Evidence of Vascular Damage in Dengue Disease: Demonstration of High Levels of Soluble Cell Adhesion Molecules and Circulating Endothelial Cells

REFERENCES

• Adams D. H., Mainolfi E., Burra P., Neuberger J. M., Ayres R., Elias E., Rothlein R. Detection of circulating intercellular adhesion molecule-1 in chronic liver diseases. Hepatology 1992; 16: 810–814, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Anderson R., Wang S., Osiowy C., Issekutz A. Activation of endothelial cells via antibody-enhanced dengue virus infection of peripheral blood monocytes. Journal of Virology 1997; 71: 4226–4232, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Avirutnan P., Malasit P., Seliger B., Bhakdi S., Husmann M. Dengue virus infection of human endothelial cells leads to chemokine production, complement activation, and apoptosis. Journal of Immunology 1998; 161: 6338–6346, [CSA]
   PubMed Web of Science ®Google Scholar
• Cardier J. E., Balogh V., Perez-Silva C., Romano E., Rivas R., Bosch N., Rothman A. L. Relationship of thrombopoietin and Interleukin-11 to thrombocytopenia associated with dengue disease. Cytokine 2006; 34: 155–160, [INFOTRIEVE], [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Cardier J. E., Marino E., Romano E., Taylor P., Liprandi F., Bosch N., Rothman A. L. Proinflammatory factors present in sera from patients with acute dengue infection induce activation and apoptosis of human microvascular endothelial cells: Possible role of TNF-alpha in endothelial cell damage in dengue. Cytokine 2005; 30: 359–365, [INFOTRIEVE], [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Cines D. B., Pollak E. S., Buck C. A., Loscalzo J., Zimmeman G. A., McEver R. P., Pober J. S., Wick T. M., Konkle B. A., Schwarts B. S., Barnathan E. S., McCrae K. R., Hug B. A., Schmidt A. M., Stern D. M. Endothelial cells in physiology and in the pathophysiology of vascular disorders. Blood 1998; 91: 3527–3561, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Dhawan R., Khanna M., Chaturvedi U. C., Mathur A. Effect of dengue virus-induced cytotoxin on capillary permeability. Journal of Experimental Pathology 1990; 71: 83–88, [INFOTRIEVE], [CSA]
   Google Scholar
• Gearing A. J., Newman W. Circulating adhesion molecules in disease. Immunology Today 1993; 14: 506–512, [INFOTRIEVE], [CROSSREF], [CSA]
   PubMedGoogle Scholar
• George F., Brouqui P., Boffa M. C., Mutin M., Drancourt M., Brisson C., Raoult D., Sampol J. Demonstration of Rickettsia conorii-induced endothelial injury in vivo by measuring circulating endothelial cells, thrombomodulin, and von Willebrand factor in patients with mediterranean spotted fever. Blood 1993; 82: 2109–2116, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Goon P. K., Boos C. J., Lip G. Y. Circulating endothelial cells: Markers of vascular dysfunction. Clinical Laboratory 2005; 51: 531–538, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Goon P. K., Lip G. Y., Boos C. J., Stonelake P. S., Blann A. D. Circulating endothelial cells, endothelial progenitor cells, and endothelial microparticles in cancer. Neoplasia 2006; 8: 79–88, [INFOTRIEVE], [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Grefte A., van der Giessen M., van Son W., The T H. Circulating cytomegalovirus (CMV)-infected endothelial cells in patients with an active CMV infection. Journal Infectious Disease 1993; 167: 270–277, [CSA]
   PubMed Web of Science ®Google Scholar
• Halstead S. Pathogenesis of dengue: Challenges to molecular biology. Science 1988; 239: 476–481, [INFOTRIEVE], [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Hober D., Poli L., Roblin B., Gestas P., Chungue E., Granic G., Imbert P., Pecarere J. L., Vergez-Pascal R., Wattre P., et al. Serum levels of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6) and interleukin 1- (IL-1-β) in dengue-infected patients. American Journal Tropical Medicine Hygiene 1993; 48: 324–331, [CSA]
   PubMed Web of Science ®Google Scholar
• Kalka C., Masuda H., Takahashi T., Gordon R., Tepper O., Gravereaux E., Pieczek A., Iwaguro H., Hayashi S., Isner J., Asahara T. Vascular endothelial growth factor165 gene transfer augments circulating endothelial progenitor cells in human subjects. Circulation Research 2000; 86: 1198–1202, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Khanna M., Chaturvedi U. C., Sharma M. C., Pandey V. C., Mathur A. Increased capillary permeability mediated by a dengue virus induced lymphokine. Immunology 1990; 69: 449–453, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Koraka P., Murgue B., Deparis X., Van Gorp E. C., Setiati T. E., Osterhaus A. D., Groen J. Elevation of soluble VCAM-1 plasma levels in children with acute dengue virus infection of varying severity. Journal Medical Virology 2004; 72: 445–450, [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Kurane I., Ennis F. A. Cytokines in dengue fever virus infections: role of cytokines in the pathogenesis of dengue hemorrhagic fever. Seminars Immunology 1994; 5: 443–448, [CSA]
   Google Scholar
• Kurane I., Rothman A. L., Livingston P. G., Green S., Gagnon S. J., Janus J., Innis B. L., Nimmannitya S., Nisalak A., Ennis F. A. Immnunopathological mechanisms of dengue hemorrhagic fever and dengue shock syndrome. Archives Virology Supplement 1994; 9: 59–64, [CSA]
   PubMedGoogle Scholar
• Labarrere C. A., Nelson D. R., Faulk W. P. Endothelial activation and development of coronary artery disease in transplanted human hearts. The Journal of the American Medical Association 1997; 278: 1169–1175, [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Lanciotti R. S., Calisher C. H., Gubler D. J., Chang G. J., Vorndam A. V. Rapid detection and typing of dengue viruses from clinical samples by using reverse transcriptase-polymerase chain reaction. Journal Clinical Microbiology 1992; 30: 545–551, [CSA]
   PubMed Web of Science ®Google Scholar
• Lin C. F., Chiu S. C., Hsiao Y. L., Wan S. W., Lei H. Y., Shiau A. L., Liu H. S., Yeh T. M., Chen S. H., Liu C. C., Lin Y. S. Expression of cytokine, chemokine, and adhesion molecules during endothelial cell activation induced by antibodies against dengue virus nonstructural protein 1. Journal of Immunology 2005; 174: 395–403, [CSA]
   PubMed Web of Science ®Google Scholar
• Lin Y. S., Lin C. F., Lei H. Y., Liu H. S., Yeh T. M., Chen S. H., Liu C. C. Antibody-mediated endothelial cell damage via nitric oxide. Curr Pharm Des 2004; 10: 213–221, [INFOTRIEVE], [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Mason J. C., Kapahi P., Haskard D. O. Detection of increased levels of circulating intercellular adhesion molecule 1 in some patients with rheumatoid arthritis but not in patients with systemic lupus erythematosus. Lack of correlation with levels of circulating vascular cell adhesion molecule 1. Arthritis Rheumatism 1993; 36: 519–527, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Most J., Zangerle R., Herold M., Fuchs D., Wachter H., Fritsch P., Dierich M. P. Elevated concentrations of circulating intercellular adhesion molecule 1 (ICAM-1) in HIV-1 infection. Journal of Acquired Immune Deficiency Syndrome 1993; 6: 221–226, [CSA]
   PubMed Web of Science ®Google Scholar
• Murgue B., Cassar O., Deparis X. Plasma concentrations of sVCAM-1 and severity of dengue infections. Journal Medical Virology 2001; 65: 97–104, [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Peyrefitte C. N., Pastorino B., Grau G. E., Lou J., Tolou H., Couissinier-Paris P. Dengue virus infection of human microvascular endothelial cells from different vascular beds promotes both common and specific functional changes. Journal of Medical Virology 2006; 78: 229–242, [INFOTRIEVE], [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Pober J. S., Cotran R. S. Cytokines and endotheial cell biology. Physiology Review 1990; 70: 427–451, [CSA]
   PubMed Web of Science ®Google Scholar
• Ramirez-Ronda C. H., Garcia C. Dengue in the Western hemisphere. Infectious Disease Clinics of North America 1994; 8: 107–128, [INFOTRIEVE], [CSA]
   PubMed Web of Science ®Google Scholar
• Remick D. G., Kunkel S. L. Pathophysiologic alterations induced by tumor necrosis factor. International Review of Experimental Pathology 1993; 34B: 7–25, [CSA]
   Google Scholar
• Sahaphong S., Riengrojpitax S., Bhamarapravati N., Chirachariyavej T. Electron microscopic study of the vascular endothelial cell in dengue hemorrhagic fever. Southeast Asian Journal Tropical Medicine Public Health 1980; 11: 194–204, [CSA]
   PubMedGoogle Scholar
• Schnittler H. J., Feldmann H. Viral hemorrhagic fever—A vascular disease?. Thrombosis Haemostasis 2003; 89: 967–972, [CSA]
   PubMed Web of Science ®Google Scholar
• Seth R., Raymond F. D., Makgoba M. W. Circulating ICAM-1 isoforms: Diagnostic prospects for inflammatory and immune disorders. Lancet 1991; 338: 83–84, [INFOTRIEVE], [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Shijubo N., Imai K., Aoki S., Hirasawa M., Sugawara H., Koba H., Tsujisaki M., Sugiyama T., Hinoda Y., Yachi A. Circulating intercellular adhesion molecule-1 (ICAM-1) antigen in sera of patients with idiopathic pulmonary fibrosis. Clinical Experimental Immunology 1992; 89: 58–62, [CSA]
   PubMed Web of Science ®Google Scholar
• Solovey A., Lin Y., Browne P., Choong S., Wayner E., Hebbel R. Circulating activated endothelial cells in sickle cell anemia. New England Journal Medicine 1997; 337: 1584–1590, [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Talavera D., Castillo A. M., Dominguez M. C., Gutierrez A. E., Meza I. IL8 release, tight junction and cytoskeleton dynamic reorganization conducive to permeability increase are induced by dengue virus infection of microvascular endothelial monolayers. General Virology 2004; 85: 1801–1813, [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Tseng C. S., Lo H. W., Teng H. C., Lo W. C., Ker C. G. Elevated levels of plasma VEGF in patients with dengue hemorrhagic fever. FEMS Immunology and Medical Microbiology 2005; 43: 99–102, [INFOTRIEVE], [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Waterman S. H., Gubler D. J. Dengue fever. Clinical Dermatology 1989; 7: 117–122, [CROSSREF], [CSA]
   PubMed Web of Science ®Google Scholar
• Yadav M., Katath K. R., Iyngkaran N., Sinniah M. Dengue hemorrhagic fever and dengue shock syndrome: Are they tumor necrosis factor-mediated disorders?. FEMS Microbiology Immunology 1991; 4: 46–49, [CSA]
   Google Scholar
• World Health Organization. Dengue Hemorrhagic Fever: Diagnosis, Treatment and Control. World Health Organization, Geneva 1986
   Google Scholar