2014
DOI: 10.1016/j.jhep.2014.02.011
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Influence of CD8 T cell priming in liver and gut on the enterohepatic circulation

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Cited by 22 publications
(20 citation statements)
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“…The down-regulated VEGF-A, was responsive to recruits macrophages (Walczak et al, 2004 ; Tanaka and Iwakiri, 2016 ), indicating the finishing of the acute immune response. Whereas, the up-regulated CCR9, a marker of gut-homing lymphocyte, suggested the entering of intestinal activated lymphocytes (Eickmeier et al, 2014 ). This may relate to hepatic inflammation, since the gut-primed T cells, preferentially migrating to the liver, could induce autoimmune disease (Eickmeier et al, 2014 ).…”
Section: Discussionmentioning
confidence: 99%
“…The down-regulated VEGF-A, was responsive to recruits macrophages (Walczak et al, 2004 ; Tanaka and Iwakiri, 2016 ), indicating the finishing of the acute immune response. Whereas, the up-regulated CCR9, a marker of gut-homing lymphocyte, suggested the entering of intestinal activated lymphocytes (Eickmeier et al, 2014 ). This may relate to hepatic inflammation, since the gut-primed T cells, preferentially migrating to the liver, could induce autoimmune disease (Eickmeier et al, 2014 ).…”
Section: Discussionmentioning
confidence: 99%
“…12 A recent study showed that gut-primed CD8 + T cells had a strong propensity to migrate to the liver, but liver-primed CD8 + T cells were incapable of migrating to gut. 13 Bliss et al observed that the gut-derived CD4 + T cells migrated to liver and induce hepatic inflammation in IL-10 knockout mice infected with Trichinella spiralis. 10 Considering the intimate relationship between gut and liver, in this study, we focus on the migration behavior of gut-derived lymphocytes to liver in NAFLD mice model.…”
Section: Discussionmentioning
confidence: 99%
“…57 Additionally, in a murine model, CD8 + T cells activated in GALT caused immune-mediated cholangitis in an antigen-dependent manner, and gut-primed CD8 + T cells activated in GALT could migrate to the liver, whereas liver-activated CD8 + T cells did not home to the intestine. 58,59 Conversely, one in vitro study showed that murine sinusoidal endothelium could induce gut trophism on CD4 + T cells. 60 In general, there are no differences in the amount of total circulating CD4 + and CD8 + T cells in the peripheral blood of patients with PSC-UC and UC compared to healthy controls.…”
Section: Recruitment Of Lymphocytes To the Livermentioning
confidence: 99%