Targeting dendritic cells to advance cross-presentation and vaccination outcomes

被引:26
作者
Macri, Christophe [1 ]
Jenika, Devi [1 ]
Ouslinis, Cassandra [1 ]
Mintern, Justine D. [1 ]
机构
[1] Univ Melbourne, Bio21 Mol Sci & Biotechnol Inst, Dept Biochem & Pharmacol, 30 Flemington Rd, Parkville, Vic 3010, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
Cross-presentation; Dendritic cells; Vaccination; Antigen presentation; C-TYPE LECTIN; CD8(+) T-CELLS; MANNOSE RECEPTOR; ANTIGEN-PRESENTATION; DC-SIGN; INDOLEAMINE 2,3-DIOXYGENASE; IFN-ALPHA; DEC-205; RESPONSES; CLEC9A;
D O I
10.1016/j.smim.2023.101762
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) are a complex network of specialised antigen-presenting cells that are critical initiators of adaptive immunity. Targeting antigen directly to DCs in situ is a vaccination strategy that selectively delivers antigen to receptors expressed by DC subtypes. This approach exploits specific DC subset functions of antigen uptake and presentation. Here, we review DC-targeted vaccination strategies that are designed to elicit effective cross-presentation for CD8+ T cell immunity. In particular, we focus on approaches that exploit receptors highly expressed by mouse and human cDCs equipped with superior cross-presentation capacity. These receptors include DEC205, Clec9A and XCR1. Targeting DC receptors Clec12A, Clec4A4 and mannose receptor is also reviewed. Outcomes of DC-targeted vaccination in mouse models through to human clinical trials is discussed. This is a promising new vaccination approach capable of directly targeting the cross-presentation pathway for prevention and treatment of tumours and infectious diseases.
引用
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页数:11
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