Mechanistic insights into the efficacy of cell penetrating peptide-based cancer vaccines

被引:38
|
作者
Grau, Morgan [1 ]
Walker, Paul R. [2 ,3 ]
Derouazi, Madiha [1 ]
机构
[1] Amal Therapeut, Geneva, Switzerland
[2] Geneva Univ Hosp, Div Oncol, Ctr Translat Res Oncohematol, Geneva, Switzerland
[3] Univ Geneva, Geneva, Switzerland
关键词
Cell penetrating peptides; Cancer vaccines; Immunotherapy; Tumor antigens; Antigen processing; MHC CLASS-I; DEPENDENT ANTITUMOR IMMUNITY; PROTEIN TRANSDUCTION DOMAIN; DENDRITIC CELLS; ANTIGEN PRESENTATION; TAT PROTEIN; CROSS-PRESENTATION; FUSION PROTEINS; DELIVERY; RESPONSES;
D O I
10.1007/s00018-018-2785-0
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
Immunotherapies are increasingly used to treat cancer, with some outstanding results. Immunotherapy modalities include therapeutic vaccination to eliminate cancer cells through the activation of patient's immune system against tumor-derived antigens. Nevertheless, the full potential of therapeutic vaccination has yet to be demonstrated clinically because many early generation vaccines elicited low-level immune responses targeting only few tumor antigens. Cell penetrating peptides (CPPs) are highly promising tools to advance the field towards clinical success. CPPs efficiently penetrate cell membranes, even when linked to antigenic cargos, which can induce both CD8 and CD4 T-cell responses. Pre-clinical studies demonstrated that targeting multiple tumor antigens, even those considered to be poorly immunogenic, led to tumor regression. Therefore, CPP-based cancer vaccines represent a flexible and powerful means to extend therapeutic vaccination to many cancer indications. Here, we review recent findings in CPP development and discuss their use in next generation immunotherapies.
引用
收藏
页码:2887 / 2896
页数:10
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