Old concepts, new tricks: How peptide vaccines are reshaping cancer immunotherapy?

被引:3
作者
Liu, Qingyang [1 ]
Wu, Peihua [1 ]
Lei, Jun [2 ,3 ]
Bai, Peng [4 ]
Zhong, Peiluan [1 ]
Yang, Min [1 ]
Wei, Pengcheng [1 ]
机构
[1] Guangxi Univ, Sch Med, Guangxi Key Lab Special Biomed, Nanning 530004, Peoples R China
[2] Wuhan Univ, Coll Life Sci, State Key Lab Virol, Hubei Key Lab Cell Homeostasis,Dept Clin Oncol,Ren, Wuhan, Peoples R China
[3] Xixi Hosp Hangzhou, Dept Lab Med, Hangzhou, Peoples R China
[4] WuXi AppTec, Vivo Pharmacol Unit, Nantong, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Peptide vaccines; Cancer; Immunotherapy; T-CELL RESPONSES; BISPECIFIC ANTIBODIES; ANTITUMOR IMMUNITY; HLA-G; ADJUVANT; VACCINATION; RESISTANCE; MELANOMA; BINDING; EPITOPE;
D O I
10.1016/j.ijbiomac.2024.135541
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
Over the past few decades, research on cancer immunotherapy has firmly established immune cells as key players in effective cancer treatment. Peptide vaccines directly targeting immune cells have demonstrated immense potential due to their specificity and applicability. However, developing peptide vaccines to generate tumorreactive T cells remains challenging, primarily due to suboptimal immunogenicity and overcoming the immunosuppressive tumor microenvironment (TME). In this review, we discuss various elements of effective peptide vaccines, including antigen selection, peptide epitope optimization, vaccine adjuvants, and the combination of multiple immunotherapies, in addition to recent advances in tumor neoantigens as well as epitopes bound by non-classical human leukocyte antigen (HLA) molecules, to increase the understanding of cancer peptide vaccines and provide multiple references for the design of subsequent T cell-based peptide vaccines.
引用
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页数:13
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