Barriers to systemic application of virus-based vectors in gene therapy: lessons from adenovirus type 5.

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 Genes

journal_title

Virus genes

authors

Jönsson F,Kreppel F

doi

10.1007/s11262-017-1498-z

subject

Has Abstract

pub_date

2017-10-01 00:00:00

pages

692-699

issue

5

eissn

0920-8569

issn

1572-994X

pii

10.1007/s11262-017-1498-z

journal_volume

53

pub_type

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