Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14250
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSaksirisampant W.
dc.contributor.authorThaisom S.
dc.contributor.authorRatanavararak M.
dc.contributor.authorThanomsub B.W.
dc.date.accessioned2021-04-05T03:33:48Z-
dc.date.available2021-04-05T03:33:48Z-
dc.date.issued2012
dc.identifier.issn144894
dc.identifier.other2-s2.0-84867330892
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14250-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84867330892&doi=10.1016%2fj.exppara.2012.08.002&partnerID=40&md5=64047f6ac7a6c4e36458fb1aa35bac0c
dc.description.abstractMice were infected with 8- or 25-infective worms of advanced third stage Gnathostoma spinigerum larvae (L3) which were obtained from natural infected eels. On day 14, 60 and 200 post infections (PI), spleen cells of infected mice were tested for lymphoproliferative responses in vitro against the mitogen and specific L3 somatic antigen in order to clarify the cellular immune status of the host upon this nematode infection. Reduced responsiveness to Con A was observed in infected mice. These depressed responses were more pronounced in chronically infected mice (day 200, PI) than in day 14 and day 60, PI. There was no significant difference of lymphoproliferative response between groups of high (25 L3) and low (8 L3)-infective dose in the chronic readily stage. Regarding to the L3 somatic Ag stimulation, the depressed response was obviously detected in high dose and chronic infection. Our results demonstrated that in this G. spinigerum-mouse system T-cell response is defective. The depression could be reversible and was associated with active infection because it was abolished by anthelmintic (ivermectin) treatment. This study shows the involvement of Th-2 response to this nematode in regulating T cell proliferation. © 2012 Elsevier Inc.
dc.subjectconcanavalin A
dc.subjectivermectin
dc.subjectmitogenic agent
dc.subjectsilver
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantigen specificity
dc.subjectarticle
dc.subjectcellular immunity
dc.subjectcontrolled study
dc.subjectdose response
dc.subjectexperimental infection
dc.subjectexperimental mouse
dc.subjectgnathostomiasis
dc.subjectimmune deficiency
dc.subjectin vitro study
dc.subjectlymphocyte proliferation
dc.subjectmale
dc.subjectmitogenicity
dc.subjectmouse
dc.subjectnonhuman
dc.subjectpriority journal
dc.subjectsingle drug dose
dc.subjectsomatic cell
dc.subjectT lymphocyte activation
dc.subjectAnimals
dc.subjectAntigens, Helminth
dc.subjectAntiparasitic Agents
dc.subjectCell Proliferation
dc.subjectConcanavalin A
dc.subjectGnathostoma
dc.subjectGnathostomiasis
dc.subjectIvermectin
dc.subjectLymphocytes
dc.subjectMale
dc.subjectMice
dc.subjectMitogens
dc.subjectSmegmamorpha
dc.subjectSpleen
dc.subjectGnathostoma spinigerum
dc.subjectMus
dc.titleGnathostoma spinigerum: Immunodepression in experimental infected mice
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationExperimental Parasitology. Vol 132, No.3 (2012), p.320-326
dc.identifier.doi10.1016/j.exppara.2012.08.002
Appears in Collections:Scopus 1983-2021

Files in This Item:
There are no files associated with this item.


Items in SWU repository are protected by copyright, with all rights reserved, unless otherwise indicated.