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Hemopoietic progenitor cells and bone marrow stromal cells in patients with autoimmune hepatitis type 1 and primary biliary cirrhosis

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Auteur
Kyriakou, D. S.; Alexandrakis, M. G.; Zachou, K.; Passam, F.; Stathakis, N. E.; Dalekos, G. N.
Date
2003
DOI
10.1016/s0168-8278(03)00387-8
Sujet
stem cell transplantation
autoimmunity
autoimmune liver diseases
autoimmune hepatitis
primary biliary cirrhosis
hemopoietic progenitor
cells
stromal cells
LONG-TERM CULTURE
STEM-CELLS
LIMITING DILUTION
IN-VITRO
TRANSPLANTATION
LIVER
DIFFERENTIATION
BLOOD
Gastroenterology & Hepatology
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Résumé
Background/Aims: Autologous hematopoietic stem cell transplantation has been used in severe cases of autoimmunity. We investigated whether hemopoietic progenitor cells and/or bone marrow (BM) microenvironment are affected in autoimmune hepatitis type-1 (AIH-1) and primary biliary cirrhosis (PBC). Methods: We studied 13 AIH-1 patients, 13 PBC patients, 12 cirrhotic controls (CC) and ten healthy controls (HC). Flow cytometry, expansion cultures, long-term BM cultures and clonogenic progenitor cell assays were used. Stromal cell function was assessed in long-term BM cultures recharged with normal CD34+ cells. Results: AIH-1 had increased CD34+, CD34+/CD38+ and CD34+/CD38- cells compared to all groups (P<0.001). PBC had lower progenitor cells compared to controls (P<0.005). No differences were found between CC and HC. Committed progenitor cells in non-adherent cell fraction were increased in AIH-1 (P<0.05) but decreased in PBC compared to controls (P<0.05). Granulocyte-macrophage colony forming units (CFU) and erythroid-burst CFU were increased in AIH-1 compared to all groups (P<0.001). PBC had these CFUs decreased compared to controls (P<0.005). Stromal cells failed to support normal hemopoiesis in PBC. Conclusions: We demonstrated for the first time that AIH-1 had increased hemopoietic progenitor cells and normal stromal function. In PBC, progenitor cells and BM microenvironment were defective. Further studies will determine the significance of these novel findings. (C) 2003 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
URI
http://hdl.handle.net/11615/30110
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