共 101 条
Strategies for Cancer Vaccine Development
被引:93
作者:

Vergati, Matteo
论文数: 0 引用数: 0
h-index: 0
机构:
NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Intrivici, Chiara
论文数: 0 引用数: 0
h-index: 0
机构:
NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Huen, Ngar-Yee
论文数: 0 引用数: 0
h-index: 0
机构:
NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Schlom, Jeffrey
论文数: 0 引用数: 0
h-index: 0
机构:
NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA

Tsang, Kwong Y.
论文数: 0 引用数: 0
h-index: 0
机构:
NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
机构:
[1] NCI, Tumor Immunol & Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
来源:
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY
|
2010年
关键词:
PROSTATE-SPECIFIC ANTIGEN;
HEAT-SHOCK PROTEINS;
T-CELL RESPONSES;
ACTIVE SPECIFIC IMMUNOTHERAPY;
TRANSFECTED DENDRITIC CELLS;
BLP25 LIPOSOME VACCINE;
AUTOLOGOUS TUMOR-CELL;
PHASE-I/II TRIAL;
MESSENGER-RNA;
CARCINOEMBRYONIC ANTIGEN;
D O I:
10.1155/2010/596432
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Treating cancer with vaccines has been a challenging field of investigation since the 1950s. Over the years, the lack of effective active immunotherapies has led to the development of numerous novel strategies. However, the use of therapeutic cancer vaccines may be on the verge of becoming an effective modality. Recent phase II/III clinical trials have achieved hopeful results in terms of overall survival. Yet despite these encouraging successes, in general, very little is known about the basic immunological mechanisms involved in vaccine immunotherapy. Gaining a better understanding of the mechanisms that govern the specific immune responses (i.e., cytotoxic T lymphocytes, CD4 T helper cells, T regulatory cells, cells of innate immunity, tumor escape mechanisms) elicited by each of the various vaccine platforms should be a concern of cancer vaccine clinical trials, along with clinical benefits. This review focuses on current strategies employed by recent clinical trials of therapeutic cancer vaccines and analyzes them both clinically and immunologically.
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