Cellular and cytokine-mediated mechanisms of inflammation and its modulation in immune-mediated liver injury - PubMed
Review
Cellular and cytokine-mediated mechanisms of inflammation and its modulation in immune-mediated liver injury
G Tiegs. Z Gastroenterol. 2007 Jan.
Abstract
The immune response to foreign or self antigens mediates liver damage during viral or autoimmune hepatitis. However, it now appears that also specific antigen-independent liver diseases, where liver damage has been attributed to occur from oxygen radical formation, seem to be mediated by cells of the innate and adaptive immune response. These liver disorders include alcoholic liver disease, non-alcoholic fatty liver disease or non-alcoholic steatohepatitis, and ischemia/reperfusion injury that impairs the function of liver grafts. Here it seems that breakdown of the gastrointestinal barrier might increase the concentration of bacterial toxins in the portal blood, which then activate cells of the innate immune system, e. g., Kupffer cells, but, depending on the nature of the toxin, probably also conventional T cells. Invariant NKT cells which specifically recognize glycolipid antigens were supposed to become activated during metabolic disorders related to obesity. However, both steatohepatitis as well as ischemia/reperfusion injury are associated with a Th1 cytokine response characterized by IFNgamma and TNFalpha elevation, that might reflect an NKT cell response on the one hand, but also conventional T lymphocytes, in particular CD4 (+) T cells, are critical for the pathophysiology of these disorders. In 1992 we described a model of T cell-dependent liver injury inducible by the T cell-mitogenic lectin concanavalin A. This model of immune-mediated liver injury was intensively used to study pathophysiological immune effector mechanisms as well as cytokine signaling important for hepatocellular apoptosis, inhibition of apoptosis and regeneration. Recently it became evident that the inflammatory response in this model is regulated by specific cytokine signals as well as by immune regulator cells. The immune-regulatory functions of the liver are of particular interest with respect to the scavenger function of this organ, being continuously exposed to foreign antigenic material from the gut which should be eliminated without causing chronic disease.
Similar articles
-
[Immunopathology of chronic liver diseases].
Meyer zum Büschenfelde KH. Meyer zum Büschenfelde KH. Verh Dtsch Ges Pathol. 1995;79:186-97. Verh Dtsch Ges Pathol. 1995. PMID: 8600684 Review. German.
-
Hepatic NKT cells: friend or foe?
Swain MG. Swain MG. Clin Sci (Lond). 2008 Apr;114(7):457-66. doi: 10.1042/CS20070328. Clin Sci (Lond). 2008. PMID: 18302533 Review.
-
Innate immune response and hepatic inflammation.
Szabo G, Mandrekar P, Dolganiuc A. Szabo G, et al. Semin Liver Dis. 2007 Nov;27(4):339-50. doi: 10.1055/s-2007-991511. Semin Liver Dis. 2007. PMID: 17979071 Review.
-
Jaeschke H. Jaeschke H. Am J Physiol Gastrointest Liver Physiol. 2006 Jun;290(6):G1083-8. doi: 10.1152/ajpgi.00568.2005. Am J Physiol Gastrointest Liver Physiol. 2006. PMID: 16687579 Review.
-
Immune disorders of the liver and bile duct.
Vierling JM. Vierling JM. Gastroenterol Clin North Am. 1992 Jun;21(2):427-49. Gastroenterol Clin North Am. 1992. PMID: 1512050 Review.
Cited by
-
Cre-inducible human CD59 mediates rapid cell ablation after intermedilysin administration.
Feng D, Dai S, Liu F, Ohtake Y, Zhou Z, Wang H, Zhang Y, Kearns A, Peng X, Zhu F, Hayat U, Li M, He Y, Xu M, Zhao C, Cheng M, Zhang L, Wang H, Yang X, Ju C, Bryda EC, Gordon J, Khalili K, Hu W, Li S, Qin X, Gao B. Feng D, et al. J Clin Invest. 2016 Jun 1;126(6):2321-33. doi: 10.1172/JCI84921. Epub 2016 May 9. J Clin Invest. 2016. PMID: 27159394 Free PMC article.
-
Yang GX, Lian ZX, Chuang YH, Moritoki Y, Lan RY, Wakabayashi K, Ansari AA, Flavell RA, Ridgway WM, Coppel RL, Tsuneyama K, Mackay IR, Gershwin ME. Yang GX, et al. Hepatology. 2008 Jun;47(6):1974-82. doi: 10.1002/hep.22226. Hepatology. 2008. PMID: 18452147 Free PMC article.
-
Zhuang Y, Li Y, Li X, Xie Q, Wu M. Zhuang Y, et al. PLoS One. 2016 Mar 3;11(3):e0149754. doi: 10.1371/journal.pone.0149754. eCollection 2016. PLoS One. 2016. PMID: 26939081 Free PMC article.
-
Li SL, Cao R, Hu XF, Xiong P, Zhao GY, Xie YN, Wang ZM, Li YK, Yang B, Yang J. Li SL, et al. Ann Transl Med. 2021 Aug;9(15):1228. doi: 10.21037/atm-21-378. Ann Transl Med. 2021. PMID: 34532365 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials