Apoptotic cell death in response to dengue virus infection: The pathogenesis of dengue haemorrhagic fever revisited

Clinical and Diagnostic Virology

Volumn 10, Issue 2-3, 1998, Pages 113-119

  Marianneau, Philippe ^a   Flamand, Marie ^a   Deubel, Vincent ^a   Desprès, Philippe ^a  

^a INSTITUT PASTEUR   (France)

Author keywords

Apoptosis; Dengue virus; Hepatocytes; Host response; Neurones

Indexed keywords

CYTOKINE;

APOPTOSIS; CONFERENCE PAPER; DENGUE; DENGUE VIRUS; HEPATOMEGALY; IMMUNE RESPONSE; LIVER CELL; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; SHOCK; VIRUS INFECTION; VIRUS REPLICATION;

ANIMALS; APOPTOSIS; CYTOKINES; DENGUE HEMORRHAGIC FEVER; DENGUE VIRUS; HUMANS; LIVER; NEURONS; PHAGOCYTOSIS;

DENGUE VIRUS; RNA VIRUSES;

EID: 0032527410     PISSN: 09280197     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0928-0197(98)00031-2     Document Type: Conference Paper

References (36)

1. Anderson R., King A.D., Innis B.L. Correlation of E protein binding with cell susceptibility to dengue 4 virus infection. J Gen Virol. 73:1992;2155-2159.
2. Anderson R., Wang S., Osiowy C., Issekutz A.C. Activation of endothelial cells via antibody-enhanced dengue virus infection of peripheral blood monocytes. J Virol. 71:1997;4226-4232.
3. Bhamarapravati N., Toochinda P., Boonyapaknavik V. Pathology of Thailand haemorrhagic fever: a study of 100 autopsy cases. Am J Trop Med Parasitol. 61:1967;500-510.
4. Bielefeldt-Ohmann H. Pathogenesis of dengue virus diseases: missing pieces in the jigsaw. Trends Microbiol. 5:1997;409-413.
5. Desprès P., Flamand M., Ceccaldi P.E., Deubel V. Human isolates of dengue type 1 induce apoptosis in mouse neuroblastoma cells. J Virol. 70:1996;4090-4096.
6. Desprès P., Frenkiel M.P., Ceccaldi P.E., Duarte dos Santos C., Deubel V. Apoptosis in the mouse central nervous system in response to infection with mouse-neurovirulent dengue viruses. J Virol. 72:1998;823-829.
7. Freedman S.R., Sharma R.J., Nabel G.J., Emerson S.G., Griffin G.E. Cellular distribution of nuclear factor kappa B binding activity in rat liver. Biochem J. 287:1992;645-649.
8. Galle P.R., Hofman W.J., Walczak H., Schaller H., Otto G., Stremmel W., Krammer P.H., Runkel L. Involvement of the CD95 (APO-1/Fas) receptor and ligand in liver damage. J Exp Med. 182:1995;1223-1230.
9. Hall W.C., Crowell T.P., Watts D.M., Barros V.L.R., Kruger H., Pinheiro F., Peters C.J. Demonstration of yellow fever and dengue antigens in formalin-fixed paraffin-embedded human liver by immunohistological analysis. Am J Trop Med Hyg. 45:1991;408-417.
10. Halstead S.B. Pathogenesis of dengue: challenges to molecular biology. Science. 239:1988;476-481.
11. Hober D., Nguyen T.L., Shen L., Do Q.H., Vu T.Q.H., Benyoucef S., Nguyen T.H., Bui T.M.P., Loan H.K., Le B.L., Bouzidi A., De Groote D., Deubel V., Wattré P. TNFα levels in plasma and whole blood culture in dengue-infected patients: relationship with virus detection and pre-existing specific antibodies. J Med Virol. 54:1998;210-218.
12. Innis B.L. Dengue and dengue haemorrhagic fever. Porterfield J.S. Exotic Viral Infections. 1995;103-146 Chapman and Hall, London.
13. Kerr J.F.R., Searle J., Halliday W.J., Roberts T., Cooksley W.G.E., Halliday J.W., Holder L., Burnett W. The nature of piecemeal necrosis in chronic active hepatitis. Lancet. 20:1979;827-828.
14. Knowles B.B., Searls D.B., Aden D.P. Human hepatoma-derived cell lines. Chisari F.V. Advances in Hepatitis Research. 1984;196-202 Masson, New York.
15. Knudsen A.B. Global strategy for the prevention and control of dengue and dengue haemorrhagic fever. Saluzzo J.F., Dodet B. Emerging Diseases: Factors in the Emergence of Arbovirus Diseases. 1997;129-140 Elsevier, Paris.
16. Kuo C.H., Tai D.I., Chang-Chien C.S., Lan C.K., Chiou S.S., Liaw Y.F. Liver biochemical tests and dengue fever. Am J Trop Med Hyg. 47:1992;265-270.
17. Kurane I., Ennis F.E. Immunity and immunopathology in dengue virus infections. Semin Immunol. 4:1992;121-127.
18. Lam K.W., Burke D.S., Siemans M., Kipperly V., Li C.Y., Lam T. Characterization of serum acid phosphatase associated with dengue hemorrhagic fever. Clin Chem. 28:1982;2296-2299.
19. Lucia H.L., Kangwanpong D. Identification of dengue virus-infected cells in paraffin-embedded tissue using in situ polymerase chain reaction and DNA hybridisation. J Virol Methods. 48:1994;1-8.
20. Majno G., Joris I. Apoptosis, oncosis and necrosis. An overview of cell death. Am J Pathol. 146:1995;3-15.
21. Marianneau P., Mégret F., Olivier R., Morens D.M., Deubel V. Dengue 1 virus binding to human hepatoma HepG2 and simian Vero cell surfaces differs. J Gen Virol. 77:1996;2547-2554.
22. Marianneau P., Cardona A., Edelman L., Deubel V., Desprès P. Dengue virus replication in human hepatoma cells activates NF-κB which in turn induces apoptotic cell death. J Virol. 71:1997;3244-3249.
23. Marianneau P, Flamand M, Courageot MP, Deubel V, Desprès P. La mort cellulaire par apoptose en réponse à l'infection par le virus de la dengue: quelles conséquences dans la pathogénie virale? Ann Biol Clin 1998 (in press).
24. Monath T.P. Pathobiology of the flaviviruses. Schlesinger S., Schlesinger M.J. The Togaviridae and Flaviviridae. 1986;375-440 Plenum, New York and London.
25. Monath T.P. Yellow fever and dengue - the interactions of virus, vector and host in the re-emergence of epidemic disease. Semin Virol. 5:1994;133-145.
26. Monath T.P., Heinz F.X. Flaviviruses. Fields B.N., Knipe D.M., Howley P.M. Fields Virology. 1996;961-1034 Lippincott-Raven Press, Philadelphia, PA.
27. Nguyen T.L., Nguyen T.H., Tieu N.T. The impact of dengue haemorrhagic fever on liver function. Res Virol. 148:1997;273-277.
28. O'Sullivan M.A., Killen H.M. The differentiation state of monocytic cells affects their susceptibility to infection and the effects of infection by dengue virus. J Gen Virol. 75:1994;2387-2392.
29. Razvi E.S., Welsh R.M. Apoptosis in viral infections. Adv Virus Res. 45:1995;1-60.
30. Rosen L., Khin M.M., U T. Recovery of virus from the liver of children with fatal dengue: reflection on the pathogenesis of the disease and its possible analogy with that of yellow fever. Res Virol. 140:1989;351-360.
31. Rothwell S.W., Putnak R., La Russa V.F. Dengue-2 infection of human bone marrow: characterisation of dengue-2 antigen-positive stroma cells. Am J Trop Med Hyg. 54:1996;503-510.
32. Schlesinger R.W. Dengue Viruses. 1977;Springer, New York.
33. Scott R.M., Nisalak A., Cheamudon U., Seridhoranakul S., Nimmannitya S. Isolation of dengue viruses from peripheral blood leukocytes of patients with hemorrhagic fever. J Infect Dis. 141:1980;1-6.
34. Searle J., Harmon B.V., Bishop C.J., Kerr J.F.R. The significance of cell death by apoptosis in hepatobiliary disease. J Gastroenterol Hepatol. 2:1987;77-96.
35. Waterman S.H., Kuno G., Gubler D.J., Sather G.E. Low rates of antigen detection and virus isolation from the peripheral blood leukocytes of dengue fever patients. Am J Trop Med Hyg. 34:1985;380-384.
36. Zinkernagel R.M., Doherty P.C. MHC-restricted cytotoxic T cells: studies on the biological role of polymorphic major transplantation antigens determining T-cell restriction-specificity, function and responsiveness. Adv Immunol. 27:1979;51-177.