Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Science 17 September 1982:
Vol. 217. no. 4565, pp. 1151 - 1153
DOI: 10.1126/science.7112121

Articles

Science, Vol 217, Issue 4565, 1151-1153
Copyright © 1982 by American Association for the Advancement of Science


articles

Quantitative autoradiographic mapping of herpes simplex virus encephalitis with a radiolabeled antiviral drug

Y Saito, RW Price, DA Rottenberg, JJ Fox, TL Su, KA Watanabe, and FS Philips

2'-Fluoro-5-methyl-l-beta-D-arabinosyluracil (FMAU) labeled with carbon-14 was used to image herpes simplex virus type 1-infected regions of rat brain by quantitative autoradiography. FMAU is a potent antiviral pyrimidine nucleoside which is selectively phosphorylated by virus-coded thymidine kinase. When the labeled FMAU was administered 6 hours before the rats were killed, the selective uptake and concentration of the drug and its metabolites by infected cells (defined by immunoperoxidase staining of viral antigens) allowed quantitative definition and mapping of HSV-1-infected structures in autoradiograms of brain sections. These results show that quantitative autoradiography can be used to characterize the local metabolism of antiviral drugs by infected cells in vivo. They also suggest that the selective uptake of drugs that exploit viral thymidine kinase for their antiviral effect can, by appropriate labeling, be used in conjunction with clinical neuroimaging techniques to define infected regions of human brain, thereby providing a new approach to the diagnosis of herpes encephalitis in man.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Molecular-Genetic Imaging Based on Reporter Gene Expression.
J. H. Kang and J.-K. Chung (2008)
J. Nucl. Med. 49, 164S-179S
   Abstract »    Full Text »    PDF »
Normal Brain Cells Contribute to the Bystander Effect in Suicide Gene Therapy of Malignant Glioma.
H. Miletic, Y. H. Fischer, T. Giroglou, M. A. Rueger, A. Winkeler, H. Li, U. Himmelreich, W. Stenzel, A. H. Jacobs, and D. von Laer (2007)
Clin. Cancer Res. 13, 6761-6768
   Abstract »    Full Text »    PDF »
Intermolecular Contact between Globular N-terminal Fold and C-terminal Domain of ApoA-I Stabilizes Its Lipid-bound Conformation: STUDIES EMPLOYING CHEMICAL CROSS-LINKING AND MASS SPECTROMETRY.
S. Bhat, M. G. Sorci-Thomas, E. T. Alexander, M. P. Samuel, and M. J. Thomas (2005)
J. Biol. Chem. 280, 33015-33025
   Abstract »    Full Text »    PDF »
Imaging Transgene Expression for Gene Therapy.
M. Sadelain and R. G. Blasberg (2001)
Journal of Pharmacy Practice 14, 376-382
   Abstract »    PDF »
Imaging Techniques for Gene Therapy: SPECT, PET, and MRI.
U. Haberkorn and A. Altmann (2001)
Journal of Pharmacy Practice 14, 383-396
   Abstract »    PDF »
Quantitative Kinetics of [124I]FIAU in Cat and Man.
A. Jacobs, I. Bräunlich, R. Graf, M. Lercher, T. Sakaki, J. Voges, V. Hesselmann, W. Brandau, K. Wienhard, and W.-D. Heiss (2001)
J. Nucl. Med. 42, 467-475
   Abstract »    Full Text »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)