Cancer vaccines: on the threshold of success

被引:43
作者
Emens, Leisha A. [1 ]
机构
[1] Johns Hopkins Univ, Dept Oncol, Tumor Immunol & Breast Canc Res Programs, Baltimore, MD 21231 USA
关键词
biomarkers; cancer vaccine; immune monitoring; immune tolerance; therapeutic resistance; tumor immunity;
D O I
10.1517/14728214.13.2.295
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Cancer vaccines are a unique approach to cancer therapy. They exert an antitumor effect by engaging the host immune response, and have great potential for circumventing the intrinsic drug resistance that limits standard cancer management. Additional advantages of cancer vaccines are exquisite specificity, low toxicity, and the potential for a durable treatment effect due to immunologic memory. Objectives: This review aims to consider the promise of cancer vaccines, review the current state of cancer vaccine development, and suggest directions for future research. Methods: The scope of this review was defined peer-reviewed information found on Medline, and information found on the Internet about Phase III clinical trials that are ongoing and not yet published. Results/conclusions: Multiple Phase III clinical trials have demonstrated the promise and challenges posed by therapeutic vaccines, and defined the next steps in their clinical development. Determining the optimal integration of cancer vaccines with chemotherapy, radiation, surgery, and biologically targeted therapies, defining predictive biomarkers of immunologic and clinical response, and combining tumor vaccines with new drugs that effectively modulate the antitumor immune response, will ensure that cancer vaccines become part of standard cancer therapy and prevention.
引用
收藏
页码:295 / 308
页数:14
相关论文
共 112 条
[21]   VACCINATION WITH IRRADIATED TUMOR-CELLS ENGINEERED TO SECRETE MURINE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR STIMULATES POTENT, SPECIFIC, AND LONG-LASTING ANTITUMOR IMMUNITY [J].
DRANOFF, G ;
JAFFEE, E ;
LAZENBY, A ;
GOLUMBEK, P ;
LEVITSKY, H ;
BROSE, K ;
JACKSON, V ;
HAMADA, H ;
PARDOLL, D ;
MULLIGAN, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3539-3543
[22]   Leveraging the activity of tumor vaccines with cytotoxic chemotherapy [J].
Emens, LA ;
Jaffee, EM .
CANCER RESEARCH, 2005, 65 (18) :8059-8064
[23]   Breast cancer vaccines: maximizing cancer treatment by tapping into host immunity [J].
Emens, LA ;
Reilly, RT ;
Jaffee, EM .
ENDOCRINE-RELATED CANCER, 2005, 12 (01) :1-17
[24]  
Emens LA, 2001, CURR OPIN MOL THER, V3, P77
[25]  
Emens Leisha A, 2005, Am J Ther, V12, P243
[26]   Recruitment of latent pools of high-avidity CD8+ T cells to the antitumor immune response [J].
Ercolini, AM ;
Ladle, BH ;
Manning, EA ;
Pfannenstiel, LW ;
Armstrong, TD ;
Machiels, JPH ;
Bieler, JG ;
Emens, LA ;
Reilly, RT ;
Jaffee, EM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (10) :1591-1602
[27]  
Ferlay J, 2004, GLOBOCAN 2002 CANC I
[28]   Dendritic cells generated from CD34+ progenitor cells with flt3 ligand, c-kit ligand, GM-CSF, IL-4, and TNF-α are functional antigen-presenting cells resembling mature monocyte-derived dendritic cells [J].
Ferlazzo, G ;
Klein, J ;
Paliard, X ;
Wei, WZ ;
Galy, A .
JOURNAL OF IMMUNOTHERAPY, 2000, 23 (01) :48-58
[29]   How much longer will tumour cells fool the immune system? [J].
Ferrone, S ;
Finerty, JF ;
Jaffee, EM ;
Nabel, GJ .
IMMUNOLOGY TODAY, 2000, 21 (02) :70-72
[30]   Engagement of the PD-1 immunoinhibitory receptor by a novel B7 family member leads to negative regulation of lymphocyte activation [J].
Freeman, GJ ;
Long, AJ ;
Iwai, Y ;
Bourque, K ;
Chernova, T ;
Nishimura, H ;
Fitz, LJ ;
Malenkovich, N ;
Okazaki, T ;
Byrne, MC ;
Horton, HF ;
Fouser, L ;
Carter, L ;
Ling, V ;
Bowman, MR ;
Carreno, BM ;
Collins, M ;
Wood, CR ;
Honjo, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (07) :1027-1034