Tapia Daniel, Reyes-Sandoval Arturo, Sanchez-Villamil Javier I
The Ragon Institute of Massachusetts General Hospital, The Massachusetts Institute of Technology and Harvard University, Cambridge, MA, USA.
Instituto Politécnico Nacional, Escuela Nacional de Ciencias Biológicas, Laboratorio Nacional de Vacunología y Virus Tropicales, Ciudad de México, México.
Arch Med Res. 2023 Apr;54(3):168-175. doi: 10.1016/j.arcmed.2023.02.003. Epub 2023 Mar 7.
The field of vaccine development has seen an increase in the number of rationally designed technologies that increase effectiveness against vaccine-resistant pathogens, while not compromising safety. Yet, there is still an urgent need to expand and further understand these platforms against complex pathogens that often evade protective responses. Nanoscale platforms have been at the center of new studies, especially in the wake of the coronavirus disease 2019 (COVID-19), with the aim of deploying safe and effective vaccines in a short time period. The intrinsic properties of protein-based nanoparticles, such as biocompatibility, flexible physicochemical characteristics, and variety have made them an attractive platform against different infectious disease agents. In the past decade, several studies have tested both lumazine synthase-, ferritin-, and albumin-based nanoplatforms against a wide range of complex pathogens in pre-clinical studies. Owed to their success in pre-clinical studies, several studies are undergoing human clinical trials or are near an initial phase. In this review we highlight the different protein-based platforms, mechanisms of synthesis, and effectiveness of these over the past decade. In addition, some challenges, and future directions to increase their effectiveness are also highlighted. Taken together, protein-based nanoscaffolds have proven to be an effective means to design rationally designed vaccines, especially against complex pathogens and emerging infectious diseases.
疫苗研发领域出现了越来越多经过合理设计的技术,这些技术提高了针对疫苗抗性病原体的有效性,同时又不影响安全性。然而,对于那些常常逃避保护性免疫反应的复杂病原体,仍然迫切需要扩展并进一步了解这些平台。纳米级平台一直是新研究的核心,尤其是在2019年冠状病毒病(COVID-19)之后,其目标是在短时间内部署安全有效的疫苗。基于蛋白质的纳米颗粒的固有特性,如生物相容性、灵活的物理化学特性和多样性,使其成为对抗不同传染病原体的有吸引力的平台。在过去十年中,多项研究在临床前研究中测试了基于核黄素合酶、铁蛋白和白蛋白的纳米平台对多种复杂病原体的效果。由于它们在临床前研究中的成功,多项研究正在进行人体临床试验或已接近初始阶段。在本综述中,我们重点介绍了过去十年中不同的基于蛋白质的平台、合成机制及其有效性。此外,还强调了一些挑战以及提高其有效性的未来方向。综上所述,基于蛋白质的纳米支架已被证明是合理设计疫苗的有效手段,尤其是针对复杂病原体和新发传染病。