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
相关论文
共 33 条
[1]  
BARRA C, 1993, J IMMUNOL, V150, P3681
[2]   BAGE - A NEW GENE ENCODING AN ANTIGEN RECOGNIZED ON HUMAN MELANOMAS BY CYTOLYTIC T-LYMPHOCYTES [J].
BOEL, P ;
WILDMANN, C ;
SENSI, ML ;
BRASSEUR, R ;
RENAULD, JC ;
COULIE, P ;
BOON, T ;
VANDERBRUGGEN, P .
IMMUNITY, 1995, 2 (02) :167-175
[3]   Identification of HLA-A2-restricted T-cell epitopes derived from the MUC1 tumor antigen for broadly applicable vaccine therapies [J].
Brossart, P ;
Heinrich, KS ;
Stuhler, G ;
Behnke, L ;
Reichardt, VL ;
Stevanovic, S ;
Muhm, A ;
Rammensee, HG ;
Kanz, L ;
Brugger, W .
BLOOD, 1999, 93 (12) :4309-4317
[4]  
Carmon L, 2000, INT J CANCER, V85, P391
[5]   CIRCULATING HUMAN MAMMARY EPITHELIAL ANTIGENS IN BREAST-CANCER [J].
CERIANI, RL ;
SASAKI, M ;
SUSSMAN, H ;
WARA, WM ;
BLANK, EW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (17) :5420-5424
[6]   Cloning and sequence analysis of human breast epithelial antigen BA46 reveals an RGD cell adhesion sequence presented on an epidermal growth factor-like domain [J].
Couto, JR ;
Taylor, MR ;
Godwin, SG ;
Ceriani, RL ;
Peterson, JA .
DNA AND CELL BIOLOGY, 1996, 15 (04) :281-286
[7]   Isolation and characterization of full and truncated forms of human breast carcinoma protein BA46 from human milk fat globule membranes [J].
Giuffrida, MG ;
Cavaletto, M ;
Giunta, C ;
Conti, A ;
Godovac-Zimmermann, J .
JOURNAL OF PROTEIN CHEMISTRY, 1998, 17 (02) :143-148
[8]   The polymorphic epithelial mucin: Potential as an immunogen for a cancer vaccine [J].
Graham, RA ;
Burchell, JM ;
TaylorPapadimitriou, J .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 1996, 42 (02) :71-80
[9]   Medin:: An integral fragment of aortic smooth muscle cell-produced lactadherin forms the most common human amyloid [J].
Häggqvist, B ;
Näslund, J ;
Sletten, K ;
Westermark, GT ;
Mucchiano, G ;
Tjernberg, LO ;
Nordstedt, C ;
Engström, U ;
Westermark, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (15) :8669-8674
[10]   Identification of a factor that links apoptotic cells to phagocytes [J].
Hanayama, R ;
Tanaka, M ;
Miwa, K ;
Shinohara, A ;
Iwamatsu, A ;
Nagata, S .
NATURE, 2002, 417 (6885) :182-187