Challenges in the development of effective peptide vaccines for cancer

被引:51
作者
Buteau, C
Markovic, SN
Celis, E
机构
[1] Mayo Clin, Dept Immunol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Oncol, Rochester, MN 55905 USA
[3] Mayo Clin, Div Hematol & Internal Med, Rochester, MN 55905 USA
[4] Mayo Clin, Div Infect Dis & Internal Med, Rochester, MN 55905 USA
关键词
D O I
10.4065/77.4.339
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The ability of the Immune system to recognize malignant cells has opened the door to development of tumor vaccines to treat or prevent various types of cancer. In the era of molecular biology, the tumor antigens recognized by the immune system have been identified, allowing the generation of subunit vaccines that may improve safety and efficacy compared with more crude vaccines such as irradiated tumor cells and tumor cell lysates. Synthetic peptides corresponding to defined antigenic epitopes for tumor-reactive lymphocytes represent one of the new types of vaccines currently being developed to treat or prevent various types of malignant disorders. The design of peptide-based vaccines to stimulate antitumor T-cell responses has many attractive features such as case of manufacturing and characterization (i.e, quality control), as well as an excellent safety profile in past clinical studies. However, ambiguous results from initial clinical trials indicate that these vaccines are far from optimal and that considerable efforts for their optimization lie ahead. We attempt to address the 8 most important challenges we currently face for developing peptide-based vaccines that would effectively induce immune responses leading to antitumor effects.
引用
收藏
页码:339 / 349
页数:11
相关论文
共 94 条
[1]   Cancer and autoimmunity: autoimmune and rheumatic features in patients with malignancies [J].
Abu-Shakra, M ;
Buskila, D ;
Ehrenfeld, M ;
Conrad, K ;
Shoenfeld, Y .
ANNALS OF THE RHEUMATIC DISEASES, 2001, 60 (05) :433-440
[2]  
Banchereau J, 2001, CANCER RES, V61, P6451
[4]  
BOON T, 1992, CANCER SURV, V13, P23
[5]   Epitope selection and development of peptide based vaccines to treat cancer [J].
Celis, E ;
Sette, A ;
Grey, HM .
SEMINARS IN CANCER BIOLOGY, 1995, 6 (06) :329-336
[6]   INDUCTION OF ANTITUMOR CYTOTOXIC T-LYMPHOCYTES IN NORMAL HUMANS USING PRIMARY CULTURES AND SYNTHETIC PEPTIDE EPITOPES [J].
CELIS, E ;
TSAI, V ;
CRIMI, C ;
DEMARS, R ;
WENTWORTH, PA ;
CHESNUT, RW ;
GREY, HM ;
SETTE, A ;
SERRA, HM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2105-2109
[7]  
Clay TM, 2001, CLIN CANCER RES, V7, P1127
[8]  
Clay TM, 1999, J IMMUNOL, V162, P1749
[9]  
Coley W.B., 1893, AM J MED SCI, V105, P487, DOI DOI 10.1097/00000441-189305000-00001
[10]   Peripheral neuropathy in cancer patients [J].
Corbo, M ;
Balmaceda, C .
CANCER INVESTIGATION, 2001, 19 (04) :369-382