Bioinspired vaccines to enhance MHC class-I antigen cross-presentation

被引:0
作者
Baljon, Jessalyn J. [1 ]
Wilson, John T. [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Vanderbilt Univ, Dept Biomed Engn, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Dept Chem & Biomol Engn, Nashville, TN 37235 USA
[3] Vanderbilt Univ, Med Ctr, Vanderbilt Inst Infect Immunol & Inflammat, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Med Ctr, Vanderbilt Inst Chem Biol, Nashville, TN 37232 USA
[5] Vanderbilt Univ, Med Ctr, Vanderbilt Ctr Immunobiol, Nashville, TN 37232 USA
[6] Vanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Nashville, TN 37232 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
CD8-ALPHA(+) DENDRITIC CELLS; CD8(+) T-CELLS; STING AGONISTS; INNATE; EFFICIENT; RESPONSES; DELIVERY; VIVO; NANOPARTICLES; DEGRADATION;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cross-presentation of exogenous antigen on MHC class-I is a crucial process for generating a CD8(+) T cell response, and is therefore an important design consideration in the development of T-cell-engaging vaccines against viruses, intracellular bacteria, and cancers. Here, we briefly summarize known cross-presentation pathways and highlight how synthetic vaccines can be engineered to enhance MHC-I presentation of exogenous peptide and protein antigens by professional antigen-presenting cells (APCs). In particular, we summarize how molecular engineering and nanotechnology are being harnessed to enhance antigen delivery to lymph nodes and to cross-presenting dendritic cells, to bypass endosomal trafficking of exogenous antigen to promote delivery of antigen to the cytosol of APCs, and to coordinate the delivery of antigen with immune-stimulating adjuvants that can act synergistically to augment antigen cross-presentation.
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页数:10
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