نتایج جستجو برای: adenoviral vectors adv

تعداد نتایج: 84187  

Journal: :Journal of immunology 2010
Peter Johannes Holst Cathrine Ørskov Allan Randrup Thomsen Jan Pravsgaard Christensen

Adenoviral vectors have been widely used for experimental gene therapy and vaccination, yet there is a surprising lack of knowledge connecting the route and dose of adenovirus administration to the induced transgene-specific immune response. We have recently demonstrated polyfunctional CD8(+) T cells and protective memory responses using adenoviral vectors, which seem to contrast with recent re...

Journal: :Circulation 2000
J M Waugh J Li-Hawkins E Yuksel M D Kuo P N Cifra P R Hilfiker R Geske M Chawla J Thomas S M Shenaq M D Dake S L Woo

BACKGROUND-These studies were initiated to confirm that high-level thrombomodulin overexpression is sufficient to limit neointima formation after mechanical overdilation injury. METHODS AND RESULTS-An adenoviral construct expressing thrombomodulin (Adv/RSV-THM) was created and functionally characterized in vitro and in vivo. The impact of local overexpression of thrombomodulin on neointima form...

Journal: :Circulation research 2006
David R Harder Richard J Roman

Vascular cytochrome P450 (CYP) 4A enzymes catalyze the synthesis of 20-hydroxyeicosatetraenoic acid (20-HETE), an eicosanoid which participates in the regulation of vascular tone by sensitizing the smooth muscle cells to constrictor and myogenic stimuli. This study was undertaken to investigate the consequences of CYP4A overexpression on blood pressure and endothelial function in rats treated w...

2014
Cristian Capasso Mariangela Garofalo Mari Hirvinen Vincenzo Cerullo

A long time has passed since the first clinical trial with adenoviral (Ad) vectors. Despite being very promising, Ad vectors soon revealed their limitations in human clinical trials. The pre-existing immunity, the marked liver tropism and the high toxicity of first generation Ad (FG-Ad) vectors have been the main challenges for the development of new approaches. Significant effort toward the de...

Journal: :Journal of virology 2008
S Sridhar A Reyes-Sandoval S J Draper A C Moore S C Gilbert G P Gao J M Wilson A V S Hill

Human adenovirus serotype 5 (AdH5) vector vaccines elicit strong immune responses to the encoded antigen and have been used in various disease models. We designed AdH5 vectors expressing antigen under the control of a human cytomegalovirus (HCMV) immediate-early promoter containing its intron A sequence. The transcriptional levels of antigen and immune responses to antigen for vectors with the ...

2006
Ji-Shi Wang Harpreet Singh Frank Zhang Tsuneo Ishizuka Huan Deng Rowena Kemp Michael S. Wolin Thomas H. Hintze Nader G. Abraham Alberto Nasjletti Michal Laniado-Schwartzman

Vascular cytochrome P450 (CYP) 4A enzymes catalyze the synthesis of 20-hydroxyeicosatetraenoic acid (20-HETE), an eicosanoid which participates in the regulation of vascular tone by sensitizing the smooth muscle cells to constrictor and myogenic stimuli. This study was undertaken to investigate the consequences of CYP4A overexpression on blood pressure and endothelial function in rats treated w...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Fumi Ohbayashi Michael A Balamotis Atsuhiro Kishimoto Emi Aizawa Arturo Diaz Paul Hasty Frank L Graham C Thomas Caskey Kohnosuke Mitani

For gene therapy of inherited diseases, targeted integration/gene repair through homologous recombination (HR) between exogenous and chromosomal DNA would be an ideal strategy to avoid potentially serious problems of random integration such as cellular transformation and gene silencing. Efficient sequence-specific modification of chromosomes by HR would also advance both biological studies and ...

Journal: :Journal of immunology 2005
Philippe Krebs Elke Scandella Bernhard Odermatt Burkhard Ludewig

Replication-deficient adenoviruses (recombinant adenovirus (rec-AdV)) expressing different transgenes are widely used vectors for gene therapy and vaccination. In this study, we describe the tolerization of transgene-specific CTL following administration of beta-galactosidase (beta gal)-recombinant adenovirus (Ad-LacZ). Using MHC class I tetramers to track beta gal-specific CTL, we found that a...

2009
John Nemunaitis

Adenoviral gene therapy for cancer, especially the use of vectors based on adenovirus serotype-5 (Ad5), has been widely investigated, and numerous gene transfer studies have been performed using replicationdefective and conditionally replicating adenoviral vectors. The data suggest that both replicationdefective and conditionally replicating adenoviral vectors are safe and welltolerated ((Licht...

Journal: :Anticancer research 2011
Deepika Srivastava Ganesh Joshi Kumaravel Somasundaram Rita Mulherkar

BACKGROUND Adenoviral mediated suicide gene therapy has been shown to have a tumoricidal effect against a variety of tumor models. Although the efficacy of this treatment regimen has been verified, the molecular mechanism of Herpes simplex virus thymidine kinase gene (HSVtk)- and ganciclovir (GCV)-induced cell death is still not well established. MATERIALS AND METHODS The mode of cell death b...

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