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Hepatocyte entry leads to degradation of autoreactive CD8 T cells.


ABSTRACT: Although most self-reactive T cells are eliminated in the thymus, mechanisms to inactivate or control T cells specific for extrathymic antigens are required and exist in the periphery. By investigating the site in which autoreactive T cells are tolerized, we identify a unique mechanism of peripheral deletion in which naïve autoreactive CD8 T cells are rapidly eliminated in the liver after intrahepatic activation. T cells actively invade hepatocytes, enter endosomal/lysosomal compartments, and are degraded. Blockade of this process leads to accumulation of autoreactive CD8 T cells in the liver and breach of tolerance, with the development of autoimmune hepatitis. Cell into cell invasion, or emperipolesis, is a long-observed phenomenon for which a physiological role has not been previously demonstrated. We propose that this "suicidal emperipolesis" is a unique mechanism of autoreactive T-cell deletion, a process critical for the maintenance of tolerance.

SUBMITTER: Benseler V 

PROVIDER: S-EPMC3189041 | biostudies-literature | 2011 Oct

REPOSITORIES: biostudies-literature

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Hepatocyte entry leads to degradation of autoreactive CD8 T cells.

Benseler Volker V   Warren Alessandra A   Vo Michelle M   Holz Lauren E LE   Tay Szun S SS   Le Couteur David G DG   Breen Eamon E   Allison Anthony C AC   van Rooijen Nico N   McGuffog Claire C   Schlitt Hans J HJ   Bowen David G DG   McCaughan Geoffrey W GW   Bertolino Patrick P  

Proceedings of the National Academy of Sciences of the United States of America 20110920 40


Although most self-reactive T cells are eliminated in the thymus, mechanisms to inactivate or control T cells specific for extrathymic antigens are required and exist in the periphery. By investigating the site in which autoreactive T cells are tolerized, we identify a unique mechanism of peripheral deletion in which naïve autoreactive CD8 T cells are rapidly eliminated in the liver after intrahepatic activation. T cells actively invade hepatocytes, enter endosomal/lysosomal compartments, and ar  ...[more]

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