Clinical grade cell manipulation

被引:15
作者
Giordano, R [1 ]
Lazzari, L [1 ]
Rebulla, P [1 ]
机构
[1] Osped Maggiore, IRCCS, Ctr Transfus & Immunol Trapianti, Franco Calori Cell Factory, I-20122 Milan, Italy
关键词
cell manipulation; cell therapy; stem cells;
D O I
10.1111/j.1423-0410.2004.00537.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the past decade, a new form of therapy based on biological rather than pharmacological intervention has been developed. The term 'cell therapy', as applied to this new therapeutic tool, means the administration of living, non-germline somatic cells to humans for diagnostic or therapeutic purposes. Cell therapy products (CTPs) are generated by ex vivo processes, which comprise cell harvesting from patients or healthy donors, in vitro manipulation and administration of the manipulated cells to patients. The aim of ex vivo processes is to obtain cell subsets with defined functional properties that are capable of replacing or repairing damaged tissues or organs. Some examples of cell therapy are transplantation of expanded haematopoietic stem cells (HSCs), adoptive immunotherapy and dendritic cell vaccination to augment or restore the immune response for the treatment of malignant or infectious diseases. The types of cells most frequently used for cell therapy include haematopoietic pluripotent progenitor and stem cells from the bone marrow and peripheral blood, T-cell clones and dendritic cells. Although CTPs should be produced according to good manufacturing practice, they differ from traditional pharmaceutical products with regard to quality control and safety aspects. These differences prompted the development of a number of documents issued by regulatory bodies, which specifically address CTPs. This review discusses several issues related to the design, construction and validation of a hospital-based facility for the production of CTPs, the implementation of cell-manipulation processes and quality control of the final products.
引用
收藏
页码:65 / 72
页数:8
相关论文
共 18 条
[1]  
*EMEA, 2001, CPMPBWP41450 EMEA
[2]  
*FDA, GUID HUM SOM CELL TH
[3]   Stem cells: A new lease on life [J].
Fuchs, E ;
Segre, JA .
CELL, 2000, 100 (01) :143-155
[4]   Clinical-grade cell purification from thawed cord blood: an example of translational research [J].
Giordano, R ;
Lazzari, L ;
Montemurro, T ;
Lecchi, L ;
Porretti, L ;
Rebulla, P .
BONE MARROW TRANSPLANTATION, 2003, 32 (09) :965-966
[5]   Comparison of different serum-free media for ex vivo expansion of HPCs from cord blood using thrombopoietin, Flt-3 ligand, IL-6, and IL-11 [J].
Lazzari, L ;
Lucchi, S ;
Porretti, L ;
Montemurro, T ;
Giordano, R ;
Lopa, R ;
Rebulla, P ;
Sirchia, G .
TRANSFUSION, 2001, 41 (05) :718-719
[6]   Long-term expansion and maintenance of cord blood haematopoietic stem cells using thrombopoietin, Flt3-ligand, interleukin (IL)-6 and IL-11 in a serum-free and stroma-free culture system [J].
Lazzari, L ;
Lucchi, S ;
Rebulla, P ;
Porretti, L ;
Puglisi, G ;
Lecchi, L ;
Sirchia, G .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 112 (02) :397-404
[7]   Presence of IgE antibodies to bovine serum albumin in a patient developing anaphylaxis after vaccination with human peptide-pulsed dendritic cells [J].
Mackensen, A ;
Dräger, R ;
Schlesier, M ;
Mertelsmann, R ;
Lindemann, A .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2000, 49 (03) :152-156
[8]   ANAPHYLAXIS TO INFUSION OF AUTOLOGOUS BONE-MARROW - AN APPARENT REACTION TO SELF, MEDIATED BY IGE ANTIBODY TO BOVINE SERUM-ALBUMIN [J].
MACY, E ;
BULPITT, K ;
CHAMPLIN, RE ;
SAXON, A .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1989, 83 (05) :871-875
[9]   Developmental potential of somatic stem cells in mammalian adults [J].
Magli, MC ;
Levantini, E ;
Giorgetti, A .
JOURNAL OF HEMATOTHERAPY & STEM CELL RESEARCH, 2000, 9 (06) :961-969
[10]   Muscle-derived hematopoietic stem cells are hematopoietic in origin [J].
McKinney-Freeman, SL ;
Jackson, KA ;
Camargo, FD ;
Ferrari, G ;
Mavilio, F ;
Goodell, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (03) :1341-1346