Transfer of a TCR gene derived from a patient with a marked antitumor response conveys highly active T-cell effector functions.
about
In vivo suppression of HIV by antigen specific T cells derived from engineered hematopoietic stem cellsAdoptive immunotherapy for cancer: building on successGene therapy with human and mouse T-cell receptors mediates cancer regression and targets normal tissues expressing cognate antigenAdoptive cell transfer: a clinical path to effective cancer immunotherapyCancer regression in patients after transfer of genetically engineered lymphocytesGenetic engineering with T cell receptorsAdoptive cell therapy for sarcomaIn vivo imaging of therapy-induced anti-cancer immune responses in humans.T-cell receptor gene therapy--ready to go viral?Engineering antigen-specific T cells from genetically modified human hematopoietic stem cells in immunodeficient mice.Adoptive transfer of vaccine-induced peripheral blood mononuclear cells to patients with metastatic melanoma following lymphodepletion.High-affinity TCRs generated by phage display provide CD4+ T cells with the ability to recognize and kill tumor cell lines.Novel human interleukin-15 agonistsLentiviral vector design for optimal T cell receptor gene expression in the transduction of peripheral blood lymphocytes and tumor-infiltrating lymphocytes.Transduction of SIV-specific TCR genes into rhesus macaque CD8+ T cells conveys the ability to suppress SIV replication.Use of the piggyBac transposon to create stable packaging cell lines for the production of clinical-grade self-inactivating γ-retroviral vectors.Rebalancing immune specificity and function in cancer by T-cell receptor gene therapy.Tumor-specific CD8+ T cells expressing interleukin-12 eradicate established cancers in lymphodepleted hostsGamma-retroviral vector design for the co-expression of artificial microRNAs and therapeutic proteins.Immunotherapy for metastatic solid cancersGene therapy using genetically modified lymphocytes targeting VEGFR-2 inhibits the growth of vascularized syngenic tumors in miceThe human application of gene therapy to re-program T-cell specificity using chimeric antigen receptorsAdoptive transfer of syngeneic T cells transduced with a chimeric antigen receptor that recognizes murine CD19 can eradicate lymphoma and normal B cells.Characterization of human T lymphocytes engineered to express interleukin-15 and herpes simplex virus-thymidine kinaseRapid production of clinical-grade gammaretroviral vectors in expanded surface roller bottles using a "modified" step-filtration process for clearance of packaging cells.Probing the effector and suppressive functions of human T cell subsets using antigen-specific engineered T cell receptorsRecognition of fresh human tumor by human peripheral blood lymphocytes transduced with a bicistronic retroviral vector encoding a murine anti-p53 TCR.Primary human T lymphocytes engineered with a codon-optimized IL-15 gene resist cytokine withdrawal-induced apoptosis and persist long-term in the absence of exogenous cytokine.Development of a genetically-modified novel T-cell receptor for adoptive cell transfer against renal cell carcinoma.Improving adoptive T cell therapy by targeting and controlling IL-12 expression to the tumor environment.Transduction of an HLA-DP4-restricted NY-ESO-1-specific TCR into primary human CD4+ lymphocytes.Genetic engineering of murine CD8+ and CD4+ T cells for preclinical adoptive immunotherapy studies.Development of a T cell receptor targeting an HLA-A*0201 restricted epitope from the cancer-testis antigen SSX2 for adoptive immunotherapy of cancer.EGFRvIII-specific chimeric antigen receptor T cells migrate to and kill tumor deposits infiltrating the brain parenchyma in an invasive xenograft model of glioblastoma.Generation of CAR T cells for adoptive therapy in the context of glioblastoma standard of care.Mouse model for pre-clinical study of human cancer immunotherapy.Augmented lymphocyte expansion from solid tumors with engineered cells for costimulatory enhancementIL-15:IL-15 receptor alpha superagonist complex: high-level co-expression in recombinant mammalian cells, purification and characterization.Increased intensity lymphodepletion and adoptive immunotherapy--how far can we go?Improving TCR Gene Therapy for Treatment of Haematological Malignancies.
P2860
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P2860
Transfer of a TCR gene derived from a patient with a marked antitumor response conveys highly active T-cell effector functions.
description
2005 nî lūn-bûn
@nan
2005 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Transfer of a TCR gene derived ...... ive T-cell effector functions.
@ast
Transfer of a TCR gene derived ...... ive T-cell effector functions.
@en
Transfer of a TCR gene derived ...... ive T-cell effector functions.
@nl
type
label
Transfer of a TCR gene derived ...... ive T-cell effector functions.
@ast
Transfer of a TCR gene derived ...... ive T-cell effector functions.
@en
Transfer of a TCR gene derived ...... ive T-cell effector functions.
@nl
prefLabel
Transfer of a TCR gene derived ...... ive T-cell effector functions.
@ast
Transfer of a TCR gene derived ...... ive T-cell effector functions.
@en
Transfer of a TCR gene derived ...... ive T-cell effector functions.
@nl
P2093
P2860
P356
P1433
P1476
Transfer of a TCR gene derived ...... ive T-cell effector functions.
@en
P2093
John Wunderlich
Mark E Dudley
Marybeth S Hughes
Morvarid Moayeri
Paul F Robbins
Richard A Morgan
Robert G Hawley
Steven A Rosenberg
Yik Y L Yu
P2860
P304
P356
10.1089/HUM.2005.16.457
P577
2005-04-01T00:00:00Z