TY  - JOUR
A1  - Tulone, C
A1  - Sponaas, AM
A1  - Raiber, EA
A1  - Tabor, AB
A1  - Langhorne, J
A1  - Chain, BM
JF  - PLOS One
KW  - Animals
KW  -  Antibody Formation
KW  -  Antigen Presentation
KW  -  Antigens
KW  -  Protozoan
KW  -  Bone Marrow Cells
KW  -  Cathepsin D
KW  -  Chimera
KW  -  Dendritic Cells
KW  -  Erythrocytes
KW  -  Histocompatibility Antigens Class II
KW  -  Immunoglobulin G
KW  -  Malaria
KW  -  Merozoite Surface Protein 1
KW  -  Merozoites
KW  -  Mice
KW  -  Parasitemia
KW  -  Phenotype
KW  -  Plasmodium chabaudi
KW  -  Protease Inhibitors
KW  -  Spleen
VL  - 6
N1  - © 2011 Tulone et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
The study was supported by the Biotechnology and Biological Sciences Research Council (BB/D005469/1) under the Selective Chemical Intervention in Biological Systems initiative and by the Medical Research Council, United Kingdom, ref. U117584248. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
ID  - discovery1329816
UR  - http://dx.doi.org/10.1371/journal.pone.0024886
IS  - 10
N2  - Merozoite Surface Protein 1 is expressed on the surface of malaria merozoites and is important for invasion of the malaria parasite into erythrocytes. MSP1-specific CD4 T cell responses and antibody can confer protective immunity in experimental models of malaria. In this study we explore the contributions of cathepsins D and E, two aspartic proteinases previously implicated in antigen processing, to generating MSP1 CD4 T-cell epitopes for presentation. The absence of cathepsin D, a late endosome/lysosomal enzyme, is associated with a reduced presentation of MSP1 both following in vitro processing of the epitope MSP1 from infected erythrocytes by bone marrow-derived dendritic cells, and following in vivo processing by splenic CD11c+ dendritic cells. By contrast, processing and presentation of the soluble recombinant protein fragment of MSP1 is unaffected by the absence of cathepsin D, but is inhibited when both cathepsin D and E are absent. The role of different proteinases in generating the CD4 T cell repertoire, therefore, depends on the context in which an antigen is introduced to the immune system.
AV  - public
Y1  - 2011/10/28/
SN  - 1932-6203
TI  - Differential requirement for cathepsin D for processing of the full length and C-terminal fragment of the malaria antigen MSP1.
ER  -