Identification of MAGE-3 epitopes presented by HLA-DR molecules to CD4+ T lymphocytes

被引:198
作者
Chaux, P
Vantomme, V
Stroobant, V
Thielemans, K
Corthals, J
Luiten, R
Eggermont, AMM
Boon, T
van der Bruggen, P
机构
[1] Catholic Univ Louvain, Ludwig Inst Canc Res, B-1200 Brussels, Belgium
[2] Free Univ Brussels, Sch Med, Physiol Lab, B-1070 Brussels, Belgium
[3] Univ Rotterdam Hosp, Dept Surg Oncol, Dr Daniel Den Hoed Canc Ctr, NL-3075 EA Rotterdam, Netherlands
关键词
human; invariant chain; peptide; tumor; histocompatibility leukocyte antigen class II;
D O I
10.1084/jem.189.5.767
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
MAGE-type genes are expressed by many tumors of different histological types and not by normal cells, except for male germline cells, which do not express major histocompatibility complex (MHC) molecules. Therefore, the antigens encoded by MAGE-type genes are strictly tumor specific and common to many tumors. We describe here the identification of the first MAGE-encoded epitopes presented by histocompatibility leukocyte antigen (HLA) class II molecules to CD4(+) T lymphocytes. Monocyte-derived dendritic cells were loaded with a MAGE-3 recombinant protein and used to stimulate autologous CD4(+) T cells. We isolated CD4(+) T cell clones that recognized two different MAGE-3 epitopes, MAGE-3(114-127) and MAGE-3(121-134), both presented by the HLA-DR13 molecule, which is expressed in 20% of Caucasians. The second epitope is also encoded by MAGE-1, -2, and -6. Our procedure should be applicable to other proteins for the identification of new tumor-specific antigens presented by HLA class II molecules. The knowledge of such antigens will be useful for evaluation of the immune response of cancer patients immunized with proteins or with recombinant viruses carrying entire genes coding for tumor antigens. The use of antigenic peptides presented by class II in addition to peptides presented by class I may also improve the efficacy of therapeutic antitumor vaccination.
引用
收藏
页码:767 / 777
页数:11
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