharose at 50% prepared in water without endonuclease. The mice are injected with 100 µl of solution.
Unless indicated otherwise, the lipopolyplexes (called LPR) used in the experiments described contain RNA control single strand PolyU (ssPolyU).
The various LPR (bare LPR, diether LPR or bare diether LPR, LPR-MN, LPR-MN diether, LPR-triMN) are obtained by mixing the corresponding liposomes (bare liposomes, diether liposomes or bare diether liposomes, liposomes MN, liposomes MN diether, liposomes triMN) with a cationic polymer (RNA complexed with the partially histidinylated polylysine and comprising one molecule of PEG 5 kDa).
The cell line 293T is a cell line derived from transformed human embryonic kidney cells.
The cell line 293T DC-SIGN corresponds to genetically modified cells 293T to express DC-SIGN, a type C lectin.
MoDCs cells are human monocyte-derived dendritic cells.
PBMCs cells are mononuclear cells of the blood.
PanDCs cells are human dendritic cells identified within the other cells of the peripheral blood (PBMCs).
The secretion of interferon-y by the lymphocytes T coming from the spleen (spleen cells) is analysed using the kit IFN-γ ELISpotPLUS kit (Mabtech, Sweden). Briefly the spleen cells to be analysed are incubated in an ELISpot plate in the presence of the antigen E749-57 or of concanavalin A (positive control) or of culture medium (negative control). The interferon-y secreted is captured by antibodies attached to the plate. After an incubation of 36 h at 37° C., the plate is washed and the cells are removed. The plate is then incubated with a biotinylated antibody directed against interferon-y then with the streptavidin coupled to the alkaline phosphatase. The presence of spots corresponding to a secretion of interferon-y is detected after incubation with the reaction buffer BCIP/NBT. The spots are analysed by an ELISpot plate reader.
The total RNA were extracted from samples of skin using the ReliPrep RNA Tissue Miniprep system kit (Z6112, Promega), by following the supplier’s instructions. The RNA were then retrotranscribed in cDNA using the GoScript Reverse Transcription system kit (A5000, Promega), by following the supplier’s instructions. The quantitative PCR reactions in real time SYBR green (qRT-PCR) were carried out on the iGenSeq platform (Hôpital de la Pitié-Salpêtrière, Paris, France) with the primers described in Table 1. The results were analysed with the 1536 Lightcycler software (Roche, Basel, Switzerland) and the expression of the genes was quantified by the relative method of ΔCT, standardised by the expression of the reference genes β-actin and GAPH.
In a first experiment, different cell lines were incubated with different concentrations of bare lipopolyplexes (LPR), of mono-mannosylated lipopolyplexes (LPR-MN) or of tri-mannosylated lipopolyplexes (LPR-triMN). The lipopolyplexes all comprise a fluorescent lipid coupled to the fluorescein. The cell lines tested express type C lectins on their surface, able to bind the sugar residues mannose, galactose or fucose. The binding of the lipopolyplexes on these receptors is analysed by flow cytometry. The tri-mannosylated lipopolyplexes target the cells 293T DCSign (
In a second experiment, three different cell lines were incubated with increasing concentrations of mono-mannosylated lipopolyplexes (LPR-MN), diether mono-mannosylated lipopolyplexes (LPR-MN diether) and tri-mannosylated lipopolyplexes (LPR-triMN).
The presence of tri-mannosylated lipids of the invention therefore provides the LPR-triMN lipopolyplexes the capacity to bind to the cells expressing lectin type receptors. This property is specific to the tri-mannosylated lipopolyplexes of the invention, and lipopolyplexes comprising mono-mannosylated lipids (LPR-MN) or mono-mannosylated lipids and diether lipids (diether LPR-MN) have a reduced binding capacity.
The dendritic cells MoDCs are placed in a culture in the presence of LPS or of increasing doses of LPR-MN or LPR-triMN comprising lipids marked with fluorescein for 6h. The analysis via cytometry makes it possible to identify the fluorescent cells MoDCs that have captured the LPR. Moreover the expression of the activation markers HLA-DR, CD80 and CD83 is also measured.
The fluorescent cells MoDCs that have captured the LPR-MN do not express activation markers significantly with respect to the activation control LPS (
The presence of tri-mannosylated lipids of the invention therefore provides the LPR-triMN with the intrinsic property of activating the dendritic cells to which they are bound. The activated dendritic cells expressing co-stimulation molecules such as CD80 allow in turn for the activation of the lymphocytes T CD4+ and CD8+. The LPR-triMN are therefore capable of stimulating an immune response even though they do not contain any immunogenic molecule of interest.
In a first step, the dendritic cells MoDCs ate placed in culture in the presence of LPR-MN containing mRNA GFP for 6 h. After these 6 h, the cells MoDCs are put into contact for an additional 12 h with either LPS (positive control of activation of MoDCs), or with LPR-MN or LPR-triMN. The lipopolyplexes used for this second stimulation do not contain encoding RNA but contain RNA single strand PolyU (ssPolyU). The expression of the GFP and of the activation markers HLA-DR, CD80 and CD83 is measured by cytometry after 18 h of culture in total.
The incubation of dendritic cells with LPR-triMN ssPolyU makes it possible to induce the activation of these cells. This experiment confirms that the LPR-triMN have an adjuvant effect provided by the presence of tri-mannosylated lipids.
In a first experiment, mice were intradermally injected with PBS, LPR-MN or LPR-triMN.
In addition, analyses via qRT-PCR conduced on skin samples show a significant increase in the number of transcription products of genes CCR7 and CXCR4 (results not shown). These receptors are known to play a role in the migration of dendritic cells of the skin to the lymph nodes (Förster et al., (1999) CCR7 coordinates the primary immune response by establishing functional microenvironments in secondary lymphoid organs. Cell 99:23-33; Kabashima et al., (2007) CXCL12-CXCR4 Engagement Is Required for Migration of Cutaneous Dendritic Cells. Am J Pathol. 171:1249-57). The results of qRT-PCR also show an increase in the transcription of genes MMP9, IL1β and PGE2R1 (results not presented), that are involved in the inflammatory response.
In a second experiment, mice were intradermally injected on the foot arch with PBS, LPR-MN or LPR-triMN comprising a lipid marked with rhodamine. The popliteal draining lymph nodes of the mice were taken 6h after injection then marked with an antibody anti-CD169 (siglec-1). The analysis via fluorescence microscopy thus makes it possible to view the location of the LPR (rhodamine signal) and of the macrophages of the subcapsular sinus (signal CD169+).
Finally in a third experiment, mice were intradermally injected on the foot arch with PBS, bare LPR, bare diether LPR, LPR-MN or LPR-triMN. The popliteal lymph nodes of the mice were taken 24 h after injection. The presence in the popliteal draining lymph nodes of dendritic cells (DCs), and more particularly of activated dendritic cells expressing the marker Ly6C (Ly6C+ cells) or Ly6G (Ly6G+ cells), was analysed by flow cytometry.
All of these experiments show that the LPR-triMN comprising the tri-mannosylated lipid of the invention can induce an immune response (recruiting and activation of the dendritic cells in the lymph nodes draining the injection site) when they are injected into mice. In these experiments, the LPR-triMN contain RNA single strand PolyU (ssPolyU) and are not used as a vector for the introduction of immunogenic molecules of interest. These experiments show that the lipopolyplexes triMN have an intrinsic in vivo adjuvant effect.
Dendritic cells MoDCs coming from HLA-A2 donors were incubated for 24 h with bare LPR, LPR-MN or LPR-triMN containing mRNA of oncoprotein E7 of the virus HPV16 (mRNA E7) or the RNA non-encoding single strand PolyU (ssPolyU). The cells MoDCs where then used to sensitise T CD3+ autologous lymphocytes in co-culture for 3 days. After 3 days of co-culture the T lymphocytes were placed in a medium enriched with IL-7 and IL-15. At D7, the sensitised T lymphocytes were put back in the presence of MoDCs that were loaded beforehand with peptides E7 restricted to HLA-A2 (allele HLA2) for 16 h. Finally the exocytosis was inhibited for 4 h before conducting an intracellular marking of interferon-γ (INF-γ) analysed by cytometry. A detection of the expression of membrane markers CD3, CD4 and CD8 was also conducted.
This experiment therefore shows that the LPR-triMN, used as a vector for the vaccination “anti-E7”, are capable of inducing a specific “anti-T7” reaction.
Mice vaccination experiments were conducted with lipopolyplexes containing mRNA encoding oncoprotein E7 of the virus HPV16. These mice were vaccinated with an equimolar mixture of LPR-E7 and of LPR-E7-DC-LAMP which makes it possible to obtain a better response to the vaccination (Mockey et al. (2007) mRNA-based cancer vaccine: Prevention of B16 melanoma progression and metastasis by systemic injection of MART1 mRNA histidylated lipopolyplexes. Cancer Gene Therapy 14, 802-814). Indeed DC-LAMP is a glycoprotein of the membrane of the lysosomes and of the late endosomes, which play a role in the loading of peptides on CMH-II, making it possible to actively induce responses Th1. The use of a chimeric nucleic acid sequence (by fusion of the sequence encoding E7 and of the sequence encoding DC-LAMP) makes it possible to orient E7 to the path of the CMH-II and to improve the immune response.
LPR containing RNA non-encoding single strand polyU (ssPolyU) were used as a control. The injections were conducted at D0, D7 and D15. At D21 the mice were sacrificed and their spleens were taken. The spleen cells isolated as such were incubated in the presence of peptides E7 and their secretion of INF-γ was analysed by ELISpot. Various modes of vaccination were compared. Groups of 5 mice were thus vaccinated with 21 µg of LPR-triMN-ssPolyU (control) intravenously or with LPR-triMN-E7/E7-DC-LAMP: 21 µg intravenously, 7 µg intradermally or 7 µg subcutaneously.
Similar experiments have been conducted to compare the effect induced by the injection of different LPR. Mice were vaccinated at D0 and D2 with PBS (control) or different LPR (bare LPR, bare diether LPR, diether LPR-MN, LPR-triMN) containing mRNA E7. At D14 the mice were sacrificed and their spleens were taken. The spleen cells isolated as such were incubated in the presence of peptides E7 and their secretion of INF-γ was analysed via ELISpot.
Furthermore, the mannosylated LPR, although positively charged, do not accumulate in the lungs (results not presented).
The LPR-triMN are therefore effective vaccination vectors for the induction of a specific T response to an antigen of interest in the vaccinated subjects.
The therapeutic effect of a vaccination with LPR-E7 was evaluated in groups of 5 mice to which were administered 50,000 cells of the syngeneic tumoural line TC-1 by intradermal injection in the ectopic position (left side). These tumour cells express oncoprotein E7.
The mice then received two intradermal injections (7 days and 9 days after the inoculation of the tumour cells) of PBS (negative control) or of 7 µg of: LPR-MN-ssPolyU, LPR-MN-E7/E7-DC-LAMP, LPR-triMN-ssPolyU or LPR-triMN-E7/E7-DC-LAMP.
The tumoural growth was evaluated every 2 days by measuring with a calliper, according to the formula (L×l2)/2. Animals for which the tumoural volume becomes critical (>2000 mm2) were sacrificed.
In order to confirm the benefit of LPR-triMN as a therapeutic vaccine, two other tumoural models were tested: the model with melanoma B16F0 (expressing MART1), and the lymphoma model of the cells EG7 expressing OVA. The therapeutic effect of a vaccination with LPR-triMN was evaluated in groups of 10 mice who were administered cells of the tumoural line B16F0 or EG7 by intradermal injection in the ectopic position (left side). The mice were then vaccinated on days 7 and 9 post-injection with PBS, LPR-triMN comprising an RNA ssPolyU or an LPR-triMN comprising an mRNA of MART1 or of OVA respectively.
These results show the interest of LPR-triMN for cancer vaccination.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1655296 | Jun 2016 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/FR2017/051481 | 6/9/2017 | WO |
