Liu Ting, Tian Yang, Zheng Aiping, Cui Chunying
Department of Pharmaceutics, School of Pharmaceutical Sciences, Capital Medical University, Beijing 100069, China.
State Key Laboratory of Toxicology and Medical Countermeasures, Institute of Pharmacology and Toxicology, Beijing 100850, China.
Polymers (Basel). 2022 Oct 6;14(19):4195. doi: 10.3390/polym14194195.
Messenger RNA (mRNA) vaccines have shown great preventive potential in response to the novel coronavirus (COVID-19) pandemic. The lipid nanoparticle (LNP), as a non-viral vector with good safety and potency factors, is applied to mRNA delivery in the clinic. Among the recently FDA-approved SARS-CoV-2 mRNA vaccines, lipid-based nanoparticles have been shown to be well-suited to antigen presentation and enhanced immune stimulation to elicit potent humoral and cellular immune responses. However, a design strategy for optimal mRNA-LNP vaccines has not been fully elaborated. In this review, we comprehensively and systematically discuss the research strategies for mRNA-LNP vaccines against COVID-19, including antigen and lipid carrier selection, vaccine preparation, quality control, and stability. Meanwhile, we also discuss the potential development directions for mRNA-LNP vaccines in the future. We also conduct an in-depth review of those technologies and scientific insights in regard to the mRNA-LNP field.
信使核糖核酸(mRNA)疫苗在应对新型冠状病毒(COVID-19)大流行方面已显示出巨大的预防潜力。脂质纳米颗粒(LNP)作为一种具有良好安全性和效力因素的非病毒载体,已应用于临床中的mRNA递送。在最近获得美国食品药品监督管理局(FDA)批准的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)mRNA疫苗中,基于脂质的纳米颗粒已被证明非常适合抗原呈递和增强免疫刺激,以引发有效的体液免疫和细胞免疫反应。然而,最佳mRNA-LNP疫苗的设计策略尚未得到充分阐述。在本综述中,我们全面且系统地讨论了针对COVID-19的mRNA-LNP疫苗的研究策略,包括抗原和脂质载体的选择、疫苗制备、质量控制和稳定性。同时,我们还讨论了mRNA-LNP疫苗未来的潜在发展方向。我们还对mRNA-LNP领域的那些技术和科学见解进行了深入综述。