Induction of HLA-A2-restricted CTL responses by a tubular structure carrying human melanoma epitopes

被引:9
作者
Ghosh, MK
Li, CL
Fayolle, C
Dadaglio, G
Murphy, A
Lemonnier, FA
Roy, P
Leclerc, C
机构
[1] Inst Pasteur, Unite Biol Regulat Immunitaires, F-75724 Paris 15, France
[2] Univ Alabama Birmingham, Sch Med, Dept Med, Div Geog Med, Birmingham, AL 35924 USA
[3] Inst Pasteur, Unite Immunol Cellulaire Antivirale, F-75724 Paris 15, France
[4] Univ London London Sch Hyg & Trop Med, Dept Infect & Trop Dis, London WC1E 7HT, England
关键词
melanoma; HHD mice; CTL responses; chimeric BTV NS1 tubules;
D O I
10.1016/S0264-410X(02)00185-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Epitope-based vaccination strategies designed to induce strong tumor-specific CD8(+) T cell responses are being widely considered for cancer immunotherapy. Here, two recombinant tubular structures, NS1-Mela 1 and NS1-Mela 2, carrying, respectively two HLA-A2 epitopes derived from human melanoma antigens were constructed and their capability to induce CTL responses in vivo were studied in HLA-A2 transgenic mice. Strong CTL responses specific for GnT-V/NA 17-A and gp100 (154-162) epitopes were generated in HLA-A2 transgenic mice immunized by the construct NS1-Mela 1 carrying these two epitopes. The second construct NS1-Mela 2 carrying both Tyrosinase (369-377 Da) and Melan-A/Mart-1 (27-35) epitopes induced a weak Tyrosinase-specific CTL response in mice but failed to induce specific CTL responses against the Melan-A/Mart-1 (27-35) epitope in the tested mice. Thus, recombinant tubular structures containing multiple tumoral epitopes may lead to new strategies for the induction of strong tumor-specific CTL responses in cancer patients. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2463 / 2473
页数:11
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