Patent Application
20220031813
The present invention relates to a composition for inhibiting formation of leukocyte extracellular traps containing lactoferrin as an active ingredient, and a composition for treating a disease associated with the formation of the leukocyte extracellular traps. The present invention also relates to a method for treating a disease associated with the formation of hemocyte extracellular traps using the composition for inhibition or the composition for treatment.
NETs (neutrophil extracellular traps) are extracellular structures that release mesh-like structures, capture bacteria, true fungi, parasitic worms and viruses, and exhibit an antibacterial action when neutrophils are activated by contamination with bacteria, the form of the segmented neutrophils and the distribution of chromatin are made unclear, then the nuclear membrane is extinguished, cytoplasm and granular components are existent in the chromatin structure in a mixed state, and the cell membrane is broken. NETs mainly involve DNAs, and histone 3 (H3) and elastase play an important role in the action of NETs. Formation of the NETs locally collects antibacterial molecules that efficiently kill microorganisms. The formation of the NETs causes NETosis of the neutrophils, but the molecular mechanism thereof has not been much clarified. The NETs are formed by the neutrophils being stimulated with TNF-α, PMA, LPS, IL-8 or the like, and NETosis caused at the time of the formation of NETs exhibits a different form from classically known necrosis or apoptosis that causes activation of caspase or fragmentation of DNAs. When the neutrophils are stimulated by LPS or PMA, autophagy is caused, and at the same time, activated oxygen is generated. This causes degradation of nuclear membrane, decondensation of chromatin, and citrullination of histone, and thus NETosis is caused (Non-patent documents 1 and 2).
It has been reported that along with the formation of the NETs, many proteins, especially, antibacterial proteins contained in azurophilic granule or type-II granule, are secreted from the neutrophils by degranulation, and proteins related to cell structure are also secreted (Non-patent document 2). These proteins are also called “NETs constructing proteins”. Reported as such proteins are neutrophil elastase, histone, myeloperoxidase, F-actin, lactoferrin, matrix metalloprotease 9, LL37, cathepsin G, BPI, proteinase 3, calprotectin, azurocidin, lysozyme C, defensin, catalase and the like (Non-patent document 3).
Lactoferrin is contained in type-II granule in the neutrophils. The neutrophils form the NETs and finally cause degranulation, and lactoferrin is released to the outside of the neutrophils (Non-patent document 1).
Lactoferrin is well preserved in mammals, and there is little difference in the function of lactoferrin among different species of mammals. Today, lactoferrin is a target of attention as a protein contained in milk for the physiological activity thereof, and is commercially available. It should be noted that milk has been reported as not having an inhibitory effect on the formation of the NETs of bovine neutrophils (Non-patent document 4).
The NETs are involved in enlargement and growth of thrombus. When the NETs are released, histone contained therein has an action of condensing platelets. Thus, platelet thrombus is formed based on the NETs. Neutrophil elastase or cathepsin G contained in the NETs degrades tissue factor pathway inhibitor and promotes blood clotting reaction. The NETs play a role of keeping the microorganisms and the like at a local site by such an action (Non-patent document 5).
The action of the NETs that is to be exhibited originally is to capture external microorganisms such as gram-positive bacteria, gram-negative bacteria, true fungi and the like, and confine and kill such external microorganisms at a local site. Owing to having such an action, the NETs are often seen in infectious diseases. However, it has also been reported that when an infectious disease becomes chronic, the NETs are formed even in the absence of external microorganisms. Systemic lupus erythematosus (SLE), which is one of chronic and intractable autoimmune diseases, is known to form autoantibody against self-DNA or related proteins and thus cause inflammation in tissues or organs. A characteristic finding regarding SLE is that many neutrophils are present in the injury site. It is known that in the serum of an SLE patient, antibacterial peptide LL37 and DNAs in the NETs are existent (Non-patent documents 6 and 7). Such a substance is recognized by B cells as autoantigen, and thus autoantibody is produced. The neutrophils in an SLE patient are more likely to cause NETosis than the neutrophils in a healthy person (Non-patent document 6). These factors are considered to induce chronic inflammation. It has been reported that the IgG fragment in the serum of a patient of anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis, which is a disease caused by autoantibody, has an ability of forming the neutrophil NETs that is about twice as high as the ability of a healthy person (Non-patent documents 8 and 9).
The relationship between the formation of the NETs and diseases has been a target of attention merely recently, more specifically, since the report by Brinkman et al. in 2004 (Non-patent document 1) was made. In the future, diseases caused by the formation of the NETs will be newly revealed. Although the formation of the NETs plays an important role in protecting a living body against infection, inhibition of the formation of the NETs is considered to be necessary to improve some disease conditions as described above.
A substance that inhibits the formation of the NETs, for example, Streptococcus, which is gram-positive bacteria such as Streptococcus pneumoniae, Staphylococcus aureus or the like have been reported to express DNase extracellularly. As substances that suppress production of antibody against histone or superoxide, diphenyleneiodoniumchloride (DPI) and catalase have been reported (Non-patent document 10).
In addition, it is known, for example, that myeloperoxidase (MPO) activity influences NETosis (Non-patent document 11) and that the phenomenon that the neutrophils form the NETs and are put to death, namely, NETosis is a different process from apoptosis or necrosis (Non-patent document 10).
There is prior art of preventing an autoimmune disease such as type I diabetes or rheumatoid arthritis by use of milk-derived basic protein fragment as an active ingredient (Patent document 1). This prior art is specialized for adjustment of immunocyte, mainly, lymphocyte, suppression of inflammatory cytokine, and the like, but is not regarding the action of inhibiting the formation of the NETs.
So far, no therapeutic drug for a disease caused by the formation of the NETs has been reported.
An object of the present invention is to provide a fundamental therapeutic drug for a disease caused by the formation of leukocyte extracellular traps, especially a safe and effective therapeutic drug, and also a therapeutic method, suitable for preservation of remission (suppression of relapse) performed for a long period of time.
As a result of active studies made for the purpose of solving the above-described problem, the present inventors found that lactoferrin exhibits a significant suppressing effect on the formation of NETs and realizes fundamental therapy of NETs-related diseases. It has also been found that the present invention significantly improves the survival rate of model animals for ANCA associated vasculitis, local Shwartzman reaction and disseminated intravascular coagulation (DIC), which diseases are caused by the formation of the NETs.
Namely, the present invention provides the following.
[1] A composition for inhibiting formation of leukocyte extracellular traps, comprising lactoferrin.
[2] The composition according to [1] above, wherein the lactoferrin is in an amount of 0.001 to 10 g/kg/day.
[3] The composition according to [1] above, wherein the lactoferrin is derived from human.
[4] The composition according to [1] above, wherein the lactoferrin is a protein selected from the group consisting of (a) to (c):
(a) a protein formed of either one of amino acid sequences of SEQ ID NOS: 1 to 5;
(b) a protein formed of either one of amino acid sequences of SEQ ID NOS: 1 to 5, in which 1 to 66 amino acids are deleted, substituted, inserted and/or added, the protein having activity of inhibiting the formation of the leukocyte extracellular traps; and
(c) a protein having an amino acid sequence having an amino acid sequence identity of 90% or greater with either one of amino acid sequences of SEQ ID NOS: 1 to 5, the protein having activity of inhibiting the formation of the leukocyte extracellular traps.
[5] The composition according to any one of [1] to [5] above, wherein the leukocytes are one selected from the group consisting of neutrophils, eosinophil granulocytes, basophil granulocytes, monocytes, macrophages, and mast cells.
[6] The composition according to [5] above, wherein the leukocytes are neutrophils.
[7] A composition for treating a disease associated with formation of leukocyte extracellular traps, the composition comprising lactoferrin.
[8] The composition according to [7] above, wherein the lactoferrin is in an amount of 0.001 to 10 g/kg/day.
[9] The composition according to [7] above, wherein the lactoferrin is derived from human.
[10] The composition according to [7] above, wherein the lactoferrin is a protein selected from the group consisting of (a) to (c):
(a) a protein formed of either one of amino acid sequences of SEQ ID NOS: 1 to 5;
(b) a protein formed of either one of amino acid sequences of SEQ ID NOS: 1 to 5, in which 1 to 66 amino acids are deleted, substituted, inserted and/or added, the protein having activity of inhibiting the formation of the leukocyte extracellular traps; and
(c) a protein having an amino acid sequence having an amino acid sequence identity of 90% or greater with either one of amino acid sequences of SEQ ID NOS: 1 to 5, the protein having activity of inhibiting the formation of the leukocyte extracellular traps.
[11] The composition according to any one of [7] to [10] above, wherein the leukocytes are one selected from the group consisting of neutrophils, eosinophil granulocytes, basophil granulocytes, monocytes, macrophages, and mast cells.
[12] The composition according to any one of [7] to [11] above, wherein the disease is one selected from the group consisting of ANCA associated vasculitis, systemic lupus erythematosus, local Shwartzman reaction, acute kidney injury (AKI) accompanied by ischemia reperfusion injury, and disseminated intravascular coagulation.
[13] The composition according to any one of [7] to [12] above, which is in a form of food.
[14] The composition according to any one of [7] to [12] above, which is in a form of an injection agent.
[15] The composition according to any one of [7] to [13] above, which is orally administrable.
[16] A method for inhibiting formation of leukocyte extracellular traps, the method comprising administering lactoferrin to a patient.
[17] A therapeutic method for a disease associated with formation of leukocyte extracellular traps, the therapeutic method comprising administering lactoferrin to a patient.
The present invention provides a therapeutic method with little side effect for a disease caused by the formation of the leukocyte extracellular traps. The method has little side effect and therefore has an advantage of being safely usable for a wide range of patients and people having possibility of becoming patients.
The compositions for inhibition and treatment according to the present invention are usable for a wide range of subjects including subjects with immune system depression such as senior people, cancer patients and the like, and subjects who have infectious diseases or complications or who had tuberculosis. The present invention provides a therapeutic drug and a therapeutic method for a disease associated with the formation of the leukocyte extracellular traps that have little side effect even if being used for a long period of time. The compositions for inhibition and treatment according to the present invention are especially useful as a drug that is usable for a long period of time for treating the above-described diseases, as a drug that suppresses relapse after an acute symptom of a subject remits, or a therapeutic drug for the above-described diseases that become chronic.
Hereinafter, the present invention will be described in detail. The following embodiments are provided to illustrate the present invention, and the present invention is not to be construed as being limited to any of the following embodiments. The present invention may be carried out in various embodiments without departing from the gist thereof.
All the documents and the patent documents including the laid-open publications, the patents and the like that are cited in the specification are incorporated herein by reference. This specification incorporates the contents of the specification and the drawings of the Japanese patent application, filed on Apr. 9, 2013, upon which the present application claims priority (Japanese Patent Application No. 2013-081243).
In a first embodiment, the present invention provides a lactoferrin-containing composition for inhibition of formation of leukocyte extracellular traps (hereinafter, referred to as the “composition for inhibition according to the present invention”).
Extracellular traps have been reported as being formed by many types of leukocytes. For example, extracellular traps have been reported as being formed by neutrophils (Brinkmann, V., et al., Science 2004; 303:1532-1535), basophil granulocytes (Yousefi, S., et al., Nat Med 2008; 14:949-953), mast cells (von Koeckritz-Blickwede M, et al., Blood 2008; 111:3070-3080), and monocytes (Webster S J, et al., J Immunol 2010; 185:2968-2979; for example, macrophages (Chow, O. A., et al., Cell Host & Microbe, Volume 8, Issue 5, 445-454, 18 Nov. 2010)), and the like.
The extracellular traps formed by such types of leukocytes have been reported to have a common feature of releasing fiber components mainly containing DNAs and granule proteins (Simon, D., et al, Allergy 68 (2013) 409-416).
The composition for inhibition according to the present invention aggregates and/or condenses the fiber components and thus can suppress the release of the fiber components (see
Lactoferrin, which is an active ingredient of the composition for inhibition according to the present invention, may be any lactoferrin derived from mammals with no specific limitation. The lactoferrin is preferably derived from mammalian milk that is drinkable by human (e.g., milk of cow, goat, sheep, human), and is more preferably derived from human milk. Alternatively, lactoferrin may be derived from neutrophils of the mammals.
Amino acid sequences of lactoferrin derived from various types of mammals are known (see Table 1 below).
In an embodiment, lactoferrin used for the composition for inhibition according to the present invention is a protein selected from the group consisting of (a) to (c) below:
(a) a protein formed of either one of amino acid sequences of SEQ ID NOS: 1 to 5;
(b) a protein formed of either one of amino acid sequences of SEQ ID NOS: 1 to 5, in which 1 to 66 amino acids are deleted, substituted, inserted and/or added, the protein having activity of inhibiting the formation of the leukocyte extracellular traps; and
(c) a protein having an amino acid sequence having an amino acid sequence identity of 90% or greater with either one of amino acid sequences of SEQ ID NOS: 1 to 5, the proteins having activity of inhibiting the formation of the leukocyte extracellular traps.
The protein of (b) or (c) above is typically a variant of either one of polypeptides of SEQ ID NOS: 1 to 5 naturally existent, but encompasses proteins that can be artificially acquired by use of a site-specific mutation induction method described in, for example, “Sambrook & Russell, Molecular Cloning: A Laboratory Manual Vol. 3, Cold Spring Harbor Laboratory Press 2001”, “Ausubel, Current Protocols in Molecular Biology, John Wiley & Sons 1987-1997”, “Nuc. Acids. Res., 10, 6487 (1982)”, “Proc. Natl. Acad. Sci. USA, 79, 6409 (1982)”, “Gene, 34, 315 (1985)”, “Nuc. Acids. Res., 13, 4431 (1985)”, “Proc. Natl. Acad. Sci. USA, 82, 488 (1985)”, and the like.
In this specification, the “protein formed of either one of amino acid sequences of SEQ ID NOS: 1 to 5, in which 1 to 66 amino acids are deleted, substituted, inserted and/or added, the protein having activity of inhibiting the formation of the leukocyte extracellular traps” encompasses proteins formed of either one of amino acid sequences of SEQ ID NOS: 1 to 5, in which, for example, 1 to 66 amino acid residues, 1 to 65 amino acid residues, 1 to 60 amino acid residues, 1 to 55 amino acid residues, 1 to 50 amino acid residues, 1 to 49 amino acid residues, 1 to 48 amino acid residues, 1 to 47 amino acid residues, 1 to 46 amino acid residues, 1 to 45 amino acid residues, 1 to 44 amino acids, 1 to 43 amino acid residues, 1 to 42 amino acid residues, 1 to 41 amino acid residues, 1 to 40 amino acid residues, 1 to 39 amino acid residues, 1 to 38 amino acid residues, 1 to 37 amino acid residues, 1 to 36 amino acid residues, 1 to 35 amino acid residues, 1 to 34 amino acid residues, 1 to 33 amino acid residues, 1 to 32 amino acid residues, 1 to 31 amino acid residues, 1 to 30 amino acid residues, 1 to 29 amino acid residues, 1 to 28 amino acid residues, 1 to 27 amino acid residues, 1 to 26 amino acid residues, 1 to 25 amino acid residues, 1 to 24 amino acid residues, 1 to 23 amino acid residues, 1 to 22 amino acid residues, 1 to 21 amino acid residues, 1 to 20 amino acid residues, 1 to 19 amino acid residues, 1 to 18 amino acid residues, 1 to 17 amino acid residues, 1 to 16 amino acid residues, 1 to 15 amino acid residues, 1 to 14 amino acid residues, 1 to 13 amino acid residues, 1 to 12 amino acid residues, 1 to 11 amino acid residues, 1 to 10 amino acid residues, 1 to 9 (1 to several) amino acid residues, 1 to 8 amino acid residues, 1 to 7 amino acid residues, 1 to 6 amino acid residues, 1 to 5 amino acid residues, 1 to 4 amino acid residues, 1 to 3 amino acid residues, 1 to 2 amino acid residues, or 1 amino acid residue is deleted, substituted, inserted and/or added, the proteins having activity of inhibiting the formation of the leukocyte extracellular traps. Generally, the number of the amino acid residues deleted, substituted, inserted and/or added is preferably as small as possible.
Such a protein encompasses proteins having an at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, at least 99.1%, at least 99.2%, at least 99.3%, at least 99.4%, at least 99.5%, at least 99.6%, at least 99.7%, at least 99.8%, or at least 99.9% amino acid sequence identity with either one of amino acid sequences of SEQ ID NOS: 1 to 5, and the proteins having activity of inhibiting the formation of the leukocyte extracellular traps. Generally, the degree of the amino acid sequence identity is preferably as high as possible.
Regarding “activity of inhibiting the formation of the leukocyte extracellular traps”, the leukocytes are derived from an organism that forms the leukocyte extracellular traps. The leukocytes are preferably derived from vertebrata, and more preferably derived from mammals. Examples of the mammals include human, cow, horse, goat, sheep, dog, and cat. Preferably, the mammal is human.
Preferably, the leukocytes are derived from the above-listed organism and also are one selected from the group consisting of neutrophils, eosinophil granulocytes, basophil granulocytes, monocytes, macrophages, and mast cells. More preferably, the leukocytes are one selected from the group consisting of neutrophils, basophil granulocytes, monocytes, macrophages, and mast cells. More preferably, the leukocytes are neutrophils.
The leukocytes are cultured in the presence of, or in the absence of, lactoferrin, and the culturing system is observed by a microscope to confirm that the formation of the extracellular traps decreases in the presence of lactoferrin. Thus, it can be confirmed that lactoferrin has activity of inhibiting the formation of the leukocyte extracellular traps can be confirmed.
Preferably, the leukocytes are treated with an extracellular trap formation stimulant (paramethoxyamphetamine (PMA), lipopolysaccharide (LPS), etc.) before lactoferrin is added thereto.
Alternatively, the culture supernatant of the culturing system is recovered, and the DNA concentration in the supernatant is measured. In this manner also, it can be confirmed that lactoferrin has activity of inhibiting the formation of the leukocyte extracellular traps. The DNA concentration is of the DNAs released into the culture supernatant mainly at the time of the formation of the extracellular traps.
In the case where the formation of the extracellular traps is inhibited by lactoferrin, the DNA concentration in the supernatant is lower than that in the absence of lactoferrin.
In this case also, it is preferable that the leukocytes are treated with an extracellular trap formation stimulant (paramethoxyamphetamine (PMA), lipopolysaccharide (LPS), etc.) before lactoferrin is added thereto.
The DNA concentration can be simply measured by use of a commercially available kit (Picogreen dsDNA assay reagent (P11496 Invitrogen)).
For the culturing conditions of each type of leukocytes and the method for confirming whether the extracellular traps have been formed, the following may be referred to: neutrophils (Brinkmann, V., et al., Science 2004; 303:1532-1535), A. K Gupta. FEBS letters 2010; 584:3193-3197, D J Novo. Antimicrob Agents Chemother. 2000; 44(4):827-34), basophil granulocytes (Yousefi, S., et al., Nat Med 2008; 14:949-953), mast cells (von Köckritz-Blickwede M, et al., Blood 2008; 111:3070-3080), monocytes (Webster S J, et al., J Immunol 2010; 185:2968-2979: for example, macrophages (Chow, O. A., et al., Cell Host & Microbe, Volume 8, Issue 5, 445-454, 18 Nov. 2010)).
The expression provided regarding an amino acid sequence of each protein of the present invention that “one or a plurality of (e.g., 2 to 9) amino acid residues are deleted, substituted, inserted and/or added” indicates that one or a plurality of amino acid residues are deleted, substituted, inserted and/or added at any position among one or a plurality of positions of the amino acid sequence. Two or more among deletion, substitution, insertion and addition may occur at the same time.
Examples of mutually substitutable amino acid residues will be shown below. Amino acid residues included in the same group are mutually substitutable. Group A: leucine, isoleucine, norleucine, valine, norvaline, alanine. 2-aminobutyric acid, methionine, o-methylserine, t-butylglycine, t-butylalanine, cyclohexylalanine: group B: aspartic acid, glutamic acid, isoaspartic acid, isoglutamic acid, 2-aminoadipic acid, 2-aminosberic acid; group C: asparagine, glutamine; group D: lysine, arginine, orthinine, 2,4-diaminobutyric acid, 2,3-diaminopropionic acid; group E: proline, 3-hydroxyproline, 4-hydroxyproline; group F: serine, threonine, homoserine; group G: phenylalanine, tyrosine.
The lactoferrin used in the present invention may be modified with a compound. For example, the lactoferrin may be a modified protein bonded with polyethyleneglycol (Japanese Patent No. 4195486, Japanese Patent No. 4261531, International Publication WO2009/113743) or a fused protein fused with another protein or a fragment thereof (e.g., protein stable in the blood, i.e., IgG, albumin or a fragment thereof, etc.) (Japanese Patent Application No. 2012-98085).
By use of the composition for inhibition according to the present invention, the formation of the leukocyte extracellular traps can be effectively inhibited. Namely, the use of the composition for inhibition according to the present invention can provide therapy of a disease associated with the formation of the leukocyte extracellular traps (hereinafter, the therapeutic method using the composition for inhibition according to the present invention will be referred to as the “therapeutic method of the present invention”).
In this specification, the term “therapy” generally indicates improving a symptom of a human or a mammal other than the human. The term “improvement” indicates that the degree of the disease is alleviated or is not deteriorated as compared with in the case where, for example, lactoferrin is not administered. The term “therapy” also encompasses “prevention”.
In this case, the target of therapy (patient) is an organism suffering, or having a risk of suffering, from a disease associated with the formation of the leukocyte extracellular traps. The target of therapy is preferably vertebrata, and is more preferably a mammal. The mammal is selected from the group consisting of human, cow, horse, goat, sheep, dog and cat. The target of therapy is still more preferably human.
Regarding the therapeutic method of the present invention, the “disease associated with the formation of the leukocyte extracellular traps” may be any disease, with no specific limitation, by which the formation of the leukocyte extracellular traps is observed to increase in the body of the patient.
Such diseases include, for example, ANCA associated vasculitis (Wegener's granulomatosis, microscopic polyangitis, allergic granulomatosis-angitis, etc.), acute kidney injury (AKI) accompanied by ischemia reperfusion injury, systemic lupus erythematosus (SLE), appendicitis, aspergillosis, pneumonia, infection with Diplococcus pneumoniae, necrotizing fasciitis, infection with Streptococcus, sepsis, preeclampsia, Crohn's disease, Schistosomiasis, periodontitis, tuberculosis, mastitis, malaria, cystic fibrosis, and thrombosis diseases such as deep venous thrombosis (von Bruhl, M. L., et al., J Exp Med. 2012 Apr. 9; 209(4):819-35), myocardial infarction (de Boer, O. J., Thromb Haemost. 2013 February; 109(2):290-7), tumor-related thrombosis (Demers, M., Proc Natl Acad Sci USA; 2012 Aug. 7; 109(32):13076-81), disseminated intravascular coagulation (DIC) (Tobias A. et al., blood, 29 Sep. 2011, vol. 118, no. 13, pp. 3708-3714), and the like (Non-patent documents 2 and 12). Vasculitis syndrome is classified into large vessel vasculitis, medium vessel vasculitis, and small vessel vasculitis, depending on the size of the vessel in which the disease occurs. The NETs-related diseases such as ANCA associated vasculitis, SLE and the like mentioned above are classified into the small vessel vasculitis. However, DIC is often developed together with a severe case of polyarteritis nodosa, which is medium vessel vasculitis (Guidelines on diagnosis and therapy of circulatory system diseases (report by the 2006-2007 joint research team)), sepsis or solid cancer. With these diseases, the cytotoxicity caused by the formation of the leukocyte extracellular traps (e.g., NETs) causes vascular endothelial dysfunction, and thus organ dysfunction is caused. With the above-mentioned thrombosis diseases, the formation of the leukocyte extracellular traps (e.g., NETs) acts as a trigger to promote cascade of the formation of thrombus. It is considered that lactoferrin suppresses the formation and release/diffusion of the leukocyte extracellular traps (e.g., NETs) to prevent vascular endothelial dysfunction, also suppresses the cascade of the formation of thrombosis to provide an action of protecting the organs, and thus has a therapeutic effect for the above-mentioned diseases.
The diseases which are targets of therapeutic method of the present invention are preferably ANCA associated vasculitis (Wegener's granulomatosis, microscopic polyangitis, allergic granulomatosis-angitis, etc.), systemic lupus erythematosus, local Shwartzman reaction, and acute kidney injury (AKI) accompanied by ischemia reperfusion injury; and are more preferably microscopic polyangitis accompanied by increase in the antibody titer of MPO-ANCA (myeloperoxidase specific anti-neutrophil cytoplasmic antibody) in the blood, allergic granulomatosis-angitis, and disseminated intravascular coagulation (DIC).
It has been reported that lactoferrin is used for treating autoimmune diseases such as type I diabetes and rheumatoid arthritis (Patent Document 1). However, the autoimmune diseases such as type I diabetes and rheumatoid arthritis are not considered to be caused mainly by the formation of the leukocyte extracellular traps. Therefore, it is highly possible that lactoferrin does not act via the formation of the extracellular traps in the therapy described in the above-described report.
Namely, according to the present invention, lactoferrin exhibits a therapeutic effect on the above-mentioned diseases by a completely novel mechanism, more specifically, a mechanism of inhibiting the formation of the leukocyte extracellular traps.
Therapy of the diseases caused by SLE or ANCA uses steroid, an immunosuppressing drug or the like. Such a therapeutic method has problems of imposing a physical load (side effect or the like) on the patient, causing the patient to suffer, and having a high risk of inducing another disease (infectious disease).
By contrast, according to the present invention, lactoferrin contained in food is used as an active ingredient. This is advantageous in causing fewer side effects, not causing the patient to suffer, and having a lower risk of inducing another disease.
In another embodiment, the present invention provides a lactoferrin-containing composition for treating a disease associated with the formation of the leukocyte extracellular traps (hereinafter, referred to as the “composition of the present invention”).
The term “composition” indicates a composition containing an additive such as a carrier or the like used in preparation of an active ingredient useful in the present invention (lactoferrin, etc.).
Regarding the composition of the present invention, the “lactoferrin” and the “disease associated with the formation of the leukocyte extracellular traps” are as described above.
The administration route of the composition of the present invention may be any of generally used routes with no specific limitation. Specific examples of the administration route include oral administration, sublingual administration, transnasal administration, pulmonary administration, administration via alimentary canal, transdermal administration, instillation, intravenous injection, subcutaneous injection, intramuscular injection, intraperitoneal injection, local injection, and surgical implant. Preferable examples of the administration route are oral administration and intravenous injection.
The composition of the present invention may be provided as a solid formulation such as capsule, tablet, powder or the like; a liquid formulation such as solution, suspension, emulsion or the like; or a semi-liquid formulation such as ointment, cream, paste or the like.
In the case of being orally administered, the composition is preferably provided as a solid formation. In the case of being injected, the composition is preferably provided as a solid formulation encompassing a formulation realized by lyophilization or a liquid formulation.
In the case of being orally administered, the composition of the present invention is more preferably prepared as an enteric formulation. Lactoferrin orally taken is known to be easily digested with pepsin in the stomach. The composition prepared as an enteric formulation is taken into the body at a higher rate (Takeuchi et al., Exp Physiol. 2006 November; 91(6):1033-40). In this case, it is desirable that lactoferrin powder is compressed in a dry state and coated with an enteric coating material because lactoferrin is thermally unstable when containing moisture (Japanese patents regarding NRL formulation: Japanese Patent No. 4050784 regarding granules, Japanese Patent No. 4592041 regarding tablets).
Lactoferrin may be taken by human or an animal other than the human as food or feed as being added to the food or feed. A method for producing such food or feed is known to a person of ordinary skill in the art. Lactoferrin may also be formulated as a solution formation, more specifically, as an injection agent.
Alternatively, such lactoferrin or lactoferrin degradation may be added to a nutrient, food, drink or the like as it is or in the form of a formulation.
Lactoferrin may be used independently or in a combination with another pharmacologically acceptable component.
For example, a composition as a formulation for oral administration such as powder, granule, tablet, capsule or the like is prepared by a normal method by use of starch, lactose, white sugar, mannitol, carboxymethycellulose, corn starch, inorganic salt or the like. For this type of composition, other than the excipients as listed above, a coating agent, a binder, a disintegrant, a surfactant, a lubricant, a fluidity enhancer, a colorant, a flavor material or the like is usable when necessary.
The composition of the present invention may contain lactoferrin, which is an active ingredient, in a therapeutically effective amount. The expression “therapeutically effective amount” refers to an amount of lactoferrin as an active agent which, when being administered to the target, alleviates or does not deteriorate the symptom of the disease associated with the formation of the leukocyte extracellular traps as compared with in the case where lactoferrin is not administered. The therapeutically effective amount” encompasses an amount that is effective for prevention.
In the case where, for example, the composition may be orally administered, the therapeutically effective amount is 0.001 to 10 g/kg/day, 0.005 to 10 g/kg/day, 0.01 to 10 g/kg/day, or 0.01 to 5 g/kg/day. In the case where the composition is administered to human, the therapeutically effective amount is generally 10 mg to 15,000 mg, 10 mg to 12,000 mg, 10 mg to 10,000 mg, 20 mg to 10,000 mg, 20 mg to 8,000 mg, 30 mg to 8,000 mg, or 30 mg to 6,000 mg per day. Such a dose per day may be administered at once or as being divided into several times to a patient who needs therapy of a disease associated with the formation of the leukocyte extracellular traps.
The dose and frequency of administration of the composition of the present invention vary in accordance with various factors including the species, body weight, gender, age, and degree of advancement of the tumor disease of the target, and the administration route to the target. A person of ordinary skill in the art such as a physician, a veterinarian, a dentist, a pharmacist or the like could determine the dose of administration in consideration of these factors.
In the above, typical values are listed regarding the therapeutically effective amount, and the dose and frequency of administration. Even a value above or below the list may sufficiently be therapeutically effective. Therefore, even a value above or below the therapeutically effective amount, or the dose or frequency of administration is encompassed in the therapeutically effective amount, or the dose or frequency of administration of the composition of the present invention.
Hereinafter, the present invention will be described in detail by way of examples. The present invention is not to be limited to any of the embodiments described in the examples.
From heathy persons, 15 ml to 20 ml of peripheral blood was sampled for one cycle of experiment with an EDTA-containing syringe (needle: 18 to 22 G). After the blood sampling, 3 ml of mono-poly resolving medium (Cat No. DSBN100, DS Pharma Biomedical Co., Ltd.) contained in 15 ml conical tube, and then 3.5 ml of the whole blood were gently stacked in the lower-layer mono-poly resolving medium. The 15 ml conical tube was centrifuged at room temperature (15 to 30° C.) at 400×g for 20 minutes by a swing-type centrifuge, and then the conical tube was taken out gently. A brown plasma layer in the top layer and a lymphocyte/monocyte layer immediately below the brown plasma layer were removed by an aspirator or the like. A transparent layer below the lymphocyte/monocyte layer was removed as much as possible. A pale pink layer below the transparent layer was taken out by a Pasteur pipette. In order to wash neutrophils, the pale pink layer was transferred to a test tube containing phosphate-buffered saline (PBS(−): 137 mM sodium chloride, 2.7 mM potassium chloride, 8.1 mM disodium hydrogenphosphate dodecahydrate, 1.47 mM potassium dihydrogenphosphate). The test tube containing the neutrophils was centrifuged at room temperature (15 to 30° C.) at 200×g for 10 minutes. The test tube was taken out, and the supernatant was discarded. 4° C. sterilized water was added to the neutrophils in the test tube and left still on ice for 30 seconds to cause hemolysis of erythrocytes mixed therein. After the hemolysis, 45 ml of PBS(−) was added to the test tube, and the test tube was centrifuged at 200×g for 10 minutes. The test tube was taken out, and the supernatant was discarded. The precipitation was suspended in culture DMEM+2% human serum Alb (serum human albumin; Product No. A9080 Sigma+4 mM L-glutamine), and left at 8° C. until immediately before being used. The neutrophils were separated in the number of 1×106/ml to 1×107/ml. The purity, which was obtained by visually counting the post-cytospin sample stained with Giemsa, was 95 to 98%.
About 1 hour after the isolation of the neutrophils described in “1. Method of isolating human neutrophils” in Example 1, the neutrophils were pre-treated. On an 8 well-μ slide (Cat. No. ib 80826 Ibidi (registered trademark)), the neutrophils were seeded in 400 μl of culture DMEM+2% human serum Alb (serum human albumin; Product No. A9080 Sigma+4 mM L-glutamine) at a rate of about 1.0×105 cells/well. Drugs (i) to (v) were each added, and pre-treatment was performed at room temperature for 30 minutes: (i) bovine lactoferrin (Product No. 123-04124 Lot: KWG6332 WAKO (registered trademark)) (stock: 100 mg/ml) diluted at 1/500, 1/5000 or 1/50000 to have final concentrations of 200 μg/ml, 20 μg/ml or 2 μg/ml; (ii) human lactoferrin (stock: 100 mg/ml, 200 μl; Cat No. SIGL6793, SIGMA) diluted at 1/500, 1/5000 or 1/50000 to have final concentrations of 200 μg/ml, 20 μg/ml or 2 μg/ml; (iii) DPI (stock: 25 mM; Product No. D2926 Sigma; attached document; solvent: DMSO) diluted at 1/2500 to have a final concentration of 10 μM; (iv) deferoxamine (Product No. D9533 Sigma) (stock: 200 mM) diluted at 1/100 to have a final concentration of 2 mM; (v) trientine (triethylenetetramine dihydrochloride (Sigma Product No. T5033; Lot: 1354380V; stock 100 mM, 100 μl)) (final concentration: 125 μM, 12.5 μM, 1.25 μM)). The pre-treatment was each performed by use of reagent at each concentration. After the pre-treatment, the neutrophils were stimulated with PMA (final concentration: 25 nM, stock: 10 mM in DMSO; Sigma Prod No. P8139).
3. Method and Results of Observation of NETosis Caused Along with the Formation of the NETs
For observation of the formation of the NETs, a confocal microscope (Leica DMI 6000B, Leica (registered trademark)) was used. The number of the neutrophils was visually countered via the microscope (in all the experiments, probe of HySOx (final concentration: 500 nM; stock: 10 mM; provided by Professor Yasuteru URANO, Bioinformatics, Biomedical Engineering, Department of Biophysical Medicine, Graduate School of Medicine, The University of Tokyo) (Kenmoku, S., et al., 2007. J Am Chem Soc 129:7313-7318; Setsukinai, K., et al., 2003. J Biol Chem 278:3170-3175) was used, and red fluorescent cells obtained by use of the probe were counted). For the quantization of the NETs, the number of mesh-like structures stained with Sytoxgreen (final concentration: 500 nM; stock: 5 mM, 5 μl; Product No. 57020) and TO-PRO-3 (final concentration: 1 μM; stock: 1 mM; Cat No. T3605 Invitrogen (registered trademark)) and released to the outside of the neutrophils was visually counted, referring to A. K Gupta. FEBS letters 2010; 584:3193-3197, D J Novo. Antimicrob Agents Chemother. 2000; 44(4):827-34 [
The observation by a scanning electron microscope was performed as follows. Eosinophil granulocytes were seeded on a glass cover or a glass bottom dish for cell culture in the number of 1×106 and pre-treated with 200 μg/ml of human lactoferrin or were not pre-treated before stimulation for NETs. Three hours later, the sample was pre-immobilized with 0.1 M phosphoric acid buffer (pH: 7.4) containing 2% glutaraldehyde at 4° C. for 1 hour. Next, the sample was post-immobilized with 0.1 M phosphoric acid buffer (pH: 7.4) containing 1% osmium tetroxide at 4° C. for 1 hour. After the immobilization, the sample was washed with 60% ethanol, with 70% ethanol, with 80% ethanol and with 95% ethanol while being gently shaken for 5 to 10 minutes, and immersed twice in 100% ethanol for 5 to 10 minutes to be dehydrated. Critical point drying was performed by substitution with isoamyl acetate for 10 to 15 minutes. The sample were covered with a layer of sublimated osmium tetroxide by use of an osmium plasma coating device (OPC80N, Filgen, Inc.) and observed by a scanning electron microscope (JSM-6320F, JEOL, Ltd.). In the case where the neutrophils were not stimulated, the neutrophils were kept spherical and no extracellular fiber was recognized. In the case where the neutrophils were stimulated with PMA, the cells were broken and many fiber components were formed. By contrast, the neutrophils pre-treated with lactoferrin were observed to form such fiber components in bundles. This indicates that the fibers of the NETs were condensed by lactoferrin [
The culture supernatant was recovered and centrifuged at 200×g for 10 minutes, and the supernatant was transferred to a new microscopic centrifuge tube. The DNA amount was measured by use of Picogreen dsDNA assay reagent (P11496 Invitrogen) in accordance with an accompanying protocol. In the case where pre-treatment was performed with human lactoferrin, the DNA concentration in the culture supernatant decreased in a concentration-dependent manner, and thus the release of the DNAs by the NETs was suppressed [
From heathy volunteer, 15 ml to 20 ml of peripheral blood was sampled for one cycle of experiment with an EDTA-containing syringe (needle: 18 to 22 G). After the blood sampling, 3 ml of mono-poly resolving medium (Cat No. DSBN100, DS Pharma Biomedical Co., Ltd.) contained in 15 ml conical tube, and then 3.5 ml of the whole blood were gently stacked in the lower-layer mono-poly resolving medium. The 15 ml conical tube was centrifuged at room temperature (15 to 30° C.) at 400×g for 20 minutes by a swing-type centrifuge, and then the conical tube was taken out gently. A brown plasma layer in the top layer and a lymphocyte/monocyte layer immediately below the brown plasma layer were removed by an aspirator or the like. A transparent layer below the lymphocyte/monocyte layer was removed as much as possible. A pale pink layer below the transparent layer was taken out by a Pasteur pipette. In order to wash the neutrophils, the pale pink layer was transferred to a test tube containing phosphate-buffered saline (PBS(−): 137 mM sodium chloride, 2.7 mM potassium chloride, 8.1 mM disodium hydrogenphosphate dodecahydrate, 1.47 mM potassium dihydrogenphosphate). The test tube containing the neutrophils was centrifuged at room temperature (15 to 30° C.) at 200×g for 10 minutes. The test tube was taken out, and the supernatant was discarded. 4° C. sterilized water was added to the neutrophils in the test tube and left still on ice for 30 seconds to cause hemolysis of erythrocytes mixed therein. After the hemolysis, 45 ml of PBS(−) was added to the test tube, and the test tube was centrifuged at 200×g for 10 minutes. The test tube was taken out, and the supernatant was discarded. The precipitation was suspended in culture DMEM+2% human serum Alb (serum human albumin; Product No. A9080 Sigma+4 mM L-glutamine), and left at 8° C. until immediately before being used. The neutrophils were separated in the number of 1×106/ml to 1×107/ml. The purity, which was obtained by visually counting the post-cytospin sample stained with Giemsa, was 95 to 98%.
About 1 hour after the isolation of the neutrophils described in “1. Method of isolating human neutrophils” in Example 2, the neutrophils were pre-treated. On an 8-well microslide (Cat. No. ib 80826 Ibidi (registered trademark)), the neutrophils were seeded in 400 μl of culture DMEM+2% human serum Alb (serum human albumin; Product No. A9080 Sigma+4 mM L-glutamine) at a rate of about 1.0×105 cells/well, and stimulated with PMA (final concentration: 25 nM, stock: 10 mM in DMSO, Sigma Prod No. P8139). At thirty minutes before the stimulation, and at every one hour or every two hours after the stimulation, 200 μg/ml of human lactoferrin (stock: 100 mg/ml, 200 μl; Cat. No. SIGL6793, SIGMA) was added to perform inhibition [
The culture supernatant was recovered and centrifuged at 200×g for 10 minutes, and the supernatant was transferred to a new microscopic centrifuge tube. The DNA amount was measured by use of Picogreen dsDNA assay reagent (P11496 Invitrogen) in accordance with an accompanying protocol. Treatment with human lactoferrin at one hour and two hours after the stimulation was a similar effect to the prior pre-treatment, the DNA concentration in the culture supernatant decreased, resulting in suppression of the release of the DNAs by the NETs [
Production of standard feed and lactoferrin-containing feed was outsourced to Oriental Kobo Kabushiki Kaisha.
The standard feed was produced as follows. The standard refined feed AIN-93M for nutrition research for mice and rats that was published in 1993 by American Institute of Nutrition (14% of casein, 0.18% of L-cystine, 46.5692% of corn starch, 15.5% of α-corn starch, 10.0% of sucrose, 4.0% of soybean oil, 5.0% of cellulose powder, 3.5% of AIN-93M mineral mixture, 1.0% of AIN-93 vitamin mixture, 0.25% of choline tartrate, 0.0008% of tert-butylhydroquinone) was solidified by a pelleter. The mice were allowed to take the feed freely. The lactoferrin-containing feed was produced as follows. Bovine lactoferrin was mixed in AIN-93M so as to have a final concentration of 2%, and the mixture was solidified by a pelleter. The mice were allowed to take the feed freely.
Six to seven week old female SCG/Kj mice having crescentic glomerulonephritis and ANCA associated vasculitis were purchased from BioResource Center, Tsukuba Institute, RIKEN, and allowed to be accustomed for 1 to 2 weeks before being used. The mice were divided into two groups. From the eighth week of age, one group of mice were fed with the lactoferrin-containing feed (n=16), and the other group of mice were fed with the standard feed (n=16). The survival rate/lifetime extension was evaluated by use of the Kaplan-Meier method. The group of mice fed with the standard feed gradually started to die from the ninth week of age. At the 18th week of age, two mice were alive. The group of mice fed with the lactoferrin-containing feed started to die from the 14th week of age, and 11 mice were alive at the 18th week of age, demonstrating a significant improvement effect on the survival rate/lifetime extension (statistically significant difference p=0.0111) [
Production of standard feed and lactoferrin-containing feed was outsourced to Oriental Kobo Kabushiki Kaisha.
The standard feed was produced as follows. The standard refined feed AIN-93M for nutrition research for mice and rats that was published in 1993 by American Institute of Nutrition (14% of casein, 0.18% of L-cystine, 46.5692% of corn starch, 15.5% of α-corn starch, 10.0% of sucrose, 4.0% of soybean oil, 5.0% of cellulose powder, 3.5% of AIN-93M mineral mixture, 1.0% of AIN-93 vitamin mixture, 0.25% of choline tartrate, 0.0008% of tert-butylhydroquinone) was solidified by a pelleter. The mice were allowed to take the feed freely. The lactoferrin-containing feed was produced as follows. Bovine lactoferrin was mixed in AIN-93M so as to have a final concentration of 2%, and the mixture was solidified by a pelleter. The mice were allowed to take the feed freely.
At least 6 week old female SCG/Kj mice were purchased from BioResource Center, Tsukuba Institute, RIKEN, and used from the eighth week of age. The mice were divided into two groups. One group of mice were fed with the lactoferrin-containing feed (n=8), and the other group of mice were fed with the standard feed (n=8). SCG/Kj mice of 8 to 17 weeks of age were caused to inhale diethylether to be anesthetized, and blood was sampled with heparin. The sampled blood was transferred to a 1.5 ml microscopic centrifuge tube, and centrifuged at 4° C. at 1000 g for 10 minutes. The supernatant was recovered to be used as plasma.
The measurement of the antibody titer of the MPO-ANCA was performed by use of ELISA (Ishida-Okawara, A., et al, Nephrol Dial Transplant 2004; 19:1708-1715) provided by Prof Kazuo SUZUKI, formerly in Department of Immunology and Inflammation Control, Graduate School of Medicine, Chiba University. The recombinant mouse MPO was seeded at a certain concentration to a 96-well ELISA plate (TOYOSHIMA) and left at 4° C. for 16 hours. After the MPO was left in this manner, the supernatant was discarded, and 300 to 400 μl of PBS(−) was put into each well for washing (the operation was performed 2 to 3 times). After the washing, 300 to 400 μl of 1% PBS(−) solution of bovine serum albumin was put into each well, left at room temperature for 2 hours, and then 300 to 400 μl of PBS(−) was put into each well for washing (the operation was performed 3 to 4 times). After the wells were left in this manner, mouse serum diluted 50-fold with PBS(−) was put into each well and reacted at room temperature for 90 minutes. After the reaction, 300 to 400 μl of PBS(−) was put into each well for washing (the operation was performed 3 to 4 times).
After the washing, anti-mouse IgG antibody labeled with alkaline phosphatase diluted 1000-fold with PBS(−) was put into each well and reacted at room temperature for 2 hours. After the reaction, 300 to 400 μl of PBS(−) was put into each well for washing (the operation was performed 2 to 3 times). 150 μl of 1 mg/ml para-nitrophenylphosphoric acid diluted with PBS(−) was put into each well and reacted for 15 to 30 minutes. An equivalent amount of 0.75 M sodium hydroxide aqueous solution was put into each well to stop the reaction. The measurement was performed at a wavelength of 405 nm. The results of the measurement performed by use of an absorptiometer were that the average antibody titer of the MPO-ANCA of the group of mice fed with the standard feed was 0.283875 and the average antibody titer of the MPO-ANCA of the group of mice fed with the lactoferrin-containing feed was 0.15625. The antibody titer of the MPO-ANCA was recognized to be lower with the group of mice fed with the lactoferrin-containing feed. Thus, the therapeutic effect was recognized (statistically significant difference p=0.0221) [
The DNA amount in the plasma was measured by use of Picogreen dsDNA assay reagent (P11496 Invitrogen) in accordance with an accompanying protocol. The group of mice fed with the lactoferrin-containing feed had a smaller DNA amount in the blood than the group of mice fed with the lactoferrin-non-containing feed. This indicates that the release of the DNAs by the NETs was significantly suppressed with the group of mice fed with the lactoferrin-containing feed (p=0.046) [
The SCG/Kj mice were put to euthanasia by cervical dislocation, and kidney samples were collected by celiotomy. A 40% paraffin block was created, and tissue sections were formed. Masson trichrome staining was performed, and subcutaneous bleeding was histologically evaluated. The tissue sections were osmosed with 10% formalin solution for 24 hours or longer to be immobilized. Formalin was washed with tap water for 1 hour or longer. The immobilized tissue sections were immersed in 60% ethanol for 1 hour, in 70% ethanol for 1 hour, in 80% ethanol for 1 hour, in 95% ethanol for 1 hour, in 100% ethanol for 1 hour 3 times, in xylene for 1 hour twice, and in paraffin (kept at 65° C.) for 1 hour 3 times. Then, the tissue block was created with an embedding tray. The tissue block was cut by a microtome into tissue sections each having a thickness of 20 to 50 nm. The tissue sections were put onto a glass slide and deparaffinized. The deparaffinization was performed as follows. The tissue sections that were completely dry on the glass slide were lightly washed with xylene for 5 minutes 3 times, with 100% ethanol for 1 minute twice, and with 95% ethanol. Then, similarly, the tissue sections were lightly washed with 80% ethanol, with 70% ethanol, with 60% ethanol and with tap water in this order. Then, the tissue sections were immersed in ion exchange water, and then were treated with the Masson trichrome staining. Then, the tissue sections were immersed in a mordanting liquid (10% trichloroacetic acid solution, 10% potassium dichromate solution) for 10 to 15 minutes, washed with tap water for 5 minutes, immersed in an iron hematoxylin solution (2 g hematoxylin, 100 ml of 100% ethanol, 0.5 g of ferric nitrate (III).9H2O, 100 ml of 25% hydrochloric acid solution) for 5 minutes, and lightly washed with water. A 1% hydrochloric acid in 70% ethanol was used for separation. The tissue sections were washed with water for 10 minutes to remove the color, and immersed in ion exchange water. The tissue sections were immersed in liquid I (90 ml of 1% Biebrich Scarlet, 10 ml of 1% acidic fuchsine, 1 ml of acetic acid) for 2 to 5 minutes, and lightly washed with water. The tissue sections were immersed in liquid II (5 g of phosphomolybdic acid, 5 g of phosphotungstic acid, 200 ml of distilled water) for 30 minutes or longer, lightly washed with water, immersed in liquid III (2.5 g of aniline blue, 2 ml of acetic acid, 100 ml of distilled water) for 5 minutes, and lightly washed with water. The tissue sections were immersed in 1% aqueous acetic acid for 5 minutes, and quickly washed with water. The tissue sections were lightly washed with 60% ethanol, with 70% ethanol, with 80% ethanol and with 95% ethanol, and then immersed in 100% ethanol for 5 minutes 3 times. The tissue sections were immersed in xylene for 5 minutes 3 times, and covered with a cover glass by use of a mounting agent. The glass slide was dried and then observed by a microscope. Separately, similar tissue sections were stained with hematoxylin-eosin. After being deparaffinized, the tissue sections were washed with running tap water for 3 to 5 minutes, and immersed in a Mayer's hematoxylin solution for 5 minutes. The tissue sections were washed with running water at 25 to 37° C. for 3 to 5 minutes, and immersed in an eosin solution for 5 minutes. The tissue sections were lightly washed with 60% ethanol, with 70% ethanol, with 80% ethanol and with 95% ethanol, and then immersed in 100% ethanol for 5 minutes 3 times. The tissue sections were immersed in xylene for 5 minutes 3 times, and covered with a cover glass by use of a mounting agent. The glass slide was dried and then observed by a microscope. With both of the staining methods, the kidney of the group of mice fed with the lactoferrin-containing feed was milder regarding interstitial fibrosis, inflammatory cell infiltration (upper) and crescent body formation (lower) of the tissues than the kidney of the group of mice fed with the lactoferrin-non-containing feed [
Six week old C57BL/6j mice were allowed to be accustomed for 2 weeks, and from the eighth week of age, fed with the lactoferrin-containing feed or control feed. At the 10th week of age, lipopolysaccharide (LPS; Sigma) derived from Escherichia coli was dissolved in PBS(−) so as to be _ mg/ml. 100 μg of the resultant solution was subcutaneously injected to each mouse by a 30 G needle. The day on which the injection was performed was set as day 1. Mouse recombinant TNF-α (R&D Systems, Inc., Product No. 410-MT) was dissolved in PBS(−) so as to be 100 μg/ml. 0.3 μg of the resultant solution was subcutaneously injected to each mouse at the same site. The day on which the injection was performed was set as day 2. On day 3, the bleeding of the site was evaluated with the naked eye. With the group of mice fed with the lactoferrin-containing feed, the range of subcutaneous bleeding was more significantly suppressed than with the control group of mice fed with the control feed. The severity of the subcutaneous bleeding was observed with the naked eye and numerically evaluated based on the range of bleeding and the state of necrosis as follows: 0: none; 1: mild; 2: moderate; 3: severe; 4: central necrosis [Table 2]. The severity of the group of mice fed with the lactoferrin-containing feed was significantly lower than that of the control group of mice fed with the control feed (p>0.0001) [
The mice produced in “1. Production of LSR model 1 and its evaluation” in Example 5 were put to euthanasia by cervical dislocation, and skin samples were taken. A 40% paraffin block was created, and tissue sections were formed. The Masson trichrome staining was performed, and subcutaneous bleeding was histologically evaluated. The tissue sections were osmosed with 10% formalin solution for 24 hours or longer to be immobilized. Formalin was washed away with tap water for 1 hour or longer. The immobilized tissue sections were immersed in 60% ethanol for 1 hour, in 70% ethanol for 1 hour, in 80% ethanol for 1 hour, in 95% ethanol for 1 hour, in 100% ethanol for 1 hour 3 times, in xylene for 1 hour twice, and in paraffin (kept at 65° C.) for 1 hour 3 times. Then, the tissue block was created with an embedding tray. The tissue block was cut by a microtome into tissue sections each having a thickness of 20 to 50 nm. The tissue sections were put onto a glass slide and deparaffinized. The deparaffinization was performed as follows. The tissue sections that were completely dry on the glass slide were lightly washed with xylene for 5 minutes 3 times, with 100% ethanol for 1 minute twice, and with 95% ethanol. Then, similarly, the tissue sections were lightly washed with 80% ethanol, with 70% ethanol, with 60% ethanol and with tap water in this order. Then, the tissue sections were immersed in ion exchange water, and then were treated with the Masson trichrome staining. Then, the tissue sections were immersed in a stain fixing solution (10% trichloroacetic acid solution, 10% potassium dichromate solution) for 10 to 15 minutes, washed with tap water for 5 minutes, immersed in an iron hematoxylin solution (2 g of hematoxylin, 100 ml of 100% ethanol, 0.5 g of ferric nitrate (III).9H2O, 100 ml of 25% hydrochloric acid solution) for 5 minutes, and lightly washed with water. A solution of 1% hydrochloric acid and 70% ethanol was used for separation. The tissue sections were washed with water for 10 minutes to remove the color, and then immersed in ion exchange water. The tissue sections were immersed in liquid I (90 ml of 1% Biebrich Scarlet, 10 ml of 1% acidic fuchsine, 1 ml of acetic acid) for 2 to 5 minutes, and lightly washed with water. The tissue sections were immersed in liquid II (5 g of phosphomolybdic acid, 5 g of phosphotungstic acid, 200 ml of distilled water) for 30 minutes or longer, lightly washed with water, immersed in liquid III (2.5 g of aniline blue, 2 ml of acetic acid, 100 ml of distilled water) for 5 minutes, and lightly washed with water. The tissue sections were immersed in 1% aqueous acetic acid for 5 minutes, and quickly washed with water. The tissue sections were lightly washed with 60% ethanol, with 70% ethanol, with 80% ethanol and with 95% ethanol, and then immersed in 100% ethanol for 5 minutes 3 times. The tissue sections were immersed in xylene for 5 minutes 3 times, and covered with a cover glass by use of a mounting agent. The glass slide was dried and then observed by a microscope. Separately, similar tissue sections were stained with hematoxylin-eosin. After being deparaffinized, the tissue sections were washed with running tap water for 3 to 5 minutes, and immersed in a Mayer's hematoxylin solution for 5 minutes. The tissue sections were washed with running water at 25 to 37° C. for 3 to 5 minutes, and immersed in an eosin solution for 5 minutes. The tissue sections were lightly washed with 60% ethanol, with 70% ethanol, with 80% ethanol and with 95% ethanol, and then immersed in 100% ethanol for 5 minutes 3 times. The tissue sections were immersed in xylene for 5 minutes 3 times, and covered with a cover glass by use of a mounting agent. The glass slide was dried and then observed by a microscope.
In both of the staining methods, the tissue sections were finally treated with specific esterase staining (chloroacetate esterase) in which only esterase in granules in such tissue sections are stained. After being deparaffinized, the tissue sections were washed with running tap water for 3 to 5 minutes, and washed with distilled water 3 times. The tissue sections were dried at room temperature for 10 to 30 minutes, and immersed in a chloroacetate esterase reaction solution for 15 to 30 minutes. The tissue sections were washed with running tap water for 3 to 5 minutes, and immersed in a Mayer's hematoxylin solution for 5 minutes. The tissue sections were washed with running water at 25 to 37° C. for 3 to 5 minutes, and immersed in an eosin solution for 5 minutes. The tissue sections were lightly washed with 60% ethanol, 70% ethanol, 80% ethanol and 95% ethanol, and then immersed in 100% ethanol for 5 minutes 3 times. The tissue sections were immersed in xylene for 5 minutes 3 times, and covered with a cover glass by use of a mounting agent. The glass slide was dried and then observed by a microscope. With the group of mice fed with the lactoferrin-non-containing feed, the subcutaneous bleeding in the top part of muscular layer and the thrombus formation in the blood vessel were significant. By contrast, with the group of mice fed with the lactoferrin-containing feed, the subcutaneous bleeding and the thrombus formation were mild. Neutrophilic infiltration in the subcutaneous tissues was observed to be suppressed by the lactoferrin-containing feed [
An air pouch was created subcutaneously on the back of each mouse to induce LSR, and the DNA concentration in the air pouch was measured and the neutrophils were observed. First, 5 ml of air was subcutaneously injected vigorously on the back with a 5 ml syringe and a 30 G needle. Three days later, 100 μg of LPS was injected into the air pouch in each mouse. Twenty four hours later, 0.3 μg of TNF-α was injected into the air pouch to each mouse, and 6 hours later, the air pouch was washed with 2 ml of sterilized PBS(−) and recovered.
The sampled lavage fluid was transferred to a 1.5 ml microscopic centrifuge tube, and centrifuged at room temperature at 6000 g for 5 minutes. The DNA concentration in the supernatant was measured by use of Picogreen dsDNA assay reagent in accordance with an accompanying protocol. The group of mice fed with the lactoferrin-containing feed had a smaller DNA amount in the blood than the group of mice fed with the lactoferrin-non-containing feed. This indicates that the release of the DNAs by the NETs was significantly suppressed with the group of mice fed with the lactoferrin-containing feed (p=0.0015) [
The neutrophils in the lavage fluid were immobilized on a glass slide by use of Cytospin 2 (Shandon), stained with 5 μM DRAQ5, and observed by a microscope. The number of the neutrophils with which the formation of the NETs was observed was smaller with the group of mice the fed with the lactoferrin-containing feed than with the control group of mice fed with the lactoferrin-non-containing feed [
80 mg/kg of histone (sigma, H9250) dissolved in physiological saline and left at 37° C. was intravenously administered to the tails of 11 week old male C57BL/6 mice to create DIC model mice (Tobias A. et al., blood, 29 Sep. 2011, vol. 118, no. 13, pp. 3708-3714). As a pre-treatment, 20 mg/kg of bovine lactoferrin was intravenously administered to the tails of the mice, and 30 minute later, histone was intravenously administered to the tails of the mice (n=8). These mice were labeled as a group of mice provided with therapy with lactoferrin. To the tails of different mice (n=8), 100 μl of physiological saline not containing bovine lactoferrin was intravenously administered, and 30 minutes later, histone was intravenously administered. These mice were labeled as a control group of mice provided with no therapy. The survival rate/lifetime extension after the administration of histone was evaluated by use of the Kaplan-Meier method. The control group of mice provided with no therapy gradually started to die about 20 minutes after the administration of histone. Two days later, two mice were alive, and 4 days later, one mouse was alive. By contrast, the 8 mice in the group provided with therapy with bovine lactoferrin were all alive even 4 days later. The significant improvement effect on the survival rate/lifetime extension was observed (
As a pre-treatment, 20 mg/kg of bovine lactoferrin was intravenously administered to the tails of 11 week old male C57BL/6 mice, and 30 minute later, 60 mg/kg of histone (sigma, H9250) dissolved in physiological saline and left at 37° C. was intravenously administered to the tails of the mice to check the effect of hemostasis on the DIC model mice (n=5) (Tobias A, et al., Blood, 2011; 118: pp. 3708-3714) (75% of the amount of histone used for improving the survival rate/lifetime extension was adopted). For control group mice without therapy (n=5), 100 μl of physiological saline not containing bovine lactoferrin was intravenously administered to the tails 30 minutes before the administration of histone. For healthy control mice (n=5), physiological saline, instead of the bovine lactoferrin used for the pre-treatment and also instead of histone, was administered. Twenty minutes after the administration of histone, the vein of the tail of each mouse was cut at a position 3 mm from the end, and immersed in a 37° C. physiological saline. At every 30 seconds, the blood was wiped off with a filter paper, and the bleeding time duration was measured (in the case where the bleeding time duration was 15 minutes or longer, the bleeding time duration was recorded as 15 minutes and a hemostasis treatment was performed) (Fuchs T A, et al., Blood, 2011; 118:3708-3714). The control group mice provided with no therapy were observed to bleed for a significantly long time (
As a pre-treatment, 20 mg/kg of bovine lactoferrin was intravenously administered to the tails of 11 week old male C57BL/6 mice, and 30 minute later, 80 mg/kg of histone (sigma, H9250) dissolved in physiological saline and left at 37° C. was intravenously administered to tails of the mice to create DIC model mice (n=4) (Tobias A., et al., Blood, 29 Sep. 2011; vol. 118: no. 13, pp. 3708-3714). For control group mice with no therapy (n=4), 100 μl of physiological saline not containing bovine lactoferrin was intravenously administered to the tails 30 minutes before histone was intravenously administered. For healthy control group mice (n=4), physiological saline, instead of the bovine lactoferrin used for the pre-treatment and also instead of histone, was administered. Ten minutes after the administration of histone (second administration of physiological saline), the mice were put to euthanasia. Lung tissues were extracted and immobilized by use of 4% paraformaldehyde. With the group of mice provided with therapy with bovine lactoferrin, the tissues were not observed to bleed almost at all, unlike with the control group of mice provided with no therapy; and the lung tissues of the group of mice provided with therapy with bovine lactoferrin had a similar color as that of the healthy control group of mice (
It has been reported that N-terminal fragment of lactoferrin is charged positive and therefore is bindable with a negatively charged DNA molecule (He J, and Furmanski P., Sequence specificity and transcriptional activation in the binding of lactoferrin to DNA. Nature. 1995; 373(6516):721-4). Thus, an experiment was performed in order to investigate whether proteins that were of different types from lactoferrin but were close to lactoferrin in the molecular weight (MW) and the isoelectric point (pI) would each inhibit the formation of the NETs. For the experiment, the following proteins were used.
Angiogenin is known as a tumor angiogenesis factor (Strydom D J, Fett J W, Lobb R R, Alderman E M, Bethune J L, Riordan J F, and Vallee B L Amino acid sequence of human tumor derived angiogenin. Biochemistry. 1985; 24:5486-94). Lactoperoxidase is heme peroxidase contained in the milk of mammals at a high concentration like lactoferrin (Sharma S, Singh A K, Kaushik S, Sinha M, Singh R P, Sharma P, Sirohi H, Kaur P, and Singh T P., Lactoperoxidase: structural insights into the function, ligand binding and inhibition. Int J Biochem Mol Biol. 2013; 4:108-28).
Crude protein isolated from bovine milk was dissolved in 10 mM sodium phosphate buffer (pH 7.0), and the obtained solution was loaded onto an SP-Sepharose column (GE Healthcare Life Sciences) equilibrated with the buffer (flow rate: 3.0 ml/min.). The protein bound to the column was washed with the buffer, and lactoperoxidase, angiogenin and lactoferrin were eluted by the linear concentration gradient of sodium chloride in the buffer (0.3 to 1.0 M).
The inhibition of the formation of the NETs was performed by measuring the DNA concentration in the culture supernatant in a similar manner to that in Example 2. The experiment was performed triplicate in three independent systems (n=3).
Neither lactoperoxidase nor angiogenin inhibited the formation of the NETs (
The present invention provides a therapeutic method with little side effect for a disease caused by the formation of the leukocyte extracellular traps. The method has little side effect and therefore has an advantage of being safely usable for a wide range of patients and people having possibility of becoming patients.
It has been confirmed with non-autoimmune disease model mice that lactoferrin has an ability of inhibiting the formation of the leukocyte extracellular traps. Therefore, according to the present invention, lactoferrin exhibits a therapeutic action by a completely novel mechanism that is different from any mechanism of actions reported in the past (Patent document 1).
| Number | Date | Country | Kind |
|---|---|---|---|
| 2013-081243 | Apr 2013 | JP | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14783295 | Oct 2015 | US |
| Child | 17402790 | US |
