CTLA-4 blockade in combination with xenogeneic DNA vaccines enhances T-cell responses, tumor immunity and autoimmunity to self antigens in animal and cellular model systems

被引:95
作者
Gregor, PD
Wolchok, JD
Ferrone, CR
Buchinshky, H
Guevara-Patiño, JA
Perales, MA
Mortazavi, F
Bacich, D
Heston, W
Latouche, JB
Sadelain, M
Allison, JP
Scher, HI
Houghton, AN
机构
[1] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[2] Cleveland Clin, Dept Canc Biol, Cleveland, OH 44106 USA
[3] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[4] Cornell Univ, Grad Sch, New York, NY 10021 USA
[5] Cornell Univ, Weill Med Sch, New York, NY 10021 USA
关键词
CTLA-4; DNA vaccine; tumor immunity;
D O I
10.1016/j.vaccine.2003.10.048
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Xenogeneic DNA vaccination can elicit tumor immunity through T cell and antibody-dependent effector mechanisms. Blockade of CTLA-4 engagement with B7 expressed on APCs has been shown to enhance T cell-dependent immunity. We investigated whether CTLA-4 blockade could increase T-cell responses and tumor immunity elicited by DNA vaccines. CTLA-4 blockade enhanced B 16 tumor rejection in mice immunized against the melanoma differentiation antigens tyrosinase-related protein 2 and gp100, and this effect was stronger when anti-CTLA-4 was administered with booster vaccinations. CTLA-4 blockade also increased the T-cell responses to prostate-specific membrane antigen (PSMA) when given with the second or third vaccination. Based on these pre-clinical studies, we suggest that anti-CTLA-4 should be tested with xenogeneic DNA vaccines against cancer and that special attention should be given to sequence and schedule of administration. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1700 / 1708
页数:9
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