Platforms for Production of Protein-Based Vaccines: From Classical to Next-Generation Strategies

被引:98
作者
Cid, Raquel [1 ]
Bolivar, Jorge [2 ]
机构
[1] ADL Bionatur Solut SA, Av Desarrollo Tecnol 11, Jerez de la Frontera 11591, Spain
[2] Univ Cadiz, Dept Biomed Biotechnol & Publ Hlth Biochem & Mol, Campus Univ Puerto Real, Puerto Real 11510, Spain
关键词
vaccine; protein expression system; alternative platform; subunit; recombinant antigen; VIRUS-LIKE PARTICLES; HEPATITIS-B SURFACE; RECOMBINANT SUBUNIT VACCINE; EXPRESSION SYSTEMS; INFLUENZA VACCINE; MESSENGER-RNA; DNA VACCINES; CELL-LINES; CIRCUMSPOROZOITE PROTEIN; RATIONAL DESIGN;
D O I
10.3390/biom11081072
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To date, vaccination has become one of the most effective strategies to control and reduce infectious diseases, preventing millions of deaths worldwide. The earliest vaccines were developed as live-attenuated or inactivated pathogens, and, although they still represent the most extended human vaccine types, they also face some issues, such as the potential to revert to a pathogenic form of live-attenuated formulations or the weaker immune response associated with inactivated vaccines. Advances in genetic engineering have enabled improvements in vaccine design and strategies, such as recombinant subunit vaccines, have emerged, expanding the number of diseases that can be prevented. Moreover, antigen display systems such as VLPs or those designed by nanotechnology have improved the efficacy of subunit vaccines. Platforms for the production of recombinant vaccines have also evolved from the first hosts, Escherichia coli and Saccharomyces cerevisiae, to insect or mammalian cells. Traditional bacterial and yeast systems have been improved by engineering and new systems based on plants or insect larvae have emerged as alternative, low-cost platforms. Vaccine development is still time-consuming and costly, and alternative systems that can offer cost-effective and faster processes are demanding to address infectious diseases that still do not have a treatment and to face possible future pandemics.
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页数:33
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共 271 条
[51]   Vaccines against enteric infections for the developing world [J].
Czerkinsky, Cecil ;
Holmgren, Jan .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2015, 370 (1671)
[52]   Anti-Infectious Human Vaccination in Historical Perspective [J].
D'Amelio, Enrico ;
Salemi, Simonetta ;
D'Amelio, Raffaele .
INTERNATIONAL REVIEWS OF IMMUNOLOGY, 2016, 35 (03) :260-290
[53]   IMMUNOGENICITY OF YEAST-DERIVED HEPATITIS-B VACCINE FROM 2 DIFFERENT PRODUCERS [J].
DAHLHANSEN, E ;
SIEBKE, JC ;
FROLAND, SS ;
DEGRE, M .
EPIDEMIOLOGY AND INFECTION, 1990, 104 (01) :143-149
[54]  
Datla M., 2012, P GAV ALL PARTN FOR
[55]   From empiricism to rational design: a personal perspective of the evolution of vaccine development [J].
De Gregorio, Ennio ;
Rappuoli, Rino .
NATURE REVIEWS IMMUNOLOGY, 2014, 14 (07) :505-514
[56]   A Novel Chimpanzee Adenovirus Vector with Low Human Seroprevalence: Improved Systems for Vector Derivation and Comparative Immunogenicity [J].
Dicks, Matthew D. J. ;
Spencer, Alexandra J. ;
Edwards, Nick J. ;
Wadell, Goran ;
Bojang, Kalifa ;
Gilbert, Sarah C. ;
Hill, Adrian V. S. ;
Cottingham, Matthew G. .
PLOS ONE, 2012, 7 (07)
[57]   Marker vaccine strategies and candidate CSFV marker vaccines [J].
Dong, Xiao-Nan ;
Chen, Ying-Hua .
VACCINE, 2007, 25 (02) :205-230
[58]   Early prediction of instability of chinese hamster ovary cell lines expressing recombinant antibodies and antibody-fusion proteins [J].
Dorai, Haimanti ;
Corisdeo, Susanne ;
Ellis, Dawn ;
Kinney, Cherylann ;
Chomo, Matt ;
Hawley-Nelson, Pam ;
Moore, Gordon ;
Betenbaugh, Michael J. ;
Ganguly, Subinay .
BIOTECHNOLOGY AND BIOENGINEERING, 2012, 109 (04) :1016-1030
[59]   Characterization of the Proteases Involved in the N-Terminal Clipping of Glucagon-Like-Peptide-1-Antibody Fusion Proteins [J].
Dorai, Haimanti ;
Santiago, Aleixo ;
Campbell, Marguerite ;
Tang, Q. Mike ;
Lewis, Michael J. ;
Wang, Yonghui ;
Lu, Qiao-Zhen ;
Wu, Shiaw-Lin ;
Hancock, William .
BIOTECHNOLOGY PROGRESS, 2011, 27 (01) :220-231
[60]   Heat-stable oral alga-based vaccine protects mice from Staphylococcus aureus infection [J].
Dreesen, Imke A. J. ;
Charpin-El Hamri, Ghislaine ;
Fussenegger, Martin .
JOURNAL OF BIOTECHNOLOGY, 2010, 145 (03) :273-280