US20120093828A1 - Vaccine compositions and methods for treatment of mucormycosis and other fungal diseases - Google Patents

Vaccine compositions and methods for treatment of mucormycosis and other fungal diseases Download PDF

Info

Publication number
US20120093828A1
US20120093828A1 US13/257,585 US201013257585A US2012093828A1 US 20120093828 A1 US20120093828 A1 US 20120093828A1 US 201013257585 A US201013257585 A US 201013257585A US 2012093828 A1 US2012093828 A1 US 2012093828A1
Authority
US
United States
Prior art keywords
ftr
mucormycosis
ftr1
oryzae
iron
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US13/257,585
Other languages
English (en)
Inventor
Ashraf S. Ibrahim
Brad J. Spellberg
Yue Fu
John E. Edwards
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Harbor Ucla Medical Center
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US13/257,585 priority Critical patent/US20120093828A1/en
Publication of US20120093828A1 publication Critical patent/US20120093828A1/en
Assigned to LOS ANGELES BIOMEDICAL RESEARCH INSTITUTE AT HARBOR-UCLA MEDICAL CENTER reassignment LOS ANGELES BIOMEDICAL RESEARCH INSTITUTE AT HARBOR-UCLA MEDICAL CENTER ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: FU, YUE, EDWARDS, JOHN E., IBRAHIM, ASHRAF S., SPELLBERG, BRAD J.
Abandoned legal-status Critical Current

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/0005—Vertebrate antigens
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/14—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from fungi, algea or lichens
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/12—Viral antigens
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/39—Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39591—Stabilisation, fragmentation
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
    • A61K48/005—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy characterised by an aspect of the 'active' part of the composition delivered, i.e. the nucleic acid delivered
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/16—Otologicals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10—Antimycotics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/04—Immunostimulants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1138—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against receptors or cell surface proteins
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2121/00—Preparations for use in therapy
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/10—Type of nucleic acid
    • C12N2310/14—Type of nucleic acid interfering N.A.

Definitions

  • This invention generally relates to compositions and methods to vaccinate subjects against infectious diseases and, more particularly, relates to compositions and methods to vaccinate subjects against opportunistic fungal diseases.
  • fungi can establish an infection in all exposed subjects, e.g., the systemic pathogens Histoplasma capsulatum and Coccidioides immitis. Others, such as Candida, Asergillus species and Zygomycetes are opportunist pathogens which ordinarily cause disease only in a compromised host. Fungi of the class Zygomycetes, order Mucorales, can cause Mucormycosis, a potentially deadly fungal infection in human. Fungi belonging to the order Mucorales are distributed into at least six families, all of which can cause mucormycosis (Ibrahim et al.
  • Rhizopus arrhizus fungi belonging to the family Mucoraceae, and specifically the species Rhizopus oryzae ( Rhizopus arrhizus ), are by far the most common cause of infection (Ribes et al., supra). Increasing cases of mucormycosis have been also reported due to infection with Cunninghamella spp.
  • mucormycosis The agents of mucormycosis almost uniformly affect immunocompromised hosts (Spellberg et al., Clin. Microbiol. Rev. 18:556-69 (2005)).
  • the major risk factors for mucormycosis include uncontrolled diabetes mellitus in ketoacidosis known as diabetes ketoacidosis (DKA), other forms of metabolic acidosis, treatment with corticosteroids, organ or bone marrow transplantation, neutropenia, trauma and burns, malignant hematological disorders, and deferoxamine chelation-therapy in subjects receiving hemodialysis.
  • DKA diabetes ketoacidosis
  • Amphotericin B remains the only antifungal agent approved for the treatment of invasive mucormycosis (Id). Because the fungus is relatively resistant to AmB, high doses are required, which frequently cause nephrotoxicity and other adverse effects (Sugar, supra). Also, in the absence of surgical removal of the infected focus (such as excision of the eye in subjects with rhinocerebral mucormycosis), antifungal therapy alone is rarely curative (Edwards, J. (1989), supra; Ibrahim et al., (2003), supra). Even when surgical debridement is combined with high-dose AmB, the mortality associated with mucormycosis exceeds 50% (Sugar, supra).
  • serum iron levels One of the underlying factors in predisposition to fungal infection is elevated serum iron levels. Subjects who have elevated available serum iron are hypersusceptible to mucormycosis. Iron is required by virtually all microbial pathogens for growth and virulence. In mammalian hosts, very little serum iron is available to microorganisms because it is highly bound to carrier proteins such as transferrin. Although sequestration of serum iron is a major host defense mechanism against pathogenic fungi, subjects treated with exogenous iron chelators e.g., deferoxamine have a markedly increased incidence of invasive mucormycosis, which is associated with a mortality of >80%. While deferoxamine is a chelator from the perspective of the human host, it predisposes subjects to mucormycosis by acting as a siderophore, supplying previously unavailable iron to the pathogenic fungi.
  • exogenous iron chelators e.g., deferoxamine
  • deferoxamine is
  • the present invention provides a vaccine composition, including an FTR polypeptide, or an antigenic fragment of the polypeptide, and a pharmaceutically acceptable carrier.
  • the invention provides a vaccine composition, including a vector having a nucleotide sequence that is substantially complimentary to at least 18 contiguous nucleotides of FTR sequence, a transcription promoter, and a transcription terminator; wherein the promoter is operably linked to the FTR nucleotide sequence, and wherein the FTR nucleotide sequence is operably linked to the transcription terminator, and a pharmaceutically acceptable carrier.
  • the vaccine compositions of the present invention can further include an adjuvant.
  • the invention provides a pharmaceutical composition for treating or preventing a fungal condition in a subject in need thereof, including an antisense, a small interfering RNA or an antibody inhibitor of FTR selected from the group consisting of a nucleotide sequence that is substantially complimentary to a portion of an FTR sequence; a nucleotide sequence that is substantially complimentary to at least 12 contiguous nucleotide bases of FTR sequence; a nucleotide RNAi sequence that is substantially complimentary to at least 18 contiguous nucleotide bases of FTR sequence; an antibody or antibody fragment thereof that specifically binds to an FTR polypeptide or a fragment thereof; and a pharmaceutically acceptable excipient or carrier.
  • an antisense, a small interfering RNA or an antibody inhibitor of FTR selected from the group consisting of a nucleotide sequence that is substantially complimentary to a portion of an FTR sequence; a nucleotide sequence that is substantially complimentary to at least 12 contiguous nucleotide bases of FTR sequence
  • the invention provides a method of treating or preventing a fungal condition, including administering to a subject having, or susceptible to having, a fungal condition an immunogenic amount of an FTR polypeptide, or an immunogenic fragment thereof.
  • the invention provides a method for treating or preventing a fungal condition in a subject in need thereof, including exposing said fungi to an antisense, a small interfering RNA or an antibody inhibitor of FTR.
  • FIG. 1 shows Rhizopus oryzae high affinity iron permease nucleotide sequence (SEQ ID NO: 1), with Genbank cDNA accession NO. AY344587.
  • FIG. 2 shows Rhizopus oryzae high affinity iron permease polypeptide sequence (SEQ ID NO:2), with Genbank protein ID. No. AAQ24109.1.
  • FIG. 3 shows amino acid sequence alignment (a) and dendrogram (b) for FTR of R. oryzae having 46% and 44% identity with FTR of C. albicans and S. cerevisiae, respectively. Box on amino acid sequence alignment indicates the conserved REGLE motif involved in a direct interaction with iron.
  • FIG. 4 shows mechanisms of iron uptake by Zygomycetes in conditions of elevated available serum iron.
  • FIG. 5 shows the FTR expression in R. oryzae grown in media with varying concentrations of iron.
  • FIG. 6 shows the growth of S. cerevisiae ftr1 mutant transformed with vector expressing FTR.
  • FIG. 7 shows high affinity iron uptake by S. cerevisiae ftr1 mutant transformed with vector expressing FTR as compared with iron uptake by wild-type S. cerevisiae and S. cerevisiae ftr1 mutant transformed with empty vector. *P ⁇ 0.05.
  • FIG. 9 shows a temporal link or an inverse correlation between percent survival and the kidney burden of R. oryzae (5 ⁇ 10 4 spores) as determined by TaqMan assay.
  • FIG. 11 shows the expression of FTR in the hematogenously disseminated mucormycosis model using DKA mice.
  • FIG. 12 shows the expression of FTR in the brains of DKA mice infected with R. oryzae expressing GFP under the control of FTR promoter.
  • A H & E stain of brain infected with R. oryzae;
  • B brain section stained with rabbit polyclonal antibody to GFP then counter stained with FITC conjugated anti-rabbit antibody; and
  • C DIC confocal image showing non-fluorescent R. oryzae at the time of infection. Arrows denote fungal elements in infected brains. Magnification, ⁇ 400.
  • FIG. 13 shows the agarose gel electrophoresis result of an RT-PCR assay showing lack of expression of FTR in R. oryzae transformed with RNA-interference plasmid (T 1 and T 3 -T 5 ) as compared to R. oryzae transformed with empty plasmid (C).
  • Primers amplifying the 18s rDNA served as a control to demonstrate the specificity of RNA interference in targeting FTR.
  • FIG. 15 shows Aspergillus fumigatus high affinity iron permease nucleotide sequence.
  • FIG. 16 shows Candida guilliermondii high affinity iron permease nucleotide sequence.
  • FIG. 17 shows Aspergillus flavus high affinity iron permease nucleotide sequences.
  • FIG. 18 shows Candida tropicalis high affinity iron permease nucleotide sequence.
  • FIG. 19 shows a conceptual model of the Rhizopus rFtr1p helical bundle protein and translocation of iron from the extracellular setting into the cytoplasm of Rhizopus species.
  • FIG. 20 shows results of an SDS-PAGE demonstrating purified synthetic/recombinant rFtr1p.
  • E. coli was transformed with a plasmid expressing 6 ⁇ -His tagged synthetic rFTR1 or with empty plasmid.
  • rFtr1p was purified by Ni-agrose column and detected at the expected size of 28 kD in the rFtr1p clone but not when E. coli was transformed with empty plasmid.
  • FIG. 22 shows that FTR1 is expressed in DKA mice infected intravenously with R. oryzae.
  • Panel (A) shows FACS analysis of R. oryzae transformed with plasmid containing the reporter gene GFP driven by either the FTR1 promoter or the constitutively expressed ACT1 promoter and grown in iron-rich or iron-depleted conditions.
  • R. oryzae M16 transformed with an empty plasmid was used as a negative control.
  • Panel (B) shows FTR1 is expressed in the brains of DKA mice infected with R. oryzae expressing GFP under the control of FTR1p.
  • tissue section was stained with rabbit polyclonal antibody to GFP then counter stained with FITC conjugated anti-rabbit antibody.
  • DIC confocal image showing non-fluorescent R. oryzae at the time of infection. Arrows denote fungal elements in infected brains. Magnification, ⁇ 400.
  • FIG. 23 shows that the disruption cassette integrates in FTR1 locus but complete elimination of FTR1 could not be achieved.
  • Panel (A) A diagram summarizing the strategy we used to achieve FTR1 disruption. PyrF (998 bp) was used as a selectable marker flanked by 606 and 710 bp fragments of FTR1-5′ UTR and FTR1-3′ UTR, respectively.
  • Panel (B) Gel electrophoresis showing integration of the disruption cassette in a representative putative ftr1 null mutant (KO) but not in the wild-type (WT) (see 5′UTR and 3′UTR).
  • Primers FTR1 P11 and FTR1 P12 were used to amplify 503 bp from the FTR1 ORF only from the wild-type but not from the putative ftr1 null mutant (see FTR1).
  • Primers PyrF P9 and PyrF P18 to test for possible reciculization of the transformed plasmid with expected band of 2094 bp were also used (see self ligation).
  • FIG. 24 shows confirmation of the lack of complete disruption of FTR1 in the multinucleated R. oryzae.
  • Panel (A) DAPI stain of swollen R. oryzae spores showing the presence of multiple nuclei with a single spore. Arrows denote nuclei. Original magnification, ⁇ 1000.
  • Panel (B) Gel electrophoresis showing lack of amplification of FTR1 after 14 passages of the putative null mutants on iron-rich medium (1000 ⁇ M FeCl3) and amplification of the FTR1 from the same isolate following growth on iron-depleted medium (i.e. 100 ⁇ M ferrioxamine) for 96 h.
  • FIG. 25 shows that reduced copy number results in compromised ability of R. oryzae to take up iron.
  • Panel (A) Quantitative PCR demonstrating reduced copy number in the putative ftr1 null mutant compared to R. oryzae PyrF-complemented strain or to the same mutant grown in iron-depleted medium.
  • Panel (B) Gel electrophoresis of samples taken from the qPCR tube showing the amplification specificity for the FTR1 product.
  • FIG. 26 shows how the reduction of FTR1 copy number reduces R. oryzae virulence in the DKA mouse models.
  • Panel (A) a representative of the putative ftr1 null mutant demonstrated comparable growth to R. oryzae PyrF-complemented strain on YPD or CSM-URA media.
  • FIG. 27 shows how inhibition of FTR1 expression reduces R. oryzae ability to take up 59 Fe in vitro.
  • A RT-PCR showing lack of expression of FTR1 in R. oryzae transformed with RNA-interference plasmid (T 1 and T 3 -T 5 ) compared to R. oryzae transformed with empty plasmid (C, control). Primers amplifying the 18s rDNA served as a control to demonstrate the integrity of starting sample and lack of PCR inhibitors.
  • B a representative of the RNAi transformants demonstrated comparable growth to the R. oryzae M16 transformed with empty plasmid on YPD or CSM-URA media.
  • C 59 Fe uptake by wild-type, R.
  • FIG. 28 shows how inhibition of FTR1 expression reduces virulence of R. oryzae in the DKA mouse models and passive immunization with anti-Ftr1p sera protects DKA mice from R. oryzae infection.
  • Panel (A) Survival of mice (n 8) infected i.v. with R. oryzae transformed with empty plasmid (control strain, 2.9 ⁇ 10 3 spores) or with RNA-i plasmid targeting expression of FTR1 (FTR1-i, 4.1 ⁇ 10 3 spores). *, P ⁇ 0.001.
  • Panel (B) Survival of mice (n 9) infected intranasally with R.
  • This invention is directed to the use of compositions and methods that directly and/or indirectly inhibit the high affinity iron permease (FTR) of pathogenic fungi, specifically those involved in the onset of mucormycosis.
  • FTR high affinity iron permease
  • High affinity iron permease is a molecule responsible for the uptake of iron in fungi; targeting and inhibition of this molecule, therefore, will impede the ability of the fungi to uptake and/or use the iron available in the surrounding environment. Inhibition of high affinity iron permease will result in iron-starvation in fungal pathogens hampering their growth and/or virulence.
  • the FTR polypeptide in, for example, R. oryzae has little or no homology with any known human proteins.
  • Three of these proteins are coiled-coil domain containing 82 (i.e., EAW66982; AAH33726.1; and NP — 079001.2), one is a CCDC82 protein (i.e., AAH18663.1) and an unnamed protein (i.e., BAB15683.1)
  • the standard BLAST search e value for identification of unique sequences from fungi compared to other organisms has been set at 10 ⁇ 8 , indicating that rFtr1p has no significant homology to the human proteome. Therefore, the compositions and methods of the current invention in targeting and inhibiting FTR will only affect the iron levels in the fungal pathogen not the host, which constitutes an effective and targeted therapy against mucormycosis.
  • the invention is directed to an immunogenic composition such as a vaccine.
  • the immunogenic composition includes an effective dose of fungal FTR polypeptide or an antigenic fragment thereof that confer protection against mucormycosis in a subject.
  • the vaccine composition of the invention induces host humoral and/or cell mediated immune response against fungal FTR.
  • a composition of the invention further includes an adjuvant that can boost the immunogenecity of the vaccine composition.
  • the invention includes an inhibitor of FTR molecule such as siRNA, for example.
  • the FTR inhibitor includes a vector expressing one or more siRNAs that include sequences sufficiently complementary to a portion of the FTR molecule for inhibiting FTR transcription or translation levels.
  • interfering RNAs against FTR of R. oryzae were prepared, which were shown to inhibit FTR expression in these fungi.
  • DKA mice it was demonstrated that R. oryzae transformants harboring anti-FTR siRNAs were less virulent than the wild type R. oryzae.
  • FTR refers to high affinity iron permease, a membrane protein responsible for iron transport in pathogenic fungi, such as, but not limited to FTR in R. oryzae, A. fumigatus, C. guilliermondii, A flavus, and C. tropicalis; and the nucleic acids encoding the same.
  • FTRs from R. oryzae, C. albicans and S. cerevisiae share percent identities of 39% or more with multiple regions of protein sequence homology.
  • the nucleotide sequence of FTR in, for example, R. oryzae is shown in FIG.
  • FTR expression or “expressing FTR” can be employed to designate indifferently expression of an FTR nucleic acid or an FTR polypeptide.
  • nucleic acid is an RNA, for example, mRNA or pre-mRNA, or DNA, such as cDNA and genomic DNA.
  • An FTR nucleic acid refers to a nucleic acid molecule (RNA, mRNA, cDNA, or genomic DNA, either single-or double-stranded) corresponding to FTR polypeptide or an immunogenic fragment thereof.
  • DNA molecules can be doubled-stranded or singled-stranded; single stranded RNA or DNA can be either the coding or sense strand, or the non-coding or antisense strand.
  • the nucleic acid molecule or nucleotide sequence can include all or a portion of the coding sequence of the gene and can further include additional non-coding sequences such as introns and non-coding 3′ and 5′ sequences (including promoter, regulatory, poly-A stretches or enhancer sequences, for example).
  • the nucleic acid molecule or nucleotide sequence can be fused to another sequence, for example, a label, a marker or a sequence that encodes a polypeptide that assists in isolation or purification of the polypeptide.
  • sequences include, but are not limited to, those that encode a selection marker (e.g.
  • the nucleic acid molecule or nucleotide sequence can include a nucleic acid molecule or nucleotide sequence which is synthesized chemically or by recombinant means, such nucleic acid molecule or nucleotide sequence is suitable for use in recombinant DNA processes and within genetically engineered protein synthesis systems.
  • polypeptide refers to a chain of two or more amino acids covalently linked by a peptide bond.
  • Particular polypeptides of interest in the context of this invention are amino acid subsequences having antigenic epitopes.
  • Antigenic epitopes are well known in the art and include sequence and/or structural determinants substantially responsible for the immunogenic properties of a polypeptide and being capable of evoking an immune response.
  • Functional domains of the FTR polypeptide are also considered to fall within the scope of the invention.
  • the REGLE motif which interacts with iron is one exemplary functional domain of the invention.
  • Another exemplary functional domain is the cell surface EXXE motif of FTR which is required for full function of FTR in Saccharomyces cerevisiae (Stearman et al., Science 271: 1552-1557 (1996)).
  • Polypeptides also undergo maturation or post-translational modification processes that can include, for example, glycosylation, proteolytic cleavage, lipidization, signal peptide cleavage, propeptide cleavage, phosphorylation, and such like.
  • immunogenic refers to a portion of a protein that is recognized by a T-cell and/or B-cell antigen receptor.
  • the immunogenic portion generally includes at least 5 amino acid residues, preferably at least 10, more preferably at least 20, and still more preferably at least 30 amino acid residues of an FTR polypeptide or a variant thereof.
  • Preferred immunogenic portions can contain a small N-and/or C-terminal fragment (e.g., 5-30 amino acids, preferably 10-25 amino acids).
  • a variant polypeptide contains at least one amino acid change compared to the target polypeptide.
  • Polypeptide variants of FTR can exhibit at least about 39%, more preferably at least about 50%, and even more preferably at least about 70% identity to the FTR polypeptide.
  • a polynucleotide variant includes a substantially homologous polynucleotide that deviates in some bases from the identified polynucleotide, usually caused by mutations such as substitution, insertion, deletion or transposition. Polynucleotide variants preferably exhibit at least about 60% (for fragments with 10 or more nucleotides), more preferably at least about 70%, 80% or 90%, and even more preferably at least about 95%, 98% or 99% identity to the identified polynucleotide.
  • fragment as used herein with reference to an FTR polypeptide is intended to refer to a polypeptide having a portion of FTR amino acid sequence.
  • Useful fragments include those that retain one or more of the biological activities of the polypeptide.
  • Such biologically active fragments can have a wide range of lengths including, for example, 4, 6, 10, 15, 20, 25, 30, 40, 50, 100, or more amino acid in length.
  • biologically active fragments also can be characterized by, for example, a motif, domain, or segment that has been identified by analysis of the polypeptide sequence using methods well known in the art.
  • Such regions can include, for example, a signal peptide, extracellular domain, transmembrane segment, ligand binding region, zinc finger domain and/or glycosylation site.
  • vacun refers to a composition that can be administered to an animal to protect the animal against an infectious disease.
  • Vaccines protect against diseases by inducing or increasing an immune response in an animal against the infectious disease.
  • An exemplary infectious disease amenable to treatment with the vaccines of the invention is mucormycosis.
  • the vaccine-mediated protection can be humoral and/or cell mediated immunity induced in host when a subject is challenged with, for example, FTR or an immunogenic portion or fragment thereof.
  • adjuvant is intended to mean a composition with the ability to enhance an immune response to an antigen generally by being delivered with the antigen at or near the site of the antigen.
  • Ability to increase an immune response is manifested by an increase in immune mediated protection.
  • Enhancement of humoral immunity can be determined by, for example, an increase in the titer of antibody raised to the antigen.
  • Enhancement of cellular immunity can be measured by, for example, a positive skin test, cytotoxic T-cell assay, ELISPOT assay for IFN-gamma or IL-2.
  • Adjuvants are well known in the art. Exemplary adjuvants include, for example, Freud's complete adjuvant, Freud's incomplete adjuvant, aluminum adjuvants, MF59 and QS21.
  • antibody refers to immunoglobulin molecules and immunologically active portion of immunoglobulin molecules.
  • Antibodies can be prepared by any of a variety of techniques known to those skilled in the art (see, for example, Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratories, Cold Spring Harbor, N.Y., 1988).
  • the present invention provides polyclonal and monoclonal antibodies that bind specifically to a polypeptide of the invention or fragment or variant thereof.
  • Monoclonal antibodies of the invention for example, include a population of antibody molecules that contain only one species of antigen binding site capable of immunoreacting with a particular epitope of a polypeptide of the invention or a fragment or variant thereof.
  • Monoclonal antibodies can be coupled to one or more therapeutic agents. Suitable agents in this regard include differentiation inducers, drugs, toxins, and derivatives thereof.
  • a therapeutic agent can be coupled (e.g., covalently bonded) to a suitable monoclonal antibody either directly or indirectly (e.g., via a linker group).
  • vector means the vehicle by which a nucleic acid can be introduced into a host cell.
  • the vector can be used for propagation or harboring a nucleic acid or for polypeptide expression of an encoded sequence.
  • vectors are known in the art and include, for example, plasmids, phages and viruses Exemplary vectors can be found described in, for example, Sambrook et al., Molecular Cloning: A Laboratory Manual, Third Ed., Cold Spring Harbor Laboratory, New York (2001); Ausubel et al., Current Protocols in Molecular Biology, John Wiley and Sons, Baltimore, Md. (1999).
  • antibody inhibitor refers to an antibody that reduces the biological activity or function of the target antigen (i.e., FTR).
  • FTR target antigen
  • Such reduction in activity or function can be, for example, in connection with a cellular component (e.g., membrane localization), or in connection with a cellular process (e.g., iron transport), or in connection with an overall process of a cell (e.g., cell growth or survival).
  • the inhibitory effects can be fungicidal (killing of fungi) or fungistatic (i.e., stopping or at least slowing fungal growth). The latter slows or prevents fungal growth such that fewer fungi are produced relative to uninhibited fungi over a given time period. From a molecular standpoint, such inhibition can equate with a reduction in the level of, or elimination of, the transcription and/or translation of FTR molecule, or reduction or elimination of activity of FTR molecule.
  • treating or “treatment,” as it is used herein is intended to mean an amelioration of a clinical symptom indicative of a fungal condition.
  • Amelioration of a clinical symptom includes, for example, a decrease or reduction in at least one symptom of a fungal condition in a treated individual compared to pretreatment levels or compared to an individual with a fungal condition.
  • the term “treating” also is intended to include the reduction in severity of a pathological condition, a chronic complication or an opportunistic fungal infection which is associated with a fungal condition. Such pathological conditions, chronic complications or opportunistic infections are exemplified below with reference to mucormycosis.
  • Mucormycosis and other such pathological conditions, chronic complications and opportunistic infections also can be found described in, for example, Merck Manual, Sixteenth Edition, 1992, and Spellberg et al., Clin. Microbio. Rev. 18:556-69 (2005).
  • preventing or “prevention,” as it is used herein is intended to mean a forestalling of a clinical symptom indicative of a fungal condition.
  • forestalling includes, for example, the maintenance of normal physiological indicators in an individual at risk of infection by a fungus or fungi prior to the development of overt symptoms of the condition or prior to diagnosis of the condition. Therefore, the term “preventing” includes the prophylactic treatment of individuals to guard them from the occurrence of a fungal condition. Preventing a fungal condition in an individual also is intended to include inhibiting or arresting the development of the fungal condition.
  • Inhibiting or arresting the development of the condition includes, for example, inhibiting or arresting the occurrence of abnormal physiological indicators or clinical symptoms such as those described above and/or well known in the art. Therefore, effective prevention of a fungal condition would include maintenance of normal body temperature, weight, psychological state as well as lack of lesions or other pathological manifestations in an individual predisposed to a fungal condition.
  • Individuals predisposed to a fungal condition include, for example, an individual with AIDS, azotemia, diabetes mellitus, bronchiectasis, emphysema, TB, lymphoma, leukemia, or burns, or an individual with a history of susceptibility to a fungal condition.
  • Inhibiting or arresting the development of the condition also includes, for example, inhibiting or arresting the progression of one or more pathological conditions, chronic complications or susceptibility to an opportunistic infection associated with a fungal condition.
  • fungal condition refers to fungal diseases, infection, or colonization including superficial mycoses (i.e., fungal diseases of skin, hair, nail and mucous membranes; for example, ringworm or yeast infection), subcutaneous mycoses (i.e., fungal diseases of subcutaneous tissues, fascia and bone; for example, mycetoma, chromomycosis, or sporotichosis), and systemic mycoses (i.e., deep-seated fungal infections generally resulting from the inhalation of air-borne spores produced by causal moulds; for example, zygomycosis, mucormycosis, coccidioidomycosis, blastomycosis, histoplasmosis, or paracoccidioidomycosis)
  • superficial mycoses i.e., fungal diseases of skin, hair, nail and mucous membranes; for example, ringworm or yeast infection
  • subcutaneous mycoses i.e., fungal diseases of subcutaneous tissues,
  • zygomycosis is intended to mean a fungal condition caused by fungi of the class Zygomycetes, comprised of the orders Mucorales and Entomophthorales.
  • the Entomophthorales are causes of subcutaneous and mucocutaneous infections known as entomophthoromycosis, which largely afflict immunocompetent hosts in developing countries.
  • Zygomycosis is also referred to as mucormycosis and the two terms are used interchangeably to refer to similar types of fungal infections.
  • Mucormycosis is intended to mean a fungal condition caused by fungi of the order Mucorales.
  • Mucormycosis is a life-threatening fungal infection almost uniformly affecting immunocompromised hosts in either developing or industrialized countries.
  • Fungi belonging to the order Mucorales are distributed into at least six families, all of which can cause cutaneous and deep infections.
  • Species belonging to the family Mucoraceae are isolated more frequently from patients with mucormycosis than any other family.
  • Rhizopus oryzae Rhizopus arrhizus
  • Mucoraceae family that cause a similar spectrum of infections include, for example, Rhizopus microsporus var. rhizopodiformis, Absidia corymbifera, Apophysomyces elegans, Mucor species, Rhizomucor pusillus and Cunninghamella spp (Cunninghamellaceae family).
  • Mucormycosis is well known in the art and includes, for example, rinocerebral mucormycosis, pulmonary mucormycosis, gastrointestinal mucormycosis, disseminated mucormycosis, bone mucormycosis, mediastinum mucormycosis, trachea mucormycosis, kidney mucormycosis, peritoneum mucormycosis, superior vena cava mucormycosis or external otitis mucormycosis.
  • Fungi belonging to the order Mucorales are currently distributed into the families of Choanephoraceae; Cunninghamellaceae; Mucoraceae; Mycotyphaceae; Phycomycetaceae; Pilobolaceae; Saksenaeaceae; Syncephalastraceae; and Umbelopsidaceae.
  • Each of these fungi families consists of one or more genera.
  • fungi belonging to the order Mucorales, family Mucoraceae are further classified into the genera of Absidia (e.g., A. corymbifera ); Actinomucor (e.g., A. elegans ); Amylomyces (e.g., A.
  • rouxii Apophysomyces; Backusella (e.g., B. circina ); Benjaminiella (e.g., B. multispora ); Chaetocladium (e.g., C. brefeldii ); Circinella (e.g., C. angarensis ); Cokeromyces (e.g., C. recurvatus ); Dicranophora (e.g., D. fulva ); Ellisomyces (e.g., E. anomalus; Helicostylum (e.g., H. elegans ); Hyphomucor (e.g., H. assamensis ); Kirkomyces (e.g., K.
  • Backusella e.g., B. circina
  • Benjaminiella e.g., B. multispora
  • Chaetocladium e.g., C. brefeldii
  • Circinella e.g.
  • Mucor e.g., M. amphibiorum
  • Parasitella e.g., P. parasitica
  • Philophora e.g., P. agaricina
  • Pilaira e.g., P. anomala
  • Pirella e.g., P. circinans
  • Rhizomucor e.g., R. endophyticus
  • Rhizopodopsis e.g., R. javensis
  • Rhizopus Sporodiniella (e.g., S. umbellata ); Syzygites (e.g., S. megalocarpus ); Thamnidium (e.g., T.
  • Rhizopus for example, consists of R. azygosporus; R. caespitosus; R. homothallicus; R. oryzae; and R. schipperae species.
  • the Choanephoraceae family consists of fungi genera Blakeslea (e.g., B. monospora ), Choanephora (e.g., C. cucurbitarum ), Gilbertella (e.g., G. hainanensis ), and Poitrasia (e.g., P. circinans ).
  • the Cunninghamellaceae family consists of genera Chlamydoabsidia (e.g., C. padenii ); Cunninghamella (e.g., C. antarctica ); Gongronella (e.g., G. butleri ); Garromyces (e.g., H. radiatus ); and Hesseltinella (e.g., H.
  • the Mycotyphaceae family consists of fungi genus Mycotypha (e.g., M. africana ).
  • the Phycomycetaceae family consists of fungi genus Phycomyces (e.g., P. blakesleeanus ) and Spinellus (e.g., S. chalybeus ).
  • the Pilobolaceae family consists of fungi genera Pilobolus (e.g., P. longipes ) and Utharomyces (e.g., U. epallocaulus ).
  • the Saksenaeaceae family consists of fungi genera Apophysomyces (e.g., A.
  • the Syncephalastraceae family consists of fungi genera Dichotomocladium (e.g., D. elegans ); Fennellomyces (e.g., F. gigacellularis ); Mycocladus (e.g., M. blakesleeanus ); Phascolomyces (e.g., P. articulosus ); Protomycocladus (e.g., P. noiralabadensis ); Syncephalastrum (e.g., S. monosporum ); Thamnostylum (e.g., T.
  • Umbelopsidaceae family consists of fungi genus Umbelopsis (e.g., U. angularis ).
  • the term “pharmaceutically acceptable carrier” includes any and all pharmaceutical grade solvents, buffers, oils, lipids, dispersion media, coatings, isotonic and absorption facilitating agents and the like that are compatible with the active ingredient. These pharmaceutically acceptable carriers can be prepared from a wide range of pharmaceutical grade materials appropriate for the chosen mode of administration, e.g., injection, intranasal administration, oral administration, etc.
  • the terms “pharmaceutical” or “pharmaceutically acceptable” further refer to compositions formulated by known techniques to be non-toxic and, when desired, used with carriers or additives that can be safely administered to humans.
  • the term “pharmaceutically 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.
  • carrier refers to a diluent, adjuvant, excipient, or vehicle with which the therapeutic is administered.
  • Such pharmaceutical carriers can be sterile liquids, such as water and oils, including those of petroleum, animal, vegetable or synthetic origin, such as peanut oil, soybean oil, mineral oil, sesame oil and the like. Water is a preferred carrier when the pharmaceutical composition is administered intravenously.
  • Saline solutions and aqueous dextrose and glycerol solutions can also be employed as liquid carriers, particularly for injectable solutions.
  • suitable pharmaceutical excipients include starch, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk, silica gel, sodium stearate, glycerol monostearate, talc, sodium chloride, dried skim milk, glycerol, propylene, glycol, water, ethanol and the like.
  • immunogenic amount refers an effective amount of a particular epitope of a polypeptide of the invention or a fragment or variant thereof that can induce the host immune response against the polypeptide or the infectious agent expressing the polypeptide. This amount is generally in the range of 20 ⁇ g to 10 mg of antigen per dose of vaccine and depends on the subject to be treated, capacity of the subject's immune system to synthesize antibodies, and the degree of protection desired. The precise amount of immunogen required can be calculated by various methods such as, for example, antibody titration.
  • effective amount refers to an amount of a compound or compositions that is sufficient to provide a desired result.
  • an effective amount refers to an amount of a compound or composition (e.g., an antigen) that is sufficient to produce or elicit a protective immune response.
  • An effective amount with respect to an immunological composition is an amount that is sufficient to elicit an immune response, whether or not the response is protective.
  • the present invention in part, relates to the discovery that FTR gene product is required for full virulence of a fungal pathogen such as R. oryzae in hematogenous dissemination or mucormycosis. Moreover, inhibition of FTR polypeptide formation in a host having mucormycosis conferred prolonged survival. As described herein, abrogation of FTR1 function resulted in diminished iron uptake and diminished virulence in vivo, and passive immunization with anti-Ftr1p antibody significantly improved survival in infected mice. As disclosed herein, passive immunotherapy against FTR1 is a viable strategy to improve outcomes of these deadly infections.
  • compositions for effective inhibition of FTR molecule and/or its function in treating mucormycosis or other fungal diseases.
  • These inhibitory compositions include vaccines, antisense, siRNA, antibodoy or any other compositions capable of effectively targeting and inhibiting the function of FTR.
  • Such compositions will reduce and/or prevent the growth of the fungus in the infected tissues and will cause organism death.
  • the compositions of the invention also are useful in prophylactic settings to decrease onset and/or prevent infection from occurring.
  • any of the FTR inhibitory compositions disclosed herein can further be supplemented and/or combined with other known antifungal therapies including, for example, Amphotericin B or iron chelators.
  • Exemplary iron chelators include Deferiprone and Deferasirox.
  • the invention provides a vaccine composition having an FTR polypeptide or an antigenic fragment or variant of the polypeptide.
  • the vaccine composition also can include an adjuvant.
  • the vaccine composition of the invention has an FTR polypeptide (SEQ ID NO: 2) shown in FIG. 2 or an antigenic fragment of the FTR polypeptide (e.g., REGLE motif), a pharmaceutically acceptable carrier and/or an adjuvant.
  • the vaccine composition has an FTR polypeptide corresponding to the nucleotides shown in FIG. 15-18 .
  • the formulation of the vaccine composition of the invention is effective in inducing protective immunity in a subject by stimulating both specific humoral (neutralizing antibodies) and effector cell mediated immune responses against fungal pathogens' FTRs.
  • the vaccine composition of the invention is also used in the treatment or prophylaxis of fungal infections such as, for example, mucormycosis.
  • the vaccine of the present invention will contain an immunoprotective quantity of FTR antigens and is prepared by methods well known in the art.
  • the preparation of vaccines is generally described in, for example, M. F. Powell and M. J. Newman, eds., “Vaccine Design (the subunit and adjuvant approach),” Plenum Press (1995); A. Robinson, M. Cranage, and M. Hudson, eds., “Vaccine Protocols (Methods in Molecular Medicine),” Humana Press (2003); and D. Ohagan, ed., “Vaccine Ajuvants: Preparation Methods and Research Protocols (Methods in Molecular Medicine),” Humana Press (2000).
  • FTR polypeptide, and peptide fragments or variants thereof can include immunogenic epitopes, which can be identified using methods known in the art and described in, for example, Geysen et al. Proc. Natl. Acad. Sci. USA 81: 3998 (1984)). Briefly, hundreds of overlapping short peptides, e.g., hexapeptides, can be synthesized covering the entire amino acid sequence of the target polypeptide (i.e., FTR). The peptides while still attached to the solid support used for their synthesis are then tested for antigenicity by an ELISA method using a variety of antisera.
  • immunogenic epitopes which can be identified using methods known in the art and described in, for example, Geysen et al. Proc. Natl. Acad. Sci. USA 81: 3998 (1984)). Briefly, hundreds of overlapping short peptides, e.g., hexapeptides, can be synthesized covering
  • Antiserum against FTR protein can be obtained by known techniques, Kohler and Milstein, Nature 256: 495-499 (1975), and can be humanized to reduce antigenicity, see, for example, U.S. Pat. No. 5,693,762, or produced in transgenic mice leaving an unrearranged human immunoglobulin gene, see, for example, U.S. Pat. No. 5,877,397.
  • the peptide can be further tested for specificity by amino acid substitution at every position and/or extension at both C and/or N terminal ends.
  • Such epitope bearing polypeptides typically contain at least six to fourteen amino acid residues of SEQ ID NO: 2, and can be produced, for example, by polypeptide synthesis using methods well known in the art or by fragmenting an FTR polypeptide.
  • FTR polypeptide can be truncated or fragmented without losing the essential qualities as an immunogenic vaccine.
  • FTR polypeptide can be truncated to yield an N-terminal fragment by truncation from the C-terminal end with preservation of the functional properties of the molecule as an immunogen.
  • C-terminal fragments can be generated by truncation from the N-terminal end with preservation of the functional properties of the molecule as an immunogen.
  • Other modifications in accord with the teachings and guidance provided herein can be made pursuant to this invention to create other FTR polypeptide functional fragments, immunogenic fragments, variants, analogs or derivatives thereof, to achieve the therapeutically useful properties described herein with the native protein.
  • the vaccine compositions of the invention further contain conventional pharmaceutical carriers. Suitable carriers are well known to those of skill in the art. These vaccine compositions can be prepared in liquid unit dose forms. Other optional components, e.g., pharmaceutical grade stabilizers, buffers, preservatives, excipients and the like can be readily selected by one of skill in the art. However, the compositions can be lyophilized and reconstituted prior to use. Alternatively, the vaccine compositions can be prepared in any manner appropriate for the chosen mode of administration, e.g., intranasal administration, oral administration, etc. The preparation of a pharmaceutically acceptable vaccine, having due regard to pH, isotonicity, stability and the like, is within the skill of the art.
  • the immunogenicity of the vaccine compositions of the invention can further be enhanced if the vaccine further comprises an adjuvant substance.
  • adjuvant substance Various methods of achieving adjuvant effect for the vaccine are known. General principles and methods are detailed in “The Theory and Practical Application of Adjuvants”, 1995, Duncan E. S. Stewart-Tull (ed.), John Wiley & Sons Ltd, ISBN 0-471-95170-6, and also in “Vaccines: New Generation Immunological Adjuvants”, 1995, Gregoriadis G et al. (eds.), Plenum Press, New York, ISBN 0-306-45283-9, both of which are hereby incorporated by reference herein.
  • Preferred adjuvants facilitate uptake of the vaccine molecules by antigen presenting cells (APCs), such as dendritic cells, and activate these cells.
  • APCs antigen presenting cells
  • Non-limiting examples are selected from the group consisting of an immune targeting adjuvant; an immune modulating adjuvant such as a toxin, a cytokine, and a mycobacterial derivative; an oil formulation; a polymer; a micelle forming adjuvant; a saponin; an immunostimulating complex matrix (ISCOM® matrix); a particle; DDA (dimethyldioctadecylammonium bromide); aluminium adjuvants; DNA adjuvants; and an encapsulating adjuvant.
  • Liposome formulations are also known to confer adjuvant effects, and therefore liposome adjuvants are included according to the invention.
  • Another aspect of the invention relates to a vaccine composition having a vector containing a nucleotide sequence that is substantially complimentary to at least 12 contiguous nucleotides of FTR sequence (e.g., SEQ ID NO: 1) shown in FIGS. 1 , 15 - 18 , a transcription promoter, and a transcription terminator; wherein the promoter is operably linked to the FTR nucleotide sequence, and wherein the FTR nucleotide sequence is operably linked to the transcription terminator.
  • FTR sequence e.g., SEQ ID NO: 1
  • the preparation of DNA vaccines is generally described in, for example, M. Saltzman, H. Shen, and J. Brandsma, eds., “DNA Vaccines (Methods in Molecular Medicine),” Humana Press (2006); H.
  • the vaccine composition further contains pharmaceutically acceptable carrier and/or adjuvant.
  • pharmaceutically acceptable carrier and/or adjuvant Combination of DNA vaccines with adjuvants have been shown to induce a stronger and more specific immune response in human (Hokey et al. Springer Semin Immun 28:267-279 (2006)).
  • the potency of DNA vaccines increases when combined with adjuvants that can provide additional immune stimuli.
  • chemokines such as, for example, MIP-1 ⁇ when used as adjuvants for DNA vaccines have the ability to recruit a variety of cells including professional antigen presenting cells (APCs) to the immunization site.
  • APCs professional antigen presenting cells
  • APCs such as, for example, GM-CSF when used as adjuvant for DNA vaccines can recruit dendritic cells and promote their survival at the immunization site.
  • Molecular adjuvants such as, for example, Fas that induce cell death can also increase the potency and efficacy of DNA vaccines.
  • Adjuvant-mediated apoptosis and necrosis have been shown to provide more antigens to APCs.
  • Other molecules such as for example, poly(lactide-co-glycolide) (PLG) and heat shock proteins have also been shown to act as adjuvants for DNA vaccines.
  • PLG poly(lactide-co-glycolide)
  • heat shock proteins have also been shown to act as adjuvants for DNA vaccines. It is well known to those skilled in the art that adjuvants can be combined with DNA vaccines as intact molecules such as, for example, intact molecules, or as vectors expressing such molecules; for example, plasmids expressing GM-CSF.
  • the vaccine compositions of the present invention can be used to treat, immunotherapeutically, subjects suffering from a variety of fungal infections. Accordingly, vaccines that contain one or more of FTR polynucleotides, polypeptides and/or antibody compositions described herein in combination with adjuvants, and that act for the purposes of prophylactic or therapeutic use, are also within the scope of the invention. In an embodiment, vaccines of the present invention will induce the body's own immune system to seek out and inhibit fungal FTR molecules.
  • Another aspect of the invention relates to a pharmaceutical composition for treating or preventing a fungal condition having an antisense, a small interfering RNA or antibody inhibitor of FTR selected from the group consisting of a nucleotide sequence that is substantially complimentary to a portion of an FTR sequence; a nucleotide sequence that is substantially complimentary to at least 12 contiguous nucleotide bases of FTR sequence; a nucleotide RNAi sequence that is substantially complimentary to at least 18 contiguous nucleotide bases of FTR sequence; an antibody or antibody fragment thereof that specifically binds to an FTR nucleotide sequence, polypeptide or a fragment thereof; and a pharmaceutically acceptable excipient or carrier.
  • the pharmaceutical composition further includes an adjuvant.
  • Antisense nucleic acid molecules of the invention can be designed using the nucleotide sequences of SEQ ID NO: 1, FIGS. 15-18 , their complementary strands, and/or a portion or variant thereof, constructed using enzymatic ligation reactions by procedures known in the art of the genetic engineering.
  • an antisense nucleic acid molecule e.g., an antisense oligonucleotide
  • an antisense nucleic acid molecule can be chemically synthesized using naturally occurring nucleotides or variously modified nucleotides designed to hybridize with a control region of a gene (e.g., promoter, enhancer, or transcription initiation region) to inhibit the expression of the FTR gene through triple-helix formation.
  • the antisense nucleic acid molecule can be designed to hybridize with the transcript of a gene (i.e., mRNA), and thus inhibit the translation of FTR by inhibiting the binding of the transcript to ribosomes.
  • a gene i.e., mRNA
  • the antisense methods and protocols are generally described in, for example, C. Stein, A. Krieg, eds., “Applied Antisense Oligonucleotide Technology” Wiley-Liss, Inc. (1998); or U.S. Pat. Nos. 5,965,722; 6,339,066; 6,358,931; and 6,359,124.
  • the present invention also provides, as antisense molecules, nucleic acids or nucleotide sequences that contain a fragment, portion or variant that hybridizes under high stringency conditions to a nucleotide sequence including a nucleotide sequence selected from SEQ ID NO: 1, FIGS. 15-18 , or their complementary strands.
  • the nucleic acid fragments of the invention are at least about 12, generally at least about 15, 18, 21, or 25 nucleotides, and can be 40, 50, 70, 100, 200, or more nucleotides in length. Longer fragments, for example, 30 or more nucleotides in length, which encode antigenic polypeptides described hereinafter, are particularly useful, such as for the generation of antibodies.
  • RNAi short interfering RNAs
  • RNAi interfering RNA
  • RNAi has been used to knock-down FTR expression in a DKA mouse model of mucormycosis infection, and in doing so it demonstrates a dramatic effect on survival and protection against the infection.
  • the RNAi approach relies on an innate cellular response to combat viral infection. In this process, double stranded mRNAs are recognized and cleaved by the dicer RNase resulting in 21-23 nucleotide long stretches of RNAi.
  • RNA-inducing silencing complex RISC
  • the single antisense strand guides the RISC to mRNA containing the complementary sequence resulting in endonucleolytic cleavage of the mRNA, see Elbashir et al. (Nature 411; 494-498 (2001)).
  • RISC RNA-inducing silencing complex
  • the present invention further provides inhibitory antibodies (monoclonal or polyclonal) and antigen-binding fragments thereof, that are capable of binding to and inhibition of FTR function.
  • the antibody inhibitors of the present invention can bind to FTR, or a portion, fragment, variant thereof, and interfere with or inhibit the protein function, i.e., iron transportation. Furthermore, such antibodies can bind to FTR and interfere with or inhibit the proper localization or conformation of the protein within the fungal membrane.
  • An antibody, or antigen-binding fragment thereof is said to “specifically bind,” “immunologically bind,” and/or is “immunologically reactive” to an FTR polypeptide of the invention if it reacts at a detectable level with the FTR polypeptide, and does not react detectably with unrelated polypeptides under similar conditions.
  • recombinant antibodies such as chimeric and humanized antibodies, including both human and non-human portions, which can be made using standard recombinant DNA techniques, are within the scope of the invention.
  • antibody also included within the term “antibody” are fragments, such as the Fab, F(ab′).
  • the FTR specific monoclonal antibodies of the invention have specific binding activity to FTR, or a functional fragment thereof, in pathogenic fungi responsible for mucormycosis.
  • Monoclonal antibodies can be prepared using methods such as, for example, hybridoma, recombinant, phage display, and combinatorial antibody technologies or a combination thereof.
  • the techniques and protocols for production of monoclonal antibodies are generally described in, for example, Harlow and lane, eds., “Antibodies: A laboratory Manual,” Cold Spring harbor Laboratory Press (1999); Harlow et al., Using Antibodies: A Laboratory Manual, Cold Spring harbor Laboratory Press (1999); C. Borrebaeck, ed., Antibody Engineering: A Practical Guide, W.H. Freeman and Co., Publishers, pp. 130-120 (1991).
  • portions or fragments or variants of the FTR nucleotide sequence identified herein can be used in various ways as polynucleotide reagents.
  • these sequences can be used to identify and express recombinant polypeptides for analysis, characterization, or therapeutic use.
  • the sequences can additionally be used as reagents in the screening and/or diagnostic assays described hereinafter, and can also be included as components of kits (e.g., diagnostic kits) for use in the screening and/or diagnostic assays.
  • compositions of the present invention in inhibiting FTR can be applied to subjects who are suffering from a wide variety of fungal infections including zygomycosis and mucormycosis.
  • the compositions of the invention can further be supplemented with other antifungal agents (e.g., Amphotericin, Deferiprone, Deferasirox).
  • the compositions of the invention can be applied prophylactically to all subjects who are at high risk of developing mucormycosis or other fungal infections (e.g., via active immunization). This would not be considered an over treatment giving the high mortality and morbidity of mucormycosis in view of the current antifungal and surgical debridement treatment.
  • the invention is also directed to host cells in which immunogenic FTR polypeptides or FTR inhibitory nucleotides (e.g., RNAi, antisense molecules) can be produced.
  • host cell is understood to refer not only to the particular subject cell but also to the progeny or potential progeny of the foregoing cell.
  • a host cell can be any prokaryotic (e.g., E. coli ) or eukaryotic cell (e.g., yeast, insect cells, or mammalian cells, such as CHO or COS cells). Other suitable host cells are known to those skilled in the art.
  • Vectors expressing such immunogenic inhibitory molecules can be introduced into prokaryotic or eukaryotic cells via conventional transfection or transformation techniques (see, Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratories, Cold Spring Harbor, N.Y., 1989).
  • any of the above-described compositions can be used for treating or prevention of a fungal condition.
  • a fungal condition is an aberrant condition or infection causes by a pathogenic fungus.
  • Symptoms of a fungal condition that can be ameliorated by a method of the invention include, for example, fever, chills, night sweats, anorexia, weight loss, malaise, depression and lung, skin or other lesions.
  • symptoms or characteristic manifestations include, for example, dissemination from a primary focus, acute or subacute presentations, progressive pneumonia, fungemia, manifestations of extrapulmonary dissemination, chronic meningitis, progressive disseminated histoplasmosis as a generalized involvement of the reticuloendothelial system (liver, spleen, bone marrow) and blastomycosis as single or multiple skin lesions.
  • Effective treatment of an individual with a fungal condition for example, will result in a reduction one or more of such symptoms in the treated individual.
  • Numerous other clinical symptoms of fungal conditions are well known in the art and also can be used as a measure of amelioration or reduction in the severity of a fungal condition using the methods of the invention described herein.
  • Diagnosis of a fungal condition can be confirmed by isolating causative fungi from, for example, sputum, urine, blood, bone marrow, or specimens from infected tissues.
  • causative fungi for example, sputum, urine, blood, bone marrow, or specimens from infected tissues.
  • fungal infections can be diagnosed histopathologically with a high degree of reliability based on distinctive morphologic characteristics of invading fungi and/or by immunohistochemistry and the like selective for identifying antigens.
  • Assessment of the activity of the infection also can be based on cultures taken from many different sites, fever, leukocyte counts, clinical and laboratory parameters related to specific involved organs (eg, liver function tests), and immunoserologic tests. The clinical significance of positive sputum cultures also can be corroborated by confirmation of tissue invasion.
  • Fungal infection, or mycoses, of humans and animals include, for example, superficial fungal infections that affect the outer layers of skin; fungal infections of the mucous membranes including the mouth (thrush), vaginal and anal regions, such as those caused by Candida albicans, and fungal infections that affect the deeper layers of skin and internal organs are capable of causing serious, often fatal illness, such as those caused by, for example, Rhizopus oryzae.
  • Fungal infections are well known in the art and include, for example, zygomycosis, mucormycosis, aspergillosis, cryptococcosis, candidiasis, histoplasmosis, coccidiomycosis, paracoccidiomycosis, fusariosis (hyalohyphomycoses), blastomycosis, penicilliosis or sporotrichosis.
  • zygomycosis mucormycosis, aspergillosis, cryptococcosis, candidiasis, histoplasmosis, coccidiomycosis, paracoccidiomycosis, fusariosis (hyalohyphomycoses), blastomycosis, penicilliosis or sporotrichosis.
  • the fungal conditions caused by fungi of the genus Candida can occur, for example, in the skin and mucous membranes of the mouth, respiratory tract and/or vagina as well as invade the bloodstream, especially in immunocompromised individuals.
  • Candidiasis also is known in the art as candidosis or moniliasis.
  • Exemplary species of the genus Candida include, for example, Candida albicans, Candida krusei, Candida tropicalis, Candida glabrata and Candida parapsilosis.
  • the fungal diseases caused by the genus Aspergillus include, for example, allergic aspergillosis, which affects asthma, cystic fibrosis and sinusitis patients; acute invasive aspergillosis, which shows increased incidence in patients with weakened immunity such as in cancer patients, patients undergoing chemotherapy and AIDS patients; disseminated invasive aspergillosis, which is widespread throughout the body, and opportunistic Aspergillus infection, which is characterized by inflammation and lesions of the ear and other organs.
  • Aspergillus is a genus of around 200 fungi.
  • Aspergillus species causing invasive disease include, for example, Aspergillus fumigatus and Aspergillus flavus.
  • Aspergillus species causing allergic disease include, for example, Aspergillus fumigatus and Aspergillus clavatus.
  • Other exemplary Aspergillus infectious species include, for example, Aspergillus terreus and Aspergillus nidulans.
  • the fungal conditions such as, for example, zygomycosis and mucormycosis which are caused by saprophytic mould fungi include rinocerebral mucormycosis, pulmonary mucormycosis, gastrointestinal mucormycosis, disseminated mucormycosis, bone mucormycosis, mediastinum mucormycosis, trachea mucormycosis, kidney mucormycosis, peritoneum mucormycosis, superior vena cava mucormycosis or external otitis mucormycosis.
  • Infectious agents causing mucormycosis are of the order Mucorales which include species from Rhizopus genus such as, for example, Rhizopus oryzae ( Rhizopus arrhizus ), Rhizopus microsporus var. rhizopodiformis; or species from Absidia genus such as, for example, Absidia corymbifera; or species from Apophysomyces genus such as, for example, Apophysomyces elegans; or species from Mucor genus such as, for example, Mucor amphibiorum; or species from Rhizomucor genus such as, for example, Rhizomucor pusillus; or species from Cunninghamell genus (in the Cunninghamellaceae family) such as, for example, Cunninghamella bertholletiae.
  • Rhizopus genus such as, for example, Rhizopus oryzae ( Rhizopus arrhizus ), Rhizopus microsporus var. rh
  • Various methods are described herein for effective inhibition of FTR molecule and/or its function in treatment of mucormycosis and other fungal diseases. These inhibiting methods involve vaccines, antisense, siRNA, antibodoy, or any other compositions capable of effectively targeting and inhibiting the function of FTR. Such methods will reduce or prevent the growth of the fungus in the infected tissues by inhibiting the main iron transporter that functions in supplying the pathogenic organism with iron.
  • An immunotherapeutic inhibition of iron transportation using a soluble FTR polypeptide or functional fragment or a variant thereof is useful in this context because: (i) the morbidity and mortality associated with mucormycosis, for example, continues to increase, even with currently available antifungal therapy; (ii) a rising incidence of antifungal resistance is associated with the increasing use of antifungal agents; iii) the population of patients at risk for serious zygomycosis, mucormycosis, candidosis, or aspergillosis, for example, is well-defined and very large, and includes, e.g., post-operative patients, transplant patients, cancer patients, low birth weight infants, subjects with diabetes ketoacidosis (DKA) and other forms of metabolic acidosis, subjects receiving treatment with corticosteroids, subjects with neutropenia, trauma, burns, and malignant hematological disorders, and subjects receiving deferoxamine chelation-therapy or hemodialysis; and iv) a high percentage of the patients
  • FTR polypeptide physically complexes with copper oxidase in yeast, transports ferric iron nearly simultaneously to the oxidation step.
  • low pH conditions cause proton-mediated displacement of ferric iron (Fe 3+ ) from serum carrier molecules, including transferrin (T). See FIG. 4 .
  • Fe 3+ is then reduced at the cell surface to ferrous iron (Fe 2+ ).
  • deferoxamine (D) directly chelates iron from transferrin, resulting in ferrioxamine (iron-deferoxamine complex).
  • Ferrioxamine then binds to unidentified receptor(s) on the surface of fungi, e.g., Zygomycetes. The fungus then liberates ferrous iron from ferrioxamine by reduction at the cell surface. In both cases, ferrous iron is reoxidized back to ferric iron by copper oxidase (Cu-oxidase).
  • the methods of the present invention in inhibiting FTR can be applied to subjects who are suffering from a wide variety of fungal infections including zygomycosis and mucormycosis.
  • the methods of the invention can further be supplemented with other antifungal agents (e.g., Amphotericin, Deferiprone, Deferasirox).
  • the methods of the invention can be applied prophylactically to all subjects who are at high risk of developing mucormycosis or other fungal infections (e.g., via active immunization). This would not be considered an over treatment giving the high mortality and morbidity of mucormycosis in view of the current antifungal and surgical debridement treatment.
  • the invention provides a method of treating or preventing disseminated mucormycosis or other fungal diseases.
  • the method includes administering an immunogenic amount of a vaccine having an FTR polypeptide (SEQ ID NO: 2) shown in FIG. 2 , or an antigenic or immunogenic fragment of the polypeptide or a variant thereof in a pharmaceutically acceptable medium.
  • FTR polypeptide SEQ ID NO: 2
  • the preparation of vaccines is generally described in, for example, M. F. Powell and M. J. Newman, eds., “Vaccine Design (the subunit and adjuvant approach),” Plenum Press (1995); A. Robinson, M. Cranage, and M.
  • the FTR polypeptide, or an antigenic or immunogenic fragment of the polypeptide or a variant thereof can be derived from different pathogenic fungal species of Zygomycetes such as Rhizopus oryzae ( Rhizopus arrhizus ), Rhizopus microsporus var.
  • rhizopodiformis Absidia corymbifera, Apophysomyces elegans, Mucor species, Rhizomucor pusillus and Cunninghamella spp (Cunninghamellaceae family); or from different Candida species such as Candida albicans, Candida krusei, Candida tropicalis, Candida glabrata, and Candida parapsilosis; or from different Aspargillus species such as Aspargillus fumigatus, Aspargillus niger, Aspargillus flavus, Aspargillus terreus, and Aspargillus nidulans.
  • Administration of a vaccine of the invention will result in inhibition of the growth and/or virulence of fungal pathogen in a subject.
  • the vaccine compositions are administrated in a manner compatible with the dosage formulation and in such amount as will be prophylactically effective with or without an adjuvant.
  • the quantity to be administered which is generally in the range of 1 to 10 mg, preferably 1 to 1000 ⁇ g of antigen per dose, depends on the subject to be treated, capacity of the subject's immune system to synthesize antibodies, and the degree of protection desired. Precise amounts of active ingredient required to be administered can depend on the judgement of the practitioner and can be peculiar to each subject.
  • the amount of polypeptide in each vaccine dose is selected as an immunogenic amount which induces an immunoprotective response. Particularly useful immunogenic amounts include an amount of FTR polypeptide that also is devoid of significant, adverse side effects.
  • Such amount will vary depending upon the immunogenic strength of an FTR polypeptide selected for vaccination.
  • Useful immunogenic amounts of an FTR polypeptide or immunogenic fragment thereof include, for example, doses ranging from about 1-1000 ⁇ g. In certain embodiments, useful immunogenic amounts of an FTR polypeptide or immunogenic fragment thereof include about 2-100 ⁇ g, and particularly useful dose ranges can range from about 4-40 ⁇ g, including for example, 5, 6, 7, 8, 9, 10, 12, 15, 20, 25, 30, 35 and 40 ⁇ g as well as all values in between the above exemplified amounts.
  • An optimal immunogenic amount for a selected FTR polypeptide vaccine of the invention can be ascertained using methods well known in the art such as determination of antibody titres and other immune responses in subjects as exemplified previously.
  • Vaccine delivery methods is further described, for example, in S. Cohen and H. Bernstein, eds., “Microparticulate Systems for the Delivery of Proteins and Vaccines (Drugs and The Pharmaceutical Sciences),” Vol. 77, Marcel Dekker, Inc. (1996).
  • Encapsulation within liposomes is described, for example, by Fullerton, U.S. Pat. No. 4,235,877.
  • Conjugation of proteins to macromolecules is disclosed, for example, by Likhite, U.S. Pat. No. 4,372,945 and by Armor et al., U.S. Pat. No. 4,474,757.
  • the vaccine compositions of the present invention include DNA vaccines encoding antigenic FTR molecules.
  • DNA vaccines can be introduced into the host cells of the subject by a variety of expression systems. These expression systems include prokaryotic, mammalian, and yeast expression systems.
  • one approach is to utilize a viral vector, such as vaccinia virus incorporating the new genetic material, to innoculate the host cells.
  • the genetic material can be incorporated in a vector or can be delivered directly to the host cells as a “naked” polynucleotide, i.e. simply as purified DNA.
  • the DNA can be stably transfected into attenuated bacteria such as Salmonella typhimurium. When a subject is orally vaccinated with the transformed Salmonella, the bacteria are transported to Peyer's patches in the gut (i.e., secondary lymphoid tissues), which then stimulate an immune response.
  • DNA vaccines can be delivered by variety of well-known delivery vehicles such as, for example, lipid monolayers, bilayers, or vesicles such as liposomes.
  • Agents such as saponins and block-copolymers, which are commonly used to permeablilize cells, can also be used with DNA vaccines.
  • DNA vaccine compositions of the invention can include pharmaceutically acceptable carriers and/or adjuvants.
  • DNA vaccine compositions as described herein can be administered by a variety of routes contemplated by the present invention.
  • routes include intranasal, oral, rectal, vaginal, intramuscular, intradermal and subcutaneous administration.
  • the DNA vaccine compositions for parenteral administration include sterile aqueous or non-aqueous solutions, suspensions or emulsions, the protein vaccine, and an adjuvant as described herein.
  • the composition can be in the form of a liquid, a slurry, or a sterile solid which can be dissolved in a sterile injectable medium before use.
  • the parenteral administration is preferably intramuscular. Intramuscular inoculation involves injection via a syringe into the muscle. This injection can be via a syringe or comparable means.
  • the vaccine composition can contain a pharmaceutically acceptable carrier and/or an adjuvant.
  • the present vaccine compositions can be administered via a mucosal route, in a suitable dose, and in a liquid form.
  • the vaccine composition can be administered in liquid, or solid form with a suitable carrier.
  • the invention also provides a method of treating or preventing a fungal condition in a subject in need thereof, including exposing said fungi to an antisense against FTR.
  • the antisense includes a nucleotide sequence that is substantially complimentary to a portion of an FTR nucleotide sequence.
  • the nucleotide sequence of the antisense is substantially complimentary to at least 12 contiguous nucleotide bases of FTR sequence.
  • the antisense oligonucleotides used in accordance with this invention can be conveniently and routinely made through the well-known technique of solid phase synthesis.
  • Equipment for such synthesis is sold by several vendors including Applied Biosystems. Any other means for such synthesis can also be employed, however the actual synthesis of the oligonucleotides are well within the talents of those skilled in the art. It is also well known to use similar techniques to prepare other oligonucleotides such as the phosphorothioates and alkylated derivatives.
  • an antisense nucleic acid molecule e.g., an antisense oligonucleotide
  • an antisense nucleic acid molecule can be chemically synthesized using naturally occurring nucleotides or variously modified nucleotides designed to hybridize with a control region of a gene (e.g., promoter, enhancer, or transcription initiation region) to inhibit the expression of the FTR gene through triple-helix formation.
  • the antisense nucleic acid molecule can be designed to hybridize with the transcript of FTR (i.e., mRNA), and thus inhibit the translation of FTR by inhibiting the binding of the transcript to ribosomes.
  • the antisense methods and protocols are generally described in, for example, C. Stein, A.
  • the antisense compositions of the invention can be delivered to a subject in need thereof with variety of means known in the art.
  • microparticles such as polystyrene microparticles, biodegradable particles, liposomes or microbubbles containing the antisense compositions in releasable form can be used for direct delivery of the compositions into tissues via injection.
  • the antisense oligonucleotides can be prepared and delivered in a viral vector such as hepatitis B virus (see, for example, Ji et al., J. Viral Hepat. 4:167 173 (1997)); in adeno-associated virus (see, for example, Xiao et al. Brain Res.
  • HVJ(Sendai virus)-liposome gene delivery system see, for example, Kaneda et al. Ann. N.Y. Acad. Sci. 811:299 308 (1997)); a “peptide vector” (see, for example, Vidal et al. CR Acad. Sci III 32):279 287 (1997)); as a gene in an episomal or plasmid vector (see, for example, Cooper et al. Proc. Natl. Acad. Sci. U.S.A. 94:6450 6455 (1997), Yew et al. Hum Gene Ther.
  • the invention also provides a method of treating or preventing a fungal condition in a subject in need thereof, including exposing said fungi to a small interfering RNA against FTR.
  • a nucleotide RNAi sequence that is substantially complimentary to at least 18 contiguous nucleotide bases of FTR sequence is used that is capable of binding to an FTR nucleotide sequence or a fragment thereof.
  • RNAi Double-stranded RNA (dsRNA) also known as small-interfering RNA (siRNA) induces sequence-specific post-transcriptional gene silencing in many organisms by a process known as RNA interference (RNAi).
  • dsRNA double-stranded RNA
  • siRNA small-interfering RNA
  • RNAi RNA interference
  • RNAi has been prepared and used to knock-down FTR expression in a DKA mouse model of mucormycosis infection, and in doing so it demonstrates a dramatic effect on survival and protection against the infection.
  • the siRNA is usually administered as a pharmaceutical composition.
  • the administration can be carried out by known methods, wherein a nucleic acid is introduced into a desired target cell in vitro or in vivo.
  • Commonly used gene transfer techniques include calcium phosphate, DEAE-dextran, electroporation and microinjection and viral methods (Graham et al. Virol. 52, 456 (1973); McCutchan et al. J. Natl. Cancer Inst. 41, 351(1968); Chu et al. Nucl. Acids Res. 15, 1311 (1987); Fraley et al. J. Biol. Chem.
  • cationic liposomes 255, 10431 (1980); Capecchi, Cell 22, 479 (1980); and cationic liposomes (Feigner et al. Proc. Natl. Acad. Sci USA 84, 7413 (1987)).
  • Commercially available cationic lipid formulations are e.g. Tfx 50TM (Promega) or Lipofectamin2000TM (Invitrogen).
  • the invention also provides a method of treating or preventing a fungal condition in a subject in need thereof, including an antibody inhibitor of FTR.
  • the antibody inhibitor of FTR is an antibody or antibody fragment that specifically binds to an FTR nucleotide polypeptide or a fragment thereof.
  • the antibody inhibitors of FTR are capable of binding to and inhibition of FTR function.
  • the antibody inhibitors of the present invention can bind to FTR, a portion, fragment, or variant thereof, and interfere with or inhibit the protein function, i.e., iron transportation. These antibodies can inhibit FTR by negatively affecting, for example, the protein's proper membrane localization, folding or conformation, its substrate binding ability.
  • the antibodies of the present invention can be generated by any suitable method known in the art.
  • Polyclonal antibodies against FTR can be produced by various procedures well known in the art.
  • an FTR peptide antigenic can be administered to various host animals including, but not limited to, rabbits, mice, rats, etc. to induce the production of sera containing polyclonal antibodies specific for the antigen.
  • adjuvants can be used to increase the immunological response, depending on the host species, and include but are not limited to, Freund's (complete and incomplete), mineral gels such as aluminum hydroxide, alum (alhydrogel), surface active substances such as lysolecithin, pluronic polyols, polyanions, peptides, oil emulsions, keyhole limpet hemocyanins, dinitrophenol, and potentially useful human adjuvants such as BCG (bacille Calmette-Guerin) and corynebacterium parvum. Such adjuvants are also well known in the art.
  • FTR peptide antigens suitable for producing antibodies of the invention can be designed, constructed and employed in accordance with well-known techniques. See, e.g., A NTIBODIES: A L ABORATORY M ANUAL, Chapter 5, p. 75-76, Harlow & Lane Eds., Cold Spring Harbor Laboratory (1988); Czemik, Methods In Enzymology, 201: 264-283 (1991); Merrifield, J. Am. Chem. Soc. 85: 21-49 (1962)). Monoclonal antibodies of the present invention can be prepared using a wide variety of techniques known in the art including the use of hybridoma, recombinant, and phage display technologies, or a combination thereof.
  • monoclonal antibodies can be produced using hybridoma techniques including those known in the art and taught, for example, in Harlow et al., Antibodies: A Laboratory Manual, (Cold Spring Harbor Laboratory Press, 2nd ed. 1988); Hammerling, et al., in: Monoclonal Antibodies and T-Cell Hybridomas 563-681 (Elsevier, N.Y., 1981) (said references incorporated by reference in their entireties).
  • the antibodies of the present invention can also be generated using various phage display methods known in the art.
  • phage display methods functional antibody domains are displayed on the surface of phage particles which carry the polynucleotide sequences encoding them.
  • phage can be utilized to display antigen binding domains expressed from a repertoire or combinatorial antibody library (e.g., human or murine).
  • Phage expressing an antigen binding domain that binds the antigen of interest can be selected or identified with antigen, e.g., using labeled antigen or antigen bound or captured to a solid surface or bead.
  • Phage used in these methods are typically filamentous phage including fd and M13 binding domains expressed from phage with Fab, Fv or disulfide stabilized Fv antibody domains recombinantly fused to either the phage gene III or gene VIII protein.
  • Examples of phage display methods that can be used to make the antibodies of the present invention include those disclosed in U.S. Pat. Nos.
  • the antibodies of the invention can be assayed for immunospecific binding by any method known in the art.
  • the immunoassays which can be used include but are not limited to competitive and non-competitive assay systems using techniques such as western blots, radioimmunoassays, ELISA (enzyme linked immunosorbent assay), “sandwich” immunoassays, immunoprecipitation assays, precipitin reactions, gel diffusion precipitin reactions, immunodiffusion assays, agglutination assays, complement-fixation assays, immunoradiometric assays, fluorescent immunoassays, protein A immunoassays, to name but a few.
  • Such assays are routine and well known in the art. See, e.g., Sambrook, Fitsch & Maniatis, Molecular Cloning: A Laboratory Manual, Second Edition Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1989).
  • Specific binding can be determined by any of a variety of measurements known to those skilled in the art including, for example, affinity (K a or K d ), association rate (k on ), dissociation rate (k off ), avidity or a combination thereof.
  • Antibodies of the present invention can also be described or specified in terms of their binding affinity to FTR.
  • Preferred binding affinities include those with a dissociation constant or K d less than 5 ⁇ 10 ⁇ 2 M, 10 ⁇ 2 M, 5 ⁇ 10 ⁇ 3 M, 10 ⁇ 3 M, 5 ⁇ 10 ⁇ 4 M, 10 ⁇ 4 M, 5 ⁇ 10 ⁇ 5 M, 10 ⁇ 5 M, 5 ⁇ 10 ⁇ 6 M, 10 ⁇ 6 M, 5 ⁇ 10 ⁇ 7 M, 10 7 M, 5 ⁇ 10 ⁇ 8 M, 10 ⁇ 8 M, 5 ⁇ 10 ⁇ 9 M, 10 ⁇ 9 M, 5 ⁇ 10 ⁇ 10 M, 10 ⁇ 10 M, 5 ⁇ 10 ⁇ 11 M, 11 ⁇ M, 5 ⁇ 10 ⁇ 12 M, 10 ⁇ 12 M, 5 ⁇ 10 ⁇ 13 M, 10 ⁇ 13 M, 5 ⁇ 10 ⁇ 14 M, 10 ⁇ 14 M, 5 ⁇ 10 ⁇ 15 M, or 10 ⁇ 15 M.
  • An exemplary approach in which the antibodies of the present invention can be used as FTR inhibitors includes binding to and inhibiting FTR polypeptides locally or systemically in the body or by direct cytotoxicity of the antibody, e.g. as mediated by complement (CDC) or by effector cells (ADCC).
  • the antibodies of this invention can be advantageously utilized in combination with other monoclonal or chimeric antibodies, or with lymphokines or hematopoietic growth factors (such as, e.g., IL-2, IL-3 and IL-7), for example, which serve to increase the number or activity of effector cells which interact with the antibodies.
  • the antibodies of the invention can be administered alone or in combination with other types of treatments such as, for example, anti-fungal therapies.
  • FTR inhibitor antibodies are administered to a human patient for therapy or prophylaxis.
  • Various delivery systems are known and can be used to administer the antibody inhibitors of the invention, e.g., encapsulation in liposomes, microparticles, microcapsules, recombinant cells capable Methods of introduction include but are not limited to intradermal, intramuscular, intraperitoneal, intravenous, subcutaneous, intranasal, epidural, and oral routes.
  • the compounds or compositions can be administered by any convenient route, for example by infusion or bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral mucosa, rectal and intestinal mucosa, etc.) and can be administered together with other biologically active agents. Administration can be systemic or local. Pulmonary administration can also be employed, e.g., by use of an inhaler or nebulizer, and formulation with an aerosolizing agent.
  • the dosage administered to a subject is typically 0.1 mg/kg to 100 mg/kg of the subject's body weight.
  • the dosage administered to a subject is between 0.1 mg/kg and 20 mg/kg of the subject's body weight, more preferably 1 mg/kg to 10 mg/kg of the subject's body weight.
  • humanized or human antibodies have a longer half-life within the human body than antibodies from other species due to the immune response to the foreign polypeptides. Thus, lower dosages of humanized antibodies and less frequent administration is often possible.
  • the dosage and frequency of administration of antibodies of the invention can be reduced by enhancing uptake and tissue penetration (e.g., into the brain) of the antibodies by modifications such as, for example, lipidation.
  • compositions of the invention including vaccine, antisense, siRNA and antibodies can be used alone or in appropriate association, as well as in combination, with each other or with other pharmaceutically active compounds.
  • Administration of the agents can be achieved in various ways, including oral, buccal, nasal, rectal, parenteral, intraperitoneal, intradermal, transdermal, subcutaneous, intravenous, intra-arterial, intracardiac, intraventricular, intracranial, intratracheal, and intrathecal administration, etc., or otherwise by implantation or inhalation.
  • compositions can be formulated into preparations in solid, semi-solid, liquid or gaseous forms, such as tablets, capsules, powders, granules, ointments, solutions, suppositories, enemas, injections, inhalants and aerosols.
  • the following methods and excipients are merely exemplary and are in no way limiting.
  • any of treatment modalities disclosed herein can be combined and administered to a subject suffering from a fungal infection or being at risk for developing a fungal infection (prophylactic vaccination or treatment).
  • a subject can first receive a vaccine of the invention to generate an immune response towards the fungi, then an antisense, siRNA and/or antibody that can target FTR of the fungi and further augment the fungal treatment.
  • the vaccine of the invention is used in combination with an antisense, siRNA and/or antibody against FTR for treating or preventing a fungal condition such as, for example, mucormycosis.
  • the antibodies of the invention are used in combination with antisense and/or siRNA for treating the fungal condition.
  • compositions of the inventions can further be combined one or more methods or compositions available for fungal therapy.
  • the compositions of the invention can be used in concert with a surgical method to treat a fungal infection.
  • the compositions of the invention can be used in combination with a drug or radiation therapy for treating a fungal condition.
  • Antifungal drugs that are useful for combination therapy with the compositions of the invention include, but are not limited to, amphotericin B, iron chelators such as, for example, deferasirox, deferiprone, POSACONAZOLE®, FLUCONAZOLE®, ITRACONAZOLE® and/or KETOCONAZOLE®.
  • Radiations useful in combination therapies for treating fungal infections include electromagnetic radiations such as, for example, near infrared radiation with specific wavelength and energy useful for treating fungal infections.
  • electromagnetic radiations such as, for example, near infrared radiation with specific wavelength and energy useful for treating fungal infections.
  • chemotherapy or irradiation is typically followed by administration of the vaccine in such a way that the formation of an effective anti-fungal immune response is not compromised by potential residual effects of the prior treatment.
  • compositions of the invention can be combined with immunocytokine treatments.
  • a vaccine generates a more effective immune response against, for example, an infection when a cytokine promoting the immune response is present at the site of the infection.
  • useful immunocytokines are those that elicit Th1 response, such as IL-2 or IL-12.
  • a subject can first receive a vaccine of the invention to generate an immune response towards a fungal infection, then an immunocytokine that can target the fungi and support the immune response in fighting the infection.
  • Preferred immunocytokines typically have, for example, an antibody moiety that recognizes a surface antigen characteristic of the fungi such as, for example, FTR. Immunocytokines typically also have a cytokine moiety such as IL-2, IL-12, or others that preferentially direct a Th1 response. Immunocytokines suitable for the invention are described in U.S. Pat. No. 5,650,150, the contents of which are hereby incorporated by reference.
  • combinations of the compositions of the invention can be administered either concomitantly, e.g., as an admixture, separately but simultaneously or concurrently; or sequentially.
  • Administration “in combination” further includes the separate administration of one of the compounds or agents given first, followed by the second.
  • compositions of the invention are used in any combination with amphotericin B, deferasirox, deferiprone, POSACONAZOLE®, FLUCONAZOLE®, ITRACONAZOLE®, and/or KETOCONAZOLE® to prophylactically treat, prevent, and/or diagnose an opportunistic fungal infection.
  • the invention therefore, provides methods of treatment, inhibition and prophylaxis by administration to a subject of an effective amount of one or more compounds or pharmaceutical compositions of the invention.
  • the compositions of the invention are substantially purified (e.g., substantially free from substances that limit their effect or produce undesired side-effects).
  • the subject is preferably an animal, including but not limited to animals such as cows, pigs, horses, chickens, cats, dogs, etc., and is preferably a mammal, and most preferably human.
  • compositions of the invention can be administered by any convenient route, for example by infusion or bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral mucosa, rectal and intestinal mucosa, etc.) and can be administered together with other biologically active agents. Administration can be systemic or local.
  • the pharmaceutical compounds or compositions of the invention can be desirable to administer the pharmaceutical compounds or compositions of the invention locally to the area in need of treatment; this can be achieved by, for example, and not by way of limitation, local infusion during surgery, topical application, e.g., in conjunction with a wound dressing after surgery, by injection, by means of a catheter, by means of a suppository, or by means of an implant, said implant being of a porous, non-porous, or gelatinous material, including membranes, such as sialastic membranes, or fibers.
  • a protein including a vaccine or antibody
  • care must be taken to use materials to which the protein does not absorb.
  • the compound or composition can be delivered in liposomes.
  • the compounds or compositions can be delivered in a controlled release system.
  • compositions are formulated in accordance with routine procedures as a pharmaceutical composition adapted for intravenous administration to human beings.
  • compositions for intravenous administration are solutions in sterile isotonic aqueous buffer.
  • the composition can also include a solubilizing agent and a local anesthetic such as lignocaine to ease pain at the site of the injection.
  • the ingredients are supplied either separately or mixed together in unit dosage form, for example, as a dry lyophilized powder or water free concentrate in a hermetically sealed container such as an ampoule indicating the quantity of active agent.
  • the compositions are to be administered by infusion, they can be dispensed with an infusion bottle containing sterile pharmaceutical grade water or saline.
  • an ampoule of sterile water for injection or saline can be provided so that the ingredients can be mixed prior to administration.
  • the compounds of the invention can also be formulated as neutral or salt forms.
  • Pharmaceutically acceptable salts include those formed with anions such as those derived from hydrochloric, phosphoric, acetic, oxalic, tartaric acids, etc., and those formed with cations such as those derived from sodium, potassium, ammonium, calcium, ferric hydroxides, isopropylamine, triethylamine, 2-ethylamino ethanol, histidine, procaine, etc.
  • the amount of the compounds or compositions of the invention which will be effective in the treatment, inhibition and prevention of a fungal disease or condition can be determined by standard clinical techniques.
  • in vitro assays can optionally be employed to help identify optimal dosage ranges.
  • the precise dose to be employed in the formulation will also depend on the route of administration, and the seriousness of the disease or condition, and should be decided according to the judgment of the practitioner and each subject's circumstances. Effective doses can be extrapolated from dose-response curves derived from in vitro or animal model test systems.
  • Example 1 describes cloning and identification of FTR.
  • Example 2 describes FTR expression in R. oryzae under iron-depleted condition.
  • Example 3 describes FTR expression in S. cerevisiae ftr1 null mutant.
  • Example 4 describes FTR function in S. cerevisiae ftr1 null mutant.
  • Example 5, describes development of animal model of mucormycosis.
  • Example describes the effect of serum iron availability on susceptibility of DKA mice to R. oryzae.
  • Example 7 describes the expression of FTR in vivo in DKA mice infected with R. oryzae.
  • Example 8 describes FTR polypeptide and its homology to other proteins.
  • Example 9 describes the role of FTR gene product in virulence of R. oryzae in the DKA mouse model of hematogenous dissemination of mucormycosis.
  • This Example describes the cloning and identification of FTR of R. oryzae which showed considerable sequence homology to high affinity iron permeases of S. cerevisiae and C. albicans ( FIG. 3 ).
  • Rhizopus oryzae 99-880 was obtained from the Fungus Testing Laboratory (University of Texas Health Science Center at San Antonio). This strain was isolated from a brain abscess in a diabetic subject with rhinocerebral mucormycosis.
  • FTR polypeptide functions as a high-affinity iron permease
  • R. oryzae mycelia were collected by filtration and used to inoculate potato dextrose broth (PDB) supplemented with the iron chelators, 1 mM ferrozine and 100 ⁇ M of 2,2′bipyridyl, to induce iron starvation.
  • the mycelia were transferred to PDB previously chelated for iron, and supplemented with varying concentrations of FeCl 3 and incubated at 37° C. for selected intervals.
  • FTR expression was induced at all time points when the organism was exposed to media deficient in FeCl 3 .
  • the addition of FeCl 3 resulted in rapid suppression of FTR expression as early as 5 minutes after exposure. Further, this suppression of FTR expression appeared to be dose dependent, with a more marked, and rapid decrease in FTR mRNA at 350 ⁇ M FeCl 3 as compared with 50 ⁇ M FeCl 3 . Consistent with these results, FTR expression was undetectable when mycelia were grown in the iron-rich medium, PDB.
  • FTR iron-dependent growth defect of a S. cerevisiae ftr1 null mutant.
  • S. cerevisiae was transformed with a plasmid containing FTR under the control of the inducible GAL1 promoter (i.e. expression only in the presence of galactose).
  • S. cerevisiae transformed with FTR grew when cultured on iron-limited medium (50 ⁇ M iron) containing galactose.
  • no growth was noted when the FTR-transformed cells were cultured on plates containing glucose, which failed to induce activation of the GAL1 promoter, and hence transcription of the FTR ( FIG. 6 ).
  • R. oryzae FTR encodes a functional polypeptide in S. cerevisiae.
  • FTR gene that is expressed in R. oryzae in iron-depleted media, suppressed in iron-rich media, and complements the growth defect of high-affinity iron permease null mutant of S. cerevisiae by rescuing the mutant's ability to take up iron in iron-poor media.
  • FTR polypeptide encodes a high-affinity R. oryzae iron permease and also justifies the production of FTR polypeptide in S. cerevisiae because R. oryzae genes can be functionally expressed in S. cerevisiae.
  • This Example shows that we have developed an animal model relevant to mucormycosis, a DKA mouse model of hematogenously disseminated R. oryzae infection.
  • mice with DKA are more susceptible to R. oryzae infection than normal mice. Seven days after intravenous challenge of 10 4 spores, all mice with DKA died, whereas 40% of infected non-diabetic mice survived ( FIG. 8 ).
  • tissue colony counts to a quantitative PCR-based (qPCR) (TaqMan) assay that was developed originally to determine disease progression in animal models of A. fumigatus.
  • the TaqMan technique was developed because the colony count method is unreliable for determining tissue fungal burden of molds since hyphal structures are disrupted by tissue homogenization, resulting in death of the fungus and inaccurately low estimate of the organ fungal burden. Indeed, as anticipated, colony counts did not increase during infection with R. oryzae and did not correlate with mortality. In contrast, a temporal correlation between increase in tissue fungal burden and onset of mortality was found when a qPCR-based (TaqMan) technique, using primers designed to amplify R.
  • This Example shows that susceptibility of DKA mice to R. oryzae is due in part to elevated available serum iron.
  • mice were infected via the tail-vein with spores of R. oryzae.
  • the mice were treated by oral gavage with 1, 3, or 10 mg/kg deferasirox (a newly FDA approved iron chelator to treat subjects with iron overload) in 0.5% hydroxypropylcellulose twice daily (bid) for seven days starting the day after infection.
  • deferasirox a newly FDA approved iron chelator to treat subjects with iron overload
  • hydroxypropylcellulose twice daily (bid) for seven days starting the day after infection.
  • Negative control mice were treated with hydroxypropylcellulose carrier (placebo) or deferasirox plus saturating ferric chloride (administered i.p.).
  • mice treated with placebo or deferasirox plus saturating ferric chloride resulted in a greater than 10-fold decrease in both brain and kidney (primary target organs) fungal burden compared to mice treated with placebo or deferasirox plus saturating ferric chloride ( FIG. 10B ).
  • kidneys of deferasirox-treated mice had no visible hyphae, whereas kidneys of mice treated with placebo or deferasirox plus saturating ferric chloride had extensively filamented fungi.
  • mice treated with saturating iron had a striking absence of neutrophil influx to the sites of infection, while neutrophil influx was prominent in the kidneys of mice treated with deferasirox (data not shown).
  • FTR polypeptide In order for FTR polypeptide to play a role in the pathogenesis of mucormycosis, it must be expressed during infection.
  • DKA diabetic ketoacidic mice infected with 10 5 spores of R. oryzae through tail vein injection.
  • the brain was chosen because it is the primary target organ in this model. Mice were sacrificed 24 or 48 h post infection and brains were collected and immediately flash frozen in liquid nitrogen prior to grinding and RNA extraction with phenol. Brains collected from uninfected DKA mice were processed in parallel and served as negative controls.
  • cDNA was analyzed by real-time PCR using the SYBR-Green method and an ABI® Prism 7000 cycler.
  • Gene-expression was normalized to R. oryzae ACT1 or 18S rRNA-expression.
  • FTR was found to have been expressed in the brains of 4 infected mice 48 h post infection but not after 24 h ( FIG. 11 ). The lack of FTR expression after 24 h of infection cannot be attributed to the presence of lower fungal elements in the brains of infected mice since the expression of both 18S rRNA and ACT1 genes were detected in these tissues.
  • the pattern of delayed FTR polypeptide expression i.e.
  • FTR polypeptide is expressed during infection and is involved in the pathogenesis of mucormycosis.
  • GFP GFP cloned reporter system for FTR expression.
  • R. oryzae was transformed with a plasmid containing GFP cloned down stream of a 2 kb fragment containing FTR promoter. This strain fluoresced green when grown in iron-depleted but not in iron-rich environments in vitro (data not shown).
  • DKA mice were infected with 1 ⁇ 10 5 spores of this R. oryzae strain grown under iron-rich conditions. Forty eight hours post infection mice were sacrificed and brains were collected, and fixed in 10% zinc formalin. Paraffin sections of the brains were stained with anti-GFP polyclonal rabbit Ab and counter stained with anti-rabbit FITC conjugated Ab.
  • a protein vaccine being utilized as a human vaccine not have significant homology to numerous human proteins.
  • coiled-coil domain containing 82 i.e., EAW66982; AAH33726.1; and NP — 079001.2
  • CCDC82 protein i.e., AAH18663.1
  • BAB 15683.1 unnamed protein
  • FTR gene product e.g., mRNA or polypeptide
  • RNA interference RNA interference
  • a 400 bp fragment of FTR ORF containing the REGLE motif was cloned in plasmid pRNAi-pdc upstream of an intron segment.
  • the reverse complement sequence of the same fragment was cloned downstream of the intron.
  • the generated plasmid was transformed into R. oryzae pyrf mutant using the biolistic® delivery system (BioRad®) and transformants were selected on minimal medium lacking uracil. Southern blot analysis showed that all obtained transformants maintained the transformed plasmid episomally (data not shown).
  • RT-PCR was used to compare expression of FTR by five selected transformants to a control strain, which was transformed with the empty plasmid. FTR expression was almost completely inhibited in 4 of the 5 transformants tested and reduced in one transformant compared to control strain ( FIG. 13 ). The expression of 18s rDNA was not altered in any transformant indicating the specificity of RNAi in inhibiting expression of FTR.
  • RNAi transformants The virulence of one of the RNAi transformants was compared to the control strain in the DKA mouse model of hematogenously disseminated mucormycosis. Mice were infected with the control strain transformed or with a transformant harboring the RNAi plasmid (FTR-i strain). There was delayed and reduced virulence of the RNAi-transformant compared to the control strain. Interestingly, we found that R. oryzae recovered from brains and kidneys of moribund mice infected with the FTR-i strain lost the RNAi plasmid since R. oryzae failed to grow on minimal medium without uracil but did grow on rich medium (potato dextrose agar). In contrast, R.
  • the rFtr1p is Exposed Extracellularly and has Limited Homology to Known Human Proteins but is conserveed Among Other Mucorales
  • a protein vaccine being utilized as a human vaccine not have significant homology to numerous human proteins.
  • EAW66982; AAH33726.1; and NP — 079001.2 one is a CCDC82 protein (i.e. AAH18663.1) and an unnamed protein (i.e. BAB15683.1).
  • AAH18663.1 a CCDC82 protein
  • BAB15683.1 an unnamed protein
  • the standard BLAST search e value for identification of unique sequences from fungi compared to other organisms has been set at 10 ⁇ 8 , (Jones et al., Proc Natl Acad Sci USA 2004; 101:7329-34 (2004)) indicating that rFtr1p has no significant homology to the human proteome.
  • rFTR1 is highly conserved among other pathogenic Mucorales including R. microsporus, R. niveus, R. stolonifer, Rhizomucor miehei, Rhizomucor pusillus, Mucor circinelloides, M. racemosus, M. rouxii, and M. plumbeus, with nucleotide homology of >70%.
  • the putative REGLE iron-binding functional motif is 100% conserved among all Mucorales. Nyilasi et al., Clin Microbiol Infect. (2008). This indicates that the proposed vaccine will be cross-immunogenic against other agents of mucormycosis.
  • R. oryzae rFtr1p has a high degree of identity with high iron permeases from a very diverse array of fungi, even beyond molds, including Aspergillus spp., C. albicans, and Cryptococcus neoformans. In all of these fungi, the core REGLE iron-binding functional motif is 100% conserved.
  • a gene was synthesized (Genscript) encoding a more hydrophilic protein by removing the signal peptide and 6 transmembrane domains that direct localization of the protein to the cell membrane. While the synthesized gene had sequence elements removed, none of the remaining sequence was altered, so as to avoid altering potential epitopes in the exposed, hydrophilic regions of the protein.
  • the synthetic gene also included a 6 ⁇ -His-tag to affinity purify the expressed protein. This gene was cloned into pQE32 expression vector and transformed into E. coli.
  • mice were immunized by SQ injection of rFtr1p (20 ⁇ g) mixed with complete Freund's adjuvant (CFA) at day 0, boosted with another dose of the antigen with incomplete Freund's adjuvant (IFA) at day 21, and bled for serum collection two weeks later.
  • CFA complete Freund's adjuvant
  • IFA incomplete Freund's adjuvant
  • FTR1 is Expressed by R. oryzae During Infection in DKA Mice
  • FTR1 FTR1 to play a role in the pathogenesis of mucormycosis, it must be expressed during infection.
  • Quantitative real time PCR qPCR was used to investigate the expression of FTR1 in the brains of DKA mice infected intravenously with 10 5 spores of R. oryzae, an inoculum that causes a 100% mortality within 2-3 days (Ibrahim et al., Antimicrob Agents Chemother 49: 721-727 (2005).
  • the brain was chosen for analysis because it is a primary target organ in this model (Ibrahim et al., Antimicrob Agents Chemother 49: 721-727 (2005)).
  • the non-parametric log-rank test was used to determine differences in survival times, whereas differences in kidney fungal burden, iron uptake, growth rate and in vivo FTR1 expression were compared by the non-parametric Wilcoxon Rank Sum test.
  • R. oryzae was transformed with a plasmid containing GFP under the control of the FTR1 promoter.
  • R. oryzae strains used in this study are listed in Table 1. Briefly, organisms were grown on potato dextrose agar (PDA) or on YPD plates [1% yeast extract (Difco Laboratories), 2% bacto-peptone (Difco), and 2% D-glucose] for 4 days at 37° C.
  • PDA was supplemented with 100 ⁇ g/ml uracil.
  • oryzae was starved for iron by growth on yeast nitrogen base (YNB) (Difco/Becton Dickinson, Sparks, Md.) supplemented with complete supplemental media without uracil (CSM-URA) (Q-Biogene), (YNB+CSM-URA) [formulation/100 ml, 1.7 g YNB without amino acids, 20 g glucose, 0.77 g CSM-URA] in the presence of 1 mM of ascorbic acid and ferrozine.
  • the sporangiospores were collected in endotoxin free PBS containing 0.01% Tween 80, washed with PBS, and counted with a hemacytometer to prepare the final inocula.
  • oryzae GFP1 M16 (pP Ftr1 -GFP) M16 transformed with a plasmid containing a FTR1 promoter driven GFP (Ibrahim et al., J Clin Invest 117: 2649-2657 (2007)).
  • R. oryzae pyrF205, ftr1 knock out, this work FTR1Ko ftr1::PyrF
  • R. oryzae M16 pFTRi- FTR1 inhibited by RNAi, FTR1Inh pdc intron
  • R. oryzae Empty M16 (pRNAi- M16 transformed with pdc intron) empty plasmid, this work
  • This strain fluoresced green when grown in iron-depleted but not iron-rich media in vitro, whereas R. oryzae transformed with GFP under the control of the constitutive actin promoter (positive control) fluoresced regardless of the iron concentration in the medium ( FIG. 22A ).
  • DKA mice were infected with the GFP reporter strain or PyrF-complemented R. oryzae grown under iron-rich conditions to suppress GFP expression prior to infection. Twenty four or 48 h post infection brains were collected and processed for histopathology. Because the paraffin embedding process abrogated the intrinsic fluorescence of the GFP protein, the sections were stained with fluorescent anti-GFP antibody.
  • FTR1 The expression of FTR1 during active infection suggested a role for FTR1 in the pathogenicity of R. oryzae.
  • transformants were grown on chemically defined medium (YNB+CSM-URA) supplemented with 1 mM FeCl 3 (iron rich) to favor the segregation of the ftr1 null allele, since FTR1 is poorly expressed in concentrations ⁇ 350 ⁇ M of FeCl 3 (Fu et al., FEMS Microbiol Lett 235: 169-176 (2004)).
  • Isolates were screened for integration of the disruption cassette with PCR primer pairs FTR1-P3/PyrF-P9 (expected 1054 bp) and PyrF-P18/FTR1-P4 (expected 1140 bp).
  • Disruption of the FTR1 locus was tested by the absence of a PCR amplification product using primers FTR1-P5/FTR1-P6 (expected 503), which amplified a segment from the ORF of FTR1 (Table 2 and FIG. 23A ).
  • PCR confirmed integration of the disruption cassette in the FTR1 locus, and absence of FTR1 ORF from several putative null mutant strains ( FIG. 23B ).
  • these amplification products were also sequenced to demonstrate that the disruption cassette had integrated into the FTR1 locus by homologous recombination (data not shown).
  • integration of the disruption cassette in the FTR1 locus was confirmed by Southern blotting (see below).
  • FTR1 FTR1 promoter expression
  • R. oryzae M16 was transformed with a plasmid containing the reporter gene GFP driven by the FTR1 promoter ( R. oryzae GFP1) as previously described (Ibrahim et al., J Clin Invest 117: 2649-2657 (2007)).
  • GFP was also cloned under the constitutively expressed actin promoter (Act1p) then transformed into R. oryzae M16 to serve as a positive control.
  • Act1p constitutively expressed actin promoter
  • Prior to studying the expression of FTR1 in vivo we examined the expression of FTR1 in vitro using FACS analysis. Briefly, R. oryzae transformed with either.
  • GFP driven by Ftr1p or Act1p were grown in YNB+CSM-URA with (iron-depleted conditions) or without (iron-replete conditions) 1 mM of ascorbic acid and ferrozine at 37° C. for 12 h. These conditions produced germlings of R. oryzae rather than hyphae. Fluorescence of 1 ml of germlings was determined using a FACSCaliber (Becton Dickinson) instrument equipped with an argon laser emitting at 488 nm. Fluorescence emission was read with 515/40 bandpass filter. Fluorescence data were collected with logarithmic amplifiers. The mean fluorescence intensities of 104 events were calculated using CELLQUEST software.
  • mice For in vivo infection, BALB/c male mice (>20 g) were rendered diabetic with a single i.p. injection of 190 mg/kg streptozotocin in 0.2 ml citrate buffer 10 days prior to fungal challenge (Ibrahim et al. Antimicrob Agents Chemother 47: 3343-3344 (2003)). Glycosuria and ketonuria were confirmed in all mice 7 days after streptozotocin treatment. Diabetic ketoacidotic mice were infected with fungal spores by tail vein injection with a target inoculum of 5 ⁇ 103 spores.
  • mice were sacrificed immediately after inhaling R. oryzae spores, and lungs were homogenized, plated on PDA containing 0.1% triton and colonies were counted following incubation at 37° C.
  • brain and kidney fungal burden (primary target organs) (Ibrahim et al., Antimicrob Agents Chemother 49: 721-727 (2005)) was determined by homogenization by rolling a pipette on organs placed in Whirl-Pak bags (Nasco, Fort Atkinson, Wis.) containing 1 ml saline. The homogenate was serially diluted in 0.85% saline and then quantitatively cultured on PDA plates containing 0.1% triton. Values were expressed as log 10 cfu g-1 tissue. To detect GFP expression, anti-GFP rabbit polyclonal antibody (Novus) was used to stain the histopathological samples then counter stained with FITC conjugated anti-rabbit antibody.
  • RNA Clean-Up kit Zymo Research
  • First-strand cDNA synthesis was performed using the Retroscript first-strand synthesis kit (Ambion).
  • FTR1 specific primers listed in Table 2 were designed with the assistance of online primer design software (Genscript). The amplification efficiency was determined by serial dilution experiments, and the resulting efficiency coefficient was used for the quantification of the products (Pfaffl et al., Nucleic Acids Res 29: e45 (2001)).
  • a gene disruption cassette encompassing a functional PyrF copy (998 bp) amplified from R. oryzae wild-type flanked by 606 and 710 bp fragments of FTR1-5′ UTR and FTR1-3′ UTR, respectively ( FIG. 23A ).
  • the gene disruption construct was PCR amplified using primers FTR1 P1/P2 (Table 2) in order to obtain a 2.3 kb disruption fragment containing only the pyrF flanked by homologous FTR1 UTR sequence ( FIG. 23A ). This was then used to transform R. oryzae M16 (pyrF mutant) with biolistic bombardment (Skory, Mol Genet Genomics 268: 397-406 (2002)).
  • the disruption cassette replaces the entire FTR1 coding region from ⁇ 16 to the stop codon, with the pyrF gene fragment.
  • Isolates obtained from two separate transformations were purified with one round of sporulation and single colony isolation on chemically defined medium (YNB+CSM-URA) supplemented with 1 mM FeCl3 (iron rich) to favor the segregation of the FTR1 null allele, since FTR1 expression in this iron concentration is suppressed (Fu et al., FEMS Microbiol Lett 235: 169-176 (2004)).
  • Isolates were tested for integration of the disruption cassette with PCR primer pairs FTR1-P3/PyrF-P9 (expected 1054 bp) and PyrF-P18/FTR1-P4 (expected 1140 bp). Disruption of FTR1 was confirmed by the absence of a PCR amplification product using primers FTR1-P5/FTR1-P6 (expected 503) to amplify the ORF of FTR1 and by Southern blot analysis.
  • transformants with confirmed integration in the FTR1 locus were further taken through 14 rounds of sporulation and single colony isolation on YNB+CSM-URA supplemented with 1 mM FeCl3.
  • FTR1 is expressed in vitro in iron-depleted conditions (FeCl 3 concentration between 0-50 ⁇ M) and suppressed in iron replete media (FeCl 3 concentrations of ⁇ 350 ⁇ M) (Fu et al., FEMS Microbiol Lett 235: 169-176 (2004)).
  • FTR1 disruption had an effect on the ability of R. oryzae to grow in media with different sources and concentration of iron
  • FeCl 3 or FeSO 4 iron complexed to deferoxamine [ferrioxamine] or heme.
  • putative ftr 1 null mutant strains had significantly less growth at 48 h in iron-depleted media (i.e. free iron at 10 ⁇ M) ( FIG. 23C ).
  • Ferrioxamine or iron complexed with heme at 100 ⁇ M (relatively depleted because iron is complexed) supported the growth of the wild-type and PyrF-complemented strains better than the putative ftr1 null mutant.
  • free iron at 1000 ⁇ M iron-rich media supported the growth of all strains equally ( FIG. 23C ) consistent with our previous findings that ftr1 is primarily expressed in iron-depleted environments.
  • putative ftr1 disruption mutants were compared to R. oryzae wild-type or R. oryzae PyrF-complemented strain by growing on plates YNB+CSM-URA supplemented with 10 or 1000 ⁇ M of FeCl3, FeSO4, or with 100 ⁇ M of heme, or ferroxamine as a source of iron. Additionally, putative ftr1 null or RNAi mutants were compared to their corresponding control strains for their growth on YPD or chemically defined medium (i.e. YNB+CSM-URA). Briefly, ten microliters of 105 spores of R.
  • oryzae spores were spotted in the center of plates and the mycelial diameter was measured after 48 h of growth for medium containing FeCl3, FeSO4, or ferroxamine or for 72 h for plates supplemented with heme. The experiment was repeated three times on different days and growth rate was expressed as increase in mycelial diameter of the fungus per hour.
  • R. oryzae is known to be coenocytic and it is generally presumed that sporangiospores are multinucleated, although the number of nuclei has not been previously described (Ma et al., PLoS Genet 5: e1000549 (2009)). Gene disruption appeared to be complicated by the presence of heterokaryotic nuclei in both the mycelium and sporangiospores, and the number of nuclei present in swollen spores using DAPI staining was determined. Briefly, to determine the number of nuclei present in R. oryzae spores, spores in YPD medium were pregerminated for 2 h at 37° C.
  • R. oryzae strain M16 had more than 10 nuclei per swollen spore ( FIG. 24A ).
  • iron-rich medium i.e. medium containing 1000 ⁇ M of FeCl 3
  • PCR analysis of the putative null mutants after 14 rounds of selection demonstrated lack of amplification of FTR1 ORF ( FIG. 24B ).
  • the null mutant had defective growth on iron limited sources for the first 48 h compared to wild-type or PyrF-complemented strains.
  • the FTR1 ORF was once again amplified by PCR.
  • FIG. 24C The Southern blot demonstrated almost complete elimination of the FTR1 band (1960 kb) from gDNA of the putative ftr1 null mutants grown on iron-rich medium, but return of the FTR1 band after growth of the same strain on iron-depleted medium ( FIG. 24C ).
  • genomic DNA was extracted with the OmniPrep lysis buffer (GBiosciences) from PyrF-complemented R. oryzae grown in YNB+CSM-URA supplemented with 1 mM FeCl3 or putative ftr1 null mutant grown in either YNB+CSM-URA supplemented with 1 mM FeCl3 or 100 ⁇ M ferrioxamine.
  • qPCR was used to quantify the copy number of FTR1 in a putative ftr1 null mutant that was passed through 14 rounds of sporulation and single colony isolation on iron-rich media, as well as the same strain after growth in iron-depleted media, and the R. oryzae PyrF-complemented strain.
  • the putative ftr1 null mutant strain grown in iron-rich media had a 60% reduction in the relative copy number of FTR1 (normalized to ACT1 gene) compared to the same strain grown in iron-depleted media or to the R. oryzae PyrF-complemented strain ( FIGS. 25A and 25B ).
  • the putative ftr1 null mutant showed reduced virulence compared to the wild-type or PyrF-complemented strain (62% vs. 100% mortality for mutant vs. control strains in mice with disseminated infection, and 44% vs. 75% mortality for mutant vs. control strains in the intranasal model) (FIG. 26 B,C).
  • the pyrF-complemented strain had similar virulence to the wild-type R. oryzae, demonstrating that restoration of the pyrF gene in its original locus does not affect virulence.
  • RNA interference was used to diminish FTR1 expression in R. oryzae.
  • RNA interference (RNAi) technology was utilized to inhibit the expression of FTR1 in R. oryzae.
  • a 450 bp fragment of FTR1 ORF containing the REGLE motif believed to interact with iron during uptake was PCR amplified and cloned as an inverted repeat under control of the Rhizopus expression vector pPdcA-Ex (Mertens et al., Archives of microbiology 186: 41-50 (2006)).
  • an intron from the Rhizopus pdcA gene (Skory, Curr Microbiol 47: 59-64 (2003)) was included between repeat to serve as a linker for stabilization of the intended dsRNA structure (Nakayashiki et al., Fungal Genet Biol 42: 275-283 (2005); Wesley et al. Plant J 27: 581-590 (2001)).
  • the generated plasmid was transformed into R. oryzae pyrF mutant using the biolistic delivery system (BioRad) and transformants were selected on minimal medium lacking uracil.
  • RNAi Inhibition of FTR1 expression by RNAi was specific, with no apparent reduction in off-site gene expression.
  • a representative RNAi transformant demonstrated similar growth to control strain when grown on either iron rich YPD or CSM-URA media (0.193 ⁇ 0.082 or 0.205 ⁇ 0.016 cm/h for the transformant vs. 0.201 ⁇ 0.087 or 0.211 ⁇ 0.011cm/h for the control strain on iron rich CSM-URA or YPD medium, respectively) ( FIG. 27B ).
  • RNAi decreased 59 Fe uptake by R. oryzae more effectively than did gene disruption, with ⁇ 50% inhibition of iron uptake at all times tested ( FIG. 27C ).
  • ftr1 putative disruption mutant or the RNAi mutant were compared to wild-type or R.
  • Cells were harvested by centrifugation, washed twice with ice cold assay buffer pH 6.1 (minimal medium+10 mM 4-morpholinepropanesulfonic acid+1 mM ferrozine), and then resuspended in assay buffer without any ferrozine to give a concentration of 108 cells per ml.
  • 50 ⁇ l of the cell suspension was added to 450 ⁇ l of chilled assay buffer without ferrozine but supplemented with 0.11M 59FeCl3, and incubated in a shaking water bath at 30° C.
  • the assay samples were chilled on ice, vortexed, vacuum filtered through Whatman GF/C filters and washed with 10 ml ice cold SSW (1 mM EDTA, 20 mM Na3-citrate pH 4.2, 1 mMKH2PO4, 1 mM CaCl2, 5 mM MgSO4, 1 mM NaCl). Filters were removed and placed in glass scintillation vials containing 10 ml scintillation fluid (Filter-count). Cell-associated 59 Fe was counted in a Packard 2200CA liquid scintillation counter (Packard Instrument Co., Downers Grove, Ill.).
  • Nonspecific uptake due to cell surface adsorption was determined by preparing parallel assays that were held on ice for 10 min before filtration and washing. The background levels of 59 Fe were subtracted before calculation of uptake rates. The experiment was carried out in triplicate and repeated three times on different days. The data is presented as specific uptake in pmole/5 ⁇ 10 6 germinated spores.
  • RNAi transformant was compared to the control strain in the DKA mouse models of hematogenously disseminated or intranasal mucormycosis.
  • the RNAi-transformant demonstrated reduced virulence compared to the control strain in both models (75% vs. 100% mortality for RNAi transformant vs. control strain in mice with disseminated infection, and 11% vs. 67% mortality for RNAi transformant vs. control in the intranasal model, p ⁇ 0.02 for both comparisons by Log Rand test) (FIG. 28 A,B).
  • mice were immunized by SQ injection of Ftr1p mixed with complete Freund's adjuvant (CFA) followed by a boost with another dose of the antigen with incomplete Freund's adjuvant (IFA) at day 21, and bled for serum collection two weeks later.
  • CFA complete Freund's adjuvant
  • IFA incomplete Freund's adjuvant
  • Another set of mice were vaccinated with supernatants collected from E. coli transformed with empty plasmid to generate non-immune control serum.
  • Antibody titers were determined using ELISA plates coated with 5 ⁇ g of synthetic recombinant Ftr1p as we previously described (Ibrahim et al., Infect Immun 73: 999-1005 (2005)). Immune or control sera (0.25 ml) were administered i.p.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Genetics & Genomics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Immunology (AREA)
  • Biomedical Technology (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Biophysics (AREA)
  • Mycology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Diabetes (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Plant Pathology (AREA)
  • Virology (AREA)
  • Physics & Mathematics (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Obesity (AREA)
US13/257,585 2009-03-19 2010-03-19 Vaccine compositions and methods for treatment of mucormycosis and other fungal diseases Abandoned US20120093828A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US13/257,585 US20120093828A1 (en) 2009-03-19 2010-03-19 Vaccine compositions and methods for treatment of mucormycosis and other fungal diseases

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US16161409P 2009-03-19 2009-03-19
US13/257,585 US20120093828A1 (en) 2009-03-19 2010-03-19 Vaccine compositions and methods for treatment of mucormycosis and other fungal diseases
PCT/US2010/000820 WO2010107500A1 (en) 2009-03-19 2010-03-19 Vaccine compositions and methods for treatment of mucormycosis and other fungal diseases

Publications (1)

Publication Number Publication Date
US20120093828A1 true US20120093828A1 (en) 2012-04-19

Family

ID=42739922

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/661,609 Expired - Fee Related US8444985B2 (en) 2009-03-19 2010-03-19 Vaccine compositions and methods for treatment of mucormycosis and other fungal diseases
US13/257,585 Abandoned US20120093828A1 (en) 2009-03-19 2010-03-19 Vaccine compositions and methods for treatment of mucormycosis and other fungal diseases

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US12/661,609 Expired - Fee Related US8444985B2 (en) 2009-03-19 2010-03-19 Vaccine compositions and methods for treatment of mucormycosis and other fungal diseases

Country Status (16)

Country Link
US (2) US8444985B2 (es)
EP (1) EP2408804A4 (es)
JP (1) JP2012520878A (es)
KR (1) KR20110139743A (es)
CN (1) CN102639557A (es)
AU (1) AU2010226320A1 (es)
CA (1) CA2755273A1 (es)
CL (1) CL2011002284A1 (es)
IL (1) IL215093A0 (es)
MA (1) MA33199B1 (es)
MX (1) MX2011009735A (es)
NZ (2) NZ595271A (es)
RU (1) RU2011142173A (es)
SG (1) SG174413A1 (es)
TN (1) TN2011000459A1 (es)
WO (1) WO2010107500A1 (es)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013040517A3 (en) * 2011-09-15 2013-07-18 Los Angeles Biomedical Research Institute At Harbor-Ucla Medical Center IMMUNOTHERAPY AND DIAGNOSIS OF MUCORMYCOSIS USING CotH

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1403092B1 (it) * 2010-12-01 2013-10-04 Univ Degli Studi Modena E Reggio Emilia Metodo per la diagnosi e/o il monitoraggio della mucormicosi.
US20160017293A1 (en) * 2012-08-15 2016-01-21 Neostem Oncology, Llc Individualized high purity hepatocellular carcinoma stem cells, methods and use of the same
CN106590685A (zh) * 2015-10-19 2017-04-26 粮华生物科技（北京）有限公司 重金属污染土壤的原位生物修复制剂和修复方法
WO2020006438A1 (en) * 2018-06-29 2020-01-02 University Of Maryland, Baltimore Methods of treating or preventing mucormycosis

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6100380A (en) * 1991-10-28 2000-08-08 Cytran, Inc. Immunomodulating peptides and methods of use
US20060094092A1 (en) * 2004-11-04 2006-05-04 Damude Howard G High arachidonic acid producing strains of Yarrowia lipolytica
US7226600B2 (en) * 2003-06-11 2007-06-05 Ultra Biotech Limited Method to prepare compositions comprising yeast treated with electromagnetic energy
US20080145384A1 (en) * 2001-01-04 2008-06-19 Finlay B Brett Enterohemorrhagic escherichia coli vaccine

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PH31594A (en) 1993-09-30 1998-11-03 Janssen Pharmaceutica Nv Oral formulations on an antifungal.
TW533205B (en) 1996-06-25 2003-05-21 Novartis Ag Substituted 3,5-diphenyl-l,2,4-triazoles and their pharmaceutical composition
DE50111949D1 (de) 2000-12-16 2007-03-15 Alstom Technology Ltd Komponente einer Strömungsmaschine
US7363166B2 (en) * 2001-03-30 2008-04-22 Council Of Scientific & Industrial Research Computational method for the identification of candidate proteins useful as anti-infectives
US7914799B2 (en) * 2001-08-27 2011-03-29 Immunitor USA, Inc. Anti-fungal composition
GB0223978D0 (en) 2002-10-15 2002-11-20 Novartis Ag Organic compound
ITMI20022447A1 (it) 2002-11-19 2004-05-20 Carlo Ghisalberti Uso di piridinoni nel trattamento della purpura capillare ed affezioni cutanee correlate.
JP2006513235A (ja) 2002-12-31 2006-04-20 ネクター セラピューティクス 真菌感染症療法のためのエアゾール化可能な医薬製剤
EP1706481A2 (en) * 2003-12-23 2006-10-04 GlaxoSmithKline Biologicals S.A. Vaccine
MX2008012252A (es) * 2006-03-24 2009-01-14 Basf Plant Science Gmbh Proteinas que se relacionan con la respuesta al estres abiotico y homologos.
CL2007002026A1 (es) * 2006-07-13 2008-06-06 Los Angeles Biomed Res Inst Composicion que comprende al menos un compuesto quelante de hierro y al menos un agente antifungico; y metodo para el tratamiento o prevencion de una condicion fungica.

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6100380A (en) * 1991-10-28 2000-08-08 Cytran, Inc. Immunomodulating peptides and methods of use
US20080145384A1 (en) * 2001-01-04 2008-06-19 Finlay B Brett Enterohemorrhagic escherichia coli vaccine
US7226600B2 (en) * 2003-06-11 2007-06-05 Ultra Biotech Limited Method to prepare compositions comprising yeast treated with electromagnetic energy
US20060094092A1 (en) * 2004-11-04 2006-05-04 Damude Howard G High arachidonic acid producing strains of Yarrowia lipolytica

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
Fu et al. FEMS Microbiol. Lett. 235: 169-176, 2004 *
Greenspan et al. Nature Biotechnology 7: 936-937, 1999 *
Lee et al. In: Abstracts of the American Society for Microbiology's 42nd Annual Interscience Conference on Antimicrobial Agents and Chemotherapy (ICAAC), #M-199, page 374, 2002 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013040517A3 (en) * 2011-09-15 2013-07-18 Los Angeles Biomedical Research Institute At Harbor-Ucla Medical Center IMMUNOTHERAPY AND DIAGNOSIS OF MUCORMYCOSIS USING CotH
US9279002B2 (en) 2011-09-15 2016-03-08 Los Angeles Biomedical Research Institute At Harbor-Ucla Medical Center Immunotherapy and diagnosis of mucormycosis using CotH

Also Published As

Publication number Publication date
WO2010107500A1 (en) 2010-09-23
CA2755273A1 (en) 2010-09-23
NZ595271A (en) 2013-08-30
TN2011000459A1 (en) 2013-03-27
JP2012520878A (ja) 2012-09-10
EP2408804A1 (en) 2012-01-25
AU2010226320A1 (en) 2011-10-13
MA33199B1 (fr) 2012-04-02
CL2011002284A1 (es) 2012-09-14
SG174413A1 (en) 2011-10-28
NZ614255A (en) 2015-03-27
IL215093A0 (en) 2011-11-30
EP2408804A4 (en) 2012-10-03
US8444985B2 (en) 2013-05-21
CN102639557A (zh) 2012-08-15
RU2011142173A (ru) 2013-04-27
MX2011009735A (es) 2011-10-19
US20100285024A1 (en) 2010-11-11
KR20110139743A (ko) 2011-12-29

Similar Documents

Publication Publication Date Title
Ibrahim et al. The high affinity iron permease is a key virulence factor required for Rhizopus oryzae pathogenesis
EP2532360B1 (en) Pharmaceutical compositions and methods to vaccinate against vaginal candidiasis
EP2448959B1 (en) Hyr1 as a target for active and passive immunization against candida
US8444985B2 (en) Vaccine compositions and methods for treatment of mucormycosis and other fungal diseases
US20160130330A1 (en) Mammalian receptors as targets for antibody and active vaccination therapy against mold infections
AU2006244401A1 (en) Pharmaceutical compositions and methods to vaccinate against disseminated candidiasis and other infectious agents
AU2012216520A1 (en) Pharmaceutical compositions and methods to vaccinate against disseminated candidiasis and other infectious agents
AU2013203750A1 (en) Pharmaceutical compositions and methods to vaccinate against disseminated candidiasis and other infectious agents

Legal Events

Date Code Title Description
AS Assignment

Owner name: LOS ANGELES BIOMEDICAL RESEARCH INSTITUTE AT HARBO

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:IBRAHIM, ASHRAF S.;SPELLBERG, BRAD J.;FU, YUE;AND OTHERS;SIGNING DATES FROM 20150219 TO 20150220;REEL/FRAME:035101/0151

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION