Optimizing targeted gene delivery: Chemical modification of viral vectors and synthesis of artificial virus vector systems

Journal Title: The AAPS Journal - Year 2006, Vol 8, Issue 4

Abstract

In comparison to classical medicines, gene therapy has the potential to mediate the highest possible level of therapeutic specificity. Every normal or diseased cell can switch on or off a gene expression cassette in a tissue-, disease-, and time-dependent fashion, by use of specific transcription factors that are active only in a given unique situation. In practice, we face the problem in realizing the concept: the delivery of nucleic acids into target cells is very ineffective and presents a formidable challenge. Key issues for future developments include improved targeting, enhanced intracellular uptake, and reduced toxicity of gene vectors. The currently used classes of vectors have complementary characteristics, such as high intracellular efficiency of viral vectors on the one hand and low immunogenicity and greater flexibility of nonviral vectors on the other hand. The merge of viral and nonviral vector technologies is highlighted as an encouraging strategy for the future; concepts include chemically modified viral vectors (“chemo-viruses”) and synthesis of virus-like systems (“synthetic viruses”). Examples for the development of vectors toward artificial synthetic viruses are presented.

Authors and Affiliations

Sabine Boeckle, Ernst Wagner

Keywords

Related Articles

Pharmacokinetically-Guided Lead Optimization of Nitrofuranylamide Anti-Tuberculosis Agents

In an effort to develop novel and more potent therapies to treat tuberculosis, a new class of chemical agents, nitrofuranylamides, is being developed. The present study examines biopharmaceutic properties and preclinical...

Detergent-resistant membrane microdomains in the disposition of the lipid signaling molecule anandamide

The endogenous cannabinoid anandamide is an agonist of the cannabinoid receptors CB1 and CB2, as well as transient receptor potential vanilloid type 1 and type 4 ion channels. In recent years, there has been a great deal...

Introduction of unsaturation into theN-n-alkyl chain of the nicotinic receptor antagonists, NONI and NDNI: Effect on affinity and selectivity

N-n-Octylnicotinium iodide (NONI) andN-n-decylnicotinium iodide (NDNI) are selective nicotinic receptor (nAChR) antagonists mediating nicotine-evoked striatal dopamine (DA) release, and inhibiting [3H]nicotine binding, r...

Introduction to the Proposals from the Global Bioanalysis Consortium Harmonization Team

At the initiative of four regional professional organizations from Europe (European Bioanalysis Forum (EBF)) and North America (AAPS, Applied Pharmaceutical Analysis (APA) APA and Calibration & validation group (...

Mechanistic Models Describing Active Renal Reabsorption and Secretion: A Simulation-Based Study

The online version of this article (doi:10.1208/s12248-012-9437-3) contains supplementary material, which is available to authorized users.

Download PDF file
  • EP ID EP681830
  • DOI  10.1208/aapsj080483
  • Views 81
  • Downloads 0

How To Cite

Sabine Boeckle, Ernst Wagner (2006). Optimizing targeted gene delivery: Chemical modification of viral vectors and synthesis of artificial virus vector systems. The AAPS Journal, 8(4), -. https://europub.co.uk/articles/-A-681830