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1.
Artif Organs ; 36(1): 86-93, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21819437

ABSTRACT

Given the xenogeneic immune reaction relevant to the molecular weight cutoff of the membrane of a bioartificial liver (BAL) system, we investigated the influence of membrane molecular weight cutoff in our BAL system in this study. Acute liver failure in beagles was induced by d-galactosamine administration. Eight beagles were divided into two groups by the membrane molecular weight cutoff of the plasma component separator. Group 1 beagles were treated with BAL containing 200 kDa retention rating membrane. Group 2 beagles were treated with BAL containing 1200 kDa retention rating membrane. Each group underwent two 6-h BAL treatments that were performed on day 1 and day 21. The hemodynamic and hematologic response, humoral immune responses, and cytotoxic immune response to BAL therapy were studied before and after treatments. All beagles remained hemodynamically and hematologically stable during BAL treatments. BAL treatment was associated with a significant decline in levels of complement; however, a longer time of level maintenance was observed in Group 2. Group 2 beagles experienced a significant increase in levels of IgG and IgM after two BAL treatments. Significant levels of canine proteins were detected in BAL medium from Group 2; only trace levels of canine proteins were detected in BAL medium from Group 1. The posttreatment viability of co-culture cells in Group 2 was lower compared with Group 1, and the viability of co-culture cells after treatments was associated with deposition of canine proteins on the cells. Xenogeneic immune response was influenced by membrane molecular weight cutoff in the BAL.


Subject(s)
Bioreactors , Liver Failure, Acute/therapy , Liver, Artificial , Membranes, Artificial , Animals , Cell Survival , Coculture Techniques , Disease Models, Animal , Dogs , Equipment Design , Galactosamine/toxicity , Hemodynamics , Hepatocytes/cytology , Immunity, Humoral , Liver Failure, Acute/chemically induced , Liver Failure, Acute/immunology , Mesenchymal Stem Cells/cytology , Molecular Weight , Swine
2.
Am J Med Sci ; 343(6): 429-34, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22008783

ABSTRACT

INTRODUCTION: To study and evaluate the immunosafety of our newly developed multilayer flat-plate bioartificial liver (BAL) in treatment of canines with acute liver failure. METHODS: Fresh porcine hepatocytes and bone marrow mesenchymal stem cells were cocultured in new BAL. Ten canine models with acute liver failure were set up through D-galactosamine administration; 24 hours after administration, the beagles were randomly allocated to a 6-hour treatment with the BAL. The beagles were divided into 2 groups by treatment times. Group 1 beagles (n = 5) received a single BAL treatment. Group 2 beagles (n = 5) received 3 BAL treatments. The hemodynamic, hematologic response and humoral immune responses to BAL therapy were studied before and after treatments. RESULTS: All beagles remained hemodynamically and hematologically stable during BAL treatments. The levels of IgG and IgM were similar before and after treatment after a single treatment. In addition, the level of CH50 in group 1 slightly decreased after the initiation of BAL treatment, and then the level recovered to baseline quickly after treatments. Time-course changes of the levels of antibodies and CH50 after 3 treatments in group 2 were similar to group 1. Only trace levels of IgG were detected in BAL medium after treatments. CONCLUSION: The multilayer flat-plate BAL showed a great immunosafety in the treatment of canines with acute liver failure and exhibited a good prospect of its use in clinic.


Subject(s)
Hepatocytes/immunology , Liver Failure, Acute/immunology , Liver Failure, Acute/surgery , Liver, Artificial , Animals , Bone Marrow Cells/cytology , Bone Marrow Cells/immunology , Coculture Techniques , Disease Models, Animal , Dogs , Equipment Design/standards , Hepatocytes/cytology , Liver Failure, Acute/pathology , Liver, Artificial/adverse effects , Mesenchymal Stem Cells/cytology , Mesenchymal Stem Cells/immunology , Random Allocation , Swine
3.
Artif Organs ; 35(3): E40-6, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21371057

ABSTRACT

Immunoisolation using semipermeable membranes has been incorporated into bioartificial liver (BAL) devices to separate cellular components of the recipient's immune system from the cells within the BAL device. This study was designed to explore the influence of membrane molecular weight cutoff on performance of the multilayer radial-flow BAL using porcine hepatocytes cocultured with mesenchymal stem cells. In this study, healthy beagles underwent 6-h treatment with a BAL containing membrane with 200 kDa retention rating or 1200 kDa retention rating. Functional markers of BAL performance were monitored before and after treatment, as well as cytotoxic immune response to BAL therapy. The results showed that hepatocyte performance levels such as albumin secretion, urea synthesis, and viability were all significantly higher in 200 kDa retention rating group compared with the 1200 kDa retention rating group after treatment (P < 0.05). Significant levels of canine proteins were detected in BAL medium from the 1200 kDa retention rating group. Fluorescence microscopy further verified that heavy deposition of canine IgG, IgM, and complement (C3) on coculture cells was obtained after BAL treatment in the 1200 kDa retention rating group. However, only trace deposits of canine immunoproteins were observed on coculture cells obtained from BAL in the 200 kDa retention rating group. Small membrane molecular weight cutoff of the BAL could reduce the transfer of xenoreactive antibodies into the BAL medium and improve the performance of the BAL.


Subject(s)
Hepatocytes/cytology , Liver, Artificial , Membranes, Artificial , Mesenchymal Stem Cells/cytology , Animals , Antibodies, Heterophile/immunology , Cell Survival , Cells, Cultured , Coculture Techniques , Dogs , Equipment Design , Hepatocytes/immunology , Mesenchymal Stem Cells/immunology , Molecular Weight , Swine
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