Background: Bone marrow stem/progenitor cells seem to be effective in liver regeneration after tissueinjury. Aim: To evaluate the feasibility and safety of the mobilization and reinfusion of CD133+stem/progenitorcells in patients with end-stage liver disease.Methods: Autologous CD133+stem/progenitor cells, mobilized with granulocyte-colony stimulating fac-tor, were collected by leukapheresis and reinfused at increasing doses through the hepatic artery startingfrom 5 × 104/kg up to 1 × 106/kg.Results: 16 subjects with Model for End-stage Liver Disease (MELD) score between 17 and 25 wereenrolled, 14 mobilized an adequate number of CD133+stem/progenitor cells and 12 were reinfused.No severe adverse events related to the procedure were reported. MELD score significantly worsenedduring mobilization in Child Turcotte Pugh-C patients. A significant improvement of liver function wasobserved 2 months after reinfusion (MELD 19.5 vs 16; P = 0.045). Overall, 5 patients underwent livertransplantation within 12 months from reinfusion and 2 died because of progressive liver failure.Conclusions: CD133+stem/progenitor cells reinfusion in patients with end-stage liver disease is feasi-ble and safe. A worsening of liver function was observed during mobilization in Child Turcotte Pugh-Cpatients. The temporary improvement of MELD score after reinfusion suggests that stem cells therapymay be a “bridge to transplant” approach for these patients.

Reinfusion of highly purified CD133+ bone marrow-derived stem/progenitor cells in patients with end-stage liver disease: a phase I clinical trial / Andreone, P; Catani, L; Margini, C; Brodosi, L; Lorenzini, S; Sollazzo, D; Nicolini, B; Giordano, R; Montemurro, T; Rizzi, S; Dan, E; Giudice, V; Viganò, M; Casadei, A; Foschi, F; Malvi, D; Bernardi, M; Conti, F; Lemoli, RM.. - In: DIGESTIVE AND LIVER DISEASE. - ISSN 1590-8658. - STAMPA. - 47:12(2015), pp. 1059-1066. [10.1016/j.dld.2015.08.018]

Reinfusion of highly purified CD133+ bone marrow-derived stem/progenitor cells in patients with end-stage liver disease: a phase I clinical trial

ANDREONE, PIETRO;CATANI, LUCIA;BRODOSI, LUCIA;SOLLAZZO, DARIA;NICOLINI, BENEDETTA;DAN, ELISA;MALVI, DEBORAH;BERNARDI, MAURO;CONTI, FABIO;
2015

Abstract

Background: Bone marrow stem/progenitor cells seem to be effective in liver regeneration after tissueinjury. Aim: To evaluate the feasibility and safety of the mobilization and reinfusion of CD133+stem/progenitorcells in patients with end-stage liver disease.Methods: Autologous CD133+stem/progenitor cells, mobilized with granulocyte-colony stimulating fac-tor, were collected by leukapheresis and reinfused at increasing doses through the hepatic artery startingfrom 5 × 104/kg up to 1 × 106/kg.Results: 16 subjects with Model for End-stage Liver Disease (MELD) score between 17 and 25 wereenrolled, 14 mobilized an adequate number of CD133+stem/progenitor cells and 12 were reinfused.No severe adverse events related to the procedure were reported. MELD score significantly worsenedduring mobilization in Child Turcotte Pugh-C patients. A significant improvement of liver function wasobserved 2 months after reinfusion (MELD 19.5 vs 16; P = 0.045). Overall, 5 patients underwent livertransplantation within 12 months from reinfusion and 2 died because of progressive liver failure.Conclusions: CD133+stem/progenitor cells reinfusion in patients with end-stage liver disease is feasi-ble and safe. A worsening of liver function was observed during mobilization in Child Turcotte Pugh-Cpatients. The temporary improvement of MELD score after reinfusion suggests that stem cells therapymay be a “bridge to transplant” approach for these patients.
2015
Reinfusion of highly purified CD133+ bone marrow-derived stem/progenitor cells in patients with end-stage liver disease: a phase I clinical trial / Andreone, P; Catani, L; Margini, C; Brodosi, L; Lorenzini, S; Sollazzo, D; Nicolini, B; Giordano, R; Montemurro, T; Rizzi, S; Dan, E; Giudice, V; Viganò, M; Casadei, A; Foschi, F; Malvi, D; Bernardi, M; Conti, F; Lemoli, RM.. - In: DIGESTIVE AND LIVER DISEASE. - ISSN 1590-8658. - STAMPA. - 47:12(2015), pp. 1059-1066. [10.1016/j.dld.2015.08.018]
Andreone, P; Catani, L; Margini, C; Brodosi, L; Lorenzini, S; Sollazzo, D; Nicolini, B; Giordano, R; Montemurro, T; Rizzi, S; Dan, E; Giudice, V; Viganò, M; Casadei, A; Foschi, F; Malvi, D; Bernardi, M; Conti, F; Lemoli, RM.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/536365
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