Concentration of Human Hematopoietic Stem Cells in Bone Marrow Transplantation: Results of a Multicenter Study Using Baxter CS 3000 plus Cell Separator

Author:

Angelini A.12,Accorsi P.1,Iacone A.1,Bonfini T.12,Refè C.3,Olivieri A.4,Bodini U.5,Bergonzi C.6,Incarbone E.7,Adorno G.8,Bertola F.9,Fattori G.10,Torlontano G.1211

Affiliation:

1. Hematology Department and Blood Transfusion Centre, Pescara

2. Chair of Hematology, G. D'Annunzio University, Chieti

3. Regional Blood Transfusion Centre, Torrette Hospital, Ancona

4. Clinic of Hematology, University of Ancona

5. Blood Transfusion Centre, “Maggiore” Hospital, Cremona

6. Department of Bone Marrow Transplantation and Hematology, “Maggiore” Hospital, Cremona

7. Immunohematology and Blood Transfusion Centre, Regina Margherita, Pediatric Hospital, Torino

8. Chair of Hematology, Tor Vergata University, Roma

9. Blood Transfusion Centre, Civil Hospital, Vicenza

10. Baxter SpA, Roma

11. I.R.C.C.S. S. Giovanni Rotondo, Foggia - Italy

Abstract

Preliminary BM processing to produce an enriched MNC fraction from large BM volumes improves subsequent pharmacological and/or immunological “ex vivo” treatment and cryopreservation. We detail on a multicenter study (6 Transplant Centers) performed to establish an effective and reliable protocol using a CS 3000 continuous flow separator on a large series of BM processed for autologous (96) and allogeneic (12) transplantation. The reduction in volume was 78.6+7.2% while 28.9+12.4% of the original nucleated cells were found in the final product. A mean of 84.3+13.2% of the starting MNC was yielded in a fraction containing over 81% MNC. Cloning efficiency indicated than the final graft was highly enriched in progenitor cells committed to the granulocyte/macrophage pathway (> 100%) as assessed in vitro (CFU-GM). Removal of RBC and PLT was 98.3+1.1 and 37.7+14.6%, respectively. The mean dose of MNC and CFU-GM was 0.6+0.37 x 108 and 0.96+1 x 108 recipient weight. The entire process was accomplished in 87.5+20 min. We concluded that this automated device is a simple and reproducible method for BM processing suitable as first step for further “ex vivo” automated negative and/or positive cell selections.

Publisher

SAGE Publications

Subject

Biomedical Engineering,Biomaterials,General Medicine,Medicine (miscellaneous),Bioengineering

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