AJTMH ASTMH Job Mart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 45(4), 1991, pp. 408-417
Copyright © 1991 by The American Society of Tropical Medicine and Hygiene

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hall, W. C.
Right arrow Articles by Peters, C. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hall, W. C.
Right arrow Articles by Peters, C. J.
Right arrowPubmed/NCBI databases
Medline Plus Health Information
*Dengue

Demonstration of Yellow Fever and Dengue Antigens in Formalin-Fixed Paraffin-Embedded Human Liver by Immunohistochemical Analysis

William C. Hall, Thomas P. Crowell, Douglas M. Watts, Vera L. R. Barros, Hever Kruger, Francisco Pinheiro AND Clarence J. Peters
Pathology Associates, Inc., Frederick, Maryland; Instituto Evandro Chagas, Belem-Para, Brazil; Department of Pathology, Centro Medico Naval, Callao, Peru; Pan American Health Organization, Washington DC; Disease Assessment Division, US Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland

Two immunohistochemical techniques to determine the presence of yellow fever and dengue antigens in fixed tissue samples were developed for the purpose of making retrospective diagnoses of these viral diseases in humans. A horseradish peroxidase label was used for one technique and an alkaline phosphatase label for the other. In the former technique, acid hematin was removed from the tissues, iron-containing pigments were counterstained with Prussian blue, and the product of the diaminobenzidine reaction was enhanced with a dilute solution of osmium tetroxide that differentiated antigen from lipofuscin. In the latter technique, alkaline phosphatase was used as the enzyme labeling system with a red chromagen that contrasted nicely with the pigments in the tissues, as mentioned above. Thus, pigment removal or differentiation from antigen was not required. Replicate sections were cut and mouse polyclonal antibodies for yellow fever and all dengue types were applied to individual sections. On samples positive for dengue antigen, monoclonal antibodies were applied to additional replicate sections to demonstrate antigen of dengue types 1 and 4. In order to test the assay, samples of formalin-fixed liver tissue from Brazilian and Peruvian individuals who had died from a variety of causes as long as eight years earlier were received in a blinded fashion for immunohistochemical analysis. The techniques appeared to be highly reliable for yellow fever diagnosis; however, not enough cases were observed to adequately evaluate the procedures for dengue diagnosis. Both procedures appeared to have similar sensitivity.




This article has been cited by other articles:


Home page
J. Virol.Home page
T. R. Prestwood, D. M. Prigozhin, K. L. Sharar, R. M. Zellweger, and S. Shresta
A Mouse-Passaged Dengue Virus Strain with Reduced Affinity for Heparan Sulfate Causes Severe Disease in Mice by Establishing Increased Systemic Viral Loads
J. Virol., September 1, 2008; 82(17): 8411 - 8421.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
B. E. Dewi, T. Takasaki, and I. Kurane
Peripheral blood mononuclear cells increase the permeability of dengue virus-infected endothelial cells in association with downregulation of vascular endothelial cadherin
J. Gen. Virol., March 1, 2008; 89(3): 642 - 652.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
Y.-R. Lee, M.-T. Liu, H.-Y. Lei, C.-C. Liu, J.-M. Wu, Y.-C. Tung, Y.-S. Lin, T.-M. Yeh, S.-H. Chen, and H.-S. Liu
MCP-1, a highly expressed chemokine in dengue haemorrhagic fever/dengue shock syndrome patients, may cause permeability change, possibly through reduced tight junctions of vascular endothelium cells
J. Gen. Virol., December 1, 2006; 87(12): 3623 - 3630.
[Abstract] [Full Text] [PDF]


Home page
J. Immunol.Home page
J.-P. Chen, H.-L. Lu, S.-L. Lai, G. S. Campanella, J.-M. Sung, M.-Y. Lu, B. A. Wu-Hsieh, Y.-L. Lin, T. E. Lane, A. D. Luster, et al.
Dengue Virus Induces Expression of CXC Chemokine Ligand 10/IFN-{gamma}-Inducible Protein 10, Which Competitively Inhibits Viral Binding to Cell Surface Heparan Sulfate.
J. Immunol., September 1, 2006; 177(5): 3185 - 3192.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1991 by the American Society of Tropical Medicine and Hygiene.