Publication:
Gnathostoma spinigerum: Immunodepression in experimental infected mice

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.date.issuedBE2555
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.format.mimetypeapplication/pdf
dc.identifier.citationExperimental Parasitology. Vol 132, No.3 (2012), p.320-326
dc.identifier.doi10.1016/j.exppara.2012.08.002
dc.identifier.issn144894
dc.identifier.other2-s2.0-84867330892
dc.identifier.urihttps://hdl.handle.net/20.500.14740/6925
dc.rights.holderScopus
dc.subject.otherConcanavalin A
dc.subject.otherIvermectin
dc.subject.otherMitogenic agent
dc.subject.otherSilver
dc.subject.otherAnimal cell
dc.subject.otherAnimal experiment
dc.subject.otherAnimal model
dc.subject.otherAnimal tissue
dc.subject.otherAntigen specificity
dc.subject.otherArticle
dc.subject.otherCellular immunity
dc.subject.otherControlled study
dc.subject.otherDose response
dc.subject.otherExperimental infection
dc.subject.otherExperimental mouse
dc.subject.otherGnathostomiasis
dc.subject.otherImmune deficiency
dc.subject.otherIn vitro study
dc.subject.otherLymphocyte proliferation
dc.subject.otherMale
dc.subject.otherMitogenicity
dc.subject.otherMouse
dc.subject.otherNonhuman
dc.subject.otherPriority journal
dc.subject.otherSingle drug dose
dc.subject.otherSomatic cell
dc.subject.otherT lymphocyte activation
dc.subject.otherAnimals
dc.subject.otherAntigens, Helminth
dc.subject.otherAntiparasitic Agents
dc.subject.otherCell Proliferation
dc.subject.otherConcanavalin A
dc.subject.otherGnathostoma
dc.subject.otherGnathostomiasis
dc.subject.otherIvermectin
dc.subject.otherLymphocytes
dc.subject.otherMale
dc.subject.otherMice
dc.subject.otherMitogens
dc.subject.otherSmegmamorpha
dc.subject.otherSpleen
dc.subject.otherGnathostoma spinigerum
dc.subject.otherMus
dc.titleGnathostoma spinigerum: Immunodepression in experimental infected mice
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84867330892&doi=10.1016%2fj.exppara.2012.08.002&partnerID=40&md5=64047f6ac7a6c4e36458fb1aa35bac0c

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