Results 281 to 290 of about 1,436,444 (347)
Some of the next articles are maybe not open access.

Retargeting CD19 CAR T cells via engineered CD19-fusion proteins.

Molecular Pharmaceutics, 2019
CD19-targeted chimeric antigen receptor (CAR) T-cells (CAR19s) show remarkable efficacy in the treatment of relapsed/refractory acute lymphocytic leukemia and Non-Hodgkin lymphoma.
Justin R. Klesmith   +9 more
semanticscholar   +3 more sources

CD19 Chimeric Antigen Receptor-Exosome Targets CD19 Positive B-lineage Acute Lymphocytic Leukemia and Induces Cytotoxicity

open access: yesCancers, 2021
CAR-T cell therapy is not without some clinical adverse effects, namely cytokine storms, due to a massive release of cytokines when CAR-T cells multiply in the body.
Shabirul Haque
exaly   +2 more sources

Retargeting CD19 Chimeric Antigen Receptor T Cells via Engineered CD19-Fusion Proteins

open access: yesMolecular Pharmaceutics, 2019
CD19-targeted chimeric antigen receptor (CAR) T-cells (CAR19s) show remarkable efficacy in the treatment of relapsed/refractory acute lymphocytic leukemia and Non-Hodgkin’s lymphoma.
Paul D Rennert   +2 more
exaly   +2 more sources

Dual CAR-T cells targeting CD19 and CD37 are effective in target antigen loss B cell tumor models.

Molecular Cancer Therapeutics, 2023
Chimeric antigen receptor T (CAR-T) cells targeting multiple antigens, may reduce the risk of immune escape following the loss of the target antigen and further increase the efficacy of treatment.
Kanae Imai   +10 more
semanticscholar   +1 more source

Trispecific CD19-CD20-CD22–targeting duoCAR-T cells eliminate antigen-heterogeneous B cell tumors in preclinical models

Science Translational Medicine, 2021
Trispecific duoCAR-T cells with optimized costimulatory domains effectively kill tumor cells in antigen-heterogeneous and antigen-replete tumor models.
D. Schneider   +12 more
semanticscholar   +1 more source

CD19 Antigen in Leukemia and Lymphoma Diagnosis and Immunotherapy

Leukemia & Lymphoma, 1995
The CD19 antigen plays an important role in clinical oncology. In normal cells, it is the most ubiquitously expressed protein in the B lymphocyte lineage. CD19 expression is induced at the point of B lineage commitment during the differentiation of the hematopoietic stem cell, and its expression continues through preB and mature B cell differentiation ...
R H, Scheuermann, E, Racila
openaire   +2 more sources

Donor-derived CD19 chimeric antigen receptor T cells

Current Opinion in Hematology, 2015
As immunotherapy matures into possible front-line therapy, new approaches are necessary to expand the capacity to treat more patients. Although most technologies for chimeric antigen receptor (CAR) therapies require autologous T cells, 'off the shelf' sources are highly desired.Sources of T cells for modification with CARs include cord blood and either
Nathan, Singh, David M, Barrett
openaire   +2 more sources

CD19: Lowering the Threshold for Antigen Receptor Stimulation of B Lymphocytes

Science, 1992
Lymphocytes must proliferate and differentiate in response to low concentrations of a vast array of antigens. The requirements of broad specificity and sensitivity conflict because the former is met by low-affinity antigen receptors, which precludes achieving the latter with high-affinity receptors.
R H, Carter, D T, Fearon
openaire   +2 more sources

CD19 Fc-Fusion Protein for Detection of Cells Expressing Anti-CD19 Chimeric Antigen Receptors.

Blood, 2010
Abstract Abstract 3756 Chimeric Antigen Receptors (CARs) consist of the antigen-recognition portion of a monoclonal antibody fused to an intracellular signaling domain that is capable of activating T cells. CARs are displayed on the surface of transduced cells, performing non-MHC-restricted antigen recognition and ...
Satiro N. De Oliveira   +3 more
openaire   +1 more source

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