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• W2899898115 abstract "In recent years, the cross talk between the liver and the immune system is being uncovered, in part by studying liver involvement in primary immune deficiencies (PID) and in part by investigating the alterations of the immune system following orthotopic liver transplantation (OLT). Here we review some of the reciprocal interactions between the liver and the immune system. Patients with PID, particularly those involving inherited defects in T and B cells or innate immunity are prone to infections and inflammatory responses that often involve the liver. Omenn's syndrome, familial hemophagocytic lymphohistiocytosis, AIRE, FOXP3 and CD25 deficiencies, common variable immunodeficiency, CD40 ligand deficiency, chronic granulomatous disease and autoimmune lymphoproliferative syndrome are some of the notable PID associated with typical hepatobiliary abnormalities. Knowledge gained from studying these PID together with laboratory and histological evaluations can assist in managing PID-associated liver dysfunction. The liver itself also has important effects on the immune system, as evident from the growing experience with patients surviving OLT. Up to 40% of pediatric patients who receive OLT suffer from post transplantation allergy, autoimmunity, and immune-mediated disorders (PTAA). PTAA is more common after liver and heart transplantations than kidney transplantations. Potential contributing factors for the increased frequency of PTAA after OLT include the age of the patients, the prolonged use of tacrolimus and the reduced regulatory immune function with a shift towards a TH2 immune response. Better understanding of the mechanisms leading to the development of PTAA after OLT will also improve the management of these conditions." @default.
• W2899898115 created "2018-11-16" @default.
• W2899898115 creator A5006022905 @default.
• W2899898115 creator A5084267840 @default.
• W2899898115 date "2019-01-01" @default.
• W2899898115 modified "2023-09-25" @default.
• W2899898115 title "Liver-associated immune abnormalities" @default.
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• W2899898115 doi "https://doi.org/10.1016/j.autrev.2018.06.016" @default.
• W2899898115 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30408587" @default.
• W2899898115 hasPublicationYear "2019" @default.
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