Current status of genetic modification of T cells for cancer treatment

被引:16
作者
Dotti, G
Heslop, HE
机构
[1] Baylor Coll Med, Methodist Hosp, Ctr Gene & Cell Therapy, Houston, TX 77030 USA
[2] Baylor Coll Med, Methodist Hosp, Dept Pediat, Houston, TX 77030 USA
[3] Baylor Coll Med, Methodist Hosp, Dept Med, Houston, TX 77030 USA
[4] Texas Childrens Hosp, Houston, TX 77030 USA
关键词
cytotoxic T cells; immunotherapy;
D O I
10.1080/14653240510027217
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Clinical studies of adoptive immunotherapy with T cells have shown activity directed at hematologic and solid malignancies and viral infections. Genetic modification of infused T cells offers the prospect of improving such therapies and has already been used to track infused T cells, insert suicide genes and redirect the immune response towards specific Ag. Pre-clinical studies are evaluating novel approaches to genetically modify T cells to confer resistance to tumor evasion mechanisms. There is also increasing interest in developing suicide gene strategies as a failsafe mechanism to eradicate genetically modified cells should adverse effects occur.
引用
收藏
页码:262 / 272
页数:11
相关论文
共 68 条
[61]  
STRAATHOF KC, 2005, BLOOD 0222
[62]   Treatment of nasopharyngeal carcinoma with Epstein-Barr virus-specific T lymphocytes [J].
Straathof, KCM ;
Bollard, CM ;
Popat, U ;
Huls, MH ;
Lopez, T ;
Morriss, MC ;
Gresik, MV ;
Gee, AP ;
Russell, HV ;
Brenner, MK ;
Rooney, CM ;
Heslop, HE .
BLOOD, 2005, 105 (05) :1898-1904
[63]   Use of suicide gene-expressing donor T-cells to control alloreactivity after haematopoietic stem cell transplantation [J].
Tiberghien, P .
JOURNAL OF INTERNAL MEDICINE, 2001, 249 (04) :369-377
[64]   Administration of herpes simplex-thymidine kinase-expressing donor T cells with a T-cell-depleted allogeneic marrow graft [J].
Tiberghien, P ;
Ferrand, C ;
Lioure, B ;
Milpied, N ;
Angonin, R ;
Deconinck, E ;
Certoux, JM ;
Robinet, E ;
Saas, P ;
Petracca, B ;
Juttner, C ;
Reynolds, CW ;
Longo, DL ;
Herve, P ;
Cahn, JY .
BLOOD, 2001, 97 (01) :63-72
[65]   A strategy for treatment of Epstein-Barr virus-positive Hodgkin's disease by targeting interleukin 12 to the tumor environment using tumor antigen-specific T cells [J].
Wagner, HJ ;
Bollard, CM ;
Vigouroux, S ;
Huls, MH ;
Anderson, R ;
Prentice, HG ;
Brenner, MK ;
Heslop, HE ;
Rooney, CM .
CANCER GENE THERAPY, 2004, 11 (02) :81-91
[66]   RECONSTITUTION OF CELLULAR-IMMUNITY AGAINST CYTOMEGALOVIRUS IN RECIPIENTS OF ALLOGENEIC BONE-MARROW BY TRANSFER OF T-CELL CLONES FROM THE DONOR [J].
WALTER, EA ;
GREENBERG, PD ;
GILBERT, MJ ;
FINCH, RJ ;
WATANABE, KS ;
THOMAS, ED ;
RIDDELL, SR .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (16) :1038-1044
[67]   RETROVIRAL EXPRESSION OF THE HUMAN IL-2 GENE IN A MURINE T-CELL LINE RESULTS IN CELL-GROWTH AUTONOMY AND TUMORIGENICITY [J].
YAMADA, G ;
KITAMURA, Y ;
SONODA, H ;
HARADA, H ;
TAKI, S ;
MULLIGAN, RC ;
OSAWA, H ;
DIAMANTSTEIN, T ;
YOKOYAMA, S ;
TANIGUCHI, T .
EMBO JOURNAL, 1987, 6 (09) :2705-2709
[68]   Targeted delivery of adenoviral vectors by cytotoxic T cells [J].
Yotnda, P ;
Savoldo, B ;
Charlet-Berguerand, N ;
Rooney, C ;
Brenner, M .
BLOOD, 2004, 104 (08) :2272-2280