免疫系统
抗原
抗原呈递
抗原提呈细胞
免疫学
T细胞
材料科学
生物
作者
Ming Qin,Guangsheng Du,Nan Qiao,Zhaofei Guo,Min Jiang,Chun‐Ting He,Sha Bai,Penghui He,Yanhua Xu,Hairui Wang,Tao Gong,Zhirong Zhang,Xun Sun
标识
DOI:10.1002/adfm.202108917
摘要
Abstract Whole‐cell vaccines that provide broad‐spectrum antigens have been explored for recent decades. But so far, they have revealed limited success in clinical trials, possibly owing to their inefficiency in targeting immune organs and antigen‐presenting cells (APCs). Herein, a facile strategy is developed to convert the whole‐cell vaccines into the nanoscale size to promote their lymphatic migration and subsequent intracellular antigen presentation to maximize immune responses. Briefly, the study designs a multiple antigen delivery platform based on alum‐induced and cancer/bacterial cell membrane coated protein antigen nanoparticles. Through a simple two‐step vortex‐sonification method, a universal carrier‐free nano‐vaccine without additional excipients could be quickly fabricated. After subcutaneous vaccination, the developed nanovaccines rapidly migrate to lymph nodes, leading to their effective uptake by lymph node‐resident APCs, and subsequent antigen presentation and activation of downstream immune processes. Overall, the described promising work offers a safe, effective, facile, and widely applicable vaccine strategy, which has great potential for clinical transformation.
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