Government-Owned Inventions; Availability for Licensing
Federal Register: May 11, 2010 (Volume 75, Number 90)
Notices
Page 26258-26260
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
DOCID:fr11my10-84
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions; Availability for Licensing
AGENCY: National Institutes of Health, Public Health Service, HHS.
ACTION: Notice.
SUMMARY: The inventions listed below are owned by an agency of the U.S.
Government and are available for licensing in the U.S. in accordance with 35 U.S.C. 207 to achieve expeditious commercialization of results of federally-funded research and development. Foreign patent applications are filed on selected inventions to extend market coverage for companies and may also be available for licensing.
ADDRESSES: Licensing information and copies of the U.S. patent applications listed below may be obtained by writing to the indicated licensing contact at the Office of Technology Transfer, National
Institutes of Health, 6011 Executive Boulevard, Suite 325, Rockville,
Maryland 20852-3804; telephone: 301/496-7057; fax: 301/402-0220. A signed Confidential Disclosure Agreement will be required to receive copies of the patent applications.
Erythroid Progenitor Cell Line for Hematological Disease Applications
Description of Invention: Plasmodium vivax (malaria) is a significant health concern in many parts of Asia, Latin America, North
Africa, and the Middle East. There is a lack of continuous culture systems for this pathogen. The subject technology is an erythroid progenitor continuous cell line (termed CD36E) identified by erythroid markers CD36, CD33, CD44, CD71, CD235, and globoside. These CD36E cells are heterozygous for Fya and Fyb (Duffy antigen). Due to recent evidence that Plasmodium vivax (P. vivax) can infect erythroid progenitor cells (reference: YX Ru et al. and T Panichakul et al.), these cells can be potentially used for culturing P. vivax and other species of malaria. This in turn could aid development of malaria related treatments and/or products. In addition, the cell line can also be used for other hematological disease applications that involve red blood cells or red blood cell precursors. The CD36E cells also produce alpha, beta, and chi hemoglobin and therefore may be used for research involving hemoglobin.
Applications:
Culture system for Plasmodium species (malaria)
Hematological diseases
Advantages: Immortalized erythroid progenitor cell line.
Development Status: In vitro data can be provided upon request.
Market:
Malaria
Anti-malaria drug screening
Hematological diseases
Hemoglobin
Inventors: Susan Wong, Neal S. Young, Ning Zhi (NHLBI).
Relevant Publications: 1. YX Ru et al. Invasion of erythroblasts by Pasmodium vivax: A new mechanism contributing to malarial anemia. Ultrastruct Pathol. 2009
Oct;33(5):236-242. [PubMed: 19895296]. 2. T Panichakul et al. Production of erythropoietic cells in vitro for continuous culture of Plasmodium vivax. Int J Parasitol. 2007
Dec;37(14):1551-1557. [PubMed: 17610880].
Patent Status: HHS Reference No. E-151-2010/0--Research Tool.
Patent protection is not being pursued for this technology.
Licensing Status: Available for biological materials licensing.
Licensing Contact: Kevin W. Chang, Ph.D.; 301-435-5018; changke@mail.nih.gov.
Collaborative Research Opportunity: The National Heart Lung and
Blood Institute, Hematology Branch, is seeking statements of capability or interest from parties interested in collaborative research to further develop, evaluate, or commercialize the CD36E cell line. Please contact Cecilia Pazman, Ph.D., at pazmance@mail.nih.gov for more information.
Parvovirus B19 Codon Optimized Structural Proteins for Vaccine and
Diagnostic Applications
Description of Invention: Parvovirus B19 (B19V) is the only known pathogenic human parvovirus. Infection by this viral pathogen can cause transient aplastic crisis in individuals with high red cell turnover, pure red cell aplasia in immunosuppressed patients, and hydrops fetalis during
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pregnancy. In children, B19V most commonly causes erythema infectiosum, or fifth's disease. Infection can also cause arthropathy and arthralgia. The virus is very erythrotropic, targeting human erythroid
(red blood) progenitors found in the blood, bone marrow, and fetal liver. Currently, there are no approved vaccines or antiviral drugs for the treatment or prevention of B19V infection.
The subject technology is a series of plasmid constructs with codon optimized B19 viral capsid genes (VP1 and VP2) that can be expressed in mammalian cells. Transfection of vectors encoding these optimized VP1 and VP2 genes into different mammalian cell lines, including 293, Cos7, and Hela cells produce virus-like particles (VLPs). The vectors include bicistronic plasmids expressing the VP1 and VP2 proteins at different ratios to produce B19V VLPs with optimal antigenicity for vaccine applications. This technology can also be used for diagnostic applications and development of a viral packaging system for producing infectious B19V virus.
Applications:
VLPs based vaccines for the prevention and/or treatment of
B19V infection
DNA based vaccines for the prevention and/or treatment of
B19V infection
B19V diagnostics
Viral packaging system
Advantages:
Codon optimized VP1 and VP2 genes for better expression in mammalian cell lines
Expression of B19V VLPs from ``nonpermissive'' cell lines
Development Status: In vitro data can be provided upon request.
Market:
B19V vaccines (VLPs and DNA)
B19V diagnostics
Inventors: Ning Zhi, Sachiko Kajigaya, and Neal S. Young (NHLBI).
Patent Status: U.S. Provisional Application No. 61/337,983 filed 12
Feb 2010 (HHS Reference No. E-011-2010/0-US-01).
Licensing Status: Available for licensing.
Licensing Contact: Kevin W. Chang, Ph.D.; 301-435-5018; changke@mail.nih.gov.
Collaborative Research Opportunity: The National Heart Lung and
Blood Institute, Hematology Branch, is seeking statements of capability or interest from parties interested in collaborative research to further develop, evaluate, or commercialize the subject technology.
Please contact Cecilia Pazman, Ph.D., at pazmance@mail.nih.gov for more information.
Optimized Expression of IL-12 Cytokine Family
Description of Invention: The IL-12 family of cytokines (IL-12, IL- 23, and IL-27) has an important role in inflammation and autoimmune diseases. IL-12 is produced by macrophages and dendritic cells in response to certain bacterial and parasitic infections and is a powerful inducer of IFN-gamma production. IL-23 is proposed to stimulate a subset of T cells to produce IL-17, which in turn induce the production of proinflammatory cytokines that lead to a protective response during infection. IL-27 appears to have duel functions as an initiator of TH1-type (cellular immunity) immune responses and as an attenuator of immune/inflammatory responses.
The present inventions provide methods for improved expression of multimeric proteins by engineering different ratios of the subunit expression units in a cell or upon expression from a multi-promoter plasmid having different strength promoters. The inventors have improved the levels and efficiency of expression of the IL-12 family of cytokines, which includes IL-12, IL-23, and IL-27, by adjusting the transcription and translation of the alpha and beta subunits that comprise the heterodimeric proteins. Optimal ratios of expression for the two (2) subunits were determined for IL-12, IL-23, and IL-27.
Applications:
Tumor treatment
Anti-viral therapy
Anti-inflammatory therapy
Advantages: Increased expression and stability of in vitro expressed IL-12, IL-23 and IL-27 cytokines
Development Status: In vitro data and data in animal models can be provided upon request
Market:
Infectious Diseases
Cancer
Inflammatory Diseases
Inventors: George N. Pavlakis and Barbara K. Felber (NCI)
Patent Status: International PCT Patent Application No. PCT/US09/ 043481 filed 11 May 2009, which published as WO 2009/140206 on 19 Nov 2009 (HHS Reference No. E-192-2008/1-PCT-02)
Licensing Status: Available for licensing.
Licensing Contact: Kevin W. Chang, Ph.D.; 301-435-5018; changke@mail.nih.gov.
Collaborative Research Opportunity: The Center for Cancer Research,
Human Retrovirus Section, is seeking statements of capability or interest from parties interested in collaborative research to further develop, evaluate, or commercialize delivery of cytokines of the IL-12 family in cancer and other indications. Please contact John D. Hewes,
Ph.D. at 301-435-3121 or hewesj@mail.nih.gov for more information.
Radiotracers for Imaging Cannabinoid Sub-Type 1 (CB1)
Receptor
Description of Invention: The present invention relates to novel radiolabeled compounds for imaging cannabinoid sub-type 1
(CB1) receptors in brains of mammals, particularly humans, using positron emission tomography (PET) or single photon emission computed tomography (SPECT). These radioligands can be used in clinical research, diagnostics, or drug discovery and development, in that, they permit understanding of the role of CB1receptors in neuropsychiatric disorders such as Parkinson's disease, Huntington's disease, Alzheimer's disease, multiple sclerosis, depression, mood disorder, anxiety, schizophrenia, drug addiction, alcohol disorder, obesity and anorexia.
Applications:
In vivo imaging of CB1receptor in mammals, particularly humans
Diagnostic imaging of CB1receptors in subjects having a neurological, neuropsychiatric, neurodegenerative or other condition and treatment
Pharmaceutical composition
Diagnostic kits
Advantages: The principal radioligand under the claim is effective for imaging CB1receptors in vivo with PET.
Development Status: Primary radioligand has been evaluated in non- human primates with PET.
Market: Radioligands may be useful for performing drug occupancy studies of CB1receptors, and for neuropsychiatric studies and investigations with imaging techniques (e.g., PET or SPECT).
Inventors: Victor W. Pike (NIMH), Sean R. Donohue (NIMH), et al.
Relevant Publications: 1. SR Donohue, C Halldin, VW Pike. Synthesis and structure-activity relationships (SARs) of 1,5-diarylpyrazole cannabinoid type-1
(CB1) receptor ligands for potential use in molecular imaging. Bioorg Med Chem. 2006 Jun 1;14(11):3712-3720. [PubMed: 16466922]. 2. SR Donohue, VW Pike, SJ Finnema, P Truong, J Andersson, B
Guly[aacute]s, C Halldin. Discovery and labeling of high affinity 3,4- diarylpyrazolines as
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candidate radioligands for in vivo imaging of cannabinoid subtype-1
(CB1) receptors. J Med Chem. 2008 Sep 25;51(18):5608-5616.
PubMed: 18754613
.
Licensing Status: Available for licensing.
Licensing Contact: Susan Ano, PhD; 301-435-5515; anos@mail.nih.gov.
Dated: May 5, 2010.
Richard U. Rodriguez,
Director, Division of Technology Development and Transfer, Office of
Technology Transfer, National Institutes of Health.
FR Doc. 2010-11173 Filed 5-10-10; 8:45 am
BILLING CODE 4140-01-P
