Acquired constitutive expression of interferon β after gene transduction enhances human immunodeficiency virus type 1-specific cytotoxic T lymphocyte activity by a RANTES-dependent mechanism

被引:7
作者
Hadida, F [1 ]
De Maeyer, E
Cremer, I
Autran, B
Baggiolini, M
Debré, P
Vieillard, V
机构
[1] Hop La Pitie Salpetriere, CNRS, UMR 7627, Lab Immunol Cellulaire, F-75013 Paris, France
[2] Inst Curie, CNRS, UMR 146, Lab Oncogenese Retrovirale & Mol, F-91405 Orsay, France
[3] Inst Curie, INSERM, U255, Lab Immunol Cellulaire & Clin, F-75005 Paris, France
[4] Univ Bern, Theodor Kocher Inst, CH-3000 Bern 9, Switzerland
[5] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
关键词
D O I
10.1089/10430349950017482
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
CTL lines directed against HIV-1 antigens were generated from infected individuals and were transduced by the HMB-K(b)HuIFN beta vector, resulting in low, constitutive expression of interferon beta (IFN-beta), The IFN-beta-transduced cells showed markedly increased HTV-1-specific, MHC class I-restricted CTL activity against HIV-1-LAI Gag, Pol, or Env antigens, This effect of IFN-P was correlated with an overexpression of RANTES and completely abrogated by RANTES-blocking antibody. The present results provide the first evidence that IFN-beta transduction of CTL lines enhances HTV-specific cytotoxic activities through an upregulation of RANTES production. The efficient elimination of HIV-infected cells by IFN-beta-transduced CTL lines makes this gene therapy approach an attractive treatment for AIDS.
引用
收藏
页码:1803 / 1810
页数:8
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