Results 1 to 10 of about 176,919 (206)

CD19-negative relapse after CAR-T cell therapy: mechanisms of antigen escape and lineage switch [PDF]

open access: yesFrontiers in Immunology
CD19 chimeric antigen receptor (CAR)-T cell therapy has transformed the treatment of relapsed/refractory B-cell malignancies, achieving high remission rates. Nonetheless, 20%-40% of patients eventually relapse, classified as either CD19+ or CD19− relapse.
Jiawen Huang, Xiaobing Huang, Duonan Yu
doaj   +2 more sources

CD19-immunoPET for noninvasive visualization of CD19 expression in B-cell lymphoma patients

open access: yesBiomarker Research
Cell- and antibody-based CD19-directed therapies have demonstrated great potential for treating B-cell non-Hodgkin lymphoma (B-NHL). However, all these approaches suffer from limited response rates and considerable toxicity.
Dominik Sonanini   +17 more
doaj   +3 more sources

A study on influence of different signal peptides on anti-tumor effect of chimeric antigen receptor (CAR) T cells [PDF]

open access: yesZhongguo aizheng zazhi, 2022
Background and purpose: Signal peptide (SP) is a short peptide chain at the N-terminal of precursor protein, which can regulate the folding and transfer of precursor protein and plays an important role in protein secretion.
LI Fan, ZHANG Qinxing, TONG Xiangwen, TIAN Gaohui, GU Lixing, XU Yao
doaj   +3 more sources

Correction: The Endocytic Adaptor Eps15 Controls Marginal Zone B Cell Numbers. [PDF]

open access: yes, 2013
Eps15 is an endocytic adaptor protein involved in clathrin and non-clathrin mediated endocytosis. In Caenorhabditis elegans and Drosophila melanogaster lack of Eps15 leads to defects in synaptic vesicle recycling and synapse formation. We generated Eps15-
Adler, Thure   +18 more
core   +8 more sources

CAR-T cell Therapies for B-cell Lymphoid Malignancies: Identifying Targets Beyond CD19

open access: yesHematology/Oncology and Stem Cell Therapy, 2022
Chimeric antigen receptors (CARs) are synthetic engineered receptors with an antigen recognition domain derived from a high-specificity monoclonal antibody that can target surface molecules on tumor cells.
Yenny M. Vanegas   +6 more
doaj   +1 more source

Transferrin epitope-CD19-CAR-T cells effectively kill lymphoma cells in vitro and in vivo

open access: yesFrontiers in Bioscience-Landmark, 2020
Chimeric antigen receptor (CAR) T cell immunotherapy has demonstrated clinical success in treatment of B-cell hematologic cancers. In this study, we compared human Transferrin epitope tagged CAR-T cells with non-tagged CAR-T cells for cytotoxicity, IFN ...
Michael Valentine   +9 more
doaj   +1 more source

Chimeric Antigen Receptor-T-Cell Therapy for B-Cell Hematological Malignancies: An Update of the Pivotal Clinical Trial Data

open access: yesPharmaceutics, 2020
Chimeric antigen receptor (CAR)-T-cell therapy is an innovative form of adoptive cell therapy that has revolutionized the treatment of certain hematological malignancies, including B-cell non-Hodgkin lymphoma (NHL) and B-cell acute lymphoblastic leukemia
Gils Roex   +8 more
doaj   +1 more source

CAR T cell therapy

open access: yesImmunological Medicine, 2021
Chimeric antigen receptor (CAR) is generated by fusing a cancer-specific antibody’s antigen recognition site with costimulatory molecules such as CD28 and CD3ζ. T cells transduced with CAR recognizes cancer-specific antigens and kill cancer cells.
Naoki Hosen
doaj   +1 more source

CD19-CAR Trials [PDF]

open access: yesThe Cancer Journal, 2014
CD19 is a B-lineage-specific transmembrane glycoprotein, the expression of which is maintained on more than 95% B-cell malignancies. This strict lineage restriction makes CD19 an ideal target for immune therapies using chimeric antigen receptors (CARs).
Carlos A, Ramos   +2 more
openaire   +2 more sources

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