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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/65972
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dc.contributor.authorSartori, Alexandria-
dc.contributor.authorKaneno, Ramon-
dc.contributor.authorBaruzzi, Nelson-
dc.contributor.authorPeraçoli, Maria Terezinha Serrão-
dc.date.accessioned2014-05-27T11:19:49Z-
dc.date.accessioned2016-10-25T18:16:02Z-
dc.date.available2014-05-27T11:19:49Z-
dc.date.available2016-10-25T18:16:02Z-
dc.date.issued1999-12-01-
dc.identifierhttp://dx.doi.org/10.1590/S0036-46651999000400002-
dc.identifier.citationRevista do Instituto de Medicina Tropical de Sao Paulo, v. 41, n. 4, p. 215-219, 1999.-
dc.identifier.issn0036-4665-
dc.identifier.urihttp://hdl.handle.net/11449/65972-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/65972-
dc.description.abstractKala-azar is the visceral form of leishmaniasis and it is caused by intracellular parasites from the complex Leishmania donovani. Golden hamster (Mesocricetus auratus) infected with Leishmania donovani develop a disease very similar to human Kala-azar. There is conspicuous hipergammaglobulinaemia and their T cells do not respond to stimulation with parasite antigens. We used this experimental model to evaluate the natural killer (NK) activity during the initial phase of the disease. Outbred hamsters infected by intravenous route with 5.106 amastigotes of L. donovani 1S showed a concurrent increase in the spleen weight and in the spleen cell number. Using the single cell assay we detected a significant increase in the percentage of NK effector cells on the 4th day of infection. Imprints from spleen and liver showed at days 14 and 28 a significant increase in the parasite burden. These results show that the increased NK activity in the beginning of the infection was not able to restrain the progression of the disease in this experimental model.en
dc.format.extent215-219-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectKala-azar-
dc.subjectLeismania donovani-
dc.subjectNatural killer activity-
dc.subjectanimal-
dc.subjectdisease course-
dc.subjectdisease model-
dc.subjectfemale-
dc.subjecthamster-
dc.subjectimmunology-
dc.subjectLeishmania donovani-
dc.subjectliver-
dc.subjectlymphocyte count-
dc.subjectlymphocyte subpopulation-
dc.subjectnatural killer cell-
dc.subjectparasitology-
dc.subjectspleen-
dc.subjectvisceral leishmaniasis-
dc.subjectAnimals-
dc.subjectCricetinae-
dc.subjectDisease Models, Animal-
dc.subjectDisease Progression-
dc.subjectFemale-
dc.subjectKiller Cells, Natural-
dc.subjectLeishmaniasis, Visceral-
dc.subjectLiver-
dc.subjectLymphocyte Count-
dc.subjectLymphocyte Subsets-
dc.subjectSpleen-
dc.titleIncreased natural killer activity does not prevent progression of experimental kala-azaren
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Microbiology Institute of Biological Sciences S. Paulo State University (UNESP), Botucatu, SP-
dc.description.affiliationHematology Center Medical School of UNESP, Botucatu, SP-
dc.description.affiliationDepto. de Microbiologia Instituto de Biociências UNESP, 18618-000 Botucatu, SP-
dc.description.affiliationUnespDepartment of Microbiology Institute of Biological Sciences S. Paulo State University (UNESP), Botucatu, SP-
dc.description.affiliationUnespHematology Center Medical School of UNESP, Botucatu, SP-
dc.description.affiliationUnespDepto. de Microbiologia Instituto de Biociências UNESP, 18618-000 Botucatu, SP-
dc.identifier.doi10.1590/S0036-46651999000400002-
dc.identifier.scieloS0036-46651999000400002-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-0033155342.pdf-
dc.relation.ispartofRevista do Instituto de Medicina Tropical de São Paulo-
dc.identifier.scopus2-s2.0-0033155342-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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