Nguyen Brian, Tolia Niraj H
Laboratory of Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institute of Health, Bethesda, MD, USA.
NPJ Vaccines. 2021 May 13;6(1):70. doi: 10.1038/s41541-021-00330-7.
Modern vaccine design has sought a minimalization approach, moving to the isolation of antigens from pathogens that invoke a strong neutralizing immune response. This approach has created safer vaccines but may limit vaccine efficacy due to poor immunogenicity. To combat global diseases such as COVID-19, malaria, and AIDS there is a clear urgency for more effective next-generation vaccines. One approach to improve the immunogenicity of vaccines is the use of nanoparticle platforms that present a repetitive array of antigen on its surface. This technology has been shown to improve antigen presenting cell uptake, lymph node trafficking, and B-cell activation through increased avidity and particle size. With a focus on design, we summarize natural platforms, methods of antigen attachment, and advancements in generating self-assembly that have led to new engineered platforms. We further examine critical parameters that will direct the usage and development of more effective platforms.
现代疫苗设计采用了一种最小化方法,转向从能引发强烈中和免疫反应的病原体中分离抗原。这种方法制造出了更安全的疫苗,但由于免疫原性较差,可能会限制疫苗效力。为应对新冠病毒、疟疾和艾滋病等全球性疾病,下一代更有效的疫苗显然刻不容缓。提高疫苗免疫原性的一种方法是使用纳米颗粒平台,该平台在其表面呈现重复排列的抗原。这项技术已被证明可通过提高亲和力和颗粒大小来改善抗原呈递细胞摄取、淋巴结运输和B细胞激活。我们重点关注设计,总结了天然平台、抗原附着方法以及产生自组装的进展,这些进展已带来了新的工程平台。我们还进一步研究了将指导更有效平台的使用和开发的关键参数。