Results 41 to 50 of about 70,663 (209)

Third-Generation Anti-CD47-Specific CAR-T Cells Effectively Kill Cancer Cells and Reduce the Genes Expression in Lung Cancer Cell Metastasis

open access: yesJournal of Immunology Research, 2021
CD47 is a cell surface glycoprotein molecule, belonging to the immunoglobulin superfamily, binding to various proteins including integrins, thrombospondin-1, and signal regulatory protein α (SIRPα).
Huyen Thi La   +3 more
doaj   +1 more source

Optimization of chimeric antigen receptor (CAR) therapy

open access: yes, 2021
In this thesis, we focused on how to improve the safety and efficacy of CAR T cell therapy. First, we studied different safeguard mechanisms for CAR T cell depletion in case of short and long-term toxicities. Second, we explored strategies for reducing a priori the risk of severe side effects upon CAR T cell administration through the generation of ...
openaire   +2 more sources

Advancements in CAR-NK therapy: lessons to be learned from CAR-T therapy

open access: yesFrontiers in Immunology, 2023
Advancements in chimeric antigen receptor engineered T-cell (CAR-T) therapy have revolutionized treatment for several cancer types over the past decade. Despite this success, obstacles including the high price tag, manufacturing complexity, and treatment-
Marisa K. Kilgour   +10 more
doaj   +1 more source

NK Cells Armed with Chimeric Antigen Receptors (CAR): Roadblocks to Successful Development [PDF]

open access: yesCells, 2021
In recent years, cell-based immunotherapies have demonstrated promising results in the treatment of cancer. Chimeric antigen receptors (CARs) arm effector cells with a weapon for targeting tumor antigens, licensing engineered cells to recognize and kill cancer cells.
Ali Bashiri Dezfouli   +6 more
openaire   +5 more sources

A BAFF ligand-based CAR-T cell targeting three receptors and multiple B cell cancers

open access: yesNature Communications, 2022
Antigen escape represents a potential drawback of chimeric antigen receptor T cell (CAR-T) therapy targeting a single tumor-associated antigen. To reduce the risk of antigen escape, here the authors report the design and characterization of a BAFF ligand
Derek P. Wong   +12 more
doaj   +1 more source

A new insight in chimeric antigen receptor-engineered T cells for cancer immunotherapy [PDF]

open access: yes, 2017
Adoptive cell therapy using chimeric antigen receptor (CAR)-engineered T cells has emerged as a very promising approach to combating cancer. Despite its ability to eliminate tumors shown in some clinical trials, CAR-T cell therapy involves some ...
Erhao Zhang, Hanmei Xu
core   +2 more sources

Clonal kinetics and single-cell transcriptional profiling of CAR-T cells in patients undergoing CD19 CAR-T immunotherapy [PDF]

open access: yes, 2020
Chimeric antigen receptor (CAR) T-cell therapy has produced remarkable anti-tumor responses in patients with B-cell malignancies. However, clonal kinetics and transcriptional programs that regulate the fate of CAR-T cells after infusion remain poorly ...
Adair, Jennifer E.   +16 more
core   +1 more source

Guanylate cyclase C as a target for prevention, detection, and therapy in colorectal cancer. [PDF]

open access: yes, 2017
INTRODUCTION: Colorectal cancer remains the second leading cause of cancer death in the United States, and new strategies to prevent, detect, and treat the disease are needed.
Aka, Allison A.   +5 more
core   +2 more sources

Chimeric Antigen Receptor (CAR) T-Cell Therapy for Thoracic Malignancies [PDF]

open access: yesJournal of Thoracic Oncology, 2018
Chimeric antigen receptor (CAR) T cells are patient T cells that are transduced with genetically engineered synthetic receptors to target a cancer cell surface antigen. The remarkable clinical response rates achieved by adoptive transfer of T cells that target CD19 in patients with leukemia and lymphoma have led to a growing number of clinical trials ...
Stefan Kiesgen   +3 more
openaire   +2 more sources

Circumventing antivector immunity: potential use of nonhuman adenoviral vectors [PDF]

open access: yes, 2014
Adenoviruses are efficient gene delivery vectors based on their ability to transduce a wide variety of cell types and drive high-level transient transgene expression. While there have been advances in modifying human adenoviral (HAdV) vectors to increase
Beard C.W.   +30 more
core   +3 more sources

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