A membrane antibody receptor for noninvasive imaging of gene expression.

Abstract

Monitoring gene expression is important to optimize gene therapy protocols and ensure that the proper tissue distribution is achieved in clinical practice. We developed a noninvasive imaging system based on the expression of artificial antibody receptors to trap hapten-labeled imaging probes. Functional membrane-bound anti-dansyl antibodies (DNS receptor) were stably expressed on melanoma cells in vitro and in vivo. A bivalent (DNS)2-diethylenetriaminepentaacetic 111Indium probe specifically bound to cells that expressed DNS receptors but not control scFv receptors. Importantly, the 111In probe preferentially localized to DNS receptors but not control receptors on tumors in mice as assessed by gamma camera imaging. By 48 h after intravenous injection, the uptake of the probe in tumors expressing DNS receptors was 72 times greater than the amount of probe in the blood. This targeting strategy may allow noninvasive assessment of the location, extent and persistence of gene expression in living animals and in the clinic.

• Authors: S R Roffler, H-E Wang, H-M Yu, W-D Chang, C-M Cheng, Y-L Lu, B-M Chen, T-L Cheng
• Journal: Gene therapy (Gene Ther) Vol. 13 Issue 5 Pg. 412-20 (Mar 2006) ISSN: 0969-7128 [Print] England
• PMID: 16267569 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• 1-myristoyl-2-(12-((5-dimethylamino-1-naphthalenesulfonyl)amino)dodecanoyl)-sn-glycero-3-phosphocholine
• Haptens
• Indium Radioisotopes
• Phosphatidylcholines
• Receptors, Cell Surface
• Receptors, Fc
• Pentetic Acid

Topics

• Animals
• Antibody Specificity
• Gene Expression
• Genetic Engineering
• Genetic Therapy (methods)
• Genetic Vectors (administration & dosage)
• Haptens
• HeLa Cells
• Humans
• Indium Radioisotopes
• Melanoma, Experimental (metabolism)
• Mice
• Mice, Inbred C57BL
• Microscopy, Phase-Contrast
• Pentetic Acid
• Phosphatidylcholines (immunology)
• Protein Binding
• Receptors, Cell Surface (metabolism)
• Receptors, Fc (metabolism)
• Retroviridae (genetics)