Gene therapy of lymphoma

被引:10
作者
Buttgereit, P [1 ]
Schmidt-Wolf, IGH [1 ]
机构
[1] Univ Bonn, Med Klin & Poliklin 1, D-53105 Bonn, Germany
来源
JOURNAL OF HEMATOTHERAPY & STEM CELL RESEARCH | 2002年 / 11卷 / 03期
关键词
D O I
10.1089/15258160260090924
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Gene therapy offers new and promising treatment for patients with hematological malignancies. Tumor cells-lymphoma cells, for example-are possible targets for gene therapy. In general, gene therapeutic approaches require efficient gene transfer into host cells and sufficient transgene expression. Although many methods of gene transfer into mammalian cells exist, most do not allow efficient DNA transfer into primary lymphocytes. In contrast to gene transfer into tumor cells and many other cell types, which can be successfully performed using a variety of methods, the efficient expression of foreign DNA in lymphoma cells presents unique problems and challenges, requiring a careful selection of the mode of gene transfer. In this review, we discuss the current strategies for gene therapy in the treatment of lymphoma. We also summarize the current gene transfer methods for lymphoma cells and efficiency of transgene expression.
引用
收藏
页码:457 / 467
页数:11
相关论文
共 94 条
  • [11] RAPID TRANSGENE EXPRESSION IN LYMPHOCYTE AND MACROPHAGE PRIMARY CULTURES AFTER PARTICLE BOMBARDMENT-MEDIATED GENE-TRANSFER
    BURKHOLDER, JK
    DECKER, J
    YANG, NS
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1993, 165 (02) : 149 - 156
  • [12] Efficient gene transfer into lymphoma cells using adenoviral vectors combined with lipofection
    Buttgereit, P
    Weineck, S
    Röpke, G
    Märten, A
    Brand, K
    Heinicke, T
    Caselmann, WH
    Huhn, D
    Schmidt-Wolf, IGH
    [J]. CANCER GENE THERAPY, 2000, 7 (08) : 1145 - 1155
  • [13] Effects of adenoviral wild-type p53 gene transfer in p53-mutated lymphoma cells
    Buttgereit, P
    Schakowski, F
    Märten, A
    Brand, K
    Renoth, S
    Ziske, C
    Schöttker, B
    Ebert, O
    Schroers, R
    Schmidt-Wolf, IGH
    [J]. CANCER GENE THERAPY, 2001, 8 (06) : 430 - 439
  • [14] Adenovirus vector infection of chronic lymphocytic leukemia B cells
    Cantwell, MJ
    Sharma, S
    Friedmann, T
    Kipps, TJ
    [J]. BLOOD, 1996, 88 (12) : 4676 - 4683
  • [15] T cell activation following infection of primary follicle center lymphoma B cells with adenovirus encoding CD154
    Cantwell, MJ
    Wierda, WG
    Lossos, IS
    Levy, R
    Kipps, TJ
    [J]. LEUKEMIA, 2001, 15 (09) : 1451 - 1457
  • [16] GENETIC MECHANISMS OF TUMOR SUPPRESSION BY THE HUMAN P53 GENE
    CHEN, PL
    CHEN, YM
    BOOKSTEIN, R
    LEE, WH
    [J]. SCIENCE, 1990, 250 (4987) : 1576 - 1580
  • [17] Cherney BW, 1997, CANCER RES, V57, P2508
  • [18] High-efficiency transfer of the T cell co-stimulatory molecule B7-2 to lymphoid cells using high-titer recombinant adeno-associated virus vectors
    Chiorini, JA
    Wendtner, CM
    Urcelay, E
    Safer, B
    Hallek, M
    Kotin, RM
    [J]. HUMAN GENE THERAPY, 1995, 6 (12) : 1531 - 1541
  • [19] On the mechanism of DNA transfection: efficient gene transfer without viruses
    Coonrod, A
    Li, FQ
    Horwitz, M
    [J]. GENE THERAPY, 1997, 4 (12) : 1313 - 1321
  • [20] COTTER FE, 1994, ONCOGENE, V9, P3049