Downstream processing for influenza vaccines and candidates: An update

• Published in: Biotechnology and bioengineering Vol. 118; no. 8; pp. 2845 - 2869
• Main Authors: B. Carvalho, Sofia, Peixoto, Cristina, T. Carrondo, Manuel J., S. Silva, Ricardo J.
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01-08-2021
• Subjects: Antigen processing; Antigens; Clinical trials; downstream processing; Humans; Influenza; Influenza Vaccines - chemistry; Influenza Vaccines - therapeutic use; Influenza, Human - epidemiology; Influenza, Human - prevention & control; manufacturing; Pandemics; purification; Three dimensional printing; Vaccination; vaccine; Vaccines; Viruses; influenza; manufacturing; vaccine; downstream processing; purification
• ISSN: 0006-3592; 1097-0290
• DOI: 10.1002/bit.27803

Seasonal and pandemic influenza outbreaks present severe health and economic burdens. To overcome limitations on influenza vaccines' availability and effectiveness, researchers chase universal vaccines providing broad, long‐lasting protection against multiple influenza subtypes, and including pandemic ones.
Novel influenza vaccine designs are under development, in clinical trials, or reaching the market, namely inactivated, or live‐attenuated virus, virus‐like particles, or recombinant antigens, searching for improved effectiveness; all these bring downstream processing (DSP) new challenges. Having to deal with new influenza strains, including pandemics, requires shorter development time, driving the development of faster bioprocesses. To cope with better upstream processes, new regulatory demands for quality and safety, and cost reduction requirements, new unit operations and integrated processes are increasing DSP efficiency for novel vaccine formats.
This review covers recent advances in DSP strategies of different influenza vaccine formats. Focus is given to the improvements on relevant state‐of‐the‐art unit operations, from harvest and clarification to purification steps, ending with sterile filtration and formulation. The development of more efficient unit operations to cope with biophysical properties of the new candidates is discussed: emphasis is given to the design of new stationary phases, 3D printing approaches, and continuous processing tools, such as continuous chromatography. The impact of the production platforms and vaccine designs on the downstream operations for the different influenza vaccine formats approved for this season are highlighted.
Influenza vaccines either in commercialization or still under development are reviewed. Here Carvalho and co‐workers discuss how different vaccine formats, presenting distinct biophysical properties, are purified. Focus is given to the improvements on relevant state‐of‐the‐art unit operations, from harvest and clarification to purification steps, ending with sterile filtration and formulation.