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1 oma cells by virus-regulated expression of a suicide gene.
2 with a CD28-containing anti-SLAMF7 CAR and a suicide gene.
3 ed with mCherry, and the inducible Caspase-9 suicide gene.
4 0-fold, suggesting that it may be a superior suicide gene.
5 and a herpes simplex virus thymidine kinase suicide gene.
6 virus thymidine kinase or cytosine deaminase suicide genes.
7 several advantages over currently available suicide genes.
8 allow selection of transduced cells, whereas suicide genes allow selective deletion of administered T
9 the incorporation of an inducible caspase-9 suicide gene allowed efficient elimination of transgenic
11 fy and to destroy tumor cells expressing the suicide gene alpha(1,3)Galactosyltransferase (alpha GT).
12 effectiveness of combination therapy using a suicide gene and cytokine genes for the treatment of met
13 term immune reconstitution did not carry the suicide gene and displayed high numbers of naive lymphoc
14 dies demonstrate the need for nonimmunogenic suicide genes and identify a strategy for detection of C
15 d herpes simplex virus thymidine kinase as a suicide gene, at different time points after sensitizati
17 ts thus show that locoregional delivery of a suicide gene by RCR vectors infused into the portal circ
18 ently deleted by using direct repeats, (iii) suicide genes can be functionally reconstituted during r
20 Therefore, (a) a lytic virus expressing a "suicide" gene can activate a prodrug; and (b) within rRp
21 T cells expressing the anti-SLAMF7 CAR plus suicide-gene construct specifically recognized SLAMF7 in
23 rleukin 6 (IL-6) and the bacterial metabolic suicide gene cytosine deaminase (205-IL6-CD) become high
25 rpes simplex virus-thymidine kinase (HSV-tk) suicide gene delivery and treatment with ganciclovir (GC
29 ablated these cells by targeting them with a suicide gene encoding herpes simplex virus thymidine kin
30 mbinant VSV (rVSV) that expressed the fusion suicide gene Escherichia coli cytosine deaminase (CD)/ur
31 ant-negative mutant rpoB gene is a potential suicide gene especially for the treatment of multidrug-r
32 d molecularly via microRNA (miRNA)-regulated suicide gene expression to enrich for specific tissues.
36 The genetic modification of T cells with a suicide gene grants a mechanism of control of adverse re
40 ly modified donor T cells with an inducible "suicide" gene have the potential to improve the safety a
41 of either reporter red florescent protein or suicide genes [herpes simplex virus-thymidine kinase (TK
42 to oocytes in transgenic mice expressing the suicide gene, herpes simplex virus thymidine kinase (HSV
47 o difficulties in the development of DT as a suicide gene in cancer gene therapy, because toxicity ap
49 ne kinase (HSV1-tk) gene is widely used as a suicide gene in combination with ganciclovir (GCV) and a
51 hymidine kinase (HSV-tk) is widely used as a suicide gene in experimental gene therapy of cancer.
52 DeltaCD34-tk is an attractive candidate as a suicide gene in man because of the ensured expression of
53 rpes simplex virus-thymidine kinase (HSV-tk) suicide gene in mouse mammary adenocarcinoma (TSA) cells
54 we assessed the efficacy of the DeltaCD34-tk suicide gene in the absence of extended ex vivo manipula
55 the transduction and regulation of a double suicide gene in tumor cells and may provide a unique app
56 city can be accomplished by RIP coupled to a suicide gene in vivo, preventing hypoglycemic death.
57 We recently constructed a novel chimeric suicide gene in which the entire coding region of HSV th
59 ified MSCs to stably express a panel of four suicide genes including TK (TK007 and TK(SR39) mutants),
60 ed: a retroviral construct incorporating the suicide gene inducible caspase-9 (CD19-CAR-Retro_ALLO) f
61 reacting T cells by T cell subset selection, suicide gene insertion or selective allodepletion, and t
63 dly applicable to introducing therapeutic or suicide genes into patient-specific iPS cells for use in
64 l injections of a plasmid in which the HSVtk suicide gene is expressed from a melanocyte-specific pro
65 sgenic mice in which a thymidine kinase (TK) suicide gene is targeted to the T cell using a CD3 promo
66 th the herpes simplex virus thymidine kinase suicide gene linked to the IL-2 promoter were used as a
67 odel, we demonstrate that early-intervention suicide-gene-mediated senescent cell ablation improves p
74 clusion, the insertion of the fusion CD/UPRT suicide gene potentiates the oncolytic efficiency of VSV
75 r stomatitis virus (VSV) able to produce the suicide gene product thymidine kinase (TK) or cytokine i
77 rpes simplex virus thymidine kinase (HSV-TK) suicide gene protocols has resulted in enhanced antitumo
78 and herpes simplex virus-1 thymidine kinase suicide genes render malignant cells sensitive to specif
83 e reconstitution associated with a different suicide gene strategy to abrogate graft-versus-host dise
85 of direct viral oncolysis to the HSV-tk/GCV suicide gene system resulted in a striking improvement i
88 divided into four main areas: 1) transfer of suicide genes that convert inactive prodrugs into cytoto
89 cancer, one improvement would be to develop suicide genes that effectively kill both dividing and no
90 in which tumor cells are transfected with a 'suicide' gene that encodes a metabolic enzyme capable of
91 Prior transduction of T lymphocytes with the suicide gene, the viral thymidine kinase (TK), permits s
94 ductase enzyme (NTR) has been widely used in suicide gene therapy (GDEPT and ADEPT) applications as a
97 , this cytokine approach was combined with a suicide gene therapy and subcutaneous B16 melanomas were
98 sent the findings on improved techniques for suicide gene therapy and various oncolytic viral therapi
101 x virus type 1 (HSV-1) thymidine kinase (TK) suicide gene therapy as a potential antitumor treatment.
102 this attribute could be exploited in cancer suicide gene therapy by using a lentiviral (LV) vector e
103 ication-competent adenovirus-mediated double-suicide gene therapy can be combined safely with convent
104 hypothesis that the effectiveness of HSV-TK suicide gene therapy can be enhanced by coexpression of
105 deficiencies, chronic granulomatous disease, suicide gene therapy for graft-versus-host disease, vira
106 d HVP22 to enhance Etk/ganciclovir (Etk/GCV) suicide gene therapy for neuroblastomas by GCV cytotoxic
108 utic potential of BVP22 and HVP22 in Etk/GCV suicide gene therapy in this tumor system is not due to
110 emonstrate that CID-regulated, caspase-based suicide gene therapy is safe and can inhibit the growth
115 e cell-based, non-viral or viral vectors for suicide gene therapy of cancer make more informed decisi
117 evelop a stem cell-based system for targeted suicide gene therapy of recurrent, metastatic, and unres
118 ible to utilize such nucleoside analogues in suicide gene therapy or protein therapy applications tha
119 or obstacle to the successful application of suicide gene therapy strategies that rely on in situ tra
122 evaluated the safety and efficacy of a novel suicide gene therapy that could potentially spare normal
125 with established liver metastases show that suicide gene therapy using TK- vaccinia virus as a vecto
128 In a mouse xenograft model of lung cancer, suicide gene therapy with LV-ARE-TK/GCV was effective co
130 udied antiglioma gene therapy strategies are suicide gene therapy, genetic immunotherapy and oncolyti
131 est the potential therapeutic efficacy of DT suicide gene therapy, we first developed a DT-resistant
135 ndidate for anti-microbial drug development, suicide-gene therapy, and cell-specific mRNA labeling te
136 Insulinoma-specific cytotoxicity using the suicide gene thymidine kinase (tk) was studied both in v
138 approach likely requires the inclusion of a suicide gene to deal with the potential development of T
139 neered human CAF cell line with an inducible suicide gene to enable selective in vivo elimination of
140 bination of tumor killing by activation of a suicide gene to release tumor antigens and in situ HSP70
141 h donor T cells expressed a thymidine kinase suicide gene, to test whether separation of GVL and graf
142 . injection of plasmids encoding hsp70 and a suicide gene transcriptionally targeted to melanocytes g
143 st disease include CD4 lymphocyte infusions, suicide gene-transfected cells, and the use of cloned T
144 aft-versus-host disease may be controlled by suicide gene transfection of the donor lymphocytes.
145 r data suggest that the HSV-tk/GCV metabolic suicide gene transfer system could serve as an adjuvant
148 road relevance to the use of the in vivo HSP/suicide gene tumor vaccine in therapy for human solid tu
149 ful for positive T-cell selection and (2) a "suicide" gene useful for elimination of transfected T ce
150 erpes simplex virus-thymidine kinase (HSVtk) suicide gene, using a murine fibrosarcoma model, in the
152 eated cells that express an NF-kappaB-driven suicide gene, we discovered that the LPS receptor Toll-l
153 pes simplex virus thymidine kinase (HSV-TK) "suicide gene," we demonstrate Smad4-responsive regulatio