Cross‐presentation of oral antigens by liver sinusoidal endothelial cells leads to CD8 T cell tolerance

Andreas Limmer(Institut für Medizinische Biometrie, Informatik und Epidemiologie), Jutta Ohl(Institut für Medizinische Informatik, Biometrie und Epidemiologie), Gerhard Wingender(Institut für Medizinische Informatik, Biometrie und Epidemiologie), Martina Berg(Institut für Medizinische Informatik, Biometrie und Epidemiologie), Frank Jüngerkes(Institut für Medizinische Informatik, Biometrie und Epidemiologie), Beatrix Schumak(Institut für Medizinische Informatik, Biometrie und Epidemiologie), Dominik Djandji(Institut für Medizinische Informatik, Biometrie und Epidemiologie), Kai Scholz(Institut für Medizinische Informatik, Biometrie und Epidemiologie), Alexandra Klevenz(German Cancer Research Center), Silke Hegenbarth(Institut für Medizinische Informatik, Biometrie und Epidemiologie), Frank Momburg(German Cancer Research Center), Günter J. Hämmerling(German Cancer Research Center), Bernd Arnold(German Cancer Research Center), Percy A. Knolle(Institut für Medizinische Informatik, Biometrie und Epidemiologie)
European Journal of Immunology
September 14, 2005
Cited by 170Open Access
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Abstract

After ingestion, oral antigens distribute systemically and provoke T cell stimulation outside the gastrointestinal tract. Within the liver, scavenger liver sinusoidal endothelial cells (LSEC) eliminate blood-borne antigens and induce T cell tolerance. Here we investigated whether LSEC contribute to oral tolerance. Oral antigens were efficiently cross-presented on H-2K(b) by LSEC to naive CD8 T cells. Cross-presentation efficiency in LSEC but not dendritic cells was increased by antigen-exposure to heat or low pH. Mechanistically, cross-presentation in LSEC requires endosomal maturation, involves hsc73 and proteasomal degradation. H-2K(b)-restricted cross-presentation of oral antigens by LSEC in vivo induced CD8 T cell priming and led to development of CD8 T cell tolerance in two independent experimental systems. Adoptive transfer of LSEC from mice fed with antigen (ovalbumin) into RAG2-/- knockout mice, previously reconstituted with naive ovalbumin-specific CD8 T cells, prevented development of specific cytotoxicity and expression of IFN-gamma in CD8 T cells. Using a new transgenic mouse line expressing H-2K(b) only on endothelial cells, we have demonstrated that oral antigen administration leads to tolerance in H-2K(b)-restricted CD8 T cells. Collectively, our data demonstrate a participation of the liver, in particular scavenger LSEC, in development of CD8 T cell tolerance towards oral antigens.


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