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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.
Afiliação
  • 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 em En | MEDLINE | ID: mdl-26115424
ABSTRACT

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.
Assuntos
Doença Enxerto-Hospedeiro/prevenção & controle; Transplante de Células-Tronco Mesenquimais; Células-Tronco Mesenquimais/imunologia; Agonistas Mieloablativos/uso terapêutico; Condicionamento Pré-Transplante/métodos; Adolescente; Adulto; Feminino; Expressão Gênica; Doença Enxerto-Hospedeiro/diagnóstico; Doença Enxerto-Hospedeiro/imunologia; Doença Enxerto-Hospedeiro/mortalidade; Humanos; Leucemia Mieloide Aguda/imunologia; Leucemia Mieloide Aguda/mortalidade; Leucemia Mieloide Aguda/patologia; Leucemia Mieloide Aguda/terapia; Masculino; Células-Tronco Mesenquimais/citologia; Pessoa de Meia-Idade; Síndromes Mielodisplásicas/imunologia; Síndromes Mielodisplásicas/mortalidade; Síndromes Mielodisplásicas/patologia; Síndromes Mielodisplásicas/terapia; PPAR gama/genética; PPAR gama/imunologia; Leucemia-Linfoma Linfoblástico de Células Precursoras/imunologia; Leucemia-Linfoma Linfoblástico de Células Precursoras/mortalidade; Leucemia-Linfoma Linfoblástico de Células Precursoras/patologia; Leucemia-Linfoma Linfoblástico de Células Precursoras/terapia; Receptor Tipo 1 de Fator de Crescimento de Fibroblastos/genética; Receptor Tipo 1 de Fator de Crescimento de Fibroblastos/imunologia; Receptor Tipo 2 de Fator de Crescimento de Fibroblastos/genética; Receptor Tipo 2 de Fator de Crescimento de Fibroblastos/imunologia; Receptor de Fator Estimulador de Colônias de Macrófagos/genética; Receptor de Fator Estimulador de Colônias de Macrófagos/imunologia; Receptor beta de Fator de Crescimento Derivado de Plaquetas/genética; Receptor beta de Fator de Crescimento Derivado de Plaquetas/imunologia; Análise de Sobrevida; Transplante Homólogo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Condicionamento Pré-Transplante / Agonistas Mieloablativos / Transplante de Células-Tronco Mesenquimais / Células-Tronco Mesenquimais / Doença Enxerto-Hospedeiro Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Condicionamento Pré-Transplante / Agonistas Mieloablativos / Transplante de Células-Tronco Mesenquimais / Células-Tronco Mesenquimais / Doença Enxerto-Hospedeiro Tipo de estudo: Diagnostic_studies / Prognostic_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article