Limmer Andreas, Ohl Jutta, Wingender Gerhard, Berg Martina, Jüngerkes Frank, Schumak Beatrix, Djandji Dominik, Scholz Kai, Klevenz Alexandra, Hegenbarth Silke, Momburg Frank, Hämmerling Günter J, Arnold Bernd, Knolle Percy A
Institut für Molekulare Medizin und Experimentelle Immunologie, Bonn, Germany.
Eur J Immunol. 2005 Oct;35(10):2970-81. doi: 10.1002/eji.200526034.
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.
Z Gastroenterol. 2006-1
Nat Rev Immunol. 2025-1
Cancer Cell Int. 2024-8-31
J Hepatol. 2024-9
J Clin Exp Hepatol. 2023
Front Cell Dev Biol. 2022-6-28