Large-scale generation of natural killer lymphocytes for clinical application

被引:68
作者
Luhm, J [1 ]
Brand, JM [1 ]
Koritke, P [1 ]
Höppner, M [1 ]
Kirchner, H [1 ]
Frohn, C [1 ]
机构
[1] Med Univ Lubeck, Sch Med, Inst Immunol & Transfus Med, D-23538 Lubeck, Germany
来源
JOURNAL OF HEMATOTHERAPY & STEM CELL RESEARCH | 2002年 / 11卷 / 04期
关键词
D O I
10.1089/15258160260194794
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Natural killer (NK) lymphocytes can be used for adoptive immunotherapeutic strategies. Alternatively, they may be employed as adjuvants for stem cell/bone marrow transplantation, either to reinduce remission, or to purge autografts of contaminating malignant cells. We developed a new protocol that enables the generation of NK cells on a clinical scale in a closed system that enables good manufacturing practice (GMP) conformity. Aside from the initial NK cell inoculum, our protocol includes activated feeder cells [irradiated peripheral blood mononuclear cells (PBMC) and no transformed blasts], cytokines [interleukin-2 (IL-2) and IL-15], human serum, and a complex basic media formulation. During the whole expansion period of approximately 14 days, the cells were handled in PTFE (Teflon) bags, whereby fresh medium was added without opening the system. The use of immortalized or virus-transformed feeder cells, as used in many other current research protocols, was completely avoided. A precise controlling of a number of environmental factors was necessary to achieve reproducible results. Increases in NK cell number ranged between 80- and 200-fold. The resulting NK cells were CD56(+), CD3(-), and CD16(+) (75%). They were highly cytotoxic against different malignant target cells and did not produce significant levels of interferon-gamma. Therefore, they belonged to the cytotoxic rather than the immunoregulatory NK subpopulation. No nonspecific activation against normal allogenous lymphocytes occurred. This work might permit the realization of future protocols for evaluating the clinical effect of NK lymphocytes in human disease.
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页码:651 / 657
页数:7
相关论文
共 31 条
[1]  
Aloe L, 1999, MICROSC RES TECHNIQ, V45, P285, DOI 10.1002/(SICI)1097-0029(19990515/01)45:4/5<285::AID-JEMT12>3.0.CO
[2]  
2-3
[3]  
Barao Isabel, 1998, Archivum Immunologiae et Therapiae Experimentalis, V46, P213
[4]   A new method for in vitro expansion of cytotoxic human CD3-CD56+ natural killer cells [J].
Carlens, S ;
Gilljam, M ;
Chambers, BJ ;
Aschan, J ;
Guven, H ;
Ljunggren, HG ;
Christensson, B ;
Dilber, MS .
HUMAN IMMUNOLOGY, 2001, 62 (10) :1092-1098
[5]   Ex vivo expansion of CD56+ cytotoxic cells from human umbilical cord blood [J].
Condiotti, R ;
Zakai, YB ;
Barak, V ;
Nagler, A .
EXPERIMENTAL HEMATOLOGY, 2001, 29 (01) :104-113
[6]   Human natural killer cells:: a unique innate immunoregulatory role for the CD56bright subset [J].
Cooper, MA ;
Fehniger, TA ;
Turner, SC ;
Chen, KS ;
Ghaheri, BA ;
Ghayur, T ;
Carson, WE ;
Caligiuri, MA .
BLOOD, 2001, 97 (10) :3146-3151
[7]   IMMUNOTHERAPY WITH INTERLEUKIN-2 (IL2) AND LYMPHOKINE-ACTIVATED NATURAL-KILLER-CELLS - IMPROVEMENT OF CLINICAL-RESPONSES IN METASTATIC RENAL-CELL CARCINOMA PATIENTS PREVIOUSLY TREATED WITH IL2 [J].
ESCUDIER, B ;
FARACE, F ;
ANGEVIN, E ;
CHARPENTIER, F ;
NITENBERG, G ;
TRIEBEL, F ;
HERCEND, T .
EUROPEAN JOURNAL OF CANCER, 1994, 30A (08) :1078-1083
[8]   LOSS OF HLA CLASS-I ANTIGENS BY MELANOMA-CELLS - MOLECULAR MECHANISMS, FUNCTIONAL-SIGNIFICANCE AND CLINICAL RELEVANCE [J].
FERRONE, S ;
MARINCOLA, FM .
IMMUNOLOGY TODAY, 1995, 16 (10) :487-494
[9]   Feasibility of the adoptive transfusion of allogenic human leukocyte antigen-matched natural killer cells in patients with renal cell carcinoma [J].
Frohn, C ;
Doehn, C ;
Durek, C ;
Böhle, A ;
Schlenke, P ;
Jocham, D ;
Kirchner, H .
JOURNAL OF IMMUNOTHERAPY, 2000, 23 (04) :499-504
[10]   NATURAL-HISTORY OF HLA EXPRESSION DURING TUMOR-DEVELOPMENT [J].
GARRIDO, F ;
CABRERA, T ;
CONCHA, A ;
GLEW, S ;
RUIZCABELLO, F ;
STERN, PL .
IMMUNOLOGY TODAY, 1993, 14 (10) :491-499