Literature DB >> 12100134

Variable product purity and functional capacity after CD34 selection: a direct comparison of the CliniMACS (v2.1) and Isolex 300i (v2.5) clinical scale devices.

Michael J Watts1, Tim C P Somervaille, Stuart J Ings, Forhad Ahmed, Asim Khwaja, Kwee Yong, David C Linch.   

Abstract

The two clinical scale devices currently available for CD34+ cell selection from peripheral blood stem cells (PBSC) apheresis products, the CliniMACS and the Isolex 300i, were compared directly by pooling and splitting two PBSC harvests collected on sequential days from 10 patients and processing half of each pooled harvest on each device. The CliniMACS product had significantly higher median CD34+ purity (90%vs 78%; P = 0.004) and lower median T-cell content (0.06%vs 0.44%; P = 0.003) compared with the Isolex 300i product. The median CD34+ yields were similar (64% and 60% respectively). However, when the functional capacities of the products were compared, the median recovery of colony-forming units was significantly greater from the Isolex 300i product (48%vs 38%; P = 0.035), as was expansion of cells in either erythroid or granulocytic lineage-specific liquid culture (2.1-fold more erythroid and 1.5-fold more granulocytic lineage progenitors on d 9 (P = 0.03 and 0.03 respectively). This was due to a higher proportion of apoptotic cells in the CliniMACS product (28%vs 18%; P = 0.007, annexin V binding). Hence, although the CliniMACS device yielded a higher purity product with fewer T cells, the Isolex 300i product contained fewer apoptotic cells and consequently had greater functional capacity in culture.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12100134     DOI: 10.1046/j.1365-2141.2002.03561.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  6 in total

Review 1.  Preparing clinical grade Ag-specific T cells for adoptive immunotherapy trials.

Authors:  D L DiGiusto; L J N Cooper
Journal:  Cytotherapy       Date:  2007       Impact factor: 5.414

2.  Manufacture of Autologous CD34+ Selected Grafts in the NIAID-Sponsored HALT-MS and SCOT Multicenter Clinical Trials for Autoimmune Diseases.

Authors:  Carolyn A Keever-Taylor; Shelly Heimfeld; Kaitlyn C Steinmiller; Richard A Nash; Keith M Sullivan; Christine W Czarniecki; Tomeka C Granderson; Julia S Goldstein; Linda M Griffith
Journal:  Biol Blood Marrow Transplant       Date:  2017-06-30       Impact factor: 5.742

3.  Evaluation of mobilized peripheral blood CD34(+) cells from patients with severe coronary artery disease as a source of endothelial progenitor cells.

Authors:  Abba C Zubair; Sunita Malik; Athena Paulsen; Masakazu Ishikawa; Christopher McCoy; Peter X Adams; David Amrani; Marco Costa
Journal:  Cytotherapy       Date:  2010-04       Impact factor: 5.414

4.  Targeted transduction of CD34+ hematopoietic progenitor cells in nonpurified human mobilized peripheral blood mononuclear cells.

Authors:  Min Liang; Nonia Pariente; Kouki Morizono; Irvin S Y Chen
Journal:  J Gene Med       Date:  2009-03       Impact factor: 4.565

5.  The angiogenic potential of CD271+ human adipose tissue-derived mesenchymal stem cells.

Authors:  Richard J P Smith; Alessandro Faroni; James R Barrow; Jamie Soul; Adam J Reid
Journal:  Stem Cell Res Ther       Date:  2021-03-02       Impact factor: 6.832

Review 6.  The ex vivo purge of cancer cells using oncolytic viruses: recent advances and clinical implications.

Authors:  Jovian J Tsang; Harold L Atkins
Journal:  Oncolytic Virother       Date:  2015-01-23
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.