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

被引:4
作者
Shi, Hua [1 ]
Ross, Ted M. [1 ,2 ,3 ,4 ]
机构
[1] Univ Georgia, Ctr Vaccines & Immunol, Athens, GA USA
[2] Univ Georgia, Dept Infect Dis, Athens, GA USA
[3] Cleveland Clin, Florida Res & Innovat Ctr, 9801 SW Discovery Way, Port St Lucie, FL 34987 USA
[4] Cleveland Clin, Lehner Res Inst, Dept Infect Biol, Cleveland, OH USA
关键词
Beta-propiolactone; formaldehyde; inactivated influenza vaccine; hemagglutinin; universal influenza vaccine; reverse transgenic rescued influenza virus; adjuvant; PANDEMIC INFLUENZA; BETA-PROPIOLACTONE; VIRUS-VACCINES; DNA; ANTIBODIES; PARTICLE; HISTORY; STEM;
D O I
10.1080/14760584.2024.2333338
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IntroductionVaccination 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 coveredThis 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 opinionThe 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.
引用
收藏
页码:409 / 418
页数:10
相关论文
共 91 条
[1]   Split inactivated COBRA vaccine elicits protective antibodies against H1N1 and H3N2 influenza viruses [J].
Allen, James D. ;
Ray, Satyajit ;
Ross, Ted M. .
PLOS ONE, 2018, 13 (09)
[2]  
Allen JD, 2021, Design and characterization of computationally optimized broadly reactive antigen (cobra) vaccines against human seasonal influenza A (H3N2) viruses
[3]   Immune history profoundly affects broadly protective B cell responses to influenza [J].
Andrews, Sarah F. ;
Huang, Yunping ;
Kaur, Kaval ;
Popova, Lyubov I. ;
Ho, Irvin Y. ;
Pauli, Noel T. ;
Dunand, Carole J. Henry ;
Taylor, William M. ;
Lim, Samuel ;
Huang, Min ;
Qu, Xinyan ;
Lee, Jane-Hwei ;
Salgado-Ferrer, Marlene ;
Krammer, Florian ;
Palese, Peter ;
Wrammert, Jens ;
Ahmed, Rafi ;
Wilson, Patrick C. .
SCIENCE TRANSLATIONAL MEDICINE, 2015, 7 (316)
[4]  
[Anonymous], 2024, Information for the 2023-2024 flu season 2024
[5]   Comparison of serology and reactogenicity between influenza subunit vaccines and whole virus or split vaccines - A review and meta-analysis of the literature [J].
Beyer, WEP ;
Palache, AM ;
Osterhaus, ADME .
CLINICAL DRUG INVESTIGATION, 1998, 15 (01) :1-12
[6]  
Bolton MJ., 2021, medRxiv
[7]   Induction of Heterosubtypic Cross-Protection against Influenza by a Whole Inactivated Virus Vaccine: The Role of Viral Membrane Fusion Activity [J].
Budimir, Natalija ;
Huckriede, Anke ;
Meijerhof, Tjarko ;
Boon, Louis ;
Gostick, Emma ;
Price, David A. ;
Wilschut, Jan ;
de Haan, Aalzen .
PLOS ONE, 2012, 7 (01)
[8]   PRINCIPLES OF SELECTIVE INACTIVATION OF VIRAL GENOME .6. INACTIVATION OF THE INFECTIVITY OF THE INFLUENZA-VIRUS BY THE ACTION OF BETA-PROPIOLACTONE [J].
BUDOWSKY, EI ;
FRIEDMAN, EA ;
ZHELEZNOVA, NV ;
NOSKOV, FS .
VACCINE, 1991, 9 (06) :398-402
[9]  
BURNET F. M., 1941, AUSTRALIAN JOUR EXP BIOL AND MED SCI, V19, P291, DOI 10.1038/icb.1941.44
[10]   Better influenza vaccines: an industry perspective [J].
Chen, Juine-Ruey ;
Liu, Yo-Min ;
Tseng, Yung-Chieh ;
Ma, Che .
JOURNAL OF BIOMEDICAL SCIENCE, 2020, 27 (01)