Clinical and immunological evaluation of patients with metastatic melanoma undergoing immunization with the HLA-Cw*0702-associated epitope MAGE-A12:170-178

被引:32
作者
Bettinotti, MP
Panelli, MC
Ruppe, E
Mocellin, S
Phan, GQ
White, DE
Marincola, FM
机构
[1] NIH, Ctr Clin, Dept Transfus Med, Bethesda, MD 20892 USA
[2] NCI, Surg Branch, Ctr Canc Res, Bethesda, MD 20892 USA
关键词
melanoma; immunotherapy; MAGE; immune response;
D O I
10.1002/ijc.11045
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients with metastatic melanoma who expressed HLA-Cw*0702 and whose tumors had demonstrable MAGE-A12 expression were immunized with the peptide MAGE-A12: 170-178 administered subcutaneously in incomplete Freund's adjuvant (IFA). The peptide was administered either every week or every 3 weeks for 4 cycles. Patients were evaluated for toxicity and for immunologic and clinical response to peptide immunization. Pre-treatment fine needle aspirates were obtained to document MAGE-A 12 expression for enrollment. MAGE-A12 mRNA was identified in 62% of specimens. Nine patients were selected for vaccination based on MAGE-A12 expression and the presence of HLA-Cw*0702. The immune response was monitored both by tetrameric HLA-Cw*0702/MAGE-A12:170-178 complexes and by analysis of interferon-gamma mRNA transcription using a quantitative real-time polymerase chain reaction assay after peptide-specific stimulation. The samples consisted of circulating lymphocytes analyzed ex vivo or after 10 to 14 days of in vitro sensitization. One of 9 patients sustained an ongoing partial clinical response. No convincing evidence of enhancement of the systemic immune response against MAGE-A 12: 170-178 could be documented. Because of the modest immunological and clinical results, the present protocol has been discontinued as new routes of administration are being considered. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:210 / 216
页数:7
相关论文
共 30 条
[1]  
Cormier JN, 1998, INT J CANCER, V75, P517, DOI 10.1002/(SICI)1097-0215(19980209)75:4<517::AID-IJC5>3.0.CO
[2]  
2-W
[3]  
Cormier JN, 1997, CANCER J, V3, P37
[4]   A monoclonal cytolytic T-lymphocyte response observed in a melanoma patient vaccinated with a tumor-specific antigenic peptide encoded by gene MAGE-3 [J].
Coulie, PG ;
Karanikas, V ;
Colau, D ;
Lurquin, C ;
Landry, C ;
Marchand, M ;
Dorval, T ;
Brichard, V ;
Boon, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (18) :10290-10295
[5]   Antigens recognized by T-lymphocytes on human tumours [J].
Coulie, PG ;
VandenEynde, BJ ;
vanderBruggen, P ;
VanPel, A ;
Boon, T .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1997, 25 (02) :544-548
[6]   STRUCTURE, CHROMOSOMAL LOCALIZATION, AND EXPRESSION OF 12 GENES OF THE MAGE FAMILY [J].
DEPLAEN, E ;
ARDEN, K ;
TRAVERSARI, C ;
GAFORIO, JJ ;
SZIKORA, JP ;
DESMET, C ;
BRASSEUR, F ;
VANDERBRUGGEN, P ;
LETHE, B ;
LURQUIN, C ;
BRASSEUR, R ;
CHOMEZ, P ;
DEBACKER, O ;
CAVENEE, W ;
BOON, T .
IMMUNOGENETICS, 1994, 40 (05) :360-369
[7]   The activation of human gene MAGE-1 in tumor cells is correlated with genome-wide demethylation [J].
DeSmet, C ;
DeBacker, O ;
Faraoni, I ;
Lurquin, C ;
Brasseur, F ;
Boon, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) :7149-7153
[8]   Cytolytic T lymphocytes raised against a human bladder carcinoma recognize an antigen encoded by gene MAGE-A12 [J].
Heidecker, L ;
Brasseur, F ;
Probst-Kepper, M ;
Guéguen, M ;
Boon, T ;
Van den Eynde, BJ .
JOURNAL OF IMMUNOLOGY, 2000, 164 (11) :6041-6045
[9]   Real-time quantitative polymerase chain reaction assessment of immune reactivity in melanoma patients after tumor peptide vaccination [J].
Kammula, US ;
Marincola, FM ;
Rosenberg, SA .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (16) :1336-1344
[10]  
Kammula US, 1999, J IMMUNOL, V163, P6867