Use este identificador para citar ou linkar para este item: https://repositorio.ufba.br/handle/ri/13828
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dc.contributor.authorAndrade, Bruno Bezerril-
dc.contributor.authorRocha, Bruno Coelho-
dc.contributor.authorReis Filho, Antonio-
dc.contributor.authorCamargo, Luís Marcelo Aranha-
dc.contributor.authorTadei, Wanderli Pedro-
dc.contributor.authorMoreira, Luciano Andrade-
dc.contributor.authorBarral, Aldina Maria Prado-
dc.contributor.authorBarral-Netto, Manoel-
dc.creatorAndrade, Bruno Bezerril-
dc.creatorRocha, Bruno Coelho-
dc.creatorReis Filho, Antonio-
dc.creatorCamargo, Luís Marcelo Aranha-
dc.creatorTadei, Wanderli Pedro-
dc.creatorMoreira, Luciano Andrade-
dc.creatorBarral, Aldina Maria Prado-
dc.creatorBarral-Netto, Manoel-
dc.date.accessioned2013-11-20T19:48:35Z-
dc.date.available2013-11-20T19:48:35Z-
dc.date.issued2009-
dc.identifier.issn1475-2875-
dc.identifier.urihttp://repositorio.ufba.br/ri/handle/ri/13828-
dc.descriptionp. 1-9pt_BR
dc.description.abstractBackground: Despite governmental and private efforts on providing malaria control, this disease continues to be a major health threat. Thus, innovative strategies are needed to reduce disease burden. The malaria vectors, through the injection of saliva into the host skin, play important role on disease transmission and may influence malaria morbidity. This study describes the humoral immune response against Anopheles (An.) darlingi saliva in volunteers from the Brazilian Amazon and addresses the association between levels of specific antibodies and clinical presentation of Plasmodium (P.) vivax infection. Methods: Adult volunteers from communities in the Rondônia State, Brazil, were screened in order to assess the presence of P. vivax infection by light microscopy and nested PCR. Non-infected volunteers and individuals with symptomatic or symptomless infection were randomly selected and plasma collected. An. darlingi salivary gland sonicates (SGS) were prepared and used to measure anti-saliva antibody levels. Plasma interleukin (IL)-10 and interferon (IFN)-γ levels were also estimated and correlated to anti-SGS levels. Results: Individuals infected with P. vivax presented higher levels of anti-SGS than non-infected individuals and antibody levels could discriminate infection. Furthermore, anti-saliva antibody measurement was also useful to distinguish asymptomatic infection from non-infection, with a high likelihood ratio. Interestingly, individuals with asymptomatic parasitaemia presented higher titers of anti-SGS and lower IFN-γ/IL-10 ratio than symptomatic ones. In P. vivax-infected asymptomatic individuals, the IFN-γ/IL-10 ratio was inversely correlated to anti-SGS titers, although not for while in symptomatic volunteers. Conclusion: The estimation of anti-An. darlingi antibody levels can indicate the probable P. vivax infection status and also could serve as a marker of disease severity in this region of Brazilian Amazon.pt_BR
dc.language.isoenpt_BR
dc.sourcehttp://dx.doi.org/10.1186/1475-2875-8-121pt_BR
dc.titleAnti-Anopheles darlingi saliva antibodies as marker of Plasmodium vivax infection and clinical immunity in the Brazilian Amazonpt_BR
dc.title.alternativeMalaria Journalpt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv. 8, n. 1pt_BR
Aparece nas coleções:Artigo Publicado em Periódico (Faculdade de Medicina)

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