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1.
Artif Organs ; 36(1): 86-93, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-21819437

RESUMO

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.


Assuntos
Reatores Biológicos , Falência Hepática Aguda/terapia , Fígado Artificial , Membranas Artificiais , Animais , Sobrevivência Celular , Técnicas de Cocultura , Modelos Animais de Doenças , Cães , Desenho de Equipamento , Galactosamina/toxicidade , Hemodinâmica , Hepatócitos/citologia , Imunidade Humoral , Falência Hepática Aguda/induzido quimicamente , Falência Hepática Aguda/imunologia , Células-Tronco Mesenquimais/citologia , Peso Molecular , Suínos
2.
Artif Organs ; 35(3): E40-6, 2011 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-21371057

RESUMO

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.


Assuntos
Hepatócitos/citologia , Fígado Artificial , Membranas Artificiais , Células-Tronco Mesenquimais/citologia , Animais , Anticorpos Heterófilos/imunologia , Sobrevivência Celular , Células Cultivadas , Técnicas de Cocultura , Cães , Desenho de Equipamento , Hepatócitos/imunologia , Células-Tronco Mesenquimais/imunologia , Peso Molecular , Suínos
3.
Am J Med Sci ; 343(6): 429-34, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22008783

RESUMO

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.


Assuntos
Hepatócitos/imunologia , Falência Hepática Aguda/imunologia , Falência Hepática Aguda/cirurgia , Fígado Artificial , Animais , Células da Medula Óssea/citologia , Células da Medula Óssea/imunologia , Técnicas de Cocultura , Modelos Animais de Doenças , Cães , Desenho de Equipamento/normas , Hepatócitos/citologia , Falência Hepática Aguda/patologia , Fígado Artificial/efeitos adversos , Células-Tronco Mesenquimais/citologia , Células-Tronco Mesenquimais/imunologia , Distribuição Aleatória , Suínos
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