用于肿瘤基因治疗的慢病毒载体研究进展(3)

2012-08-26 23:47

  [2]HAASE A T. Viral gene expression and pathogenesis in three emerging diseases: HIV and AIDS; HTLV?Ⅰ and HAM/TSP; and HHV?8 and Kaposi’s sarcoma[J]. FEMS Immunol Med Microbiol, 1997,18:301?305.

  [3]ZAULI G, GIBELLINI D. He human immunodeficiency virus type?1 (HIV?1) Tat protein and Bcl?2 gene expression[J]. Leuk Lymphoma, 1996,23:551?560.

  [4]GORLICH D, MATTAJ I W. Nucleocytoplasmic transport[J]. Science, 1996,5:1513?1519.

  [5]THESLEFF I A. The role of growth factors in tooth development[J]. Int Rev Cytol, 2002,217:93?135.

  [6]ZUFFEREY R, NAGY D, MANDEL R J, et al. Mutiply attenuated lentiviral vector achieved efficient gene delivery in vivo[J]. Nat Biotechnol, 1997,15(9):871?875.

  [7]SCHERR M, EDER M. Gene transfer into hematopoietic stem cells using lentiviral vectors[J]. Curt Gene Ther, 2002,2(1):45?55.

  [8]NALDINI L, BLOMER U, GALLAY P, et al. In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector[J]. Science, 1996, 272:263?267.

  [9]KAFRI T, BLOMER U, PETERSON DA, et al. Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors[J]. Nat Genet, 1997,17:314?317.

  [10]TRONO D. Lentiviral vectors: turning a deadly foe into a therapeutic agent[J]. Gene Ther, 2000,7(1):20?23.

  [11]ANTHONY S, WHITEHEAD P R, ANDREY A K. Use of recombinant lentivirus pseudotyped with vesicular stomatitis virus glycoprotein G for efficient generation of human anti?cancer chimeric T cells by transduction of human peripheral blood lymphocytes in vitro[J]. Virol J, 2006,3(8):1?10.

  [12]杨宇,吴江,杨欣,等. 携强绿色荧光蛋白重组慢病毒的构建及其在原代培养SD大鼠皮层神经细胞中的表达[J]. 吉林大学学报:医学版, 2007,33(2):237?241.

  [13]WONG L F, GOODHEAD L, PRAT C, et al.Lentivirus?mediated gene transfer to the central nervous system: therapeutic and research applications[J]. Hum Gene Ther, 2006,17(1):1?9.

  [14]马晓生,姜建元,吕飞舟,等. 腺病毒和慢病毒载体感染骨髓间质干细胞的比较[J]. 中华医学杂志, 2006,86(47):3340?3344.

  [15]李振宇,徐开林,潘秀英,等. 慢病毒载体介导绿色荧光蛋白基因在小鼠T淋巴细胞中的表达[J]. 中国实验血液学杂志, 2007,15(1):125?128.

  [16]陈香梅,徐开林,潘秀英,等. 携带绿色荧光蛋白基因的逆转录病毒载体的构建及其介导的T 细胞基因转移研究[J]. 中国实验血液学杂志, 2005,13:641?644.

  [17]林健,戴学军,王伟民,等. 慢病毒在大鼠胶质瘤细胞基因转导中的应用[J]. 中国微侵袭神经外科杂志, 2007,12(8):358?362.

  [18]MAY C, RIVELLA S, CALLEGARI J, et al. Therapeutic haemoglobin synthesis in beta?thalassaemic mice expressing lentivirus?encoded human beta?globin[J]. Nature, 2000,406(6791):82?86.

  [19]CARROLL R, LIN J T, DACQUEL E J, et al. A human immunodeficiency virus type?1 (HIV?1)?based retroviral vector system utilizing stable HIV?1 pakaging cell lines[J]. J Virol, 1994,68(9):6047?6051.

  [20]GORBEAU P, KRAUS G, WONG?STAAL F. Efficient gene transfer by a human immunoddficiency virus type?1 (HIV?1)?derived vector utilizing a stable HIV pakaging cell line[J]. Proc Nat1 Acad Sci USA, 1996,93(24):14070?14075.

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