An alternative open reading frame of the human macrophage colony-stimulating factor gene is independently translated and codes for an antigenic peptide of 14 amino acids recognized by tumor-infiltrating CD8 T lymphocytes

被引:82
作者
Probst-Kepper, M
Stroobant, V
Kridel, R
Gaugler, B
Landry, C
Brasseur, F
Cosyns, JP
Weynand, B
Boon, T
Van den Eynde, BJ
机构
[1] Catholic Univ Louvain, Ludwig Inst Canc Res, B-1200 Brussels, Belgium
[2] Catholic Univ Louvain, Cellular Genet Unit, B-1200 Brussels, Belgium
[3] Catholic Univ Louvain, Dept Pathol, B-1200 Brussels, Belgium
[4] German Res Ctr Biotechnol, Mol Immunol Grp, D-38124 Braunschweig, Germany
关键词
renal cell carcinoma; HLA-B35; translation; peptide binding; natural peptide;
D O I
10.1084/jem.193.10.1189
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We show that cytotoxic T lymphocytes (CTLs) infiltrating a kidney tumor recognize a peptide encoded by an alternative open reading frame (ORF) of the macrophage colony-stimulating factor (M-CSF) gene. Remarkably, this alternative ORF, which is translated in many tumors concurrently with the major ORF, is also translated in some tissues that do not product M-CSF, such as liver and kidney. Such a dissociation of the translation of two overlapping ORFs from the same gene is unexpected. The antigenic peptide encoded by the alternative ORF is presented by human histocompatibility leukocyte antigen (HLA)-B(*)3501 and has a length of 14 residues. peptide elution indicated that tumor cells naturally present this 14 mer, which is the longest peptide known to be recognized by CTL.s. Binding studies of peptide analogues suggest that it binds by its two extremities and bulges out of the HLA groove to compensate for its length.
引用
收藏
页码:1189 / 1198
页数:10
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