US20140127310A1 - Treatment of disease with poly-n-acetylglucosamine nanofibers - Google Patents

Treatment of disease with poly-n-acetylglucosamine nanofibers Download PDF

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US20140127310A1
US20140127310A1 US14/111,703 US201214111703A US2014127310A1 US 20140127310 A1 US20140127310 A1 US 20140127310A1 US 201214111703 A US201214111703 A US 201214111703A US 2014127310 A1 US2014127310 A1 US 2014127310A1
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snag nanofibers
snag
infection
disease
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John N. Vournakis
Sergio Finkielsztein
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Marine Polymer Technologies Inc
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Marine Polymer Technologies Inc
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
    • A61K31/726—Glycosaminoglycans, i.e. mucopolysaccharides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00—Bandages or dressings; Absorbent pads
    • A61F13/01—Non-adhesive bandages or dressings
    • A61F13/01008—Non-adhesive bandages or dressings characterised by the material
    • A61F13/01017—Non-adhesive bandages or dressings characterised by the material synthetic, e.g. polymer based
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
    • A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0014—Skin, i.e. galenical aspects of topical compositions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A61K9/0024—Solid, semi-solid or solidifying implants, which are implanted or injected in body tissue
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K9/0012—Galenical forms characterised by the site of application
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    • A61P17/00—Drugs for dermatological disorders
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
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Definitions

  • compositions comprising shortened fibers of poly-N-acetylglucosamine and/or a derivative thereof (“sNAG nanofibers”) and the use of such compositions in the treatment of disease.
  • Defensins are small (3-4 kDa), cysteine-rich cationic peptides found in mammals, insects, and plants that are classified into different families ( ⁇ , ⁇ , and ⁇ ) based on their pattern of disulfide bonding. These small peptides are important effectors of innate immunity and consequently play an important role in the body's battle against various diseases.
  • a number of diseases are incurable at this time or have suboptimal treatments available, due to only partial effectiveness of such treatments or side effects associated with such treatments.
  • Such diseases include, among others, cancer, some viral diseases, some fungal diseases, inflammatory bowel diseases (e.g., Crohn's disease), and dermatological diseases such as psoriasis and dermatitis.
  • sNAG nanofibers examples include, but are not limited to, solid tumor cancers, skin cancer, viral infections, yeast infections, fungal infections, inflammatory bowel disease, Crohn's disease, dermatitis and psoriasis.
  • described herein is a method for treating a viral infection in a subject, comprising administering a composition comprising sNAG nanofibers to a subject having (e.g., diagnosed with) a viral infection (e.g., an HSV infection).
  • a method for preventing a viral disease in a human subject comprising administering a composition comprising sNAG nanofibers to a subject at risk of developing a viral disease (e.g., a symptom of an HSV infection such as a cold sore or a lesion).
  • the sNAG nanofiber composition is topically administered to the subject (e.g., to the skin or mucous membrane).
  • the subject is a human.
  • a method for treating a solid tumor in a subject comprising administering a composition comprising sNAG nanofibers to a subject diagnosed with a solid tumor.
  • all or part of the solid tumor has been removed from the subject (e.g., surgically removed), and the sNAG nanofibers are administered to the site of the solid tumor before, during, and/or after the removal of all or part of the solid tumor.
  • the subject is a human.
  • a method for treating a skin cancer in a subject comprising topically administering a composition comprising sNAG nanofibers to a human subject diagnosed with a skin cancer.
  • all or part of the skin cancer has been removed from the subject (e.g., surgically removed), and the sNAG nanofibers are administered to the site of the skin cancer before, during, and/or after the removal of all or part of the skin cancer.
  • the subject is a human.
  • a method for treating inflammatory bowel disease in a subject comprising administering a composition comprising sNAG nanofibers to a subject with inflammatory bowel disease (e.g., diagnosed with inflammatory bowel disease).
  • a method for treating Crohn's disease in a subject comprising administering a composition comprising sNAG nanofibers to a subject with Crohn's disease (e.g., a subject diagnosed with Crohn's disease).
  • the sNAG nanofiber composition is topically administered to the subject (e.g., rectally via a suppository).
  • the subject is a human.
  • the sNAG nanofibers contemplated in the methods described herein may be of varying lengths, widths and molecular weights as described in Section 5.1, infra. In certain embodiments, the majority (and in certain embodiments, at least or more than 60%, 70%, 80%, 90%, 95% or 99%) of the sNAG nanofibers, or 100% of the sNAG nanofibers, are between about 1 to 15 ⁇ m in length.
  • the majority (and in certain embodiments, at least or more than 60%, 70%, 80%, 90%, 95% or 99%) of the sNAG nanofibers, or 100% of the sNAG nanofibers are between about 2 to 10 ⁇ m, 4 to 7 ⁇ m, 4 to 10 ⁇ m, or 5 to 10 ⁇ m in length.
  • the sNAG nanofibers of the described length can be obtained, for example, as described below in Section 5.2, infra.
  • the sNAG nanofibers were produced by irradiation, e.g., gamma irradiation, of poly-N-acetylglucosamine or a derivative thereof.
  • the sNAG nanofibers are produced by irradiation of the poly- ⁇ -1 ⁇ 4-N-acetylglucosamine in the form of dried fibers (e.g., at 500-2,000 kgy), or irradiation of the poly- ⁇ -1 ⁇ 4-N-acetylglucosamine in the form of wet fibers (e.g., at 100-500 kgy).
  • the sNAG nanofibers are derived from microalgae. In another embodiment, the sNAG nanofibers are not derived from crustaceans. In yet another embodiment, the sNAG nanofibers may be derived from microalgae, crustaceans (e.g., shrimp), fungus or any other source.
  • the sNAG nanofibers comprise N-acetylglucosamine monosaccharides and/or glucosamine monosaccharides, wherein more than 60%, 70%, 80%, 90%, 95%, or 99% of the monosaccharides of the sNAG nanofibers are N-acetylglucosamine monosaccharides.
  • the sNAG nanofibers comprise N-acetylglucosamine monosaccharides and/or glucosamine monosaccharides, wherein more than 70% of the monosaccharides of the sNAG nanofibers are N-acetylglucosamine monosaccharides.
  • the sNAG nanofibers used in the methods described herein are non-reactive in a biocompatibility test or tests.
  • the sNAG nanofibers used in the methods described herein may be non-reactive when tested in an elution test, an intramuscular implantation test, an intracutaneous test, or a systemic test.
  • the compositions described herein are non-reactive when tested in an elution test, an intramuscular implantation test, an intracutaneous test, or a systemic test.
  • the sNAG nanofibers used in the methods described herein have Grade 0 or Grade 1 when tested in an elution test, an intramuscular implantation test, an intracutaneous test, or a systemic test.
  • the sNAG nanofibers used in the methods described herein are at most mildly reactive when tested in an elution test, an intramuscular implantation test, an intracutaneous test, or a systemic test.
  • the sNAG nanofibers or compositions comprising such nanofibers are non-reactive as determined by an intramuscular implantation test.
  • the compositions described herein do not cause an allergenic reaction or an irritation, e.g., at the site of application.
  • the compositions described herein cause at most a mild allergenic reaction or a mild irritation, e.g., at the site of application.
  • the sNAG nanofibers used in the methods described herein increase the metabolic rate of serum-starved human umbilical cord vein endothelial cells in a MTT assay and/or do not rescue apoptosis of serum-starved human umbilical cord vein endothelial cells in a trypan blue exclusion test. In some embodiments, the sNAG nanofibers increase the metabolic rate of serum-starved human umbilical cord vein endothelial cells in a MTT assay and do not rescue apoptosis of serum-starved human umbilical cord vein endothelial cells in a trypan blue exclusion test.
  • compositions described herein are topical, e.g., topical on the skin; topical at the site of a wound, a surgery, a viral infection, a fungal infection, or a symptom of an infection (e.g., a swelling, a blister, a rash, a lesion); and topical to a body surface such as the skin, mucous membranes (e.g., vagina, anus, throat, eyes, ears), or the surface of other tissues.
  • the sNAG nanofibers or compositions comprising such nanofibers are formulated as a dressing, a bandage, a mat, a spray, a liquid, a suspension (e.g., a thick suspension), a membrane, a powder, an ointment, a cream, a paste, a suppository, or a gel.
  • the sNAG nanofibers or compositions comprising such nanofibers are formulated as a suspension, a cream, a liquid solution, a gel, an ointment, a membrane, a powder, a spray, or a suppository.
  • the sNAG nanofibers or compositions comprising such nanofibers are formulated as a suspension (e.g., a thick suspension).
  • compositions comprising the sNAG nanofibers are not solid or barrier-forming.
  • compositions for use in the methods described herein comprise sNAG nanofibers.
  • the compositions described herein comprise sNAG nanofibers and one or more additional active ingredients useful in preventing and/or treating solid tumor cancers, skin cancer, viral infections, viral diseases, yeast infections, fungal infections, fungal diseases, inflammatory bowel disease, Crohn's disease, dermatitis and psoriasis.
  • the compositions described herein do not comprise any additional anti-bacterial agent (e.g., an antibiotic).
  • the compositions described herein comprise the sNAG nanofibers as the only active ingredient and do not comprise any additional active ingredients.
  • compositions described herein are administered in conjunction with one or more additional therapies. In other embodiments, the compositions described herein are not administered in conjunction with any other therapy.
  • sNAG nanofiber As used herein, the terms “sNAG nanofiber,” “sNAG,” “Taliderm,” or “Talymed” (formerly known as “Taliderm”) are used interchangeably to refer to shortened fibers of poly-N-acetylglucosamine and/or derivatives thereof. In a preferred embodiment, sNAG nanofibers consist entirely of shortened fibers of poly-N-acetylglucosamine and/or derivatives thereof. Taliderm or Talymed are examples of sNAG nanofibers which are membranes consisting entirely of shortened fibers of poly-N-acetylglucosamine and/or derivatives thereof.
  • the term “about” means a range around a given value wherein the resulting value is the same or substantially the same (e.g., within 10%, 5% or 1%) as the expressly recited value. In one embodiment, “about” means within 10% of a given value or range. In another embodiment, the term “about” means within 5% of a given value or range. In another embodiment, the term “about” means within 1% of a given value or range.
  • disease and “disorder” are used interchangeably to refer to a condition in a subject.
  • exemplary diseases/disorders that can be treated or prevented in accordance with the methods described herein include, without limitation, solid tumor cancers, skin cancers, viral diseases, yeast diseases, fungal diseases, inflammatory bowel disease, and Crohn's disease, psoriasis and dermatitis.
  • the disease is the pathological state resulting from infection by a virus, a yeast, or a fungus, respectively.
  • infection means the invasion by, multiplication and/or presence of a pathogen (e.g., a virus, yeast, or fungus) in a cell or a subject.
  • pathogen e.g., a virus, yeast, or fungus
  • log refers to log 10 .
  • the term “subject” and “patient” are used interchangeably to refer to an animal (e.g., cow, horse, sheep, pig, chicken, turkey, quail, cat, dog, mouse, rat, rabbit, guinea pig, etc.).
  • the subject is a mammal such as a non-primate and a primate (e.g., monkey and human).
  • the subject is a human.
  • an “effective amount” in the context of administering a sNAG nanofiber or composition thereof to a subject refers to the amount of a sNAG nanofiber or composition thereof that results in a beneficial or therapeutic effect.
  • an “effective amount” of a sNAG nanofiber or composition thereof refers to an amount of a sNAG nanofiber or composition thereof which is sufficient to achieve at least one, two, three, four or more of the following effects: (i) reduction or amelioration of the severity of a disease in the subject or population of subjects or a symptom associated therewith; (ii) reduction of the duration of a disease in the subject or population of subjects or a symptom associated therewith; (iii) prevention of the progression of a disease in the subject or population of subjects or a symptom associated therewith; (iv) regression of a disease in the subject or population of subjects or a symptom associated therewith; (v) prevention of the development or onset of a disease in the subject or population of subjects or a a symptom associated therewith;
  • premature human infant refers to a human infant born at less than 37 weeks of gestational age.
  • human infant refers to a newborn to 1 year old human.
  • premature human infant refers to a newborn to 1 year old year human who was born of less than 37 weeks gestational age (e.g., before 37 weeks, 36 weeks, 35 weeks, 34 weeks, 33 weeks, 32 weeks, 31 weeks, 30 weeks, 29 weeks, 28 weeks, or less than 28 weeks of pregnancy).
  • human toddler refers to a human that is 1 years to 3 years old.
  • human child refers to a human that is 1 year to 18 years old.
  • human adult refers to a human that is 18 years or older.
  • yielderly human refers to a human 65 years or older.
  • low expression in the context of expression of a gene (e.g., based on the level of protein or peptide produced by the gene) refers to an expression that is less than the “normal” expression of the gene.
  • “low expression” refers to expression of a gene that is less than 99%, less than 95%, less than 90%, less than 85%, less than 75%, less than 70%, less than 65%, less than 60%, less than 55%, less than 50%, less than 45%, less than 40%, less than 35%, less than 30%, less than 25%, or less than 20% of the “normal” expression of the gene.
  • “low expression” refers to expression of a gene that is about 20-fold, about 15-fold, about 10-fold, about 5-fold, about 4-fold, about 3-fold, about 2-fold, or about 1.5 fold less than the “normal” expression of the gene.
  • the term “majority” refers to greater than 50%, including, e.g., 50.5%, 51%, 55%, etc.
  • the terms “therapies” and “therapy” can refer to any protocol(s), method(s), compositions, formulations, and/or agent(s) that can be used in the prevention and/or treatment of an infection with a pathogen or a disease or a symptom thereof, or a disease described herein (such as Crohn's disease, inflammatory bowel disease, psoriasis, dermatitis, and solid tumor).
  • a pathogen may be a virus, a fungus, or an yeast.
  • the terms “therapies” and “therapy” refer to drug therapy, adjuvant therapy, radiation, surgery, biological therapy, supportive therapy, and/or other therapies useful in treatment and/or prevention of an infection with a pathogen or a disease, or a symptom thereof, or a disease described herein.
  • the term “therapy” refers to a therapy other than a sNAG nanofiber or a pharmaceutical composition thereof.
  • an “additional therapy” and “additional therapies” refer to a therapy other than a treatment using a sNAG nanofiber or a pharmaceutical composition thereof.
  • a therapy includes the use of a sNAG nanofiber as an adjuvant therapy. For example, using a sNAG nanofiber in conjunction with a drug therapy, biological therapy, surgery, and/or supportive therapy.
  • FIG. 1 Nanofibers stimulate Akt1 activation, an upstream regulator of Ets1.
  • A Western blot analysis of phospho-Akt in response to NAG and sNAG stimulation of serum starved EC.
  • B RT-PCR analysis of EC infected either with scrambled control (“SCR”) or Akt1 shRNA lentiviruses and assessed for expression of Ets1 and S26 as a loading control.
  • C Schematic of a signal transduction pathway transducing a signal from sNAG nanofibers to Akt1, Ets1 and Defensins.
  • FIG. 2 Delayed wound healing in Akt1 null animals is partially rescued by Taliderm treatment.
  • A Representative images of wounded WT and AKT 1 null mice with and without treatment of Taliderm.
  • B H&E staining of representative mouse skin sections from day 3 wounds.
  • FIG. 3 sNAG nanofibers stimulate cytokine and defensin expression in primary endothelial cells.
  • A Immunohistochemisty of EC treated with or without sNAG using an antibody directed against ⁇ -defensin.
  • B ELISA showing that nanofiber treatment of EC results in the secretion of ⁇ -defensins 1-3 (serum starved, treated with 5 ⁇ g/ml or 10 ⁇ g/ml sNAG).
  • FIG. 4 sNAG nanofibers stimulate defensin expression in primary endothelial cells in an Akt1 dependent manner.
  • A serum starved EC
  • ss serum starved EC
  • PD PD98059
  • PI3K inhibitor PI3K inhibitor
  • SCR scrambled control
  • Akt1 Akt1
  • FIG. 5 sNAG nanofibers stimulate ⁇ -defensin 3 expression in mouse keratinocytes.
  • A Immunofluorescent staining with ⁇ -defensin 3 (visible as bright staining in the upper right hand panel; see, e.g., thick white arrows) and Involucrin antibodies of paraffin embedded mouse cutaneous wound sections from WT and Akt1 null animals on Day 3.
  • FIG. 6 Akt1 dependent transcription factor binding sites. Schematic of Akt1 dependent transcription factor binding sites. Using Genomatix software, 500 bp upstream of the transcription start site was analyzed for conserved sites on the mRNA of DEF1, 4, and 5 (ETS-black ovals; FKHD-striped ovals; CREB-white ovals; NFKB-checkered ovals).
  • FIG. 7 sNAG treatment results in expression and secretion of defensins in vitro.
  • A RTPCR analysis of serum starved (“SS”) primary endothelial cells treated with sNAG (50 ⁇ g/ml) for the times indicated and assessed for expression of ⁇ -defensin 3 and ⁇ -defensin 1.
  • B Immunofluorescent labeling of endothelial cells either serum starved (untreated) or treated with sNAG nanofibers (10 ⁇ g/ml for 5 hrs). Antibodies are directed against ⁇ -defensin 5 (FITC, upper left hand panel), ⁇ -defensin 3 (Texas Red, upper right hand panel).
  • Nuclei are stained with TOPRO-3 (Blue, lower left hand panel). Lower right hand panel represents triple overlay.
  • C Immunofluorescent labeling of keratinocytes (HaCat) that are either serum starved (untreated) or treated with sNAG nanofibers (10 ⁇ g/ml for 5 hours). Antibodies are directed against ⁇ -defensin 5 (FITC, upper left hand panel), ⁇ -defensin 3 (Texas Red, upper right hand panel). Nuclei are stained with TOPRO-3 (Blue, lower left hand panel).
  • FIG. 8 sNAG induced defensin expression is dependent on Akt1.
  • A Quantitative RT-PCR analyses using primers directed against ⁇ -defensin 1 from total RNA isolated from serum starved endothelial cells treated with or without sNAG for 3 hours, with or without pretreatment with PD098059 (“PD”) (50 ⁇ M), wortmannin (“WTM”) (100 nm). Quantitation is relative to the S26 protein subunit.
  • PD098059 50 ⁇ M
  • WTM wortmannin
  • D Quantitative RT-PCR analyses of serum starved endothelial cells infected with a scrambled control (SCR) or Akt1 shRNA lentiviruses, treated with or without sNAG and assessed for ⁇ -defensin 4 expression. Quantitation is shown relative to S26.
  • E Quantitation of ⁇ -defensin 3 expression from total RNA isolated from serum starved endothelial cells infected with a scrambled control (SCR) or Akt1 shRNA lentiviruses, treated with or without sNAG. Quantitation is shown relative to S26. All experiments were done in at least triplicate and repeated at least three independent times and p values are shown.
  • FIG. 9 sNAG induced defensin expression in vivo requires Akt1.
  • B Paraffin embedded section from WT treated with sNAG harvested on day 3.
  • C Quantitation of ⁇ -defensin 3 expression from paraffin embedded sections was performed using NIH ImageJ software. Experiments were repeated three independent times and p values are shown.
  • FIG. 10 sNAG treatment increases wound closure in wild type mice. H&E staining of wound tissue sections derived from C57Bl6 wild type animals either untreated or treated with sNAG membrane. The day post-wound is indicated to the left of each panel. The solid black line follows the keratinocyte cell layer indicating wound closure. Black arrows indicate the margin of the wound bed.
  • FIG. 11 sNAG treatment reduces bacterial infection in an Akt1 dependent manner.
  • A Tissue gram staining of S. aureus infected wounds from WT mice. WT mice were wounded using a 4 mm biopsy punch. Immediately after wounding mice were inoculated with 1 ⁇ 10 9 cfu/ml. 30 minutes post-infection, mice in the treated group were treated with Taliderm. Skin samples were taken 5 days post-treatment and sectioned for analysis. Tissue gram staining was performed. Dark purple staining indicates gram-positive bacteria and neutrophils that have engulfed bacteria. Sections under 20 ⁇ and 40 ⁇ magnification are shown.
  • B Tissue gram staining of paraffin embedded S.
  • Wild type mice that were sNAG treated show a significant (p ⁇ 0.01) decrease in bacteria load in the wound beds as compared to Akt1 null animals. All experiments were repeated three independent times and the p values are shown.
  • D CFU quantitated from infected wounds at day 3 post wounding in a similar fashion described in (C). sNAG treatment of infected wounds shows a significant decrease in CFU of both WT and Akt1 null animals on day 3, but the WT animals show an approximate 10 fold difference compared to a 2 fold difference in Akt1 animals.
  • E Quantitation of CFUs in S. aureus cultures that were either untreated or treated with various amounts of sNAG nanofibers. Each experiment was performed three independent times and p values are shown.
  • FIG. 12 Rapid induction of defensin expression by sNAG treatment of S. aureus infected wounds.
  • B Quantitation of ⁇ -defensin 3 expression from paraffin embedded sections using NIH ImageJ software. S. aureus infected wounds that were treated with sNAG show a significant increase (p ⁇ 0.05) in ⁇ -defensin 3 staining. Experiments were repeated three independent times and p values are shown.
  • FIG. 13 Antibodies against ⁇ -defensin 3 impedes antibacterial effects of sNAG treatment.
  • sNAG treated wounds were treated with either ⁇ -defensin 3 antibody or isotype control goat IgG antibody prior to sNAG treatment.
  • ⁇ -defensin 3 application significantly increased (p ⁇ 0.05) CFU.
  • FIG. 14 Effect of irradiation on chemical and physical structure of poly-N-acetylglucosamine (“pGlcNAc”) fibers.
  • A Correlation between molecular weight of pGlcNAc and irradiation level/formulation for irradiation.
  • B Infrared (IR) spectrum of non-irradiated pGlcNAc slurry (top line), pGlcNAc slurry irradiated at 100 kGy (bottom line), and pGlcNAc slurry irradiated at 200 kGy (middle line).
  • C Scanning electron microscopic (SEM) analyses of pGlcNAc.
  • D Scanning electron microscopic (SEM) analyses of sNAG.
  • FIG. 15 pGlcNAc did not affect metabolic rate.
  • the identity for each of the four bars is as follows: serum starvation (SS), VEGF, and pGlcNAc (NAG) at 50 and 100 ⁇ g/ml.
  • FIG. 16 pGlcNAc protected human umbilical vein endothelial cell (EC) from cell death induced by serum deprivation.
  • EC human umbilical vein endothelial cell
  • the identity for each of the five bars is as follows: serum starvation (SS), VEGF, and pGlcNAc (NAG) at 50, 100, and 250 ⁇ g/ml.
  • FIG. 17 sNAG induced marked increase in metabolic rate. Identity for each of the five bars (from left to right) is as follows: serum starvation (SS), VEGF, and sNAG at 50, 100 and 200 ⁇ g/ml.
  • FIG. 18 sNAG did not protect EC from cell death induced by serum deprivation.
  • identity for each of the five bars is as follows: serum starvation (SS), VEGF, and sNAG at 50, 100 and 200 ⁇ g/ml.
  • FIG. 19 Numeric Pain Intensity Scale.
  • FIG. 20 Schematic showing experimental set up for the 3% DSS (dextran sodium sulphate)-induced inflammatory bowel disease (in particular, ulcerative colitis) in a mouse model.
  • DSS distal sodium sulphate
  • FIG. 21 sNAG treatment decreased inflammation in an animal model of inflammatory bowel disease.
  • A H&E staining of a section of intestinal epithelium from a control group of 10 mice administered 3% DSS via drinking water for 7 days (day 0 to day 7), and saline via rectal suppository at day 0 and day 3 (100 ⁇ l).
  • B H&E staining of a section of intestinal epithelium from a test group of 10 mice administered 3% DSS via drinking water for 7 days (day 0 to day 7), and sNAG via rectal suppository at day 0 and day 3 (100 ⁇ l total with 12 ⁇ g/ ⁇ l sNAG).
  • Thin arrow and bracket point to the site of edema, and thick arrow points to the site of leukocytic infiltration.
  • FIG. 22 sNAG treatment decreased fibrosis in an animal model of inflammatory bowel disease.
  • A staining for fibrosis of a section of intestinal epithelium from a control group of 10 mice administered 3% DSS via drinking water for 7 days (day 0 to day 7), and saline via rectal suppository at day 0 and day 3 (100 ⁇ l).
  • B staining for fibrosis of a section of intestinal epithelium from a test group of 10 mice administered 3% DSS via drinking water for 7 days (day 0 to day 7), and sNAG via rectal suppository at day 0 and day 3 (100 ⁇ l total with 12 ⁇ g/ ⁇ l sNAG).
  • sNAG nanofibers can stimulate expression of defensins, which may boost the innate immune response. It is widely accepted that defensins are important players in innate immunity. As demonstrated in the examples presented in Sections 6.1 and 6.2, infra, the inventors of the present invention have found that sNAG nanofibers can increase the expression of both ⁇ - and ⁇ -type defensins in endothelial cells and ⁇ -type defensins in keratinocytes in vitro and in a wound healing model in vivo.
  • Akt1 appears to be important for sNAG-dependent defensin expression in vitro and in vivo, in a wound healing model.
  • TLRs Toll-like receptors
  • TLRs Toll-like receptors
  • TLRs are highly conserved receptors that activate innate immunity.
  • Recent work has linked human defensin expression to TLR activation, in particular, stimulation of TLRs can lead to increased defensin synthesis.
  • sNAG nanofibers may act as a stimulator of innate immunity.
  • sNAG nanofibers as a novel method for preventing and/or treating of infections and diseases for which an increase in expression and/or secretion of one or more of defensins and Toll-like receptors may be beneficial.
  • treatment of viral, yeast or fungal infections with sNAG nanofibers decreases the pathogen count in patients.
  • the use of sNAG nanofibers enhances wound closure while simultaneously eradicating, decreasing or preventing a viral, a fungal or an yeast infection of the wound.
  • the sNAG nanofibers can be used in treating a dermatological condition such as dermatitis or psoriasis by, for example, alleviating one or more symptoms of such diseases.
  • a dermatological condition such as dermatitis or psoriasis
  • the sNAG nanofibers can be used in treating an Inflammatory Bowel Disease (e.g., Crohn's disease) by, for example, alleviating one or more symptoms of such diseases.
  • an Inflammatory Bowel Disease e.g., Crohn's disease
  • sNAG nanofibers can be effective to treat viral infections.
  • sNAG nanofibers are effective to treat HSV infection when administered topically to human patients.
  • Example 8 infra, demonstrates that topical administration of sNAG nanofibers to cold sores reduces the pain associated with cold sores and reduces the duration of the cold sores in human patients. Cold sores are typically caused by HSV-1 infection,
  • described herein are uses of sNAG nanofibers to treat viral infections, in particular, topical viral infections.
  • sNAG nanofibers to treat an HSV infection, or to treat and/or prevent a symptom associated with an HSV infection (e.g., a cold sore or a lesion) by topical administration of sNAG nanofibers to a patient (e.g., at the site of HSV infection or the site of a symptom of HSV infection, or at the site where a symptom of infection is known to occur).
  • a symptom associated with an HSV infection e.g., a cold sore or a lesion
  • sNAG nanofibers can be effective to treat inflammatory bowel disease (IBD).
  • IBD inflammatory bowel disease
  • the inventors found that sNAG nanofibers are effective to treat IBD in an animal model of IBD when administered rectally (such as via a suppository).
  • Example 9, infra demonstrates that administration of sNAG nanofibers reduces inflammation and fibrosis associated with IBD in a mouse model of IBD.
  • sNAG nanofibers to treat IBD, such as ulcerative colitis and Crohn's disease.
  • sNAG nanofibers to treat IBD (e.g., ulcerative colitis, or Crohn's disease) by topical administration of sNAG nanofibers to a patient (e.g., to the anus or rectally via a suppository, a cream, a suspension, a liquid solution, a gel, or an ointment).
  • IBD ulcerative colitis, or Crohn's disease
  • topical administration of sNAG nanofibers to a patient (e.g., to the anus or rectally via a suppository, a cream, a suspension, a liquid solution, a gel, or an ointment).
  • sNAG nanofiber compositions comprise fibers of poly-N-acetylglucosamine and/or a derivative(s) thereof, the majority of which are less than 30 microns in length and at least 1 micron in length as measured by any method known to one skilled in the art, for example, by scanning electron microscopy (“SEM”).
  • SEM scanning electron microscopy
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers are less than about 30, 25, 20, 15, 12, 10, 9, 8, 7, 6, 5, 4, or 3 microns in length, and at least 1 micron in length as measured by any method known to one skilled in the art, for example, by SEM.
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers are less than about 15 microns or less than about 12 microns in length, and at least 1 micron in length as measured by any method known to one skilled in the art, for example, by SEM.
  • all (100%) of the sNAG nanofibers are less than about 15 microns or less than about 10 microns in length, and at least 1 micron in length as measured by any method known to one skilled in the art, for example, by SEM.
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers are equal to or less than 14, 13, 12, 11, 10, 9, 8 or 7 microns in length, and at least 1 micron in length as measured by any method known to one skilled in the art, for example, by SEM.
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers are between 1 to 15, 2 to 15, 2 to 14, 1 to 12, 2 to 12, 1 to 10, 2 to 10, 3 to 12, 3 to 10, 4 to 12, 4 to 10, 5 to 12, 5 to 10, 1 to 9, 2 to 9, 3 to 9, 1 to 8, 2 to 8, 3 to 8, 4 to 8, 1 to 7, 2 to 7, 3 to 7, 4 to 7, 1 to 6, 1 to 5, 1 to 4, or 1 to 3 microns in length as measured by any method known to one skilled in the art, for example, by SEM.
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers are about 8, 7, 6, 5, 4, 3 or 2 microns in length as measured by any method known to one skilled in the art, for example, by SEM.
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers are between about 2 to about 10 microns, about 3 to about 8 microns, about 4 to about 7 microns, about 4 to about 10 microns, or about 5 to about 10 microns in length as measured by any method known to one skilled in the art, for example, by SEM.
  • all (100%) of the sNAG nanofibers are between about 2 to about 10 microns, about 3 to about 8 microns, about 4 to about 7 microns, about 4 to about 10 microns, or about 5 to about 10 microns in length as measured by any method known to one skilled in the art, for example, by SEM.
  • the sNAG nanofibers fibers are in a range between 0.005 to 5 microns in thickness and/or diameter as determined by electron microscopy.
  • the sNAG nanofibers are about 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.2, 2.4, 2.6, 2.8, 3 or 4 microns in thickness and/or diameter on average, or any range in between (e.g., 0.02 to 2 microns, 0.02 to 1 microns, 0.02 to 0.75 microns, 0.02 to 0.5 microns, 0.02 to 0.5 microns, 0.05 to 1 microns, 0.05 to 0.75
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers have a thickness or diameter of about 0.02 to 1 microns.
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers have a thickness or diameter of about 0.05 to 0.5 microns. In specific embodiments, all (100%) of the sNAG nanofibers have a thickness or diameter of about 0.02 to 1 microns or about 0.05 to 0.5 microns.
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers have a thickness or diameter of about 0.02 to 2 microns, 0.02 to 1 microns, 0.02 to 0.75 microns, 0.02 to 0.5 microns, 0.02 to 0.5 microns, 0.05 to 1 microns, 0.05 to 0.75 microns, 0.05 to 0.5 microns, 0.1 to 1 microns, 0.1 to 0.75 microns, or 0.1 to 0.5 microns.
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers are between 1 and 15 microns, or between (or in the range of) 1 to 10 microns, 2 to 10 microns, 3 to 10 microns, 4 to 10 microns, 4 to 7 microns, 5 to 10 microns, or 5 to 15 microns in length and have a thickness or diameter of about 0.02 to 1 microns.
  • the molecular weight of the sNAG nanofibers is less than 100 kDa, 90 kDa, 80 kDa, 75 kDa, 70 kDa, 65 kDa, 60 kDa, 55 kDa, 50 kDa, 45 kDA, 40 kDa, 35 kDa, 30 kDa, or 25 kDa.
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers have a molecular weight between about 5 kDa to 100 kDa, about 10 kDa to 100 kDa, about 20 kDa to 100 kDa, about 10 kDa to 80 kDa, about 20 kDa to 80 kDa, 20 kDa to 75 kDa, about 25 kDa to about 75 kDa, about 30 kDa to about 80 kDa, about 30 kDa to about 75 kDa, about 40 kda to about 80 kDa, about 40 kDa to
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the sNAG nanofibers have a molecular weight of about 60 kDa.
  • 1% to 5%, 5% to 10%, 5% to 15%, 20% to 30% or 25% to 30% of the sNAG nanofibers are deacetylated. In some embodiments, 1%, 5%, 10%, 15%, 20%, 25%, or 30% of the sNAG nanofibers are deacetylated. In other embodiments, less than 30%, 25%, 20%, 15%, 10%, 5%, 4%, 3%, 2% or 1% of the sNAG nanofibers are deacetylated.
  • sNAG nanofibers equal to or more than 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 99%, or all (100%), of the sNAG nanofibers are deacetylated. In other embodiments, less than 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 99%, or 100% of the sNAG nanofibers are deacetylated.
  • 70% to 80%, 75% to 80%, 75% to 85%, 85% to 95%, 90% to 95%, 90% to 99% or 95% to 100% of the sNAG nanofibers are acetylated. In some embodiments, 70%, 75%, 80%, 85%, 90%, 95%, 98%, 99% or 100% of the sNAG nanofibers are acetylated. In other embodiments, more than 70%, 75%, 80%, 85%, 90%, 95%, 97%, 98%, 99%, 99.5% or 99.9% of the sNAG nanofibers are acetylated.
  • equal to or more than 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 97%, 98% or 99%, or all (100%), of the sNAG nanofibers are acetylated. In other embodiments, less than 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 97%, 98%, 99%, or 100% of the sNAG nanofibers are acetylated.
  • the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.9%, or 100%) of the sNAG nanofibers are between (or in the range of) 2 to 12 microns, 2 to 10 microns, 4 to 15 microns, 4 to 10 microns, 5 to 15 microns, or 5 to 10 microns, and such sNAG nanofibers are at least 70%, 75%, 80%, 85%, 90%, 95%, 97%, 98%, 99% or 100% acetylated.
  • the sNAG nanofibers comprise at least one glucosamine monosaccharide, and may further comprise at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 99% of the N-acetylglucosamine monosaccharides. In other embodiments, the sNAG nanofibers comprise at least one N-acetylglucosamine monosaccharide, and may further comprise at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 99% of glucosamine monosaccharides.
  • the sNAG nanofibers increase the metabolic rate of serum-starved human umbilical cord vein endothelial cells (“EC”) in a MTT assay.
  • a MTT assay is a laboratory test and a standard colorimetric assay (an assay which measures changes in color) for measuring cellular proliferation (cell growth). Briefly, yellow MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, a tetrazole) is reduced to purple formazan in the mitochondria of living cells. This reduction takes place only when mitochondrial reductase enzymes are active, and therefore conversion can be directly related to the number of viable (living) cells.
  • the MTT assay is described in Example 6, infra, where it is utilized to assess the effect of sNAG nanofibers on the metabolic rate of EC cells.
  • the metabolic rate of cells may also be determined by other techniques commonly known to the skilled artisan.
  • the sNAG nanofibers do not rescue apoptosis of serum-starved EC in a trypan blue exclusion test.
  • a trypan blue exclusion test is a dye exclusion test used to determine the number of viable cells present in a cell suspension. It is based on the principle that live cells possess intact cell membranes that exclude certain dyes, such as trypan blue, Eosin, or propidium, whereas dead cells do not.
  • the trypan blue assay is described in Example 6, infra, where it is utilized to assess the effect of sNAG nanofibers on cell viability of EC cells. The viability of cells may also be determined by other techniques commonly known to the skilled artisan.
  • compositions comprising the sNAG nanofibers are described, wherein the sNAG nanofibers increase the metabolic rate of serum-starved human umbilical cord vein endothelial cells in a MTT assay and/or do not rescue apoptosis of serum-starved human umbilical cord vein endothelial cells in a trypan blue exclusion test.
  • the sNAG nanofibers increase the metabolic rate of serum-starved human umbilical cord vein endothelial cells in a MTT assay and do not rescue apoptosis of serum-starved human umbilical cord vein endothelial cells in a trypan blue exclusion test.
  • the sNAG nanofibers are biocompatible. Biocompatibility may be determined by a variety of techniques, including, but not limited to such procedures as the elution test, intramuscular implantation, or intracutaneous or systemic injection into animal subjects. Such tests are described in U.S. Pat. No. 6,686,342 (see, e.g., Example 10), which is incorporated by reference herein in its entirety. Some of the biocompatibility tests are described in Example 7, infra, which show that sNAG nanofibers are non-reactive in such tests.
  • the sNAG nanofibers used in the methods described herein are non-reactive in a biocompatibility test or tests.
  • the sNAG nanofibers used in the methods described herein may be non-reactive when tested in an elution test, an intramuscular implantation test, an intracutaneous test, and/or a systemic test.
  • the sNAG nanofibers used in the methods described herein have Grade 0 or Grade 1 test score when tested in an elution test, an intramuscular implantation test, an intracutaneous test, or a systemic test.
  • the sNAG nanofibers used in the methods described herein are at most mildly reactive when tested in an elution test, an intramuscular implantation test, an intracutaneous test, and/or a systemic test.
  • the compositions described herein do not cause an allergenic reaction or an irritation.
  • the compositions described herein cause at most a mild allergenic reaction or a mild irritation, e.g., at the site of application.
  • the relevant tests and evaluation of test results are described in, e.g., U.S. Pat. No. 6,686,342, which is incorporated herein by reference in its entirety, and in Section 6.8, infra.
  • the sNAG nanofibers are non-reactive when tested in an intramuscular implantation test.
  • an intramuscular implantation test is an intramuscular implantation test—ISO 4 week implantation, as described in Section 6.8.3, infra.
  • the sNAG nanofibers have a test score equal to “0” and/or are at most a negligible irritant as determined by intracutaneous injection test.
  • the sNAG nanofibers elicit no intradermal reaction (i.e., Grade I reaction) in Kligman test and/or have a weak allergenic potential as determined by Kligman test.
  • Example 7, infra shows that sNAG nanofibers are non-reactive in an intramuscular implantation test, an intracutaneous injection test, and Kligman test.
  • the sNAG nanofibers are immunoneutral (i.e., they do not elicit an immune response).
  • the sNAG nanofibers are biodegradable.
  • the sNAG nanofibers preferably degrade within about 1 day, 2 days, 3 days, 5 days, 7 days (1 week), 8 days, 10 days, 12 days, 14 days (2 weeks), 17 days, 21 days (3 weeks), 25 days, 28 days (4 weeks), 30 days, 1 month, 35 days, 40 days, 45 days, 50 days, 55 days, 60 days, 2 months, 65 days, 70 days, 75 days, 80 days, 85 days, 90 days, 3 months, 95 days, 100 days or 4 months after administration or implantation into a patient.
  • the sNAG nanofibers do not cause a detectable foreign body reaction.
  • a foreign body reaction which may occur during wound healing, includes accumulation of exudate at the site of injury, infiltration of inflammatory cells to debride the area, and the formation of granulation tissue. The persistent presence of a foreign body can inhibit full healing. Rather than the resorption and reconstruction that occurs in wound healing, the foreign body reaction is characterized by the formation of foreign body giant cells, encapsulation of the foreign object, and chronic inflammation. Encapsulation refers to the firm, generally avascular collagen shell deposited around a foreign body, effectively isolating it from the host tissues.
  • treatment of a site e.g., a wound or a site of a bacterial infection in a wound
  • treatment of a site (e.g., a wound or a site of a bacterial infection in a wound) with the sNAG nanofibers does not elicit a detectable foreign body reaction in 1 day, 3 days, 5 days, 7 days, 10 days or 14 days after treatment.
  • treatment of a site (e.g., a wound) with the sNAG nanofibers does not elicit a foreign body encapsulations in 1 day, 3 days, 5 days, 7 days, 10 days or 14 days after treatment.
  • the sNAG nanofibers (i) comprise fibers, wherein majority of the fibers are between about 1 and 15 microns in length, and (ii) (a) increase the metabolic rate of serum-starved EC in a MTT assay and/or do not rescue apoptosis of serum-starved EC in a trypan blue exclusion test, and (b) are non-reactive when tested in an intramuscular implantation test.
  • the sNAG nanofibers (i) comprise fibers, wherein majority of the fibers are between about 1 and 12 microns in length, and (ii) (a) increase the metabolic rate of serum-starved EC in a MTT assay and/or do not rescue apoptosis of serum-starved EC in a trypan blue exclusion test, and (b) are non-reactive when tested in an intramuscular implantation test.
  • the sNAG nanofibers (i) comprise fibers, wherein majority of the fibers are between (or in the range of) 1 to 10 microns, 2 to 10 microns, 4 to 10 microns, 5 to 10 microns, or 5 to 15 microns in length, and (ii) (a) increase the metabolic rate of serum-starved EC in a MTT assay and/or do not rescue apoptosis of serum-starved EC in a trypan blue exclusion test, and (b) are non-reactive when tested in an intramuscular implantation test.
  • the sNAG nanofibers (i) comprise fibers, wherein majority of the fibers are between about 4 and 10 microns in length, and (ii) (a) increase the metabolic rate of serum-starved EC in a MTT assay and/or do not rescue apoptosis of serum-starved EC in a trypan blue exclusion test, and (b) are non-reactive when tested in an intramuscular implantation test.
  • the sNAG nanofibers (i) comprise fibers, wherein majority of the fibers are between about 4 and 7 microns in length, and (ii) (a) increase the metabolic rate of serum-starved EC in a MTT assay and/or do not rescue apoptosis of serum-starved EC in a trypan blue exclusion test, and (b) are non-reactive when tested in an intramuscular implantation test.
  • the sNAG nanofibers do not have a direct effect on the growth or survival of bacteria, such as S. aureus , as determined by one skilled in the art. In other embodiments, sNAG nanofibers do not have a direct effect on the growth or survival of bacteria, such as S. aureus , as determined by the methods set forth in Section 6.2.2.5, infra. In some embodiments, the sNAG nanofibers do not have a direct effect in vitro on bacterial growth or survival. In one embodiment, the sNAG nanofibers do not have a direct effect (e.g., in vitro) on growth or survival of gram-negative bacteria.
  • the sNAG nanofibers do not have a direct effect (e.g., in vitro) on growth or survival of gram-positive bacteria. In yet another embodiment, the sNAG nanofibers do not have a direct effect (e.g., in vitro) on growth or survival of either gram-positive or gram-negative bacteria.
  • the sNAG nanofibers (i) comprise fibers, wherein majority of the fibers are between (or in the range of) about 1 and 15 microns, 1 and 12 microns, 1 and 10 microns, 4 and 10 microns, 4 and 15 microns, 5 and 10 microns, 5 and 15 microns, or 4 and 7 microns in length, (ii) do not have an effect on bacterial growth or survival of Staphylococcus aureus bacterial cultures in vitro, and (iii) are non-reactive when tested in a biocompatibility test (e.g., an intramuscular implantation test).
  • a biocompatibility test e.g., an intramuscular implantation test.
  • the sNAG nanofibers induce a certain pattern of gene expression (RNA or protein expression as determined by, e.g., RT-PCR, microarray or ELISA) in a cell, tissue or organ treated with or exposed to a sNAG nanofiber composition.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of one or more defensin proteins, one or more defensin-like proteins, and/or one or more Toll-like receptors.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of one or more proteins that are known to have an anti-bacterial effect.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of one or more ⁇ -defensins (e.g., DEFA1 (i.e., ⁇ -defensin 1), DEFA1B, DEFA3, DEFA4, DEFA5, DEFA6), one or more ⁇ -defensins (e.g., DEFB1 (i.e., ⁇ -defensin 1), DEFB2, DEFB4, DEFB103A, DEFB104A, DEFB105B, DEFB107B, DEFB108B, DEFB110, DEFB112, DEFB114, DEFB118, DEFB119, DEFB123, DEFB124, DEFB125, DEFB126, DEFB127, DEFB128, DEFB129, DEFB131, DEFB136), and/or one or more ⁇ -defensins (e.g., DEFT1P).
  • DEFA1 i.e., ⁇ -defensin 1
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of one or more of DEFA1, DEFA3, DEFA4, DEFA5, DEFB1, DEFB3, DEFB103A, DEFB104A, DEFB108B, DEFB112, DEFB114, DEFB118, DEFB119, DEFB123, DEFB124, DEFB125, DEFB126, DEFB128, DEFB129 and DEFB131.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of one or more Toll receptors (e.g., TLR1, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TLR10, TLR11, and/or TLR12).
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of one or more of IL-1, CEACAM3, SPAG11, SIGIRR (IL1-like receptor), IRAK1, IRAK2, IRAK4, TBK1, TRAF6 and IKKi.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of one or more of IRAK2, SIGIRR, TLR1, TLR2, TLR4, TLR7, TLR8, TLR10 and TRAF6.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of at least one of the above-listed gene products.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of one or more of the above-listed genes in the amount equal to or more than about 0.25 fold, 0.5 fold, 1 fold, 1.5 fold, 2 fold, 2.5 fold, 3 fold, 3.5 fold, 4 fold, 4.5 fold, 5 fold, 6 fold, 7 fold, 8 fold, 9 fold, 10 fold, 12 fold, 15 fold or 20 fold as compared to the level of expression of the one or more of the above-listed genes in a cell, tissue or organ of a subject before treatment with the sNAG nanofibers (e.g., a known average level of expression of the one or more of the above-listed genes).
  • a known average level of expression of the one or more of the above-listed genes e.g., a known average level of expression of the one or more of the above-listed genes.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of one or more of the above-listed genes in the amount equal to or more than about 10%, 25%, 50%, 75%, 100%, 125%, 150%, 175%, 200%, 225%, 250%, 275%, 300%, 350%, 400%, 450%, 500%, 550%, 600%, 650%, 700%, 750%, 800%, 900% or 1000% the level of expression of the one or more of the above-listed genes in a cell, tissue or organ of a subject before treatment with the sNAG nanofibers (e.g., a known average level of expression of the one or more of the above-listed genes).
  • a known average level of expression of the one or more of the above-listed genes e.g., a known average level of expression of the one or more of the above-listed genes.
  • the sNAG nanofibers but not long poly-N-acetylglucosamine, chitin and/or chitosan induce expression of the one or more genes listed above, as determined by a method known to one skilled in the art, or described herein.
  • long poly-N-acetylglucosamine, chitin and/or chitosan do not induce expression of the one or more genes listed above or induce lower level (e.g., more than 1.25 fold, 1.5 fold, 2 fold, 2.5 fold, 3 fold, 3.5 fold, 4 fold, 4.5 fold, 5 fold, 6 fold, 7 fold, 8 fold, 9 fold, or 10 fold lower) of expression of the one or more genes listed above as compared to the level of expression of the one or more genes listed above induced by the sNAG nanofibers, as determined by a method known to one skilled in the art, or described herein.
  • lower level e.g., more than 1.25 fold, 1.5 fold, 2 fold, 2.5 fold, 3 fold, 3.5 fold, 4 fold, 4.5 fold, 5 fold, 6 fold, 7 fold, 8 fold, 9 fold, or 10 fold lower
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce a gene expression profile that is consistent with, similar to, about the same as, or equivalent to one or more gene expression profiles demonstrated in Tables I, II, III, V, VIII and IX, Sections 6.2-6.5, infra.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of one or more of the genes shown to be upregulated by sNAG treatment in Tables I, II, III, V, VIII and IX, Sections 6.2-6.5, infra.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce expression of the majority or all of the genes shown to be upregulated by sNAG treatment in Tables I, II, III, V, VIII and IX, Sections 6.2-6.5, infra.
  • gene expression levels are measured at 1 hour, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 10 hours, 12 hours, 14 hours, 16 hours, 18 hours, 20 hours, 24 hours, 48 hours, 3 days or 5 days after treatment of a cell, tissue or organ with a sNAG nanofiber composition by a method known to one skilled in the art, or described herein.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce a gene expression profile that differs from the profile induced by long poly-N-acetylglucosamine polymers or fibers.
  • a gene expression profile induced by the sNAG nanofibers is consistent with, similar to, about the same as, or equivalent to that shown in Tables I, II, III, V, VIII and IX, Sections 6.2-6.5, infra
  • gene expression profile induced by long poly-N-acetylglucosamine polymers or fibers is consistent with, similar to, about the same with, or equivalent to that shown in Table VIII and/or IX, Section 6.5, infra.
  • the sNAG nanofibers or a composition comprising the sNAG nanofibers induce a gene expression profile that differs from the gene expression profile induced by chitin or chitosan.
  • the sNAG nanofibers are obtained by irradiating poly-N-acetylglucosamine and/or a derivative thereof. See Section 5.1.1, infra, regarding poly-N-acetylglucosamine and derivatives thereof and Section 5.2, infra, regarding methods for producing the sNAG nanofibers using irradiation. Irradiation may be used to reduce the length of poly-N-acetylglucosamine fibers and/or poly-N-acetylglucosamine derivative fibers to form shortened poly- ⁇ -1 ⁇ 4-N-acetylglucosamine fibers and/or shortened poly-N-acetylglucosamine derivative fibers, i.e.
  • sNAG nanofibers Specifically, irradiation may be used to reduce the length and molecular weight of poly-N-acetylglucosamine or a derivative thereof without disturbing its microstructure.
  • the infrared spectrum (IR) of sNAG nanofibers is similar to, about the same as, or equivalent to that of the non-irradiated poly- ⁇ -1 ⁇ 4-N-acetylgulcosamine or a derivative thereof.
  • the sNAG nanofibers are not derived from chitin or chitosan.
  • the compositions described herein may be derived from chitin or chitosan, or the sNAG nanofibers may be derived from chitin or chitosan.
  • U.S. Pat. Nos. 5,622,834; 5,623,064; 5,624,679; 5,686,115; 5,858,350; 6,599,720; 6,686,342; 7,115,588 and U.S. Patent Pub. 2009/0117175 (each of which is incorporated herein by reference) describe the poly-N-acetylglucosamine and derivatives thereof, and methods of producing the same.
  • the poly-N-acetylglucosamine has a ⁇ -1 ⁇ 4 configuration.
  • the poly-N-acetylglucosamine has a ⁇ -1 ⁇ 4 configuration.
  • the poly-N-acetylglucosamine and derivatives thereof may be in the form of a polymer or in the form of a fiber.
  • Poly-N-acetylglucosamine can, for example, be produced by, and may be purified from, microalgae, preferably diatoms.
  • the diatoms which may be used as starting sources for the production of the poly-N-acetylglucosamine include, but are not limited to members of the Coscinodiscus genus, the Cyclotella genus, and the Thalassiosira genus.
  • Poly-N-acetylglucosamine may be obtained from diatom cultures via a number of different methods, including the mechanical force method and chemical/biological method known in the art (see, e.g., U.S. Pat. Nos.
  • the poly-N-acetylglucosamine is not derived from one or more of the following: a shell fish, a crustacean, an insect, a fungi or yeasts.
  • poly- ⁇ -1 ⁇ 4-N-acetylglucosamine is derived from a process comprising a) treating a microalgae comprising a cell body and a poly- ⁇ -1 ⁇ 4-N-acetylglucosamine polymer fiber with a biological agent (such as hydrofluoric) capable of separating the N-acetylglucosamine polymer fiber from the cell body for a sufficient time so that the poly- ⁇ -1 ⁇ 4-N-acetylglucosamine polymer fiber is released from the cell body; b) segregating the poly- ⁇ -1 ⁇ 4-N-acetylglucosamine polymer fiber from the cell body; and c) removing contaminants from the segregated poly- ⁇ -1 ⁇ 4-N-acetylglucosamine polymer fiber, so that the poly- ⁇ -1 ⁇ 4-N-acetylglucosamine polymer is isolated and purified.
  • a biological agent such as hydrofluoric
  • the poly- ⁇ -1 ⁇ 4-N-acetylglucosamine may be derived from one or more of the following: a shell fish, a crustacean, an insect, a fungi or yeasts.
  • the compositions described herein do not comprise chitin or chitosan.
  • One or more of the monosaccharide units of the poly-N-acetylglucosamine may be deacetylated. In certain embodiments, 1% to 5%, 5% to 10%, 5% to 15%, 20% to 30% or 25% to 30% of the poly-N-acetylglucosamine is deacetylated. In some embodiments, 1%, 5%, 10%, 15%, 20%, 25%, or 30% of the poly-N-acetylglucosamine is deacetylated. In other embodiments, less than 30%, 25%, 20%, 15%, 10%, 5%, 4%, 3%, 2% or 1% of the poly-N-acetylglucosamine is deacetylated.
  • a poly-N-acetylglucosamine composition comprises 70% to 80%, 75% to 80%, 75% to 85%, 85% to 95%, 90% to 95%, 90% to 99% or 95% to 100% of acetylated glucosamine (i.e., N-acetylglucosamine) monosaccharides.
  • a poly-N-acetylglucosamine composition comprises 70%, 75%, 80%, 85%, 90%, 95%, 97%, 98%, 99% or 100% of acetylated glucosamine (i.e., N-acetylglucosamine) monosaccharides.
  • a poly-N-acetylglucosamine composition comprises more than 70%, 75%, 80%, 85%, 90%, 95%, 97%, 98%, 99%, 99.5% or 99.9% of the acetylated glucosamine.
  • a poly-N-acetylglucosamine composition comprises equal to or more than 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 97%, 98%, or 99%, or all (100%), of the acetylated glucosamine.
  • a poly-N-acetylglucosamine composition comprises less than 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 99%, or 100% of the acetylated glucosamine.
  • a poly-N-acetylglucosamine composition comprises at least one glucosamine monosaccharide, and may further comprise at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 99% of N-acetylglucosamine monosaccharides.
  • a poly-N-acetylglucosamine composition comprises at least one N-acetylglucosamine monosaccharide, and may further comprise at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95% or 99% of glucosamine monosaccharides.
  • Derivatives of poly-N-acetylglucosamine may also be used in a composition described herein. Derivatives of poly-N-acetylglucosamine and methods of making such derivatives are described in U.S. Pat. No. 5,623,064 (see, e.g., Section 5.4), which is incorporated by reference herein in its entirety. Derivatives of poly-N-acetylglucosamine may include, but are not limited to, partially or completely deacetylated poly-N-acetylglucosamine, or its deacetylated derivatives.
  • poly-N-acetylglucosamine may be derivatized by being sulfated, phosphorylated and/or nitrated.
  • Poly-N-acetylglucosamine derivatives include, e.g., sulfated poly-N-acetylglucosamine derivatives, phosphorylated poly-N-acetylglucosamine derivatives, or nitrated poly-N-acetylglucosamine derivatives.
  • one or more of the monosaccharide units of the poly-N-acetylglucosamine may contain one or more sulfonyl groups one or more O-acyl groups.
  • one or more of the monosaccharides of the deacetylated poly-N-acetylglucosamine may contain an N-acyl group.
  • One or more of the monosaccharides of the poly-N-acetylglucosamine or of its deacetylated derivative may contain an O-alkyl group.
  • One or more of the monosaccharide units of the poly-N-acetylglucosamine may be an alkali derivative.
  • One or more of the monosaccharide units of the deacetylated derivative of poly-N-acetylglucosamine may contain an N-alkyl group.
  • One or more of the monosaccharide units of the deacetylated derivative of poly-N-acetylglucosamine may contain at least one deoxyhalogen derivative.
  • One or more of the monosaccharide units of the deacetylated derivative of poly-N-acetylglucosamine may form a salt.
  • One or more of the monosaccharide units of the deacetylated derivative of poly-N-acetylglucosamine may form a metal chelate. In a specific embodiment, the metal is zinc.
  • One or more of the monosaccharide units of the deacetylated derivative of poly-N-acetylglucosamine may contain an N-alkylidene or an N-arylidene group.
  • the derivative is an acetate derivative. In another embodiment, the derivative is not an acetate derivative. In one embodiment the poly-N-acetylglucosamine or deacetylated poly-N-acetylglucosamine is derivatized with lactic acid. Wherein, in another embodiment, the derivative is not derivatized with lactic acid.
  • poly-N-acetylglucosamine polymers or fibers, and any derivatives of poly-N-acetylglucosamine polymers or fibers described above can be irradiated as dry polymers or fibers or polymer or fiber membranes.
  • poly-N-acetylglucosamine polymers or fibers, and any derivatives of poly-N-acetylglucosamine polymers or fibers described above can be irradiated when wet.
  • the methods of making sNAG nanofibers by irradiation and the sNAG nanofibers so produced have been described in U.S. Patent Pub. No. 2009/0117175, which is incorporated by reference herein in its entirety.
  • the poly-N-acetylglucosamine polymers or fibers are formulated into a suspension/slurry or wet cake for irradiation. Irradiation can be performed prior to, concurrently with or following the formulation of the polymers or fibers into its final formulation, such as a dressing.
  • the polymer or fiber content of suspensions/slurries and wet cakes can vary, for example from about 0.5 mg to about 50 mg of polymer or fiber per 1 ml of distilled water are used for slurries and from about 50 mg to about 1000 mg of polymer or fiber per 1 ml of distilled water are use for wet cake formulations.
  • the polymer or fiber may first be lyophilized, frozen in liquid nitrogen, and pulverized, to make it more susceptible to forming a suspension/slurry or wet cake. Also, the suspensions/slurries can be filtered to remove water such that a wet cake is formed.
  • the polymer or fiber is irradiated as a suspension comprising about 0.5 mg, 1 mg, 2 mg, 3 mg, 4 mg, 5 mg, 6 mg, 7 mg, 8 mg, 9 mg, 10 mg, 12 mg, 15 mg, 18 mg, 20 mg, 25 mg or 50 mg of polymer or fiber per ml of distilled water, or any range in between the foregoing embodiments (e.g., 1-10 mg/ml, 5-15 mg/ml, 2-8 mg/ml, 20-50 mg/ml, etc.).
  • the polymer or fiber is irradiated as a wet cake, comprising about 50-1,000 mg polymer or fiber per 1 ml of distilled water.
  • the wet cake comprises about 50, 100, 200, 300, 400, 500, 600, 700, 800, 900 or 1000 mg of polymer or fiber per 1 ml distilled water, or any range in between (e.g., 100-500 mg/ml, 300-600 mg/ml, 50-1000 mg/ml, etc.).
  • the irradiation is preferably in the form of gamma radiation, e-beam radiation, or x-rays.
  • Two sources of irradiation are preferred: radioactive nuclides and electricity.
  • the radioactive nuclides are cobalt-60 and cesium-137. Both of these nuclides emit gamma rays, which are photons containing no mass.
  • the gamma rays have energies from 0.66 to 1.3 MeV. Using electricity, electrons are generated and accelerated to energies up to 10 MeV or higher.
  • Electron energy can be converted to x-rays by placing a metal (usually tungsten or tantalum) target in the electron beam path. Conversion to x-rays is limited to electrons with energies up to 5 MeV. X-rays are photons with no mass and can penetrate polymers or fibers similar to gamma rays. There is only about 8% efficiency in the conversion of electron energy to x-ray energy. High powered electron beam machines are needed in x-ray production facilities to account for the low conversion efficiency.
  • the irradiation is gamma irradiation.
  • the absorbed dose of radiation is the energy absorbed per unit weight of product, measured in gray (gy) or kilogray (kgy).
  • the preferred absorbed dose is about 500-2,000 kgy of radiation, most preferably about 750-1,250 kgy or about 900-1,100 kgy of radiation.
  • the preferred absorbed dose is about 100-500 kgy of radiation, most preferably about 150-250 kgy or about 200-250 kgy of radiation.
  • the dose of radiation can be described in terms of its effect on the length of the polymers or fibers.
  • the dose of radiation used preferably reduces the length of the polymer or fiber by anywhere from about 10% to 90% of the starting length of the polymer or fiber, respectively.
  • the average length is reduced by about 10%, by about 20%, by about 30%, by about 40%, by about 50%, by about 60%, by about 70%, by about 80%, or by about 90%, or any range in between (e.g., 20-40%, 30-70%, and so on and so forth).
  • the dose of radiation used preferably reduces the length of the polymer or fiber to anywhere from 1 to 100 microns.
  • the average length of the polymer or fiber is reduced to less than about 15 microns, less than about 14 microns, less than about 13 microns, less than about 12 microns, less than about 11 microns, less than about 10 microns, less than about 8 microns, less than about 7 microns, less than about 5 microns, less than about 4 microns, less than about 3 microns, less than 2 microns, or less than 1 microns.
  • the length of the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the polymers or fibers is reduced to no greater than about 20 microns, no greater than about 15 microns, no greater than about 12 microns, no greater than about 10 microns, no greater than about 8 microns, no greater than about 7 microns, or no greater than about 5 microns.
  • irradiation of the polymers or fibers reduces the length of the majority (and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%; 90% to 95%, or 95% to 99%) of the fibers to anywhere between about 1 to 20 microns, between about 1 to 15 microns, between about 2 to 15 microns, between about 1 to 12 microns, between about 2 to 12 microns, between about 1 to 10 microns, between about 2 to 10 microns, between about 1 to 8 microns, between about 2 to 8 microns, between about 1 to 7 microns, between about 2 to 7 microns, between about 3 to 8 microns, between about 4 to 10 microns, between about 4 to 7 microns, between about 5 to 10 microns
  • the dose of radiation can also be described in terms of its effect on the molecular weight of the polymer or fiber.
  • the dose of radiation used preferably reduces the molecular weight of the polymer or fiber by anywhere from about 10% to 90% of the starting weight of the polymer or fiber.
  • the average molecular weight is reduced by about 10%, by about 20%, by about 30%, by about 40%, by about 50%, by about 60%, by about 70%, by about 80%, or by about 90%, or any range in between (e.g., 20-40%, 30-70%, and so on and so forth).
  • the dose of radiation used preferably reduces the molecular weight of the polymer or fiber to anywhere from 1,000 to 1,000,000 daltons.
  • the average molecular weight of the polymer or fiber is reduced to less than 1,000,000 daltons, less than 750,000 daltons, less than 500,000 daltons, less than 300,000 daltons, less than 200,000 daltons, less than 100,000 daltons, less than 90,000 daltons, less than 80,000 daltons, less than 70,000 daltons, less than 60,000 daltons, less than 50,000 daltons, less than 25,000 daltons, less than 10,000 daltons, or less than 5,000 daltons.
  • the average molecular weight is reduced to no less than 500 daltons, no less than 1,000 daltons, no less than 2,000 daltons, no less 3,500 daltons, no less than 5,000 daltons, no less than 7,500 daltons, no less than 10,000 daltons, no less than 25,000 daltons, no less than 50,000 daltons, no less than 60,000 daltons or no less than 100,000 daltons.
  • irradiation of the polymer or fiber reduces the average molecular weight to anywhere between 10,000 to 100,000 daltons, between 1,000 and 25,000 daltons, between 50,000 and 500,000 daltons, between 25,000 and 100,000 daltons, between 30,000 and 90,000 daltons, between about 40,000 and 80,000 daltons, between about 25,000 and 75,000 daltons, between about 50,000 and 70,000 daltons, or between about 55,000 and 65,000 daltons and so on and so forth.
  • irradiation of the polymers or fibers reduces the molecular weight of the majority and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the fibers to anywhere between about 20,000 and 100,000 daltons, about 25,000 and 75,000 daltons, about 30,000 and 90,000 daltons, about 40,000 and 80,000 daltons, about 50,000 and 70,000 daltons, or about 55,000 and 65,000 daltons.
  • irradiation of the polymers or fibers reduces the molecular weight of the majority and in certain embodiments, at least 60%, 70%, 80%, 90%, 95%, 98%, 99%, 99.5%, 99.8%, 99.9%, or 100%, or between 55% to 65%, 55% to 75%, 65% to 75%, 75% to 85%, 75% to 90%, 80% to 95%, 90% to 95%, or 95% to 99%) of the fibers to about 60,000 daltons.
  • compositions e.g., dressings and other compositions described herein.
  • the sNAG nanofibers may be formulated in a variety of compositions for topical administration as described herein.
  • a composition comprising the sNAG nanofibers may be formulated as a cream, a membrane, a film, a liquid solution, a suspension (e.g., a thick suspension), a powder, a paste, an ointment, a suppository, a gelatinious composition, an aerosol, a gel, or a spray.
  • a composition comprising the sNAG nanofibers is formulated as an ultra-thin membrane.
  • a composition comprising the sNAG nanofibers is formulated as a dressing, a mat, or a bandage.
  • compositions comprising sNAG nanofibers are not solid or barrier-forming.
  • Solid formulations suitable for solution in, or suspension in, liquids prior to administration are also contemplated. It is also possible that such compositions are incorporated in or coated on implantable devices, such as orthopedic implants (for hip, knee, shoulder; pins, screws, etc.), cardiovascular implants (stents, catheters, etc.) and the like where the antibacterial activity would be of benefit.
  • implantable devices such as orthopedic implants (for hip, knee, shoulder; pins, screws, etc.), cardiovascular implants (stents, catheters, etc.) and the like where the antibacterial activity would be of benefit.
  • a composition comprising the sNAG nanofibers may include one or more of pharmaceutically acceptable excipients.
  • Suitable excipients may include water, saline, salt solution, dextrose, glycerol, ethanol and the like, or combinations thereof.
  • Suitable excipients also include starch, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate, oil (including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil and the like), talc, sodium chloride, dried skim milk, propylene, glycol and the like.
  • a composition comprising the sNAG nanofibers may include one or more of wetting agents, emulsifying agents, pH buffering agents, and other agents.
  • the sNAG nanofiber compositions may also be incorporated in a physiologically acceptable carrier, for example in a physiologically acceptable carrier suitable for topical application.
  • physiologically acceptable means approved by a regulatory agency of the Federal or a state government or listed in the U.S. Pharmacopeia or other generally recognized pharmacopeia for use in animals, and more particularly in humans. Examples of suitable pharmaceutical carriers are described in “Remington's Pharmaceutical Sciences” by E. W. Martin.
  • the final amount of the sNAG nanofibers in a composition may vary.
  • the amount of the sNAG nanofibers in a composition (e.g., prepared for administration to a patient) may be greater than or equal to about 50%, about 60%, about 70%, about 75%, about 80%, about 85%, about 90%, about 95%, about 98%, or about 99% weight by volume.
  • the amount of the sNAG nanofibers in a composition is about 95%, about 98%, about 99, or about 100%.
  • the amount of the sNAG nanofibers in a composition may be about 50%-100%, about 60%-100%, about 70%-100%, about 75%-100%, about 80%-100%, about 90%-100%, about 95%-100%, about 70%-95%, about 75%-95%, about 80%-95%, about 90%-95%, about 70%-90%, about 75%-90%, or about 80%-90% weight/volume.
  • a composition may comprise more than 30%, 40%, 50%, 60%, 70%, 75%, 80%, 90%, 95% or 99% solution of the sNAG nanofibers.
  • a sNAG nanofiber composition may be formulated into a wound dressing.
  • a sNAG nanofiber composition is formulated as a wound dressing in the form of a barrier, a membrane, or a film.
  • a sNAG nanofiber composition may be added to dressing backings, such as barriers, membranes, or films.
  • a barrier, membrane, or film can be supplied in a variety of standard sizes, which can be further cut and sized to the area being treated.
  • the backing can be a conventional dressing material, such as a bandage or gauze to which a polymer or fiber is added or coated on, prior to application to the patient.
  • the sNAG nanofibers can be formulated as a barrier, membrane, or film made out of strings, microbeads, microspheres, or microfibrils, or the composition can be formulated as a barrier-forming mat.
  • at least 75%, at least 85%, at least 90%, or at least 95% of a dressing is composed of the sNAG nanofibers.
  • a dressing does not contain a conventional dressing material such as a gauze or bandage.
  • the sNAG nanofiber itself is formulated as a wound dressing.
  • a composition comprising the sNAG nanofibers may further comprise any suitable natural or synthetic polymers or fibers.
  • suitable polymers or fibers include cellulose polymers, xanthan, polyaramides, polyamides, polyimides, polyamide/imides, polyamidehydrazides, polyhydrazides, polyimidazoles, polybenzoxazoles, polyester/amide, polyester/imide, polycarbonate/amides, polycarbonate/imides, polysulfone/amides, polysulfone imides, and the like, copolymers and blends thereof.
  • Other suitable classes of polymers or fibers include polyvinyledene fluorides and polyacrylonitriles. Examples of these polymers or fibers include those described in U.S. Pat. Nos.
  • the polymers or fibers can include at least one of either of cellulose polymers, polyamides, polyaramides, polyamide/imides or polyimides.
  • the polymers or fibers include polyaramides, polyester, urethan and polytetrafluoroethylene.
  • the compositions described herein comprise more than one type of polymer (e.g., the sNAG nanofiber and cellulose).
  • the sNAG nanofiber is the only active ingredient in a composition.
  • a composition comprises one or more additional active ingredients, e.g., an anti-viral agent, an anti-fungal agent, an anti-yeast agent, a chemotherapeutic agent or any other agent.
  • the additional active ingredient is one or more of an anti-viral agent, an anti-fungal agent, an anti-yeast agent, a defensin peptide, a defensin-like peptide, or a Toll-receptor-like peptide), or a growth factor.
  • the additional active ingredient is a growth factor such as one or more of PDGF-AA, PDGF-AB, PDGF-BB, PDGF-CC, PDGF-DD, FGF-1, FGF-2, FGF-5, FGF-7, FGF-10, EGF, TGF- ⁇ , (HB-EGF), amphiregulin, epiregulin, betacellulin, neuregulins, epigen, VEGF-A, VEGF-B, VEGF-C, VEGF-D, VEGF-E, placenta growth factor (PLGF), angiopoietin-1, angiopoietin-2, IGF-I, IGF-II, hepatocyte growth factor (HGF), and macrophage-stimulating protein (MSP).
  • the additional active ingredient is an agent that boost the immune system, a pain relief agent, or a fever relief agent.
  • the additional active ingredient is an anti-viral agent.
  • Any anti-viral agents well-known to one of skill in the art may be used in a sNAG nanofiber composition.
  • Non-limiting examples of anti-viral agents include proteins, polypeptides, peptides, fusion proteins antibodies, nucleic acid molecules, organic molecules, inorganic molecules, and small molecules that inhibit and/or reduce the attachment of a virus to its receptor, the internalization of a virus into a cell, the replication of a virus, or release of virus from a cell.
  • anti-viral agents include, but are not limited to, nucleoside analogs (e.g., zidovudine, acyclovir, gangcyclovir, vidarabine, idoxuridine, trifluridine, and ribavirin), foscarnet, amantadine, peramivir, rimantadine, saquinavir, indinavir, ritonavir, alpha-interferons and other interferons, AZT, zanamivir (Relenza®), and oseltamivir (Tamiflu®).
  • nucleoside analogs e.g., zidovudine, acyclovir, gangcyclovir, vidarabine, idoxuridine, trifluridine, and ribavirin
  • foscarnet e.g., amantadine, peramivir, rimantadine, saquinavir, indinavir, ritonavir
  • influenza virus vaccines e.g., Fluarix® (GlaxoSmithKline), FluMist® (MedImmune Vaccines), Fluvirin® (Chiron Corporation), Flulaval® (GlaxoSmithKline), Afluria® (CSL Biotherapies Inc.), Agriflu® (Novartis) or Fluzone® (Aventis Pasteur).
  • influenza virus vaccines e.g., Fluarix® (GlaxoSmithKline), FluMist® (MedImmune Vaccines), Fluvirin® (Chiron Corporation), Flulaval® (GlaxoSmithKline), Afluria® (CSL Biotherapies Inc.), Agriflu® (Novartis) or Fluzone® (Aventis Pasteur).
  • the additional active ingredient is an anti-cancer agent.
  • the anti-cancer agent is a chemotherapeutic agent. Any anti-cancer agents known to one of skill in the art may be used in a sNAG nanofiber composition.
  • anti-cancer agents include: acivicin; anthracyclin; anthramycin; azacitidine (Vidaza); bisphosphonates (e.g., pamidronate (Aredria), sodium clondronate (Bonefos), zoledronic acid (Zometa), alendronate (Fosamax), etidronate, ibandornate, cimadronate, risedromate, and tiludromate); carboplatin; chlorambucil; cisplatin; cytarabine (Ara-C); daunorubicin hydrochloride; decitabine (Dacogen); demethylation agents, docetaxel; doxorubicin; EphA2 inhibitors; etoposide; camrabine; fluorouracil; gemcitabine; histone deacetylase inhibitors (HDACs); interleukin II (including recombinant interleukin
  • WO 02/098370 which is incorporated herein by reference in its entirety
  • melphalan methotrexate; mitomycin; oxaliplatin; paclitaxel; puromycin; riboprine; spiroplatin; tegafur; teniposide; vinblastine sulfate; vincristine sulfate; vorozole; zeniplatin; zinostatin; and zorubicin hydrochloride.
  • the additional active ingredient is an anti-angiogenic agent.
  • anti-angiogenic agents include proteins, polypeptides, peptides, conjugates, antibodies (e.g., human, humanized, chimeric, monoclonal, polyclonal, Fvs, ScFvs, Fab fragments, F(ab)2 fragments, and antigen-binding fragments thereof) such as antibodies that specifically bind to TNF- ⁇ , nucleic acid molecules (e.g., antisense molecules or triple helices), organic molecules, inorganic molecules, and small molecules that reduce or inhibit angiogenesis.
  • nucleic acid molecules e.g., antisense molecules or triple helices
  • organic molecules e.g., inorganic molecules, and small molecules that reduce or inhibit angiogenesis.
  • the additional active ingredient is not an anti-angiogenic agent.
  • the additional active ingredient is an anti-inflammatory agent.
  • anti-inflammatory agents include non-steroidal anti-inflammatory drugs (NSAIDs) (e.g., celecoxib (CELEBREXTM), diclofenac (VOLTARENTM), etodolac (LODINETM), fenoprofen (NALFONTM), indomethacin (INDOCINTM), ketoralac (TORADOLTM), oxaprozin (DAYPROTM), nabumentone (RELAFENTM), sulindac (CLINORILTM), tolmentin (TOLECTINTM), rofecoxib (VIOXXTM), naproxen (ALEVETM, NAPROSYNTM), ketoprofen (ACTRONTM) and nabumetone (RELAFENTM)), steroidal anti-inflammatory drugs (e.g., glucocorticoids, dexamethasone (DECADRONTM), corticosteroids (e.g., glucocortic
  • the additional active ingredient is an alkylating agent, a nitrosourea, an antimetabolite, an anthracyclin, a topoisomerase II inhibitor, or a mitotic inhibitor.
  • Alkylating agents include, but are not limited to, busulfan, cisplatin, carboplatin, cholormbucil, cyclophosphamide, ifosfamide, decarbazine, mechlorethamine, mephalen, and themozolomide.
  • Nitrosoureas include, but are not limited to carmustine (BCNU) and lomustine (CCNU).
  • Antimetabolites include but are not limited to 5-fluorouracil, capecitabine, methotrexate, gemcitabine, cytarabine, and fludarabine.
  • Anthracyclins include but are not limited to daunorubicin, doxorubicin, epirubicin, idarubicin, and mitoxantrone.
  • Topoisomerase II inhibitors include, but are not limited to, topotecan, irinotecan, etopiside (VP-16), and teniposide.
  • Mitotic inhibitors include, but are not limited to taxanes (paclitaxel, docetaxel), and the vinca alkaloids (vinblastine, vincristine, and vinorelbine).
  • a sNAG nanofiber composition may contain collagen, although in certain aspects a sNAG nanofiber composition does not contain collagen.
  • a sNAG nanofiber composition does not comprise any additional therapy. In certain embodiments, a sNAG nanofiber composition does not comprise any additional anti-viral agent, anti-cancer agent, anti-fungal agent, anti-yeast agent, anti-inflammatory agent, chemotherapeutic agent, anti-angiogenic agent, a defensin peptide, a defensin-like peptide, a Toll-receptor-like peptide, or a growth factor.
  • the additional active ingredient is not an anti-bacterial agent (e.g., an antibiotic, a defensin peptide, a defensin-like peptide, or a Toll-receptor-like peptide), or a growth factor.
  • an anti-bacterial agent e.g., an antibiotic, a defensin peptide, a defensin-like peptide, or a Toll-receptor-like peptide
  • a growth factor e.g., an antibiotic, a defensin peptide, a defensin-like peptide, or a Toll-receptor-like peptide
  • the additional active ingredient is not a growth factor, such as PDGF-AA, PDGF-AB, PDGF-BB, PDGF-CC, PDGF-DD, FGF-1, FGF-2, FGF-5, FGF-7, FGF-10, EGF, TGF- ⁇ , (HB-EGF), amphiregulin, epiregulin, betacellulin, neuregulins, epigen, VEGF-A, VEGF-B, VEGF-C, VEGF-D, VEGF-E, placenta growth factor (PLGF), angiopoietin-1, angiopoietin-2, IGF-I, IGF-II, hepatocyte growth factor (HGF), and macrophage-stimulating protein (MSP).
  • the additional active ingredient is not an agents that boost the immune system, a pain relief agent, or a fever relief agent.
  • the additional active ingredient is not an antibiotic from one of the following classes of antibiotics: microlides (e.g., erythromycin, azithromycin), aminoglycosides (e.g., amikacin, gentamicin, neomycin, streptomycin), cephalosporins (e.g., cefadroxil, cefaclor, cefotaxime, cefepime), fluoroquinolones (e.g., ciprofloxacin, levofloxacin), penicillins (e.g., penicillin, ampicillin, amoxicillin), tetracyclines (e.g., tetracycline, doxycycline), and carbapenems (e.g., meropenem, imipenem).
  • microlides e.g., erythromycin, azithromycin
  • aminoglycosides e.g., amikacin, gentamicin, neomycin, strept
  • the additional active ingredient is not vancomycin, sulfa drug (e.g., co-trimoxazole/trimethoprim-sulfamethoxazole), tetracycline (e.g., doxycycline, minocycline), clindamycin, oxazolidinones (e.g., linezolid), daptomycin, teicoplanin, quinupristin/dalfopristin (synercid), tigecycline, allicin, bacitracin, nitrofurantoin, hydrogen peroxide, novobiocin, netilmicin, methylglyoxal, bee defensin-1, tobramycin, chlorhexidine digluconate, chlorhexidine gluconate, levofloxacin, zinc, and/or silver.
  • sulfa drug e.g., co-trimoxazole/trimethoprim-sulfamethoxazo
  • a sNAG nanofiber composition does not comprise a significant amount of protein material.
  • the protein content of a sNAG nanofiber composition is no greater than 0.1%, 0.5% or 1% by weight. In other embodiments, the protein content of the composition is undetectable by Coomassie staining.
  • zinc is also included in a sNAG nanofiber composition.
  • zinc also plays a role in wound healing (see Andrews et al., 1999, Adv Wound Care 12:137-8).
  • the zinc is preferably added in the form of a salt, such as zinc oxide, zinc sulphate, zinc acetate or zinc gluconate.
  • compositions described herein can be used to prevent and/or treat infections and/or diseases for which an increase in defensin production and/or secretion is beneficial.
  • diseases may be the result of a defensin deficiency or may derive benefit from increased presence of defensins.
  • compositions described herein are used to treat and/or prevent a disease which is associated with no or low level of expression of one or more defensin peptides; or a mutation/deletion/low gene copy number (“GCN”) in a gene or genes encoding one or more of defensin peptides.
  • GCN mutation/deletion/low gene copy number
  • Exemplary defensin genes that may be mutated/deleted/have low GCN/not expressed or whose expression may be low or altered include any of the known ⁇ -defensins (e.g., DEFA1, DEFA1B, DEFA3, DEFA4, DEFA5, DEFA6), any of the known ⁇ -defensins (e.g., DEFB1, DEFB2, DEFB4, DEFB103A, DEFB104A, DEFB105B, DEFB107B, DEFB108B, DEFB110, DEFB112, DEFB114, DEFB118, DEFB119, DEFB123, DEFB124, DEFB125, DEFB126, DEFB127, DEFB128, DEFB129, DEFB131, DEFB136), and any of the known ⁇ -defensins (e.g., DEFT1P).
  • DEFA1, DEFA1B, DEFA3, DEFA4, DEFA5, DEFA6 any of the known ⁇ -defensins (e.g., DEFB1,
  • compositions described herein are used to treat or prevent a disease or infection which is associated with no, low, or altered level of expression of or a mutation/deletion/low GCN of one or more of the above-listed genes.
  • the compositions described herein are used to treat or prevent a disease or infection which is associated with no, low, or altered level of expression of or a mutation/deletion/low GCN of one or more of DEFA1, DEFA3, DEFA4, DEFA5; DEFB1, DEFB3, DEFB103A, DEFB104A, DEFB108B, DEFB112, DEFB114, DEFB118, DEFB119, DEFB123, DEFB124, DEFB125, DEFB126, DEFB128, DEFB129 and DEFB131.
  • compositions described herein are used to treat or prevent a disease or infection which is associated with no, low, or altered level of expression of or a mutation/deletion/low GCN of one or more Toll receptors (e.g., TLR1, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TLR10, TLR11, and/or TLR12).
  • Toll receptors e.g., TLR1, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TLR10, TLR11, and/or TLR12.
  • compositions described herein are used to treat or prevent a disease or infection which is associated with no, low, or altered level of expression of or a mutation/deletion/low GCN of one or more of IL-1, CEACAM3, SPAG11, SIGIRR (IL1-like receptor), IRAK1, IRAK2, IRAK4, TBK1, TRAF6 and MG.
  • the compositions described herein are used to treat or prevent a disease or infection which is associated with no, low, or altered level of expression of or a mutation/deletion/low GCN of one or more of IRAK2, SIGIRR, TLR1, TLR2, TLR4, TLR7, TLR8, TLR10 and TRAF6.
  • a low level of expression of a gene is a level that is lower (e.g., more than 1.25 fold, 1.5 fold, 2 fold, 2.5 fold, 3 fold, 3.5 fold, 4 fold, 4.5 fold, 5 fold, 6 fold, 7 fold, 8 fold, 9 fold, 10 fold lower) than the “normal” level of expression.
  • An altered level of expression of a gene is a level that differs (e.g., by more than 20%, 25%, 30%, 50%, 75%, 100%, 150%, 200%, 250%, 300%) from the “normal” level of expression.
  • the expression of one or more defensin genes in a patient to be administered a composition described herein may be less than less than 90%, less than 75%, less than 60%, less than 50%, less than 30% or less than 20% of the “normal” expression of one or more defensin genes.
  • the “normal” expression of one or more defensin genes is: (i) the average expression level known to be found in subjects not displaying symptoms or not diagnosed with the disease or infection to be treated; (ii) the average expression level detected in three, five, ten, twenty, twenty-five, fifty or more subjects not displaying symptoms or not diagnosed with the disease or infection to be treated; and/or (iii) the level of expression detected in a patient to be administered a composition described herein before the onset of the disease or infection.
  • compositions described herein are used to treat a solid tumor cancer.
  • the ability of sNAG nanofibers to induce alpha and beta defensins may contribute to the anti-cancer activity of the sNAG nanofibers.
  • Human alpha and beta defensins e.g., beta-defensin 1 have been shown to have anti-cancer activity.
  • Exemplary solid tumor cancers that can be treated with the compositions described herein include, without limitation, bone and connective tissue sarcomas, brain cancer, breast cancer, ovarian cancer, kidney cancer, pancreatic cancer, esophageal cancer, stomach cancer, ovarian cancer, lung cancer (e.g., small cell lung cancer (SCLC), non-small cell lung cancer (NSCLC), throat cancer, and mesothelioma), liver cancer, and prostate cancer.
  • SCLC small cell lung cancer
  • NSCLC non-small cell lung cancer
  • throat cancer e.g., mesothelioma
  • liver cancer e.g., liver cancer, and prostate cancer.
  • the compositions described herein are used to treat a cancer caused by or associated with a viral infection.
  • the compositions described herein are used to treat Kaposi's sarcoma.
  • treatment of a subject having a solid tumor by administration of a composition described herein results in one or more of the following: reduction in the size of the solid tumor; prevention of the metastasis of the solid tumor; prevention of the recurrence of the solid tumor; reduction in the duration and/or severity of one or more symptoms associated with the solid tumor; reduction in the number of symptoms associated with the solid tumor; prevention of the increase in the size of the solid tumor; reduction/inhibition of proliferation of cancer cells of the solid tumor; reduction in organ failure associated with the solid tumor; reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject; an increase the survival of the subject; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • compositions described herein are used to treat skin cancer.
  • exemplary skin cancers that can be treated with the compositions described herein include, without limitation, melanoma, basal cell carcinoma, and squamous cell carcinoma.
  • treatment of a subject having a skin cancer by administration of a composition described herein results in one or more of the following: reduction in the size of the skin cancer; prevention of the metastasis of the skin cancer; prevention of the recurrence of the skin cancer; reduction in the duration and/or severity of one or more symptoms associated with the skin cancer; reduction in the number of symptoms associated with the skin cancer; reduction in organ failure associated with the skin cancer; reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject; an increase the survival of the subject; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • compositions described herein are used to treat inflammatory bowel disease (IBD).
  • IBD inflammatory bowel disease
  • the ability of sNAG nanofibers to induce alpha and beta defensins may contribute to the anti-IBD activity of the sNAG nanofibers.
  • Alpha and beta defensins have been shown to have anti-IBD activity.
  • IBD includes, but is not limited to, Crohn's disease and ulcerative colitis.
  • treatment of a subject having IBD by administration of a composition described herein results in one or more of the following: prevention of the recurrence of IBD; reduction in the duration and/or severity of one or more symptoms associated with IBD; reduction in the number of symptoms associated with the IBD; reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • compositions described herein prevent the onset or development of one or more of the above-listed symptoms or other symptoms known in the art, or reduce duration and/or severity of one or more of these symptoms.
  • compositions described herein are used to treat ulcerative colitis. Symptoms of ulcerative colitis may include above listed symptoms of IBD, and may also include defecation often mucus-like and with blood, tenesmus, and/or fever.
  • Example 9 shows that sNAG nanofibers are effective to treat IBD based on the data obtained in an animal model of IBD.
  • a composition comprising sNAG nanofibers that can be used to treat IBD can be any sNAG composition described herein.
  • a composition comprising sNAG nanofibers that can be used to treat IBD is the same or similar to the composition described in Example 9.
  • compositions described herein are used to treat Crohn's disease (e.g., ileal Crohn's disease).
  • Crohn's disease e.g., ileal Crohn's disease
  • the ability of sNAG nanofibers to induce alpha and beta defensins may contribute to the anti-Crohn's disease activity of the sNAG nanofibers.
  • Alpha and beta defensins have been shown to have anti-Crohn's disease activity.
  • treatment of a subject having Crohn's disease by administration of a composition described herein results in one or more of the following: prevention of the recurrence of the Crohn's disease; reduction in the duration and/or severity of one or more symptoms associated with the Crohn's disease; reduction in the number of symptoms associated with the Crohn's disease; reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • Crohn's disease Some of the symptoms of Crohn's disease include abdominal pain, vomiting, diarrhea, rectal bleeding, severe internal cramps/muscle spasms in the region of the pelvis, weight loss and various associated complaints or diseases like arthritis, pyoderma gangrenosum, and primary sclerosing cholangitis. Symptoms of Crohn's disease also may include defecation often porridge-like and sometimes steatorrhea, fever, fistulae, flatulence, bloating, perianal discomfort such itchiness and pain, fecal incontinence, aphthous ulcers of the mouth, and/or weight loss. In some embodiments, the compositions described herein prevent the onset or development of one or more of the above-listed symptoms or other symptoms known in the art, or reduce duration and/or severity of one or more of these symptoms.
  • the compositions described herein are used to prevent and/or treat mucositis.
  • Mucositis is the painful inflammation and ulceration of the mucous membranes lining the digestive tract (e.g., as an adverse effect of chemotherapy or radiotherapy treatment for cancer). Mucositis can occur anywhere along the gastrointestinal tract, for example, in the mouth (i.e., oral mucositis).
  • the compositions described herein are administered topically to a patient (e.g., a patient diagnosed with or displaying symptoms of mucositis) to treat mucositis (e.g., administered topically on the inflamed or ulcerated area of the mouth, or administered topically to the anus or rectal area such as via a cream, a suppository, a suspension, a liquid solution, a gel, or an ointment).
  • the compositions described herein are administered at the site, or in proximity to the site, of an inflammation or ulcer caused by or associated with mucositis (e.g., in the mouth).
  • compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of mucositis subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • treatment of a subject having mucositis by administration of a composition described herein results in one or more of the following: prevention or reduction of frequency of the recurrence of the mucositis; reduction in the duration and/or severity of one or more symptoms associated with mucositis (e.g., pain, ulceration); reduction in the number of symptoms associated with mucositis; reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • prevention or reduction of frequency of the recurrence of the mucositis results in one or more of the following: prevention or reduction of frequency of the recurrence of the mucositis; reduction in the duration and/or severity of one or more symptoms associated with mucositis (e.g., pain, ulceration); reduction in the number of symptoms associated with mucositis; reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject
  • compositions described herein are used to prevent and/or treat a viral infection or a disease caused by or associated therewith.
  • beta defensins e.g., beta-defensin 1
  • Beta defensins e.g., beta-defensin 1
  • viruses which can cause infection or disease to be prevented and/or treated with the compositions described herein include, without limitation, respiratory syncytial virus (RSV), influenza virus (influenza A virus, influenza B virus, or influenza C virus), human metapneumovirus (HMPV), rhinovirus, parainfluenza virus, SARS Coronavirus, human immunodeficiency virus (HIV), hepatitis virus (A, B, C), ebola virus, herpes simplex virus (e.g., HSV-1, HSV-2, HSV-6, HSV-7), varicella, varicella zoster virus, human papillomavirus (HPV), parapox virus, morbilli, echovirus, adenovirus, Epstein Barr virus, Coxsackie virus, enterovirus, rubella, variola major, and variola minor.
  • RSV respiratory syncytial virus
  • influenza virus influenza A virus, influenza B virus, or influenza C virus
  • HMPV human metapneu
  • prevention of a viral infection in a subject or a disease caused by or associated therewith by administration of a composition described herein results in one or more of the following: prevention of the development or onset of a disease caused by or associated with viral infection; and/or prevention of the spread of a viral infection or a disease caused by or associated therewith from the subject to another subject or population of subjects.
  • treatment of a subject having a viral infection or a disease caused by or associated therewith by administration of a composition described herein results in one or more of the following: prevention of the recurrence of the viral infection or a disease caused by or associated therewith; reduction in the number of symptoms associated with the viral infection or a disease caused by or associated therewith; reduction in organ failure associated with the viral infection or a disease caused by or associated therewith; reduction of the severity and/or duration of the viral infection or a disease caused by or associated therewith; reduction of the severity and/or duration of one or more symptoms of the viral infection or a disease caused by or associated therewith; reduction in viral load or count (e.g., by more than about 0.25 log, 0.5 log, 0.75 log, 1 log, 1.5 log, 2 logs, 2.5 logs, 3 logs, 4 logs, 5 logs, 6 logs, 7 logs, 8 logs, 9 logs, or 10 logs); reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject;
  • compositions described herein are not used to prevent and/or treat an HIV infection or a disease caused by or associated with an HIV infection.
  • Symptoms of a viral infection may include but are not limited to fever, chills, headache, stiff neck, irritability, enlarged glands, diarrhea, nausea, vomiting, a skin or a mucous membrane abnormality associated with a viral infection (e.g, a rash, an ulceration, a cold sore, a lesion, a swelling, redness, itching, a papule, a vesicle, a pustule, a blister, a crust) and/or pain associated with such abnormality, abdominal pain, sore throat, ear pain, cough, weight loss, fatigue, body aches, and/or other flu-like symptoms.
  • the compositions described herein prevent the onset or development of one or more of the above-listed symptoms or other symptoms known in the art, or reduce duration and/or severity of one or more of these symptoms.
  • compositions described herein are used to prevent and/or treat a viral infection of a wound (e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn).
  • a viral infection of a wound e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn.
  • the compositions described herein are not used to prevent and/or treat a viral infection of a wound.
  • wounds There are two types of wounds, open and closed. Open wounds are classified according to the object that caused the wound. For example, incisions or incised wounds (including surgical wounds) are caused by a clean, sharp-edged object such as a knife, a razor or a glass splinter.
  • Lacerations are irregular wounds caused by a blunt impact to soft tissue which lies over hard tissue (e.g., laceration of the skin covering the skull) or tearing of skin and other tissues such as caused by childbirth.
  • Abrasions or grazes are superficial wounds in which the topmost layer of the skin (the epidermis) is scraped off.
  • Puncture wounds are caused by an object puncturing the skin, such as a nail or needle.
  • Penetration wounds are caused by an object such as a knife entering the body.
  • Gunshot wounds are caused by a bullet or similar projectile driving into (e.g., entry wound) and/or through the body (e.g., exit wound). In a medical context, all stab wounds and gunshot wounds are considered open wounds.
  • Open wounds also include burn wounds induced by thermal, chemical, or electrical injury. Closed wounds include contusions (more commonly known as a bruise, caused by blunt force trauma that damages tissue under the skin), hematoma (also called a blood tumor, caused by damage to a blood vessel that in turn causes blood to collect under the skin), and crushing injuries (caused by a great or extreme amount of force applied over a long period of time).
  • contusions more commonly known as a bruise, caused by blunt force trauma that damages tissue under the skin
  • hematoma also called a blood tumor, caused by damage to a blood vessel that in turn causes blood to collect under the skin
  • crushing injuries caused by a great or extreme amount of force applied over a long period of time).
  • the sNAG compositions described herein are used to prevent and/or treat a topical viral infection in a patient (e.g., in a patient diagnosed with viral infection or displaying a symptom of a viral infection).
  • the compositions described herein are used to prevent and/or treat a viral infection or a symptom of a viral infection on the skin, mucous membranes (e.g., eyes, ears, throat, vagina, anus), or the surface of other tissues.
  • the compositions described herein are administered directly to the skin, mucous membrane (e.g., eyes, ears, throat, oral cavity, vagina, anus), or the surface of other tissues.
  • compositions described herein are used to treat vesicular (such as a vesicle, a pustule or a blister), ulcer or crust stages of a viral infection (e.g., herpes simplex virus infection or varicella zoster infection).
  • vesicular such as a vesicle, a pustule or a blister
  • ulcer or crust stages of a viral infection e.g., herpes simplex virus infection or varicella zoster infection.
  • the compositions described herein are used to treat prodrome, erythema/macule or papule/edema stages of a viral infection (e.g., herpes simplex virus infection or varicella zoster infection).
  • compositions described herein are administered at the site or in the proximity to the site of a viral infection or at the site or in the proximity to the site of a symptom of a viral infection (e.g., to a cold sore, lesion, blister, pustule, ulcer, rash, swelling, or crust associated with a viral infection).
  • a symptom of a viral infection e.g., to a cold sore, lesion, blister, pustule, ulcer, rash, swelling, or crust associated with a viral infection.
  • treatment of a subject having a topical viral infection by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of a topical viral infection (e.g., an itching, a lesion, an ulcer, a blister, a papule, a rush, a crust, or any other symptom of a topical viral infection described herein or known in the art); reduction of pain associated with a symptom of a topical viral infection; reduction in the number of symptoms associated with a topical viral infection; prevention or reduction of frequency of the recurrence of a symptom of a topical viral infection; prevention of the spread of a topical viral infection from the subject to another subject; prevention of the onset or development of one or more of the symptoms of a topical viral infection described herein or known in the art; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy (e.g., another anti-viral therapy) in the subject.
  • another therapy
  • the sNAG compositions described herein are formulated in a non-barrier form for use in the treatment of topical viral infections.
  • the compositions described herein are formulated in the form of a liquid solution, a suspension (e.g., a thick suspension), a cream, or an ointment for use in the treatment of topical viral infections.
  • the sNAG compositions described herein are not in a solid form when used in the treatment of topical viral infections.
  • the sNAG compositions described herein are barrier-forming and/or solid for use in the treatment of topical viral infections.
  • Example 8 infra, shows that sNAG nanofibers are effective to treat topical viral infections based on the data obtained on human patients.
  • Example 8 shows that sNAG nanofibers are effective to treat an HSV infection, such as a cold sore caused by or associated with an HSV infection, in human patients.
  • a composition comprising sNAG nanofibers that can be used to treat a topical viral infection can be any sNAG composition described herein.
  • a composition comprising sNAG nanofibers that can be used to treat a topical viral infection can be the same or similar to the composition described in Example 8.
  • Viral infections and diseases/conditions of the skin associated with viral infections include, but are not limited to, measles (morbilli), German measles (rubella), chickenpox (varicella), fifth disease (erythema infectiosum, due to parvovirus), Roseola, infectious mononucleosis or glandular fever (Epstein Barr virus), enterovirus infections, Pityriasis rosea (possibly caused by herpes 6 or 7), hand, foot and mouth disease (due to Coxsackie infection), Gianotto-Crosti syndrome (papular acrodermatitits occurring in children; most often caused by infectious mononucleosis due to Epstein Barr virus or hepatitis B), Laterothoracic exanthem (asymmetric periflexural exanthem of childhood or APEC), smallpox, cowpox, epidermodysplasia verruciformis, skin conditions caused by or associated with
  • compositions described herein are used to prevent and/or treat an infection with a herpes simplex virus (e.g., HSV-1, HSV-2), or a disease or condition caused by a herpes simplex virus (e.g., HSV-1, HSV-2).
  • a herpes simplex virus e.g., HSV-1, HSV-2
  • a disease or condition caused by a herpes simplex virus e.g., HSV-1, HSV-2
  • Symptoms of Herpes simplex virus type 1 may include blisters or lesions in the mouth, throat, lips (e.g., peri-oral cold sores)
  • symptoms of herpes simplex virus type 2 (HSV-2) may include blisters or lesions (e.g., papules and/or vesicles) on the outer surface of genitals.
  • HSV HSV
  • Both types of HSV reside in a latent state in the sensory nerves of the skin.
  • the virus spreads down the nerves and out into the skin or mucous membranes where it multiplies, causing the clinical lesion. After each attack it recedes up the nerve fiber and becomes dormant again.
  • Primary infections of type 1 occur mainly in infants and young children and are usually mild or subclinical. In crowded, underdeveloped areas of the world up to 100% of children have been infected by the age of 5.
  • Type 2 is usually sexually acquired, after puberty and is less often asymptomatic.
  • the virus is shed in saliva and genital secretions, during a clinical attack and for some days or weeks afterwards.
  • the amount shed from active lesions is 100 to 1,000 times greater than when it is inactive.
  • Spread of HSV is usually by direct contact with infected secretions. Where immunity is deficient infections tend to occur more frequently and to be more pronounced and persistent. Recurrence may be triggered by: minor trauma; other infections including coryza, ultraviolet radiation (sun exposure); hormonal factors (premenstrual flares occur); emotional stress; operations or procedures performed on the face (including dentistry).
  • the compositions described herein are administered topically to treat HSV-1 infection or a lesion or a cold sore associated with HSV-1 infection (e.g., administered orally or peri-orally).
  • compositions described herein are administered topically to treat HSV-2 infection or a genital lesion associated with HSV-2 infection (e.g., administered topically in the genital area, such as vaginally).
  • treatment of a subject having an HSV infection or a disease caused by or associated therewith by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of an HSV infection (e.g., a cold sore, a lesion, or any other symptom of an HSV infection described herein or known in the art); reduction in the number of symptoms associated with an HSV infection, reduction of pain associated with a symptom of an HSV infection (e.g., a cold sore or a lesion); prevention or reduction of frequency of the recurrence of a symptom of an HSV infection; prevention of the spread of an HSV infection from the subject to another subject; prevention of the onset of development of one or more symptoms of an HSV infection;
  • a composition described herein is administered to a human infant, a human toddler, a human child, a human adult, and/or an elderly human who has an HSV infection or a symptom of an HSV infection.
  • the compositions described herein are administered topically on a surface area (e.g., peri-oral, oral or genital area of the skin or mucous membranes) at the time when the surface area starts to tingle, itch or swell (wherein tingling, itching or swelling at the surface area is associated with an HSV infection (e.g., HSV-1 or HSV-2)).
  • a surface area e.g., peri-oral, oral or genital area of the skin or mucous membranes
  • compositions described herein are administered topically at the site, or in proximity to the site, of a cold sore or lesion (e.g., a peri-oral, oral or genital lesion on the skin or on a mucous membrane) (wherein the cold sore or lesion is associated with an HSV infection (e.g., HSV-1 or HSV-2)).
  • a cold sore or lesion e.g., a peri-oral, oral or genital lesion on the skin or on a mucous membrane
  • HSV infection e.g., HSV-1 or HSV-2
  • Example 8 shows that a sNAG nanofiber composition was effective to treat cold sores associated with HSV infection in human patients when applied topically at the site of the cold sore in a patient, and that treatment of HSV-associated cold sores with a sNAG nanofiber composition resulted in reduction of the severity and duration of the cold sores, and of the pain associated with the cold sores.
  • the compositions described herein are used to treat vesicular (such as a vesicle, a pustule or a blister), ulcer or crust stages of an HSV (e.g., HSV-1 or HSV-2) infection.
  • compositions described herein are used to treat prodrome, erythema/macule or papule/edema stages of an HSV (e.g., HSV-1 or HSV-2) infection.
  • compositions described herein are administered in combination with an anti-viral drug (e.g., acyclovir or any other anti-viral drug described herein or known in the art) in the treatment of an HSV infection.
  • an anti-viral drug e.g., acyclovir or any other anti-viral drug described herein or known in the art
  • the compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of an HSV infection subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • compositions described herein are used to prevent and/or treat an infection with varicella virus, or a disease or condition caused by varicella virus (herpes zoster, shingles, or chickenpox).
  • varicella virus or a disease or condition caused by varicella virus (herpes zoster, shingles, or chickenpox).
  • varicella infection see Shingles, Clinical Knowledge Summaries (2008)
  • nerve cells usually sensory cells.
  • Herpes zoster or shingles is characterized by distribution in a single dermatome. It may not affect all of the dermatome but usually it is confined to the area of one dermatome and does not therefore cross the midline.
  • Herpes zoster Symptoms of herpes zoster include, without limitation, a rash, which consists of macules and papules, and develops into vesicular lesions in a dermatomal distribution (most commonly on the chest), and pain. The rash tends to last 7-10 days, and healing can take 2-4 weeks. More extensive disease may occur in immune compromised patients (for example, with lymphomas and HIV). Herpes zoster can occur at any age, but it is more common in the elderly, and slightly more common in females (although chickenpox affects both sexes equally). Skin complications can include secondary infection, scarring and changes in pigmentation. The elderly are more likely to have complications due to herpes zoster (especially postherpetic neuralgia).
  • compositions described herein are administered topically to treat herpes zoster infection or chickenpox (e.g., administered on the skin).
  • compositions described herein are administered at the site, or in proximity to the site, of a rash (e.g., a macule or papule on the skin) (wherein the rash is associated with herpes zoster infection).
  • treatment of a subject having herpes zoster infection or a disease caused by or associated therewith by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of herpes zoster infection (e.g., a rash, or any other symptom of herpes zoster infection listed herein or known in the art); reduction in the number of symptoms associated with herpes zoster infection; reduction of pain associated with a symptom of herpes zoster infection; prevention or reduction of frequency of the recurrence of a symptom of herpes zoster infection; prevention of the spread of herpes zoster infection from the subject to another subject; prevention of the onset or development of a symptom of herpes zoster infection; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy (e.g., another anti-viral therapy) in the subject.
  • another therapy e.g., another anti-vir
  • composition described herein is administered to a human infant, a human toddler, a human child, a human adult, and/or an elderly human who has herpes zoster infection or a symptom of herpes zoster infection.
  • compositions described herein are administered in combination with an anti-viral drug (e.g., acyclovir or any other anti-viral drug described herein or known in the art) in the treatment of herpes zoster infection.
  • compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of herpes zoster infection subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • compositions described herein are used to prevent and/or treat molluscum contagiosum infection.
  • Molluscum contagiosum is common and usually affects infants and young children, and, only rarely, adults (see Molluscum contagiosum. Clinical Knowledge Summaries (2008)).
  • Symptoms of molluscum contagiosum include, but are not limited to, clusters of small papules, particularly, in the warm moist places such as the axilla, groin or behind the knees.
  • the papules range in size from 1-6 mm and may be white, pink or brown. They often have a waxy, pinkish look and are umbilicated (a central depression of the surface).
  • compositions described herein are administered topically to treat molluscum contagiosum infection (e.g., administered on the skin).
  • compositions described herein are administered at the site, or in proximity to the site, of a rash (e.g., a macule or papule on the skin) (wherein the rash is associated with molluscum contagiosum infection).
  • a rash e.g., a macule or papule on the skin
  • the rash is associated with molluscum contagiosum infection.
  • treatment of a subject having molluscum contagiosum or a disease caused by or associated therewith by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of molluscum contagiosum (e.g., a rash, or any other symptom of molluscum contagiosum listed herein or known in the art); reduction in the number of symptoms of molluscum contagiosum; reduction of pain associated with a symptom of molluscum contagiosum; prevention or reduction of frequency of the recurrence of a symptom of molluscum contagiosum; prevention of the spread of molluscum contagiosum from the subject to another subject; prevention of the onset or development of a symptom of molluscum contagiosum; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • a symptom of molluscum contagiosum e.g., a rash, or any
  • composition described herein is administered to a human infant, a human toddler, a human child, a human adult, and/or an elderly human who has molluscum contagiosum or a symptom of molluscum contagiosum.
  • compositions described herein are administered in combination with a known therapy (e.g., squeezing, piercing, curettage, cryotherapy, wart paints such as salicylic acid and podophyllin; immunomodulatory agent such as imiquimod cream; 1% hydrocortisone cream; or fusidic acid cream 2%) in the treatment of molluscum contagiosum infection.
  • a known therapy e.g., squeezing, piercing, curettage, cryotherapy, wart paints such as salicylic acid and podophyllin; immunomodulatory agent such as imiquimod cream; 1% hydrocortisone cream; or fusidic acid cream 2
  • compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of molluscum contagiosum infection subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • compositions described herein are used to prevent and/or treat human papillomavirus or warts or verrucae associated with human papillomavirus. More than 80 HPV subtypes are known (see Warts and verrucae, Clinical Knowledge Summaries (June 2009)), of which 20 can affect the genital tract. The presentation and appearance of HPV infection varies according to the site of infection. For example, plantar warts occur on pressure-bearing areas and are flattened rather than raised. Warts are most common in childhood and are spread by direct contact or auto-inoculation; it may take up to 12 months for the wart to appear.
  • compositions described herein are administered topically to treat HPV infection or warts or verrucae associated with HPV infection (e.g., administered on the skin).
  • compositions described herein are administered at the site, or in proximity to the site, of a wart or verricuae (wherein the wart or verricuae is caused by or associated with HPV).
  • treatment of a subject having HPV infection or a disease caused by or associated therewith by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of HPV infection (e.g., a wart, a verricuae, or any other symptom of HPV infection described herein or known in the art); reduction in the number of symptoms associated with HPV infection; reduction of pain associated with a symptom of HPV infection; prevention or reduction of frequency of the recurrence of a symptom of HPV infection; prevention of the spread of HPV infection from the subject to another subject; prevention of the onset or development of a symptom of HPV infection; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • a symptom of HPV infection e.g., a wart, a verricuae, or any other symptom of HPV infection described herein or known in the art
  • reduction in the number of symptoms associated with HPV infection
  • a composition described herein is administered to a human infant, a human toddler, a human child, a human adult, and/or an elderly human who has HPV infection or a symptom of HPV infection.
  • the compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of HPV infection subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • compositions described herein are used to prevent and/or treat orf.
  • Orf is contracted from sheep and goats (see Orf, Health Protection Agency (2010)). It is caused by a parapox virus, which infects mainly young lambs and goats that contract the infection from one another (or possibly from persistence of the virus in the pastures). Human lesions are caused by direct inoculation of infected material. It may occur in farmers, butchers, vets, children who bottle-feed lambs and possibly even children who play in pastures where sheep have grazed. The incubation period of parapox virus is 5 or 6 days. Orf lesions are usually solitary but multiple lesions do occur.
  • Orf lesions are usually small, firm, red or reddish-blue, forming a lump that enlarges to form a flat-topped, blood-tinged pustule or blister.
  • the fully developed lesion is usually 2 or 3 cm in diameter but may be as large as 5 cm; and although there appears to be pus under the white skin, incising this will reveal firm, red tissue underneath.
  • the lesion is sometimes irritable during the early stages and is often tender. They usually occur on the fingers, hands or forearms, but may also occur on the face. Red lymph lines may occur on the medial side of the elbow up to the axilla. There may be a mild fever associated with orf.
  • compositions described herein are administered topically to treat orf (e.g., administered on the skin).
  • compositions described herein are administered at the site, or in proximity to the site, of a lesion, a pustule or a blister (wherein the lesion, pustule or blister is caused by or associated with orf).
  • treatment of a subject having orf by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of orf (e.g., a lesion, a pustule, a blister, or any other symptom of orf described herein or known in the art); reduction in the number of symptoms associated with off; reduction of pain associated with a symptom of orf; prevention or reduction of frequency of the recurrence of a symptom of off; prevention of the spread of off from the subject to another subject; prevention of the onset or development of a symptom of orf; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • a symptom of orf e.g., a lesion, a pustule, a blister, or any other symptom of orf described herein or known in the art
  • reduction in the number of symptoms associated with off e.g., a lesion, a pustule, a blister,
  • a composition described herein is administered to a human infant, a human toddler, a human child, a human adult, and/or an elderly human who has orf or a symptom of orf.
  • the compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of orf subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • compositions described herein are used to treat viral infections that produce rashes.
  • viral infections that produce rashes include, but are not limited to, measles (morbilli), German measles (rubella), chickenpox (varicella virus), fifth disease (erythema infectiosum, due to parvovirus), Roseola (erythema subitum, due to herpes virus 6), Pityriasis rosea (the cause is unknown but it may be caused by herpes virus types 6 and 7), echovirus and adenovirus infections, Epstein Barr virus of infectious mononucleosis or glandular fever, and primary HIV infection.
  • the compositions described herein are used to treat nonspecific rashes associated with viral infections (e.g., erythematous rash such as erythematous blotchy eruption).
  • the compositions described herein are administered at the site of a rash caused by or associated with a viral infection or in proximity to the site of a rash caused by or associated with a viral infection.
  • the compositions described herein reduce the severity of rashes, the duration of rashes, and/or pain associated with rashes caused by a viral infection.
  • compositions described herein are used to prevent and/or treat hand, foot and mouth disease or an infection caused by Coxsackie virus or enterovirus.
  • Hand, foot and mouth disease is common, mild and brief, most often affecting young children during the summer months (see Hand, foot and mouth disease, Clinical Knowledge Summaries (March 2010)).
  • Hand, foot and mouth disease is caused by Coxsackie virus A16, although it can also be due to enterovirus 71. Incubation period of such viruses is 3-5 days. Symptoms of hand, foot and mouth disease include small, flat blisters on the hands and feet, oral ulcers, that are sometimes painful, and the disease may be accompanied by a mild fever or a rash on the buttocks (in young children).
  • compositions described herein are administered topically to treat hand, foot and mouth disease or a condition caused by or associated with Coxsackie virus or enterovirus infection (e.g., administered on the skin).
  • compositions described herein are administered at the site, or in proximity to the site, of a blister, ulcer or rash (wherein the blister, ulcer or rash is associated with hand, foot and mouth disease or a condition caused by or associated with Coxsackie virus or enterovirus infection).
  • treatment of a subject having hand, foot and mouth disease by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of hand, foot and mouth disease (e.g., a rash, a blister, an ulcer or any other symptom of hand, foot and mouth disease described herein or known in the art); reduction in the number of symptoms of hand, foot and mouth disease; reduction of pain associated with a symptom of hand, foot and mouth disease; prevention or reduction of frequency of the recurrence of a symptom of hand, foot and mouth disease; prevention of the spread of hand, foot and mouth disease from the subject to another subject; prevention of the onset or development of a symptom of hand, foot and mouth disease; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • a symptom of hand, foot and mouth disease e.g., a rash, a blister, an ulcer or any other symptom of hand, foot and mouth disease described herein or known in
  • a composition described herein is administered to a human infant, a human toddler, a human child, a human adult, and/or an elderly human who has hand, foot and mouth disease or a symptom of hand, foot and mouth disease.
  • the compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of hand, foot and mouth disease subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • compositions described herein are used to prevent and/or treat Crosti-Gianotti syndrome.
  • Crosti-Gianotti syndrome is a response of the skin to viral infection with a papular rash which lasts for several weeks. This condition is also known as papulovesicular acrodermatitis of childhood, papular acrodermatitis of childhood and acrodermatitis papulosa infantum.
  • Crosti-Gianotti syndrome can be caused by Hepatitis B virus, Epstein Barr virus, Coxsackie viruses, Echoviruses, or Respiratory syncytial virus. It affects children between 6 and 12 months. In this condition, a profuse eruption of dull red spots may develop over 3 or 4 days.
  • compositions described herein are administered topically to treat Crosti-Gianotti syndrome (e.g., administered on the skin).
  • compositions described herein are administered at the site, or in proximity to the site, of a red spot, eruption or rash (wherein the red spot, eruption or rash is associated with Crosti-Gianotti syndrome or an infection caused by Hepatitis B virus, Epstein Barr virus, Coxsackie viruses, Echoviruses, or Respiratory syncytial virus).
  • treatment of a subject having Crosti-Gianotti syndrome by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of Crosti-Gianotti syndrome (e.g., a red spot, an eruption, a rash or any other symptom of Crosti-Gianotti syndrome described herein or known in the art); reduction in the number of symptoms associated with Crosti-Gianotti syndrome; reduction of pain associated with a symptom of Crosti-Gianotti syndrome; prevention or reduction of frequency of the recurrence of a symptom of Crosti-Gianotti syndrome; prevention of the spread of Crosti-Gianotti syndrome from the subject to another subject; prevention of the onset or development of a symptom of Crosti-Gianotti; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • a symptom of Crosti-Gianotti syndrome e.g., a red spot, an eruption, a
  • a composition described herein is administered to a human infant (particularly, to an infant between 6 and 12 months of age), a human toddler, a human child, a human adult, and/or an elderly human who has Crosti-Gianotti syndrome or a symptom thereof.
  • the compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of Crosti-Gianotti syndrome subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • compositions described herein are used to prevent and/or treat herpes gladiatorum or “scrum pox.”
  • Herpes gladiatorum is primarily transmitted by direct skin-to-skin contact and abrasions may facilitate a portal of entry (see Becker et al., Am J Sports Med. 16(6):665-9 (1988)).
  • the majority of lesions due to herpes gladiatorum occur on the head or face, followed by the trunk and extremities.
  • Symptoms of herpes gladiatorum include, but are not limited to, prodromal itching or burning sensation, which may be followed by clustered vesicles on an erythematous base which heal with crusts over about 1 to 2 weeks.
  • herpes gladiatorum symptoms include, without limitation, headache, malaise, sore throat and fever. Recurrent episodes may follow the initial infection. Accurate diagnosis can be made by viral immunofluorescence, and cultures can be obtained by gently breaking an intact vesicle and firmly rubbing the swab tip across the base of the erosion. Accordingly, in some embodiments, the compositions described herein are administered topically to treat herpes gladiatorum infection (e.g., administered on the skin).
  • compositions described herein are administered at the site, or in proximity to the site, of an itching, a lesion, a vesicle or a crust (wherein the site of itching, a lesion, a vesicle or a crust is caused by or associated with herpes gladiatorum infection).
  • compositions described herein are administered in combination with an anti-viral drug (e.g., acyclovir or any other anti-viral drug described herein or known in the art) in the treatment of herpes gladiatorum infection.
  • treatment of a subject having herpes gladiatorum by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of herpes gladiatorum (e.g., an itching, a lesion, a vesicle, a crust, or any other symptom of HPV infection described herein or known in the art); reduction in the number of symptoms associated with herpes gladiatorum; reduction of pain associated with a symptom of herpes gladiatorum; prevention of the recurrence of a symptom of herpes gladiatorum; prevention of the spread of herpes gladiatorum from the subject to another subject; prevention of the onset or development of a symptom of herpes gladiatorum; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • a symptom of herpes gladiatorum e.g., an itching, a lesion, a vesicle,
  • a composition described herein is administered to a human infant, a human toddler, a human child, a human adult, and/or an elderly human who has herpes gladiatorum or a symptom of herpes gladiatorum.
  • a composition described herein is administered to an athlete (e.g., professional athlete) for a prophylactic and/or therapeutic purpose.
  • the compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of herpes gladiatorum infection subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • compositions described herein are used to prevent and/or treat common warts associated with a viral infection (e.g., plantar warts, warts in calluses).
  • a viral infection e.g., plantar warts, warts in calluses.
  • the compositions described herein are administered at the site, or in proximity to the site, of a wart caused by or associated with a viral infection or in proximity to the site of a wart caused by or associated with a viral infection.
  • the compositions described herein reduce the number of warts, the severity of warts, the duration of warts and/or the pain associated with warts caused by a viral infection.
  • compositions described herein are used to prevent and/or treat viral infections in immunocompromised patients (e.g., HIV-infected patients).
  • the compositions described herein are used to treat gastroenteritis (e.g., gastroenteritis caused by or associated with a viral infection, or gastroenteritis caused by or associated with a protozoal infection).
  • gastroenteritis e.g., gastroenteritis caused by or associated with a viral infection, or gastroenteritis caused by or associated with a protozoal infection.
  • viruses that can cause gastroenteritis include but are not limited to rotavirus, noravirus, adenovirus, and astrovirus.
  • protozoa that can cause gastroeneteritis include but are not limited to Giardia lamblia , cryptosporidium, and Entamoeba histolytica .
  • the compositions described herein are administered rectally (e.g., as a cream or suppository) to treat gastroenteritis.
  • treatment of a subject having gastroenteritis by administration of a composition described herein results in one or more of the following: prevention of the recurrence of gastroenteritis; reduction in the duration and/or severity of one or more symptoms associated with gastroenteritis; reduction in the number of symptoms associated with gastroenteritis; reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • compositions described herein are used to prevent and/or treat a fungal infection or a disease caused by or associated therewith.
  • beta defensins e.g., beta-defensin 1
  • Beta defensins e.g., beta-defensin 1
  • Exemplary fungi which can cause infection or disease to be prevented and/or treated with the compositions described herein include, without limitation, Blastomyces, Paracoccidioides, Sporothrix, Cryptococcus, Candida, Aspergillus, Histoplasma, Cryptococcus, Bipolaris, Cladophialophora, Cladosporium, Drechslera, Exophiala, Fonsecaea, Phialophora, Xylohypha, Ochroconis, Rhinocladiella, Scolecobasidium , and Wangiella .
  • prevention of a fungal infection in a subject or a disease caused by or associated therewith by administration of a composition described herein results in one or more of the following: prevention of the development or onset of a disease caused by or associated with fungal infection; and/or prevention of the spread of a fungal infection or a disease caused by or associated therewith from the subject to another subject or population of subjects.
  • treatment of a subject having a fungal infection or a disease caused by or associated therewith by administration of a composition described herein results in one or more of the following: prevention of the recurrence of the fungal infection or a disease caused by or associated therewith; reduction in the number of symptoms associated with the fungal infection or a disease caused by or associated therewith; reduction in organ failure associated with the fungal infection or a disease caused by or associated therewith; reduction of the duration and/or severity of the fungal infection or a disease caused by or associated therewith; reduction of the duration and/or severity of one or more symptoms of the fungal infection or a disease caused by or associated therewith; reduction in fungal cell count; reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject; an increase the survival of the subject; enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject; prevention of the spread of a fungus from a cell, tissue, organ of the subject to another cell, tissue, organ of the subject; prevention
  • Symptoms of a fungal infection with jock itch may include itching in the groin are and/or a red scaly rash.
  • Symptoms of athlete's foot may include scaling, flaking of the skin, itching of the feet and/or yellowish toenails.
  • Symptoms of a vaginal infection may include itching and irritation, burning with urination, and/or thick vaginal discharge.
  • Symptoms of fungal gastroenteritis may include vomiting and/or diarrhea.
  • Symptoms of a fungal infection of the lungs may include fever, cough and/or symptoms of pneumonia.
  • Symptoms of mouth yeast infection may include yellow-white patchy lesions/sores in the mouth or tongue.
  • Symptoms of Candidiasis of the genitalia include itching, burning, soreness, irritation and/or discharge.
  • the compositions described herein prevent the onset or development of one or more of the above-listed symptoms or other symptoms known in the art, or reduce duration and/or severity of one or more of these symptoms.
  • compositions described herein are used to prevent and/or treat Athlete's foot, jock itch, ringworm, or a fungal infection of nail, scalp or hair.
  • fungal infections can cause reddening, peeling, blistering, and scaling of the skin, itching, deformation and brittleness of affected nails, and/or brittle hair. They are caused by dermatophytes, a group of fungi that includes Trichophyton, Microsporum , and Epidermophyton species. Dermatophytes feed on keratin and rarely penetrate below the skin. Athlete's foot ( tinea pedis ) is found between the toes and sometimes covers the bottom of the foot.
  • Jock itch ( tinea cruris ) may extend from the groin to the inner thigh.
  • Scalp and hair infection ( tinea capitis ) affects hair shaft, primarily in children.
  • Finger or toenail infection ( tinea unguium ) typically affects toenails but may also affect fingernails.
  • Ringworm of the body ( tinea corporis ) can be found anywhere on the body.
  • Barber's itch tinea barbae ) affects the bearded portion of the face.
  • the compositions described herein are administered topically to treat any of the above-listed fungal infections (such as Athlete's foot, jock itch, nail, scalp and hair infections).
  • compositions described herein are administered at the site, or in the proximity to the site, of reddening, peeling, blistering, or scaling of the skin, or itching, deformation or brittleness of the nail (wherein such symptoms are associated with a fungal infection).
  • treatment of a subject having one of the above-listed fungal infections by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of the fungal infection (e.g., itching, reddening, peeling, blistering, or any other symptom of the fungal infection described herein or known in the art); reduction in the number of symptoms of the fungal infection; reduction of pain associated with a symptom of the fungal infection; prevention of the recurrence of a symptom of the fungal infection; prevention of the spread of the fungal infection from the subject to another subject; prevention of the onset or development of a symptom of the fungal infection; and/or enhancement or improvement of the prophylactic and/or therapeutic effect(s) of another therapy (e.g., anti-fungal therapy) in the subject.
  • another therapy e.g., anti-fungal therapy
  • a composition described herein is administered to a human infant, a human toddler, a human child, a human adult, and/or an elderly human who has one of the above-listed fungal infections or a symptom thereof.
  • the compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of a fungal infection subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • the compositions described herein are used to prevent and/or treat Sporotrichosis.
  • Sporotrichosis is a condition caused by the fungus Sporothrix schenckii , which is not a dermatophyte. It is an infection of the skin and subcutaneous tissue that has been abraded by thorny plants, pine needles, and sphagnum moss where this fungus normally resides.
  • the compositions described herein are administered topically to treat Aporotrichosis.
  • the compositions described herein are administered at the site, or in the proximity to the site, of Sporotrichosis infection.
  • treatment of a subject having Sporotrichosis by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of Sporotrichosis, reduction in the number of symptoms of Sporotrichosis; reduction of pain associated with a symptom of Sporotrichosis; prevention or reduction of frequency of the recurrence of a symptom of Sporotrichosis; prevention of the spread of Sporotrichosis from the subject to another subject; prevention of the onset or development of a symptom of Sporotrichosis; and/or enhancement or improvement of the prophylactic and/or therapeutic effect(s) of another therapy (e.g., anti-fungal therapy) in the subject.
  • another therapy e.g., anti-fungal therapy
  • compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of Sporotrichosis subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • compositions described herein are used to prevent and/or treat a fungal infection of a wound (e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn). In another specific embodiment, the compositions described herein are not used to prevent and/or treat a fungal infection of a wound.
  • a wound e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn.
  • the compositions described herein are not used to prevent and/or treat a fungal infection of a wound.
  • compositions described herein are used to prevent and/or treat a yeast infection or a disease caused by or associated therewith.
  • the ability of sNAG nanofibers to induce beta defensins may contribute to the anti-yeast activity of the sNAG nanofibers.
  • Beta defensins have been shown to have anti-yeast activity.
  • Exemplary yeast which can cause infection or disease to be prevented and/or treated with the compositions described herein include, without limitation, Aciculoconidium, Botryoascus, Brettanomyces, Bullera, Bulleromyces, Candida, Citeromyces, Clavispora, Cryptococcus, Cystofilobasidium, Debaromyces, Debaryomyces, Dekkera, Dipodascus, Endomyces, Endomycopsis, Erythrobasidium, Fellomyces, Filobasidium, Guilliermondella, Hanseniaspora, Hansenula, Hasegawaea, Hyphopichia, Issatchenkia, Kloeckera, Kluyveromyces, Komagataella, Leucosporidium, Lipomyces, Lodderomyces, Malassezia - Mastigomyces, Metschnikowia, Mrakia, Nadsonia, Octosporomyces, Oosporidium,
  • prevention of a yeast infection of a subject or a disease caused by or associated therewith by administration of a composition described herein results in one or more of the following: prevention of the development or onset of a disease caused by or associated with a yeast infection; and/or prevention of the spread of a yeast infection or a disease caused by or associated therewith from the subject to another subject or population of subjects.
  • treatment of a subject having a yeast infection or a disease caused by or associated therewith by administration of a composition described herein results in one or more of the following: prevention of the recurrence of the yeast infection or a disease caused by or associated therewith; reduction in the number of symptoms associated with the yeast infection or a disease caused by or associated therewith; reduction in organ failure associated with the yeast infection or a disease caused by or associated therewith; reduction of the duration and/or severity of the yeast infection or a disease caused by or associated therewith; reduction of the duration and/or severity of one or more symptoms of the yeast infection or a disease caused by or associated therewith; reduction in yeast cell count; reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject; an increase the survival of the subject; enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject; prevention of the spread of a yeast from a cell, tissue, organ of the subject to another cell, tissue, organ of the subject; prevention of the development or onset of a
  • compositions described herein are used to prevent and/or treat Candidiasis.
  • Candidiasis is a common yeast infection that is due primarily to the overgrowth of Candida albicans and other species of Candida , which are part of the normal flora. In the mouth, candidiasis causes redness and white patches and is called “thrush.” In children, Candida can cause diaper rash. In women, it can cause genital itching and vaginal discharge that is referred to as a “yeast infection.” Candidiasis can also cause a variety of other infections, including nail infections, and can become systemic—especially in those who are immunocompromised. It is currently the fourth most common cause of hospital-acquired septicemia in the United States.
  • compositions described herein are administered topically to treat Candidiasis (e.g, administered topically to the skin or topically to the genital area, such as intravaginally).
  • compositions described herein are administered at the site, or in the proximity to the site, of redness, white patches or genital itching (wherein such symptoms are associated with Candidiasis).
  • treatment of a subject having Candidiasis by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of Candidiasis, reduction in the number of symptoms of Candidiasis; reduction of pain associated with a symptom of Candidiasis; prevention or reduction of frequency of the recurrence of a symptom of Candidiasis; prevention of the spread of Candidiasis from the subject to another subject; prevention of the onset or development of a symptom of Candidiasis; and/or enhancement or improvement of the prophylactic and/or therapeutic effect(s) of another therapy (e.g., anti-yeast therapy) in the subject.
  • another therapy e.g., anti-yeast therapy
  • compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of a Candida infection subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • the compositions described herein are used to prevent and/or treat Tinea versicolor .
  • Symptoms of Tinea versicolor include, but are not limited to, multicolored patches or lesions on the skin. It is a condition that is common in young adults.
  • the compositions described herein are administered topically to treat Tinea versicolor .
  • the compositions described herein are administered at the site, or in the proximity to the site, of Tinea versicolor infection.
  • treatment of a subject having Tinea versicolor by administration of a composition described herein results in one or more of the following: reduction of the severity and/or duration of a symptom of Tinea versicolor , reduction in the number of symptoms of Tinea versicolor ; reduction of pain associated with a symptom of Tinea versicolor ; prevention or reduction of frequency of the recurrence of a symptom of Tinea versicolor ; prevention of the spread of Tinea versicolor from the subject to another subject; prevention of the onset or development of a symptom of Tinea versicolor ; and/or enhancement or improvement of the prophylactic and/or therapeutic effect(s) of another therapy (e.g., anti-yeast therapy) in the subject.
  • another therapy e.g., anti-yeast therapy
  • compositions described herein can be administered daily (e.g., once or twice a day) until the symptoms of a Tinea versicolor infection subside (e.g., for 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12 days, 2 weeks, 3 weeks, 4 weeks, or more than 4 weeks).
  • the compositions described herein are used to prevent and/or treat osteomyelitis.
  • Osteomyelitis is an infection of the bone or bone marrow, which can be caused by a bacteria or a fungus
  • Osteomyeltitis can be diagnosed based on radiologic results showing a lytic center with a ring of sclerosis, and culture of material can taken from a bone biopsy to identify the specific pathogen.
  • the compositions described herein are administered to a patient having (e.g., diagnosed with) osteomyelitis to treat osteomyelitis.
  • the compositions described herein are used to treat osteomyelitis caused by a fungal infection.
  • compositions described herein are used to treat an infection, wherein the infection is not caused by a bacteria.
  • the compositions described herein are used to treat osteomyelitis caused by any infection (including, but not limited to, a bacterial infection).
  • the compostions described herein are administered topically to a surface of a tissue (e.g., to the surface of a bone or in proximity to the surface of a bone) of a patient after surgery.
  • the compositions described herein can be administered to an area of the knee after knee replacement surgery, to an area of the hip after hip replacement surgery, or to an area of the elbow after elbow replacement surgery.
  • treatment of a subject having osteomyelitis by administration of a composition described herein results in one or more of the following: reduction in the duration and/or severity of one or more symptoms associated with osteomyelitis (e.g., pain, inflammation); reduction in the number of symptoms associated with osteomyelitis; prevention or reduction of frequency or recurrence of osteomyelitis; reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • one or more symptoms associated with osteomyelitis e.g., pain, inflammation
  • reduction in the number of symptoms associated with osteomyelitis e.g., prevention or reduction of frequency or recurrence of osteomyelitis
  • reduction of the incidence of hospitalization of the subject reducing of the hospitalization length of the subject
  • enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject e.g., depression, depression, depression, depression, depression, depression, depression,
  • compositions described herein are used to prevent and/or treat a yeast infection of a wound (e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn). In another specific embodiment, the compositions described herein are not used to prevent and/or treat a yeast infection of a wound.
  • a wound e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn.
  • the compositions described herein are not used to prevent and/or treat a yeast infection of a wound.
  • a subject treated for a viral infection, a fungal infection or an yeast infection (such as any of the viral, fungal or yeast infections described herein) using the sNAG compositions described herein does not have a bacterial infection.
  • a subject treated for a viral, a fungal, or an yeast infection (such as any of the viral, fungal or yeast infections described herein) using the sNAG compositions described herein has both a bacterial infection and a viral, a fungal or an yeast infection.
  • such infections are in the same location in the subject's organism. Mother embodiments, such infections are in different locations in the subject's organism.
  • the compositions described herein are used to treat skin diseases. Without being bound by any mechanism of action, the ability of sNAG nanofibers to induce beta defensins may contribute to the activity of the sNAG nanofibers in treatment of skin diseases. Beta defensins have been shown to have activity in skin diseases.
  • the compositions described herein are used to treat dermatitis (e.g., atopic dermatitis). In a specific embodiment, the compositions are used to prevent and/or treat atopic dermatitis in a premature human infant, a human infant, a human toddler, or a human child.
  • compositions described herein are used to treat psoriasis (e.g., Psoriasis vulgaris, Psoriasis erythroderma, Pustular psoriasis, nail psoriasis, or guttate psoriasis).
  • psoriasis e.g., Psoriasis vulgaris, Psoriasis erythroderma, Pustular psoriasis, nail psoriasis, or guttate psoriasis.
  • the compositions are used to treat psoriasis in a premature human infant, a human infant, a human toddler, or a human child.
  • treatment of a subject having a skin disease by administration of a composition described herein results in one or more of the following: prevention of the recurrence of the skin disease; reduction in the number of symptoms associated with the skin disease; reduction in the severity or duration of one or more symptoms associated with the skin disease; reduction of the incidence of hospitalization of the subject; reduction of the hospitalization length of the subject; and/or enhancement or improvement of the prophylactic or therapeutic effect(s) of another therapy in the subject.
  • Symptoms of dermatitis include but are not limited to rashes (e.g., a bumpy rash), blisters, redness of the skin, swelling, itching, skin lesions, oozing, and/or scarring. Such symptoms often appear on the neck, wrist, forearm, thigh or ankle; but may also appear on the genital area. Common symptoms of atopic dermatitis include but are not limited to dry, itchy, and/or red skin.
  • Symptoms of psoriasis include but are not limited to plaques (e.g., raised areas of inflamed skin covered with silvery white scaly skin), itching, swelling, pain, pustules (e.g., raised bumps filled with noninfectious pus), smooth inflamed patches of skin, small scaly lesions, and/or thickening and discoloring of the nails.
  • the compositions described herein prevent the onset or development of one or more of the above-listed symptoms or other symptoms known in the art, or reduce duration and/or severity of one or more of these symptoms.
  • composition described herein is not used to prevent and/or treat a bacterial infection or a disease caused by or associated therewith. In one embodiment, composition described herein is not used to prevent and/or treat S. aureus infection or a disease caused by or associated with such infection. In another specific embodiment, a composition described herein is not used to prevent and/or treat a bacterial infection of a wound (e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn).
  • a wound e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn.
  • the disease to be treated and/or prevented by administration of a composition described herein is not a wound (e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn).
  • a wound e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn.
  • a composition described herein may be administered to a na ⁇ ve subject, i.e., a subject that does not have a disease or infection. In one embodiment, a composition described herein is administered to a na ⁇ ve subject that is at risk of acquiring a disease or infection.
  • a sNAG nanofiber composition described herein may be administered to a patient who has been diagnosed with a disease or infection.
  • a composition described herein may be administered to a patient who displays one or more symptoms of a disease or infection.
  • a patient is diagnosed with a disease or infection prior to administration of a composition described herein
  • the compositions described herein are administered to patients diagnosed with an infection.
  • the compositions described herein may be administered to a patient when a pathogen (e.g., virus, fungi or yeast) is detected in a biological sample taken from the patient.
  • a biological sample is obtained from the site or area to be treated by the compositions described herein or an area to which the compositions described herein are to be administered.
  • a swab is used to collect cells or pus from the site of the suspected infection to detect an infection.
  • a fluid is aspirated from the suspected site of an infection (e.g., a wound) to detect an infection.
  • a tissue biopsy is performed to detect an infection.
  • a wound culture may be performed to detect an infection.
  • the biological sample is obtained from blood, urine, sputum or feces of the patient.
  • a blood or a urine test may be performed to detect an infection (e.g., when an infection is suspected to have spread into the blood or other tissues/organs).
  • the collected sample e.g., cells, tissues or fluid
  • DNA detection methods such as PCR for presence of one or more types of bacteria.
  • immunofluorescence analysis, serology, culture e.g., blood agar culture
  • any other test known and/or practiced in the art may be used for laboratory diagnosis of an infection.
  • the compositions described herein may be administered to a patient diagnosed with or displaying one or more symptoms of a disease, e.g., a cancer, an IBD, Crohn's disease, dermatitis, psoriasis or an infection (e.g., viral, yeast or fungi infection).
  • a patient is diagnosed with a disease (e.g., one of the diseases listed above) or displays one or more symptoms of a disease prior to administration of a composition described herein.
  • a disease may be diagnosed by any method known to a skilled artisan, including evaluation of the patient's symptoms and/or detection of a pathogen in a biological sample of the patient (e.g., as described above).
  • the compositions described herein may be administered to a patient diagnosed with a disease by a treating physician or another medical professional.
  • a patient may use the compositions described herein upon detection of one or more symptoms of a disease.
  • a subject to be administered a composition described herein is a subject with no or low level of expression of one or more defensin peptides or a mutation/deletion in a gene or genes encoding one or more defensin peptides.
  • a subject to be administered a composition described herein is a subject with no or low or altered level of expression of one or more ⁇ -defensins (e.g., DEFA1, DEFA1B, DEFA3, DEFA4, DEFA5, DEFA6), one or more ⁇ -defensins (e.g., DEFB1, DEFB2, DEFB4, DEFB103A, DEFB104A, DEFB105B, DEFB107B, DEFB108B, DEFB110, DEFB112, DEFB114, DEFB118, DEFB119, DEFB123, DEFB124, DEFB125, DEFB126, DEFB127, DEFB128, DEFB129, DEFB131, DEFB136), and/or one or more 9-defensins (e.g., DEFT1P).
  • ⁇ -defensins e.g., DEFA1, DEFA1B, DEFA3, DEFA4, DEFA5, DEFA6
  • ⁇ -defensins e.g., DEFB
  • a subject to be administered a composition described herein is a subject with no or low or altered level of expression of one or more of DEFA1, DEFA3, DEFA4, DEFA5, DEFB1, DEFB3, DEFB103A, DEFB104A, DEFB108B, DEFB112, DEFB114, DEFB118, DEFB119, DEFB123, DEFB124, DEFB125, DEFB126, DEFB128, DEFB129 and DEFB131.
  • a subject to be administered a composition described herein is a subject with no or low or altered level of expression of one or more Toll receptors (e.g., TLR1, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TLR10, TLR11, and/or TLR12).
  • a subject to be administered a composition described herein is a subject with no or low or altered level of expression of one or more of IL-1, CEACAM3, SPAG11, SIGIRR (IL1-like receptor), IRAK1, IRAK2, IRAK4, TBK1, TRAF6 and IKKi.
  • a subject to be administered a composition described herein is a subject with no or low or altered level of expression of one or more of IRAK2, SIGIRR, TLR1, TLR2, TLR4, TLR7, TLR8, TLR10 and TRAF6.
  • a low level of expression of a gene is a level that is lower (e.g., more than 1.25 fold, 1.5 fold, 2 fold, 2.5 fold, 3 fold, 3.5 fold, 4 fold, 4.5 fold, 5 fold, 6 fold, 7 fold, 8 fold, 9 fold, 10 fold lower) than the normal level of expression.
  • An altered level of expression of a gene is a level that differs (e.g., by more than 20%, 25%, 30%, 50%, 75%, 100%, 150%, 200%, 250%, 300%) from the normal level of expression.
  • the “normal” expression of one or more defensin genes is: (i) the average expression level known to be found in subjects not displaying symptoms or not diagnosed with the disease or infection to be treated; (ii) the average expression level detected in three, five, ten, twenty, twenty-five, fifty or more subjects not displaying symptoms or not diagnosed with the disease or infection to be treated; and/or (iii) the level of expression detected in a patient to be administered a composition described herein before the onset of the disease or infection.
  • a composition described herein is administered to a patient who has been diagnosed with a solid tumor cancer, such as bone and connective tissue sarcomas, brain cancer, breast cancer, ovarian cancer, kidney cancer, pancreatic cancer, esophageal cancer, stomach cancer, lung cancer (e.g., small cell lung cancer (SCLC), non-small cell lung cancer (NSCLC), throat cancer, and mesothelioma), liver cancer, and prostate cancer.
  • a composition described herein is administered to a patient who has been diagnosed with Kaposi's sarcoma.
  • a composition described herein is administered to a patient who has been diagnosed with a skin cancer, such as melanoma, basal cell carcinoma, and squamous cell carcinoma.
  • a skin cancer such as melanoma, basal cell carcinoma, and squamous cell carcinoma.
  • a composition described herein is administered to a patient who has (e.g., has been diagnosed with) inflammatory bowel disease (e.g., ulcerative colitis) or displays one, two or more symptoms of inflammatory bowel disease.
  • inflammatory bowel disease e.g., ulcerative colitis
  • a composition described herein is administered to a patient who has (e.g., has been diagnosed with) Crohn's disease (e.g., ileal Crohn's disease) or displays one or more symptoms of Crohn's disease.
  • Crohn's disease e.g., ileal Crohn's disease
  • a composition described herein is administered to a patient who has (e.g., has been diagnosed with) a disease caused by a virus or an infection associated with a virus (such as any disease caused by a virus or an infection associated with a virus described herein), e.g., the patient has been infected by respiratory syncytial virus (RSV), influenza virus (influenza A virus, influenza B virus, or influenza C virus), human metapneumovirus (HMPV), rhinovirus, parainfluenza virus, SARS Coronavirus, human immunodeficiency virus (HIV), hepatitis virus (A, B, C), ebola virus, herpes simplex virus (e.g., HSV-1, HSV-2), rubella, variola major, and/or variola minor.
  • RSV respiratory syncytial virus
  • influenza virus influenza A virus, influenza B virus, or influenza C virus
  • HMPV human metapneumovirus
  • rhinovirus parainfluenza virus
  • a composition described herein is administered to a patient who displays one, two or more symptoms of a disease caused by a virus or an infection associated with a virus (such as any disease caused by a virus or an infection associated with a virus described herein).
  • a composition described herein is administered to a patient who has (e.g., has been diagnosed with) a wound (e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn) that has been infected by a virus.
  • a wound e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn
  • a composition described herein is not administered to a patient who has been diagnosed with a wound that has been infected by a virus.
  • a composition described herein is administered to a patient who has (e.g., has been diagnosed with) a disease caused by a fungus or an infection associated with a fungus (any disease caused by a fungus or an infection associated with a fungus described herein); e.g., the patient has been infected by Blastomyces, Paracoccidioides, Sporothrix, Cryptococcus, Candida, Aspergillus, Histoplasma, Cryptococcus, Bipolaris, Cladophialophora, Cladosporium, Drechslera, Exophiala, Fonsecaea, Phialophora, Xylohypha, Ochroconis, Rhinocladiella, Scolecobasidium , and/or Wangiella .
  • a composition described herein is administered to a patient who displays one, two or more symptoms of a disease caused by a fungus or an infection associated with a fungus (such as any disease caused by a virus or an infection associated with a fungus described herein).
  • a composition described herein is administered to a patient who has (e.g., has been diagnosed with) a wound (e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn) that has been infected by a fungus.
  • a wound e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn
  • a composition described herein is not administered to a patient who has been diagnosed with a wound that has been infected by a fungus.
  • a composition described herein is administered to a patient who has (e.g., has been diagnosed with) a disease caused by a yeast or an infection associated with a yeast, e.g., the patient has been infected by Aciculoconidium, Botryoascus, Brettanomyces, Bullera, Bulleromyces, Candida, Citeromyces, Clavispora, Cryptococcus, Cystofilobasidium, Debaromyces, Debaryomyces, Dekkera, Dipodascus, Endomyces, Endomycopsis, Erythrobasidium, Fellomyces, Filobasidium, Guilliermondella, Hanseniaspora, Hansenula, Hasegawaea, Hyphopichia, Issatchenkia, Kloeckera, Kluyveromyces, Komagataella, Leucosporidium, Lipomyces, Lodderomyces, Malassezia - Mastigo
  • a composition described herein is administered to a patient who has (e.g., has been diagnosed with) a wound (e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn) that has been infected by a yeast.
  • a wound e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn
  • a composition described herein is not administered to a patient who has been diagnosed with a wound that has been infected by a yeast.
  • a composition described herein is administered to a patient who has (e.g., has been diagnosed with) a skin disease or displays one, two or more symptoms of a skin disease.
  • a composition described herein is administered to a patient who has been diagnosed with dermatitis (e.g., atopic dermatitis) or displays one, two or more symptoms of dermatitis.
  • a composition described herein is administered to a patient who has been diagnosed with psoriasis or displays one, two or more symptoms of psoriasis.
  • a composition described herein is administered to an immunosuppressed patient, and/or a patient susceptible to acute or chronic disease or infection (e.g., an HIV positive patient, or a patient immunosuppressed as a result of cancer treatment or a transplantation procedure).
  • a composition described herein is administered to a patient diagnosed with cystic fibrosis.
  • a composition described herein is administered to a patient with a disease or infection before symptoms of the disease or infection manifest or before symptoms of the disease or infection become severe (e.g., before the patient requires treatment or hospitalization). In some embodiments, a composition described herein is administered to a patient with a disease or infection after symptoms of the disease or infection manifest or after symptoms of the disease or infection become severe (e.g., after the patient requires treatment or hospitalization).
  • a subject to be administered a composition described herein is an animal.
  • the animal is a bird.
  • the animal is a canine.
  • the animal is a feline.
  • the animal is a horse.
  • the animal is a cow.
  • the animal is a mammal, e.g., a horse, swine, mouse, or primate, preferably a human.
  • a subject to be administered a composition described herein is a human adult. In certain embodiments, a subject to be administered a composition described herein is a human adult more than 50 years old. In certain embodiments, a subject to be administered a composition described herein is an elderly human subject.
  • a subject to be administered a composition described herein is a human toddler. In certain embodiments, a subject to be administered a composition described herein is a human child. In certain embodiments, a subject to be administered a composition described herein is a human infant. In certain embodiments, a subject to be administered a composition described herein is a premature human infant.
  • a composition described herein is not administered to a subject to prevent and/or treat a bacterial infection or a disease caused by or associated therewith. In one embodiment, a composition described herein is not administered to a subject to prevent and/or treat S. aureus infection or a disease caused by or associated with such infection. In another specific embodiment, a composition described herein is not administered to a subject to prevent and/or treat a bacterial infection of a wound (e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn).
  • a wound e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn.
  • a composition described herein is not administered to a subject to treat a wound (e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn).
  • a wound e.g., an open wound such as an incision, a laceration, a penetration, an abrasion, or a burn.
  • methods are described herein for treating or preventing an infection and/or a disease or a symptom thereof, wherein a composition comprising the sNAG nanofibers is topically administered to a patient in need of such treatment.
  • a sNAG nanofiber composition is applied topically to tissue or organ which has an increased risk of an infection or a disease.
  • an effective amount of the sNAG nanofibers and/or a sNAG nanofiber composition is administered to a subject.
  • a composition comprising the sNAG nanofibers is administered topically to the site of an infection or a disease in a patient or to the site affected by an infection or a disease.
  • a composition comprising the sNAG nanofibers is administered topically to the site and around the site of an infection or a disease in a patient or to the site affected by an infection or a disease.
  • a composition comprising sNAG nanofibers is applied in proximity to the site of an infection or disease in a patient or in proximity to the site affected by an infection or a disease.
  • a composition comprising the sNAG nanofibers is administered topically to the site at high risk of an infection or a disease associated with such infection.
  • the sNAG nanofiber compositions described herein may be administered by any of the many suitable means of topical administration which are well known to those skilled in the art, including but not limited to topically to the skin, topically to any other surface of the body (e.g., mucosal surface), by inhalation, intranasally, vaginally, rectally, buccally, or sublingually.
  • the mode of topical administration may vary depending upon the infection or disease to be treated or prevented.
  • the sNAG nanofiber compositions can be formulated for the various types of topical administration.
  • the compositions disclosed herein are applied topically, for example to the skin of a patient in need of such treatment or to another tissue of a patient in need of such treatment.
  • the compositions may be applied directly to the site of a disease or infection and/or in the proximity to the site of a disease or infection.
  • the compositions may be applied directly to a site where a disease or infection might potentially develop (e.g., to an open wound).
  • a composition comprising sNAG nanofibers is applied to the skin of a patient.
  • a composition may be applied topically to the skin of a patient for treating or preventing a disease or infection of the skin.
  • a composition described herein may be applied topically to a mucosal surface of a patient.
  • a composition may be applied topically to the oral mucosa for treating or preventing a disease or infection of the mouth or gums.
  • a composition described herein may be applied topically to a genital, urinal or anal surface/area of a patient.
  • a composition may be applied topically to genital, urinal or anal surface/area for treating or preventing a genital, urinal or anal disease or infection.
  • compositions comprising sNAG nanofibers are not solid or barrier-forming.
  • a composition described herein may be applied as a spray into the oral cavity and/or respiratory system of a patient.
  • a composition may be applied as a spray for treating or preventing a disease or infection of the mouth, nose, gums, throat or lungs.
  • the composition may be formulated to be administered as an inhaler.
  • a composition described herein may be applied as a suppository in the rectum, vagina or urethra of a patient.
  • such composition may be applied as a suppository for treating or preventing a disease or infection of the digestive tract, urinary tract or reproductive tract.
  • a composition described herein may be applied topically with a syringe or another type of applicator (e.g., a spatula, a cotton swab, a tube such as a squeeze tube) suitable for topical delivery of the composition to the patient.
  • a composition described herein formulated as a suspension e.g., thick suspension
  • a liquid solution, a cream, an ointment, or a gel can be administered topically to the skin, mucous membrane or other surface tissue of a patient via an applicator (e.g., syringe).
  • a composition described herein may be applied at the site of a surgical procedure.
  • such composition may be sprayed, applied as a cream, suspension (e.g., a thick suspension), liquid solution, ointment, gel, membrane, or powder, or coated on the surface of the tissue or organ to be subjected to a surgical procedure or that has been subjected to the surgical procedure.
  • a composition described herein is applied at the site of the surgical incision, at the site of the excised tissue, or at the site of surgical stitches or sutures.
  • Such administration of a composition described herein may prevent a postsurgical infection or may prevent recurrence of a disease for which the surgery was indicated.
  • a composition described herein may be used during or after a surgical procedure which is known to pose high risk of a viral, yeast, or fungal infection.
  • Surgical procedures that are known to pose high risk of an infection include bowel resection, gastrointestinal surgical procedures, kidney surgery, etc.
  • a composition described herein may be applied at the site of any of the above-listed or other surgical procedures.
  • a composition described herein may be coated on a device, for example an oral hygiene product, a catheter, a surgical instrument or another product, to be used in or inserted into a patient, in order to treat or prevent a disease or infection in a patient.
  • a device for example an oral hygiene product, a catheter, a surgical instrument or another product, to be used in or inserted into a patient, in order to treat or prevent a disease or infection in a patient.
  • the compositions disclosed herein are applied topically to the site of a solid tumor or skin cancer.
  • the compositions are applied directly to the solid tumor or skin cancer itself.
  • the compositions are applied directly to the site of a solid tumor or skin cancer, wherein all or part of the tumor or skin cancer has been removed (e.g., surgically removed).
  • the compositions disclosed herein are topically administered to the site and/or around the site from which a solid tumor or skin cancer has been excised or removed.
  • compositions may be sprayed, applied as a suspension, liquid solution, cream, ointment, gel, membrane, or powder, or coated on the surface of an organ or tissue from which a solid tumor was excised.
  • the compositions described herein are sprayed or coated at and around the site or sites of removed or excised solid tumor or skin cancer.
  • methods contemplated herein include a step that includes detection/diagnosis of a disease or an infection in a patient.
  • detection/diagnosis involves a test or assay for one or more pathogen (e.g., a virus, a fungi, or an yeast) in a biological sample of the patient.
  • pathogen e.g., a virus, a fungi, or an yeast
  • diagnosis involves assessing whether the patient has one or more symptoms of a disease (e.g., IBD, Crohn's disease, cancer, dermatitis, psoriasis, or a disease associated with a viral, fungal, or yeast infection).
  • compositions described herein may exhibit sustained release properties and/or may be administered in a formulation resulting in a sustained release of such compositions.
  • the sNAG nanofibers biodegrade over time as described in Section 5.1, supra, and these properties of sNAG nanofibers may lead to or contribute to sustained release of the compositions described herein.
  • the compositions described herein are formulated to display sustained release capabilities using any methods known in the art.
  • the compositions described herein may exhibit sustained release over a time period equal to or more than about 6 hours, 12 hours, 18 hours, 24 hours (1 day), 2 days, 3 days, 5 days, 7 days (1 week), 10 days, 14 days (2 weeks), 3 weeks or 4 weeks after administration of the composition to the patient.
  • Contemplated treatment regimes include a single dose or a single application of a sNAG nanofiber composition; two doses or two applications of a sNAG nanofiber composition; or a regiment of multiple doses or multiple applications of a sNAG nanofiber composition.
  • a dose or an application may be administered hourly, daily, weekly or monthly.
  • a dose of a sNAG nanofiber composition may be administered once a day, twice a day, three times a day, four times a day, once a week, 2 times a week, 3 times a week, every other day, once in 2 weeks, once in 3 weeks, once in 4 weeks, once a month, or once in two months.
  • a sNAG nanofiber composition may be administered for a duration equal to or greater than 2 days, 3 days, 4 days, 5 days, 1 week, 2 weeks, 3 weeks, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 9 months, 1 year, 1.5 years, 2 years, 2.5 years, 3 years, 4 years, 5 years, 7 years, 10 years or more.
  • a sNAG fiber composition is administered to a patient once or twice a day for a duration equal to or greater than 2 days, 3 days, 4 days, 5 days, 1 week, 2 weeks, 3 weeks, 1 month, 2 months, 3 months, 4 months, 5 months, 6 months, 9 months, or 1 year.
  • a sNAG nanofiber composition does not cause any side effects or causes only mild side effects during the duration of the treatment. In another embodiment, a sNAG nanofiber composition does not cause irritation (e.g., moderate or severe irritation) or allergy (e.g., moderate or severe allergy).
  • irritation e.g., moderate or severe irritation
  • allergy e.g., moderate or severe allergy
  • the concentration of sNAG nanofibers in a composition may vary.
  • an effective amount of sNAG nanofibers are used in the compositions described herein to treat the diseases described herein.
  • An effective amount may be an amount sufficient to achieve one or more of the effects described herein, for example an amount effective to treat a disease or reduce or eradicate one or more symptoms of a disease.
  • a composition may comprise about 0.2 to 20 mg/cm 2 of sNAG nanofibers per dose/application of the composition in a form suitable for topical delivery to a patient.
  • a composition described herein comprises about 0.25 to 20 mg/cm 2 , about 0.5 to 20 mg/cm 2 , about 1 to 20 mg/cm 2 , about 1 to 15 mg/cm 2 , about 1 to 12 mg/cm 2 , about 1 to 10 mg/cm 2 , about 1 to 8 mg/cm 2 , about 1 to 5 mg/cm 2 , about 2 to 8 mg/cm 2 , or about 2 to 6 mg/cm 2 of sNAG nanofibers per dose/application of the composition in a form suitable for topical delivery to a patient.
  • compositions described herein can comprise about 5 to 50 mg/ml of sNAG nanofibers per dose/application of the composition in a form suitable for topical delivery to a patient.
  • a composition described herein comprises about 5 to 40 mg/ml, about 5 to 35 mg/ml, about 10 to 50 mg/ml, about 10 to 40 mg/ml, about 10 to 35 mg/ml, about 10 to 30 mg/ml, about 15 to 40 mg/ml, about 15 to 35 mg/ml, about 15 to 30 mg/ml, or about 20 to 30 mg/ml of sNAG nanofibers per dose/application of the composition in a form suitable for topical delivery to a patient.
  • a composition described herein comprises about 10 mg/ml, 12 mg/ml, 15 mg/ml, 20 mg/ml, 25 mg/ml or 30 mg/ml of sNAG nanofibers per dose/application of the composition in a form suitable for topical delivery to a patient.
  • compositions described herein can comprise an amount of total solution or suspension (comprising sNAG nanofibers) in the range of about 50 to 100 ⁇ l, 50 to 200 ⁇ l, 50 to 250 ⁇ l, 50 to 300 ⁇ l, 50 to 350 ⁇ l, 50 to 400 ⁇ l, 50 to 450 ⁇ l, 50 to 500 ⁇ l, 100 to 200 ⁇ l, 100 to 300 ⁇ l, 100 to 400 ⁇ l, 100 to 500 ⁇ l per 0.5 cm 2 or 1 cm 2 of the surface to be treated in a patient (e.g., skin, mucosal surface or other tissue surface).
  • the total solution or suspension can comprise saline, buffer, solution (e.g., Hank buffer solution), or any other physiologically compatible solution.
  • the sNAG nanofibers described herein or compositions thereof may be administered to a subject in combination with one or more other therapies.
  • the one or more other therapies may be beneficial in the treatment or prevention of a disease or may ameliorate a symptom or condition associated with a disease.
  • the therapies are administered less than 5 minutes apart, less than 30 minutes apart, 1 hour apart, at about 1 hour apart, at about 1 to about 2 hours apart, at about 2 hours to about 3 hours apart, at about 3 hours to about 4 hours apart, at about 4 hours to about 5 hours apart, at about 5 hours to about 6 hours apart, at about 6 hours to about 7 hours apart, at about 7 hours to about 8 hours apart, at about 8 hours to about 9 hours apart, at about 9 hours to about 10 hours apart, at about 10 hours to about 11 hours apart, at about 11 hours to about 12 hours apart, at about 12 hours to 18 hours apart, 18 hours to 24 hours apart, 24 hours to 36 hours apart, 36 hours to 48 hours apart, 48 hours to 52 hours apart, 52 hours to 60 hours apart, 60 hours to 72 hours apart, 72 hours to 84 hours apart, 84 hours to 96 hours apart, or 96 hours to 120 hours part.
  • two or more therapies are administered within the same patent visit.
  • the one or more therapies is surgery.
  • surgery is performed to remove all or part of a solid tumor or skin cancer, and a composition described herein is administered to the site of the tumor before, during, and/or after the surgery.
  • the one or more therapies is radiation therapy.
  • the one or more therapies is an anti-viral agent.
  • Any anti-viral agents well-known to one of skill in the art may used in combination with the sNAG nanofibers described herein or compositions thereof.
  • Non-limiting examples of anti-viral agents include proteins, polypeptides, peptides, fusion proteins antibodies, nucleic acid molecules, organic molecules, inorganic molecules, and small molecules that inhibit and/or reduce the attachment of a virus to its receptor, the internalization of a virus into a cell, the replication of a virus, or release of virus from a cell.
  • anti-viral agents include, but are not limited to, nucleoside analogs (e.g., zidovudine, acyclovir, gangcyclovir, vidarabine, idoxuridine, trifluridine, and ribavirin), foscarnet, amantadine, peramivir, rimantadine, saquinavir, indinavir, ritonavir, alpha-interferons and other interferons, AZT, zanamivir (Relenza®), and oseltamivir (Tamiflu®).
  • nucleoside analogs e.g., zidovudine, acyclovir, gangcyclovir, vidarabine, idoxuridine, trifluridine, and ribavirin
  • foscarnet e.g., amantadine, peramivir, rimantadine, saquinavir, indinavir, ritonavir
  • influenza virus vaccines e.g., Fluarix® (GlaxoSmithKline), FluMist® (MedImmune Vaccines), Fluvirin® (Chiron Corporation), Flulaval® (GlaxoSmithKline), Afluria® (CSL Biotherapies Inc.), Agriflu® (Novartis) or Fluzone® (Aventis Pasteur).
  • influenza virus vaccines e.g., Fluarix® (GlaxoSmithKline), FluMist® (MedImmune Vaccines), Fluvirin® (Chiron Corporation), Flulaval® (GlaxoSmithKline), Afluria® (CSL Biotherapies Inc.), Agriflu® (Novartis) or Fluzone® (Aventis Pasteur).
  • the one or more therapies is an anti-cancer agent.
  • the anti-cancer agent is a chemotherapeutic agent. Any anti-cancer agents known to one of skill in the art may used in combination with the sNAG nanofibers described herein or compositions thereof.
  • anti-cancer agents include: acivicin; anthracyclin; anthramycin; azacitidine (Vidaza); bisphosphonates (e.g., pamidronate (Aredria), sodium clondronate (Bonefos), zoledronic acid (Zometa), alendronate (Fosamax), etidronate, ibandornate, cimadronate, risedromate, and tiludromate); carboplatin; chlorambucil; cisplatin; cytarabine (Ara-C); daunorubicin hydrochloride; decitabine (Dacogen); demethylation agents, docetaxel; doxorubicin; EphA2 inhibitors; etoposide; camrabine; fluorouracil; gemcitabine; histone deacetylase inhibitors (HDACs); interleukin H (including recombinant interleukin
  • WO 02/098370 which is incorporated herein by reference in its entirety
  • melphalan methotrexate; mitomycin; oxaliplatin; paclitaxel; puromycin; riboprine; spiroplatin; tegafur; teniposide; vinblastine sulfate; vincristine sulfate; vorozole; zeniplatin; zinostatin; and zorubicin hydrochloride.
  • cancer therapies include, but are not limited to angiogenesis inhibitors; antisense oligonucleotides; apoptosis gene modulators; apoptosis regulators; BCR/ABL antagonists; beta lactam derivatives; casein kinase inhibitors (ICOS); estrogen agonists; estrogen antagonists; glutathione inhibitors; HMG CoA reductase inhibitors; immunostimulant peptides; insulin-like growth factor-1 receptor inhibitor; interferon agonists; interferons; interleukins; lipophilic platinum compounds; matrilysin inhibitors; matrix metalloproteinase inhibitors; mismatched double stranded RNA; nitric oxide modulators; oligonucleotides; platinum compounds; protein kinase C inhibitors, protein tyrosine phosphatase inhibitors; purine nucleoside phosphorylase inhibitors; raf antagonists; signal transduction inhibitors; signal transduction modulators; translation inhibitors;
  • the therapy(ies) used in combination with the sNAG nanofibers described herein or compositions thereof is an anti-angiogenic agent.
  • anti-angiogenic agents include proteins, polypeptides, peptides, conjugates, antibodies (e.g., human, humanized, chimeric, monoclonal, polyclonal, Fvs, ScFvs, Fab fragments, F(ab)2 fragments, and antigen-binding fragments thereof) such as antibodies that specifically bind to TNF- ⁇ , nucleic acid molecules (e.g., antisense molecules or triple helices), organic molecules, inorganic molecules, and small molecules that reduce or inhibit angiogenesis.
  • nucleic acid molecules e.g., antisense molecules or triple helices
  • organic molecules e.g., inorganic molecules, and small molecules that reduce or inhibit angiogenesis.
  • anti-angiogenic agents can be found, e.g., in U.S. Publication No. 2005/0002934 A1 at paragraphs 277-282, which is incorporated by reference in its entirety.
  • the therapy(ies) used in accordance with the invention is not an anti-angiogenic agent.
  • the therapy(ies) used in combination with the sNAG nanofibers described herein or compositions thereof is an anti-inflammatory agent.
  • anti-inflammatory agents include non-steroidal anti-inflammatory drugs (NSAIDs) (e.g., celecoxib (CELEBREXTM), diclofenac (VOLTARENTM), etodolac (LODINETM), fenoprofen (NALFONTM), indomethacin (INDOCINTM), ketoralac (TORADOLTM), oxaprozin (DAYPROTM), nabumentone (RELAFENTM), sulindac (CLINORILTM), tolmentin (TOLECTINTM), rofecoxib (VIOXXTM), naproxen (ALEVETM, NAPROSYNTM), ketoprofen (ACTRONTM) and nabumetone (RELAFENTM)), steroidal anti-inflammatory drugs (e.g., glucocorticoids, dexac (LODINE
  • the therapy(ies) used in combination with the sNAG nanofibers described herein or compositions thereof is an alkylating agent, a nitrosourea, an antimetabolite, an anthracyclin, a topoisomerase II inhibitor, or a mitotic inhibitor.
  • Alkylating agents include, but are not limited to, busulfan, cisplatin, carboplatin, cholormbucil, cyclophosphamide, ifosfamide, decarbazine, mechlorethamine, mephalen, and themozolomide.
  • Nitrosoureas include, but are not limited to carmustine (BCNU) and lomustine (CCNU).
  • Antimetabolites include but are not limited to 5-fluorouracil, capecitabine, methotrexate, gemcitabine, cytarabine, and fludarabine.
  • Anthracyclins include but are not limited to daunorubicin, doxorubicin, epirubicin, idarubicin, and mitoxantrone.
  • Topoisomerase II inhibitors include, but are not limited to, topotecan, irinotecan, etopiside (VP-16), and teniposide.
  • Mitotic inhibitors include, but are not limited to taxanes (paclitaxel, docetaxel), and the vinca alkaloids (vinblastine, vincristine, and vinorelbine).
  • the therapy(ies) used in combination with the sNAG nanofibers described herein or compositions thereof is an anti-pain medication (e.g., an analgesic). In some embodiments, the therapy(ies) used in combination with the sNAG nanofibers described herein or compositions thereof is an anti-fever medication.
  • a pharmaceutical pack or kit comprising one or more of the sNAG nanofiber compositions described herein.
  • the pack or kit may comprise one or more containers filled with one or more ingredients comprising the compositions described herein.
  • the composition is preferably contained within a sealed, water proof, sterile package which facilitates removal of the composition without contamination.
  • Materials from which containers may be made include aluminum foil, plastic, or another conventional material that is easily sterilized.
  • the kit can contain material for a single administration or for multiple administrations of the composition, preferably wherein the material for each administration is provided in a separate, waterproof, sterile package.
  • a container having dual compartments is provided.
  • a first compartment contains any of the above-described sNAG nanofiber compositions described herein, while the second compartment contains another active agent such as another agent to be used in combination with the sNAG nanofiber composition.
  • the composition in the first compartment can be readily combined with the agent in the second compartment for subsequent administration to a patient.
  • the kit can also contain an applicator for administration of one or more of the sNAG nanofiber compositions described herein, and/or for administration of another active agent such as another agent to be used in combination with the sNAG nanofiber composition.
  • the kit comprises an applicator for topical administration of a sNAG nanofiber composition.
  • applicators for topical administration of a sNAG nanofiber composition include, without limitation, a syringe, a spatula, a tube (a squeeze tube), and a cotton swab.
  • kits designed for emergency or military use can also contain disposable pre-sterilized instruments, such as scissors, scalpel, clamp, tourniquet, elastic or inelastic bandages, or the like.
  • kit or pack can be a notice in the form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals or biological products, which notice reflects approval by the agency of manufacture, use or sale for human administration.
  • a kit can comprise a notice regarding FDA approval and/or instructions for use.
  • kits encompassed herein can be used in the above applications and methods.
  • sNAG nanofibers are produced and supplied by Marine Polymer Technologies and formed into suitable patches for wound treatment.
  • Wildtype C57 Black and Akt1 null mice were housed at the Medical University of South Carolina animal facilities. Wildtype and Akt1 null mice, ages ranging from eight to 12 weeks, were anesthetized with 50% pure oxygen and 50% isoflurane gas. Immediately before wounding, Nair Hair Removal Lotion was applied to their dorsum to remove any unwanted hair. A dorsal 4 mm circular area of skin was removed using an excision biopsy punch. Taliderm was placed onto each wound at day 0 or wounds were left untreated.
  • Paraffin-embedded sections were sectioned and placed on microscope slides for staining. Slides were washed with xylenes to remove paraffin and rehydrated through a series of graded alcohols. The sections were then incubated in 0.1% Triton x100 for permeabilization. Sections were incubated in a boiling Antigen Retrival solution. 1% Animal serum was used for blocking before incubating in the primary goat antibody, ⁇ -defensin 3 1:400 dilution. The sections were then incubated in the primary antibody overnight at 4° in a humidity chamber. An immunofluorescent secondary Donkey ⁇ -goat 488 antibody 1:200 dilution was used, followed by nuclear staining with TOPRO-3. Images were captured using confocal microscopy.
  • Hematoxylin and eosin staining was used to visualize basic structures such as the epidermis, dermis, muscle, and blood vessels and to determine the orientation and approximate location in the wound. H&E staining was also used to begin to identify which cell types are stimulated by Taliderm in an Akt1-independent manner.
  • sNAG Nanofibers Stimulate Akt1 Activation, an Upstream Regulator of Ets1.
  • FIG. 1A shows a Western blot analysis of phospho-Akt in response to NAG and sNAG stimulation of serum starved EC.
  • FIG. 1B shows RT-PCR analysis of EC infected either with scrambled control or Akt1 shRNA lentiviruses and assessed for expression of Ets1 and S26 as a loading control.
  • FIG. 1C illustrates a signal transduction pathway transducing a signal from sNAG nanofibers to Akt1, Ets1 and Defensins.
  • FIG. 2A shows representative images of wounded WT and AKT1 null mice with and without treatment of Taliderm.
  • FIG. 2B shows H&E staining of representative mouse skin sections from day 3 wounds. H&E staining of wildtype and Akt1 wound excisions indicate a Taliderm dependent increase in keratinocyte proliferation and migration. The dashed lines indicate the area of keratinocyte proliferation across the wound margin. In both the wildtype and Akt1 treated wounds there is an an evident increase in reepithelization across the wound margin compared to the wildytpe and Akt1 control. This indicates that Taliderm increases kertainoctye recruitment independent of the Akt1 pathway.
  • Taliderm induces a complete reepithlization of the epidermis across the wound margin, there is still substantial lack of revascularization in the underlying tissue compared to the wildtype. This is evident by substantial hemorrhaging and infiltration of red blood cells in the Akt1 aminals.
  • sNAG Nanofibers Stimulate Cytokine and Defensin Expression in Primary Endothelial Cells.
  • FIG. 3A shows immunohistochemistry of EC treated with or without sNAG using an antibody directed against ⁇ -defensin.
  • FIG. 3B presents ELISA showing that nanofiber treatment of EC results in the secretion of ⁇ -defensins 1-3.
  • sNAG Nanofibers Stimulate Defensin Expression in Primary Endothelial Cells in an Akt1 Dependent Manner.
  • FIGS. 4A and 4B show quantitative RT-PCR analyses of serum starved EC treated with or without sNAG, with or without PD98059 (MAPK inhibitor), Wortmannin (PI3K inhibitor) or infected with a scrambled control or Akt1 shRNA lentiviruses and assessed for expression of the genes indicated.
  • PD98059 MAPK inhibitor
  • Wortmannin PI3K inhibitor
  • sNAG Nanofibers Stimulate ⁇ -Defensin 3 Expression in Mouse Keratinocytes.
  • FIG. 5A shows immunofluorescent staining with ⁇ -defensin 3 and Involucrin antibodies of paraffin embedded mouse cutaneous wound sections from WT and Akt1 null animals on Day 3.
  • a cutaneous wound healing model was developed in both WT and Akt1 null mice to assess the effects of Taliderm in vivo.
  • FIG. 5B shows quantification of ⁇ -defensin 3 immunofluorescent staining using NIHImageJ software.
  • 5C shows immunofluorescent staining of WT and Akt1 null treated and untreated keratinocytes with ⁇ -Defensin 3 and TOPRO-3. Notice the increase in green ⁇ -Defensin 3 staining in WT and Akt1 Taliderm treated wounds.
  • the immunofluorescent labeling of wound sections illustrates that Taliderm treated wounds show an increase in ⁇ -defensin 3 expression in an Akt1 dependent manner.
  • the Akt1 treated wounds show a reasonable increase in ⁇ -defensin 3
  • the wildtype treated wounds illustrate a more remarkable increase. This indicates that ⁇ -defensin 3 expression is not only increased by application of the nanofiber, but is at least partially dependent on the Akt1 pathway.
  • ⁇ -defensin 3 expression seems limited to the keratinocytes indicating this expression is keratinocyte specific.
  • FIG. 6 shows schematic of Akt1 dependent transcription factor binding sites. Using Genomatix software, 500 bp upstream of the transcription start site was analyzed for conserved sites on the mRNA of DEF1, 4, and 5.
  • Nanofiber treatment resulted in marked increases in the expression of genes involved in cellular recruitment, such as IL-1 (a known Ets1 target), VEGF and several defensins ( ⁇ 3, ⁇ 1, ⁇ 4, and ⁇ 5), small anti-microbial peptides recently shown to act as chemoattractants.
  • IL-1 a known Ets1 target
  • VEGF vascular endothelial growth factor
  • defensins ⁇ 3, ⁇ 1, ⁇ 4, and ⁇ 5
  • shRNAs small anti-microbial peptides
  • Akt1 null mice exhibited a delayed wound healing phenotype that is partially rescued by Taliderm nanofibers.
  • Taliderm treated wounds also showed an increase in defensin expression that is Akt1 dependent.
  • Taliderm acts to increase anti-microbial peptide expression in keratinocytes in an Akt1 dependent manner suggesting the essential role of Akt1 in the function of sNAG nanofibers. This correlates with the results from other studies in the laboratory (Buff, Muise-Helmericks, unpublished) that inhibition of the PI3K/Akt1 pathway and Akt1 knockdown using shRNAs results in decreased expression of these chemotactic factors.
  • FIG. 2B H&E staining of 8 mm wound excisions ( FIG. 2B ) indicated that Taliderm acts independent of Akt1 in wound reepithelization. Even though the new keratinocytes span the entire wound margin, the underlying tissue did not demonstrate the same stimulation in vascular growth. This indicates the that absence of Akt1 is responsible for leaky blood vessels and the large amount of floating red blood cells in the dermis. This suggests that Taliderm is dependent on the Akt1 pathway for an increase in vascularization.
  • sNAG nanofibers such as Taliderm
  • sNAG nanofibers treatment of endothelial cells activate an Akt1/Ets1 dependent pathway leading to changes in cell motility and cytokine secretion
  • Taliderm treated wounds show increased expression of ⁇ -defensin 3 in an AKT1 dependent manner
  • treatment of Akt1 null animals with Taliderm partially rescues the phenotype, leading to markedly increased keratinocyte proliferation/migration
  • bioinformatics analysis indicates that ETS1 is likely involved in the sNAG activated pathway leading to increased wound healing and cytokine secretion.
  • sNAG nanofibers have a potent anti-bacterial effect against Staphylococcus aureus in vivo, which is indirect and defensin-dependent.
  • This example also shows that sNAG nanofibers induce expression of defensins in vitro in keratinocytes and endothelial cells and in vivo in cutaneous wounds, in an Akt-1 dependent manner, and increase the kinetics of wound closure.
  • EBM2 Endothelial basal medium 2
  • EC growth medium 2 SingleQuots as described by Lonza procedures and 1% penicillin/streptomycin (Invitrogen).
  • Serum starvation was performed at 80-90% confluency in EBM2 supplemented with 0.1% fetal calf serum (Valley Biomedical) for 24 hours followed by stimulation with highly purified pGlcNAc (50 ⁇ g/ml) nanofibers (sNAG) in sterile water (provided by Marine Polymer Technologies, Inc., Danvers, Mass., USA).
  • the pGlcNAc diatom-derived nanofibers used in this study are short biodegradable fibers derived from a longer form (NAG), and have an average length of 4-7 ⁇ m and a polymer molecular weight of approximately 60,000 Da.
  • NAG neurodegradable fibers derived from a longer form
  • PD098059 50 ⁇ M
  • wortmannin 100 nM
  • cells were pre-treated for 45 minutes prior to 3 hour stimulation with sNAG (50 ⁇ g/ml).
  • Mission shRNA lentiviral constructs directed against Akt1 were purchased from Sigma/Aldrich.
  • a scrambled pLKO.1 shRNA vector was purchased from Addgene.
  • Lentiviruses were propagated in 293T cells, maintained in DMEM supplemented as above. Lentiviral production was performed using psPAX2 and pMD2.G packaging vectors purchased from Addgene using the protocol for producing lentiviral particles from Addgene.
  • For infection of target cells 7.5 ⁇ 10 5 cells were plated on 100 mm 2 plates and allowed to incubate overnight. The next day, cells were transduced using a final concentration of 1 ⁇ g/ml polybrene and either scrambled control or Akt1 shRNA lentiviruses. After transduction, endothelial cells were serum starved overnight and stimulated with sNAG (50 g/ml) for 3 hours. All infections were monitored for appropriate knockdown by RT-PCR.
  • RNA was extracted with RNAsol (Teltest, Inc.) following manufacturer's instructions.
  • cDNA was synthesized from 2 ⁇ g total RNA with a Superscript First Strand Synthesis Kit (Invitrogen), using Oligo(dT) following the manufacturer's instructions.
  • PCR reactions contained equal amounts of cDNA and 1.25 ⁇ M of the appropriate primer pair (Sigma-Proligo, St. Louis, Mo., USA). All primer sequences used in these analyses are as follows:
  • Cycling conditions were: 94° C. for 5 min; 30-35 cycles of 94° C. for 1 min, 55-65° C. (based on primer T m ) for 1 min, 72° C. for 1 min; 72° C. for 7 min and cooled to 4° C. Cycle number was empirically determined to be within the linear range of the assay for each primer pair used. All semi-quantitative RT-PCR was performed with the ribosomal protein subunit S26 primers as internal controls. Products were visualized on a BioRad Molecular Imaging System (Hercules, Calif., USA). Real time PCR was performed using a Brilliant CYBR green QPCR kit in combination with an Mx3000P Real-Time PCR system both purchased from Stratagene. Primers detecting the ribosomal subunit S26 were used as internal controls.
  • Wild Type C57Bl/6 and Akt1 ⁇ / ⁇ [43] were used in all experiments.
  • the Akt1 null animals were created using an insertional mutagenesis strategy at the translational start site that blocks expression of the entire protein. Wounding was performed on anesthetized adult male mice between 8-12 weeks old. Two full thickness cutaneous wounds were created using a 4 mm biopsy punch (Miltex), to create two identical wounds on each flank. Mice were anesthetized using an O 2 /Isoflurane vaporizing anesthesia machine (VetEquip, Inc.). Isoflurane was used at 4% for induction; 2% for surgery. Prior to surgery hair was removed by depilation and the area was washed and sterilized using 70% ethanol.
  • Wounds were either treated with sNAG membrane moistened with distilled water or left untreated. On days 3 and 5 animals were euthanized and entire wounds were harvested including the surrounding skin using an 8 mm biopsy punch (Miltex). Wounds were fixed in 4% paraformaldehyde overnight at 4°, embedded in paraffin, and sectioned for analysis.
  • H&E Hematoxylin and Eosin Staining
  • H&E staining was performed in the Histology Core Facility at the Medical University of South Carolina, Department of Regenerative Medicine and Cell Biology. Briefly, sections were cleared in xylene, rehydrated through a series of graded alcohols, placed in Hematoxylin followed by acid alcohol. Samples were then placed in ammonia water, rinsed in ethanol and exposed to Eosin before dehydrating through graded alcohols and clearing in xylene. Sections were mounted using Cytoseal-XYL (Richard-Allan Scientific). H&E sections were visualized using an Olympus BX40 microscope (4 ⁇ objective lens, 0.13) and captured using an Olympus Camera (Model DP25) and DP2-BSW acquisition software.
  • mice between 8-12 weeks were wounded as described above.
  • One mL of S. aureus was spun at 10,000 rpm, re-suspended in sterile PBS, and 15 ⁇ l was used to innoculate each wound.
  • sNAG membranes were applied to the treated group thirty minutes post inoculation. Mice were euthanized on day 3 and 5 post wounding and wounds were harvested using an 8 mm biopsy punch. One wound per animal was fixed overnight in 4% paraformaldehyde at 4° C.
  • CFU colony forming units
  • S. aureus cultures in solution were treated with varying concentrations of sNAG (10 ⁇ l and 20 ⁇ l of 10.8 mg/ml sNAG) for three hours. Cultures were then plated overnight at 37° and CFU/ml were determined.
  • Wild Type male mice were wounded and infected with 15 ul of S. aureus as described above. After inoculation, one wound was treated with 0.2 ug/mL of ⁇ -defensin 3 antibody (Santa Cruz) while the other was treated with 0.2 ug/mL of normal goat IgG control antibody (Santa Cruz). sNAG membranes were applied to all mice after antibody treatment on day 0. Antibody was applied every 24 hours. Mice were euthanized on day 3 and wounds were harvested using an 8 mm biopsy punch. Wounds were fixed overnight in 4% paraformaldehyde at 4° C., embedded in paraffin, sectioned, and analyzed using tissue gram stain. CFU/ml quantitation was performed from wounds harvested on day 3 as described above.
  • Paraffin embedded tissue sections were rehydrated through xylene and a series of graded alcohols. Sections were treated with 0.01% Triton-X100 and subjected to antigen retrieval using antigen unmasking solution (Vector Laboratories) in a pressure cooker for 5 min and allowed to cool. Skin sections were labeled with ⁇ -defensin 3 goat polyclonal antibody (Santa Cruz), involucrin rabbit polyclonal antibody (Santa Cruz), and TO-PRO 3-iodide (Molecular Probes). Sections were incubated in primary antibody overnight at 4° and appropriate secondary immunofluorescent antibodies (Invitrogen) for 1 hour at room temperature. Control sections for each antibody were stained without primary antibody.
  • Tissue sections were visualized using an Olympus FluroView laser scanning confocal microscope (Model IX70) and captured at ambient temperature using an Olympus camera (Model FV5-ZM) and Fluoview 5.0 acquisition software. All tissue sections were imaged using 60 ⁇ oil immersion lens (Olympus Immersion Oil)
  • HUVECs were either serum starved or treated with sNAG for 5 hours in culture and stained with antibodies directed against ⁇ -defensin 5 (FITC), ⁇ -defensin 3 (Texas Red), or TOPRO 3 (Blue). Images were taken using immunofluorescent microscopy. Cell culture defensin expression was visualized using a Zeiss Axiovert 100M confocal microscope and was captured at ambient temperature, using water as the medium, using LSM 510 camera (Zeiss Fluor 63 ⁇ W/1.2A objective).
  • FITC ⁇ -defensin 5
  • Texas Red Texas Red
  • TOPRO 3 Blue
  • Endothelial cells were serum starved prior to stimulation with sNAG (50 ⁇ l/ml) for a given time course. Cells were then lysed and subjected to Western blot analysis.
  • the antibodies used for Western blot analysis are as follows: anti-p85 subunit of PI3K and phosphospecific Akt antibody (Cell Signaling Technologies).
  • Endothelial cells express both ⁇ -type and ⁇ -type defensins when stimulated with sNAG.
  • endothelial cells treated with sNAG show an up-regulation of ⁇ -defensin 3 and ⁇ -defensin 1 mRNA expression within 1 hour of stimulation. Similar up-regulation of ⁇ -defensin 4 and 5 by sNAG treatment was also observed (data not shown).
  • Custom gene arrays containing over 25 different defensin genes were used to confirm the expression of the ⁇ -type defensins in primary endothelial cells and the n-type defensins in keratinocytes.
  • sNAG stimulation of endothelial cells was shown to increase the expression specifically of ⁇ -defensins 1, 4 and 5 and ⁇ -defensin 3.
  • sNAG stimulation of human keratinocytes increased expression of ⁇ -defensin like genes, several of which are listed in Table 1.
  • sNAG stimulated endothelial cells were subjected to immunofluorescence using antibodies directed against both ⁇ and ⁇ defensins. As shown in FIG. 7B , both ⁇ -defensin 3 and ⁇ -defensin 5 are up-regulated upon sNAG stimulation in this cell type. However, stimulation of primary human keratinocytes (HaCat) with sNAG did not cause increased expression of ⁇ -defensin but does cause an increase in the expression of ⁇ -defensin 3 ( FIG. 7C ). Taken together, these experiments suggest that sNAG stimulation results in an up-regulation of defensin peptides in both primary keratinocytes and primary endothelial cells.
  • sNAG treatment of endothelial cells for a short time course leads to phosphorylation of Akt1, a standard indicator of its activation ( FIG. 8C ).
  • Akt1 a standard indicator of its activation
  • lentiviral delivery of shRNA directed against Akt1 was used. Quantitative RT-PCR of serum starved endothelial cells infected with scrambled (SCR) control or Akt1 shRNA followed with sNAG treatment confirms that Akt1 expression is required for sNAG-dependent ⁇ -defensin expression ( FIG. 8D ).
  • ⁇ -defensins are known to be expressed in epithelial cells
  • lentiviral delivery of shRNA directed against Akt1 was used in human keratinocytes (HaCat).
  • sNAG treatment of serum starved keratinocytes infected with scrambled (SCR) control leads to a significant increase in ⁇ -defensin 3 expression that is abrogated by Akt1 knockdown ( FIG. 8E ).
  • FIG. 9A To better visualize the epidermal layers that are expressing ⁇ -defensin 3, FIG. 9A
  • FIG. 9B shows a representative image of a sNAG treated wild type wound harvested on day 3.
  • Quantitative analyses shown in FIG. 9C shows an approximate 5-fold increase in ⁇ -defensin 3 expression in sNAG treated wild type animals and that Akt1 is required for this increase.
  • sNAGs were tested for a similar affect in wild type animals. Excisional wounds were created in wild type animals which were either treated with the membrane form of sNAG or left untreated. Tissue sections were taken at 1, 3 and 5 days post wounding and subjected to H&E staining. As shown in FIG. 10 , sNAG treatment of wild type wounds results in complete closure, as visualized by the solid line, at day 3 post wounding. This occurs two days earlier than in the control wounds. Akt1 null animals display a delay in wound closure; these animals do not fully close the wound until 7 days post wounding.
  • Defensin peptides are known to possess antimicrobial properties that are active against gram-positive and gram-negative bacteria. Since treatment of endothelial cells with sNAG increases defensin expression (both ⁇ - and ⁇ -type) and treatment of cutaneous wounds with sNAG dramatically increases ⁇ -defensin 3 expression in vivo, the antimicrobial efficacy of sNAG treatment in bacterially infected wounds was assessed.
  • sNAG decreases bacterial load in cutaneous wounds
  • wild type and Akt1 null animals were subjected to cutaneous wound healing, followed by infection with Staphylococcus aureus .
  • Infected wounds were either treated with sNAG or left untreated for 3 and 5 days post infection.
  • tissue gram staining in FIGS. 11A and 11B wild type animals treated with sNAG show a significant reduction in gram positive staining by day 5 post wounding as compared with untreated wounds.
  • gram stained tissue derived from untreated wounds in Akt1 null animals at 5 days post wounding show an accumulation of neutrophils which stain gram positive ( FIG. 11B ), indicating a potential lack of bacterial clearance in these animals that is not rescued by sNAG treatment.
  • CFU colony forming units
  • the sNAG treated Akt1 null animals show a 2-fold decrease in CFU as compared to untreated Akt1 null animals.
  • the Akt1 null animals have a lower bacterial load per wound which may be reflective of an Akt1-dependent effect on other processes in addition to defensin expression.
  • sNAG treatment had no direct effect on the growth of S. aureus , indicating that sNAG is not directly inhibiting bacterial growth and may then be working via the up-regulation of defensins.
  • FIG. 11 F-G shows the results of these experiments. Infected mice treated with ⁇ -defensin 3 peptide have a decreased bacterial load, an approximate 7.5 fold decrease in viable bacteria ( FIG. 11G ), similar to that shown in wild type mice treated with sNAG.
  • wounds were created, infected with S. aureus and treated with sNAG as described above.
  • the wounds were either treated with a ⁇ -defensin 3 antibody or an isotype control; one application each day for three days.
  • Wound sections were obtained and stained for gram positive bacteria. As shown in FIG. 13A , sections derived from wounds treated with ⁇ -defensin antibody have more gram positive bacteria than those treated with isotype control antibodies. Each section shown was derived from the wound area directly under the scab.
  • sNAG marine diatom derived nanofiber
  • Defensins are an essential component of the innate immune system. These peptides possess anti-microbial properties that are active against gram-positive and negative bacteria, fungi, and many viruses. Defensins are small (3-4 kDa), cysteine-rich cationic peptides found in mammals, insects, and plants that are classified into different families ( ⁇ , ⁇ , and ⁇ ) based on their pattern of disulfide bonding. ⁇ -defensins are thought to be specific to neutrophils, are found in very high concentrations (comprising approximately 5-7% of the total cellular protein) (Ganz, T. and R. I. Lehrer, 1994, Curr Opin Immunol.
  • ⁇ -defensins are found in epithelial cell types such as keratinocytes, mucosal epithelial cells (Harder, J., et al., 1997, Nature 387(6636):861; and Harder, J., et al., 2001, J Biol Chem.
  • hDEFB1 Human ⁇ -defensin 1
  • hDEFB1 Human ⁇ -defensin 1
  • Defensin expression and secretion could be extremely important for creating wound therapeutics.
  • the anti-microbial action by defensins is considered part of innate immunity and is non-specific and broad spectrum. Therefore acquired bacterial resistance, as seen with the overuse of antibiotics, is not an issue.
  • the skin is in constant contact with injury and infection and functions not only as a mechanical barrier but also maintains the ability to mount an active defense against infection.
  • the expression of ⁇ -defensin in the outer layers of skin supports their role in cutaneous innate immunity.
  • sNAG specifically stimulates the expression of three different ⁇ -defensins (1, 4 and 5) in endothelial cells. This is shown by RT-PCR, gene array analysis, immunofluorescence and ELISA (data not shown).
  • the interaction between endothelial cells and leukocytes in tissue repair is one of the initial and most important steps in wound healing.
  • ⁇ -defensin 1 expression is controlled at the level of transcription, in part, by the Ets-family member PU.1.
  • Ets-family member PU.1 is a downstream target of Akt1 in the B-cell lineage.
  • sNAG treatment has resulted in a series of downstream activities; hemostasis, cell migration, cell proliferation, increased wound closure, and as described here, stimulation of the innate immune response resulting in anti-bacterial functions.
  • sNAG Nanofibers Upregulate Expression of a Number of Defensins and Toll Receptor Genes
  • This example demonstrates that a number of defensins and Toll-like receptors are up-regulated by sNAG treatment of human endothelial cells.
  • Human Chip probes were printed on epoxy slides.
  • HUVEC cells were cultured as described in section 6.2, and treated with sNAG nanofibers (“sNAG”) for 5 hours.
  • RNA was extracted with RNAsol (Teltest, Inc.) following manufacturer's instructions, amplified using Amino Allyl MessageAMPTM II aRNA amplification kit (Applied Biosystems), and labeled.
  • the slides were prepared for hybridization with aRNA by soaking in blocking solution (Sigma Tris-buffered saline pH8.0, in 1000 ml dH 2 O, 1% BSAw/v, NaN 3 to 0.05%) at RT O/N, then rinsed and dryed.
  • Samples containing labeled target aRNA from sNAG-treated cells were hybridized with the slides (65 ul/slide; denatured at 95° C. for 5 min; hybridized for 48 hours at 37° C. in 0.1% SDS and 5 ⁇ SSC and 1% BSA), rinsed and dryed.
  • the slides were scanned and hybridization detected using Perkin-Elmer Scan Array equipment and ScanArray Express software V3.0, updated.
  • microarray data was analyzed using Agilent GeneSpring GX v. 11 Bioinformation Data Analysis.
  • TLR Toll-like receptors
  • SEGIRR Single IG IL-1-related receptor
  • TRAF6 TRAF6 receptor associated factor 6
  • Positive controls 1433Z (Tyrosine-3-monohydrogenase/tryptophan 5 monohydrogenase actition protein); GAPD (glyceraldehydes-3-phosphate dehydrogenase); RPL13A (Ribosomal protein L13a); UBC (Ubiquitin C); ACTB (Actin B).
  • TLRs Toll-like receptors
  • Drosophila lack an adaptive immune system but are still resistant to microbial infections.
  • This host defense is the result of an innate immune system that provides protection by synthesizing the antimicrobial peptides dToll and 18-wheeler which are induced by TLRs.
  • PI3K/Akt pathway is a key component in TLR signal transduction, controlling cellular responses to pathogens.
  • TLR1 Triacyl lipopeptides from bacteria and 7.6 mycobacteria TLR4 LPS, viral proteins, Hsp60 ( Chlamydia ) 5.064 TLR7 synthetic compounds 3.271 TLR8 synthetic compounds 2.067 TRAF6 Downstream signalling modulator 6.167 SIGRR IL-1 receptor related TLR modulator 5.895
  • sNAG nanofibers differ from long p-GlcNAc fibers in their effect on gene expression, and specifically in their effect on expression of some of the defensins and Toll-like receptors.
  • Human Defensin Chip probes (concentration: 20 uM, quantity 18-20, solvent: SSC based spotting buffer) were printed on epoxy slides using standard techniques.
  • HUVEC and HaCat cells were cultured as described in section 6.2, and treated with either long fibers (“LNAG”) or sNAG nanofibers (“sNAG”), for 2 hours or 20 hours.
  • RNA was extracted with RNAsol (Teltest, Inc.) following manufacturer's instructions, and amplified using Amino Allyl MessageAMPTM II aRNA amplification kit (Applied Biosystems). During RNA amplification, aRNA from cells treated with LNAG and aRNA from cells treated with sNAG was differentially labeled with Cy3 or Cy5 fluorescent dyes.
  • the slides were prepared for hybridization with aRNA by soaking in blocking solution (Sigma Tris-buffered saline pH8.0, in 1000 ml dH 2 O, 1% BSAw/v, NaN 3 to 0.05%) at RT O/N, then rinsed and dryed.
  • Samples containing equal amounts of differentially labeled target aRNA from LNAG and sNAG-treated cells were mixed, hybridized with the slides (65 ul/slide; denatured at 95° C. for 5 min; hybridized for 48 hours at 37° C. in 0.1% SDS and 5 ⁇ SSC and 1% BSA), rinsed and dryed.
  • the following exemplary graphs in Table VII illustrate experimental set up:
  • SIGIRR Single IG IL-1-related receptor
  • IRAK2 IL-1 receptor-associated
  • Negative controls three random sequences (1, 2, 3). Positive controls: 1433Z (Tyrosine-3-monohydrogenase/tryptophan 5 monohydrogenase actition protein); GAPD (glyceraldehydes-3-phosphate dehydrogenase); RPL13A (Ribosomal protein L13a); UBC (Ubiquitin C); ACTB (Actin B).
  • Tables VIII and IX show gene expression in human umbilical vein endothelial cells (“HUVEC”) after 2 h or 24 h exposure to either LNAG fibers or sNAG nanofibers.
  • Table IX shows gene expression in human keratinocyte cell line (HaCat) after 2 h or 24 h exposure to either LNAG fibers or sNAG nanofibers.
  • LNAG long poly-N-acetylglucosamine fibers
  • sNAG gene expression profile induced by sNAG nanofibers
  • LNAG and sNAG differ in their effect on expression of defensin genes and Toll receptor genes.
  • the sNAG membrane is derived from microalgal pGlcNAc fibers produced as previously described (see Vournakis et al. U.S. Pat. Nos. 5,623,064; and 5,624,679, the content of each of which is incorporated herein by reference in its entirety). Briefly, microalgae were cultured in unique bioreactor conditions using a defined growth media. Following the harvest of microalgae from high-density cultures, fibers were isolated via a stepwise separation and purification process resulting in batches of pure fibers suspended in water for injections (wfi).
  • Fibers were formulated into patches by concentration and oven drying, and were packaged and sterilized by gamma-irradiation. Fiber dimensions average 20-50 nm ⁇ 1-2 nm ⁇ 100 ⁇ m. Batches of fibers were individually quality controlled using chemical and physical test parameters, and each batch met strict purity criteria prior to release. Final batches were required to be substantially free of proteins, metal ions, and other components. The fibers were then shortened by irradiation to produce sNAG membranes. Briefly, the starting material contained 60 g of pGlcNAc slurry at a concentration of 1 mg/mL. The concentration of the pGlcNAc slurry was confirmed by filtering 5 mL into a 0.2 um filter.
  • pGlcNAc was irradiated under different conditions: as a dry, lyophilized material; as a dry membrane; as a concentrated slurry (30:70 weight by volume); and as a dilute slurry (5 mg/ml).
  • a suitable molecular weight reduction (to a molecular weight of 500,000-1,000,000 daltons) was achieved at an irradiation dose of 1,000 kgy for dry polymer, and 200 kgy for wet polymer ( FIG. 14A ).
  • the chemical and physical structure of the fibers was maintained throughout irradiation as verified by infrared (IR) spectrum ( FIG. 14B ), elemental assay, and scanning electron microscopes (SEMs) analysis. Microscopic observation of irradiated fibers showed a decrease in the particle length ( FIGS. 14C and 14D ). The majority of the fibers are less than about 15 ⁇ m in length, with an average length of about 4 um.
  • Serum starvation was performed at 80-90% confluency in RPMI-1640 supplemented with 0.1% fetal calf serum (Gibco BRL) for 24 h followed by stimulation with VEGF 165 (20 ng/ml, R&D Systems) or with highly purified pGlcNAc nanofibers or sNAG nanofibers in sterile water (provided by Marine Polymer Technologies, Inc., Danvers, Mass., USA) with the amounts indicated in the figure descriptions.
  • pGlcNAc did not result in a higher metabolic rate as measured by MTT assays, indicating that this polymeric material was not causing marked increases in cellular proliferation.
  • sNAG at 50, 100 or 200 ⁇ g/ml resulted in a higher metabolic rate of EC than VEGF ( FIG. 17 ).
  • test article comprising sNAG produced as previously described in Section 6.2.1 supra. was utilized.
  • the test article was supplied sterile by Marine Polymer Technologies, Inc.
  • test article Biocompatibility of the test article was tested in mouse fibroblast L929 mammalian cells. No biological reactivity (Grade 0) was observed in the L929 cells at 48 hours, post exposure to the test article. The observed cellular response obtained from the positive control article (Grade 4) and negative control article (Grade 0) confirmed the suitability of the test system. Based on the criteria of the protocol, the test article is considered non-toxic and meets the requirements of the Elution Test, International Organization for Standardization (ISO) 10993-5 guidelines. See Table X below.
  • Intramuscular Implantation Test ISO—4 Week Implantation (“Intramuscular Implantation Test”) was used. Briefly, the test article was implanted in the paravertebral muscle tissue of New Zealand White rabbits for a period of 4 weeks. The test article was then evaluated separately using two control articles: positive control Surgicel (Johnson and Johnson, NJ) and negative control High Density Polyethylene (Negative Control Plastic).
  • the test article measured approximately 1 mm to in width and 10 mm in length.
  • the two control articles were prepared.
  • the positive control, Surgicel (C1) measured approximately 1 mm in width by 10 mm in length and was received sterile.
  • Negative Control Plastic measured approximately 1 mm in width by 10 mm in length and was sterilized by dipping in 70% ethanol.
  • Each animal was weighed prior to implantation. On the day of the test, the dorsal sides of the animals were clipped free of fur and loose hair was removed by means of a vacuum. Each animal was appropriately anesthetized. Prior to implantation, the area was swabbed with a surgical preparation solution.
  • test article strips were surgically implanted into each of the paravertebral muscles of each rabbit, approximately 2.5 cm from the midline and parallel to the spinal column and approximately 2.5 cm from each other.
  • the test article strips were implanted on one side of the spine.
  • positive control article strips (Surgicel) were implanted in the contralateral muscle of each animal.
  • Two negative control strips (Negative Control Plastic) were implanted caudal (toward the tail) to the test article and to C1 control implant sites on either side of the spine (total of four strips). A total of at least eight test article strips and eight of each control article strips are required for evaluation.
  • the animals were maintained for a period of 4 weeks. The animals were observed daily for this period to ensure proper healing of the implant sites and for clinical signs of toxicity. Observations included all clinical manifestations. At the end of the observation period, the animals were weighed. Each animal was sacrificed by an injectable barbiturate. Sufficient time was allowed to elapse for the tissue to be cut without bleeding.
  • the paravertebral muscles in which the test or control articles were implanted were excised in toto from each animal.
  • the muscle tissue was removed by carefully slicing around the implant sites with a scalpel and lifting out the tissue.
  • the excised implant tissues were examined grossly, but without using excessive invasive procedures that might have disrupted the integrity of this tissue for histopathological evaluation.
  • the tissues were placed in properly labeled containers containing 10% neutral buffered formalin.
  • each of the implant sites was excised from the larger mass of tissue.
  • the implant site, containing the implanted material, was examined macroscopically.
  • Each site was examined for signs of inflammation, encapsulation, hemorrhaging, necrosis, and discoloration using the following scale:
  • the relative size of the involved area was scored by assessing the width of the area from the implant/tissue interface to unaffected areas which have the characteristics of normal tissue and normal vascularity. Relative size of the involved area was scored using the following scale:
  • the pathology observer reviews the calculated level of bioreactivity. Based on the observation of all factors (e.g., relative size, pattern of response, inflammatory vs. resolution), the pathology observer may revise the Bioreactivity Rating. Justification for the modification to the rating is presented in the narrative report (A descriptive narrative report regarding the biocompatibility of the test material is provided by the pathology observer).
  • test article was non-reactive when implanted for 4 weeks (Bioreactivity Rating of 0.2) when compared to positive control Surgicel; and non-reactive (Bioreactivity Rating of 0.0) when compared to negative control High Density Polyethylene (Negative Control Plastic).
  • Table XI shows results of the macroscopic evaluation of the test article and control implant sites indicated no significant signs of inflammation, encapsulation, hemorrhage, necrosis, or discoloration at the 4 week time period. Some test sites and the majority of the positive control, Surgicel, were not seen macroscopically and serial sections were submitted for microscopic evaluation.
  • Table XII shows results of the microscopic evaluation of the test article implant sites indicated no significant signs of inflammation, fibrosis, hemorrhage, necrosis, or degeneration as compared to each of the control article sites.
  • the Bioreactivity Rating for the 4 week time period was 0.2, (C1—Surgicel) and 0.0 (C2—Negative Control Plastic) indicating no reaction as compared to either of control implant sites.
  • sNAG nanofibers have a potent anti-viral effect, in particular, against Herpes Simplex Virus, in vivo.
  • this example shows that sNAG nanofibers are effective to treat cold sores associated with HSV infection when administered topically, at the site of herpes infection, to human patients.
  • topical treatment of human patients with compositions comprising sNAG nanofibers reduces painfulness and duration of cold sore symptoms associated with HSV infection.
  • Herpes simplex labialis is a common infection that is estimated to affect 20% to 40% of the population (Spruance, 1992; Löwhagen, 2002). The majority of these infections are due to herpes simplex type I, with a smaller number being attributed to herpes simplex type II.
  • herpes gingivostomatitis Most individuals suffer primary infection with herpes gingivostomatitis early in life. Following primary infection, the virus establishes itself in the trigeminal sensory ganglia as a chronic latent infection. Reactivation of the virus is common and typically presents as herpes labialis along the vermillion border of the lip. Primary infection with herpes simplex is marked by a long period of viral multiplication and shedding (Harmenberg, 2010). After viral replication is terminated, the lesions heal rapidly. Recurrent herpes labialis is generally cleared more rapidly than primary infection due to acquired immune response. Unfortunately, the vigorous immune response results in significant inflammation leading to clinical symptoms including pain, redness and swelling.
  • Recurrent herpes is marked by distinct stages (Harmenberg, 2010).
  • the stages occur in a predictable sequence as follows: prodrome, redness, papule, vesicle, ulcer, hard crust, dry flaking residual swelling, and normal healed skin.
  • the disease is most severe during the vesicular, ulcer and crust stages that are also referred to as the ulcerative or classical lesions.
  • the primary objective of this study was to explore the efficacy of sNAG nanofibers in the treatment of herpes labialis pen-oral lesions, and to explore the duration and intensity of pain of herpes labialis peri-oral lesions in subjects treated with sNAG nanofibers.
  • sNAG nanofibers were supplied in five white plastic tubes containing 200 microliters each (with sNAG concentration of 50 ing/mL).
  • the sNAG nanofibers (the majority of the sNAG nanofibers used were between about 1 to 15 microns in length) were applied to the cold sore once a night for five (5) consecutive nights, immediately prior to bedtime.
  • Subjects participating in the study had their herpetic ulcer evaluated by the study team based upon a Cold Sore Clinical Rating scale as shown in Table XV.
  • FIG. 19 shows Numeric Pain Intensity Scale utilized in the study.
  • Table XVI shows the Investigator End-of-Study Global Assessment of Therapy, including the question posed to the Investigator and the scale by which the effectiveness of therapy was measured.
  • Table XVII shows the Subject End-of-Study Global Assessment of Therapy, including the question posed to the subject and the scale by which the effectiveness of therapy was measured.
  • Table XVII also shows that the subjects were asked “Was this cold score recurrence resolved faster than prior events?” and the subjects could reply “Yes” or “No” to this question.
  • Pre” assessment is assessment of pain according to Numeric Pain Intensity Scale (see FIG. 19) before treatment with sNAG nanofibers.
  • Post” assessment is assessment of pain according to Numeric Pain Intensity Scale (see FIG. 19) within about 1 hour after treatment with sNAG nanofibers.
  • sNAG nanofibers are effective to treat and/or prevent the development of inflammatory bowel disease.
  • rectal administration of sNAG nanofibers is effective to treat and/or prevent inflammation associated with chemically-induced inflammatory bowel disease in an animal model of the disease.
  • IBD inflammatory bowel disease
  • UC ulcerative colitis
  • the model used in this study is the DSS-induced ulcerative colitis that consists of administration of 3% DSS (dextran sodium sulphate) via drinking water for 7 days to a mouse.
  • DSS distal endothelial growth factor
  • the peak of the inflammatory reaction is observed on day 7 and is followed by a period of repair of the injured colonic tissue and ultimately regeneration or progression to chronic disease and development of fibrosis.
  • the Chart showing experimental set up is presented in FIG. 20 .
  • DSS was administered via drinking water to all of the animals (mice) used in the study.
  • FIGS. 21 and 22 show that in the DSS-induced mouse model of inflammatory bowel disease, treatment with sNAG nanofibers resulted in: significant reduction in the inflammatory reaction (as judged by published histological criteria) compared to the control mice; and protective effects in the subacute phase of DSS-colitis, acting in concert with repair mechanisms to support tissue remodeling including the intestinal epithelium.
  • FIG. 21 shows improved histological findings related to the inflammatory process in the mice administered sNAG nanofibers but not in control mice.
  • sNAG-treated group mice but not control mice displayed decreased edema (see FIGS. 21A and 21B ; the area of edema is indicated by a thin arrow and a bracket), and reduced leukocytic infiltration (see FIGS. 21A and 21B ; the leukocytic infiltration is indicated by a thick arrow).
  • FIG. 22 shows staining for fibrosis in sections from mice treated with sNAG nanofibers and from control mice. The differences in the inflammatory response between sNAG-treated mice and control mice are evident. In particular, the control group shows signs of increased fibrosis (see FIG. 22A ), whereas sNAG-treated group does not (see FIG. 22B ).
  • sNAG nanofibers are effective to treat and/or prevent inflammation associated with inflammatory bowel disease in an animal model of the disease.

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JP6328690B2 (ja) 2018-05-23
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IL266368A (he) 2019-06-30
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