Gene transfer in haematological malignancy

被引:6
作者
Brenner, MK
机构
[1] St. Jude Children's Research Hospital, Memphis, TN
[2] Cell and Gene Therapy Program, St. Jude Children's Research Hospital, Memphis, TN 38105-2794
关键词
cytotoxic T cells; gene therapy; haematological malignancies; haematopoietic stem cells; vectors;
D O I
10.3109/07853899608999113
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although gene transfer was first suggested to treat inherited monogenic disorders, at present most clinical protocols are intended to treat patients with malignant disease. Although current vector technologies profoundly limit the potential therapeutic applications of gene transfer, the technique is already being successfully used to complement longer established therapies. This article reviews current and forthcoming applications of gene transfer to treat haematological malignancies.
引用
收藏
页码:491 / 497
页数:7
相关论文
共 56 条
[11]   INVIVO GENE-TRANSFER WITH RETROVIRAL VECTOR PRODUCER CELLS FOR TREATMENT OF EXPERIMENTAL BRAIN-TUMORS [J].
CULVER, KW ;
RAM, Z ;
WALLBRIDGE, S ;
ISHII, H ;
OLDFIELD, EH ;
BLAESE, RM .
SCIENCE, 1992, 256 (5063) :1550-1552
[12]  
DEFABRITIIS P, 1989, BONE MARROW TRANSPL, V4, P669
[13]   GENETIC MARKING SHOWS THAT PH(+) CELLS PRESENT IN AUTOLOGOUS TRANSPLANTS OF CHRONIC MYELOGENOUS LEUKEMIA (CML) CONTRIBUTE TO RELAPSE AFTER AUTOLOGOUS BONE-MARROW IN CML [J].
DEISSEROTH, AB ;
ZU, ZF ;
CLAXTON, D ;
HANANIA, EG ;
FU, SQ ;
ELLERSON, D ;
GOLDBERG, L ;
THOMAS, M ;
JANICEK, K ;
ANDERSON, WF ;
HESTER, J ;
KORBLING, M ;
DURETT, A ;
MOEN, R ;
BERENSON, R ;
HEIMFELD, S ;
HAMER, J ;
CALVERT, L ;
TIBBITS, P ;
TALPAZ, M ;
KANTARJIAN, H ;
CHAMPLIN, R ;
READING, C .
BLOOD, 1994, 83 (10) :3068-3076
[14]   GENE-TRANSFER INTO HEMATOPOIETIC-CELLS - IMPLICATIONS FOR CANCER-THERAPY [J].
DUNBAR, CE ;
BODINE, DM ;
SORRENTINO, B ;
DONAHUE, R ;
MCDONAGH, K ;
COTTLERFOX, M ;
OSHAUGHNESSY, J ;
COWAN, K ;
CARTER, C ;
DOREN, S ;
CASSELL, A ;
NIENHUIS, AW .
GENE THERAPY FOR NEOPLASTIC DISEASES, 1994, 716 :216-224
[15]   INTERLEUKIN-2 PRODUCTION BY TUMOR-CELLS BYPASSES T-HELPER FUNCTION IN THE GENERATION OF AN ANTITUMOR RESPONSE [J].
FEARON, ER ;
PARDOLL, DM ;
ITAYA, T ;
GOLUMBEK, P ;
LEVITSKY, HI ;
SIMONS, JW ;
KARASUYAMA, H ;
VOGELSTEIN, B ;
FROST, P .
CELL, 1990, 60 (03) :397-403
[16]  
FUJIWARA T, 1993, CANCER RES, V53, P4129
[17]   SELECTIVE PURGING BY HUMAN INTERLEUKIN-2 ACTIVATED LYMPHOCYTES OF BONE MARROWS CONTAMINATED WITH A LYMPHOMA LINE OR AUTOLOGOUS LEUKEMIC-CELLS [J].
GAMBACORTIPASSERINI, C ;
RIVOLTINI, L ;
FIZZOTTI, M ;
RODOLFO, M ;
SENSI, ML ;
CASTELLI, C ;
ORAZI, A ;
POLLI, N ;
BREGNI, M ;
SIENA, S ;
BORIN, L ;
POGLIANI, E ;
CORNEO, GM ;
PARMIANI, G .
BRITISH JOURNAL OF HAEMATOLOGY, 1991, 78 (02) :197-205
[18]   INTERLEUKIN-2 GENE-TRANSFER INTO TUMOR-CELLS ABROGATES TUMORIGENICITY AND INDUCES PROTECTIVE IMMUNITY [J].
GANSBACHER, B ;
ZIER, K ;
DANIELS, B ;
CRONIN, K ;
BANNERJI, R ;
GILBOA, E .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (04) :1217-1224
[19]   AUTOLOGOUS BONE-MARROW TRANSPLANTATION FOLLOWING HIGH-DOSE CHEMOTHERAPY FOR THE TREATMENT OF ADULT PATIENTS WITH ACUTE MYELOID-LEUKEMIA [J].
GOLDSTONE, AH ;
ANDERSON, CC ;
LINCH, DC ;
FRANKLIN, IM ;
BOUGHTON, BJ ;
CAWLEY, JC ;
RICHARDS, JDM .
BRITISH JOURNAL OF HAEMATOLOGY, 1986, 64 (03) :529-537
[20]   TREATMENT OF ESTABLISHED RENAL-CANCER BY TUMOR-CELLS ENGINEERED TO SECRETE INTERLEUKIN-4 [J].
GOLUMBEK, PT ;
LAZENBY, AJ ;
LEVITSKY, HI ;
JAFFEE, LM ;
KARASUYAMA, H ;
BAKER, M ;
PARDOLL, DM .
SCIENCE, 1991, 254 (5032) :713-716