RCA-free production of third generation adenoviral vectors

نویسندگان

چکیده

Adenoviruses (Ad) have a long history as DNA-transfer vehicles in various medical applications including vivo gene therapy [1]. In this context, the favorable safety profile of Ad has been considered major benefit, since lack integration into host cell genome eliminates potential risks associated with insertional mutagenesis. This is combined comparatively high packaging capacity for foreign DNA, which relevant projects where therapeutic expression cassette too large other vectors such adeno-associated viruses. Further advantages include infectivity, high-titer virus production, excellent stability, and broad tissue tropism. 

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Construction of first-generation adenoviral vectors.

Genetically modified adenoviruses (Ads) make attractive vectors for the delivery of exogenous DNA to mammalian cells for basic science and gene therapy applications. Ad vector production consists of (1) cloning a trangene into an infectious plasmid by in vivo recombination in bacteria, (2) rescuing and propagating the vector in complementing cells, and (3) purifying the vector. All of this can ...

متن کامل

Production of Rca

Concrete pavement recycling is a relatively simple process that involves breaking, removing and crushing hardened concrete from an acceptable source to produce recycled concrete aggregate (RCA). The formal process of RCA production typically involves an initial evaluation of the existing source concrete; pavement preparation, which may include removal of an asphalt overlay; pavement breaking, r...

متن کامل

Adenoviral Vectors for Hemophilia Gene Therapy

Hemophilia is an inherited blood clotting disorder resulting from deficiency of blood coagulation factors. Current standard of care for hemophilia patients is frequent intravenous infusions of the missing coagulation factor. Gene therapy for hemophilia involves the introduction of a normal copy of the deficient coagulation factor gene thereby potentially offering a definitive cure for the bleed...

متن کامل

Efficient generation of recombinant adenoviral vectors by Cre-lox recombination in vitro.

BACKGROUND Although recombinant adenovirus vectors are attractive for use in gene expression studies and therapeutic applications, the construction of these vectors remains relatively time-consuming. We report here a strategy that simplifies the production of adenoviruses using the Cre-loxP system. MATERIALS AND METHODS Full-length recombinant adenovirus DNA was generated in vitro by Cre-medi...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Cell & gene therapy insights

سال: 2022

ISSN: ['2059-7800', '2397-0545']

DOI: https://doi.org/10.18609/cgti.2022.215