Autores: Behairy Behairy E, El-Araby Hanaa A, Abd El kader Hasan H, Ehsan Nermin A, Salem Menan E, Zakaria Haidy M, Khedr Mohammed A
Background: T-cell populations regulate the balance of immune responses. The CD (Cluster of differentiation) 4+CD25+ regulatory T cells (Tregs) are crucial for maintaining negative control of various immune responses. There are different T-cell subpopulations with regulatory functions, as natural killer T cells, CD8+ and CD28. The forkhead box P3 (FOXP3) regulates Treg development and is required for its suppressive function. Aim: To evaluate the hepatic expression of the intrahepatic Tregs, Ig (immunoglobulin) Gand IgM plasma cells in autoimmune hepatitis (AIH) and other chronic liver diseases (CLDs). Material and methods: This study included 100 pediatric patients; 50 AIH and 50 CLDs other than AIH. All patients were subjected to routine investigations of CLDs plus immune-staining of liver tissue for FOXp3, IgG and IgM plasma cells, CD4 and CD8 T-cells. Results: The FOXP3+ T cells in patients with AIH (6.3 ± 5) were significantly higher than that in the non-AIH (2.1 ± 2.6). FOXP3+ T cells were abundant in liver tissue with marked inflammatory cellular infiltrate. CD4+ and CD8+ infiltrating the liver tissue and IgG positive cells were significantly higher in AIH group, while the expression of IgM positive cells showed no significant difference. The IgG/IgM was significantly higher in the AIH treatment responders (3 ± 3) than non-responders (1.6 ± 0.5), while there was no significant difference regarding the intrahepatic expression of FOXP3+, CD4+, CD8+ cells, T-cells, IgG and IgM plasma cells. Conclusion: Intrahepatic Tregs were in-creased in number in patients with AIH in the initial presentation, and their presence is associated with increased activity and inflammation in liver biopsy.
Palabras clave: Cluster of differentiation chronic liver diseases forkhead box P3 immunoglobulin
2016-10-21 | 235 visitas | Evalua este artículo 0 valoraciones
Vol. 15 Núm.5. Septiembre-Octubre 2016 Pags. 682-690 Ann Hepatol 2016; 15(5)