2011
DOI: 10.1016/j.vaccine.2011.03.038
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A human challenge model for dengue infection reveals a possible protective role for sustained interferon gamma levels during the acute phase of illness

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Cited by 98 publications
(85 citation statements)
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“…[29][30][31][32][33][34][35] As our results suggest, DENV-2 seems to be more immunogenic than the other serotypes, and generates a stronger pro-inflammatory immunologic response, which is necessary to control viral infection. Much of the antiviral potential of effector cells of the innate and adaptive immune system (natural killer cells and cytotoxic T cells) is caused by production of antiviral cytokines such as IFN-γ and TNF-α at the site of the infection.…”
Section: Discussionmentioning
confidence: 99%
See 2 more Smart Citations
“…[29][30][31][32][33][34][35] As our results suggest, DENV-2 seems to be more immunogenic than the other serotypes, and generates a stronger pro-inflammatory immunologic response, which is necessary to control viral infection. Much of the antiviral potential of effector cells of the innate and adaptive immune system (natural killer cells and cytotoxic T cells) is caused by production of antiviral cytokines such as IFN-γ and TNF-α at the site of the infection.…”
Section: Discussionmentioning
confidence: 99%
“…30 Recently, a human challenge model for dengue infection showed a possible protective role for sustained IFN-γ levels during the acute phase of illness. 31 Significantly higher gene expression of TNF-α and IFN-γ in response to DENV-2 and DENV-3 heterologous challenge in DENV-1 primary immune cases was found, and the highest response was to DENV-2 Although DENV-1/DENV-2 and DENV-1/DENV-3 sequences of dengue infection were associated with severe illness during the 1981 (DENV-2) and 2001 (DENV-3) epidemics, respectively, greater severity was observed during the 1981 epidemic. Previous studies demonstrated that in 1981, 98% of DHF cases occurred during a secondary DENV-1/DENV-2 infection while in 2001, 73% of DHF cases occurred during a secondary DENV-1/DENV-3 infection.…”
Section: Discussionmentioning
confidence: 99%
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“…Los receptores AXL son expresados por los fibroblastos cutá-neos, los queratinocitos epidermicos, los macrófagos, las Infectología al Día células del endotelio vascular; mientras que los receptores Tyro 3 son expresados por las neuronas del SNC 37,38 . La activación de los receptores TAM, junto con la respuesta del interferon β (INF-β), reducen la permeabilidad de la BHE, contribuyendo al buen funcionamiento de ésta 39,40 e impidiendo la entrada del virus al SNC. En infecciones por flavivirus se ha observado, una regulación negativa de los receptores TAM, en especial de los AXL 38,39 ; esto produce una disminución de la integridad de la BHE en su capa basal, pérdida de la unión de células endoteliales de la microvasculatura cerebral, permitiendo la entrada y replicación del virus al SNC 38 .…”
Section: Virus Del Zika Y Su Neurotropismounclassified
“…It is anticipated that efficacy studies will further elucidate the role of neutralizing antibodies and what constitutes a human immuno-protection profile. Cell-mediated immunity's role in immuno-protective and pathogenic immune responses is also under exploration [23][24][25]. It is likely that a single correlate of protection can be defined for all DENV serotypes, but surrogates (i.e.…”
Section: Dengue Vaccine Development Challengesmentioning
confidence: 99%