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灭活重组流感疫苗:下一代流感疫苗的有前途方向。

Inactivated recombinant influenza vaccine: the promising direction for the next generation of influenza vaccine.

机构信息

Center for Vaccines and Immunology, University of Georgia, Athens, GA, USA.

Department of Infectious Diseases, University of Georgia, Athens, GA, USA.

出版信息

Expert Rev Vaccines. 2024 Jan-Dec;23(1):409-418. doi: 10.1080/14760584.2024.2333338. Epub 2024 Mar 25.


DOI:10.1080/14760584.2024.2333338
PMID:38509022
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11056089/
Abstract

INTRODUCTION: Vaccination is the most effective method to control the prevalence of seasonal influenza and the most widely used influenza vaccine is the inactivated influenza vaccine (IIV). Each season, the influenza vaccine must be updated to be most effective against current circulating variants. Therefore, developing a universal influenza vaccine (UIV) that can elicit both broad and durable protection is of the utmost importance. AREA COVERED: This review summarizes and compares the available influenza vaccines in the market and inactivation methods used for manufacturing IIVs. Then, we discuss the latest progress of the UIV development in the IIV format and the challenges to address for moving these vaccine candidates to clinical trials and commercialization. The literature search was based on the Centers for Disease Control and Prevention (CDC) and the PubMed databases. EXPERT OPINION: The unmet need for UIV is the primary aim of developing the next generation of influenza vaccines. The IIV has high antigenicity and a refined manufacturing process compared to most other formats. Developing the UIV in IIV format is a promising direction with advanced biomolecular technologies and next-generation adjuvant. It also inspires the development of universal vaccines for other infectious diseases.

摘要

简介:接种疫苗是控制季节性流感流行的最有效方法,而应用最广泛的流感疫苗为灭活流感疫苗(IIV)。为了使疫苗对当前流行的变异株最有效,每年都需要更新流感疫苗。因此,开发一种能引发广泛而持久保护的通用流感疫苗(UIV)至关重要。

涵盖领域:本综述总结并比较了目前市场上可获得的流感疫苗和用于制造 IIV 的灭活方法。然后,我们讨论了以 IIV 为形式的 UIV 开发的最新进展,以及为将这些疫苗候选物推向临床试验和商业化需要解决的挑战。文献检索基于疾病控制与预防中心(CDC)和 PubMed 数据库。

专家意见:开发下一代流感疫苗的主要目标是满足对 UIV 的未满足需求。与大多数其他形式相比,IIV 具有较高的抗原性和经过改良的制造工艺。利用先进的生物分子技术和新一代佐剂在 IIV 形式中开发 UIV 是一个很有前途的方向。它也为其他传染病的通用疫苗的开发提供了灵感。

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引用本文的文献

[1]
Insect-specific virus platforms for arbovirus vaccine development.

Front Immunol. 2025-3-14

[2]
Dissecting immunological mechanisms underlying influenza viral nucleoprotein-induced mucosal immunity against diverse viral strains.

Emerg Microbes Infect. 2024-12

本文引用的文献

[1]
A recombinant chimeric influenza virus vaccine expressing the consensus H3 hemagglutinin elicits broad hemagglutination inhibition antibodies against divergent swine H3N2 influenza viruses.

Vaccine. 2023-10-6

[2]
A mosaic influenza virus-like particles vaccine provides broad humoral and cellular immune responses against influenza A viruses.

NPJ Vaccines. 2023-9-7

[3]
Recombinant Protein Vaccines Formulated with Enantio-Specific Cationic Lipid R-DOTAP Induce Protective Cellular and Antibody-Mediated Immune Responses in Mice.

Viruses. 2023-2-4

[4]
Homologous peptides derived from influenza A, B and C viruses induce variable CD8 T cell responses with cross-reactive potential.

Clin Transl Immunology. 2022-10-19

[5]
An inactivated multivalent influenza A virus vaccine is broadly protective in mice and ferrets.

Sci Transl Med. 2022-7-13

[6]
Adenoviral-Vectored Centralized Consensus Hemagglutinin Vaccine Provides Broad Protection against H2 Influenza a Virus.

Vaccines (Basel). 2022-6-10

[7]
Safety and immunogenicity of a quadrivalent, inactivated, split-virion influenza vaccine (IIV4-W) in healthy people aged 3-60 years: a phase III randomized clinical noninferiority trial.

Hum Vaccin Immunother. 2022-11-30

[8]
Antigenic and virological properties of an H3N2 variant that continues to dominate the 2021-22 Northern Hemisphere influenza season.

Cell Rep. 2022-5-31

[9]
Inactivated Whole Virus Particle Influenza Vaccine Induces Anti-Neuraminidase Antibodies That May Contribute to Cross-Protection against Heterologous Virus Infection.

Vaccines (Basel). 2022-5-19

[10]
Methods of Inactivation of Highly Pathogenic Viruses for Molecular, Serology or Vaccine Development Purposes.

Pathogens. 2022-2-19

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