Co-expression of bfl-1 enhances host response in the herpes simplex virus-thymidine kinase/ganciclovir gene therapy system

被引:24
作者
Kwon, GY
Jeong, J
Woo, JK
Choi, HY
Lee, MJ
Ko, JK
Shim, YH
Kim, CW
机构
[1] Seoul Natl Univ, Coll Med, Inst Canc Res, Tumor Immun Med Res Ctr,Dept Pathol,Chongno Gu, Seoul 110799, South Korea
[2] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pathol,Kangnam Ku, Seoul 135710, South Korea
[3] Konkuk Univ, Coll Sci, Dept Biol Sci, Seoul, South Korea
关键词
gene therapy; herpes simplex virus; thymidine kinase; ganciclovir; bfl-1;
D O I
10.1016/S0006-291X(03)00417-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Anticancer suicide gene therapy using herpes simplex virus-thymidine kinase (HSV-tk) and ganciclovir (GCV) features the unique advantage of being able to elicit brisk host immune response against tumors and the host response reportedly can be potentiated with the co-expression of other appropriate immune- or apoptosis-related genes. We introduced a novel antiapoptotic gene, bfl-1, to test its applicability in the HSV-tk/GCV system. CT-26 murine colon cancer cells transfected with HSV-tk, alone or in combination with bcl-xL or bfl-1, were either grown in vitro or injected into syngeneic mice, followed by GCV administration. The co-expression of bfl-1 was associated with the upregulation of CD95 and CD40 ligand (CD40L) in vitro and with pronounced intratumoral T-lymphocyte infiltration in vivo. These results add to the previous findings that antiapoptotic genes can be used as an adjunctive component in the HSV-tk/GCV system to enhance host immune response against tumors. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:756 / 763
页数:8
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