Receptor affinity and extracellular domain modifications affect tumor recognition by ROR1-specific chimeric antigen receptor T cells.
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Mesothelin-Targeted CARs: Driving T Cells to Solid TumorsAdoptive immunotherapy for acute leukemia: New insights in chimeric antigen receptorsStrategies for combining immunotherapy with radiation for anticancer therapyAdoptive T-cell therapy for cancer: The era of engineered T cellsAdoptive T-cell therapy for LeukemiaConcise review: humanized models of tumor immunology in the 21st century: convergence of cancer research and tissue engineeringChimeric antigen receptor-engineered T cells for cancer immunotherapy: progress and challengesAntigen-Specific T-Cell Activation Independently of the MHC: Chimeric Antigen Receptor-Redirected T CellsRecent advances in T-cell engineering for use in immunotherapySmart CARs engineered for cancer immunotherapyDesigning chimeric antigen receptors to effectively and safely target tumorsReengineering chimeric antigen receptor T cells for targeted therapy of autoimmune diseaseSilencing of Receptor Tyrosine Kinase ROR1 Inhibits Tumor-Cell Proliferation via PI3K/AKT/mTOR Signaling Pathway in Lung AdenocarcinomaAn Optimized GD2-Targeting Retroviral Cassette for More Potent and Safer Cellular Therapy of Neuroblastoma and Other CancersRedirecting Specificity of T cells Using the Sleeping Beauty System to Express Chimeric Antigen Receptors by Mix-and-Matching of VL and VH Domains Targeting CD123+ TumorsPreserved Activity of CD20-Specific Chimeric Antigen Receptor-Expressing T Cells in the Presence of Rituximab.A tandem CD19/CD20 CAR lentiviral vector drives on-target and off-target antigen modulation in leukemia cell lines.ROR1 expression as a biomarker for predicting prognosis in patients with colorectal cancer.Emerging immunotherapeutics in adenocarcinomas: A focus on CAR-T cellsCAR-modified T-cell therapy for cancer: an updated review.Chimeric antigen receptor-modified T cells derived from defined CD8+ and CD4+ subsets confer superior antitumor reactivity in vivo.Versatile strategy for controlling the specificity and activity of engineered T cells.Inclusion of Strep-tag II in design of antigen receptors for T-cell immunotherapy.Universal artificial antigen presenting cells to selectively propagate T cells expressing chimeric antigen receptor independent of specificity.Chimeric antigen receptor for adoptive immunotherapy of cancer: latest research and future prospects.The human application of gene therapy to re-program T-cell specificity using chimeric antigen receptorsThermoreversible poly(ethylene glycol)-g-chitosan hydrogel as a therapeutic T lymphocyte depot for localized glioblastoma immunotherapy.Tumor antigen ROR1 targeted drug delivery mediated selective leukemic but not normal B-cell cytotoxicity in chronic lymphocytic leukemia.Safety of targeting ROR1 in primates with chimeric antigen receptor-modified T cells.Nature Biotechnology's academic spinouts of 2013.DNAM-1-based chimeric antigen receptors enhance T cell effector function and exhibit in vivo efficacy against melanoma.Chimeric antigen receptors with mutated IgG4 Fc spacer avoid fc receptor binding and improve T cell persistence and antitumor efficacySleeping Beauty Transposition of Chimeric Antigen Receptors Targeting Receptor Tyrosine Kinase-Like Orphan Receptor-1 (ROR1) into Diverse Memory T-Cell Populations.Targeting of folate receptor β on acute myeloid leukemia blasts with chimeric antigen receptor-expressing T cellsIGF1R- and ROR1-Specific CAR T Cells as a Potential Therapy for High Risk Sarcomas.Chimeric antigen receptor-engineered T cells for the treatment of metastatic prostate cancer.Affinity-Tuned ErbB2 or EGFR Chimeric Antigen Receptor T Cells Exhibit an Increased Therapeutic Index against Tumors in MiceTuning Sensitivity of CAR to EGFR Density Limits Recognition of Normal Tissue While Maintaining Potent Antitumor Activity.Fully human CD19-specific chimeric antigen receptors for T-cell therapy.The nonsignaling extracellular spacer domain of chimeric antigen receptors is decisive for in vivo antitumor activity.
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Receptor affinity and extracellular domain modifications affect tumor recognition by ROR1-specific chimeric antigen receptor T cells.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 25 April 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Receptor affinity and extracel ...... eric antigen receptor T cells.
@en
Receptor affinity and extracel ...... eric antigen receptor T cells.
@nl
type
label
Receptor affinity and extracel ...... eric antigen receptor T cells.
@en
Receptor affinity and extracel ...... eric antigen receptor T cells.
@nl
prefLabel
Receptor affinity and extracel ...... eric antigen receptor T cells.
@en
Receptor affinity and extracel ...... eric antigen receptor T cells.
@nl
P2093
P2860
P1476
Receptor affinity and extracel ...... eric antigen receptor T cells.
@en
P2093
Christoph Rader
Daniel Sommermeyer
Maria-Teresa Lupo-Stanghellini
Michael C Jensen
Michael Hudecek
Paula L Kosasih
Stanley R Riddell
P2860
P304
P356
10.1158/1078-0432.CCR-13-0330
P407
P577
2013-04-25T00:00:00Z