CA1336816C - Wound healing - Google Patents
Wound healingInfo
- Publication number
- CA1336816C CA1336816C CA000607968A CA607968A CA1336816C CA 1336816 C CA1336816 C CA 1336816C CA 000607968 A CA000607968 A CA 000607968A CA 607968 A CA607968 A CA 607968A CA 1336816 C CA1336816 C CA 1336816C
- Authority
- CA
- Canada
- Prior art keywords
- pdgf
- egf
- purified
- wound
- healing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/18—Growth factors; Growth regulators
- A61K38/1808—Epidermal growth factor [EGF] urogastrone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Abstract
A method for healing an external wound of a mammal includes administering to the mammal a composition containing purified EGF and purified PDGF in a weight to weight ratio of at least 5:1.
Description
1 3368 ~ 6 WOUND HEALING
Backqround of the Invention This invention relates to healing wounds.
Growth factors are polypeptide hormones which stimulate a defined population of target cells.
Examples of growth factors include platelet-derived growth factor (PDGF), insulin-like growth factor, transforming growth factor beta (TGF-B), transforming growth factor alpha, epidermal growth factor (EGF), and fibroblast growth factor. PDGF is a cationic, heat-stable protein found in the granules of circulating platelets which is known to stimulate in vitro protein synthesis and collagen production by fibroblasts. It is also known to act as an in vitro mitogen and chemotactic agent for fibroblasts, and smaoth muscle cells.
It has been proposed to use PDGF to promote in vivo wound healing. For example, Grotendorst (1984) J.
Trauma 24:549-52 describes adding PDGF to Hunt-Schilling wire mesh chambers impregnated with a collagen gel and implanted in the backs of rats; PDGF was found to increase the amount of new collagen synthesized.
However, Leitzel et al. (1985) J. Dermatol. Surg. Oncol.
11:617-22 were unable to accelerate normal wound healing in hamsters using PDGF alone or in combination with FGF
and EGF.
Michaeli, et al. (1984) In Soft and Hard Tissue Repair (Hunt, T.K. et al., Eds), Praeger Publishers, New York, pp. 380-394, report that application of a partially purified preparation of PDGF obtained from platelet-rich plasma stimulated angiogenesis when implanted in rabbit corneas. Because PDGF is not an angiogenic growth factor the investigators suggested that an unknown factor in their partially purified PDGF
preparation was responsible for the angiogenic effect.
Backqround of the Invention This invention relates to healing wounds.
Growth factors are polypeptide hormones which stimulate a defined population of target cells.
Examples of growth factors include platelet-derived growth factor (PDGF), insulin-like growth factor, transforming growth factor beta (TGF-B), transforming growth factor alpha, epidermal growth factor (EGF), and fibroblast growth factor. PDGF is a cationic, heat-stable protein found in the granules of circulating platelets which is known to stimulate in vitro protein synthesis and collagen production by fibroblasts. It is also known to act as an in vitro mitogen and chemotactic agent for fibroblasts, and smaoth muscle cells.
It has been proposed to use PDGF to promote in vivo wound healing. For example, Grotendorst (1984) J.
Trauma 24:549-52 describes adding PDGF to Hunt-Schilling wire mesh chambers impregnated with a collagen gel and implanted in the backs of rats; PDGF was found to increase the amount of new collagen synthesized.
However, Leitzel et al. (1985) J. Dermatol. Surg. Oncol.
11:617-22 were unable to accelerate normal wound healing in hamsters using PDGF alone or in combination with FGF
and EGF.
Michaeli, et al. (1984) In Soft and Hard Tissue Repair (Hunt, T.K. et al., Eds), Praeger Publishers, New York, pp. 380-394, report that application of a partially purified preparation of PDGF obtained from platelet-rich plasma stimulated angiogenesis when implanted in rabbit corneas. Because PDGF is not an angiogenic growth factor the investigators suggested that an unknown factor in their partially purified PDGF
preparation was responsible for the angiogenic effect.
Lawrence et al. 203 Ann. Surgery 142, 1986 demonstrate a synerglstlc wound heallng actlvlty when TGF-B, PDGF and EGF are used together at 100 ng/ml each but not wlth PDGF ln comblnatlon wlth EGF alone. Lynch et al. 84 Proc. Nat. Acad. Scl, USA 7696, 1987 state that a preparatlon contalnlng equal amounts (5ng/mm ) of EGF and PDGF dld not elicit wound heallng actlvity greater than that brought about by EGF or PDGF alone.
Summary of the Invention In general, the lnventlon features heallng an external wound ln a mammal, e.g., a human patient, by applylng to the wound an effective amount of a composition that includes a combination of purified EGF and purified PDGF, in a welght to welght ratio of at least 5:1, preferably at least 10:1. Preferably, the EGF is recombinant human EGF, but can also be of another mammalian species, e.g., rat. EGF can be isolated from natural sources or, more preferably, produced by recombinant cells or solid phase peptide synthesis. The composition of the invention aids in healing the wound, at least in part, by promoting the growth of epithelial and connective tissue and the synthesls of total proteln and collagen. Wound heallng uslng the composltlon of the lnventlon ls more effectlve than that achleved ln the absence of treatment (l.e. wlthout applying exogenous agents) or by treatment with purlfled PDGF alone, or purlfled EGF alone.
In another aspect the lnventlon features a commerclal package comprlslng the above composltlon together wlth lnstructions for the use thereof ln the treatment of an external wound of a mammal.
In preferred embodlments of the lnvention, the i~
2a 60412-1989 composltlon ls prepared by comblning, ln a pharmaceutlcally acceptable carrler substance, e.g., commerclally avallable lnert gels, llqulds, or other slow release dellvery systems (e.g., sallne supplemented wlth albumln or methyl cellulose), purlfled EGF and PDGF (both of whlch are commerclally avallable) ln a _ 3 _ 1 33681 6 weight-to-weight ratio of between 5:1 and 10:1, or greater than 10:1. The purified PDGF may be obtained from human platelets or by recombinant DNA technology.
Thus, by the term "PDGF" we mean both platelet-derived and recombinant materials of mammalian, preferably primate, origin; most preferably, the primate is a human, but can also be a chimpanzee or other primate.
Recombinant PDGF can be recombinant heterodimer, made by inserting into cultured prokaryotic or eukaryotic cells DNA sequences encoding both subunits, and then allowing the translated subunits to be processed by the cells to form heterodimer, or DNA encoding just one of the subunits (preferably the beta or "2" chain) can be inserted into cells, which then are cultured to produce homodimeric-PDGF (PDGF-~ or PDGF-2 homodimer).
The term "purified" as used herein refers to PDGF or EGF which, prior to mixing with the other, is 95% or greater, by weight, PDGF or EGF, i.e., is substantially free of other proteins, lipids, and carbohydrates with which it is naturally associated.
A purified protein preparation will generally yield a single major band on a polyacrylamide gel for each PDGF or EGF component. Most preferably, the purified PDGF or EGF used in the composition of the invention is pure as judged by amino-terminal amino acid sequence analysis.
The invention also features healing an external wound by applying at least 500ng/150mm2 of EGF to the wound, preferably at least 5000ng/150mm2, in combination with purified PDGF.
The composition of the invention provides a fast, effective method for healing external wounds of mammals, e.g., bed sores, lacerations, corneal wounds and burns. The composition enhances connective tissue formation compared to natural healing (i.e. no exogenous agents added) or pure PDGF or EGF alone. Unlike pure PDGF alone, the composition promotes a significant increase in both new connective tissue and epithelial tissue. The epithelial layer obtained is thicker than that created by natural healing or by EFG alone, and also contains more epithelial projections connecting it to the new connective tissue; it is thus more firmly bound and protective.
Other features and advantages of the invention will be apparent from the following description of the preferred embodiments thereof, and from the claims.
Description of the Preferred Embodiments We now describe preferred embodiments of the invention.
External wounds, e.g., bed sores, diabetic ulcers and burns, are treated, according to the invention, with PDGF/EGF mixtures prepared by combining pure PDGF and EGF. Recombinant human EGF is commercially available from Amgen (Thousand Oaks, California) and Collaborative Research (Bedford, MA).
Purified recombinant PDGF and purified PDGF derived from human platelets are commercially available from PDGF, Inc. (Boston, MA), Collaborative Research (Waltham, MA), and Amgen Corp. Purified PDGF can also be prepared as follows.
Five hundred to l000 units of washed human platelet pellets are suspended in lM NaCl (2ml per platelet unit) and heated at 100C for 15 minutes. The supernatant is then separated by centrifugation and the precipitàte extracted twice with the lM NaCl.
The extracts are combined and dialyzed against 0.08M NaCl-0.OlM sodium phosphate buffer (pH 7.4) and mixed overnight at 4C with CM-Sephadex C-50 ~ 0 ~
133681 k equilibrated with the buffer. The mixture is then poured into a column (5 x 100 cm), washed extensively with 0.08M NaCl-O.OlM sodium phosphate buffer (pH 7.4), and eluted with lM NaCl while 10 ml fractions are collected.
Active fractions are pooled and dialyzed against 0.3M NaCl-O.OlM sodium phosphate buffer (pH
7.4), centrifuged, and pass~d at 4C through a 2.5 x 25 ~ cm column of Blue Sepharose~r(Pharmacia) equilibrated with 0.3M NaCl-O.OlM sodium phosphate buffer (pH 7.4).
The column is then washed with the buffer and partially purified PDGF eluted with a 1:1 solution of lM NaCl and ethylene glycol.
The partially purified PDGF fractions are diluted (1:1) with lM NaCl, dialyzed against lM acetic acid, and lyophilized. The lyophilized samples are dissolved in 0.8M NaCl-O.OlM sodium phosphate buffer (pH
7.4) and passed through a 1.2 x 40 cm column of CM-Sephadex C-50 equilibrated with the buffer. PDGF is then eluted with a NaCl gradient (0.08 to 1~).
The active fractions are combined, dialyzed against lM acetic acid, lyophilized, and dissolved in a small volume of lM acetic acid. O.5 ml portions~are applied to a 1.2 x 100 cm column of Biogel P-150 (100 to 200 mesh) equilibrated with lM acetic acid. The PDGF is then eluted with lM acetic acid while 2 ml fractions are collected.
Each active fraction containing 100 to 200 mg of protein is lyophilized, dissolved in 100 ml of 0.4%
trifluoroacetic acid, and subjected to reverse phase high performance liquid chromatography on a phenyl Bondapak column (Waters). Elution with a linear acetonitrile gradient (O to 60%) yields pure PDGF.
PDGF made by recombinant DNA technology can be prepared as follows:
Platelet-derived growth factor (PDGF) derived from human platelets contains two polypeptide sequences (PDGF-l and PDGF-2 polypeptides; Antoniades, H.N, and Hunkapiller, M. (1983) Science 220:963-965). PDGF-l is encoded by a gene localized in chromosome 7 (Betsholtz, C. et al., Nature 320:695-699), and PDGF-2 is encoded by the sis oncogene (Doolittle, R. et al. (1983) Science 22I:275-277) localized in chromosome 22 (Dalla-Favera, R. (1982) Science 218:686-688). The sis gene encodes the transforming protein of the Simian Sarcoma Virus (SSV) which is closely related to PDGF-2 polypeptide.
The human cellular c-sis also encodes the PDGF-2 chain (Rao, C.D. et al. (1986) Proc. Natl. Acad. Sci. USA
83:2392-2396). Because the two polypeptide chains of PDGF are coded by two different genes localized in separate chromosomes, the possibility exists that human PDGF consists of a disulfide-linked heterodimer of PDGF-l and PDGF-2, or a mixture of the two homodimers (homodimer of PDGF-l and homodimer of PDGF-2), or a mixture of the heterodimer and the two homodimers.
Mammalian cells in culture infected with the Simian Sarcoma Virus, which contains the gene encoding the PDGF-2 chain, were shown to synthesize the PDGF-2 polypeptide and to process it into a disulfide-linked homodimer (Robbins, K. et al. (1983) Nature 305:605-608). In addition, PDGF-2 homodimer reacts with antisera raised against human PDGF. Furthermore, the functional properties of the secreted PDGF-2 homodimer are similar to those of platelet-derived PDGF in that it stimulates DNA synthesis in cultured fibroblasts, it induces phosphorylation at the tyrosine residue of a 185 kd cell membrane protein, and it is capable of competing with human (125I)-PDGF for binding to specific cell surface PDGF receptors (Owen, A. et al. (1984) Science 225:54-56). Similar properties were shown for the sis/PDGF-2 gene product derived from cultured normal human cells (for example, human arterial endothelial cells), or from human malignant cells expressing the sis/PDGF-2 gene (Antoniades, H. et al. (1985) Cancer Cells 3:145-151).
The recombinant PDGF-2 homodimer (referred to as recombinant PDGF herein) is obtained by the introduction of cDNA clones of c-sis/PDGF-2 gene into mouse cells using an expression vector. The c-sis/PDGF-2 clone used for the expression was obtained from normal human cultured endothelial cel1s (Collins, T., et al. (1985) Nature 216:748-750).
Wound Healing To determine the effectiveness of PDGF/EGF
mixtures in promoting wound healing, the following experiments were performed.
Young white Yorkshire pigs (Parson's Farm, Hadley, MA) weighing between 10 and 15 kg were fasted for at least 6 hours prior to surgery and then anesthetized. Under aseptic conditions, the back and thoracic areas were clipped, shaved, and washed with mild soap and water. The area to be wounded was then disinfected with 70~ alcohol.
Wounds measuring 1 cm x 2 cm were induced at a depth of 0.5 mm using a modified Castroviejo electrokeratome (Storz, St. Louis, MO, as modified by Brownells, Inc.). The wounds resulted in complete removal of the epithelium, as well as a portion of the underlying dermis (comparable to a second degree burn injury). Individual wounds were separated by at least 15 mm of unwounded skin. Wounds receiving identical treatment were organized as a group and separated from other groups by at least 3 cm. Wounds receiving no - 8 - 13368~6 growth factor treatment were separated from wounds receiving such treatment by at least 10 cm.
The wounds were treated directly with a single application of the following growth factors suspended in biocompatible gel: 1) 500 ng pure human PDGF (purified by high performance liquid chromatography) or recombinant PDGF alone; 2) 500 ng pure recombinant PDGF
in combination with up to 5000 ng human, mouse, or recombinant EGF; 3) 500 ng human, mouse, or recombinant to 5000 ng recombinant human EGF alone.
Following wounding, biopsy specimens were taken on days 3 through 10. Biopsy specimens for histologic evaluation were taken as wedges approximately 3 mm deep and placed in 10% formalin. Specimens for biochemical analysis and autoradiography were obtained using an electrokeratome. The final dimensions of the specimens were 1.5 mm x 10 mm x 1.5 mm. Three specimens per wound were collected for biochemical analysis. Following collection, the specimens were frozen in liquid nitrogen and stored at -80C. The biopsy specimens were analyzed as follows.
Histologic Evaluation Histologic specimens were prepared using standard paraffin impregnating and embedding techniques. Four micron sections were made and stained using filtered Harris hemotoxylin and alcoholic eosin;
they were then observed under a microscope. All specimens were scored blindly by two investigators at equally distributed points throughout the sections. The widths of the epithelial and connective tissue layers were scored using a grid placed within the ocular of the microscope; the measurement was then converted into millimeters using a micrometer viewed under the same conditions. Cell density was determined by counting the number of nuclei per grid area.
1 3368 1 ~
g Collaqen and Protein Determination Hydroxy-proline content (i.e., collagen) was determined in the 1.5 mm wide frozen cross-sections by separating the newly formed wound tissue from the remaining tissue under a dissecting microscope. The wound tissue was hydrolized in 6M HCl overnight at 120C
and hydroxyproline analyses were performed on the hydrolysate as described previously (Switzer et al., Anal. Biochem. 39, 487 (1971).
Protein content of the tissue extract in concentrated ammonium hydroxide was measured by the Bradford method (Bradford (1976) Anal. Biochem.
72:248-54), with bovine serum albumin as a standard.
Results The results from histologic evaluation indicated that wounds treated with the combination of recombinant EGF and PDGF in a weight to weight ratio of 5:1 to 10:1 had thicker connective tissue with more collagen (about 2.0 fold increase over controls) and epithelial layers (about 0.8 fold increase over controls), and more extensive epithelial projections connecting these layers, than wounds receiving no treatment, human or recombinant EGF alone, or pure PDGF
alone. The PDGF/EGF treated wounds also had greater cellularity, protein and collagen contents.
Dosaqe To determine the appropriate dosage of purified PDGF and EGF, the above-described experiments were repeated except that the wounds were treated with 5 ng, 10 ng, 20 ng, and 30 ng purified PDGF and EGF per square millimeter of wound dispersed in 30~1 of biocompatible gel. The results showed that optimum effects were produced when the PDGF content was 4 ng/mm2 or higher and EGF was 20 ng/mm2 or higher.
To determine the appropriate ratio of pure PDGF
to EGF, combinations in which the weight to weight ratio of PDGF to EGF ranged from 1:10 to 25:1 were evaluated as described above. Optimum results were achieved with ratios greater than 1:5.
Other embodiments are within the following claims.
Summary of the Invention In general, the lnventlon features heallng an external wound ln a mammal, e.g., a human patient, by applylng to the wound an effective amount of a composition that includes a combination of purified EGF and purified PDGF, in a welght to welght ratio of at least 5:1, preferably at least 10:1. Preferably, the EGF is recombinant human EGF, but can also be of another mammalian species, e.g., rat. EGF can be isolated from natural sources or, more preferably, produced by recombinant cells or solid phase peptide synthesis. The composition of the invention aids in healing the wound, at least in part, by promoting the growth of epithelial and connective tissue and the synthesls of total proteln and collagen. Wound heallng uslng the composltlon of the lnventlon ls more effectlve than that achleved ln the absence of treatment (l.e. wlthout applying exogenous agents) or by treatment with purlfled PDGF alone, or purlfled EGF alone.
In another aspect the lnventlon features a commerclal package comprlslng the above composltlon together wlth lnstructions for the use thereof ln the treatment of an external wound of a mammal.
In preferred embodlments of the lnvention, the i~
2a 60412-1989 composltlon ls prepared by comblning, ln a pharmaceutlcally acceptable carrler substance, e.g., commerclally avallable lnert gels, llqulds, or other slow release dellvery systems (e.g., sallne supplemented wlth albumln or methyl cellulose), purlfled EGF and PDGF (both of whlch are commerclally avallable) ln a _ 3 _ 1 33681 6 weight-to-weight ratio of between 5:1 and 10:1, or greater than 10:1. The purified PDGF may be obtained from human platelets or by recombinant DNA technology.
Thus, by the term "PDGF" we mean both platelet-derived and recombinant materials of mammalian, preferably primate, origin; most preferably, the primate is a human, but can also be a chimpanzee or other primate.
Recombinant PDGF can be recombinant heterodimer, made by inserting into cultured prokaryotic or eukaryotic cells DNA sequences encoding both subunits, and then allowing the translated subunits to be processed by the cells to form heterodimer, or DNA encoding just one of the subunits (preferably the beta or "2" chain) can be inserted into cells, which then are cultured to produce homodimeric-PDGF (PDGF-~ or PDGF-2 homodimer).
The term "purified" as used herein refers to PDGF or EGF which, prior to mixing with the other, is 95% or greater, by weight, PDGF or EGF, i.e., is substantially free of other proteins, lipids, and carbohydrates with which it is naturally associated.
A purified protein preparation will generally yield a single major band on a polyacrylamide gel for each PDGF or EGF component. Most preferably, the purified PDGF or EGF used in the composition of the invention is pure as judged by amino-terminal amino acid sequence analysis.
The invention also features healing an external wound by applying at least 500ng/150mm2 of EGF to the wound, preferably at least 5000ng/150mm2, in combination with purified PDGF.
The composition of the invention provides a fast, effective method for healing external wounds of mammals, e.g., bed sores, lacerations, corneal wounds and burns. The composition enhances connective tissue formation compared to natural healing (i.e. no exogenous agents added) or pure PDGF or EGF alone. Unlike pure PDGF alone, the composition promotes a significant increase in both new connective tissue and epithelial tissue. The epithelial layer obtained is thicker than that created by natural healing or by EFG alone, and also contains more epithelial projections connecting it to the new connective tissue; it is thus more firmly bound and protective.
Other features and advantages of the invention will be apparent from the following description of the preferred embodiments thereof, and from the claims.
Description of the Preferred Embodiments We now describe preferred embodiments of the invention.
External wounds, e.g., bed sores, diabetic ulcers and burns, are treated, according to the invention, with PDGF/EGF mixtures prepared by combining pure PDGF and EGF. Recombinant human EGF is commercially available from Amgen (Thousand Oaks, California) and Collaborative Research (Bedford, MA).
Purified recombinant PDGF and purified PDGF derived from human platelets are commercially available from PDGF, Inc. (Boston, MA), Collaborative Research (Waltham, MA), and Amgen Corp. Purified PDGF can also be prepared as follows.
Five hundred to l000 units of washed human platelet pellets are suspended in lM NaCl (2ml per platelet unit) and heated at 100C for 15 minutes. The supernatant is then separated by centrifugation and the precipitàte extracted twice with the lM NaCl.
The extracts are combined and dialyzed against 0.08M NaCl-0.OlM sodium phosphate buffer (pH 7.4) and mixed overnight at 4C with CM-Sephadex C-50 ~ 0 ~
133681 k equilibrated with the buffer. The mixture is then poured into a column (5 x 100 cm), washed extensively with 0.08M NaCl-O.OlM sodium phosphate buffer (pH 7.4), and eluted with lM NaCl while 10 ml fractions are collected.
Active fractions are pooled and dialyzed against 0.3M NaCl-O.OlM sodium phosphate buffer (pH
7.4), centrifuged, and pass~d at 4C through a 2.5 x 25 ~ cm column of Blue Sepharose~r(Pharmacia) equilibrated with 0.3M NaCl-O.OlM sodium phosphate buffer (pH 7.4).
The column is then washed with the buffer and partially purified PDGF eluted with a 1:1 solution of lM NaCl and ethylene glycol.
The partially purified PDGF fractions are diluted (1:1) with lM NaCl, dialyzed against lM acetic acid, and lyophilized. The lyophilized samples are dissolved in 0.8M NaCl-O.OlM sodium phosphate buffer (pH
7.4) and passed through a 1.2 x 40 cm column of CM-Sephadex C-50 equilibrated with the buffer. PDGF is then eluted with a NaCl gradient (0.08 to 1~).
The active fractions are combined, dialyzed against lM acetic acid, lyophilized, and dissolved in a small volume of lM acetic acid. O.5 ml portions~are applied to a 1.2 x 100 cm column of Biogel P-150 (100 to 200 mesh) equilibrated with lM acetic acid. The PDGF is then eluted with lM acetic acid while 2 ml fractions are collected.
Each active fraction containing 100 to 200 mg of protein is lyophilized, dissolved in 100 ml of 0.4%
trifluoroacetic acid, and subjected to reverse phase high performance liquid chromatography on a phenyl Bondapak column (Waters). Elution with a linear acetonitrile gradient (O to 60%) yields pure PDGF.
PDGF made by recombinant DNA technology can be prepared as follows:
Platelet-derived growth factor (PDGF) derived from human platelets contains two polypeptide sequences (PDGF-l and PDGF-2 polypeptides; Antoniades, H.N, and Hunkapiller, M. (1983) Science 220:963-965). PDGF-l is encoded by a gene localized in chromosome 7 (Betsholtz, C. et al., Nature 320:695-699), and PDGF-2 is encoded by the sis oncogene (Doolittle, R. et al. (1983) Science 22I:275-277) localized in chromosome 22 (Dalla-Favera, R. (1982) Science 218:686-688). The sis gene encodes the transforming protein of the Simian Sarcoma Virus (SSV) which is closely related to PDGF-2 polypeptide.
The human cellular c-sis also encodes the PDGF-2 chain (Rao, C.D. et al. (1986) Proc. Natl. Acad. Sci. USA
83:2392-2396). Because the two polypeptide chains of PDGF are coded by two different genes localized in separate chromosomes, the possibility exists that human PDGF consists of a disulfide-linked heterodimer of PDGF-l and PDGF-2, or a mixture of the two homodimers (homodimer of PDGF-l and homodimer of PDGF-2), or a mixture of the heterodimer and the two homodimers.
Mammalian cells in culture infected with the Simian Sarcoma Virus, which contains the gene encoding the PDGF-2 chain, were shown to synthesize the PDGF-2 polypeptide and to process it into a disulfide-linked homodimer (Robbins, K. et al. (1983) Nature 305:605-608). In addition, PDGF-2 homodimer reacts with antisera raised against human PDGF. Furthermore, the functional properties of the secreted PDGF-2 homodimer are similar to those of platelet-derived PDGF in that it stimulates DNA synthesis in cultured fibroblasts, it induces phosphorylation at the tyrosine residue of a 185 kd cell membrane protein, and it is capable of competing with human (125I)-PDGF for binding to specific cell surface PDGF receptors (Owen, A. et al. (1984) Science 225:54-56). Similar properties were shown for the sis/PDGF-2 gene product derived from cultured normal human cells (for example, human arterial endothelial cells), or from human malignant cells expressing the sis/PDGF-2 gene (Antoniades, H. et al. (1985) Cancer Cells 3:145-151).
The recombinant PDGF-2 homodimer (referred to as recombinant PDGF herein) is obtained by the introduction of cDNA clones of c-sis/PDGF-2 gene into mouse cells using an expression vector. The c-sis/PDGF-2 clone used for the expression was obtained from normal human cultured endothelial cel1s (Collins, T., et al. (1985) Nature 216:748-750).
Wound Healing To determine the effectiveness of PDGF/EGF
mixtures in promoting wound healing, the following experiments were performed.
Young white Yorkshire pigs (Parson's Farm, Hadley, MA) weighing between 10 and 15 kg were fasted for at least 6 hours prior to surgery and then anesthetized. Under aseptic conditions, the back and thoracic areas were clipped, shaved, and washed with mild soap and water. The area to be wounded was then disinfected with 70~ alcohol.
Wounds measuring 1 cm x 2 cm were induced at a depth of 0.5 mm using a modified Castroviejo electrokeratome (Storz, St. Louis, MO, as modified by Brownells, Inc.). The wounds resulted in complete removal of the epithelium, as well as a portion of the underlying dermis (comparable to a second degree burn injury). Individual wounds were separated by at least 15 mm of unwounded skin. Wounds receiving identical treatment were organized as a group and separated from other groups by at least 3 cm. Wounds receiving no - 8 - 13368~6 growth factor treatment were separated from wounds receiving such treatment by at least 10 cm.
The wounds were treated directly with a single application of the following growth factors suspended in biocompatible gel: 1) 500 ng pure human PDGF (purified by high performance liquid chromatography) or recombinant PDGF alone; 2) 500 ng pure recombinant PDGF
in combination with up to 5000 ng human, mouse, or recombinant EGF; 3) 500 ng human, mouse, or recombinant to 5000 ng recombinant human EGF alone.
Following wounding, biopsy specimens were taken on days 3 through 10. Biopsy specimens for histologic evaluation were taken as wedges approximately 3 mm deep and placed in 10% formalin. Specimens for biochemical analysis and autoradiography were obtained using an electrokeratome. The final dimensions of the specimens were 1.5 mm x 10 mm x 1.5 mm. Three specimens per wound were collected for biochemical analysis. Following collection, the specimens were frozen in liquid nitrogen and stored at -80C. The biopsy specimens were analyzed as follows.
Histologic Evaluation Histologic specimens were prepared using standard paraffin impregnating and embedding techniques. Four micron sections were made and stained using filtered Harris hemotoxylin and alcoholic eosin;
they were then observed under a microscope. All specimens were scored blindly by two investigators at equally distributed points throughout the sections. The widths of the epithelial and connective tissue layers were scored using a grid placed within the ocular of the microscope; the measurement was then converted into millimeters using a micrometer viewed under the same conditions. Cell density was determined by counting the number of nuclei per grid area.
1 3368 1 ~
g Collaqen and Protein Determination Hydroxy-proline content (i.e., collagen) was determined in the 1.5 mm wide frozen cross-sections by separating the newly formed wound tissue from the remaining tissue under a dissecting microscope. The wound tissue was hydrolized in 6M HCl overnight at 120C
and hydroxyproline analyses were performed on the hydrolysate as described previously (Switzer et al., Anal. Biochem. 39, 487 (1971).
Protein content of the tissue extract in concentrated ammonium hydroxide was measured by the Bradford method (Bradford (1976) Anal. Biochem.
72:248-54), with bovine serum albumin as a standard.
Results The results from histologic evaluation indicated that wounds treated with the combination of recombinant EGF and PDGF in a weight to weight ratio of 5:1 to 10:1 had thicker connective tissue with more collagen (about 2.0 fold increase over controls) and epithelial layers (about 0.8 fold increase over controls), and more extensive epithelial projections connecting these layers, than wounds receiving no treatment, human or recombinant EGF alone, or pure PDGF
alone. The PDGF/EGF treated wounds also had greater cellularity, protein and collagen contents.
Dosaqe To determine the appropriate dosage of purified PDGF and EGF, the above-described experiments were repeated except that the wounds were treated with 5 ng, 10 ng, 20 ng, and 30 ng purified PDGF and EGF per square millimeter of wound dispersed in 30~1 of biocompatible gel. The results showed that optimum effects were produced when the PDGF content was 4 ng/mm2 or higher and EGF was 20 ng/mm2 or higher.
To determine the appropriate ratio of pure PDGF
to EGF, combinations in which the weight to weight ratio of PDGF to EGF ranged from 1:10 to 25:1 were evaluated as described above. Optimum results were achieved with ratios greater than 1:5.
Other embodiments are within the following claims.
Claims (8)
1. A use for healing an external wound of a mammal of a wound-healing amount of a composition comprising purified epidermal growth factor (EGF) and purified platelet-derived growth factor (PDGF) wherein said EGF and said PDGF are present in a weight to weight ratio of at least 5:1 respectively.
2. A use of claim 1 wherein the weight to weight ratio of said EGF to said PDGF in said composition is at least 10:1.
3. A wound healing composition comprising purified EGF and purified PDGF, in a weight to weight ratio of at least 5:1.
4. The composition of claim 3 wherein said ratio is at least 10:1.
5. A method for preparing a composition for healing wounds, comprising mixing purified EGF and purified PDGF in a weight to weight ratio of at least 5:1.
6. A use for healing an external wound of a wound-healing amount of a composition comprising purified PDGF and purified EGF, wherein said EGF is present in said composition at a concentration of at least 500 ng/150 mm2 in said wound.
7. A use of claim 6, said EGF being present at a concentration of at least 5000 ng/150 mm2 in said wound.
8. A commercial package comprising a composition according to claim 3 or 4 together with instructions for the use thereof in the treatment of an external wound of a mammal.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/231,145 US5034375A (en) | 1988-08-10 | 1988-08-10 | Process of wound healing using PDGF and EGF |
US231,145 | 1988-08-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1336816C true CA1336816C (en) | 1995-08-29 |
Family
ID=22867921
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000607968A Expired - Lifetime CA1336816C (en) | 1988-08-10 | 1989-08-10 | Wound healing |
Country Status (7)
Country | Link |
---|---|
US (1) | US5034375A (en) |
EP (1) | EP0382841B1 (en) |
JP (1) | JPH075481B2 (en) |
AU (1) | AU4319789A (en) |
CA (1) | CA1336816C (en) |
DE (1) | DE68912758T2 (en) |
WO (1) | WO1990001331A1 (en) |
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ATE212554T1 (en) * | 1990-11-27 | 2002-02-15 | American Nat Red Cross | TISSUE COVERING AND GROWTH FACTOR CONTAINING COMPOUNDS TO PROMOTE ACCELERATED WOUND HEALING |
US6117425A (en) * | 1990-11-27 | 2000-09-12 | The American National Red Cross | Supplemented and unsupplemented tissue sealants, method of their production and use |
JPH04305528A (en) * | 1991-02-22 | 1992-10-28 | Dai Ichi Seiyaku Co Ltd | Proliferation stimulant for keratinocyte and dermal fibroblast |
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EP0639980A1 (en) * | 1992-02-26 | 1995-03-01 | Allergan, Inc. | Use of platelet derived growth factor in ophthalmic wound healing |
CN1141058A (en) * | 1993-11-09 | 1997-01-22 | 纽罗斯菲里斯控股有限公司 | In situ modification and manipulation of stem cells of the central nervous system |
US6762336B1 (en) | 1998-01-19 | 2004-07-13 | The American National Red Cross | Hemostatic sandwich bandage |
DE10014557A1 (en) * | 2000-03-23 | 2001-10-04 | Lohmann Therapie Syst Lts | Wound dressing with reduced tendency to overgrow |
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HK1077740A1 (en) | 2001-12-20 | 2006-02-24 | Ct Ingenieria Genetica Biotech | Use of epidermal growth factor in the manufacture of a pharmaceutical injection composition for preventing diabetic limb amputation |
TWI348912B (en) * | 2002-03-12 | 2011-09-21 | Method and composition for treating skin wounds with epidermal growth factor | |
US20060155234A1 (en) * | 2002-09-10 | 2006-07-13 | American National Red Cross | Hemostatic dressing |
DE102004018347A1 (en) * | 2004-04-06 | 2005-10-27 | Manfred Dr. Schmolz | Wound healing-promoting messenger mix |
US7473678B2 (en) | 2004-10-14 | 2009-01-06 | Biomimetic Therapeutics, Inc. | Platelet-derived growth factor compositions and methods of use thereof |
WO2007061889A2 (en) * | 2005-11-17 | 2007-05-31 | Biomimetic Therapeutics, Inc. | Maxillofacial bone augmentation using rhpdgf-bb and a biocompatible matrix |
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CA2641860C (en) | 2006-02-09 | 2015-07-14 | Biomimetic Therapeutics, Inc. | Compositions and methods for treating bone |
US9161967B2 (en) | 2006-06-30 | 2015-10-20 | Biomimetic Therapeutics, Llc | Compositions and methods for treating the vertebral column |
JP5484047B2 (en) | 2006-06-30 | 2014-05-07 | バイオミメティック セラピューティクス, エルエルシー | PDGF-biomatrix composition and method for treating rotator cuff injury |
MX2009001323A (en) * | 2006-08-04 | 2009-07-22 | Stb Lifesaving Technologies In | Solid dressing for treating wounded tissue. |
US8106008B2 (en) | 2006-11-03 | 2012-01-31 | Biomimetic Therapeutics, Inc. | Compositions and methods for arthrodetic procedures |
US20080195476A1 (en) * | 2007-02-09 | 2008-08-14 | Marchese Michael A | Abandonment remarketing system |
US20090075891A1 (en) * | 2007-08-06 | 2009-03-19 | Macphee Martin | Methods and dressings for sealing internal injuries |
WO2009052221A2 (en) * | 2007-10-15 | 2009-04-23 | The Regents Of The University Of Colorado | Methods for extracting platelets and compositions obtained therefrom |
CN102014977B (en) | 2008-02-07 | 2015-09-02 | 生物模拟治疗有限责任公司 | For compositions and the method for Distraction Osteogenesis |
AU2009291828C1 (en) * | 2008-09-09 | 2016-03-17 | Biomimetic Therapeutics, Llc | Platelet-derived growth factor compositions and methods for the treatment of tendon and ligament injuries |
JP6144049B2 (en) | 2010-02-22 | 2017-06-07 | バイオミメティック セラピューティクス,リミテッド ライアビリティ カンパニー | Platelet-derived growth factor compositions and methods for treating tendon disorders |
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KR101777910B1 (en) * | 2015-04-30 | 2017-09-13 | 주식회사 제네웰 | A composition for wound healing, method of producing the same and dressing using the same |
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ATE85080T1 (en) * | 1984-02-17 | 1993-02-15 | Genentech Inc | HUMAN TRANSFORMATIONAL GROWTH FACTOR AND PRECURSORS OR FRAGMENTS THEREOF, CELLS, DNA, VECTORS AND METHODS FOR THEIR PRODUCTION, COMPOSITIONS AND PRODUCTS CONTAINING THEM, AND ANTIBODIES AND DIAGNOSTIC METHODS DERIVED THEREOF. |
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US4702908A (en) * | 1985-11-01 | 1987-10-27 | Thorbecke G Jeanette | Composition containing platelet factor 4 and method for restoring suppressed immune responses |
NZ222413A (en) * | 1986-11-05 | 1991-06-25 | Ethicon Inc | Compositions containing a polypeptide growth factor and a water-soluble cellulose polymer stabiliser |
NZ226171A (en) * | 1987-09-18 | 1990-06-26 | Ethicon Inc | Gel formulation containing polypeptide growth factor |
-
1988
- 1988-08-10 US US07/231,145 patent/US5034375A/en not_active Expired - Lifetime
-
1989
- 1989-08-10 EP EP89910545A patent/EP0382841B1/en not_active Expired - Lifetime
- 1989-08-10 JP JP1509811A patent/JPH075481B2/en not_active Expired - Lifetime
- 1989-08-10 DE DE68912758T patent/DE68912758T2/en not_active Expired - Lifetime
- 1989-08-10 WO PCT/US1989/003490 patent/WO1990001331A1/en active IP Right Grant
- 1989-08-10 AU AU43197/89A patent/AU4319789A/en not_active Abandoned
- 1989-08-10 CA CA000607968A patent/CA1336816C/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
EP0382841A1 (en) | 1990-08-22 |
WO1990001331A1 (en) | 1990-02-22 |
AU4319789A (en) | 1990-03-05 |
JPH03500782A (en) | 1991-02-21 |
US5034375A (en) | 1991-07-23 |
DE68912758T2 (en) | 1994-06-01 |
EP0382841B1 (en) | 1994-01-26 |
DE68912758D1 (en) | 1994-03-10 |
JPH075481B2 (en) | 1995-01-25 |
EP0382841A4 (en) | 1991-01-02 |
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