Provided herein are compositions and methods for the treatment of a disease, such as cancer, using a chimeric antigen receptor or genetically-modified cells comprising a chimeric antigen receptor having specificity for CD20. The invention provides polynucleotides encoding such chimeric antigen receptors, and genetically-modified cells comprising such chimeric antigen receptors. Also provided are methods for making such genetically-modified cells and pharmaceutical compositions comprising the same. The invention further provides methods for treating a disease (e.g., cancer) in a subject by administering such genetically-modified cells or compositions. The main embodiments concern CARs with an scFv specific for CD20, the hinge and transmembrane domains from CD8, the costimulatory cytoplasmic or signalling domain from co-stimulatory molecules Novell (N1) or Novel6 (N6) and the CD3zeta intracellular signaling domain.
Nucleic Acid Molecules Encoding An Engineered Antigen Receptor And An Inhibitory Nucleic Acid Molecule And Methods Of Use Thereof
The present disclosure provides nucleic acid molecules encoding an engineered antigen receptor, such as a chimeric antigen receptor or exogenous T cell receptor, and an inhibitory nucleic acid molecule, such as an RNA interference molecule. The present disclosure further relates to nucleic acids, DNA constructs, vectors, pharmaceutical compositions, genetically-modified cells, and methods of treatment that utilize the nucleic acid molecules of the invention.
Methods Of Preparing Populations Of Genetically-Modified Immune Cells
- Durham NC, US Aaron Martin - Carrboro NC, US Melissa Samo - Raleigh NC, US
Assignee:
Precision BioSciences, Inc. - Durham NC
International Classification:
C12N 15/88 C12N 5/0783 C12N 15/62
Abstract:
The present disclosure provides methods for preparing a population of genetically-modified immune cells. The methods include contacting a population of immune cells with lipid nanoparticles in the presence of an apolipoprotein. The lipid nanoparticles include mRNA encoding an engineered nuclease having specificity for a recognition sequence in the genome of the immune cells. The mRNA is delivered into the immune cells and the engineered nuclease is expressed, generating a cleavage site at the recognition sequence. Further provided are populations of genetic ally-modified immune cells produced according to the disclosed methods, pharmaceutical compositions containing such cells, and methods of treating diseases with the genetically-modified immune cells.
The present invention encompasses methods of cancer immunotherapy, and particularly methods of allogeneic cellular immunotherapy, using particular lymphodepletion regimens in combination with particular populations of chimeric antigen receptor T cells expressing anti CD19 CAR PBCAR0191, anti CD20 CAR PBCAR20A or anti BCMA CAR PBCAR269A.
Engineered Meganucleases With Recognition Sequences Found In The Human Beta-2 Microglobulin Gene
- Durham NC, US Christina Pham - Durham NC, US Aaron Martin - Carrboro NC, US Derek Jantz - Durham NC, US James Jefferson Smith - Morrisville NC, US Michael G. Nicholson - Chapel Hill NC, US
Disclosed herein are recombinant meganucleases engineered to recognize and cleave a recognition sequence present in the human beta-2 microglobulin gene. The disclosure further relates to the use of such recombinant meganucleases in methods for producing genetically-modified eukaryotic cells, and to a population of genetically-modified T cells having reduced cell-surface expression of beta-2 microglobulin.
Co-Stimulatory Domains For Use In Genetically-Modified Cells
The present disclosure provides novel co-stimulatory domains useful in genetically-modified cells to promote cell proliferation and/or promote cytokine secretion after antigen recognition. For example, disclosed herein are genetically-modified cells comprising a chimeric antigen receptor or an inducible regulatory construct incorporating the co-stimulatory domains disclosed herein. Also disclosed herein are plasmids and viral vectors comprising a nucleic acid sequence encoding the co-stimulatory domains, and methods of administering compositions comprising the novel co-stimulatory domains to subjects in order to reduce the symptoms, progression, or occurrence of disease, such as cancer.
Nucleic Acid Molecules Encoding An Engineered Antigen Receptor And An Inhibitory Nucleic Acid Molecule And Methods Of Use Thereof
The present disclosure provides nucleic acid molecules encoding an engineered antigen receptor, such as a chimeric antigen receptor or exogenous T cell receptor, and an inhibitory nucleic acid molecule, such as an RNA interference molecule. The present disclosure further relates to nucleic acids, DNA constructs, vectors, pharmaceutical compositions, genetically-modified cells, and methods of treatment that utilize the nucleic acid molecules of the invention.
Nucleic Acid Molecules Encoding An Engineered Antigen Receptor And An Inhibitory Nucleic Acid Molecule And Methods Of Use Thereof
The present disclosure provides nucleic acid molecules encoding an engineered antigen receptor, such as a chimeric antigen receptor or exogenous T cell receptor, and an inhibitory nucleic acid molecule, such as an RNA interference molecule. The present disclosure further relates to nucleic acids, DNA constructs, vectors, pharmaceutical compositions, genetically-modified cells, and methods of treatment that utilize the nucleic acid molecules of the invention.
Abdominal Hernia Appendicitis Breast Disorders Cholelethiasis or Cholecystitis Gastrointestinal Hemorrhage
Languages:
English Spanish
Description:
Dr. Martin graduated from the A.T. Still University of Health Sciences/ Kirksville College of Osteopathic Medicine in 2005. He works in Grants Pass, OR and specializes in General Surgery. Dr. Martin is affiliated with Asante Three Rivers Medical Center.
Security researcher Aaron Martin linked this activity to an undocumented malware botnet he dubbed "Brutus," which controlled at least 20,000 IP addresses across cloud services and residential networks.
Date: May 27, 2024
Category: Business
Source: Google
State Police: Fights Break Out At Met Life Stadium During Summer Jam Concert
Wewe arrived here about 4:30-5 oclock, whenwe got here they had everybody standing outside in a mob, said Aaron Martin. They wouldnt let us in. When I asked him what was going on they said there was some sort of riot but they wouldnt elaborate.
Another reason Oculus Rift is unlikely to revolutionise marketing in 2015 is that consumers are embedded in a social world, where they share with others constantly. In its current format, the Oculus Rift is fundamentally unsociable, notes Collectives head of strategy, Aaron Martin.
Of course, our students love Lafayette, said Aaron Martin, director of Communications and Marketing at UL. Last month, it was named the happiest town in the nation by The Wall Street Journal.
New Iberia will continue to maintain a colony of about 240 chimpanzees not owned by NIH, said Aaron Martin, director of communications at the University of Louisiana at Lafayette. They are made available to pharmaceutical companies for research.
Thankfully, Saving Hope, from Being Erica and Degrassi Next Generation writer Aaron Martin and Rookie Blue co-creator Morwyn Brebner, avoids most of the obvious pitfalls, judging from the early evidence of tonight's. Saving Hope is neither mawkish nor overly sentimental, though it can be sappy at ti