The hematopoietic system-specific minor histocompatibility antigen HA-1 shows aberrant expression in epithelial cancer cells

被引:67
作者
Klein, CA
Wilke, M
Pool, J
Vermeulen, C
Blokland, E
Burghart, E
Krostina, S
Wendler, N
Passlick, B
Riethmüeller, G
Goulmy, E
机构
[1] Leiden Univ, Med Ctr, Dept Immunohematol & Blood Transfus, NL-2333 ZA Leiden, Netherlands
[2] Univ Munich, Klinikum Innenstadt, Dept Immunol, D-80336 Munich, Germany
[3] Univ Munich, Klinikum Innenstadt, Chirurg Klin, D-80336 Munich, Germany
关键词
stem cell transplantation; graft-versus-tumor; carcinomas; cytotoxic T cells; minimal residual disease;
D O I
10.1084/jem.20011838
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Allogeneic stem cell transplantation (SCT) can induce curative graft-versus-tumor reactions in patients with hematological malignancies and solid tumors. The graft-versus-tumor reaction after human histocompatibility leukocyte antigen (HLA)-identical SCT is mediated by alloimmune donor T cells specific for polymorphic minor histocompatibility antigens (mHags). Among these, the mHag HA-1 was found to be restricted to the hematopoietic system. Here, we report on the HA-1 ribonucleic acid expression by microdissected carcinoma tissues and by single disseminated tumor cells isolated from patients with various epithelial tumors. The HA-1 peptide is molecularly defined, as it forms an immunogenic peptide ligand with HLA-A2 on the cell membrane of carcinoma cell lines. HA-1-specific cytotoxic T cells lyse epithelial tumor cell lines in vitro, whereas normal epithelial cells are not recognized. Thus, HA-1-specific immunotherapy combined with HLA-identical allogeneic SCT may now be feasible for patients with HA-1(+) carcinomas.
引用
收藏
页码:359 / 368
页数:10
相关论文
共 31 条
[1]   Potential allogeneic graft-versus-tumor effect in a patient with ovarian cancer [J].
Bay, JO ;
Choufi, B ;
Pomel, C ;
Dauplat, J ;
Durando, X ;
Tournilhac, O ;
Travade, P ;
Plagne, R ;
Blaise, D .
BONE MARROW TRANSPLANTATION, 2000, 25 (06) :681-682
[2]   Graft-versus-tumour and graft-versus-leukaemia effect in patient with concurrent breast cancer and acute myelocytic leukaemia [J].
BenYosef, R ;
Or, R ;
Nagler, A ;
Slavin, S .
LANCET, 1996, 348 (9036) :1242-1243
[3]   THE ESSENTIALS OF DNA METHYLATION [J].
BIRD, A .
CELL, 1992, 70 (01) :5-8
[4]   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
[5]  
BORN MB, 1996, LANCET, V347, P1377
[6]   Cytokeratin-positive cells in the bone marrow and survival of patients with stage I, II, or III breast cancer. [J].
Braun, S ;
Pantel, K ;
Muller, P ;
Janni, W ;
Hepp, F ;
Kentenich, CRM ;
Gastroph, S ;
Wischnik, A ;
Dimpfl, T ;
Kindermann, G ;
Riethmuller, G ;
Schlimok, G .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (08) :525-533
[7]  
BUTTURINI A, 1988, BONE MARROW TRANSPL, V3, P185
[8]  
Chaux P, 1999, J IMMUNOL, V163, P2928
[9]   Regression of metastatic renal-cell carcinoma after nonmyeloablative allogeneic peripheral-blood stem-cell transplantation [J].
Childs, R ;
Chernoff, A ;
Contentin, N ;
Bahceci, E ;
Schrump, D ;
Leitman, S ;
Read, EJ ;
Tisdale, J ;
Dunbar, C ;
Linehan, WM ;
Young, NS ;
Barrett, AJ ;
Clave, E ;
Epperson, D ;
Mayo, V .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (11) :750-758
[10]  
De Smet C, 1999, MOL CELL BIOL, V19, P7327