Abstract: Compounds that either produced a higher proportion or greater absolute number of phenotypically identified nave, stem cell memory, central memory T cells, adaptive NK cells, and type I NKT cells are identified. Compositions and methods for modulating immune cells including T, NK, and NKT cells for adoptive cell therapies with improved efficacy are provided.
Type:
Grant
Filed:
January 20, 2017
Date of Patent:
August 24, 2021
Assignee:
FATE THERAPEUTICS, INC.
Inventors:
Jonathan Rosen, Betsy Rezner, Bahram Valamehr, Ryan Bjordahl, Eigen Peralta
Abstract: Compositions are described for direct protein delivery into multiple cell types in the mammalian inner ear. The compositions are used to deliver protein(s) (such as gene editing factors) editing of genetic mutations associated with deafness or associated disorders thereof. The delivery of genome editing proteins for gene editing and correction of genetic mutations protect or restore hearing from genetic deafness. Methods of treatment include the intracellular delivery of these molecules to a specific therapeutic target.
Type:
Grant
Filed:
October 29, 2015
Date of Patent:
July 27, 2021
Assignees:
Massachusetts Eye and Ear Infirmary, President and Fellows of Harvard College
Inventors:
Zheng-Yi Chen, David R. Liu, Margie Li, David B. Thompson, John Zuris
Abstract: The present application provides materials and methods for treating a patient with Usher Syndrome Type 2A, both ex vivo and in vivo; materials and methods for editing a USH2A gene in a human cell; materials and methods for editing an USH2A gene containing an IVS40 mutation; materials and methods for treating a patient with an USH2A gene containing an IVS40 mutation; and a method for deleting a sequence comprising an IVS40 mutation within a USH2A gene of a cell. The present application also provides one or more gRNAs or sgRNAs for editing an USH2A gene containing an IVS40 mutation. The present application provides a therapeutic for treating a patient with Usher Syndrome Type 2A. The present application also provides a kit for treating a patient with Usher Syndrome Type 2A.
Type:
Grant
Filed:
June 18, 2020
Date of Patent:
July 27, 2021
Assignees:
BAYER HEALTHCARE LLC, CRISPR THERAPEUTICS AG
Inventors:
Albena Kantardzhieva, Akiko Noma, Abraham Scaria
Abstract: Described is a liquid composition containing naked RNA, such as mRNA encoding a polypeptide, for use in the treatment or prevention of ligament or tendon lesions as well as a method for treating ligament or tendon lesions comprising the administration of a liquid composition containing naked RNA, such as mRNA encoding a polypeptide, which is beneficial in the process of healing the ligament or tendon lesions.
Abstract: Compositions comprising liposomes composed of whole cell membrane fraction are provided. The liposomes may be attached to, or encapsulate a pharmaceutical agent. Also provided are methods of generating and using these liposomes.
Type:
Grant
Filed:
April 2, 2019
Date of Patent:
July 20, 2021
Assignee:
Techmon Research & Development Foundation Limited
Abstract: The invention relates to cancer therapeutics, in particular, the system of making cancer cells more susceptible to effector cells by introduction of cellular therapy targets into the cancer cells.
Abstract: The present disclosure provides methods for re-stimulating TIL populations that lead to improved phenotype and increased metabolic health of the TILs and provides methods of assaying for TIL populations to determine suitability for more efficacious infusion after re-stimulation.
Abstract: A nucleic acid encoding a chimeric antigen receptor (CAR) comprising a single-chain variable fragment (scFv) operatively linked to a signaling domain that polarizes a macrophage to an M1 macrophage; wherein the nucleic acid is operatively linked to a macrophage specific promoter; and wherein the scFv is specific for a human antigen. Monocytes or macrophages comprising such a nucleic acid.
Abstract: A method and device for transfecting a cell to introduce an exogenous material into the cell. The method includes exposing the cell to a region of unsteady flow in the presence of an electric field to encourage introduction of the exogenous material into a cell without lysing the cell.
Type:
Grant
Filed:
November 2, 2018
Date of Patent:
July 6, 2021
Assignee:
INDEE. PTY. LTD.
Inventors:
Ryan Pawell, Amy Twite, Geoff Facer, Katherine Lau, Adrian Lievano, Julyana Acevedo
Abstract: Disclosed herein are compositions and methods for modulating the production of a protein in a target cell. The compositions and methods disclosed herein are capable of ameliorating diseases associated with protein or enzyme deficiencies.
Type:
Grant
Filed:
November 16, 2020
Date of Patent:
July 6, 2021
Assignee:
TRANSLATE BIO, INC.
Inventors:
Braydon Charles Guild, Frank DeRosa, Michael Heartlein
Abstract: The present invention relates to a method for producing renal cells, comprising overexpressing Hnf1b and Pax8, and optionally Hnf4a and/or Emx2 in differentiated cells.
Type:
Grant
Filed:
January 25, 2017
Date of Patent:
June 29, 2021
Assignee:
Albert-Ludwigs-Universitaet Freiburg
Inventors:
Soeren Lienkamp, Michael Kaminski, Sebastian Arnold, Gerd Walz
Abstract: The present invention provides compositions for use in recovering and/or ameliorating deterioration of physiological functions due to aging. Provided are: a cell overexpressing GDF6 protein or an miR-17 family member; a composition for use in treating a senescence-related condition, containing GDF6 protein; a composition for use in treating a senescence-related condition, containing a human expression vector for GDF6 protein or an miR-17 family member; and a composition for use in treating a senescence-related condition, containing a cell secreting GDF6 protein.
Abstract: In a method p for controlling translocation of a target polymer molecule through a nanopore, a clamp is reversibly bound to a sequential plurality of polymer subunits along the target polymer molecule length and the molecule and clamp are disposed in an ionic solution that is in fluidic communication with the nanopore. A constant translocation force is applied across the nanopore to induce travel of the target polymer molecule into the nanopore, until the clamp abuts the nanopore aperture and stops further travel of the target polymer molecule into the nanopore. Then a voltage control pulse is applied across the nanopore and/or a thermal control pulse is applied at the nanopore, with a pulse duration that steps the clamp along the target polymer molecule by no more than one polymer subunit in a direction opposite that of travel into the nanopore. No fuel is provided to the clamp.
Type:
Grant
Filed:
June 28, 2018
Date of Patent:
June 15, 2021
Assignee:
President and Fellows of Harvard College
Inventors:
Daniel Branton, Stephen Jordan Fleming, Jene A. Golovchenko
Abstract: Upon administration of rAAV vectors the humoral immune response (neutralizing antibodies) is the first barrier that needs to be overcome. Surprisingly it was found that by using immunoadsorption for depletion of immunoglobulins from the blood (plasma), subjects can be highly efficiently treated with rAAV vectors, i.e. obtain highly efficient transduction after rAAV vector administration, in spite of the presence of high levels of nAb.
Abstract: Disclosed herein are methods for selectively expanding cells expressing chimeric antigen receptors and enriching cells expressing chimeric antigen receptors in compositions and methods of treating HIV infection in subjects by administering the expanded and/or enriched cells.
Type:
Grant
Filed:
January 27, 2017
Date of Patent:
June 15, 2021
Assignee:
The Regents of the University of California
Inventors:
Otto O. Yang, Ayub Ali, Hwee Ng, Scott G. Kitchen, Jerome A. Zack, Irvin Chen
Abstract: The present disclosure provides methods for re-stimulating TIL populations that lead to improved phenotype and increased metabolic health of the TILs and provides methods of assaying for TIL populations to determine suitability for more efficacious infusion after re-stimulation.
Abstract: Disclosed are compositions and methods comprising one or more recombinant influenza viruses. Recombinant influenza viruses with mutated polymerases and/or rearranged genomes are disclosed. Constructs comprising different influenza nucleic acid sequences are also provided. Methods of inducing protecting immunity with the recombinant influenza viruses are disclosed. Also disclosed are methods of plasmid-free production of influenza virus comprising amplicons comprising one or more of influenza genes.
Type:
Grant
Filed:
May 28, 2013
Date of Patent:
June 8, 2021
Assignee:
UNIVERSITY OF MARYLAND, COLLEGE PARK
Inventors:
Daniel R. Perez, Hongjun Chen, Yibin Cai, Lindomar Jose Pena, Matthew Angel
Abstract: This invention generally relates to cationic oil-in-water emulsions that can be used to deliver nucleic acid molecules, such as an RNA molecule. The emulsion particles comprise an oil core and a cationic lipid. The emulsion particles have an average diameter of about 80 nm to about 180 nm, and the emulsion have an N/P ratio of at least 1.1:1.
Type:
Grant
Filed:
May 2, 2019
Date of Patent:
June 8, 2021
Assignee:
GlaxoSmithKline Biologicals SA
Inventors:
Luis Brito, Michelle C. Archer, Andrew Geall, Derek O'Hagan, Manmohan Singh
Abstract: Described herein are novel preparations of functionalized erythroid cells and related compositions, reagents, and methods for use in human pharmaceutical and veterinary applications.
Type:
Grant
Filed:
February 16, 2018
Date of Patent:
June 1, 2021
Assignee:
Rubius Therapeutics, Inc.
Inventors:
Tom Wickham, Tiffany F. Chen, Xuqing Zhang, Carolyn Sayre, Jordi Mata-Fink, Sivan Elloul, Billy Law, Lenka Hoffman, Kristian Eric Teichert, Shamael Rabia Dastagir
Abstract: The present invention relates to polymers comprising a characteristic combination of alkylene amine moieties which are useful as vehicles for transfecting a cell with a nucleic acid. The present invention furthermore relates to a composition comprising a nucleic acid and such a polymer, and to a method of transfecting a cell using said composition. Furthermore, the present invention relates to pharmaceutical compositions and uses.
Type:
Grant
Filed:
December 18, 2015
Date of Patent:
June 1, 2021
Assignee:
ethris GmbH
Inventors:
Christian Dohmen, Christian Plank, Carsten Rudolph