Nel André E, Miller Jeff F
Division of NanoMedicine, Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California 90095, United States.
California NanoSystems Institute, University of California, Los Angeles, Los Angeles, California 90095, United States.
ACS Nano. 2021 Apr 27;15(4):5793-5818. doi: 10.1021/acsnano.1c01845. Epub 2021 Apr 1.
At the time of preparing this Perspective, large-scale vaccination for COVID-19 is in progress, aiming to bring the pandemic under control through vaccine-induced herd immunity. Not only does this vaccination effort represent an unprecedented scientific and technological breakthrough, moving us from the rapid analysis of viral genomes to design, manufacture, clinical trial testing, and use authorization within the time frame of less than a year, but it also highlights rapid progress in the implementation of nanotechnology to assist vaccine development. These advances enable us to deliver nucleic acid and conformation-stabilized subunit vaccines to regional lymph nodes, with the ability to trigger effective humoral and cellular immunity that prevents viral infection or controls disease severity. In addition to a brief description of the design features of unique cationic lipid and virus-mimicking nanoparticles for accomplishing spike protein delivery and presentation by the cognate immune system, we also discuss the importance of adjuvancy and design features to promote cooperative B- and T-cell interactions in lymph node germinal centers, including the use of epitope-based vaccines. Although current vaccine efforts have demonstrated short-term efficacy and vaccine safety, key issues are now vaccine durability and adaptability against viral variants. We present a forward-looking perspective of how vaccine design can be adapted to improve durability of the immune response and vaccine adaptation to overcome immune escape by viral variants. Finally, we consider the impact of nano-enabled approaches in the development of COVID-19 vaccines for improved vaccine design against other infectious agents, including pathogens that may lead to future pandemics.
在撰写本综述时,针对新冠病毒(COVID-19)的大规模疫苗接种正在进行,旨在通过疫苗诱导的群体免疫来控制疫情。这项疫苗接种工作不仅代表了前所未有的科技突破,使我们在不到一年的时间内从对病毒基因组的快速分析推进到疫苗设计、生产、临床试验测试及使用授权,还凸显了纳米技术在助力疫苗研发方面的快速进展。这些进展使我们能够将核酸疫苗和构象稳定的亚单位疫苗递送至区域淋巴结,从而激发有效的体液免疫和细胞免疫,预防病毒感染或控制疾病严重程度。除了简要描述用于实现刺突蛋白递送并由相关免疫系统呈递的独特阳离子脂质和病毒模拟纳米颗粒的设计特点外,我们还讨论了佐剂的重要性以及促进淋巴结生发中心B细胞和T细胞协同相互作用的设计特点,包括基于表位的疫苗的使用。尽管目前的疫苗接种工作已证明了短期疗效和疫苗安全性,但当前的关键问题是疫苗的持久性以及对病毒变异株的适应性。我们提出了一个前瞻性观点,即如何调整疫苗设计以提高免疫反应的持久性,并使疫苗能够适应以克服病毒变异株导致的免疫逃逸。最后,我们考虑了纳米技术在新冠疫苗研发中的作用,以改进针对其他传染病病原体(包括可能引发未来大流行的病原体)的疫苗设计。