Associations between hepcidin and immune response in individuals with hyperbilirubinaemia and severe malaria due to Plasmodium vivax infection.

dc.creatorMendonça, Vitor Rosa Ramos de
dc.creatorSouza, Ligia C. L
dc.creatorGarcia, Gabriela Barreto Caldas
dc.creatorMagalhães, Belisa Maria Lopes
dc.creatorGonçalves, Marilda de Souza
dc.creatorLacerda, Marcus Vinícius Guimarães de
dc.creatorBarral Netto, Manoel
dc.date2016-03-28T17:59:35Z
dc.date2016-03-28T17:59:35Z
dc.date2015
dc.date.accessioned2023-09-26T20:19:14Z
dc.date.available2023-09-26T20:19:14Z
dc.identifierMENDONÇA, V. R. R. Associations between hepcidin and immune response in individuals with hyperbilirubinaemia and severe malaria due to Plasmodium vivax infection. Malaria Journal, v.14, n. 1, p. 407-417, 2015.
dc.identifier1475-2875
dc.identifier10.1186/s12936-015-0930-x
dc.identifierhttps://www.arca.fiocruz.br/handle/icict/13370
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8854145
dc.descriptionBACKGROUND: Hyperbilirubinaemia (bilirubin >51.3 µmol/L) alone is not indicative of severe malaria, and the immune response underlying hyperbilirubinaemia remains largely unexplored. Liver damage associated with hyperbilirubinaemia may alter the expression of hepcidin, which regulates systemic iron by degrading ferroportin. For this study, the association between hepcidin and the levels of cytokines and chemokines in the serum of individuals with mild and severe vivax malaria and subjects with malaria with isolated hyperbilirubinaemia was evaluated. METHODS: Cytokines/chemokines and hepcidin were measured in individuals with mild (n = 72) and severe (n = 17) vivax malaria, as well as in the serum of subjects with vivax malaria with isolated hyperbilirubinaemia (n = 14) from the Brazilian Amazon between 2009 and 2013 by multiplex assay and ELISA, respectively. The polymorphism 744 G > T in the ferroportin gene was identified by restriction fragment-length polymorphism analysis and the restriction enzyme PvuII. RESULTS: The polymorphism at position 744 G > T in the ferroportin gene was typed and no differences in the distributions of genotypes or alleles were observed between the study groups. Subjects with severe malaria had higher levels of interleukin (IL)-2 and IL-13 than subjects with hyperbilirubinaemia. No differences in the expression of immune markers were observed between subjects with mild malaria and those with hyperbilirubinaemia. However, hepcidin levels were higher in individuals with severe malaria and hyperbilirubinaemia than those with mild malaria (p = 0.0002 and p = 0.0004, respectively) and cut-off values of hepcidin differentiated these groups from subjects with mild malaria. Hepcidin was positively associated with IL-6 and IL-10 levels and with parasitaemia in subjects with mild malaria and with IFN-γ in subjects with severe malaria. CONCLUSIONS: Malaria in the presence of hyperbilirubinaemia produces a less robust inflammatory response compared to severe cases of malaria. Hepcidin levels are positively associated with immune markers in vivax malaria outcomes.
dc.formatapplication/pdf
dc.languageeng
dc.publisherBioMed Central
dc.rightsopen access
dc.subjectMalaria
dc.subjectPlasmodium vivax
dc.subjectImmune response
dc.subjectHepcidin
dc.subjectHyperbilirubinemia
dc.titleAssociations between hepcidin and immune response in individuals with hyperbilirubinaemia and severe malaria due to Plasmodium vivax infection.
dc.typeArticle


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