Please use this identifier to cite or link to this item: https://doi.org/10.3389/fimmu.2018.01875
Title: A plasmodium cross-stage antigen contributes to the development of experimental cerebral malaria
Authors: Fernandes, 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
Keywords: 3' untranslated region
animal cell
animal tissue
Article
bioluminescence
cerebral malaria
controlled study
enzyme linked immunospot assay
fluorescence microscopy
mouse
nonhuman
nuclear magnetic resonance imaging
parasitemia
Plasmodium
animal
CD8+ T lymphocyte
cerebral malaria
cross presentation
disease model
disease predisposition
gene
gene expression
genetics
growth, development and aging
immunology
life cycle stage
metabolism
parasitology
pathology
Plasmodium berghei
reporter gene
parasite antigen
Animals
Antigens, Protozoan
CD8-Positive T-Lymphocytes
Cross-Priming
Disease Models, Animal
Disease Susceptibility
Gene Expression
Genes, Protozoan
Genes, Reporter
Life Cycle Stages
Magnetic Resonance Imaging
Malaria, Cerebral
Mice
Plasmodium berghei
Issue Date: 2018
Citation: Fernandes, 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
Rights: Attribution 4.0 International
Abstract: Cerebral 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.
Source Title: Frontiers in Immunology
URI: https://scholarbank.nus.edu.sg/handle/10635/178068
ISSN: 16643224
DOI: 10.3389/fimmu.2018.01875
Rights: Attribution 4.0 International
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