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Construction and application of adenoviral vectors

Journal

MOLECULAR THERAPY-NUCLEIC ACIDS
Volume 34, Issue -, Pages -

Publisher

CELL PRESS
DOI: 10.1016/j.omtn.2023.09.004

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Adenoviral vectors have been widely used as vaccine candidates against infectious diseases and in cancer gene therapy. However, they face challenges such as poor targeting and immune response, which can be overcome through further research and technological development.
Adenoviral vectors have been widely used as vaccine candidates or potential vaccine candidates against infectious diseases due to the convenience of genome manipulation, their ability to accommodate large exogenous gene fragments, easy access of obtaining high-titer of virus, and high efficiency of transduc-tion. At the same time, adenoviral vectors have also been used extensively in clinical research for cancer gene therapy and treatment of diseases caused by a single gene defect. However, application of adenovirus also faces a series of challenges such as poor targeting, strong immune response against the vector itself, and they cannot be used repeatedly. It is believed that these problems will be solved gradually with further research and technological development in related fields. Here, we review the construction methods of adenoviral vectors, including gutless adenovirus and discuss application of adenoviral vectors as prophylactic vaccines for infectious pathogens and their application prospects as therapeutic vaccines for cancer and other kinds of chronic infectious disease such as human papillomavirus, hepatitis B virus, and hepatitis C virus.

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