نتایج جستجو برای: lentiviral vector

تعداد نتایج: 200877  

Journal: :Addiction biology 2015
Eduardo Karahanian Mario Rivera-Meza Lutske Tampier María Elena Quintanilla Mario Herrera-Marschitz Yedy Israel

Previous studies suggest that acetaldehyde generated from ethanol in the brain is reinforcing. The present studies tested the feasibility of achieving a long-term reduction of chronic and post-deprivation binge ethanol drinking by a single administration into the brain ventral tegmental area (VTA) of a lentiviral vector that codes for aldehyde dehydrogenase-2 (ALDH2), which degrades acetaldehyd...

2013
Hélio A. Tomás Ana F. Rodrigues Paula M. Alves Ana S. Coroadinha

Lentiviral vectors (LV) are efficient vehicles for gene transfer in mammalian cells due to their capacity to stably express a gene of interest in non-dividing and dividing cells. Their use has exponentially grown in the last years both in research and in gene therapy protocols, reaching 12% of the viral vector based clinical trials in 2011 [1]. This chapter reviews and discusses the state of th...

Journal: :Nucleic acids research 2002
Barbara Mitta Markus Rimann Markus U Ehrengruber Martin Ehrbar Valentin Djonov Jens Kelm Martin Fussenegger

In recent years, lentiviral expression systems have gained an unmatched reputation among the gene therapy community for their ability to deliver therapeutic transgenes into a wide variety of difficult-to-transfect/transduce target tissues (brain, hematopoietic system, liver, lung, retina) without eliciting significant humoral immune responses. We have cloned a construction kit-like self-inactiv...

2017
Eric W F W Alton Jeffery M Beekman A Christopher Boyd June Brand Marianne S Carlon Mary M Connolly Mario Chan Sinead Conlon Heather E Davidson Jane C Davies Lee A Davies Johanna F Dekkers Ann Doherty Sabrina Gea-Sorli Deborah R Gill Uta Griesenbach Mamoru Hasegawa Tracy E Higgins Takashi Hironaka Laura Hyndman Gerry McLachlan Makoto Inoue Stephen C Hyde J Alastair Innes Toby M Maher Caroline Moran Cuixiang Meng Michael C Paul-Smith Ian A Pringle Kamila M Pytel Andrea Rodriguez-Martinez Alexander C Schmidt Barbara J Stevenson Stephanie G Sumner-Jones Richard Toshner Shu Tsugumine Marguerite W Wasowicz Jie Zhu

We have recently shown that non-viral gene therapy can stabilise the decline of lung function in patients with cystic fibrosis (CF). However, the effect was modest, and more potent gene transfer agents are still required. Fuson protein (F)/Hemagglutinin/Neuraminidase protein (HN)-pseudotyped lentiviral vectors are more efficient for lung gene transfer than non-viral vectors in preclinical model...

2012
Dubravka Škalamera Mareike Dahmer Amy S. Purdon Benjamin M. Wilson Max V. Ranall Antje Blumenthal Brian Gabrielli Thomas J. Gonda

The bottleneck in elucidating gene function through high-throughput gain-of-function genome screening is the limited availability of comprehensive libraries for gene overexpression. Lentiviral vectors are the most versatile and widely used vehicles for gene expression in mammalian cells. Lentiviral supernatant libraries for genome screening are commonly generated in the HEK293T cell line, yet v...

Journal: :Blood 2001
J Dyall J B Latouche S Schnell M Sadelain

Dendritic cells (DCs) are professional antigen-presenting cells that are highly effective adjuvants for immunizing against pathogens and tumor antigens. The potential merit of genetic approaches to loading DCs with antigens is to express high and sustained levels of proteins that can be subsequently processed and presented to T lymphocytes. Replication-defective oncoretroviruses are able to eff...

2016
Alexander Falkenhagen Sabah Asad Stanley E Read Sadhna Joshi

BACKGROUND Recombinant proteins of therapeutic use are ideally produced in human cells to ensure appropriate co- and post-translational modifications. However, purification of secreted proteins from the culture media is impeded by low expression from transfected cell lines and the presence of serum proteins. Here we describe a simple and cost-effective approach based on lentiviral vector-mediat...

Journal: :Human gene therapy 2003
Xianzheng Zhou Yan Cui Xin Huang Zhiwei Yu Amy M Thomas Zhaohui Ye Drew M Pardoll Elizabeth M Jaffee Linzhao Cheng

In this report, we evaluated the efficiency of stable gene transfer into established CD8(+) human tumor antigen-specific cytotoxic T cell (CTL) lines and peripheral blood lymphocytes (PBL) by oncoretroviral and lentiviral vectors. In the oncoretroviral vector, the green fluorescent protein (GFP) reporter gene was regulated by the murine stem cell virus (MSCV) promoter. In three human immunodefi...

2017
Magdalena Winiarska Dominika Nowis Malgorzata Firczuk Agnieszka Zagozdzon Magdalena Gabrysiak Radoslaw Sadowski Joanna Barankiewicz Michal Dwojak Jakub Golab

Gene transfer into normal quiescent human B cells is a challenging procedure. The present study aimed to investigate whether it is possible to increase the levels of transgene expression by using various types of promoters to drive the expression of selected genes‑of‑interest. To produce lentiviral particles, the present study used the 2nd generation psPAX2 packaging vector and the vesicular st...

Journal: :AIDS Research and Therapy 2004
Akhil Banerjea Ming-Jie Li Leila Remling John Rossi Ramesh Akkina

BACKGROUND: RNA based antiviral approaches against HIV-1 are among the most promising for long-term gene therapy. These include ribozymes, aptamers (decoys), and small interfering RNAs (siRNAs). Lentiviral vectors are ideal for transduction of such inhibitory RNAs into hematopoietic stem cells due to their ability to transduce non-dividing cells and their relative refractiveness to gene silenci...

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