CYTOTOXIC T-CELLS ISOLATED FROM OVARIAN MALIGNANT ASCITES RECOGNIZE A PEPTIDE DERIVED FROM THE HER-2/NEU PROTOONCOGENE

被引:121
作者
IOANNIDES, CG
FISK, B
FAN, D
BIDDISON, WE
WHARTON, JT
OBRIAN, CA
机构
[1] NIH,BETHESDA,MD 20892
[2] NIND,NEUROIMMUNOL BRANCH,MOLEC IMMUNOL SECT,BETHESDA,MD 20892
[3] MD ANDERSON CANC CTR,DEPT CELL BIOL,HOUSTON,TX 77030
关键词
D O I
10.1006/cimm.1993.1233
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The HER-2/neu proto-oncogene encodes a transmembrane receptor protein whose expression is enhanced in a number of breast and ovarian tumors and correlates with tumor aggressiveness, suggesting that it may play an important role in tumor growth. Recent evidence suggests that HER-2/neu may be a potential candidate for targeted immune intervention. In this report we show that cytotoxic T lymphocytes (CTL) expanded from tumor-associated lymphocytes with HLA-A2+ and HER-2/neu+ tumors can specifically recognize synthetic peptides corresponding to amino acids 971-980 of HER-2/neu protein. This sequence includes a potential amphiphilic are containing both Rothbard’s epitope motifs and HLA-A2 anchor residues. Our study provides the first direct evidence of HER-2/neu-reactive CTL in humans. The fact that these HER-2/neu peptide-reactive CTL show significantly lower reactivity with corresponding EGF-R peptides offers new perspectives for understanding the recognition of self-antigens by tumor-reactive T cells. © 1993 Academic Press, Inc.
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收藏
页码:225 / 234
页数:10
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