Abstract: Novel hexon isolated from simian adenovirus serotype 19 encoded in the polynucleotide defined as SEQ ID NO: 3, hepervariable region thereof, chimeric adenovirus comprising the same, and therapeutic use thereof provides a solution to the problem of safety and effective systemic treatment for developing gene therapeutic agents using adenovirus.
Abstract: This disclosure provides modified cytosine deaminases (CDs). The disclosure further relates to cells and vector expressing or comprising such modified CDs and methods of using such modified CDs in the treatment of disease and disorders.
Type:
Grant
Filed:
May 9, 2014
Date of Patent:
July 31, 2018
Assignee:
Tocagen Inc.
Inventors:
Harry E. Gruber, Douglas J. Jolly, Omar D. Perez, Christopher R. Logg
Abstract: The present invention relates to a transduced T cell precursor prepared by introducing a gene construct comprising a polynucleotide encoding C/EBP (CCAAT/enhancer binding protein) to a T cell precursor and overexpressing the C/EBP thereby, wherein the transduced T cell precursor is capable of differentiating into a regulatory T cell and an induced regulatory T cell differentiated therefrom. The transduced T cell precursor and the induced regulatory T cell may be useful for preventing and treating autoimmune diseases, inflammatory diseases and graft rejections caused by the malfunction of immune response.
Type:
Grant
Filed:
June 23, 2015
Date of Patent:
July 24, 2018
Assignee:
SEOUL NATIONAL UNIVERSITY R&DB FOUNDATION
Abstract: The invention relates to an oncolytic adenovirus for the treatment of cancer, containing a human DNA sequence isolating a promoter conferring selective expression on an adenoviral gene. Said adenovirus can also contain a sequence that optimizes the protein translation of an adenoviral gene regulated by a promoter conferring tumor selectivity. The invention is suitable for use in the treatment of cancer.
Type:
Grant
Filed:
May 2, 2016
Date of Patent:
July 10, 2018
Assignee:
DNATRIX, INC.
Inventors:
Ramon Alemany Bonastre, Juan Jose Rojas Exposito, Manel Maria Cascallo Piqueras
Abstract: The present inventors successfully introduced genes into stem cells of airway epithelial tissues using simian immunodeficiency virus vectors pseudotyped with F and HN, which are envelope glycoproteins of Sendai virus. Gene transfer into airway epithelial tissue stem cells using a vector of the present invention is useful for gene therapy of genetic respiratory diseases such as cystic fibrosis. Furthermore, it is possible to select respiratory organs such as the lungs as production tissues for providing proteins that are deficient due to genetic diseases.
Type:
Grant
Filed:
November 17, 2014
Date of Patent:
July 10, 2018
Assignee:
ID PHARMA CO., LTD.
Inventors:
Katsuyuki Mitomo, Makoto Inoue, Hitoshi Iwasaki, Mamoru Hasegawa, Eric W. Alton, Uta Griesenbach
Abstract: A method for stem or progenitor cell culture. More precisely, the invention relates to a method for cell culture using one or more I?I (inter-alpha trypsin inhibitor or inter-alpha inhibitor) protein(s) or part(s) thereof as a component in a cell culture media or a coating on a cell culture surface material. Furthermore the invention relates to a cell culture media and a cell culture coating/matrix provided with one or more I?I proteins(s) or part(s) thereof.
Type:
Grant
Filed:
October 7, 2016
Date of Patent:
July 3, 2018
Assignee:
GE HEALTHCARE BIO-SCIENCES AB
Inventors:
Sara Pijuan Galito, Christoffer Tamm, Cecilia Anneren
Abstract: Methods and compositions are provided for delivering a polynucleotide encoding a gene of interest to a target cell using a virus. The virus envelope comprises a cell-specific binding determinant that recognizes and binds to a component on the target cell surface, leading to endocytosis of the virus. A separate fusogenic molecule is also present on the envelope and facilitates delivery of the polynucleotide across the membrane and into the cytosol of the target cell. The methods and related compositions can be used for treating patients having suffering from a wide range of conditions, including infection, such as HIV; cancers, such as non-Hodgkin's lymphoma and breast cancer; and hematological disorders, such as severe combined immunodeficiency.
Abstract: The present invention relates generally to constructs and their use in gene expression or gene regulation assays. More particularly, the present invention provides expression vectors and/or reporter vectors providing kinetics of protein expression with improved temporal correlation to promoter activity. Even more particularly, the invention provides expression vectors comprising a transcribable polynucleotide which comprises a sequence of nucleotides encoding a RNA element that modulates the stability of a transcript corresponding to the transcribable polynucleotide. The present invention provides, inter alia, novel vectors, useful for identifying and analysing cis- and trans-acting regulatory sequences/factors as well as vectors and genetically modified cell lines or organisms that are particularly useful for drug screening and drug discovery.
Abstract: A method for stem or progenitor cell culture. More precisely, the invention relates to a method for cell culture using one or more I?I (inter-alpha trypsin inhibitor or inter-alpha inhibitor) protein(s) or part(s) thereof as a component in a cell culture media or a coating on a cell culture surface material. Furthermore the invention relates to a cell culture media and a cell culture coating/matrix provided with one or more I?I proteins(s) or part(s) thereof.
Type:
Grant
Filed:
October 7, 2016
Date of Patent:
May 22, 2018
Assignee:
GE HEALTHCARE BIO-SCIENCES AB
Inventors:
Sara Pijuan Galito, Christoffer Tamm, Cecilia Anneren
Abstract: Methods and compositions related to the use of a protein with kynureninase activity are described. For example, in certain aspects there may be disclosed a modified kynureninase capable of degrading kynurenine. Furthermore, certain aspects of the invention provide compositions and methods for the treatment of cancer with kynurenine depletion using the disclosed proteins or nucleic acids.
Type:
Grant
Filed:
August 28, 2015
Date of Patent:
May 22, 2018
Assignee:
BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
Inventors:
George Georgiou, Everett Stone, Nicholas Marshall, John Blazeck, Wei-Cheng Lu
Abstract: The present invention provides a method of preparing adult red blood cells from stem cells in vitro using certain transcription factors for use in medicine, transfusions and transplants. The invention also provides blood compositions with cells prepared by the method.
Abstract: A method for stem or progenitor cell culture. More precisely, the invention relates to a method for cell culture using one or more I?I (inter-alpha trypsin inhibitor or inter-alpha inhibitor) protein(s) or part(s) thereof as a component in a cell culture media or a coating on a cell culture surface material. Furthermore the invention relates to a cell culture media and a cell culture coating/matrix provided with one or more I?I proteins(s) or part(s) thereof.
Type:
Grant
Filed:
June 22, 2016
Date of Patent:
April 17, 2018
Assignee:
GE HEALTHCARE BIO-SCIENCES AB
Inventors:
Sara Pijuan Galito, Christoffer Tamm, Cecilia Anneren
Abstract: This disclosure provides for compositions and methods for the use of designed nucleic acid-targeting nucleic acids, Argonautes, and complexes thereof.
Type:
Grant
Filed:
April 10, 2014
Date of Patent:
February 27, 2018
Assignee:
Caribou Biosciences, Inc.
Inventors:
John Van Der Oost, Daniƫl Christianus Swarts, Andrew Paul May, Rachel E. Haurwitz
Abstract: The present invention provides a method for inducing differentiation of a human pluripotent stem cell into an intermediate mesoderm cell without the use of a growth factor. Such method comprises performing culture in a medium containing a specific compound, so as to induce differentiation of a human pluripotent stem cell into an intermediate mesoderm cell.
Abstract: The present invention relates to the use of one or more cas genes for modulating resistance in a cell against a target nucleic acid or a transcription product thereof.
Type:
Grant
Filed:
June 6, 2012
Date of Patent:
January 30, 2018
Assignee:
DUPONT NUTRITION BIOSCIENCES APS
Inventors:
Rodolphe Barrangou, Patrick Boyaval, Philippe Horvath, Christophe Fremaux, Dennis A. Romero
Abstract: The present invention is directed generally to cell culture media useful for introducing macromolecules and compounds (e.g., nucleic acid molecules) into cells (e.g., eukaryotic cells) in the presence of said media. Cells containing introduced materials can be further cultured in the media. In particular, the invention allows introduction of nucleic acid molecules (e.g., vectors) into cells (particularly eukaryotic cells) and expression of proteins encoded by the nucleic acid molecules in the cells. The invention obviates the need to change the cell culture medium each time a different procedure is performed with the cells (e.g., culturing cells vs. transfecting cells). The invention thus provides efficient and high throughput methods to transform/transfect culture and cells avoiding the need for multiple manipulations and transfers of cells during transfection and expression studies.
Type:
Grant
Filed:
August 15, 2013
Date of Patent:
January 30, 2018
Assignee:
LifeTechnologies Corporation
Inventors:
Valentina C. Ciccarone, Dale Gruber, Shelly Bennett
Abstract: The present invention relates to novel hybrid promoters comprising a caulimovirus promoter operably linked to one or more of an EF1?, Act8, Act2 or Act11 promoter. The present invention also relates to novel DNA constructs comprising at least one expression cassette which comprises the hybrid promoter thereof. The present invention further relates to transgenic plants/seeds comprising such DNA constructs.
Type:
Grant
Filed:
April 22, 2016
Date of Patent:
January 2, 2018
Assignee:
Monsanto Technology LLC
Inventors:
Karen L. Fincher, Stanislaw Flasinski, Jack Q. Wilkinson
Abstract: Disclosed are genetic delivery systems that utilize genetic elements of the piggyBac family transposon system, and methods of introducing nucleic acid into target cells using the genetic delivery systems.
Type:
Grant
Filed:
July 11, 2014
Date of Patent:
December 12, 2017
Assignee:
University of South Alabama
Inventors:
Victor Solodushko, Brian Fouty, Vira Bitko
Abstract: Transgenic microalgae expressing at least one exogenous biologically active protein. The protein-expressing microalgae are used for the oral delivery of the biologically active protein to the target organism in its intact and functional form. The exogenous protein, expressed in algae, is characterized by being biologically active, exerting at least one specific activity having a beneficial effect on the subject consuming the algae. The transgenic microalgae are used as animal food for aquatic or land animals welfare or as food supplement for human healthcare.
Type:
Grant
Filed:
February 23, 2015
Date of Patent:
November 28, 2017
Assignee:
TRANSALGAE ISRAEL LTD.
Inventors:
Shiri Moshitzky, Doron Eisenstadt, Guy Levi, Ofra Chen