Aspects of cancer immunotherapy

被引:10
作者
Mckenzie, IF [1 ]
Apostolopoulos, V [1 ]
Plebanski, M [1 ]
Pietersz, GA [1 ]
Loveland, BE [1 ]
机构
[1] Austin Res Inst, Heidelberg, Vic 3084, Australia
关键词
antigen presenting cells; dendritic cells; H-2K(b); MHC class I; MUC1; peptide-MHC interactions; tumour immunotherapy; vaccine;
D O I
10.1046/j.0818-9641.2002.01140.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cancer immunotherapy has traditionally undergone a 'revolution' every decade, from the use of Bacille Calmette-Guerin by scarification in the 1970s, to interleukin-2 therapies in the 1980s, and monoclonal antibody treatments in the early 1990s. Usually the early reports on the use of such agents were encouraging, but when more patients were studied in multiple centres, the initial promising results could not be confirmed. Now in a new century, we have more reagents and methods available than ever before - indeed, with such a plethora of reagents it is difficult to envisage them being fully and appropriately tested within the next decade, by which time there will be even more reagents to test. However, there have been three major advances which should lead to substantial progress in cancer immunotherapy: (1) the widespread use of genetic engineering, enabling identification of candidate vaccine proteins and manipulation of their sequences; (2) the production of antigens, antibodies and cytokines in large amounts by recombinant technologies, and (3) an understanding of the mode of presentation of peptides by major histocompatibility complex Class I and Class II molecules and their recognition by T cells. Despite these advances, there are major problems facing cancer immunotherapy, such as the ability of tumours to mutate and evade the immune system and the difficulty of precisely defining the interactions of effector cells in mediating 'rejection' or destruction of a tumour. There are clearly immunological similarities with diseases such as malaria and schistosomiasis, where the invading foreign organisms can use a variety of strategies to resist an elicited immune response. The failure to find a suitable vaccine for these diseases must lead to some pessimism for the development of immunotherapy for an autologous tumour. However, there are promising studies now in progress which should give an indication of the most important directions to follow. This review provides a commentary on aspects of cancer immunotherapy and in particular will deal with: (1) the selection of antigens as vaccine components; (2) the modes of presentation of antigens, particularly by major histocompatibility complex Class I molecules; and (3) new modes of delivery of vaccine immunogens.
引用
收藏
页码:79 / 85
页数:7
相关论文
共 55 条
[1]   MUC1-specific immune responses in human MUC1 transgenic mice immunized with various human MUC1 vaccines [J].
Acres, B ;
Apostolopoulos, V ;
Balloul, JM ;
Wreschner, D ;
Xing, PX ;
Ali-Hadji, D ;
Bizouarne, N ;
Kieny, MP ;
McKenzie, IFC .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2000, 48 (10) :588-594
[2]   Peptide mimics of a tumor antigen induce functional cytotoxic T cells [J].
Apostolopoulos, V ;
Lofthouse, SA ;
Popovski, V ;
Chelvanayagam, G ;
Sandrin, MS ;
McKenzie, IFC .
NATURE BIOTECHNOLOGY, 1998, 16 (03) :276-280
[3]   MUC1 cross-reactive Galα(1,3)Gal antibodies in humans switch immune responses from cellular to humoral [J].
Apostolopoulos, V ;
Osinski, C ;
McKenzie, IFC .
NATURE MEDICINE, 1998, 4 (03) :315-320
[4]   Crystal structure of a non-canonical low-affinity peptide complexed with MHC class I: A new approach for vaccine design [J].
Apostolopoulos, V ;
Yu, MM ;
Corper, AL ;
Teyton, L ;
Pietersz, GA ;
McKenzie, IFC ;
Wilson, IA .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 318 (05) :1293-1305
[5]   Crystal structure of a non-canonical high affinity peptide complexed with MHC class I: A novel use of alternative anchors [J].
Apostolopoulos, V ;
Yu, MM ;
Corper, AL ;
Li, WJ ;
McKenzie, IFC ;
Teyton, L ;
Wilson, IA .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 318 (05) :1307-1316
[6]   PRODUCTION OF ANTI-BREAST CANCER MONOCLONAL-ANTIBODIES USING A GLUTATHIONE-S-TRANSFERASE-MUC1 BACTERIAL FUSION PROTEIN [J].
APOSTOLOPOULOS, V ;
XING, PX ;
TRAPANI, JA ;
MCKENZIE, IFC .
BRITISH JOURNAL OF CANCER, 1993, 67 (04) :713-720
[7]   Cell-mediated immune responses to MUC1 fusion protein coupled to mannan [J].
Apostolopoulos, V ;
Pietersz, GA ;
McKenzie, IFC .
VACCINE, 1996, 14 (09) :930-938
[8]   OXIDATIVE REDUCTIVE CONJUGATION OF MANNAN TO ANTIGEN SELECTS FOR T-1 OR T-2 IMMUNE-RESPONSES [J].
APOSTOLOPOULOS, V ;
PIETERSZ, GA ;
LOVELAND, BE ;
SANDRIN, MS ;
MCKENZIE, IFC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (22) :10128-10132
[9]  
Apostolopoulos V, 1997, J IMMUNOL, V159, P5211
[10]   THE IMMUNOGENICITY OF MUC1 PEPTIDES AND FUSION PROTEIN [J].
APOSTOLOPOULOS, V ;
PIETERSZ, GA ;
XING, PX ;
LEES, CJ ;
MICHAEL, M ;
BISHOP, J ;
MCKENZIE, IFC .
CANCER LETTERS, 1995, 90 (01) :21-26