Patent Application
20240366734
A keloid is a type of scar resulting from abnormal hyperplasia of skin fibrosis. The main cause is the excessive accumulation of extracellular matrix, which leads to the formation of a large scar. The scar not only has a conspicuous appearance, but also causes excessive inflammatory reaction, itching, and pain, and even leading to impaired peripheral tissue function.
Keloids occur in the high-tension positions of the human body, such as the anterior chest, suprapubic region, and upper arm. The shape of the scar is mostly crab or dumbbell shaped. Its structure, flexibility and strength are also different from normal tissues. Although a keloid scar can be removed by clinical surgery, the recurrence rate in patients is still more than 60%.
Studies have shown that the pathogenesis of keloids, in addition to family genetic factors, is mostly related to keloid fibroblasts. Compared to fibroblasts isolated from normal wound tissues, keloid fibroblasts excessively secrete extracellular matrix components, especially collagen, fibronectin, elastin, and proteoglycans, and some growth factors including vascular endothelial growth factor (VEGF), transforming growth factor (TGF), platelet-derived growth factor (PDGF), and connective tissue growth factor (CTGF). Hyperplasia of fibrous tissues in wounds of keloid patients makes the granulation tissues too large, beyond the original areas of the wounds, forming keloid scars. In addition, the expression of connexins and apoptotic genes in keloid fibroblasts is lower than normal, so the degree of apoptosis is relatively low. Also, in the scar tissue of a keloid, increase of collagen and glycosaminoglycan components causes the collagen bundles to be thickened and form a whorls arrangement. Further, the metabolic activity of the wound tissue is higher than normal tissues, resulting in hypoxia in the wound tissue, so it is easy to form a keloid under such high oxygen consumption and hypoxia expansion.
Current treatments of keloid mainly target keloid scars. There are many treatments including pressure dressing, local injection of steroid, laser rejuvenation, and external application of drugs. Treatments are selected according to the degree of scars such that the recurrences of keloid cannot be prevented resulting in high recurrence rates. In addition, there is currently no single treatment for all types of keloid patients, and some treatments may even cause side effects. Therefore, it is important to develop pharmaceutical compositions and treatment methods that are suitable for most keloid patients, are safe and effective, and can reduce the recurrence rates.
In one aspect, described herein is a method of treating a keloid in a subject. The method comprises: applying a pharmaceutical composition to a keloid or an area at risk of forming a keloid in a subject, wherein the composition includes an effective amount of a hyaluronan and an effective amount of a collagen, the weight ratio per unit volume of the hyaluronan to the collagen being greater than 1 (e.g., 1.5-1000, 1.5-3.5, 2-5, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.5, 5, 5.5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 200, 300, 400, 500, 600, 700, 800, 900, or 1000). In some embodiments, the area at risk of forming a keloid is an area from which a keloid scar has been surgically removed.
In some embodiments, the pharmaceutical composition is produced by a procedure including: mixing a hyaluronan, a 0.001M-0.1M phosphate buffer solution at pH 7±2, and a 0.1%-0.9% NaCl solution to form a hyaluronan solution; providing a collagen solution; mixing the hyaluronan solution and the collagen solution at below 4° C. to obtain a mixture such that the weight ratio per unit volume of hyaluronan to collagen in the mixture is greater than 1; and adjusting the pH of the mixture to 7±1. The pH of the hyaluronan solution can be below 6. In some embodiments, the pH of the collagen solution is below 6.
In some embodiments, the pharmaceutical composition further includes an additive selected from the group consisting of a nutrient, a biological active agent, an antimicrobial agent, a cell, an extracellular matrix component, and an excipient.
In some embodiments, the molecular weight of the hyaluronan is 4 to 5000 kDa (e.g., 4 to 20, 20 to 100, 100 to 500, 500 to 1000, 1000 to 2000, 2000 to 2500, 2500 to 5000, 5, 10, 50, 100, 200, 300, 400, 500, 750, 1000, 1500, 1800, 2000, 2500, 3000, 3500, 4000, 4500, or 5000 kDa).
In some embodiments, the concentration of the hyaluronan solution can be 3 to 1000 mg/ml (e.g., 3 to 200 mg/ml). In some embodiments, the concentration of the collagen solution can be 0.03 to 500 mg/ml (e.g., 1 to 100 mg/ml).
In some embodiments, the pharmaceutical composition is capable of reducing the gene expression of plasminogen activator inhibitor-1 (PAI-1), serpin peptidase inhibitor, clade B (Ovalbumin), plasminogen activator inhibitor-2 (PAI-2), collagen type1, fibronectin, alpha-smooth muscle actin (α-SMA), or connective tissue growth factor (CTGF) in keloid fibroblasts.
In some embodiments, the biological active agent is selected from the group consisting of an epidermal growth factor, fibroblast growth factor (FGF), vascular endothelial growth factor (VEGF), connective tissue growth factor (CTGF), platelet-derived growth factor (PDGF), insulin-like growth factor, nerve growth factor, hepatocyte growth factor, colony-stimulating factor, stem call factor, keratinocyte growth factor, granulocyte colony-stimulating factor, granulocyte macrophage colony-stimulating factor, glial-derived neurotropic factor, ciliary neurotrophic factor, endothelial-monocyte activating polypeptide, epithelial neutrophil activating peptide, erythropoietin, bone morphogenetic protein, brain-derived neurotrophic factor, BRAK, transforming growth factor beta (TGF-β), and tumor necrosis factor.
In some embodiments, the extracellular matrix component is selected from the group consisting of a collagen, hyaluronan, gelatin, fibronectin, elastin, tenascin, laminin, vitronectin, heparan sulfate, chondroitin, chondroitin sulfate, keratin, keratan sulfate, dermatan sulfate, carrageenan, heparin, chitin, chitosan, alginate, agarose, agar, cellulose, glycogen, fibrin, fibrinogen, clotting enzymes, polyglutamic acid, and synthetic polymer or derivative thereof.
In some embodiments, the antimicrobial agent is an antibiotic, anti-microbial protein, or an anti-microbial peptide. In some embodiments, the cell is a stem cell, satellite cell, precursor cell, or tissue cell. In some embodiments, the excipient is vaseline, glycerin or lecithin. In some embodiments, the nutrient is a carbohydrate, amino acid, peptide, protein, fatty acid, lipid, vitamin, or mineral.
In another aspect, a pharmaceutical composition for treating or preventing a keloid in a subject is described herein. The composition includes an effective amount of a hyaluronan and an effective amount of a collagen, the weight ratio per unit volume of the hyaluronan to the collagen being greater than 1.
The details of one or more embodiments are set forth in the accompanying drawing and the description below. Other features, objects, and advantages of the embodiments will be apparent from the description and drawing, and from the claims.
It was unexpectedly discovered that various compositions containing hyaluronan and collagen restored the morphology, migration, contractility, and expression of keloid-associated genes of keloid fibroblasts to normal levels or close to normal levels. Therefore, the compositions can be used to treat keloids or reduce the risk of keloids.
Accordingly, described herein is a pharmaceutical composition for treating keloids. The composition contains an effective amount of a hyaluronan and an effective amount of a collagen, the weight ratio per unit volume of the hyaluronan to the collagen being greater than 1 (e.g., 1.5-1000, 1.5-3.5, 2-5, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.5, 5, 5.5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 200, 300, 400, 500, 600, 700, 800, 900, or 1000).
The composition can further contain one or more components including a nutrient, a bioactive agent, an antimicrobial agent, a cell, an extracellular matrix component, and an excipient.
Any of the naturally-occurring collagens or their functional variants can be used for preparing the pharmaceutical composition. Collagen can be isolated and purified from collagen-rich tissues such as skin, tendon, ligament, and bone of humans and animals. Methods for isolating and purifying collagen are well known in the art. See, e.g., U.S. Pat. No. 5,512,291; US Patent Publication 20040138695; Methods in Enzymology, vol. 82, pp. 33-64, 1982; The Preparation of Highly Purified Insoluble Collagen, Oneson, I., et al., Am. Leather Chemists Assoc., Vol. LXV, pp. 440-450, 1970; U.S. Pat. No. 6,090,996. Collagen can also be prepared by recombinant technology, such as those described by Advanced Tissue Sciences (La Jolla, Calif.) or purchased from various venders (e.g., Fibrogen; South San Francisco, Calif.). The term “collagen” refers to the above-mentioned molecules, degraded/hydrated molecules (also named gelatin) and their derivatives. To make a collagen solution, collagen can be dissolved in acetic acid (e.g., 0.1M to 0.5M), HCl (e.g., 0.001 to 0.05 N), or water.
The term “hyaluronan” refers to a naturally-occurring anionic, non-sulfated glycosaminoglycan including repeated disaccharide units of N-acetylglucosamine and D-glucuronic acid, and its derivatives. Naturally-occurring hyaluronan (also known as hyaluronic acid or hyaluronate) can be isolated from its natural sources, e.g., capsules of Streptococci, rooster comb, cartilage, synovial joints fluid, umbilical cord, skin tissue and vitreous of eyes, via conventional methods. See, e.g., Guillermo Lago et al. Carbohydrate Polymers 62 (4): 321-326, 2005; and Ichika Amagai et al. Fisheries Science 75 (3): 805-810, 2009. Alternatively, it can be purchased from a commercial vendor, e.g., Genzyme Corporation, Lifecore Biomedical, LLC and Hyaluron Contract Manufacturing. Derivatives of naturally-occurring hyaluronan include, but are not limited to, hyaluronan esters, adipic dihydrazide-modified hyaluronan, hyaluronan amide products, crosslinked hyaluronic acid, hemiesters of succinic acid or heavy metal salts thereof hyaluronic acid, partial or total esters of hyaluronic acid, sulphated hyaluronic acid, N-sulphated hyaluronic acid, and amines or diamines modified hyaluronic acid. They can be obtained by chemically modifying one or more of its functional groups (e.g., carboxylic acid group, hydroxyl group, reducing end group, N-acetyl group). A carboxyl group can be modified via esterification or reactions mediated by carbodiimide and bishydrazide. Modifications of hydroxyl groups include, but are not limited to, sulfation, esterification, isourea coupling, cyanogen bromide activation, and periodate oxidation. A reducing end group can be modified by reductive amination. It also can be linked to a phospholipid, a dye (e.g., a fluorophore or chromophore), or an agent suitable for preparation of affinity matrices. Derivatives of naturally-occurring hyaluronan can also be obtained by crosslinking, using a crosslinking agent (e.g., bisepoxide, divinylsulfone, biscarbodiimide, small homobifunctional linker, formaldehyde, cyclohexyl isocyanide, and lysine ethyl ester, metal cation, hydrazide, or a mixture thereof) or via internal esterification, photo-crosslinking, or surface plasma treatment. The molecular weight of the hyaluronan can range from 4 kDa to 5000 kDa (e.g., 4 to 20, 20 to 100, 100 to 500, 500 to 1000, 1000 to 2000, 2000 to 2500, 2500 to 5000, 5, 10, 50, 100, 200, 300, 400, 500, 750, 1000, 1500, 1800, 2000, 2500, 3000, 3500, 4000, 4500, or 5000 kDa). To make a hyaluronan solution, hyaluronan can be dissolved in a phosphate buffer solution (e.g., 0.001˜0.1 M at pH 7±2) with NaCl (e.g., 0.1˜0.9%). The concentration of hyaluronan can be in the range of 3 to 1000 mg/mL. A preferred range of hyaluronan is 3 to 200 mg/mL.
The term “nutrient” refers to a source of nourishment essential for cell growth. It can be an amino acid, vitamin, mineral, carbon source (e.g., glucose), fatty acid, or a mixture thereof. In one example, the nutrient in the pharmaceutical composition is a cell growth medium, e.g., Minimum Essential Medium, Basal Medium Eagle, Dulbecco's Modified Eagle's medium, Ham's Nutrient Mixtures F-10 or F-12, Medium 199, RPMI medium, Ames' Media, BGJb Medium (Fitton-Jackson Modification), Click's Medium, CMRL-1066 Medium, Fischer's Medium, Glascow Minimum Essential Medium, Iscove's Modified Dulbecco's Medium, L-15 Medium, McCoy's 5A Modified Medium, NCTC Medium, Swim's S-77 Medium, Waymouth Medium, or William's Medium E.
A bioactive agent is any agent (e.g., peptide, polypeptide, oligosaccharide, polysaccharide, or small molecule) that improves cell viability, promotes cell proliferation, or induces cell differentiation. In one example, the bioactive agent is a growth factor, such as epidermal growth factor, fibroblast growth factor, vascular endothelial growth factor, connective tissue growth factor, platelet-derived growth factor, insulin-like growth factor, nerve growth factor, hepatocyte growth factor, colony-stimulating factors, stem cell factor, serotonin, and von Willebrand factor, transforming growth factor, keratinocyte growth factor, granulocyte colony-stimulating factor, granulocyte/macrophage colony stimulating factor, glial derived neurotrophic factor, ciliary neurotrophic factor, endothelial-monocyte activating polypeptide, epithelial neutrophil activating peptide, erythropoietin, bone morphogenetic proteins, brain-derived neurotrophic factor. In another example, the bioactive agent is a cytokine or chemokine, including, but are not limited to, IL-2, breast-expressed chemokine (e.g., BRAK), kidney-expressed chemokine (e.g., CXCL14). The bioactive agent can also be a cell differentiation factor, such as dexamethasone, sodium pyruvate, ascorbic acid-2-phosphate, retinoic acid, proline, insulin, transferrin, selenous acid, linoleic acid, and bovine serum albumin, and TGF-β3. In a preferred example, the differentiation factor is a compound that promotes chondrogenesis of mesenchymal stem cells (see those disclosed in U.S. Pat. No. 5,908,784), osteogenesis (e.g., dexamethasone, ascorbic acid, β-glycerol phosphate), adipogenesis (e.g., insulin, isobutyl-methyl xanthine, dexamethasone, indomethacin), cardiomyogenic differentiation (e.g., activin A, BMP-4), endothelial cell differentiation (e.g., EBM-2, dexamethasone, and VEGF), smooth muscle cell differentiation (e.g., PDGF-BB), neural induction (e.g., bFGF, EGF, and B27 supplement, DMSO, butylated hydroxyanisole, forskolin, valproic acid, KCl, K252a, and N2 supplement) and endodermal lineage differentiation (e.g., dexamethasone, HGF, and FGF-4). The bioactive agent can also be a Chinese herbal medicine or an active ingredient thereof.
Extracellular matrix components include, but are not limited to, gelatin, collagen, hyaluronan, fibronectin, elastin, tenacin, laminin, vitronectin, polypeptides, heparan sulfate, chondroitin, chondroitin sulfate, keratan, keratan sulfate, dermatan sulfate, carrageenan, heparin, chitin, chitosan, alginate, agarose, agar, cellulose, methyl cellulose, carboxyl methyl cellulose, glycogen and derivatives thereof. In addition, the extracellular matrix component can be fibrin, fibrinogen, thrombin, polyglutamic acid, a synthetic polymer (e.g., acrylate, polylactic acid, polyglycolic acid, or poly(lactic-co-glycolic acid), or a cross-linking agent (e.g., genipin, glutaraldehyde, formaldehyde, or epoxide).
One or more excipients can be included in the pharmaceutical composition to provide lubrication and moisture insulation. The presence of the excipient can also serve as a cream to bind and smooth the epithelial layer for healing of wounds. Lecithin, petroleum jelly, glycerol, glycerine, and glycerin are exemplary excipients that can be included in the cell tissue gel. Other excipients are also known and available in the art.
Cell such as stem cells, satellite cells, precursor cells, or any tissue cells can be included in the pharmaceutical composition.
The pharmaceutical composition can also include one or more antimicrobial agents, e.g., an antibiotic, anti-microbial protein, or an anti-microbial peptide.
The pharmaceutical composition can be in the form of a liquid, cream, gel, jelly, paste, ointment, spray, colloid, foam, sponge, matrix, dressing, pad, granule, suspension or powder.
To make the pharmaceutical composition, a hyaluronan solution and a collagen solution can be mixed at below 4° C. to produce a mixture that contain hyaluronan and collagen at the desired weight ratio per unit volume. A preferred weight ratio of hyaluronan to collagen ranges from 1.5 to 1000. One or more other components (e.g., nutrients, bioactive agents, antimicrobial agents, cells, extracellular matrix components, and excipients) can be added to the mixture. The pH of the final mixture is then adjusted to neutral or near neutral (e.g., 7±1) to form the pharmaceutical composition, which has a gelatinous consistency. The concentration of the hyaluronan solution can be 3 to 1000 mg/ml (e.g., 3 to 100 mg/ml, 5 mg/ml to 10 mg/ml, 7 mg/ml to 15 mg/ml, 10 to 25 mg/ml, 15 to 35 mg/ml, 25 to 50 mg/ml, 35 to 65 mg/ml, 50 to 75 mg/ml, 65 to 85 mg/ml, 75 to 95 mg/ml, 85 to 105 mg/ml, 100 to 400 mg/ml, 250 to 550 mg/ml, 400 to 700 mg/ml, 550 to 850 mg/ml, 700 to 1000 mg/ml, 0.5 mg/ml, 1 mg/ml, 1.5 mg/ml, 3 mg/ml, 5 mg/ml, 10 mg/ml, 15 mg/ml, 20 mg/ml, 25 mg/ml, 30 mg/ml, 35 mg/ml, 45 mg/ml, 50 mg/ml, 55 mg/ml, 60 mg/ml, 65 mg/ml, 70 mg/ml, 75 mg/ml, 80 mg/ml, 85 mg/ml, 90 mg/ml, 95 mg/ml, 100 mg/ml, 200 mg/ml, 300 mg/ml, 400 mg/ml, 500 mg/ml, 600 mg/ml, 700 mg/ml, 800 mg/ml, 900 mg/ml, or 1000 mg/ml). A preferred range for the hyaluronan is 3 to 200 mg/ml. The concentration of the collagen solution can be 0.03 to 500 mg/ml (e.g., 0.03 to 1 mg/ml, 1 to 2.5 mg/ml, 2.5 to 5 mg/ml, 5 mg/ml to 10 mg/ml, 7 mg/ml to 15 mg/ml, 10 to 25 mg/ml, 15 to 35 mg/ml, 25 to 50 mg/ml, 35 to 65 mg/ml, 50 to 75 mg/ml, 65 to 85 mg/ml, 75 to 95 mg/ml, 85 to 105 mg/ml, 100 to 200 mg/ml, 150 to 250 mg/ml, 200 to 300 mg/ml, 250 to 350 mg/ml, 300 to 400 mg/ml, 350 to 450 mg/ml, 400 to 500 mg/ml, 0.5 mg/ml, 1 mg/ml, 1.5 mg/ml, 3 mg/ml, 5 mg/ml, 10 mg/ml, 15 mg/ml, 20 mg/ml, 25 mg/ml, 30 mg/ml, 35 mg/ml, 45 mg/ml, 50 mg/ml, 55 mg/ml, 60 mg/ml, 65 mg/ml, 70 mg/ml, 75 mg/ml, 80 mg/ml, 85 mg/ml, 90 mg/ml, 95 mg/ml, 100 mg/ml, 200 mg/ml, 300 mg/ml, 400 mg/ml, or 500 mg/ml). A preferred range for the collagen is 1 to 100 mg/ml.
The pharmaceutical composition can be administered to a patient to treat, prevent, or reduce the reoccurrence of a keloid. The composition can be injected to or applied topically over a keloid or an area at risk of developing a keloid. In particular, the composition can be administered to an area from which a keloid has been removed surgically to aid wound healing and reduce the risk of a keloid forming at the same area.
The composition can be applied to a subject as often as needed, e.g., 1 to 5 times daily, 1 to 5 times per week, 1 to 5 times per month, for a suitable treatment period, e.g., 1 to 4 week, 1 to 12 months, or 1 to 3 years.
“Treating” refers to administration of a composition to a subject, who is suffering from or is at risk for developing a disorder, with the purpose to cure, alleviate, relieve, remedy, delay the onset of, prevent, or ameliorate the disorder, the symptom of the disorder, the disease state secondary to the disorder, or the predisposition toward the disorder. An “effective amount” refers to an amount of the composition that is capable of producing a medically desirable result in a treated subject. The treatment method can be performed alone or in conjunction with other drugs or therapies.
The specific examples below are to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever. Without further elaboration, it is believed that one skilled in the art can, based on the description herein, utilize the present disclosure to its fullest extent. All publications cited herein are herein incorporated by reference in their entirety.
A hyaluronan solution was prepared by mixing hyaluronan, a phosphate buffer solution (0.001 to 0.1 M and pH 7±2), and a NaCl solution (0.1 to 0.9%). A collagen solution was mixed with the hyaluronan solution in each of the centrifuge tubes in the weight ratios shown in Tables 1, 2, and 3. A mixture containing fetal bovine serum and a cell culture medium was added to each tube so that the final volume in each tube was the same. Subsequently, the pH of each tube was measured with a pH acid-base test paper, and the pH was adjusted to neutral (pH 7.0) with HCl and NaOH. The mixing steps were carried out at below 4° C.
Previous studies suggested that keloid fibroblasts exhibit fusiform attachment under normal culturing conditions. In order to understand the effect of various compositions containing hyaluronan and collagen on the morphology of keloid fibroblasts, normal fibroblasts (NF) and keloid fibroblasts (KF) were cultured in the control groups and experimental groups of Tables 1-3, and in a culture medium (10 mL DMEM, 10% FBS, 1% penicillin/streptomycin). The fibroblasts were stained with 0.5% crystal violet and observed under an electron microscope.
As shown in
Previous studies have shown that keloid fibroblasts have higher migration potential than normal fibroblasts. A study was carried out in order to understand the effect of various compositions containing hyaluronan and collagen on the migration of keloid fibroblasts. 100 μL of each composition of the groups was apply to coating on a culture dish and an O-ring (inner diameter 4 mm, outer diameter 6 mm) was placed in the center of the culture dish. Normal fibroblasts or keloid fibroblasts were placed inside the O-ring respectively in each coated dish. The O-ring was removed after the cells attached, and the cells continued to culture for four days. The cells were than stained with crystal violet and observed. Cell migration areas were calculated.
As shown in
Previous studies have shown that keloid fibroblasts have stronger contractile force than normal fibroblasts. A study was carried out in order to understand the effect of various compositions containing hyaluronan and collagen on the contractile force of keloid fibroblasts.
Normal or keloid fibroblasts were each added to the various compositions containing hyaluronan and collagen. After mixing uniformly, 50 μL of each was dropped onto the center of a culture dish in a half-spherical shape, which was placed at 37° C. in an incubator for 2 hours. After 2 hours of gelation, the area (A0) of the half-sphere was recorded. After 800 μL of culture medium was added, the fibroblasts started to contract the composition and the half-sphere was shrunken. After 48 hours, the area (A) of the half-sphere was recorded. The following formula was used to calculate the percentage of cell contractile force: X=[(A0−A)/A0]×100%. A higher percentage of shrinkage indicated a stronger contractile force.
As shown in
Previous studies have demonstrated that tension factors (e.g., PAI-1, PAI-2 and α-SMA), growth factor CTGF, and extracellular matrix components (collagen I and fibronectin) are associated with the formation of keloid. A study was carried out in order to understand the effect of various compositions containing hyaluronan and collagen on keloid fibroblasts on the molecular level.
Normal and keloid fibroblasts were separately cultured in the plane culture group, control group, and experimental groups described in Table 1. After four days of culturing, total RNA was extracted from the fibroblasts. The total RNA was then reverse transcribed into cDNA and analyzed by quantitative polymerase chain reaction (PCR). In the plane culture group, cells were cultured on the surface of a standard culture dish.
As shown in
In summary, compositions containing hyaluronan and collagen with a weight ratio greater than 1 were shown to improve the morphology, migration, and contractility of keloid fibroblasts to normal levels. The expression levels of keloid-associated genes were also modulated to be close to those in normal fibroblasts by the compositions. Therefore, the compositions can reduce hyperplasia of healing wound tissues in keloid patients such that the skin is closer to normal skin without abnormal protrusions. Furthermore, the compositions can be used to treat patients after surgical removal of keloid scars to prevent hyperplasia of the healing tissues.
All of the features disclosed in this specification may be combined in any combination. Each feature disclosed in this specification may be replaced by an alternative feature serving the same, equivalent, or similar purpose. Thus, unless expressly stated otherwise, each feature disclosed is only an example of a generic series of equivalent or similar features.
From the above description, one skilled in the art can easily ascertain the essential characteristics of the described embodiments, and without departing from the spirit and scope thereof, can make various changes and modifications of the embodiments to adapt it to various usages and conditions. Thus, other embodiments are also within the claims.
This application is a continuation of U.S. application Ser. No. 16/642,233, filed on Feb. 26, 2020, which is a National Stage of International Application No. PCT/US2018/049017, filed on Aug. 31, 2018, which claims the benefit of U.S. Provisional Application No. 62/553,267, filed on Sep. 1, 2017, the contents of all above applications being hereby incorporated by reference herein in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62553267 | Sep 2017 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16642233 | Feb 2020 | US |
| Child | 18662966 | US |
