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dc.creatorGAMA, Mônica Elinor Alves-
dc.creatorGOMES, Claudia Maria de Castro-
dc.creatorSILVEIRA, Fernando Tobias-
dc.creatorAURENTI, Márcia Dalastra-
dc.creatorGONÇALVES, Eloisa da Graça do Rosario-
dc.creatorSILVA, Antônio Rafael da-
dc.creatorCORBETT, Carlos Eduardo Pereira-
dc.date.accessioned2017-02-17T14:44:51Z-
dc.date.available2017-02-17T14:44:51Z-
dc.date.issued2013-12-
dc.identifier.citationGAMA, Monica Elinor Alves et al. Severe visceral leishmaniasis in children: the relationship between cytokine patterns and clinical features. Revista da Sociedade Brasileira de Medicina Tropical, Uberaba, v. 46, n. 6, p. 741-745, dez. 2013. Disponível em: <http://www.scielo.br/pdf/rsbmt/v46n6/0037-8682-rsbmt-46-06-741.pdf>. Acesso em: 17 fev. 2017. <http://dx.doi.org/10.1590/0037-8682-0203-2013>.pt_BR
dc.identifier.issn0037-8682pt_BR
dc.identifier.urihttp://repositorio.ufpa.br/jspui/handle/2011/7722-
dc.description.abstractIntroduction: The relationship between severe clinical manifestations of visceral leishmaniasis (VL) and immune response profi les has not yet been clarifi ed, despite numerous studies on the subject. This study aimed to investigate the relationship between cytokine profi les and the presence of immunological markers associated with clinical manifestations and, particularly, signs of severity, as defi ned in a protocol drafted by the Ministry of Health (Brazil). Methods: We conducted a prospective, descriptive study between May 2008 and December 2009. This study was based on an assessment of all pediatric patients with VL who were observed in a reference hospital in Maranhão. Results: Among 27 children, 55.5% presented with more than one sign of severity or warning sign. Patients without signs of severity or warning signs and patients with only one warning sign had the highest interferon-gamma (IFN-γ) levels, although their interleukin 10 (IL-10) levels were also elevated. In contrast, patients with the features of severe disease had the lowest IFN-γ levels. Three patients who presented with more than two signs of severe disease died; these patients had undetectable interleukin 2 (IL-2) and IFN-γ levels and low IL-10 levels, which varied between 0 and 36.8pg/mL. Conclusions: Our results showed that disease severity was associated with low IFN-γ levels and elevated IL-10 levels. However, further studies with larger samples are needed to better characterize the relationship between disease severity and cytokine levels, with the aim of identifying immunological markers of active-disease severity.pt_BR
dc.description.provenanceSubmitted by Luciana Alcantara (lalcantara@ufpa.br) on 2017-02-17T14:44:40Z No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Artigo_SevereVisceralLeishmaniasis.pdf: 686000 bytes, checksum: ddd904a475ac02d94fa4b1024beb4be1 (MD5)en
dc.description.provenanceApproved for entry into archive by Luciana Alcantara (lalcantara@ufpa.br) on 2017-02-17T14:44:51Z (GMT) No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Artigo_SevereVisceralLeishmaniasis.pdf: 686000 bytes, checksum: ddd904a475ac02d94fa4b1024beb4be1 (MD5)en
dc.description.provenanceMade available in DSpace on 2017-02-17T14:44:51Z (GMT). No. of bitstreams: 2 license_rdf: 0 bytes, checksum: d41d8cd98f00b204e9800998ecf8427e (MD5) Artigo_SevereVisceralLeishmaniasis.pdf: 686000 bytes, checksum: ddd904a475ac02d94fa4b1024beb4be1 (MD5) Previous issue date: 2013-12en
dc.languageporpt_BR
dc.publisherUniversidade Federal do Parápt_BR
dc.relation.ispartofRevista da Sociedade Brasileira de Medicina Tropicalpt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectLeishmaniose visceralpt_BR
dc.subjectCriançaspt_BR
dc.subjectCitocinaspt_BR
dc.subjectPediatriapt_BR
dc.subjectHospitalização infantilpt_BR
dc.titleSevere visceral leishmaniasis in children: the relationship between cytokine patterns and clinical featurespt_BR
dc.typeArtigo de Periódicopt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.initialsUFPApt_BR
dc.citation.volume46pt_BR
dc.citation.issue6pt_BR
dc.citation.spage741pt_BR
dcterms.citation.epage745pt_BR
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