Generation of cellular immune responses to antigenic tumor peptides

被引:24
作者
Pietersz, GA
Apostolopoulos, V
McKenzie, IFC
机构
[1] Austin Res Inst, Heidelberg, Vic 3084, Australia
[2] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
关键词
tumor antigens; vaccines; class I presentation; class II presentation; peptides; toxins; adjuvants; antigen targeting; clinical trials; CTL epitopes;
D O I
10.1007/PL00000691
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tumor immunotherapy is currently receiving close scrutiny. However, with the identification of tumor antigens and their production by recombinant means, the use of cytokines and knowledge of major histocompatibility complex (MHC) class I and class II presentation has provided ample reagents for use and clear indications of how they should be used. At this time, much attention is focused on using peptides to be presented by MHC class I molecules to both induce and be targets for CD8(+) cytolytic T cells. Many peptides generated endogenously or given exogenously can enter the class I pathway, but a number of other methods of entering this pathway are also known and are discussed in detail herein. While the review concentrates on inducing cytotoxic T cells (CTLs), it is becoming increasingly apparent that other modes of immunotherapy would be desirable, such as class II presentation to induce increased helper activity (for CTL), but also activating macrophages to be effective against tumor cells.
引用
收藏
页码:290 / 310
页数:21
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