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针对新发传染病的有前景的疫苗制剂。

Promising Vaccine Formulations for Emerging Infectious Diseases.

作者信息

Park Pil-Gu, Lee Seok-Yong, Youn Hyewon, Hong Kee-Jong

机构信息

Department of Life Science, Gachon University, Seongnam 13120, Republic of Korea.

Department of Nuclear Medicine, Cancer Imaging Center, Seoul National University Hospital, Seoul 03080, Republic of Korea.

出版信息

Int J Mol Sci. 2025 May 20;26(10):4893. doi: 10.3390/ijms26104893.


DOI:10.3390/ijms26104893
PMID:40430032
Abstract

Emerging infectious diseases (EIDs) are one of the greatest threats to human health today, thus requiring an urgent response. Vaccines are one of the most effective means of preventing the spread of infectious diseases, and their usefulness in responding to EIDs has been clearly proven through the process of overcoming the global COVID-19 pandemic. As the characteristics of various vaccine formulations differ, it is necessary to apply the most appropriate one according to the EID response strategy. In this review, we first consider which vaccine formulation is the most suitable for EID vaccines by comparing the pros and cons of different vaccine formulations, and then we discuss the utility of mRNA vaccine formulations, which are considered the most promising for EID vaccines.

摘要

新发传染病(EIDs)是当今人类健康面临的最大威胁之一,因此需要紧急应对。疫苗是预防传染病传播的最有效手段之一,通过战胜全球新冠疫情的过程,疫苗在应对新发传染病方面的效用已得到明确证明。由于各种疫苗制剂的特性不同,有必要根据新发传染病应对策略应用最合适的疫苗制剂。在本综述中,我们首先通过比较不同疫苗制剂的优缺点,考量哪种疫苗制剂最适合用于新发传染病疫苗,然后讨论被认为在新发传染病疫苗方面最具潜力的mRNA疫苗制剂的效用。

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Promising Vaccine Formulations for Emerging Infectious Diseases.

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[10]
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本文引用的文献

[1]
Revolutionizing mRNA Vaccines Through Innovative Formulation and Delivery Strategies.

Biomolecules. 2025-3-1

[2]
Clinical advancements in mRNA vaccines against viral infections.

Clin Immunol. 2025-2

[3]
Phase 1 clinical trial of Hantaan and Puumala virus DNA vaccines delivered by needle-free injection.

NPJ Vaccines. 2024-11-17

[4]
Development of Thermally Stable mRNA-LNP Delivery Systems: Current Progress and Future Prospects.

Mol Pharm. 2024-12-2

[5]
Recent Advances in Lipid Nanoparticles and Their Safety Concerns for mRNA Delivery.

Vaccines (Basel). 2024-10-8

[6]
Equivalence of freeze-dried and liquid-frozen formulations of MVA-BN as smallpox and mpox vaccine.

Hum Vaccin Immunother. 2024-12-31

[7]
Safety and Immunogenicity of a DNA Vaccine With Subtype C gp120 Protein Adjuvanted With MF59 or AS01B: A Phase 1/2a HIV-1 Vaccine Trial.

J Acquir Immune Defic Syndr. 2024-8-1

[8]
The next-generation DNA vaccine platforms and delivery systems: advances, challenges and prospects.

Front Immunol. 2024

[9]
DNA Vaccines: History, Molecular Mechanisms and Future Perspectives.

J Mol Biol. 2023-12-1

[10]
Safety and Immunogenicity of Inactivated Whole Virion COVID-19 Vaccine CoviVac in Clinical Trials in 18-60 and 60+ Age Cohorts.

Viruses. 2023-8-29

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