Peptide compounds and methods of treating diseases thereof

Abstract

The present application provides peptide compounds and methods of treating diseases thereof. Isolated peptides are capable of reducing the amount of dexamethasone-induced weight loss of the spleen and / or thymus in a mouse. Use of the plurality of isolated peptides for the treatment of inflammatory or degenerative diseases.

Description

[0001] This application is a divisional application of application number CN 202180017719.4 (PCT application number is PCT / IL2021 / 050044), application date January 14, 2021, and invention name “Peptide compounds and methods for treating diseases thereof”.

[0002] Related Applications

[0003] This application claims priority to Israel Patent Application No. 272074 filed on January 15, 2020, the contents of which are incorporated herein by reference.

[0004] Sequence Listing Statement

[0005] An ASCII file entitled 84727SequenceListing.txt, created on January 13, 2021, comprising 12,288 bytes, was filed concurrently with the filing of this application and is incorporated herein by reference.

[0006] Technical field and background technology

[0007] The present invention, in some embodiments thereof, relates to compositions and methods of use for treating inflammatory and autoimmune diseases.

[0008] There is an unmet need for new compositions that can attenuate cellular and immune stress responses in normal tissues in a specific, safe, and effective manner, thereby reducing the severity of stress-related degenerative diseases and stress-induced inflammation.

[0009] The peptide LPPLPYP (SEQ ID NO: 42, also known as Stressin-1 and IPL344) is a short 7-amino acid peptide that protects various cell types from pro-apoptotic stress and activates the Akt signaling system. The structure of IPL344 is similar to the binding sites of adaptor proteins. It has been proposed that its mechanism of action involves mimicking these proteins and activating cytoprotective processes through Akt and other pathways.

[0010] International patent application publication numbers: WO 2006 / 021954 and WO 2012 / 160563 disclose that the LPPLPYP (SEQ ID NO: 42) peptide is used for treating diseases such as ALS. Summary of the invention

[0011] According to one aspect of the present invention, there is provided an isolated peptide consisting of 5 or 7 amino acids, wherein the isolated peptide consists of an amino acid sequence represented by the molecular formula X1-X2-X3-X4-X5-X6-X7, i.e., SEQ ID NO: 45, wherein

[0012] (i) X1 is selected from the group consisting of leucine, d-leucine, d-valine, d-arginine and lack thereof;

[0013] (ii) X2 is selected from the group consisting of dimethylproline (dMP), proline, α-aminoisobutyric acid (Aib) and d-proline;

[0014] (iii) X3 is selected from the group consisting of dimethylproline, proline, α-aminoisobutyric acid and d-proline;

[0015] (iv) X4 is selected from the group consisting of histidine, serine, valine, leucine, d-leucine and threonine;

[0016] (v) X5 is proline or alanine;

[0017] (vi) X6 is selected from the group consisting of tyrosine, d-valine, d-aspartic acid, tryptophan and phenylalanine; and

[0018] (vii) X7 is selected from the group consisting of proline, dMP, d-proline and lack thereof;

[0019] The peptide is capable of reducing the amount of dexamethasone-induced spleen and / or thymus weight loss in a mouse, provided that the peptide does not consist of the sequence set forth in SEQ ID NO 42, 43 or 44.

[0020] According to one aspect of the present invention, a pharmaceutical composition is provided, which comprises the peptide disclosed herein as an active agent and a physiologically acceptable carrier.

[0021] According to one aspect of the present invention, an isolated peptide of no more than 10 amino acids is provided, wherein the isolated peptide comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-33 and 34, wherein the peptide is capable of reducing the amount of dexamethasone-induced spleen and / or thymus weight loss in a mouse.

[0022] According to some embodiments of the invention, the peptide consists of an amino acid sequence selected from the group consisting of SEQ ID NOs: 6-33 and 34.

[0023] According to some embodiments of the present invention, the peptide consists of an amino acid sequence selected from the group consisting of SEQ ID NOs: 6-12 and 13.

[0024] According to some embodiments of the invention, the peptide comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-4 and 5.

[0025] According to some embodiments of the present invention, the peptide consists of the amino acid sequence selected from the group consisting of SEQ ID NOs: 1-33 and 34.

[0026] According to some embodiments of the present invention, the peptide is a stapled peptide.

[0027] According to some embodiments of the present invention, the peptide is a cyclic peptide.

[0028] According to some embodiments of the invention, the order of the sequence is reversed and all of the amino acids are in D-form.

[0029] According to some embodiments of the invention, the peptide is linked to a cell penetrating moiety.

[0030] According to some embodiments of the invention, the cell penetrating moiety is linked to an N-terminus of the peptide.

[0031] According to some embodiments of the present invention, the peptide is used in treating diseases associated with cell apoptosis.

[0032] According to some embodiments of the present invention, the disease associated with cell apoptosis is an inflammatory disease or a degenerative disease.

[0033] According to some embodiments of the present invention, the inflammatory disease is an autoimmune disease.

[0034] According to some embodiments of the present invention, the degenerative disease is a neurodegenerative disease.

[0035] According to some embodiments of the present invention, the disease associated with cell apoptosis is selected from the group consisting of age-related macular degeneration (AMD), retinitis pigmentosa, stroke and myocardial infarction.

[0036] Unless otherwise defined, all technical and / or scientific terms used herein have the same meaning as commonly understood by those of ordinary skill in the art to which the invention belongs. Although methods and materials similar or equivalent to the methods and materials described herein can be used for the execution or testing of embodiments of the present invention, exemplary methods and / or materials are described below. In the event of a conflict, the patent specification, including definitions, shall prevail. In addition, these materials, methods and examples are illustrative only and are not necessarily meant to be limiting. DETAILED DESCRIPTION

[0037] The present invention, in some embodiments thereof, relates to compositions and methods of use for treating inflammatory and autoimmune diseases.

[0038] Before describing in detail at least one embodiment of the present invention, it should be understood that the scope of application of the present invention is not necessarily limited to the details described below or shown by this example. The present invention can be implemented or carried out in various ways.

[0039] The polyproline peptide LPPLPYP (SEQ ID NO: 42), also known as IPL344 and Stressin-1) is a short 7-amino acid peptide that can protect various types of cells from pro-apoptotic stress and activate the Akt signaling system. It is a candidate drug for the treatment of degenerative, inflammatory and autoimmune diseases.

[0040] In studying the contribution of individual amino acids of the peptides, the inventors surprisingly found that specific amino acid substitutions of the core sequence significantly improved the reduction in the amount of dexamethasone-induced spleen and / or thymus weight loss in mice, while other substitutions and / or deletions severely abolished the reduction. In addition, these peptides can also minimize the dexamethasone-induced reduction in spleen and thymus cell numbers.

[0041] The inventors found that most of these peptides conform to the molecular formula set forth in SEQ ID NO: 45 and proposed that these peptides could be used to treat degenerative, inflammatory and autoimmune diseases.

[0042] While further simplifying the present invention for the implementation of the present invention, the inventors noticed that replacing proline with the synthetic amino acid Aib at a specific position also resulted in peptides having enhanced improvements in reducing the amount of dexamethasone-induced spleen and / or thymus weight loss in mice, and minimizing dexamethasone-induced reductions in spleen and thymus cell numbers.

[0043] The term "peptide" as used herein refers to a polymer of natural or synthetic amino acids, including natural peptides (degradation products, synthetic polypeptides or recombinant polypeptides) and peptidomimetics (usually synthetic peptides), as well as peptoids and hemi-peptides. These polypeptide analogs, for example, may have modifications that make the polypeptide more stable in vivo or more permeable to cells.

[0044] The present invention also includes derivatives (modification and / or addition of chemical functions on the amino acid side chains without chemical changes on the peptide chain) and analogs (modification and / or addition of chemical functions on the peptide chain, for example, N-terminal or C-terminal modifications or peptide bond modifications).

[0045] These modifications include, but are not limited to, N-terminal modifications, C-terminal modifications, peptide bond modifications, including, but not limited to, CH2-NH, CH2-S, CH2-S=O, O=C-NH, CH2-O, CH2-CH2, S=C-NH, CH=CH or CF=CH, main chain modifications, residue modifications. Methods for preparing peptoid compounds are well known in the art, for example, in "Quantitative Drug Design", CA Ramsden Gd, F. Choplin Pergamon Press (1992) Chapter 17.2, which is incorporated herein by reference as if fully described herein. Further details are provided below.

[0046] The intrapeptide chemical bonds (-CO-NH) may be replaced, for example, by N-methylated bonds (-N(CH3)-CO-), ester bonds (-C(R)HCOOC(R)-N-), ketomethylene bonds (-CO-CH2-), alpha-aza bonds (-NH-N(R)-CO-), where R is an alkyl group, such as a methyl group, amine bonds (-CH2-NH-), hydroxyethylene bonds (-CH(OH)-CH2-), thioamide bonds (-CS-NH-), olefinic double bonds (-CH=CH-), reverse amide bonds (-NH-CO-), and peptide derivatives (-N(R)-CH2-CO-), where R is a "normal" side chain naturally present on a carbon atom.

[0047] These modifications can occur on any chemical bond in the peptide chain, or even on multiple (2-3) chemical bonds simultaneously.

[0048] The unnatural amino acids are summarized in Table 2 below.

[0049] The term "amino acid" or "amino acids (plural)" as used in this specification and claims is understood to include the 20 naturally occurring amino acids; these amino acids are often post-translationally modified in vivo, for example, hydroxyproline, phosphoserine and phosphothreonine; other less common amino acids include, but are not limited to, 2-aminoadipic acid, hydroxylysine, isodesmosine, nor-valine, nor-leucine and ornithine. In addition, the term "amino acid" includes both D- and L-amino acids (stereoisomers).

[0050] Tables 1 and 2 below list natural amino acids (Table 1) and unconventional or modified amino acids (Table 2) that can be used with the present invention.

[0051] Table 1

[0052] Amino Acid Three-Letter Abbreviation One-letter notation Alanine Ala A Arginine Arg R Asparagine Asn N Aspartic acid Asp D Cysteine Cys C Glutamine Gln Q Glutamic Acid Glu E Glycine Gly G Histidine His H Isoleucine Ile I Leucine Leu L Lysine Lys K Methionine Met M Phenylalanine Phe F Proline Pro P Serine Ser S Threonine Thr T Tryptophan Trp W Tyrosine Tyr Y Valine Val V Any of the above amino acids XA X

[0053] Table 2

[0054]

[0055]

[0056]

[0057]

[0058]

[0059] As previously mentioned, the N-terminus and C-terminus of the peptides of the present invention may be protected by functional groups. Suitable functional groups are described in Green and Wuts, "Protective Groups in Organic Synthesis", John Wiley and Sons, Chapters 5 and 7, 1991, the teachings of which are incorporated herein by reference. Preferred protecting groups are those that facilitate transport of the compound to which they are attached to cells, for example, by reducing the hydrophilicity of the compound and increasing the lipophilicity of the compound.

[0060] These moieties can be cleaved in vivo by hydrolysis or enzymes in cells. Hydroxyl protecting groups include esters, carbonates and carbamate protecting groups. Amine protecting groups include alkoxy and aryloxycarbonyl, N-terminal protecting groups as described above. Carboxylic acid protecting groups include aliphatic esters, benzyl esters and aryl esters, C-terminal protecting groups as described above. In one embodiment, the carboxylic acid groups in the side chains of one or more glutamic acid or aspartic acid residues in the peptides of the present invention are preferably protected using methyl, ethyl, benzyl or substituted benzyl esters.

[0061] Examples of N-terminal protecting groups include acyl (-CO-R1) and alkoxycarbonyl or aryloxycarbonyl (-CO-O-R1), wherein R1 is aliphatic, substituted aliphatic, benzyl, substituted benzyl, aromatic or a substituted aromatic group. Specific examples of acyl include acetyl, (ethyl)-CO-, n-propyl-CO-, isopropyl-CO-, n-butyl-CO-, sec-butyl-CO-, t-butyl-CO-, hexyl, lauroyl, palmitoyl, myristyl, stearyl, oleoylphenyl-CO-, substituted phenyl-CO-, benzyl-CO- and (substituted benzyl)-CO-. Examples of alkoxycarbonyl and aryloxycarbonyl groups include CH3-O-CO-, (ethyl)-O-CO-, n-propyl-O-CO-, isopropyl-O-CO-, n-butyl-O-CO-, sec-butyl-O-CO-, t-butyl-O-CO-, phenyl-O-CO-, substituted phenyl-O-CO- and benzyl-O-CO-, (substituted benzyl)-O-CO-. Adamantane, decalin, myristoyl, toluene, biphenyl, cinnamyl, nitrobenzoyl, tolyl, furanyl, benzoyl, cyclohexane, norbornane, Z-hexyl. To promote N-acylation, 1 to 4 glycine residues may be present at the N-terminus of the molecule.

[0062] The C-terminal carboxyl group of the compound can be protected, for example, amide (i.e., the C-terminal hydroxyl group is replaced by -NH2, -NHR2 and -NR2R3) or ester (i.e., the C-terminal hydroxyl group is replaced by -OR2). R2 and R3 are respectively aliphatic, substituted aliphatic, benzyl, substituted benzyl, aryl or substituted aryl. In addition, R2 and R3 can form a C4 to C8 heterocyclic ring in combination with the nitrogen atom, and there are also about 0-2 heteroatoms, such as nitrogen, oxygen or sulfur.

[0063] Examples of suitable heterocycles include piperidinyl, pyrrolidinyl, morpholino, thiomorpholino or piperazinyl. Examples of C-terminal protecting groups include -NH2, -NHCH3, -N(CH3)2, -NH(ethyl), -N(ethyl), -N(methyl)(ethyl), -NH(benzyl), -N(C1-C4 alkyl)(benzyl), -NH(phenyl), N(C1-C4 alkyl)(phenyl), -OCH3, -O(ethyl), -O(N-propyl), -O(n-butyl), -O(isopropyl), -O(sec-butyl), -O(tert-butyl), -Obenzyl and -Ophenyl.

[0064] The peptides of the present invention may also include non-amino acid moieties, for example, hydrophobic moieties attached to the peptide (various linear, branched, cyclic, polycyclic or hexacyclic hydrocarbons and hydrocarbon derivatives); non-peptide permeants; various protective groups, particularly where the compound is linear, attached to the termini of the compound to reduce degradation. Chemical (non-amino acid) groups present in the compound may be included to improve various physiological properties, such as; reduced degradation or clearance; reduced rejection by various cell pumps, increased immunogenic activity, improved various modes of administration (such as attachment of various sequences, allowing penetration of various barriers, passage through the intestine, etc.); increased specificity, increased affinity, reduced toxicity, etc.

[0065] The amino acid sequence assembly of peptide of the present invention is connected to other non-amino acid reagents, can be by covalent connection, by non-covalent connection, for example, by covalent connection on hydrophobic polymer, hydrophobic polymer can be degraded or cut, produce the compound that can release slowly; By the amino acid part of peptide is wrapped in liposome or micelle to produce the final peptide of the present invention. Combination can be by capturing the amino acid sequence in other components (liposome, micelle) or dipping the amino acid sequence in polymer to produce the final peptide of the present invention.

[0066] According to certain embodiments, the peptide is linked to a cell penetrating moiety.

[0067] As used herein, the term "cell penetrating moiety" refers to a moiety (e.g., a lipid, such as palmitic acid) that enhances the translocation of an attached peptide across a cell membrane. In certain embodiments, the cell penetrating moiety is not a peptide moiety. This moiety can be attached to the N-terminus or the C-terminus.

[0068] The peptides of the present invention may be linear or cyclic (cyclization may improve stability). Cyclization may occur by any known method. When the compound is composed primarily of amino acids, cyclization may be by N-terminal to C-terminal, N-terminal to side chain and N-terminal to main chain, C-terminal to side chain, C-terminal to main chain, side chain to main chain, side chain to side chain, and main chain to main chain cyclization. Peptide cyclization may also be carried out by non-amino acid organic moieties contained in the peptide.

[0069] The inventors of the present invention also contemplate stapled peptides.

[0070] The term "stapled peptide" as used herein refers to a peptide having a selected number of standard or non-standard amino acids and further having at least two moieties capable of reacting to promote carbon-carbon bond formation, which moieties have been contacted with an agent to produce at least one cross-linker between at least two moieties, for example, to modulate the stability of the peptide.

[0071] As used herein, the term "staple" introduces at least two peptides that can react to promote the formation of carbon-carbon bonds, which can be contacted with a reagent to produce at least one cross-linker between at least two groups. Staples provide constraints for secondary structures (such as alpha helical structures). The length and geometry of the cross-linker can be optimized to increase the yield of the desired secondary structure content. For example, the constraints provided can prevent the secondary structure from unfolding and / or can strengthen the shape of the secondary structure. For example, a secondary structure that is prevented from unfolding is more stable.

[0072] The peptides of the present invention can be biochemically synthesized using standard solid phase techniques. These methods include exclusive solid phase synthesis, partial solid phase synthesis, fragment condensation, and classical solution synthesis. Solid phase peptide synthesis procedures are well known in the art and are further described by John Morrow Stewart and Janis Dillaha Young, Solid Phase Peptide Synthesis (Second Edition, Pierce Chemical Company, 1984).

[0073] The inventors also considered liquid phase techniques to be particularly suitable for small peptides.

[0074] Anderson Biopolymers 2000; 55(3): 227-50 describes large scale peptide synthesis.

[0075] The synthesized peptides can be purified by preparative high performance liquid chromatography [Creighton T. (1983) Proteins, Structure and Molecular Principles, WH Freeman and Co. NY] and their composition can be confirmed by amino acid sequencing.

[0076] Recombinant technology can also be used to produce the peptides of the present invention. In order to produce the peptides of the present invention using recombinant technology, the polynucleotide encoding the peptides of the present invention is connected to a nucleic acid expression vector, the vector includes a polynucleotide sequence under the transcriptional control of a cis-regulatory sequence (e.g., a promoter sequence), the cis-regulatory sequence is suitable for directing constitutive, tissue-specific or inducible transcription of the peptides of the present invention in a host cell.

[0077] In addition to being synthesized in host cells, the peptides of the present invention can also be synthesized using in vitro expression systems. These methods and components of the systems are well known in the art.

[0078] The peptides described herein are able to reduce the amount of dexamethasone-induced spleen and / or thymus weight loss in mice - for example, after injection (IP) of 100 μg of dexamethasone. In addition, they can minimize dexamethasone-induced reductions in spleen and thymus cell numbers.

[0079] In another embodiment, the peptides described herein are capable of interfering with and blocking the secretion of TNF-α and IL-6 by macrophages in response to innate activators such as lipopolysaccharide (LPS) and CpG oligonucleotides.

[0080] In addition or alternately, the peptides described herein can or reduce, prevent or inhibit apoptosis of eukaryotic cells. The mechanism by which the peptides of the invention mediate stress responses is not considered, and it is not desired to be constrained by any theory or mechanism of action, assuming that the peptides may be able to activate the Akt-CREB axis. The peptides can be tested by analyzing their ability to activate Akt kinases and / or cAMP response element binding protein (CREB) transcription factors, see Herkel et al., Immunology, 2017, pp. 151, 474-480, the contents of which are incorporated herein by reference.

[0081] Measurement of apoptosis: Apoptosis is an active, genetically directed self-destructive process associated with characteristic morphological and biochemical changes. Typical features of apoptosis are condensation of the nucleus and cytoplasm and fragmentation of dying cells into membrane-bound apoptotic bodies. Another characteristic of apoptotic cell death is the degradation of chromosomal DNA into oligonuclear fragments following activation of specific nucleases.

[0082] "Inhibition of apoptosis" or "inhibition of apoptosis activity" refers to any reduction in the number of cells undergoing apoptosis relative to an untreated control (i.e., cells not contacted with the peptide of the present invention). Preferably, at least 25% reduction, more preferably at least 50% reduction, more preferably at least 65% reduction, most preferably at least 80% reduction.

[0083] Flow cytometry provides many possibilities for detecting apoptosis. Different staining methods have been established and implemented, some staining the cell surface and some staining the inside of the cell.

[0084] In addition to observing apoptotic cells shrinking and having a higher intracellular granularity, the first method is to use DNA-specific fluorescent stains (such as propidium iodide [PI], ethidium bromide [EtBr]). Once the lethal knockout is induced, the DNA begins to change its characteristics. Apoptotic DNA not only includes DNA fragments (which appear as shorter bands in agarose gels, called DNA ladders), but is also partially digested into single nucleotides, so that fluorescent pigments such as PI or EtBr can stain less DNA (Nicoletti et al., 1991). This is usually done by FACScan TM (from Becton Dickinson, USA) was observed as a left shift (called sub-G1 peak) on the detection channel of a specific fluorescent pigment.

[0085] Another method is terminal deoxynucleotidyltransferase (TdT)-mediated DNA strand break end labeling (TUNEL). The TUNEL method detects DNA strand breaks in cells during apoptosis. TdT is an enzyme that catalyzes the addition of deoxyribonucleotide triphosphates to the 3'-OH end of double-stranded or single-stranded DNA. Unlike normal cells, under the action of TdT, the nucleus of apoptotic cells includes exogenous nucleotides (dUTP)-DIG. Anti-DIG antibody fragments with conjugated fluorescent pigments can display apoptotic cells. The increase in apoptotic cells will lead to more DNA fragments, resulting in brighter fluorescence. The advantage of this method is that the specificity is very high (Gavrieli et al., 1992). The disadvantage of this method is that it is expensive and can only be used for a small number of samples due to time constraints. Therefore, it is not suitable for large screening projects.

[0086] In the early stages of apoptosis, the loss of cell membrane polarity and the increase of phosphatidylserine (PS) outside the cell membrane provide a new pathway for apoptosis. Annexin V is a calcium-dependent phospholipid binding protein that has a high affinity for PS and maintains the integrity of the cell membrane in the early and middle stages of apoptosis. Annexin-FITC binding is enhanced in early and middle apoptotic cells, and PI staining is mainly negative. Late apoptotic stages and necrotic cells are double positive, which is due to the disintegration of the cell membrane, resulting in PS and PI staining of intracellular nucleic acids. This method is costly and labor-intensive.

[0087] Other methods for measuring apoptosis in vivo and in vitro are disclosed in US Pat. Nos. 6,726,895 and 6,723,567.

[0088] Provided is an isolated peptide consisting of 5 or 7 amino acids, wherein the isolated peptide consists of an amino acid sequence represented by a molecular formula X1-X2-X3-X4-X5-X6-X7, i.e., SEQ ID NO: 45, wherein

[0089] (i) X1 is selected from the group consisting of leucine, d-leucine, d-valine, d-arginine and lack thereof;

[0090] (ii) X2 is selected from the group consisting of dimethylproline (dMP), proline, α-aminoisobutyric acid (Aib) and d-proline;

[0091] (iii) X3 is selected from the group consisting of dimethylproline, proline, α-aminoisobutyric acid and d-proline;

[0092] (iv) X4 is selected from the group consisting of histidine, serine, valine, leucine, d-leucine and threonine;

[0093] (v) X5 is proline or alanine;

[0094] (vi) X6 is selected from the group consisting of tyrosine, d-valine, d-aspartic acid, tryptophan and phenylalanine; and

[0095] (vii) X7 is selected from the group consisting of proline, dMP, d-proline and lack thereof;

[0096] The peptide is capable of reducing the amount of dexamethasone-induced spleen and / or thymus weight loss in a mouse, provided that the peptide does not consist of the sequence set forth in SEQ ID NO 42, 43 or 44

[0097] The peptides according to this aspect of the invention may be 5 or 7 amino acids in length. Thus, when X1 is absent, X7 is also absent.

[0098] Examples of peptides contemplated by this aspect of the invention are set forth in SEQ ID NOs: 6-34.

[0099] In one embodiment, the peptide consists of any one of the sequences set forth in SEQ ID NOs: 6-34.

[0100] In another embodiment, the peptide consists of one of the sequences set forth in SEQ ID NOs: 6-13.

[0101] It is noted that in this aspect of the invention, the amino acids are listed according to the formula in SEQ ID NO: 45, and conservative / non-conservative mutations are not considered except for the specified mutations. In addition, when a specific stereoisomer appears in the formula, it is obvious that it cannot be replaced by another stereoisomer.

[0102] According to another aspect of the present invention, an isolated peptide of no more than 10 amino acids is provided, wherein the isolated peptide comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 1-33 and 34, wherein the peptide is capable of reducing the amount of dexamethasone-induced spleen and / or thymus weight loss in a mouse.

[0103] In one embodiment, the peptides of this aspect of the invention are 10 amino acids in length.

[0104] In one embodiment, the peptide of this aspect of the invention is 9 amino acids in length.

[0105] In one embodiment, the peptide of this aspect of the invention is 8 amino acids in length.

[0106] In one embodiment, the peptide of this aspect of the invention is 7 amino acids in length.

[0107] In one embodiment, the peptide of this aspect of the invention is 6 amino acids in length.

[0108] In one embodiment, the peptide of this aspect of the invention is 5 amino acids in length.

[0109] Examples of such peptides include the peptides listed in SEQ ID NOs: 1-34, and more specifically, the peptides listed in SEQ ID NOs: 1-5.

[0110] For any peptide described herein, the present invention also contemplates retro-inverso peptides, which are protease resistant peptides composed of D-amino acids in reverse order, resulting in a change in the peptide backbone but unchanged side chain orientation.

[0111] The peptides described herein can be used to treat a myriad of diseases, including those associated with stress-related responses. These include pathological conditions such as neurodegenerative diseases (such as stroke, Parkinson's disease and Alzheimer's disease), myocardial infarction, exposure to radiation or chemotherapeutic agents, inflammation, injury (such as burns and central nervous system damage), cellular aging, hyperthermia, epilepsy, hypoxia (such as ischemia and stroke), and transplanted tissues and organs prior to transplantation.

[0112] These conditions also include autoimmune diseases, which are characterized by an immune state of the individual against at least one normal component of the body. These phenomena are particularly observed in pathologies, including but not limited to infections associated with systemic lupus erythematosus disease (SLE), Gougerot-Sjogren syndrome (or Sjogren's disease), and rheumatoid polyarthritis, as well as pathologies such as sarcoidosis and osteopenia, spondyloarthritis, etc. Scleroderma, multiple sclerosis, amyotrophic lateral sclerosis (ALS), hyperthyroidism, Addison's disease, autoimmune hemolytic anemia, Crohn's disease, Goodpastures syndrome, Graves' disease, Hashimoto's thyroiditis, idiopathic purpura hemorrhage, insulin-dependent diabetes mellitus, myasthenia, pemphigus vulgaris, pernicious anemia, poststreptococcal glomerulonephritis, psoriasis and spontaneous infertility, as well as immediate or delayed phenomena observed during transplant rejection and graft-versus-host disease. In another embodiment, the peptides of the present invention can be used to treat ischemia or myocardial infarction.

[0113] According to certain embodiments, the disease is ALS.

[0114] Other diseases contemplated by the present invention include, but are not limited to, Alzheimer's disease, Parkinson's disease, secondary degeneration following trauma, stroke, CNS intoxication, glaucoma, macular degeneration, type 1 diabetes, systemic lupus erythematosus, autoimmune uveitis, graft-versus-host disease, transplant rejection, arthritis, systemic inflammatory response syndrome (SIRS), inflammatory bowel disease (IBD), adult respiratory distress syndrome (ARDS), psoriasis, atherosclerosis, myocardial infarction, radiation sickness, hyperthermia, hypoxia, fulminant hepatotoxicity, renal failure, infertility, and many other conditions.

[0115] Transplant rejection refers to an individual's immune state to foreign components (body fluids such as blood, cerebrospinal fluid, cells, tissues, organs, antibodies, etc.) intentionally implanted into the patient's body.

[0116] As used herein, the terms "degenerative condition," "degenerative disease," and "degenerative condition" refer to any disorder, disease, or condition characterized by inappropriate cell proliferation or inappropriate cell death, or in some cases both, or abnormal or unregulated apoptosis. These conditions also include conditions in which, despite being appropriate and regulated at the single cell level, excessive apoptosis is associated with organ dysfunction or failure.

[0117] In one embodiment, the peptides are used to prevent cell death in non-malignant tissues or cells of a subject suffering from a neoplastic disease and receiving chemotherapy and / or radiotherapy for the treatment of cancer.

[0118] As used herein, the terms "inflammatory disease" and "inflammatory condition" refer to any disease or condition in which an excessive or unregulated inflammatory response results in excessive inflammatory symptoms, host tissue damage, or loss of tissue function.

[0119] In one embodiment, the inflammatory disease or condition is an autoimmune disease.

[0120] In another embodiment, the inflammatory disease or condition has an etiology associated with the production of at least one pro-inflammatory cytokine selected from IL-6 and TNF-α.

[0121] In another embodiment, the disease or condition is selected from the group consisting of Alzheimer's disease, Parkinson's disease, secondary degeneration after trauma, stroke, central nervous system poisoning, glaucoma, macular degeneration, myocardial infarction, radiation sickness, hyperthermia, hypoxia, fulminant toxic liver, renal failure and infertility.

[0122] In another embodiment, the disease includes retinitis pigmentosa and macular degeneration.

[0123] In another embodiment, the disease comprises stroke or myocardial infarction.

[0124] The peptide may be provided alone or as a part of a pharmaceutical composition, mixed with a suitable carrier or excipient.

[0125] As used herein, "pharmaceutical composition" refers to a composition prepared by combining one or more active ingredients described herein with other chemical components (such as physiologically suitable carriers and excipients). The purpose of a pharmaceutical composition is to facilitate administration of a compound to an organism.

[0126] The “active ingredient” here refers to the peptide responsible for the biological effect.

[0127] Hereinafter, the terms "physiologically acceptable carrier" and "pharmaceutically acceptable carrier" are used interchangeably and refer to a carrier or diluent that does not cause significant irritation to an organism and does not impair the biological activity and properties of the given compound. Adjuncts are included under these terms.

[0128] Preparation of pharmaceutical compositions containing peptides or polypeptides as active ingredients is well known in the art. Typically, these compositions are prepared as indicative solutions or suspensions, however, solid forms that can be suspended or solubilized prior to injection can also be prepared. The formulations can also be emulsified. The active therapeutic ingredient is mixed with an inorganic and / or organic carrier that is pharmaceutically acceptable and compatible with the active ingredient. A carrier is a pharmaceutically acceptable excipient that contains more or less inert substances when added to a pharmaceutical composition to give the composition an appropriate consistency or form. Suitable carriers are, for example, water, saline, glucose, glycerol, ethanol or the like and combinations thereof. In addition, if desired, the composition can include a small amount of auxiliary substances, such as wetting agents or emulsifiers and pH buffers, which can enhance the effectiveness of the active ingredient.

[0129] The toxicity and therapeutic effects of the peptides described herein can be determined by standard pharmaceutical procedures in cell culture or experimental animals, for example, by determining the IC50 (the concentration that provides 50% inhibition) and LD50 (the lethal dose that causes 50% death of experimental animals) of the target compound. The data obtained from these cell culture assays and animal studies can be used to formulate a range of doses for human use. The dose may vary depending on the dosage form used and the route of administration. The specific formulation, route of administration and dose can be selected by the individual physician based on the patient's condition. (See Fingl et al., 1975).

[0130] The amount of the activating agent used in the drug delivery composition of the present invention is the amount that effectively realizes the purpose of the specific activating agent for the target indication. The amount of the activating agent in the composition is usually a pharmacologically, biologically, therapeutically or chemically effective amount. However, when the composition is used in a dosage unit form, the usage amount can be smaller, because the dosage unit form can include multiple compounds or activating agents in a single composition, and can also include a pharmaceutically, biologically, therapeutically or chemically effective split amount. Then, the total effective dose can be administered in a cumulative unit, wherein the total effective dose is an activating agent.

[0131] The therapeutically effective amount of the peptide of the present invention is an amount that can exert anti-apoptotic activity and / or anti-inflammatory activity when administered to a patient. Assays for detecting the anti-apoptotic activity of the peptide of the present invention include, but are not limited to, DNA staining with specific fluorescent dyes (such as propidium iodide and ethidium bromide), Annexin V assay, TUNEL assay, etc.; some non-limiting examples of such assays are presented in the examples below. Assays for detecting the activity of anti-inflammatory peptides are also well known in the art.

[0132] Although the appropriate dosage of the peptides of the present invention varies depending on the route of administration, age, weight, sex or condition of the patient and should ultimately be determined by a physician, a dosage suitable for adults (e.g., intravenous administration) may generally be between about 2-6 mg body weight, preferably between about 2-4 mg / kg.

[0133] The pharmaceutical composition of the present invention comprises one or more compounds of the present invention, and one or more adjuvants or diluents. In one embodiment, one or more of the compounds or solvents or salts of the compounds.

[0134] The term "pharmaceutically acceptable salt" as used herein refers to a salt that is substantially non-toxic to organisms. Typical pharmaceutically acceptable salts include those prepared by reacting the compounds of the present invention with pharmaceutically acceptable mineral acids or organic acids. Such salts are also referred to as acid addition salts.

[0135] Compositions comprising the compound and an active agent have utility in delivering the active agent to a selected biological system and in increasing or improving the bioavailability of the active agent compared to not using the active agent. Delivery can be improved by delivering a more active agent over a period of time, or delivering the active agent over a specific period of time (e.g., accelerated or delayed delivery) or over a period of time (e.g., sustained delivery).

[0136] Thus, the pharmaceutical compositions used according to the present invention may be formulated in a conventional manner using one or more physiologically acceptable carriers including adjuvants and auxiliaries which facilitate processing of the active compounds into preparations which can be used for pharmaceutical purposes. The correct formulation depends on the chosen route of administration.

[0137] The pharmaceutical composition may be administered locally or systemically by any conventional and appropriate route, including but not limited to oral, intraperitoneal, parenteral, intravenous, intramuscular, subcutaneous, transdermal, intrathecal, topical, rectal, buccal, by inhalation, or intranasal.

[0138] For injection, the compounds of the invention can be formulated in aqueous solution, preferably in a physiologically compatible buffer, such as Hank's solution, Ringer's solution, or physiological saline buffer. For transmucosal administration, penetrants are appropriate to the barrier to be permeated in the formulation. Such penetrants, such as DMSO or polyethylene glycol, are generally known in the art.

[0139] Pharmaceutical compositions for oral administration include push-fit capsules made of gelatin and soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol. The push-fit capsules may contain the active ingredient in a mixture with fillers such as lactose, binders such as starches, lubricants such as talc or magnesium stearate and, optionally, stabilizers.

[0140] In soft capsules, the active compound can be dissolved or suspended in a suitable liquid, such as a fatty oil, liquid paraffin or liquid polyethylene glycol. In addition, a stabilizer can also be added. The dosage of all oral preparations should be compatible with the selected route of administration.

[0141] Alternatively, the compounds of the invention may be incorporated into oral liquid preparations, for example, aqueous or oil suspensions, solutions, emulsions, syrups or elixirs. In addition, formulations containing these compounds may be constituted with water or other suitable carriers as dry products before use. Such liquid preparations may contain conventional additives, such as suspending agents, such as sorbitol syrup, methylcellulose, glucose / sugar syrup, gelatin, hydroxyethylcellulose, carboxymethylcellulose, aluminum stearate gel and hydrogenated edible fats; emulsifiers, such as lecithin, sorbitol monooleate or acacia; non-aqueous carriers (which may include edible oils), such as almond oil, fractionated coconut oil, oily esters, propylene glycol and ethanol; preservatives, such as methyl or propyl parabens and sorbic acid.

[0142] For administration by inhalation, the peptides used according to the invention are conveniently provided in the form of an aerosol spray from a pressurized bag or atomizer using a suitable propellant, for example, dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane or carbon dioxide. In the case of a pressurized aerosol, the dosage unit can be determined by providing a valve to deliver a metered amount. Capsules and powder boxes, for example made of gelatin, for use in inhalers or inhalers, can include a powdered mixture of the peptide and a suitable powdered matrix, such as lactose or starch, when formulated.

[0143] The pharmaceutical compositions of the present invention can also be used for topical and local applications. The term "topical" as used herein means "related to a specific surface area", such as skin and mucous membranes, and local preparations applied to a certain area of ​​the surface will only affect the area to which they are applied. The formulations of the peptides / peptide analogs can be administered topically as gels, ointments, creams, lotions and sustained-release formulations including transdermal patches, and may include liposomes and any other pharmaceutically acceptable carriers suitable for topical administration. The pharmaceutical compositions described herein may also include suitable gel phase solid carriers or excipients. Examples of such carriers or excipients include, but are not limited to, calcium carbonate, calcium phosphate, various sugars, starches, cellulose derivatives, gelatin and polymers, such as polyethylene glycol.

[0144] If desired, the compositions of the present invention may be presented in a package or dispenser device, such as a reagent kit approved by the FDA, which may include one or more unit dosage forms containing active ingredients. For example, the package may include metal or plastic foil, such as a blister pack. The package or dispenser device may be accompanied by regulatory instructions. The package or dispenser may also be accompanied by precautions associated with the container, in a form specified by a government agency that regulates the manufacture, use or sale of controlled drugs, and the precautions reflect the approval of the agency to the form of ingredients or human or veterinary regulatory agencies. For example, such precautions may be a prescription drug label approved by the U.S. Food and Drug Administration or an approved product instruction sheet. As described above, compositions of the present invention formulations prepared in compatible pharmaceutical carriers may also be prepared, placed in appropriate containers, and labeled for treatment of specified conditions.

[0145] Here, "approximately" means ±10%.

[0146] The terms "comprise", "comprising", "includes", "including", "having" and their conjugations mean "including but not limited to".

[0147] The term "consisting of" means "including and limited to."

[0148] The term "consisting essentially of" means that the composition, method or structure may include additional ingredients, steps and / or parts, but only if these additional ingredients, steps and / or parts do not materially change the basic and novel characteristics of the claimed composition, method or structure.

[0149] As used herein, the singular forms "a", "an" and "the" include plural forms unless the context clearly dictates otherwise. For example, the term "a compound" or "at least one compound" may include a plurality of compounds, including mixtures thereof.

[0150] Throughout the application, various embodiments of the present invention may be presented in range format. It should be understood that the description in range format is merely for convenience and brevity and should not be construed as an inflexible limitation on the scope of the invention. Therefore, the description of a range should be considered to have explicitly disclosed all possible subranges and individual values ​​within the range. For example, describing a range, such as 1 to 6, should be considered to have specifically disclosed subranges, such as 1 to 3, 1 to 4, 1 to 5, 2 to 4, 2 to 6, 3 to 6, etc., as well as individual numbers within the range, such as 1, 2, 3, 4, 5 and 6. This has nothing to do with the breadth of the range.

[0151] Whenever a numerical range is presented herein, it is meant to include any cited number (fractional or integer) within the presented range. The terms "ranging / ranges between" the first presented number and the second presented number, and "ranging / ranges from" the first presented number "to" the second presented number can be used interchangeably herein to include all fractions and integers between the first presented number and the second presented number.

[0152] Here, "method" refers to the ways, means, techniques and procedures to complete a task, including but not limited to the ways, means, techniques and procedures known to practitioners of chemistry, pharmacology, biology, biochemistry and medicine or developed from known ways, means, techniques and procedures.

[0153] As used herein, the term "treating" includes abrogating, substantially inhibiting, slowing or reversing the progression of a disease, substantially ameliorating the clinical or aesthetic symptoms of a disease, or substantially preventing the appearance of clinical or aesthetic symptoms of a disease.

[0154] It is worth noting that certain features of the present invention, for the sake of clarity, may be described in the context of separate embodiments, or may be provided in combination in a single embodiment. Conversely, various features of the present invention (described in the context of a single embodiment for the sake of simplicity) may also be provided separately or in any suitable sub-combination, or as appropriate for any other described embodiment of the present invention. Certain features described in the context of various embodiments cannot be considered essential features of those embodiments, unless the embodiments are invalid without these elements.

[0155]

[0066] Various embodiments and aspects of the present invention as described hereinabove and in the claims section below find experimental support in the following examples.

[0156] Example

[0157] Reference is now made to the following examples, which together with the above descriptions illustrate some embodiments of the invention in a non-limiting fashion.

[0158] Generally, the nomenclature used herein and the laboratory procedures utilized in the present invention include molecular, biochemical, microbiological and recombinant DNA techniques. Such techniques are explained in detail in the literature. For example, see Sambrook et al. (1989), "Molecular Cloning: A Laboratory Manual"; Ausubel, RM, ed., "Current Protocols in Molecular Biology," Volumes I-III (1994); Ausubel et al., "Current Protocols in Molecular Biology," John Wiley and Sons, Baltimore, Maryland (1989); Perbal, "A Practical Guide to Molecular Cloning," John Wiley & Sons, Baltimore, Maryland (1989); Wiley and Sons, New York (1988); Watson et al., "Recombinant DNA", Scientific American Books, New York; Birren et al., ed., "Genome Analysis: A Laboratory Manual Series", Vols. 1-4, Cold Spring Harbor Laboratory Press, New York (1998); U.S. Patent Nos.: 4,666,828; 4,683,202; 4,801,531; 5,192,659 and 5,272,057; "Cell Biology: A Laboratory Manual", Vols. I-III Cellis, JE, ed., (1994); "Animal Cell Culture - A Manual of Basic Techniques", Freshney, Wiley-Liss, NY (1994), 3rd edition; "Current Protocols in Immunology" Vols. I-III, Coligan JE, ed. (1994); Stites et al., eds., Basic and Clinical Immunology (8th ed.), Appleton & Lange, Norwalk, CT (1994); Mishell & Shiigi, eds., Selected Methods in Cellular Immunology, WH Freeman & Co., New York (1980); Available immunoassays are extensively described in the patent and scientific literature, see, e.g., U.S. Pat. Nos. 3,791,932; 3,839,153; 3,850, 752; 3,850,578; 3,853,987; 3,867,517; 3,879,262; 3,901,654; 3,935,074; 3,984,533; 3,996,345; 4,034,074; 4,098,876; 4,879,219; 5,011,771 and 5,281,521; "Oligonucleotide Synthesis" Gait, MJ, ed. (1984); "Nucleic Acid Hybridization" Hames, BD and Higgins SJ, ed. (1985); "Transcription and Translation" Hames, BD and Higgins S.J., ed. (1984); "Animal Cell Culture" Freshney, RI, ed. (1986); "Immobilized Cells and Enzymes" IRL Press, (1986); "A Practical Guide to Molecular Cloning" Perbal, B., (1984) and "Methods in Enzymology" Volumes 1-317, Academic Press; "PCR Protocols: A Methods Guide and Applications", Academic Press, San Diego, CA (1990); Marshak et al., "Protein Purification and Characterization Strategies - A Laboratory Course Manual" CSHL Press (1996); all of the above are incorporated herein by reference. Other general references are provided throughout the document. The procedures therein are believed to be well known in the art and are provided for the convenience of the reader. All information contained therein is incorporated herein by reference. .

[0159] Example 1

[0160] method:

[0161] Dexamethasone is a corticosteroid drug that induces apoptosis in immune cells and lymphoid tissue cells. BALB / c mice were used to examine the ability of candidate peptides to rescue lymphocytes from apoptosis. Mice were injected intraperitoneally with 100 μg of dexamethasone. Dexamethasone-treated mice were immediately injected with candidate peptides (200 μg peptide / mouse) 24 hours after dexamethasone treatment. Mice were sacrificed 48 hours after the first treatment. The spleen and thymus were weighed and the whole cell count of both organs was counted.

[0162] The peptides used in the screening were SEQ ID NOs: 1 to 13. The peptide of SEQ ID NO: 42 was used as a positive control. The peptides of SEQ ID NOs: 35 to 41 were used as negative controls.

[0163] result:

[0164] The results are summarized in Tables 3 and 4.

[0165] Table 3

[0166]

[0167] Table 4

[0168]

[0169] Dexamethasone induced a decrease in spleen and thymus weight, a 50% decrease in spleen cell number, and a 60% decrease in thymus cell number compared with normal mice.

[0170] All peptides in Table 3 showed significant improvement over SEQ ID NO: 42. All peptides in Table 4 showed reduced effects compared to SEQ ID NO: 42.

[0171] Although the present invention has been described in conjunction with its specific embodiments, it is obvious that many alternatives, modifications and variations are obvious to those skilled in the art. Therefore, it is intended to include all such alternatives, modifications and variations that are consistent with the spirit and broad scope of the appended claims.

[0172] All publications, patents, and patent applications mentioned in this specification are hereby incorporated by reference in their entirety into this specification, just as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference into this specification. In addition, citation or identification of any reference in this application shall not be construed as an admission that the reference is prior art to the present invention. To the extent that section headings are used, they should not be construed as necessarily limiting.

[0173] Furthermore, the priority document of the present application is incorporated herein by reference in its entirety.

Claims

1. An isolated peptide, characterized in that: The isolated peptide consists of the amino acid sequence represented by SEQ ID NO:

1.

2. A pharmaceutical composition, characterized in that: The pharmaceutical composition comprises the peptide as claimed in claim 1 as an active agent and a physiologically acceptable carrier.

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