dc.creator | Silva, Mayara Marques Carneiro da | |
dc.creator | Gil, Laura Helena Vega Gonzales | |
dc.creator | Marques, Ernesto Torres de Azevedo | |
dc.creator | Calzavara-Silva, Carlos Eduardo | |
dc.date | 2017-12-12T12:41:16Z | |
dc.date | 2017-12-12T12:41:16Z | |
dc.date | 2013 | |
dc.date.accessioned | 2023-09-27T00:07:08Z | |
dc.date.available | 2023-09-27T00:07:08Z | |
dc.identifier | SILVA, M. M. C. da et al. Potential biomarkers for the clinical prognosis of severe dengue. Memorias Do Instituto Oswaldo Cruz, v. 108, n. 6, p. 755–762, set. 2013. | |
dc.identifier | 1678-8060 | |
dc.identifier | https://www.arca.fiocruz.br/handle/icict/23617 | |
dc.identifier | 10.1590/0074-0276108062013012 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/8897622 | |
dc.description | Currently, several assays can confirm acute dengue infection at the point-of-care. However, none of these assays can predict the severity of the disease symptoms. A prognosis test that predicts the likelihood of a dengue patient to develop a severe form of the disease could permit more efficient patient triage and treatment. We hypothesise that mRNA expression of apoptosis and innate immune response-related genes will be differentially regulated during the early stages of dengue and might predict the clinical outcome. Aiming to identify biomarkers for dengue prognosis, we extracted mRNA from the peripheral blood mononuclear cells of mild and severe dengue patients during the febrile stage of the disease to measure the expression levels of selected genes by quantitative polymerase chain reaction. The selected candidate biomarkers were previously identified by our group as differentially expressed in microarray studies. We verified that the mRNA coding for CFD, MAGED1, PSMB9, PRDX4 and FCGR3B were differentially expressed between patients who developed clinical symptoms associated with the mild type of dengue and patients who showed clinical symptoms associated with severe dengue. We suggest that this gene expression panel could putatively serve as biomarkers for the clinical prognosis of dengue haemorrhagic fever. | |
dc.format | application/pdf | |
dc.language | eng | |
dc.rights | open access | |
dc.subject | dengue | |
dc.subject | biomarcadores | |
dc.subject | apoptose | |
dc.subject | imunidade inata | |
dc.subject | PCR quantitativa em tempo real | |
dc.subject | Dengue | |
dc.subject | biomarkers | |
dc.subject | apoptosis | |
dc.subject | innate immunity | |
dc.subject | quantitative real-time PCR | |
dc.subject | Antígenos de Neoplasias | |
dc.subject | genética | |
dc.subject | Cisteína Endopeptidases | |
dc.subject | genética | |
dc.subject | Glicoproteínas de Membrana | |
dc.subject | genética | |
dc.subject | Proteínas de Neoplasias | |
dc.subject | genética | |
dc.subject | Peroxirredoxinas | |
dc.subject | genética | |
dc.subject | Receptores de IgG | |
dc.subject | genética | |
dc.subject | Receptores de Interleucina-1 | |
dc.subject | genética | |
dc.subject | Dengue Grave | |
dc.subject | diagnóstico | |
dc.subject | Índice de Gravidade de Doença | |
dc.subject | Biomarcadores | |
dc.subject | Proteínas Reguladoras de Apoptose | |
dc.subject | genética | |
dc.subject | Proteínas Ligadas por GPI | |
dc.subject | genética | |
dc.subject | Expressão Gênica | |
dc.subject | Humanos | |
dc.subject | Imunidade Inata | |
dc.subject | genética | |
dc.subject | Leucócitos Mononucleares | |
dc.subject | imunologia | |
dc.subject | Leucócitos Mononucleares | |
dc.subject | patologia | |
dc.subject | Análise em Microsséries | |
dc.subject | Prognóstico | |
dc.subject | RNA Mensageiro | |
dc.subject | isolamento & purificação | |
dc.subject | Reação em Cadeia da Polimerase em Tempo Real | |
dc.subject | Sorotipagem | |
dc.title | Potential biomarkers for the clinical prognosis of severe dengue | |
dc.type | Article | |