Literature DB >> 31758807

State-of-the-art human adenovirus vectorology for therapeutic approaches.

Jian Gao1, Kemal Mese1, Oskar Bunz1, Anja Ehrhardt1.   

Abstract

Human adenoviruses (Ads) have long been studied in the basic virology field and are exploited as vectors for gene therapy, vaccination, and oncolytic therapy. Ads are usually mild pathogens, but they can cause severe infections and symptoms in immunocompromised individuals. Ads show a large natural diversity and a broad spectrum of hosts. However, replication-competent and replication-deficient Ad vectors with therapeutic applications have been built mainly starting from human Ad type 5, because generating vectors from other human and animal Ads has proven challenging. This review provides an updated overview of vectors that are not derived from human Ad type 5. We discuss genetic engineering techniques for getting access to the natural diversity of human Ads and for vectorization of alternative Ad types. A catalogue of currently available vectorized human Ads and translational applications thereof is also compiled. We conclude with a perspective on Ad vectorology that looks into the future of Ad vectors in translational medicine.
© 2019 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.

Entities:  

Keywords:  adenoviral vector; adenovirus; assembly; cloning; gene therapy; genome engineering; oncolytic virus; vaccination; vector production; virus type

Mesh:

Year:  2019        PMID: 31758807     DOI: 10.1002/1873-3468.13691

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  22 in total

Review 1.  Role of Adenoviruses in Cancer Therapy.

Authors:  Sintayehu Tsegaye Tseha
Journal:  Front Oncol       Date:  2022-06-09       Impact factor: 5.738

2.  Preparation and identification of a single domain antibody specific for adenovirus vectors and its application to the immunoaffinity purification of adenoviruses.

Authors:  Yi Cheng; Yanxia Hao; Fuxiang Bao; Huimin Zhang; Yanlong Liu; Kexin Ao; Shan Fu; Qiyao Wu; Zhi Wang
Journal:  AMB Express       Date:  2022-06-20       Impact factor: 4.126

3.  E1B-55K Is a Phosphorylation-Dependent Transcriptional and Posttranscriptional Regulator of Viral Gene Expression in Human Adenovirus C5 Infection.

Authors:  Paloma Hidalgo; Yasel Garcés; Eduardo Mundo; Raúl E López; Luca D Bertzbach; Thomas Dobner; Ramón A González
Journal:  J Virol       Date:  2022-01-12       Impact factor: 6.549

4.  Overcoming Immunological Challenges to Helper-Dependent Adenoviral Vector-Mediated Long-Term CFTR Expression in Mouse Airways.

Authors:  Huibi Cao; Rongqi Duan; Jim Hu
Journal:  Genes (Basel)       Date:  2020-05-18       Impact factor: 4.096

Review 5.  Advances in Oral Subunit Vaccine Design.

Authors:  Hans Van der Weken; Eric Cox; Bert Devriendt
Journal:  Vaccines (Basel)       Date:  2020-12-22

6.  iMATCH: an integrated modular assembly system for therapeutic combination high-capacity adenovirus gene therapy.

Authors:  Dominik Brücher; Nicole Kirchhammer; Sheena N Smith; Jatina Schumacher; Nina Schumacher; Jonas Kolibius; Patrick C Freitag; Markus Schmid; Fabian Weiss; Corina Keller; Melanie Grove; Urs F Greber; Alfred Zippelius; Andreas Plückthun
Journal:  Mol Ther Methods Clin Dev       Date:  2021-01-20       Impact factor: 6.698

Review 7.  Understanding and addressing barriers to successful adenovirus-based virotherapy for ovarian cancer.

Authors:  Rebeca Gonzalez-Pastor; Peter S Goedegebuure; David T Curiel
Journal:  Cancer Gene Ther       Date:  2020-09-19       Impact factor: 5.987

Review 8.  Novel vectors and approaches for gene therapy in liver diseases.

Authors:  Sheila Maestro; Nicholas D Weber; Nerea Zabaleta; Rafael Aldabe; Gloria Gonzalez-Aseguinolaza
Journal:  JHEP Rep       Date:  2021-04-30

Review 9.  Expanding the Spectrum of Adenoviral Vectors for Cancer Therapy.

Authors:  Jian Gao; Wenli Zhang; Anja Ehrhardt
Journal:  Cancers (Basel)       Date:  2020-05-02       Impact factor: 6.639

10.  Curative in vivo hematopoietic stem cell gene therapy of murine thalassemia using large regulatory elements.

Authors:  Hongjie Wang; Aphrodite Georgakopoulou; Chang Li; Zhinan Liu; Sucheol Gil; Ashvin Bashyam; Evangelia Yannaki; Achilles Anagnostopoulos; Amit Pande; Zsuzsanna Izsvák; Thalia Papayannopoulou; André Lieber
Journal:  JCI Insight       Date:  2020-08-20
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