Characterization of novel breast carcinoma-associated BA46-derived peptides in HLA-A2.1/Db-β2m transgenic mice

被引:29
作者
Carmon, L
Bobilev-Priel, I
Brenner, B
Bobilev, D
Paz, A
Bar-Haim, E
Tirosh, B
Klein, T
Fridkin, M
Lemonnier, F
Tzehoval, E
Eisenbach, L [1 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[2] Tel Aviv Univ, Sackler Fac Med, Rabin Med Ctr, Inst Oncol, IL-69978 Tel Aviv, Israel
[3] Ben Gurion Univ Negev, Fac Hlth Sci, Soroka Med Ctr, Dept Oncol, IL-84105 Beer Sheva, Israel
[4] Tel Aviv Univ, Sackler Fac Med, Rabin Med Ctr, Tissue Typing Lab, IL-69978 Tel Aviv, Israel
[5] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
[6] Inst Pasteur, Antiviral Cellular Immun Unit, AIDS Retrovirus Dept, Paris, France
关键词
D O I
10.1172/JCI200214071
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
The human milk fat globule membrane protein BA46 (lactadherin) is highly overexpressed in human breast tumors, making it a potential target for tumor immunotherapy. We have identified BA46-derived peptides that contain the motif recognized by the MHC class I molecule HLA-A2.1 and that are processed and presented by human breast carcinoma cells. In mice lacking normal class I molecules but expressing an HLA-A2.1/D-b-beta2 microglobulin single chain (HHD mice), three peptides elicited specific CTL activity. Two of these peptides also stimulated cytotoxic activity in peripheral blood lymphocytes from HLA-A2.1-positive breast carcinoma patients. Adoptive transfer of HHD-derived bulk CTLs to nude mice bearing human breast carcinoma transplants reduced tumor growth. These peptides therefore represent naturally processed BA46-derived CTL epitopes that can be used in peptide-based antitumor vaccines.
引用
收藏
页码:453 / 462
页数:10
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