Patent Application
20160074475
The invention is comprised within the field of the methods for stabilizing and targeting compounds of therapeutic interest in a specific manner to target tissues. The invention is particularly based on the capacity of apolipoprotein A to target compounds of therapeutic interest to all those tissues having on their surface binding sites with high affinity for said protein.
The development of new forms of therapy using macromolecules as active ingredients has generated the need to develop effective forms of stabilizing and targeting said molecules to their suitable cell targets. Examples of therapy requiring the specific targeting to a target tissue include therapies based on the use of specific growth factors or on the use of genes which are used to replace absent or deficient genes in the target tissue. The tissue-specific systems that are not based on viral vectors frequently suffer from the problem of their low or nil cell specificity.
Different systems have been described for targeting therapeutic compounds to liver cells based on lipid vesicles containing the therapeutic compound therein and the targeting of which is given by the presence on the surface of the vesicles of molecules showing affinity for liver cell membranes.
For example, WO07130873 describes methods for targeting microvesicles to liver cells by means of incorporating on the surface of said capsules a compound which is specifically recognized by asialoglycoprotein, hyaluronan, N-acetyl-galactosamine or mannose receptors present in liver cells. WO02086091 describes methods for targeting nanovesicles to liver cells by means of incorporating the hepatitis B virus coat protein in said nanovesicles. WO200473684 describes a method for targeting partially hydrophobic compounds to liver cells based on phospholipid discoidal vesicles comprising ApoA-I on their surface. Lou et al (World J. Gastroenterol., 2005, 11:954-959) have described a method for targeting a lipophilic antitumor compound to the hepatocellular carcinoma cells using high density lipoprotein (HDL) as a specific carrier based on the capacity of HDL to accommodate hydrophobic compounds such as cholesterol.
Finally, Kim et al (Molecular Therapy, 2007, 15:1145-1152) have described a method for targeting interfering RNA to liver cells based on liposomes including interfering RNAs and containing ApoA-I on their surface. However, these methods have the drawback that they only allow carrying hydrophobic compounds since said compounds are housed inside vesicles or artificial membranes in contact with the hydrophobic fraction of the phospholipids.
Alternatively, it is possible to carry hydrophilic compounds to the liver by means of using conjugates of said compounds to agents which are specifically captured by the liver. For example, Kramer et al (J. Biol. Chem., 1992, 267:18598-18604) have described methods for targeting therapeutic compounds (the cytostatic agent chlorambucil and the prolyl-4 hydroxylase I-nitrobenzo-2-oxa-1,3-diazol-β-Ala-Phe-5-oxaproline-Gly inhibitor) to liver cells by means of the conjugation of said compounds to bile acids. However, this type of conjugation only allows carrying to the liver, which excludes its use for the administration of compounds to other tissues of therapeutic interest.
WO04082720 describes methods for targeting compounds with therapeutic activity to liver cells by means of incorporating said compounds in pseudoviral particles formed by the hepatitis B virus coat protein. However, these vehicles have the problem of showing a reduced plasma half-life which requires a continuous administration or an administration at high doses to reach sustained therapeutic plasma levels. Furthermore, the viral proteins forming the pseudoviral particles generate a humoral immune response.
WO8702061A describes methods for targeting compounds to tissues expressing the LDL receptor by means of using fusion proteins formed by the apoliprotein B or E receptor binding region and an active component.
The problem of the short half-life of the interferon has been dealt with by WO07021494, which describes fusion proteins formed by albumin and interferon. These fusions reach plasma half-lives of about 14 days.
Therefore, there is a need for suitable vehicles for specifically targeting therapeutic compounds to liver cells and which allow reaching a long plasma half-life of the conjugates.
In a first aspect, the invention relates to a conjugate comprising
In a second aspect, the invention relates to a polynucleotide or a gene construct comprising a polynucleotide encoding a conjugate according to the invention wherein the compound of therapeutic interest (ii) is a polypeptide which forms a single chain with component (i).
In successive aspects, the invention relates to a vector comprising a polynucleotide or a gene construct according to the invention and to a host cell comprising a polynucleotide, a gene construct or a vector according to the invention or a nanolipoparticle comprising the conjugate of the invention.
In another aspect, the invention relates to a conjugate, a polynucleotide, a gene construct, a vector, a host cell or a nanolipoparticle according to the invention for its use in medicine.
In another aspect, the invention relates to a conjugate, a polynucleotide, a gene construct, a vector, a host cell or a nanolipoparticle according to the invention for the treatment of liver diseases or of diseases associated with the immune system.
In another aspect, the invention relates to a composition comprising:
In another aspect, the invention relates to a combination of the invention for its use in medicine and, in particular, for the treatment of cancer.
The authors of the present invention have observed that the conjugates formed by an Apo A protein or a functionally equivalent variant thereof and a molecule of therapeutic interest show, after their administration to patients, a serum half-life greater than that observed in patients to whom the molecule of therapeutic interest has been administered without conjugation. Additionally, the conjugates of Apo A and the molecule of therapeutic interest are specifically carried to the liver of the patient, which enormously facilitates the treatment of liver diseases and the reduction of side-effects due to the action of the therapeutic molecule in other tissues.
Thus, in a first aspect, the invention relates to a conjugate comprising
Without intending to be linked to any theory, it is believed that the affinity of the conjugates for liver tissue is due to the fact that said tissue has specific receptors for the Apo A proteins the natural function of which is to capture HDLs having ApoA-I on their surface. In addition, the longer half-life of the conjugates seems to be related to the long half-life that the Apo A molecules show in the organism (in the order of 35 hours in humans or 10 hours in mice in the case of ApoA-I). Furthermore, there are other cells expressing specific receptors for ApoA-I on their surface, which allows the carrying to other tissues.
In the context of the present invention, “Apo A protein” is understood as any member of the Apo A family forming part of the high density lipoproteins (HDLs) and which is capable of interacting specifically with receptors on the surface of liver cells, thus ensuring its capacity to carry the molecules of interest coupled to said Apo A protein to this organ. The Apo A molecules which can be used in the present invention are preferably selected from the group of ApoA-I, ApoA-II, ApoA-III, ApoA-IV and ApoA-V or of functionally equivalent variants thereof.
In a preferred embodiment, the Apo A protein which is used in the present invention is the ApoA-I protein. In the context of the present invention, ApoA-I is understood as the mature form of the pre-proApoA-I protein forming part of the high density lipoproteins (HDLs). ApoA-I is synthesized as a precursor (pre-proApoA-I) containing a secretion signal sequence which is eliminated to give rise to the precursor. The signal sequence is made up of 18 amino acids, the propeptide of 6 amino acids and the mature form of the protein of 243 amino acids. The mature form of the protein which lacks a signal peptide and is processed is preferably used. In a preferred embodiment, the ApoA-I protein is of human origin and its amino acid sequence is that shown in SEQ ID NO:1 (access number in UniProt P02647). In another preferred embodiment, the ApoA-I protein is of murine origin, in particular from mouse, and its amino acid sequence is that shown in SEQ ID NO:2 (access number in UniProt Q00623). In another preferred embodiment, the ApoA-I protein is of murine origin, in particular from rat, and its amino acid sequence is that shown in SEQ ID NO:3 (access number in UniProt P04639).
A functionally equivalent variant of ApoA-I is understood as all those polypeptides resulting from the insertion, substitution or deletion of one or more amino acids of the previously mentioned human or murine ApoA-I sequence and substantially maintaining intact the capacity to interact with the so-called “scavenger receptor class B type I” (SR-BI) forming the HDL receptor present in liver cells. The capacity to interact with the HDL receptor is determined essentially as has been described by Monaco et al (EMBO J., 1987, 6:3253-3260) by means of studies of ApoA-I binding to the hepatocyte membrane or by means of determining the capacity of ApoA-I or of its variant to inhibit the binding of HDL to the hepatocyte membrane receptors. The dissociation constant of the binding of the variant of ApoA-I to the hepatocyte membranes is preferably at least 10−8 M, 10−7 M, 10−6M, 10−5M or 10−4M.
Variants of ApoA-I contemplated in the context of the present invention include polypeptides showing at least 60%, 65%, 70%, 72%, 74%, 76%, 78%, 80%, 90% or 95% similarity or identity with the ApoA-I polypeptides. The degree of identity between two polypeptides is determined using computer algorithms and methods that are widely known by persons skilled in the art. The identity between two amino acid sequences is preferably determined using the BLASTP algorithm (BLAST Manual, Altschul, S. et al., NCBI NLM NIH Bethesda, Md. 20894, Altschul, S., et al., J., 1990, Mol. Biol. 215:403-410).
The variants of ApoA-I used in the context of the invention preferably have a long serum half-life with respect to native ApoA-I, which allows reaching serum ApoA-I levels greater than those observed with ApoA-I. Methods for determining the serum half-life of a protein and, in particular of ApoA-I, are known in the art and include, among others, using the methods based on metabolic labeling with labeled proteins described by Eisenberg, S. et al (J. Lipid Res., 1973, 14:446-458), by Blum et al. (J. Clin. Invest., 1977, 60:795-807) and by Graversen et al (J Cardiovasc Pharmacol., 2008, 51:170-177). An example of said variants which shows a longer half-life is, for example, the variant called Milano (which contains the mutation R173C).
In the context of the present invention, “compounds of therapeutic interest” are understood as any compound which is capable of preventing or eliminating the symptoms of a disease. The invention initially contemplates the use of any therapeutic compound which is susceptible to covalent modification without substantially losing its biological activity, such that it can be conjugated to ApoA-I or to the functionally equivalent variant thereof. Thus, the invention contemplates the use of small organic molecules, peptides, peptidomimetics, peptoids, proteins, polypeptides, glycoproteins, oligosaccharides, nucleic acids and the like as a therapeutically effective component.
By way of example, compounds which can be conjugated to ApoA-I or to the functionally equivalent variant thereof include antibiotics, cholinesterase agents, atropine, scopolamine, sympathomimetic drugs, hypnotic drugs, sedatives, antiepileptic drugs, opioids, analgesics, anti-inflamatory drugs, histamines, lipid derivatives, antiasthmatic drugs, antipyretic-analgesic drugs, xanthines, osmotic diuretics, mercurial compounds, thiazides and sulfonamides, carbonic anhydrase inhibitors, organic nitrates, antihypertensives, cardiac glycosides, antiarrhythmic drugs, oxytocin, prostaglandins, alkaloids, tocolytic agents, antihelminthics, antiprotozoal drugs, antimalarial drugs, amebicides, sulfonamides, penicillins, trimetropin, cephalosporins, sulfamethoxazole, antimycotics, quinolones, antiviral drugs, antibiotics, aminoglycosides, tetracyclines, chloramphenicol, erythromycin, alkylating agents, hormones, antimetabolites, antibiotics, radioactive isotopes, azathioprine, chlorambucil, cyclophosphamide, methotrexate, anticoagulants, thrombolytic drugs, antiplatelet drugs, adenohypophyseal hormones, thyroid and antithyroid hormones, estrogens and progesterone, androgens, adrenocorticotropin, insulin, parathyroid hormone, steroid derivative of vitamin D, vitamins, (hydrosoluble vitamins such as vitamin B complex and ascorbic acid or liposoluble vitamins such as vitamins A, D, K or E), antihistaminic drugs, antitumor, antiviral, antifungal compounds. Compounds which are useful for the treatment of diseases affecting or having their origin in the liver are preferably used.
In a preferred embodiment, component (ii) of the conjugates of the invention comprises a polypeptide chain. In a preferred embodiment, polypeptide ApoA-I and the polypeptide forming component (ii) form a single polypeptide chain. The present invention contemplates the two relative orientations of both polypeptides. Thus, in a preferred embodiment, the C-terminal end of component (i) is bound to the N-terminal end of component (ii). In another preferred embodiment, the N-terminal end of component (i) is bound to the C-terminal end of component (ii). Preferably, when the ApoA-I conjugates are formed by a single polypeptide chain, they are not formed by
Polypeptides which can be carried to the liver using the conjugates of the invention include erythropoietin (EPO), leptins, adrenocorticotropin-releasing hormone (CRH), somatotropic hormone-releasing hormone (GHRH), gonadotropin-releasing hormone (GnRH), thyrotropin-releasing hormone (TRH), prolactin-releasing hormone (PRH), melatonin-releasing hormone (MRH), prolactin-inhibiting hormone (PIH), somatostatin, adrenocorticotropin hormone (ACTH), somatotropic hormone or growth hormone (GH), luteinizing hormone (LH), follicle-stimulating hormone (FSH), thyrotropin (TSH or thyroid-stimulating hormone), prolactin, oxytocin, antidiuretic hormone (ADH or vasopressin), melatonin, Müllerian inhibiting factor, calcitonin, parathyroid hormone, gastrin, cholecystokinin (CCK), Arg-vasopressin, thyroid hormones, azoxymethane, triiodothyronine, LIF, amphiregulin, soluble thrombomodulin, SCF, osteogenic protein 1, BMPs, MGF, MGSA, heregulins, melanotropin, secretin, insulin-like growth factor I (IGF-I), insulin-like growth factor II (IGF-II), atrial natriuretic peptide (ANP), human chorionic gonadotropin (hCG), insulin, glucagon, somatostatin, pancreatic polypeptide (PP), leptin, neuropeptide Y, renin, angiotensin I, angiotensin II, factor VIII, factor IX, tissue factor, factor VII, factor X, thrombin, factor V, factor XI, factor XIII, interleukin 1 (IL-1), interleukin 2 (IL-2), interleukin 3 (IL-3), interleukin 4 (IL-4), interleukin 5 (IL-5), interleukin 6 (IL-6), interleukin 7 (IL-7), interleukin 8 (IL-8), interleukin 9 (IL-9), interleukin 10 (IL-10), interleukin 11 (IL-11), interleukin 12 (IL-12), interleukin 13 (IL-13), interleukin 14 (IL-14), interleukin 15 (IL-15) interleukin 16 (IL-16), interleukin 24 (IL-24), tumor necrosis factor alpha (TNF-α), interferons alpha, beta, gamma, CD3, CD134, CD137, ICAM-1, LFA-1, LFA-3, chemokines including RANTES 1α, MIP-1α, MIP-1β, nerve growth factor (NGF), WT1 protein encoded by the Wilms' tumor suppressor gene, platelet-derived growth factor (PDGF), transforming growth factor beta (TGF-beta), bone morphogenetic proteins (BMPs), fibroblast growth factors (FGF and KGF), epidermal growth factor (EGF and related factors), vascular endothelial growth factor (VEGF), granulocyte colony-stimulating factor (GM-CSF), glial growth factor, keratinocyte growth factor, endothelial growth factor, glial-cell line-derived, neurotrophic factor (GDNF), alpha 1-antitrypsin, tumor necrosis factor, granulocyte-macrophage colony-stimulating factor (GM-CSF), cardiotrophin-1 (CT-1), oncostatin M (OSM), serpin (A1, A2, A3, A4, A5, A6, A7, A8, A9, A10, A11, A12, A13, B1, B2, B3, B4, B5, B6, B7, B8, B9, B10, B11, B12, B13, C1, D1, E1, E2, F1, F2, G1, H1, I1 and I2), cyclosporine, fibrinogen, the EDA domain of fibronectin, lactoferrin, tissue-type plasminogen activator (tPA), chymotrypsin, immunoglobins, hirudin, superoxide dismutase, imiglucerase, β-Glucocerebrosidase, alglucosidase-α, α-L-iduronidase, iduronate-2-sulfatase, galsulfase, human α-galactosidase A, α-1 proteinase inhibitor, lactase, pancreatic enzymes (lipase, amylase, protease), adenosine deaminase, immunoglobulins, albumin, Botulinum toxins type A and B, collagenase, human deoxyribonuclease I, hyaluronidase, papain, L-asparaginase, lepirudin, streptokinase, porphobilinogen deaminase (PBGD), cell transforming factor beta (TGF-β) inhibitor peptides, IL10 inhibitors, FoxP3 inhibitors, TNFα inhibitors, VEGF inhibitors, PD-1 inhibitors and CD152 inhibitors.
In a preferred embodiment, component (ii) of the conjugate of the invention is an interferon (IFN). Interferons are classified as interferon of type I, of type II and of type III. Type I interferons are a polypeptide family with cytokine activity which were originally discovered as a result their inhibitory activity on the viral infection of cell lines in vitro (Pestka, S., Krause, C. D. and Walter, M. R. 2004. Immunol Rev. 202:8-32) and which are characterized in that they are bound to the so-called IFN-α receptor (IFNAR). Depending on the homology of their sequences, type I interferons are classified as interferon-α (IFN-α), interferon-β (IFN-β) and interferon-ω (IFN-ω). IFN-α and IFN-β share a single dimeric receptor which is expressed on the surface of most nucleated cells. The function of these cytokines is very important in the immune response against multiple types of viral infections, given that they start up mechanisms promoting the death by apoptosis of the infected cells and viral replication inhibition while at the same time they favor antigen presentation. It has recently been experimentally documented that it also carries out its functions by directly activating the activities of T, B and NK cells as well as of dendritic cells in the immune response (Le Bon A. et al., 2003. Nat. Immunol. 4:1009-1015; Le Bon A. et al., 2006. J. Immunol. 176:4682-4689; Le Bon A. et al., 2006. J Immunol. 176:2074-8). Type II interferons are characterized in that they are bound to the interferon gamma receptor (IFNGR) and include IFN-γ as a single member. Type III interferons transduce their signal through a complex formed by the IL-10 receptor 2 (IL10R2) and the IFN lambda 1 receptor (IFNLR1) and is formed by three interferons lambda called IFN-λ1, IFN-λ2 and IFN-λ3.
In a preferred embodiment, component (ii) is a type I interferon, such as IFN-α, IFN-β, IFN-δ, IFN-ε, IFN-κ, IFN-τ and IFN-ω. In a particular embodiment, at least one type I interferon comprised in the composition of the invention is selected from the group comprising interferon-alpha (IFN-α) and interferon-beta (IFN-β). When the type I interferon is IFN-α, the latter can correspond to any interferon encoded by any gene member of the family of human IFN-α genes. In a particular embodiment, at least one type I interferon is an IFN-α selected from the group of IFN-α2a, IFN-α2b, IFN-α4, IFN-α5, IFN-α8 and combinations thereof, including its combination with other substances in pharmaceutical formulations. In an even more particular embodiment, the interferon is IFN-α1, preferably of human origin. In a preferred embodiment, the interferon is IFN-α5.
A list of species of type I interferon, particularly IFN-α and IFN-β which can be used according to the invention, can be found in Bekisz et al. (Growth Factors, 2004; 22: 243-251) and in Petska et al. (Immunological Reviews, 2004; 202: 8-32). Additionally, the invention provides the use of combinations of conjugates comprising more than one type of interferon, such as for example IFN-αn1 (lymphoblastoid derivative) or IFN-α3 (combination of interferons produced by human leukocytes stimulated with the Sendai virus (or another virus) or viral particles).
The origin of the type I interferon used is not a critical aspect of the invention. This can be of natural origin, extracted and purified from biological fluids or tissues, or produced by means of conventional recombinant genetic engineering and methods, such as those described in Sambrook and Russel (“Molecular Cloning: to Laboratory manual” of J. Sambrook, D. W. Russel Eds. 2001, third edition, Cold Spring Harbor, N.Y.), by synthesis processes or by any other conventional technique described in the state of the art.
In a particular embodiment of the invention, at least one type I interferon comprised in the composition of the invention is in pegylated form. Some examples for preparing pegylated forms of interferon can be found in U.S. Pat. No. 5,762,923 and U.S. Pat. No. 5,766,582. In addition, it is also possible to use some of the interferon forms which are already commercially available, either pegylated or non-pegylated forms. These include, without involving any limitation, ROFERON-A (human recombinant IFN-α2a) and PEGASYS (pegylated IFN-α) from Hoffmann La Roche Inc., INTRON-A (human recombinant IFN-α2b) and PEG-INTRON (pegylated IFN-α2b) from Schering Corp., ALFERON-N (IFN-α3n, combination of interferons of natural origin) from Interferon Sciences, or IFNERGEN (IFN-αcon1) from InterMune Pharmaceuticals Inc., the sequence of which is a consensus sequence that does not exactly correspond with a natural sequence. IFN-β formulations, such as for example AVONEX (IFN-β1a) from Biogen Idec, REBIF (IFN-β1a) from EMD Serono, Inc, and BETASERON (IFN-β1b) from Bayer Health Care are also included.
In a preferred embodiment, the conjugate of the invention is formed by ApoA-I fused through its C-terminal end and by means of a flexible linker with the N-terminal end of an interferon α1 molecule. In another preferred embodiment, the conjugate of the invention is formed by an interferon α1 molecule fused through its C-terminal end and by means of a flexible linker with the N-terminal end of a ApoA-I molecule.
In another preferred embodiment, component (ii) is a TGF-beta inhibitor. TGF-beta inhibitors which can form part of the conjugates according to the invention include the peptide inhibitors selected from TGF-beta1 receptor sequences which are bound to the receptor binding site in TGF-β1, thus blocking the binding to the receptor. These types of peptides have been described in WO200031135, the entire content of which is incorporated by reference. In a preferred embodiment, the TGF-β1 inhibitor peptide is derived from the TGF-β1 type III receptor. In an even more preferred embodiment, the inhibitor peptide is peptide p144 having the sequence TSLDASIIWAMMQN (SEQ ID NO:4).
The invention likewise provides the use of inhibitor peptides inhibiting the interaction between TGFβ1 and the TGFβ1 receptor and the signaling occurring in response to said interaction, identified as phage-displayed gene libraries as they have been described in WO200519244, the entire content of which is incorporated by reference. In a preferred embodiment, the inhibitor peptide is peptide p17 characterized by the sequence KRIWFIPRSSWYERA (SEQ ID NO:5), as well as truncated variants thereof and which substantially conserve the capacity to inhibit the interaction between TGFβ1 and its receptor as they have been described in WO2007048857, the entire content of which is incorporated in the present invention.
The conjugates object of the invention comprising the Apo A protein and a second component with a peptide nature can contain a bond directly connecting the Apo A protein and said second component or, alternatively, can contain an additional amino acid sequence acting as a linker between the Apo A protein and said second component with a peptide nature. According to the invention, said non-natural intermediate amino acid sequence acts as a hinge region between domains, allowing them to move independently from one another while they maintain the three-dimensional shape of the individual domains. In this sense, a preferred non-natural intermediate amino acid sequence according to the invention would be a hinge region characterized by a structural ductility allowing this movement. In a particular embodiment, said non-natural intermediate amino acid sequence is a non-natural flexible linker. In a preferred embodiment, said flexible linker is a flexible linker peptide with a length of 20 amino acids or less. In a more preferred embodiment, the linker peptide comprises 2 amino acids or more selected from the group consisting of glycine, serine, alanine and threonine. In a preferred embodiment of the invention, said flexible linker is a polyglycine linker. Possible examples of linker/spacer sequences include SGGTSGSTSGTGST (SEQ ID NO:6), AGSSTGSSTGPGSTT (SEQ ID NO:7) or GGSGGAP (SEQ ID NO:8). These sequences have been used for binding designed coiled helixes to other protein domains (Muller, K. M., Arndt, K. M. and Alber, T., Meth. Enzymology, 2000, 328: 261-281). Said linker preferably comprises or consists of the amino acid sequence GGGVEGGG (SEQ ID NO: 9).
The effect of the linker region is providing space between the Apo A protein and component (ii). It is thus ensured that the secondary structure of Apo A is not affected by the presence of component (ii) and vice versa. The spacer preferably has a peptide nature. The linker peptide preferably comprises at least two amino acids, at least three amino acids, at least five amino acids, at least ten amino acids, at least 15 amino acids, at least 20 amino acids, at least 30 amino acids, at least 40 amino acids, at least 50 amino acids, at least 60 amino acids, at least 70 amino acids, at least 80 amino acids, at least 90 amino acids or approximately 100 amino acids.
The linker can be bound to components flanking the two components of the conjugates of the invention by means of covalent bonds and preferably the spacer is essentially non-immunogenic and/or does not comprise any cysteine residue. In a similar manner, the three-dimensional structure of the spacer is preferably linear or substantially linear.
Preferred examples of spacer or linker peptides include those which have been used for binding proteins without substantially deteriorating the function of the bound proteins or at least without substantially deteriorating the function of one of the bound proteins. More preferably, the spacers or linkers have been used for binding proteins comprising structures with coiled helixes.
The linker can include residues 53-56 of tetranectin, forming a β sheet in tetranectin, and residues 57-59 forming a turn in the tetranectin (Nielsen, B. B. et al., FEBS Lett. 412: 388-396, 1997). The sequence of the segment is GTKVHMK (SEQ ID NO:10). This linker has the advantage that when it is present in native tetranectin, it binds the trimerization domain with the CRD domain, and therefore it is suitable for connecting the trimerization domain to another domain in general. Furthermore, the resulting construct is not expected to be more immunogenic than the construct without a linker.
Alternatively, a subsequence from the connecting strand 3 from human fibronectin can be chosen as a linker, corresponding to amino acids 1992-2102 (SWISSPROT numbering, entry P02751). The subsequence PGTSGQQPSVGQQ (SEQ ID NO:11) corresponding to amino acids number 2037-2049 is preferably used, and within that subsequence fragment GTSGQ (SEQ ID NO:52) corresponding to amino acids 2038-2042 is more preferable. This construct has the advantage that it not very prone to proteolytic cleavage and is not very immunogenic because fibronectin is present at high concentrations in plasma.
Alternatively, a suitable peptide linker can be based on the 10 amino acid residue sequence of the upper hinge region of murine IgG3. This peptide (PKPSTPPGSS, SEQ ID NO: 12) has been used to produce antibodies dimerized by means of a coiled helix (Pack P. and Pluckthun, A., 1992, Biochemistry 31:1579-1584) and can be useful as a spacer peptide according to the present invention. A corresponding sequence of the upper hinge region of human IgG3 can be even more preferable. Human IgG3 sequences are not expected to be immunogenic in human beings.
In a preferred embodiment, the linker peptide is selected from the group of the peptide of sequence APAETKAEPMT (SEQ ID NO:13) and of the peptide of sequence GAP.
Alternatively, the two components of the conjugates of the invention can be connected by a peptide the sequence of which contains a cleavage target for a protease, thus allowing the separation of ApoA-I from component (ii). Protease cleavage sites suitable for their incorporation into the polypeptides of the invention include enterokinase (cleavage site DDDDK, SEQ ID NO:14), factor Xa (cleavage site IEDGR, SEQ ID NO:15), thrombin (cleavage site LVPRGS, SEQ ID NO:16), TEV protease (cleavage site ENLYFQG, SEQ ID NO:17), PreScission protease (cleavage site LEVLFQGP, SEQ ID NO:18), inteins and the like. In a preferred embodiment, the cleavage site is a protease cleavage site expressed in tumor tissues, in inflamed tissues or in liver such that the separation of Apo A and of component (ii) takes place once the conjugate has reached the liver. In a preferred embodiment, the linker contains a matrix metalloprotease-9 recognition site (cleavage site LFPTS, SEQ ID NO:19).
The conjugates of the invention can be obtained using any method known for a person skilled in the art. It is thus possible to obtain the ApoA protein or the variant of said protein by any standard method. For example, the ApoA-I protein can be purified from serum samples of individuals or of laboratory animals (WO9807751, WO9811140, Jackson et al., 1976, Biochim Biophys Acta. 420:342-349, Borresen, A. L. and Kindt, T. J., 1978, J. Immunogenet. 5:5-12 and Forgez, P, and Chapman, M. J., 1982, J. Biochem. Biophys. Methods, 6:283-96). Alternatively, the ApoA-I protein can be obtained from cDNA by means of expression in a heterologous organism such as, for example, E. coli, S. cerevisiae, P. pastoris, insect cells using methods known in the art such as those described in WO07023476, WO9525786, WO8702062, Feng et al., (Protein. Expr. Purif., 2006, 46:337-42), Pyle et al., 1996 Biochemistry. 35:12046-52), Brissette et al., (Protein Expr. Purif. 1991, 2:296-303) and Bonen, D. K. (J. Biol. Chem., 1997, 272:5659-67).
Once there is a sufficient amount of purified ApoA protein, it must be conjugated to the therapeutic compound of interest. The conjugation of therapeutically active component (ii) to the Apo A molecule can be carried out in different ways. One possibility is the direct conjugation of a functional group to the therapeutically active component in a position which does not interfere with the activity of said component. As understood in the present invention, functional groups relates to a group of specific atoms in a molecule which are responsible for a characteristic chemical reaction of said molecule. Examples of functional groups include, but are not limited to hydroxy, aldehyde, alkyl, alkenyl, alkynyl, amide, carboxamide, primary, secondary, tertiary and quaternary amines, aminoxy, azide, azo (diimide), benzyl, carbonate, ester, ether, glyoxylyl, haloalkyl, haloformyl, imine, imide, ketone, maleimide, isocyanide, isocyanate, carbonyl, nitrate, nitrite, nitro, nitroso, peroxide, phenyl, phosphine, phosphate, phosphono, pyridyl, sulfide, sulfonyl, sulfinyl, thioester, thiol and oxidized 3,4-dihydroxyphenylalanine (DOPA) groups. Examples of said groups are maleimide or glyoxylyl groups which react specifically with thiol groups in the Apo A molecule and oxidized 3,4-dihydroxyphenylalanine (DOPA) groups which react with primary amine groups in the Apo A molecule.
Another possibility is to conjugate therapeutically active component (ii) to the Apo A molecule by means of the use of homo- or heterobifunctional groups. The bifunctional group can be conjugated first to the therapeutically active compound and, then, conjugated to the Apo A protein or, alternatively, it is possible to conjugate the bifunctional group to the Apo A protein and then, conjugate it to the therapeutically active compound. Illustrative examples of theses types of conjugates include the conjugates known as ketone-oxime (described in US20050255042) in which the first component of the conjugate comprises an aminoxy group which is bound to a ketone group present in a heterobifunctional group which is in turn bound to an amino group in the second component of the conjugate.
In other embodiments, the agent which is used to conjugate components (i) and (ii) of the conjugates of the invention can be photolytically, chemically, thermally or enzymatically processed. It is particularly interesting to use linking agents which can be hydrolyzed by enzymes which are in the cell target, so that the therapeutically active compound is only released in the inside of the cell. Examples of types linking agents which can be intracellularly processed have been described in WO04054622, WO06107617, WO07046893 and WO07112193.
In a preferred embodiment, component (ii) of the conjugate of the invention is a compound with a peptide nature, including both oligopeptides and peptides. Methods for chemically modifying a polypeptide chain are widely known for a person skilled in the art and include methods based on the conjugation through the thiol groups present in the cysteine moieties, methods based on the conjugation through the primary amino groups present in lysine moieties (U.S. Pat. No. 6,809,186), methods based on the conjugation through the N- and C-terminal moieties. Reagents suitable for modifying polypeptides to allow their coupling to other compounds include: glutaraldehyde (it allows binding compounds to the N-terminal end of polypeptides), carbodiimide (it allows binding the compound to the C-terminal end of a polypeptide), succinimide esters (for example MBS, SMCC) which allow activating the N-terminal end and cysteine moieties, benzidine (BDB), which allows activating tyrosine moieties, periodate, which allows activating carbohydrate moieties in the proteins which are glycosylated.
In the particular case in which component ApoA and the therapeutic compound of interest form a single peptide chain, it is possible to express the conjugate in a single step using a gene construct of the invention encoding said conjugate, for which said construct is introduced in a vector suitable for its expression in a heterologous organism together with transcription and, optionally, translation control elements. The transcription and, optionally, translation control elements present in the expression cassette of the invention include promoters, which direct the transcription of the nucleotide sequence to which they are operatively linked and other sequences which are necessary or suitable for the transcription and its suitable regulation in time and place, for example, initiation and termination signals, cleavage sites, polyadenylation signal, replication origin, transcriptional enhancers, transcriptional silencers, etc. Said elements, as well as the vectors used for constructing the expression cassettes and the recombinant vectors according to the invention are generally chosen according to the host cells to be used.
In another aspect, the invention relates to a polynucleotide encoding a polypeptide of the invention. A person skilled in the art will understand that the polynucleotides of the invention will only encode the conjugates in which component (ii) has a peptide nature and in which the polypeptide Apo A forms a single peptide chain, regardless of the relative orientation and regardless of the fact that both components are directly connected or separated by a spacer region.
In another aspect, the invention relates to a gene construct comprising a polynucleotide of the invention. The construct preferably comprises the polynucleotide of the invention located under the operative control of sequences regulating the expression of the polynucleotide of the invention. A person skilled in the art will understand that the polynucleotides of the invention must access the nucleus of a target tissue and there be transcribed and translated to give rise to the biologically active fusion protein. For this reason, when the active ingredient which is administered is a polynucleotide, the latter must preferably encode the precursor form pre-proApoA1 or the precursor form of the ApoA1 variant, such that after its expression it is secreted as a result of the signal sequence and it is processed to give rise to the mature ApoA1.
In the event that the conjugate formed by Apo A fused through its C-terminal end with an interferon molecule is to be expressed, it is preferable for the polynucleotide encoding it to be preceded by a sequence encoding the ApoA1 signal sequence. In the event that the conjugate formed by an interferon molecule fused through its C-terminal end with the N-terminal end of a ApoA molecule is to be expressed, it is preferable for the polynucleotide encoding it to be preceded by a sequence encoding the interferon α1 signal sequence.
In principle, any promoter can be used for the gene constructs of the present invention provided that said promoter is compatible with the cells in which the polynucleotide is to be expressed. Thus, promoters suitable for the embodiment of the present invention include, without being necessarily limited to, constitutive promoters such as the derivatives of the genomes of eukaryotic viruses such as the polyoma virus, adenovirus, SV40, CMV, avian sarcoma virus, hepatitis B virus, the promoter of the metallothionein gene, the promoter of the herpes simplex virus thymidine kinase gene, retrovirus LTR regions, the promoter of the immunoglobulin gene, the promoter of the actin gene, the promoter of the EF-1alpha gene as well as inducible promoters in which the expression of the protein depends on the addition of a molecule or an exogenous signal, such as the tetracycline system, the NFκB/UV light system, the Cre/Lox system and the promoter of heat shock genes, the regulatable promoters of RNA polymerase II described in WO/2006/135436 as well as tissue-specific promoters. In a preferred embodiment, the gene constructs of the invention contain the expression-enhancing regions present in promoter regions of predominantly hepatic expression genes such as human serum albumin genes, prothrombin genes, the alpha-1-microglobulin genes or aldolase genes, either in a single copy in the form of several copies thereof and either in an isolated form or in combination with other liver-specific expression elements such as cytomegalovirus, alpha-1-antitrypsin or albumin promoters.
Other examples of promoters which are tissue-specific include the promoter of the albumin gene (Miyatake et al., 1997, J. Virol, 71:5124-32), the core promoter of hepatitis virus (Sandig et al, 1996, Gene Ther., 3:1002-9); the promoter of the alpha-phetoprotein gene (Arbuthnot et al., 1996, Hum. GeneTher., 7:1503-14), and the promoter of the globulin-binding protein which binds to thyroxine (Wang, L., et al., 1997, Proc. Natl. Acad. Sci. USA 94:11563-11566).
The polynucleotides of the invention or the gene constructs forming them can form part of a vector. Thus, in another aspect, the invention relates to a vector comprising a polynucleotide or a gene construct of the invention. A person skilled in the art will understand that there is no limitation as regards the type of vector which can be used because said vector can be a cloning vector suitable for propagation and for obtaining the polynucleotides or suitable gene constructs or expression vectors in different heterologous organisms suitable for purifying the conjugates. Thus, suitable vectors according to the present invention include expression vectors in prokaryotes such as pUC18, pUC19, Bluescript and their derivatives, mp18, mp19, pBR322, pMB9, CoIE1, pCR1, RP4, phages and shuttle vectors such as pSA3 and pAT28, expression vectors in yeasts such as vectors of the type of 2 micron plasmids, integration plasmids, YEP vectors, centromeric plasmids and the like, expression vectors in insect cells such as the pAC series and pVL series vectors, expression vectors in plants such as vectors of expression in plants such as pIBI, pEarleyGate, pAVA, pCAMBIA, pGSA, pGWB, pMDC, pMY, pORE series vectors and the like and expression vectors in superior eukaryotic cells based on viral vectors (adenoviruses, viruses associated to adenoviruses as well as retroviruses and lentiviruses) as well as non-viral vectors such as pSilencer 4.1-CMV (Ambion), pcDNA3, pcDNA3.1/hyg pHCMV/Zeo, pCR3.1, pEF1/His, pIND/GS, pRc/HCMV2, pSV40/Zeo2, pTRACER-HCMV, pUB6/V5-His, pVAX1, pZeoSV2, pCI, pSVL and pKSV-10, pBPV-1, pML2d and pTDT1.
The vector of the invention can be used to transform, transfect or infect cells which can be transformed, transfected or infected by said vector. Said cells can be prokaryotic or eukaryotic. By way of example, the vector wherein said DNA sequence is introduced can be a plasmid or a vector which, when it is introduced in a host cell, is integrated in the genome of said cell and replicates together with the chromosome (or chromosomes) in which it has been integrated. Said vector can be obtained by conventional methods known by the persons skilled in the art (Sambrok et al., 2001, mentioned above).
Therefore, in another aspect, the invention relates to a cell comprising a polynucleotide, a gene construct or a vector of the invention, for which said cell has been able to be transformed, transfected or infected with a construct or vector provided by this invention. The transformed, transfected or infected cells can be obtained by conventional methods known by persons skilled in the art (Sambrok et al., 2001, mentioned above). In a particular embodiment, said host cell is an animal cell transfected or infected with a suitable vector.
Host cells suitable for the expression of the conjugates of the invention include, without being limited to, mammal, plant, insect, fungal and bacterial cells. Bacterial cells include, without being limited to, Gram-positive bacterial cells such as species of the Bacillus, Streptomyces and Staphylococcus genus and Gram-negative bacterial cells such as cells of the Escherichia and Pseudomonas genus. Fungal cells preferably include cells of yeasts such as Saccharomyces, Pichia pastoris and Hansenula polymorpha. Insect cells include, without being limited to, Drosophila cells and Sf9 cells. Plant cells include, among others, cells of crop plants such as cereals, medicinal, ornamental or bulbous plants. Suitable mammal cells in the present invention include epithelial cell lines (porcine, etc.), osteosarcoma cell lines (human, etc.), neuroblastoma cell lines (human, etc.), epithelial carcinomas (human, etc.), glial cells (murine, etc.), hepatic cell lines (from monkey, etc.), CHO (Chinese Hamster Ovary) cells, COS cells, BHK cells, HeLa cells, 911, AT1080, A549, 293 or PER.C6, NTERA-2 human ECC cells, D3 cells of the mESC line, human embryonic stem cells such as HS293 and BGV01, SHEF1, SHEF2 and HS181, NIH3T3 cells, 293T, REH and MCF-7 and hMSC cells.
In another aspect, the invention relates to a nanolipoparticle that comprises a conjugate according to the invention.
As used herein, the term “nanolipoparticle” is equivalent to the terms “lipoprotein” or “lipoprotein particle” and can be used interchangeably. By “nanolipoparticle” is understood herein any hidrosoluble particule, formed by a core of apolar lipids (such as esterified cholesterol and triglycerides) coated by an external polar coat formed by apolipoprtoeins, phospholipids and free cholesterol.
The nanolipoparticles or liporpteins are classified according to their density as chylomicrons, very low density lipoproteins (VLDL), intermediate density lipoproteins (IDL), low density lipoproteins (LDL) and high density lipoproteins (HDL). The features of th different lipoproteins is shown in Table 1.
In a particular, embodiment, the nanolipoparticles according to the invention is an HDL which composition is given in Table 1 and wherein the protein fraction is formed by Apo A, Apo C, Apo D and Apo E.
The nanoparticules of the invention may be obtained using methods known to a skilled artisan. By way of example, the nanolipoparticles may be obtained in vitro by the addition of cholesterol and phosphatidylcholine to the conjugate of the invention as described by Lerch, et al. (Vox Sang, 1996, 71: 155-164) or in vivo by the use of a transgenic non-human animal which expresses in the liver the conjugate of the invention, resulting in the secretion to the serum of nanoparticles from where they can be isolated.
The conjugates of the invention are useful for carrying compounds of therapeutic interest to the liver and stabilizing them. Therefore, in another aspect, the invention relates to a pharmaceutical preparation comprising a therapeutically effective amount of a conjugate, of a polynucleotide, of a gene construct, of a vector, or a host cell or of a nanolipoparticle according to the invention and a pharmaceutically acceptable carrier or excipient.
In another aspect, the invention relates to a polypeptide of the invention, a polynucleotide of the invention, a gene construct of the invention, a vector of the invention, a nanolipoparticle of the invention or a pharmaceutical composition for its use in medicine.
For the use in medicine, the conjugates of the invention can be found in the form of prodrug, salt, solvate or clathrate, either in an isolated form or in combination with additional active agents. The combinations of compounds according to the present invention can be formulated together with an excipient which is acceptable from the pharmaceutical point of view. Preferred excipients for their use in the present invention include sugars, starches, celluloses, gums and proteins. In a particular embodiment, the pharmaceutical composition of the invention will be formulated in a solid pharmaceutical dosage form (for example tablets, capsules, coated tablets, granules, suppositories, crystalline or amorphous sterile solids which can be reconstituted to provide liquid forms etc.), liquid pharmaceutical dosage form (for example solutions, suspensions, emulsions, elixirs, lotions, unguents etc.) or semisolid pharmaceutical dosage form (gels, ointments, creams and the like). The pharmaceutical compositions of the invention can be administered by any route including, without being limited to, oral, intravenous, intramuscular, intra-arterial, intramedullary, intrathecal, intraventricular, transdermal, subcutaneous, intraperitoneal, intranasal, enteral, topical, sublingual or rectal route. A review of the different forms of administration of active ingredients, of the excipients to be used and of the processes for manufacturing them can be found in Tratado de Farmacia Galénica, C. Fauli i Trillo, Luzan 5, S. A. de Ediciones, 1993 and in Remington's Pharmaceutical Sciences (A. R. Gennaro, Ed.), 20th edition, Williams & Wilkins Pa., USA (2000) Examples of pharmaceutically acceptable vehicles are known in the state of the art and include phosphate-buffered saline solutions, water, emulsions, such as oil/water emulsions, different types of wetting agents, sterile solutions, etc. The compositions comprising said vehicles can be formulated by conventional processes known in the state of the art.
In the event that nucleic acids (the polynucleotides of the invention, the vectors or the gene constructs) are administered, the invention provides pharmaceutical compositions especially prepared for the administration of said nucleic acids. The pharmaceutical compositions can comprise said nucleic acids in naked form, i.e., in the absence of compounds protecting the nucleic acids from their degradation by the nucleases of the organism, which involves the advantage that the toxicity associated to the reagents used for the transfection is eliminated. Suitable routes of administration for the naked compounds include intravascular, intratumoral, intracranial, intraperitoneal, intrasplenic, intramuscular, subretinal, subcutaneous, mucosal, topical and oral route (Templeton, 2002, DNA Cell Biol., 21:857-867). Alternatively, the nucleic acids can be administered forming part of liposomes, conjugated to cholesterol or conjugated to compounds which can promote the translocation through cell membranes such as peptide Tat derived from the HIV-1 TAT protein, the third helix of the homeodomain of the D. melanogaster Antennapedia protein, the VP22 protein of the herpes simplex virus, arginine oligomers and peptides such as those described in WO07069090 (Lindgren, A. et al., 2000, Trends Pharmacol. Sci, 21:99-103, Schwarze, S. R. et al., 2000, Trends Pharmacol. Sci., 21:45-48, Lundberg, M et al., 2003, Mol. Therapy 8:143-150 and Snyder, E. L. and Dowdy, S. F., 2004, Pharm. Res. 21:389-393). Alternatively, the polynucleotide can be administered forming part of a plasmid vector or of a viral vector, preferably vectors based on adenoviruses, in adeno-associated viruses or in retroviruses, such as viruses based on the murine leukemia virus (MLV) or in lentiviruses (HIV, FIV, EIAV).
In another embodiment, the compositions and polynucleotides of the invention are administered by means of the so-called “hydrodynamic administration”, as has been described by Liu, F., et al., (Gene Ther, 1999, 6:1258-66). According to said method, the compounds are intravascularly introduced in the organism at a high rate and volume, which results in high transfection levels with a more diffused distribution. It has been demonstrated that the efficacy of the intracellular access depends directly on the volume of fluid administered and on the rate of the injection (Liu et al., 1999, Science, 305:1437-1441). In mice, the administration has been optimized in values of 1 ml/10 g of body weight in a period of 3-5 seconds (Hodges et al., 2003, Exp. Opin. Biol. Ther, 3:91-918). The exact mechanism allowing in vivo cell transfection with polynucleotides after their hydrodynamic administration is not completely known. In the case of mice, it is believed that the administration through the tail vein takes place at a rate exceeding the heart rate, which causes the administered fluid to accumulate in the superior vena cava. This fluid subsequently accesses the vessels in the organs and, subsequently, through fenestrations in said vessels, it accesses the extravascular space. The polynucleotide thus comes into contact with the cells of the target organ before it is mixed with blood, thus reducing the possibilities of degradation by nucleases.
The compositions of the invention can be administered in doses of less than 10 mg per kilogram of body weight, preferably less than 5, 2, 1, 0.5, 0.1, 0.05, 0.01, 0.005, 0.001, 0.0005, 0,0001, 0.00005 or 0.00001 mg per kg of body weight and less than 200 nmol of RNA agent, i.e., about 4.4×1016 copies per kg of body weight or less than 1500, 750, 300, 150, 75, 15, 7.5, 1.5, 0.75, 0.15 or 0.075 nmol per kg of body weight. The unit doses can be administered by injection, by inhalation or by topical administration. The bifunctional polynucleotides and compositions of the invention can be administered directly in the organ in which the target mRNA is expressed, in which case doses of between 0.00001 mg to 3 mg per organ, or preferably between 0.0001 and 0.001 mg per organ, about 0.03 and 3.0 mg per organ, about 0.1 and 3.0 mg per organ or between 0.3 and 3.0 mg per organ are administered.
The dose depends on the severity and response of the condition to be treated and can vary between several days and several months or until it is observed that the condition remits. The optimal dosage can be determined by carrying out periodic measurements of the concentrations of the agent in the organism of the patient. The optimal dose can be determined from the EC50 values obtained by means of prior in vitro or in vivo assays in animal models. The unit dose can be administered once a day or less than once a day, preferably less than once every 2, 4, 8 or 30 days. Alternatively, it is possible to administer an initial dose followed by one or several maintenance doses, generally of a smaller amount than the initial dose. The maintenance regimen can involve treating the patient with doses ranging between 0.01 μg and 1.4 mg/kg of body weight per day, for example 10, 1, 0.1, 0.01, 0.001, or 0.00001 mg per kg of body weight per day. The maintenance doses are preferably administered at most once every 5, 10 or 30 days. The treatment must be continued for a time period which will vary according to the type of disorder that the patient suffers from, its severity and the condition of the patient. After the treatment, the evolution of the patient must be monitored to determine if the dose must be increased in the event that the disease does not respond to the treatment or the dose is decreased if an improvement of the disease is observed or if undesirable side effects are observed.
The daily dose can be administered in a single dose or in two or more doses according to the particular circumstances. If a repeated administration or frequent administrations are desired, the implantation of an administration device such as a pump, a semi-permanent (intravenous, intraperitoneal, intracisternal or intracapsular) catheter or a reservoir is recommendable.
The conjugates of the invention, the polynucleotides encoding them, the gene constructs and vectors comprising said polynucleotides and the nanolipoparticles of the invention can be used in methods of therapeutic treatment given the capacity of said conjugates of carrying a compound of therapeutic interest to a target tissue. A person skilled in the art will understand that the diseases which can be treated with the compounds of the invention will depend (i) on the active component which is associated to Apo A and (ii) on the tissue to which said conjugates are carried. Table 2 describes, in a non-limiting manner, possible diseases which can be treated with said conjugates and the active ingredient which would have to be incorporated to the conjugate:
The conjugates of the invention have the capacity to be targeted to the organs or tissues in which there is expression of surface molecules with sufficient affinity for ApoA and with the capacity to be internalized after the binding with said polypeptide. Said surface molecules include SR-B1 (scavenger receptor B type 1), SR-A1 (scavenger receptor A type 1), SR-A2 (scavenger receptor A type 1) and SR-C (scavenger receptor C). The therapeutically active compounds can thus be carried to said target organs or tissues. These organs include not only the liver, but also all the cells expressing on their surface sufficient amounts of the SR-BI receptor. Example 7 of the present invention thus illustrates the presence of the SR-BI receptor in different populations of the immune system and, in particular, in CD4+ T cells, in CD8+ T cells, in NK cells; in dendritic cells and in monocytes/macrophages. The invention thus also provides the use of the conjugates of the invention for the treatment of diseases associated to the immune system. Additionally, the expression of the SR-BI receptor in osteoclasts (Brodeur et al., 2008, J. Bone Miner Res. 23:326-37), in endothelial cells (Yeh et al., 2002, Atherosclerosis, 161:95-103), intestinal epithelium (Cai, S. F. et al., 2001, J. Lipid Res. 42:902-909), in the bile duct epithelium (Miguel et al., Gut., 2003, 52:1017-1024), in adipose tissue (Acton et al., 1994, J. Biol. Chem., 269:21003-21009) and in the lung (Acton et al., 1994, J. Biol. Chem., 269:21003-21009) is known.
Therefore, the conjugates of the present invention are suitable for carrying compounds of therapeutic interest to the previously indicated compartments. Thus, considering the target organ, the conjugates of the invention can be used for the treatment of liver diseases such as intrahepatic cholestasis, fatty liver (alcoholic fatty liver, Reye's syndrome), hepatic vein thrombosis, hepatoventricular degeneration, hepatomegaly, hepatopulmonary syndrome, hepatorenal syndrome, portal hypertension, hepatic abscesses, cirrhosis (alcoholic, biliary, experimental cirrhosis), alcoholic liver diseases (fatty liver, hepatitis, cirrhosis), parasitic diseases (echinococcosis, fascioliasis, amebic abscesses), jaundice (hemolytic, hepatocellular and cholestatic), hepatitis (alcoholic hepatitis, chronic hepatitis, autoimmune hepatitis, hepatitis B, hepatitis C, hepatitis D, drug-induced hepatitis, toxic hepatitis, viral hepatitis (hepatitis A, B, C, D and E), Wilson's disease, granulomatous hepatosis, secondary biliary cirrhosis, primary biliary cirrhosis, hepatic encephalopathy, portal hypertension, hepatocellular adenoma, hemangioma, gallstones, hepatic neoplasms (angiomyolipoma, calcified liver metastases, cystic liver metastases, fibrolamellar hepatocarcinoma, focal nodular hyperplasia, hepatic adenoma, hepatobiliary cystadenoma, hepatoblastoma, hepatocellular carcinoma, hepatoma, liver cancer, hepatic hemangioendothelioma, regenerative nodular hyperplasia, benign liver tumors, hepatic cysts (simple cysts, polycystic cysts, hepatobiliary cystadenoma, mesenchymal liver tumors [mesenchymal hamartoma, infantile hemangioendothelioma, hemangioma, peliosis hepatis, lipomas, inflammatory pseudotumor], epithelial bile duct tumors, bile duct hamartoma, bile duct adenoma, malignant liver tumors [hepatocellular, hepatoblastoma, hepatocellular carcinoma, cholangiocellular cancer, cholangiocarcinoma, cystadenocarcinoma, capillary tumors, angiosarcoma, Kaposi's sarcoma, hemangioendothelioma, embryonal sarcoma, fibrosarcoma, leiomyosarcoma, rhabdomyosarcoma, carcinosarcoma, teratoma, squamous carcinoma, primary lymphoma]), erythrohepatic porphyria, hepatic porphyria (acute intermittent porphyria, late cutaneous porphyria), Zellweger syndrome.
The conjugates of the invention can be used for the treatment of immune system diseases such as:
The conjugates of the invention can be used for the treatment of capillary endothelium diseases such as arteriosclerosis, obliterative arteriopathy, Raynaud's disease due to connectivitis, primitive hypertension and secondary pulmonary hypertension, diabetic microangiopathy, Buerger's disease, systemic sclerosis, vasculitis and all the diseases characterized by endothelial damage with the subsequent ischemia.
The conjugates of the invention can be used for the treatment of bone diseases such as dysplasias characterized by an abnormal bone growth. Representative examples of such conditions are achondroplasia, cleidocranial dysostosis, enchondromatosis, fibrous dysplasia, Gaucher's disease, hypophosphatemic rickets, Marfan syndrome, hereditary multiple exostoses, neurofibromatosis, osteogenesis imperfecta, osteopetrosis, osteopoikilosis, sclerotic lesions, fractures, periodontal disease, pseudoarthrosis, pyogenic osteomyelitis, conditions resulting in osteopenia such as anemic conditions, osteopenia caused by steroids and heparin, bone marrow disorders, scurvy, malnutrition, calcium deficiency, idiopathic osteoporosis, congenital osteopenia, alcoholism, Cushing's disease, acromegaly, hypogonadism, transient regional osteoporosis and osteomalacia.
The conjugates of the invention can be used for the treatment of intestinal epithelium diseases such as malabsorption syndromes, Crohn's disease, intestinal diverticular disease, paralytic ileus and intestinal obstruction.
The conjugates of the invention can be used for the treatment of respiratory diseases such as nasal vestibulitis, non-allergic rhinitis (for example, acute rhinitis, chronic rhinitis, atrophic rhinitis, vasomotor rhinitis), nasal polyps, sinusitis, juvenile angiofibromas, nose cancer and juvenile papillomas, vocal cord polyps, nodules, contact ulcers, vocal cord paralysis, laryngoceles, pharyngitis, tonsillitis, tonsillar cellulitis, parapharyngeal abscesses, laryngitis, laryngocele, throat cancer (for example, nasopharyngeal cancer, tonsil cancer, larynx cancer), lung cancer (squamous cell carcinoma, microcytic carcinoma, macrocytic carcinoma, adenocarcinoma), allergic disorders (eosinophilic pneumonia, allergic alveolitis, allergic interstitial pneumonia, allergic bronchopulmonary aspergillosis, asthma, Wegener's granulomatosis, Goodpasture's syndrome, pneumonia (for example, bacterial pneumonia (for example, that caused by Streptococcus pneumoniae, by Staphylococcus aureus, by Gram-negative bacteria such as Klebsiella and Pseudomonas spp, that caused by Mycoplasma pneumoniae, by Haemophilus influenzae, by Legionella pneumophil and by Chlamydia psittaci and viral pneumonias (for example, influenza or chicken pox), bronchiolitis, polio, laryngotracheobronchitis (also called croup syndrome), respiratory infection due to syncytial viruses, mumps, erythema infectiosum, roseola infantum, rubella, fungal pneumonia, (for example histoplasmosis, coccidioidomycosis, blastomycosis and fungal infections in immunosuppressed patients such as cryptococcosis caused by Cryptococcus neoformans; aspergillosis caused by Aspergillus spp.; candidiasis, caused by Candida; and mucormycosis), infection due to Pneumocystis carinii, atypical pneumonias (for example, those caused by Mycoplasma and Chlamydia spp.), opportunistic pneumonia, nosocomial pneumonia, chemical pneumonitis and aspiration pneumonia, pleural disorders (for example pleurisy, pleural effusion and pneumothorax (for example simple spontaneous pneumothorax, complex spontaneous pneumothorax, tension pneumotorax), obstructive respiratory tract disease (for example asthma, chronic obstructive pulmonary disease, emphysema, chronic or acute bronchitis), occupational pulmonary diseases (for example silicosis, black lung disease, asbestosis, berylliosis, occupational asthma, byssinosis and benign pneumoconiosis), infiltrative pulmonary disease such as pulmonary fibrosis, fibrosing alveolitis, idiopathic pulmonary fibrosis, desquamative interstitial pneumonia, lymphoid interstitial pneumonia, histiocytosis X (for example Letterer-Siwe disease, Hand-Schuller-Christian disease, eosinophilic granuloma), idiopathic pulmonary hemosiderosis, sarcoidosis and pulmonary alveolar proteinosis, acute respiratory distress syndrome, edema, pulmonary embolism, bronchitis (for example, viral, bacterial bronchitis), bronchiectasis, atelectasis, lung abscesses and cystic fibrosis.
In a preferred embodiment, the invention contemplates that the therapeutically active component is an interferon. In that case, the conjugates or the polynucleotides encoding them will be useful for the treatment of liver diseases responding to interferon, such as chronic hepatitis C, chronic hepatitis B, hepatocarcinoma, cirrhosis, fibrosis.
In addition, given the presence of SR-BI receptors in immune system cells, the conjugates of the invention can be used to target therapeutically active compounds to said cells. Thus, in a preferred embodiment, the conjugates of the invention containing interferon as the therapeutically active compound can be used as an adjuvant for enhancing the immune response of a vaccine. The vaccine can be a vaccine targeted against an organism capable of triggering an infectious disease, a vaccine targeted against a tumor or a vaccine targeted against an allergen. The vaccines can contain a component of an infectious agent, a tumor or an allergen (peptide, polypeptide, glycopeptide, multiepitope peptide, fragment, etc.) or can be a gene vaccine formed by a nucleic acid encoding a polypeptide of said organism, tumor or allergen.
In another embodiment, the conjugates of the invention comprise a TGF-β1 peptide inhibitor. These conjugates can be used in the treatment of diseases or pathological disorders associated to an excess or deregulated expression of TGF-β1, such as (i) fibrosis associated with the loss of function of an organ or a tissue, for example, pulmonary fibrosis, hepatic fibrosis (cirrhosis), cardiac fibrosis, renal fibrosis, corneal fibrosis, etc., as well as (ii) surgical and aesthetic complications, for example, fibrosis associated with cutaneous and peritoneal surgery, fibrosis associated with burns, osteoarticular fibrosis, keloids, etc.
The authors of the present invention have shown that the administration of the conjugates of the invention comprising a TGF-β1 peptide inhibitor together with IL-12 results in a stimulation of the induction of IFN-gamma mediated by IL-12. Given that IFN-γ is a known antitumor agent, the findings of the inventors opens up the way for a new antitumor treatment based on the combination of an immunostimulating cytokine and to a conjugate according to the invention comprising a TGF-β1 inhibitor peptide.
Therefore, in another aspect, the invention relates to a composition comprising
Immunostimulating cytokines which can be administered together with the Apo A conjugates comprising the TGF-β1 inhibitor peptides include, but are not limited to, IL-12, IL-2, IL-15, IL-18, IL-24, GM-CSF, TNF-α, CD40 ligand, IFN-α, IFN-β, IFN-γ. In a preferred embodiment, the stimulating cytokine is IL-12.
TGF-β1 inhibitor peptides that may form component (b) of the composition of the invention are essentially the same as those that form part of the conjugate of the invention as described previously. Thus, the TGF-β1 inhibitor peptides may be, without limitation, peptide p144 (SEQ ID NO:4) or peptide p17 (SEQ ID NO:5). The peptides forming part of the conjugate and forming the second component of the invention may be the same or different.
A “cytotoxic agent”, as used herein, is a compound capable of selectively or non-selectively killing or inhibiting the growth of a cell. Examples include paclitaxel, cytochalasin B, gramicidin D, ethidium bromide, emetine, mitomycin, etoposide, tenoposide, vincristine, vinblastine, colchicin, doxorubicin, daunorubicin, dihydroxy anthracin dione, mitoxantrone, mithramycin, actinomycin D, 1-dehydrotestosterone, glucocorticoids, procaine, tetracaine, lidocaine, propranolol, puromycin, epirubicin, and cyclophosphamide and analogs or homologs thereof, antimetabolites (e.g., methotrexate, 6-mercaptopurine, 6-thioguanine, cytarabine, 5-fluorouracil decarbazine), alkylating agents (e.g., mechlorethamine, thioepa chlorambucil, melphalan, carmustine (BCNU) and lomustine (CCNU), busulfan, dibromomannitol, streptozotocin, mitomycin C, and cisdichlorodiamine platinum (II) (DDP) cisplatin), anthracyclines (e.g., daunorubicin and doxorubicin), antibiotics (e.g., dactinomycin), bleomycin.
In another aspect, the compositions of the invention can be used for the treatment of different types of tumors including, but not limited to, hematological cancers (leukemias or lymphomas, for example), neurological tumors (astrocytomas or glioblastomas, for example), melanoma, breast cancer, lung cancer, head and neck cancer, gastrointestinal tumors (stomach, pancreas or colon cancer, for example), liver cancer (for example, hepatocellular carcinoma), renal cell cancer, genitourinary tumors (ovarian cancer, vaginal cancer, cervical cancer, bladder cancer, testicle cancer, prostate cancer, for example) bone tumors and vascular tumors.
Thus, in another aspect, the invention relates to a composition of the invention for the treatment of cancer. In another aspect, the invention relates to a method for the treatment of cancer which comprises the administration to a subject in need thereof of a composition according to the invention. In another aspect, the invention relates to the use of a composition of the invention for the preparation of a medicament for the treatment of cancer.
The therapeutically effective amounts of the components of the composition of the invention as described herein to be used will depend, for example, upon the therapeutic objectives, the route of administration, and the condition of the patient. Accordingly, it is preferred for the therapist to titer the dosage and modify the route of administration as required to obtain the optimal therapeutic effect. A typical daily dosage might range from about 0.01 mg/kg to up to 250 mg/kg or more, daily, every 2 days, every 3 days, every 4 days, every 5 days, every 6 days or weekly.
Administration of the composition may carried out by different means. For example components (a) and (b) of the composition may be administered sequentially, separately and/or simultaneously. In one embodiment, components (a) and (b) of the composition are administered simultaneously (optionally repeatedly). In one embodiment the separate formulations are administered sequentially (optionally repeatedly). In one embodiment the separate formulations separately (optionally repeatedly). The skilled person will understand that where the separate formulations of components (a) and (b) are administered sequentially or serially, that this could be administration of component (a) followed by component (b) or component (b) followed by component (a). In one embodiment the separate formulations of components (a) and (b) may be administered in alternative dosing patterns. Where the administration of the separate formulations of components (a) and (b) of the composition of the invention is sequential or separate, the delay in administering the second formulation should not be such as to lose the beneficial effect of the combination therapy.
The invention is illustrated below based on the following examples which are provided by way of a non-limiting illustration of the scope of the invention.
1.1 RNA extraction:
Total RNA from mice liver or from brain of treated mice was isolated from individual samples using TRI reagent (Sigma, Madrid, Spain). The concentration and purity of the samples were determined by the absorbance at 260 and 280 nm with background correction at 320 nm in a spectrophotometer (Biophotometer, Eppendorf).
1.2 RT-PCR Synthesis of Total cDNA:
The total RNA (3 μg) was treated with DNase I and retrotranscribed to cDNA with M-MLV RT in the presence of RNase OUT (all the reagents were from Invitrogen, Carlsbed, Calif.). 25 μl of liver total cDNA were obtained. The reaction was incubated for 1 hour at 37° C., denatured for 1 minute at 95° C. and taken to 4° C. The samples were used immediately for PCR or stored at −20° C.
1.3 Obtaining and Cloning Murine Apolipoprotein A1(mApoA1) cDNA:
The sense primer 5′-ATGAAAGCTGTGGTGCTGGC-3′ (FwATGmApoA1) (SEQ ID NO: 20) and the antisense primer 5′-TCACTGGGCAGTCAGAGTCT-3′ (RvTGAmApoA1) (SEQ ID NO: 21) were designed. The mApoA1 cDNA (795 total nucleotides, 72 nucleotides encoding the signal peptide and 723 nucleotides encoding the native protein) was amplified by means of PCR on the liver total cDNA, using BioTaq DNA polymerase (Bioline, London, United Kingdom): 5 minutes at 94° C., 30 cycles of 40 seconds at 94° C., 40 seconds at 55° C. and 40 seconds at 72° C., followed by 7 minutes at 72° C. in a 2720 Thermal cycler (Applied Biosystems, Foster City, USA). The PCR product was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified by means of a QIAquick Gel Extraction Kit (Qiagen, Valencia, Calif.). The purified cDNA of mApoA1 was cloned, according to the instructions provided by the manufacturer, into the expression vector pcDNA™ 3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV-mApoA1. Finally, the sequence obtained was confirmed by means of sequencing.
1.4 Obtaining and Cloning of Murine Interferon Alpha 1 (mIFNα1) cDNA:
The sense primer 5′-ATGGCTAGGCTCTGTGCTTT-3′ (FwATGmIFNα1) (SEQ ID NO: 22) and the antisense primer 5′-TCATTTCTCTTCTCTCAGTC-3′ (RvTGAmIFNα1) (SEQ ID NO:23) were designed. The mIFNα1 cDNA (570 total nucleotides, 69 nucleotides encoding the signal peptide and 501 nucleotides encoding the native protein) was amplified by means of PCR on the liver total cDNA, using BioTaq DNA polymerase (Bioline, London, United Kingdom). The amplification conditions were: 5 minutes at 94° C., 30 cycles of 40 seconds at 94° C., 40 seconds at 55° C. and 40 seconds at 72° C., followed by 7 minutes at 72° C. in a 2720 Thermal cycler (Applied Biosystems Foster City, USA). The PCR product was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified by means of a QIAquick Gel Extraction Kit (Qiagen, Valencia, Calif.). The purified cDNA of mIFNα1 was cloned, according to the provided instructions, into the expression vector pcDNA™ 3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV-mIFNα1. Finally, the sequence was confirmed by means of sequencing.
1.5.1 C-Terminal Fusion of the mIFNα1 Gene to the mApoA1 Gene: Apo-IFN
The antisense primer 5′-GGCGCGCCCTGGGCAGTCAGAGTCTCGC-3′ (RvAscImApoA1) (SEQ ID NO:24) was designed, which introduces the 9-nucleotide sequence (GGCGCGCCC) which forms a restriction site for the AscI enzyme in 3′ of the ApoA1 gene and eliminates the stop codon. This added restriction sequence will be translated into a short binding peptide GAP, which will provide certain mobility to the constituent proteins. The sense primer 5′GGCGCGCCCTGTGACCTGCC TCAGACTCA-3′ (FwAscImIFNα1) (SEQ ID NO:25) was designed, which introduces the AscI restriction sequence in 5′ of the sequence encoding the mature mIFNα1 protein (i.e., elimination of the signal peptide sequence).
Amplification was carried out by PCR, using pCMV-mApoA1 as a template, and the primers FwATGmApoA1 and RvAscImApoA1, with the BioTaq DNA polymerase enzyme (Bioline, London, United Kingdom), 5 minutes at 94° C., 30 cycles of 40 seconds at 94° C., 40 seconds at 57° C. and 40 seconds at 72° C., followed by 7 minutes at 72° C. in a 2720 Thermal cycler (Applied Biosystems Foster City, USA). The PCR product (804 nucleotides) was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified by means of a QIAquick Gel Extraction Kit (Qiagen, Valencia, Calif.). The purified DNA of mApoA1-AscI was cloned, according to the provided instructions, into the expression vector pcDNA™3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV-mApoA1-AscI. Finally, the sequence was confirmed by means of sequencing.
In parallel, amplification was carried out by PCR using pCMV-mIFNα1 as a template and the primers FwAscImIFNα1 and RvTGAmIFNα1. The BioTaq DNA polymerase enzyme (Bioline, London, United Kingdom) and the following amplification conditions were used: 5 minutes at 94° C., 30 cycles of 40 seconds at 94° C., 40 seconds at 57° C. and 40 seconds at 72° C., followed by 7 minutes at 72° C. in a 2720 Thermal cycler (Applied Biosystems Foster City, USA). The PCR product (510 nucleotides) was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified by means of a QIAquick Gel Extraction Kit (Qiagen, Valencia, Calif.). The purified DNA of AscI-mIFNα1 was cloned, according to the provided instructions, into the expression vector pcDNA™3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV-AscI-mIFNα1. Finally, the sequence was confirmed by means of sequencing.
To carry out the gene fusion, the plasmids pCMV-mApoA1-AscI and pCMV-AscI-mIFNα1 were digested independently for 1.5 hours at 37° C. with the AscI/PmeI enzymes, 1×BSA and Buffer 4 (New England Biolabs), using the restriction site PmeI present in the pcDNA 3.1 V5-His TOPO® TA skeleton. Both digestions were migrated in 1% agarose gel and the corresponding bands were purified to the open vector pCMV-mApoA1-AscI and to the pCMV-AscI-mIFNα1 insert. The product was ligated in a 1:3 (vector:insert) ratio using T4 DNA ligase High Concentration and a 2× Rapid Ligation Buffer (Promega Madison, Wl, USA) as a buffer solution, incubating the mixture for 10 minutes at room temperature. Top10 bacteria (Invitrogen, Carlsbed, Calif.) were subsequently transformed. The transformed bacteria were selected by their growth in Petri dishes with LB medium with ampicillin, since the vector contains a gene resistant to this antibiotic. The plasmid DNA of the positive bacteria was extracted by means of the MiniPrep technique (Qiagen, Germany) to subsequently digest 2 μg of said plasmid with the AscI/PmeI enzymes (New England Biolabs) and separate by electrophoresis the result of said digestion in 1% agarose gel to verify the presence of the insert. The resulting 6825 nt plasmid will hereinafter be called pCMV-Apo-IFN (pCMV-AF).
1.5.2 N-Terminal Fusion of the mIFNα1 Gene to the mApoA1 Gene: IFN-Apo
The antisense primer 5′-GGGCGCGCCTTTCTCTTCTCTCAGTCTTC-3′ (RvAscImIFNα1) (SEQ ID NO:26) was designed, which introduces the 9-nucleotide sequence (GGCGCGCCC) which forms a restriction site for the AscI enzyme in 3′ of the mIFNα1 gene and eliminates the stop codon. The sense primer 5′-CCAGGCGCGCCGGATGAACCCCAGTCCCAATG-3′ (FwAscImApoA1) (SEQ ID NO:27) was designed, which introduces the AscI restriction sequence in 5′ of the sequence encoding the mature mApoA1 protein (i.e., elimination of the signal peptide sequence). This primer includes 3 nucleotides in 5′ to allow the cleavage with AscI.
Amplification was carried out by PCR using pCMV-mApoA1 as a template, and the primers FwAscImApoA1 and RvTGAmApoA1, with the BioTaq DNA polymerase enzyme (Bioline, London, United Kingdom), using the following amplification conditions: 5 minutes at 94° C., 30 cycles of 40 seconds at 94° C., 40 seconds at 57° C. and 40 seconds at 72° C., followed by 7 minutes at 72° C. in a 2720 Thermal cycler (Applied Biosystems Foster City, USA). The PCR product (732 nucleotides) was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified by means of a QIAquick Gel Extraction Kit (Qiagen, Valencia, Calif.). The purified DNA of AscI-mApoA1 was cloned, according to the provided instructions, into the expression vector pcDNA™ 3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV-AscI-mApoA1. Finally, the sequence was confirmed by means of sequencing.
In parallel, amplification was carried out by using PCR pCMV-mIFNα1 as a template and the primers FwATGmIFNα1 and RvAscImIFNα1 with the BioTaq DNA polymerase enzyme (Bioline, London, United Kingdom) and the following conditions: 5 minutes at 94° C., 30 cycles of 40 seconds at 94° C., 40 seconds at 57° C. and 40 seconds at 72° C., followed by 7 minutes at 72° C. in a 2720 Thermal cycler (Applied Biosystems Foster City, USA). The PCR product (576 nucleotides) was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified by means of a QIAquick Gel Extraction Kit (Qiagen, Valencia, Calif.). The purified DNA of mIFNα1-AscI was cloned, according to the provided instructions, in the expression vector pcDNA™ 3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV-mIFNα1-AscI. Finally, the sequence was confirmed by means of sequencing.
To carry out the gene fusion, plasmids pCMV-AscI-mApoA1 and pCMV-mIFNα1-AscI were digested independently for 1.5 hours at 37° C. with the AscI/PmeI enzymes, 1×BSA and Buffer 4 (New England Biolabs), using the restriction site PmeI present in the pcDNA 3.1 V5-His TOPO® TA skeleton. Both digestions were migrated in a 1% agarose gel and the corresponding bands were purified to the open vector pCMV-mIFNα1-AscI and to the pCMV-AscI-mApoA1 insert. The product was ligated in a 1:3 (vector:insert) ratio using T4 DNA ligase High Concentration and 2× Rapid Ligation Buffer (Promega Madison, Wl, USA) as a buffer solution, incubating the mixture for 10 minutes at room temperature. Top10 bacteria (Invitrogen, Carlsbed, Calif.) were subsequently transformed. The transformed bacteria were selected by their growth in Petri dishes with LB medium with ampicillin, since the vector contains a gene resistant to this antibiotic. The plasmid DNA of positive bacteria was extracted by means of the MiniPrep technique (Qiagen, Germany) to subsequently digest 2 μg of said plasmid with the AscI/PmeI enzymes (New England Biolabs) and separate by electrophoresis the result of said digestion in a 1% agarose gel to verify the presence of the insert. The resulting 6822-nucleotide plasmid will hereinafter be called pCMV-IFN-Apo (pCMV-IA).
1.5.3 C-Terminal Fusion of Peptide p17 to the mApoA1 Gene:
The primer 5′-TCACGCACGCTCATACCAAGAACTCCTAGGAATAAACCAAATACGCTTGGGCGC GCCCTGGGC-3′ (RvmApoA1p17) (SEQ ID NO:28) was designed. It was amplified by PCR, with the Easy-A High Fidelity PCR cloning enzyme (Stratagene, La Jolla, Calif.) using pCMV-mApoA1-AscI as a template and the primers FwATGmApoA1 and RvmApoA1p17. The following conditions were used: 1 minute at 95° C., 30 cycles of 40 seconds at 95° C., 40 seconds at 60° C. and 1 minute at 72° C., followed by 7 minutes at 72° C. in a 2720 Thermal cycler (Applied Biosystems Foster City, USA). The PCR product was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified by means of a QIAquick Gel Extraction Kit (Qiagen, Valencia, Calif.). The purified DNA of mApoA1-AscI-p17 was cloned, according to the provided instructions, in the expression vector pcDNA™3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV-mApoA1-AscI-p17. Finally, the sequence was confirmed by means of sequencing.
1.5.4 C-Terminal Fusion of Peptide p144 to the mApoA1 Gene:
The primer 5′-TCAATTCTGCATCATGGCCCAGATTATCGAGGCGTCCAGCGAGGTGGGCGCGCC CTGGGC-3′ (RvmApoA1p144) (SEQ ID NO:29) was designed. It was amplified by PCR, with the Easy-A High Fidelity PCR cloning enzyme (Stratagene, La Jolla, Calif.) using pCMV-mApoA1-AscI as a template and the primers FwATGmApoA1 and RvmApoA1p144. The following conditions were used: 1 minute at 95° C., 30 cycles of 40 seconds at 95° C., 40 seconds at 65° C. and 1 minute at 72° C., followed by 7 minutes at 72° C. in a 2720 Thermal cycler (Applied Biosystems Foster City, USA). The PCR product was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified by means of QIAquick Gel Extraction Kit (Qiagen, Valencia, Calif.). The purified DNA of mApoA1-AscI-p144 was cloned, according to the provided instructions, in the expression vector pcDNA™3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV-mApoA1-AscI-p144. Finally, the sequence was confirmed by means of sequencing.
1.5.5 Cloning the Gene Sequence of the mApoA1 Signal Peptide:
To construct plasmids which will serve as a control in the fusion mApoA1 and peptide fusion experiments, the gene fusion of the mApoA1 signal peptide sequence (SPmApoA1) with peptides p17 and p144 is carried out (without adding the sequence for AscI), and thus ensuring that the secretion of the peptide is the same as that of mApoA1-peptides. The primer 5′-TTGCTGCCATACGTGCCAAG-3′ (RvSPmApoA1) (SEQ ID NO:30) was designed, which together with the primer FwATGmApoA1 is used to amplify SPmApoA1, using pCMV-mApoA1 as a template. The PCR product (72 nucleotides) was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified by means of QIAquick Gel Extraction Kit (Qiagen, Valencia, Calif.). The purified DNA of SPmApoA1 was cloned, according to the provided instructions, in the expression vector pcDNA™ 3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV-SPmApoA1. Finally, the sequence was confirmed by means of sequencing.
1.5.6 C-Terminal Fusion of Peptide p17 to the mApoA1 Signal Peptide Gene Sequence:
The primer 5′-TCACGCACGCTCATACCAAGAACTCCTAGGAATAAACCAAATACGCTTTTGCTG CCAGAAATGCCG-3′ (RvSPmApoA1p17) (SEQ ID NO:31) was designed, which together with the primer FwATGmApoA1 was used to amplify SPmApoA1-p17, starting from the pCMV-mApoA1 template. The PCR product (120 nucleotides) was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified by means of QIAquick Gel Extraction Kit (Qiagen, Valencia, Calif.). The purified DNA of SPmApoA1-p17 was cloned, according to the provided instructions, in the expression vector pcDNA™3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV SPmApoA1-p17. Finally, the sequence was confirmed by means of sequencing.
1.5.7 C-Terminal Fusion of Peptide p144 to the mApoA1 Signal Peptide Gene Sequence
The primer 5′-TCATTCTGCATCATGGCCCAGATTATCGAGGCGTCCAGCGAGGTTTGCTGCCAG AAATGCCG-3′ (RvSPmApoA1p144) (SEQ ID NO:32) was designed, which together with the primer FwATGmApoA1 was used to amplify SPmApoA1-p144, starting from the pCMV-mApoA1 template. The PCR product (117 nucleotides) was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified by means of QIAquick Gel Extraction Kit (Qiagen, Valencia, Calif.). The purified DNA of SPmApoA1-p144 was cloned, according to the provided instructions, in the expression vector pcDNA™ 3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV-SPmApoA1-p144. Finally, the sequence was confirmed by means of sequencing.
1.5.8 Introduction of MMP9 Sequence in pCMV-mApoA1-AscI-p144:
For the purpose of providing the fusion protein generated from this gene with the possibility of release by the cleavage of peptide p144, the proteases capable of cleaving the amino acid sequence of the fusion protein, releasing the complete p144 were studied by means of the MEROPS database (http://merops.sanger.ac.uk/). The result of the search gave as a candidate metalloprotease-9 (MMP9), which carried out the cleavage leaving an amino acid S in the p144 sequence. The use of this protease further conferred to the construct the capacity of release of this TGF-β inhibitor in the sites where its inhibition is necessary (localized, and not systemic, inhibition), since its presence in carcinomas has been described. The DNA sequence CTTTTCCCGACGTCT (SEQ ID NO:51) (amino acids: LFPTS, SEQ ID NO:19) will be translated into said cleavage site: LFPT-S TSLDASIIWAMMQN (SEQ ID NO:4).
The primers 5′-CCAGGCGCGCCGCTTTTCCCGACGTCTACCTCGCTGGACGCCTC-3′ (FwMMp9AscIp144) (SEQ ID NO:33) and 5′-TCAATTCTGCATCATGGCCCA-3′ (RvMMp9AscIp144) (SEQ ID NO:34) were designed. Amplification was carried out by means of the Easy-A High Fidelity PCR cloning enzyme (Stratagene, La Jolla, Calif.), using pCMV-SPmApoA1-p144 as a template. The PCR was performed with the following conditions: 2 minutes at 94° C., 30 cycles of 40 seconds at 94° C., 45 seconds at 54° C. and 40 seconds at 72° C., followed by 7 minutes at 72° C. in a 2720 Thermal cycler (Applied Biosystems Foster City, USA). The PCR product was migrated in an Agarose D-1 low EEO 1% agarose gel (Pronadisa, Madrid, Spain), and the gel fragment was purified (70 nucleotides), PerfectPrep DNA Cleanup (Eppendorf, Germany). The purified DNA of DNA AscI-MMP9-p144 was cloned, according to the instructions provided by the manufacturer, in the expression vector pcDNA™ 3.1/V5-His TOPO® TA (Invitrogen, Carlsbed, Calif.), which will be called pCMV-AscI-MMP9-p144. Finally, the sequence was confirmed by means of sequencing.
To carry out the gene fusion, plasmids pCMV-mApoA1-AscI-p144 and pCMV-AscI-MMp9-p144 were digested independently with the AscI/PmeI restriction enzymes, the latter being present in the pcDNA 3.1 V5-His TOPO® TA skeleton. The digestion was performed for 1.5 hours at 37° C. with the AscI/PmeI enzymes, 1×BSA and Buffer 4 (New England Biolabs, Beverly, USA). Both digestions were migrated in a 1% agarose gel and the corresponding bands were purified to the open vector pCMV-mApoA1-AscI-p144 and to the pCMV-AscI-MMp9-p1441 insert. The product was ligated in a 1:3 (vector:insert) ration using T4 DNA ligase High Concentration and 2× Rapid Ligation Buffer (Promega Madison, Wl, USA) as a buffer solution, incubating the mixture for 10 minutes at room temperature. Top10 bacteria (Invitrogen, Carlsbed, Calif.) were subsequently transformed. The transformed bacteria were selected by their growth in Petri dishes with LB medium with ampicillin, since the vector contains a gene resistant to this antibiotic. The plasmid DNA of the positive bacteria was extracted by means of the MiniPrep technique (Qiagen, Germany) to subsequently digest 2 μg of said plasmid with the AccI/PmeI enzymes (New England Biolabs) and separate by electrophoresis the result of said digestion in a 1% agarose gel to verify the presence of the insert. The resulting 6324-nucleotide plasmid will hereinafter be called pCMV-mApoA1-AscI-MMP9-p144.
1.5.9 Introduction of Linker Sequence in pCMV-mApoA1-p144:
For the purpose of providing the fusion protein generated from this gene with the possibility of movements between the protein and peptide p144, the DNA sequence (GCACCAGCAGAAACAAAAGCAGAACCAATGAC, SEQ ID NO:53) encoding a flexible extended linker the sequence of which translated to amino acids is APAETKAEPMT (SEQ ID NO:13) was introduced, which adopts a CCCCCCCCCCC (coil) structure, and exists as a binding peptide in the native pyruvate ferredoxin oxidoreductase (1b0pA—2).
The primers 5′-CGCGCCGGCACCAGCAGAAACAAAAGCAGAACCAATGACAACC TCGCTGGACGCCTCGATAATCTGGGCCATGATGCAGAATTGAGC-3′ (FwLINKERp144) (SEQ ID NO:35) and 5′-GGCCGCTCAATTCTGCATCATGGCCCAGATTATCGAGGCGTCCAGCGAGGTTGT CATTGGTTCTGCTTTTGTTTCTGCTGGTGCCGG-3′ (RvLINKERp144) (SEQ ID NO:36) were designed at a 100 mM concentration each. 10 μl of each primer were mixed and hybridized in a thermal cycler: 2 minutes at 95° C., 10 minutes at 52° C. and taken to 4° C. The hybridization of these primers is complete in the sequence corresponding to the linker and to p144, but leaves sticky ends compatible with the cleavage by AscI in 5′, and compatible with NotI in 3′.
The plasmid pCMV-mApoA1-AscI-p144 was digested with AscI (Buffer 4, New England Biolabs), the DNA was purified, with PerfectPrep DNA Cleanup (Eppendorf, Germany), and it was subsequently digested with NotI (Buffer 3 and BSA, New England Biolabs), due to the incompatibility of digestion buffers. A 1% agarose gel was migrated, the open vector was purified with PerfectPrep DNA Cleanup (Eppendorf, Germany). The product was ligated in a 1:3 (vector:insert) ratio using T4 DNA ligase High Concentration and 2× Rapid Ligation Buffer (Promega Madison, Wl, USA) as a buffer solution, incubating the mixture for 10 minutes at room temperature. Top10 bacteria (Invitrogen, Carlsbed, Calif.) were subsequently transformed. The transformed bacteria were selected by their growth in Petri dishes with LB medium with ampicillin, since the vector contains a gene resistant to this antibiotic. The resulting 6373-nucleotide plasmid will hereinafter be called pCMV-mApoA1-AscI-LINKER-p144. Finally, the sequence was confirmed by means of sequencing.
The experiments have been conducted in female immunocompetent BALB/c and C57BL/6 mice between 5-7 weeks (Harlan, Barcelona, Spain). The animals were treated according to the indications and ethical rules of the Centro de Investigación Médica Aplicada (CIMA, Pamplona, Spain), under specific external pathogen-free conditions.
Each DNA plasmid (20 μg) was resuspended in 1.8 ml of 0.9% saline (Braun) introduced through the tail vein by means of a hydrodynamic injection (Liu et al., 1999, Gene Ther., 6:1258-1266), using 27.5G needles and 2.5 ml syringes (Becton-Dickinson, Spain). Blood samples were obtained by a retro-orbital route, after anesthesia by inhalation of isoflurane (Forane, Abbott). The serum was recovered by means of two consecutive centrifugations at 9.1×g for 5 minutes and stored at −20° C. Parenteral anesthesia was carried out by a 200 μl/mouse intraperitoneal injection with a 9:1 mixture of ketamine (Imalgene) and xylazine (Rompun). The temperatures were measured by abdominal contact with the ThermoKlinik thermometer (Artsana, Grandate, Italy).
Blood was extracted from mice to tubes with 0.5% heparin (Mayne) as final concentration. To determine: i) total white blood cells, a 1:1000 dilution of the whole blood was performed in vessels with 20 ml of Isoton II Diluent solution and 3 drops of Zap-Oglobin II Lytic Reagent were added 2 minutes before their measurement, ii) total red blood cells, a 1:50000 dilution of the whole blood was performed in vessels with 10 ml of Isoton II Diluent solution, iii) platelets, the whole blood was diluted 1:25 in a tube with 500 μl of Isoton II Diluent solution, centrifuged for 1.5 minutes 600 g at 4° C., and supernatant was transferred in a 1:400 dilution to a vessel with 20 ml of Isoton II Diluent the samples were analyzed in a Z1 Coulter Particle Counter with the settings recommended for each case by the manufacturer (all the material and reagents were from Beckman Coulter).
To analyze the anti-tumor efficacy of the gene transfer, two vaccination protocols were carried out:
The CT26 cell lines is derived from a BALB/c mouse colorectal adenocarcinoma and was introduced by the carcinogen N-nitroso-N-methyl-urethane, cultured in complete RPMI-1640 medium (Gibco-BRL, Paisley, UK), supplemented with 10% fetal calf serum (FCS) inactivated at 56° C., 2 mM glutamine, 100 U/ml streptomycin, 100 mg/ml penicillin, 1% 5×10−3 β-mercaptoethanol. The cell lines MC38 (murine adenocarcinoma cells), L929 (cells derived from mouse fibroblasts) and 293 (embryonic human kidney cells stably transfected with the E1 region belonging to the human adenovirus type 5, ECACC no. 85120602) cultured in complete DMEM (supplemented with 10% fetal calf serum (FCS) inactivated at 56° C., 2 mM glutamine, 100 U/ml streptomycin, 100 mg/ml penicillin)
The cells described were cultured in humidified incubating chambers at 37° C. and in a 5% CO2 atmosphere. The culture bottles and plates were from Greiner Bio-one (Essen, Germany).
2.4 Determination of mIFNα1, IFNγ, and Neopterin:
The mIFNα1 levels were measured by ELISA in NUNC maxisorp flat 96-well plates. The anti-mIFNα1 neutralizing Ab antibody (RMMA-1, PBL) was diluted 1/1000 in PBS1×, it was plated 100 μl/well and incubated 0/N at 4° C. in a humid atmosphere. After five washings in PBS1×-0.1% Tween-20 (pH 7.2-7.4), the plate was blocked with 300 μl/well of the PBS1×1% BSA solution for 1 hour at room temperature. The serum samples were diluted 1/100 in PBS1×1% BSA solution and incubated for 1 hour at room temperature. After five washings in PBS1×-0.1% Tween-20, it was incubated for 1 hour with 100 W/well of rabbit anti-IFNα polyclonal antibody (PBL), diluted 1/1000 in PBS1×1% BSA solution. After five washings in PBS1×-0.1% Tween-20, 100 μl/well of HRP-conjugated donkey α-rabbit IgG (Southern Biotech, Birmingham, Calif., USA) were added, dilution 1/4000 in PBS 1×1% BSA solution, 1 hour at room temperature. After five washings in PBS1×-0.1% Tween-20, 100 μl/well of BD OptEIA substrate solution (BD) were added, after 15 minutes at room temperature and in darkness, 50 μl of 2N H2SO4 were added. Finally, the absorbance at 450 nm was measured, and it was corrected at 540 nm.
The IFNγ levels in serum were measured with IFN-γ ELISA Set (BD Biosciences, San Diego, Calif.). The neopterin levels in serum were measured with Neopterin ELISA (IBL, Hamburg), according to the instructions provided by the manufacturer.
2 μl of cDNA were incubated with the specific primers of Table 1 using iQ SYBR Green Supermix (Bio-Rad, Hercules, Calif.). Murine actin was used to standardize the gene expression, because its expression is not affected by mIFNα1 or mApoA1. The mRNA values were represented by the formula 2ΔCt, where ΔCt indicates the difference in the threshold cycle between mActin and the target genes.
Female BALB/c mice (N=3/group) were immunized by means of a hydrodynamic injection as has been previously described, on day 0 with 20 μg of pCMV-LacZ and with 20 μg of each construction to study: (i) pCMV-mApoA1 ii) pCMV-IFNα1 iii) pCMV-mApo-IFN iv) pCMV-mIFN-ApoA1 dissolved in 0.9% physiological saline (Braun). On day 7, splenocytes from non-immunized BALB/c mice spleen were isolated and the red blood cells were lysed with ACK solution (Cambrex, Walkersville, Md.). The obtained splenocytes were divided into two groups and one of them was incubated for 30 minutes at 37° C. with RPMI 1640 medium and 9 μM of peptide TPHPARIGL (cytotoxic epitope derived from β-galactosidase, Proimmune Ltd., Oxford, United Kingdom). The second group received the same treatment without the peptide. The splenocytes loaded with the peptide were labeled with 2.5 μM CFSE (CFSEhigh) (Molecular Probes, Eugene, Oreg.). The control splenocytes were labeled with 0.25 μM CFSE (CFSElow). Finally, both populations were mixed in a 1:1 ratio and 107 cells were injected intravenously into naïve mice or into the immunized mice. After 24 hours, the animals were sacrificed. The extracted spleens were broken up and the ratio of CFSEhigh and CFSElow cells was analyzed by means of flow cytometry using FACSalibur (Becton Dickinson, Mountain View, Calif., USA). The percentage of specific lysis was calculated according to the following formula:
Splenocytes from C57BL/6 mice spleen were isolated. The extracted and broken up spleens were divided into 8 groups, of which four groups were incubated for 10 minutes with rabbit anti-SR-B1 polyclonal antibody (Novus Biologicals Littleton, Colo.) and with the BD Pharmigen antibodies: i) R-PE-Conjugated Rat Anti-Mouse CD4 (L3T4) Monoclonal Antibody to define the CD4+ cell populations and APC-Conjugated Rat Anti-Mouse CD8a (Ly-2) Monoclonal Antibody, to define the CD8+ cell populations. ii) APC-Conjugated Mouse Anti-Mouse NK-1.1 (NKR-P1B and NKR-P1C) Monoclonal Antibody to define the NK cell population. iii) APC-Rat Anti-Mouse CD11b to define the monocyte cell population iv) APC-CD11c to define the dendritic cell population. The other four groups were used as a control, being incubated for 10 minutes with the respective antibodies, without anti-SRB1. The labeled splenocytes were washed in PBS and 5% fetal bovine serum and were incubated for 10 minutes with FITC-Conjugated Donkey Anti-Rabbit IgG Antibody (Jackson ImmunoResearch, West Grove, Pa.). The samples thus stained were studied by flow cytometry using FACSalibur (Becton Dickinson, Mountain View, Calif., USA).
24 hours after the hydrodynamic injection with the plasmids mApoA1, IFNα1, Apo-IFN, IFN-Apo or ApoAI-linker-P144, blood was extracted from mice to tubes with 0.5% heparin (Mayne) as final concentration, and the plasma was extracted immediately by centrifugation (5000 g, 20 minutes).
The sodium bromide (NaBr) solutions at different densities were prepared in a final volume of 25 mL in distilled water. EDTA at a final concentration of 0.05% (w/v) was added. NaBr (Fluka) was added to obtain the solutions: 0.225 g (ρ=1.006 g/ml), 1.431 g (ρ=1.04 g/ml), 7.085 g (ρ=1.21 g/ml) and 13.573 g (ρ=1.4 g/ml). Due to the fact that NaBr is a highly hygroscopic salt, the density was verified and corrected by adding distilled water when necessary.
The method of sequential separation of lipoproteins by flotation after ultracentrifugation was performed with small modifications of the protocol described by Rodriguez-Sureda et al (Analytical Biochemistry 303, 73-77 (2002)) in Ultracentrifuge Optima MAX, with TLA100.4 rotor (Beckman Coulter), from 2-4 mL of mouse plasmas (unified according to the samples) at the following densities: VLDL<1.006 g/mL, LDL 1.006-1.04 g/mL and HDL 1.04-1.21 g/mL. i) Isolation of VLDL: 400 μl of mouse plasma were transferred to 3 ml polycarbonate tubes and 1100 μl of a ρ=1.006 g/ml NaBr solution were added. The samples were centrifuged for 2 hours, 4° C., 336000 g. Approximately 650 μl of supernatant were collected with a pipette and stored at −20° C. ii) Isolation of LDL: The remaining volume of sediment was taken to a density of 1.04 by adding the volume calculated by the formula of the ρ=1.4 g/ml NaBr solution:
The volume was taken to 1.5 ml with the ρ=1.04 g/ml NaBr solution and the samples were centrifuged for 2.5 hours, 4° C., 336000 g. 300-400 μl of supernatant were collected with a pipette and stored at −20° C. iii) Isolation of HDL: approximately 800 μl of sediment were transferred to a new tube, and the density was adjusted to 1.21 g/mL as has already been described, and taken to a volume of 1.5 mL with the ρ=1.21 g/ml NaBr solution. The samples were centrifuged for 3.5 hours, 4° C., 336000 g, and a supernatant fraction of approximately 400 ul corresponding to HDL, and the sediment fraction corresponding to the lipoprotein-free plasma (LDP) were collected and stored at −20° C.
2.9 Electrophoresis and Immunoblotting Against mApo A1:
25 μl of HDL or LDP fraction for each of the samples were separated in 4-20% Tris-hepes PAGE LongLife iGels (Nusep) gradient gels, transferred to nitrocellulose membrane (Whatman). The protein was detected with the goat polyclonal antibody against mApoA1, 1:200 dilution (Goat polyclonal anti-Apolipoprotein A1, Santa Cruz Biotechnology) and antibody against goat IgG, 1:20000 dilution (Anti-goat IgG (whole molecule)-HRP conjugated, Sigma-Aldrich). The membrane was developed with ECL Plus Western Blotting Detection Reagent (Amersham).
The IFN activity units of the HDL fractions isolated from mouse plasma containing Apo-IFN and IFN-Apo were calculated by means of an activity bioassay, measuring the capacity of IFN to protect the cells against the cytopathic activity of the encephalomyocarditis lytic virus (EMCV) over a wide range of plated IFN concentrations by the successive dilution of the samples. On this dilution, 3×105 L929 cells/well were plated in 96-well Cellstar cell culture plates (Greiner bio-one) and incubated 0/N at 37° C. 5% CO2 to reach the monolayer of adherent cells. Then, the same amount of pfu/well of EMCV was added and incubated for 24 hours until achieving the lysis of the untreated cells used as control. At this point, the viable cells protected by the IFN effect are measured by luminometry with the ViaLight Plus Kit developing solution (Lonza) following the manufacturer's instructions. The reading is plotted to generate a dose-response curve (Prism 5, GraphPad Software, Inc.) from which the potency of the IFN preparations in terms of antiviral activity units can be calculated with reference to the dilutions of a rIFNα recombinant protein standard (PBL) used in each assay.
2.11 Experiments with rIFN and Isolated HDL IFN-Apo Fractions:
10000 IU of mouse rIFN alpha (CHO derived mouse, Hycult Biotechnol) or 10000 IU of HDL IFN-Apo measured by activity bioassay was retro-orbitally injected into mice.
The statistical analysis of the data was performed using the Prism 5 computer program (GraphPad Software, Inc.). The tumor appearance data were represented in Kaplan-Meier graphs and analyzed by means of the log-rank test. The data studied at different times was analyzed by means of repeated-measures ANOVA followed by the Bonferroni test. The remaining parameters were analyzed by means of ANOVA and followed by Dunnett's post hoc analysis for carrying out multiple comparisons. p<0.05 values were considered to be significant.
To compare the levels of serum murine IFNα levels, plasmids expressing apolipoprotein AI (ApoAI), murine interferon alpha 1 (IFNα1), Apo-IFN (fusion of ApoAI and IFNα1) or IFN-Apo (fusion of IFNα1 and ApoAI) are administered to groups of four mice by means of a hydrodynamic injection Sera obtained after 6 hours and on day 1, 3, 6 and 9 were analyzed by means of a sandwich ELISA. The sera of the mice which received the control plasmid expressing ApoAI did not have detectable IFNα levels, indicating that the hydrodynamic administration per se or the expression of ApoAI did not induce the expression of the endogenous IFNα (
The difference in the serum IFNα levels can be explained by the increase of the plasma half-life of the fusion proteins with respect to IFNα or by the increase of the expression of these proteins. To distinguish between these two alternatives, the messenger RNA (mRNA) kinetics of these constructs was analyzed. To that end, the livers of the mice which had received a hydrodynamic injection with plasmids expressing ApoAI, IFNα 1, Apo-IFN and IFN-Apo on day 0, 1, 3 and 6 were collected. The RNA of these samples was extracted and a quantitative RT-PCR was performed. As can be observed in
To verify i) that the chimeric proteins maintained the biological activity of IFNα and ii) that the more sustained levels were correlated with a higher biological activity, two parameters which increase after the administration of IFNα were analyzed. These parameters were studied three days after the administration of plasmids, at which time IFNα produced by the construct with IFNα1 was no longer detected but that produced by the chimeric constructs was detected. Firstly, the serum neopterin levels were analyzed. Neopterin is a catabolite product of GTP, synthesized by the macrophages stimulated by type I and II interferons. The three plasmids containing the IFNα sequence increased the serum neopterin levels but only the chimeric constructs increased significantly (
The activity of the type I interferons is mediated by proteins encoded by interferon-stimulated genes (ISGs). After IFNα binds to their membrane receptor, a signaling cascade is activated which results in the activation of ISG transcription. To verify if the chimeric constructs also induce these genes, the mRNA levels of four of these genes was analyzed on day 3 after the hydrodynamic administration. The genes which were analyzed are IRF1, 2′-5′ OAS, USP18, ISG15, M×1. As can be observed in
To explore the immunostimulating activity of the constructs, the increase of the number and activity of spleen cells was analyzed first. To that end, the plasmids were injected by means of a hydrodynamic injection and six days later, the spleens were broken up, the total cells were counted and after labeling the splenocytes with antibodies to identify the main lymphocyte populations and with an activation marker (CD69), they were analyzed by means of flow cytometry. The injection of constructs with IFNα significantly increased the number of splenocytes. The construct encoding for IFN-Apo is considerably emphasized in this assay (
To verify the adjuvant effect of IFN-Apo, the increase of the cytotoxic activity induced by a DNA vaccine was analyzed in presence of the different constructs. The LacZ gene encoding the immunogenic β-galactosidase protein was chosen as an antigen model. The plasmid encoding this protein was injected together with plasmids encoding ApoA1, IFNα1, Apo-IFN or IFN-Apo. Seven days after the gene vaccination, splenocytes labeled with 2.5 μM CFSE and loaded with the cytotoxic epitope H2Kd TPHPARIGL, derived from the β-galactosidase protein, were intravenously injected. As an internal control, splenocytes were injected with 0.25 μM CFSE without peptide. After twenty-four hours, the specific lysis of the splenocytes loaded with the cytotoxic epitope was quantified by flow cytometry. In
The increase in the adjuvant activity can be due to the increase in the stability of IFNα or due to the fact that the ApoAI fraction of IFN-Apo allows a higher interaction of IFNα with immune system cells. To explore the latter hypothesis, the presence of the main receptor for ApoAI, SR-BI, was analyzed in different immune system populations. Splenocytes from a naïve mouse were isolated and labeled with an anti-SRB-I antibody and with an antibody for defining the population. The following antibodies were used: anti-CD4, as a marker of CD4+ T cell marker; anti-CD8, as a CD8+ T cell marker; anti-CD49b, as an NK cell marker; anti-CD11b, as a monocytes/macrophages marker; and anti-CD11c, as a dendritic cell marker. The SRB-I receptor was detected in all the analyzed populations. In the immune system effector cells (CD4+ T, CD8+ T and NK cells), the percentage of cells expressing this receptor ranges between 15% and 28%. This percentage rises up to more than 50% in cells with antigen-presenting capacity such as monocytes and dendritic cells (
After demonstrating that IFN-Apo has a higher adjuvant activity than IFN, it was evaluated if this effect translates into a higher antitumor efficacy in a vaccination protocol. To that end, BALB/c mice received a hydrodynamic injection with the Apo, IFN or IFN-Apo plasmids and on the following day they were vaccinated with the cytotoxic peptide AH-1 in Freund's incomplete adjuvant. This peptide is presented by the CT26 tumor line, which was inoculated into the different experimental groups 9 days after the vaccination. Most of the mice of the control group, which received the vaccination plus the hydrodynamic injection with the Apo plasmid, developed a subcutaneous tumor in the inoculation site of the CT26 tumor cells. Mice which received IFN in addition to the vaccination present a behavior which does not differ significantly from that of the control group. However, about 60% of the mice which received the vaccination and the IFN-Apo plasmid were capable of rejecting the tumor cells and did not present tumors throughout the 30 days of the experiment (
One of the limitations of the IFN is its considerably hematological toxicity, which can lead to the suspension of the treatment in certain patients who develop an intense leukopenia and/or thrombocytopenia. The evolution was analyzed then, after the hydrodynamic administration of the different constructs, of the leukocytes and platelets in blood. It is observed in
Another of the main adverse effects of the IFN, which limits its use in certain patients, is neuropsychiatric disorders. To study the effect of the new fusion molecules in the central nervous system, BALB/c mice were injected with the plasmids encoding the different constructs and after 24 hours, the mice were sacrificed and their brain extracted. The increase in the interferon-induced genes (ISGs) in the different groups (
About 97% of the apolipoprotein AI present in the blood, circulate in the form of a macromolecular lipoprotein complex called high density lipoproteins. To study if the fusion protein was capable of being incorporated into HDLs, 24 hours after injecting the plasmids encoding IFN and the IFN-Apo molecules by hydrodynamic route, the HDLs were isolated from the serum by means of differential centrifugation in NaBr gradient. An IFN bioassay, i.e., an assay of protection from the cytopatic effect of a virus, was performed with these fractions, in which cells previously incubated with the samples with IFN in serial dilutions are compared with a cytopathic virus. If there is interferon in the samples, the virus will not be capable of lysing the pretreated cells. The HDLs obtained from mice which received the plasmid encoding IFN were not capable of protecting the cells from the cytopatic effect of the encephalomyelitis virus, indicating that IFN does not circulate bound to the HDLs. In contrast, the two IFN-Apo molecules can indeed be detected by this technique in the HDLs (
The possibility of purifying HDLs containing IFN-Apo from the sera of mice to which the plasmid encoding IFN-Apo was administered allows providing physiological IFN-Apo nanolipoparticles to study the properties both in vitro and in vivo thereof. HDL with IFN-Apo was purified and the equivalent to 10000 IU of IFN per mouse was administered. On day 3, the leukocyte and platelet count in blood was analyzed. The dose administered of recombinant IFN was not capable of causing a decrease of these parameters. But the mice which received the HDLs of IFN-Apo presented significantly higher levels (
Interleukin 12 (IL12) is an immunostimulating cytokine with a potent antitumor activity. Its activity is essentially mediated by IFNγ. The production of this mediator is regulated by TGFβ, therefore its blocking by means of the inhibitor peptides p17 or p144 can increase IFNγ induction and, therefore, the antitumor activity of IL12. To study if chimeric constructs formed by ApoAI and the TGFβ inhibitor peptides, bound by means of different peptide sequences, can increase I112-mediated IFNγ induction, a plasmid encoding murine IL12 and plasmids encoding the different constructs were administered by means of a hydrodynamic injection. ApoAI was used as a control. Two constructs were generated with p17: i) spP17, containing the sequence encoding peptide p17 preceded by the ApoAI signal peptide, the release of peptide p17 to the extracellular medium being achieved. ii) ApoAI-P17, containing the gene encoding ApoAI followed by three binding amino acids (GAP), and the sequence encoding p17. The constructs spP144 and ApoAI-P144 were generated with p144, substituting the sequence encoding p17 with that of p144. Another two constructs were furthermore generated: i) ApoAI-MMP9-P144, containing a target for metalloproteinase 9 (MMP9) as a binding peptide. ii) ApoAI-linker-P144, containing a sequence with extended conformation as a binding peptide.
Four days after the hydrodynamic injection, the serum IFNγ levels were analyzed by means of ELISA. The injection of plasmids encoding for IL12 and ApoAI generated detectable IFNγ levels. The injection of the constructs with p17 did not increase these levels (
To verify the biological activity of the constructs with the TGFβ inhibitor peptides in an independent experimental model, BALB/c mice were vaccinated with the cytotoxic epitope H2Kd AH1 (SPSYVYHQF, SEQ ID NO:54) with Freund's incomplete adjuvant. Seven days later, the different constructs were administered by means of a hydrodynamic injection. After another seven days, 5×105 CT26 cells were inoculated subcutaneously. The percentage of tumor-free animals was analyzed over time. In the group which had received the vaccine and the control construct expressing ApoAI, all the mice developed a subcutaneous tumor in the CT26 cell inoculation site. However, more than 50% of the mice which had received one of the two constructs expressing p17 remained tumor-free at the end of the experiment (
To study if the ApoAI-linker-P144 protein forms complexes with HDLs, the fraction containing the HDLs was isolated from a serum of a mouse to which the plasmid encoding the ApoAI-linker-P144 was administered by hydrodynamic route. To that end the serum was subjected to a differential centrifugation in NaBr gradient. Once the HDLs were purified, a western blot was performed to detect apolipoprotein AI. In addition to the major band corresponding to the endogenous apolipoprotein AI, a band with a greater height corresponding to the ApoAI-linker-P144 molecule was detected (
The purification of HDLs containing ApoAI-linker-P144 allows obtaining physiological nanolipoparticles with the capacity to inhibit TGFβ activity. To show their in vivo activity, HDLs purified from an animal expressing ApoAI-linker-P144 were inoculated into mice to which a hydrodynamic injection with a plasmid expressing interleukin 12 in response to the administration of doxycycline is simultaneously administered. As positive control, the plasmid ApoAI-linker-P144 was coadministered. The IFNγ levels obtained after the administration of the HDLs are similar to those obtained after the hydrodynamic injection (
| Number | Date | Country | Kind |
|---|---|---|---|
| P200801796 | Jun 2008 | ES | national |
This application is the Divisional of U.S. patent application Ser. No. 12/997,829, filed Dec. 13, 2010, which is the National Stage of International Application No. PCT/ES2009/070224, which designates the U.S., filed Jun. 12, 2009, which claims the benefit of ES P200801796, filed Jun. 13, 2008, the contents of all of which are incorporated by reference herein.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12997829 | Dec 2010 | US |
| Child | 14947164 | US |
