Zeng Jieming, Wu Chunxiao, Wang Shu
Institute of Bioengineering and Nanotechnology, Singapore.
Department of Biological Sciences, National University of Singapore, Singapore.
Sci Rep. 2015 Oct 16;5:15262. doi: 10.1038/srep15262.
Human pluripotent stem cells (hPSCs) provide a promising platform to produce dendritic cell (DC) vaccine. To streamline the production process, we investigated a unique antigen-loading strategy that suits this novel platform. Specifically, we stably modified hPSCs using tumour antigen genes in the form of a full-length tumour antigen gene or an artificial tumour antigen epitope-coding minigene. Such antigenically modified hPSCs were able to differentiate into tumour antigen-presenting DCs. Without conventional antigen-loading, DCs derived from the minigene-modified hPSCs were ready to prime a tumour antigen-specific T cell response and further expand these specific T cells in restimulation processes. These expanded tumour antigen-specific T cells were potent effectors with central memory or effector memory phenotype. Thus, we demonstrated that immunocompetent tumour antigen-loaded DCs can be directly generated from antigenically modified hPSCs. Using such strategy, we can completely eliminate the conventional antigen-loading step and significantly simplify the production of DC vaccine from hPSCs.
人多能干细胞(hPSCs)为生产树突状细胞(DC)疫苗提供了一个很有前景的平台。为了简化生产流程,我们研究了一种适用于这个新平台的独特抗原加载策略。具体而言,我们使用全长肿瘤抗原基因或人工肿瘤抗原表位编码小基因形式的肿瘤抗原基因对hPSCs进行稳定修饰。这种抗原修饰的hPSCs能够分化为呈递肿瘤抗原的DC。无需传统的抗原加载,源自小基因修饰hPSCs的DC即可启动肿瘤抗原特异性T细胞反应,并在再刺激过程中进一步扩增这些特异性T细胞。这些扩增的肿瘤抗原特异性T细胞是具有中枢记忆或效应记忆表型的强效效应细胞。因此,我们证明了具有免疫活性的负载肿瘤抗原的DC可以直接从抗原修饰的hPSCs产生。使用这种策略,我们可以完全省去传统的抗原加载步骤,并显著简化从hPSCs生产DC疫苗的过程。