Targeting Costimulatory Molecules to Improve Antitumor Immunity

被引:73
作者
Capece, Daria [1 ]
Verzella, Daniela [1 ]
Fischietti, Mariafausta [1 ]
Zazzeroni, Francesca [1 ]
Alesse, Edoardo [1 ]
机构
[1] Univ Aquila, Dept Expt Med, I-67100 Laquila, Italy
来源
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY | 2012年
关键词
ANTI-CD40; MONOCLONAL-ANTIBODY; T-CELL RESPONSES; PHASE-II TRIAL; COLONY-STIMULATING FACTOR; UNRESECTABLE STAGE-III; B7; FAMILY-MEMBER; CTLA-4; BLOCKADE; DENDRITIC CELLS; ANTIGEN-4; PD-1;
D O I
10.1155/2012/926321
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 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
The full activation of T cells necessitates the concomitant activation of two signals, the engagement of T-cell receptor by peptide/major histocompatibility complex II and an additional signal delivered by costimulatory molecules. The best characterized costimulatory molecules belong to B7/CD28 and TNF/TNFR families and play crucial roles in the modulation of immune response and improvement of antitumor immunity. Unfortunately, tumors often generate an immunosuppressive microenvironment, where T-cell response is attenuated by the lack of costimulatory molecules on the surface of cancer cells. Thus, targeting costimulatory pathways represent an attractive therapeutic strategy to enhance the antitumor immunity in several human cancers. Here, latest therapeutic approaches targeting costimulatory molecules will be described.
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页数:17
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