An immunodominant SSX-2-derived epitope recognized by CD4+ T cells in association with HLA-DR

被引:30
|
作者
Ayyoub, M
Hesdorffer, CS
Montes, M
Merlo, A
Speiser, D
Rimoldi, D
Cerottini, JC
Ritter, G
Scanlan, M
Old, LJ
Valmori, D
机构
[1] Columbia Univ Coll Phys & Surg, Dept Med, Ludwig Inst Clin Trial Ctr, Div Med Oncol, New York, NY 10032 USA
[2] Univ Lausanne Hosp, Ludwig Inst Canc Res, Div Clin Oncoimmunol, Lausanne, Switzerland
[3] Mem Sloan Kettering Canc Ctr, Ludwig Inst Canc Res, New York Branch, New York, NY 10021 USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 2004年 / 113卷 / 08期
关键词
D O I
10.1172/JCI200420667
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Ectopic gene expression in tumors versus normal somatic tissues provides opportunities for the specific immunotargeting of cancer cells. SSX gene products are expressed in tumors of different histological types and can be recognized by tumor-reactive CTLs from cancer patients. Here, we report the identification of an SSX-2-derived immunodominant T cell epitope recognized by CD4(+) T cells from melanoma patients in association with HLA-DR. The epitope maps to the 37-58 region of the protein, encompassing the sequence of the previously defined HLA-A2-restricted immunodominant epitope SSX-2(41-49). SSX-2(37-58)-specific CD4(+) T cells were detected among circulating lymphocytes from the majority of melanoma patients analyzed and among tumor-infiltrating lymphocytes, but not in healthy donors. Together, our data suggest a dominant role of the 37-58 sequence in the induction of cellular CD4(+)T cell responses against SSX antigens and will be instrumental for both the onset and the monitoring of upcoming cancer-vaccine trials using SSX-derived immunogens.
引用
收藏
页码:1225 / 1233
页数:9
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