Please use this identifier to cite or link to this item: https://doi.org/10.3389/fimmu.2018.01875
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dc.titleA plasmodium cross-stage antigen contributes to the development of experimental cerebral malaria
dc.contributor.authorFernandes, P
dc.contributor.authorHowland, S.W
dc.contributor.authorHeiss, K
dc.contributor.authorHoffmann, A
dc.contributor.authorHernández-Castañeda, M.A
dc.contributor.authorObrová, K
dc.contributor.authorFrank, R
dc.contributor.authorWiedemann, P
dc.contributor.authorBendzus, M
dc.contributor.authorRénia, L
dc.contributor.authorMueller, A.-K
dc.date.accessioned2020-10-20T04:59:52Z
dc.date.available2020-10-20T04:59:52Z
dc.date.issued2018
dc.identifier.citationFernandes, P, Howland, S.W, Heiss, K, Hoffmann, A, Hernández-Castañeda, M.A, Obrová, K, Frank, R, Wiedemann, P, Bendzus, M, Rénia, L, Mueller, A.-K (2018). A plasmodium cross-stage antigen contributes to the development of experimental cerebral malaria. Frontiers in Immunology 9 (AUG) : 1875. ScholarBank@NUS Repository. https://doi.org/10.3389/fimmu.2018.01875
dc.identifier.issn16643224
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178068
dc.description.abstractCerebral malaria is a complex neurological syndrome caused by an infection with Plasmodium falciparum parasites and is exclusively attributed to a series of host-parasite interactions at the pathological blood-stage of infection. In contrast, the preceding intra-hepatic phase of replication is generally considered clinically silent and thereby excluded from playing any role in the development of neurological symptoms. In this study, however, we present an antigen PbmaLS_05 that is presented to the host immune system by both pre-erythrocytic and intra-erythrocytic stages and contributes to the development of cerebral malaria in mice. Although deletion of the endogenous PbmaLS_05 prevented the development of experimental cerebral malaria (ECM) in susceptible mice after both sporozoite and infected red blood cell (iRBC) infections, we observed significant differences in contribution of the host immune response between both modes of inoculation. Moreover, PbmaLS_05-specific CD8+ T cells contributed to the development of ECM after sporozoite but not iRBC-infection, suggesting that pre-erythrocytic antigens like PbmaLS_05 can also contribute to the development of cerebral symptoms. Our data thus highlight the importance of the natural route of infection in the study of ECM, with potential implications for vaccine and therapeutic strategies against malaria. © 2018 Fernandes, Howland, Heiss, Hoffmann, Hernández-Castañeda, Obrová, Frank, Wiedemann, Bendzus, Rénia and Mueller.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subject3' untranslated region
dc.subjectanimal cell
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectbioluminescence
dc.subjectcerebral malaria
dc.subjectcontrolled study
dc.subjectenzyme linked immunospot assay
dc.subjectfluorescence microscopy
dc.subjectmouse
dc.subjectnonhuman
dc.subjectnuclear magnetic resonance imaging
dc.subjectparasitemia
dc.subjectPlasmodium
dc.subjectanimal
dc.subjectCD8+ T lymphocyte
dc.subjectcerebral malaria
dc.subjectcross presentation
dc.subjectdisease model
dc.subjectdisease predisposition
dc.subjectgene
dc.subjectgene expression
dc.subjectgenetics
dc.subjectgrowth, development and aging
dc.subjectimmunology
dc.subjectlife cycle stage
dc.subjectmetabolism
dc.subjectparasitology
dc.subjectpathology
dc.subjectPlasmodium berghei
dc.subjectreporter gene
dc.subjectparasite antigen
dc.subjectAnimals
dc.subjectAntigens, Protozoan
dc.subjectCD8-Positive T-Lymphocytes
dc.subjectCross-Priming
dc.subjectDisease Models, Animal
dc.subjectDisease Susceptibility
dc.subjectGene Expression
dc.subjectGenes, Protozoan
dc.subjectGenes, Reporter
dc.subjectLife Cycle Stages
dc.subjectMagnetic Resonance Imaging
dc.subjectMalaria, Cerebral
dc.subjectMice
dc.subjectPlasmodium berghei
dc.typeArticle
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.description.doi10.3389/fimmu.2018.01875
dc.description.sourcetitleFrontiers in Immunology
dc.description.volume9
dc.description.issueAUG
dc.description.page1875
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