Apoptosis in tissues from fatal dengue shock syndrome

Journal of Clinical Virology

Volumn 40, Issue 1, 2007, Pages 50-54

  Limonta, Daniel ^a,b   Capó, Virginia ^b   Torres, Griselda ^b   Pérez, Ana B ^a   Guzmán, María G ^a  

^a Virology Department   (Cuba)

^b INSTITUTO DE MEDICINA TROPICAL PEDRO KOURÍ   (Cuba)

Author keywords

Apoptosis; Cuba; Dengue; Immunohistochemistry; Leakage; Shock

Indexed keywords

VIRUS ANTIGEN;

ADULT; APOPTOSIS; ARTICLE; BRAIN CELL; BRAIN HYPOXIA; BRAIN ISCHEMIA; BRAIN NERVE CELL; BRAIN TISSUE; CLINICAL ARTICLE; CONTROLLED STUDY; CUBA; DENGUE; DENGUE SHOCK SYNDROME; DENGUE VIRUS; ENDOTHELIUM CELL; EPIDEMIC; FEMALE; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; IMMUNOLOCALIZATION; INTESTINE; LEUKOCYTE; LIVER; LIVER CELL; LUNG PARENCHYMA; MALE; NICK END LABELING; PATHOGENESIS; PRIORITY JOURNAL; VASCULAR ENDOTHELIUM;

ADULT; ANTIGENS, VIRAL; APOPTOSIS; BRAIN; CUBA; DENGUE HEMORRHAGIC FEVER; DENGUE VIRUS; DISEASE OUTBREAKS; FEMALE; HUMANS; IN SITU NICK-END LABELING; INTESTINES; LIVER; LUNG; MALE; MIDDLE AGED;

EID: 34548126493     PISSN: 13866532     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcv.2007.04.024     Document Type: Article

References (25)

1. Avirutnan P., Malasit P., Seliger B., et al. Dengue virus infection of human endothelial cells leads to chemokine production, complement activation, and apoptosis. J Immunol 161 11 (1998) 6338-6346
2. Avirutnan P., Punyadee N., Noisakran S., et al. Vascular leakage in severe dengue virus infections: a potential role for the nonstructural viral protein NS1 and complement. J Infect Dis 193 8 (2006) 1078-1088
3. Cardier J.E., Marino E., Romano E., et al. 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 30 6 (2005) 359-365
4. Clyde K., Kyle J.L., and Harris E. Recent advances in deciphering viral and host determinants of dengue virus replication and pathogenesis. J Virol 80 23 (2006) 11418-11431
5. Courageot M.P., Catteau A., and Despres P. Mechanisms of dengue virus-induced cell death. Adv Virus Res 60 (2003) 157-186
6. Couvelard A., Marianneau P., Bedel C., et al. Report of a fatal case of dengue infection with hepatitis: demonstration of dengue antigens in hepatocytes and liver apoptosis. Hum Pathol 30 9 (1999) 1106-1110
7. Despres P., Frenkiel M.P., Ceccaldi P.E., et al. Apoptosis in the mouse central nervous system in response to infection with mouse-neurovirulent dengue viruses. J Virol 72 1 (1998) 823-829
8. Green S., and Rothman A. Immunopathological mechanisms in dengue and dengue hemorrhagic fever. Curr Opin Infect Dis 19 5 (2006) 429-436
9. Gubler D.J. Dengue and dengue hemorrhagic fever. Clin Microbiol Rev 11 3 (1998) 480-496
10. Guzman M.G., and Kouri G. Dengue: an update. Lancet Infect Dis 2 1 (2002) 33-42
11. Guzman M.G., Alvarez M., Rodriguez R., et al. Fatal dengue hemorrhagic fever in Cuba, 1997. Int J Infect Dis 3 3 (1999) 130-135
12. Hotchkiss R.S., Tinsley K.W., Swanson P.E., et al. Endothelial cell apoptosis in sepsis. Crit Care Med 30 5 Suppl. (2002) S225-S228
13. Huerre M.R., Lan N.T., Marianneau P., et al. Liver histopathology and biological correlates in five cases of fatal dengue fever in Vietnamese children. Virchows Arch 438 2 (2001) 107-115
14. Hughes J., Nangaku M., Alpers C.E., et al. C5b-9 membrane attack complex mediates endothelial cell apoptosis in experimental glomerulonephritis. Am J Physiol Renal Physiol 278 5 (2000) F747-F757
15. Jessie K., Fong M.Y., Devi S., et al. Localization of dengue virus in naturally infected human tissues, by immunohistochemistry and in situ hybridization. J Infect Dis 189 8 (2004) 1411-1418
16. Li J.H., Kluger M.S., Madge L.A., et al. Interferon-gamma augments CD95(APO-1/Fas) and pro-caspase-8 expression and sensitizes human vascular endothelial cells to CD95-mediated apoptosis. Am J Pathol 161 4 (2002) 1485-1495
17. Lin C.F., Lei H.Y., Shiau A.L., et al. Endothelial cell apoptosis induced by antibodies against dengue virus nonstructural protein 1 via production of nitric oxide. J Immunol 169 2 (2002) 657-664
18. Lin C.F., Lei H.Y., Shiau A.L., et al. Antibodies from dengue patient sera cross-react with endothelial cells and induce damage. J Med Virol 69 1 (2003) 82-90
19. Matsuda T., Almasan A., Tomita M., et al. Dengue virus-induced apoptosis in hepatic cells is partly mediated by Apo2 ligand/tumour necrosis factor-related apoptosis-inducing ligand. J Gen Virol 86 Pt 4 (2005) 1055-1065
20. Miagostovich M.P., Ramos R.G., Nicol A.F., et al. Retrospective study on dengue fatal cases. Clin Neuropathol 16 4 (1997) 204-208
21. Mongkolsapaya J., Dejnirattisai W., Xu X.N., et al. Original antigenic sin and apoptosis in the pathogenesis of dengue hemorrhagic fever. Nat Med 9 7 (2003) 921-927
22. Myint K.S., Endy T.P., Mongkolsirichaikul D., et al. Cellular immune activation in children with acute dengue virus infections is modulated by apoptosis. J Infect Dis 194 5 (2006) 600-607
23. PAHO. Dengue and dengue hemorrhagic fever in the Americas: guidelines for prevention and control (1994), PAHO, Washington, DC
24. Pelegrino J.L., Arteaga E., Rodriguez A.J., et al. Normalizacion de tecnicas inmunohistoquimicas para la deteccion de antigenos del virus dengue en tejidos embebidos en parafina. Rev Cubana Med Trop 49 2 (1997) 100-107
25. Won S.J., Kim D.Y., and Gwang B.J. Cellular and molecular pathways of ischemic neuronal death. Biochem Mol Biol 35 (2002) 67-86