Cancer vaccines and immunotherapy

被引:53
作者
Dermime, S
Armstrong, A
Hawkins, RE
Stern, PL
机构
[1] Christie Hosp NHS Trust, Paterson Inst Canc Res, Dept Immunol, Manchester M20 4BX, Lancs, England
[2] Univ Manchester, Crc Dept Med Oncol, Manchester, Lancs, England
[3] Univ Manchester, CRC Dept Immunol, Manchester, Lancs, England
关键词
D O I
10.1093/bmb/62.1.149
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
It is now clear that many human tumour antigens can be recognised by the immune system. These tumour antigens can be classified into several groups including cancer-testis, differentiation, tissue specific, over-expressed, and viral-associated antigens. In many cases, there is a known molecular basis of carcinogenesis which provides the explanation for the differentiated expression of these antigens in tumours compared with normal cells. Improved understanding of the biology of the immune response, particularly of immune recognition and activation of T-cells, allow better design of vaccines. Pre-clinical comparative studies allow evaluation of optimal vaccine strategies which can then be delivered to the clinic. Currently, a range of cancer vaccines are being tested including those using tumour cells, proteins, peptides, viral vectors, DNA or dendritic cells. Ultimately, this research should give rise to an entirely new modality of cancer treatments.
引用
收藏
页码:149 / 162
页数:14
相关论文
共 51 条
[1]
Dendritic cells pulsed with RNA are potent antigen-presenting cells in vitro and in vivo [J].
Boczkowski, D ;
Nair, SK ;
Snyder, D ;
Gilboa, E .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :465-472
[2]
Recombinant viruses as a tool for therapeutic vaccination against human cancers [J].
Bonnet, MC ;
Tartaglia, J ;
Verdier, F ;
Kourilsky, P ;
Lindberg, A ;
Klein, M ;
Moingeon, P .
IMMUNOLOGY LETTERS, 2000, 74 (01) :11-25
[3]
Multiple mechanisms underlie HLA dysregulation in cervical cancer [J].
Brady, CS ;
Bartholomew, JS ;
Burt, DJ ;
Duggan-Keen, MF ;
Glenville, S ;
Telford, N ;
Little, AM ;
Davidson, JA ;
Jimenez, P ;
Ruiz-Cabello, F ;
Garrido, F ;
Stern, PL .
TISSUE ANTIGENS, 2000, 55 (05) :401-411
[4]
Origin, maturation and antigen presenting function of dendritic cells [J].
Cella, M ;
Sallusto, F ;
Lanzavecchia, A .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) :10-16
[5]
Induction of ErbB-2/neu-specific protective and therapeutic antitumor immunity using genetically modified dendritic cells: enhanced efficacy by cotransduction of gene encoding IL-12 [J].
Chen, Y ;
Emtage, P ;
Zhu, Q ;
Foley, R ;
Muller, W ;
Hitt, M ;
Gauldie, J ;
Wan, Y .
GENE THERAPY, 2001, 8 (04) :316-323
[6]
Why are dendritic cells central to cancer immunotherapy? [J].
Colaco, CALS .
MOLECULAR MEDICINE TODAY, 1999, 5 (01) :14-17
[7]
COLEY W, 1996, B J HOPKINS HOSP, V7, P57
[8]
Ehrlich P., 1909, Ned. Tijdschr. Geneeskd, V5, P273
[9]
Dendritic cells injected via different routes induce immunity in cancer patients [J].
Fong, L ;
Brockstedt, D ;
Benike, C ;
Wu, L ;
Engleman, EG .
JOURNAL OF IMMUNOLOGY, 2001, 166 (06) :4254-4259
[10]
Altered peptide ligand vaccination with Flt3 ligand expanded dendritic cells for tumor immunotherapy [J].
Fong, L ;
Hou, YF ;
Rivas, A ;
Benike, C ;
Yuen, A ;
Fisher, GA ;
Davis, MM ;
Engleman, EG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8809-8814