Government-Owned Inventions; Availability for Licensing, 48544-48546 [2015-19912]
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Federal Register / Vol. 80, No. 156 / Thursday, August 13, 2015 / Notices
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BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions;
Availability for Licensing
National Institutes of Health,
Notice.
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. 209 and 37 CFR part 404 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.
FOR FURTHER INFORMATION CONTACT:
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
SUMMARY:
BILLING CODE 4151–17–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute on Aging; Notice of
Closed Meeting
tkelley on DSK3SPTVN1PROD with NOTICES
[FR Doc. 2015–19946 Filed 8–12–15; 8:45 am]
ACTION:
[FR Doc. 2015–19855 Filed 8–12–15; 8:45 am]
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
Jkt 235001
Dated: August 10, 2015.
Melanie J. Gray,
Program Analyst, Office of Federal Advisory
Committee Policy.
HHS.
Dated: July 30, 2015.
John W. Gill,
Deputy Assistant Secretary, ASA.
16:56 Aug 12, 2015
Name of Committee: National Institute on
Aging Special Emphasis Panel; Physiological
Studies on Aging.
Date: September 28, 2015.
Time: 12:00 p.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institute on Aging,
Gateway Building, Suite 2C212, 7201
Wisconsin Avenue, Bethesda, MD 20892,
(Telephone Conference Call).
Contact Person: Maurizio Grimaldi, Ph.D.,
MD Scientific Review Officer, National
Institute on Aging, National Institutes of
Health, 7201 Wisconsin Avenue, Room
2C218, Bethesda, MD 20892, 301–496–9374,
grimaldim2@mail.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.866, Aging Research,
National Institutes of Health, HHS)
AGENCY:
EXEMPTIONS CLAIMED FOR THIS SYSTEM:
VerDate Sep<11>2014
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
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be required to receive copies of the
patent applications.
SUPPLEMENTARY INFORMATION:
Technology descriptions follow.
Rabbit Antisera to Various Matrix,
Matricellular, and Other Secreted
Proteins
Description of Technology: The
extracellular matrix (ECM) is composed
of a group of proteins that regulate many
cellular functions, such as cell shape,
adhesion, migration, proliferation, and
differentiation. Deregulation of ECM
protein production or function
contributes to many pathological
conditions, including asthma, chronic
obstructive pulmonary disease,
arthrosclerosis, and cancer. Scientists at
the NIH have developed antisera against
various ECM components such as
proteoglycan, sialoprotein, collagen, etc.
(https://www.nidcr.nih.gov/Research/
NIDCRLaboratories/CranioSkeletal/
Antisera.htm). These antisera can be
used as research tools to study the
biology of extracellular matrix
molecules.
Potential Commercial Applications:
Studying the biology of extracellular
matrix molecules.
Development Stage: Early-stage.
Inventor: Larry Fisher (NIDCR).
Intellectual Property: HHS Reference
No. E–135–2008/0—Research Tool.
Patent protection is not being pursued
for this technology.
Licensing Contact: Sally Hu, Ph.D.,
M.B.A.; 301–435–5606; hus@
mail.nih.gov
Collaborative Research Opportunity:
The National Institute for Dental and
Craniofacial Research is seeking
statements of capability or interest from
parties interested in collaborative
research to further develop, evaluate or
commercialize antibodies for studying
the biology of extracellular matrix
molecules. For collaboration
opportunities, please contact David
Bradley, Ph.D. at bradleyda@
nidcr.nih.gov.
mNFHcre Transgenic Mice
Description of Technology: Knockout
mouse is a valuable model to study
biological functions of target genes.
When Cre expressing mice are bred with
mice containing a loxP-flanked gene, the
gene between the loxP sites will be
deleted in the offsprings. Scientists at
the NIH have generated mNF–H-cre
transgenic mouse lines that express Cre
recombinase under the control of the
promoter of the neurofilament-H gene,
which is expressed in the late stage of
neuronal maturation. The transgenic
mice express cre in neurons (but not
astrocytes) with highest expression in
E:\FR\FM\13AUN1.SGM
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Federal Register / Vol. 80, No. 156 / Thursday, August 13, 2015 / Notices
the cortex and hippocampus. The mNF–
H-cre transgenic mouse line can be used
to generate conditional knockout mice
with targeted excision of neuronspecific genes during the late stage of
mouse development. This mouse model
will be useful for the study of neuronal
functions of particular genes.
Potential Commercial Applications:
Generating conditional knockout mice
for neurobiological, neurodevelopmental, or aging studies
involving neurons of the brain and the
spinal cord.
Competitive Advantages: Transgenic
mice express Cre recombinase
selectively in neurons (but not in
astrocytes) in the late stage of brain
development.
Development Stage: In vivo data
available (animal)
Inventor: Ashok Kulkarni (NIDCR)
Publications
1. Hirasawa M,et al. Neuron-specific
expression of Cre recobinase during the late
phase of brain development. Neurosci Res.
2001 Jun; 40(2):125–32. [PMID 11377750].
2. Hirasawa M, et al. Perinatal abrogation
of Cdk5 expression in brain results in
neuronal migration defects. Proc Natl Acad
Sci USA. 2004 Apr 20; 101(16):6249–54.
[PMID 15067135]
Intellectual Property: HHS Reference
No. E–293–2009/0—Research Tool.
Patent protection is not being pursued
for this technology.
Licensing Contact: Sally Hu, Ph.D.,
M.B.A.; 301–435–5606; hus@
mail.nih.gov
Collaborative Research Opportunity:
The National Institute for Dental and
Craniofacial Research is seeking
statements of capability or interest from
parties interested in collaborative
research to further develop, evaluate or
commercialize knockout mice for
neurobiological studies. For
collaboration opportunities, please
contact David Bradley, Ph.D. at
bradleyda@nidcr.nih.gov.
tkelley on DSK3SPTVN1PROD with NOTICES
Novel Vaccine for Prevention and
Treatment of Chlamydia Infection
Description of Technology: The
invention provides novel vectors,
attenuated pathogens, compositions,
methods and kits for preventing and/or
treating chlamydia infections.
Chlamydia trachomatis is an obligate
intracellular human pathogen with a
unique biphasic developmental growth
cycle. It’s the etiological agent of
trachoma, the world’s leading cause of
preventable blindness and the most
common cause of bacterial sexually
transmitted disease. C. trachomatis
isolates maintain a highly conserved
plasmid and naturally occurring
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16:56 Aug 12, 2015
Jkt 235001
plasmidless clinical isolates are rare,
implicating its importance in
chlamydial pathogenesis.
Understanding the plasmid’s role in
chlamydial pathogenesis at a molecular
level is an important objective for the
future control of chlamydial infections.
The NIAID inventor had studied
chlamydia strains in both non-human
primate and murine infectious models
providing evidence that plasmids play
an important role in chlamydial
pathogenesis. In addition, the study
results of macaque model of trachoma
supports the use of plasmid-deficient
organisms as novel live-attenuated
chlamydial vaccines.
Potential Commercial Applications:
Novel live-attenuated chlamydial
vaccines.
Competitive Advantages
• Virulence attenuated vectors that
can be used as vaccines against
chlamydia.
• Combination of vector with
attenuated pathogenic agent improves
the stability and replicative capacity of
the pathogen.
• Features nucleic acids, attenuated
pathogens, compositions, methods and
kits to treat and prevent chlamydia
infections.
Development Stage
• In vitro data available.
• In vivo data available (animal).
• In vivo data available (human).
• Prototype.
Inventor: Harlan D. Caldwell (NIAID).
Publications
1. Song L, et al. Chlamydia trachomatis
plasmid-encoded Pgp4 is a transcriptional
regulator of virulence associated genes. Infect
Immun. 2013 Mar;81(3):636–44. [PMID
23319558].
2. Kari L, et al. A live-attenuated
chlamydial vaccine protects against trachoma
in nonhuman primates. J Exp Med. 2011 Oct
24;208(11):2217–23. [PMID 21987657].
Intellectual Property: HHS Reference
No. E–133–2012/0—
• US Provisional Application No. 61/
753,320 filed 16 Jan 2013.
• PCT Application No. PCT/US2014/
011799 filed 16 Jan 2014, which
published as WO 2014/113541 on 24 Jul
2014.
Licensing Contact: Peter Soukas; 301–
435–4646; ps193c@nih.gov.
Collaborative Research Opportunity:
The National Institute of Allergy and
Infectious Diseases, Laboratory of
Clinical Infectious Diseases, is seeking
statements of capability or interest from
parties interested in collaborative
research to further develop, evaluate or
commercialize chlamydia vaccine. For
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48545
collaboration opportunities, please
contact Harlan D. Caldwell, Ph.D. at
hcaldwell@niaid.nih.gov.
Anti-CD47 Antibodies for the Treatment
of Cancer
Summary: Researchers at the National
Cancer Institute found that CD47
enhances renewal of breast cancer stem
cells, and antibody targeting of CD47
forces these stem cells to differentiate.
Description of Technology: High
expression of CD47, a cell surface
receptor on several types of cancer cells,
has been identified as a ‘don’t eat me
signal’ that inhibits their killing by
macrophages, cytotoxic T cells, and NK
cells. Conversely, the CD47 antibody
B6H12 that blocks SIRPa binding
enhances macrophage-dependent
clearance of tumors in several mouse
models, although others have shown
that such clearance can be independent
of SIRPa signaling.
Cancer stems cells (CSCs) are
tumorigenic cells that are difficult to
target with conventional
chemotherapies due to their
undifferentiated state. Stem cells also
play an important role in the
pathogenesis of cancer. CSCs have been
reported to express elevated CD47
levels, but the role of CD47 in directly
regulating cancer stem cell function has
not been examined.
Researchers at the National Cancer
Institute’s Laboratory of Pathology
found in nonmalignant cells and tissues
that the absence of CD47 enhances stem
cell renewal in vitro and in vivo by
increasing expression of four stem cell
transcription factors (see related
technologies below). Conversely, cancer
stem cells often express high levels of
CD47, and decreasing CD47 is
associated with loss of stem cell
characteristics. More recently, they
discovered methods to force
differentiation of breast cancer stem
cells by targeting the receptor CD47.
These methods disrupt EGF receptor
signaling and up-regulate tumor
suppressor gene expression in breast
cancer stem cells from triple negative
breast cancers, but have no effect on
normal mammary epithelial cells.
Potential Commercial Applications
• Treatment for breast cancer and
other cancers.
• Antibodies for biomedical research.
Competitive Advantages: Monoclonal
antibodies that directly target CD47expressing cancers.
Development Stage: Pre-clinical (in
vivo).
Inventors: David D. Roberts and
Sukhbir Kaur (NCI).
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48546
Federal Register / Vol. 80, No. 156 / Thursday, August 13, 2015 / Notices
Publication
Kaur S, et al. Role of CD47 in triple
negative breast cancer. FASEB J. 2015
April;29(1 Supplement); Abstract 890.5.
[https://www.fasebj.org/content/29/1_
Supplement/890.5]
Intellectual Property: HHS Reference
No. E–263–2014/0—US Application No.
62/062,675 filed October 10, 2014.
tkelley on DSK3SPTVN1PROD with NOTICES
Related Technologies
• HHS Reference No. E–227–2006/
5—US Patent 8,236,313 issued August
7, 2012; US Patent 8,557,788 issued
October 15, 2013; US Patent 8,865,672
issued October 21, 2014.
• HHS Reference No. E–153–2008/
0—US Patent No. 8,951,527 issued
February 10, 2015.
• HHS Reference No. E–086–2012/
1—US Patent Application No. 61/
735,701 filed December 11, 2012.
• HHS Reference No. E–296–2011/
0—Application PCT/US2014/025989
filed March 13, 2014.
Licensing Contact: Jaime M. Greene;
301–435–5559; jaime.greene@
mail.nih.gov.
Collaborative Research Opportunity:
The National Cancer Institute, Center for
Cancer Research, Laboratory of
Pathology, is seeking statements of
capability or interest from parties
interested in collaborative research to
further develop, evaluate or
commercialize methods to differentiate
cancer stem cells. For collaboration
opportunities, please contact John D.
Hewes, Ph.D. at hewesj@mail.nih.gov.
Prevention or Treatment of Viral
Infections by Inhibition of the Histone
Methyltransferases EZH1/2
Description of Technology: Herpes
simplex viral infections, including
herpes simplex virus type 1 (HSV–1)
and type 2 (HSV–2), are exceptionally
common worldwide. These viruses
establish lifelong persistent infections
with cycles of lytic reactivation to
produce recurrent diseases including
oral and genital lesions, herpetic
keratitis/blindness, congenitaldevelopmental syndromes, and viral
encephalitis. Infection with HSV–2
increases the rate of human
immunodeficiency virus (HIV)
transmission in coinfected individuals.
DNA replication inhibitors are typically
used to treat herpesvirus infections.
However, these compounds do not
completely suppress infection, viral
shedding, reactivation from latency, and
the inflammation that contributes to
diseases such as keratitis. An unmet
need continues to exist for methods of
preventing or treating herpesviral
infections. The application claims
methods of preventing or treating
VerDate Sep<11>2014
16:56 Aug 12, 2015
Jkt 235001
herpesviral infection of a host,
comprising administering to the host an
effective amount of an inhibitor of the
EZH1/2 histone methyltransferase
activities. The application is not limited
to herpes simplex virus but rather is
applicable to other viral infections as
well.
Potential Commercial Applications
• HSV therapeutics
• HSV vaccines
Competitive Advantages
• Low-cost production
• Ease of synthesis
Development Stage
• In vitro data available
• In vivo data available (animal)
Inventors: Thomas M. Kristie and
Jesse H. Arbuckle (NIAID)
Intellectual Property: HHS Reference
E–141–2015/0—US Provisional Patent
Application 62/155,704 filed 01 May
2015
Related Technologies
• HHS Reference E–275–2008/0—US
Patent Number 8,916,596 issued 23 Dec
2014; US Application No. 14/543,321
filed 17 Nov 2014; PCT Application No.
PCT/US2009/051557 filed 23 Jul 2009
• HHS Reference E–184–2010/0—US
Patent Number 8,871,789 issued 28 Oct
2014; PCT Application No. PCT/
US2011/044835 filed 21 Jul 2011
Licensing Contact: Peter Soukas; 301–
435–4646; ps193c@nih.gov
Dated: August 7, 2015.
Richard U. Rodriguez,
Acting Director, Office of Technology
Transfer, National Institutes of Health.
[FR Doc. 2015–19912 Filed 8–12–15; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Diabetes and
Digestive and Kidney Diseases; Notice
of Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of a meeting of the Board
of Scientific Counselors, NIDDK.
The meeting will be open to the
public as indicated below, with
attendance limited to space available.
Individuals who plan to attend and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the meeting.
PO 00000
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The meeting will be closed to the
public as indicated below in accordance
with the provisions set forth in section
552b(c)(6), Title 5 U.S.C., as amended
for the review, discussion, and
evaluation of individual intramural
programs and projects conducted by the
NATIONAL INSTITUTE OF DIABETES
AND DIGESTIVE AND KIDNEY
DISEASES, including consideration of
personnel qualifications and
performance, and the competence of
individual investigators, the disclosure
of which would constitute a clearly
unwarranted invasion of personal
privacy.
Name of Committee: Board of Scientific
Counselors, NIDDK.
Date: September 10–11, 2015.
Open: September 10, 2015, 8:00 a.m. to
8:20 a.m.
Agenda: Introductions and Overview.
Place: National Institutes of Health,
Building 5, Room 127, 5 Memorial Drive,
Bethesda, MD 20892.
Closed: September 10, 2015, 8:20 a.m. to
5:00 p.m.
Agenda: To review and evaluate personal
qualifications and performance, and
competence of individual investigators.
Place: National Institutes of Health,
Building 5, Room 127, 5 Memorial Drive,
Bethesda, MD 20892.
Closed: September 11, 2015, 8:00 a.m. to
4:00 p.m.
Agenda: To review and evaluate personal
qualifications and performance, and
competence of individual investigators.
Place: National Institutes of Health,
Building 5, Room 127, 5 Memorial Drive,
Bethesda, MD 20892.
Contact Person: Michael W. Krause, Ph.D.,
Scientific Director, National Institute of
Diabetes and Digestive and Kidney Diseases,
National Institute of Health, Building 5,
Room B104, Bethesda, MD 20892–1818, (301)
402–4633, mwkrause@helix.nih.gov.
In the interest of security, NIH has
instituted stringent procedures for entrance
onto the NIH campus. All visitor vehicles,
including taxicabs, hotel, and airport shuttles
will be inspected before being allowed on
campus. Visitors will be asked to show one
form of identification (for example, a
government-issued photo ID, driver’s license,
or passport) and to state the purpose of their
visit.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.847, Diabetes,
Endocrinology and Metabolic Research;
93.848, Digestive Diseases and Nutrition
Research; 93.849, Kidney Diseases, Urology
and Hematology Research, National Institutes
of Health, HHS)
Dated: August 10, 2015.
Melanie J. Gray,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2015–19940 Filed 8–12–15; 8:45 am]
BILLING CODE 4140–01–P
E:\FR\FM\13AUN1.SGM
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Agencies
[Federal Register Volume 80, Number 156 (Thursday, August 13, 2015)]
[Notices]
[Pages 48544-48546]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-19912]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Government-Owned Inventions; Availability for Licensing
AGENCY: National Institutes of Health, 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. 209 and 37 CFR part 404 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.
FOR FURTHER INFORMATION CONTACT: 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.
SUPPLEMENTARY INFORMATION: Technology descriptions follow.
Rabbit Antisera to Various Matrix, Matricellular, and Other Secreted
Proteins
Description of Technology: The extracellular matrix (ECM) is
composed of a group of proteins that regulate many cellular functions,
such as cell shape, adhesion, migration, proliferation, and
differentiation. Deregulation of ECM protein production or function
contributes to many pathological conditions, including asthma, chronic
obstructive pulmonary disease, arthrosclerosis, and cancer. Scientists
at the NIH have developed antisera against various ECM components such
as proteoglycan, sialoprotein, collagen, etc. (https://www.nidcr.nih.gov/Research/NIDCRLaboratories/CranioSkeletal/Antisera.htm). These antisera can be used as research tools to study
the biology of extracellular matrix molecules.
Potential Commercial Applications: Studying the biology of
extracellular matrix molecules.
Development Stage: Early-stage.
Inventor: Larry Fisher (NIDCR).
Intellectual Property: HHS Reference No. E-135-2008/0--Research
Tool. Patent protection is not being pursued for this technology.
Licensing Contact: Sally Hu, Ph.D., M.B.A.; 301-435-5606;
hus@mail.nih.gov
Collaborative Research Opportunity: The National Institute for
Dental and Craniofacial Research is seeking statements of capability or
interest from parties interested in collaborative research to further
develop, evaluate or commercialize antibodies for studying the biology
of extracellular matrix molecules. For collaboration opportunities,
please contact David Bradley, Ph.D. at bradleyda@nidcr.nih.gov.
mNFHcre Transgenic Mice
Description of Technology: Knockout mouse is a valuable model to
study biological functions of target genes. When Cre expressing mice
are bred with mice containing a loxP-flanked gene, the gene between the
loxP sites will be deleted in the offsprings. Scientists at the NIH
have generated mNF-H-cre transgenic mouse lines that express Cre
recombinase under the control of the promoter of the neurofilament-H
gene, which is expressed in the late stage of neuronal maturation. The
transgenic mice express cre in neurons (but not astrocytes) with
highest expression in
[[Page 48545]]
the cortex and hippocampus. The mNF-H-cre transgenic mouse line can be
used to generate conditional knockout mice with targeted excision of
neuron-specific genes during the late stage of mouse development. This
mouse model will be useful for the study of neuronal functions of
particular genes.
Potential Commercial Applications: Generating conditional knockout
mice for neurobiological, neuro-developmental, or aging studies
involving neurons of the brain and the spinal cord.
Competitive Advantages: Transgenic mice express Cre recombinase
selectively in neurons (but not in astrocytes) in the late stage of
brain development.
Development Stage: In vivo data available (animal)
Inventor: Ashok Kulkarni (NIDCR)
Publications
1. Hirasawa M,et al. Neuron-specific expression of Cre
recobinase during the late phase of brain development. Neurosci Res.
2001 Jun; 40(2):125-32. [PMID 11377750].
2. Hirasawa M, et al. Perinatal abrogation of Cdk5 expression in
brain results in neuronal migration defects. Proc Natl Acad Sci USA.
2004 Apr 20; 101(16):6249-54. [PMID 15067135]
Intellectual Property: HHS Reference No. E-293-2009/0--Research
Tool. Patent protection is not being pursued for this technology.
Licensing Contact: Sally Hu, Ph.D., M.B.A.; 301-435-5606;
hus@mail.nih.gov
Collaborative Research Opportunity: The National Institute for
Dental and Craniofacial Research is seeking statements of capability or
interest from parties interested in collaborative research to further
develop, evaluate or commercialize knockout mice for neurobiological
studies. For collaboration opportunities, please contact David Bradley,
Ph.D. at bradleyda@nidcr.nih.gov.
Novel Vaccine for Prevention and Treatment of Chlamydia Infection
Description of Technology: The invention provides novel vectors,
attenuated pathogens, compositions, methods and kits for preventing
and/or treating chlamydia infections.
Chlamydia trachomatis is an obligate intracellular human pathogen
with a unique biphasic developmental growth cycle. It's the etiological
agent of trachoma, the world's leading cause of preventable blindness
and the most common cause of bacterial sexually transmitted disease. C.
trachomatis isolates maintain a highly conserved plasmid and naturally
occurring plasmidless clinical isolates are rare, implicating its
importance in chlamydial pathogenesis. Understanding the plasmid's role
in chlamydial pathogenesis at a molecular level is an important
objective for the future control of chlamydial infections. The NIAID
inventor had studied chlamydia strains in both non-human primate and
murine infectious models providing evidence that plasmids play an
important role in chlamydial pathogenesis. In addition, the study
results of macaque model of trachoma supports the use of plasmid-
deficient organisms as novel live-attenuated chlamydial vaccines.
Potential Commercial Applications: Novel live-attenuated chlamydial
vaccines.
Competitive Advantages
Virulence attenuated vectors that can be used as vaccines
against chlamydia.
Combination of vector with attenuated pathogenic agent
improves the stability and replicative capacity of the pathogen.
Features nucleic acids, attenuated pathogens,
compositions, methods and kits to treat and prevent chlamydia
infections.
Development Stage
In vitro data available.
In vivo data available (animal).
In vivo data available (human).
Prototype.
Inventor: Harlan D. Caldwell (NIAID).
Publications
1. Song L, et al. Chlamydia trachomatis plasmid-encoded Pgp4 is
a transcriptional regulator of virulence associated genes. Infect
Immun. 2013 Mar;81(3):636-44. [PMID 23319558].
2. Kari L, et al. A live-attenuated chlamydial vaccine protects
against trachoma in nonhuman primates. J Exp Med. 2011 Oct
24;208(11):2217-23. [PMID 21987657].
Intellectual Property: HHS Reference No. E-133-2012/0--
US Provisional Application No. 61/753,320 filed 16 Jan
2013.
PCT Application No. PCT/US2014/011799 filed 16 Jan 2014,
which published as WO 2014/113541 on 24 Jul 2014.
Licensing Contact: Peter Soukas; 301-435-4646; ps193c@nih.gov.
Collaborative Research Opportunity: The National Institute of
Allergy and Infectious Diseases, Laboratory of Clinical Infectious
Diseases, is seeking statements of capability or interest from parties
interested in collaborative research to further develop, evaluate or
commercialize chlamydia vaccine. For collaboration opportunities,
please contact Harlan D. Caldwell, Ph.D. at hcaldwell@niaid.nih.gov.
Anti-CD47 Antibodies for the Treatment of Cancer
Summary: Researchers at the National Cancer Institute found that
CD47 enhances renewal of breast cancer stem cells, and antibody
targeting of CD47 forces these stem cells to differentiate.
Description of Technology: High expression of CD47, a cell surface
receptor on several types of cancer cells, has been identified as a
`don't eat me signal' that inhibits their killing by macrophages,
cytotoxic T cells, and NK cells. Conversely, the CD47 antibody B6H12
that blocks SIRP[alpha] binding enhances macrophage-dependent clearance
of tumors in several mouse models, although others have shown that such
clearance can be independent of SIRP[alpha] signaling.
Cancer stems cells (CSCs) are tumorigenic cells that are difficult
to target with conventional chemotherapies due to their
undifferentiated state. Stem cells also play an important role in the
pathogenesis of cancer. CSCs have been reported to express elevated
CD47 levels, but the role of CD47 in directly regulating cancer stem
cell function has not been examined.
Researchers at the National Cancer Institute's Laboratory of
Pathology found in nonmalignant cells and tissues that the absence of
CD47 enhances stem cell renewal in vitro and in vivo by increasing
expression of four stem cell transcription factors (see related
technologies below). Conversely, cancer stem cells often express high
levels of CD47, and decreasing CD47 is associated with loss of stem
cell characteristics. More recently, they discovered methods to force
differentiation of breast cancer stem cells by targeting the receptor
CD47. These methods disrupt EGF receptor signaling and up-regulate
tumor suppressor gene expression in breast cancer stem cells from
triple negative breast cancers, but have no effect on normal mammary
epithelial cells.
Potential Commercial Applications
Treatment for breast cancer and other cancers.
Antibodies for biomedical research.
Competitive Advantages: Monoclonal antibodies that directly target
CD47-expressing cancers.
Development Stage: Pre-clinical (in vivo).
Inventors: David D. Roberts and Sukhbir Kaur (NCI).
[[Page 48546]]
Publication
Kaur S, et al. Role of CD47 in triple negative breast cancer.
FASEB J. 2015 April;29(1 Supplement); Abstract 890.5. [https://www.fasebj.org/content/29/1_Supplement/890.5]
Intellectual Property: HHS Reference No. E-263-2014/0--US
Application No. 62/062,675 filed October 10, 2014.
Related Technologies
HHS Reference No. E-227-2006/5--US Patent 8,236,313 issued
August 7, 2012; US Patent 8,557,788 issued October 15, 2013; US Patent
8,865,672 issued October 21, 2014.
HHS Reference No. E-153-2008/0--US Patent No. 8,951,527
issued February 10, 2015.
HHS Reference No. E-086-2012/1--US Patent Application No.
61/735,701 filed December 11, 2012.
HHS Reference No. E-296-2011/0--Application PCT/US2014/
025989 filed March 13, 2014.
Licensing Contact: Jaime M. Greene; 301-435-5559;
jaime.greene@mail.nih.gov.
Collaborative Research Opportunity: The National Cancer Institute,
Center for Cancer Research, Laboratory of Pathology, is seeking
statements of capability or interest from parties interested in
collaborative research to further develop, evaluate or commercialize
methods to differentiate cancer stem cells. For collaboration
opportunities, please contact John D. Hewes, Ph.D. at
hewesj@mail.nih.gov.
Prevention or Treatment of Viral Infections by Inhibition of the
Histone Methyltransferases EZH1/2
Description of Technology: Herpes simplex viral infections,
including herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2), are
exceptionally common worldwide. These viruses establish lifelong
persistent infections with cycles of lytic reactivation to produce
recurrent diseases including oral and genital lesions, herpetic
keratitis/blindness, congenital-developmental syndromes, and viral
encephalitis. Infection with HSV-2 increases the rate of human
immunodeficiency virus (HIV) transmission in coinfected individuals.
DNA replication inhibitors are typically used to treat herpesvirus
infections. However, these compounds do not completely suppress
infection, viral shedding, reactivation from latency, and the
inflammation that contributes to diseases such as keratitis. An unmet
need continues to exist for methods of preventing or treating
herpesviral infections. The application claims methods of preventing or
treating herpesviral infection of a host, comprising administering to
the host an effective amount of an inhibitor of the EZH1/2 histone
methyltransferase activities. The application is not limited to herpes
simplex virus but rather is applicable to other viral infections as
well.
Potential Commercial Applications
HSV therapeutics
HSV vaccines
Competitive Advantages
Low-cost production
Ease of synthesis
Development Stage
In vitro data available
In vivo data available (animal)
Inventors: Thomas M. Kristie and Jesse H. Arbuckle (NIAID)
Intellectual Property: HHS Reference E-141-2015/0--US Provisional
Patent Application 62/155,704 filed 01 May 2015
Related Technologies
HHS Reference E-275-2008/0--US Patent Number 8,916,596
issued 23 Dec 2014; US Application No. 14/543,321 filed 17 Nov 2014;
PCT Application No. PCT/US2009/051557 filed 23 Jul 2009
HHS Reference E-184-2010/0--US Patent Number 8,871,789
issued 28 Oct 2014; PCT Application No. PCT/US2011/044835 filed 21 Jul
2011
Licensing Contact: Peter Soukas; 301-435-4646; ps193c@nih.gov
Dated: August 7, 2015.
Richard U. Rodriguez,
Acting Director, Office of Technology Transfer, National Institutes of
Health.
[FR Doc. 2015-19912 Filed 8-12-15; 8:45 am]
BILLING CODE 4140-01-P