Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
SHR Neuro Krebs Kardio Lipid Stoffw Microb
Stephen, TL; Fabri, M; Groneck, L; Rohn, TA; Hafke, H; Robinson, N; Rietdorf, J; Schrama, D; Becker, JC; Plum, G; Kronke, M; Kropshofer, H; Kalka-Moll, WM.
Transport of Streptococcus pneumoniae capsular polysaccharide in MHC class II tubules
PLOS PATHOG. 2007; 3(3):
Doi: 10.1371/journal.ppat.0030032
[OPEN ACCESS]
Web of Science
PubMed
FullText
FullText_MUG
Google Scholar
- Co-Autor*innen der Med Uni Graz
- Becker Jürgen Christian
- Schrama David
- Altmetrics:
- Dimensions Citations:
- Plum Analytics:
- Scite (citation analytics):
- Abstract:
- Bacterial capsular polysaccharides are virulence factors and are considered T cell-independent antigens. However, the capsular polysaccharide Sp1 from Streptococcus pneumoniae serotype 1 has been shown to activate CD4(+) T cells in a major histocompatibility complex (MHC) class II-dependent manner. The mechanism of carbohydrate presentation to CD4(+) T cells is unknown. We show in live murine dendritic cells (DCs) that Sp1 translocates from lysosomal compartments to the plasma membrane in MHCII-positive tubules. Sp1 cell surface presentation results in reduction of self-peptide presentation without alteration of the MHCII self peptide repertoire. In DM-deficient mice, retrograde transport of Sp1/MHCII complexes resulting in T cell-dependent immune responses to the polysaccharide in vitro and in vivo is significantly reduced. The results demonstrate the capacity of a bacterial capsular polysaccharide antigen to use DC tubules as a vehicle for its transport as an MHCII/saccharide complex to the cell surface for the induction of T cell activation. Furthermore, retrograde transport requires the functional role of DM in self peptide-carbohydrate exchange. These observations open new opportunities for the design of vaccines against microbial encapsulated pathogens.
- Find related publications in this database (using NLM MeSH Indexing)
- Animals -
- Antigen Presentation -
- Antigens, Bacterial - metabolism
- Antigens, Differentiation, B-Lymphocyte - metabolism
- Autoantigens - metabolism
- Bacterial Capsules - metabolism
- Biological Transport -
- CD4-Positive T-Lymphocytes - immunology
- Dendritic Cells - physiology
- Endosomes - metabolism
- HLA-D Antigens - physiology
- Histocompatibility Antigens Class II - metabolism Histocompatibility Antigens Class II - physiology
- Lymphocyte Activation -
- Mice -
- Mice, Inbred C57BL -
- Streptococcus pneumoniae - immunology