Polymorphisms in Plasmodium vivax circumsporozoite protein (CSP) influence parasite burden and cytokine balance in a pre-amazon endemic area from Brazil

xmlui.dri2xhtml.METS-1.0.item-date
2016xmlui.mirage2.itemSummaryView.MetaData
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http://patua.iec.gov.br/handle/iec/2430xmlui.dri2xhtml.METS-1.0.item-author
Ribeiro, Bruno de Paulo
Cassiano, Gustavo Capatti
Souza, Rodrigo Medeiros de
Cysne, Dalila Nunes
Grisotto, Marcos Augusto Grigolin
Santos, Ana Paula Silva de Azevedo dos
Marinho, Cláudio Romero Farias
Machado, Ricardo Luiz Dantas
Nascimento, Flávia Raquel Fernandes
xmlui.dri2xhtml.METS-1.0.item-abstract
Mechanisms involved in severe P. vivax malaria remain unclear. Parasite polymorphisms, parasite load and host cytokine profile may influence the course of infection. In this study, we investigated the influence of circumsporozoite protein (CSP) polymorphisms on parasite load and cytokine profile in patients with vivax malaria. A cross-sectional study was carried out in three cities: São Luís, Cedral and Buriticupu, Maranhão state, Brazil, areas of high prevalence of P. vivax. Interleukin (IL)-2, IL-4, IL-10, IL-6, IL-17, tumor necrosis factor alpha (TNF-α, interferon gamma (IFN-γ and transforming growth factor beta (TGF-β were quantified in blood plasma of patients and in supernatants from peripheral blood mononuclear cell (PBMC) cultures. Furthermore, the levels of cytokines and parasite load were correlated with VK210, VK247 and P. vivax-like CSP variants. Patients infected with P. vivax showed increased IL-10 and IL-6 levels, which correlated with the parasite load, however, in multiple comparisons, only IL-10 kept this association. A regulatory cytokine profile prevailed in plasma, while an inflammatory profile prevailed in PBMC culture supernatants and these patterns were related to CSP polymorphisms. VK247 infected patients showed higher parasitaemia and IL-6 concentrations, which were not associated to IL-10 anti-inflammatory effect. By contrast, in VK210 patients, these two cytokines showed a strong positive correlation and the parasite load was lower. Patients with the VK210 variant showed a regulatory cytokine profile in plasma, while those infected with the VK247 variant have a predominantly inflammatory cytokine profile and higher parasite loads, which altogether may result in more complications in infection. In conclusion, we propose that CSP polymorphisms is associated to the increase of non-regulated inflammatory immune responses, which in turn may be associated with the outcome of infection.
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RIBEIRO, Bruno de Paulo et al. Polymorphisms in Plasmodium vivax circumsporozoite protein (CSP) influence parasite burden and cytokine balance in a pre-amazon endemic area from Brazil. PLoS Neglected Tropical Diseases, v. 10, n. 3, p. 1-9, 2016.xmlui.dri2xhtml.METS-1.0.item-decsPrimary
Malária Vivax / parasitologiaPlasmodium vivax / imunologia
Plasmodium vivax / genética
Polimorfismo Genético
Polimorfismo de Fragmento de Restrição
Variação Genética
Genótipo
Citocinas