HUMAN LYMPHOCYTES-T RECOGNIZE A PEPTIDE OF SINGLE POINT-MUTATED, ONCOGENIC RAS PROTEINS

被引:214
|
作者
JUNG, S
SCHLUESENER, HJ
机构
[1] Department of Neurology, Neuroimmunology Branch, University of Würzburg
[2] Department of Neurology, Neuroimmunology Branch, University of Würzburg, D-8700 Würzburg
来源
JOURNAL OF EXPERIMENTAL MEDICINE | 1991年 / 173卷 / 01期
关键词
D O I
10.1084/jem.173.1.273
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
P21ras proteins are thought to play an important role in cell proliferations and differentiation. Single nucleotide mutations in the encoding cellular photo-oncogenes often result in p21ras proteins with transforming activity. Such activated ras oncogenes have been demonstrated in a variety of human malignancies and also in preneoplastic changes. Using a synthetic peptide corresponding to amino acids 5-16 of mutated p21ras proteins with an exchange of the normal glycine at position 12 by valine, it is shown here that human CD4+ T cells specifically recognize the mutated protein sequence and can be generated as antigen-specific T lymphocyte lines. The fact that these T lines did not crossreact to the sequence of normal p21ras proteins offers new perspectives for specific immunotherapy of human malignancies and even precancerous lesions.
引用
收藏
页码:273 / 276
页数:4
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