Abstract:
:Currently, virus-based vectors, namely derivatives of the adenovirus, are frequently used in a wide variety of ex vivo or local gene therapeutic applications. However, the efficacy of virus-based vectors in systemic applications is presently still extremely limited. Complex interactions of the various vector types with the patient's organism hinder successful vector deployment. Exemplary, here we summarize barriers to systemic application of Adenovirus-based vectors leading either to acute toxic effects or rapid vector neutralization and discuss strategies to overcome these barriers aiming to develop more efficient vector types.
journal_name
Virus Genesjournal_title
Virus genesauthors
Jönsson F,Kreppel Fdoi
10.1007/s11262-017-1498-zsubject
Has Abstractpub_date
2017-10-01 00:00:00pages
692-699issue
5eissn
0920-8569issn
1572-994Xpii
10.1007/s11262-017-1498-zjournal_volume
53pub_type
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