Separation of dendritic cells from highly purified human monocytes by counterflow centrifugation induces tissue factor expression
| Autor: | Gérard Potron, Jacky Bernard, Matthieu Broussas, Jean‐C. Adjizian, Pascale Cornillet-Lefebvre, Philippe Nguyen |
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| Rok vydání: | 2000 |
| Předmět: |
Anions
medicine.medical_treatment Immunology Centrifugation Cell Separation Biology Monocytes Thromboplastin Tissue factor Antigen medicine Animals Humans Immunology and Allergy RNA Messenger Antigens Cells Cultured Phospholipids Coagulants Reverse Transcriptase Polymerase Chain Reaction Monocyte Dendritic Cells Hematology Leukapheresis Dendritic cell Immunotherapy Fetal Blood Molecular biology In vitro medicine.anatomical_structure Cattle Tumor necrosis factor alpha |
| Zdroj: | Transfusion. 40:1088-1094 |
| ISSN: | 1537-2995 0041-1132 |
| Popis: | BACKGROUND: In vitro generation of dendritic cells (DCs) from human monocytes represents a promising tool in immunotherapy. However, it is not known whether the separation of DCs from monocytes induces tissue factor expression and therefore may trigger coagulation in patients receiving these DC preparations. The aim of this study is thus to analyze tissue factor expression on monocyte-derived DCs and to compare their ability to trigger thrombin generation to that of macrophages obtained from the same monocytes. STUDY DESIGN AND METHODS: Human monocytes are separated by leukapheresis and washed by using counterflow centrifugation in sterile, endotoxin-free conditions. Macrophages are grown from human monocytes in the presence of GM–CSF alone and immature DCs are grown in the presence of GM–CSF plus IL-4 for 5 days with fetal calf serum (IDC-FCS). Immature DCs are also grown from human monocytes for 7 days in the presence of GM–CSF plus IL-4 with human group AB serum (IDC-HS). The addition of prostaglandin E2 and TNFα in this culture medium at Day 5 leads to mature DCs (MDC-HS). Tissue factor mRNA expression is studied by RT-PCR analysis. Tissue factor antigen is measured by ELISA in cell lysates and by direct flow cytometry. The procoagulant activity of intact cells is assessed by using an amidolytic assay or a chronometric assay. RESULTS: IDC-FCS express tissue factor mRNA and antigen and trigger thrombin generation. Procoagulant activity of IDC-FCS is dependent on both tissue factor expression and exposure to anionic phospholipid. Monocyte-derived macrophages cultured for 5 days with GM–CSF alone express lower levels of tissue factor mRNA, tissue factor antigen, and procoagulant activity than IDC-FCS. IDC-HS and MDC-HS also express high levels of tissue factor mRNA and antigen and support procoagulant activity. CONCLUSION: Monocyte-derived DCs express a high level of functional tissue factor and support procoagulant activity. This finding should be taken into account in clinical trials. |
| Databáze: | OpenAIRE |
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