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Analysis of multipotent mesenchymal stromal cells used for acute graft-versus-host disease prophylaxis.
Kuzmina, Larisa A; Petinati, Nataliya A; Shipounova, Irina N; Sats, Natalia V; Bigildeev, Alexey E; Zezina, Ekaterina A; Popova, Maria D; Drize, Nina J; Parovichnikova, Elena N; Savchenko, Valery G.
  • Kuzmina LA; Federal Government Budget Institution National Research Center for Hematology, Ministry of Health, Moscow, Russia.
  • Petinati NA; Federal Government Budget Institution National Research Center for Hematology, Ministry of Health, Moscow, Russia.
  • Shipounova IN; Federal Government Budget Institution National Research Center for Hematology, Ministry of Health, Moscow, Russia.
  • Sats NV; Federal Government Budget Institution National Research Center for Hematology, Ministry of Health, Moscow, Russia.
  • Bigildeev AE; Federal Government Budget Institution National Research Center for Hematology, Ministry of Health, Moscow, Russia.
  • Zezina EA; Department of Molecular Immunology, Faculty of Biology, Moscow State University, Moscow, Russia.
  • Popova MD; Department of Molecular Immunology, Faculty of Biology, Moscow State University, Moscow, Russia.
  • Drize NJ; Federal Government Budget Institution National Research Center for Hematology, Ministry of Health, Moscow, Russia.
  • Parovichnikova EN; Federal Government Budget Institution National Research Center for Hematology, Ministry of Health, Moscow, Russia.
  • Savchenko VG; Federal Government Budget Institution National Research Center for Hematology, Ministry of Health, Moscow, Russia.
Eur J Haematol ; 96(4): 425-34, 2016 Apr.
Article en En | MEDLINE | ID: mdl-26115424
BACKGROUND: Multipotent mesenchymal stromal cells (MSCs) are used for prophylaxis of acute graft-versus-host disease (aGvHD) after allogeneic hematopoietic cell transplantation (allo-HCT). Not all samples of MSC are efficient for aGvHD prevention. The suitability of MSCs for aGvHD prophylaxis was studied. METHODS: MSCs were derived from the bone marrow (BM) of HCT donor and cultivated for no more than three passages. The characteristics of donor BM samples including colony-forming unit fibroblast (CFU-F) concentration, growth parameters of MSCs, and the relative expression levels (REL) of different genes were analyzed. MSCs were injected intravenously precisely at the moment of blood cell reconstitution. RESULTS: MSCs infusion induced a significant threefold decrease in aGvHD development and improved overall survival compared with the standard prophylaxis group. In ineffective MSC samples (9.4%), a significant decrease in total cell production and the REL of CSF1, FGFR1, and PDGFRB was observed. In all studied BM samples, the cumulative MSC production and CFU-F concentrations decreased with age. The expression levels of FGFR2, PPARG, and VEGF differed by age. CONCLUSIONS: A universal single indicator for the prediction of MSC eligibility for aGvHD prophylaxis was not identified. A multiparameter mathematical model for selecting MSC samples effective for the prevention of aGvHD was proposed.
Asunto(s)
Enfermedad Injerto contra Huésped/prevención & control; Trasplante de Células Madre Mesenquimatosas; Células Madre Mesenquimatosas/inmunología; Agonistas Mieloablativos/uso terapéutico; Acondicionamiento Pretrasplante/métodos; Adolescente; Adulto; Femenino; Expresión Génica; Enfermedad Injerto contra Huésped/diagnóstico; Enfermedad Injerto contra Huésped/inmunología; Enfermedad Injerto contra Huésped/mortalidad; Humanos; Leucemia Mieloide Aguda/inmunología; Leucemia Mieloide Aguda/mortalidad; Leucemia Mieloide Aguda/patología; Leucemia Mieloide Aguda/terapia; Masculino; Células Madre Mesenquimatosas/citología; Persona de Mediana Edad; Síndromes Mielodisplásicos/inmunología; Síndromes Mielodisplásicos/mortalidad; Síndromes Mielodisplásicos/patología; Síndromes Mielodisplásicos/terapia; PPAR gamma/genética; PPAR gamma/inmunología; Leucemia-Linfoma Linfoblástico de Células Precursoras/inmunología; Leucemia-Linfoma Linfoblástico de Células Precursoras/mortalidad; Leucemia-Linfoma Linfoblástico de Células Precursoras/patología; Leucemia-Linfoma Linfoblástico de Células Precursoras/terapia; Receptor Tipo 1 de Factor de Crecimiento de Fibroblastos/genética; Receptor Tipo 1 de Factor de Crecimiento de Fibroblastos/inmunología; Receptor Tipo 2 de Factor de Crecimiento de Fibroblastos/genética; Receptor Tipo 2 de Factor de Crecimiento de Fibroblastos/inmunología; Receptor de Factor Estimulante de Colonias de Macrófagos/genética; Receptor de Factor Estimulante de Colonias de Macrófagos/inmunología; Receptor beta de Factor de Crecimiento Derivado de Plaquetas/genética; Receptor beta de Factor de Crecimiento Derivado de Plaquetas/inmunología; Análisis de Supervivencia; Trasplante Homólogo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Acondicionamiento Pretrasplante / Agonistas Mieloablativos / Trasplante de Células Madre Mesenquimatosas / Células Madre Mesenquimatosas / Enfermedad Injerto contra Huésped Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Acondicionamiento Pretrasplante / Agonistas Mieloablativos / Trasplante de Células Madre Mesenquimatosas / Células Madre Mesenquimatosas / Enfermedad Injerto contra Huésped Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Año: 2016 Tipo del documento: Article