Hemopoietic progenitor cells and bone marrow stromal cells in patients with autoimmune hepatitis type 1 and primary biliary cirrhosis
- PMID: 14568247
- DOI: 10.1016/s0168-8278(03)00387-8
Hemopoietic progenitor cells and bone marrow stromal cells in patients with autoimmune hepatitis type 1 and primary biliary cirrhosis
Abstract
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.
Similar articles
-
Assessment of bone marrow stem cell reserve and function and stromal cell function in patients with autoimmune cytopenias.Blood. 2000 Nov 1;96(9):3272-5. Blood. 2000. PMID: 11050013
-
Autoimmune hepatitis type 1 and primary biliary cirrhosis have distinct bone marrow cytokine production.J Autoimmun. 2005 Dec;25(4):283-8. doi: 10.1016/j.jaut.2005.08.002. Epub 2005 Oct 20. J Autoimmun. 2005. PMID: 16242912
-
Markers of cell activation and apoptosis in bone marrow mononuclear cells of patients with autoimmune hepatitis type 1 and primary biliary cirrhosis.J Hepatol. 2005 Mar;42(3):393-9. doi: 10.1016/j.jhep.2004.11.023. J Hepatol. 2005. PMID: 15710223
-
Immunodysregulation of HIV disease at bone marrow level.Autoimmun Rev. 2005 Nov;4(8):486-90. doi: 10.1016/j.autrev.2005.04.014. Autoimmun Rev. 2005. PMID: 16214083 Review.
-
Clinical significance of long-term cultures of myeloid blood cells.Crit Rev Oncol Hematol. 1987;7(2):125-38. doi: 10.1016/s1040-8428(87)80022-7. Crit Rev Oncol Hematol. 1987. PMID: 3311425 Review.
Cited by
-
Erythrocyte count is associated with prognosis in Chinese patients with primary biliary cholangitis.Exp Ther Med. 2020 Mar;19(3):2075-2082. doi: 10.3892/etm.2020.8446. Epub 2020 Jan 13. Exp Ther Med. 2020. PMID: 32104268 Free PMC article.
-
IFN-γ-STAT1-iNOS Induces Myeloid Progenitors to Acquire Immunosuppressive Activity.Front Immunol. 2017 Sep 22;8:1192. doi: 10.3389/fimmu.2017.01192. eCollection 2017. Front Immunol. 2017. PMID: 29018448 Free PMC article.
-
Autoantibodies and autoantigens in autoimmune hepatitis: important tools in clinical practice and to study pathogenesis of the disease.J Autoimmune Dis. 2004 Oct 15;1(1):2. doi: 10.1186/1740-2557-1-2. J Autoimmune Dis. 2004. PMID: 15679907 Free PMC article.
-
Distinct microRNAs expression profile in primary biliary cirrhosis and evaluation of miR 505-3p and miR197-3p as novel biomarkers.PLoS One. 2013 Jun 12;8(6):e66086. doi: 10.1371/journal.pone.0066086. Print 2013. PLoS One. 2013. PMID: 23776611 Free PMC article.
-
Double reactivity against actin and alpha-actinin defines a severe form of autoimmune hepatitis type 1.J Clin Immunol. 2006 Nov;26(6):495-505. doi: 10.1007/s10875-006-9045-z. Epub 2006 Sep 26. J Clin Immunol. 2006. PMID: 17001515
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials